ketcher-macromolecules 2.19.0-rc.3 → 2.19.0
This diff represents the content of publicly available package versions that have been released to one of the supported registries. The information contained in this diff is provided for informational purposes only and reflects changes between package versions as they appear in their respective public registries.
- package/dist/index.js +1 -1
- package/dist/index.modern.js +1 -1
- package/package.json +1 -1
package/dist/index.js
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@@ -44,7 +44,7 @@ var _asyncToGenerator__default = /*#__PURE__*/_interopDefaultLegacy(_asyncToGene
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var _objectWithoutProperties__default = /*#__PURE__*/_interopDefaultLegacy(_objectWithoutProperties);
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var MuiButton__default = /*#__PURE__*/_interopDefaultLegacy(MuiButton);
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var monomersData = "1',2'-Di-Deoxy-Ribose\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n -0.8526 1.5410 0.0000 O 0 0\n -0.3405 0.1310 0.0000 C 0 0 1 0 0 0\n 0.3301 2.4636 0.0000 C 0 0\n 1.1586 0.1823 0.0000 C 0 0 2 0 0 0\n 1.5731 1.6239 0.0000 C 0 0\n 2.0777 -1.0008 0.0000 O 0 0\n -1.1818 -1.1087 0.0000 C 0 0\n -2.6787 -1.0008 0.0000 O 0 0\n -3.3525 -1.9937 0.0000 R# 0 0\n 3.2666 -0.8378 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 1\n 3 5 1 0\n 4 5 1 0\n 4 6 1 6\n 6 10 1 0\n 7 8 1 0\n 8 9 1 0\nM RGP 2 9 1 10 2\nM END\n> <Name>\n1',2'-Di-Deoxy-Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n12ddR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n2,5-Ribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.6295 -1.1398 0.0000 O 0 0\n -0.8657 0.3416 0.0000 C 0 0 1 0 0 0\n 0.8523 -1.3729 0.0000 C 0 0 2 0 0 0\n 0.4701 1.0240 0.0000 C 0 0 2 0 0 0\n 1.5319 -0.0356 0.0000 C 0 0 1 0 0 0\n 0.6566 2.2094 0.0000 O 0 0\n 3.0119 0.1971 0.0000 O 0 0\n -2.2027 1.0176 0.0000 C 0 0\n 1.3982 -2.4414 0.0000 R# 0 0\n -3.4595 0.1971 0.0000 O 0 0\n -4.5303 0.7385 0.0000 R# 0 0\n 3.7667 -0.7357 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 8 10 1 0\n 10 11 1 0\n 7 12 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\n2,5-Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n25R\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n6-amino-hexanol (3' end)\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n -3.6321 -0.5320 0.0000 C 0 0\n -2.3982 0.3223 0.0000 C 0 0\n -1.0410 -0.3184 0.0000 C 0 0\n 0.1930 0.5359 0.0000 C 0 0\n 1.5502 -0.1048 0.0000 C 0 0\n 2.7842 0.7494 0.0000 C 0 0\n 4.1414 0.1087 0.0000 N 0 0\n 5.1280 0.7918 0.0000 R# 0 0\n -4.9894 0.1087 0.0000 O 0 0\n -5.9760 -0.5743 0.0000 R# 0 0\n 4.2400 -1.0872 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 1 9 1 0\n 9 10 1 0\n 7 11 1 0\nM RGP 3 8 2 10 1 11 3\nM END\n> <Name>\n6-amino-hexanol (3' end)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n3A6\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]H\n\n$$$$\n3-FAM\n SciTegic07272112182D\n\n 38 42 0 0 1 0 999 V2000\n -11.6944 -6.1247 0.0000 R# 0 0\n -10.4944 -6.1250 0.0000 O 0 0\n -9.7428 -4.8259 0.0000 C 0 0\n -8.2420 -4.8264 0.0000 C 0 0\n -7.4897 -6.1250 0.0000 O 0 0\n -7.4904 -3.5273 0.0000 C 0 0\n -6.2897 -6.1240 0.0000 R# 0 0\n -5.9896 -3.5276 0.0000 C 0 0\n -5.2380 -2.2286 0.0000 C 0 0\n -3.7372 -2.2289 0.0000 C 0 0\n -2.9856 -0.9298 0.0000 N 0 0\n -1.4848 -0.9303 0.0000 C 0 0\n -0.7333 0.3689 0.0000 C 0 0\n -0.8854 -1.9698 0.0000 O 0 0\n 1.5152 1.6705 0.0000 C 0 0\n 0.7667 0.3706 0.0000 C 0 0\n -1.4848 1.6670 0.0000 C 0 0\n -0.7363 2.9669 0.0000 C 0 0\n 0.7637 2.9686 0.0000 C 0 0\n 3.1364 3.4756 0.0000 O 0 0\n 2.9814 1.9837 0.0000 C 0 0\n 1.7654 4.0841 0.0000 C 0 0\n 1.5144 5.2576 0.0000 O 0 0\n 6.0184 1.4243 0.0000 O 0 0\n 5.0455 0.2826 0.0000 C 0 0\n 3.5703 0.5543 0.0000 C 0 0\n 4.0410 3.1094 0.0000 C 0 0\n 5.5162 2.8377 0.0000 C 0 0\n 6.4886 3.9794 0.0000 C 0 0\n 3.5383 4.5229 0.0000 C 0 0\n 4.5112 5.6646 0.0000 C 0 0\n 5.9864 5.3928 0.0000 C 0 0\n 5.5474 -1.1307 0.0000 C 0 0\n 4.5745 -2.2724 0.0000 C 0 0\n 3.0993 -2.0007 0.0000 C 0 0\n 2.5971 -0.5873 0.0000 C 0 0\n 6.7647 6.3061 0.0000 O 0 0\n 4.9763 -3.4032 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 4 6 1 0\n 5 7 1 0\n 6 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 12 14 2 0\n 16 13 2 0\n 13 17 1 0\n 15 16 1 0\n 17 18 2 0\n 18 19 1 0\n 19 22 1 0\n 15 19 2 0\n 21 15 1 0\n 20 21 1 0\n 20 22 1 0\n 22 23 2 0\n 26 21 1 0\n 21 27 1 0\n 24 25 1 0\n 24 28 1 0\n 27 30 2 0\n 28 27 1 0\n 29 28 2 0\n 30 31 1 0\n 31 32 2 0\n 29 32 1 0\n 33 25 2 0\n 26 25 1 0\n 36 26 2 0\n 33 34 1 0\n 34 35 2 0\n 35 36 1 0\n 32 37 1 0\n 34 38 1 0\nM RGP 2 1 1 7 2\nM END\n> <Name>\n3-FAM\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n3FAM\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n3'-Thiol-Modifier 6 S-S from Glen Research\n SciTegic07272112182D\n\n 18 17 0 0 1 0 999 V2000\n -8.4293 -0.6995 0.0000 C 0 0\n -7.1591 0.0999 0.0000 C 0 0\n -9.7571 0.0000 0.0000 O 0 0\n -5.8312 -0.5996 0.0000 O 0 0\n -4.5610 0.1999 0.0000 C 0 0\n -3.2332 -0.4996 0.0000 C 0 0\n -1.9630 0.2998 0.0000 C 0 0\n -0.6351 -0.3997 0.0000 S 0 0\n 0.6351 0.3997 0.0000 S 0 0\n 1.9629 -0.2998 0.0000 C 0 0\n 3.2332 0.4996 0.0000 C 0 0\n 4.5610 -0.1999 0.0000 C 0 0\n 5.8312 0.5996 0.0000 O 0 0\n 7.1591 -0.0999 0.0000 C 0 0\n 8.4292 0.6995 0.0000 C 0 0\n 9.7571 0.0000 0.0000 O 0 0\n -10.7727 -0.6392 0.0000 R# 0 0\n 10.7728 0.6392 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 3 17 1 0\n 16 18 1 0\nM RGP 2 17 1 18 2\nM END\n> <Name>\n3'-Thiol-Modifier 6 S-S from Glen Research\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n3SS6\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n4-Thio-Ribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.1017 -1.0663 0.0000 S 0 0\n -0.5897 0.3436 0.0000 C 0 0 1 0 0 0\n 0.0809 -1.9889 0.0000 C 0 0 2 0 0 0\n 0.9095 0.2924 0.0000 C 0 0 2 0 0 0\n 1.3239 -1.1493 0.0000 C 0 0 1 0 0 0\n 1.8285 1.4755 0.0000 O 0 0\n 2.4518 -1.5589 0.0000 O 0 0\n -1.4310 1.5834 0.0000 C 0 0\n 0.0399 -3.1881 0.0000 R# 0 0\n -2.9279 1.4755 0.0000 O 0 0\n -3.6017 2.4684 0.0000 R# 0 0\n 3.0174 1.3125 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 12 1 0\n 8 10 1 0\n 10 11 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\n4-Thio-Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n4sR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n6-amino-hexanol (5' end)\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 3.6322 -0.5320 0.0000 C 0 0\n 2.3981 0.3223 0.0000 C 0 0\n 1.0410 -0.3184 0.0000 C 0 0\n -0.1930 0.5358 0.0000 C 0 0\n -1.5502 -0.1048 0.0000 C 0 0\n -2.7842 0.7494 0.0000 C 0 0\n -4.1414 0.1087 0.0000 N 0 0\n -5.1280 0.7918 0.0000 R# 0 0\n 4.9894 0.1087 0.0000 O 0 0\n 5.9760 -0.5743 0.0000 R# 0 0\n -4.2400 -1.0872 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 1 9 1 0\n 9 10 1 0\n 7 11 1 0\nM RGP 3 8 1 10 2 11 3\nM END\n> <Name>\n6-amino-hexanol (5' end)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5A6\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]H\n\n$$$$\n5'-6FAM (6-carboxyfluorescein)\n SciTegic07272112182D\n\n 36 39 0 0 1 0 999 V2000\n -23.5563 -25.6056 0.0000 C 0 0\n -24.3065 -26.9045 0.0000 C 0 0\n -23.5568 -28.2037 0.0000 C 0 0\n -22.0569 -28.2039 0.0000 C 0 0\n -21.3066 -26.9050 0.0000 C 0 0\n -22.0563 -25.6059 0.0000 C 0 0\n -21.3061 -24.3070 0.0000 C 0 0\n -22.0558 -23.0078 0.0000 C 0 0\n -23.5558 -23.0075 0.0000 C 0 0\n -24.3061 -24.3064 0.0000 O 0 0\n -21.3056 -21.7089 0.0000 C 0 0\n -22.0553 -20.4097 0.0000 C 0 0\n -23.5553 -20.4094 0.0000 C 0 0\n -24.3055 -21.7083 0.0000 C 0 0\n -24.1570 -29.2428 0.0000 O 0 0\n -24.1551 -19.3701 0.0000 O 0 0\n -19.8053 -24.3073 0.0000 C 0 0\n -19.0570 -23.0072 0.0000 C 0 0\n -17.5570 -23.0051 0.0000 C 0 0\n -16.8052 -24.3031 0.0000 C 0 0\n -17.5533 -25.6032 0.0000 C 0 0\n -19.0534 -25.6053 0.0000 C 0 0\n -16.8057 -21.7059 0.0000 C 0 0\n -15.3049 -21.7059 0.0000 N 0 0\n -17.4054 -20.6664 0.0000 O 0 0\n -14.5536 -20.4067 0.0000 C 0 0\n -13.0528 -20.4067 0.0000 C 0 0\n -12.3015 -19.1075 0.0000 C 0 0\n -10.8006 -19.1075 0.0000 C 0 0\n -10.0494 -17.8083 0.0000 C 0 0\n -8.5486 -17.8083 0.0000 C 0 0\n -7.7973 -16.5091 0.0000 O 0 0\n -6.5973 -16.5091 0.0000 R# 0 0\n -19.7993 -26.9076 0.0000 C 0 0\n -20.7993 -26.9108 0.0000 O 0 0\n -19.1963 -27.9451 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 2 0\n 9 10 1 0\n 1 6 2 0\n 1 10 1 0\n 6 7 1 0\n 8 11 1 0\n 8 9 1 0\n 9 14 2 0\n 11 12 2 0\n 12 13 1 0\n 13 14 1 0\n 3 15 1 0\n 13 16 2 0\n 7 17 1 0\n 17 18 2 0\n 17 22 1 0\n 18 19 1 0\n 19 20 2 0\n 20 21 1 0\n 21 22 2 0\n 19 23 1 0\n 23 24 1 0\n 23 25 2 0\n 24 26 1 0\n 26 27 1 0\n 27 28 1 0\n 28 29 1 0\n 29 30 1 0\n 30 31 1 0\n 31 32 1 0\n 32 33 1 0\n 22 34 1 0\n 34 35 1 0\n 34 36 2 0\nM RGP 1 33 2\nM END\n> <Name>\n5'-6FAM (6-carboxyfluorescein)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5FAM\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]H\n\n$$$$\n4-Formylbenzamidehexanol (5' end)\n SciTegic07272112182D\n\n 20 20 0 0 1 0 999 V2000\n -26.0016 11.8824 0.0000 H 0 0\n -25.0016 11.8792 0.0000 C 0 0\n -24.2557 10.5767 0.0000 C 0 0\n -25.0076 9.2788 0.0000 C 0 0\n -24.2595 7.9786 0.0000 C 0 0\n -22.7596 7.9765 0.0000 C 0 0\n -22.0084 6.6772 0.0000 C 0 0\n -20.5076 6.6770 0.0000 N 0 0\n -19.7564 5.3778 0.0000 C 0 0\n -18.2555 5.3777 0.0000 C 0 0\n -17.5044 4.0783 0.0000 C 0 0\n -16.0035 4.0783 0.0000 C 0 0\n -15.2523 2.7790 0.0000 C 0 0\n -13.7514 2.7790 0.0000 C 0 0\n -13.0003 1.4796 0.0000 O 0 0\n -22.6081 5.6378 0.0000 O 0 0\n -22.0077 9.2744 0.0000 C 0 0\n -22.7557 10.5745 0.0000 C 0 0\n -24.3986 12.9166 0.0000 O 0 0\n -11.8004 1.4796 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 7 16 2 0\n 6 17 1 0\n 17 18 2 0\n 3 18 1 0\n 2 19 2 0\n 15 20 1 0\nM RGP 1 20 2\nM END\n> <Name>\n4-Formylbenzamidehexanol (5' end)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5FBC6\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]H\n\n$$$$\n2-(methylamino)acetamide (GeneTools 5'-cap for PMO)\n SciTegic07272112182D\n\n 7 6 0 0 1 0 999 V2000\n 3.3003 4.3894 0.0000 O 0 0\n 3.9000 3.3500 0.0000 C 0 0\n 3.1500 2.0500 0.0000 C 0 0\n 3.9000 0.7500 0.0000 N 0 0\n 3.3003 -0.2894 0.0000 C 0 0\n 5.1000 3.3500 0.0000 N 0 0\n 5.1000 0.7500 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 2 6 1 0\n 4 7 1 0\nM RGP 1 7 2\nM END\n> <Name>\n2-(methylamino)acetamide (GeneTools 5'-cap for PMO)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5cGT\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]H\n\n$$$$\n5-ethynyl-uracil\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.8621 -1.2489 0.0000 C 0 0\n 2.4620 -2.2881 0.0000 C 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\n 2 10 1 0\n 10 11 3 0\nM RGP 1 9 1\nM END\n> <Name>\n5-ethynyl-uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5eU\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-fluoro-uracil\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.7117 -0.9884 0.0000 F 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\n 2 10 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-fluoro-uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5fU\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-iodo-uracil\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.7117 -0.9884 0.0000 I 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\n 2 10 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-iodo-uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5iU\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-methyl-cytidine\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 2.6489 0.0000 C 0 0\n -0.3882 2.6490 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3883 0.0509 0.0000 C 0 0\n 1.1117 0.0509 0.0000 N 0 0\n 3.0618 1.3499 0.0000 N 0 0\n -0.9884 -0.9883 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.7118 3.6882 0.0000 C 0 0\n 1 2 1 0\n 1 6 2 0\n 1 7 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 6 1 0\n 5 8 2 0\n 2 10 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-methyl-cytidine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5meC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-tris-propynyl-uracil\n SciTegic07272112182D\n\n 19 19 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.8621 -1.2489 0.0000 C 0 0\n 2.6125 -2.5487 0.0000 C 0 0\n 3.3628 -3.8485 0.0000 C 0 0\n 4.8637 -3.8494 0.0000 N 0 0\n 5.6140 -5.1492 0.0000 C 0 0\n 5.6172 -2.5515 0.0000 C 0 0\n 7.1149 -5.1502 0.0000 C 0 0\n 7.1180 -2.5541 0.0000 C 0 0\n 8.3148 -5.1510 0.0000 C 0 0\n 8.3181 -2.5563 0.0000 C 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\n 2 10 1 0\n 10 11 3 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 13 15 1 0\n 14 16 1 0\n 15 17 1 0\n 16 18 3 0\n 17 19 3 0\nM RGP 1 9 1\nM END\n> <Name>\n5-tris-propynyl-uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5tpU\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nAdenine\n SciTegic07272112182D\n\n 11 12 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 C 0 0\n -0.0787 -2.2532 0.0000 N 0 0\n 2.1768 -0.1209 0.0000 N 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n 1 10 1 0\n 1 6 2 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 1 0\n 7 11 1 0\n 8 9 2 0\nM RGP 1 11 1\nM END\n> <Name>\nAdenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nA\n\n> <MonomerCode>\nA\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nCytosine\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 2.6489 0.0000 C 0 0\n -0.3882 2.6490 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3883 0.0509 0.0000 C 0 0\n 1.1117 0.0509 0.0000 N 0 0\n 3.0618 1.3499 0.0000 N 0 0\n -0.9884 -0.9883 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1 2 1 0\n 1 6 2 0\n 1 7 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 6 1 0\n 5 8 2 0\nM RGP 1 9 1\nM END\n> <Name>\nCytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nC\n\n> <MonomerCode>\nC\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2'-O-Tris-trifluoromethoxyethyl ribose\n SciTegic07272112182D\n\n 28 28 0 0 1 0 999 V2000\n -4.4125 2.2734 0.0000 O 0 0\n -3.9005 3.6833 0.0000 C 0 0 1 0 0 0\n -3.2299 1.3508 0.0000 C 0 0 2 0 0 0\n -2.4014 3.6321 0.0000 C 0 0 2 0 0 0\n -1.9869 2.1905 0.0000 C 0 0 1 0 0 0\n -1.4822 4.8152 0.0000 O 0 0\n -0.5797 1.6761 0.0000 O 0 0\n -4.7418 4.9231 0.0000 C 0 0\n -3.2709 0.1515 0.0000 R# 0 0\n -6.2387 4.8152 0.0000 O 0 0\n -6.9125 5.8082 0.0000 R# 0 0\n -0.2934 4.6522 0.0000 R# 0 0\n -0.3201 0.1978 0.0000 C 0 0\n 1.0894 -0.3174 0.0000 C 0 0\n 1.3489 -1.7956 0.0000 O 0 0\n 2.7585 -2.3109 0.0000 C 0 0\n 3.0181 -3.7891 0.0000 C 0 0\n 3.9091 -1.3475 0.0000 C 0 0\n 1.5836 -3.2910 0.0000 C 0 0\n 4.1451 -4.2011 0.0000 F 0 0\n 2.2514 -4.4311 0.0000 F 0 0\n 3.2249 -4.9711 0.0000 F 0 0\n 5.0367 -1.7584 0.0000 F 0 0\n 3.7017 -0.1655 0.0000 F 0 0\n 4.8289 -0.5766 0.0000 F 0 0\n 0.4570 -2.8778 0.0000 F 0 0\n 0.6625 -4.0600 0.0000 F 0 0\n 1.7547 -4.2762 0.0000 F 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 12 1 0\n 8 10 1 0\n 10 11 1 0\n 7 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 16 18 1 0\n 16 19 1 0\n 17 20 1 0\n 17 21 1 0\n 17 22 1 0\n 18 23 1 0\n 18 24 1 0\n 18 25 1 0\n 19 26 1 0\n 19 27 1 0\n 19 28 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\n2'-O-Tris-trifluoromethoxyethyl ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nFMOE\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nGuanine\n SciTegic07272112182D\n\n 12 13 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 C 0 0\n -0.0787 -2.2532 0.0000 N 0 0\n 2.1768 -0.1209 0.0000 O 0 0\n -0.9527 3.3542 0.0000 N 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n 1 10 2 0\n 1 6 1 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 5 11 1 0\n 7 8 1 0\n 7 12 1 0\n 8 9 2 0\nM RGP 1 12 1\nM END\n> <Name>\nGuanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nG\n\n> <MonomerCode>\nG\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nInosine\n SciTegic07272112182D\n\n 11 12 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 C 0 0\n -0.0787 -2.2532 0.0000 N 0 0\n 2.1768 -0.1209 0.0000 O 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n 1 10 2 0\n 1 6 1 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 1 0\n 7 11 1 0\n 8 9 2 0\nM RGP 1 11 1\nM END\n> <Name>\nInosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nIn\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2,'4'-locked-Ribose\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n -0.9702 0.0384 0.0000 O 0 0\n 0.5413 -0.5559 0.0000 C 0 0 1 0 0 0\n -1.5602 -1.0669 0.0000 C 0 0 2 0 0 0\n 1.9236 0.0726 0.0000 C 0 0 2 0 0 0\n -0.2063 -1.7187 0.0000 C 0 0 1 0 0 0\n 1.5616 1.5445 0.0000 O 0 0\n 0.3744 0.9413 0.0000 C 0 0\n -2.6751 -0.6231 0.0000 R# 0 0\n -0.9999 1.5445 0.0000 O 0 0\n -1.1323 2.7372 0.0000 R# 0 0\n 2.4387 2.3633 0.0000 R# 0 0\n 0.6245 -2.0152 0.0000 C 0 0\n 0.0798 -3.2622 0.0000 O 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 1\n 3 5 1 0\n 3 8 1 6\n 4 5 1 0\n 6 11 1 0\n 7 9 1 0\n 9 10 1 0\n 2 12 1 6\n 12 13 1 0\n 5 13 1 1\n 4 6 1 1\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n2,'4'-locked-Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nLR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2'-O-Methoxyethyl ribose\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2340 0.0328 0.0000 O 0 0\n -1.7220 1.4427 0.0000 C 0 0 1 0 0 0\n -1.0514 -0.8898 0.0000 C 0 0 2 0 0 0\n -0.2229 1.3915 0.0000 C 0 0 2 0 0 0\n 0.1916 -0.0500 0.0000 C 0 0 1 0 0 0\n 0.6962 2.5746 0.0000 O 0 0\n 1.5988 -0.5644 0.0000 O 0 0\n -2.5633 2.6825 0.0000 C 0 0\n -1.0923 -2.0891 0.0000 R# 0 0\n -4.0602 2.5746 0.0000 O 0 0\n -4.7341 3.5674 0.0000 R# 0 0\n 1.8851 2.4118 0.0000 R# 0 0\n 1.8584 -2.0426 0.0000 C 0 0\n 3.2680 -2.5578 0.0000 C 0 0\n 3.5275 -4.0361 0.0000 O 0 0\n 4.6546 -4.4481 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 12 1 0\n 8 10 1 0\n 10 11 1 0\n 7 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\n2'-O-Methoxyethyl ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nMOE\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nTest-6-AP-Phosphate\n Ketcher 9272311252D 1 1.00000 0.00000 0\n\n 13 12 0 0 0 0 0 0 0 0999 V2000\n 8.5250 -7.0500 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0\n 9.0248 -7.9162 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 9.5250 -7.0500 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 9.0248 -6.1838 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 7.5250 -7.0500 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0\n 6.5250 -7.0500 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0\n 5.5250 -7.0500 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0\n 4.5250 -7.0500 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0\n 7.7838 -8.0159 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 6.5250 -8.0500 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 5.5250 -8.0500 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 4.2662 -8.0159 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 3.6590 -6.5500 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 1 2 2 0 0 0\n 1 3 1 0 0 0\n 1 4 1 0 0 0\n 1 5 1 0 0 0\n 5 6 1 0 0 0\n 6 7 1 0 0 0\n 7 8 1 0 0 0\n 5 9 1 0 0 0\n 6 10 1 0 0 0\n 7 11 1 0 0 0\n 8 12 1 0 0 0\n 8 13 1 0 0 0\nM RGP 6 3 2 9 6 10 5 11 4 12 3 13 1\nM END\n> <Name>\nTest-6-AP-Phosphate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nTest-6-Ph\n\n> <MonomerCode>\nP\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]Cl\n[R3]H\n[R4]O\n[R5]H\n[R6]O\n\n$$$$\nPhosphate\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n -0.2399 0.0000 0.0000 P 0 0\n -1.4399 0.0000 0.0000 R# 0 0\n 0.3598 -1.0394 0.0000 O 0 0\n 0.9601 0.0000 0.0000 R# 0 0\n 0.3598 1.0394 0.0000 O 0 0\n 1 2 1 0\n 1 3 2 0\n 1 4 1 0\n 1 5 1 0\nM RGP 2 2 1 4 2\nM END\n> <Name>\nPhosphate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nP\n\n> <MonomerCode>\nP\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\n2-(methylamino)ethanol (PHONA sugar)\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 1.1375 -0.1688 0.0000 N 0 0\n 2.4375 0.5812 0.0000 C 0 0\n 3.4769 -0.0185 0.0000 R# 0 0\n -0.1625 0.5812 0.0000 C 0 0\n -1.4625 -0.1688 0.0000 C 0 0\n -2.7625 0.5812 0.0000 O 0 0\n -3.8019 -0.0185 0.0000 R# 0 0\n 1.1375 -1.3688 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 1 8 1 0\nM RGP 3 3 2 7 1 8 3\nM END\n> <Name>\n2-(methylamino)ethanol (PHONA sugar)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nPONA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]H\n\n$$$$\nRibose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.1017 -1.0663 0.0000 O 0 0\n -0.5897 0.3436 0.0000 C 0 0 1 0 0 0\n 0.0809 -1.9889 0.0000 C 0 0 2 0 0 0\n 0.9095 0.2924 0.0000 C 0 0 2 0 0 0\n 1.3239 -1.1493 0.0000 C 0 0 1 0 0 0\n 1.8285 1.4755 0.0000 O 0 0\n 2.4518 -1.5589 0.0000 O 0 0\n -1.4310 1.5834 0.0000 C 0 0\n 0.0399 -3.1881 0.0000 R# 0 0\n -2.9279 1.4755 0.0000 O 0 0\n -3.6017 2.4684 0.0000 R# 0 0\n 3.0174 1.3125 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 12 1 0\n 8 10 1 0\n 10 11 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\nRibose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nR\n\n> <MonomerCode>\nR\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nR Propanetriol (GNA sugar)\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 0.2258 -0.3260 0.0000 C 0 0 1 0 0 0\n 0.9760 -1.6259 0.0000 C 0 0\n 2.1760 -1.6267 0.0000 R# 0 0\n 0.9740 0.9749 0.0000 O 0 0\n 2.1741 0.9778 0.0000 R# 0 0\n -1.2751 -0.3249 0.0000 C 0 0\n -2.0254 0.9749 0.0000 O 0 0\n -3.2253 0.9758 0.0000 R# 0 0\n 1 2 1 6\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 1 6 1 0\n 6 7 1 0\n 7 8 1 0\nM RGP 3 3 3 5 2 8 1\nM END\n> <Name>\nR Propanetriol (GNA sugar)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRGNA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nS Propanetriol (GNA sugar)\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 0.2258 -0.3260 0.0000 C 0 0 2 0 0 0\n 0.9760 -1.6259 0.0000 C 0 0\n 2.1760 -1.6267 0.0000 R# 0 0\n 0.9740 0.9749 0.0000 O 0 0\n 2.1741 0.9778 0.0000 R# 0 0\n -1.2751 -0.3249 0.0000 C 0 0\n -2.0254 0.9749 0.0000 O 0 0\n -3.2253 0.9758 0.0000 R# 0 0\n 1 2 1 1\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 1 6 1 0\n 6 7 1 0\n 7 8 1 0\nM RGP 3 3 3 5 2 8 1\nM END\n> <Name>\nS Propanetriol (GNA sugar)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSGNA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nThymine\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.7117 -0.9884 0.0000 C 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\n 2 10 1 0\nM RGP 1 9 1\nM END\n> <Name>\nThymine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nT\n\n> <MonomerCode>\nT\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nUracil\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\nM RGP 1 9 1\nM END\n> <Name>\nUracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nU\n\n> <MonomerCode>\nU\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2'-3'-Unlocked-ribose\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 0.6066 -1.3510 0.0000 O 0 0\n -0.6923 -2.1029 0.0000 C 0 0 2 0 0 0\n 0.6057 0.1499 0.0000 C 0 0 1 0 0 0\n 1.9045 0.9019 0.0000 C 0 0\n -0.6915 -3.6037 0.0000 C 0 0\n -1.7320 -1.5039 0.0000 R# 0 0\n -0.6932 0.9018 0.0000 C 0 0\n -0.6925 2.4027 0.0000 O 0 0\n -1.7310 3.0037 0.0000 R# 0 0\n 1.9036 2.4027 0.0000 O 0 0\n -1.7299 -4.2050 0.0000 O 0 0\n 2.9422 3.0039 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 3 4 1 6\n 2 5 1 6\n 2 6 1 0\n 3 7 1 0\n 7 8 1 0\n 8 9 1 0\n 4 10 1 0\n 5 11 1 0\n 10 12 1 0\nM RGP 3 6 3 9 1 12 2\nM END\n> <Name>\n2'-3'-Unlocked-ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nUNA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nalpha-FANA\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.1017 -1.0663 0.0000 O 0 0\n -0.5897 0.3436 0.0000 C 0 0 1 0 0 0\n 0.0809 -1.9889 0.0000 C 0 0 2 0 0 0\n 0.9095 0.2924 0.0000 C 0 0 2 0 0 0\n 1.3239 -1.1493 0.0000 C 0 0 2 0 0 0\n 1.8285 1.4755 0.0000 O 0 0\n -1.4310 1.5834 0.0000 C 0 0\n 0.0399 -3.1881 0.0000 R# 0 0\n -2.9279 1.4755 0.0000 O 0 0\n -3.6017 2.4684 0.0000 R# 0 0\n 3.0174 1.3125 0.0000 R# 0 0\n 2.4518 -1.5589 0.0000 F 0 0\n 1 2 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 3 8 1 6\n 4 5 1 0\n 4 6 1 1\n 6 11 1 0\n 7 9 1 0\n 9 10 1 0\n 5 12 1 6\n 1 3 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\nalpha-FANA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\naFR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Amino-Ribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.1017 -1.0663 0.0000 O 0 0\n -0.5897 0.3436 0.0000 C 0 0 1 0 0 0\n 0.0809 -1.9889 0.0000 C 0 0 2 0 0 0\n 0.9095 0.2924 0.0000 C 0 0 2 0 0 0\n 1.3239 -1.1493 0.0000 C 0 0 1 0 0 0\n 1.8285 1.4755 0.0000 N 0 0\n 2.4518 -1.5589 0.0000 O 0 0\n -1.4310 1.5834 0.0000 C 0 0\n 0.0399 -3.1881 0.0000 R# 0 0\n -2.9279 1.4755 0.0000 O 0 0\n -3.6017 2.4684 0.0000 R# 0 0\n 3.0174 1.3125 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 12 1 0\n 8 10 1 0\n 10 11 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\n3-Amino-Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\naR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5'-12-amino-dodecanol\n SciTegic07272112182D\n\n 16 15 0 0 1 0 999 V2000\n -8.4583 0.0000 0.0000 N 0 0\n -7.1263 -0.6916 0.0000 C 0 0\n -5.8608 0.1153 0.0000 C 0 0\n -4.5288 -0.5764 0.0000 C 0 0\n -3.2634 0.2305 0.0000 C 0 0\n -1.9315 -0.4611 0.0000 C 0 0\n -0.6660 0.3458 0.0000 C 0 0\n 0.6659 -0.3458 0.0000 C 0 0\n -9.4700 -0.6452 0.0000 R# 0 0\n 1.9314 0.4611 0.0000 C 0 0\n 3.2634 -0.2305 0.0000 C 0 0\n 4.5289 0.5764 0.0000 C 0 0\n 5.8608 -0.1153 0.0000 C 0 0\n 7.1263 0.6916 0.0000 C 0 0\n 8.4583 0.0000 0.0000 O 0 0\n 9.4701 0.6452 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 1 9 1 0\n 8 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\nM RGP 2 9 1 16 2\nM END\n> <Name>\n5'-12-amino-dodecanol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nam12\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n5'-6-amino-hexanol\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n -4.5654 0.0000 0.0000 N 0 0\n -3.2082 -0.6407 0.0000 C 0 0\n -5.5520 -0.6831 0.0000 R# 0 0\n -1.9742 0.2136 0.0000 C 0 0\n -0.6170 -0.4271 0.0000 C 0 0\n 0.6170 0.4271 0.0000 C 0 0\n 1.9742 -0.2136 0.0000 C 0 0\n 3.2082 0.6407 0.0000 C 0 0\n 4.5654 0.0000 0.0000 O 0 0\n 5.5520 0.6830 0.0000 R# 0 0\n 1 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 2 1 1 0\nM RGP 2 3 1 10 2\nM END\n> <Name>\n5'-6-amino-hexanol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nam6\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nBoranophosphate\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n -0.2399 0.0000 0.0000 P 0 0\n -1.4399 0.0000 0.0000 R# 0 0\n 0.3598 -1.0394 0.0000 O 0 0\n 0.9601 0.0000 0.0000 R# 0 0\n 0.3598 1.0394 0.0000 B 0 0\n 1 2 1 0\n 1 3 2 0\n 1 4 1 0\n 1 5 1 0\nM RGP 2 2 1 4 2\nM END\n> <Name>\nBoranophosphate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbP\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nN-benzyl-adenine\n SciTegic07272112182D\n\n 18 20 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 C 0 0\n -0.0787 -2.2532 0.0000 N 0 0\n 2.4638 -0.2109 0.0000 N 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n 3.5776 0.7950 0.0000 C 0 0\n 5.0060 0.3343 0.0000 C 0 0\n 7.8594 -0.5925 0.0000 C 0 0\n 7.5474 0.8747 0.0000 C 0 0\n 6.1207 1.3381 0.0000 C 0 0\n 5.3181 -1.1330 0.0000 C 0 0\n 6.7448 -1.5963 0.0000 C 0 0\n 1 10 1 0\n 1 6 2 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 1 0\n 7 11 1 0\n 8 9 2 0\n 10 12 1 0\n 12 13 1 0\n 16 13 2 0\n 13 17 1 0\n 14 15 2 0\n 15 16 1 0\n 17 18 2 0\n 14 18 1 0\nM RGP 1 11 1\nM END\n> <Name>\nN-benzyl-adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbaA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-cyclopropyl-4-dimethylamino-cytosine\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 2.6489 0.0000 C 0 0\n -0.3882 2.6490 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3883 0.0509 0.0000 C 0 0\n 1.1117 0.0509 0.0000 N 0 0\n 3.3626 1.3468 0.0000 N 0 0\n -0.9884 -0.9883 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.8621 3.9486 0.0000 C 0 0\n 3.1144 4.6215 0.0000 C 0 0\n 1.8143 5.3694 0.0000 C 0 0\n 3.9611 0.3067 0.0000 C 0 0\n 3.9644 2.3849 0.0000 C 0 0\n 1 2 1 0\n 1 6 2 0\n 1 7 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 6 1 0\n 5 8 2 0\n 2 10 1 0\n 10 11 1 0\n 10 12 1 0\n 12 11 1 0\n 7 13 1 0\n 7 14 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-cyclopropyl-4-dimethylamino-cytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncdaC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nT-clamp OMe\n SciTegic07272112182D\n\n 20 23 0 0 1 0 999 V2000\n 6.0065 0.0000 0.0000 N 0 0\n 4.8065 0.0000 0.0000 R# 0 0\n 6.8882 -1.2135 0.0000 C 0 0\n 6.8882 1.2135 0.0000 C 0 0\n 8.3140 0.7500 0.0000 C 0 0\n 8.3140 -0.7500 0.0000 C 0 0\n 9.6130 -1.5000 0.0000 C 0 0\n 9.3808 -3.0307 0.0000 N 0 0\n 8.0105 -3.6408 0.0000 C 0 0\n 6.7969 -2.7592 0.0000 N 0 0\n 10.9120 -0.7500 0.0000 N 0 0\n 9.6130 1.5000 0.0000 C 0 0\n 10.9120 0.7500 0.0000 C 0 0\n 12.2111 1.5000 0.0000 C 0 0\n 12.2111 3.0000 0.0000 C 0 0\n 10.9120 3.7500 0.0000 C 0 0\n 9.6130 3.0000 0.0000 C 0 0\n 13.5124 0.7523 0.0000 O 0 0\n 14.5508 1.3538 0.0000 C 0 0\n 7.8851 -4.8343 0.0000 N 0 0\n 1 2 1 0\n 1 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 3 1 0\n 7 11 1 0\n 5 12 1 0\n 12 13 1 0\n 13 11 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 16 17 1 0\n 17 12 2 0\n 14 18 1 0\n 18 19 1 0\n 9 20 1 0\nM RGP 1 2 1\nM END\n> <Name>\nT-clamp OMe\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nclA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-cyclopropyl-cytosine\n SciTegic07272112182D\n\n 12 13 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 2.6489 0.0000 C 0 0\n -0.3882 2.6490 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3883 0.0509 0.0000 C 0 0\n 1.1117 0.0509 0.0000 N 0 0\n 3.0618 1.3499 0.0000 N 0 0\n -0.9884 -0.9883 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.8621 3.9486 0.0000 C 0 0\n 3.1144 4.6215 0.0000 C 0 0\n 1.8143 5.3694 0.0000 C 0 0\n 1 2 1 0\n 1 6 2 0\n 1 7 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 6 1 0\n 5 8 2 0\n 2 10 1 0\n 10 11 1 0\n 10 12 1 0\n 12 11 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-cyclopropyl-cytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncpC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-cyclopropyl-uracil\n SciTegic07272112182D\n\n 12 13 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.8621 -1.2489 0.0000 C 0 0\n 1.8185 -2.6698 0.0000 C 0 0\n 3.1164 -1.9177 0.0000 C 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\n 2 10 1 0\n 10 11 1 0\n 10 12 1 0\n 12 11 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-cyclopropyl-uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncpU\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN-cyclopropylmethyl-adenine\n SciTegic07272112182D\n\n 15 17 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 C 0 0\n -0.0787 -2.2532 0.0000 N 0 0\n 2.4638 -0.2109 0.0000 N 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n 3.5776 0.7950 0.0000 C 0 0\n 5.0060 0.3343 0.0000 C 0 0\n 6.3863 0.6744 0.0000 C 0 0\n 5.9228 -0.7522 0.0000 C 0 0\n 1 10 1 0\n 1 6 2 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 1 0\n 7 11 1 0\n 8 9 2 0\n 10 12 1 0\n 12 13 1 0\n 13 14 1 0\n 13 15 1 0\n 15 14 1 0\nM RGP 1 11 1\nM END\n> <Name>\nN-cyclopropylmethyl-adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncpmA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nDeoxy-Ribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.8788 -1.2080 0.0000 O 0 0\n -0.3668 0.2019 0.0000 C 0 0 1 0 0 0\n 0.3038 -2.1307 0.0000 C 0 0 2 0 0 0\n 1.1323 0.1506 0.0000 C 0 0 2 0 0 0\n 1.5468 -1.2910 0.0000 C 0 0\n 2.0515 1.3338 0.0000 O 0 0\n -1.2081 1.4417 0.0000 C 0 0\n 0.2628 -3.3299 0.0000 R# 0 0\n -2.7050 1.3338 0.0000 O 0 0\n -3.3788 2.3267 0.0000 R# 0 0\n 3.2403 1.1709 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 3 8 1 6\n 4 5 1 0\n 4 6 1 1\n 6 11 1 0\n 7 9 1 0\n 9 10 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\nDeoxy-Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nN,N-dimethyl-Adenine\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 C 0 0\n -0.0787 -2.2532 0.0000 N 0 0\n 2.4638 -0.2109 0.0000 N 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n 3.3544 0.5933 0.0000 C 0 0\n 2.7154 -1.3842 0.0000 C 0 0\n 1 10 1 0\n 1 6 2 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 1 0\n 7 11 1 0\n 8 9 2 0\n 10 12 1 0\n 10 13 1 0\nM RGP 1 11 1\nM END\n> <Name>\nN,N-dimethyl-Adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndaA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-deaza-8-aza-7-bromo-2-amino-Adenine\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 N 0 0\n -0.0787 -2.2532 0.0000 C 0 0\n 2.1768 -0.1209 0.0000 N 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n -0.9527 3.3542 0.0000 N 0 0\n 0.8922 -2.9584 0.0000 Br 0 0\n 1 10 1 0\n 1 6 2 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 1 0\n 7 11 1 0\n 8 9 2 0\n 5 12 1 0\n 9 13 1 0\nM RGP 1 11 1\nM END\n> <Name>\n7-deaza-8-aza-7-bromo-2-amino-Adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndabA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2,4-Difluoro-Benzene\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 2.6489 0.0000 C 0 0\n -0.3882 2.6490 0.0000 C 0 0\n -1.1382 1.3500 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n 3.0618 1.3499 0.0000 F 0 0\n -0.9884 -0.9883 0.0000 F 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 1 7 1 0\n 5 8 1 0\n 4 9 1 0\nM RGP 1 9 1\nM END\n> <Name>\n2,4-Difluoro-Benzene\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndfB\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5- 1,2-Dierucyl-rac-glycerol (Genzyme)\n SciTegic07272112182D\n\n 51 50 0 0 1 0 999 V2000\n 29.4991 -4.8473 0.0000 C 0 0\n 30.2517 -3.5488 0.0000 C 0 0\n 30.2465 -6.1488 0.0000 O 0 0\n 29.5043 -2.2473 0.0000 O 0 0\n 31.7525 -3.5488 0.0000 C 0 0\n 32.5037 -2.2494 0.0000 O 0 0\n 33.7037 -2.2494 0.0000 R# 0 0\n 30.2569 -0.9489 0.0000 C 0 0\n 29.5095 0.3526 0.0000 C 0 0\n 30.2621 1.6511 0.0000 C 0 0\n 29.5147 2.9526 0.0000 C 0 0\n 30.2673 4.2511 0.0000 C 0 0\n 29.5199 5.5526 0.0000 C 0 0\n 30.2725 6.8511 0.0000 C 0 0\n 29.5251 8.1526 0.0000 C 0 0\n 30.2777 9.4511 0.0000 C 0 0\n 29.5303 10.7526 0.0000 C 0 0\n 30.2829 12.0510 0.0000 C 0 0\n 29.5355 13.3525 0.0000 C 0 0\n 30.2881 14.6510 0.0000 C 0 0\n 29.4939 -7.4473 0.0000 C 0 0\n 30.2413 -8.7488 0.0000 C 0 0\n 29.4887 -10.0473 0.0000 C 0 0\n 30.2361 -11.3488 0.0000 C 0 0\n 29.4835 -12.6473 0.0000 C 0 0\n 30.2309 -13.9488 0.0000 C 0 0\n 29.4783 -15.2473 0.0000 C 0 0\n 30.2257 -16.5487 0.0000 C 0 0\n 29.4731 -17.8472 0.0000 C 0 0\n 30.2205 -19.1487 0.0000 C 0 0\n 29.4679 -20.4472 0.0000 C 0 0\n 30.2153 -21.7487 0.0000 C 0 0\n 29.4627 -23.0472 0.0000 C 0 0\n 30.2101 -24.3487 0.0000 C 0 0\n 31.7109 -24.3531 0.0000 C 0 0\n 29.5407 15.9525 0.0000 C 0 0\n 28.0399 15.9569 0.0000 C 0 0\n 32.4583 -25.6546 0.0000 C 0 0\n 33.9591 -25.6590 0.0000 C 0 0\n 34.7065 -26.9605 0.0000 C 0 0\n 36.2074 -26.9649 0.0000 C 0 0\n 36.9548 -28.2664 0.0000 C 0 0\n 38.4556 -28.2709 0.0000 C 0 0\n 39.0532 -29.3115 0.0000 C 0 0\n 27.2925 17.2584 0.0000 C 0 0\n 25.7917 17.2629 0.0000 C 0 0\n 25.0443 18.5643 0.0000 C 0 0\n 23.5434 18.5688 0.0000 C 0 0\n 22.7960 19.8703 0.0000 C 0 0\n 21.2952 19.8747 0.0000 C 0 0\n 20.6976 20.9153 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 5 1 0\n 5 6 1 0\n 6 7 1 0\n 4 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 19 20 1 0\n 3 21 1 0\n 21 22 1 0\n 22 23 1 0\n 23 24 1 0\n 24 25 1 0\n 25 26 1 0\n 26 27 1 0\n 27 28 1 0\n 28 29 1 0\n 29 30 1 0\n 30 31 1 0\n 31 32 1 0\n 32 33 1 0\n 33 34 2 0\n 34 35 1 0\n 20 36 2 0\n 36 37 1 0\n 35 38 1 0\n 38 39 1 0\n 39 40 1 0\n 40 41 1 0\n 41 42 1 0\n 42 43 1 0\n 43 44 1 0\n 37 45 1 0\n 45 46 1 0\n 46 47 1 0\n 47 48 1 0\n 48 49 1 0\n 49 50 1 0\n 50 51 1 0\nM RGP 1 7 2\nM END\n> <Name>\n5- 1,2-Dierucyl-rac-glycerol (Genzyme)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndier\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]H\n\n$$$$\n2'-O,4'-ethylene bridged Ribose\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -1.7962 0.2830 0.0000 O 0 0\n -0.2126 -0.1654 0.0000 C 0 0 1 0 0 0\n -0.7491 -0.5569 0.0000 C 0 0 2 0 0 0\n 1.0867 0.5840 0.0000 C 0 0 2 0 0 0\n 0.6934 -0.7266 0.0000 C 0 0 1 0 0 0\n 1.9988 1.7614 0.0000 O 0 0\n -0.5224 1.2978 0.0000 C 0 0\n -1.2125 -1.6638 0.0000 R# 0 0\n -1.9499 1.7614 0.0000 O 0 0\n -2.2001 2.9350 0.0000 R# 0 0\n 3.1880 1.6005 0.0000 R# 0 0\n 1.2940 -2.2554 0.0000 O 0 0\n 0.4041 -1.8438 0.0000 C 0 0\n -0.0222 -3.0111 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 1\n 3 5 1 0\n 3 8 1 6\n 4 5 1 0\n 6 11 1 0\n 7 9 1 0\n 9 10 1 0\n 4 6 1 1\n 5 12 1 1\n 2 13 1 6\n 13 14 1 0\n 14 12 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n2'-O,4'-ethylene bridged Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\neR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nN-ethyl-adenine\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 C 0 0\n -0.0787 -2.2532 0.0000 N 0 0\n 2.4638 -0.2109 0.0000 N 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n 3.5776 0.7950 0.0000 C 0 0\n 4.7197 0.4267 0.0000 C 0 0\n 1 10 1 0\n 1 6 2 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 1 0\n 7 11 1 0\n 8 9 2 0\n 10 12 1 0\n 12 13 1 0\nM RGP 1 11 1\nM END\n> <Name>\nN-ethyl-adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\neaA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2'-Flu0ro-Ribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.1017 -1.0663 0.0000 O 0 0\n -0.5897 0.3436 0.0000 C 0 0 1 0 0 0\n 0.0809 -1.9889 0.0000 C 0 0 2 0 0 0\n 0.9095 0.2924 0.0000 C 0 0 2 0 0 0\n 1.3239 -1.1493 0.0000 C 0 0 1 0 0 0\n 1.8285 1.4755 0.0000 O 0 0\n 2.4518 -1.5589 0.0000 F 0 0\n -1.4310 1.5834 0.0000 C 0 0\n 0.0399 -3.1881 0.0000 R# 0 0\n -2.9279 1.4755 0.0000 O 0 0\n -3.6017 2.4684 0.0000 R# 0 0\n 3.0174 1.3125 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 12 1 0\n 8 10 1 0\n 10 11 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\n2'-Flu0ro-Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nhexitol\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.2871 -0.9728 0.0000 O 0 0\n -0.5356 0.3254 0.0000 C 0 0 1 0 0 0\n 0.9644 0.3237 0.0000 C 0 0 2 0 0 0\n 1.7128 -0.9762 0.0000 C 0 0\n 0.9613 -2.2744 0.0000 C 0 0 1 0 0 0\n -0.5387 -2.2726 0.0000 C 0 0\n -1.2872 1.6245 0.0000 C 0 0\n -2.7880 1.6241 0.0000 O 0 0\n -3.3890 2.6628 0.0000 R# 0 0\n 1.7136 1.6241 0.0000 O 0 0\n 1.5602 -3.3144 0.0000 R# 0 0\n 2.9136 1.6260 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 1 6 1 0\n 2 7 1 6\n 7 8 1 0\n 8 9 1 0\n 3 10 1 1\n 5 11 1 6\n 10 12 1 0\nM RGP 3 9 1 11 3 12 2\nM END\n> <Name>\nhexitol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nhx\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2,'4'-locked-Ribose (alpha-L-LNA)\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n -0.9702 0.0384 0.0000 O 0 0\n 0.5413 -0.5559 0.0000 C 0 0 1 0 0 0\n -1.5602 -1.0669 0.0000 C 0 0 2 0 0 0\n 1.9236 0.0726 0.0000 C 0 0 1 0 0 0\n -0.2063 -1.7187 0.0000 C 0 0 2 0 0 0\n 1.5616 1.5445 0.0000 O 0 0\n 0.6245 -2.0152 0.0000 C 0 0\n -2.6751 -0.6231 0.0000 R# 0 0\n 2.4387 2.3633 0.0000 R# 0 0\n 0.3744 0.9413 0.0000 C 0 0\n 0.0798 -3.2622 0.0000 O 0 0\n -0.9999 1.5445 0.0000 O 0 0\n -1.1323 2.7372 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 3 8 1 6\n 4 5 1 0\n 6 9 1 0\n 2 10 1 0\n 5 11 1 6\n 4 6 1 6\n 10 12 1 0\n 7 11 1 0\n 12 13 1 0\nM RGP 3 8 3 9 2 13 1\nM END\n> <Name>\n2,'4'-locked-Ribose (alpha-L-LNA)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nlLR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2'-O-Methyl-Ribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.3493 -0.8393 0.0000 O 0 0\n -0.8372 0.5706 0.0000 C 0 0 1 0 0 0\n -0.1666 -1.7620 0.0000 C 0 0 2 0 0 0\n 0.6619 0.5193 0.0000 C 0 0 2 0 0 0\n 1.0764 -0.9223 0.0000 C 0 0 1 0 0 0\n 1.5811 1.7025 0.0000 O 0 0\n 2.4836 -1.4367 0.0000 O 0 0\n -1.6785 1.8103 0.0000 C 0 0\n -0.2077 -2.9612 0.0000 R# 0 0\n -3.1754 1.7025 0.0000 O 0 0\n -3.8492 2.6954 0.0000 R# 0 0\n 2.7699 1.5395 0.0000 R# 0 0\n 2.6911 -2.6186 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 12 1 0\n 8 10 1 0\n 10 11 1 0\n 7 13 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\n2'-O-Methyl-Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nN-Methyl-Adenine\n SciTegic07272112182D\n\n 12 13 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 C 0 0\n -0.0787 -2.2532 0.0000 N 0 0\n 2.4638 -0.2109 0.0000 N 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n 3.3544 0.5933 0.0000 C 0 0\n 1 10 1 0\n 1 6 2 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 1 0\n 7 11 1 0\n 8 9 2 0\n 10 12 1 0\nM RGP 1 11 1\nM END\n> <Name>\nN-Methyl-Adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmeA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nmorpholino\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.4725 -0.9529 0.0000 O 0 0\n -0.4712 0.5471 0.0000 C 0 0 1 0 0 0\n 0.8284 1.2959 0.0000 C 0 0\n 2.1268 0.5448 0.0000 N 0 0\n 2.1255 -0.9552 0.0000 C 0 0\n 0.8258 -1.7041 0.0000 C 0 0 2 0 0 0\n -1.7719 1.2960 0.0000 C 0 0\n 0.8248 -2.9041 0.0000 R# 0 0\n -3.0712 0.5448 0.0000 O 0 0\n -4.1112 1.1437 0.0000 R# 0 0\n 3.1666 1.1439 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 1 6 1 0\n 2 7 1 6\n 6 8 1 6\n 7 9 1 0\n 9 10 1 0\n 4 11 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\nmorpholino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmph\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nSodium Phosphate\n SciTegic07272112182D\n\n 6 4 0 0 1 0 999 V2000\n -0.1999 -0.6333 0.0000 P 0 0\n -1.3999 -0.6333 0.0000 R# 0 0\n 0.3998 -1.6727 0.0000 O 0 0\n 1.0001 -0.6333 0.0000 R# 0 0\n 0.3998 0.4061 0.0000 O 0 5\n -0.1999 3.1667 0.0000 Na 0 3\n 1 2 1 0\n 1 3 2 0\n 1 4 1 0\n 1 5 1 0\nM CHG 2 5 -1 6 1\nM RGP 2 2 1 4 2\nM END\n> <Name>\nSodium Phosphate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnaP\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nSodium Phosporothioate\n SciTegic07272112182D\n\n 6 4 0 0 1 0 999 V2000\n -0.1999 -0.6333 0.0000 P 0 0\n -1.3999 -0.6333 0.0000 R# 0 0\n 0.3998 -1.6727 0.0000 O 0 0\n 1.0001 -0.6333 0.0000 R# 0 0\n 0.3998 0.4061 0.0000 S 0 5\n -0.1999 3.1667 0.0000 Na 0 3\n 1 2 1 0\n 1 3 2 0\n 1 4 1 0\n 1 5 1 0\nM CHG 2 5 -1 6 1\nM RGP 2 2 1 4 2\nM END\n> <Name>\nSodium Phosporothioate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnasP\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\n5-Propynyl-Cytosine\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 2.6489 0.0000 C 0 0\n -0.3882 2.6490 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3883 0.0509 0.0000 C 0 0\n 1.1117 0.0509 0.0000 N 0 0\n 3.0618 1.3499 0.0000 N 0 0\n -0.9884 -0.9883 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.8622 3.9487 0.0000 C 0 0\n 2.6126 5.2484 0.0000 C 0 0\n 3.2127 6.2877 0.0000 C 0 0\n 1 2 1 0\n 1 6 2 0\n 1 7 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 6 1 0\n 5 8 2 0\n 2 10 1 0\n 10 11 3 0\n 11 12 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-Propynyl-Cytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nprpC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-propynyl Uracil\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.8621 -1.2489 0.0000 C 0 0\n 2.6125 -2.5487 0.0000 C 0 0\n 3.2124 -3.5880 0.0000 C 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\n 2 10 1 0\n 10 11 3 0\n 11 12 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-propynyl Uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nprpU\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-O-beta-hydroxy-ethoxy-methyl Ribose (Qiagen)\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.5533 0.3762 0.0000 O 0 0\n -2.0412 1.7861 0.0000 C 0 0 1 0 0 0\n -1.3706 -0.5464 0.0000 C 0 0 2 0 0 0\n -0.5421 1.7349 0.0000 C 0 0 2 0 0 0\n -0.1276 0.2932 0.0000 C 0 0 1 0 0 0\n 0.3770 2.9180 0.0000 O 0 0\n 1.2795 -0.2212 0.0000 O 0 0\n -2.8825 3.0258 0.0000 C 0 0\n -1.4117 -1.7458 0.0000 R# 0 0\n -4.3794 2.9180 0.0000 O 0 0\n -5.0532 3.9109 0.0000 R# 0 0\n 1.5659 2.7550 0.0000 R# 0 0\n 1.5391 -1.6994 0.0000 C 0 0\n 2.9487 -2.2146 0.0000 O 0 0\n 3.2082 -3.6929 0.0000 C 0 0\n 4.6177 -4.2081 0.0000 C 0 0\n 4.8253 -5.3900 0.0000 O 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 12 1 0\n 8 10 1 0\n 10 11 1 0\n 7 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\n2-O-beta-hydroxy-ethoxy-methyl Ribose (Qiagen)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nqR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nPhosporothioate\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n -0.2399 0.0000 0.0000 P 0 0\n -1.4399 0.0000 0.0000 R# 0 0\n 0.3598 -1.0394 0.0000 O 0 0\n 0.9601 0.0000 0.0000 R# 0 0\n 0.3598 1.0394 0.0000 S 0 0\n 1 2 1 0\n 1 3 2 0\n 1 4 1 0\n 1 5 1 0\nM RGP 2 2 1 4 2\nM END\n> <Name>\nPhosporothioate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nsP\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nRibose\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n -0.2355 -2.0711 0.0000 O 0 0\n -1.4490 -1.1894 0.0000 C 0 0\n 0.9781 -1.1894 0.0000 C 0 0 2 0 0 0\n -0.9855 0.2372 0.0000 C 0 0 1 0 0 0\n 0.5145 0.2372 0.0000 C 0 0 1 0 0 0\n -1.8686 1.4475 0.0000 O 0 0\n 1.3977 1.4475 0.0000 O 0 0\n 2.1193 -1.5602 0.0000 R# 0 0\n -3.0619 1.3203 0.0000 R# 0 0\n 2.5909 1.3203 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 3 5 1 0\n 3 8 1 6\n 4 5 1 0\n 4 6 1 6\n 5 7 1 1\n 6 9 1 0\n 7 10 1 0\nM RGP 3 8 3 9 1 10 2\nM END\n> <Name>\nRibose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ntR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-trifluoromethyl-uracil\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.8621 -1.2489 0.0000 C 0 0\n 3.0621 -1.2497 0.0000 F 0 0\n 1.2617 -2.2879 0.0000 F 0 0\n 2.4615 -2.2884 0.0000 F 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\n 2 10 1 0\n 10 11 1 0\n 10 12 1 0\n 10 13 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-trifluoromethyl-uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ntfU\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nAlanine\n SciTegic07272112182D\n\n 7 6 0 0 1 0 999 V2000\n -1.2549 -0.3920 0.0000 N 0 0\n -0.2720 0.2633 0.0000 C 0 0 1 0 0 0\n -0.3103 1.7393 0.0000 C 0 0\n 1.0523 -0.3920 0.0000 C 0 0\n 1.0829 -1.5722 0.0000 O 0 0\n 2.0353 0.2633 0.0000 R# 0 0\n -2.3334 0.0905 0.0000 R# 0 0\n 2 1 1 0\n 2 3 1 1\n 2 4 1 0\n 4 5 2 0\n 4 6 1 0\n 1 7 1 0\nM RGP 2 6 2 7 1\nM END\n> <Name>\nAlanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nA\n\n> <MonomerCode>\nA\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nTest-6-AP-Peptide\n Ketcher 9272310562D 1 1.00000 0.00000 0\n\n 23 22 0 0 1 0 0 0 0 0999 V2000\n 12.7761 -7.9506 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.7754 -9.0509 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.7276 -9.6021 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.7271 -10.4818 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 14.4899 -9.1629 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 11.8233 -9.6021 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0\n 11.8239 -7.3994 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 11.8245 -6.2991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 10.8724 -5.7479 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 10.1101 -6.1871 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 10.8728 -4.8682 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 11.0606 -9.1637 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 12.7904 -5.7903 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.7564 -6.2991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 14.7564 -6.2991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 15.2564 -5.4331 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 12.7904 -4.7903 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 15.6224 -6.7991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 15.6224 -7.7991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 16.4884 -8.2991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 14.7564 -8.2991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 16.4884 -9.2991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 17.3544 -9.7991 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 2 1 1 1 0 0\n 2 3 1 0 0 0\n 3 4 2 0 0 0\n 3 5 1 0 0 0\n 2 6 1 0 0 0\n 1 7 1 0 0 0\n 7 8 1 0 0 0\n 8 9 1 0 0 0\n 9 10 1 0 0 0\n 9 11 2 0 0 0\n 6 12 1 0 0 0\n 8 13 1 0 0 0\n 13 14 1 0 0 0\n 14 15 1 0 0 0\n 15 16 1 0 0 0\n 13 17 1 0 0 0\n 15 18 1 0 0 0\n 18 19 1 0 0 0\n 19 20 1 0 0 0\n 19 21 1 0 0 0\n 20 22 1 0 0 0\n 22 23 1 0 0 0\nM RGP 6 5 2 10 3 12 1 16 5 17 4 23 6\nM END\n\n> <Name>\nTest-6-AP-Peptide\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTest-6-P\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]N\n[R4]Cl\n[R5]F\n[R6]Br\n\n$$$$\n2-aminoadipic acid\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 0.8445 0.0123 0.0000 C 0 0\n 0.8436 -1.4885 0.0000 C 0 0 1 0 0 0\n 2.1425 -2.2405 0.0000 C 0 0\n 2.1418 -3.4405 0.0000 O 0 0\n 3.1823 -1.6414 0.0000 R# 0 0\n -0.4552 -2.2405 0.0000 N 0 0\n -0.4543 0.7643 0.0000 C 0 0\n -0.4535 2.2651 0.0000 C 0 0\n -1.7523 3.0170 0.0000 C 0 0\n -2.7921 2.4179 0.0000 R# 0 0\n -1.7517 4.2171 0.0000 O 0 0\n -1.4956 -1.6424 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 1 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 9 11 2 0\n 6 12 1 0\nM RGP 3 5 2 10 3 12 1\nM END\n> <Name>\n2-aminoadipic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAad\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\n2-aminobutanoic acid\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n -0.0318 1.5208 0.0000 C 0 0\n -0.0326 0.0200 0.0000 C 0 0 1 0 0 0\n 1.2663 -0.7320 0.0000 C 0 0\n 1.2656 -1.9320 0.0000 O 0 0\n 2.3061 -0.1329 0.0000 R# 0 0\n -1.3315 -0.7320 0.0000 N 0 0\n -1.0703 2.1220 0.0000 C 0 0\n -2.3718 -0.1339 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 1 7 1 0\n 6 8 1 0\nM RGP 2 5 2 8 1\nM END\n> <Name>\n2-aminobutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAbu\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-aminocapric acid\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n 1.3727 -1.2230 0.0000 C 0 0\n 1.3719 -2.7239 0.0000 C 0 0 1 0 0 0\n 2.6708 -3.4758 0.0000 C 0 0\n 2.6701 -4.6759 0.0000 O 0 0\n 3.7105 -2.8768 0.0000 R# 0 0\n 0.0730 -3.4758 0.0000 N 0 0\n -0.9674 -2.8778 0.0000 R# 0 0\n 0.0739 -0.4711 0.0000 C 0 0\n 0.0748 1.0298 0.0000 C 0 0\n -1.2240 1.7816 0.0000 C 0 0\n -1.2232 3.2825 0.0000 C 0 0\n -2.5221 4.0344 0.0000 C 0 0\n -2.5213 5.5353 0.0000 C 0 0\n -3.5597 6.1366 0.0000 C 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 6 7 1 0\n 1 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\nM RGP 2 5 2 7 1\nM END\n> <Name>\n2-aminocapric acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAca\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nalpha-aminoisobutyric acid (2-aminoalanine)\n SciTegic07272112182D\n\n 8 7 0 0 0 0 999 V2000\n -0.7185 1.1362 0.0000 C 0 0\n -0.1279 0.1134 0.0000 C 0 0\n -1.1506 -0.4772 0.0000 N 0 0\n -2.1736 0.1133 0.0000 R# 0 0\n 0.8950 -0.4772 0.0000 C 0 0\n 0.8951 -1.6582 0.0000 O 0 0\n 1.9179 0.1135 0.0000 R# 0 0\n 0.4626 1.1363 0.0000 C 0 0\n 2 1 1 0\n 3 2 1 0\n 3 4 1 0\n 2 5 1 0\n 5 6 2 0\n 5 7 1 0\n 8 2 1 0\nM RGP 2 4 1 7 2\nM END\n> <Name>\nalpha-aminoisobutyric acid (2-aminoalanine)\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAib\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-aminopimelic acid\n SciTegic07272112182D\n\n 13 12 0 0 1 0 999 V2000\n 0.8990 -0.6122 0.0000 C 0 0\n 0.8982 -2.1130 0.0000 C 0 0 1 0 0 0\n 2.1971 -2.8650 0.0000 C 0 0\n 2.1964 -4.0650 0.0000 O 0 0\n 3.2369 -2.2659 0.0000 R# 0 0\n -0.4007 -2.8650 0.0000 N 0 0\n -0.3998 0.1398 0.0000 C 0 0\n -0.3989 1.6406 0.0000 C 0 0\n -1.6977 2.3925 0.0000 C 0 0\n -1.6969 3.8933 0.0000 C 0 0\n -1.4410 -2.2669 0.0000 R# 0 0\n -0.6571 4.4924 0.0000 R# 0 0\n -2.7355 4.4946 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 1 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 6 11 1 0\n 10 12 1 0\n 10 13 2 0\nM RGP 3 5 2 11 1 12 3\nM END\n> <Name>\n2-aminopimelic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nApm\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\ngamma-amino-beta-hydroxybenzenepentanoic acid\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n 0.7404 -1.8505 0.0000 C 0 0\n 0.1498 -0.8277 0.0000 C 0 0 1 0 0 0\n 0.7404 0.1952 0.0000 O 0 0\n -1.0313 -0.8277 0.0000 C 0 0 2 0 0 0\n -1.6218 0.1952 0.0000 C 0 0\n -1.0313 1.2181 0.0000 C 0 0\n 0.1498 1.2181 0.0000 C 0 0\n 0.7404 2.2410 0.0000 C 0 0\n 0.1499 3.2638 0.0000 C 0 0\n -1.0312 3.2638 0.0000 C 0 0\n -1.6218 2.2410 0.0000 C 0 0\n -1.6218 -1.8505 0.0000 N 0 0\n -1.6570 -2.9283 0.0000 R# 0 0\n 1.9214 -1.8505 0.0000 C 0 0\n 2.5121 -0.8277 0.0000 R# 0 0\n 2.5120 -2.8734 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 6\n 2 4 1 0\n 4 5 1 1\n 6 5 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 6 2 0\n 4 12 1 0\n 12 13 1 0\n 1 14 1 0\n 14 15 1 0\n 14 16 2 0\nM RGP 2 13 1 15 2\nM END\n> <Name>\ngamma-amino-beta-hydroxybenzenepentanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nApp\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-aminosuberic acid\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n 1.3729 -1.0086 0.0000 C 0 0\n 1.3720 -2.5095 0.0000 C 0 0 1 0 0 0\n 2.6709 -3.2614 0.0000 C 0 0\n 2.6702 -4.4614 0.0000 O 0 0\n 3.7107 -2.6624 0.0000 R# 0 0\n 0.0732 -3.2614 0.0000 N 0 0\n 0.0741 -0.2566 0.0000 C 0 0\n 0.0749 1.2442 0.0000 C 0 0\n -1.2239 1.9961 0.0000 C 0 0\n -1.2230 3.4969 0.0000 C 0 0\n -0.9672 -2.6634 0.0000 R# 0 0\n -2.5219 4.2489 0.0000 C 0 0\n -3.5617 3.6498 0.0000 R# 0 0\n -2.5212 5.4489 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 1 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 6 11 1 0\n 12 10 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 3 5 2 11 1 13 3\nM END\n> <Name>\n2-aminosuberic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAsu\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\n2-carboxyazetidine\n SciTegic07272112182D\n\n 8 8 0 0 1 0 999 V2000\n 0.0331 0.2591 0.0000 C 0 0 2 0 0 0\n -0.4189 1.3503 0.0000 C 0 0\n -1.5101 0.8983 0.0000 C 0 0\n -1.0581 -0.1929 0.0000 N 0 0\n -1.5101 -1.2841 0.0000 R# 0 0\n 1.1243 -0.1929 0.0000 C 0 0\n 2.0613 0.5261 0.0000 R# 0 0\n 1.2785 -1.3639 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 4 3 1 0\n 1 4 1 1\n 4 5 1 0\n 1 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 2 5 1 7 2\nM END\n> <Name>\n2-carboxyazetidine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAze\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nbeta-Alanine\n SciTegic07272112182D\n\n 7 6 0 0 0 0 999 V2000\n 0.1914 0.5523 0.0000 C 0 0\n 1.3074 0.1657 0.0000 C 0 0\n 1.5305 -0.9942 0.0000 O 0 0\n 2.2002 0.9389 0.0000 R# 0 0\n -0.7015 -0.2209 0.0000 C 0 0\n -1.8176 0.1657 0.0000 N 0 0\n -2.7104 -0.6075 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 5 6 1 0\n 6 7 1 0\nM RGP 2 4 2 7 1\nM END\n> <Name>\nbeta-Alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBal\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nbutanoic acid\n SciTegic07272112182D\n\n 6 5 0 0 1 0 999 V2000\n 3.3003 4.3894 0.0000 C 0 0\n 3.9000 3.3500 0.0000 C 0 0\n 3.1500 2.0500 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1000 0.7500 0.0000 R# 0 0\n 3.3003 -0.2894 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\nM RGP 1 5 2\nM END\n> <Name>\nbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBua\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n4-amino-3-hydroxybutanoic acid\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n -1.2501 0.5906 0.0000 C 0 0\n -2.2731 0.0000 0.0000 N 0 0\n -3.2959 0.5906 0.0000 R# 0 0\n -0.2273 0.0000 0.0000 C 0 0 1 0 0 0\n -0.2273 -1.1812 0.0000 O 0 0\n 0.7955 0.5906 0.0000 C 0 0\n 1.8184 0.0000 0.0000 C 0 0\n 1.8184 -1.1811 0.0000 O 0 0\n 2.8413 0.5906 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 6\n 4 6 1 0\n 6 7 1 0\n 7 8 2 0\n 7 9 1 0\nM RGP 2 3 1 9 2\nM END\n> <Name>\n4-amino-3-hydroxybutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBux\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nCysteine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.4457 -1.1333 0.0000 C 0 0\n 0.1453 -0.3840 0.0000 C 0 0 2 0 0 0\n 0.1430 1.1168 0.0000 C 0 0\n -1.1573 1.8661 0.0000 S 0 0\n -1.1551 -1.1333 0.0000 N 0 0\n 1.4475 -2.3333 0.0000 O 0 0\n 2.4842 -0.5320 0.0000 R# 0 0\n -2.1942 -0.5331 0.0000 R# 0 0\n -1.1591 3.0661 0.0000 R# 0 0\n 6 1 2 0\n 1 2 1 0\n 1 7 1 0\n 2 5 1 0\n 2 3 1 1\n 3 4 1 0\n 5 8 1 0\n 4 9 1 0\nM RGP 3 7 2 8 1 9 3\nM END\n> <Name>\nCysteine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nC\n\n> <MonomerCode>\nC\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\ngamma-amino-beta-hydroxycyclohexanepentanoic acid\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -0.2371 -1.5700 0.0000 C 0 0 1 0 0 0\n 0.6555 -2.3431 0.0000 C 0 0 2 0 0 0\n 1.7711 -1.9566 0.0000 C 0 0\n 1.9943 -0.7972 0.0000 R# 0 0\n 2.6637 -2.7297 0.0000 O 0 0\n 0.4323 -3.5026 0.0000 O 0 0\n -1.3528 -1.9566 0.0000 N 0 0\n -2.2454 -1.1835 0.0000 R# 0 0\n -0.0140 -0.4106 0.0000 C 0 0\n -0.9066 0.3624 0.0000 C 0 0\n -0.6834 1.5218 0.0000 C 0 0\n -1.5759 2.2948 0.0000 C 0 0\n -1.3527 3.4542 0.0000 C 0 0\n -0.2370 3.8408 0.0000 C 0 0\n 0.6555 3.0677 0.0000 C 0 0\n 0.4324 1.9082 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 3 5 2 0\n 2 6 1 6\n 1 7 1 0\n 7 8 1 0\n 1 9 1 1\n 9 10 1 0\n 10 11 1 0\n 12 11 1 0\n 13 12 1 0\n 14 13 1 0\n 15 14 1 0\n 15 16 1 0\n 11 16 1 0\nM RGP 2 4 2 8 1\nM END\n> <Name>\ngamma-amino-beta-hydroxycyclohexanepentanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nCap\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-cyclohexylalanine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n 1.0999 0.2895 0.0000 C 0 0\n 1.0990 -1.2114 0.0000 C 0 0 1 0 0 0\n 2.3979 -1.9634 0.0000 C 0 0\n 2.3972 -3.1634 0.0000 O 0 0\n 3.4377 -1.3643 0.0000 R# 0 0\n -0.1999 -1.9634 0.0000 N 0 0\n -0.1990 1.0414 0.0000 C 0 0\n -1.2401 -1.3653 0.0000 R# 0 0\n -1.5000 3.2903 0.0000 C 0 0\n -0.2003 2.5413 0.0000 C 0 0\n -1.4973 0.2903 0.0000 C 0 0\n -2.7970 1.0391 0.0000 C 0 0\n -2.7982 2.5391 0.0000 C 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 1 7 1 0\n 6 8 1 0\n 10 7 1 0\n 7 11 1 0\n 9 10 1 0\n 11 12 1 0\n 12 13 1 0\n 9 13 1 0\nM RGP 2 5 2 8 1\nM END\n> <Name>\n3-cyclohexylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nCha\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\ncitrullin\n SciTegic07272112182D\n\n 13 12 0 0 1 0 999 V2000\n 0.8990 -0.6122 0.0000 C 0 0\n 0.8982 -2.1130 0.0000 C 0 0 1 0 0 0\n 2.1971 -2.8650 0.0000 C 0 0\n 2.1964 -4.0650 0.0000 O 0 0\n 3.2369 -2.2659 0.0000 R# 0 0\n -0.4007 -2.8650 0.0000 N 0 0\n -0.3998 0.1398 0.0000 C 0 0\n -1.4410 -2.2669 0.0000 R# 0 0\n -0.3989 1.6406 0.0000 C 0 0\n -1.6977 2.3925 0.0000 N 0 0\n -1.6969 3.8933 0.0000 C 0 0\n -0.6571 4.4924 0.0000 N 0 0\n -2.7355 4.4946 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 1 7 1 0\n 6 8 1 0\n 9 7 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 5 2 8 1\nM END\n> <Name>\ncitrullin\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nCit\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-sulfoalanine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 0.5437 0.7780 0.0000 C 0 0\n 0.5429 -0.7228 0.0000 C 0 0 1 0 0 0\n 1.8417 -1.4748 0.0000 C 0 0\n 1.8410 -2.6748 0.0000 O 0 0\n 2.8815 -0.8757 0.0000 R# 0 0\n -0.7560 -1.4748 0.0000 N 0 0\n -1.7964 -0.8767 0.0000 R# 0 0\n -0.7551 1.5300 0.0000 S 0 0\n -0.7544 2.7300 0.0000 O 0 0\n -1.7949 0.9309 0.0000 O 0 0\n -1.7940 2.1307 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 6 7 1 0\n 1 8 1 0\n 8 9 2 0\n 8 10 2 0\n 8 11 1 0\nM RGP 2 5 2 7 1\nM END\n> <Name>\n3-sulfoalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nCya\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nAspartic acid\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.6310 -1.5578 0.0000 C 0 0\n 1.6327 -2.7392 0.0000 O 0 0\n 0.3507 -0.8201 0.0000 C 0 0 1 0 0 0\n -0.9295 -1.5578 0.0000 N 0 0\n -1.9525 -0.9669 0.0000 R# 0 0\n 0.3485 0.6575 0.0000 C 0 0\n -0.9317 1.3952 0.0000 C 0 0\n -1.9542 0.8032 0.0000 O 0 0\n -0.9335 2.5766 0.0000 O 0 0\n 2.6534 -0.9658 0.0000 R# 0 0\n 0.0851 3.1751 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 7 8 2 0\n 7 9 1 0\n 1 10 1 0\n 9 11 1 0\nM RGP 3 5 1 10 2 11 3\nM END\n> <Name>\nAspartic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD\n\n> <MonomerCode>\nD\n\n> <MonomerNaturalAnalogCode>\nD\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\n2,4-diaminobutanoic acid\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 0.3641 0.6909 0.0000 C 0 0\n 0.3632 -0.8099 0.0000 C 0 0 1 0 0 0\n 1.6621 -1.5619 0.0000 C 0 0\n 1.6614 -2.7619 0.0000 O 0 0\n 2.7019 -0.9628 0.0000 R# 0 0\n -0.9356 -1.5619 0.0000 N 0 0\n -1.9760 -0.9638 0.0000 R# 0 0\n -0.9347 1.4429 0.0000 C 0 0\n -0.9339 2.9437 0.0000 N 0 0\n -1.9725 3.5449 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 6 7 1 0\n 1 8 1 0\n 8 9 1 0\n 9 10 1 0\nM RGP 3 5 2 7 1 10 3\nM END\n> <Name>\n2,4-diaminobutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDab\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\ndiaminopimelic acid\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n 0.8356 -0.3752 0.0000 C 0 0\n 0.8363 -1.8760 0.0000 C 0 0\n 2.1360 -2.6267 0.0000 C 0 0\n 2.1366 -3.8266 0.0000 O 0 0\n 3.1751 -2.0264 0.0000 R# 0 0\n -0.4632 -2.6267 0.0000 N 0 0\n -0.4641 0.3753 0.0000 C 0 0\n -0.4649 1.8761 0.0000 C 0 0\n -1.7646 2.6267 0.0000 C 0 0\n -1.7653 4.1275 0.0000 C 0 0\n -0.4637 -3.8268 0.0000 R# 0 0\n -0.7262 4.7276 0.0000 O 0 0\n -2.8045 4.7277 0.0000 O 0 0\n -0.2031 -1.2765 0.0000 N 0 0\n 2 1 1 0\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 1 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 6 11 1 0\n 10 12 1 0\n 10 13 2 0\n 2 14 1 0\nM RGP 2 5 2 11 1\nM END\n> <Name>\ndiaminopimelic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDpm\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2,3-diaminopropanoic acid\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 0.1449 1.1182 0.0000 C 0 0\n 0.1441 -0.3826 0.0000 C 0 0 1 0 0 0\n 1.4430 -1.1346 0.0000 C 0 0\n 1.4423 -2.3346 0.0000 O 0 0\n 2.4827 -0.5355 0.0000 R# 0 0\n -1.1548 -1.1346 0.0000 N 0 0\n -2.1952 -0.5365 0.0000 R# 0 0\n -1.1539 1.8702 0.0000 N 0 0\n -1.1532 3.0702 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 6 7 1 0\n 1 8 1 0\n 8 9 1 0\nM RGP 3 5 2 7 1 9 3\nM END\n> <Name>\n2,3-diaminopropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDpr\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\n2,7-diaminosuberic acid (2,7-diaminooctanedioic acid)\n SciTegic07272112182D\n\n 15 14 0 0 1 0 999 V2000\n 1.3903 -2.7806 0.0000 C 0 0 1 0 0 0\n 2.6907 -3.5299 0.0000 C 0 0\n 2.6925 -4.7299 0.0000 O 0 0\n 3.7292 -2.9286 0.0000 R# 0 0\n 0.0899 -3.5299 0.0000 N 0 0\n -0.9492 -2.9297 0.0000 R# 0 0\n 1.3880 -1.2798 0.0000 C 0 0\n 0.0877 -0.5305 0.0000 C 0 0\n 0.0854 0.9703 0.0000 C 0 0\n -1.2150 1.7195 0.0000 C 0 0\n -1.2173 3.2203 0.0000 C 0 0\n -2.5178 3.9696 0.0000 C 0 0\n -3.5562 3.3684 0.0000 O 0 0\n -2.5194 5.1696 0.0000 O 0 0\n -0.1788 3.8216 0.0000 N 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 5 6 1 0\n 1 7 1 1\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 12 14 2 0\n 11 15 1 0\nM RGP 2 4 2 6 1\nM END\n> <Name>\n2,7-diaminosuberic acid (2,7-diaminooctanedioic acid)\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDsu\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nGlutamic acid\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 0.3442 -1.4777 0.0000 C 0 0 1 0 0 0\n 1.6244 -2.2154 0.0000 C 0 0\n 1.6261 -3.3968 0.0000 O 0 0\n 2.6469 -1.6234 0.0000 R# 0 0\n -0.9361 -2.2154 0.0000 N 0 0\n -1.9591 -1.6245 0.0000 R# 0 0\n 0.3419 -0.0001 0.0000 C 0 0\n -0.9383 0.7375 0.0000 C 0 0\n -0.9406 2.2151 0.0000 C 0 0\n -1.9642 2.8049 0.0000 O 0 0\n 0.0819 2.8071 0.0000 O 0 0\n 0.0729 3.9885 0.0000 R# 0 0\n 2 1 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 5 6 1 0\n 1 7 1 1\n 7 8 1 0\n 8 9 1 0\n 9 10 2 0\n 9 11 1 0\n 11 12 1 0\nM RGP 3 4 2 6 1 12 3\nM END\n> <Name>\nGlutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nE\n\n> <MonomerCode>\nE\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nS-ethylthiocysteine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.8932 -2.0181 0.0000 C 0 0\n 0.5928 -1.2688 0.0000 C 0 0 2 0 0 0\n 0.5905 0.2320 0.0000 C 0 0\n -0.7098 0.9813 0.0000 S 0 0\n -0.7076 -2.0181 0.0000 N 0 0\n 1.8950 -3.2181 0.0000 O 0 0\n 2.9317 -1.4168 0.0000 R# 0 0\n -1.7467 -1.4179 0.0000 R# 0 0\n -0.7121 2.4821 0.0000 S 0 0\n -2.0125 3.2313 0.0000 C 0 0\n -2.0144 4.4314 0.0000 C 0 0\n 6 1 2 0\n 1 2 1 0\n 1 7 1 0\n 2 5 1 0\n 2 3 1 1\n 3 4 1 0\n 5 8 1 0\n 4 9 1 0\n 9 10 1 0\n 10 11 1 0\nM RGP 2 7 2 8 1\nM END\n> <Name>\nS-ethylthiocysteine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nEdc\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nPhenylalanine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.2052 2.5398 0.0000 C 0 0\n -1.5064 3.2860 0.0000 C 0 0\n -2.8032 2.5322 0.0000 C 0 0\n -2.7988 1.0322 0.0000 C 0 0\n -1.4976 0.2861 0.0000 C 0 0\n -0.2008 1.0398 0.0000 C 0 0\n 1.0995 0.2905 0.0000 C 0 0\n 1.1018 -1.2103 0.0000 C 0 0 2 0 0 0\n -0.1986 -1.9596 0.0000 N 0 0\n 2.4022 -1.9596 0.0000 C 0 0\n 2.4040 -3.1596 0.0000 O 0 0\n 3.4407 -1.3583 0.0000 R# 0 0\n -1.2376 -1.3593 0.0000 R# 0 0\n 1 2 1 0\n 1 6 2 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 1\n 8 9 1 0\n 8 10 1 0\n 10 11 2 0\n 10 12 1 0\n 9 13 1 0\nM RGP 2 12 2 13 1\nM END\n> <Name>\nPhenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nF\n\n> <MonomerCode>\nF\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nGlycine\n SciTegic07272112182D\n\n 6 5 0 0 1 0 999 V2000\n -0.3363 0.5346 0.0000 C 0 0\n 0.9929 -0.1107 0.0000 C 0 0\n 1.0782 -1.2890 0.0000 O 0 0\n 1.9709 0.5520 0.0000 R# 0 0\n -1.3260 -0.1107 0.0000 N 0 0\n -2.3797 0.4238 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 5 6 1 0\nM RGP 2 4 2 6 1\nM END\n> <Name>\nGlycine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nG\n\n> <MonomerCode>\nG\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\ngamma-glutamic acid\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 3.1627 -0.1074 0.0000 R# 0 0\n 2.1394 -1.8796 0.0000 O 0 0\n 2.1394 -0.6982 0.0000 C 0 0\n 1.1162 -0.1074 0.0000 C 0 0\n 0.0931 -0.6982 0.0000 C 0 0\n -2.9765 -0.1074 0.0000 R# 0 0\n -1.9534 -0.6982 0.0000 N 0 0\n 0.0929 1.6649 0.0000 R# 0 0\n -1.9534 1.6648 0.0000 O 0 0\n -0.9302 1.0741 0.0000 C 0 0\n -0.9302 -0.1075 0.0000 C 0 0 2 0 0 0\n 3 1 1 0\n 3 2 2 0\n 4 3 1 0\n 5 4 1 0\n 11 5 1 0\n 7 6 1 0\n 11 7 1 0\n 10 8 1 0\n 10 9 2 0\n 11 10 1 6\nM RGP 3 1 2 6 1 8 3\nM END\n> <Name>\ngamma-glutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nGgu\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\ngamma-carboxyglutamic acid\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n -2.0450 1.9399 0.0000 O 0 0\n -3.0677 0.1688 0.0000 R# 0 0\n -2.0451 0.7591 0.0000 C 0 0\n -2.0452 -1.6023 0.0000 R# 0 0\n -1.0226 -1.0121 0.0000 N 0 0\n -0.0001 -1.6024 0.0000 O 0 0\n 2.0450 -1.6025 0.0000 R# 0 0\n 1.0225 -1.0121 0.0000 C 0 0\n 3.0678 0.1686 0.0000 O 0 0\n 2.0452 1.9396 0.0000 O 0 0\n 2.0452 0.7590 0.0000 C 0 0\n 1.0226 0.1687 0.0000 C 0 0\n 0.0000 0.7591 0.0000 C 0 0\n -1.0226 0.1687 0.0000 C 0 0 1 0 0 0\n 3 1 2 0\n 3 2 1 0\n 14 3 1 6\n 5 4 1 0\n 14 5 1 0\n 8 6 2 0\n 8 7 1 0\n 12 8 1 0\n 11 9 1 0\n 11 10 2 0\n 12 11 1 0\n 13 12 1 0\n 14 13 1 0\nM RGP 3 2 3 4 1 7 2\nM END\n> <Name>\ngamma-carboxyglutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nGla\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\nglycolic acid\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n 0.5500 -0.5500 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 0.7003 1.7894 0.0000 O 0 0\n 2.5000 0.7500 0.0000 R# 0 0\n 1.1497 -1.5894 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\nM RGP 1 4 2\nM END\n> <Name>\nglycolic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nGlc\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\npyroglutamic acid\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n 9.1574 -4.5963 0.0000 C 0 0 1 0 0 0\n 7.6654 -4.4422 0.0000 C 0 0\n 7.3510 -2.9755 0.0000 C 0 0\n 8.6486 -2.2231 0.0000 C 0 0\n 9.9062 -5.8940 0.0000 C 0 0\n 8.7719 -1.0295 0.0000 O 0 0\n 9.3065 -6.9335 0.0000 O 0 0\n 9.7651 -3.2249 0.0000 N 0 0\n 11.1062 -5.8940 0.0000 R# 0 0\n 5 1 1 0\n 1 8 1 0\n 1 2 1 6\n 2 3 1 0\n 3 4 1 0\n 4 6 2 0\n 5 7 2 0\n 5 9 1 0\n 4 8 1 0\nM RGP 1 9 2\nM END\n> <Name>\npyroglutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nGlp\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nHistidine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n 1.8978 -1.6508 0.0000 C 0 0\n 1.8993 -2.5957 0.0000 O 0 0\n 0.8739 -1.0609 0.0000 C 0 0 1 0 0 0\n -0.1500 -1.6508 0.0000 N 0 0\n -0.9683 -1.1782 0.0000 R# 0 0\n 0.8720 0.1209 0.0000 C 0 0\n -0.1501 0.7098 0.0000 C 0 0\n -0.2771 1.8841 0.0000 C 0 0\n -1.4330 2.1263 0.0000 N 0 0\n -2.0205 1.1016 0.0000 C 0 0\n -1.2277 0.2263 0.0000 N 0 0\n 2.7155 -1.1774 0.0000 R# 0 0\n -2.0317 3.1449 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 8 7 2 0\n 9 8 1 0\n 10 9 1 0\n 11 7 1 0\n 11 10 2 0\n 1 12 1 0\n 9 13 1 0\nM RGP 3 5 1 12 2 13 3\nM END\n> <Name>\nHistidine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nH\n\n> <MonomerCode>\nH\n\n> <MonomerNaturalAnalogCode>\nH\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nhomoarginine\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n 2.6779 -3.2569 0.0000 C 0 0\n 1.3775 -2.5077 0.0000 C 0 0 2 0 0 0\n 1.3753 -1.0068 0.0000 C 0 0\n 0.0749 -0.2576 0.0000 C 0 0\n 0.0771 -3.2569 0.0000 N 0 0\n 2.6797 -4.4570 0.0000 O 0 0\n -1.2301 3.4933 0.0000 N 0 0\n -2.5305 4.2425 0.0000 C 0 0\n -3.5690 3.6414 0.0000 N 0 0\n -2.5322 5.4425 0.0000 N 0 0\n 3.7164 -2.6557 0.0000 R# 0 0\n -0.9620 -2.6568 0.0000 R# 0 0\n 0.0726 1.2433 0.0000 C 0 0\n -1.2278 1.9924 0.0000 C 0 0\n 6 1 2 0\n 1 2 1 0\n 1 11 1 0\n 2 5 1 0\n 2 3 1 1\n 3 4 1 0\n 7 8 1 0\n 8 10 2 0\n 8 9 1 0\n 5 12 1 0\n 4 13 1 0\n 13 14 1 0\n 7 14 1 0\nM RGP 2 11 2 12 1\nM END\n> <Name>\nhomoarginine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHar\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nhomocysteine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.6657 -1.5600 0.0000 C 0 0\n 0.3653 -0.8107 0.0000 C 0 0 2 0 0 0\n 0.3630 0.6901 0.0000 C 0 0\n -0.9396 2.9402 0.0000 S 0 0\n -0.9351 -1.5600 0.0000 N 0 0\n 1.6675 -2.7600 0.0000 O 0 0\n 2.7042 -0.9587 0.0000 R# 0 0\n -1.9742 -0.9598 0.0000 R# 0 0\n -1.9794 3.5393 0.0000 R# 0 0\n -0.9373 1.4394 0.0000 C 0 0\n 6 1 2 0\n 1 2 1 0\n 1 7 1 0\n 2 5 1 0\n 2 3 1 1\n 5 8 1 0\n 4 9 1 0\n 3 10 1 0\n 4 10 1 0\nM RGP 3 7 2 8 1 9 3\nM END\n> <Name>\nhomocysteine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHcy\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nhomohistidine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n 1.8022 -2.6822 0.0000 C 0 0\n 0.5019 -1.9329 0.0000 C 0 0 2 0 0 0\n 0.4996 -0.4321 0.0000 C 0 0\n -0.8031 1.8154 0.0000 C 0 0\n -0.0518 4.1233 0.0000 C 0 0\n -2.0160 2.6978 0.0000 C 0 0\n 0.4109 2.6965 0.0000 N 0 0\n -1.5517 4.1242 0.0000 N 0 0\n -0.7985 -2.6822 0.0000 N 0 0\n 1.8041 -3.8822 0.0000 O 0 0\n 2.8409 -2.0810 0.0000 R# 0 0\n -1.8377 -2.0820 0.0000 R# 0 0\n -0.8008 0.3172 0.0000 C 0 0\n 10 1 2 0\n 1 2 1 0\n 1 11 1 0\n 2 9 1 0\n 2 3 1 1\n 6 4 2 0\n 7 4 1 0\n 7 5 2 0\n 5 8 1 0\n 8 6 1 0\n 9 12 1 0\n 3 13 1 0\n 4 13 1 0\nM RGP 2 11 2 12 1\nM END\n> <Name>\nhomohistidine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHhs\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nH\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-hydroxyisovaleric acid\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 9.4238 -6.6063 0.0000 C 0 0\n 8.8334 -7.6296 0.0000 O 0 0\n 8.6853 -5.3265 0.0000 C 0 0 1 0 0 0\n 7.2077 -5.3296 0.0000 N 0 0\n 9.4237 -4.0465 0.0000 C 0 0\n 8.8333 -3.0233 0.0000 C 0 0\n 10.6051 -4.0465 0.0000 C 0 0\n 10.6052 -6.6063 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 3 5 1 1\n 5 6 1 0\n 5 7 1 0\n 1 8 1 0\nM RGP 1 8 2\nM END\n> <Name>\n2-hydroxyisovaleric acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHiv\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nhomoserine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.4457 -1.1333 0.0000 C 0 0\n 1.4475 -2.3333 0.0000 O 0 0\n -1.1551 -1.1333 0.0000 N 0 0\n 0.1453 -0.3840 0.0000 C 0 0 1 0 0 0\n 0.1430 1.1168 0.0000 C 0 0\n -1.1573 1.8661 0.0000 C 0 0\n 2.4842 -0.5320 0.0000 R# 0 0\n -2.1942 -0.5331 0.0000 R# 0 0\n -1.1591 3.0661 0.0000 O 0 0\n 2 1 2 0\n 1 4 1 0\n 1 7 1 0\n 4 3 1 0\n 4 5 1 1\n 5 6 1 0\n 3 8 1 0\n 6 9 1 0\nM RGP 2 7 2 8 1\nM END\n> <Name>\nhomoserine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHse\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-hydroxypentanoic acid\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 1.3000 0.7500 0.0000 C 0 0\n 0.7003 1.7894 0.0000 O 0 0\n -0.6500 -0.5500 0.0000 O 0 0\n 0.5500 -0.5500 0.0000 C 0 0 1 0 0 0\n 1.3000 -1.8500 0.0000 C 0 0\n 0.5500 -3.1500 0.0000 C 0 0\n 2.5000 0.7500 0.0000 R# 0 0\n 1.1497 -4.1894 0.0000 C 0 0\n 2 1 2 0\n 1 4 1 0\n 1 7 1 0\n 4 3 1 0\n 4 5 1 6\n 5 6 1 0\n 6 8 1 0\nM RGP 1 7 2\nM END\n> <Name>\n2-hydroxypentanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHva\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n5-hydroxylysine\n SciTegic07272112182D\n\n 13 12 0 0 1 0 999 V2000\n 2.1031 -2.6885 0.0000 C 0 0\n 0.8027 -1.9392 0.0000 C 0 0 2 0 0 0\n 0.8004 -0.4384 0.0000 C 0 0\n -0.5000 0.3109 0.0000 C 0 0\n -0.5022 1.8117 0.0000 C 0 0\n -1.8026 2.5609 0.0000 C 0 0\n -1.8049 4.0617 0.0000 N 0 0\n -0.4977 -2.6885 0.0000 N 0 0\n 2.1049 -3.8885 0.0000 O 0 0\n 3.1416 -2.0873 0.0000 R# 0 0\n -1.5368 -2.0884 0.0000 R# 0 0\n -2.8447 4.6608 0.0000 R# 0 0\n 0.5363 2.4129 0.0000 O 0 0\n 9 1 2 0\n 1 2 1 0\n 1 10 1 0\n 2 8 1 0\n 2 3 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 8 11 1 0\n 7 12 1 0\n 5 13 1 0\nM RGP 3 10 2 11 1 12 3\nM END\n> <Name>\n5-hydroxylysine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHyl\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\n4-hydroxyproline\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n 0.2044 1.3597 0.0000 C 0 0\n -1.2773 1.5932 0.0000 C 0 0 2 0 0 0\n -1.9573 0.2561 0.0000 C 0 0\n -0.8958 -0.8036 0.0000 N 0 0\n 0.4401 -0.1216 0.0000 C 0 0 2 0 0 0\n 1.7742 -0.8036 0.0000 C 0 0\n 1.8362 -2.0021 0.0000 O 0 0\n 2.7813 -0.1510 0.0000 R# 0 0\n -1.0827 -1.9890 0.0000 R# 0 0\n -1.8230 2.6620 0.0000 O 0 0\n 1 2 1 0\n 5 1 1 1\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 6 8 1 0\n 4 9 1 0\n 2 10 1 6\nM RGP 2 8 2 9 1\nM END\n> <Name>\n4-hydroxyproline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHyp\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nIsoleucine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n -1.2557 1.6681 0.0000 C 0 0\n 0.0245 0.9304 0.0000 C 0 0 1 0 0 0\n 0.0268 -0.5472 0.0000 C 0 0 2 0 0 0\n -1.2536 -1.2849 0.0000 N 0 0\n -2.2766 -0.6940 0.0000 R# 0 0\n 1.3069 -1.2849 0.0000 C 0 0\n 1.3086 -2.4664 0.0000 O 0 0\n 2.3294 -0.6930 0.0000 R# 0 0\n 1.0470 1.5223 0.0000 C 0 0\n -1.2574 2.8495 0.0000 C 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 3 6 1 0\n 6 7 2 0\n 6 8 1 0\n 2 9 1 6\n 1 10 1 0\nM RGP 2 5 1 8 2\nM END\n> <Name>\nIsoleucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nI\n\n> <MonomerCode>\nI\n\n> <MonomerNaturalAnalogCode>\nI\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nisovaline\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n -0.2631 1.6583 0.0000 C 0 0\n -0.2625 0.1806 0.0000 C 0 0 2 0 0 0\n -1.5417 -0.5583 0.0000 N 0 0\n -1.5423 -1.7399 0.0000 R# 0 0\n 1.0172 -0.5583 0.0000 C 0 0\n 1.0177 -1.7397 0.0000 O 0 0\n 2.0402 0.0326 0.0000 R# 0 0\n 0.8209 0.4757 0.0000 C 0 0\n -1.2863 2.2491 0.0000 C 0 0\n 2 1 1 1\n 3 2 1 0\n 3 4 1 0\n 2 5 1 0\n 5 6 2 0\n 5 7 1 0\n 2 8 1 0\n 1 9 1 0\nM RGP 2 4 1 7 2\nM END\n> <Name>\nisovaline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nIva\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nLysine\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 2.1478 -2.4874 0.0000 C 0 0\n 0.8474 -1.7382 0.0000 C 0 0 2 0 0 0\n 0.8451 -0.2373 0.0000 C 0 0\n -0.4553 0.5119 0.0000 C 0 0\n -0.4575 2.0128 0.0000 C 0 0\n -1.7579 2.7619 0.0000 C 0 0\n -1.7602 4.2628 0.0000 N 0 0\n -0.4530 -2.4874 0.0000 N 0 0\n 2.1495 -3.6875 0.0000 O 0 0\n 3.1863 -1.8862 0.0000 R# 0 0\n -1.4921 -1.8873 0.0000 R# 0 0\n -2.8000 4.8619 0.0000 R# 0 0\n 9 1 2 0\n 1 2 1 0\n 1 10 1 0\n 2 8 1 0\n 2 3 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 8 11 1 0\n 7 12 1 0\nM RGP 3 10 2 11 1 12 3\nM END\n> <Name>\nLysine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nK\n\n> <MonomerCode>\nK\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nLeucine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 0.3626 0.9903 0.0000 C 0 0\n -0.9395 2.9396 0.0000 C 0 0\n -0.9377 1.7396 0.0000 C 0 0\n -1.9763 1.1383 0.0000 C 0 0\n 0.3649 -0.5105 0.0000 C 0 0 1 0 0 0\n 1.6653 -1.2598 0.0000 C 0 0\n 1.6671 -2.4598 0.0000 O 0 0\n -0.9355 -1.2598 0.0000 N 0 0\n 2.7038 -0.6585 0.0000 R# 0 0\n -1.9746 -0.6596 0.0000 R# 0 0\n 3 1 1 0\n 5 1 1 1\n 3 2 1 0\n 3 4 1 0\n 5 8 1 0\n 5 6 1 0\n 6 7 2 0\n 6 9 1 0\n 8 10 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\nLeucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nL\n\n> <MonomerCode>\nL\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nlactic acid\n SciTegic07272112182D\n\n 6 5 0 0 1 0 999 V2000\n 0.5500 -0.5500 0.0000 C 0 0 1 0 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 0.7003 1.7894 0.0000 O 0 0\n 2.5000 0.7500 0.0000 R# 0 0\n 1.1497 -1.5894 0.0000 O 0 0\n -0.6500 -0.5500 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 1 6 1 1\nM RGP 1 4 2\nM END\n> <Name>\nlactic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLac\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nMethionine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.6657 -1.5600 0.0000 C 0 0\n -0.9351 -1.5600 0.0000 N 0 0\n 1.6675 -2.7600 0.0000 O 0 0\n 0.3653 -0.8107 0.0000 C 0 0 1 0 0 0\n 0.3630 0.6901 0.0000 C 0 0\n -0.9373 1.4394 0.0000 C 0 0\n -1.9794 3.5393 0.0000 C 0 0\n -0.9396 2.9402 0.0000 S 0 0\n 2.7042 -0.9587 0.0000 R# 0 0\n -1.9742 -0.9598 0.0000 R# 0 0\n 3 1 2 0\n 1 4 1 0\n 1 9 1 0\n 4 2 1 0\n 4 5 1 1\n 5 6 1 0\n 6 8 1 0\n 8 7 1 0\n 2 10 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\nMethionine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nM\n\n> <MonomerCode>\nM\n\n> <MonomerNaturalAnalogCode>\nM\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nmercaptoacetic acid\n SciTegic07272112182D\n\n 6 5 0 0 1 0 999 V2000\n 0.5500 1.3000 0.0000 C 0 0\n 1.3000 0.0000 0.0000 C 0 0\n 0.7003 -1.0394 0.0000 O 0 0\n 2.5000 0.0000 0.0000 R# 0 0\n 1.3000 2.6000 0.0000 S 0 0\n 0.7003 3.6394 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 5 6 1 0\nM RGP 2 4 2 6 3\nM END\n> <Name>\nmercaptoacetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nMaa\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n[R3]H\n\n$$$$\nmercaptobutanoic acid (GMBA)\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 0.5500 1.3000 0.0000 C 0 0 1 0 0 0\n 1.3000 0.0000 0.0000 C 0 0\n 0.7003 -1.0394 0.0000 O 0 0\n 2.5000 0.0000 0.0000 R# 0 0\n -0.9508 1.3031 0.0000 S 0 0\n -1.5494 2.3432 0.0000 R# 0 0\n 1.3000 2.6000 0.0000 C 0 0\n 0.7003 3.6394 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 5 6 1 0\n 1 7 1 1\n 7 8 1 0\nM RGP 2 4 2 6 3\nM END\n> <Name>\nmercaptobutanoic acid (GMBA)\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nMba\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n[R3]H\n\n$$$$\n4-methyl-3-hydroxyproline\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n 0.0644 0.9085 0.0000 C 0 0\n 0.8995 1.7437 0.0000 O 0 0\n 0.2491 -0.2580 0.0000 C 0 0 1 0 0 0\n 1.3016 -0.7942 0.0000 C 0 0\n 2.2921 -0.1510 0.0000 R# 0 0\n 1.3634 -1.9737 0.0000 O 0 0\n -0.8032 -0.7942 0.0000 N 0 0\n -0.9879 -1.9608 0.0000 R# 0 0\n -1.6383 0.0409 0.0000 C 0 0\n -1.1022 1.0932 0.0000 C 0 0\n -1.6384 2.1456 0.0000 C 0 0\n 1 2 1 0\n 3 1 1 1\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\n 7 3 1 0\n 7 8 1 0\n 9 7 1 0\n 10 9 1 0\n 1 10 1 0\n 10 11 1 0\nM RGP 2 5 2 8 1\nM END\n> <Name>\n4-methyl-3-hydroxyproline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nMhp\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nmercaptopropanoic acid\n SciTegic07272112182D\n\n 7 6 0 0 1 0 999 V2000\n 0.5500 1.3000 0.0000 C 0 0 1 0 0 0\n 1.3000 0.0000 0.0000 C 0 0\n 0.7003 -1.0394 0.0000 O 0 0\n 2.5000 0.0000 0.0000 R# 0 0\n 1.3000 2.6000 0.0000 S 0 0\n 0.7003 3.6394 0.0000 R# 0 0\n -0.6500 1.3000 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 5 6 1 0\n 1 7 1 6\nM RGP 2 4 2 6 3\nM END\n> <Name>\nmercaptopropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nMpa\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n[R3]H\n\n$$$$\nAsparagine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.8929 -1.4175 0.0000 C 0 0\n 1.8947 -2.5989 0.0000 O 0 0\n 0.6127 -0.6799 0.0000 C 0 0 1 0 0 0\n -0.6676 -1.4175 0.0000 N 0 0\n -1.6907 -0.8266 0.0000 R# 0 0\n 0.6104 0.7978 0.0000 C 0 0\n -0.6698 1.5354 0.0000 C 0 0\n -1.6922 0.9434 0.0000 N 0 0\n -0.6716 2.7168 0.0000 O 0 0\n 2.9153 -0.8255 0.0000 R# 0 0\n -2.5341 1.7724 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 7 8 1 0\n 7 9 2 0\n 1 10 1 0\n 8 11 1 0\nM RGP 3 5 1 10 2 11 3\nM END\n> <Name>\nAsparagine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nN\n\n> <MonomerCode>\nN\n\n> <MonomerNaturalAnalogCode>\nN\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\n3-naphthylalanine\n SciTegic07272112182D\n\n 17 18 0 0 1 0 999 V2000\n 1.8370 -0.7903 0.0000 C 0 0\n 1.8392 -2.2912 0.0000 C 0 0 1 0 0 0\n 3.1396 -3.0405 0.0000 C 0 0\n 0.5388 -3.0405 0.0000 N 0 0\n 3.1415 -4.2404 0.0000 O 0 0\n 4.1781 -2.4393 0.0000 R# 0 0\n -0.5003 -2.4402 0.0000 R# 0 0\n -2.0658 1.4514 0.0000 C 0 0\n -3.3671 2.1976 0.0000 C 0 0\n -3.3714 3.6975 0.0000 C 0 0\n -2.0746 4.4513 0.0000 C 0 0\n -0.7734 3.7051 0.0000 C 0 0\n -0.7689 2.2052 0.0000 C 0 0\n 0.5322 1.4589 0.0000 C 0 0\n 0.5367 -0.0410 0.0000 C 0 0\n -0.7602 -0.7949 0.0000 C 0 0\n -2.0614 -0.0487 0.0000 C 0 0\n 2 1 1 1\n 4 2 1 0\n 2 3 1 0\n 3 5 2 0\n 3 6 1 0\n 4 7 1 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 14 15 2 0\n 15 16 1 0\n 16 17 2 0\n 8 13 2 0\n 8 17 1 0\n 13 14 1 0\n 15 1 1 0\nM RGP 2 6 2 7 1\nM END\n> <Name>\n3-naphthylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNal\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nnorleucine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 0.3630 0.6901 0.0000 C 0 0\n -0.9373 1.4394 0.0000 C 0 0\n -0.9396 2.9402 0.0000 C 0 0\n 0.3653 -0.8107 0.0000 C 0 0 1 0 0 0\n 1.6657 -1.5600 0.0000 C 0 0\n 1.6675 -2.7600 0.0000 O 0 0\n -0.9351 -1.5600 0.0000 N 0 0\n 2.7042 -0.9587 0.0000 R# 0 0\n -1.9742 -0.9598 0.0000 R# 0 0\n -1.9794 3.5393 0.0000 C 0 0\n 2 1 1 0\n 4 1 1 1\n 2 3 1 0\n 4 7 1 0\n 4 5 1 0\n 5 6 2 0\n 5 8 1 0\n 7 9 1 0\n 3 10 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\nnorleucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNle\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nnitrotyrosine\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n 0.3609 -1.4586 0.0000 C 0 0\n 1.3835 -0.8682 0.0000 R# 0 0\n -0.6616 -0.8683 0.0000 C 0 0 2 0 0 0\n -0.6616 0.3125 0.0000 C 0 0\n 0.3609 0.9029 0.0000 C 0 0\n 0.3608 2.0837 0.0000 C 0 0\n 1.3834 2.6741 0.0000 C 0 0\n 2.4059 2.0838 0.0000 C 0 0\n 3.4285 2.6742 0.0000 O 0 0\n 2.4060 0.9030 0.0000 C 0 0\n 1.3835 0.3126 0.0000 C 0 0\n -1.6842 -1.4586 0.0000 N 0 0\n -2.7068 -0.8684 0.0000 N 0 0\n -2.7068 0.3124 0.0000 O 0 0\n -3.7293 -1.4588 0.0000 O 0 0\n -1.6841 -2.6394 0.0000 R# 0 0\n 0.3610 -2.6393 0.0000 O 0 0\n 1 2 1 0\n 1 3 1 0\n 3 4 1 1\n 4 5 1 0\n 6 5 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 8 10 1 0\n 10 11 2 0\n 11 5 1 0\n 3 12 1 0\n 12 13 1 0\n 13 14 2 0\n 13 15 2 0\n 12 16 1 0\n 17 1 2 0\nM RGP 2 2 2 16 1\nM END\n> <Name>\nnitrotyrosine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNty\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nnorvaline\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.4457 -1.1333 0.0000 C 0 0\n 0.1453 -0.3840 0.0000 C 0 0 2 0 0 0\n 0.1430 1.1168 0.0000 C 0 0\n -1.1573 1.8661 0.0000 C 0 0\n 1.4475 -2.3333 0.0000 O 0 0\n -1.1551 -1.1333 0.0000 N 0 0\n 2.4842 -0.5320 0.0000 R# 0 0\n -2.1942 -0.5331 0.0000 R# 0 0\n -1.1591 3.0661 0.0000 C 0 0\n 5 1 2 0\n 1 2 1 0\n 1 7 1 0\n 2 6 1 0\n 2 3 1 1\n 3 4 1 0\n 6 8 1 0\n 4 9 1 0\nM RGP 2 7 2 8 1\nM END\n> <Name>\nnorvaline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNva\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-carboxyocthydroindole\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n 2.0870 -0.8839 0.0000 C 0 0\n 3.0775 -0.2406 0.0000 R# 0 0\n 1.0346 -0.3477 0.0000 C 0 0 2 0 0 0\n 0.8498 0.8189 0.0000 C 0 0\n -0.3168 1.0037 0.0000 C 0 0\n -0.8529 -0.0487 0.0000 C 0 0\n -2.0324 -0.1106 0.0000 C 0 0\n -2.6757 0.8800 0.0000 C 0 0\n -2.1395 1.9323 0.0000 C 0 0\n -0.9601 1.9942 0.0000 C 0 0\n -0.0178 -0.8839 0.0000 N 0 0\n -0.2025 -2.0504 0.0000 R# 0 0\n 2.1488 -2.0633 0.0000 O 0 0\n 1 2 1 0\n 1 3 1 0\n 3 4 1 1\n 4 5 1 0\n 6 5 1 0\n 7 6 1 0\n 8 7 1 0\n 9 8 1 0\n 10 5 1 0\n 10 9 1 0\n 6 11 1 0\n 3 11 1 0\n 11 12 1 0\n 13 1 2 0\nM RGP 2 2 2 12 1\nM END\n> <Name>\n2-carboxyocthydroindole\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOic\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nL-ornithine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.8932 -2.0181 0.0000 C 0 0\n 0.5928 -1.2688 0.0000 C 0 0 2 0 0 0\n 0.5905 0.2320 0.0000 C 0 0\n -0.7098 0.9813 0.0000 C 0 0\n -2.0125 3.2313 0.0000 N 0 0\n -0.7076 -2.0181 0.0000 N 0 0\n 1.8950 -3.2181 0.0000 O 0 0\n 2.9317 -1.4168 0.0000 R# 0 0\n -1.7467 -1.4179 0.0000 R# 0 0\n -2.0144 4.4314 0.0000 R# 0 0\n -0.7121 2.4821 0.0000 C 0 0\n 7 1 2 0\n 1 2 1 0\n 1 8 1 0\n 2 6 1 0\n 2 3 1 1\n 3 4 1 0\n 6 9 1 0\n 5 10 1 0\n 4 11 1 0\n 11 5 1 0\nM RGP 3 8 2 9 1 10 3\nM END\n> <Name>\nL-ornithine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOrn\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nProline\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n 0.0018 1.6555 0.0000 C 0 0\n -1.4799 1.8890 0.0000 C 0 0\n -2.1599 0.5519 0.0000 C 0 0\n -1.0984 -0.5079 0.0000 N 0 0\n 0.2376 0.1741 0.0000 C 0 0 2 0 0 0\n 1.5717 -0.5079 0.0000 C 0 0\n 1.6336 -1.7063 0.0000 O 0 0\n 2.5787 0.1448 0.0000 R# 0 0\n -1.2852 -1.6933 0.0000 R# 0 0\n 1 2 1 0\n 5 1 1 1\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 6 8 1 0\n 4 9 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\nProline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nP\n\n> <MonomerCode>\nP\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\npenicillamine (3-mercaptovaline)\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.3220 -1.5015 0.0000 C 0 0\n 0.0231 -0.7495 0.0000 C 0 0 2 0 0 0\n 1.0637 1.3504 0.0000 C 0 0\n 0.0239 0.7513 0.0000 C 0 0\n 0.0252 1.9513 0.0000 C 0 0\n 1.3213 -2.7015 0.0000 O 0 0\n -1.2758 -1.5015 0.0000 N 0 0\n 2.3618 -0.9024 0.0000 R# 0 0\n -2.3162 -0.9034 0.0000 R# 0 0\n -1.2749 1.5033 0.0000 S 0 0\n -1.2742 2.7033 0.0000 R# 0 0\n 6 1 2 0\n 1 2 1 0\n 1 8 1 0\n 2 7 1 0\n 2 4 1 1\n 4 3 1 0\n 4 5 1 0\n 7 9 1 0\n 4 10 1 0\n 10 11 1 0\nM RGP 3 8 2 9 1 11 3\nM END\n> <Name>\npenicillamine (3-mercaptovaline)\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPen\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\n2-phenylglycine\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.1105 -1.1869 0.0000 C 0 0 1 0 0 0\n 1.1883 -1.9388 0.0000 C 0 0\n 1.1876 -3.1389 0.0000 O 0 0\n -1.4095 -1.9388 0.0000 N 0 0\n 2.2281 -1.3398 0.0000 R# 0 0\n -2.4498 -1.3407 0.0000 R# 0 0\n 1.1953 2.5605 0.0000 C 0 0\n -0.1018 3.3139 0.0000 C 0 0\n -1.4027 2.5674 0.0000 C 0 0\n -1.4067 1.0675 0.0000 C 0 0\n -0.1097 0.3140 0.0000 C 0 0\n 1.1914 1.0606 0.0000 C 0 0\n 4 1 1 0\n 1 2 1 0\n 2 3 2 0\n 2 5 1 0\n 4 6 1 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 10 11 2 0\n 11 12 1 0\n 7 12 2 0\n 1 11 1 1\nM RGP 2 5 2 6 1\nM END\n> <Name>\n2-phenylglycine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhg\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nPiperazine quinazolinone acetic acid, 2-(4-oxo-6-piperazin-1-yl-quinazolin-3-yl)acetic acid\n SciTegic07272112182D\n\n 22 24 0 0 1 0 999 V2000\n 1.0933 1.6152 0.0000 C 0 0\n -0.0398 2.5980 0.0000 C 0 0\n -1.4576 2.1082 0.0000 C 0 0\n -1.7421 0.6354 0.0000 C 0 0\n -0.6090 -0.3475 0.0000 C 0 0\n 0.8087 0.1425 0.0000 C 0 0\n 1.9419 -0.8404 0.0000 C 0 0\n 3.3596 -0.3504 0.0000 N 0 0\n 3.6442 1.1223 0.0000 C 0 0\n 2.5111 2.1052 0.0000 C 0 0\n -3.4430 -1.3280 0.0000 C 0 0\n -4.8599 -1.8203 0.0000 C 0 0\n -5.9946 -0.8392 0.0000 N 0 0\n -5.7124 0.6340 0.0000 C 0 0\n -4.2954 1.1262 0.0000 C 0 0\n -3.1606 0.1453 0.0000 N 0 0\n -7.1282 -1.2330 0.0000 R# 0 0\n 4.4954 -1.3315 0.0000 C 0 0\n 5.9133 -0.8392 0.0000 C 0 0\n 1.7143 -2.0185 0.0000 O 0 0\n 6.1389 0.3393 0.0000 R# 0 0\n 6.8214 -1.6237 0.0000 O 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 7 8 1 0\n 8 9 1 0\n 9 10 2 0\n 1 6 1 0\n 1 10 1 0\n 6 7 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 11 16 1 0\n 4 16 1 0\n 13 17 1 0\n 8 18 1 0\n 18 19 1 0\n 7 20 2 0\n 19 21 1 0\n 19 22 2 0\nM RGP 2 17 1 21 2\nM END\n> <Name>\nPiperazine quinazolinone acetic acid, 2-(4-oxo-6-piperazin-1-yl-quinazolin-3-yl)acetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPqa\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nGlutamine\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 1.6237 -2.2154 0.0000 C 0 0\n 1.6254 -3.3969 0.0000 O 0 0\n 0.3435 -1.4777 0.0000 C 0 0 1 0 0 0\n -0.9368 -2.2154 0.0000 N 0 0\n -1.9598 -1.6245 0.0000 R# 0 0\n 0.3413 -0.0001 0.0000 C 0 0\n -0.9389 0.7376 0.0000 C 0 0\n -0.9411 2.2152 0.0000 C 0 0\n 0.0813 2.8071 0.0000 N 0 0\n -1.9648 2.8050 0.0000 O 0 0\n 2.6462 -1.6235 0.0000 R# 0 0\n 0.0799 3.9885 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 8 10 2 0\n 1 11 1 0\n 9 12 1 0\nM RGP 3 5 1 11 2 12 3\nM END\n> <Name>\nGlutamine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nQ\n\n> <MonomerCode>\nQ\n\n> <MonomerNaturalAnalogCode>\nQ\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nArginine\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n 1.7718 -2.5891 0.0000 C 0 0\n 1.7732 -3.5337 0.0000 O 0 0\n 0.7483 -1.9994 0.0000 C 0 0 1 0 0 0\n -0.2752 -2.5891 0.0000 N 0 0\n -1.0932 -2.1168 0.0000 R# 0 0\n 0.7464 -0.8182 0.0000 C 0 0\n -0.2771 -0.2284 0.0000 C 0 0\n -0.2789 0.9529 0.0000 C 0 0\n -1.3024 1.5426 0.0000 N 0 0\n -1.3042 2.7238 0.0000 C 0 0\n -0.4868 3.1971 0.0000 N 0 0\n -2.1227 3.1955 0.0000 N 0 0\n 2.5892 -2.1159 0.0000 R# 0 0\n -0.4883 4.3786 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 10 12 2 0\n 1 13 1 0\n 11 14 1 0\nM RGP 3 5 1 13 2 14 3\nM END\n> <Name>\nArginine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nR\n\n> <MonomerCode>\nR\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nSerine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.3671 -1.0829 0.0000 C 0 0\n 1.3689 -2.2643 0.0000 O 0 0\n 0.0869 -0.3452 0.0000 C 0 0 1 0 0 0\n -1.1934 -1.0829 0.0000 N 0 0\n -2.2165 -0.4920 0.0000 R# 0 0\n 0.0847 1.1324 0.0000 C 0 0\n -0.9391 1.7222 0.0000 O 0 0\n 2.3896 -0.4909 0.0000 R# 0 0\n -0.9481 2.9036 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 1 8 1 0\n 7 9 1 0\nM RGP 3 5 1 8 2 9 3\nM END\n> <Name>\nSerine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nS\n\n> <MonomerCode>\nS\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nsarcosine (N-methylglycine)\n SciTegic07272112182D\n\n 7 6 0 0 0 0 999 V2000\n 0.0000 0.6750 0.0000 C 0 0\n 1.0229 0.0844 0.0000 C 0 0\n 2.0458 0.6749 0.0000 R# 0 0\n 1.0228 -1.0968 0.0000 O 0 0\n -1.0229 0.0844 0.0000 N 0 0\n -2.0457 0.6750 0.0000 C 0 0\n -1.0229 -1.0967 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\n 5 1 1 0\n 5 6 1 0\n 5 7 1 0\nM RGP 2 3 2 7 1\nM END\n> <Name>\nsarcosine (N-methylglycine)\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nSar\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n1-amino-1-carboxycyclopentane\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n 1.0834 0.6054 0.0000 C 0 0\n -0.1301 -0.2763 0.0000 C 0 0 1 0 0 0\n -1.3437 0.6051 0.0000 C 0 0\n -0.8803 2.0318 0.0000 C 0 0\n 0.6197 2.0320 0.0000 C 0 0\n -1.4300 -0.9996 0.0000 N 0 0\n 1.1702 -0.9996 0.0000 C 0 0\n 1.1712 -2.1996 0.0000 O 0 0\n 2.2090 -0.3991 0.0000 R# 0 0\n -2.4695 -0.4001 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 1\n 3 4 1 0\n 4 5 1 0\n 1 5 1 0\n 2 6 1 0\n 2 7 1 0\n 7 8 2 0\n 7 9 1 0\n 6 10 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\n1-amino-1-carboxycyclopentane\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nSpg\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nstatin (4-amino-3-hydroxy-6-methylheptanoic acid)\n SciTegic07272112182D\n\n 13 12 0 0 1 0 999 V2000\n -1.6523 -1.7716 0.0000 R# 0 0\n -1.6523 -0.5905 0.0000 N 0 0\n -0.6295 0.0000 0.0000 C 0 0 1 0 0 0\n -0.6295 1.1811 0.0000 C 0 0\n -1.6524 1.7717 0.0000 C 0 0\n -2.6752 1.1811 0.0000 C 0 0\n -1.6523 2.9528 0.0000 C 0 0\n 0.3934 -0.5906 0.0000 C 0 0 1 0 0 0\n 0.3934 -1.7717 0.0000 O 0 0\n 1.4162 -0.0001 0.0000 C 0 0\n 2.4391 -0.5905 0.0000 C 0 0\n 2.4391 -1.7716 0.0000 O 0 0\n 3.4620 0.0000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 1\n 4 5 1 0\n 5 6 1 0\n 5 7 1 0\n 3 8 1 0\n 8 9 1 6\n 8 10 1 0\n 10 11 1 0\n 11 12 2 0\n 11 13 1 0\nM RGP 2 1 1 13 2\nM END\n> <Name>\nstatin (4-amino-3-hydroxy-6-methylheptanoic acid)\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nSta\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nThreonine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.0488 -1.2558 0.0000 C 0 0\n 1.0481 -2.4369 0.0000 O 0 0\n -0.2297 -0.5156 0.0000 C 0 0 1 0 0 0\n -1.5081 -1.2558 0.0000 N 0 0\n -2.5321 -0.6672 0.0000 R# 0 0\n -0.2289 0.9614 0.0000 C 0 0 2 0 0 0\n 0.7944 1.5510 0.0000 O 0 0\n -1.2510 1.5531 0.0000 C 0 0\n 2.0720 -0.6661 0.0000 R# 0 0\n 0.7866 2.7318 0.0000 R# 0 0\n 2 1 2 0\n 3 1 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 1\n 6 8 1 0\n 1 9 1 0\n 7 10 1 0\nM RGP 3 5 1 9 2 10 3\nM END\n> <Name>\nThreonine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nT\n\n> <MonomerCode>\nT\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\n3-thienylalanine\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n 0.8925 0.4864 0.0000 C 0 0\n 0.8948 -1.0144 0.0000 C 0 0 1 0 0 0\n 2.1952 -1.7637 0.0000 C 0 0\n -0.4056 -1.7637 0.0000 N 0 0\n 2.1969 -2.9637 0.0000 O 0 0\n 3.2337 -1.1625 0.0000 R# 0 0\n -1.4447 -1.1635 0.0000 R# 0 0\n -2.7811 1.7319 0.0000 C 0 0\n -2.0350 3.0332 0.0000 C 0 0\n -0.5669 2.7257 0.0000 S 0 0\n -0.4056 1.2344 0.0000 C 0 0\n -1.7742 0.6202 0.0000 C 0 0\n 2 1 1 1\n 4 2 1 0\n 2 3 1 0\n 3 5 2 0\n 3 6 1 0\n 4 7 1 0\n 8 9 2 0\n 9 10 1 0\n 10 11 1 0\n 11 12 2 0\n 8 12 1 0\n 11 1 1 0\nM RGP 2 6 2 7 1\nM END\n> <Name>\n3-thienylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nThi\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -1.4700 3.5026 0.0000 C 0 0\n -2.7681 2.7511 0.0000 C 0 0\n -2.7664 1.2510 0.0000 C 0 0\n -1.4665 0.5026 0.0000 C 0 0\n -0.1683 1.2542 0.0000 C 0 0\n -0.1701 2.7542 0.0000 C 0 0\n -1.4646 -0.9974 0.0000 C 0 0\n -0.1647 -1.7458 0.0000 N 0 0\n 1.1334 -0.9943 0.0000 C 0 0 1 0 0 0\n 1.1317 0.5057 0.0000 C 0 0\n 2.4326 -1.7458 0.0000 C 0 0\n 3.4721 -1.1463 0.0000 R# 0 0\n 2.4323 -2.9458 0.0000 O 0 0\n -0.1633 -2.9459 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 5 6 1 0\n 1 6 2 0\n 5 10 1 0\n 4 5 2 0\n 4 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 1\n 9 11 1 0\n 11 12 1 0\n 11 13 2 0\n 8 14 1 0\nM RGP 2 12 2 14 1\nM END\n> <Name>\n1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTic\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-methylvaline\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.1685 -1.2160 0.0000 C 0 0\n -0.1303 -0.4641 0.0000 C 0 0 2 0 0 0\n -1.1680 1.6379 0.0000 C 0 0\n -0.1295 1.0368 0.0000 C 0 0\n 0.9103 1.6358 0.0000 C 0 0\n 1.1678 -2.4161 0.0000 O 0 0\n -1.4292 -1.2160 0.0000 N 0 0\n 2.2083 -0.6170 0.0000 R# 0 0\n -2.4696 -0.6180 0.0000 R# 0 0\n -0.1282 2.2367 0.0000 C 0 0\n 6 1 2 0\n 1 2 1 0\n 1 8 1 0\n 2 7 1 0\n 2 4 1 1\n 4 3 1 0\n 4 5 1 0\n 7 9 1 0\n 4 10 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\n3-methylvaline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTle\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nepsilon-N-trimethyllysine\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n 2.3251 -3.2251 0.0000 C 0 0\n 1.0248 -2.4758 0.0000 C 0 0 2 0 0 0\n 1.0225 -0.9750 0.0000 C 0 0\n -0.2779 -0.2257 0.0000 C 0 0\n -0.2802 1.2751 0.0000 C 0 0\n -1.5805 2.0243 0.0000 C 0 0\n -1.5828 3.5251 0.0000 N 0 3\n -0.2756 -3.2251 0.0000 N 0 0\n 2.3269 -4.4251 0.0000 O 0 0\n 3.3637 -2.6238 0.0000 R# 0 0\n -1.3148 -2.6249 0.0000 R# 0 0\n -2.6226 4.1243 0.0000 C 0 0\n -0.5443 4.1264 0.0000 C 0 0\n -1.5841 4.7252 0.0000 C 0 0\n 9 1 2 0\n 1 2 1 0\n 1 10 1 0\n 2 8 1 0\n 2 3 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 8 11 1 0\n 7 12 1 0\n 7 13 1 0\n 7 14 1 0\nM CHG 1 7 1\nM RGP 2 10 2 11 1\nM END\n> <Name>\nepsilon-N-trimethyllysine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTml\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-thiazolylalanine\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n 0.8925 0.4863 0.0000 C 0 0\n 0.8948 -1.0144 0.0000 C 0 0 1 0 0 0\n 2.1952 -1.7637 0.0000 C 0 0\n -0.4056 -1.7637 0.0000 N 0 0\n 2.1970 -2.9637 0.0000 O 0 0\n 3.2337 -1.1625 0.0000 R# 0 0\n -1.4447 -1.1635 0.0000 R# 0 0\n -0.5669 2.7257 0.0000 N 0 0\n -0.4057 1.2344 0.0000 C 0 0\n -1.7742 0.6202 0.0000 C 0 0\n -2.7811 1.7319 0.0000 S 0 0\n -2.0350 3.0333 0.0000 C 0 0\n 2 1 1 1\n 4 2 1 0\n 2 3 1 0\n 3 5 2 0\n 3 6 1 0\n 4 7 1 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 1 0\n 8 12 2 0\n 9 1 1 0\nM RGP 2 6 2 7 1\nM END\n> <Name>\n3-thiazolylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTza\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nValine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.1543 -0.9675 0.0000 C 0 0\n -0.1446 -0.2156 0.0000 C 0 0 2 0 0 0\n -1.1823 1.8865 0.0000 C 0 0\n -0.1438 1.2853 0.0000 C 0 0\n 0.8960 1.8843 0.0000 C 0 0\n 1.1536 -2.1676 0.0000 O 0 0\n -1.4435 -0.9675 0.0000 N 0 0\n 2.1941 -0.3685 0.0000 R# 0 0\n -2.4838 -0.3695 0.0000 R# 0 0\n 6 1 2 0\n 1 2 1 0\n 1 8 1 0\n 2 7 1 0\n 2 4 1 1\n 4 3 1 0\n 4 5 1 0\n 7 9 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\nValine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nV\n\n> <MonomerCode>\nV\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nTryptophan\n SciTegic07272112182D\n\n 17 18 0 0 1 0 999 V2000\n 2.0938 -2.3551 0.0000 C 0 0\n 2.0952 -3.3000 0.0000 O 0 0\n 1.0698 -1.7652 0.0000 C 0 0 1 0 0 0\n 0.0459 -2.3551 0.0000 N 0 0\n -0.7723 -1.8826 0.0000 R# 0 0\n 1.0680 -0.5835 0.0000 C 0 0\n 0.0458 0.0055 0.0000 C 0 0\n -1.0319 -0.4779 0.0000 C 0 0\n -1.8246 0.3978 0.0000 N 0 0\n -1.2370 1.4216 0.0000 C 0 0\n -0.0810 1.1793 0.0000 C 0 0\n 0.7068 2.0591 0.0000 C 0 0\n 0.3387 3.1814 0.0000 C 0 0\n -0.8173 3.4238 0.0000 C 0 0\n -1.6051 2.5438 0.0000 C 0 0\n 2.9114 -1.8818 0.0000 R# 0 0\n -3.0061 0.3887 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 8 7 2 0\n 9 8 1 0\n 10 9 1 0\n 11 7 1 0\n 11 10 2 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 15 10 1 0\n 14 15 2 0\n 1 16 1 0\n 9 17 1 0\nM RGP 3 5 1 16 2 17 3\nM END\n> <Name>\nTryptophan\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nW\n\n> <MonomerCode>\nW\n\n> <MonomerNaturalAnalogCode>\nW\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nalpha-amino-2,4-dioxopyrimidinepropanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n 1.3004 -0.1276 0.0000 C 0 0\n 1.3027 -1.6284 0.0000 C 0 0 1 0 0 0\n 2.6030 -2.3777 0.0000 C 0 0\n 0.0023 -2.3777 0.0000 N 0 0\n 2.6048 -3.5777 0.0000 O 0 0\n 3.6416 -1.7764 0.0000 R# 0 0\n -1.0369 -1.7774 0.0000 R# 0 0\n -1.3056 2.8679 0.0000 N 0 0\n -0.0044 2.1216 0.0000 C 0 0\n 0.0000 0.6217 0.0000 N 0 0\n -1.2969 -0.1321 0.0000 C 0 0\n -2.5980 0.6141 0.0000 C 0 0\n -2.6025 2.1140 0.0000 C 0 0\n -3.6435 2.7110 0.0000 O 0 0\n 1.0330 2.7248 0.0000 O 0 0\n 2 1 1 1\n 4 2 1 0\n 2 3 1 0\n 3 5 2 0\n 3 6 1 0\n 4 7 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 8 13 1 0\n 13 14 2 0\n 9 15 2 0\n 10 1 1 0\nM RGP 2 6 2 7 1\nM END\n> <Name>\nalpha-amino-2,4-dioxopyrimidinepropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nWil\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nTyrosine\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n 2.2957 -1.9502 0.0000 C 0 0\n 2.2972 -2.8951 0.0000 O 0 0\n 1.2718 -1.3602 0.0000 C 0 0 1 0 0 0\n 0.2479 -1.9502 0.0000 N 0 0\n -0.5703 -1.4776 0.0000 R# 0 0\n 1.2701 -0.1785 0.0000 C 0 0\n 0.2461 0.4114 0.0000 C 0 0\n 0.2426 1.5925 0.0000 C 0 0\n -0.7820 2.1801 0.0000 C 0 0\n -1.8031 1.5866 0.0000 C 0 0\n -1.7996 0.4055 0.0000 C 0 0\n -0.7751 -0.1820 0.0000 C 0 0\n -2.6228 2.0566 0.0000 O 0 0\n 3.1134 -1.4768 0.0000 R# 0 0\n -2.6319 3.2381 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 8 7 1 0\n 9 8 2 0\n 10 9 1 0\n 11 10 2 0\n 12 7 2 0\n 12 11 1 0\n 10 13 1 0\n 1 14 1 0\n 13 15 1 0\nM RGP 3 5 1 14 2 15 3\nM END\n> <Name>\nTyrosine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nY\n\n> <MonomerCode>\nY\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nN-Terminal Acetic Acid\n SciTegic07272112182D\n\n 4 3 0 0 1 0 999 V2000\n 0.7003 1.7894 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 0.7003 -0.2894 0.0000 O 0 0\n 2.5000 0.7500 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\nM RGP 1 4 2\nM END\n> <Name>\nN-Terminal Acetic Acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nac\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nC-Terminal amine\n SciTegic07272112182D\n\n 2 1 0 0 1 0 999 V2000\n 2.5000 0.7500 0.0000 N 0 0\n 1.3000 0.7500 0.0000 R# 0 0\n 1 2 1 0\nM RGP 1 2 1\nM END\n> <Name>\nC-Terminal amine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nam\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nD-Alanine\n SciTegic07272112182D\n\n 7 6 0 0 1 0 999 V2000\n -1.2546 -0.3919 0.0000 N 0 0\n -0.2719 0.2632 0.0000 C 0 0 2 0 0 0\n -0.3102 1.7388 0.0000 C 0 0\n 1.0520 -0.3919 0.0000 C 0 0\n 1.0826 -1.5717 0.0000 O 0 0\n 2.0347 0.2632 0.0000 R# 0 0\n -2.3327 0.0905 0.0000 R# 0 0\n 2 1 1 0\n 2 3 1 6\n 2 4 1 0\n 4 5 2 0\n 4 6 1 0\n 1 7 1 0\nM RGP 2 6 2 7 1\nM END\n> <Name>\nD-Alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Cysteine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.4457 -1.1333 0.0000 C 0 0\n 0.1453 -0.3840 0.0000 C 0 0 1 0 0 0\n 0.1430 1.1168 0.0000 C 0 0\n -1.1573 1.8661 0.0000 S 0 0\n -1.1551 -1.1333 0.0000 N 0 0\n 1.4475 -2.3333 0.0000 O 0 0\n 2.4842 -0.5320 0.0000 R# 0 0\n -2.1942 -0.5331 0.0000 R# 0 0\n -1.1591 3.0661 0.0000 R# 0 0\n 6 1 2 0\n 1 2 1 0\n 1 7 1 0\n 2 5 1 0\n 2 3 1 6\n 3 4 1 0\n 5 8 1 0\n 4 9 1 0\nM RGP 3 7 2 8 1 9 3\nM END\n> <Name>\nD-Cysteine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Aspartic acid\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.6248 -1.5501 0.0000 C 0 0\n 1.6266 -2.7315 0.0000 O 0 0\n 0.3445 -0.8123 0.0000 C 0 0 2 0 0 0\n -0.9357 -1.5501 0.0000 N 0 0\n -1.9587 -0.9592 0.0000 R# 0 0\n 0.3423 0.6652 0.0000 C 0 0\n -0.9379 1.4029 0.0000 C 0 0\n -1.9604 0.8110 0.0000 O 0 0\n -0.9397 2.5843 0.0000 O 0 0\n 2.6472 -0.9581 0.0000 R# 0 0\n 0.1468 3.0978 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 7 8 2 0\n 7 9 1 0\n 1 10 1 0\n 9 11 1 0\nM RGP 3 5 1 10 2 11 3\nM END\n> <Name>\nD-Aspartic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndD\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nD\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Glutamic acid\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 0.3441 -1.4777 0.0000 C 0 0 2 0 0 0\n 1.6244 -2.2154 0.0000 C 0 0\n 1.6261 -3.3969 0.0000 O 0 0\n 2.6468 -1.6235 0.0000 R# 0 0\n -0.9362 -2.2154 0.0000 N 0 0\n -1.9591 -1.6245 0.0000 R# 0 0\n 0.3420 -0.0001 0.0000 C 0 0\n -0.9383 0.7376 0.0000 C 0 0\n -0.9404 2.2152 0.0000 C 0 0\n -1.9642 2.8050 0.0000 O 0 0\n 0.0820 2.8071 0.0000 O 0 0\n 0.0730 3.9885 0.0000 R# 0 0\n 2 1 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 5 6 1 0\n 1 7 1 6\n 7 8 1 0\n 8 9 1 0\n 9 10 2 0\n 9 11 1 0\n 11 12 1 0\nM RGP 3 4 2 6 1 12 3\nM END\n> <Name>\nD-Glutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndE\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Phenylalanine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.2052 2.5398 0.0000 C 0 0\n -1.5064 3.2860 0.0000 C 0 0\n -2.8032 2.5322 0.0000 C 0 0\n -2.7988 1.0322 0.0000 C 0 0\n -1.4976 0.2861 0.0000 C 0 0\n -0.2008 1.0398 0.0000 C 0 0\n 1.0995 0.2905 0.0000 C 0 0\n 1.1018 -1.2103 0.0000 C 0 0 1 0 0 0\n -0.1986 -1.9596 0.0000 N 0 0\n 2.4022 -1.9596 0.0000 C 0 0\n 2.4040 -3.1596 0.0000 O 0 0\n 3.4407 -1.3583 0.0000 R# 0 0\n -1.2376 -1.3593 0.0000 R# 0 0\n 1 2 1 0\n 1 6 2 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 6\n 8 9 1 0\n 8 10 1 0\n 10 11 2 0\n 10 12 1 0\n 9 13 1 0\nM RGP 2 12 2 13 1\nM END\n> <Name>\nD-Phenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndF\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Histidine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n 1.8978 -1.6509 0.0000 C 0 0\n 1.8993 -2.5957 0.0000 O 0 0\n 0.8738 -1.0609 0.0000 C 0 0 2 0 0 0\n -0.1501 -1.6509 0.0000 N 0 0\n -0.9683 -1.1782 0.0000 R# 0 0\n 0.8720 0.1209 0.0000 C 0 0\n -0.1501 0.7098 0.0000 C 0 0\n -0.2770 1.8841 0.0000 C 0 0\n -1.4331 2.1263 0.0000 N 0 0\n -2.0206 1.1017 0.0000 C 0 0\n -1.2276 0.2263 0.0000 N 0 0\n 2.7155 -1.1775 0.0000 R# 0 0\n -2.0316 3.1449 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 8 7 2 0\n 9 8 1 0\n 10 9 1 0\n 11 7 1 0\n 11 10 2 0\n 1 12 1 0\n 9 13 1 0\nM RGP 3 5 1 12 2 13 3\nM END\n> <Name>\nD-Histidine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndH\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nH\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Lysine\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 1.7076 -1.9282 0.0000 C 0 0\n 1.7090 -2.8727 0.0000 O 0 0\n 0.6840 -1.3385 0.0000 C 0 0 2 0 0 0\n -0.3395 -1.9282 0.0000 N 0 0\n -1.1574 -1.4558 0.0000 R# 0 0\n 0.6823 -0.1571 0.0000 C 0 0\n -0.3413 0.4325 0.0000 C 0 0\n -0.3430 1.6139 0.0000 C 0 0\n -1.3666 2.2036 0.0000 C 0 0\n -1.3680 3.1481 0.0000 N 0 0\n 2.5250 -1.4549 0.0000 R# 0 0\n -2.3921 3.7373 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 1 11 1 0\n 10 12 1 0\nM RGP 3 5 1 11 2 12 3\nM END\n> <Name>\nD-Lysine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndK\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Leucine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 0.3626 0.9903 0.0000 C 0 0\n -0.9395 2.9396 0.0000 C 0 0\n -0.9377 1.7396 0.0000 C 0 0\n -1.9763 1.1383 0.0000 C 0 0\n 0.3649 -0.5105 0.0000 C 0 0 2 0 0 0\n 1.6653 -1.2598 0.0000 C 0 0\n 1.6671 -2.4598 0.0000 O 0 0\n -0.9355 -1.2598 0.0000 N 0 0\n 2.7038 -0.6585 0.0000 R# 0 0\n -1.9746 -0.6596 0.0000 R# 0 0\n 3 1 1 0\n 5 1 1 6\n 3 2 1 0\n 3 4 1 0\n 5 8 1 0\n 5 6 1 0\n 6 7 2 0\n 6 9 1 0\n 8 10 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\nD-Leucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndL\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Methionine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.6657 -1.5600 0.0000 C 0 0\n -0.9351 -1.5600 0.0000 N 0 0\n 1.6675 -2.7600 0.0000 O 0 0\n 0.3653 -0.8107 0.0000 C 0 0 2 0 0 0\n 0.3630 0.6901 0.0000 C 0 0\n -0.9373 1.4394 0.0000 C 0 0\n -1.9794 3.5393 0.0000 C 0 0\n -0.9396 2.9402 0.0000 S 0 0\n 2.7042 -0.9587 0.0000 R# 0 0\n -1.9742 -0.9598 0.0000 R# 0 0\n 3 1 2 0\n 1 4 1 0\n 1 9 1 0\n 4 2 1 0\n 4 5 1 6\n 5 6 1 0\n 6 8 1 0\n 8 7 1 0\n 2 10 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\nD-Methionine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndM\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nM\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Asparagine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.9098 -1.3951 0.0000 C 0 0\n 1.9116 -2.5765 0.0000 O 0 0\n 0.6296 -0.6575 0.0000 C 0 0 2 0 0 0\n -0.6507 -1.3951 0.0000 N 0 0\n -1.6738 -0.8042 0.0000 R# 0 0\n 0.6273 0.8201 0.0000 C 0 0\n -0.6529 1.5578 0.0000 C 0 0\n -1.6753 0.9658 0.0000 N 0 0\n -0.6547 2.7392 0.0000 O 0 0\n 2.9322 -0.8032 0.0000 R# 0 0\n -2.7030 1.5487 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 7 8 1 0\n 7 9 2 0\n 1 10 1 0\n 8 11 1 0\nM RGP 3 5 1 10 2 11 3\nM END\n> <Name>\nD-Asparagine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndN\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nN\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Proline\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n 0.0018 1.6555 0.0000 C 0 0\n -1.4799 1.8890 0.0000 C 0 0\n -2.1599 0.5519 0.0000 C 0 0\n -1.0984 -0.5079 0.0000 N 0 0\n 0.2376 0.1741 0.0000 C 0 0 1 0 0 0\n 1.5717 -0.5079 0.0000 C 0 0\n 1.6336 -1.7063 0.0000 O 0 0\n 2.5787 0.1448 0.0000 R# 0 0\n -1.2852 -1.6933 0.0000 R# 0 0\n 1 2 1 0\n 5 1 1 6\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 6 8 1 0\n 4 9 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\nD-Proline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndP\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Glutamine\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 1.6243 -2.2154 0.0000 C 0 0\n 1.6260 -3.3969 0.0000 O 0 0\n 0.3442 -1.4777 0.0000 C 0 0 2 0 0 0\n -0.9362 -2.2154 0.0000 N 0 0\n -1.9592 -1.6245 0.0000 R# 0 0\n 0.3419 -0.0001 0.0000 C 0 0\n -0.9383 0.7376 0.0000 C 0 0\n -0.9405 2.2152 0.0000 C 0 0\n 0.0820 2.8071 0.0000 N 0 0\n -1.9641 2.8050 0.0000 O 0 0\n 2.6468 -1.6235 0.0000 R# 0 0\n 0.0730 3.9885 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 8 10 2 0\n 1 11 1 0\n 9 12 1 0\nM RGP 3 5 1 11 2 12 3\nM END\n> <Name>\nD-Glutamine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndQ\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nQ\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Arginine\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n 1.7724 -2.5892 0.0000 C 0 0\n 1.7737 -3.5337 0.0000 O 0 0\n 0.7488 -1.9994 0.0000 C 0 0 2 0 0 0\n -0.2747 -2.5892 0.0000 N 0 0\n -1.0926 -2.1168 0.0000 R# 0 0\n 0.7470 -0.8181 0.0000 C 0 0\n -0.2766 -0.2284 0.0000 C 0 0\n -0.2784 0.9529 0.0000 C 0 0\n -1.3019 1.5426 0.0000 N 0 0\n -1.3037 2.7239 0.0000 C 0 0\n -0.4863 3.1972 0.0000 N 0 0\n -2.1222 3.1954 0.0000 N 0 0\n 2.5898 -2.1159 0.0000 R# 0 0\n -0.4953 4.3786 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 10 12 2 0\n 1 13 1 0\n 11 14 1 0\nM RGP 3 5 1 13 2 14 3\nM END\n> <Name>\nD-Arginine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Serine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.3671 -1.0829 0.0000 C 0 0\n 1.3689 -2.2643 0.0000 O 0 0\n 0.0868 -0.3452 0.0000 C 0 0 2 0 0 0\n -1.1933 -1.0829 0.0000 N 0 0\n -2.2164 -0.4920 0.0000 R# 0 0\n 0.0846 1.1324 0.0000 C 0 0\n -0.9391 1.7221 0.0000 O 0 0\n 2.3895 -0.4908 0.0000 R# 0 0\n -0.9482 2.9036 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 1 8 1 0\n 7 9 1 0\nM RGP 3 5 1 8 2 9 3\nM END\n> <Name>\nD-Serine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndS\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Valine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.1543 -0.9675 0.0000 C 0 0\n -0.1446 -0.2156 0.0000 C 0 0 1 0 0 0\n -1.1823 1.8865 0.0000 C 0 0\n -0.1438 1.2853 0.0000 C 0 0\n 0.8960 1.8843 0.0000 C 0 0\n 1.1536 -2.1676 0.0000 O 0 0\n -1.4435 -0.9675 0.0000 N 0 0\n 2.1941 -0.3685 0.0000 R# 0 0\n -2.4838 -0.3695 0.0000 R# 0 0\n 6 1 2 0\n 1 2 1 0\n 1 8 1 0\n 2 7 1 0\n 2 4 1 6\n 4 3 1 0\n 4 5 1 0\n 7 9 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\nD-Valine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndV\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Isoleucine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n -1.2557 1.6681 0.0000 C 0 0\n 0.0245 0.9304 0.0000 C 0 0 2 0 0 0\n 0.0268 -0.5472 0.0000 C 0 0 1 0 0 0\n -1.2536 -1.2849 0.0000 N 0 0\n -2.2766 -0.6940 0.0000 R# 0 0\n 1.3069 -1.2849 0.0000 C 0 0\n 1.3086 -2.4664 0.0000 O 0 0\n 2.3294 -0.6930 0.0000 R# 0 0\n 1.0470 1.5223 0.0000 C 0 0\n -1.2574 2.8495 0.0000 C 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 3 6 1 0\n 6 7 2 0\n 6 8 1 0\n 2 9 1 1\n 1 10 1 0\nM RGP 2 5 1 8 2\nM END\n> <Name>\nD-Isoleucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndI\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nI\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Threonine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.0488 -1.2558 0.0000 C 0 0\n 1.0481 -2.4369 0.0000 O 0 0\n -0.2297 -0.5156 0.0000 C 0 0 2 0 0 0\n -1.5081 -1.2558 0.0000 N 0 0\n -2.5321 -0.6672 0.0000 R# 0 0\n -0.2289 0.9614 0.0000 C 0 0 1 0 0 0\n 0.7944 1.5510 0.0000 O 0 0\n -1.2510 1.5531 0.0000 C 0 0\n 2.0720 -0.6661 0.0000 R# 0 0\n 0.7866 2.7318 0.0000 R# 0 0\n 2 1 2 0\n 3 1 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 6\n 6 8 1 0\n 1 9 1 0\n 7 10 1 0\nM RGP 3 5 1 9 2 10 3\nM END\n> <Name>\nD-Threonine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndT\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Tryptophan\n SciTegic07272112182D\n\n 17 18 0 0 1 0 999 V2000\n 2.0938 -2.3551 0.0000 C 0 0\n 2.0951 -3.3000 0.0000 O 0 0\n 1.0698 -1.7651 0.0000 C 0 0 2 0 0 0\n 0.0458 -2.3551 0.0000 N 0 0\n -0.7723 -1.8826 0.0000 R# 0 0\n 1.0680 -0.5835 0.0000 C 0 0\n 0.0458 0.0056 0.0000 C 0 0\n -1.0319 -0.4778 0.0000 C 0 0\n -1.8247 0.3977 0.0000 N 0 0\n -1.2370 1.4216 0.0000 C 0 0\n -0.0810 1.1792 0.0000 C 0 0\n 0.7068 2.0591 0.0000 C 0 0\n 0.3388 3.1814 0.0000 C 0 0\n -0.8172 3.4238 0.0000 C 0 0\n -1.6051 2.5439 0.0000 C 0 0\n 2.9114 -1.8817 0.0000 R# 0 0\n -3.0060 0.3887 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 8 7 2 0\n 9 8 1 0\n 10 9 1 0\n 11 7 1 0\n 11 10 2 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 15 10 1 0\n 14 15 2 0\n 1 16 1 0\n 9 17 1 0\nM RGP 3 5 1 16 2 17 3\nM END\n> <Name>\nD-Tryptophan\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndW\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nW\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Tyrosine\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n 2.2956 -1.9503 0.0000 C 0 0\n 2.2970 -2.8952 0.0000 O 0 0\n 1.2717 -1.3603 0.0000 C 0 0 2 0 0 0\n 0.2478 -1.9503 0.0000 N 0 0\n -0.5703 -1.4776 0.0000 R# 0 0\n 1.2701 -0.1786 0.0000 C 0 0\n 0.2461 0.4115 0.0000 C 0 0\n 0.2427 1.5926 0.0000 C 0 0\n -0.7819 2.1801 0.0000 C 0 0\n -1.8030 1.5867 0.0000 C 0 0\n -1.7996 0.4056 0.0000 C 0 0\n -0.7751 -0.1820 0.0000 C 0 0\n -2.6227 2.0568 0.0000 O 0 0\n 3.1134 -1.4770 0.0000 R# 0 0\n -2.6317 3.2381 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 8 7 1 0\n 9 8 2 0\n 10 9 1 0\n 11 10 2 0\n 12 7 2 0\n 12 11 1 0\n 10 13 1 0\n 1 14 1 0\n 13 15 1 0\nM RGP 3 5 1 14 2 15 3\nM END\n> <Name>\nD-Tyrosine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndY\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nfmoc N-Terminal Protection Group\n SciTegic07272112182D\n\n 18 20 0 0 1 0 999 V2000\n 0.0842 -0.3368 0.0000 C 0 0\n 1.3810 -1.0892 0.0000 C 0 0\n 2.4977 -0.0877 0.0000 C 0 0\n 1.8903 1.2838 0.0000 C 0 0\n 0.3989 1.1298 0.0000 C 0 0\n -0.7138 2.1357 0.0000 C 0 0\n -2.1412 1.6749 0.0000 C 0 0\n -2.4560 0.2083 0.0000 C 0 0\n -1.3433 -0.7975 0.0000 C 0 0\n 1.6892 -2.5561 0.0000 C 0 0\n 3.1148 -3.0224 0.0000 C 0 0\n 4.2315 -2.0208 0.0000 C 0 0\n 3.9225 -0.5530 0.0000 C 0 0\n 2.6389 2.5816 0.0000 C 0 0\n 1.8889 3.8816 0.0000 O 0 0\n 2.6389 5.1816 0.0000 C 0 0\n 2.0393 6.2211 0.0000 O 0 0\n 3.8389 5.1816 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 1 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 1 9 1 0\n 2 10 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 2 0\n 3 13 1 0\n 4 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 2 0\n 16 18 1 0\nM RGP 1 18 2\nM END\n> <Name>\nfmoc N-Terminal Protection Group\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nfmoc\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nN-Methyl-Alanine\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n -0.0001 1.6241 0.0000 C 0 0\n -0.0001 0.4428 0.0000 C 0 0 1 0 0 0\n 1.0229 -0.1476 0.0000 C 0 0\n 2.0457 0.4430 0.0000 R# 0 0\n 1.0230 -1.3286 0.0000 O 0 0\n -1.0229 -0.1476 0.0000 N 0 0\n -2.0458 0.4427 0.0000 C 0 0\n -1.0227 -1.3288 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 1 0\n 3 5 2 0\n 6 2 1 0\n 6 7 1 0\n 6 8 1 0\nM RGP 2 4 2 8 1\nM END\n> <Name>\nN-Methyl-Alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Cysteine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.5613 -0.9000 0.0000 C 0 0\n 0.2609 -0.1507 0.0000 C 0 0 2 0 0 0\n 0.2586 1.3501 0.0000 C 0 0\n -1.0418 2.0994 0.0000 S 0 0\n -1.0395 -0.9000 0.0000 N 0 0\n 1.5630 -2.1000 0.0000 O 0 0\n 2.5998 -0.2987 0.0000 R# 0 0\n -1.0401 -2.1000 0.0000 R# 0 0\n -1.0435 3.2994 0.0000 R# 0 0\n -2.0786 -0.2998 0.0000 C 0 0\n 6 1 2 0\n 1 2 1 0\n 1 7 1 0\n 2 5 1 0\n 2 3 1 1\n 3 4 1 0\n 5 8 1 0\n 4 9 1 0\n 5 10 1 0\nM RGP 3 7 2 8 1 9 3\nM END\n> <Name>\nN-Methyl-Cysteine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nN-Methyl-Aspartic acid\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.7504 -1.0361 0.0000 C 0 0\n 0.4500 -0.2869 0.0000 C 0 0 2 0 0 0\n 0.4477 1.2140 0.0000 C 0 0\n -0.8526 1.9632 0.0000 C 0 0\n -0.8544 3.1632 0.0000 O 0 0\n -1.8912 1.3620 0.0000 R# 0 0\n 1.7522 -2.2362 0.0000 O 0 0\n -0.8504 -1.0361 0.0000 N 0 0\n 2.7889 -0.4349 0.0000 R# 0 0\n -0.8510 -2.2362 0.0000 R# 0 0\n -1.8895 -0.4360 0.0000 C 0 0\n 7 1 2 0\n 1 2 1 0\n 1 9 1 0\n 2 8 1 0\n 2 3 1 1\n 3 4 1 0\n 4 6 1 0\n 4 5 2 0\n 8 10 1 0\n 8 11 1 0\nM RGP 3 6 3 9 2 10 1\nM END\n> <Name>\nN-Methyl-Aspartic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeD\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nD\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\nN-Methyl-Glutamic acid\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 0.4350 -0.8758 0.0000 C 0 0 1 0 0 0\n 0.4328 0.6250 0.0000 C 0 0\n -0.8676 1.3743 0.0000 C 0 0\n -0.8699 2.8751 0.0000 C 0 0\n 1.7354 -1.6251 0.0000 C 0 0\n 0.1686 3.4764 0.0000 R# 0 0\n -1.9097 3.4742 0.0000 O 0 0\n 1.7372 -2.8251 0.0000 O 0 0\n -0.8654 -1.6251 0.0000 N 0 0\n 2.7739 -1.0238 0.0000 R# 0 0\n -0.8660 -2.8251 0.0000 R# 0 0\n -1.9045 -1.0249 0.0000 C 0 0\n 5 1 1 0\n 1 9 1 0\n 1 2 1 1\n 2 3 1 0\n 3 4 1 0\n 4 7 2 0\n 4 6 1 0\n 5 8 2 0\n 5 10 1 0\n 9 11 1 0\n 9 12 1 0\nM RGP 3 6 3 10 2 11 1\nM END\n> <Name>\nN-Methyl-Glutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeE\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\nN-Methyl-Phenylalanine\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -0.1860 2.7672 0.0000 C 0 0\n -1.4858 3.5162 0.0000 C 0 0\n -2.7841 2.7651 0.0000 C 0 0\n -2.7828 1.2651 0.0000 C 0 0\n -1.4831 0.5162 0.0000 C 0 0\n -0.1848 1.2673 0.0000 C 0 0\n 1.1140 0.5153 0.0000 C 0 0\n 1.1132 -0.9855 0.0000 C 0 0 2 0 0 0\n -0.1857 -1.7375 0.0000 N 0 0\n 2.4121 -1.7375 0.0000 C 0 0\n 2.4114 -2.9375 0.0000 O 0 0\n 3.4519 -1.1384 0.0000 R# 0 0\n -1.2253 -1.1383 0.0000 R# 0 0\n -0.1850 -2.9375 0.0000 C 0 0\n 1 2 1 0\n 1 6 2 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 1\n 8 9 1 0\n 8 10 1 0\n 10 11 2 0\n 10 12 1 0\n 9 13 1 0\n 9 14 1 0\nM RGP 2 12 2 13 1\nM END\n> <Name>\nN-Methyl-Phenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeF\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Histidine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n 2.2265 -1.5358 0.0000 C 0 0\n 0.9260 -0.7865 0.0000 C 0 0 2 0 0 0\n 0.9237 0.7143 0.0000 C 0 0\n -0.3744 1.4623 0.0000 C 0 0\n -2.7498 1.9600 0.0000 C 0 0\n -0.5355 2.9536 0.0000 C 0 0\n -1.7429 0.8482 0.0000 N 0 0\n -2.0037 3.2612 0.0000 N 0 0\n -0.3744 -1.5358 0.0000 N 0 0\n 2.2283 -2.7358 0.0000 O 0 0\n 3.2649 -0.9346 0.0000 R# 0 0\n -0.3751 -2.7357 0.0000 R# 0 0\n -1.4135 -0.9355 0.0000 C 0 0\n 10 1 2 0\n 1 2 1 0\n 1 11 1 0\n 2 9 1 0\n 2 3 1 1\n 3 4 1 0\n 6 4 2 0\n 7 4 1 0\n 7 5 2 0\n 5 8 1 0\n 8 6 1 0\n 9 12 1 0\n 9 13 1 0\nM RGP 2 11 2 12 1\nM END\n> <Name>\nN-Methyl-Histidine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeH\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nH\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Isoleucine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n -1.1567 1.9262 0.0000 C 0 0\n -1.1560 3.1262 0.0000 C 0 0\n 0.1413 -0.3266 0.0000 C 0 0 1 0 0 0\n 1.4401 -1.0786 0.0000 C 0 0\n 1.4394 -2.2786 0.0000 O 0 0\n -1.1576 -1.0786 0.0000 N 0 0\n 0.1421 1.1742 0.0000 C 0 0 1 0 0 0\n 1.1819 1.7733 0.0000 C 0 0\n 2.4799 -0.4795 0.0000 R# 0 0\n -2.1973 -0.4794 0.0000 R# 0 0\n -1.1570 -2.2785 0.0000 C 0 0\n 1 7 1 0\n 1 2 1 0\n 3 7 1 0\n 3 6 1 0\n 3 4 1 1\n 4 5 2 0\n 4 9 1 0\n 7 8 1 6\n 6 10 1 0\n 6 11 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\nN-Methyl-Isoleucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeI\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nI\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Lysine\n SciTegic07272112182D\n\n 13 12 0 0 1 0 999 V2000\n 2.1827 -2.2038 0.0000 C 0 0\n 0.8823 -1.4545 0.0000 C 0 0 2 0 0 0\n 0.8800 0.0463 0.0000 C 0 0\n -0.4204 0.7956 0.0000 C 0 0\n -0.4227 2.2964 0.0000 C 0 0\n -1.7230 3.0456 0.0000 C 0 0\n -1.7253 4.5464 0.0000 N 0 0\n -0.4181 -2.2038 0.0000 N 0 0\n 2.1844 -3.4038 0.0000 O 0 0\n 3.2212 -1.6025 0.0000 R# 0 0\n -0.4187 -3.4038 0.0000 R# 0 0\n -2.7651 5.1456 0.0000 R# 0 0\n -1.4572 -1.6036 0.0000 C 0 0\n 9 1 2 0\n 1 2 1 0\n 1 10 1 0\n 2 8 1 0\n 2 3 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 8 11 1 0\n 7 12 1 0\n 8 13 1 0\nM RGP 3 10 2 11 1 12 3\nM END\n> <Name>\nN-Methyl-Lysine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeK\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nN-Methyl-Leucine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 0.4492 1.2148 0.0000 C 0 0\n -0.8489 3.1668 0.0000 C 0 0\n -0.8496 1.9667 0.0000 C 0 0\n -1.8894 1.3677 0.0000 C 0 0\n 0.4484 -0.2861 0.0000 C 0 0 1 0 0 0\n 1.7473 -1.0380 0.0000 C 0 0\n 1.7466 -2.2381 0.0000 O 0 0\n -0.8505 -1.0380 0.0000 N 0 0\n 2.7870 -0.4390 0.0000 R# 0 0\n -1.8902 -0.4389 0.0000 R# 0 0\n -0.8499 -2.2380 0.0000 C 0 0\n 3 1 1 0\n 5 1 1 1\n 3 2 1 0\n 3 4 1 0\n 5 8 1 0\n 5 6 1 0\n 6 7 2 0\n 6 9 1 0\n 8 10 1 0\n 8 11 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\nN-Methyl-Leucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeL\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Methionine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.7507 -1.3091 0.0000 C 0 0\n -0.8500 -1.3091 0.0000 N 0 0\n 1.7525 -2.5091 0.0000 O 0 0\n 0.4504 -0.5598 0.0000 C 0 0 1 0 0 0\n 0.4481 0.9410 0.0000 C 0 0\n -0.8523 1.6903 0.0000 C 0 0\n -1.8944 3.7902 0.0000 C 0 0\n -0.8546 3.1911 0.0000 S 0 0\n 2.7893 -0.7078 0.0000 R# 0 0\n -0.8506 -2.5091 0.0000 R# 0 0\n -1.8891 -0.7089 0.0000 C 0 0\n 3 1 2 0\n 1 4 1 0\n 1 9 1 0\n 4 2 1 0\n 4 5 1 1\n 5 6 1 0\n 6 8 1 0\n 8 7 1 0\n 2 10 1 0\n 2 11 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\nN-Methyl-Methionine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeM\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nM\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Asparagine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.7504 -1.0361 0.0000 C 0 0\n 0.4500 -0.2869 0.0000 C 0 0 2 0 0 0\n 0.4477 1.2140 0.0000 C 0 0\n 1.7522 -2.2362 0.0000 O 0 0\n -0.8504 -1.0361 0.0000 N 0 0\n -0.8526 1.9632 0.0000 C 0 0\n -0.8544 3.1632 0.0000 O 0 0\n -1.8912 1.3620 0.0000 N 0 0\n 2.7889 -0.4349 0.0000 R# 0 0\n -0.8510 -2.2362 0.0000 R# 0 0\n -1.8895 -0.4360 0.0000 C 0 0\n 4 1 2 0\n 1 2 1 0\n 1 9 1 0\n 2 5 1 0\n 2 3 1 1\n 3 6 1 0\n 6 8 1 0\n 6 7 2 0\n 5 10 1 0\n 5 11 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\nN-Methyl-Asparagine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeN\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nN\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Glutamine\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 1.7354 -1.6251 0.0000 C 0 0\n 0.4350 -0.8758 0.0000 C 0 0 2 0 0 0\n 0.4328 0.6250 0.0000 C 0 0\n -0.8676 1.3743 0.0000 C 0 0\n 1.7372 -2.8251 0.0000 O 0 0\n 0.1686 3.4764 0.0000 N 0 0\n -0.8654 -1.6251 0.0000 N 0 0\n -1.9097 3.4742 0.0000 O 0 0\n -0.8699 2.8751 0.0000 C 0 0\n 2.7739 -1.0238 0.0000 R# 0 0\n -0.8660 -2.8251 0.0000 R# 0 0\n -1.9045 -1.0249 0.0000 C 0 0\n 5 1 2 0\n 1 2 1 0\n 1 10 1 0\n 2 7 1 0\n 2 3 1 1\n 3 4 1 0\n 4 9 1 0\n 9 6 1 0\n 9 8 2 0\n 7 11 1 0\n 7 12 1 0\nM RGP 2 10 2 11 1\nM END\n> <Name>\nN-Methyl-Glutamine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeQ\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nQ\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Arginine\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n 2.2317 -2.5715 0.0000 C 0 0\n 0.9313 -1.8222 0.0000 C 0 0 2 0 0 0\n 0.9291 -0.3214 0.0000 C 0 0\n -0.3713 0.4279 0.0000 C 0 0\n -0.3736 1.9287 0.0000 C 0 0\n -0.3691 -2.5715 0.0000 N 0 0\n 2.2335 -3.7715 0.0000 O 0 0\n -1.6740 2.6779 0.0000 N 0 0\n -1.6763 4.1787 0.0000 C 0 0\n -2.7161 4.7779 0.0000 N 0 0\n -0.6377 4.7800 0.0000 N 0 0\n 3.2702 -1.9702 0.0000 R# 0 0\n -0.3697 -3.7715 0.0000 R# 0 0\n -1.4082 -1.9713 0.0000 C 0 0\n 7 1 2 0\n 1 2 1 0\n 1 12 1 0\n 2 6 1 0\n 2 3 1 1\n 3 4 1 0\n 4 5 1 0\n 5 8 1 0\n 8 9 1 0\n 9 11 1 0\n 9 10 2 0\n 6 13 1 0\n 6 14 1 0\nM RGP 2 12 2 13 1\nM END\n> <Name>\nN-Methyl-Arginine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Serine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.4164 -0.5167 0.0000 C 0 0\n 1.4181 -1.7167 0.0000 O 0 0\n -1.1844 -0.5167 0.0000 N 0 0\n 0.1160 0.2326 0.0000 C 0 0 1 0 0 0\n 0.1137 1.7334 0.0000 C 0 0\n -0.9261 2.3325 0.0000 O 0 0\n 2.4549 0.0846 0.0000 R# 0 0\n -1.1850 -1.7167 0.0000 R# 0 0\n -2.2235 0.0835 0.0000 C 0 0\n 2 1 2 0\n 1 4 1 0\n 1 7 1 0\n 4 3 1 0\n 4 5 1 1\n 5 6 1 0\n 3 8 1 0\n 3 9 1 0\nM RGP 2 7 2 8 1\nM END\n> <Name>\nN-Methyl-Serine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeS\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Threonine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.3011 -0.7501 0.0000 C 0 0\n -1.2996 -0.7501 0.0000 N 0 0\n 1.3029 -1.9501 0.0000 O 0 0\n 0.0008 -0.0009 0.0000 C 0 0 1 0 0 0\n 1.0370 2.1012 0.0000 C 0 0\n -0.0015 1.5000 0.0000 C 0 0 1 0 0 0\n -1.0413 2.0990 0.0000 O 0 0\n 2.3397 -0.1489 0.0000 R# 0 0\n -1.3003 -1.9502 0.0000 R# 0 0\n -2.3388 -0.1500 0.0000 C 0 0\n 3 1 2 0\n 4 1 1 1\n 1 8 1 0\n 4 2 1 0\n 4 6 1 0\n 6 5 1 0\n 6 7 1 6\n 2 9 1 0\n 2 10 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\nN-Methyl-Threonine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeT\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Valine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.3011 0.7502 0.0000 C 0 0\n 0.0011 0.0002 0.0000 C 0 0 2 0 0 0\n -1.0421 -2.0992 0.0000 C 0 0\n -0.0020 -1.5005 0.0000 C 0 0\n 1.0362 -2.1024 0.0000 C 0 0\n 2.3405 0.1505 0.0000 O 0 0\n -1.2989 0.7502 0.0000 N 0 0\n 1.3011 1.9502 0.0000 R# 0 0\n -1.2989 1.9502 0.0000 R# 0 0\n -2.3382 0.1505 0.0000 C 0 0\n 6 1 2 0\n 1 2 1 0\n 1 8 1 0\n 2 7 1 0\n 2 4 1 6\n 4 3 1 0\n 4 5 1 0\n 7 9 1 0\n 7 10 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\nN-Methyl-Valine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeV\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Tryptophan\n SciTegic07272112182D\n\n 17 18 0 0 1 0 999 V2000\n 2.4311 -2.7154 0.0000 C 0 0\n 2.4328 -3.9155 0.0000 O 0 0\n -0.1698 -2.7154 0.0000 N 0 0\n 1.1306 -1.9662 0.0000 C 0 0 1 0 0 0\n 1.1284 -0.4655 0.0000 C 0 0\n -0.1698 0.2826 0.0000 C 0 0\n -1.5385 -0.3313 0.0000 C 0 0\n -0.3308 1.7733 0.0000 C 0 0\n -1.7989 2.0810 0.0000 C 0 0\n 0.6697 2.8906 0.0000 C 0 0\n 0.2023 4.3159 0.0000 C 0 0\n -1.2658 4.6238 0.0000 C 0 0\n -2.2664 3.5063 0.0000 C 0 0\n -2.5452 0.7808 0.0000 N 0 0\n 3.4695 -2.1143 0.0000 R# 0 0\n -0.1705 -3.9155 0.0000 R# 0 0\n -1.2088 -2.1153 0.0000 C 0 0\n 2 1 2 0\n 1 4 1 0\n 1 15 1 0\n 4 3 1 0\n 4 5 1 1\n 5 6 1 0\n 7 6 2 0\n 8 6 1 0\n 14 7 1 0\n 8 9 2 0\n 8 10 1 0\n 9 14 1 0\n 13 9 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 2 0\n 3 16 1 0\n 3 17 1 0\nM RGP 2 15 2 16 1\nM END\n> <Name>\nN-Methyl-Tryptophan\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeW\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nW\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Tyrosine\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n 2.6718 -1.9575 0.0000 C 0 0\n 0.0710 -1.9575 0.0000 N 0 0\n 2.6736 -3.1576 0.0000 O 0 0\n 1.3714 -1.2083 0.0000 C 0 0 1 0 0 0\n 1.3692 0.2926 0.0000 C 0 0\n 0.0688 1.0418 0.0000 C 0 0\n -1.2281 0.2881 0.0000 C 0 0\n -2.5293 1.0343 0.0000 C 0 0\n -1.2369 3.2880 0.0000 C 0 0\n 0.0644 2.5418 0.0000 C 0 0\n -2.5336 2.5343 0.0000 C 0 0\n -3.5747 3.1312 0.0000 O 0 0\n 3.7103 -1.3564 0.0000 R# 0 0\n 0.0703 -3.1576 0.0000 R# 0 0\n -0.9680 -1.3573 0.0000 C 0 0\n 3 1 2 0\n 1 4 1 0\n 1 13 1 0\n 4 2 1 0\n 4 5 1 1\n 5 6 1 0\n 10 6 1 0\n 7 6 2 0\n 7 8 1 0\n 8 11 2 0\n 11 9 1 0\n 9 10 2 0\n 11 12 1 0\n 2 14 1 0\n 2 15 1 0\nM RGP 2 13 2 14 1\nM END\n> <Name>\nN-Methyl-Tyrosine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeY\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nPNA Adenine\n SciTegic07272112182D\n\n 22 23 0 0 0 0 999 V2000\n -4.0177 -3.1348 0.0000 R# 0 0\n -2.8711 -3.4186 0.0000 N 0 0\n -2.0522 -2.5674 0.0000 C 0 0\n -0.9056 -2.8511 0.0000 C 0 0\n -0.0867 -2.0001 0.0000 N 0 0\n -0.4142 -0.8653 0.0000 C 0 0\n -1.5608 -0.5816 0.0000 O 0 0\n 0.4047 -0.0142 0.0000 C 0 0\n 0.0771 1.1205 0.0000 N 0 0\n -1.0335 1.5226 0.0000 C 0 0\n -0.9944 2.7030 0.0000 N 0 0\n 0.1404 3.0305 0.0000 C 0 0\n 0.8026 2.0526 0.0000 C 0 0\n 1.9807 2.1371 0.0000 N 0 0\n 2.4966 3.1995 0.0000 C 0 0\n 1.8343 4.1775 0.0000 N 0 0\n 0.6562 4.0930 0.0000 C 0 0\n -0.0059 5.0710 0.0000 N 0 0\n 1.0598 -2.2838 0.0000 C 0 0\n 1.3874 -3.4186 0.0000 C 0 0\n 0.5685 -4.2696 0.0000 O 0 0\n 2.5340 -3.7022 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 6 8 1 0\n 8 9 1 0\n 9 10 1 0\n 11 10 2 0\n 12 11 1 0\n 13 12 2 0\n 9 13 1 0\n 13 14 1 0\n 15 14 2 0\n 16 15 1 0\n 12 17 1 0\n 17 16 2 0\n 17 18 1 0\n 5 19 1 0\n 19 20 1 0\n 20 21 2 0\n 20 22 1 0\nM RGP 2 1 1 22 2\nM END\n> <Name>\nPNA Adenine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\npnA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nPNA Cytosine\n SciTegic07272112182D\n\n 20 20 0 0 0 0 999 V2000\n -3.3034 -4.1754 0.0000 R# 0 0\n -3.0802 -3.0156 0.0000 N 0 0\n -1.9642 -2.6289 0.0000 C 0 0\n -1.7410 -1.4691 0.0000 C 0 0\n -0.6250 -1.0825 0.0000 N 0 0\n -0.4018 0.0773 0.0000 C 0 0\n -1.2946 0.8505 0.0000 O 0 0\n 0.7143 0.4640 0.0000 C 0 0\n 0.9374 1.6238 0.0000 N 0 0\n 2.0535 2.0104 0.0000 C 0 0\n 2.9463 1.2372 0.0000 O 0 0\n 2.2767 3.1702 0.0000 N 0 0\n 1.3838 3.9434 0.0000 C 0 0\n 1.6070 5.1032 0.0000 N 0 0\n 0.2678 3.5568 0.0000 C 0 0\n 0.0446 2.3969 0.0000 C 0 0\n 0.2679 -1.8557 0.0000 C 0 0\n 0.0447 -3.0156 0.0000 C 0 0\n -1.0713 -3.4022 0.0000 O 0 0\n 0.9375 -3.7887 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 6 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 2 0\n 12 10 1 0\n 13 12 2 0\n 13 14 1 0\n 15 13 1 0\n 16 15 2 0\n 9 16 1 0\n 5 17 1 0\n 17 18 1 0\n 18 19 2 0\n 18 20 1 0\nM RGP 2 1 1 20 2\nM END\n> <Name>\nPNA Cytosine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\npnC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nPNA Guanine\n SciTegic07272112182D\n\n 23 24 0 0 0 0 999 V2000\n -3.9874 -4.5541 0.0000 R# 0 0\n -3.7641 -3.3943 0.0000 N 0 0\n -2.6481 -3.0076 0.0000 C 0 0\n -2.4249 -1.8478 0.0000 C 0 0\n -1.3088 -1.4613 0.0000 N 0 0\n -1.0856 -0.3015 0.0000 C 0 0\n -1.9783 0.4718 0.0000 O 0 0\n 0.0305 0.0851 0.0000 C 0 0\n 0.2537 1.2449 0.0000 N 0 0\n -0.5533 2.1072 0.0000 C 0 0\n 0.0174 3.1413 0.0000 N 0 0\n 1.1772 2.9181 0.0000 C 0 0\n 1.3232 1.7460 0.0000 C 0 0\n 2.4113 1.2865 0.0000 N 0 0\n 3.3532 1.9990 0.0000 C 0 0\n 4.4414 1.5396 0.0000 N 0 0\n 3.2072 3.1711 0.0000 N 0 0\n 2.1191 3.6306 0.0000 C 0 0\n 1.9731 4.8026 0.0000 O 0 0\n -0.4160 -2.2345 0.0000 C 0 0\n -0.6393 -3.3943 0.0000 C 0 0\n -1.7553 -3.7809 0.0000 O 0 0\n 0.2536 -4.1676 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 6 8 1 0\n 8 9 1 0\n 9 10 1 0\n 11 10 2 0\n 12 11 1 0\n 13 12 2 0\n 9 13 1 0\n 13 14 1 0\n 15 14 2 0\n 15 16 1 0\n 17 15 1 0\n 12 18 1 0\n 18 17 1 0\n 18 19 2 0\n 5 20 1 0\n 20 21 1 0\n 21 22 2 0\n 21 23 1 0\nM RGP 2 1 1 23 2\nM END\n> <Name>\nPNA Guanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\npnG\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nPNA Thymine\n SciTegic07272112182D\n\n 21 21 0 0 0 0 999 V2000\n -3.2737 -4.3815 0.0000 R# 0 0\n -3.0505 -3.2217 0.0000 N 0 0\n -1.9345 -2.8351 0.0000 C 0 0\n -1.7113 -1.6753 0.0000 C 0 0\n -0.5952 -1.2887 0.0000 N 0 0\n -0.3720 -0.1288 0.0000 C 0 0\n -1.2649 0.6444 0.0000 O 0 0\n 0.7440 0.2577 0.0000 C 0 0\n 0.9672 1.4176 0.0000 N 0 0\n 2.0833 1.8041 0.0000 C 0 0\n 2.9761 1.0309 0.0000 O 0 0\n 2.3065 2.9639 0.0000 N 0 0\n 1.4137 3.7372 0.0000 C 0 0\n 1.6369 4.8970 0.0000 O 0 0\n 0.2977 3.3506 0.0000 C 0 0\n -0.5952 4.1238 0.0000 C 0 0\n 0.0745 2.1908 0.0000 C 0 0\n 0.2976 -2.0619 0.0000 C 0 0\n 0.0743 -3.2217 0.0000 C 0 0\n -1.0417 -3.6084 0.0000 O 0 0\n 0.9672 -3.9949 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 6 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 2 0\n 12 10 1 0\n 13 12 1 0\n 13 14 2 0\n 15 13 1 0\n 15 16 1 0\n 17 15 2 0\n 9 17 1 0\n 5 18 1 0\n 18 19 1 0\n 19 20 2 0\n 19 21 1 0\nM RGP 2 1 1 21 2\nM END\n> <Name>\nPNA Thymine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\npnT\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nSelenoCysteine\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 1.2682 -0.7312 0.0000 C 0 0\n -0.0321 0.0180 0.0000 C 0 0 2 0 0 0\n -0.0344 1.5189 0.0000 C 0 0\n -1.0742 2.1179 0.0000 Se 0 0\n -1.3325 -0.7312 0.0000 N 0 0\n 1.2700 -1.9313 0.0000 O 0 0\n 2.3068 -0.1300 0.0000 R# 0 0\n -2.3717 -0.1311 0.0000 R# 0 0\n 6 1 2 0\n 1 2 1 0\n 1 7 1 0\n 2 5 1 0\n 2 3 1 1\n 3 4 1 0\n 5 8 1 0\nM RGP 2 7 2 8 1\nM END\n> <Name>\nSelenoCysteine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nseC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nTest-6-AP-Chem\nKetcher 9272311162D 1 1.00000 0.00000 0\n\n 22 21 0 0 0 0 0 0 0 0999 V2000\n 12.0838 -6.5500 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0\n 11.1373 -6.1032 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 10.2767 -6.6989 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.3303 -6.2522 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.4697 -6.8478 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.5233 -6.4011 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.6627 -6.9968 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.7162 -6.5500 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 12.7718 -6.0736 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 5.0282 -7.0264 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 7.0233 -5.5351 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.0233 -4.5351 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.3162 -3.8280 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.5750 -2.8621 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.6091 -2.6032 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.8679 -1.6373 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 4.8679 -1.6373 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 10.2767 -7.6989 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 7.5750 -2.8621 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 8.4697 -7.8478 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.9697 -8.7139 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.9697 -9.7139 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 1 2 1 0 0 0\n 2 3 1 0 0 0\n 3 4 1 0 0 0\n 4 5 1 0 0 0\n 5 6 1 0 0 0\n 6 7 1 0 0 0\n 7 8 1 0 0 0\n 1 9 1 0 0 0\n 8 10 1 0 0 0\n 6 11 1 0 0 0\n 11 12 1 0 0 0\n 12 13 1 0 0 0\n 13 14 1 0 0 0\n 14 15 1 0 0 0\n 15 16 1 0 0 0\n 16 17 1 0 0 0\n 3 18 1 0 0 0\n 14 19 1 0 0 0\n 5 20 1 0 0 0\n 20 21 1 0 0 0\n 21 22 1 0 0 0\nM RGP 6 9 2 10 1 17 3 18 5 19 4 22 6\nM END\n> <Name>\nTest-6-AP-Chem\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nTest-6-Ch\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]I\n[R3]Br\n[R4]Cl\n[R5]O\n[R6]H\n\n$$$$\n6-amino-hexanol\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 4.5654 0.0000 0.0000 N 0 0\n 3.2082 0.6407 0.0000 C 0 0\n 1.9742 -0.2135 0.0000 C 0 0\n 0.6170 0.4271 0.0000 C 0 0\n -0.6170 -0.4271 0.0000 C 0 0\n -1.9741 0.2135 0.0000 C 0 0\n -3.2082 -0.6407 0.0000 C 0 0\n -4.5654 0.0000 0.0000 O 0 0\n 5.5520 0.6831 0.0000 R# 0 0\n -5.5520 -0.6831 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 1 9 1 0\n 8 10 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\n6-amino-hexanol\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nA6OH\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nAzide\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 3.0997 0.9106 0.0000 O 0 0\n 2.5000 1.9500 0.0000 C 0 0\n 3.2500 3.2500 0.0000 C 0 0\n 2.5000 4.5500 0.0000 C 0 0\n 3.2500 5.8500 0.0000 C 0 0\n 2.5000 7.1500 0.0000 N 0 0\n 3.2500 8.4499 0.0000 N 0 3\n 3.8497 9.4894 0.0000 N 0 5\n 1.3000 1.9500 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 2 0\n 2 9 1 0\nM CHG 2 7 1 8 -1\nM RGP 1 9 1\nM END\n> <Name>\nAzide\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nAz\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n\n$$$$\nEthylene Glycol\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n -1.3000 0.3899 0.0000 O 0 0\n 0.0000 -0.3601 0.0000 C 0 0\n -2.3394 -0.2098 0.0000 R# 0 0\n 1.3000 0.3899 0.0000 C 0 0\n 2.3394 -0.2098 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 4 5 1 0\nM RGP 2 3 1 5 2\nM END\n> <Name>\nEthylene Glycol\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nEG\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n4-(N-maleimidomethyl)cyclohexane-1-carboxylate\n SciTegic07272112182D\n\n 17 18 0 0 1 0 999 V2000\n 4.8398 3.5052 0.0000 C 0 0\n 5.5875 2.2049 0.0000 C 0 0\n 7.0875 2.2023 0.0000 C 0 0\n 7.8397 3.5000 0.0000 C 0 0\n 7.0920 4.8003 0.0000 C 0 0\n 5.5920 4.8030 0.0000 C 0 0\n 4.8375 0.9049 0.0000 C 0 0\n 5.4372 -0.1345 0.0000 O 0 0\n 3.6375 0.9049 0.0000 R# 0 0\n 7.8420 6.1003 0.0000 C 0 0\n 7.0920 7.4003 0.0000 N 0 0\n 7.7107 8.7528 0.0000 C 0 0\n 5.6109 7.5356 0.0000 C 0 0\n 5.2965 9.0023 0.0000 C 0 0\n 6.5942 9.7545 0.0000 C 0 0\n 8.8856 8.9973 0.0000 O 0 0\n 4.8148 6.6378 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 1 6 1 0\n 2 7 1 0\n 7 8 2 0\n 7 9 1 0\n 5 10 1 0\n 10 11 1 0\n 12 11 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 2 0\n 12 15 1 0\n 12 16 2 0\n 13 17 2 0\nM RGP 1 9 1\nM END\n> <Name>\n4-(N-maleimidomethyl)cyclohexane-1-carboxylate\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nMCC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n\n$$$$\nDiethylene Glycol\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n -3.8999 -0.3833 0.0000 O 0 0\n -2.5999 0.3667 0.0000 C 0 0\n -1.3000 -0.3833 0.0000 C 0 0\n 0.0000 0.3667 0.0000 O 0 0\n 1.3000 -0.3833 0.0000 C 0 0\n 2.6000 0.3667 0.0000 C 0 0\n 3.9000 -0.3833 0.0000 O 0 0\n 4.9394 0.2164 0.0000 R# 0 0\n -4.9394 0.2164 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 1 9 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\nDiethylene Glycol\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nPEG2\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nSMCC linker from Pierce\n SciTegic07272112182D\n\n 18 19 0 0 1 0 999 V2000\n 0.4966 -1.0108 0.0000 C 0 0\n -0.8438 -1.6860 0.0000 C 0 0\n -2.0992 -0.8637 0.0000 N 0 0\n -4.4215 -0.2334 0.0000 C 0 0\n -3.4845 -1.4048 0.0000 C 0 0\n -2.1504 0.6228 0.0000 C 0 0\n -3.5970 1.0196 0.0000 C 0 0\n -1.2090 1.3667 0.0000 O 0 0\n -3.7953 -2.5638 0.0000 O 0 0\n -4.0204 2.1426 0.0000 R# 0 0\n 1.9171 1.1645 0.0000 C 0 0\n 3.1730 0.3443 0.0000 C 0 0\n 3.0908 -1.1534 0.0000 C 0 0\n 1.7526 -1.8310 0.0000 C 0 0\n 0.5789 0.4870 0.0000 C 0 0\n 4.5135 1.0196 0.0000 C 0 0\n 5.5173 0.3621 0.0000 O 0 0\n 4.5813 2.2177 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 5 3 1 0\n 3 6 1 0\n 4 5 1 0\n 6 7 1 0\n 4 7 1 0\n 6 8 2 0\n 5 9 2 0\n 7 10 1 0\n 14 1 1 0\n 1 15 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 11 15 1 0\n 12 16 1 0\n 16 17 2 0\n 16 18 1 0\nM RGP 2 10 1 18 2\nM END\n> <Name>\nSMCC linker from Pierce\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nSMCC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nSM(PEG)2 linker from Pierce\n SciTegic07272112182D\n\n 24 24 0 0 1 0 999 V2000\n 0.9955 -0.0240 0.0000 N 0 0\n 2.1808 -0.9447 0.0000 C 0 0\n 3.5711 -0.3794 0.0000 C 0 0\n 4.7564 -1.3000 0.0000 C 0 0\n 6.1443 -0.7358 0.0000 N 0 0\n 8.5647 -0.5561 0.0000 C 0 0\n 7.4197 -1.5251 0.0000 C 0 0\n 6.5009 0.7213 0.0000 C 0 0\n 7.9968 0.8323 0.0000 C 0 0\n 5.7256 1.6372 0.0000 O 0 0\n 7.5086 -2.7219 0.0000 O 0 0\n 8.6283 1.8526 0.0000 R# 0 0\n 2.0167 -2.1334 0.0000 O 0 0\n -0.3947 -0.5893 0.0000 C 0 0\n -1.5801 0.3313 0.0000 C 0 0\n -2.9705 -0.2339 0.0000 O 0 0\n -4.1556 0.6867 0.0000 C 0 0\n -5.5460 0.1214 0.0000 C 0 0\n -6.7313 1.0422 0.0000 O 0 0\n -8.1216 0.4769 0.0000 C 0 0\n -9.3068 1.3976 0.0000 C 0 0\n -10.6971 0.8323 0.0000 C 0 0\n -10.8610 -0.3565 0.0000 R# 0 0\n -11.6448 1.5683 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 7 5 1 0\n 5 8 1 0\n 6 7 1 0\n 8 9 1 0\n 6 9 1 0\n 8 10 2 0\n 7 11 2 0\n 9 12 1 0\n 2 13 2 0\n 1 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 19 20 1 0\n 20 21 1 0\n 21 22 1 0\n 22 23 1 0\n 22 24 2 0\nM RGP 2 12 2 23 1\nM END\n> <Name>\nSM(PEG)2 linker from Pierce\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nSMPEG2\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]H\n\n$$$$\nDipropanol-disulfide\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n -6.8609 -0.6650 0.0000 R# 0 0\n -5.8620 0.0000 0.0000 O 0 0\n -4.5166 -0.6653 0.0000 C 0 0\n -3.2673 0.1663 0.0000 C 0 0\n -1.9220 -0.4990 0.0000 C 0 0\n -0.6726 0.3327 0.0000 S 0 0\n 0.6726 -0.3327 0.0000 S 0 0\n 1.9220 0.4990 0.0000 C 0 0\n 3.2673 -0.1663 0.0000 C 0 0\n 4.5166 0.6653 0.0000 C 0 0\n 5.8620 0.0000 0.0000 O 0 0\n 6.8609 0.6650 0.0000 R# 0 0\n 6 7 1 0\n 2 3 1 0\n 7 8 1 0\n 8 9 1 0\n 3 4 1 0\n 9 10 1 0\n 10 11 1 0\n 4 5 1 0\n 11 12 1 0\n 1 2 1 0\n 5 6 1 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\nDipropanol-disulfide\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nSS3\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nHexynyl alcohol\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 1.4606 0.1503 0.0000 O 0 0\n 2.2118 -1.1490 0.0000 C 0 0\n 0.2606 0.1503 0.0000 R# 0 0\n 3.7126 -1.1491 0.0000 C 0 0\n 4.4638 -2.4484 0.0000 C 0 0\n 5.9647 -2.4484 0.0000 C 0 0\n 6.7158 -3.7477 0.0000 C 0 0\n 7.3165 -4.7866 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 3 0\nM RGP 1 3 1\nM END\n> <Name>\nHexynyl alcohol\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nhxy\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nSymmetric Doubler\n SciTegic07272112182D\n\n 23 22 0 0 1 0 999 V2000\n 5.1451 -1.0717 0.0000 C 0 0\n 3.9656 -0.1437 0.0000 C 0 0\n 2.5718 -0.7004 0.0000 N 0 0\n 1.3922 0.2275 0.0000 C 0 0\n -0.0015 -0.3292 0.0000 C 0 0\n -1.1811 0.5987 0.0000 C 0 0\n -2.5749 0.0420 0.0000 N 0 0\n -3.7544 0.9700 0.0000 C 0 0\n -5.1483 0.4133 0.0000 C 0 0\n -0.2189 -1.8141 0.0000 O 0 0\n -6.3278 1.3412 0.0000 C 0 0\n -7.7215 0.7845 0.0000 C 0 0\n -8.9011 1.7124 0.0000 C 0 0\n -10.2948 1.1557 0.0000 O 0 0\n 6.5389 -0.5150 0.0000 C 0 0\n 7.7185 -1.4429 0.0000 C 0 0\n 9.1122 -0.8862 0.0000 C 0 0\n 10.2918 -1.8141 0.0000 O 0 0\n -3.5831 2.1577 0.0000 O 0 0\n 4.1370 1.0440 0.0000 O 0 0\n -1.3338 -2.2581 0.0000 R# 0 0\n 11.4062 -1.3690 0.0000 R# 0 0\n -11.2381 1.8977 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 5 10 1 0\n 9 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 1 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 8 19 2 0\n 2 20 2 0\n 10 21 1 0\n 18 22 1 0\n 14 23 1 0\nM RGP 3 21 1 22 2 23 3\nM END\n> <Name>\nSymmetric Doubler\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nsDBL\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]H\n\n$$$$\nD-Pyl\n SciTegic07272112182D\n\n 19 19 0 0 1 0 999 V2000\n -2.0487 -3.8600 0.0000 R# 0 0\n -1.0256 -4.4508 0.0000 N 0 0\n -0.0024 -3.8600 0.0000 C 0 0 1 0 0 0\n 1.0208 -4.4508 0.0000 C 0 0\n 2.0439 -3.8600 0.0000 R# 0 0\n 1.0208 -5.6322 0.0000 O 0 0\n -0.0024 -2.6786 0.0000 C 0 0\n 0.5883 -1.6554 0.0000 C 0 0\n -0.0024 -0.6322 0.0000 C 0 0\n 0.5883 0.3909 0.0000 C 0 0\n -0.0024 1.4141 0.0000 N 0 0\n 0.5883 2.4373 0.0000 C 0 0\n -0.0024 3.4604 0.0000 C 0 0 1 0 0 0\n 1.7698 2.4373 0.0000 O 0 0\n -1.1768 3.5839 0.0000 C 0 0\n -1.4223 4.7390 0.0000 C 0 0\n -0.3997 5.3294 0.0000 C 0 0\n 0.4779 4.5392 0.0000 N 0 0\n -2.0122 2.7484 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\n 3 7 1 6\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 12 14 2 0\n 17 18 2 0\n 16 17 1 0\n 15 16 1 0\n 13 15 1 1\n 18 13 1 0\n 15 19 1 0\nM RGP 2 1 1 5 2\nM END\n> <Name>\nD-Pyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndPyl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-SelenoCysteine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n -1.9326 -0.3282 0.0000 R# 0 0\n -0.9095 -0.9190 0.0000 N 0 0\n 0.1137 -0.3282 0.0000 C 0 0 1 0 0 0\n 1.1369 -0.9190 0.0000 C 0 0\n 2.1600 -0.3282 0.0000 R# 0 0\n 1.1369 -2.1004 0.0000 O 0 0\n 0.1137 0.8532 0.0000 C 0 0\n -0.9095 1.4440 0.0000 Se 0 0\n -0.9095 2.6254 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\n 3 7 1 6\n 7 8 1 0\n 8 9 1 0\nM RGP 3 1 1 5 2 9 3\nM END\n> <Name>\nD-SelenoCysteine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndSec\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nPyl\n SciTegic07272112182D\n\n 19 19 0 0 1 0 999 V2000\n -2.0487 -3.8600 0.0000 R# 0 0\n -1.0256 -4.4508 0.0000 N 0 0\n -0.0024 -3.8600 0.0000 C 0 0 2 0 0 0\n 1.0208 -4.4508 0.0000 C 0 0\n 2.0439 -3.8600 0.0000 R# 0 0\n 1.0208 -5.6322 0.0000 O 0 0\n -0.0024 -2.6786 0.0000 C 0 0\n 0.5883 -1.6554 0.0000 C 0 0\n -0.0024 -0.6322 0.0000 C 0 0\n 0.5883 0.3909 0.0000 C 0 0\n -0.0024 1.4141 0.0000 N 0 0\n 0.5883 2.4373 0.0000 C 0 0\n -0.0024 3.4604 0.0000 C 0 0 1 0 0 0\n 1.7698 2.4373 0.0000 O 0 0\n -1.1768 3.5839 0.0000 C 0 0\n -1.4223 4.7390 0.0000 C 0 0\n -0.3997 5.3294 0.0000 C 0 0\n 0.4779 4.5392 0.0000 N 0 0\n -2.0122 2.7484 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\n 3 7 1 1\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 12 14 2 0\n 17 18 2 0\n 16 17 1 0\n 15 16 1 0\n 13 15 1 1\n 18 13 1 0\n 15 19 1 0\nM RGP 2 1 1 5 2\nM END\n> <Name>\nPyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPyl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nC-Terminal NMe\n SciTegic07272112182D\n\n 3 2 0 0 0 0 999 V2000\n 8.3795 -8.3427 0.0000 N 0 0\n 8.8579 -7.5142 0.0000 C 0 0\n 7.4230 -8.3427 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\nM RGP 1 3 1\nM END\n> <Name>\nC-Terminal NMe\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNMe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nC-Terminal OMe\n SciTegic07272112182D\n\n 3 2 0 0 0 0 999 V2000\n 8.4509 -11.5165 0.0000 O 0 0\n 8.9293 -10.6879 0.0000 C 0 0\n 7.4944 -11.5165 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\nM RGP 1 3 1\nM END\n> <Name>\nC-Terminal OMe\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOMe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nC-Terminal OtBu\n SciTegic07272112182D\n\n 6 5 0 0 0 0 999 V2000\n 7.7323 -15.8067 0.0000 O 0 0\n 6.7756 -15.8067 0.0000 R# 0 0\n 8.2105 -14.9781 0.0000 C 0 0\n 7.7322 -14.1496 0.0000 C 0 0\n 8.6888 -14.1496 0.0000 C 0 0\n 9.1673 -14.9780 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 3 4 1 0\n 3 5 1 0\n 3 6 1 0\nM RGP 1 2 1\nM END\n> <Name>\nC-Terminal OtBu\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOtBu\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nC-Terminal Oxa\n SciTegic07272112182D\n\n 6 6 0 0 0 0 999 V2000\n 16.7858 -10.6257 0.0000 C 0 0\n 17.3477 -9.8523 0.0000 C 0 0\n 18.2570 -10.1478 0.0000 N 0 0\n 18.2569 -11.1038 0.0000 C 0 0\n 17.3476 -11.3992 0.0000 O 0 0\n 15.8290 -10.6257 0.0000 R# 0 0\n 2 1 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 0\nM RGP 1 6 1\nM END\n> <Name>\nC-Terminal Oxa\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOxa\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nC-Terminal OBz\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 15.2550 -7.2049 0.0000 C 0 0\n 16.2116 -7.2049 0.0000 C 0 0\n 14.7767 -6.3766 0.0000 O 0 0\n 16.6900 -6.3764 0.0000 C 0 0\n 17.6438 -6.3774 0.0000 C 0 0\n 18.1239 -7.2070 0.0000 C 0 0\n 17.6479 -8.0312 0.0000 C 0 0\n 16.6920 -8.0368 0.0000 C 0 0\n 13.8202 -6.3766 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 4 2 2 0\n 5 4 1 0\n 6 5 2 0\n 7 6 1 0\n 8 7 2 0\n 2 8 1 0\n 3 9 1 0\nM RGP 1 9 1\nM END\n> <Name>\nC-Terminal OBz\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOBz\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nC-Terminal methyl\n SciTegic07272112182D\n\n 2 1 0 0 0 0 999 V2000\n 2.8000 0.7500 0.0000 C 0 0\n 1.3000 0.7500 0.0000 R# 0 0\n 1 2 1 0\nM RGP 1 2 1\nM END\n> <Name>\nC-Terminal methyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n-Me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nL-allo-Isoleucine\n SciTegic09012117322D\n\n 10 9 0 0 1 0 999 V2000\n -1.3038 -3.1492 0.0000 C 0 0\n -1.3015 -1.6492 0.0000 C 0 0\n -0.0011 -0.8999 0.0000 C 0 0 1 0 0 0\n 1.2971 -1.6515 0.0000 C 0 0\n 0.0012 0.6009 0.0000 C 0 0 2 0 0 0\n -1.2992 1.3502 0.0000 N 0 0\n -2.5981 0.5999 0.0000 R# 0 0\n 1.3016 1.3502 0.0000 C 0 0\n 2.5998 0.5986 0.0000 R# 0 0\n 1.3039 2.8501 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 0\n 3 4 1 6\n 3 5 1 0\n 5 6 1 6\n 6 7 1 0\n 5 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 2 7 1 9 2\nM END\n> <Name>\nL-allo-Isoleucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\naIle\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nI\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Gamma glutamic acid\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n -3.2036 -1.0674 0.0000 R# 0 0\n -1.7036 -1.0637 0.0000 N 0 0\n -0.9556 0.2375 0.0000 C 0 0 2 0 0 0\n 0.5452 0.2367 0.0000 C 0 0\n 1.2958 -1.0629 0.0000 C 0 0\n 2.7966 -1.0637 0.0000 C 0 0\n 3.5468 0.2352 0.0000 R# 0 0\n 3.5468 -2.3626 0.0000 O 0 0\n -1.7062 1.5371 0.0000 C 0 0\n -0.9560 2.8360 0.0000 R# 0 0\n -3.2062 1.5379 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 6 8 2 0\n 3 9 1 0\n 9 10 1 0\n 9 11 2 0\nM RGP 3 1 1 7 2 10 3\nM END\n> <Name>\nD-Gamma glutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-gGlu\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\nD-Norleucine\n SciTegic09012117322D\n\n 10 9 0 0 1 0 999 V2000\n -2.2134 3.6741 0.0000 C 0 0\n -0.9137 2.9252 0.0000 C 0 0\n -0.9114 1.4244 0.0000 C 0 0\n 0.3890 0.6751 0.0000 C 0 0\n 0.3913 -0.8257 0.0000 C 0 0 1 0 0 0\n -0.9091 -1.5750 0.0000 N 0 0\n -2.2080 -0.8247 0.0000 R# 0 0\n 1.6917 -1.5750 0.0000 C 0 0\n 2.9898 -0.8234 0.0000 R# 0 0\n 1.6939 -3.0749 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 6\n 5 6 1 0\n 6 7 1 0\n 5 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 2 7 1 9 2\nM END\n> <Name>\nD-Norleucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Nle\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Homophenylalanine\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -2.0402 2.2498 0.0000 R# 0 0\n -0.7413 3.0001 0.0000 N 0 0\n 0.5591 2.2509 0.0000 C 0 0 2 0 0 0\n 0.5568 0.7500 0.0000 C 0 0\n -0.7436 0.0008 0.0000 C 0 0\n -0.7458 -1.5001 0.0000 C 0 0\n -2.0444 -2.2508 0.0000 C 0 0\n -2.0436 -3.7508 0.0000 C 0 0\n -0.7441 -4.5001 0.0000 C 0 0\n 0.5545 -3.7494 0.0000 C 0 0\n 0.5536 -2.2494 0.0000 C 0 0\n 1.8595 3.0001 0.0000 C 0 0\n 3.1577 2.2486 0.0000 R# 0 0\n 1.8618 4.5001 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 10 11 2 0\n 6 11 1 0\n 3 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 1 1 13 2\nM END\n> <Name>\nD-Homophenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-hPhe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-4-Hydroxyproline\n SciTegic09012117322D\n\n 10 10 0 0 1 0 999 V2000\n -1.9677 -2.9458 0.0000 O 0 0\n -1.2857 -1.6098 0.0000 C 0 0 1 0 0 0\n 0.1960 -1.3762 0.0000 C 0 0\n 0.4318 0.1051 0.0000 C 0 0 1 0 0 0\n -0.9043 0.7871 0.0000 N 0 0\n -1.1378 2.2688 0.0000 R# 0 0\n -1.9657 -0.2728 0.0000 C 0 0\n 1.7658 0.7871 0.0000 C 0 0\n 3.0246 -0.0286 0.0000 R# 0 0\n 1.8432 2.2851 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 4 3 1 0\n 4 5 1 0\n 5 6 1 0\n 5 7 1 0\n 2 7 1 0\n 4 8 1 1\n 8 9 1 0\n 8 10 2 0\nM RGP 2 6 1 9 2\nM END\n> <Name>\nD-4-Hydroxyproline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Hyp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Norvaline\n SciTegic09012117322D\n\n 9 8 0 0 1 0 999 V2000\n -1.1596 -3.3327 0.0000 C 0 0\n -1.1574 -1.8327 0.0000 C 0 0\n 0.1431 -1.0834 0.0000 C 0 0\n 0.1453 0.4174 0.0000 C 0 0 1 0 0 0\n -1.1550 1.1667 0.0000 N 0 0\n -2.4540 0.4164 0.0000 R# 0 0\n 1.4458 1.1667 0.0000 C 0 0\n 2.7439 0.4151 0.0000 R# 0 0\n 1.4480 2.6666 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 4 3 1 1\n 4 5 1 0\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 2 6 1 8 2\nM END\n> <Name>\nD-Norvaline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Nva\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Ornithine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n -2.0065 -1.2951 0.0000 R# 0 0\n -0.7076 -2.0454 0.0000 N 0 0\n 0.5928 -1.2962 0.0000 C 0 0 2 0 0 0\n 0.5905 0.2047 0.0000 C 0 0\n -0.7099 0.9540 0.0000 C 0 0\n -0.7121 2.4548 0.0000 C 0 0\n -2.0125 3.2041 0.0000 N 0 0\n -2.0148 4.7041 0.0000 R# 0 0\n 1.8932 -2.0454 0.0000 C 0 0\n 3.1913 -1.2939 0.0000 R# 0 0\n 1.8955 -3.5454 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 3 9 1 0\n 9 10 1 0\n 9 11 2 0\nM RGP 3 1 1 8 3 10 2\nM END\n> <Name>\nD-Ornithine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Orn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nPyroglutamic acid\n SciTegic09012117322D\n\n 10 10 0 0 1 0 999 V2000\n -0.9899 -1.9779 0.0000 R# 0 0\n -0.7563 -0.4962 0.0000 N 0 0\n 0.5796 0.1858 0.0000 C 0 0 1 0 0 0\n 0.3439 1.6671 0.0000 C 0 0\n -1.1378 1.9007 0.0000 C 0 0\n -1.8178 0.5636 0.0000 C 0 0\n -3.2992 0.3279 0.0000 O 0 0\n 1.9137 -0.4962 0.0000 C 0 0\n 3.1725 0.3195 0.0000 R# 0 0\n 1.9912 -1.9942 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 2 6 1 0\n 6 7 2 0\n 3 8 1 1\n 8 9 1 0\n 8 10 2 0\nM RGP 2 1 1 9 2\nM END\n> <Name>\nPyroglutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPyr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Pyroglutamic acid\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n 3.1202 -2.0921 0.0000 R# 0 0\n 1.6281 -2.2462 0.0000 C 0 0\n 1.0161 -3.6157 0.0000 O 0 0\n 0.7500 -1.0323 0.0000 C 0 0 1 0 0 0\n 1.2135 0.3943 0.0000 C 0 0\n 0.0000 1.2760 0.0000 C 0 0\n -1.2135 0.3943 0.0000 C 0 0\n -2.6401 0.8578 0.0000 O 0 0\n -0.7500 -1.0323 0.0000 N 0 0\n 1 2 1 0\n 2 3 2 0\n 4 2 1 6\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 2 0\n 7 9 1 0\n 4 9 1 0\nM RGP 1 1 2\nM END\n> <Name>\nD-Pyroglutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Pyr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n3-Chloro-L-phenylalanine\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8032 -0.2585 0.0000 Cl 0 0\n -2.5064 -1.0123 0.0000 C 0 0\n -2.5107 -2.5123 0.0000 C 0 0\n -1.2139 -3.2661 0.0000 C 0 0\n 0.0873 -2.5199 0.0000 C 0 0\n 0.0917 -1.0199 0.0000 C 0 0\n 1.3921 -0.2706 0.0000 C 0 0\n 1.3944 1.2302 0.0000 C 0 0 2 0 0 0\n 0.0940 1.9795 0.0000 N 0 0\n -1.2049 1.2292 0.0000 R# 0 0\n 2.6948 1.9795 0.0000 C 0 0\n 3.9929 1.2279 0.0000 R# 0 0\n 2.6970 3.4795 0.0000 O 0 0\n -1.2051 -0.2661 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 6\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\n 6 14 2 0\n 2 14 1 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n3-Chloro-L-phenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe3Cl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n4-Chloro-L-phenylalanine\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8113 -3.0442 0.0000 Cl 0 0\n -2.5101 -2.2980 0.0000 C 0 0\n -1.2133 -3.0518 0.0000 C 0 0\n 0.0879 -2.3056 0.0000 C 0 0\n 0.0923 -0.8056 0.0000 C 0 0\n 1.3927 -0.0563 0.0000 C 0 0\n 1.3950 1.4445 0.0000 C 0 0 2 0 0 0\n 0.0946 2.1938 0.0000 N 0 0\n -1.2043 1.4435 0.0000 R# 0 0\n 2.6954 2.1938 0.0000 C 0 0\n 3.9936 1.4422 0.0000 R# 0 0\n 2.6977 3.6938 0.0000 O 0 0\n -1.2045 -0.0518 0.0000 C 0 0\n -2.5057 -0.7980 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n4-Chloro-L-phenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe4Cl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\np-Aminophenylalanine\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8113 -3.0442 0.0000 N 0 0\n -2.5101 -2.2980 0.0000 C 0 0\n -1.2133 -3.0518 0.0000 C 0 0\n 0.0879 -2.3056 0.0000 C 0 0\n 0.0923 -0.8056 0.0000 C 0 0\n 1.3927 -0.0563 0.0000 C 0 0\n 1.3950 1.4445 0.0000 C 0 0 2 0 0 0\n 0.0946 2.1938 0.0000 N 0 0\n -1.2043 1.4435 0.0000 R# 0 0\n 2.6954 2.1938 0.0000 C 0 0\n 3.9936 1.4422 0.0000 R# 0 0\n 2.6977 3.6938 0.0000 O 0 0\n -1.2045 -0.0518 0.0000 C 0 0\n -2.5057 -0.7980 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\np-Aminophenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe4NH\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nO-tert-Butyl-L-serine\n SciTegic09012117322D\n\n 12 11 0 0 1 0 999 V2000\n -2.1692 2.9989 0.0000 C 0 0\n -0.8695 2.2501 0.0000 C 0 0\n 0.4287 3.0016 0.0000 C 0 0\n -0.8710 3.7500 0.0000 C 0 0\n -0.8672 0.7492 0.0000 O 0 0\n 0.4332 -0.0001 0.0000 C 0 0\n 0.4355 -1.5009 0.0000 C 0 0 2 0 0 0\n -0.8649 -2.2502 0.0000 N 0 0\n -2.1638 -1.4999 0.0000 R# 0 0\n 1.7359 -2.2502 0.0000 C 0 0\n 3.0341 -1.4986 0.0000 R# 0 0\n 1.7382 -3.7501 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 1 0\n 5 6 1 0\n 7 6 1 1\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\nO-tert-Butyl-L-serine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nSertBu\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nO-Benzyl-L-tyrosine\n SciTegic07272112182D\n\n 21 22 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 1 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -2.6003 1.4977 0.0000 O 0 0\n -3.8990 0.7455 0.0000 C 0 0\n -5.2003 1.4932 0.0000 C 0 0\n -6.4994 0.7432 0.0000 C 0 0\n -7.7985 1.4932 0.0000 C 0 0\n -7.7985 2.9932 0.0000 C 0 0\n -6.4995 3.7432 0.0000 C 0 0\n -5.2004 2.9933 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 11 16 1 0\n 8 17 1 0\n 17 18 2 0\n 5 18 1 0\n 3 19 1 0\n 19 20 1 0\n 19 21 2 0\nM RGP 2 1 1 20 2\nM END\n> <Name>\nO-Benzyl-L-tyrosine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyr_Bn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-(1-naphthyl)-alanine\n SciTegic09012117322D\n\n 17 18 0 0 1 0 999 V2000\n -1.5241 2.2924 0.0000 R# 0 0\n -0.2254 3.0427 0.0000 N 0 0\n 1.0751 2.2934 0.0000 C 0 0 1 0 0 0\n 1.0728 0.7926 0.0000 C 0 0\n -0.2276 0.0433 0.0000 C 0 0\n -1.5244 0.7971 0.0000 C 0 0\n -2.8256 0.0509 0.0000 C 0 0\n -2.8300 -1.4491 0.0000 C 0 0\n -1.5331 -2.2028 0.0000 C 0 0\n -1.5375 -3.7029 0.0000 C 0 0\n -0.2407 -4.4567 0.0000 C 0 0\n 1.0606 -3.7104 0.0000 C 0 0\n 1.0649 -2.2105 0.0000 C 0 0\n -0.2319 -1.4567 0.0000 C 0 0\n 2.3755 3.0427 0.0000 C 0 0\n 3.6736 2.2912 0.0000 R# 0 0\n 2.3778 4.5427 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 5 14 1 0\n 9 14 1 0\n 3 15 1 0\n 15 16 1 0\n 15 17 2 0\nM RGP 2 1 1 16 2\nM END\n> <Name>\n3-(1-naphthyl)-alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n1Nal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-epsilon-tert-Boc-L-lysine\n SciTegic09012117322D\n\n 18 17 0 0 1 0 999 V2000\n -2.8247 -6.4583 0.0000 C 0 0\n -2.8225 -4.9583 0.0000 C 0 0\n -4.1206 -4.2068 0.0000 C 0 0\n -4.1225 -5.7065 0.0000 C 0 0\n -1.5221 -4.2090 0.0000 O 0 0\n -1.5198 -2.7082 0.0000 C 0 0\n -2.8179 -1.9567 0.0000 O 0 0\n -0.2194 -1.9589 0.0000 N 0 0\n -0.2171 -0.4581 0.0000 C 0 0\n 1.0833 0.2911 0.0000 C 0 0\n 1.0856 1.7919 0.0000 C 0 0\n 2.3860 2.5412 0.0000 C 0 0\n 2.3883 4.0420 0.0000 C 0 0 2 0 0 0\n 1.0879 4.7913 0.0000 N 0 0\n -0.2110 4.0410 0.0000 R# 0 0\n 3.6887 4.7913 0.0000 C 0 0\n 4.9868 4.0397 0.0000 R# 0 0\n 3.6910 6.2913 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 1 0\n 5 6 1 0\n 6 7 2 0\n 6 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 13 12 1 6\n 13 14 1 0\n 14 15 1 0\n 13 16 1 0\n 16 17 1 0\n 16 18 2 0\nM RGP 2 15 1 17 2\nM END\n> <Name>\nN-epsilon-tert-Boc-L-lysine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLysBoc\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nL-allo-Threonine\n SciTegic09012117322D\n\n 9 8 0 0 1 0 999 V2000\n 1.1521 2.0015 0.0000 C 0 0\n -0.1460 1.2499 0.0000 C 0 0 2 0 0 0\n -1.4457 1.9988 0.0000 O 0 0\n -0.1437 -0.2509 0.0000 C 0 0 2 0 0 0\n -1.4441 -1.0002 0.0000 N 0 0\n -2.7430 -0.2499 0.0000 R# 0 0\n 1.1567 -1.0002 0.0000 C 0 0\n 2.4548 -0.2487 0.0000 R# 0 0\n 1.1589 -2.5001 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 2 4 1 0\n 4 5 1 1\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 2 6 1 8 2\nM END\n> <Name>\nL-allo-Threonine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\naThr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-3-naphthylalanine\n SciTegic07272112182D\n\n 17 18 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 2 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -2.5981 1.5000 0.0000 C 0 0\n -3.8971 0.7500 0.0000 C 0 0\n -3.8971 -0.7500 0.0000 C 0 0\n -2.5981 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 8 13 1 0\n 13 14 2 0\n 5 14 1 0\n 3 15 1 0\n 15 16 1 0\n 15 17 2 0\nM RGP 2 1 1 16 2\nM END\n> <Name>\nD-3-naphthylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-2Nal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-3-thienylalanine\n SciTegic09012117322D\n\n 12 12 0 0 1 0 999 V2000\n -1.7045 -1.0135 0.0000 R# 0 0\n -0.4057 -1.7638 0.0000 N 0 0\n 0.8947 -1.0145 0.0000 C 0 0 2 0 0 0\n 0.8925 0.4863 0.0000 C 0 0\n -0.4056 1.2343 0.0000 C 0 0\n -0.5668 2.7256 0.0000 C 0 0\n -2.0349 3.0333 0.0000 C 0 0\n -2.7811 1.7320 0.0000 C 0 0\n -1.7742 0.6202 0.0000 S 0 0\n 2.1951 -1.7638 0.0000 C 0 0\n 3.4933 -1.0124 0.0000 R# 0 0\n 2.1974 -3.2638 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 5 9 1 0\n 3 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 1 1 11 2\nM END\n> <Name>\nD-3-thienylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-2Thi\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-allo-4-hydroxyproline\n SciTegic09012117322D\n\n 10 10 0 0 1 0 999 V2000\n -1.9677 -2.9458 0.0000 O 0 0\n -1.2857 -1.6098 0.0000 C 0 0 2 0 0 0\n 0.1960 -1.3762 0.0000 C 0 0\n 0.4318 0.1051 0.0000 C 0 0 1 0 0 0\n -0.9043 0.7871 0.0000 N 0 0\n -1.1378 2.2688 0.0000 R# 0 0\n -1.9657 -0.2728 0.0000 C 0 0\n 1.7658 0.7871 0.0000 C 0 0\n 3.0246 -0.0286 0.0000 R# 0 0\n 1.8432 2.2851 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 4 3 1 0\n 4 5 1 0\n 5 6 1 0\n 5 7 1 0\n 2 7 1 0\n 4 8 1 1\n 8 9 1 0\n 8 10 2 0\nM RGP 2 6 1 9 2\nM END\n> <Name>\nD-allo-4-hydroxyproline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-aHyp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-allo-Isoleucine\n SciTegic09012117322D\n\n 10 9 0 0 1 0 999 V2000\n -1.3038 -3.1492 0.0000 C 0 0\n -1.3015 -1.6492 0.0000 C 0 0\n -0.0011 -0.8999 0.0000 C 0 0 2 0 0 0\n 1.2971 -1.6515 0.0000 C 0 0\n 0.0012 0.6009 0.0000 C 0 0 1 0 0 0\n -1.2992 1.3502 0.0000 N 0 0\n -2.5981 0.5999 0.0000 R# 0 0\n 1.3016 1.3502 0.0000 C 0 0\n 2.5998 0.5986 0.0000 R# 0 0\n 1.3039 2.8501 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 0\n 3 4 1 1\n 3 5 1 0\n 5 6 1 1\n 6 7 1 0\n 5 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 2 7 1 9 2\nM END\n> <Name>\nD-allo-Isoleucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-aIle\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nI\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-2-phenylglycine\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -2.7098 1.1911 0.0000 R# 0 0\n -1.4094 1.9388 0.0000 N 0 0\n -0.1105 1.1868 0.0000 C 0 0 1 0 0 0\n 1.1884 1.9388 0.0000 C 0 0\n 2.4881 1.1899 0.0000 R# 0 0\n 1.1875 3.4388 0.0000 O 0 0\n -0.1097 -0.3140 0.0000 C 0 0\n -1.4067 -1.0674 0.0000 C 0 0\n -1.4028 -2.5674 0.0000 C 0 0\n -0.1018 -3.3140 0.0000 C 0 0\n 1.1953 -2.5606 0.0000 C 0 0\n 1.1913 -1.0606 0.0000 C 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\n 3 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 7 12 1 0\nM RGP 2 1 1 5 2\nM END\n> <Name>\nD-2-phenylglycine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Phg\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nO-tert-Butyl-D-serine\n SciTegic09012117322D\n\n 12 11 0 0 1 0 999 V2000\n -2.1692 2.9989 0.0000 C 0 0\n -0.8695 2.2501 0.0000 C 0 0\n 0.4287 3.0016 0.0000 C 0 0\n -0.8710 3.7500 0.0000 C 0 0\n -0.8672 0.7492 0.0000 O 0 0\n 0.4332 -0.0001 0.0000 C 0 0\n 0.4355 -1.5009 0.0000 C 0 0 1 0 0 0\n -0.8649 -2.2502 0.0000 N 0 0\n -2.1638 -1.4999 0.0000 R# 0 0\n 1.7359 -2.2502 0.0000 C 0 0\n 3.0341 -1.4986 0.0000 R# 0 0\n 1.7382 -3.7501 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 1 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\nO-tert-Butyl-D-serine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDSertB\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\np-Methylphenylalanine\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8113 -3.0442 0.0000 C 0 0\n -2.5101 -2.2980 0.0000 C 0 0\n -1.2133 -3.0518 0.0000 C 0 0\n 0.0879 -2.3056 0.0000 C 0 0\n 0.0923 -0.8056 0.0000 C 0 0\n 1.3927 -0.0563 0.0000 C 0 0\n 1.3950 1.4445 0.0000 C 0 0 2 0 0 0\n 0.0946 2.1938 0.0000 N 0 0\n -1.2043 1.4435 0.0000 R# 0 0\n 2.6954 2.1938 0.0000 C 0 0\n 3.9936 1.4422 0.0000 R# 0 0\n 2.6977 3.6938 0.0000 O 0 0\n -1.2045 -0.0518 0.0000 C 0 0\n -2.5057 -0.7980 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\np-Methylphenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe4Me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nO-Benzyl-L-serine\n SciTegic09012117322D\n\n 15 15 0 0 1 0 999 V2000\n 1.2919 -5.2492 0.0000 R# 0 0\n 2.5886 -6.0033 0.0000 N 0 0\n 3.8912 -5.2578 0.0000 C 0 0 1 0 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 2.5951 -3.0039 0.0000 O 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 5.1894 -6.0109 0.0000 C 0 0\n 6.4897 -5.2632 0.0000 R# 0 0\n 5.1873 -7.5109 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 7 12 1 0\n 3 13 1 0\n 13 14 1 0\n 13 15 2 0\nM RGP 2 1 1 14 2\nM END\n> <Name>\nO-Benzyl-L-serine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nSer_Bn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nO-tert-Butyl-L-tyrosine\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -5.1332 -2.6056 0.0000 C 0 0\n -3.8304 -1.8621 0.0000 C 0 0\n -3.8234 -0.3621 0.0000 C 0 0\n -5.1258 -1.1058 0.0000 C 0 0\n -2.5340 -2.6181 0.0000 O 0 0\n -1.2305 -1.8742 0.0000 C 0 0\n 0.0664 -2.6280 0.0000 C 0 0\n 1.3676 -1.8818 0.0000 C 0 0\n 1.3720 -0.3818 0.0000 C 0 0\n 2.6724 0.3675 0.0000 C 0 0\n 2.6747 1.8683 0.0000 C 0 0 2 0 0 0\n 1.3742 2.6176 0.0000 N 0 0\n 0.0754 1.8673 0.0000 R# 0 0\n 3.9751 2.6176 0.0000 C 0 0\n 5.2732 1.8660 0.0000 R# 0 0\n 3.9773 4.1176 0.0000 O 0 0\n 0.0752 0.3720 0.0000 C 0 0\n -1.2261 -0.3742 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 11 10 1 6\n 11 12 1 0\n 12 13 1 0\n 11 14 1 0\n 14 15 1 0\n 14 16 2 0\n 9 17 1 0\n 17 18 2 0\n 6 18 1 0\nM RGP 2 13 1 15 2\nM END\n> <Name>\nO-tert-Butyl-L-tyrosine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyrtBu\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nL-allo-4-hydroxyproline\n SciTegic09012117322D\n\n 10 10 0 0 1 0 999 V2000\n -1.9677 -2.9458 0.0000 O 0 0\n -1.2857 -1.6098 0.0000 C 0 0 1 0 0 0\n 0.1960 -1.3762 0.0000 C 0 0\n 0.4318 0.1051 0.0000 C 0 0 2 0 0 0\n -0.9043 0.7871 0.0000 N 0 0\n -1.1378 2.2688 0.0000 R# 0 0\n -1.9657 -0.2728 0.0000 C 0 0\n 1.7658 0.7871 0.0000 C 0 0\n 3.0246 -0.0286 0.0000 R# 0 0\n 1.8432 2.2851 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 4 3 1 0\n 4 5 1 0\n 5 6 1 0\n 5 7 1 0\n 2 7 1 0\n 4 8 1 6\n 8 9 1 0\n 8 10 2 0\nM RGP 2 6 1 9 2\nM END\n> <Name>\nL-allo-4-hydroxyproline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\naHyp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nHomophenylalanine\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -2.0402 2.2498 0.0000 R# 0 0\n -0.7413 3.0001 0.0000 N 0 0\n 0.5591 2.2509 0.0000 C 0 0 1 0 0 0\n 0.5568 0.7500 0.0000 C 0 0\n -0.7436 0.0008 0.0000 C 0 0\n -0.7458 -1.5001 0.0000 C 0 0\n -2.0444 -2.2508 0.0000 C 0 0\n -2.0436 -3.7508 0.0000 C 0 0\n -0.7441 -4.5001 0.0000 C 0 0\n 0.5545 -3.7494 0.0000 C 0 0\n 0.5536 -2.2494 0.0000 C 0 0\n 1.8595 3.0001 0.0000 C 0 0\n 3.1577 2.2486 0.0000 R# 0 0\n 1.8618 4.5001 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 10 11 2 0\n 6 11 1 0\n 3 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 1 1 13 2\nM END\n> <Name>\nHomophenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nhPhe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-3-(1-naphthyl)-alanine\n SciTegic09012117322D\n\n 17 18 0 0 1 0 999 V2000\n -1.5241 2.2924 0.0000 R# 0 0\n -0.2254 3.0427 0.0000 N 0 0\n 1.0751 2.2934 0.0000 C 0 0 2 0 0 0\n 1.0728 0.7926 0.0000 C 0 0\n -0.2276 0.0433 0.0000 C 0 0\n -1.5244 0.7971 0.0000 C 0 0\n -2.8256 0.0509 0.0000 C 0 0\n -2.8300 -1.4491 0.0000 C 0 0\n -1.5331 -2.2028 0.0000 C 0 0\n -1.5375 -3.7029 0.0000 C 0 0\n -0.2407 -4.4567 0.0000 C 0 0\n 1.0606 -3.7104 0.0000 C 0 0\n 1.0649 -2.2105 0.0000 C 0 0\n -0.2319 -1.4567 0.0000 C 0 0\n 2.3755 3.0427 0.0000 C 0 0\n 3.6736 2.2912 0.0000 R# 0 0\n 2.3778 4.5427 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 5 14 1 0\n 9 14 1 0\n 3 15 1 0\n 15 16 1 0\n 15 17 2 0\nM RGP 2 1 1 16 2\nM END\n> <Name>\nD-3-(1-naphthyl)-alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-1Nal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-allo-Threonine\n SciTegic09012117322D\n\n 9 8 0 0 1 0 999 V2000\n 1.1521 2.0015 0.0000 C 0 0\n -0.1460 1.2499 0.0000 C 0 0 1 0 0 0\n -1.4457 1.9988 0.0000 O 0 0\n -0.1437 -0.2509 0.0000 C 0 0 1 0 0 0\n -1.4441 -1.0002 0.0000 N 0 0\n -2.7430 -0.2499 0.0000 R# 0 0\n 1.1567 -1.0002 0.0000 C 0 0\n 2.4548 -0.2487 0.0000 R# 0 0\n 1.1589 -2.5001 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 2 4 1 0\n 4 5 1 6\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 2 6 1 8 2\nM END\n> <Name>\nD-allo-Threonine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-aThr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-2-Amino-3-cyclohexyl-propionic acid\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 2 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 5 10 1 0\n 3 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\nD-2-Amino-3-cyclohexyl-propionic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Cha\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-penicillamine (3-mercaptovaline)\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.2973 1.4333 0.0000 C 0 0\n -0.0008 0.6818 0.0000 C 0 0\n -0.0024 2.1818 0.0000 C 0 0\n -1.3012 1.4310 0.0000 S 0 0\n -1.3035 2.9310 0.0000 R# 0 0\n 0.0014 -0.8191 0.0000 C 0 0 1 0 0 0\n -1.2990 -1.5683 0.0000 N 0 0\n -2.5978 -0.8180 0.0000 R# 0 0\n 1.3018 -1.5683 0.0000 C 0 0\n 2.6000 -0.8168 0.0000 R# 0 0\n 1.3041 -3.0683 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 6 2 1 0\n 6 7 1 6\n 7 8 1 0\n 6 9 1 0\n 9 10 1 0\n 9 11 2 0\nM RGP 3 5 3 8 1 10 2\nM END\n> <Name>\nD-penicillamine (3-mercaptovaline)\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Pen\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\n4-Chloro-D-phenylalanine\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8113 -3.0442 0.0000 Cl 0 0\n -2.5101 -2.2980 0.0000 C 0 0\n -1.2133 -3.0518 0.0000 C 0 0\n 0.0879 -2.3056 0.0000 C 0 0\n 0.0923 -0.8056 0.0000 C 0 0\n 1.3927 -0.0563 0.0000 C 0 0\n 1.3950 1.4445 0.0000 C 0 0 1 0 0 0\n 0.0946 2.1938 0.0000 N 0 0\n -1.2043 1.4435 0.0000 R# 0 0\n 2.6954 2.1938 0.0000 C 0 0\n 3.9936 1.4422 0.0000 R# 0 0\n 2.6977 3.6938 0.0000 O 0 0\n -1.2045 -0.0518 0.0000 C 0 0\n -2.5057 -0.7980 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 1\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n4-Chloro-D-phenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDPhe4C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nO-Benzyl-D-serine\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n 1.2919 -5.2492 0.0000 R# 0 0\n 2.5886 -6.0033 0.0000 N 0 0\n 3.8912 -5.2578 0.0000 C 0 0 2 0 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 2.5951 -3.0039 0.0000 O 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 5.1894 -6.0109 0.0000 C 0 0\n 6.4897 -5.2632 0.0000 R# 0 0\n 5.1873 -7.5109 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 7 12 1 0\n 3 13 1 0\n 13 14 1 0\n 13 15 2 0\nM RGP 2 1 1 14 2\nM END\n> <Name>\nO-Benzyl-D-serine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDSerBn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nMesylate\n SciTegic07272112182D\n\n 5 4 0 0 0 0 999 V2000\n -0.2000 0.7500 0.0000 C 0 0\n 1.3000 0.7500 0.0000 S 0 0\n 2.8000 0.7500 0.0000 R# 0 0\n 2.0496 -0.5493 0.0000 O 0 0\n 2.0496 2.0493 0.0000 O 0 0\n 1 2 1 0\n 2 4 2 0\n 2 5 2 0\n 2 3 1 0\nM RGP 1 3 2\nM END\n> <Name>\nMesylate\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nMsO\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nPerhydroindolic acid\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n -0.2550 2.6034 0.0000 R# 0 0\n -0.0213 1.1217 0.0000 N 0 0\n -1.0820 0.0623 0.0000 C 0 0 1 0 0 0\n -2.5799 0.1419 0.0000 C 0 0\n -3.3978 -1.1155 0.0000 C 0 0\n -2.7178 -2.4526 0.0000 C 0 0\n -1.2199 -2.5322 0.0000 C 0 0\n -0.4020 -1.2748 0.0000 C 0 0 1 0 0 0\n 1.0789 -1.0416 0.0000 C 0 0\n 1.3147 0.4398 0.0000 C 0 0 1 0 0 0\n 2.6487 1.1217 0.0000 C 0 0\n 3.9075 0.3061 0.0000 R# 0 0\n 2.7262 2.6197 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 0\n 3 4 1 6\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 6\n 3 8 1 0\n 8 9 1 0\n 10 9 1 0\n 10 2 1 0\n 10 11 1 6\n 11 12 1 0\n 11 13 2 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\nPerhydroindolic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOic3aS\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nPipecolic acid\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n -0.9064 2.1749 0.0000 R# 0 0\n -0.9082 0.6749 0.0000 N 0 0\n -2.2081 -0.0735 0.0000 C 0 0\n -2.2099 -1.5735 0.0000 C 0 0\n -0.9118 -2.3251 0.0000 C 0 0\n 0.3882 -1.5766 0.0000 C 0 0\n 0.3900 -0.0766 0.0000 C 0 0 1 0 0 0\n 1.6891 0.6749 0.0000 C 0 0\n 2.9885 -0.0744 0.0000 R# 0 0\n 1.6887 2.1749 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 7 6 1 0\n 7 2 1 0\n 7 8 1 6\n 8 9 1 0\n 8 10 2 0\nM RGP 2 1 1 9 2\nM END\n> <Name>\nPipecolic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPip\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-(2-pyridyl)-alanine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 1 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 3 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\n3-(2-pyridyl)-alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n3Pal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-(4-Pyridyl)-alanine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 1 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 3 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\n3-(4-Pyridyl)-alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n4Pal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nAlpha-cyclohexylglycine\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -2.7098 1.1911 0.0000 R# 0 0\n -1.4094 1.9388 0.0000 N 0 0\n -0.1105 1.1868 0.0000 C 0 0 1 0 0 0\n -0.1097 -0.3140 0.0000 C 0 0\n -1.4067 -1.0674 0.0000 C 0 0\n -1.4028 -2.5674 0.0000 C 0 0\n -0.1018 -3.3140 0.0000 C 0 0\n 1.1953 -2.5606 0.0000 C 0 0\n 1.1913 -1.0606 0.0000 C 0 0\n 1.1884 1.9388 0.0000 C 0 0\n 2.4881 1.1899 0.0000 R# 0 0\n 1.1875 3.4388 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 4 9 1 0\n 3 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 1 1 11 2\nM END\n> <Name>\nAlpha-cyclohexylglycine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nChg\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-3-(2-pyridyl)-alanine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 2 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 3 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\nD-3-(2-pyridyl)-alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-3Pal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Isovaline\n SciTegic09012117322D\n\n 9 8 0 0 1 0 999 V2000\n -2.0770 1.3017 0.0000 C 0 0\n -0.5770 1.3004 0.0000 C 0 0\n 0.1731 0.0004 0.0000 C 0 0 1 0 0 0\n -0.5777 -1.2982 0.0000 C 0 0\n -1.3569 -0.0009 0.0000 N 0 0\n -2.1066 -1.3001 0.0000 R# 0 0\n 1.6739 -0.0009 0.0000 C 0 0\n 2.4247 1.2977 0.0000 R# 0 0\n 2.4235 -1.3001 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 0\n 3 4 1 1\n 3 5 1 0\n 5 6 1 0\n 3 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 2 6 1 8 2\nM END\n> <Name>\nD-Isovaline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDaMeAb\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Alpha-cyclohexylglycine\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -2.7098 1.1911 0.0000 R# 0 0\n -1.4094 1.9388 0.0000 N 0 0\n -0.1105 1.1868 0.0000 C 0 0 2 0 0 0\n -0.1097 -0.3140 0.0000 C 0 0\n -1.4067 -1.0674 0.0000 C 0 0\n -1.4028 -2.5674 0.0000 C 0 0\n -0.1018 -3.3140 0.0000 C 0 0\n 1.1953 -2.5606 0.0000 C 0 0\n 1.1913 -1.0606 0.0000 C 0 0\n 1.1884 1.9388 0.0000 C 0 0\n 2.4881 1.1899 0.0000 R# 0 0\n 1.1875 3.4388 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 4 9 1 0\n 3 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 1 1 11 2\nM END\n> <Name>\nD-Alpha-cyclohexylglycine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Chg\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Citrullin\n SciTegic09012117322D\n\n 13 12 0 0 1 0 999 V2000\n -0.4064 4.6171 0.0000 N 0 0\n -1.7046 3.8656 0.0000 C 0 0\n -3.0043 4.6145 0.0000 O 0 0\n -1.7024 2.3648 0.0000 N 0 0\n -0.4020 1.6155 0.0000 C 0 0\n -0.3998 0.1146 0.0000 C 0 0\n 0.9006 -0.6347 0.0000 C 0 0\n 0.9028 -2.1354 0.0000 C 0 0 1 0 0 0\n -0.3975 -2.8848 0.0000 N 0 0\n -1.6965 -2.1344 0.0000 R# 0 0\n 2.2032 -2.8848 0.0000 C 0 0\n 3.5014 -2.1332 0.0000 R# 0 0\n 2.2054 -4.3848 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 6\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\nD-Citrullin\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Cit\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-2,4-diaminobutanoic acid\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n -2.2080 -0.8247 0.0000 R# 0 0\n -0.9092 -1.5750 0.0000 N 0 0\n 0.3913 -0.8257 0.0000 C 0 0 2 0 0 0\n 0.3890 0.6751 0.0000 C 0 0\n -0.9114 1.4244 0.0000 C 0 0\n -0.9137 2.9252 0.0000 N 0 0\n -2.2133 3.6741 0.0000 R# 0 0\n 1.6917 -1.5750 0.0000 C 0 0\n 2.9898 -0.8235 0.0000 R# 0 0\n 1.6939 -3.0750 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 3 1 1 7 3 9 2\nM END\n> <Name>\nD-2,4-diaminobutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Dab\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Pipecolic acid\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n -0.9064 2.1749 0.0000 R# 0 0\n -0.9082 0.6749 0.0000 N 0 0\n -2.2081 -0.0735 0.0000 C 0 0\n -2.2099 -1.5735 0.0000 C 0 0\n -0.9118 -2.3251 0.0000 C 0 0\n 0.3882 -1.5766 0.0000 C 0 0\n 0.3900 -0.0766 0.0000 C 0 0 2 0 0 0\n 1.6891 0.6749 0.0000 C 0 0\n 2.9885 -0.0744 0.0000 R# 0 0\n 1.6887 2.1749 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 7 6 1 0\n 7 2 1 0\n 7 8 1 1\n 8 9 1 0\n 8 10 2 0\nM RGP 2 1 1 9 2\nM END\n> <Name>\nD-Pipecolic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Pip\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -0.1815 3.2137 0.0000 R# 0 0\n -0.1833 1.7137 0.0000 N 0 0\n -1.4832 0.9652 0.0000 C 0 0\n -1.4850 -0.5348 0.0000 C 0 0\n -2.7849 -1.2832 0.0000 C 0 0\n -2.7867 -2.7832 0.0000 C 0 0\n -1.4886 -3.5348 0.0000 C 0 0\n -0.1886 -2.7863 0.0000 C 0 0\n -0.1869 -1.2863 0.0000 C 0 0\n 1.1131 -0.5379 0.0000 C 0 0\n 1.1148 0.9621 0.0000 C 0 0 2 0 0 0\n 2.4140 1.7137 0.0000 C 0 0\n 3.7134 0.9644 0.0000 R# 0 0\n 2.4136 3.2137 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\n 9 10 1 0\n 11 10 1 0\n 11 2 1 0\n 11 12 1 1\n 12 13 1 0\n 12 14 2 0\nM RGP 2 1 1 13 2\nM END\n> <Name>\nD-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Tic\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-3-(2-Pyridyl)-alanine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 2 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 N 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 3 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\nD-3-(2-Pyridyl)-alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-2Pal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-2-aminobutanoic acid\n SciTegic09012117322D\n\n 8 7 0 0 1 0 999 V2000\n -1.3017 2.2489 0.0000 C 0 0\n -0.0020 1.5001 0.0000 C 0 0\n 0.0003 -0.0008 0.0000 C 0 0 1 0 0 0\n -1.3001 -0.7500 0.0000 N 0 0\n -2.5990 0.0002 0.0000 R# 0 0\n 1.3007 -0.7500 0.0000 C 0 0\n 2.5988 0.0015 0.0000 R# 0 0\n 1.3029 -2.2500 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 3 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 2 5 1 7 2\nM END\n> <Name>\nD-2-aminobutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Abu\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-2,3-diaminopropanoic acid\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n -2.4540 -0.4164 0.0000 R# 0 0\n -1.1551 -1.1667 0.0000 N 0 0\n 0.1453 -0.4174 0.0000 C 0 0 2 0 0 0\n 0.1431 1.0834 0.0000 C 0 0\n -1.1573 1.8327 0.0000 N 0 0\n -1.1596 3.3327 0.0000 R# 0 0\n 1.4457 -1.1667 0.0000 C 0 0\n 2.7439 -0.4151 0.0000 R# 0 0\n 1.4480 -2.6667 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 3 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 3 1 1 6 3 8 2\nM END\n> <Name>\nD-2,3-diaminopropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Dap\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nCarboxybenzyl\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 2.5951 -3.0039 0.0000 O 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 10 11 2 0\n 6 11 1 0\nM RGP 1 1 2\nM END\n> <Name>\nCarboxybenzyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nCbz\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nC-Terminal ethyl\n SciTegic07272112182D\n\n 3 2 0 0 0 0 999 V2000\n 4.8501 1.2990 0.0000 C 0 0\n 4.0993 0.0004 0.0000 C 0 0\n 2.5993 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\nM RGP 1 3 1\nM END\n> <Name>\nC-Terminal ethyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n-Et\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nEthanamine\n SciTegic07272112182D\n\n 4 3 0 0 0 0 999 V2000\n 7.6505 -0.5497 0.0000 C 0 0\n 6.1505 -0.5497 0.0000 C 0 0\n 5.3993 0.7496 0.0000 N 0 0\n 3.8993 0.7496 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\nM RGP 1 4 1\nM END\n> <Name>\nEthanamine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNHEt\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nEthanol\n SciTegic07272112182D\n\n 4 3 0 0 0 0 999 V2000\n 7.6505 -0.5497 0.0000 C 0 0\n 6.1505 -0.5497 0.0000 C 0 0\n 5.3993 0.7496 0.0000 O 0 0\n 3.8993 0.7496 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\nM RGP 1 4 1\nM END\n> <Name>\nEthanol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOEt\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nTosyl\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n -5.5976 6.6982 0.0000 C 0 0\n -4.8480 5.3989 0.0000 C 0 0\n -5.5984 4.1001 0.0000 C 0 0\n -4.8488 2.8009 0.0000 C 0 0\n -3.3488 2.8004 0.0000 C 0 0\n -2.5984 4.0992 0.0000 C 0 0\n -3.3480 5.3985 0.0000 C 0 0\n -2.5988 1.5004 0.0000 S 0 0\n -1.0988 1.5004 0.0000 R# 0 0\n -3.3484 0.2011 0.0000 O 0 0\n -1.8486 0.2015 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 2 7 1 0\n 5 8 1 0\n 8 9 1 0\n 8 10 2 0\n 8 11 2 0\nM RGP 1 9 2\nM END\n> <Name>\nTosyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTos\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n(4S)-1,3-thiazolidine-4-carboxylic acid\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n -1.3565 1.9415 0.0000 R# 0 0\n -1.1229 0.4598 0.0000 N 0 0\n -2.1844 -0.6001 0.0000 C 0 0\n -1.5044 -1.9371 0.0000 S 0 0\n -0.0227 -1.7036 0.0000 C 0 0\n 0.2131 -0.2222 0.0000 C 0 0 2 0 0 0\n 1.5471 0.4598 0.0000 C 0 0\n 2.8060 -0.3559 0.0000 R# 0 0\n 1.6246 1.9578 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 6 5 1 0\n 6 2 1 0\n 6 7 1 1\n 7 8 1 0\n 7 9 2 0\nM RGP 2 1 1 8 2\nM END\n> <Name>\n(4S)-1,3-thiazolidine-4-carboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Thz\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nDeamino-Cysteine\n SciTegic07272112182D\n\n 6 5 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 S 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 3.9000 2.2500 0.0000 R# 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\nM RGP 1 5 2\nM END\n> <Name>\nDeamino-Cysteine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDACys\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n4-aminobutanoic acid\n SciTegic07272112182D\n\n 8 7 0 0 0 0 999 V2000\n 14.5529 1.2997 0.0000 O 0 0\n 13.8033 2.5990 0.0000 C 0 0\n 14.5542 3.8975 0.0000 O 0 0\n 12.3025 2.5990 0.0000 C 0 0\n 11.5513 1.2997 0.0000 C 0 0\n 10.0505 1.2997 0.0000 C 0 0\n 9.2992 0.0004 0.0000 N 0 0\n 7.7992 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\nM RGP 1 8 1\nM END\n> <Name>\n4-aminobutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDADab\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-cyanoacetic acid\n SciTegic07272112182D\n\n 6 5 0 0 0 0 999 V2000\n 2.8000 0.7500 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 0.5504 2.0493 0.0000 O 0 0\n 0.5500 -0.5500 0.0000 C 0 0\n 1.3000 -1.8500 0.0000 C 0 0\n 2.0496 -3.1493 0.0000 N 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 3 0\nM RGP 1 1 2\nM END\n> <Name>\n2-cyanoacetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAGlyC\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-cyclopentylacetic acid\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 2.5157 -3.6164 0.0000 R# 0 0\n 1.0157 -3.6164 0.0000 C 0 0\n 0.2661 -2.3171 0.0000 O 0 0\n 0.2657 -4.9164 0.0000 C 0 0\n 1.0144 -6.2142 0.0000 C 0 0\n 0.4067 -7.5856 0.0000 C 0 0\n 1.5232 -8.5873 0.0000 C 0 0\n 2.8209 -7.8350 0.0000 C 0 0\n 2.5065 -6.3683 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 5 9 1 0\nM RGP 1 1 2\nM END\n> <Name>\n2-cyclopentylacetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAGlyP\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-hydroxyacetic acid\n SciTegic07272112182D\n\n 6 5 0 0 0 0 999 V2000\n 9.7009 0.0004 0.0000 O 0 0\n 8.9513 1.2997 0.0000 C 0 0\n 9.7021 2.5983 0.0000 O 0 0\n 7.4505 1.2997 0.0000 C 0 0\n 6.6992 0.0004 0.0000 O 0 0\n 5.1992 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\nM RGP 1 6 1\nM END\n> <Name>\n2-hydroxyacetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAGlyO\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-(thiophen-2-yl)acetic acid\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 2.5157 -3.6164 0.0000 R# 0 0\n 1.0157 -3.6164 0.0000 C 0 0\n 0.2661 -2.3171 0.0000 O 0 0\n 0.2657 -4.9164 0.0000 C 0 0\n 1.0144 -6.2142 0.0000 C 0 0\n 0.4067 -7.5856 0.0000 C 0 0\n 1.5232 -8.5873 0.0000 C 0 0\n 2.8209 -7.8350 0.0000 C 0 0\n 2.5065 -6.3683 0.0000 S 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 5 9 1 0\nM RGP 1 1 2\nM END\n> <Name>\n2-(thiophen-2-yl)acetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAGlyT\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n(2R)-2-amino-3-(1-formyl-1H-indol-3-yl)propanoic acid\n SciTegic07272112182D\n\n 18 19 0 0 1 0 999 V2000\n -0.9963 2.1750 0.0000 R# 0 0\n 0.3026 2.9253 0.0000 N 0 0\n 1.6030 2.1761 0.0000 C 0 0 2 0 0 0\n 1.6007 0.6752 0.0000 C 0 0\n 0.3026 -0.0728 0.0000 C 0 0\n -1.0661 0.5411 0.0000 C 0 0\n -2.0728 -0.5709 0.0000 N 0 0\n -3.5621 -0.4074 0.0000 C 0 0\n -4.1668 0.9654 0.0000 O 0 0\n -1.3266 -1.8711 0.0000 C 0 0\n -1.7940 -3.2964 0.0000 C 0 0\n -0.7933 -4.4139 0.0000 C 0 0\n 0.6747 -4.1061 0.0000 C 0 0\n 1.1422 -2.6808 0.0000 C 0 0\n 0.1415 -1.5633 0.0000 C 0 0\n 2.9034 2.9253 0.0000 C 0 0\n 4.2016 2.1738 0.0000 R# 0 0\n 2.9057 4.4253 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 1 0\n 8 9 2 0\n 7 10 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 15 2 0\n 5 15 1 0\n 10 15 1 0\n 3 16 1 0\n 16 17 1 0\n 16 18 2 0\nM RGP 2 1 1 17 2\nM END\n> <Name>\n(2R)-2-amino-3-(1-formyl-1H-indol-3-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDTrpFo\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nW\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-sulfanylacetic acid\n SciTegic07272112182D\n\n 5 4 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 S 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 2.6000 -1.5000 0.0000 R# 0 0\n 3.8993 0.7496 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 3 5 2 0\nM RGP 1 4 2\nM END\n> <Name>\n2-sulfanylacetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDANcy\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nDeamino-Phenylalanine\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 0.3451 -1.7039 0.0000 O 0 0\n 1.8451 -1.7039 0.0000 C 0 0\n 2.5947 -0.4046 0.0000 O 0 0\n 2.5951 -3.0039 0.0000 C 0 0\n 4.0951 -3.0039 0.0000 R# 0 0\n 1.8451 -4.3039 0.0000 C 0 0\n 2.5951 -5.6039 0.0000 C 0 0\n 1.8474 -6.9042 0.0000 C 0 0\n 2.5997 -8.2020 0.0000 C 0 0\n 4.0997 -8.1994 0.0000 C 0 0\n 4.8474 -6.8990 0.0000 C 0 0\n 4.0951 -5.6013 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 4 6 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 7 12 1 0\nM RGP 1 5 2\nM END\n> <Name>\nDeamino-Phenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAPhe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-(3,5-dimethylphenyl)acetic acid\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 1.1572 0.8886 0.0000 C 0 0\n -0.3428 0.8912 0.0000 C 0 0\n -1.0906 2.1915 0.0000 C 0 0\n -2.5906 2.1941 0.0000 C 0 0\n -3.3383 3.4945 0.0000 C 0 0\n -3.3428 0.8964 0.0000 C 0 0\n -2.5951 -0.4039 0.0000 C 0 0\n -3.3451 -1.7039 0.0000 C 0 0\n -2.5951 -3.0039 0.0000 C 0 0\n -1.0951 -3.0039 0.0000 R# 0 0\n -3.3447 -4.3032 0.0000 O 0 0\n -1.0951 -0.4065 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 9 11 2 0\n 7 12 2 0\n 2 12 1 0\nM RGP 1 10 2\nM END\n> <Name>\n2-(3,5-dimethylphenyl)acetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAPhg3\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nDeamino-Leucine\n SciTegic07272112182D\n\n 8 7 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 1.3000 2.2500 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.2000 0.0000 0.0000 C 0 0\n 5.2000 -1.5000 0.0000 R# 0 0\n 6.4992 0.7496 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 1 7 2\nM END\n> <Name>\nDeamino-Leucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDALeu\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n(2R)-2-hydroxypropanoic acid\n SciTegic07272112182D\n\n 6 5 0 0 1 0 999 V2000\n 1.3000 2.2500 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0 1 0 0 0\n 0.0007 0.0004 0.0000 O 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 2.6000 -1.5000 0.0000 R# 0 0\n 3.8993 0.7496 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 4 6 2 0\nM RGP 1 5 2\nM END\n> <Name>\n(2R)-2-hydroxypropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-OAla\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n(2S)-2-hydroxy-3-methylbutanoic acid\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 1.3000 2.2500 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0 2 0 0 0\n 2.6000 -1.5000 0.0000 O 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 3.9000 2.2500 0.0000 R# 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 4 2 1 0\n 4 5 1 1\n 4 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 1 7 2\nM END\n> <Name>\n(2S)-2-hydroxy-3-methylbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nL-OVal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nN-Terminal 1-phenylmethanamine\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 3.8926 -3.7566 0.0000 R# 0 0\n 2.5951 -3.0039 0.0000 N 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\nM RGP 1 1 2\nM END\n> <Name>\nN-Terminal 1-phenylmethanamine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNHBn-\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nBenzaldehyde\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 3.8976 -0.7553 0.0000 R# 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 2.5951 -3.0031 0.0000 O 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\nM RGP 1 1 2\nM END\n> <Name>\nBenzaldehyde\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBz\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nN-Terminal ethyl\n SciTegic07272112182D\n\n 3 2 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 2.5993 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\nM RGP 1 3 2\nM END\n> <Name>\nN-Terminal ethyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nEt-\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nN-Terminal methyl\n SciTegic07272112182D\n\n 2 1 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 R# 0 0\n 1 2 1 0\nM RGP 1 2 2\nM END\n> <Name>\nN-Terminal methyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nMe-\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n(2R)-2-amino-3-(4-ethoxyphenyl)propanoic acid\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -5.6925 -2.6973 0.0000 C 0 0\n -4.3898 -1.9538 0.0000 C 0 0\n -3.0933 -2.7099 0.0000 O 0 0\n -1.7898 -1.9660 0.0000 C 0 0\n -0.4930 -2.7198 0.0000 C 0 0\n 0.8083 -1.9736 0.0000 C 0 0\n 0.8127 -0.4736 0.0000 C 0 0\n 2.1131 0.2757 0.0000 C 0 0\n 2.1153 1.7765 0.0000 C 0 0 1 0 0 0\n 0.8149 2.5258 0.0000 N 0 0\n -0.4839 1.7755 0.0000 R# 0 0\n 3.4157 2.5258 0.0000 C 0 0\n 4.7139 1.7743 0.0000 R# 0 0\n 3.4180 4.0258 0.0000 O 0 0\n -0.4842 0.2802 0.0000 C 0 0\n -1.7854 -0.4660 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 9 8 1 1\n 9 10 1 0\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\n 7 15 1 0\n 15 16 2 0\n 4 16 1 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2R)-2-amino-3-(4-ethoxyphenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDTyrEt\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-6-acetamidohexanoic acid\n SciTegic09012117322D\n\n 14 13 0 0 1 0 999 V2000\n -3.8101 -3.4803 0.0000 C 0 0\n -2.5119 -4.2318 0.0000 C 0 0\n -2.5142 -5.7319 0.0000 O 0 0\n -1.2115 -3.4826 0.0000 N 0 0\n -1.2092 -1.9817 0.0000 C 0 0\n 0.0912 -1.2325 0.0000 C 0 0\n 0.0935 0.2684 0.0000 C 0 0\n 1.3938 1.0176 0.0000 C 0 0\n 1.3961 2.5184 0.0000 C 0 0 2 0 0 0\n 0.0957 3.2677 0.0000 N 0 0\n -1.2032 2.5174 0.0000 R# 0 0\n 2.6965 3.2677 0.0000 C 0 0\n 3.9947 2.5161 0.0000 R# 0 0\n 2.6988 4.7677 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 9 8 1 6\n 9 10 1 0\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2S)-2-amino-6-acetamidohexanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLys_Ac\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Terminal methanol\n SciTegic07272112182D\n\n 3 2 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 O 0 0\n 2.5993 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\nM RGP 1 3 2\nM END\n> <Name>\nN-Terminal methanol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOMe-\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n(2S)-2-amino-4-methoxy-4-oxobutanoic acid\n SciTegic09012117322D\n\n 11 10 0 0 1 0 999 V2000\n -2.0126 3.6129 0.0000 C 0 0\n -0.7128 2.8641 0.0000 O 0 0\n -0.7106 1.3632 0.0000 C 0 0\n -2.0087 0.6117 0.0000 O 0 0\n 0.5899 0.6139 0.0000 C 0 0\n 0.5921 -0.8869 0.0000 C 0 0 2 0 0 0\n -0.7082 -1.6362 0.0000 N 0 0\n -2.0072 -0.8859 0.0000 R# 0 0\n 1.8926 -1.6362 0.0000 C 0 0\n 3.1907 -0.8846 0.0000 R# 0 0\n 1.8948 -3.1361 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 6 5 1 1\n 6 7 1 0\n 7 8 1 0\n 6 9 1 0\n 9 10 1 0\n 9 11 2 0\nM RGP 2 8 1 10 2\nM END\n> <Name>\n(2S)-2-amino-4-methoxy-4-oxobutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAspOMe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nD\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-(dimethylamino)benzoic acid\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n -7.8462 -2.7911 0.0000 C 0 0\n -7.1003 -4.0925 0.0000 N 0 0\n -7.8549 -5.3889 0.0000 C 0 0\n -5.5995 -4.0982 0.0000 C 0 0\n -4.8518 -5.3986 0.0000 C 0 0\n -3.3518 -5.4012 0.0000 C 0 0\n -2.5995 -4.1034 0.0000 C 0 0\n -3.3473 -2.8031 0.0000 C 0 0\n -4.8473 -2.8005 0.0000 C 0 0\n -2.5972 -1.5031 0.0000 C 0 0\n -1.0972 -1.5031 0.0000 R# 0 0\n -3.3468 -0.2038 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\n 8 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 1 11 2\nM END\n> <Name>\n3-(dimethylamino)benzoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNMe23A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-amino-3-phenylprop-2-enoic acid\n SciTegic07272112182D\n\n 13 13 0 0 0 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 2 1 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 3 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\n2-amino-3-phenylprop-2-enoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPheaDH\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n4-amino-3-hydroxy-6-methylheptanoic acid\n SciTegic09012117322D\n\n 13 12 0 0 0 0 999 V2000\n -3.5226 -2.6969 0.0000 C 0 0\n -2.7715 -1.3985 0.0000 C 0 0\n -3.5208 -0.0990 0.0000 C 0 0\n -1.2707 -1.3987 0.0000 C 0 0\n -0.5192 -0.0996 0.0000 C 0 0\n -1.2716 1.1990 0.0000 N 0 0\n -2.7716 1.1976 0.0000 R# 0 0\n 0.9817 -0.0999 0.0000 C 0 0\n 1.7310 -1.3993 0.0000 O 0 0\n 1.7331 1.1993 0.0000 C 0 0\n 3.2339 1.1990 0.0000 C 0 0\n 3.9832 -0.1004 0.0000 R# 0 0\n 3.9850 2.4974 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 5 8 1 0\n 8 9 1 0\n 8 10 1 0\n 10 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 7 1 12 2\nM END\n> <Name>\n4-amino-3-hydroxy-6-methylheptanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nSta3xi\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-amino-3-(4-methoxyphenyl)prop-2-enoic acid\n SciTegic07272112182D\n\n 15 15 0 0 0 0 999 V2000\n -4.7686 -2.1340 0.0000 C 0 0\n -3.4728 -2.8897 0.0000 O 0 0\n -2.1693 -2.1457 0.0000 C 0 0\n -0.8725 -2.8995 0.0000 C 0 0\n 0.4287 -2.1534 0.0000 C 0 0\n 0.4331 -0.6534 0.0000 C 0 0\n 1.7335 0.0959 0.0000 C 0 0\n 1.7358 1.5968 0.0000 C 0 0\n 0.4354 2.3460 0.0000 N 0 0\n -0.8635 1.5957 0.0000 R# 0 0\n 3.0362 2.3460 0.0000 C 0 0\n 4.3343 1.5945 0.0000 R# 0 0\n 3.0384 3.8460 0.0000 O 0 0\n -0.8637 0.1004 0.0000 C 0 0\n -2.1650 -0.6458 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 7 6 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\n 6 14 1 0\n 14 15 2 0\n 3 15 1 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n2-amino-3-(4-methoxyphenyl)prop-2-enoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyrabD\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-aminopropan-1-ol\n SciTegic07272112182D\n\n 6 5 0 0 1 0 999 V2000\n 2.6000 -1.5000 0.0000 N 0 0\n 2.6000 0.0000 0.0000 C 0 0 1 0 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 0.0007 0.0004 0.0000 O 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 1 0\n 2 5 1 0\n 5 6 1 0\nM RGP 1 6 2\nM END\n> <Name>\n(2R)-2-aminopropan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAlaol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-amino-2-methylpropan-1-ol\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 5.1965 -1.5117 0.0000 R# 0 0\n 6.6965 -1.5117 0.0000 N 0 0\n 7.4478 -0.2124 0.0000 C 0 0\n 6.6951 1.0860 0.0000 C 0 0\n 5.1951 1.0844 0.0000 O 0 0\n 8.9486 -0.2108 0.0000 C 0 0\n 9.7027 -1.5074 0.0000 C 0 0\n 11.2027 -1.5027 0.0000 C 0 0\n 11.9486 -0.2013 0.0000 C 0 0\n 11.1945 1.0954 0.0000 C 0 0\n 9.6945 1.0906 0.0000 C 0 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 10 11 2 0\n 11 6 1 0\n 1 2 1 0\nM RGP 1 1 1\nM END\n> <Name>\n2-amino-2-methylpropan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDPhgol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2R,3R)-2-aminobutane-1,3-diol\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 1.3000 2.2500 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0 1 0 0 0\n 0.0007 0.0004 0.0000 O 0 0\n 2.6000 0.0000 0.0000 C 0 0 1 0 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 2.5969 -1.5008 0.0000 N 0 0\n 1.2968 -2.2490 0.0000 R# 0 0\n 2 1 1 6\n 2 3 1 0\n 2 4 1 0\n 4 5 1 1\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\nM RGP 1 8 1\nM END\n> <Name>\n(2R,3R)-2-aminobutane-1,3-diol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDThrol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\naminomethanol\n SciTegic07272112182D\n\n 4 3 0 0 0 0 999 V2000\n 7.6505 -0.5497 0.0000 O 0 0\n 6.1505 -0.5497 0.0000 C 0 0\n 5.3993 0.7496 0.0000 N 0 0\n 3.8993 0.7496 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\nM RGP 1 4 1\nM END\n> <Name>\naminomethanol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nGly-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-aminopropan-1-ol\n SciTegic07272112182D\n\n 6 5 0 0 1 0 999 V2000\n 6.7009 2.5990 0.0000 C 0 0\n 7.4505 1.2997 0.0000 C 0 0 1 0 0 0\n 8.9513 1.2997 0.0000 C 0 0\n 9.7021 2.5983 0.0000 O 0 0\n 6.6992 0.0004 0.0000 N 0 0\n 5.1992 0.0004 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 1 0\n 2 5 1 0\n 5 6 1 0\nM RGP 1 6 1\nM END\n> <Name>\n(2S)-2-aminopropan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAla-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2,6-diaminohexan-1-ol\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 16.0614 1.7064 0.0000 N 0 0\n 14.5614 1.7047 0.0000 C 0 0\n 13.8087 3.0031 0.0000 C 0 0\n 12.3079 3.0015 0.0000 C 0 0\n 11.5552 4.2999 0.0000 C 0 0\n 10.0544 4.2983 0.0000 C 0 0 1 0 0 0\n 9.3017 5.5967 0.0000 C 0 0\n 7.8017 5.5951 0.0000 O 0 0\n 9.3031 2.9990 0.0000 N 0 0\n 7.8031 2.9990 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 6 5 1 6\n 6 7 1 0\n 7 8 1 0\n 6 9 1 0\n 9 10 1 0\nM RGP 1 10 1\nM END\n> <Name>\n(2S)-2,6-diaminohexan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLys-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-2-phenylethan-1-ol\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n 5.1951 1.0844 0.0000 O 0 0\n 6.6951 1.0860 0.0000 C 0 0\n 7.4478 -0.2124 0.0000 C 0 0 1 0 0 0\n 6.6965 -1.5117 0.0000 N 0 0\n 5.1965 -1.5117 0.0000 R# 0 0\n 8.9486 -0.2108 0.0000 C 0 0\n 9.7027 -1.5074 0.0000 C 0 0\n 11.2027 -1.5027 0.0000 C 0 0\n 11.9486 -0.2013 0.0000 C 0 0\n 11.1945 1.0954 0.0000 C 0 0\n 9.6945 1.0906 0.0000 C 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 3 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 10 11 2 0\n 6 11 1 0\nM RGP 1 5 1\nM END\n> <Name>\n(2S)-2-amino-2-phenylethan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhg-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n[(2S)-pyrrolidin-2-yl]methanol\n SciTegic07272112182D\n\n 8 8 0 0 1 0 999 V2000\n 3.1247 -2.0836 0.0000 O 0 0\n 1.6332 -2.2426 0.0000 C 0 0\n 0.7500 -1.0323 0.0000 C 0 0 2 0 0 0\n 1.2135 0.3943 0.0000 C 0 0\n 0.0000 1.2760 0.0000 C 0 0\n -1.2135 0.3943 0.0000 C 0 0\n -0.7500 -1.0323 0.0000 N 0 0\n -1.6317 -2.2458 0.0000 R# 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 7 8 1 0\nM RGP 1 8 1\nM END\n> <Name>\n[(2S)-pyrrolidin-2-yl]methanol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPro-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-3-methylbutan-1-ol\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 1.3000 2.2500 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0 1 0 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 2.5969 -1.5008 0.0000 N 0 0\n 1.2968 -2.2490 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 4 2 1 0\n 4 5 1 1\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\nM RGP 1 8 1\nM END\n> <Name>\n(2S)-2-amino-3-methylbutan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nVal-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-aminopropanal\n SciTegic07272112182D\n\n 6 5 0 0 1 0 999 V2000\n 2.6000 -1.5000 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0 2 0 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 0.0007 0.0004 0.0000 R# 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 3 4 1 0\n 2 5 1 0\n 5 6 2 0\nM RGP 1 4 1\nM END\n> <Name>\n(2S)-2-aminopropanal\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAla-al\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN''-[(4S)-4-amino-5-oxopentyl]guanidine\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 18.1103 -2.2565 0.0000 N 0 0\n 17.3622 -0.9564 0.0000 C 0 0\n 18.1145 0.3414 0.0000 N 0 0\n 15.8614 -0.9547 0.0000 N 0 0\n 15.1087 -2.2531 0.0000 C 0 0\n 13.6079 -2.2515 0.0000 C 0 0\n 12.8552 -3.5499 0.0000 C 0 0\n 11.3544 -3.5483 0.0000 C 0 0 2 0 0 0\n 10.6031 -2.2490 0.0000 N 0 0\n 9.1031 -2.2490 0.0000 R# 0 0\n 10.6017 -4.8467 0.0000 C 0 0\n 9.1017 -4.8451 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 1\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 2 0\nM RGP 1 10 1\nM END\n> <Name>\nN''-[(4S)-4-amino-5-oxopentyl]guanidine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nArg-al\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(3S)-3-amino-4-oxobutanoic acid\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 8.9597 1.7014 0.0000 O 0 0\n 9.7079 3.0015 0.0000 C 0 0\n 11.2079 3.0031 0.0000 O 0 0\n 8.9552 4.2999 0.0000 C 0 0\n 7.4544 4.2983 0.0000 C 0 0 2 0 0 0\n 6.7032 2.9990 0.0000 N 0 0\n 5.2032 2.9990 0.0000 R# 0 0\n 6.7017 5.5967 0.0000 C 0 0\n 5.2017 5.5951 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 5 4 1 6\n 5 6 1 0\n 6 7 1 0\n 5 8 1 0\n 8 9 2 0\nM RGP 1 7 1\nM END\n> <Name>\n(3S)-3-amino-4-oxobutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAsp-al\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nN\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2,6-diaminohexanal\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 16.0614 1.7064 0.0000 N 0 0\n 14.5614 1.7047 0.0000 C 0 0\n 13.8087 3.0031 0.0000 C 0 0\n 12.3079 3.0015 0.0000 C 0 0\n 11.5552 4.2999 0.0000 C 0 0\n 10.0544 4.2983 0.0000 C 0 0 2 0 0 0\n 9.3031 2.9990 0.0000 N 0 0\n 7.8031 2.9990 0.0000 R# 0 0\n 9.3017 5.5967 0.0000 C 0 0\n 7.8017 5.5951 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 6 5 1 6\n 6 7 1 0\n 7 8 1 0\n 6 9 1 0\n 9 10 2 0\nM RGP 1 8 1\nM END\n> <Name>\n(2S)-2,6-diaminohexanal\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLys-al\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-pyrrolidine-2-carbaldehyde\n SciTegic07272112182D\n\n 8 8 0 0 1 0 999 V2000\n 1.6317 -2.2458 0.0000 R# 0 0\n 3.1317 -2.2458 0.0000 N 0 0\n 4.0134 -3.4593 0.0000 C 0 0\n 5.4400 -2.9958 0.0000 C 0 0\n 5.4399 -1.4958 0.0000 C 0 0\n 4.0134 -1.0323 0.0000 C 0 0 1 0 0 0\n 3.5533 0.3936 0.0000 C 0 0\n 4.5586 1.5069 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 6 5 1 0\n 6 2 1 0\n 6 7 1 6\n 7 8 2 0\nM RGP 1 1 1\nM END\n> <Name>\n(2S)-pyrrolidine-2-carbaldehyde\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPro-al\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nC-Terminal 1-phenylmethanamine\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 3.8926 -3.7566 0.0000 R# 0 0\n 5.3926 -3.7566 0.0000 N 0 0\n 6.1439 -5.0559 0.0000 C 0 0\n 7.6447 -5.0559 0.0000 C 0 0\n 8.3974 -6.3533 0.0000 C 0 0\n 9.8974 -6.3503 0.0000 C 0 0\n 10.6447 -5.0497 0.0000 C 0 0\n 9.8920 -3.7522 0.0000 C 0 0\n 8.3920 -3.7553 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\nM RGP 1 1 1\nM END\n> <Name>\nC-Terminal 1-phenylmethanamine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n-NHBn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-4-methanesulfonylbutanoic acid\n SciTegic09012117322D\n\n 12 11 0 0 1 0 999 V2000\n 0.4287 3.0016 0.0000 C 0 0\n -0.8695 2.2501 0.0000 S 0 0\n -2.1692 2.9989 0.0000 O 0 0\n -0.8710 3.7500 0.0000 O 0 0\n -0.8672 0.7492 0.0000 C 0 0\n 0.4332 -0.0001 0.0000 C 0 0\n 0.4355 -1.5009 0.0000 C 0 0 2 0 0 0\n -0.8649 -2.2502 0.0000 N 0 0\n -2.1638 -1.4999 0.0000 R# 0 0\n 1.7359 -2.2502 0.0000 C 0 0\n 3.0341 -1.4986 0.0000 R# 0 0\n 1.7382 -3.7501 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 2 0\n 2 5 1 0\n 5 6 1 0\n 7 6 1 1\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-4-methanesulfonylbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nMet_O2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nM\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(2-methylphenyl)propanoic acid\n SciTegic09012117322D\n\n 14 14 0 0 1 0 999 V2000\n 1.0137 3.0583 0.0000 C 0 0\n -0.2832 2.3045 0.0000 C 0 0\n -1.5844 3.0507 0.0000 C 0 0\n -2.8813 2.2970 0.0000 C 0 0\n -2.8769 0.7970 0.0000 C 0 0\n -1.5756 0.0508 0.0000 C 0 0\n -0.2788 0.8045 0.0000 C 0 0\n 1.0216 0.0552 0.0000 C 0 0\n 1.0238 -1.4456 0.0000 C 0 0 2 0 0 0\n -0.2765 -2.1949 0.0000 N 0 0\n -1.5754 -1.4446 0.0000 R# 0 0\n 2.3242 -2.1949 0.0000 C 0 0\n 3.6224 -1.4433 0.0000 R# 0 0\n 2.3265 -3.6949 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 2 7 1 0\n 7 8 1 0\n 9 8 1 1\n 9 10 1 0\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2S)-2-amino-3-(2-methylphenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe2Me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(3,4-dichlorophenyl)propanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -3.5578 -3.0413 0.0000 Cl 0 0\n -2.2566 -2.2951 0.0000 C 0 0\n -0.9598 -3.0489 0.0000 C 0 0\n 0.3415 -2.3027 0.0000 C 0 0\n 0.3458 -0.8027 0.0000 C 0 0\n 1.6463 -0.0534 0.0000 C 0 0\n 1.6485 1.4474 0.0000 C 0 0 2 0 0 0\n 0.3481 2.1967 0.0000 N 0 0\n -0.9508 1.4464 0.0000 R# 0 0\n 2.9489 2.1967 0.0000 C 0 0\n 4.2471 1.4452 0.0000 R# 0 0\n 2.9512 3.6967 0.0000 O 0 0\n -0.9510 -0.0489 0.0000 C 0 0\n -2.2522 -0.7951 0.0000 C 0 0\n -3.5491 -0.0413 0.0000 Cl 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\n 14 15 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(3,4-dichlorophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe34d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-bromophenyl)propanoic acid\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8113 -3.0442 0.0000 Br 0 0\n -2.5101 -2.2980 0.0000 C 0 0\n -1.2133 -3.0518 0.0000 C 0 0\n 0.0879 -2.3056 0.0000 C 0 0\n 0.0923 -0.8056 0.0000 C 0 0\n 1.3927 -0.0563 0.0000 C 0 0\n 1.3950 1.4445 0.0000 C 0 0 2 0 0 0\n 0.0946 2.1938 0.0000 N 0 0\n -1.2043 1.4435 0.0000 R# 0 0\n 2.6954 2.1938 0.0000 C 0 0\n 3.9936 1.4422 0.0000 R# 0 0\n 2.6977 3.6938 0.0000 O 0 0\n -1.2045 -0.0518 0.0000 C 0 0\n -2.5057 -0.7980 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-bromophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe4Br\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-iodophenyl)propanoic acid\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8113 -3.0442 0.0000 I 0 0\n -2.5101 -2.2980 0.0000 C 0 0\n -1.2133 -3.0518 0.0000 C 0 0\n 0.0879 -2.3056 0.0000 C 0 0\n 0.0923 -0.8056 0.0000 C 0 0\n 1.3927 -0.0563 0.0000 C 0 0\n 1.3950 1.4445 0.0000 C 0 0 2 0 0 0\n 0.0946 2.1938 0.0000 N 0 0\n -1.2043 1.4435 0.0000 R# 0 0\n 2.6954 2.1938 0.0000 C 0 0\n 3.9936 1.4422 0.0000 R# 0 0\n 2.6977 3.6938 0.0000 O 0 0\n -1.2045 -0.0518 0.0000 C 0 0\n -2.5057 -0.7980 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-iodophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe_4I\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-{4-[(4S)-2,6-dioxo-1,3-diazinane-4-amido]phenyl}propanoic acid\n SciTegic07272112182D\n\n 24 25 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 1 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -2.6003 1.4977 0.0000 N 0 0\n -3.8990 0.7455 0.0000 C 0 0\n -3.8964 -0.7545 0.0000 O 0 0\n -5.2003 1.4932 0.0000 C 0 0 2 0 0 0\n -6.4994 0.7432 0.0000 C 0 0\n -7.7985 1.4932 0.0000 C 0 0\n -9.0975 0.7432 0.0000 O 0 0\n -7.7985 2.9932 0.0000 N 0 0\n -6.4995 3.7432 0.0000 C 0 0\n -6.4995 5.2432 0.0000 O 0 0\n -5.2004 2.9933 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 1 0\n 10 11 2 0\n 12 10 1 6\n 12 13 1 0\n 13 14 1 0\n 14 15 2 0\n 14 16 1 0\n 16 17 1 0\n 17 18 2 0\n 17 19 1 0\n 12 19 1 0\n 8 20 1 0\n 20 21 2 0\n 5 21 1 0\n 3 22 1 0\n 22 23 1 0\n 22 24 2 0\nM RGP 2 1 1 23 2\nM END\n> <Name>\n(2S)-2-amino-3-{4-[(4S)-2,6-dioxo-1,3-diazinane-4-amido]phenyl}propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe4SD\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(phosphonooxy)propanoic acid\n SciTegic09012117322D\n\n 12 11 0 0 1 0 999 V2000\n 0.4287 3.0016 0.0000 O 0 0\n -0.8695 2.2501 0.0000 P 0 0\n -0.8710 3.7500 0.0000 O 0 0\n -2.1692 2.9989 0.0000 O 0 0\n -0.8672 0.7492 0.0000 O 0 0\n 0.4332 -0.0001 0.0000 C 0 0\n 0.4355 -1.5009 0.0000 C 0 0 2 0 0 0\n -0.8649 -2.2502 0.0000 N 0 0\n -2.1638 -1.4999 0.0000 R# 0 0\n 1.7359 -2.2502 0.0000 C 0 0\n 3.0341 -1.4986 0.0000 R# 0 0\n 1.7382 -3.7501 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\n 5 6 1 0\n 7 6 1 1\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(phosphonooxy)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nSerPO3\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S,3R)-2-amino-3-(phosphonooxy)butanoic acid\n SciTegic09012117322D\n\n 13 12 0 0 1 0 999 V2000\n 1.5982 0.6937 0.0000 C 0 0\n 0.3000 -0.0579 0.0000 C 0 0 1 0 0 0\n -1.0004 0.6914 0.0000 O 0 0\n -1.0027 2.1922 0.0000 P 0 0\n -1.0042 3.6922 0.0000 O 0 0\n 0.2955 2.9438 0.0000 O 0 0\n -2.3024 2.9411 0.0000 O 0 0\n 0.3023 -1.5587 0.0000 C 0 0 2 0 0 0\n -0.9981 -2.3080 0.0000 N 0 0\n -2.2970 -1.5577 0.0000 R# 0 0\n 1.6027 -2.3080 0.0000 C 0 0\n 2.9009 -1.5564 0.0000 R# 0 0\n 1.6050 -3.8079 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 4 6 1 0\n 4 7 2 0\n 2 8 1 0\n 8 9 1 1\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n(2S,3R)-2-amino-3-(phosphonooxy)butanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nThrPO3\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(4R)-1,3-thiazolidine-4-carboxylic acid\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n -1.3565 1.9415 0.0000 R# 0 0\n -1.1229 0.4598 0.0000 N 0 0\n -2.1844 -0.6001 0.0000 C 0 0\n -1.5044 -1.9371 0.0000 S 0 0\n -0.0227 -1.7036 0.0000 C 0 0\n 0.2131 -0.2222 0.0000 C 0 0 1 0 0 0\n 1.5471 0.4598 0.0000 C 0 0\n 2.8060 -0.3559 0.0000 R# 0 0\n 1.6246 1.9578 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 6 5 1 0\n 6 2 1 0\n 6 7 1 6\n 7 8 1 0\n 7 9 2 0\nM RGP 2 1 1 8 2\nM END\n> <Name>\n(4R)-1,3-thiazolidine-4-carboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nThz\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(1-methyl-1H-indol-3-yl)propanoic acid\n SciTegic09012117322D\n\n 17 18 0 0 1 0 999 V2000\n -3.8091 0.3532 0.0000 C 0 0\n -2.3178 0.5140 0.0000 N 0 0\n -1.3111 -0.5980 0.0000 C 0 0\n 0.0575 0.0158 0.0000 C 0 0\n 1.3557 -0.7322 0.0000 C 0 0\n 1.3580 -2.2330 0.0000 C 0 0 2 0 0 0\n 0.0576 -2.9823 0.0000 N 0 0\n -1.2413 -2.2320 0.0000 R# 0 0\n 2.6584 -2.9823 0.0000 C 0 0\n 3.9566 -2.2308 0.0000 R# 0 0\n 2.6606 -4.4823 0.0000 O 0 0\n -0.1035 1.5064 0.0000 C 0 0\n 0.8972 2.6238 0.0000 C 0 0\n 0.4298 4.0491 0.0000 C 0 0\n -1.0382 4.3570 0.0000 C 0 0\n -2.0389 3.2395 0.0000 C 0 0\n -1.5715 1.8142 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 6 5 1 1\n 6 7 1 0\n 7 8 1 0\n 6 9 1 0\n 9 10 1 0\n 9 11 2 0\n 4 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 15 2 0\n 15 16 1 0\n 16 17 2 0\n 2 17 1 0\n 12 17 1 0\nM RGP 2 8 1 10 2\nM END\n> <Name>\n(2S)-2-amino-3-(1-methyl-1H-indol-3-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTrp_Me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nW\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-hydroxy-2,6-dimethylphenyl)propanoic acid\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -1.2401 1.0645 0.0000 C 0 0\n -1.2430 0.0645 0.0000 C 0 0\n -2.5442 -0.6817 0.0000 C 0 0\n -2.5486 -2.1817 0.0000 C 0 0\n -3.8499 -2.9279 0.0000 O 0 0\n -1.2518 -2.9355 0.0000 C 0 0\n 0.0494 -2.1893 0.0000 C 0 0\n 1.3463 -2.9431 0.0000 C 0 0\n 0.0538 -0.6893 0.0000 C 0 0\n 1.3542 0.0600 0.0000 C 0 0\n 1.3565 1.5608 0.0000 C 0 0 2 0 0 0\n 0.0561 2.3101 0.0000 N 0 0\n -0.8098 1.8099 0.0000 R# 0 0\n 2.6569 2.3101 0.0000 C 0 0\n 3.9550 1.5586 0.0000 R# 0 0\n 2.6591 3.8101 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\n 6 7 1 0\n 7 8 1 0\n 7 9 2 0\n 2 9 1 0\n 9 10 1 0\n 11 10 1 6\n 11 12 1 0\n 12 13 1 0\n 11 14 1 0\n 14 15 1 0\n 14 16 2 0\nM RGP 2 13 1 15 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-hydroxy-2,6-dimethylphenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyr26d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-hydroxy-3-iodophenyl)propanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -3.5578 -3.0413 0.0000 O 0 0\n -2.2566 -2.2951 0.0000 C 0 0\n -0.9598 -3.0489 0.0000 C 0 0\n 0.3415 -2.3027 0.0000 C 0 0\n 0.3458 -0.8027 0.0000 C 0 0\n 1.6463 -0.0534 0.0000 C 0 0\n 1.6485 1.4474 0.0000 C 0 0 2 0 0 0\n 0.3481 2.1967 0.0000 N 0 0\n -0.9508 1.4464 0.0000 R# 0 0\n 2.9489 2.1967 0.0000 C 0 0\n 4.2471 1.4452 0.0000 R# 0 0\n 2.9512 3.6967 0.0000 O 0 0\n -0.9510 -0.0489 0.0000 C 0 0\n -2.2522 -0.7951 0.0000 C 0 0\n -3.5491 -0.0413 0.0000 I 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\n 14 15 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-hydroxy-3-iodophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyr_3I\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-hydroxy-3-nitrophenyl)propanoic acid\n SciTegic09012117322D\n\n 17 17 0 0 1 0 999 V2000\n -1.0001 -3.6609 0.0000 N 0 3\n -2.3000 -4.4094 0.0000 O 0 5\n 0.2977 -4.4129 0.0000 O 0 0\n -0.9989 -2.1601 0.0000 C 0 0\n 0.3024 -1.4139 0.0000 C 0 0\n -2.2957 -1.4063 0.0000 C 0 0\n 0.3068 0.0860 0.0000 C 0 0\n -3.5969 -2.1525 0.0000 O 0 0\n -2.2913 0.0936 0.0000 C 0 0\n -0.9900 0.8398 0.0000 C 0 0\n 1.6072 0.8353 0.0000 C 0 0\n 1.6095 2.3361 0.0000 C 0 0 2 0 0 0\n 0.3090 3.0854 0.0000 N 0 0\n 2.9099 3.0854 0.0000 C 0 0\n -0.9899 2.3351 0.0000 R# 0 0\n 4.2080 2.3339 0.0000 R# 0 0\n 2.9122 4.5854 0.0000 O 0 0\n 2 1 1 0\n 1 3 2 0\n 4 1 1 0\n 5 4 2 0\n 6 4 1 0\n 7 5 1 0\n 8 6 1 0\n 6 9 2 0\n 10 7 2 0\n 7 11 1 0\n 9 10 1 0\n 12 11 1 6\n 12 13 1 0\n 12 14 1 0\n 13 15 1 0\n 14 16 1 0\n 14 17 2 0\nM CHG 2 1 1 2 -1\nM RGP 2 15 1 16 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-hydroxy-3-nitrophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyr3NO\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-[4-(4-hydroxyphenoxy)phenyl]propanoic acid\n SciTegic07272112182D\n\n 21 22 0 0 1 0 999 V2000\n -6.7347 0.4258 0.0000 O 0 0\n -5.4404 -0.3325 0.0000 C 0 0\n -5.4500 -1.8325 0.0000 C 0 0\n -4.1558 -2.5908 0.0000 C 0 0\n -2.8520 -1.8491 0.0000 C 0 0\n -1.5555 -2.6051 0.0000 O 0 0\n -0.2520 -1.8612 0.0000 C 0 0\n 1.0449 -2.6149 0.0000 C 0 0\n 2.3461 -1.8687 0.0000 C 0 0\n 2.3505 -0.3687 0.0000 C 0 0\n 3.6509 0.3806 0.0000 C 0 0\n 3.6532 1.8814 0.0000 C 0 0 2 0 0 0\n 2.3528 2.6307 0.0000 N 0 0\n 1.0539 1.8804 0.0000 R# 0 0\n 4.9536 2.6307 0.0000 C 0 0\n 6.2517 1.8792 0.0000 R# 0 0\n 4.9558 4.1307 0.0000 O 0 0\n 1.0537 0.3851 0.0000 C 0 0\n -0.2476 -0.3611 0.0000 C 0 0\n -2.8424 -0.3491 0.0000 C 0 0\n -4.1366 0.4092 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 12 11 1 6\n 12 13 1 0\n 13 14 1 0\n 12 15 1 0\n 15 16 1 0\n 15 17 2 0\n 10 18 1 0\n 18 19 2 0\n 7 19 1 0\n 5 20 1 0\n 20 21 2 0\n 2 21 1 0\nM RGP 2 14 1 16 2\nM END\n> <Name>\n(2S)-2-amino-3-[4-(4-hydroxyphenoxy)phenyl]propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyrPh4\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-[4-(sulfooxy)phenyl]propanoic acid\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -3.8234 -0.3621 0.0000 O 0 0\n -3.8304 -1.8621 0.0000 S 0 0\n -5.1332 -2.6056 0.0000 O 0 0\n -5.1258 -1.1058 0.0000 O 0 0\n -2.5340 -2.6181 0.0000 O 0 0\n -1.2305 -1.8742 0.0000 C 0 0\n 0.0664 -2.6280 0.0000 C 0 0\n 1.3676 -1.8818 0.0000 C 0 0\n 1.3720 -0.3818 0.0000 C 0 0\n 2.6724 0.3675 0.0000 C 0 0\n 2.6747 1.8683 0.0000 C 0 0 2 0 0 0\n 1.3742 2.6176 0.0000 N 0 0\n 0.0754 1.8673 0.0000 R# 0 0\n 3.9751 2.6176 0.0000 C 0 0\n 5.2732 1.8660 0.0000 R# 0 0\n 3.9773 4.1176 0.0000 O 0 0\n 0.0752 0.3720 0.0000 C 0 0\n -1.2261 -0.3742 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 2 0\n 2 5 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 11 10 1 6\n 11 12 1 0\n 12 13 1 0\n 11 14 1 0\n 14 15 1 0\n 14 16 2 0\n 9 17 1 0\n 17 18 2 0\n 6 18 1 0\nM RGP 2 13 1 15 2\nM END\n> <Name>\n(2S)-2-amino-3-[4-(sulfooxy)phenyl]propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyrSO3\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-hydroxy-3-methylbutanoic acid\n SciTegic09012117322D\n\n 10 9 0 0 1 0 999 V2000\n 1.1669 1.7265 0.0000 C 0 0\n -0.1312 0.9749 0.0000 C 0 0\n -0.1328 2.4749 0.0000 C 0 0\n -1.4310 1.7238 0.0000 O 0 0\n -0.1290 -0.5259 0.0000 C 0 0 2 0 0 0\n -1.4294 -1.2752 0.0000 N 0 0\n -2.7283 -0.5249 0.0000 R# 0 0\n 1.1715 -1.2752 0.0000 C 0 0\n 2.4696 -0.5236 0.0000 R# 0 0\n 1.1737 -2.7751 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 5 2 1 0\n 5 6 1 1\n 6 7 1 0\n 5 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 2 7 1 9 2\nM END\n> <Name>\n(2S)-2-amino-3-hydroxy-3-methylbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nVal3OH\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-methylpentanoic acid\n SciTegic09012117322D\n\n 10 9 0 0 1 0 999 V2000\n -1.3038 -3.1492 0.0000 C 0 0\n -1.3015 -1.6492 0.0000 C 0 0\n -0.0011 -0.8999 0.0000 C 0 0\n 1.2971 -1.6515 0.0000 C 0 0\n 0.0012 0.6009 0.0000 C 0 0 2 0 0 0\n -1.2992 1.3502 0.0000 N 0 0\n -2.5981 0.5999 0.0000 R# 0 0\n 1.3016 1.3502 0.0000 C 0 0\n 2.5998 0.5986 0.0000 R# 0 0\n 1.3039 2.8501 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 3 1 0\n 5 6 1 6\n 6 7 1 0\n 5 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 2 7 1 9 2\nM END\n> <Name>\n(2S)-2-amino-3-methylpentanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nxiIle\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nI\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-(methylamino)benzoic acid\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n -3.0031 1.0801 0.0000 C 0 0\n -1.5031 1.0823 0.0000 N 0 0\n -0.7554 2.3826 0.0000 R# 0 0\n -0.7500 -0.2160 0.0000 C 0 0\n -1.5000 -1.5150 0.0000 C 0 0\n -0.7500 -2.8140 0.0000 C 0 0\n 0.7500 -2.8140 0.0000 C 0 0\n 1.5000 -1.5150 0.0000 C 0 0\n 0.7500 -0.2160 0.0000 C 0 0\n 1.5031 1.0823 0.0000 C 0 0\n 0.7554 2.3826 0.0000 R# 0 0\n 3.0031 1.0801 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\n 9 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 3 1 11 2\nM END\n> <Name>\n2-(methylamino)benzoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNMe2Ab\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-(methylamino)propanoic acid\n SciTegic09012117322D\n\n 8 7 0 0 0 0 999 V2000\n -3.1201 -0.9815 0.0000 C 0 0\n -1.9857 0.0000 0.0000 N 0 0\n -2.2690 1.4730 0.0000 R# 0 0\n -0.5675 -0.4910 0.0000 C 0 0\n 0.5675 0.4910 0.0000 C 0 0\n 1.9857 0.0000 0.0000 C 0 0\n 2.2690 -1.4730 0.0000 R# 0 0\n 3.1200 0.9815 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 2 3 1 7 2\nM END\n> <Name>\n3-(methylamino)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNMebAl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-2-methyl-3-phenylpropanoic acid\n SciTegic09012117322D\n\n 14 14 0 0 1 0 999 V2000\n -1.1169 -3.0644 0.0000 C 0 0\n -0.3686 -1.7645 0.0000 C 0 0 1 0 0 0\n -1.1211 -0.4659 0.0000 C 0 0\n -0.3737 0.8355 0.0000 C 0 0\n -1.1239 2.1344 0.0000 C 0 0\n -0.3742 3.4336 0.0000 C 0 0\n 1.1257 3.4339 0.0000 C 0 0\n 1.8761 2.1350 0.0000 C 0 0\n 1.1263 0.8358 0.0000 C 0 0\n -1.8986 -1.7630 0.0000 N 0 0\n -2.6481 -0.4636 0.0000 R# 0 0\n 1.1322 -1.7630 0.0000 C 0 0\n 1.8805 -0.4630 0.0000 R# 0 0\n 1.8843 -3.0608 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\n 2 10 1 0\n 10 11 1 0\n 2 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2S)-2-amino-2-methyl-3-phenylpropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\naMePhe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-methylpyrrolidine-2-carboxylic acid\n SciTegic09012117322D\n\n 10 10 0 0 1 0 999 V2000\n -0.6481 -1.6527 0.0000 C 0 0\n 0.0642 -0.3326 0.0000 C 0 0 1 0 0 0\n 0.6126 1.0636 0.0000 C 0 0\n -0.5457 2.0166 0.0000 C 0 0\n -1.8100 1.2094 0.0000 C 0 0\n -1.4330 -0.2425 0.0000 N 0 0\n -2.3861 -1.4008 0.0000 R# 0 0\n 1.5490 -0.2425 0.0000 C 0 0\n 2.3560 -1.5069 0.0000 R# 0 0\n 2.2409 1.0884 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 2 6 1 0\n 6 7 1 0\n 2 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 2 7 1 9 2\nM END\n> <Name>\n(2S)-2-methylpyrrolidine-2-carboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\naMePro\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(3,4-dihydroxyphenyl)-2-methylpropanoic acid\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -1.4451 3.4938 0.0000 C 0 0\n -0.6968 2.1938 0.0000 C 0 0 1 0 0 0\n -1.4494 0.8952 0.0000 C 0 0\n -0.7019 -0.4062 0.0000 C 0 0\n -1.4522 -1.7051 0.0000 C 0 0\n -0.7025 -3.0043 0.0000 C 0 0\n 0.7975 -3.0046 0.0000 C 0 0\n 1.5472 -4.3038 0.0000 O 0 0\n 1.5478 -1.7058 0.0000 C 0 0\n 3.0478 -1.7061 0.0000 O 0 0\n 0.7981 -0.4066 0.0000 C 0 0\n -2.2268 2.1922 0.0000 N 0 0\n -2.9763 0.8929 0.0000 R# 0 0\n 0.8040 2.1922 0.0000 C 0 0\n 1.5523 0.8922 0.0000 R# 0 0\n 1.5561 3.4901 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 7 9 1 0\n 9 10 1 0\n 9 11 2 0\n 4 11 1 0\n 2 12 1 0\n 12 13 1 0\n 2 14 1 0\n 14 15 1 0\n 14 16 2 0\nM RGP 2 13 1 15 2\nM END\n> <Name>\n(2S)-2-amino-3-(3,4-dihydroxyphenyl)-2-methylpropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\naMeTy3\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S,3R,4R)-2-amino-3-hydroxy-4-methyloct-6-enoic acid\n SciTegic09012117322D\n\n 14 13 0 0 1 0 999 V2000\n -3.0691 4.9815 0.0000 C 0 0\n -1.7694 4.2325 0.0000 C 0 0\n -1.7672 2.7317 0.0000 C 0 0\n -0.4668 1.9824 0.0000 C 0 0\n -0.4646 0.4816 0.0000 C 0 0 1 0 0 0\n -1.7627 -0.2700 0.0000 C 0 0\n 0.8358 -0.2678 0.0000 C 0 0 1 0 0 0\n 2.1340 0.4838 0.0000 O 0 0\n 0.8380 -1.7685 0.0000 C 0 0 2 0 0 0\n -0.4623 -2.5178 0.0000 N 0 0\n -1.7613 -1.7674 0.0000 R# 0 0\n 2.1384 -2.5178 0.0000 C 0 0\n 3.4366 -1.7663 0.0000 R# 0 0\n 2.1406 -4.0178 0.0000 O 0 0\n 2 1 1 0\n 2 3 2 0\n 3 4 1 0\n 5 4 1 0\n 5 6 1 6\n 7 5 1 0\n 7 8 1 1\n 7 9 1 0\n 9 10 1 1\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2S,3R,4R)-2-amino-3-hydroxy-4-methyloct-6-enoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBmt\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3-(benzylsulfanyl)propanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n 1.2919 -5.2492 0.0000 R# 0 0\n 2.5886 -6.0033 0.0000 N 0 0\n 3.8912 -5.2578 0.0000 C 0 0 1 0 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 2.5951 -3.0039 0.0000 S 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 5.1894 -6.0109 0.0000 C 0 0\n 6.4897 -5.2632 0.0000 R# 0 0\n 5.1873 -7.5109 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 7 12 1 0\n 3 13 1 0\n 13 14 1 0\n 13 15 2 0\nM RGP 2 1 1 14 2\nM END\n> <Name>\n(2R)-2-amino-3-(benzylsulfanyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nCys_Bn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(1-methyl-1H-imidazol-4-yl)propanoic acid\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -3.9438 -1.4499 0.0000 C 0 0\n -2.4525 -1.6111 0.0000 N 0 0\n -1.7063 -2.9124 0.0000 C 0 0\n -0.2382 -2.6048 0.0000 N 0 0\n -0.0770 -1.1135 0.0000 C 0 0\n 1.2211 -0.3655 0.0000 C 0 0\n 1.2234 1.1353 0.0000 C 0 0 2 0 0 0\n -0.0770 1.8846 0.0000 N 0 0\n -1.3759 1.1343 0.0000 R# 0 0\n 2.5238 1.8846 0.0000 C 0 0\n 3.8220 1.1331 0.0000 R# 0 0\n 2.5261 3.3846 0.0000 O 0 0\n -1.4455 -0.4994 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 2 0\n 2 13 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(1-methyl-1H-imidazol-4-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHis1Me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nH\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-aminopent-4-enoic acid\n SciTegic09012117322D\n\n 9 8 0 0 1 0 999 V2000\n -2.4540 0.4164 0.0000 R# 0 0\n -1.1550 1.1667 0.0000 N 0 0\n 0.1453 0.4174 0.0000 C 0 0 1 0 0 0\n 0.1431 -1.0834 0.0000 C 0 0\n -1.1574 -1.8327 0.0000 C 0 0\n -1.1596 -3.3327 0.0000 C 0 0\n 1.4458 1.1667 0.0000 C 0 0\n 2.7439 0.4151 0.0000 R# 0 0\n 1.4480 2.6666 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 3 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 2 1 1 8 2\nM END\n> <Name>\n(2S)-2-aminopent-4-enoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nGlyall\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-2-cyclopropylacetic acid\n SciTegic09012117322D\n\n 9 9 0 0 1 0 999 V2000\n -2.7445 0.3715 0.0000 R# 0 0\n -1.4441 1.1192 0.0000 N 0 0\n -0.1452 0.3672 0.0000 C 0 0 1 0 0 0\n -0.1444 -1.1228 0.0000 C 0 0\n -0.8909 -2.4239 0.0000 C 0 0\n 0.6090 -2.4198 0.0000 C 0 0\n 1.1537 1.1192 0.0000 C 0 0\n 2.4534 0.3702 0.0000 R# 0 0\n 1.1529 2.6192 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 4 6 1 0\n 3 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 2 1 1 8 2\nM END\n> <Name>\n(2S)-2-amino-2-cyclopropylacetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nGlycPr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(3S)-3-aminooxolan-2-one\n SciTegic07272112182D\n\n 8 8 0 0 1 0 999 V2000\n 3.1247 -2.0836 0.0000 R# 0 0\n 4.6247 -2.0836 0.0000 N 0 0\n 5.3747 -3.3807 0.0000 C 0 0 1 0 0 0\n 4.7626 -4.7501 0.0000 C 0 0\n 5.8759 -5.7554 0.0000 C 0 0\n 7.1760 -5.0073 0.0000 O 0 0\n 6.8662 -3.5396 0.0000 C 0 0\n 7.8715 -2.4263 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 7 8 2 0\nM RGP 1 1 1\nM END\n> <Name>\n(3S)-3-aminooxolan-2-one\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHsl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-4-(2-aminophenyl)-4-oxobutanoic acid\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -3.0073 -1.4547 0.0000 N 0 0\n -1.7078 -2.2040 0.0000 C 0 0\n -1.7070 -3.7040 0.0000 C 0 0\n -0.4075 -4.4533 0.0000 C 0 0\n 0.8911 -3.7025 0.0000 C 0 0\n 0.8902 -2.2025 0.0000 C 0 0\n -0.4092 -1.4533 0.0000 C 0 0\n -0.4070 0.0476 0.0000 C 0 0\n -1.7051 0.7991 0.0000 O 0 0\n 0.8934 0.7969 0.0000 C 0 0\n 0.8957 2.2977 0.0000 C 0 0 2 0 0 0\n -0.4047 3.0470 0.0000 N 0 0\n -1.7036 2.2967 0.0000 R# 0 0\n 2.1961 3.0470 0.0000 C 0 0\n 3.4943 2.2954 0.0000 R# 0 0\n 2.1984 4.5470 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 2 7 1 0\n 7 8 1 0\n 8 9 2 0\n 8 10 1 0\n 11 10 1 6\n 11 12 1 0\n 12 13 1 0\n 11 14 1 0\n 14 15 1 0\n 14 16 2 0\nM RGP 2 13 1 15 2\nM END\n> <Name>\n(2S)-2-amino-4-(2-aminophenyl)-4-oxobutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAspPh2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nD\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-aziridine-2-carboxylic acid\n SciTegic09012117322D\n\n 7 7 0 0 1 0 999 V2000\n -2.6157 1.1160 0.0000 R# 0 0\n -1.5553 0.0552 0.0000 N 0 0\n -1.1673 -1.3938 0.0000 C 0 0\n -0.1065 -0.3333 0.0000 C 0 0 1 0 0 0\n 1.3321 0.0552 0.0000 C 0 0\n 2.3945 -1.0037 0.0000 R# 0 0\n 1.7183 1.5046 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 4 3 1 0\n 4 2 1 0\n 4 5 1 6\n 5 6 1 0\n 5 7 2 0\nM RGP 2 1 1 6 2\nM END\n> <Name>\n(2S)-aziridine-2-carboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAzi\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-Aminobenzoic acid\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n -3.0718 1.2967 0.0000 R# 0 0\n -1.5718 1.2989 0.0000 N 0 0\n -0.8187 0.0006 0.0000 C 0 0\n -1.5687 -1.2984 0.0000 C 0 0\n -0.8187 -2.5974 0.0000 C 0 0\n 0.6813 -2.5974 0.0000 C 0 0\n 1.4313 -1.2984 0.0000 C 0 0\n 0.6813 0.0006 0.0000 C 0 0\n 1.4344 1.2989 0.0000 C 0 0\n 0.6867 2.5992 0.0000 R# 0 0\n 2.9344 1.2967 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 3 8 1 0\n 8 9 1 0\n 9 10 1 0\n 9 11 2 0\nM RGP 2 1 1 10 2\nM END\n> <Name>\n2-Aminobenzoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n2Abz\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-Aminobenzoic acid\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n -4.1342 0.0728 0.0000 R# 0 0\n -2.8331 0.8193 0.0000 N 0 0\n -1.5349 0.0663 0.0000 C 0 0\n -1.5349 -1.4338 0.0000 C 0 0\n -0.2359 -2.1837 0.0000 C 0 0\n 1.0632 -1.4337 0.0000 C 0 0\n 1.0632 0.0663 0.0000 C 0 0\n -0.2359 0.8163 0.0000 C 0 0\n 2.3614 0.8193 0.0000 C 0 0\n 3.6617 0.0716 0.0000 R# 0 0\n 2.3593 2.3193 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 3 8 1 0\n 7 9 1 0\n 9 10 1 0\n 9 11 2 0\nM RGP 2 1 1 10 2\nM END\n> <Name>\n3-Aminobenzoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n3Abz\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n4-Aminobenzoic acid\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n -4.0902 1.1834 0.0000 R# 0 0\n -3.3420 -0.1167 0.0000 N 0 0\n -1.8412 -0.1198 0.0000 C 0 0\n -1.0912 -1.4189 0.0000 C 0 0\n 0.4088 -1.4189 0.0000 C 0 0\n 1.1588 -0.1198 0.0000 C 0 0\n 0.4088 1.1792 0.0000 C 0 0\n -1.0912 1.1792 0.0000 C 0 0\n 2.6596 -0.1167 0.0000 C 0 0\n 3.4119 -1.4145 0.0000 R# 0 0\n 3.4078 1.1834 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 3 8 1 0\n 6 9 1 0\n 9 10 1 0\n 9 11 2 0\nM RGP 2 1 1 10 2\nM END\n> <Name>\n4-Aminobenzoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n4Abz\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n1-aminocyclopropane-1-carboxylic acid\n SciTegic07272112182D\n\n 8 8 0 0 0 0 999 V2000\n -2.7619 -0.1359 0.0000 R# 0 0\n -1.4625 0.6134 0.0000 N 0 0\n -0.1626 -0.1562 0.0000 C 0 0\n -0.9129 -1.4551 0.0000 C 0 0\n 0.5871 -1.4554 0.0000 C 0 0\n 1.1376 0.6134 0.0000 C 0 0\n 2.4363 -0.1374 0.0000 R# 0 0\n 1.1389 2.1134 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 5 1 0\n 3 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 2 1 1 7 2\nM END\n> <Name>\n1-aminocyclopropane-1-carboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAc3c\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n1-aminocyclohexane-1-carboxylic acid\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n -2.7175 0.4554 0.0000 R# 0 0\n -1.4181 1.2047 0.0000 N 0 0\n -0.1182 0.4961 0.0000 C 0 0\n -1.4174 -0.2537 0.0000 C 0 0\n -1.4175 -1.7537 0.0000 C 0 0\n -0.1186 -2.5039 0.0000 C 0 0\n 1.1805 -1.7541 0.0000 C 0 0\n 1.1807 -0.2541 0.0000 C 0 0\n 1.1820 1.2047 0.0000 C 0 0\n 2.4807 0.4540 0.0000 R# 0 0\n 1.1833 2.7047 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 3 8 1 0\n 3 9 1 0\n 9 10 1 0\n 9 11 2 0\nM RGP 2 1 1 10 2\nM END\n> <Name>\n1-aminocyclohexane-1-carboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAc6c\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R,3S,4S)-2-amino-3-hydroxy-4-methyloct-6-enoic acid\n SciTegic09012117322D\n\n 14 13 0 0 1 0 999 V2000\n -3.0691 4.9815 0.0000 C 0 0\n -1.7694 4.2325 0.0000 C 0 0\n -1.7672 2.7317 0.0000 C 0 0\n -0.4668 1.9824 0.0000 C 0 0\n -0.4646 0.4816 0.0000 C 0 0 2 0 0 0\n -1.7627 -0.2700 0.0000 C 0 0\n 0.8358 -0.2678 0.0000 C 0 0 2 0 0 0\n 2.1340 0.4838 0.0000 O 0 0\n 0.8380 -1.7685 0.0000 C 0 0 1 0 0 0\n -0.4623 -2.5178 0.0000 N 0 0\n -1.7613 -1.7674 0.0000 R# 0 0\n 2.1384 -2.5178 0.0000 C 0 0\n 3.4366 -1.7663 0.0000 R# 0 0\n 2.1406 -4.0178 0.0000 O 0 0\n 2 1 1 0\n 2 3 2 0\n 3 4 1 0\n 5 4 1 0\n 5 6 1 1\n 7 5 1 0\n 7 8 1 6\n 7 9 1 0\n 9 10 1 6\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2R,3S,4S)-2-amino-3-hydroxy-4-methyloct-6-enoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Bmt\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-6-[(diaminomethylidene)amino]hexanoic acid\n SciTegic09012117322D\n\n 14 13 0 0 1 0 999 V2000\n -3.8101 -3.4803 0.0000 N 0 0\n -2.5119 -4.2318 0.0000 C 0 0\n -2.5142 -5.7319 0.0000 N 0 0\n -1.2115 -3.4826 0.0000 N 0 0\n -1.2092 -1.9817 0.0000 C 0 0\n 0.0912 -1.2325 0.0000 C 0 0\n 0.0935 0.2684 0.0000 C 0 0\n 1.3938 1.0176 0.0000 C 0 0\n 1.3961 2.5184 0.0000 C 0 0 1 0 0 0\n 0.0957 3.2677 0.0000 N 0 0\n -1.2032 2.5174 0.0000 R# 0 0\n 2.6965 3.2677 0.0000 C 0 0\n 3.9947 2.5161 0.0000 R# 0 0\n 2.6988 4.7677 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 9 8 1 1\n 9 10 1 0\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2R)-2-amino-6-[(diaminomethylidene)amino]hexanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-hArg\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3-(4-fluorophenyl)propanoic acid\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8113 -3.0442 0.0000 F 0 0\n -2.5101 -2.2980 0.0000 C 0 0\n -1.2133 -3.0518 0.0000 C 0 0\n 0.0879 -2.3056 0.0000 C 0 0\n 0.0923 -0.8056 0.0000 C 0 0\n 1.3927 -0.0563 0.0000 C 0 0\n 1.3950 1.4445 0.0000 C 0 0 1 0 0 0\n 0.0946 2.1938 0.0000 N 0 0\n -1.2043 1.4435 0.0000 R# 0 0\n 2.6954 2.1938 0.0000 C 0 0\n 3.9936 1.4422 0.0000 R# 0 0\n 2.6977 3.6938 0.0000 O 0 0\n -1.2045 -0.0518 0.0000 C 0 0\n -2.5057 -0.7980 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 1\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2R)-2-amino-3-(4-fluorophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDPhe4F\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3-(2-methyl-1H-indol-3-yl)propanoic acid\n SciTegic07272112182D\n\n 17 18 0 0 1 0 999 V2000\n -1.7477 1.9238 0.0000 C 0 0\n -1.4399 0.4557 0.0000 C 0 0\n -2.4466 -0.6562 0.0000 N 0 0\n -1.7004 -1.9565 0.0000 C 0 0\n -2.1678 -3.3818 0.0000 C 0 0\n -1.1672 -4.4993 0.0000 C 0 0\n 0.3009 -4.1914 0.0000 C 0 0\n 0.7683 -2.7661 0.0000 C 0 0\n -0.2323 -1.6487 0.0000 C 0 0\n -0.0712 -0.1581 0.0000 C 0 0\n 1.2269 0.5899 0.0000 C 0 0\n 1.2292 2.0907 0.0000 C 0 0 1 0 0 0\n -0.0712 2.8400 0.0000 N 0 0\n -1.3701 2.0897 0.0000 R# 0 0\n 2.5296 2.8400 0.0000 C 0 0\n 3.8277 2.0884 0.0000 R# 0 0\n 2.5318 4.3400 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\n 9 10 1 0\n 2 10 2 0\n 10 11 1 0\n 12 11 1 1\n 12 13 1 0\n 13 14 1 0\n 12 15 1 0\n 15 16 1 0\n 15 17 2 0\nM RGP 2 14 1 16 2\nM END\n> <Name>\n(2R)-2-amino-3-(2-methyl-1H-indol-3-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDTrp2M\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nW\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n 3.5418 -9.1526 0.0000 O 0 0\n 2.7937 -7.8525 0.0000 C 0 0\n 1.2937 -7.8508 0.0000 O 0 0\n 3.5464 -6.5540 0.0000 C 0 0 1 0 0 0\n 5.0472 -6.5557 0.0000 C 0 0\n 5.7999 -5.2572 0.0000 C 0 0\n 7.2999 -5.2568 0.0000 C 0 0\n 8.0495 -3.9575 0.0000 C 0 0\n 7.2990 -2.6587 0.0000 C 0 0\n 8.0486 -1.3594 0.0000 O 0 0\n 5.7990 -2.6592 0.0000 C 0 0\n 5.0486 -1.3604 0.0000 O 0 0\n 5.0495 -3.9584 0.0000 C 0 0\n 2.7951 -5.2547 0.0000 N 0 0\n 1.2951 -5.2547 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 4 2 1 0\n 4 5 1 6\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 9 11 1 0\n 11 12 1 0\n 11 13 2 0\n 6 13 1 0\n 4 14 1 0\n 14 15 1 0\nM RGP 1 15 1\nM END\n> <Name>\n(2R)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDTyr3O\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2R)-2-amino-3-(4-methoxyphenyl)propanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -4.7686 -2.1340 0.0000 C 0 0\n -3.4728 -2.8897 0.0000 O 0 0\n -2.1693 -2.1457 0.0000 C 0 0\n -0.8725 -2.8995 0.0000 C 0 0\n 0.4287 -2.1534 0.0000 C 0 0\n 0.4331 -0.6534 0.0000 C 0 0\n 1.7335 0.0959 0.0000 C 0 0\n 1.7358 1.5968 0.0000 C 0 0 1 0 0 0\n 0.4354 2.3460 0.0000 N 0 0\n -0.8635 1.5957 0.0000 R# 0 0\n 3.0362 2.3460 0.0000 C 0 0\n 4.3343 1.5945 0.0000 R# 0 0\n 3.0384 3.8460 0.0000 O 0 0\n -0.8637 0.1004 0.0000 C 0 0\n -2.1650 -0.6458 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 8 7 1 1\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\n 6 14 1 0\n 14 15 2 0\n 3 15 1 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n(2R)-2-amino-3-(4-methoxyphenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDTyrMe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3-methylpentanoic acid\n SciTegic09012117322D\n\n 10 9 0 0 1 0 999 V2000\n -1.3038 -3.1492 0.0000 C 0 0\n -1.3015 -1.6492 0.0000 C 0 0\n -0.0011 -0.8999 0.0000 C 0 0\n 1.2971 -1.6515 0.0000 C 0 0\n 0.0012 0.6009 0.0000 C 0 0 1 0 0 0\n -1.2992 1.3502 0.0000 N 0 0\n -2.5981 0.5999 0.0000 R# 0 0\n 1.3016 1.3502 0.0000 C 0 0\n 2.5998 0.5986 0.0000 R# 0 0\n 1.3039 2.8501 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 3 1 0\n 5 6 1 1\n 6 7 1 0\n 5 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 2 7 1 9 2\nM END\n> <Name>\n(2R)-2-amino-3-methylpentanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDxiIle\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nI\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-6-[(propan-2-yl)amino]hexanoic acid\n SciTegic09012117322D\n\n 14 13 0 0 1 0 999 V2000\n -2.5142 -5.7319 0.0000 C 0 0\n -2.5119 -4.2318 0.0000 C 0 0\n -3.8101 -3.4803 0.0000 C 0 0\n -1.2115 -3.4826 0.0000 N 0 0\n -1.2092 -1.9817 0.0000 C 0 0\n 0.0912 -1.2325 0.0000 C 0 0\n 0.0935 0.2684 0.0000 C 0 0\n 1.3938 1.0176 0.0000 C 0 0\n 1.3961 2.5184 0.0000 C 0 0 2 0 0 0\n 0.0957 3.2677 0.0000 N 0 0\n -1.2032 2.5174 0.0000 R# 0 0\n 2.6965 3.2677 0.0000 C 0 0\n 3.9947 2.5161 0.0000 R# 0 0\n 2.6988 4.7677 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 9 8 1 6\n 9 10 1 0\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2S)-2-amino-6-[(propan-2-yl)amino]hexanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLysiPr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nC-Terminal toluene\n SciTegic07272112182D\n\n 8 8 0 0 0 0 999 V2000\n 2.5951 -3.0031 0.0000 R# 0 0\n 4.0951 -3.0031 0.0000 C 0 0\n 4.8464 -1.7038 0.0000 C 0 0\n 6.3464 -1.7017 0.0000 C 0 0\n 7.0945 -0.4016 0.0000 C 0 0\n 6.3427 0.8964 0.0000 C 0 0\n 4.8427 0.8943 0.0000 C 0 0\n 4.0945 -0.4058 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 3 8 1 0\nM RGP 1 1 1\nM END\n> <Name>\nC-Terminal toluene\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n-Bn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nPhenyl\n SciTegic07272112182D\n\n 7 7 0 0 0 0 999 V2000\n 2.5981 -1.5000 0.0000 R# 0 0\n 4.0981 -1.5000 0.0000 C 0 0\n 4.8481 -2.7990 0.0000 C 0 0\n 6.3481 -2.7990 0.0000 C 0 0\n 7.0981 -1.5000 0.0000 C 0 0\n 6.3481 -0.2010 0.0000 C 0 0\n 4.8481 -0.2010 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 2 7 1 0\nM RGP 1 1 1\nM END\n> <Name>\nPhenyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPh\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nTert-butyloxycarbonyl\n SciTegic07272112182D\n\n 8 7 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 1.3000 2.2500 0.0000 C 0 0\n 0.0011 1.5002 0.0000 C 0 0\n 2.6000 0.0000 0.0000 O 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 3.9000 2.2500 0.0000 R# 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 1 0\n 5 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 1 7 2\nM END\n> <Name>\nTert-butyloxycarbonyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBoc\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-cyclohexylacetic acid\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 1.2948 -3.7516 0.0000 R# 0 0\n 2.5951 -3.0039 0.0000 C 0 0\n 3.8926 -3.7566 0.0000 O 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 5 10 1 0\nM RGP 1 1 2\nM END\n> <Name>\n2-cyclohexylacetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAChg\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n3,3-diphenylpropanoic acid\n SciTegic07272112182D\n\n 17 18 0 0 0 0 999 V2000\n 5.1935 -3.0096 0.0000 R# 0 0\n 3.8934 -3.7577 0.0000 C 0 0\n 3.8917 -5.2577 0.0000 O 0 0\n 2.5949 -3.0050 0.0000 C 0 0\n 2.5966 -1.5042 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8990 -0.7582 0.0000 C 0 0\n 3.9042 0.7419 0.0000 C 0 0\n 5.2058 1.4875 0.0000 C 0 0\n 6.5023 0.7331 0.0000 C 0 0\n 6.4972 -0.7669 0.0000 C 0 0\n 5.1956 -1.5125 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 10 11 2 0\n 6 11 1 0\n 5 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 15 2 0\n 15 16 1 0\n 16 17 2 0\n 12 17 1 0\nM RGP 1 1 2\nM END\n> <Name>\n3,3-diphenylpropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDADip\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n3,3-dimethylbutanoic acid\n SciTegic07272112182D\n\n 8 7 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 1.3000 2.2500 0.0000 C 0 0\n 0.0011 1.5002 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 3.9000 2.2500 0.0000 R# 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 1 0\n 5 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 1 7 2\nM END\n> <Name>\n3,3-dimethylbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAGlyB\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n4-phenylbutanoic acid\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 2.5909 -6.0056 0.0000 R# 0 0\n 3.8912 -5.2578 0.0000 C 0 0\n 5.1887 -6.0105 0.0000 O 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 2.5951 -3.0039 0.0000 C 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 7 12 1 0\nM RGP 1 1 2\nM END\n> <Name>\n4-phenylbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAhPhe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-(4-methoxyphenyl)acetic acid\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n -0.1391 7.2331 0.0000 C 0 0\n -1.6391 7.2378 0.0000 O 0 0\n -2.3945 5.9409 0.0000 C 0 0\n -3.8945 5.9435 0.0000 C 0 0\n -4.6468 4.6458 0.0000 C 0 0\n -3.8990 3.3455 0.0000 C 0 0\n -4.6490 2.0455 0.0000 C 0 0\n -3.8990 0.7455 0.0000 C 0 0\n -2.3990 0.7455 0.0000 R# 0 0\n -4.6486 -0.5538 0.0000 O 0 0\n -2.3990 3.3428 0.0000 C 0 0\n -1.6468 4.6406 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 8 10 2 0\n 6 11 1 0\n 11 12 2 0\n 3 12 1 0\nM RGP 1 9 2\nM END\n> <Name>\n2-(4-methoxyphenyl)acetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAnTyr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-(4-chlorophenyl)acetic acid\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n -1.6422 7.2386 0.0000 Cl 0 0\n -2.3945 5.9409 0.0000 C 0 0\n -3.8945 5.9435 0.0000 C 0 0\n -4.6468 4.6458 0.0000 C 0 0\n -3.8990 3.3455 0.0000 C 0 0\n -4.6490 2.0455 0.0000 C 0 0\n -3.8990 0.7455 0.0000 C 0 0\n -2.3990 0.7455 0.0000 R# 0 0\n -4.6486 -0.5538 0.0000 O 0 0\n -2.3990 3.3428 0.0000 C 0 0\n -1.6468 4.6406 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 7 9 2 0\n 5 10 1 0\n 10 11 2 0\n 2 11 1 0\nM RGP 1 8 2\nM END\n> <Name>\n2-(4-chlorophenyl)acetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAPhg4\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n(2R)-2-hydroxy-3-methylbutanoic acid\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 1.3000 2.2500 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0 1 0 0 0\n 2.6000 -1.5000 0.0000 O 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 3.9000 2.2500 0.0000 R# 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 4 2 1 0\n 4 5 1 6\n 4 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 1 7 2\nM END\n> <Name>\n(2R)-2-hydroxy-3-methylbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-OVal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n(2S)-2-hydroxy-4-methylpentanoic acid\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 1.3000 2.2500 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0 2 0 0 0\n 3.9000 2.2500 0.0000 O 0 0\n 5.2000 0.0000 0.0000 C 0 0\n 5.2000 -1.5000 0.0000 R# 0 0\n 6.4992 0.7496 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 5 4 1 0\n 5 6 1 6\n 5 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 1 8 2\nM END\n> <Name>\n(2S)-2-hydroxy-4-methylpentanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOLeu\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nN-Terminal toluene\n SciTegic07272112182D\n\n 8 8 0 0 0 0 999 V2000\n 2.5951 -3.0031 0.0000 R# 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 3 8 1 0\nM RGP 1 1 2\nM END\n> <Name>\nN-Terminal toluene\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBn-\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nN-Terminal phenylmethanol\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 3.8926 -3.7566 0.0000 R# 0 0\n 2.5951 -3.0039 0.0000 O 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\nM RGP 1 1 2\nM END\n> <Name>\nN-Terminal phenylmethanol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOBn-\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nDeamino-Lysine\n SciTegic07272112182D\n\n 10 9 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 N 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.2000 0.0000 0.0000 C 0 0\n 6.5000 0.7500 0.0000 C 0 0\n 6.5000 2.2500 0.0000 R# 0 0\n 7.7999 0.0000 0.0000 C 0 0\n 7.7999 -1.5000 0.0000 O 0 0\n 9.0992 0.7496 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 6 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 1 7 2\nM END\n> <Name>\nDeamino-Lysine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDALys\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n4-(dimethylamino)benzoic acid\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n -7.1102 -3.6899 0.0000 C 0 0\n -5.6102 -3.6946 0.0000 N 0 0\n -4.8648 -4.9963 0.0000 C 0 0\n -4.8549 -2.3977 0.0000 C 0 0\n -3.3549 -2.4003 0.0000 C 0 0\n -2.6026 -1.1026 0.0000 C 0 0\n -3.3504 0.1977 0.0000 C 0 0\n -4.8504 0.2003 0.0000 C 0 0\n -5.6026 -1.0974 0.0000 C 0 0\n -2.6003 1.4977 0.0000 C 0 0\n -1.1003 1.4977 0.0000 R# 0 0\n -3.3499 2.7970 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 1 11 2\nM END\n> <Name>\n4-(dimethylamino)benzoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNMe24A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-amino-3-(3-nitrophenyl)prop-2-enoic acid\n SciTegic07272112182D\n\n 16 16 0 0 0 0 999 V2000\n -4.5486 -1.0149 0.0000 O 0 5\n -3.2461 -0.2709 0.0000 N 0 3\n -3.2396 1.2290 0.0000 O 0 0\n -1.9501 -1.0278 0.0000 C 0 0\n -1.9545 -2.5278 0.0000 C 0 0\n -0.6577 -3.2816 0.0000 C 0 0\n 0.6436 -2.5354 0.0000 C 0 0\n 0.6480 -1.0354 0.0000 C 0 0\n 1.9484 -0.2861 0.0000 C 0 0\n 1.9506 1.2147 0.0000 C 0 0\n 0.6502 1.9640 0.0000 N 0 0\n -0.6487 1.2137 0.0000 R# 0 0\n 3.2510 1.9640 0.0000 C 0 0\n 4.5492 1.2124 0.0000 R# 0 0\n 3.2533 3.4640 0.0000 O 0 0\n -0.6489 -0.2816 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 9 8 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 13 15 2 0\n 8 16 2 0\n 4 16 1 0\nM CHG 2 1 -1 2 1\nM RGP 2 12 1 14 2\nM END\n> <Name>\n2-amino-3-(3-nitrophenyl)prop-2-enoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPheNO2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-amino-2-methylpropan-1-ol\n SciTegic07272112182D\n\n 7 6 0 0 0 0 999 V2000\n 6.7009 2.5990 0.0000 C 0 0\n 7.4505 1.2997 0.0000 C 0 0\n 8.2007 2.5986 0.0000 C 0 0\n 8.9513 1.2997 0.0000 C 0 0\n 9.7021 2.5983 0.0000 O 0 0\n 6.6992 0.0004 0.0000 N 0 0\n 5.1992 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 2 6 1 0\n 6 7 1 0\nM RGP 1 7 1\nM END\n> <Name>\n2-amino-2-methylpropan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAib-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n[(2R)-pyrrolidin-2-yl]methanol\n SciTegic07272112182D\n\n 8 8 0 0 1 0 999 V2000\n 3.1247 -2.0836 0.0000 O 0 0\n 1.6332 -2.2426 0.0000 C 0 0\n 0.7500 -1.0323 0.0000 C 0 0 1 0 0 0\n 1.2135 0.3943 0.0000 C 0 0\n 0.0000 1.2760 0.0000 C 0 0\n -1.2135 0.3943 0.0000 C 0 0\n -0.7500 -1.0323 0.0000 N 0 0\n -1.6317 -2.2458 0.0000 R# 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 7 8 1 0\nM RGP 1 8 1\nM END\n> <Name>\n[(2R)-pyrrolidin-2-yl]methanol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDProol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-4-methylpentan-1-ol\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 11.2079 3.0031 0.0000 C 0 0\n 9.7079 3.0015 0.0000 C 0 0\n 8.9597 1.7014 0.0000 C 0 0\n 8.9552 4.2999 0.0000 C 0 0\n 7.4544 4.2983 0.0000 C 0 0 1 0 0 0\n 6.7017 5.5967 0.0000 C 0 0\n 5.2017 5.5951 0.0000 O 0 0\n 6.7032 2.9990 0.0000 N 0 0\n 5.2032 2.9990 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 5 4 1 6\n 5 6 1 0\n 6 7 1 0\n 5 8 1 0\n 8 9 1 0\nM RGP 1 9 1\nM END\n> <Name>\n(2S)-2-amino-4-methylpentan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLeu-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-3-phenylpropan-1-ol\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n 3.8912 -5.2570 0.0000 O 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 2.5951 -3.0039 0.0000 C 0 0 2 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n -0.0041 -2.9953 0.0000 R# 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 3 11 1 0\n 11 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n(2S)-2-amino-3-phenylpropan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S,3S)-2-aminobutane-1,3-diol\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 1.3000 2.2500 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0 2 0 0 0\n 0.0007 0.0004 0.0000 O 0 0\n 2.6000 0.0000 0.0000 C 0 0 2 0 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 2.5969 -1.5008 0.0000 N 0 0\n 1.2968 -2.2490 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 2 4 1 0\n 4 5 1 6\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\nM RGP 1 8 1\nM END\n> <Name>\n(2S,3S)-2-aminobutane-1,3-diol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nThr-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-aminoacetaldehyde\n SciTegic07272112182D\n\n 5 4 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\nM RGP 1 1 1\nM END\n> <Name>\n2-aminoacetaldehyde\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nGly-al\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-4-methylpentanal\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 11.2079 3.0031 0.0000 C 0 0\n 9.7079 3.0015 0.0000 C 0 0\n 8.9597 1.7014 0.0000 C 0 0\n 8.9552 4.2999 0.0000 C 0 0\n 7.4544 4.2983 0.0000 C 0 0 2 0 0 0\n 6.7032 2.9990 0.0000 N 0 0\n 5.2032 2.9990 0.0000 R# 0 0\n 6.7017 5.5967 0.0000 C 0 0\n 5.2017 5.5951 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 5 4 1 6\n 5 6 1 0\n 6 7 1 0\n 5 8 1 0\n 8 9 2 0\nM RGP 1 7 1\nM END\n> <Name>\n(2S)-2-amino-4-methylpentanal\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLeu-al\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-3-phenylpropanal\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n 1.2951 -5.2547 0.0000 R# 0 0\n 1.2956 -3.7547 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 1 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 3 11 1 0\n 11 12 2 0\nM RGP 1 1 1\nM END\n> <Name>\n(2S)-2-amino-3-phenylpropanal\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe-al\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-6-{[bis(ethylamino)methylidene]amino}hexanoic acid\n SciTegic09012117322D\n\n 18 17 0 0 1 0 999 V2000\n -2.8981 -7.0008 0.0000 C 0 0\n -2.8959 -5.5008 0.0000 C 0 0\n -1.5954 -4.7515 0.0000 N 0 0\n -1.5932 -3.2507 0.0000 C 0 0\n -0.2927 -2.5014 0.0000 N 0 0\n -0.2905 -1.0006 0.0000 C 0 0\n 1.0099 -0.2514 0.0000 C 0 0\n 1.0122 1.2494 0.0000 C 0 0\n 2.3126 1.9987 0.0000 C 0 0\n 2.3149 3.4995 0.0000 C 0 0 2 0 0 0\n 1.0145 4.2488 0.0000 N 0 0\n -0.2844 3.4985 0.0000 R# 0 0\n 3.6153 4.2488 0.0000 C 0 0\n 4.9134 3.4972 0.0000 R# 0 0\n 3.6176 5.7488 0.0000 O 0 0\n -2.8904 -2.4961 0.0000 N 0 0\n -2.8865 -0.9953 0.0000 C 0 0\n -4.1831 -0.2410 0.0000 C 0 0\n 1 2 1 0\n 3 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 10 9 1 6\n 10 11 1 0\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 13 15 2 0\n 4 16 2 0\n 16 17 1 0\n 17 18 1 0\nM RGP 2 12 1 14 2\nM END\n> <Name>\n(2S)-2-amino-6-{[bis(ethylamino)methylidene]amino}hexanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLhArgE\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-4-methanesulfinylbutanoic acid\n SciTegic09012117322D\n\n 11 10 0 0 1 0 999 V2000\n 0.3495 3.3425 0.0000 C 0 0\n -0.9487 2.5910 0.0000 S 0 0\n -2.2484 3.3398 0.0000 O 0 0\n -0.9464 1.0901 0.0000 C 0 0\n 0.3540 0.3409 0.0000 C 0 0\n 0.3563 -1.1600 0.0000 C 0 0 2 0 0 0\n -0.9441 -1.9092 0.0000 N 0 0\n 1.6567 -1.9092 0.0000 C 0 0\n -2.2430 -1.1590 0.0000 R# 0 0\n 2.9549 -1.1577 0.0000 R# 0 0\n 1.6590 -3.4092 0.0000 O 0 0\n 1 2 1 0\n 3 2 2 0\n 2 4 1 0\n 4 5 1 0\n 6 5 1 1\n 6 7 1 0\n 6 8 1 0\n 7 9 1 0\n 8 10 1 0\n 8 11 2 0\nM RGP 2 9 1 10 2\nM END\n> <Name>\n(2S)-2-amino-4-methanesulfinylbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nMet_O\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nM\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-2-(4-hydroxyphenyl)acetic acid\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.0993 4.4423 0.0000 O 0 0\n -0.1001 2.9423 0.0000 C 0 0\n -1.3996 2.1930 0.0000 C 0 0\n -1.4004 0.6930 0.0000 C 0 0\n -0.1018 -0.0577 0.0000 C 0 0\n 1.1977 0.6916 0.0000 C 0 0\n 1.1985 2.1916 0.0000 C 0 0\n -0.0995 -1.5586 0.0000 C 0 0 2 0 0 0\n -1.3999 -2.3078 0.0000 N 0 0\n -2.6988 -1.5575 0.0000 R# 0 0\n 1.2009 -2.3078 0.0000 C 0 0\n 2.4990 -1.5563 0.0000 R# 0 0\n 1.2031 -3.8078 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 2 7 1 0\n 8 5 1 0\n 8 9 1 1\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n(2S)-2-amino-2-(4-hydroxyphenyl)acetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nnTyr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S,3aR,7aS)-octahydro-1H-indole-2-carboxylic acid\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n -0.2550 2.6034 0.0000 R# 0 0\n -0.0213 1.1217 0.0000 N 0 0\n -1.0820 0.0623 0.0000 C 0 0 1 0 0 0\n -2.5799 0.1419 0.0000 C 0 0\n -3.3978 -1.1155 0.0000 C 0 0\n -2.7178 -2.4526 0.0000 C 0 0\n -1.2199 -2.5322 0.0000 C 0 0\n -0.4020 -1.2748 0.0000 C 0 0 2 0 0 0\n 1.0789 -1.0416 0.0000 C 0 0\n 1.3147 0.4398 0.0000 C 0 0 1 0 0 0\n 2.6487 1.1217 0.0000 C 0 0\n 3.9075 0.3061 0.0000 R# 0 0\n 2.7262 2.6197 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 0\n 3 4 1 6\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 1\n 3 8 1 0\n 8 9 1 0\n 10 9 1 0\n 10 2 1 0\n 10 11 1 6\n 11 12 1 0\n 11 13 2 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\n(2S,3aR,7aS)-octahydro-1H-indole-2-carboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOic3aR\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(2-fluorophenyl)propanoic acid\n SciTegic09012117322D\n\n 14 14 0 0 1 0 999 V2000\n 1.0137 3.0583 0.0000 F 0 0\n -0.2832 2.3045 0.0000 C 0 0\n -1.5844 3.0507 0.0000 C 0 0\n -2.8813 2.2970 0.0000 C 0 0\n -2.8769 0.7970 0.0000 C 0 0\n -1.5756 0.0508 0.0000 C 0 0\n -0.2788 0.8045 0.0000 C 0 0\n 1.0216 0.0552 0.0000 C 0 0\n 1.0238 -1.4456 0.0000 C 0 0 2 0 0 0\n -0.2765 -2.1949 0.0000 N 0 0\n -1.5754 -1.4446 0.0000 R# 0 0\n 2.3242 -2.1949 0.0000 C 0 0\n 3.6224 -1.4433 0.0000 R# 0 0\n 2.3265 -3.6949 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 2 7 1 0\n 7 8 1 0\n 9 8 1 1\n 9 10 1 0\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2S)-2-amino-3-(2-fluorophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe_2F\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(3-fluorophenyl)propanoic acid\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8032 -0.2585 0.0000 F 0 0\n -2.5064 -1.0123 0.0000 C 0 0\n -2.5107 -2.5123 0.0000 C 0 0\n -1.2139 -3.2661 0.0000 C 0 0\n 0.0873 -2.5199 0.0000 C 0 0\n 0.0917 -1.0199 0.0000 C 0 0\n 1.3921 -0.2706 0.0000 C 0 0\n 1.3944 1.2302 0.0000 C 0 0 2 0 0 0\n 0.0940 1.9795 0.0000 N 0 0\n -1.2049 1.2292 0.0000 R# 0 0\n 2.6948 1.9795 0.0000 C 0 0\n 3.9929 1.2279 0.0000 R# 0 0\n 2.6970 3.4795 0.0000 O 0 0\n -1.2051 -0.2661 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 6\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\n 6 14 2 0\n 2 14 1 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n(2S)-2-amino-3-(3-fluorophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe_3F\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-fluorophenyl)propanoic acid\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8113 -3.0442 0.0000 F 0 0\n -2.5101 -2.2980 0.0000 C 0 0\n -1.2133 -3.0518 0.0000 C 0 0\n 0.0879 -2.3056 0.0000 C 0 0\n 0.0923 -0.8056 0.0000 C 0 0\n 1.3927 -0.0563 0.0000 C 0 0\n 1.3950 1.4445 0.0000 C 0 0 2 0 0 0\n 0.0946 2.1938 0.0000 N 0 0\n -1.2043 1.4435 0.0000 R# 0 0\n 2.6954 2.1938 0.0000 C 0 0\n 3.9936 1.4422 0.0000 R# 0 0\n 2.6977 3.6938 0.0000 O 0 0\n -1.2045 -0.0518 0.0000 C 0 0\n -2.5057 -0.7980 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-fluorophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe_4F\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-nitrophenyl)propanoic acid\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -3.2553 -2.6153 0.0000 N 0 3\n -3.2623 -4.1153 0.0000 O 0 5\n -4.5511 -1.8597 0.0000 O 0 0\n -1.9519 -1.8714 0.0000 C 0 0\n -0.6550 -2.6252 0.0000 C 0 0\n -1.9475 -0.3714 0.0000 C 0 0\n 0.6462 -1.8790 0.0000 C 0 0\n -0.6462 0.3748 0.0000 C 0 0\n 0.6506 -0.3790 0.0000 C 0 0\n 1.9510 0.3703 0.0000 C 0 0\n 1.9533 1.8711 0.0000 C 0 0 2 0 0 0\n 0.6529 2.6204 0.0000 N 0 0\n 3.2537 2.6204 0.0000 C 0 0\n -0.6460 1.8701 0.0000 R# 0 0\n 4.5518 1.8689 0.0000 R# 0 0\n 3.2559 4.1204 0.0000 O 0 0\n 2 1 1 0\n 1 3 2 0\n 4 1 1 0\n 5 4 2 0\n 4 6 1 0\n 7 5 1 0\n 6 8 2 0\n 9 7 2 0\n 9 8 1 0\n 10 9 1 0\n 11 10 1 6\n 11 12 1 0\n 11 13 1 0\n 14 12 1 0\n 13 15 1 0\n 13 16 2 0\nM CHG 2 1 1 2 -1\nM RGP 2 14 1 15 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-nitrophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe4NO\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-methyl-3-phenylbutanoic acid\n SciTegic09012117322D\n\n 15 15 0 0 1 0 999 V2000\n 2.0773 -1.0021 0.0000 C 0 0\n 0.7791 -0.2505 0.0000 C 0 0\n 2.0792 0.4978 0.0000 C 0 0\n 0.7814 1.2503 0.0000 C 0 0 2 0 0 0\n -0.5190 1.9996 0.0000 N 0 0\n -1.8179 1.2493 0.0000 R# 0 0\n 2.0818 1.9996 0.0000 C 0 0\n 3.3799 1.2480 0.0000 R# 0 0\n 2.0841 3.4996 0.0000 O 0 0\n -0.5213 -0.9998 0.0000 C 0 0\n -1.8197 -0.2486 0.0000 C 0 0\n -3.1194 -0.9975 0.0000 C 0 0\n -3.1207 -2.4974 0.0000 C 0 0\n -1.8223 -3.2486 0.0000 C 0 0\n -0.5226 -2.4998 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 4 2 1 0\n 4 5 1 6\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\n 7 9 2 0\n 2 10 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 15 2 0\n 10 15 1 0\nM RGP 2 6 1 8 2\nM END\n> <Name>\n(2S)-2-amino-3-methyl-3-phenylbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhebbd\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid\n SciTegic09012117322D\n\n 17 18 0 0 1 0 999 V2000\n 1.1222 4.8834 0.0000 O 0 0\n 0.1216 3.7659 0.0000 C 0 0\n -1.3465 4.0738 0.0000 C 0 0\n -2.3471 2.9564 0.0000 C 0 0\n -1.8797 1.5311 0.0000 C 0 0\n -2.6260 0.2308 0.0000 N 0 0\n -1.6193 -0.8812 0.0000 C 0 0\n -0.2507 -0.2673 0.0000 C 0 0\n 1.0476 -1.0153 0.0000 C 0 0\n 1.0498 -2.5161 0.0000 C 0 0 2 0 0 0\n -0.2506 -3.2655 0.0000 N 0 0\n -1.5495 -2.5151 0.0000 R# 0 0\n 2.3501 -3.2655 0.0000 C 0 0\n 3.6483 -2.5139 0.0000 R# 0 0\n 2.3524 -4.7655 0.0000 O 0 0\n -0.4117 1.2232 0.0000 C 0 0\n 0.5890 2.3407 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 10 9 1 1\n 10 11 1 0\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 13 15 2 0\n 8 16 1 0\n 5 16 1 0\n 16 17 2 0\n 2 17 1 0\nM RGP 2 12 1 14 2\nM END\n> <Name>\n(2S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTrp5OH\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nW\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(1-methoxy-1H-indol-3-yl)propanoic acid\n SciTegic09012117322D\n\n 18 19 0 0 1 0 999 V2000\n -4.1668 -0.9653 0.0000 C 0 0\n -3.5621 0.4074 0.0000 O 0 0\n -2.0728 0.5709 0.0000 N 0 0\n -1.0661 -0.5411 0.0000 C 0 0\n 0.3025 0.0728 0.0000 C 0 0\n 1.6007 -0.6752 0.0000 C 0 0\n 1.6030 -2.1761 0.0000 C 0 0 2 0 0 0\n 0.3026 -2.9254 0.0000 N 0 0\n -0.9963 -2.1750 0.0000 R# 0 0\n 2.9034 -2.9254 0.0000 C 0 0\n 4.2016 -2.1739 0.0000 R# 0 0\n 2.9056 -4.4253 0.0000 O 0 0\n 0.1415 1.5633 0.0000 C 0 0\n 1.1422 2.6808 0.0000 C 0 0\n 0.6748 4.1060 0.0000 C 0 0\n -0.7932 4.4139 0.0000 C 0 0\n -1.7939 3.2964 0.0000 C 0 0\n -1.3265 1.8712 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 1\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 16 17 1 0\n 17 18 2 0\n 3 18 1 0\n 13 18 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(1-methoxy-1H-indol-3-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTrpOme\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nW\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-hydroxy-3,5-diiodophenyl)propanoic acid\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -3.4976 -2.7570 0.0000 O 0 0\n -2.1964 -2.0108 0.0000 C 0 0\n -0.8995 -2.7646 0.0000 C 0 0\n -0.9039 -4.2646 0.0000 I 0 0\n 0.4017 -2.0184 0.0000 C 0 0\n 0.4061 -0.5184 0.0000 C 0 0\n 1.7065 0.2309 0.0000 C 0 0\n 1.7088 1.7317 0.0000 C 0 0 2 0 0 0\n 0.4084 2.4810 0.0000 N 0 0\n -0.8905 1.7307 0.0000 R# 0 0\n 3.0092 2.4810 0.0000 C 0 0\n 4.3073 1.7295 0.0000 R# 0 0\n 3.0114 3.9810 0.0000 O 0 0\n -0.8907 0.2354 0.0000 C 0 0\n -2.1920 -0.5108 0.0000 C 0 0\n -3.4888 0.2430 0.0000 I 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 3 5 1 0\n 5 6 2 0\n 6 7 1 0\n 8 7 1 6\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\n 6 14 1 0\n 14 15 2 0\n 2 15 1 0\n 15 16 1 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-hydroxy-3,5-diiodophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyr35d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -3.5578 -3.0413 0.0000 O 0 0\n -2.2566 -2.2951 0.0000 C 0 0\n -0.9598 -3.0489 0.0000 C 0 0\n 0.3415 -2.3027 0.0000 C 0 0\n 0.3458 -0.8027 0.0000 C 0 0\n 1.6463 -0.0534 0.0000 C 0 0\n 1.6485 1.4474 0.0000 C 0 0 2 0 0 0\n 0.3481 2.1967 0.0000 N 0 0\n -0.9508 1.4464 0.0000 R# 0 0\n 2.9489 2.1967 0.0000 C 0 0\n 4.2471 1.4452 0.0000 R# 0 0\n 2.9512 3.6967 0.0000 O 0 0\n -0.9510 -0.0489 0.0000 C 0 0\n -2.2522 -0.7951 0.0000 C 0 0\n -3.5491 -0.0413 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\n 14 15 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyr3OH\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-methoxyphenyl)propanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -4.7686 -2.1340 0.0000 C 0 0\n -3.4728 -2.8897 0.0000 O 0 0\n -2.1693 -2.1457 0.0000 C 0 0\n -0.8725 -2.8995 0.0000 C 0 0\n 0.4287 -2.1534 0.0000 C 0 0\n 0.4331 -0.6534 0.0000 C 0 0\n 1.7335 0.0959 0.0000 C 0 0\n 1.7358 1.5968 0.0000 C 0 0 2 0 0 0\n 0.4354 2.3460 0.0000 N 0 0\n -0.8635 1.5957 0.0000 R# 0 0\n 3.0362 2.3460 0.0000 C 0 0\n 4.3343 1.5945 0.0000 R# 0 0\n 3.0384 3.8460 0.0000 O 0 0\n -0.8637 0.1004 0.0000 C 0 0\n -2.1650 -0.6458 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 8 7 1 6\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\n 6 14 1 0\n 14 15 2 0\n 3 15 1 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-methoxyphenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyr_Me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-[4-(phosphonooxy)phenyl]propanoic acid\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -3.8234 -0.3621 0.0000 O 0 0\n -3.8304 -1.8621 0.0000 P 0 0\n -5.1258 -1.1058 0.0000 O 0 0\n -5.1332 -2.6056 0.0000 O 0 0\n -2.5340 -2.6181 0.0000 O 0 0\n -1.2305 -1.8742 0.0000 C 0 0\n 0.0664 -2.6280 0.0000 C 0 0\n 1.3676 -1.8818 0.0000 C 0 0\n 1.3720 -0.3818 0.0000 C 0 0\n 2.6724 0.3675 0.0000 C 0 0\n 2.6747 1.8683 0.0000 C 0 0 2 0 0 0\n 1.3742 2.6176 0.0000 N 0 0\n 0.0754 1.8673 0.0000 R# 0 0\n 3.9751 2.6176 0.0000 C 0 0\n 5.2732 1.8660 0.0000 R# 0 0\n 3.9773 4.1176 0.0000 O 0 0\n 0.0752 0.3720 0.0000 C 0 0\n -1.2261 -0.3742 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 11 10 1 6\n 11 12 1 0\n 12 13 1 0\n 11 14 1 0\n 14 15 1 0\n 14 16 2 0\n 9 17 1 0\n 17 18 2 0\n 6 18 1 0\nM RGP 2 13 1 15 2\nM END\n> <Name>\n(2S)-2-amino-3-[4-(phosphonooxy)phenyl]propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyrPO3\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-4-hydroxypyrrolidine-2-carboxylic acid\n SciTegic09012117322D\n\n 10 10 0 0 1 0 999 V2000\n -1.9677 -2.9458 0.0000 O 0 0\n -1.2857 -1.6098 0.0000 C 0 0\n 0.1960 -1.3762 0.0000 C 0 0\n 0.4318 0.1051 0.0000 C 0 0 2 0 0 0\n -0.9043 0.7871 0.0000 N 0 0\n -1.1378 2.2688 0.0000 R# 0 0\n -1.9657 -0.2728 0.0000 C 0 0\n 1.7658 0.7871 0.0000 C 0 0\n 3.0246 -0.0286 0.0000 R# 0 0\n 1.8432 2.2851 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 4 3 1 0\n 4 5 1 0\n 5 6 1 0\n 5 7 1 0\n 2 7 1 0\n 4 8 1 6\n 8 9 1 0\n 8 10 2 0\nM RGP 2 6 1 9 2\nM END\n> <Name>\n(2S)-4-hydroxypyrrolidine-2-carboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nxiHyp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-hydroxybutanoic acid\n SciTegic09012117322D\n\n 9 8 0 0 1 0 999 V2000\n 1.1521 2.0015 0.0000 C 0 0\n -0.1460 1.2499 0.0000 C 0 0\n -1.4457 1.9988 0.0000 O 0 0\n -0.1437 -0.2509 0.0000 C 0 0 2 0 0 0\n -1.4441 -1.0002 0.0000 N 0 0\n -2.7430 -0.2499 0.0000 R# 0 0\n 1.1567 -1.0002 0.0000 C 0 0\n 2.4548 -0.2487 0.0000 R# 0 0\n 1.1589 -2.5001 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 4 2 1 0\n 4 5 1 1\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 2 6 1 8 2\nM END\n> <Name>\n(2S)-2-amino-3-hydroxybutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nxiThr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n4-(methylamino)benzoic acid\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n -3.7490 1.3013 0.0000 C 0 0\n -3.0008 0.0011 0.0000 N 0 0\n -3.7531 -1.2966 0.0000 R# 0 0\n -1.5000 -0.0019 0.0000 C 0 0\n -0.7500 -1.3010 0.0000 C 0 0\n 0.7500 -1.3010 0.0000 C 0 0\n 1.5000 -0.0019 0.0000 C 0 0\n 0.7500 1.2971 0.0000 C 0 0\n -0.7500 1.2971 0.0000 C 0 0\n 3.0008 0.0011 0.0000 C 0 0\n 3.7531 -1.2966 0.0000 R# 0 0\n 3.7490 1.3013 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 3 1 11 2\nM END\n> <Name>\n4-(methylamino)benzoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNMe4Ab\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-hydroxyphenyl)-2-methylpropanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -1.2419 3.3801 0.0000 C 0 0\n -0.4936 2.0800 0.0000 C 0 0 1 0 0 0\n -1.2462 0.7815 0.0000 C 0 0\n -0.4987 -0.5200 0.0000 C 0 0\n -1.2490 -1.8188 0.0000 C 0 0\n -0.4993 -3.1180 0.0000 C 0 0\n 1.0007 -3.1184 0.0000 C 0 0\n 1.7504 -4.4176 0.0000 O 0 0\n 1.7510 -1.8195 0.0000 C 0 0\n 1.0013 -0.5203 0.0000 C 0 0\n -2.0236 2.0785 0.0000 N 0 0\n -2.7731 0.7792 0.0000 R# 0 0\n 1.0072 2.0785 0.0000 C 0 0\n 1.7555 0.7785 0.0000 R# 0 0\n 1.7593 3.3763 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 7 9 1 0\n 9 10 2 0\n 4 10 1 0\n 2 11 1 0\n 11 12 1 0\n 2 13 1 0\n 13 14 1 0\n 13 15 2 0\nM RGP 2 12 1 14 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-hydroxyphenyl)-2-methylpropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\naMeTyr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-8-oxodecanoic acid\n SciTegic09012117322D\n\n 15 14 0 0 1 0 999 V2000\n -3.5597 6.0494 0.0000 C 0 0\n -2.2600 5.3005 0.0000 C 0 0\n -2.2577 3.7997 0.0000 C 0 0\n -3.5558 3.0481 0.0000 O 0 0\n -0.9573 3.0504 0.0000 C 0 0\n -0.9550 1.5496 0.0000 C 0 0\n 0.3454 0.8003 0.0000 C 0 0\n 0.3477 -0.7004 0.0000 C 0 0\n 1.6481 -1.4497 0.0000 C 0 0\n 1.6504 -2.9505 0.0000 C 0 0 2 0 0 0\n 0.3500 -3.6998 0.0000 N 0 0\n -0.9489 -2.9496 0.0000 R# 0 0\n 2.9508 -3.6998 0.0000 C 0 0\n 4.2489 -2.9483 0.0000 R# 0 0\n 2.9531 -5.1998 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 10 9 1 1\n 10 11 1 0\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 13 15 2 0\nM RGP 2 12 1 14 2\nM END\n> <Name>\n(2S)-2-amino-8-oxodecanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAoda\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-benzoylphenyl)propanoic acid\n SciTegic07272112182D\n\n 21 22 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 1 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.6003 1.4977 0.0000 C 0 0\n -2.6030 2.9977 0.0000 O 0 0\n -3.8990 0.7455 0.0000 C 0 0\n -5.2007 1.4909 0.0000 C 0 0\n -6.4972 0.7364 0.0000 C 0 0\n -6.4920 -0.7636 0.0000 C 0 0\n -5.1903 -1.5091 0.0000 C 0 0\n -3.8939 -0.7546 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 8 11 1 0\n 11 12 2 0\n 11 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 16 17 1 0\n 17 18 2 0\n 13 18 1 0\n 3 19 1 0\n 19 20 1 0\n 19 21 2 0\nM RGP 2 1 1 20 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-benzoylphenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBpa\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3-(methylsulfanyl)propanoic acid\n SciTegic09012117322D\n\n 9 8 0 0 1 0 999 V2000\n -1.1596 -3.3327 0.0000 C 0 0\n -1.1574 -1.8327 0.0000 S 0 0\n 0.1431 -1.0834 0.0000 C 0 0\n 0.1453 0.4174 0.0000 C 0 0 2 0 0 0\n -1.1550 1.1667 0.0000 N 0 0\n -2.4540 0.4164 0.0000 R# 0 0\n 1.4458 1.1667 0.0000 C 0 0\n 2.7439 0.4151 0.0000 R# 0 0\n 1.4480 2.6666 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 4 3 1 6\n 4 5 1 0\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 2 6 1 8 2\nM END\n> <Name>\n(2R)-2-amino-3-(methylsulfanyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nCys_Me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3,3-diphenylpropanoic acid\n SciTegic07272112182D\n\n 19 20 0 0 1 0 999 V2000\n -2.6668 1.7759 0.0000 R# 0 0\n -1.3676 2.5255 0.0000 N 0 0\n -0.0676 1.7755 0.0000 C 0 0 1 0 0 0\n -0.0676 0.2748 0.0000 C 0 0\n 1.2314 -0.4771 0.0000 C 0 0\n 1.2334 -1.9771 0.0000 C 0 0\n 2.5334 -2.7254 0.0000 C 0 0\n 3.8314 -1.9737 0.0000 C 0 0\n 3.8295 -0.4737 0.0000 C 0 0\n 2.5295 0.2746 0.0000 C 0 0\n -1.3686 -0.4736 0.0000 C 0 0\n -1.3718 -1.9737 0.0000 C 0 0\n -2.6724 -2.7210 0.0000 C 0 0\n -3.9699 -1.9684 0.0000 C 0 0\n -3.9668 -0.4684 0.0000 C 0 0\n -2.6662 0.2790 0.0000 C 0 0\n 1.2324 2.5255 0.0000 C 0 0\n 1.2324 4.0255 0.0000 R# 0 0\n 2.5317 1.7759 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 4 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 11 16 1 0\n 3 17 1 0\n 17 18 1 0\n 17 19 2 0\nM RGP 2 1 1 18 2\nM END\n> <Name>\n(2S)-2-amino-3,3-diphenylpropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDip\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-6-[(diaminomethyl)amino]hexanoic acid\n SciTegic09012117322D\n\n 14 13 0 0 1 0 999 V2000\n -2.5142 -5.7319 0.0000 N 0 0\n -2.5119 -4.2318 0.0000 C 0 0\n -3.8101 -3.4803 0.0000 N 0 0\n -1.2115 -3.4826 0.0000 N 0 0\n -1.2092 -1.9817 0.0000 C 0 0\n 0.0912 -1.2325 0.0000 C 0 0\n 0.0935 0.2684 0.0000 C 0 0\n 1.3938 1.0176 0.0000 C 0 0\n 1.3961 2.5184 0.0000 C 0 0 2 0 0 0\n 0.0957 3.2677 0.0000 N 0 0\n -1.2032 2.5174 0.0000 R# 0 0\n 2.6965 3.2677 0.0000 C 0 0\n 3.9947 2.5161 0.0000 R# 0 0\n 2.6988 4.7677 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 9 8 1 6\n 9 10 1 0\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2S)-2-amino-6-[(diaminomethyl)amino]hexanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nhArg\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(1-benzyl-1H-imidazol-4-yl)propanoic acid\n SciTegic09012117322D\n\n 19 20 0 0 1 0 999 V2000\n 0.2119 -2.7206 0.0000 R# 0 0\n 1.5107 -3.4708 0.0000 N 0 0\n 2.8111 -2.7215 0.0000 C 0 0 1 0 0 0\n 2.8089 -1.2207 0.0000 C 0 0\n 1.5107 -0.4727 0.0000 C 0 0\n 1.3494 1.0186 0.0000 C 0 0\n -0.1097 1.3062 0.0000 N 0 0\n -0.7270 2.6742 0.0000 C 0 0\n -2.2203 2.8245 0.0000 C 0 0\n -2.8392 4.1909 0.0000 C 0 0\n -4.3320 4.3381 0.0000 C 0 0\n -5.2058 3.1189 0.0000 C 0 0\n -4.5869 1.7526 0.0000 C 0 0\n -3.0942 1.6053 0.0000 C 0 0\n -0.8648 0.0249 0.0000 C 0 0\n 0.1422 -1.0869 0.0000 N 0 0\n 4.1115 -3.4708 0.0000 C 0 0\n 5.4097 -2.7192 0.0000 R# 0 0\n 4.1138 -4.9708 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 9 14 1 0\n 7 15 1 0\n 15 16 2 0\n 5 16 1 0\n 3 17 1 0\n 17 18 1 0\n 17 19 2 0\nM RGP 2 1 1 18 2\nM END\n> <Name>\n(2S)-2-amino-3-(1-benzyl-1H-imidazol-4-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHis1Bn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nH\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(1-methyl-1H-imidazol-5-yl)propanoic acid\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n 0.5030 3.4455 0.0000 C 0 0\n -0.6088 2.4385 0.0000 N 0 0\n -2.0769 2.7461 0.0000 C 0 0\n -2.8231 1.4448 0.0000 N 0 0\n -1.8161 0.3331 0.0000 C 0 0\n -0.4476 0.9472 0.0000 C 0 0\n 0.8506 0.1992 0.0000 C 0 0\n 0.8528 -1.3016 0.0000 C 0 0 2 0 0 0\n -0.4476 -2.0509 0.0000 N 0 0\n -1.7464 -1.3006 0.0000 R# 0 0\n 2.1532 -2.0509 0.0000 C 0 0\n 3.4514 -1.2994 0.0000 R# 0 0\n 2.1555 -3.5509 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 2 6 1 0\n 6 7 1 0\n 8 7 1 1\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n(2S)-2-amino-3-(1-methyl-1H-imidazol-5-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHis3Me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nH\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2,6-diamino-5-hydroxyhexanoic acid\n SciTegic09012117322D\n\n 12 11 0 0 1 0 999 V2000\n -2.0635 -4.4369 0.0000 N 0 0\n -2.0613 -2.9369 0.0000 C 0 0\n -0.7609 -2.1876 0.0000 C 0 0\n 0.5373 -2.9391 0.0000 O 0 0\n -0.7587 -0.6868 0.0000 C 0 0\n 0.5417 0.0626 0.0000 C 0 0\n 0.5440 1.5634 0.0000 C 0 0 2 0 0 0\n -0.7565 2.3126 0.0000 N 0 0\n -2.0553 1.5623 0.0000 R# 0 0\n 1.8443 2.3126 0.0000 C 0 0\n 3.1425 1.5611 0.0000 R# 0 0\n 1.8465 3.8126 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 3 5 1 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2,6-diamino-5-hydroxyhexanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHyl5xi\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-{[1,1'-biphenyl]-4-yl}propanoic acid\n SciTegic07272112182D\n\n 19 20 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 1 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.5987 1.5004 0.0000 C 0 0\n -2.6012 3.0004 0.0000 C 0 0\n -3.9015 3.7484 0.0000 C 0 0\n -5.1993 2.9963 0.0000 C 0 0\n -5.1969 1.4963 0.0000 C 0 0\n -3.8967 0.7484 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 8 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 11 16 1 0\n 3 17 1 0\n 17 18 1 0\n 17 19 2 0\nM RGP 2 1 1 18 2\nM END\n> <Name>\n(2S)-2-amino-3-{[1,1'-biphenyl]-4-yl}propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBip\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-aminobut-2-enoic acid\n SciTegic09012117322D\n\n 8 7 0 0 0 0 999 V2000\n -1.3017 2.2489 0.0000 C 0 0\n -0.0020 1.5001 0.0000 C 0 0\n 0.0003 -0.0008 0.0000 C 0 0\n -1.3001 -0.7500 0.0000 N 0 0\n -2.5990 0.0002 0.0000 R# 0 0\n 1.3007 -0.7500 0.0000 C 0 0\n 2.5988 0.0015 0.0000 R# 0 0\n 1.3029 -2.2500 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 3 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 2 5 1 7 2\nM END\n> <Name>\n2-aminobut-2-enoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAbu23D\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3,3-diphenylpropanoic acid\n SciTegic07272112182D\n\n 19 20 0 0 1 0 999 V2000\n -2.6668 1.7759 0.0000 R# 0 0\n -1.3676 2.5255 0.0000 N 0 0\n -0.0676 1.7755 0.0000 C 0 0 2 0 0 0\n -0.0676 0.2748 0.0000 C 0 0\n 1.2314 -0.4771 0.0000 C 0 0\n 1.2334 -1.9771 0.0000 C 0 0\n 2.5334 -2.7254 0.0000 C 0 0\n 3.8314 -1.9737 0.0000 C 0 0\n 3.8295 -0.4737 0.0000 C 0 0\n 2.5295 0.2746 0.0000 C 0 0\n -1.3686 -0.4736 0.0000 C 0 0\n -1.3718 -1.9737 0.0000 C 0 0\n -2.6724 -2.7210 0.0000 C 0 0\n -3.9699 -1.9684 0.0000 C 0 0\n -3.9668 -0.4684 0.0000 C 0 0\n -2.6662 0.2790 0.0000 C 0 0\n 1.2324 2.5255 0.0000 C 0 0\n 1.2324 4.0255 0.0000 R# 0 0\n 2.5317 1.7759 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 4 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 11 16 1 0\n 3 17 1 0\n 17 18 1 0\n 17 19 2 0\nM RGP 2 1 1 18 2\nM END\n> <Name>\n(2R)-2-amino-3,3-diphenylpropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Dip\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-aminoprop-2-enoic acid\n SciTegic07272112182D\n\n 7 6 0 0 0 0 999 V2000\n 2.6000 -1.5000 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 0.0007 0.0004 0.0000 R# 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 3.9000 2.2500 0.0000 R# 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 2 5 1 0\n 5 6 1 0\n 5 7 2 0\nM RGP 2 4 1 6 2\nM END\n> <Name>\n2-aminoprop-2-enoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDha\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-6-{[bis(ethylamino)methylidene]amino}hexanoic acid\n SciTegic09012117322D\n\n 18 17 0 0 1 0 999 V2000\n -2.8981 -7.0008 0.0000 C 0 0\n -2.8959 -5.5008 0.0000 C 0 0\n -1.5954 -4.7515 0.0000 N 0 0\n -1.5932 -3.2507 0.0000 C 0 0\n -0.2927 -2.5014 0.0000 N 0 0\n -0.2905 -1.0006 0.0000 C 0 0\n 1.0099 -0.2514 0.0000 C 0 0\n 1.0122 1.2494 0.0000 C 0 0\n 2.3126 1.9987 0.0000 C 0 0\n 2.3149 3.4995 0.0000 C 0 0 1 0 0 0\n 1.0145 4.2488 0.0000 N 0 0\n -0.2844 3.4985 0.0000 R# 0 0\n 3.6153 4.2488 0.0000 C 0 0\n 4.9134 3.4972 0.0000 R# 0 0\n 3.6176 5.7488 0.0000 O 0 0\n -2.8904 -2.4961 0.0000 N 0 0\n -2.8865 -0.9953 0.0000 C 0 0\n -4.1831 -0.2410 0.0000 C 0 0\n 1 2 1 0\n 3 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 10 9 1 1\n 10 11 1 0\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 13 15 2 0\n 4 16 2 0\n 16 17 1 0\n 17 18 1 0\nM RGP 2 12 1 14 2\nM END\n> <Name>\n(2R)-2-amino-6-{[bis(ethylamino)methylidene]amino}hexanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDhArgE\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-4-[(S)-methanesulfinyl]butanoic acid\n SciTegic09012117322D\n\n 11 10 0 0 1 0 999 V2000\n 0.3495 3.3425 0.0000 C 0 0\n -0.9487 2.5910 0.0000 S 0 0 2 0 0 0\n -2.2484 3.3398 0.0000 O 0 0\n -0.9464 1.0901 0.0000 C 0 0\n 0.3540 0.3409 0.0000 C 0 0\n 0.3563 -1.1600 0.0000 C 0 0 1 0 0 0\n -0.9441 -1.9092 0.0000 N 0 0\n 1.6567 -1.9092 0.0000 C 0 0\n -2.2430 -1.1590 0.0000 R# 0 0\n 2.9549 -1.1577 0.0000 R# 0 0\n 1.6590 -3.4092 0.0000 O 0 0\n 2 1 1 1\n 3 2 2 0\n 2 4 1 0\n 4 5 1 0\n 6 5 1 6\n 6 7 1 0\n 6 8 1 0\n 7 9 1 0\n 8 10 1 0\n 8 11 2 0\nM RGP 2 9 1 10 2\nM END\n> <Name>\n(2R)-2-amino-4-[(S)-methanesulfinyl]butanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDMetSO\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nM\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3-(1-benzyl-1H-imidazol-4-yl)propanoic acid\n SciTegic09012117322D\n\n 19 20 0 0 1 0 999 V2000\n 0.2119 -2.7206 0.0000 R# 0 0\n 1.5107 -3.4708 0.0000 N 0 0\n 2.8111 -2.7215 0.0000 C 0 0 2 0 0 0\n 2.8089 -1.2207 0.0000 C 0 0\n 1.5107 -0.4727 0.0000 C 0 0\n 1.3494 1.0186 0.0000 C 0 0\n -0.1097 1.3062 0.0000 N 0 0\n -0.7270 2.6742 0.0000 C 0 0\n -2.2203 2.8245 0.0000 C 0 0\n -2.8392 4.1909 0.0000 C 0 0\n -4.3320 4.3381 0.0000 C 0 0\n -5.2058 3.1189 0.0000 C 0 0\n -4.5869 1.7526 0.0000 C 0 0\n -3.0942 1.6053 0.0000 C 0 0\n -0.8648 0.0249 0.0000 C 0 0\n 0.1422 -1.0869 0.0000 N 0 0\n 4.1115 -3.4708 0.0000 C 0 0\n 5.4097 -2.7192 0.0000 R# 0 0\n 4.1138 -4.9708 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 9 14 1 0\n 7 15 1 0\n 15 16 2 0\n 5 16 1 0\n 3 17 1 0\n 17 18 1 0\n 17 19 2 0\nM RGP 2 1 1 18 2\nM END\n> <Name>\n(2R)-2-amino-3-(1-benzyl-1H-imidazol-4-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDHis1B\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nH\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-2-(4-hydroxyphenyl)acetic acid\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.0993 4.4423 0.0000 O 0 0\n -0.1001 2.9423 0.0000 C 0 0\n -1.3996 2.1930 0.0000 C 0 0\n -1.4004 0.6930 0.0000 C 0 0\n -0.1018 -0.0577 0.0000 C 0 0\n 1.1977 0.6916 0.0000 C 0 0\n 1.1985 2.1916 0.0000 C 0 0\n -0.0995 -1.5586 0.0000 C 0 0 1 0 0 0\n -1.3999 -2.3078 0.0000 N 0 0\n -2.6988 -1.5575 0.0000 R# 0 0\n 1.2009 -2.3078 0.0000 C 0 0\n 2.4990 -1.5563 0.0000 R# 0 0\n 1.2031 -3.8078 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 2 7 1 0\n 8 5 1 0\n 8 9 1 6\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n(2R)-2-amino-2-(4-hydroxyphenyl)acetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-nTyr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3-[4-(carbamoylamino)phenyl]propanoic acid\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -4.1249 -0.4271 0.0000 N 0 0\n -4.1319 -1.9271 0.0000 C 0 0\n -5.4347 -2.6706 0.0000 O 0 0\n -2.8355 -2.6832 0.0000 N 0 0\n -1.5320 -1.9393 0.0000 C 0 0\n -0.2351 -2.6931 0.0000 C 0 0\n 1.0661 -1.9469 0.0000 C 0 0\n 1.0705 -0.4469 0.0000 C 0 0\n 2.3709 0.3024 0.0000 C 0 0\n 2.3731 1.8032 0.0000 C 0 0 1 0 0 0\n 1.0727 2.5525 0.0000 N 0 0\n -0.2261 1.8022 0.0000 R# 0 0\n 3.6735 2.5525 0.0000 C 0 0\n 4.9717 1.8010 0.0000 R# 0 0\n 3.6758 4.0525 0.0000 O 0 0\n -0.2264 0.3069 0.0000 C 0 0\n -1.5276 -0.4393 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 10 9 1 1\n 10 11 1 0\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 13 15 2 0\n 8 16 1 0\n 16 17 2 0\n 5 17 1 0\nM RGP 2 12 1 14 2\nM END\n> <Name>\n(2R)-2-amino-3-[4-(carbamoylamino)phenyl]propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDPhe4u\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n1,3 Propanediol\n SciTegic07272112182D\n\n 7 6 0 0 0 0 999 V2000\n 1.3000 0.7500 0.0000 O 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.2000 0.0000 0.0000 C 0 0\n 6.5000 0.7500 0.0000 O 0 0\n 0.0007 0.0004 0.0000 R# 0 0\n 7.7992 0.0004 0.0000 R# 0 0\n 3 2 1 0\n 4 3 1 0\n 5 4 1 0\n 1 6 1 0\n 5 7 1 0\n 1 2 1 0\nM RGP 2 6 1 7 2\nM END\n> <Name>\n1,3 Propanediol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noC3o\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n1,3-Diaza-2-oxophenoxazin\n SciTegic07272112182D\n\n 16 18 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5000 0.4019 0.0000 O 0 0\n 6.0000 0.4019 0.0000 C 0 0\n 6.7500 1.7010 0.0000 C 0 0\n 6.7500 -0.8971 0.0000 C 0 0\n 8.2500 -0.8971 0.0000 C 0 0\n 9.0000 0.4019 0.0000 C 0 0\n 8.2500 1.7010 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 6 7 1 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 7 1 0\n 11 13 2 0\n 13 14 1 0\n 14 15 2 0\n 15 16 1 0\n 16 12 2 0\nM RGP 1 8 1\nM END\n> <Name>\n1,3-Diaza-2-oxophenoxazin\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ntCo\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n1,3-Dihydroxy-2-propoxymethyl (ganciclovir sugar)\n SciTegic09012117322D\n\n 10 9 0 0 1 0 999 V2000\n 1.5583 0.3008 0.0000 C 0 0\n -1.0386 -2.7040 0.0000 C 0 0\n 0.2603 -1.9520 0.0000 O 0 0\n 0.2594 -0.4512 0.0000 C 0 0 2 0 0 0\n -1.0394 0.3008 0.0000 C 0 0\n -1.0378 -4.2040 0.0000 R# 0 0\n 1.5575 1.8016 0.0000 O 0 0\n -1.0386 1.8016 0.0000 O 0 0\n 2.8556 2.5531 0.0000 R# 0 0\n -2.3367 2.5532 0.0000 R# 0 0\n 2 3 1 0\n 4 3 1 6\n 4 1 1 0\n 4 5 1 0\n 2 6 1 0\n 1 7 1 0\n 5 8 1 0\n 7 9 1 0\n 8 10 1 0\nM RGP 3 6 3 9 2 10 1\nM END\n> <Name>\n1,3-Dihydroxy-2-propoxymethyl (ganciclovir sugar)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndhp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n1,4 Butanediol\n SciTegic09012117322D\n\n 8 7 0 0 0 0 999 V2000\n -3.2715 0.0000 0.0000 O 0 0\n -1.8941 -0.5960 0.0000 C 0 0\n -0.6887 0.2980 0.0000 C 0 0\n 0.6887 -0.2980 0.0000 C 0 0\n 1.8942 0.5961 0.0000 C 0 0\n 3.2715 0.0000 0.0000 O 0 0\n -4.4764 -0.8936 0.0000 R# 0 0\n 4.4763 0.8936 0.0000 R# 0 0\n 3 2 1 0\n 4 3 1 0\n 5 4 1 0\n 6 5 1 0\n 1 7 1 0\n 6 8 1 0\n 1 2 1 0\nM RGP 2 7 1 8 2\nM END\n> <Name>\n1,4 Butanediol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noC4o\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n1,5 Pentanediol\n SciTegic07272112182D\n\n 9 8 0 0 0 0 999 V2000\n 1.3000 0.7500 0.0000 O 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.2000 0.0000 0.0000 C 0 0\n 6.5000 0.7500 0.0000 C 0 0\n 7.7999 0.0000 0.0000 C 0 0\n 9.0999 0.7500 0.0000 O 0 0\n 0.0007 0.0004 0.0000 R# 0 0\n 10.3992 0.0004 0.0000 R# 0 0\n 3 2 1 0\n 4 3 1 0\n 5 4 1 0\n 6 5 1 0\n 7 6 1 0\n 1 8 1 0\n 7 9 1 0\n 1 2 1 0\nM RGP 2 8 1 9 2\nM END\n> <Name>\n1,5 Pentanediol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noC5o\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n1,6 Hexanediol\n SciTegic07272112182D\n\n 10 9 0 0 0 0 999 V2000\n 1.9742 -0.2136 0.0000 C 0 0\n 3.2082 0.6407 0.0000 C 0 0\n 4.5654 0.0000 0.0000 O 0 0\n 5.7987 0.8538 0.0000 R# 0 0\n -4.5654 0.0000 0.0000 O 0 0\n -3.2082 -0.6407 0.0000 C 0 0\n -5.7987 -0.8538 0.0000 R# 0 0\n -1.9742 0.2136 0.0000 C 0 0\n -0.6170 -0.4271 0.0000 C 0 0\n 0.6170 0.4271 0.0000 C 0 0\n 1 10 1 0\n 2 1 1 0\n 3 2 1 0\n 3 4 1 0\n 5 7 1 0\n 5 6 1 0\n 6 8 1 0\n 8 9 1 0\n 9 10 1 0\nM RGP 2 4 2 7 1\nM END\n> <Name>\n1,6 Hexanediol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noC6o\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n1,7 Heptanediol\n SciTegic07272112182D\n\n 11 10 0 0 0 0 999 V2000\n 1.3000 0.7500 0.0000 O 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.2000 0.0000 0.0000 C 0 0\n 6.5000 0.7500 0.0000 C 0 0\n 7.7999 0.0000 0.0000 C 0 0\n 9.0999 0.7500 0.0000 C 0 0\n 10.3999 0.0000 0.0000 C 0 0\n 11.6999 0.7500 0.0000 O 0 0\n 0.0007 0.0004 0.0000 R# 0 0\n 12.9992 0.0004 0.0000 R# 0 0\n 3 2 1 0\n 4 3 1 0\n 5 4 1 0\n 6 5 1 0\n 7 6 1 0\n 8 7 1 0\n 9 8 1 0\n 1 10 1 0\n 9 11 1 0\n 1 2 1 0\nM RGP 2 10 1 11 2\nM END\n> <Name>\n1,7 Heptanediol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noC7o\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n1,11 Undecanediol\n SciTegic07272112182D\n\n 15 14 0 0 0 0 999 V2000\n 1.3000 0.7500 0.0000 O 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.2000 0.0000 0.0000 C 0 0\n 6.5000 0.7500 0.0000 C 0 0\n 7.7999 0.0000 0.0000 C 0 0\n 9.0999 0.7500 0.0000 C 0 0\n 10.3999 0.0000 0.0000 C 0 0\n 11.6999 0.7500 0.0000 C 0 0\n 12.9999 0.0000 0.0000 C 0 0\n 14.2999 0.7500 0.0000 C 0 0\n 15.5999 0.0000 0.0000 C 0 0\n 16.8999 0.7500 0.0000 O 0 0\n 0.0007 0.0004 0.0000 R# 0 0\n 18.1991 0.0004 0.0000 R# 0 0\n 3 2 1 0\n 4 3 1 0\n 5 4 1 0\n 6 5 1 0\n 7 6 1 0\n 8 7 1 0\n 9 8 1 0\n 10 9 1 0\n 11 10 1 0\n 12 11 1 0\n 13 12 1 0\n 1 14 1 0\n 13 15 1 0\n 1 2 1 0\nM RGP 2 14 1 15 2\nM END\n> <Name>\n1,11 Undecanediol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noC11o\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n1,12 Dodecanediol\n SciTegic09012117322D\n\n 16 15 0 0 0 0 999 V2000\n -8.4582 0.0000 0.0000 O 0 0\n -7.1263 -0.6916 0.0000 C 0 0\n -5.8608 0.1153 0.0000 C 0 0\n -4.5288 -0.5764 0.0000 C 0 0\n -3.2634 0.2305 0.0000 C 0 0\n -1.9315 -0.4611 0.0000 C 0 0\n -0.6660 0.3458 0.0000 C 0 0\n 0.6660 -0.3458 0.0000 C 0 0\n 1.9314 0.4611 0.0000 C 0 0\n 3.2634 -0.2305 0.0000 C 0 0\n 4.5289 0.5764 0.0000 C 0 0\n 5.8608 -0.1153 0.0000 C 0 0\n 7.1263 0.6916 0.0000 C 0 0\n 8.4583 0.0000 0.0000 O 0 0\n -9.7230 -0.8065 0.0000 R# 0 0\n 9.7230 0.8065 0.0000 R# 0 0\n 2 1 1 0\n 3 2 1 0\n 4 3 1 0\n 5 4 1 0\n 6 5 1 0\n 7 6 1 0\n 8 7 1 0\n 9 8 1 0\n 10 9 1 0\n 11 10 1 0\n 12 11 1 0\n 13 12 1 0\n 14 13 1 0\n 1 15 1 0\n 14 16 1 0\nM RGP 2 15 1 16 2\nM END\n> <Name>\n1,12 Dodecanediol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noC12o\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n1-Methyl-pseudouracil\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 C 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 2.7991 0.0000 N 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 7.0981 4.0981 0.0000 C 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 3 7 2 0\n 5 8 2 0\n 2 9 1 0\n 4 10 1 0\nM RGP 1 9 1\nM END\n> <Name>\n1-Methyl-pseudouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm1Yra\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n1-Methyladenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 N 0 0\n 6.4176 -8.3053 0.0000 C 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 5 1 0\n 4 10 2 0\n 3 11 1 0\n 7 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n1-Methyladenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm1A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n1-Methylguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 6.4176 -8.3053 0.0000 C 0 0\n 3.5643 -9.2321 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 O 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 1 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 9 10 1 0\n 3 11 1 0\n 2 12 1 0\n 6 13 2 0\nM RGP 1 10 1\nM END\n> <Name>\n1-Methylguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm1G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-O-(6-aminohexyl)ribose\n SciTegic07272112182D\n\n 20 20 0 0 1 0 999 V2000\n -2.4816 0.4041 0.0000 C 0 0 1 0 0 0\n -2.0660 -1.0372 0.0000 C 0 0 2 0 0 0\n -3.3083 -1.8779 0.0000 C 0 0 1 0 0 0\n -4.4917 -0.9561 0.0000 O 0 0\n -3.9808 0.4542 0.0000 C 0 0 2 0 0 0\n -4.8230 1.6933 0.0000 C 0 0\n -3.3584 -3.3770 0.0000 R# 0 0\n -1.5585 1.5842 0.0000 O 0 0\n -0.6563 -1.5446 0.0000 O 0 0\n -6.3199 1.5842 0.0000 O 0 0\n -7.1631 2.8247 0.0000 R# 0 0\n -0.0731 1.3755 0.0000 R# 0 0\n 0.4906 -0.5765 0.0000 C 0 0\n 1.9027 -1.0848 0.0000 C 0 0\n 3.0496 -0.1167 0.0000 C 0 0\n 4.4617 -0.6250 0.0000 C 0 0\n 5.6086 0.3431 0.0000 C 0 0\n 7.0207 -0.1652 0.0000 C 0 0\n 8.1676 0.8029 0.0000 N 0 0\n 9.5790 0.2949 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 5 6 1 6\n 3 7 1 6\n 1 8 1 1\n 2 9 1 1\n 6 10 1 0\n 10 11 1 0\n 8 12 1 0\n 9 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 19 20 1 0\nM RGP 4 7 3 11 1 12 2 20 4\nM END\n> <Name>\n2-O-(6-aminohexyl)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnC62r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n[R4]H\n\n$$$$\n2,2-Dimethylguanine\n SciTegic07272112182D\n\n 14 15 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 O 0 0\n 3.5672 -9.2336 0.0000 N 0 0\n 4.6832 -10.2358 0.0000 C 0 0\n 2.1414 -9.6994 0.0000 C 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 5 1 0\n 4 10 2 0\n 2 11 1 0\n 11 12 1 0\n 11 13 1 0\n 7 14 1 0\nM RGP 1 14 1\nM END\n> <Name>\n2,2-Dimethylguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm22G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2,3-Oxetanearabinose\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n -1.1982 -1.2308 0.0000 O 0 0\n -0.5767 0.1344 0.0000 C 0 0 1 0 0 0\n -0.0918 -2.2437 0.0000 C 0 0 2 0 0 0\n 0.9137 -0.0347 0.0000 C 0 0 1 0 0 0\n 1.2134 -1.5045 0.0000 C 0 0 2 0 0 0\n 0.7420 1.4469 0.0000 O 0 0\n -1.3178 1.4366 0.0000 C 0 0\n -2.8186 1.4469 0.0000 O 0 0\n -0.2610 -3.7341 0.0000 R# 0 0\n 1.9462 2.3412 0.0000 R# 0 0\n 2.6674 -1.1365 0.0000 O 0 0\n 2.3418 0.3277 0.0000 C 0 0\n -3.5605 2.7505 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 6\n 7 8 1 0\n 3 9 1 6\n 6 10 1 0\n 5 11 1 6\n 11 12 1 0\n 12 4 1 0\n 8 13 1 0\nM RGP 3 9 3 10 2 13 1\nM END\n> <Name>\n2,3-Oxetanearabinose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nox23ar\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2,4-BNANC (oxyamino-BNA)\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -0.8920 0.6779 0.0000 C 0 0\n -1.6870 -0.5951 0.0000 O 0 0\n 0.1846 2.2096 0.0000 C 0 0\n -0.2862 1.3495 0.0000 O 0 0\n 0.6105 0.6233 0.0000 C 0 0 1 0 0 0\n 0.2157 -0.3666 0.0000 C 0 0 1 0 0 0\n -0.7913 -1.6686 0.0000 C 0 0 1 0 0 0\n -0.4485 -0.3707 0.0000 O 0 0\n 3.1410 -0.5951 0.0000 O 0 0\n -1.4549 -3.0138 0.0000 R# 0 0\n -1.3230 2.0348 0.0000 N 0 0\n 1.7058 -0.1970 0.0000 C 0 0 2 0 0 0\n 4.2112 0.4560 0.0000 R# 0 0\n -3.1861 -0.5441 0.0000 R# 0 0\n 4 11 1 0\n 5 1 1 6\n 1 2 1 0\n 5 12 1 0\n 12 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 5 1 0\n 7 10 1 6\n 5 3 1 0\n 6 4 1 6\n 11 3 1 0\n 12 9 1 1\n 9 13 1 0\n 2 14 1 0\nM RGP 3 10 3 13 2 14 1\nM END\n> <Name>\n2,4-BNANC (oxyamino-BNA)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbnanc\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2,4-BNANCMe (N-Methyl-oxyamino BNA)\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n -0.7065 0.5190 0.0000 C 0 0\n -1.5015 -0.7540 0.0000 O 0 0\n 0.3701 2.0507 0.0000 C 0 0\n -0.1007 1.1907 0.0000 O 0 0\n 0.7960 0.4644 0.0000 C 0 0 1 0 0 0\n 0.4011 -0.5255 0.0000 C 0 0 1 0 0 0\n -0.6058 -1.8275 0.0000 C 0 0 1 0 0 0\n -0.2630 -0.5296 0.0000 O 0 0\n 3.3265 -0.7540 0.0000 O 0 0\n -1.2694 -3.1727 0.0000 R# 0 0\n -1.1376 1.8760 0.0000 N 0 0\n 1.8913 -0.3558 0.0000 C 0 0 2 0 0 0\n 4.3967 0.2971 0.0000 R# 0 0\n -2.5966 2.2242 0.0000 C 0 0\n -3.0006 -0.7030 0.0000 R# 0 0\n 4 11 1 0\n 5 1 1 6\n 1 2 1 0\n 5 12 1 0\n 12 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 5 1 0\n 7 10 1 6\n 5 3 1 0\n 6 4 1 6\n 11 3 1 0\n 12 9 1 1\n 9 13 1 0\n 11 14 1 0\n 2 15 1 0\nM RGP 3 10 3 13 2 15 1\nM END\n> <Name>\n2,4-BNANCMe (N-Methyl-oxyamino BNA)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbnancm\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Aminoadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 3.8763 7.7649 0.0000 C 0 0\n 2.7616 6.7611 0.0000 N 0 0\n 3.0736 5.2939 0.0000 C 0 0\n 4.5003 4.8305 0.0000 C 0 0\n 5.6149 5.8343 0.0000 C 0 0\n 5.3029 7.3015 0.0000 N 0 0\n 2.1923 4.0811 0.0000 N 0 0\n 3.0741 2.8677 0.0000 C 0 0\n 4.5007 3.3313 0.0000 N 0 0\n 7.0415 5.3709 0.0000 N 0 0\n 3.5643 9.2321 0.0000 N 0 0\n 0.6923 4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 1 6 1 0\n 3 7 1 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\n 5 10 1 0\n 1 11 1 0\n 7 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n2-Aminoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-(Methoxy)amino LNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n -1.7278 0.2031 0.0000 C 0 0\n -0.3497 0.0282 0.0000 N 0 0\n -0.8666 -0.8784 0.0000 C 0 0 1 0 0 0\n 1.2843 0.0329 0.0000 C 0 0 2 0 0 0\n 0.5255 -1.1421 0.0000 C 0 0 2 0 0 0\n 0.6808 -2.4041 0.0000 C 0 0 1 0 0 0\n -0.6888 -2.2493 0.0000 O 0 0\n -1.1921 0.5947 0.0000 C 0 0\n 1.7467 -3.4595 0.0000 R# 0 0\n 2.3504 1.0606 0.0000 O 0 0\n 3.7936 0.6516 0.0000 R# 0 0\n 0.3813 1.3433 0.0000 O 0 0\n -0.3892 2.6302 0.0000 C 0 0\n -2.6188 1.0606 0.0000 O 0 0\n -2.9295 2.5281 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 6\n 6 9 1 6\n 3 1 1 0\n 5 2 1 6\n 4 10 1 1\n 10 11 1 0\n 2 12 1 0\n 12 13 1 0\n 8 14 1 0\n 14 15 1 0\nM RGP 3 9 3 11 2 15 1\nM END\n> <Name>\n2-(Methoxy)amino LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmon2ln\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-(Methoxyethoxy)amino LNA (N-MOE)\n SciTegic09012117322D\n\n 18 19 0 0 1 0 999 V2000\n 1.8450 1.6552 0.0000 C 0 0 1 0 0 0\n -0.3106 0.7551 0.0000 C 0 0 2 0 0 0\n -1.1662 1.8411 0.0000 C 0 0 1 0 0 0\n 0.2110 1.6591 0.0000 O 0 0\n 1.0801 0.4842 0.0000 C 0 0 1 0 0 0\n 2.9164 2.6773 0.0000 O 0 0\n -2.4698 2.5830 0.0000 R# 0 0\n 1.2288 -0.7785 0.0000 C 0 0\n -0.1399 -0.6167 0.0000 N 0 0\n 4.3575 2.2610 0.0000 R# 0 0\n -1.1939 -1.6825 0.0000 O 0 0\n -0.7981 -3.1303 0.0000 C 0 0\n -1.8533 -4.1974 0.0000 C 0 0\n -1.4576 -5.6452 0.0000 O 0 0\n -2.5122 -6.7119 0.0000 C 0 0\n 1.0038 1.9936 0.0000 C 0 0\n -0.3322 2.6773 0.0000 O 0 0\n -0.4089 4.1754 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 0\n 5 1 1 0\n 3 7 1 6\n 5 8 1 0\n 2 9 1 1\n 8 9 1 0\n 1 6 1 6\n 9 11 1 0\n 6 10 1 0\n 14 15 1 0\n 13 14 1 0\n 12 13 1 0\n 11 12 1 0\n 5 16 1 1\n 16 17 1 0\n 17 18 1 0\nM RGP 3 7 3 10 2 18 1\nM END\n> <Name>\n2-(Methoxyethoxy)amino LNA (N-MOE)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmoeon2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-(R)-Methyl-cLNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -1.7573 0.3923 0.0000 C 0 0\n -0.3792 0.2175 0.0000 C 0 0 2 0 0 0\n -0.8961 -0.6891 0.0000 C 0 0 1 0 0 0\n 1.2548 0.2221 0.0000 C 0 0 2 0 0 0\n 0.4960 -0.9529 0.0000 C 0 0 2 0 0 0\n 0.6513 -2.2149 0.0000 C 0 0 1 0 0 0\n -0.7183 -2.0601 0.0000 O 0 0\n -1.2216 0.7840 0.0000 C 0 0\n 1.7172 -3.2702 0.0000 R# 0 0\n 2.3209 1.2498 0.0000 O 0 0\n 3.7640 0.8408 0.0000 R# 0 0\n 0.3758 1.5136 0.0000 C 0 0\n -2.6483 1.2498 0.0000 O 0 0\n -2.9590 2.7173 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 5 4 1 6\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 6\n 6 9 1 6\n 3 1 1 0\n 5 2 1 0\n 4 10 1 1\n 10 11 1 0\n 2 12 1 1\n 8 13 1 0\n 13 14 1 0\nM RGP 3 9 3 11 2 14 1\nM END\n> <Name>\n2-(R)-Methyl-cLNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRmclna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Amino-N6-imidazoylpropyladenine\n SciTegic07272112182D\n\n 20 22 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0031 -3.0008 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 2.5981 1.5000 0.0000 N 0 0\n 1.3039 -3.7494 0.0000 C 0 0\n 1.3070 -5.2502 0.0000 C 0 0\n 2.6078 -5.9988 0.0000 C 0 0\n 2.6109 -7.4996 0.0000 N 0 0\n 3.8244 -8.3594 0.0000 C 0 0\n 3.3609 -9.7860 0.0000 N 0 0\n 1.8609 -9.7860 0.0000 C 0 0\n 1.3974 -8.3594 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 7 8 2 0\n 5 8 1 0\n 6 9 1 0\n 4 10 1 0\n 7 10 1 0\n 10 11 1 0\n 2 12 1 0\n 9 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 2 0\n 18 19 1 0\n 19 20 2 0\n 16 20 1 0\nM RGP 1 11 1\nM END\n> <Name>\n2-Amino-N6-imidazoylpropyladenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nimpr6n\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Aminoribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.9146 -0.3813 0.0000 C 0 0 2 0 0 0\n 0.4172 0.3089 0.0000 C 0 0 2 0 0 0\n 1.4851 -0.7445 0.0000 C 0 0 2 0 0 0\n 0.8134 -2.0856 0.0000 C 0 0 1 0 0 0\n -0.6697 -1.8612 0.0000 O 0 0\n 0.6383 1.7907 0.0000 O 0 0\n -2.2528 0.2924 0.0000 C 0 0\n 1.5036 -3.4174 0.0000 R# 0 0\n 2.0334 2.3417 0.0000 R# 0 0\n 2.9650 -0.4996 0.0000 N 0 0\n -2.3396 1.7907 0.0000 O 0 0\n -3.6793 2.4652 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 7 11 1 0\n 11 12 1 0\nM RGP 3 8 3 9 2 12 1\nM END\n> <Name>\n2-Aminoribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-C-Methylribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.0259 -0.3236 0.0000 C 0 0 2 0 0 0\n 0.3059 0.3666 0.0000 C 0 0 2 0 0 0\n 1.3739 -0.6867 0.0000 C 0 0 2 0 0 0\n 0.7021 -2.0279 0.0000 C 0 0 1 0 0 0\n -0.7810 -1.8035 0.0000 O 0 0\n 0.5270 1.8485 0.0000 O 0 0\n -2.3641 0.3502 0.0000 C 0 0\n 1.3923 -3.3596 0.0000 R# 0 0\n 1.9221 2.3995 0.0000 R# 0 0\n 2.3084 -1.8600 0.0000 O 0 0\n 1.8808 0.7250 0.0000 C 0 0\n -2.4508 1.8485 0.0000 O 0 0\n -3.7906 2.5230 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 3 11 1 0\n 7 12 1 0\n 12 13 1 0\nM RGP 3 8 3 9 2 13 1\nM END\n> <Name>\n2-C-Methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nBcm2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Chloro-N6-cyclopentyladenine\n SciTegic07272112182D\n\n 17 19 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 7.0433 -5.3736 0.0000 N 0 0\n 3.5643 -9.2321 0.0000 Cl 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 8.1571 -6.3795 0.0000 C 0 0\n 9.6092 -6.0582 0.0000 C 0 0\n 10.3546 -7.3599 0.0000 C 0 0\n 9.3469 -8.4710 0.0000 C 0 0\n 7.9788 -7.8561 0.0000 C 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 5 1 0\n 4 10 1 0\n 2 11 1 0\n 7 12 1 0\n 10 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 13 1 0\nM RGP 1 12 1\nM END\n> <Name>\n2-Chloro-N6-cyclopentyladenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncl2cyp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Chloroadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 6.9961 1.8908 0.0000 C 0 0\n 6.9965 3.3900 0.0000 N 0 0\n 5.5699 3.8536 0.0000 C 0 0\n 4.6882 2.6402 0.0000 N 0 0\n 5.5695 1.4274 0.0000 C 0 0\n 8.1107 0.8870 0.0000 C 0 0\n 5.2575 -0.0398 0.0000 N 0 0\n 6.3721 -1.0436 0.0000 C 0 0\n 7.7987 -0.5802 0.0000 N 0 0\n 3.1882 2.6402 0.0000 R# 0 0\n 9.5374 1.3504 0.0000 N 0 0\n 6.0601 -2.5108 0.0000 Cl 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 5 1 2 0\n 1 6 1 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 6 2 0\n 4 10 1 0\n 6 11 1 0\n 8 12 1 0\nM RGP 1 10 1\nM END\n> <Name>\n2-Chloroadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncl2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Deoxy-2-methoxypropyl\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2590 0.0451 0.0000 O 0 0\n -1.7470 1.4550 0.0000 C 0 0 1 0 0 0\n -1.0764 -0.8776 0.0000 C 0 0 2 0 0 0\n -0.2479 1.4037 0.0000 C 0 0 2 0 0 0\n 0.1666 -0.0379 0.0000 C 0 0 1 0 0 0\n 0.6713 2.5869 0.0000 O 0 0\n -2.5882 2.6948 0.0000 C 0 0\n -4.0852 2.5869 0.0000 O 0 0\n -4.9274 3.8281 0.0000 R# 0 0\n -1.1277 -2.3767 0.0000 R# 0 0\n 1.5738 -0.5523 0.0000 C 0 0\n 2.1574 2.3832 0.0000 R# 0 0\n 1.8333 -2.0305 0.0000 C 0 0\n 3.2429 -2.5458 0.0000 C 0 0\n 3.5024 -4.0240 0.0000 O 0 0\n 4.9112 -4.5390 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-Deoxy-2-methoxypropyl\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmopr2d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Fluoroadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n 0.0000 3.0000 0.0000 F 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n 2.5981 -1.5000 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 4 1 0\n 3 10 1 0\n 7 11 1 0\n 1 12 1 0\nM RGP 1 11 1\nM END\n> <Name>\n2-Fluoroadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfl2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Iodoadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n 0.0000 3.0000 0.0000 I 0 0\n 2.5981 -1.5000 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 4 1 0\n 7 10 1 0\n 3 11 1 0\n 1 12 1 0\nM RGP 1 10 1\nM END\n> <Name>\n2-Iodoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nio2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Methoxyadenine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 7.0416 -5.3709 0.0000 N 0 0\n 3.5672 -9.2336 0.0000 O 0 0\n 4.6832 -10.2358 0.0000 C 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 5 1 0\n 7 10 1 0\n 4 11 1 0\n 2 12 1 0\n 12 13 1 0\nM RGP 1 10 1\nM END\n> <Name>\n2-Methoxyadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmo2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Methoxyethylamino\n SciTegic07272112182D\n\n 7 6 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.2000 0.0000 0.0000 O 0 0\n 6.4992 0.7496 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\n2-Methoxyethylamino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmoen\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n2-Methyladenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 3.5643 -9.2321 0.0000 C 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 9 11 1 0\n 2 12 1 0\nM RGP 1 11 1\nM END\n> <Name>\n2-Methyladenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Methylguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 5.5695 -1.4273 0.0000 C 0 0\n 4.6882 -2.6401 0.0000 N 0 0\n 5.5700 -3.8536 0.0000 C 0 0\n 6.9965 -3.3899 0.0000 N 0 0\n 6.9961 -1.8907 0.0000 C 0 0\n 5.2575 0.0399 0.0000 N 0 0\n 8.1108 -0.8870 0.0000 C 0 0\n 7.7988 0.5802 0.0000 N 0 0\n 6.3722 1.0436 0.0000 C 0 0\n 3.1882 -2.6401 0.0000 R# 0 0\n 9.5374 -1.3504 0.0000 O 0 0\n 6.0570 2.5110 0.0000 N 0 0\n 4.6297 2.9724 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 1 2 0\n 1 6 1 0\n 5 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 6 2 0\n 2 10 1 0\n 7 11 2 0\n 9 12 1 0\n 12 13 1 0\nM RGP 1 10 1\nM END\n> <Name>\n2-Methylguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Methylseleno-2-deoxyribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.1828 -0.4514 0.0000 C 0 0 2 0 0 0\n 0.1490 0.2388 0.0000 C 0 0 2 0 0 0\n 1.2170 -0.8145 0.0000 C 0 0 2 0 0 0\n 0.5452 -2.1557 0.0000 C 0 0 1 0 0 0\n -0.9379 -1.9313 0.0000 O 0 0\n -2.5210 0.2223 0.0000 C 0 0\n 0.3701 1.7207 0.0000 O 0 0\n 1.7652 2.2716 0.0000 R# 0 0\n 1.2354 -3.4875 0.0000 R# 0 0\n 2.6946 -0.5669 0.0000 Se 0 0\n 3.2204 0.8380 0.0000 C 0 0\n -2.6077 1.7207 0.0000 O 0 0\n -3.9475 2.3952 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 3 10 1 1\n 10 11 1 0\n 6 12 1 0\n 12 13 1 0\nM RGP 3 8 2 9 3 13 1\nM END\n> <Name>\n2-Methylseleno-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nse2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Methylthio-2-deoxyribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.1828 -0.4514 0.0000 C 0 0 2 0 0 0\n 0.1490 0.2388 0.0000 C 0 0 2 0 0 0\n 1.2170 -0.8145 0.0000 C 0 0 2 0 0 0\n 0.5452 -2.1557 0.0000 C 0 0 1 0 0 0\n -0.9379 -1.9313 0.0000 O 0 0\n -2.5210 0.2223 0.0000 C 0 0\n 0.3701 1.7207 0.0000 O 0 0\n -2.6077 1.7207 0.0000 O 0 0\n -3.9475 2.3952 0.0000 R# 0 0\n 1.7652 2.2716 0.0000 R# 0 0\n 1.2354 -3.4875 0.0000 R# 0 0\n 2.6946 -0.5669 0.0000 S 0 0\n 3.2204 0.8380 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\n 3 12 1 1\n 12 13 1 0\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n2-Methylthio-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nms2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Methylthioadenine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 3.5672 -9.2336 0.0000 S 0 0\n 4.6832 -10.2358 0.0000 C 0 0\n 7.0416 -5.3709 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 2 10 1 0\n 10 11 1 0\n 6 12 1 0\n 9 13 1 0\nM RGP 1 13 1\nM END\n> <Name>\n2-Methylthioadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nms2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-N-Methylcarbamoylribose\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -1.9948 -0.0515 0.0000 O 0 0\n -1.4827 1.3584 0.0000 C 0 0 1 0 0 0\n -0.8121 -0.9742 0.0000 C 0 0 2 0 0 0\n 0.0164 1.3070 0.0000 C 0 0 2 0 0 0\n 0.4308 -0.1346 0.0000 C 0 0 1 0 0 0\n 0.9355 2.4902 0.0000 O 0 0\n -2.3240 2.5981 0.0000 C 0 0\n -3.8209 2.4902 0.0000 O 0 0\n -4.6632 3.7315 0.0000 R# 0 0\n -0.8634 -2.4733 0.0000 R# 0 0\n 1.8380 -0.6489 0.0000 O 0 0\n 2.4216 2.2866 0.0000 R# 0 0\n 2.0976 -2.1271 0.0000 C 0 0\n 3.5072 -2.6424 0.0000 N 0 0\n 0.9475 -3.0901 0.0000 O 0 0\n 3.7665 -4.1198 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 13 15 2 0\n 14 16 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-N-Methylcarbamoylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmnc2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-4-(Imidazo-1-yl) butylribose\n SciTegic07272112182D\n\n 21 22 0 0 1 0 999 V2000\n -3.8016 -2.0204 0.0000 C 0 0 2 0 0 0\n -2.4699 -1.3302 0.0000 C 0 0 2 0 0 0\n -1.4019 -2.3835 0.0000 C 0 0 2 0 0 0\n -2.0736 -3.7247 0.0000 C 0 0 1 0 0 0\n -3.5568 -3.5003 0.0000 O 0 0\n -5.1399 -1.3466 0.0000 C 0 0\n -2.2488 0.1517 0.0000 O 0 0\n -0.8536 0.7027 0.0000 R# 0 0\n 0.0757 -2.1358 0.0000 O 0 0\n -1.3834 -5.0564 0.0000 R# 0 0\n 0.6019 -0.7302 0.0000 C 0 0\n 2.0821 -0.4822 0.0000 C 0 0\n 2.6082 0.9234 0.0000 C 0 0\n 4.0884 1.1715 0.0000 C 0 0\n 4.6145 2.5771 0.0000 N 0 0\n 6.0516 2.9599 0.0000 C 0 0\n 6.1146 4.4586 0.0000 N 0 0\n 4.7087 4.9815 0.0000 C 0 0\n 3.7769 3.8061 0.0000 C 0 0\n -5.2266 0.1517 0.0000 O 0 0\n -6.5664 0.8262 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 3 9 1 1\n 4 10 1 6\n 9 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 2 0\n 17 18 1 0\n 18 19 2 0\n 19 15 1 0\n 6 20 1 0\n 20 21 1 0\nM RGP 3 8 2 10 3 21 1\nM END\n> <Name>\n2-O-4-(Imidazo-1-yl) butylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nimbu2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(2,2,3,3,3-Pentafluoropropyl)ribose\n SciTegic07272112182D\n\n 20 20 0 0 1 0 999 V2000\n -3.0073 -1.1253 0.0000 C 0 0 2 0 0 0\n -1.6755 -0.4351 0.0000 C 0 0 2 0 0 0\n -0.6076 -1.4885 0.0000 C 0 0 2 0 0 0\n -1.2793 -2.8296 0.0000 C 0 0 1 0 0 0\n -2.7624 -2.6052 0.0000 O 0 0\n -4.3455 -0.4516 0.0000 C 0 0\n -1.4545 1.0467 0.0000 O 0 0\n -0.0593 1.5977 0.0000 R# 0 0\n 0.8701 -1.2408 0.0000 O 0 0\n -0.5891 -4.1614 0.0000 R# 0 0\n 1.3962 0.1648 0.0000 C 0 0\n 2.8764 0.4129 0.0000 C 0 0\n 3.8304 -0.7446 0.0000 F 0 0\n 2.3512 -0.9922 0.0000 F 0 0\n 3.4025 1.8185 0.0000 C 0 0\n 3.9277 3.2235 0.0000 F 0 0\n 2.4485 2.9760 0.0000 F 0 0\n 4.8819 2.0664 0.0000 F 0 0\n -4.4323 1.0467 0.0000 O 0 0\n -5.7721 1.7212 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 3 9 1 1\n 4 10 1 6\n 9 11 1 0\n 11 12 1 0\n 12 15 1 0\n 12 13 1 0\n 12 14 1 0\n 15 18 1 0\n 15 17 1 0\n 15 16 1 0\n 6 19 1 0\n 19 20 1 0\nM RGP 3 8 2 10 3 20 1\nM END\n> <Name>\n2-O-(2,2,3,3,3-Pentafluoropropyl)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfl5pr2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(2-Acetamide)ribose\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.1567 -0.6707 0.0000 C 0 0 2 0 0 0\n -0.8249 0.0195 0.0000 C 0 0 2 0 0 0\n 0.2430 -1.0338 0.0000 C 0 0 2 0 0 0\n -0.4287 -2.3750 0.0000 C 0 0 1 0 0 0\n -1.9118 -2.1506 0.0000 O 0 0\n -0.6039 1.5014 0.0000 O 0 0\n -3.4949 0.0031 0.0000 C 0 0\n 0.2615 -3.7068 0.0000 R# 0 0\n -3.5817 1.5014 0.0000 O 0 0\n -4.9215 2.1759 0.0000 R# 0 0\n 1.7207 -0.7861 0.0000 O 0 0\n 0.7913 2.0524 0.0000 R# 0 0\n 2.2468 0.6194 0.0000 C 0 0\n 3.7270 0.8675 0.0000 C 0 0\n 4.2528 2.2723 0.0000 O 0 0\n 4.6810 -0.2900 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 2 0\n 14 16 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-(2-Acetamide)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnac2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(2-Amino)ethylribose\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -1.9316 -0.2576 0.0000 O 0 0\n -1.4196 1.1523 0.0000 C 0 0 1 0 0 0\n -0.7490 -1.1802 0.0000 C 0 0 2 0 0 0\n 0.0796 1.1010 0.0000 C 0 0 2 0 0 0\n 0.4940 -0.3406 0.0000 C 0 0 1 0 0 0\n 0.9987 2.2842 0.0000 O 0 0\n -2.2608 2.3921 0.0000 C 0 0\n -3.7578 2.2842 0.0000 O 0 0\n -4.6000 3.5255 0.0000 R# 0 0\n -0.8003 -2.6793 0.0000 R# 0 0\n 1.9012 -0.8549 0.0000 O 0 0\n 2.4848 2.0805 0.0000 R# 0 0\n 2.1607 -2.3332 0.0000 C 0 0\n 3.5703 -2.8484 0.0000 C 0 0\n 3.8297 -4.3258 0.0000 N 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-(2-Amino)ethylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nne2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(2-Fluoroethyl)ribose\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -1.8446 -0.6900 0.0000 C 0 0 2 0 0 0\n -0.5129 0.0002 0.0000 C 0 0 2 0 0 0\n 0.5551 -1.0531 0.0000 C 0 0 2 0 0 0\n -0.1166 -2.3943 0.0000 C 0 0 1 0 0 0\n -1.5998 -2.1699 0.0000 O 0 0\n -3.1829 -0.0163 0.0000 C 0 0\n -0.2918 1.4820 0.0000 O 0 0\n 1.1033 2.0330 0.0000 R# 0 0\n 2.0327 -0.8055 0.0000 O 0 0\n 0.5736 -3.7261 0.0000 R# 0 0\n 2.5589 0.6001 0.0000 C 0 0\n 4.0390 0.8482 0.0000 C 0 0\n 4.5649 2.2530 0.0000 F 0 0\n -3.2696 1.4820 0.0000 O 0 0\n -4.6094 2.1566 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 3 9 1 1\n 4 10 1 6\n 9 11 1 0\n 11 12 1 0\n 12 13 1 0\n 6 14 1 0\n 14 15 1 0\nM RGP 3 8 2 10 3 15 1\nM END\n> <Name>\n2-O-(2-Fluoroethyl)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfle2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(2-Formaldoximino)ethylribose\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.5633 0.3990 0.0000 O 0 0\n -2.0512 1.8089 0.0000 C 0 0 1 0 0 0\n -1.3806 -0.5236 0.0000 C 0 0 2 0 0 0\n -0.5521 1.7576 0.0000 C 0 0 2 0 0 0\n -0.1377 0.3160 0.0000 C 0 0 1 0 0 0\n 0.3670 2.9408 0.0000 O 0 0\n -2.8925 3.0487 0.0000 C 0 0\n -4.3894 2.9408 0.0000 O 0 0\n -5.2317 4.1821 0.0000 R# 0 0\n -1.4319 -2.0228 0.0000 R# 0 0\n 1.2695 -0.1984 0.0000 O 0 0\n 1.8531 2.7371 0.0000 R# 0 0\n 1.5290 -1.6766 0.0000 C 0 0\n 2.9387 -2.1918 0.0000 C 0 0\n 3.1982 -3.6700 0.0000 O 0 0\n 4.6078 -4.1853 0.0000 N 0 0\n 4.8671 -5.6627 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 2 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-(2-Formaldoximino)ethylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmenoe2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(2-Phenoxyethyl)ribose\n SciTegic07272112182D\n\n 21 22 0 0 1 0 999 V2000\n -3.9854 -1.4750 0.0000 C 0 0 2 0 0 0\n -2.6541 -0.7840 0.0000 C 0 0 2 0 0 0\n -1.6070 -1.8403 0.0000 C 0 0 2 0 0 0\n -2.2564 -3.1783 0.0000 C 0 0 1 0 0 0\n -3.7397 -2.9548 0.0000 O 0 0\n -2.4225 0.6962 0.0000 O 0 0\n -5.3241 -0.8021 0.0000 C 0 0\n -1.5575 -4.5055 0.0000 R# 0 0\n -1.0236 1.2374 0.0000 R# 0 0\n -0.1270 -1.5913 0.0000 O 0 0\n 1.8783 0.0635 0.0000 C 0 0\n 0.3983 -0.1855 0.0000 C 0 0\n 2.4037 1.4694 0.0000 O 0 0\n 3.8837 1.7183 0.0000 C 0 0\n 4.4108 3.1227 0.0000 C 0 0\n 5.8905 3.3684 0.0000 C 0 0\n 6.8432 2.2098 0.0000 C 0 0\n 6.3161 0.8055 0.0000 C 0 0\n 4.8364 0.5597 0.0000 C 0 0\n -5.4117 0.6962 0.0000 O 0 0\n -6.7519 1.3699 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 11 12 1 0\n 10 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 2 0\n 15 16 1 0\n 16 17 2 0\n 17 18 1 0\n 18 19 2 0\n 19 14 1 0\n 7 20 1 0\n 20 21 1 0\nM RGP 3 8 3 9 2 21 1\nM END\n> <Name>\n2-O-(2-Phenoxyethyl)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nphoe2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(2-Trifluoro)ethylribose\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.4630 -0.7363 0.0000 C 0 0 2 0 0 0\n -1.1312 -0.0461 0.0000 C 0 0 2 0 0 0\n -0.0632 -1.0994 0.0000 C 0 0 2 0 0 0\n -0.7350 -2.4406 0.0000 C 0 0 1 0 0 0\n -2.2181 -2.2161 0.0000 O 0 0\n -0.9101 1.4358 0.0000 O 0 0\n -3.8012 -0.0625 0.0000 C 0 0\n -0.0448 -3.7723 0.0000 R# 0 0\n 0.4850 1.9868 0.0000 R# 0 0\n 1.4144 -0.8517 0.0000 O 0 0\n 1.9405 0.5539 0.0000 C 0 0\n 3.4207 0.8020 0.0000 C 0 0\n 4.9002 1.0492 0.0000 F 0 0\n 4.3748 -0.3555 0.0000 F 0 0\n 3.9466 2.2068 0.0000 F 0 0\n -3.8879 1.4358 0.0000 O 0 0\n -5.2277 2.1103 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 11 10 1 0\n 11 12 1 0\n 12 15 1 0\n 12 14 1 0\n 12 13 1 0\n 7 16 1 0\n 16 17 1 0\nM RGP 3 8 3 9 2 17 1\nM END\n> <Name>\n2-O-(2-Trifluoro)ethylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfl3e2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(3,3,3-Trifluoropropyl)ribose\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -2.6639 -1.2218 0.0000 C 0 0 2 0 0 0\n -1.3321 -0.5316 0.0000 C 0 0 2 0 0 0\n -0.2641 -1.5849 0.0000 C 0 0 2 0 0 0\n -0.9359 -2.9261 0.0000 C 0 0 1 0 0 0\n -2.4190 -2.7017 0.0000 O 0 0\n -1.1110 0.9502 0.0000 O 0 0\n -4.0021 -0.5481 0.0000 C 0 0\n -0.2457 -4.2579 0.0000 R# 0 0\n 0.2841 1.5012 0.0000 R# 0 0\n 1.2135 -1.3373 0.0000 O 0 0\n 3.2198 0.3164 0.0000 C 0 0\n 1.7396 0.0683 0.0000 C 0 0\n 3.7459 1.7220 0.0000 C 0 0\n 5.2253 1.9699 0.0000 F 0 0\n 2.7919 2.8795 0.0000 F 0 0\n 4.2711 3.1270 0.0000 F 0 0\n -4.0888 0.9502 0.0000 O 0 0\n -5.4286 1.6247 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 11 12 1 0\n 10 12 1 0\n 11 13 1 0\n 13 14 1 0\n 13 15 1 0\n 13 16 1 0\n 7 17 1 0\n 17 18 1 0\nM RGP 3 8 3 9 2 18 1\nM END\n> <Name>\n2-O-(3,3,3-Trifluoropropyl)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfl3pr2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(4-Aminobutyl)ribose\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.5868 -1.0670 0.0000 C 0 0 2 0 0 0\n -1.2550 -0.3768 0.0000 C 0 0 2 0 0 0\n -0.1871 -1.4301 0.0000 C 0 0 2 0 0 0\n -0.8588 -2.7713 0.0000 C 0 0 1 0 0 0\n -2.3419 -2.5469 0.0000 O 0 0\n -1.0340 1.1050 0.0000 O 0 0\n -3.9250 -0.3933 0.0000 C 0 0\n -0.1686 -4.1031 0.0000 R# 0 0\n 0.3612 1.6560 0.0000 R# 0 0\n 1.2906 -1.1825 0.0000 O 0 0\n 3.8230 1.8768 0.0000 C 0 0\n 3.2969 0.4712 0.0000 C 0 0\n 1.8167 0.2231 0.0000 C 0 0\n 5.3032 2.1248 0.0000 C 0 0\n 5.8290 3.5297 0.0000 N 0 0\n -4.0118 1.1050 0.0000 O 0 0\n -5.3516 1.7795 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 12 13 1 0\n 11 12 1 0\n 10 13 1 0\n 11 14 1 0\n 14 15 1 0\n 7 16 1 0\n 16 17 1 0\nM RGP 3 8 3 9 2 17 1\nM END\n> <Name>\n2-O-(4-Aminobutyl)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnbu2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(6-(N-glutaryl-GalNAc3)aminohexylribose\n SciTegic09012117322D\n\n124127 0 0 1 0 999 V2000\n 11.7833 -3.3225 0.0000 C 0 0\n 10.8292 -2.1641 0.0000 C 0 0\n 11.3545 -0.7581 0.0000 C 0 0\n 10.4003 0.4003 0.0000 C 0 0\n 8.9198 0.1541 0.0000 C 0 0\n 7.9656 1.3126 0.0000 C 0 0\n 6.4851 1.0664 0.0000 N 0 0\n 5.5310 2.2249 0.0000 C 0 0\n 6.0573 3.6295 0.0000 O 0 0\n -3.7798 3.3088 0.0000 O 0 0\n -3.2532 4.7142 0.0000 C 0 0\n -1.7729 4.9618 0.0000 C 0 0\n -0.8189 3.8033 0.0000 N 0 0\n -1.2464 6.3671 0.0000 C 0 0\n 0.2339 6.6147 0.0000 O 0 0\n -2.3073 3.5281 0.0000 C 0 0\n -1.3523 2.3704 0.0000 O 0 0\n -5.2601 3.0613 0.0000 C 0 0\n -5.7867 1.6558 0.0000 C 0 0\n -1.8764 0.9642 0.0000 C 0 0\n -0.9213 -0.1935 0.0000 C 0 0\n 0.7605 8.0201 0.0000 C 0 0\n 2.2408 8.2677 0.0000 C 0 0\n 2.7674 9.6731 0.0000 C 0 0\n 1.8138 10.8309 0.0000 O 0 0\n 0.8026 -10.4496 0.0000 C 0 0\n 0.2784 -11.8559 0.0000 C 0 0\n 1.2336 -13.0137 0.0000 C 0 0\n 0.7094 -14.4200 0.0000 C 0 0\n -1.4454 -1.5999 0.0000 C 0 0\n -0.4903 -2.7576 0.0000 N 0 0\n -2.9247 -1.8485 0.0000 O 0 0\n -1.0145 -4.1638 0.0000 C 0 0\n -0.0593 -5.3216 0.0000 C 0 0\n -0.5835 -6.7279 0.0000 C 0 0\n 0.3716 -7.8856 0.0000 N 0 0\n -0.1525 -9.2919 0.0000 C 0 0\n -1.6317 -9.5405 0.0000 O 0 0\n -7.2670 1.4083 0.0000 C 0 0\n -8.2207 2.5661 0.0000 O 0 0\n -13.8143 -4.9560 0.0000 C 0 0\n -15.2946 -5.2035 0.0000 C 0 0\n -15.8212 -6.6090 0.0000 C 0 0\n -17.3015 -6.8565 0.0000 C 0 0\n -7.7936 0.0028 0.0000 N 0 0\n -11.8074 -3.3030 0.0000 N 0 0\n -13.2877 -3.5506 0.0000 C 0 0\n -14.2413 -2.3928 0.0000 O 0 0\n 10.2684 14.8795 0.0000 C 0 0\n 10.7950 16.2849 0.0000 C 0 0\n 12.2753 16.5325 0.0000 C 0 0\n 12.8019 17.9379 0.0000 C 0 0\n 4.2477 9.9206 0.0000 N 0 0\n 4.7743 11.3261 0.0000 C 0 0\n 6.2546 11.5736 0.0000 C 0 0\n 6.7812 12.9791 0.0000 C 0 0\n 8.2615 13.2266 0.0000 N 0 0\n 8.7881 14.6319 0.0000 C 0 0\n 7.8345 15.7898 0.0000 O 0 0\n -11.2808 -1.8976 0.0000 C 0 0\n -9.8005 -1.6500 0.0000 C 0 0\n -9.2739 -0.2447 0.0000 C 0 0\n 0.6616 4.0495 0.0000 C 0 0\n 1.1880 5.4542 0.0000 O 0 0\n 1.6158 2.8910 0.0000 C 0 0\n 3.0963 3.1372 0.0000 C 0 0\n 4.0505 1.9787 0.0000 C 0 0\n 7.3996 -4.6122 0.0000 C 0 0 2 0 0 0\n 8.7310 -3.9212 0.0000 C 0 0 2 0 0 0\n 9.7780 -4.9774 0.0000 C 0 0 2 0 0 0\n 9.1286 -6.3155 0.0000 C 0 0 1 0 0 0\n 7.6455 -6.0920 0.0000 O 0 0\n 6.0609 -3.9393 0.0000 C 0 0\n 8.9625 -2.4410 0.0000 O 0 0\n 10.3614 -1.8997 0.0000 R# 0 0\n 11.2580 -4.7284 0.0000 O 0 0\n 9.8276 -7.6427 0.0000 R# 0 0\n 16.8113 21.2461 0.0000 C 0 0 2 0 0 0\n 15.8557 22.4022 0.0000 C 0 0 1 0 0 0\n 14.3766 22.1527 0.0000 C 0 0 1 0 0 0\n 13.8532 20.7471 0.0000 C 0 0 2 0 0 0\n 14.8088 19.5909 0.0000 C 0 0 1 0 0 0\n 16.2879 19.8404 0.0000 O 0 0\n 14.2822 18.1854 0.0000 O 0 0\n 13.4209 23.3089 0.0000 O 0 0\n 16.3792 23.8080 0.0000 O 0 0\n 18.2907 21.4988 0.0000 C 0 0\n 18.8122 22.9052 0.0000 O 0 0\n 1.5665 -19.5470 0.0000 C 0 0 2 0 0 0\n 0.0868 -19.7930 0.0000 C 0 0 1 0 0 0\n -0.8661 -18.6346 0.0000 C 0 0 1 0 0 0\n -0.3394 -17.2302 0.0000 C 0 0 2 0 0 0\n 1.1404 -16.9840 0.0000 C 0 0 1 0 0 0\n 2.0933 -18.1424 0.0000 O 0 0\n 1.6645 -15.5776 0.0000 O 0 0\n -2.3458 -18.8807 0.0000 O 0 0\n -0.4398 -21.1974 0.0000 O 0 0\n 2.5177 -20.7079 0.0000 C 0 0\n 1.9889 -22.1116 0.0000 O 0 0\n -21.3167 -10.1578 0.0000 C 0 0 2 0 0 0\n -22.2684 -8.9983 0.0000 C 0 0 1 0 0 0\n -21.7401 -7.5945 0.0000 C 0 0 1 0 0 0\n -20.2601 -7.3500 0.0000 C 0 0 2 0 0 0\n -19.3084 -8.5094 0.0000 C 0 0 1 0 0 0\n -19.8367 -9.9134 0.0000 O 0 0\n -17.8281 -8.2620 0.0000 O 0 0\n -22.6917 -6.4350 0.0000 O 0 0\n -23.7483 -9.2427 0.0000 O 0 0\n -21.8482 -11.5613 0.0000 C 0 0\n -23.3285 -11.8037 0.0000 O 0 0\n 12.3727 20.5004 0.0000 N 0 0\n 9.9386 21.4121 0.0000 O 0 0\n 11.4182 21.6586 0.0000 C 0 0\n 11.9441 23.0633 0.0000 C 0 0\n -1.2953 -16.0730 0.0000 N 0 0\n -3.7308 -15.1651 0.0000 O 0 0\n -2.7754 -16.3214 0.0000 C 0 0\n -3.2996 -17.7269 0.0000 C 0 0\n -19.7344 -5.9442 0.0000 N 0 0\n -20.1629 -3.3806 0.0000 O 0 0\n -20.6883 -4.7855 0.0000 C 0 0\n -22.1678 -5.0325 0.0000 C 0 0\n 5.9733 -2.4410 0.0000 O 0 0\n 4.6331 -1.7674 0.0000 R# 0 0\n113114 1 0\n112113 2 0\n111113 1 0\n117118 1 0\n116117 2 0\n115117 1 0\n121122 1 0\n120121 2 0\n119121 1 0\n 1 76 1 0\n 2 1 1 0\n 3 2 1 0\n 4 3 1 0\n 5 4 1 0\n 6 5 1 0\n 6 7 1 0\n 8 9 2 0\n 7 8 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 12 14 1 0\n 14 15 1 0\n 12 16 1 0\n 16 17 1 0\n 10 18 1 0\n 18 19 1 0\n 17 20 1 0\n 20 21 1 0\n 15 22 1 0\n 22 23 1 0\n 23 24 1 0\n 24 25 2 0\n 27 26 1 0\n 28 27 1 0\n 29 28 1 0\n 95 29 1 0\n 21 30 1 0\n 30 31 1 0\n 30 32 2 0\n 33 31 1 0\n 34 33 1 0\n 35 34 1 0\n 35 36 1 0\n 37 26 1 0\n 37 38 2 0\n 19 39 1 0\n 39 40 2 0\n 42 41 1 0\n 43 42 1 0\n 44 43 1 0\n106 44 1 0\n 47 41 1 0\n 47 48 2 0\n 45 39 1 0\n 50 49 1 0\n 51 50 1 0\n 52 51 1 0\n 84 52 1 0\n 54 53 1 0\n 55 54 1 0\n 56 55 1 0\n 56 57 1 0\n 57 58 1 0\n 58 49 1 0\n 58 59 2 0\n 53 24 1 0\n 36 37 1 0\n 46 47 1 0\n 46 60 1 0\n 60 61 1 0\n 61 62 1 0\n 62 45 1 0\n 63 64 2 0\n 63 65 1 0\n 65 66 1 0\n 66 67 1 0\n 8 67 1 0\n 68 69 1 0\n 69 70 1 0\n 70 71 1 0\n 71 72 1 0\n 72 68 1 0\n 68 73 1 6\n 69 74 1 1\n 74 75 1 0\n 70 76 1 1\n 71 77 1 6\n 78 79 1 0\n 79 80 1 0\n 80 81 1 0\n 81 82 1 0\n 82 83 1 0\n 83 78 1 0\n 82 84 1 1\n 80 85 1 1\n 79 86 1 1\n 78 87 1 1\n 87 88 1 0\n 81111 1 6\n 89 90 1 0\n 90 91 1 0\n 91 92 1 0\n 92 93 1 0\n 93 94 1 0\n 94 89 1 0\n 93 95 1 6\n 91 96 1 6\n 90 97 1 6\n 89 98 1 6\n 98 99 1 0\n 92115 1 1\n100101 1 0\n101102 1 0\n102103 1 0\n103104 1 0\n104105 1 0\n105100 1 0\n104106 1 6\n102107 1 6\n101108 1 6\n100109 1 6\n109110 1 0\n103119 1 1\n 63 13 1 0\n 73123 1 0\n123124 1 0\nM RGP 3 75 2 77 3 124 1\nM END\n> <Name>\n2-O-(6-(N-glutaryl-GalNAc3)aminohexylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nGalNAc\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(N-Methylacetamide)ribose\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.4939 -0.8190 0.0000 C 0 0 2 0 0 0\n -1.1622 -0.1288 0.0000 C 0 0 2 0 0 0\n -0.0942 -1.1821 0.0000 C 0 0 2 0 0 0\n -0.7659 -2.5233 0.0000 C 0 0 1 0 0 0\n -2.2491 -2.2989 0.0000 O 0 0\n -0.9411 1.3530 0.0000 O 0 0\n -3.8322 -0.1453 0.0000 C 0 0\n -0.0757 -3.8551 0.0000 R# 0 0\n 0.4541 1.9040 0.0000 R# 0 0\n 1.3834 -0.9345 0.0000 O 0 0\n 3.9159 2.1248 0.0000 N 0 0\n 3.3898 0.7192 0.0000 C 0 0\n 1.9096 0.4711 0.0000 C 0 0\n 5.3953 2.3727 0.0000 C 0 0\n 4.3438 -0.4383 0.0000 O 0 0\n -3.9189 1.3530 0.0000 O 0 0\n -5.2587 2.0275 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 12 13 1 0\n 11 12 1 0\n 10 13 1 0\n 11 14 1 0\n 12 15 2 0\n 7 16 1 0\n 16 17 1 0\nM RGP 3 8 3 9 2 17 1\nM END\n> <Name>\n2-O-(N-Methylacetamide)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnma\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(Pyren-1-yl)methylribose\n SciTegic07272112182D\n\n 29 33 0 0 1 0 999 V2000\n -5.0170 -2.3487 0.0000 C 0 0 2 0 0 0\n -3.6856 -1.6577 0.0000 C 0 0 2 0 0 0\n -2.6386 -2.7139 0.0000 C 0 0 2 0 0 0\n -3.2880 -4.0519 0.0000 C 0 0 1 0 0 0\n -4.7712 -3.8284 0.0000 O 0 0\n -3.4541 -0.1775 0.0000 O 0 0\n -6.3556 -1.6757 0.0000 C 0 0\n -2.5891 -5.3791 0.0000 R# 0 0\n -6.4433 -0.1775 0.0000 O 0 0\n -7.7835 0.4962 0.0000 R# 0 0\n -2.0551 0.3637 0.0000 R# 0 0\n -1.1586 -2.4650 0.0000 O 0 0\n 0.8468 -0.8102 0.0000 C 0 0\n -0.6333 -1.0591 0.0000 C 0 0\n 1.7995 -1.9688 0.0000 C 0 0\n 3.2792 -1.7230 0.0000 C 0 0\n 3.8063 -0.3186 0.0000 C 0 0\n 2.8536 0.8400 0.0000 C 0 0\n 1.3738 0.5942 0.0000 C 0 0\n 3.3806 2.2443 0.0000 C 0 0\n 2.4279 3.4029 0.0000 C 0 0\n 0.9481 3.1572 0.0000 C 0 0\n 0.4211 1.7528 0.0000 C 0 0\n 5.2860 -0.0729 0.0000 C 0 0\n 5.8130 1.3315 0.0000 C 0 0\n 4.8603 2.4901 0.0000 C 0 0\n 5.3873 3.8945 0.0000 C 0 0\n 4.4346 5.0531 0.0000 C 0 0\n 2.9549 4.8073 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 12 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 13 14 1 0\n 12 14 1 0\n 13 15 2 0\n 15 16 1 0\n 16 17 2 0\n 17 18 1 0\n 18 19 2 0\n 19 13 1 0\n 18 20 1 0\n 20 21 2 0\n 21 22 1 0\n 22 23 2 0\n 23 19 1 0\n 17 24 1 0\n 24 25 1 0\n 25 26 2 0\n 26 20 1 0\n 26 27 1 0\n 27 28 1 0\n 28 29 2 0\n 29 21 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n2-O-(Pyren-1-yl)methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\npyren1\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(S)-Methyl MOE\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.4939 -0.8190 0.0000 C 0 0 2 0 0 0\n -1.1622 -0.1288 0.0000 C 0 0 2 0 0 0\n -0.0942 -1.1821 0.0000 C 0 0 2 0 0 0\n -0.7659 -2.5233 0.0000 C 0 0 1 0 0 0\n -2.2491 -2.2989 0.0000 O 0 0\n -0.9411 1.3530 0.0000 O 0 0\n -3.8322 -0.1453 0.0000 C 0 0\n -0.0757 -3.8551 0.0000 R# 0 0\n 1.3834 -0.9345 0.0000 O 0 0\n 0.4541 1.9040 0.0000 R# 0 0\n 1.9096 0.4711 0.0000 C 0 0\n 3.3898 0.7192 0.0000 C 0 0 2 0 0 0\n 4.3438 -0.4383 0.0000 C 0 0\n 3.9159 2.1248 0.0000 O 0 0\n 5.3953 2.3727 0.0000 C 0 0\n -3.9189 1.3530 0.0000 O 0 0\n -5.2587 2.0275 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 9 1 1\n 1 7 1 6\n 4 8 1 6\n 6 10 1 0\n 9 11 1 0\n 11 12 1 0\n 12 13 1 1\n 12 14 1 0\n 14 15 1 0\n 7 16 1 0\n 16 17 1 0\nM RGP 3 8 3 10 2 17 1\nM END\n> <Name>\n2-O-(S)-Methyl MOE\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSm2moe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[(dimethylaminooxy)ethyl]ribose (DMAOE)\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -2.9344 -1.1208 0.0000 C 0 0 2 0 0 0\n -1.6027 -0.4306 0.0000 C 0 0 2 0 0 0\n -0.5347 -1.4839 0.0000 C 0 0 2 0 0 0\n -1.2064 -2.8251 0.0000 C 0 0 1 0 0 0\n -2.6896 -2.6007 0.0000 O 0 0\n -1.3816 1.0513 0.0000 O 0 0\n -4.2727 -0.4470 0.0000 C 0 0\n -0.5162 -4.1568 0.0000 R# 0 0\n 0.0136 1.6023 0.0000 R# 0 0\n 0.9429 -1.2362 0.0000 O 0 0\n 2.9493 0.4174 0.0000 C 0 0\n 1.4691 0.1694 0.0000 C 0 0\n 3.4754 1.8230 0.0000 O 0 0\n 4.9556 2.0711 0.0000 N 0 0\n 5.9096 0.9136 0.0000 C 0 0\n 5.4814 3.4759 0.0000 C 0 0\n -4.3594 1.0513 0.0000 O 0 0\n -5.6992 1.7258 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 11 12 1 0\n 13 11 1 0\n 10 12 1 0\n 14 16 1 0\n 14 15 1 0\n 13 14 1 0\n 7 17 1 0\n 17 18 1 0\nM RGP 3 8 3 9 2 18 1\nM END\n> <Name>\n2-O-[(dimethylaminooxy)ethyl]ribose (DMAOE)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndmaoe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Allylribose\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -1.8446 -0.6900 0.0000 C 0 0 2 0 0 0\n -0.5129 0.0002 0.0000 C 0 0 2 0 0 0\n 0.5551 -1.0531 0.0000 C 0 0 2 0 0 0\n -0.1166 -2.3943 0.0000 C 0 0 1 0 0 0\n -1.5998 -2.1699 0.0000 O 0 0\n -0.2918 1.4820 0.0000 O 0 0\n -3.1829 -0.0163 0.0000 C 0 0\n 0.5736 -3.7261 0.0000 R# 0 0\n -3.2696 1.4820 0.0000 O 0 0\n -4.6094 2.1566 0.0000 R# 0 0\n 1.1033 2.0330 0.0000 R# 0 0\n 2.0327 -0.8055 0.0000 O 0 0\n 4.5649 2.2530 0.0000 C 0 0\n 4.0390 0.8482 0.0000 C 0 0\n 2.5589 0.6001 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 12 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 14 15 1 0\n 13 14 2 0\n 12 15 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n2-O-Allylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nallyl2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Aminooxyethylribose (AOE)\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2224 -0.8464 0.0000 C 0 0 2 0 0 0\n -0.8907 -0.1562 0.0000 C 0 0 2 0 0 0\n 0.1773 -1.2095 0.0000 C 0 0 2 0 0 0\n -0.4944 -2.5507 0.0000 C 0 0 1 0 0 0\n -1.9776 -2.3263 0.0000 O 0 0\n -0.6696 1.3256 0.0000 O 0 0\n -3.5607 -0.1727 0.0000 C 0 0\n 0.1958 -3.8825 0.0000 R# 0 0\n -3.6474 1.3256 0.0000 O 0 0\n -4.9872 2.0002 0.0000 R# 0 0\n 1.6549 -0.9619 0.0000 O 0 0\n 0.7255 1.8766 0.0000 R# 0 0\n 2.1811 0.4437 0.0000 C 0 0\n 3.6612 0.6918 0.0000 C 0 0\n 4.1874 2.0974 0.0000 O 0 0\n 5.6667 2.3453 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-Aminooxyethylribose (AOE)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\naoe2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Aminopentylribose\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -2.9120 0.7423 0.0000 O 0 0\n -2.3999 2.1522 0.0000 C 0 0 1 0 0 0\n -1.7293 -0.1803 0.0000 C 0 0 2 0 0 0\n -0.9008 2.1009 0.0000 C 0 0 2 0 0 0\n -0.4863 0.6593 0.0000 C 0 0 1 0 0 0\n 0.0183 3.2841 0.0000 O 0 0\n -3.2412 3.3920 0.0000 C 0 0\n -4.7381 3.2841 0.0000 O 0 0\n -5.5803 4.5253 0.0000 R# 0 0\n -1.7806 -1.6795 0.0000 R# 0 0\n 0.9209 0.1449 0.0000 O 0 0\n 1.5044 3.0804 0.0000 R# 0 0\n 1.1804 -1.3333 0.0000 C 0 0\n 2.5900 -1.8485 0.0000 C 0 0\n 2.8495 -3.3267 0.0000 C 0 0\n 4.2591 -3.8420 0.0000 C 0 0\n 4.5186 -5.3202 0.0000 C 0 0\n 5.9274 -5.8352 0.0000 N 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-Aminopentylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnC52r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Aminopropylribose\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2224 -0.8464 0.0000 C 0 0 2 0 0 0\n -0.8907 -0.1562 0.0000 C 0 0 2 0 0 0\n 0.1773 -1.2095 0.0000 C 0 0 2 0 0 0\n -0.4944 -2.5507 0.0000 C 0 0 1 0 0 0\n -1.9776 -2.3263 0.0000 O 0 0\n -0.6696 1.3256 0.0000 O 0 0\n -3.5607 -0.1727 0.0000 C 0 0\n 0.1958 -3.8825 0.0000 R# 0 0\n 0.7255 1.8766 0.0000 R# 0 0\n 1.6549 -0.9619 0.0000 O 0 0\n 4.1874 2.0974 0.0000 C 0 0\n 3.6612 0.6918 0.0000 C 0 0\n 2.1811 0.4437 0.0000 C 0 0\n 5.6667 2.3453 0.0000 N 0 0\n -3.6474 1.3256 0.0000 O 0 0\n -4.9872 2.0002 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 12 13 1 0\n 11 12 1 0\n 10 13 1 0\n 11 14 1 0\n 7 15 1 0\n 15 16 1 0\nM RGP 3 8 3 9 2 16 1\nM END\n> <Name>\n2-O-Aminopropylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnpr2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Benzyloxyethylribose\n SciTegic07272112182D\n\n 22 23 0 0 1 0 999 V2000\n -4.0441 -2.2530 0.0000 C 0 0 2 0 0 0\n -2.7127 -1.5620 0.0000 C 0 0 2 0 0 0\n -1.6657 -2.6183 0.0000 C 0 0 2 0 0 0\n -2.3151 -3.9563 0.0000 C 0 0 1 0 0 0\n -3.7983 -3.7328 0.0000 O 0 0\n -5.3827 -1.5801 0.0000 C 0 0\n -2.4812 -0.0818 0.0000 O 0 0\n -5.4704 -0.0818 0.0000 O 0 0\n -6.8105 0.5919 0.0000 R# 0 0\n -1.0822 0.4593 0.0000 R# 0 0\n -0.1856 -2.3694 0.0000 O 0 0\n -1.6162 -5.2835 0.0000 R# 0 0\n 0.3397 -0.9635 0.0000 C 0 0\n 1.8197 -0.7145 0.0000 C 0 0\n 2.3450 0.6913 0.0000 O 0 0\n 3.8251 0.9403 0.0000 C 0 0\n 4.3504 2.3462 0.0000 C 0 0\n 5.8293 2.5971 0.0000 C 0 0\n 6.3514 4.0033 0.0000 C 0 0\n 5.3947 5.1586 0.0000 C 0 0\n 3.9158 4.9077 0.0000 C 0 0\n 3.3937 3.5015 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 3 11 1 1\n 4 12 1 6\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 2 0\n 18 19 1 0\n 19 20 2 0\n 20 21 1 0\n 21 22 2 0\n 22 17 1 0\nM RGP 3 9 1 10 2 12 3\nM END\n> <Name>\n2-O-Benzyloxyethylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbnoe2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Benzylribose\n SciTegic07272112182D\n\n 19 20 0 0 1 0 999 V2000\n -3.1268 -0.8718 0.0000 C 0 0 2 0 0 0\n -1.7954 -0.1808 0.0000 C 0 0 2 0 0 0\n -0.7484 -1.2370 0.0000 C 0 0 2 0 0 0\n -1.3978 -2.5750 0.0000 C 0 0 1 0 0 0\n -2.8810 -2.3515 0.0000 O 0 0\n -1.5639 1.2994 0.0000 O 0 0\n -4.4654 -0.1988 0.0000 C 0 0\n -0.6989 -3.9023 0.0000 R# 0 0\n -0.1649 1.8406 0.0000 R# 0 0\n 0.7316 -0.9881 0.0000 O 0 0\n 2.7370 0.6667 0.0000 C 0 0\n 1.2570 0.4178 0.0000 C 0 0\n 3.2640 2.0711 0.0000 C 0 0\n 4.7438 2.3169 0.0000 C 0 0\n 5.6965 1.1582 0.0000 C 0 0\n 5.1694 -0.2461 0.0000 C 0 0\n 3.6897 -0.4919 0.0000 C 0 0\n -4.5531 1.2994 0.0000 O 0 0\n -5.8933 1.9731 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 11 12 1 0\n 10 12 1 0\n 11 13 2 0\n 13 14 1 0\n 14 15 2 0\n 15 16 1 0\n 16 17 2 0\n 17 11 1 0\n 7 18 1 0\n 18 19 1 0\nM RGP 3 8 3 9 2 19 1\nM END\n> <Name>\n2-O-Benzylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbn2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Butylribose\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2224 -0.8464 0.0000 C 0 0 2 0 0 0\n -0.8907 -0.1562 0.0000 C 0 0 2 0 0 0\n 0.1773 -1.2095 0.0000 C 0 0 2 0 0 0\n -0.4944 -2.5507 0.0000 C 0 0 1 0 0 0\n -1.9776 -2.3263 0.0000 O 0 0\n -0.6696 1.3256 0.0000 O 0 0\n -3.5607 -0.1727 0.0000 C 0 0\n 0.1958 -3.8825 0.0000 R# 0 0\n 0.7255 1.8766 0.0000 R# 0 0\n 1.6549 -0.9619 0.0000 O 0 0\n 4.1874 2.0974 0.0000 C 0 0\n 3.6612 0.6918 0.0000 C 0 0\n 2.1811 0.4437 0.0000 C 0 0\n 5.6667 2.3453 0.0000 C 0 0\n -3.6474 1.3256 0.0000 O 0 0\n -4.9872 2.0002 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 12 13 1 0\n 11 12 1 0\n 10 13 1 0\n 11 14 1 0\n 7 15 1 0\n 15 16 1 0\nM RGP 3 8 3 9 2 16 1\nM END\n> <Name>\n2-O-Butylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbu2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Dimethylaminocarbamoylribose\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.2687 0.0472 0.0000 O 0 0\n -1.7567 1.4571 0.0000 C 0 0 1 0 0 0\n -1.0861 -0.8754 0.0000 C 0 0 2 0 0 0\n -0.2576 1.4058 0.0000 C 0 0 2 0 0 0\n 0.1569 -0.0358 0.0000 C 0 0 1 0 0 0\n 0.6616 2.5890 0.0000 O 0 0\n -2.5979 2.6969 0.0000 C 0 0\n -4.0949 2.5890 0.0000 O 0 0\n -4.9371 3.8303 0.0000 R# 0 0\n -1.1374 -2.3745 0.0000 R# 0 0\n 1.5641 -0.5501 0.0000 O 0 0\n 2.1477 2.3853 0.0000 R# 0 0\n 1.8236 -2.0284 0.0000 C 0 0\n 3.2332 -2.5436 0.0000 N 0 0\n 0.6735 -2.9913 0.0000 O 0 0\n 3.4926 -4.0210 0.0000 C 0 0\n 4.3833 -1.5807 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 13 15 2 0\n 14 16 1 0\n 14 17 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-Dimethylaminocarbamoylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2nc2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Dimethylaminoethylribose\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.4126 -1.0379 0.0000 C 0 0 2 0 0 0\n -1.0809 -0.3477 0.0000 C 0 0 2 0 0 0\n -0.0129 -1.4010 0.0000 C 0 0 2 0 0 0\n -0.6846 -2.7422 0.0000 C 0 0 1 0 0 0\n -2.1678 -2.5178 0.0000 O 0 0\n -0.8598 1.1342 0.0000 O 0 0\n -3.7509 -0.3641 0.0000 C 0 0\n 0.0056 -4.0740 0.0000 R# 0 0\n 0.5354 1.6852 0.0000 R# 0 0\n 1.4647 -1.1533 0.0000 O 0 0\n 3.4711 0.5003 0.0000 C 0 0\n 1.9909 0.2522 0.0000 C 0 0\n 3.9972 1.9059 0.0000 N 0 0\n 3.0431 3.0634 0.0000 C 0 0\n 5.4766 2.1539 0.0000 C 0 0\n -3.8376 1.1342 0.0000 O 0 0\n -5.1774 1.8087 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 11 12 1 0\n 10 12 1 0\n 13 15 1 0\n 13 14 1 0\n 11 13 1 0\n 7 16 1 0\n 16 17 1 0\nM RGP 3 8 3 9 2 17 1\nM END\n> <Name>\n2-O-Dimethylaminoethylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2e2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Ethoxymethylribose\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2590 0.0451 0.0000 O 0 0\n -1.7470 1.4550 0.0000 C 0 0 1 0 0 0\n -1.0764 -0.8776 0.0000 C 0 0 2 0 0 0\n -0.2479 1.4037 0.0000 C 0 0 2 0 0 0\n 0.1666 -0.0379 0.0000 C 0 0 1 0 0 0\n 0.6713 2.5869 0.0000 O 0 0\n -2.5882 2.6948 0.0000 C 0 0\n -4.0852 2.5869 0.0000 O 0 0\n -4.9274 3.8281 0.0000 R# 0 0\n -1.1277 -2.3767 0.0000 R# 0 0\n 1.5738 -0.5523 0.0000 O 0 0\n 2.1574 2.3832 0.0000 R# 0 0\n 1.8333 -2.0305 0.0000 C 0 0\n 3.2429 -2.5458 0.0000 O 0 0\n 3.5024 -4.0240 0.0000 C 0 0\n 4.9112 -4.5390 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-Ethoxymethylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\neom2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Ethylribose\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -1.5185 -0.5291 0.0000 C 0 0 2 0 0 0\n -0.1867 0.1611 0.0000 C 0 0 2 0 0 0\n 0.8812 -0.8922 0.0000 C 0 0 2 0 0 0\n 0.2095 -2.2334 0.0000 C 0 0 1 0 0 0\n -1.2736 -2.0090 0.0000 O 0 0\n 0.0343 1.6430 0.0000 O 0 0\n -2.8567 0.1447 0.0000 C 0 0\n 0.8997 -3.5651 0.0000 R# 0 0\n 2.3589 -0.6445 0.0000 O 0 0\n 1.4295 2.1940 0.0000 R# 0 0\n 2.8850 0.7611 0.0000 C 0 0\n 4.3644 1.0090 0.0000 C 0 0\n -2.9435 1.6430 0.0000 O 0 0\n -4.2833 2.3175 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 9 1 1\n 1 7 1 6\n 4 8 1 6\n 6 10 1 0\n 9 11 1 0\n 11 12 1 0\n 7 13 1 0\n 13 14 1 0\nM RGP 3 8 3 10 2 14 1\nM END\n> <Name>\n2-O-Ethylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ne2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Isopropylribose\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -1.6473 -0.6570 0.0000 C 0 0 2 0 0 0\n -0.3155 0.0332 0.0000 C 0 0 2 0 0 0\n 0.7525 -1.0201 0.0000 C 0 0 2 0 0 0\n 0.0807 -2.3613 0.0000 C 0 0 1 0 0 0\n -1.4024 -2.1369 0.0000 O 0 0\n -0.0944 1.5151 0.0000 O 0 0\n -2.9855 0.0168 0.0000 C 0 0\n 0.7709 -3.6930 0.0000 R# 0 0\n -3.0722 1.5151 0.0000 O 0 0\n -4.4120 2.1896 0.0000 R# 0 0\n 1.3007 2.0661 0.0000 R# 0 0\n 2.2301 -0.7724 0.0000 O 0 0\n 4.2356 0.8811 0.0000 C 0 0\n 2.7563 0.6332 0.0000 C 0 0\n 1.8022 1.7906 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 12 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 13 14 1 0\n 12 14 1 0\n 14 15 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n2-O-Isopropylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nipr2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Methyl carbocyclic ribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.1828 -0.4514 0.0000 C 0 0 2 0 0 0\n 0.1490 0.2388 0.0000 C 0 0 2 0 0 0\n 1.2170 -0.8145 0.0000 C 0 0 2 0 0 0\n 0.5452 -2.1557 0.0000 C 0 0 1 0 0 0\n -0.9379 -1.9313 0.0000 C 0 0\n 0.3701 1.7207 0.0000 O 0 0\n -2.5210 0.2223 0.0000 C 0 0\n 1.2354 -3.4875 0.0000 R# 0 0\n 1.7652 2.2716 0.0000 R# 0 0\n 2.6946 -0.5669 0.0000 O 0 0\n 3.2204 0.8380 0.0000 C 0 0\n -2.6077 1.7207 0.0000 O 0 0\n -3.9475 2.3952 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 10 11 1 0\n 7 12 1 0\n 12 13 1 0\nM RGP 3 8 3 9 2 13 1\nM END\n> <Name>\n2-O-Methyl carbocyclic ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc4m\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Methyl-4-thioribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.1828 -0.4514 0.0000 C 0 0 2 0 0 0\n 0.1490 0.2388 0.0000 C 0 0 2 0 0 0\n 1.2170 -0.8145 0.0000 C 0 0 2 0 0 0\n 0.5452 -2.1557 0.0000 C 0 0 1 0 0 0\n -0.9379 -1.9313 0.0000 S 0 0\n 0.3701 1.7207 0.0000 O 0 0\n -2.5210 0.2223 0.0000 C 0 0\n 1.2354 -3.4875 0.0000 R# 0 0\n -2.6077 1.7207 0.0000 O 0 0\n -3.9475 2.3952 0.0000 R# 0 0\n 2.6946 -0.5669 0.0000 O 0 0\n 1.7652 2.2716 0.0000 R# 0 0\n 3.2204 0.8380 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-Methyl-4-thioribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns4m\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Methylaminoethylribose (MMAE)\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2590 0.0451 0.0000 O 0 0\n -1.7470 1.4550 0.0000 C 0 0 1 0 0 0\n -1.0764 -0.8776 0.0000 C 0 0 2 0 0 0\n -0.2479 1.4037 0.0000 C 0 0 2 0 0 0\n 0.1666 -0.0379 0.0000 C 0 0 1 0 0 0\n 0.6713 2.5869 0.0000 O 0 0\n -2.5882 2.6948 0.0000 C 0 0\n -4.0852 2.5869 0.0000 O 0 0\n -4.9274 3.8281 0.0000 R# 0 0\n -1.1277 -2.3767 0.0000 R# 0 0\n 1.5738 -0.5523 0.0000 O 0 0\n 2.1574 2.3832 0.0000 R# 0 0\n 1.8333 -2.0305 0.0000 C 0 0\n 3.2429 -2.5458 0.0000 C 0 0\n 3.5024 -4.0240 0.0000 N 0 0\n 4.9112 -4.5390 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-Methylaminoethylribose (MMAE)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmne2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-N-[2-(methylsulfanyl)ethyl]acetamidoribose\n SciTegic07272112182D\n\n 20 20 0 0 1 0 999 V2000\n -3.5566 -1.4808 0.0000 C 0 0 2 0 0 0\n -2.2248 -0.7906 0.0000 C 0 0 2 0 0 0\n -1.1569 -1.8440 0.0000 C 0 0 2 0 0 0\n -1.8286 -3.1851 0.0000 C 0 0 1 0 0 0\n -3.3117 -2.9607 0.0000 O 0 0\n -2.0038 0.6912 0.0000 O 0 0\n -4.8948 -0.8071 0.0000 C 0 0\n -1.1384 -4.5169 0.0000 R# 0 0\n -4.9816 0.6912 0.0000 O 0 0\n -6.3214 1.3657 0.0000 R# 0 0\n -0.6086 1.2422 0.0000 R# 0 0\n 0.3208 -1.5963 0.0000 O 0 0\n 2.8532 1.4629 0.0000 N 0 0\n 2.3271 0.0574 0.0000 C 0 0\n 0.8469 -0.1907 0.0000 C 0 0\n 4.3334 1.7110 0.0000 C 0 0\n 3.2811 -1.1001 0.0000 O 0 0\n 4.8595 3.1166 0.0000 C 0 0\n 6.3397 3.3647 0.0000 S 0 0\n 6.8655 4.7695 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 12 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 14 15 1 0\n 13 14 1 0\n 12 15 1 0\n 13 16 1 0\n 14 17 2 0\n 16 18 1 0\n 18 19 1 0\n 19 20 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n2-O-N-[2-(methylsulfanyl)ethyl]acetamidoribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmseac\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Nonylribose\n SciTegic07272112182D\n\n 21 21 0 0 1 0 999 V2000\n -4.2203 -2.0781 0.0000 C 0 0 2 0 0 0\n -2.8885 -1.3879 0.0000 C 0 0 2 0 0 0\n -1.8205 -2.4412 0.0000 C 0 0 2 0 0 0\n -2.4923 -3.7824 0.0000 C 0 0 1 0 0 0\n -3.9754 -3.5580 0.0000 O 0 0\n -2.6674 0.0939 0.0000 O 0 0\n -5.5585 -1.4044 0.0000 C 0 0\n -1.8021 -5.1142 0.0000 R# 0 0\n -5.6452 0.0939 0.0000 O 0 0\n -6.9850 0.7685 0.0000 R# 0 0\n -1.2723 0.6449 0.0000 R# 0 0\n -0.3429 -2.1936 0.0000 O 0 0\n 2.1895 0.8657 0.0000 C 0 0\n 1.6634 -0.5399 0.0000 C 0 0\n 0.1832 -0.7880 0.0000 C 0 0\n 3.6697 1.1138 0.0000 C 0 0\n 4.1959 2.5194 0.0000 C 0 0\n 5.6760 2.7674 0.0000 C 0 0\n 6.2022 4.1730 0.0000 C 0 0\n 7.6823 4.4211 0.0000 C 0 0\n 8.2082 5.8259 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 12 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 14 15 1 0\n 13 14 1 0\n 12 15 1 0\n 13 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 19 20 1 0\n 20 21 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n2-O-Nonylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nC92r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Pentylribose\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.5868 -1.0670 0.0000 C 0 0 2 0 0 0\n -1.2550 -0.3768 0.0000 C 0 0 2 0 0 0\n -0.1871 -1.4301 0.0000 C 0 0 2 0 0 0\n -0.8588 -2.7713 0.0000 C 0 0 1 0 0 0\n -2.3419 -2.5469 0.0000 O 0 0\n -1.0340 1.1050 0.0000 O 0 0\n -3.9250 -0.3933 0.0000 C 0 0\n -0.1686 -4.1031 0.0000 R# 0 0\n 0.3612 1.6560 0.0000 R# 0 0\n 1.2906 -1.1825 0.0000 O 0 0\n 3.8230 1.8768 0.0000 C 0 0\n 3.2969 0.4712 0.0000 C 0 0\n 1.8167 0.2231 0.0000 C 0 0\n 5.3032 2.1248 0.0000 C 0 0\n 5.8290 3.5297 0.0000 C 0 0\n -4.0118 1.1050 0.0000 O 0 0\n -5.3516 1.7795 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 12 13 1 0\n 11 12 1 0\n 10 13 1 0\n 11 14 1 0\n 14 15 1 0\n 7 16 1 0\n 16 17 1 0\nM RGP 3 8 3 9 2 17 1\nM END\n> <Name>\n2-O-Pentylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nC52r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Phenylribose\n SciTegic07272112182D\n\n 18 19 0 0 1 0 999 V2000\n -2.2444 -1.1524 0.0000 C 0 0 2 0 0 0\n -0.9131 -0.4614 0.0000 C 0 0 2 0 0 0\n 0.1340 -1.5177 0.0000 C 0 0 2 0 0 0\n -0.5154 -2.8556 0.0000 C 0 0 1 0 0 0\n -1.9987 -2.6321 0.0000 O 0 0\n -0.6815 1.0188 0.0000 O 0 0\n -3.5831 -0.4795 0.0000 C 0 0\n 0.1835 -4.1829 0.0000 R# 0 0\n -3.6707 1.0188 0.0000 O 0 0\n -5.0109 1.6925 0.0000 R# 0 0\n 1.6140 -1.2687 0.0000 O 0 0\n 0.7174 1.5600 0.0000 R# 0 0\n 2.1393 0.1372 0.0000 C 0 0\n 3.6182 0.3881 0.0000 C 0 0\n 4.1403 1.7943 0.0000 C 0 0\n 3.1836 2.9496 0.0000 C 0 0\n 1.7047 2.6986 0.0000 C 0 0\n 1.1826 1.2925 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 16 17 1 0\n 17 18 2 0\n 18 13 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-Phenylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nph2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Propargylribose\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -2.0488 0.7379 0.0000 C 0 0 2 0 0 0\n -0.5488 0.7379 0.0000 C 0 0 2 0 0 0\n -0.0853 -0.6887 0.0000 C 0 0 2 0 0 0\n -1.2988 -1.5704 0.0000 C 0 0 1 0 0 0\n -2.5123 -0.6887 0.0000 O 0 0\n -2.9270 1.9518 0.0000 C 0 0\n 0.3293 1.9518 0.0000 O 0 0\n 1.8215 1.7991 0.0000 R# 0 0\n 1.3406 -1.1487 0.0000 O 0 0\n -1.2988 -3.0704 0.0000 R# 0 0\n 2.4545 -0.1429 0.0000 C 0 0\n 3.8828 -0.6037 0.0000 C 0 0\n -4.4192 1.7991 0.0000 R# 0 0\n 5.3103 -1.0642 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 3 9 1 1\n 4 10 1 6\n 9 11 1 0\n 11 12 1 0\n 6 13 1 0\n 12 14 3 0\nM RGP 3 8 2 10 3 13 1\nM END\n> <Name>\n2-O-Propargylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nprparg\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Propylribose\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -1.8446 -0.6900 0.0000 C 0 0 2 0 0 0\n -0.5129 0.0002 0.0000 C 0 0 2 0 0 0\n 0.5551 -1.0531 0.0000 C 0 0 2 0 0 0\n -0.1166 -2.3943 0.0000 C 0 0 1 0 0 0\n -1.5998 -2.1699 0.0000 O 0 0\n -0.2918 1.4820 0.0000 O 0 0\n -3.1829 -0.0163 0.0000 C 0 0\n 0.5736 -3.7261 0.0000 R# 0 0\n 1.1033 2.0330 0.0000 R# 0 0\n 2.0327 -0.8055 0.0000 O 0 0\n 4.5649 2.2530 0.0000 C 0 0\n 4.0390 0.8482 0.0000 C 0 0\n 2.5589 0.6001 0.0000 C 0 0\n -3.2696 1.4820 0.0000 O 0 0\n -4.6094 2.1566 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 12 13 1 0\n 11 12 1 0\n 10 13 1 0\n 7 14 1 0\n 14 15 1 0\nM RGP 3 8 3 9 2 15 1\nM END\n> <Name>\n2-O-Propylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\npr2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[2-(1-Imidizolyl)ethyl] ribose\n SciTegic07272112182D\n\n 19 20 0 0 1 0 999 V2000\n -2.9212 -1.4749 0.0000 C 0 0 2 0 0 0\n -1.5894 -0.7847 0.0000 C 0 0 2 0 0 0\n -0.5215 -1.8381 0.0000 C 0 0 2 0 0 0\n -1.1932 -3.1792 0.0000 C 0 0 1 0 0 0\n -2.6763 -2.9548 0.0000 O 0 0\n -1.3684 0.6971 0.0000 O 0 0\n -4.2594 -0.8012 0.0000 C 0 0\n -0.5030 -4.5110 0.0000 R# 0 0\n -4.3462 0.6971 0.0000 O 0 0\n -5.6860 1.3716 0.0000 R# 0 0\n 0.9562 -1.5904 0.0000 O 0 0\n 0.0268 1.2481 0.0000 R# 0 0\n 1.4823 -0.1848 0.0000 C 0 0\n 2.9625 0.0633 0.0000 C 0 0\n 3.4886 1.4689 0.0000 N 0 0\n 4.9258 1.8517 0.0000 C 0 0\n 4.9887 3.3503 0.0000 C 0 0\n 3.5828 3.8733 0.0000 N 0 0\n 2.6510 2.6978 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 2 0\n 17 18 1 0\n 18 19 2 0\n 19 15 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-[2-(1-Imidizolyl)ethyl] ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nime2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[2-(2-Methoxyethoxy)ethoxy]ethylribose (TriMOE)\n SciTegic07272112182D\n\n 22 22 0 0 1 0 999 V2000\n -4.6607 -2.3543 0.0000 C 0 0 2 0 0 0\n -3.3289 -1.6641 0.0000 C 0 0 2 0 0 0\n -2.2609 -2.7174 0.0000 C 0 0 2 0 0 0\n -2.9327 -4.0586 0.0000 C 0 0 1 0 0 0\n -4.4158 -3.8341 0.0000 O 0 0\n -3.1078 -0.1822 0.0000 O 0 0\n -5.9989 -1.6805 0.0000 C 0 0\n -2.2425 -5.3903 0.0000 R# 0 0\n -1.7127 0.3688 0.0000 R# 0 0\n -0.7833 -2.4697 0.0000 O 0 0\n 1.2230 -0.8160 0.0000 C 0 0\n -0.2571 -1.0641 0.0000 C 0 0\n 1.7492 0.5895 0.0000 O 0 0\n 3.2294 0.8376 0.0000 C 0 0\n 3.7555 2.2432 0.0000 C 0 0\n 5.2357 2.4913 0.0000 O 0 0\n 5.7618 3.8969 0.0000 C 0 0\n 7.2420 4.1449 0.0000 C 0 0\n 7.7681 5.5505 0.0000 O 0 0\n 9.2475 5.7985 0.0000 C 0 0\n -6.0856 -0.1822 0.0000 O 0 0\n -7.4254 0.4923 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 11 12 1 0\n 10 12 1 0\n 13 14 1 0\n 11 13 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 19 20 1 0\n 7 21 1 0\n 21 22 1 0\nM RGP 3 8 3 9 2 22 1\nM END\n> <Name>\n2-O-[2-(2-Methoxyethoxy)ethoxy]ethylribose (TriMOE)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ntrimoe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[2-((N,N-diethyl)aminooxy)ethyl]ribose\n SciTegic07272112182D\n\n 20 20 0 0 1 0 999 V2000\n -3.6522 -1.3653 0.0000 C 0 0 2 0 0 0\n -2.3204 -0.6751 0.0000 C 0 0 2 0 0 0\n -1.2525 -1.7284 0.0000 C 0 0 2 0 0 0\n -1.9242 -3.0696 0.0000 C 0 0 1 0 0 0\n -3.4073 -2.8452 0.0000 O 0 0\n -2.0994 0.8067 0.0000 O 0 0\n -4.9905 -0.6916 0.0000 C 0 0\n -1.2340 -4.4014 0.0000 R# 0 0\n -5.0772 0.8067 0.0000 O 0 0\n -6.4170 1.4812 0.0000 R# 0 0\n 0.2252 -1.4808 0.0000 O 0 0\n -0.7042 1.3577 0.0000 R# 0 0\n 0.7513 -0.0752 0.0000 C 0 0\n 2.2315 0.1729 0.0000 C 0 0\n 2.7576 1.5785 0.0000 O 0 0\n 4.2378 1.8265 0.0000 N 0 0\n 5.1947 0.6704 0.0000 C 0 0\n 4.7639 3.2321 0.0000 C 0 0\n 6.6738 0.9200 0.0000 C 0 0\n 6.2433 3.4801 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 18 1 0\n 16 17 1 0\n 17 19 1 0\n 18 20 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-[2-((N,N-diethyl)aminooxy)ethyl]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ne2noe2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[2-((N-Isopropyl-N-methyl)aminooxy)ethyl]ribose\n SciTegic07272112182D\n\n 20 20 0 0 1 0 999 V2000\n -3.3509 1.2004 0.0000 O 0 0\n -2.8388 2.6103 0.0000 C 0 0 1 0 0 0\n -2.1682 0.2778 0.0000 C 0 0 2 0 0 0\n -1.3397 2.5590 0.0000 C 0 0 2 0 0 0\n -0.9252 1.1174 0.0000 C 0 0 1 0 0 0\n -0.4205 3.7422 0.0000 O 0 0\n -3.6801 3.8501 0.0000 C 0 0\n -5.1770 3.7422 0.0000 O 0 0\n -6.0192 4.9835 0.0000 R# 0 0\n -2.2195 -1.2213 0.0000 R# 0 0\n 0.4820 0.6031 0.0000 O 0 0\n 1.0656 3.5385 0.0000 R# 0 0\n 0.7415 -0.8752 0.0000 C 0 0\n 2.1511 -1.3904 0.0000 C 0 0\n 2.4106 -2.8686 0.0000 O 0 0\n 3.8202 -3.3839 0.0000 N 0 0\n 4.9703 -2.4209 0.0000 C 0 0\n 4.0797 -4.8621 0.0000 C 0 0\n 5.4885 -5.3771 0.0000 C 0 0\n 2.9296 -5.8251 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 16 18 1 0\n 18 19 1 0\n 18 20 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-[2-((N-Isopropyl-N-methyl)aminooxy)ethyl]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\niprmno\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[2-(Guanidinium)ethyl]ribose\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -2.9344 -1.1208 0.0000 C 0 0 2 0 0 0\n -1.6027 -0.4306 0.0000 C 0 0 2 0 0 0\n -0.5347 -1.4839 0.0000 C 0 0 2 0 0 0\n -1.2064 -2.8251 0.0000 C 0 0 1 0 0 0\n -2.6896 -2.6007 0.0000 O 0 0\n -1.3816 1.0513 0.0000 O 0 0\n -4.2727 -0.4470 0.0000 C 0 0\n -0.5162 -4.1568 0.0000 R# 0 0\n -4.3594 1.0513 0.0000 O 0 0\n -5.6992 1.7258 0.0000 R# 0 0\n 0.9429 -1.2362 0.0000 O 0 0\n 0.0136 1.6023 0.0000 R# 0 0\n 1.4691 0.1694 0.0000 C 0 0\n 2.9493 0.4174 0.0000 C 0 0\n 3.4754 1.8230 0.0000 N 0 0\n 4.9556 2.0711 0.0000 C 0 0\n 5.4814 3.4759 0.0000 N 0 0\n 5.9096 0.9136 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 2 0\n 16 18 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-[2-(Guanidinium)ethyl]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nguane2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[2-(Methylthio)ethyl]ribose\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2224 -0.8464 0.0000 C 0 0 2 0 0 0\n -0.8907 -0.1562 0.0000 C 0 0 2 0 0 0\n 0.1773 -1.2095 0.0000 C 0 0 2 0 0 0\n -0.4944 -2.5507 0.0000 C 0 0 1 0 0 0\n -1.9776 -2.3263 0.0000 O 0 0\n -0.6696 1.3256 0.0000 O 0 0\n -3.5607 -0.1727 0.0000 C 0 0\n 0.1958 -3.8825 0.0000 R# 0 0\n -3.6474 1.3256 0.0000 O 0 0\n -4.9872 2.0002 0.0000 R# 0 0\n 1.6549 -0.9619 0.0000 O 0 0\n 0.7255 1.8766 0.0000 R# 0 0\n 2.1811 0.4437 0.0000 C 0 0\n 3.6612 0.6918 0.0000 C 0 0\n 4.1874 2.0974 0.0000 S 0 0\n 5.6667 2.3453 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-[2-(Methylthio)ethyl]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmse2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[2-(methylsulfinyl)ethyl]ribose\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.3974 0.3384 0.0000 O 0 0\n -1.8854 1.7483 0.0000 C 0 0 1 0 0 0\n -1.2148 -0.5842 0.0000 C 0 0 2 0 0 0\n -0.3862 1.6970 0.0000 C 0 0 2 0 0 0\n 0.0282 0.2554 0.0000 C 0 0 1 0 0 0\n 0.5329 2.8802 0.0000 O 0 0\n -2.7266 2.9881 0.0000 C 0 0\n -4.2236 2.8802 0.0000 O 0 0\n -5.0658 4.1215 0.0000 R# 0 0\n -1.2661 -2.0833 0.0000 R# 0 0\n 1.4354 -0.2589 0.0000 O 0 0\n 2.0190 2.6765 0.0000 R# 0 0\n 1.6949 -1.7372 0.0000 C 0 0\n 3.1045 -2.2524 0.0000 C 0 0\n 3.3640 -3.7306 0.0000 S 0 0\n 2.2139 -4.6936 0.0000 C 0 0\n 4.7729 -4.2456 0.0000 O 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 15 17 2 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-[2-(methylsulfinyl)ethyl]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmsoe2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[2-[2-(N,N-dimethyl)aminoethoxy]ethyl]ribose\n SciTegic07272112182D\n\n 20 20 0 0 1 0 999 V2000\n -3.7572 -1.6462 0.0000 C 0 0 2 0 0 0\n -2.4255 -0.9560 0.0000 C 0 0 2 0 0 0\n -1.3575 -2.0093 0.0000 C 0 0 2 0 0 0\n -2.0292 -3.3505 0.0000 C 0 0 1 0 0 0\n -3.5124 -3.1261 0.0000 O 0 0\n -2.2044 0.5258 0.0000 O 0 0\n -5.0955 -0.9725 0.0000 C 0 0\n -1.3390 -4.6823 0.0000 R# 0 0\n -5.1822 0.5258 0.0000 O 0 0\n -6.5220 1.2004 0.0000 R# 0 0\n -0.8093 1.0768 0.0000 R# 0 0\n 0.1201 -1.7617 0.0000 O 0 0\n 2.1264 -0.1080 0.0000 C 0 0\n 0.6463 -0.3561 0.0000 C 0 0\n 2.6526 1.2976 0.0000 O 0 0\n 4.1328 1.5457 0.0000 C 0 0\n 4.6589 2.9512 0.0000 C 0 0\n 6.1391 3.1993 0.0000 N 0 0\n 7.0931 2.0418 0.0000 C 0 0\n 6.6649 4.6041 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 12 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 13 14 1 0\n 15 13 1 0\n 12 14 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 20 1 0\n 18 19 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n2-O-[2-[2-(N,N-dimethyl)aminoethoxy]ethyl]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndmaeoe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[3-(N,N-Dimethyl)aminopropyl]ribose\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -2.9344 -1.1208 0.0000 C 0 0 2 0 0 0\n -1.6027 -0.4306 0.0000 C 0 0 2 0 0 0\n -0.5347 -1.4839 0.0000 C 0 0 2 0 0 0\n -1.2064 -2.8251 0.0000 C 0 0 1 0 0 0\n -2.6896 -2.6007 0.0000 O 0 0\n -1.3816 1.0513 0.0000 O 0 0\n -4.2727 -0.4470 0.0000 C 0 0\n -0.5162 -4.1568 0.0000 R# 0 0\n -4.3594 1.0513 0.0000 O 0 0\n -5.6992 1.7258 0.0000 R# 0 0\n 0.9429 -1.2362 0.0000 O 0 0\n 0.0136 1.6023 0.0000 R# 0 0\n 1.4691 0.1694 0.0000 C 0 0\n 2.9493 0.4174 0.0000 C 0 0\n 3.4754 1.8230 0.0000 C 0 0\n 4.9556 2.0711 0.0000 N 0 0\n 5.9096 0.9136 0.0000 C 0 0\n 5.4814 3.4759 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 18 1 0\n 16 17 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-[3-(N,N-Dimethyl)aminopropyl]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2npr2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[(2-Methoxy)ethyl]-4-thioribose\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2224 -0.8464 0.0000 C 0 0 2 0 0 0\n -0.8907 -0.1562 0.0000 C 0 0 2 0 0 0\n 0.1773 -1.2095 0.0000 C 0 0 2 0 0 0\n -0.4944 -2.5507 0.0000 C 0 0 1 0 0 0\n -1.9776 -2.3263 0.0000 S 0 0\n -0.6696 1.3256 0.0000 O 0 0\n -3.5607 -0.1727 0.0000 C 0 0\n 0.1958 -3.8825 0.0000 R# 0 0\n 1.6549 -0.9619 0.0000 O 0 0\n 0.7255 1.8766 0.0000 R# 0 0\n 2.1811 0.4437 0.0000 C 0 0\n 3.6612 0.6918 0.0000 C 0 0\n 4.1874 2.0974 0.0000 O 0 0\n 5.6667 2.3453 0.0000 C 0 0\n -3.6474 1.3256 0.0000 O 0 0\n -4.9872 2.0002 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 9 1 1\n 1 7 1 6\n 4 8 1 6\n 6 10 1 0\n 9 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 7 15 1 0\n 15 16 1 0\nM RGP 3 8 3 10 2 16 1\nM END\n> <Name>\n2-O-[(2-Methoxy)ethyl]-4-thioribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns4moe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[(Dimethylamino)ethylcarbamoyl]ribose\n SciTegic07272112182D\n\n 20 20 0 0 1 0 999 V2000\n -3.0819 1.1713 0.0000 O 0 0\n -2.5699 2.5812 0.0000 C 0 0 1 0 0 0\n -1.8992 0.2486 0.0000 C 0 0 2 0 0 0\n -1.0707 2.5299 0.0000 C 0 0 2 0 0 0\n -0.6563 1.0883 0.0000 C 0 0 1 0 0 0\n -0.1516 3.7131 0.0000 O 0 0\n -3.4111 3.8210 0.0000 C 0 0\n -4.9081 3.7131 0.0000 O 0 0\n -5.7503 4.9543 0.0000 R# 0 0\n -1.9506 -1.2505 0.0000 R# 0 0\n 0.7509 0.5739 0.0000 O 0 0\n 1.3345 3.5094 0.0000 R# 0 0\n 1.0104 -0.9043 0.0000 C 0 0\n 2.4200 -1.4196 0.0000 N 0 0\n -0.1397 -1.8673 0.0000 O 0 0\n 2.6795 -2.8978 0.0000 C 0 0\n 4.0891 -3.4130 0.0000 C 0 0\n 4.3487 -4.8913 0.0000 N 0 0\n 5.7575 -5.4062 0.0000 C 0 0\n 3.1986 -5.8542 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 13 15 2 0\n 14 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 18 20 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-[(Dimethylamino)ethylcarbamoyl]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2nenc\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[(N,N-dimethyl)acetamido]ribose\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -2.6585 -1.0014 0.0000 C 0 0 2 0 0 0\n -1.3267 -0.3112 0.0000 C 0 0 2 0 0 0\n -0.2587 -1.3645 0.0000 C 0 0 2 0 0 0\n -0.9305 -2.7057 0.0000 C 0 0 1 0 0 0\n -2.4136 -2.4813 0.0000 O 0 0\n -3.9967 -0.3276 0.0000 C 0 0\n -1.1056 1.1707 0.0000 O 0 0\n -4.0834 1.1707 0.0000 O 0 0\n -5.4232 1.8452 0.0000 R# 0 0\n 0.2895 1.7217 0.0000 R# 0 0\n 1.2189 -1.1168 0.0000 O 0 0\n -0.2403 -4.0374 0.0000 R# 0 0\n 1.7450 0.2888 0.0000 C 0 0\n 3.2252 0.5368 0.0000 C 0 0\n 3.7513 1.9424 0.0000 N 0 0\n 5.2307 2.1904 0.0000 C 0 0\n 4.1793 -0.6207 0.0000 O 0 0\n 2.7973 3.0999 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 3 11 1 1\n 4 12 1 6\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 14 17 2 0\n 15 18 1 0\nM RGP 3 9 1 10 2 12 3\nM END\n> <Name>\n2-O-[(N,N-dimethyl)acetamido]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndmac\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[N-[2-(Dimethylamino)ethyl]acetamido]ribose\n SciTegic07272112182D\n\n 21 21 0 0 1 0 999 V2000\n -3.9039 -1.5860 0.0000 C 0 0 2 0 0 0\n -2.5722 -0.8958 0.0000 C 0 0 2 0 0 0\n -1.5042 -1.9491 0.0000 C 0 0 2 0 0 0\n -2.1759 -3.2902 0.0000 C 0 0 1 0 0 0\n -3.6591 -3.0658 0.0000 O 0 0\n -5.2422 -0.9122 0.0000 C 0 0\n -2.3511 0.5861 0.0000 O 0 0\n -5.3289 0.5861 0.0000 O 0 0\n -6.6687 1.2606 0.0000 R# 0 0\n -0.9559 1.1371 0.0000 R# 0 0\n -0.0266 -1.7014 0.0000 O 0 0\n -1.4857 -4.6220 0.0000 R# 0 0\n 0.4996 -0.2958 0.0000 C 0 0\n 1.9798 -0.0477 0.0000 C 0 0\n 2.5059 1.3578 0.0000 N 0 0\n 3.9861 1.6059 0.0000 C 0 0\n 2.9338 -1.2052 0.0000 O 0 0\n 4.5122 3.0115 0.0000 C 0 0\n 5.9924 3.2596 0.0000 N 0 0\n 6.9464 2.1021 0.0000 C 0 0\n 6.5182 4.6644 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 3 11 1 1\n 4 12 1 6\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 14 17 2 0\n 16 18 1 0\n 18 19 1 0\n 19 21 1 0\n 19 20 1 0\nM RGP 3 9 1 10 2 12 3\nM END\n> <Name>\n2-O-[N-[2-(Dimethylamino)ethyl]acetamido]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndmaeac\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Phenylthio-2-deoxyribose\n SciTegic07272112182D\n\n 18 19 0 0 1 0 999 V2000\n -2.2444 -1.1524 0.0000 C 0 0 2 0 0 0\n -0.9131 -0.4614 0.0000 C 0 0 2 0 0 0\n 0.1340 -1.5177 0.0000 C 0 0 2 0 0 0\n -0.5154 -2.8556 0.0000 C 0 0 1 0 0 0\n -1.9987 -2.6321 0.0000 O 0 0\n -3.5831 -0.4795 0.0000 C 0 0\n -0.6815 1.0188 0.0000 O 0 0\n 0.7174 1.5600 0.0000 R# 0 0\n 0.1835 -4.1829 0.0000 R# 0 0\n 1.6140 -1.2687 0.0000 S 0 0\n 2.1393 0.1372 0.0000 C 0 0\n 3.6182 0.3881 0.0000 C 0 0\n 4.1403 1.7943 0.0000 C 0 0\n 3.1836 2.9496 0.0000 C 0 0\n 1.7047 2.6986 0.0000 C 0 0\n 1.1826 1.2925 0.0000 C 0 0\n -3.6707 1.0188 0.0000 O 0 0\n -5.0109 1.6925 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 3 10 1 1\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 16 11 1 0\n 6 17 1 0\n 17 18 1 0\nM RGP 3 8 2 9 3 18 1\nM END\n> <Name>\n2-Phenylthio-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nphs2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Thio LNA\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n 0.6312 -2.0624 0.0000 C 0 0\n 0.0863 -3.3094 0.0000 S 0 0\n 0.5482 -0.6031 0.0000 C 0 0 1 0 0 0\n 1.9307 0.0252 0.0000 C 0 0 2 0 0 0\n -0.1994 -1.7658 0.0000 C 0 0 2 0 0 0\n -1.5533 -1.1139 0.0000 C 0 0 1 0 0 0\n -0.9631 -0.0086 0.0000 O 0 0\n 0.3822 0.8942 0.0000 C 0 0\n -2.9468 -0.5588 0.0000 R# 0 0\n 1.5689 1.4971 0.0000 O 0 0\n 2.6655 2.5205 0.0000 R# 0 0\n -0.9922 1.4971 0.0000 O 0 0\n -1.1582 2.9879 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 6\n 3 1 1 0\n 5 2 1 1\n 4 10 1 1\n 10 11 1 0\n 8 12 1 0\n 12 13 1 0\nM RGP 3 9 3 11 2 13 1\nM END\n> <Name>\n2-Thio LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns2lna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Thio-(R)-cEt\n SciTegic09012117322D\n\n 14 15 0 0 1 0 999 V2000\n 1.1233 0.2604 0.0000 C 0 0 1 0 0 0\n -1.0323 -0.6397 0.0000 C 0 0 2 0 0 0\n -1.8879 0.4463 0.0000 C 0 0 1 0 0 0\n -0.5108 0.2643 0.0000 O 0 0\n 0.3584 -0.9107 0.0000 C 0 0 1 0 0 0\n 2.1947 1.2825 0.0000 O 0 0\n -3.1915 1.1882 0.0000 R# 0 0\n 0.5071 -2.1734 0.0000 C 0 0 2 0 0 0\n -0.8617 -2.0116 0.0000 S 0 0\n 1.5675 -3.2343 0.0000 C 0 0\n 3.6357 0.8661 0.0000 R# 0 0\n 0.2821 0.5988 0.0000 C 0 0\n -1.0539 1.2825 0.0000 O 0 0\n -1.1307 2.7806 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 0\n 5 1 1 0\n 3 7 1 6\n 5 8 1 0\n 2 9 1 1\n 8 9 1 0\n 1 6 1 6\n 8 10 1 1\n 6 11 1 0\n 5 12 1 1\n 12 13 1 0\n 13 14 1 0\nM RGP 3 7 3 11 2 14 1\nM END\n> <Name>\n2-Thio-(R)-cEt\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRs2cEt\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Thio-(S)-cEt\n SciTegic09012117322D\n\n 14 15 0 0 1 0 999 V2000\n 1.1233 0.2604 0.0000 C 0 0 1 0 0 0\n -1.0323 -0.6397 0.0000 C 0 0 2 0 0 0\n -1.8879 0.4463 0.0000 C 0 0 1 0 0 0\n -0.5108 0.2643 0.0000 O 0 0\n 0.3584 -0.9107 0.0000 C 0 0 1 0 0 0\n 2.1947 1.2825 0.0000 O 0 0\n -3.1915 1.1882 0.0000 R# 0 0\n 0.5071 -2.1734 0.0000 C 0 0 1 0 0 0\n -0.8617 -2.0116 0.0000 S 0 0\n 1.5675 -3.2343 0.0000 C 0 0\n 3.6357 0.8661 0.0000 R# 0 0\n 0.2821 0.5988 0.0000 C 0 0\n -1.0539 1.2825 0.0000 O 0 0\n -1.1307 2.7806 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 0\n 5 1 1 0\n 3 7 1 6\n 5 8 1 0\n 2 9 1 1\n 8 9 1 0\n 1 6 1 6\n 8 10 1 6\n 6 11 1 0\n 5 12 1 1\n 12 13 1 0\n 13 14 1 0\nM RGP 3 7 3 11 2 14 1\nM END\n> <Name>\n2-Thio-(S)-cEt\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSs2cEt\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Thiocytosine\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.5981 -1.5000 0.0000 R# 0 0\n 0.0000 -3.0000 0.0000 S 0 0\n 2.5981 1.5000 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 0\n 6 8 2 0\n 2 9 1 0\nM RGP 1 7 1\nM END\n> <Name>\n2-Thiocytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns2C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Thiothymine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 S 0 0\n 4.5000 0.4019 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\nM RGP 1 8 1\nM END\n> <Name>\n2-Thiothymine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns2T\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Thiouracil\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 2.5981 1.5000 0.0000 S 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\nM RGP 1 8 1\nM END\n> <Name>\n2-Thiouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns2U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-alpha-C-Ethyl-2-deoxyribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.1828 -0.4514 0.0000 C 0 0 2 0 0 0\n 0.1490 0.2388 0.0000 C 0 0 2 0 0 0\n 1.2170 -0.8145 0.0000 C 0 0 2 0 0 0\n 0.5452 -2.1557 0.0000 C 0 0 1 0 0 0\n -0.9379 -1.9313 0.0000 O 0 0\n 0.3701 1.7207 0.0000 O 0 0\n -2.5210 0.2223 0.0000 C 0 0\n 1.2354 -3.4875 0.0000 R# 0 0\n 1.7652 2.2716 0.0000 R# 0 0\n 2.6946 -0.5669 0.0000 C 0 0\n 3.2204 0.8380 0.0000 C 0 0\n -2.6077 1.7207 0.0000 O 0 0\n -3.9475 2.3952 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 10 11 1 0\n 7 12 1 0\n 12 13 1 0\nM RGP 3 8 3 9 2 13 1\nM END\n> <Name>\n2-alpha-C-Ethyl-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nAe2d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-alpha-C-Methyl-2-deoxyribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.1351 -1.0500 0.0000 O 0 0\n -0.6231 0.3599 0.0000 C 0 0 1 0 0 0\n 0.0475 -1.9727 0.0000 C 0 0 2 0 0 0\n 0.8761 0.3086 0.0000 C 0 0 2 0 0 0\n 1.2905 -1.1330 0.0000 C 0 0 1 0 0 0\n 1.7952 1.4918 0.0000 O 0 0\n -1.4643 1.5997 0.0000 C 0 0\n -2.9613 1.4918 0.0000 O 0 0\n -3.8035 2.7330 0.0000 R# 0 0\n -0.0038 -3.4718 0.0000 R# 0 0\n 2.7004 -1.6451 0.0000 C 0 0\n 3.2813 1.2881 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-alpha-C-Methyl-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nAm2d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-(Dimethylamino)propylaminoadenine\n SciTegic07272112182D\n\n 18 19 0 0 0 0 999 V2000\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2578 0.0000 C 0 0\n 5.1894 6.0109 0.0000 N 0 0\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n 2.5972 1.5031 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 5.1872 7.5109 0.0000 C 0 0\n 6.4897 5.2632 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 5 10 2 0\n 8 11 1 0\n 11 12 1 0\n 12 13 2 0\n 9 13 1 0\n 10 14 1 0\n 6 15 1 0\n 11 16 1 0\n 1 15 1 0\n 4 17 1 0\n 4 18 1 0\nM RGP 1 16 1\nM END\n> <Name>\n3-(Dimethylamino)propylaminoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2nprn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n3-Chloro HNA\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.5573 -0.8976 0.0000 O 0 0\n -0.8058 0.4006 0.0000 C 0 0 1 0 0 0\n 0.6942 0.3989 0.0000 C 0 0 2 0 0 0\n 1.4427 -0.9010 0.0000 C 0 0 2 0 0 0\n 0.6912 -2.1992 0.0000 C 0 0 1 0 0 0\n -0.8088 -2.1975 0.0000 C 0 0\n 1.4396 -3.4991 0.0000 R# 0 0\n 2.9427 -0.9028 0.0000 Cl 0 0\n 1.4434 1.6993 0.0000 O 0 0\n -1.5574 1.6997 0.0000 C 0 0\n 2.9434 1.7016 0.0000 R# 0 0\n -3.0582 1.6993 0.0000 O 0 0\n -3.8094 2.9977 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 6\n 4 8 1 1\n 3 9 1 1\n 2 10 1 6\n 9 11 1 0\n 10 12 1 0\n 12 13 1 0\nM RGP 3 7 3 11 2 13 1\nM END\n> <Name>\n3-Chloro HNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nclhna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Deaza-3-allylguanine\n SciTegic07272112182D\n\n 15 16 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 0.0031 3.0008 0.0000 C 0 0\n 1.3039 3.7494 0.0000 C 0 0\n 1.3070 5.2494 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 7 8 2 0\n 5 8 1 0\n 6 9 2 0\n 2 10 1 0\n 4 11 1 0\n 7 11 1 0\n 11 12 1 0\n 3 13 1 0\n 13 14 1 0\n 14 15 2 0\nM RGP 1 12 1\nM END\n> <Name>\n3-Deaza-3-allylguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc3ally\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n3-Deazaadenine\n SciTegic07272112182D\n\n 11 12 0 0 0 0 999 V2000\n 5.9498 4.1210 0.0000 C 0 0\n 6.2618 2.6538 0.0000 C 0 0\n 7.6885 2.1904 0.0000 C 0 0\n 7.0645 5.1248 0.0000 C 0 0\n 8.4911 4.6614 0.0000 N 0 0\n 8.8031 3.1942 0.0000 C 0 0\n 7.6888 0.6912 0.0000 N 0 0\n 6.2623 0.2275 0.0000 C 0 0\n 5.3805 1.4410 0.0000 N 0 0\n 10.2297 2.7308 0.0000 N 0 0\n 3.8805 1.4410 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 3 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 2 1 0\n 6 10 1 0\n 9 11 1 0\nM RGP 1 11 1\nM END\n> <Name>\n3-Deazaadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc3A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n3-Deazaguanine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 7 8 2 0\n 5 8 1 0\n 6 9 2 0\n 2 10 1 0\n 4 11 1 0\n 7 11 1 0\n 11 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n3-Deazaguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc3G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n3-Deoxy-3-amino-2-O-methylribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.1828 -0.4514 0.0000 C 0 0 2 0 0 0\n 0.1490 0.2388 0.0000 C 0 0 2 0 0 0\n 1.2170 -0.8145 0.0000 C 0 0 2 0 0 0\n 0.5452 -2.1557 0.0000 C 0 0 1 0 0 0\n -0.9379 -1.9313 0.0000 O 0 0\n -2.5210 0.2223 0.0000 C 0 0\n 0.3701 1.7207 0.0000 N 0 0\n -2.6077 1.7207 0.0000 O 0 0\n -3.9475 2.3952 0.0000 R# 0 0\n 1.7652 2.2716 0.0000 R# 0 0\n 1.2354 -3.4875 0.0000 R# 0 0\n 2.6946 -0.5669 0.0000 O 0 0\n 3.2204 0.8380 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\n 3 12 1 1\n 12 13 1 0\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n3-Deoxy-3-amino-2-O-methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn3m\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Deoxy-3-amino-2-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6450 -0.4268 0.0000 C 0 0 2 0 0 0\n 0.6867 0.2634 0.0000 C 0 0 2 0 0 0\n 1.7547 -0.7899 0.0000 C 0 0\n 1.0830 -2.1310 0.0000 C 0 0 1 0 0 0\n -0.4002 -1.9066 0.0000 O 0 0\n -1.9833 0.2470 0.0000 C 0 0\n 0.9078 1.7453 0.0000 N 0 0\n 2.3029 2.2963 0.0000 R# 0 0\n 1.7731 -3.4628 0.0000 R# 0 0\n -2.0700 1.7453 0.0000 O 0 0\n -3.4098 2.4198 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 6 10 1 0\n 10 11 1 0\nM RGP 3 8 2 9 3 11 1\nM END\n> <Name>\n3-Deoxy-3-amino-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn3d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Deoxy-3-amino-2-fluororibose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.9146 -0.3813 0.0000 C 0 0 2 0 0 0\n 0.4172 0.3089 0.0000 C 0 0 2 0 0 0\n 1.4851 -0.7445 0.0000 C 0 0 2 0 0 0\n 0.8134 -2.0856 0.0000 C 0 0 1 0 0 0\n -0.6697 -1.8612 0.0000 O 0 0\n -2.2528 0.2924 0.0000 C 0 0\n 0.6383 1.7907 0.0000 N 0 0\n 2.0334 2.3417 0.0000 R# 0 0\n 1.5036 -3.4174 0.0000 R# 0 0\n 2.9650 -0.4996 0.0000 F 0 0\n -2.3396 1.7907 0.0000 O 0 0\n -3.6793 2.4652 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 3 10 1 1\n 6 11 1 0\n 11 12 1 0\nM RGP 3 8 2 9 3 12 1\nM END\n> <Name>\n3-Deoxy-3-amino-2-fluororibose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn3fl2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Deoxy-3-amino-4-carboxyl-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6576 0.1670 0.0000 C 0 0 2 0 0 0\n 0.8424 0.1670 0.0000 C 0 0 2 0 0 0\n 1.3059 -1.2595 0.0000 C 0 0\n 0.0924 -2.1412 0.0000 C 0 0 1 0 0 0\n -1.1212 -1.2595 0.0000 O 0 0\n -1.5358 1.3810 0.0000 C 0 0\n 1.7205 1.3810 0.0000 N 0 0\n -3.0278 1.2268 0.0000 R# 0 0\n 3.2127 1.2282 0.0000 R# 0 0\n 0.0924 -3.6412 0.0000 R# 0 0\n -0.9237 2.7504 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 7 9 1 0\n 4 10 1 6\n 6 11 2 0\nM RGP 3 8 1 9 2 10 3\nM END\n> <Name>\n3-Deoxy-3-amino-4-carboxyl-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn3co4d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Deoxy-3-methylene-2-O-methylribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.1828 -0.4514 0.0000 C 0 0 2 0 0 0\n 0.1490 0.2388 0.0000 C 0 0 2 0 0 0\n 1.2170 -0.8145 0.0000 C 0 0 2 0 0 0\n 0.5452 -2.1557 0.0000 C 0 0 1 0 0 0\n -0.9379 -1.9313 0.0000 O 0 0\n -2.5210 0.2223 0.0000 C 0 0\n 0.3701 1.7207 0.0000 C 0 0\n -2.6077 1.7207 0.0000 O 0 0\n -3.9475 2.3952 0.0000 R# 0 0\n 1.7652 2.2716 0.0000 R# 0 0\n 1.2354 -3.4875 0.0000 R# 0 0\n 2.6946 -0.5669 0.0000 O 0 0\n 3.2204 0.8380 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\n 3 12 1 1\n 12 13 1 0\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n3-Deoxy-3-methylene-2-O-methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nme3m\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\n3-Deoxy-3-methylene-2-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6450 -0.4268 0.0000 C 0 0 2 0 0 0\n 0.6867 0.2634 0.0000 C 0 0 2 0 0 0\n 1.7547 -0.7899 0.0000 C 0 0\n 1.0830 -2.1310 0.0000 C 0 0 1 0 0 0\n -0.4002 -1.9066 0.0000 O 0 0\n -1.9833 0.2470 0.0000 C 0 0\n 0.9078 1.7453 0.0000 C 0 0\n 2.3029 2.2963 0.0000 R# 0 0\n 1.7731 -3.4628 0.0000 R# 0 0\n -2.0700 1.7453 0.0000 O 0 0\n -3.4098 2.4198 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 6 10 1 0\n 10 11 1 0\nM RGP 3 8 2 9 3 11 1\nM END\n> <Name>\n3-Deoxy-3-methylene-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nme3d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\n3-Deoxy-3-methylene-2-fluororibose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.9146 -0.3813 0.0000 C 0 0 2 0 0 0\n 0.4172 0.3089 0.0000 C 0 0 2 0 0 0\n 1.4851 -0.7445 0.0000 C 0 0 2 0 0 0\n 0.8134 -2.0856 0.0000 C 0 0 1 0 0 0\n -0.6697 -1.8612 0.0000 O 0 0\n -2.2528 0.2924 0.0000 C 0 0\n 0.6383 1.7907 0.0000 C 0 0\n -2.3396 1.7907 0.0000 O 0 0\n -3.6793 2.4652 0.0000 R# 0 0\n 2.0334 2.3417 0.0000 R# 0 0\n 1.5036 -3.4174 0.0000 R# 0 0\n 2.9650 -0.4996 0.0000 F 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\n 3 12 1 1\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n3-Deoxy-3-methylene-2-fluororibose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nme3fl2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\n3-Deoxy-3-methyleneribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.9146 -0.3813 0.0000 C 0 0 2 0 0 0\n 0.4172 0.3089 0.0000 C 0 0 2 0 0 0\n 1.4851 -0.7445 0.0000 C 0 0 2 0 0 0\n 0.8134 -2.0856 0.0000 C 0 0 1 0 0 0\n -0.6697 -1.8612 0.0000 O 0 0\n -2.2528 0.2924 0.0000 C 0 0\n 0.6383 1.7907 0.0000 C 0 0\n -2.3396 1.7907 0.0000 O 0 0\n -3.6793 2.4652 0.0000 R# 0 0\n 2.0334 2.3417 0.0000 R# 0 0\n 1.5036 -3.4174 0.0000 R# 0 0\n 2.9650 -0.4996 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\n 3 12 1 1\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n3-Deoxy-3-methyleneribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nme3r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\n3-Deoxy-3-thio-2-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6450 -0.4268 0.0000 C 0 0 2 0 0 0\n 0.6867 0.2634 0.0000 C 0 0 2 0 0 0\n 1.7547 -0.7899 0.0000 C 0 0\n 1.0830 -2.1310 0.0000 C 0 0 1 0 0 0\n -0.4002 -1.9066 0.0000 O 0 0\n -1.9833 0.2470 0.0000 C 0 0\n 0.9078 1.7453 0.0000 S 0 0\n -2.0700 1.7453 0.0000 O 0 0\n -3.4098 2.4198 0.0000 R# 0 0\n 2.3029 2.2963 0.0000 R# 0 0\n 1.7731 -3.4628 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n3-Deoxy-3-thio-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns3d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Deoxyribose (2,5 connectivity)\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -1.0009 -0.2740 0.0000 C 0 0 2 0 0 0\n -0.0525 0.8882 0.0000 C 0 0\n 1.3458 0.3453 0.0000 C 0 0 2 0 0 0\n 1.2616 -1.1523 0.0000 C 0 0 1 0 0 0\n -0.1887 -1.5350 0.0000 O 0 0\n 2.6071 1.1540 0.0000 O 0 0\n -2.4966 -0.1868 0.0000 C 0 0\n 2.4238 -2.1007 0.0000 R# 0 0\n 3.9400 0.4660 0.0000 R# 0 0\n -3.1710 1.1540 0.0000 O 0 0\n -4.6685 1.2412 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 0\n 3 6 1 1\n 1 7 1 6\n 4 8 1 6\n 3 2 1 0\n 6 9 1 0\n 7 10 1 0\n 10 11 1 0\nM RGP 3 8 3 9 2 11 1\nM END\n> <Name>\n3-Deoxyribose (2,5 connectivity)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n25d3r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Fluoro HNA\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.5573 -0.8976 0.0000 O 0 0\n -0.8058 0.4006 0.0000 C 0 0 1 0 0 0\n 0.6942 0.3989 0.0000 C 0 0 2 0 0 0\n 1.4427 -0.9010 0.0000 C 0 0 2 0 0 0\n 0.6912 -2.1992 0.0000 C 0 0 1 0 0 0\n -0.8088 -2.1975 0.0000 C 0 0\n 1.4396 -3.4991 0.0000 R# 0 0\n 2.9427 -0.9028 0.0000 F 0 0\n 1.4434 1.6993 0.0000 O 0 0\n -1.5574 1.6997 0.0000 C 0 0\n 2.9434 1.7016 0.0000 R# 0 0\n -3.0582 1.6993 0.0000 O 0 0\n -3.8094 2.9977 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 6\n 4 8 1 1\n 3 9 1 1\n 2 10 1 6\n 9 11 1 0\n 10 12 1 0\n 12 13 1 0\nM RGP 3 7 3 11 2 13 1\nM END\n> <Name>\n3-Fluoro HNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfhna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Methyl-alpha-L-LNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -0.4476 -0.4896 0.0000 C 0 0 2 0 0 0\n -0.0232 0.8433 0.0000 C 0 0 1 0 0 0\n 0.6412 -1.3962 0.0000 C 0 0 1 0 0 0\n 2.0234 -1.3733 0.0000 C 0 0 1 0 0 0\n 1.0122 -0.4208 0.0000 O 0 0\n 1.2845 1.6145 0.0000 O 0 0\n 3.4222 -1.9149 0.0000 R# 0 0\n 2.5763 0.8521 0.0000 R# 0 0\n -1.5203 -1.1722 0.0000 C 0 0\n -0.5300 -2.1308 0.0000 O 0 0\n -1.8131 0.1227 0.0000 C 0 0\n -1.9766 1.6145 0.0000 O 0 0\n -3.3492 2.2194 0.0000 R# 0 0\n -1.2996 1.6312 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 0\n 4 7 1 1\n 6 8 1 0\n 1 9 1 0\n 3 10 1 1\n 9 10 1 0\n 1 11 1 1\n 11 12 1 0\n 12 13 1 0\n 2 14 1 1\nM RGP 3 7 3 8 2 13 1\nM END\n> <Name>\n3-Methyl-alpha-L-LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm3ALln\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Methylcytosine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 2.7991 0.0000 N 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 0.2010 0.0000 C 0 0\n 8.5981 1.5000 0.0000 N 0 0\n 7.0981 4.0981 0.0000 C 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 4.0981 4.0981 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 2 0\n 5 7 2 0\n 4 8 1 0\n 2 9 1 0\n 1 10 2 0\nM RGP 1 9 1\nM END\n> <Name>\n3-Methylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm3C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n3-Methyluracil\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 2.2500 -4.2990 0.0000 C 0 0\n 3.7500 -4.2990 0.0000 C 0 0\n 4.5000 -3.0000 0.0000 C 0 0\n 3.7500 -1.7010 0.0000 N 0 0\n 2.2500 -1.7010 0.0000 C 0 0\n 1.5000 -3.0000 0.0000 N 0 0\n 4.5000 -0.4019 0.0000 C 0 0\n 4.5000 -5.5981 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 6.0000 -3.0000 0.0000 O 0 0\n 1.5000 -0.4019 0.0000 O 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 4 7 1 0\n 2 8 1 0\n 6 9 1 0\n 3 10 2 0\n 5 11 2 0\nM RGP 1 9 1\nM END\n> <Name>\n3-Methyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm3U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n3-N-(p-Methoxybenzyl)thymine\n SciTegic07272112182D\n\n 19 20 0 0 0 0 999 V2000\n 0.0000 3.0000 0.0000 R# 0 0\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 O 0 0\n -2.5981 -1.5000 0.0000 C 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 2.5951 -3.0039 0.0000 C 0 0\n 3.8915 -3.7585 0.0000 C 0 0\n 3.8864 -5.2585 0.0000 C 0 0\n 2.5847 -6.0040 0.0000 C 0 0\n 1.2883 -5.2495 0.0000 C 0 0\n 1.2935 -3.7495 0.0000 C 0 0\n 2.5765 -7.5048 0.0000 O 0 0\n 1.2738 -8.2484 0.0000 C 0 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 2 7 1 0\n 7 8 2 0\n 3 9 2 0\n 6 10 1 0\n 1 4 1 0\n 2 11 1 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 15 2 0\n 15 16 1 0\n 16 17 2 0\n 17 12 1 0\n 15 18 1 0\n 18 19 1 0\nM RGP 1 1 1\nM END\n> <Name>\n3-N-(p-Methoxybenzyl)thymine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmo4bn3\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n3-O-FEt ANA\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.4844 -1.0542 0.0000 O 0 0\n -1.7329 0.2440 0.0000 C 0 0 1 0 0 0\n -0.2329 0.2423 0.0000 C 0 0 2 0 0 0\n 0.5156 -1.0576 0.0000 C 0 0 2 0 0 0\n -0.2359 -2.3558 0.0000 C 0 0 1 0 0 0\n -1.7359 -2.3541 0.0000 C 0 0\n 0.5126 -3.6557 0.0000 R# 0 0\n 2.0164 -1.0563 0.0000 O 0 0\n 0.5164 1.5427 0.0000 O 0 0\n -2.4845 1.5431 0.0000 C 0 0\n 2.0164 1.5450 0.0000 R# 0 0\n 2.7665 0.2437 0.0000 C 0 0\n 4.2673 0.2450 0.0000 C 0 0\n 5.0170 1.5442 0.0000 F 0 0\n -3.9853 1.5427 0.0000 O 0 0\n -4.7365 2.8411 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 6\n 4 8 1 1\n 3 9 1 1\n 2 10 1 6\n 9 11 1 0\n 8 12 1 0\n 12 13 1 0\n 13 14 1 0\n 10 15 1 0\n 15 16 1 0\nM RGP 3 7 3 11 2 16 1\nM END\n> <Name>\n3-O-FEt ANA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfleana\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-O-MOE-ANA\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.8678 -1.1452 0.0000 O 0 0\n -2.1163 0.1530 0.0000 C 0 0 1 0 0 0\n -0.6163 0.1513 0.0000 C 0 0 2 0 0 0\n 0.1322 -1.1486 0.0000 C 0 0 2 0 0 0\n -0.6193 -2.4468 0.0000 C 0 0 1 0 0 0\n -2.1193 -2.4451 0.0000 C 0 0\n 0.1292 -3.7467 0.0000 R# 0 0\n 0.1330 1.4517 0.0000 O 0 0\n -2.8679 1.4521 0.0000 C 0 0\n 1.6330 1.4540 0.0000 R# 0 0\n 1.6330 -1.1473 0.0000 O 0 0\n 2.3831 0.1527 0.0000 C 0 0\n 3.8839 0.1540 0.0000 C 0 0\n 4.6340 1.4540 0.0000 O 0 0\n 6.1340 1.4553 0.0000 C 0 0\n -4.3687 1.4517 0.0000 O 0 0\n -5.1199 2.7501 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 6\n 4 11 1 1\n 3 8 1 1\n 2 9 1 6\n 8 10 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 9 16 1 0\n 16 17 1 0\nM RGP 3 7 3 10 2 17 1\nM END\n> <Name>\n3-O-MOE-ANA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmoe3an\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-O-Methyl-ANA\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -1.8212 -0.9263 0.0000 O 0 0\n -1.0697 0.3719 0.0000 C 0 0 1 0 0 0\n 0.4303 0.3701 0.0000 C 0 0 2 0 0 0\n 1.1788 -0.9298 0.0000 C 0 0 2 0 0 0\n 0.4273 -2.2280 0.0000 C 0 0 1 0 0 0\n -1.0727 -2.2262 0.0000 C 0 0\n 1.1758 -3.5279 0.0000 R# 0 0\n 2.6796 -0.9284 0.0000 O 0 0\n 1.1796 1.6706 0.0000 O 0 0\n -1.8213 1.6709 0.0000 C 0 0\n 2.6796 1.6728 0.0000 R# 0 0\n 3.4293 0.3708 0.0000 C 0 0\n -3.3221 1.6706 0.0000 O 0 0\n -4.0733 2.9689 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 6\n 4 8 1 1\n 3 9 1 1\n 2 10 1 6\n 9 11 1 0\n 8 12 1 0\n 10 13 1 0\n 13 14 1 0\nM RGP 3 7 3 11 2 14 1\nM END\n> <Name>\n3-O-Methyl-ANA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm3ana\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-O-methoxyethyl ribose (2,5 connectivity)\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -0.2254 -1.5142 0.0000 C 0 0 2 0 0 0\n 0.7240 -0.3530 0.0000 C 0 0 2 0 0 0\n 2.1218 -0.8971 0.0000 C 0 0 2 0 0 0\n 2.0363 -2.3946 0.0000 C 0 0 1 0 0 0\n 0.5856 -2.7761 0.0000 O 0 0\n -1.7211 -1.4257 0.0000 C 0 0\n 0.3400 1.0952 0.0000 O 0 0\n -1.1084 1.4884 0.0000 C 0 0\n 3.3805 -0.0843 0.0000 O 0 0\n 3.1976 -3.3441 0.0000 R# 0 0\n 4.7156 -0.7679 0.0000 R# 0 0\n -1.4931 2.9391 0.0000 C 0 0\n -2.9415 3.3322 0.0000 O 0 0\n -3.3260 4.7821 0.0000 C 0 0\n -2.3942 -0.0843 0.0000 O 0 0\n -3.8916 0.0043 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 3 9 1 1\n 4 10 1 6\n 9 11 1 0\n 8 12 1 0\n 12 13 1 0\n 13 14 1 0\n 6 15 1 0\n 15 16 1 0\nM RGP 3 10 3 11 2 16 1\nM END\n> <Name>\n3-O-methoxyethyl ribose (2,5 connectivity)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n25moe3\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-ara FHNA\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.5573 -0.8976 0.0000 O 0 0\n -0.8058 0.4006 0.0000 C 0 0 1 0 0 0\n 0.6942 0.3989 0.0000 C 0 0 2 0 0 0\n 1.4427 -0.9010 0.0000 C 0 0 1 0 0 0\n 0.6912 -2.1992 0.0000 C 0 0 1 0 0 0\n -0.8088 -2.1975 0.0000 C 0 0\n 1.4396 -3.4991 0.0000 R# 0 0\n 2.9427 -0.9028 0.0000 F 0 0\n 1.4434 1.6993 0.0000 O 0 0\n -1.5574 1.6997 0.0000 C 0 0\n 2.9434 1.7016 0.0000 R# 0 0\n -3.0582 1.6993 0.0000 O 0 0\n -3.8094 2.9977 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 6\n 4 8 1 6\n 3 9 1 1\n 2 10 1 6\n 9 11 1 0\n 10 12 1 0\n 12 13 1 0\nM RGP 3 7 3 11 2 13 1\nM END\n> <Name>\n3-ara FHNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nafhna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-beta-C-Methyl-2-deoxyribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.3033 -0.5714 0.0000 C 0 0 2 0 0 0\n 0.7136 0.5313 0.0000 C 0 0 2 0 0 0\n 2.0766 -0.0951 0.0000 C 0 0\n 1.9020 -1.5850 0.0000 C 0 0 1 0 0 0\n 0.4312 -1.8793 0.0000 O 0 0\n -0.7029 0.9851 0.0000 O 0 0\n -1.7910 -0.3940 0.0000 C 0 0\n 3.0047 -2.6019 0.0000 R# 0 0\n -0.9309 1.9588 0.0000 R# 0 0\n 1.8558 1.5036 0.0000 C 0 0\n -2.3831 0.9851 0.0000 O 0 0\n -3.8725 1.1628 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 0\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 2 10 1 6\n 7 11 1 0\n 11 12 1 0\nM RGP 3 8 3 9 2 12 1\nM END\n> <Name>\n3-beta-C-Methyl-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nBcm3d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-beta-C-Methylribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.5636 -0.6206 0.0000 C 0 0 2 0 0 0\n 0.4533 0.4821 0.0000 C 0 0 2 0 0 0\n 1.8162 -0.1443 0.0000 C 0 0 2 0 0 0\n 1.6417 -1.6341 0.0000 C 0 0 1 0 0 0\n 0.1708 -1.9285 0.0000 O 0 0\n -0.9633 0.9359 0.0000 O 0 0\n -2.0514 -0.4432 0.0000 C 0 0\n 2.7443 -2.6510 0.0000 R# 0 0\n -2.6434 0.9359 0.0000 O 0 0\n -4.1329 1.1136 0.0000 R# 0 0\n -1.1912 1.9096 0.0000 R# 0 0\n 1.5954 1.4544 0.0000 C 0 0\n 3.1241 0.5901 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 0\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 2 12 1 6\n 3 13 1 1\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n3-beta-C-Methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nBcm3r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n4,5,6-Trihydrouracil\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.5981 -1.5000 0.0000 R# 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 0\n 6 8 2 0\n 2 9 1 0\nM RGP 1 7 1\nM END\n> <Name>\n4,5,6-Trihydrouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nh456U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n4-Acetylamino-2-deoxyribose\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -0.2580 0.2861 0.0000 C 0 0 2 0 0 0\n 1.0738 0.9763 0.0000 C 0 0 2 0 0 0\n 2.1417 -0.0770 0.0000 C 0 0\n 1.4700 -1.4182 0.0000 C 0 0 1 0 0 0\n -0.0131 -1.1938 0.0000 N 0 0\n 1.2949 2.4582 0.0000 O 0 0\n -1.5962 0.9598 0.0000 C 0 0\n 2.1602 -2.7500 0.0000 R# 0 0\n -1.6830 2.4582 0.0000 O 0 0\n -3.0227 3.1327 0.0000 R# 0 0\n 2.6900 3.0092 0.0000 R# 0 0\n -1.0674 -2.2583 0.0000 C 0 0\n -0.6717 -3.7052 0.0000 C 0 0\n -2.5184 -1.8780 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 5 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n4-Acetylamino-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nacn4d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n4-Acetylcytosine\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -2.5981 -1.5000 0.0000 R# 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5972 1.5031 0.0000 N 0 0\n 2.5951 3.0039 0.0000 C 0 0\n 1.2948 3.7517 0.0000 C 0 0\n 3.8926 3.7566 0.0000 O 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 4 8 2 0\n 2 9 1 0\n 9 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 1 7 1\nM END\n> <Name>\n4-Acetylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nac4C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n4-Cyanoethylthiothymidine\n SciTegic07272112182D\n\n 14 14 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 C 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 N 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0008 2.9969 0.0000 S 0 0\n 1.5000 0.4019 0.0000 O 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 4.5000 5.5981 0.0000 C 0 0\n 6.7494 1.6961 0.0000 C 0 0\n 8.2502 1.6930 0.0000 C 0 0\n 8.9988 0.3922 0.0000 C 0 0\n 9.7469 -0.9079 0.0000 N 0 0\n 13 14 3 0\n 1 2 2 0\n 3 4 1 0\n 4 5 2 0\n 1 5 1 0\n 5 6 1 0\n 3 7 2 0\n 2 8 1 0\n 3 8 1 0\n 8 9 1 0\n 1 10 1 0\n 6 11 1 0\n 11 12 1 0\n 12 13 1 0\nM RGP 1 9 1\nM END\n> <Name>\n4-Cyanoethylthiothymidine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncnes4T\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n4-Deoxouracil\n SciTegic07272112182D\n\n 8 8 0 0 0 0 999 V2000\n 2.2500 -4.2990 0.0000 C 0 0\n 3.7500 -4.2990 0.0000 C 0 0\n 4.5000 -3.0000 0.0000 C 0 0\n 1.5000 -3.0000 0.0000 N 0 0\n 2.2500 -1.7010 0.0000 C 0 0\n 3.7500 -1.7010 0.0000 N 0 0\n 1.5000 -0.4019 0.0000 O 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 2 0\n 5 7 2 0\n 4 8 1 0\nM RGP 1 8 1\nM END\n> <Name>\n4-Deoxouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nd4U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n4-Hexan-6-ol-5-methylcytosine\n SciTegic07272112182D\n\n 18 18 0 0 0 0 999 V2000\n -4.9930 -0.8266 0.0000 C 0 0\n -3.6174 -1.4246 0.0000 C 0 0\n -2.4117 -0.5323 0.0000 C 0 0\n -2.5816 0.9581 0.0000 N 0 0\n -3.9572 1.5561 0.0000 C 0 0\n -4.1271 3.0464 0.0000 O 0 0\n -1.0340 -1.1278 0.0000 N 0 0\n -5.1629 0.6638 0.0000 N 0 0\n -3.4475 -2.9150 0.0000 C 0 0\n -6.5386 1.2618 0.0000 R# 0 0\n 0.1711 -0.2333 0.0000 C 0 0\n 1.5487 -0.8288 0.0000 C 0 0\n 2.7538 0.0657 0.0000 C 0 0\n 4.1314 -0.5298 0.0000 C 0 0\n 5.3365 0.3647 0.0000 C 0 0\n 6.7141 -0.2308 0.0000 C 0 0\n 7.9193 0.6638 0.0000 O 0 0\n 9.2961 0.0686 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 3 7 1 0\n 8 1 1 0\n 8 5 1 0\n 2 9 1 0\n 8 10 1 0\n 7 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\nM RGP 2 10 1 18 2\nM END\n> <Name>\n4-Hexan-6-ol-5-methylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noC64m5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n4-Methylcytosine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 2.5981 1.5000 0.0000 O 0 0\n -0.0031 -3.0008 0.0000 N 0 0\n -1.3032 -3.7490 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 3 1 0\n 3 7 1 0\n 2 8 2 0\n 4 9 1 0\n 9 10 1 0\nM RGP 1 7 1\nM END\n> <Name>\n4-Methylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm4C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n4-N-Hydroxcytosine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n 2.5981 1.5000 0.0000 O 0 0\n -0.0031 -3.0008 0.0000 N 0 0\n -1.3032 -3.7490 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 3 1 0\n 2 7 2 0\n 4 8 1 0\n 8 9 1 0\n 3 10 1 0\nM RGP 1 10 1\nM END\n> <Name>\n4-N-Hydroxcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noh4C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n4-Thio-2-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6450 -0.4268 0.0000 C 0 0 2 0 0 0\n 0.6867 0.2634 0.0000 C 0 0 2 0 0 0\n 1.7547 -0.7899 0.0000 C 0 0\n 1.0830 -2.1310 0.0000 C 0 0 1 0 0 0\n -0.4002 -1.9066 0.0000 S 0 0\n -1.9833 0.2470 0.0000 C 0 0\n 0.9078 1.7453 0.0000 O 0 0\n 2.3029 2.2963 0.0000 R# 0 0\n 1.7731 -3.4628 0.0000 R# 0 0\n -2.0700 1.7453 0.0000 O 0 0\n -3.4098 2.4198 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 6 10 1 0\n 10 11 1 0\nM RGP 3 8 2 9 3 11 1\nM END\n> <Name>\n4-Thio-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns4d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n4-Thiothymidine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 S 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5000 0.4019 0.0000 C 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 2 8 2 0\n 5 9 1 0\n 3 10 1 0\nM RGP 1 10 1\nM END\n> <Name>\n4-Thiothymidine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns4T\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n4-Thiouracil\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 C 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 N 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 S 0 0\n 1.5000 0.4019 0.0000 O 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1 2 2 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 0\n 5 6 2 0\n 3 7 2 0\n 2 8 1 0\n 3 8 1 0\n 8 9 1 0\nM RGP 1 9 1\nM END\n> <Name>\n4-Thiouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns4U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5,6-Dihydrothymine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 7.0981 4.0981 0.0000 C 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 2 0\n 3 8 2 0\n 6 9 1 0\n 2 10 1 0\nM RGP 1 10 1\nM END\n> <Name>\n5,6-Dihydrothymine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nh56T\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5,6-Dimethyluracil\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 1.5000 0.4019 0.0000 C 0 0\n 4.5000 0.4019 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 4 10 1 0\n 5 11 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5,6-Dimethyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm6T\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5,6-Propylene uracil\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.2135 0.2752 0.0000 C 0 0\n 3.0000 -0.6065 0.0000 C 0 0\n 1.7865 0.2752 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\n 4 12 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5,6-Propylene uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\npr56U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-(2-Bromovinyl)uracil\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 7.0958 4.1004 0.0000 C 0 0\n 6.3436 5.3990 0.0000 C 0 0\n 7.0909 6.6996 0.0000 Br 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 4 7 1 0\n 7 8 2 0\n 8 9 1 0\n 3 10 2 0\n 5 11 2 0\n 2 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n5-(2-Bromovinyl)uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbrviny\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-(Propargylamine)cytosine\n SciTegic07272112182D\n\n 13 13 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 N 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5004 0.4012 0.0000 C 0 0\n 5.2508 -0.8985 0.0000 C 0 0\n 6.0012 -2.1983 0.0000 C 0 0\n 5.2520 -3.4978 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 6 7 1 0\n 2 8 2 0\n 5 9 1 0\n 9 10 3 0\n 10 11 1 0\n 11 12 1 0\n 3 13 1 0\nM RGP 1 13 1\nM END\n> <Name>\n5-(Propargylamine)cytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnpry5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-(R)-Methyl-(R)-cEt BNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 0.3816 -2.3581 0.0000 C 0 0 1 0 0 0\n 0.7121 -1.0088 0.0000 O 0 0\n -0.3195 -1.1665 0.0000 C 0 0 1 0 0 0\n 1.3019 0.5151 0.0000 C 0 0 2 0 0 0\n -0.0669 0.2276 0.0000 C 0 0 2 0 0 0\n -1.1895 0.8248 0.0000 C 0 0 1 0 0 0\n -1.5357 -0.5094 0.0000 O 0 0\n 2.6434 1.1422 0.0000 O 0 0\n -1.1965 0.0610 0.0000 C 0 0 1 0 0 0\n -1.7929 2.1980 0.0000 R# 0 0\n -2.6880 -0.0977 0.0000 C 0 0\n 3.8764 0.2879 0.0000 R# 0 0\n -0.1556 1.1422 0.0000 O 0 0\n 0.5995 -3.8421 0.0000 C 0 0\n -0.5704 2.5837 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 6\n 4 8 1 6\n 3 9 1 0\n 6 10 1 1\n 9 11 1 1\n 3 1 1 0\n 5 2 1 1\n 8 12 1 0\n 9 13 1 0\n 1 14 1 6\n 13 15 1 0\nM RGP 3 10 3 12 2 15 1\nM END\n> <Name>\n5-(R)-Methyl-(R)-cEt BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5R6Rm5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-(R)-Methyl-(S)-cEt BNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 0.3816 -2.3581 0.0000 C 0 0 2 0 0 0\n 0.7121 -1.0088 0.0000 O 0 0\n -0.3195 -1.1665 0.0000 C 0 0 1 0 0 0\n 1.3019 0.5151 0.0000 C 0 0 2 0 0 0\n -0.0669 0.2276 0.0000 C 0 0 2 0 0 0\n -1.1895 0.8248 0.0000 C 0 0 1 0 0 0\n -1.5357 -0.5094 0.0000 O 0 0\n 2.6434 1.1422 0.0000 O 0 0\n -1.1965 0.0610 0.0000 C 0 0 1 0 0 0\n -1.7929 2.1980 0.0000 R# 0 0\n -2.6880 -0.0977 0.0000 C 0 0\n 3.8764 0.2879 0.0000 R# 0 0\n -0.1556 1.1422 0.0000 O 0 0\n 0.5995 -3.8421 0.0000 C 0 0\n -0.5704 2.5837 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 6\n 4 8 1 6\n 3 9 1 0\n 6 10 1 1\n 9 11 1 1\n 3 1 1 0\n 5 2 1 1\n 8 12 1 0\n 9 13 1 0\n 1 14 1 1\n 13 15 1 0\nM RGP 3 10 3 12 2 15 1\nM END\n> <Name>\n5-(R)-Methyl-(S)-cEt BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5R6Sm5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-(S)-Methyl-(R)-cEt BNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 0.3816 -2.3581 0.0000 C 0 0 1 0 0 0\n 0.7121 -1.0088 0.0000 O 0 0\n -0.3195 -1.1665 0.0000 C 0 0 1 0 0 0\n 1.3019 0.5151 0.0000 C 0 0 2 0 0 0\n -0.0669 0.2276 0.0000 C 0 0 2 0 0 0\n -1.1895 0.8248 0.0000 C 0 0 1 0 0 0\n -1.5357 -0.5094 0.0000 O 0 0\n 2.6434 1.1422 0.0000 O 0 0\n -1.1965 0.0610 0.0000 C 0 0 2 0 0 0\n -1.7929 2.1980 0.0000 R# 0 0\n -2.6880 -0.0977 0.0000 C 0 0\n 3.8764 0.2879 0.0000 R# 0 0\n -0.1556 1.1422 0.0000 O 0 0\n 0.5995 -3.8421 0.0000 C 0 0\n -0.5704 2.5837 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 6\n 4 8 1 6\n 3 9 1 0\n 6 10 1 1\n 9 11 1 6\n 3 1 1 0\n 5 2 1 1\n 8 12 1 0\n 9 13 1 0\n 1 14 1 6\n 13 15 1 0\nM RGP 3 10 3 12 2 15 1\nM END\n> <Name>\n5-(S)-Methyl-(R)-cEt BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5S6Rm5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-(S)-Methyl-(S)-cEt BNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 0.3816 -2.3581 0.0000 C 0 0 2 0 0 0\n 0.7121 -1.0088 0.0000 O 0 0\n -0.3195 -1.1665 0.0000 C 0 0 1 0 0 0\n 1.3019 0.5151 0.0000 C 0 0 2 0 0 0\n -0.0669 0.2276 0.0000 C 0 0 2 0 0 0\n -1.1895 0.8248 0.0000 C 0 0 1 0 0 0\n -1.5357 -0.5094 0.0000 O 0 0\n 2.6434 1.1422 0.0000 O 0 0\n -1.1965 0.0610 0.0000 C 0 0 2 0 0 0\n -1.7929 2.1980 0.0000 R# 0 0\n -2.6880 -0.0977 0.0000 C 0 0\n 3.8764 0.2879 0.0000 R# 0 0\n -0.1556 1.1422 0.0000 O 0 0\n 0.5995 -3.8421 0.0000 C 0 0\n -0.5704 2.5837 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 6\n 4 8 1 6\n 3 9 1 0\n 6 10 1 1\n 9 11 1 6\n 3 1 1 0\n 5 2 1 1\n 8 12 1 0\n 9 13 1 0\n 1 14 1 1\n 13 15 1 0\nM RGP 3 10 3 12 2 15 1\nM END\n> <Name>\n5-(S)-Methyl-(S)-cEt BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5S6Sm5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Allyluracil\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 7.0958 4.1004 0.0000 C 0 0\n 6.3436 5.3990 0.0000 C 0 0\n 7.0909 6.6996 0.0000 C 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 2 7 1 0\n 4 8 1 0\n 8 9 1 0\n 9 10 2 0\n 5 11 2 0\n 3 12 2 0\nM RGP 1 7 1\nM END\n> <Name>\n5-Allyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nallyl5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Aminohexylcytosine\n SciTegic07272112182D\n\n 16 16 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.4977 0.3997 0.0000 C 0 0\n 3.7455 -0.8990 0.0000 C 0 0\n 4.4932 -2.2003 0.0000 C 0 0\n 3.7409 -3.4990 0.0000 C 0 0\n 4.4887 -4.8003 0.0000 C 0 0\n 3.7364 -6.0990 0.0000 C 0 0\n 4.4837 -7.3996 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 6 7 1 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5-Aminohexylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnC65C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Aminohexyluracil\n SciTegic07272112182D\n\n 17 17 0 0 0 0 999 V2000\n -4.2493 1.5455 0.0000 N 0 0\n -4.6630 0.1037 0.0000 C 0 0\n -3.6212 -0.9755 0.0000 N 0 0\n -2.1657 -0.6129 0.0000 C 0 0\n -1.7520 0.8289 0.0000 C 0 0\n -2.7938 1.9081 0.0000 C 0 0\n -2.3801 3.3499 0.0000 O 0 0\n -4.0349 -2.4173 0.0000 R# 0 0\n -6.1185 -0.2590 0.0000 O 0 0\n -0.2949 1.1888 0.0000 C 0 0\n 0.7459 0.1075 0.0000 C 0 0\n 2.2030 0.4673 0.0000 C 0 0\n 3.2438 -0.6139 0.0000 C 0 0\n 4.7009 -0.2541 0.0000 C 0 0\n 5.7417 -1.3354 0.0000 C 0 0\n 7.1988 -0.9755 0.0000 N 0 0\n 8.2390 -2.0562 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\nM RGP 2 8 1 17 2\nM END\n> <Name>\n5-Aminohexyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnC65U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n5-Aminopropyluracil\n SciTegic07272112182D\n\n 13 13 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.4977 0.3997 0.0000 C 0 0\n 3.7455 -0.8990 0.0000 C 0 0\n 4.4932 -2.2003 0.0000 C 0 0\n 3.7413 -3.4983 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5-Aminopropyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnpr5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Bromocytosine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5000 0.4019 0.0000 Br 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 6 7 1 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5-Bromocytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbr5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Bromouracil\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5000 0.4019 0.0000 Br 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5-Bromouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbr5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Chlorocytosine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 2.2500 -4.2990 0.0000 C 0 0\n 3.7500 -4.2990 0.0000 C 0 0\n 4.5000 -3.0000 0.0000 C 0 0\n 1.5000 -3.0000 0.0000 N 0 0\n 2.2500 -1.7010 0.0000 C 0 0\n 3.7500 -1.7010 0.0000 N 0 0\n 1.5000 -0.4019 0.0000 O 0 0\n 6.0000 -3.0000 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 4.5000 -5.5981 0.0000 Cl 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 2 0\n 5 7 2 0\n 3 8 1 0\n 4 9 1 0\n 2 10 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-Chlorocytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncl5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Chlorouracil\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 2.2500 -4.2990 0.0000 C 0 0\n 3.7500 -4.2990 0.0000 C 0 0\n 4.5000 -3.0000 0.0000 C 0 0\n 1.5000 -3.0000 0.0000 N 0 0\n 2.2500 -1.7010 0.0000 C 0 0\n 3.7500 -1.7010 0.0000 N 0 0\n 1.5000 -0.4019 0.0000 O 0 0\n 6.0000 -3.0000 0.0000 O 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 4.5000 -5.5981 0.0000 Cl 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 5 7 2 0\n 3 8 2 0\n 4 9 1 0\n 2 10 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-Chlorouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncl5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Cyanouracil\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n 2.5988 1.5004 0.0000 C 0 0\n 0.0000 3.0000 0.0000 O 0 0\n -2.5981 -1.5000 0.0000 O 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 3.8978 2.2504 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 2 7 1 0\n 3 8 2 0\n 5 9 2 0\n 4 10 1 0\n 7 11 3 0\nM RGP 1 10 1\nM END\n> <Name>\n5-Cyanouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nCN5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-DBCO-U (ethylene carbamoyl hexylamino linker)\n SciTegic07272112182D\n\n 45 48 0 0 0 0 999 V2000\n 21.4447 15.6293 0.0000 R# 0 0\n 25.1948 14.3302 0.0000 C 0 0\n 23.6947 14.3302 0.0000 C 0 0\n 22.9447 15.6293 0.0000 N 0 0\n 23.6947 16.9283 0.0000 C 0 0\n 25.1947 16.9283 0.0000 N 0 0\n 25.9447 15.6293 0.0000 C 0 0\n 27.4447 15.6293 0.0000 O 0 0\n 22.9447 18.2274 0.0000 O 0 0\n 25.9425 13.0289 0.0000 C 0 0\n 25.1903 11.7302 0.0000 C 0 0\n 25.9381 10.4289 0.0000 C 0 0\n 27.4381 10.4264 0.0000 O 0 0\n 25.1859 9.1302 0.0000 N 0 0\n 25.9336 7.8289 0.0000 C 0 0\n 25.1814 6.5302 0.0000 C 0 0\n 25.9292 5.2290 0.0000 C 0 0\n 25.1770 3.9303 0.0000 C 0 0\n 25.9247 2.6290 0.0000 C 0 0\n 25.1725 1.3303 0.0000 C 0 0\n 25.9203 0.0290 0.0000 N 0 0\n 25.1681 -1.2697 0.0000 C 0 0\n 25.9158 -2.5710 0.0000 C 0 0\n 23.6681 -1.2671 0.0000 O 0 0\n 25.1636 -3.8697 0.0000 C 0 0\n 25.9114 -5.1709 0.0000 C 0 0\n 25.1591 -6.4696 0.0000 C 0 0\n 25.9069 -7.7709 0.0000 C 0 0\n 25.1529 -9.0726 0.0000 N 0 0\n 27.4069 -7.7735 0.0000 O 0 0\n 23.6665 -8.8717 0.0000 C 0 0\n 22.4733 -9.7808 0.0000 C 0 0\n 22.2724 -11.2673 0.0000 C 0 0\n 25.8611 -11.7522 0.0000 C 0 0\n 26.0620 -10.2658 0.0000 C 0 0\n 21.2841 -8.8633 0.0000 C 0 0\n 19.8963 -9.4325 0.0000 C 0 0\n 19.6954 -10.9190 0.0000 C 0 0\n 20.8823 -11.8362 0.0000 C 0 0\n 27.0504 -12.6698 0.0000 C 0 0\n 28.4381 -12.1005 0.0000 C 0 0\n 28.6390 -10.6140 0.0000 C 0 0\n 27.4521 -9.6968 0.0000 C 0 0\n 24.6680 -12.6613 0.0000 C 0 0\n 23.1815 -12.4604 0.0000 C 0 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 2 7 1 0\n 7 8 2 0\n 1 4 1 0\n 5 9 2 0\n 2 10 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 2 0\n 12 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 19 20 1 0\n 20 21 1 0\n 21 22 1 0\n 22 23 1 0\n 22 24 2 0\n 23 25 1 0\n 25 26 1 0\n 26 27 1 0\n 27 28 1 0\n 28 29 1 0\n 28 30 2 0\n 29 31 1 0\n 31 32 1 0\n 32 33 2 0\n 34 35 2 0\n 35 29 1 0\n 32 36 1 0\n 36 37 2 0\n 37 38 1 0\n 38 39 2 0\n 39 33 1 0\n 34 40 1 0\n 40 41 2 0\n 41 42 1 0\n 42 43 2 0\n 43 35 1 0\n 34 44 1 0\n 44 45 3 0\n 45 33 1 0\nM RGP 1 1 1\nM END\n> <Name>\n5-DBCO-U (ethylene carbamoyl hexylamino linker)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nDBCOnC\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Deoxy-2-O-methylribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.2827 0.5989 0.0000 C 0 0 2 0 0 0\n 0.2173 0.5989 0.0000 C 0 0 2 0 0 0\n 0.6809 -0.8276 0.0000 C 0 0 2 0 0 0\n -0.5327 -1.7093 0.0000 C 0 0 1 0 0 0\n -1.7462 -0.8276 0.0000 O 0 0\n -2.1608 1.8129 0.0000 C 0 0\n 1.0955 1.8129 0.0000 O 0 0\n 2.5877 1.6601 0.0000 R# 0 0\n -0.5327 -3.2093 0.0000 R# 0 0\n 2.1067 -1.2877 0.0000 O 0 0\n 3.2200 -0.2824 0.0000 C 0 0\n -3.6530 1.6601 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 3 10 1 1\n 10 11 1 0\n 6 12 1 0\nM RGP 3 8 2 9 3 12 1\nM END\n> <Name>\n5-Deoxy-2-O-methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nd5m\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Deoxy-2-O-methyoxyethylribose\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -2.4562 0.6440 0.0000 C 0 0 2 0 0 0\n -0.9562 0.6440 0.0000 C 0 0 2 0 0 0\n -0.4927 -0.7826 0.0000 C 0 0 2 0 0 0\n -1.7062 -1.6642 0.0000 C 0 0 1 0 0 0\n -2.9197 -0.7826 0.0000 O 0 0\n -3.3343 1.8580 0.0000 C 0 0\n -0.0781 1.8580 0.0000 O 0 0\n 1.4141 1.7052 0.0000 R# 0 0\n 0.9332 -1.2426 0.0000 O 0 0\n -1.7062 -3.1642 0.0000 R# 0 0\n 2.0471 -0.2367 0.0000 C 0 0\n 3.4754 -0.6975 0.0000 C 0 0\n 4.5893 0.3083 0.0000 O 0 0\n 6.0169 -0.1523 0.0000 C 0 0\n -4.8265 1.7052 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 3 9 1 1\n 4 10 1 6\n 9 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 6 15 1 0\nM RGP 3 8 2 10 3 15 1\nM END\n> <Name>\n5-Deoxy-2-O-methyoxyethylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nd5moe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Deoxy-5-amino-2-O-methylribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.1828 -0.4514 0.0000 C 0 0 2 0 0 0\n 0.1490 0.2388 0.0000 C 0 0 2 0 0 0\n 1.2170 -0.8145 0.0000 C 0 0 2 0 0 0\n 0.5452 -2.1557 0.0000 C 0 0 1 0 0 0\n -0.9379 -1.9313 0.0000 O 0 0\n -2.5210 0.2223 0.0000 C 0 0\n 0.3701 1.7207 0.0000 O 0 0\n -2.6077 1.7207 0.0000 N 0 0\n -3.9475 2.3952 0.0000 R# 0 0\n 1.7652 2.2716 0.0000 R# 0 0\n 1.2354 -3.4875 0.0000 R# 0 0\n 2.6946 -0.5669 0.0000 O 0 0\n 3.2204 0.8380 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\n 3 12 1 1\n 12 13 1 0\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n5-Deoxy-5-amino-2-O-methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn5m\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Deoxy-5-amino-2-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6450 -0.4268 0.0000 C 0 0 2 0 0 0\n 0.6867 0.2634 0.0000 C 0 0 2 0 0 0\n 1.7547 -0.7899 0.0000 C 0 0\n 1.0830 -2.1310 0.0000 C 0 0 1 0 0 0\n -0.4002 -1.9066 0.0000 O 0 0\n -1.9833 0.2470 0.0000 C 0 0\n 0.9078 1.7453 0.0000 O 0 0\n 2.3029 2.2963 0.0000 R# 0 0\n 1.7731 -3.4628 0.0000 R# 0 0\n -2.0700 1.7453 0.0000 N 0 0\n -3.4098 2.4198 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 6 10 1 0\n 10 11 1 0\nM RGP 3 8 2 9 3 11 1\nM END\n> <Name>\n5-Deoxy-5-amino-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn5d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Deoxy-5-amino-2-fluororibose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.9146 -0.3813 0.0000 C 0 0 2 0 0 0\n 0.4172 0.3089 0.0000 C 0 0 2 0 0 0\n 1.4851 -0.7445 0.0000 C 0 0 2 0 0 0\n 0.8134 -2.0856 0.0000 C 0 0 1 0 0 0\n -0.6697 -1.8612 0.0000 O 0 0\n -2.2528 0.2924 0.0000 C 0 0\n 0.6383 1.7907 0.0000 O 0 0\n -2.3396 1.7907 0.0000 N 0 0\n -3.6793 2.4652 0.0000 R# 0 0\n 2.0334 2.3417 0.0000 R# 0 0\n 1.5036 -3.4174 0.0000 R# 0 0\n 2.9650 -0.4996 0.0000 F 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\n 3 12 1 1\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n5-Deoxy-5-amino-2-fluororibose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn5fl2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Deoxy-5-aminoribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.9146 -0.3813 0.0000 C 0 0 2 0 0 0\n 0.4172 0.3089 0.0000 C 0 0 2 0 0 0\n 1.4851 -0.7445 0.0000 C 0 0 2 0 0 0\n 0.8134 -2.0856 0.0000 C 0 0 1 0 0 0\n -0.6697 -1.8612 0.0000 O 0 0\n -2.2528 0.2924 0.0000 C 0 0\n 0.6383 1.7907 0.0000 O 0 0\n -2.3396 1.7907 0.0000 N 0 0\n -3.6793 2.4652 0.0000 R# 0 0\n 2.0334 2.3417 0.0000 R# 0 0\n 1.5036 -3.4174 0.0000 R# 0 0\n 2.9650 -0.4996 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\n 3 12 1 1\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n5-Deoxy-5-aminoribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn5r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Deoxy-5-thioribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6450 -0.4268 0.0000 C 0 0 2 0 0 0\n 0.6867 0.2634 0.0000 C 0 0 2 0 0 0\n 1.7547 -0.7899 0.0000 C 0 0\n 1.0830 -2.1310 0.0000 C 0 0 1 0 0 0\n -0.4002 -1.9066 0.0000 O 0 0\n -1.9833 0.2470 0.0000 C 0 0\n 0.9078 1.7453 0.0000 O 0 0\n -2.0700 1.7453 0.0000 S 0 0\n -3.4098 2.4198 0.0000 R# 0 0\n 2.3029 2.2963 0.0000 R# 0 0\n 1.7731 -3.4628 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n5-Deoxy-5-thioribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns5d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Ethyluracil\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 7.0958 4.1004 0.0000 C 0 0\n 6.3440 5.3983 0.0000 C 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 2 7 1 0\n 4 8 1 0\n 8 9 1 0\n 3 10 2 0\n 5 11 2 0\nM RGP 1 7 1\nM END\n> <Name>\n5-Ethyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ne5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Ethynylcytosine\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 N 0 0\n -2.5981 -1.5000 0.0000 O 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 0.0000 3.0000 0.0000 N 0 0\n 2.5988 1.5004 0.0000 C 0 0\n 3.8985 2.2508 0.0000 C 0 0\n 5.1976 3.0009 0.0000 C 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 2 0\n 6 8 1 0\n 3 9 1 0\n 2 10 1 0\n 10 11 3 0\n 11 12 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5-Ethynylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nethy5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Fluorocytosine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -2.5981 -1.5000 0.0000 R# 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 F 0 0\n 2.5981 1.5000 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 4 8 2 0\n 3 9 1 0\n 2 10 1 0\nM RGP 1 7 1\nM END\n> <Name>\n5-Fluorocytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfl5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Formyl-2-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6576 0.1670 0.0000 C 0 0 2 0 0 0\n 0.8424 0.1670 0.0000 C 0 0 2 0 0 0\n 1.3059 -1.2595 0.0000 C 0 0\n 0.0924 -2.1412 0.0000 C 0 0 1 0 0 0\n -1.1212 -1.2595 0.0000 O 0 0\n -1.5358 1.3810 0.0000 C 0 0\n 1.7205 1.3810 0.0000 O 0 0\n 3.2127 1.2282 0.0000 R# 0 0\n 0.0924 -3.6412 0.0000 R# 0 0\n -3.0278 1.2268 0.0000 R# 0 0\n -0.9237 2.7504 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 6 10 1 0\n 6 11 2 0\nM RGP 3 8 2 9 3 10 1\nM END\n> <Name>\n5-Formyl-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5formD\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Formylcytosine\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 8.5981 1.5000 0.0000 N 0 0\n 7.0958 4.1004 0.0000 C 0 0\n 6.3440 5.3983 0.0000 O 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 3 1 0\n 5 7 1 0\n 4 8 1 0\n 8 9 2 0\n 3 10 2 0\n 2 11 1 0\nM RGP 1 11 1\nM END\n> <Name>\n5-Formylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nform5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Formyluracil\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 7.0958 4.1004 0.0000 C 0 0\n 6.3440 5.3983 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 5 7 2 0\n 3 8 2 0\n 2 9 1 0\n 4 10 1 0\n 10 11 2 0\nM RGP 1 9 1\nM END\n> <Name>\n5-Formyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nform5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Hydroxycytosine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 2.2500 -4.2990 0.0000 C 0 0\n 3.7500 -4.2990 0.0000 C 0 0\n 4.5000 -3.0000 0.0000 C 0 0\n 3.7500 -1.7010 0.0000 N 0 0\n 2.2500 -1.7010 0.0000 C 0 0\n 1.5000 -3.0000 0.0000 N 0 0\n 1.5000 -0.4019 0.0000 O 0 0\n 6.0000 -3.0000 0.0000 N 0 0\n 4.5000 -5.5981 0.0000 O 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 2 0\n 3 8 1 0\n 2 9 1 0\n 6 10 1 0\nM RGP 1 10 1\nM END\n> <Name>\n5-Hydroxycytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noh5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Hydroxymethylcytosine\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 8.5981 1.5000 0.0000 N 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 7.0958 4.1004 0.0000 C 0 0\n 6.3440 5.3983 0.0000 O 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 1 2 0\n 5 7 1 0\n 3 8 2 0\n 6 9 1 0\n 9 10 1 0\n 2 11 1 0\nM RGP 1 11 1\nM END\n> <Name>\n5-Hydroxymethylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nhm5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Hydroxyuracil\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 2.2500 -4.2990 0.0000 C 0 0\n 3.7500 -4.2990 0.0000 C 0 0\n 4.5000 -3.0000 0.0000 C 0 0\n 3.7500 -1.7010 0.0000 N 0 0\n 2.2500 -1.7010 0.0000 C 0 0\n 1.5000 -3.0000 0.0000 N 0 0\n 1.5000 -0.4019 0.0000 O 0 0\n 6.0000 -3.0000 0.0000 O 0 0\n 4.5000 -5.5981 0.0000 O 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 2 0\n 3 8 2 0\n 2 9 1 0\n 6 10 1 0\nM RGP 1 10 1\nM END\n> <Name>\n5-Hydroxyuracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noh5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Hyroxymethyluracil\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 7.0958 4.1004 0.0000 C 0 0\n 6.3440 5.3983 0.0000 O 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 2 0\n 5 7 2 0\n 3 8 2 0\n 6 9 1 0\n 9 10 1 0\n 2 11 1 0\nM RGP 1 11 1\nM END\n> <Name>\n5-Hyroxymethyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nohm5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Iodocytosine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5000 0.4019 0.0000 I 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 6 7 1 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5-Iodocytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nio5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Isopropyluracil\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.4977 0.3997 0.0000 C 0 0\n 3.7459 -0.8983 0.0000 C 0 0\n 5.9977 0.3970 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\n 10 11 1 0\n 10 12 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5-Isopropyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nipr5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Methoxyuracil\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 7.0958 4.1004 0.0000 O 0 0\n 6.3440 5.3983 0.0000 C 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 3 7 2 0\n 5 8 2 0\n 6 9 1 0\n 9 10 1 0\n 2 11 1 0\nM RGP 1 11 1\nM END\n> <Name>\n5-Methoxyuracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmo5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Methyl-2-O-methylribose\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -0.9132 -0.4085 0.0000 C 0 0 2 0 0 0\n 0.4186 0.2817 0.0000 C 0 0 2 0 0 0\n 1.4866 -0.7716 0.0000 C 0 0 2 0 0 0\n 0.8148 -2.1128 0.0000 C 0 0 1 0 0 0\n -0.6683 -1.8883 0.0000 O 0 0\n 0.6397 1.7636 0.0000 O 0 0\n -2.2514 0.2653 0.0000 C 0 0\n 1.5050 -3.4445 0.0000 R# 0 0\n 2.0348 2.3146 0.0000 R# 0 0\n -2.3381 1.7636 0.0000 O 0 0\n 2.9642 -0.5239 0.0000 O 0 0\n 3.4901 0.8809 0.0000 C 0 0\n -3.6779 2.4381 0.0000 R# 0 0\n -3.5052 -0.5582 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 0\n 2 6 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 7 10 1 0\n 3 11 1 1\n 11 12 1 0\n 10 13 1 0\n 7 14 1 0\nM RGP 3 8 3 9 2 13 1\nM END\n> <Name>\n5-Methyl-2-O-methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm5m\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Methyldeoxyribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.3753 -0.3787 0.0000 C 0 0 2 0 0 0\n 0.9565 0.3115 0.0000 C 0 0 2 0 0 0\n 2.0244 -0.7418 0.0000 C 0 0\n 1.3527 -2.0830 0.0000 C 0 0 1 0 0 0\n -0.1304 -1.8586 0.0000 O 0 0\n 1.1776 1.7933 0.0000 O 0 0\n -1.7135 0.2950 0.0000 C 0 0\n 2.0429 -3.4148 0.0000 R# 0 0\n 2.5727 2.3443 0.0000 R# 0 0\n -1.8003 1.7933 0.0000 O 0 0\n -3.1400 2.4679 0.0000 R# 0 0\n -2.9673 -0.5284 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 0\n 2 6 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 7 10 1 0\n 10 11 1 0\n 7 12 1 0\nM RGP 3 8 3 9 2 11 1\nM END\n> <Name>\n5-Methyldeoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm5d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Thiazolecytidine\n SciTegic07272112182D\n\n 14 15 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n -2.5981 1.5000 0.0000 O 0 0\n 2.5987 -1.5004 0.0000 C 0 0\n 3.9511 -0.8815 0.0000 N 0 0\n 4.9531 -1.9978 0.0000 C 0 0\n 4.2010 -3.2956 0.0000 C 0 0\n 2.7343 -2.9815 0.0000 S 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 1 6 1 0\n 6 7 1 0\n 4 8 2 0\n 1 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 9 1 0\n 3 14 1 0\nM RGP 1 14 1\nM END\n> <Name>\n5-Thiazolecytidine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nthiz5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Thiazoleuridine\n SciTegic07272112182D\n\n 14 15 0 0 0 0 999 V2000\n 2.5981 -1.5000 0.0000 R# 0 0\n 4.0981 -1.5000 0.0000 N 0 0\n 4.8481 -2.7990 0.0000 C 0 0\n 6.3481 -2.7990 0.0000 N 0 0\n 7.0981 -1.5000 0.0000 C 0 0\n 6.3481 -0.2010 0.0000 C 0 0\n 4.8481 -0.2010 0.0000 C 0 0\n 8.5981 -1.5000 0.0000 O 0 0\n 4.0981 -4.0981 0.0000 O 0 0\n 7.0985 1.0987 0.0000 C 0 0\n 8.5791 1.2390 0.0000 S 0 0\n 8.8886 2.7067 0.0000 C 0 0\n 7.5884 3.4546 0.0000 C 0 0\n 6.4753 2.4492 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 2 7 1 0\n 5 8 2 0\n 3 9 2 0\n 6 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 10 2 0\nM RGP 1 1 1\nM END\n> <Name>\n5-Thiazoleuridine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nthiz5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Thienyl-6-azauracil\n SciTegic07272112182D\n\n 14 15 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 N 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 5.9814 0.2657 0.0000 C 0 0\n 6.2956 -1.2010 0.0000 C 0 0\n 4.9978 -1.9531 0.0000 C 0 0\n 3.8815 -0.9511 0.0000 S 0 0\n 4.5004 0.4013 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 1 0\n 10 14 2 0\n 5 14 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5-Thienyl-6-azauracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nthien5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Trifluoromethylcytosine\n SciTegic07272112182D\n\n 13 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 N 0 0\n -2.5981 -1.5000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 N 0 0\n 2.5988 1.5004 0.0000 C 0 0\n 3.8983 0.7513 0.0000 F 0 0\n 2.5983 3.0004 0.0000 F 0 0\n 3.8975 2.2511 0.0000 F 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 2 0\n 3 8 1 0\n 2 9 1 0\n 9 10 1 0\n 9 11 1 0\n 9 12 1 0\n 6 13 1 0\nM RGP 1 13 1\nM END\n> <Name>\n5-Trifluoromethylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfl3mC\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Vinyluracil\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 7.0958 4.1004 0.0000 C 0 0\n 6.3440 5.3983 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 2 7 1 0\n 3 8 2 0\n 5 9 2 0\n 4 10 1 0\n 10 11 2 0\nM RGP 1 7 1\nM END\n> <Name>\n5-Vinyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nvinyl5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-[(Methylamino)methyl]uridine\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 4.4977 0.3997 0.0000 C 0 0\n 3.7455 -0.8990 0.0000 N 0 0\n 4.4928 -2.1996 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 2 7 2 0\n 6 8 2 0\n 3 9 1 0\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-[(Methylamino)methyl]uridine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmnm5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-(p-Nitrobenzylthio)purine\n SciTegic07272112182D\n\n 21 23 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 7.0433 -5.3736 0.0000 S 0 0\n 8.1571 -6.3795 0.0000 C 0 0\n 9.5855 -5.9188 0.0000 C 0 0\n 10.7002 -6.9226 0.0000 C 0 0\n 12.1268 -6.4592 0.0000 C 0 0\n 9.8976 -4.4516 0.0000 C 0 0\n 11.3242 -3.9882 0.0000 C 0 0\n 12.4388 -4.9920 0.0000 C 0 0\n 13.8672 -4.5313 0.0000 N 0 3\n 14.1818 -3.0647 0.0000 O 0 5\n 14.9804 -5.5367 0.0000 O 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 9 10 1 0\n 6 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 2 0\n 14 15 1 0\n 13 16 1 0\n 16 17 2 0\n 17 18 1 0\n 18 15 2 0\n 18 19 1 0\n 19 20 1 0\n 19 21 2 0\nM CHG 2 19 1 20 -1\nM RGP 1 10 1\nM END\n> <Name>\n6-(p-Nitrobenzylthio)purine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnobn6p\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Aminohexyl-2-aminoguanine\n SciTegic09012117322D\n\n 21 22 0 0 0 0 999 V2000\n -4.6234 -0.1544 0.0000 C 0 0\n -4.5733 1.3448 0.0000 C 0 0\n -5.9828 1.8556 0.0000 N 0 0\n -6.9045 0.6722 0.0000 C 0 0\n -6.0638 -0.5701 0.0000 N 0 0\n -3.3501 -0.9473 0.0000 N 0 0\n -2.0267 -0.2411 0.0000 C 0 0\n -1.9767 1.2581 0.0000 N 0 0\n -3.2500 2.0510 0.0000 C 0 0\n -3.1999 3.5502 0.0000 O 0 0\n -6.5745 -1.9804 0.0000 R# 0 0\n -0.7511 -1.0318 0.0000 N 0 0\n 9.6429 -1.3604 0.0000 R# 0 0\n 8.4154 0.9292 0.0000 R# 0 0\n 0.5719 -0.3233 0.0000 C 0 0\n 1.8476 -1.1141 0.0000 C 0 0\n 3.1706 -0.4056 0.0000 C 0 0\n 4.4462 -1.1963 0.0000 C 0 0\n 5.7693 -0.4878 0.0000 C 0 0\n 7.0449 -1.2786 0.0000 C 0 0\n 8.3680 -0.5701 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 1 0\n 9 2 1 0\n 9 10 2 0\n 5 11 1 0\n 7 12 1 0\n 21 13 1 0\n 21 14 1 0\n 12 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 19 20 1 0\n 20 21 1 0\nM RGP 3 11 1 13 2 14 3\nM END\n> <Name>\n6-Aminohexyl-2-aminoguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnC6n2G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]H\n\n$$$$\n6-Aminohexyl-8-aminoadenine\n SciTegic09012117322D\n\n 21 22 0 0 0 0 999 V2000\n 0.4096 -0.5840 0.0000 C 0 0\n 1.6691 -1.4002 0.0000 C 0 0\n 3.0061 -0.7183 0.0000 C 0 0\n 4.2656 -1.5345 0.0000 C 0 0\n 5.6026 -0.8527 0.0000 C 0 0\n 6.8621 -1.6689 0.0000 C 0 0\n 8.1991 -0.9870 0.0000 N 0 0\n 9.4579 -1.8028 0.0000 R# 0 0\n 8.2766 0.5110 0.0000 R# 0 0\n -4.5277 0.1792 0.0000 C 0 0\n -3.7094 1.4364 0.0000 C 0 0\n -2.2616 1.0470 0.0000 N 0 0\n -2.1847 -0.4510 0.0000 C 0 0\n -3.5857 -0.9870 0.0000 N 0 0\n -6.0256 0.2594 0.0000 N 0 0\n -6.7051 1.5967 0.0000 C 0 0\n -5.8867 2.8538 0.0000 N 0 0\n -4.3889 2.7736 0.0000 C 0 0\n -3.5705 4.0307 0.0000 N 0 0\n -3.9756 -2.4355 0.0000 R# 0 0\n -0.9274 -1.2658 0.0000 N 0 0\n 21 1 1 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 7 9 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 10 1 0\n 10 15 1 0\n 15 16 2 0\n 16 17 1 0\n 17 18 2 0\n 18 11 1 0\n 18 19 1 0\n 14 20 1 0\n 13 21 1 0\nM RGP 3 8 2 9 3 20 1\nM END\n> <Name>\n6-Aminohexyl-8-aminoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnC6n8A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]H\n\n$$$$\n6-Aza-5-propynyluracil\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 N 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5004 0.4012 0.0000 C 0 0\n 5.2508 -0.8985 0.0000 C 0 0\n 6.0008 -2.1976 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\n 10 11 3 0\n 11 12 1 0\nM RGP 1 8 1\nM END\n> <Name>\n6-Aza-5-propynyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nz6pry5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Azacytosine\n SciTegic09012117322D\n\n 9 9 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 2.5981 1.5000 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 6 7 1 0\n 3 8 1 0\n 2 9 2 0\nM RGP 1 8 1\nM END\n> <Name>\n6-Azacytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nz5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Azathymine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 N 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5000 0.4019 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\nM RGP 1 8 1\nM END\n> <Name>\n6-Azathymine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nz5T\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Azauracil\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 2.5981 1.5000 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\nM RGP 1 8 1\nM END\n> <Name>\n6-Azauracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nz6U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Chloroguanine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 Cl 0 0\n 3.5643 -9.2321 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 2 11 1 0\n 9 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n6-Chloroguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncl6G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Chloropurine\n SciTegic07272112182D\n\n 11 12 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 Cl 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 9 11 1 0\nM RGP 1 11 1\nM END\n> <Name>\n6-Chloropurine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncl6pur\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Cyclohexyladenine\n SciTegic07272112182D\n\n 17 19 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0433 -5.3736 0.0000 N 0 0\n 8.1571 -6.3795 0.0000 C 0 0\n 9.5854 -5.9211 0.0000 C 0 0\n 10.6965 -6.9288 0.0000 C 0 0\n 10.3795 -8.3949 0.0000 C 0 0\n 8.9513 -8.8533 0.0000 C 0 0\n 7.8401 -7.8457 0.0000 C 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 11 1 0\n 9 17 1 0\nM RGP 1 17 1\nM END\n> <Name>\n6-Cyclohexyladenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncyh6A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Cyclopentyladenine\n SciTegic07272112182D\n\n 16 18 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0433 -5.3736 0.0000 N 0 0\n 8.1571 -6.3795 0.0000 C 0 0\n 9.6092 -6.0582 0.0000 C 0 0\n 10.3546 -7.3599 0.0000 C 0 0\n 9.3469 -8.4710 0.0000 C 0 0\n 7.9788 -7.8561 0.0000 C 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 11 1 0\n 9 16 1 0\nM RGP 1 16 1\nM END\n> <Name>\n6-Cyclopentyladenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncyp6A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Ethyladenine\n SciTegic07272112182D\n\n 14 15 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0433 -5.3736 0.0000 O 0 0\n 8.1571 -6.3795 0.0000 C 0 0\n 9.5847 -5.9190 0.0000 C 0 0\n 3.5643 -9.2321 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 10 11 1 0\n 11 12 1 0\n 2 13 1 0\n 9 14 1 0\nM RGP 1 14 1\nM END\n> <Name>\n6-Ethyladenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ne6A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Methoxypurine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0433 -5.3736 0.0000 O 0 0\n 8.1565 -6.3790 0.0000 C 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 10 11 1 0\n 9 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n6-Methoxypurine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmo6pur\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Methylguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0433 -5.3736 0.0000 O 0 0\n 8.1565 -6.3790 0.0000 C 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 3.5643 -9.2321 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 10 11 1 0\n 9 12 1 0\n 2 13 1 0\nM RGP 1 12 1\nM END\n> <Name>\n6-Methylguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm6G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Methylpurine\n SciTegic07272112182D\n\n 11 12 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 C 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 9 11 1 0\nM RGP 1 11 1\nM END\n> <Name>\n6-Methylpurine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm6pur\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Methylthioguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0433 -5.3736 0.0000 S 0 0\n 8.1565 -6.3790 0.0000 C 0 0\n 3.5643 -9.2321 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 10 11 1 0\n 2 12 1 0\n 9 13 1 0\nM RGP 1 13 1\nM END\n> <Name>\n6-Methylthioguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nms6G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Methylthiopurine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0433 -5.3736 0.0000 S 0 0\n 8.1565 -6.3790 0.0000 C 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 10 11 1 0\n 9 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n6-Methylthiopurine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nms6pur\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Methyluracil\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 1.5000 0.4019 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 4 10 1 0\nM RGP 1 8 1\nM END\n> <Name>\n6-Methyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm6U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Thioguanine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 7.0416 -5.3709 0.0000 S 0 0\n 3.5643 -9.2321 0.0000 N 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 5 1 0\n 7 10 1 0\n 4 11 2 0\n 2 12 1 0\nM RGP 1 10 1\nM END\n> <Name>\n6-Thioguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns6G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Thiopurine\n SciTegic07272112182D\n\n 11 12 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 7.0416 -5.3709 0.0000 S 0 0\n 1 2 1 0\n 2 3 2 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 1 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 9 10 1 0\n 6 11 2 0\nM RGP 1 10 1\nM END\n> <Name>\n6-Thiopurine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns6puri\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-beta-Hydroxycarbo-2-deoxyribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.5239 -0.1789 0.0000 C 0 0 2 0 0 0\n 0.8079 0.5113 0.0000 C 0 0 2 0 0 0\n 1.8758 -0.5420 0.0000 C 0 0\n 1.2041 -1.8832 0.0000 C 0 0 1 0 0 0\n -0.2790 -1.6588 0.0000 C 0 0 2 0 0 0\n 1.0289 1.9932 0.0000 O 0 0\n -1.8621 0.4949 0.0000 C 0 0\n 1.8943 -3.2149 0.0000 R# 0 0\n -1.9489 1.9932 0.0000 O 0 0\n -3.2887 2.6677 0.0000 R# 0 0\n 2.4241 2.5442 0.0000 R# 0 0\n -1.3324 -2.7267 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 5 12 1 6\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n6-beta-Hydroxycarbo-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nBcoh4d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n7-Azaguanine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 N 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 O 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 3.5643 -9.2321 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 1 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 2 0\n 9 11 1 0\n 2 12 1 0\nM RGP 1 11 1\nM END\n> <Name>\n7-Azaguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nz7G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Deaza-7-cyanoadenine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n -3.1875 -2.6385 0.0000 C 0 0\n -3.6507 -4.0652 0.0000 N 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 7 8 2 0\n 5 8 1 0\n 6 9 1 0\n 4 10 1 0\n 7 10 1 0\n 10 11 1 0\n 8 12 1 0\n 12 13 3 0\nM RGP 1 11 1\nM END\n> <Name>\n7-Deaza-7-cyanoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc7cn7A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Deaza-7-iodo-2-aminoadenine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n 2.5981 1.5000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n -3.1882 -2.6402 0.0000 I 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 7 8 2 0\n 5 8 1 0\n 6 9 1 0\n 2 10 1 0\n 4 11 1 0\n 7 11 1 0\n 11 12 1 0\n 8 13 1 0\nM RGP 1 12 1\nM END\n> <Name>\n7-Deaza-7-iodo-2-aminoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc7io7n\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Deaza-7-iodoadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n -3.1882 -2.6402 0.0000 I 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 7 8 2 0\n 5 8 1 0\n 6 9 1 0\n 4 10 1 0\n 7 10 1 0\n 10 11 1 0\n 8 12 1 0\nM RGP 1 11 1\nM END\n> <Name>\n7-Deaza-7-iodoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc7io7A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Deaza-7-iodoguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n -3.1882 -2.6402 0.0000 I 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 7 8 2 0\n 5 8 1 0\n 6 9 2 0\n 2 10 1 0\n 4 11 1 0\n 7 11 1 0\n 11 12 1 0\n 8 13 1 0\nM RGP 1 12 1\nM END\n> <Name>\n7-Deaza-7-iodoguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc7io7G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Deaza-7-propyne-2-aminoadenine\n SciTegic07272112182D\n\n 15 16 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n -3.1875 -2.6385 0.0000 C 0 0\n -3.6510 -4.0660 0.0000 C 0 0\n -4.1142 -5.4927 0.0000 C 0 0\n 2.5981 1.5000 0.0000 N 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 7 8 2 0\n 5 8 1 0\n 6 9 1 0\n 4 10 1 0\n 7 10 1 0\n 10 11 1 0\n 8 12 1 0\n 12 13 3 0\n 13 14 1 0\n 2 15 1 0\nM RGP 1 11 1\nM END\n> <Name>\n7-Deaza-7-propyne-2-aminoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc7py7N\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Deaza-7-propynyladenine\n SciTegic07272112182D\n\n 14 15 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n -3.1875 -2.6385 0.0000 C 0 0\n -3.6510 -4.0660 0.0000 C 0 0\n -4.1142 -5.4927 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 7 8 2 0\n 5 8 1 0\n 6 9 1 0\n 4 10 1 0\n 7 10 1 0\n 10 11 1 0\n 8 12 1 0\n 12 13 3 0\n 13 14 1 0\nM RGP 1 11 1\nM END\n> <Name>\n7-Deaza-7-propynyladenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc7py7A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Deazaadenine\n SciTegic07272112182D\n\n 11 12 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 C 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n 2.5981 -1.5000 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 4 1 0\n 7 10 1 0\n 1 11 1 0\nM RGP 1 10 1\nM END\n> <Name>\n7-Deazaadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc7A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Deazaguanine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 5.9498 4.1210 0.0000 N 0 0\n 6.2618 2.6538 0.0000 C 0 0\n 7.6885 2.1904 0.0000 C 0 0\n 7.0645 5.1248 0.0000 C 0 0\n 8.4911 4.6614 0.0000 N 0 0\n 8.8031 3.1942 0.0000 C 0 0\n 7.6888 0.6912 0.0000 C 0 0\n 6.2623 0.2275 0.0000 C 0 0\n 5.3805 1.4410 0.0000 N 0 0\n 10.2297 2.7308 0.0000 O 0 0\n 6.7525 6.5920 0.0000 N 0 0\n 3.8805 1.4410 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 1 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 3 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 2 1 0\n 6 10 2 0\n 4 11 1 0\n 9 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n7-Deazaguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc7G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Methyl 8-dihydroguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n 0.6924 -4.0811 0.0000 C 0 0\n 2.5981 -1.5000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 5 1 0\n 9 10 1 0\n 7 11 1 0\n 1 12 2 0\n 3 13 1 0\nM RGP 1 10 1\nM END\n> <Name>\n7-Methyl 8-dihydroguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm7h8G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Methylguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -2.4133 -1.7530 0.0000 N 0 3\n 0.0000 3.0000 0.0000 N 0 0\n 2.5981 -1.5000 0.0000 O 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n 0.6924 -4.0811 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 5 1 0\n 3 10 1 0\n 1 11 2 0\n 9 12 1 0\n 7 13 1 0\nM CHG 1 9 1\nM RGP 1 12 1\nM END\n> <Name>\n7-Methylguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm7G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Nitro-1,3-diaza-2-oxophenothiazin\n SciTegic07272112182D\n\n 19 21 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5000 0.4019 0.0000 S 0 0\n 6.0000 0.4019 0.0000 C 0 0\n 6.7500 1.7010 0.0000 C 0 0\n 6.7500 -0.8971 0.0000 C 0 0\n 8.2500 -0.8971 0.0000 C 0 0\n 9.0000 0.4019 0.0000 C 0 0\n 8.2500 1.7010 0.0000 C 0 0\n 9.0031 -2.1953 0.0000 N 0 3\n 8.2553 -3.4957 0.0000 O 0 5\n 10.5031 -2.1932 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 6 7 1 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 7 1 0\n 11 13 2 0\n 13 14 1 0\n 14 15 2 0\n 15 16 1 0\n 16 12 2 0\n 14 17 1 0\n 17 18 1 0\n 17 19 2 0\nM CHG 2 17 1 18 -1\nM RGP 1 8 1\nM END\n> <Name>\n7-Nitro-1,3-diaza-2-oxophenothiazin\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ntCnitr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Aminoadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n -2.5532 -4.4223 0.0000 N 0 0\n 2.5981 -1.5000 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 5 1 0\n 9 10 1 0\n 8 11 1 0\n 1 12 1 0\nM RGP 1 10 1\nM END\n> <Name>\n8-Aminoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn8A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Aminoguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n 2.5981 -1.5000 0.0000 O 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n -2.5532 -4.4223 0.0000 N 0 0\n 0.0000 3.0000 0.0000 N 0 0\n 1 2 1 0\n 2 3 2 0\n 1 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 3 1 0\n 5 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 4 2 0\n 1 10 2 0\n 7 11 1 0\n 8 12 1 0\n 3 13 1 0\nM RGP 1 11 1\nM END\n> <Name>\n8-Aminoguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn8G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Aza-3-deazaguanine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 N 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 7 8 2 0\n 5 8 1 0\n 6 9 2 0\n 2 10 1 0\n 4 11 1 0\n 7 11 1 0\n 11 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n8-Aza-3-deazaguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nz8c3G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Azaadenine\n SciTegic07272112182D\n\n 11 12 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 N 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 5 1 0\n 4 10 1 0\n 7 11 1 0\nM RGP 1 11 1\nM END\n> <Name>\n8-Azaadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nz8A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Bromoadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n -2.5532 -4.4223 0.0000 Br 0 0\n 2.5981 -1.5000 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 4 1 0\n 7 10 1 0\n 8 11 1 0\n 1 12 1 0\nM RGP 1 10 1\nM END\n> <Name>\n8-Bromoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbr8A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Bromoguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n 0.0000 3.0000 0.0000 N 0 0\n 2.5981 -1.5000 0.0000 O 0 0\n -2.5532 -4.4223 0.0000 Br 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 4 1 0\n 3 10 1 0\n 1 11 2 0\n 8 12 1 0\n 7 13 1 0\nM RGP 1 13 1\nM END\n> <Name>\n8-Bromoguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbr8G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Chloroadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 6.9961 1.8908 0.0000 C 0 0\n 6.9965 3.3900 0.0000 N 0 0\n 5.5699 3.8536 0.0000 C 0 0\n 4.6882 2.6402 0.0000 N 0 0\n 5.5695 1.4274 0.0000 C 0 0\n 8.1107 0.8870 0.0000 C 0 0\n 5.2575 -0.0398 0.0000 N 0 0\n 6.3721 -1.0436 0.0000 C 0 0\n 7.7987 -0.5802 0.0000 N 0 0\n 3.1882 2.6402 0.0000 R# 0 0\n 9.5374 1.3504 0.0000 N 0 0\n 5.1065 5.2802 0.0000 Cl 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 5 1 2 0\n 1 6 1 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 6 2 0\n 4 10 1 0\n 6 11 1 0\n 3 12 1 0\nM RGP 1 10 1\nM END\n> <Name>\n8-Chloroadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncl8A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Oxo-9-thioguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 6.9961 1.8908 0.0000 C 0 0\n 6.9965 3.3900 0.0000 S 0 0\n 5.5699 3.8536 0.0000 C 0 0\n 4.6882 2.6402 0.0000 N 0 0\n 5.5695 1.4274 0.0000 C 0 0\n 8.1107 0.8870 0.0000 C 0 0\n 5.2575 -0.0398 0.0000 N 0 0\n 6.3721 -1.0436 0.0000 C 0 0\n 7.7987 -0.5802 0.0000 N 0 0\n 6.0601 -2.5108 0.0000 N 0 0\n 3.1882 2.6402 0.0000 R# 0 0\n 9.5374 1.3504 0.0000 O 0 0\n 5.1065 5.2802 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 2 0\n 1 6 1 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 6 1 0\n 8 10 1 0\n 4 11 1 0\n 6 12 2 0\n 3 13 2 0\nM RGP 1 11 1\nM END\n> <Name>\n8-Oxo-9-thioguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\no8s9G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Oxoadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n -2.5532 -4.4223 0.0000 O 0 0\n 2.5981 -1.5000 0.0000 N 0 0\n 1 2 1 0\n 1 3 2 0\n 3 4 1 0\n 4 5 2 0\n 4 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 3 1 0\n 5 9 1 0\n 9 2 2 0\n 6 10 1 0\n 7 11 2 0\n 1 12 1 0\nM RGP 1 10 1\nM END\n> <Name>\n8-Oxoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\no8A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Oxoguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 6.9961 1.8908 0.0000 C 0 0\n 6.9965 3.3900 0.0000 N 0 0\n 5.5699 3.8536 0.0000 C 0 0\n 4.6882 2.6402 0.0000 N 0 0\n 5.5695 1.4274 0.0000 C 0 0\n 8.1107 0.8870 0.0000 C 0 0\n 5.2575 -0.0398 0.0000 N 0 0\n 6.3721 -1.0436 0.0000 C 0 0\n 7.7987 -0.5802 0.0000 N 0 0\n 9.5374 1.3504 0.0000 O 0 0\n 5.1065 5.2802 0.0000 O 0 0\n 6.0601 -2.5108 0.0000 N 0 0\n 3.1882 2.6402 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 2 0\n 1 6 1 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 6 1 0\n 6 10 2 0\n 3 11 2 0\n 8 12 1 0\n 4 13 1 0\nM RGP 1 13 1\nM END\n> <Name>\n8-Oxoguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\no8G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Thioguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n -2.5532 -4.4223 0.0000 S 0 0\n 2.5981 -1.5000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 5 1 0\n 9 10 1 0\n 8 11 2 0\n 1 12 2 0\n 3 13 1 0\nM RGP 1 10 1\nM END\n> <Name>\n8-Thioguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns8G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n9-Allylguanine\n SciTegic07272112182D\n\n 16 17 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n 0.0000 3.0000 0.0000 N 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n -2.5532 -4.4223 0.0000 O 0 0\n 0.6890 -4.0818 0.0000 C 0 0\n 2.5981 -1.5000 0.0000 O 0 0\n 0.2235 -5.5086 0.0000 C 0 0\n 1.2251 -6.6252 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 5 1 0\n 3 10 1 0\n 9 11 1 0\n 8 12 2 0\n 7 13 1 0\n 1 14 2 0\n 13 15 1 0\n 15 16 2 0\nM RGP 1 11 1\nM END\n> <Name>\n9-Allylguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nallyl9\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-methyl-cLNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -1.7573 0.3923 0.0000 C 0 0\n -0.3792 0.2175 0.0000 C 0 0 1 0 0 0\n -0.8961 -0.6891 0.0000 C 0 0 1 0 0 0\n 1.2548 0.2221 0.0000 C 0 0 2 0 0 0\n 0.4960 -0.9529 0.0000 C 0 0 2 0 0 0\n 0.6513 -2.2149 0.0000 C 0 0 1 0 0 0\n -0.7183 -2.0601 0.0000 O 0 0\n -1.2216 0.7840 0.0000 C 0 0\n 1.7172 -3.2702 0.0000 R# 0 0\n 2.3209 1.2498 0.0000 O 0 0\n 3.7640 0.8408 0.0000 R# 0 0\n 0.3758 1.5136 0.0000 C 0 0\n -2.6483 1.2498 0.0000 O 0 0\n -2.9590 2.7173 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 5 4 1 6\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 6\n 6 9 1 6\n 3 1 1 0\n 5 2 1 0\n 4 10 1 1\n 10 11 1 0\n 2 12 1 6\n 8 13 1 0\n 13 14 1 0\nM RGP 3 9 3 11 2 14 1\nM END\n> <Name>\n(2S)-methyl-cLNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSmclna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(5R)-5-Methyl-LNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n 0.3972 -2.1683 0.0000 C 0 0\n -0.1631 -3.4084 0.0000 O 0 0\n 0.3322 -0.7081 0.0000 C 0 0 1 0 0 0\n 1.7223 -0.0968 0.0000 C 0 0 2 0 0 0\n -0.4298 -1.8615 0.0000 C 0 0 2 0 0 0\n -1.7755 -1.1928 0.0000 C 0 0 1 0 0 0\n -1.1717 -0.0949 0.0000 O 0 0\n 1.9043 1.4079 0.0000 O 0 0\n 0.1808 0.7908 0.0000 C 0 0 1 0 0 0\n -3.1621 -0.6206 0.0000 R# 0 0\n 1.3983 1.6670 0.0000 C 0 0\n 3.2919 1.9775 0.0000 R# 0 0\n -1.1873 1.4079 0.0000 O 0 0\n -1.3378 2.9003 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 6\n 4 8 1 1\n 3 9 1 0\n 6 10 1 6\n 9 11 1 6\n 3 1 1 0\n 5 2 1 1\n 8 12 1 0\n 9 13 1 0\n 13 14 1 0\nM RGP 3 10 3 12 2 14 1\nM END\n> <Name>\n(5R)-5-Methyl-LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRm5lna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(5R)-5-methyl-alpha-L-LNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n 0.3322 -0.7081 0.0000 C 0 0 2 0 0 0\n 1.7223 -0.0968 0.0000 C 0 0 1 0 0 0\n -0.4298 -1.8615 0.0000 C 0 0 1 0 0 0\n -1.7755 -1.1928 0.0000 C 0 0 1 0 0 0\n -1.1717 -0.0949 0.0000 O 0 0\n 1.9043 1.4079 0.0000 O 0 0\n -3.1621 -0.6206 0.0000 R# 0 0\n 3.2919 1.9775 0.0000 R# 0 0\n 0.3972 -2.1683 0.0000 C 0 0\n -0.1631 -3.4084 0.0000 O 0 0\n 0.1808 0.7908 0.0000 C 0 0 2 0 0 0\n -1.1873 1.4079 0.0000 O 0 0\n -1.3378 2.9003 0.0000 R# 0 0\n 1.3983 1.6670 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 1\n 2 6 1 6\n 4 7 1 6\n 6 8 1 0\n 1 9 1 0\n 3 10 1 6\n 9 10 1 0\n 1 11 1 0\n 11 12 1 0\n 12 13 1 0\n 11 14 1 6\nM RGP 3 7 3 8 2 13 1\nM END\n> <Name>\n(5R)-5-methyl-alpha-L-LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRm5ALl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(5R)-Me-2O-MOE\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -1.9392 -0.7878 0.0000 C 0 0 2 0 0 0\n -0.6075 -0.0976 0.0000 C 0 0 2 0 0 0\n 0.4605 -1.1509 0.0000 C 0 0 2 0 0 0\n -0.2112 -2.4921 0.0000 C 0 0 1 0 0 0\n -1.6944 -2.2677 0.0000 O 0 0\n -3.2775 -0.1141 0.0000 C 0 0 2 0 0 0\n -0.3864 1.3842 0.0000 O 0 0\n 1.0087 1.9352 0.0000 R# 0 0\n 0.4790 -3.8239 0.0000 R# 0 0\n -3.3642 1.3842 0.0000 O 0 0\n -4.7040 2.0587 0.0000 R# 0 0\n 1.9381 -0.9033 0.0000 O 0 0\n 2.4643 0.5023 0.0000 C 0 0\n 3.9445 0.7504 0.0000 C 0 0\n 4.4706 2.1560 0.0000 O 0 0\n 5.9499 2.4039 0.0000 C 0 0\n -4.5312 -0.9375 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 6\n 1 6 1 0\n 2 7 1 1\n 7 8 1 0\n 3 12 1 1\n 4 9 1 6\n 6 10 1 0\n 10 11 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 6 17 1 1\nM RGP 3 8 2 9 3 11 1\nM END\n> <Name>\n(5R)-Me-2O-MOE\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRm5moe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(5S)-2-Fluoro-5-methylribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.4000 -1.8204 0.0000 O 0 0\n -0.6449 -0.3405 0.0000 C 0 0 1 0 0 0\n 1.0831 -2.0448 0.0000 C 0 0 2 0 0 0\n 0.6869 0.3497 0.0000 C 0 0 2 0 0 0\n 1.7549 -0.7036 0.0000 C 0 0 1 0 0 0\n 0.9080 1.8316 0.0000 O 0 0\n 3.2348 -0.4587 0.0000 F 0 0\n -1.9831 0.3332 0.0000 C 0 0 1 0 0 0\n 1.7734 -3.3766 0.0000 R# 0 0\n -2.0698 1.8316 0.0000 O 0 0\n 2.3031 2.3826 0.0000 R# 0 0\n -3.4096 2.5061 0.0000 R# 0 0\n -3.2369 -0.4902 0.0000 C 0 0\n 2 1 1 6\n 1 3 1 0\n 2 4 1 0\n 2 8 1 0\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 11 1 0\n 8 10 1 0\n 10 12 1 0\n 8 13 1 6\nM RGP 3 9 3 11 2 12 1\nM END\n> <Name>\n(5S)-2-Fluoro-5-methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSm5fl2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(5S)-5-Methyl-alpha-L-LNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n 0.3322 -0.7081 0.0000 C 0 0 2 0 0 0\n 1.7223 -0.0968 0.0000 C 0 0 1 0 0 0\n -0.4298 -1.8615 0.0000 C 0 0 1 0 0 0\n -1.7755 -1.1928 0.0000 C 0 0 1 0 0 0\n -1.1717 -0.0949 0.0000 O 0 0\n 1.9043 1.4079 0.0000 O 0 0\n -3.1621 -0.6206 0.0000 R# 0 0\n 3.2919 1.9775 0.0000 R# 0 0\n 0.3972 -2.1683 0.0000 C 0 0\n -0.1631 -3.4084 0.0000 O 0 0\n 0.1808 0.7908 0.0000 C 0 0 1 0 0 0\n -1.1873 1.4079 0.0000 O 0 0\n -1.3378 2.9003 0.0000 R# 0 0\n 1.3983 1.6670 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 1\n 2 6 1 6\n 4 7 1 6\n 6 8 1 0\n 1 9 1 0\n 3 10 1 6\n 9 10 1 0\n 1 11 1 0\n 11 12 1 0\n 12 13 1 0\n 11 14 1 1\nM RGP 3 7 3 8 2 13 1\nM END\n> <Name>\n(5S)-5-Methyl-alpha-L-LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSm5ALl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(5S)-5-Vinyl-BNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 1.8111 -1.6646 0.0000 C 0 0\n 1.9118 -3.0216 0.0000 O 0 0\n 1.0560 -0.4130 0.0000 C 0 0 1 0 0 0\n 1.9848 0.7883 0.0000 C 0 0 2 0 0 0\n 0.9381 -1.7904 0.0000 C 0 0 2 0 0 0\n -0.5636 -1.8463 0.0000 C 0 0 1 0 0 0\n -0.5581 -0.5934 0.0000 O 0 0\n 0.9773 1.9207 0.0000 O 0 0\n -0.1677 0.4656 0.0000 C 0 0 2 0 0 0\n -2.0550 -2.0065 0.0000 R# 0 0\n -1.5358 -0.1515 0.0000 C 0 0\n -2.7542 0.7235 0.0000 C 0 0\n 1.4688 3.3379 0.0000 R# 0 0\n -0.5354 1.9207 0.0000 O 0 0\n -1.9783 2.3306 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 6\n 4 8 1 1\n 3 9 1 0\n 6 10 1 6\n 9 11 1 6\n 3 1 1 0\n 5 2 1 1\n 11 12 2 0\n 8 13 1 0\n 9 14 1 0\n 14 15 1 0\nM RGP 3 10 3 13 2 15 1\nM END\n> <Name>\n(5S)-5-Vinyl-BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSvinyl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(5S)-5-methyl-LNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n 0.3972 -2.1683 0.0000 C 0 0\n -0.1631 -3.4084 0.0000 O 0 0\n 0.3322 -0.7081 0.0000 C 0 0 1 0 0 0\n 1.7223 -0.0968 0.0000 C 0 0 2 0 0 0\n -0.4298 -1.8615 0.0000 C 0 0 2 0 0 0\n -1.7755 -1.1928 0.0000 C 0 0 1 0 0 0\n -1.1717 -0.0949 0.0000 O 0 0\n 1.9043 1.4079 0.0000 O 0 0\n 0.1808 0.7908 0.0000 C 0 0 2 0 0 0\n -3.1621 -0.6206 0.0000 R# 0 0\n 1.3983 1.6670 0.0000 C 0 0\n 3.2919 1.9775 0.0000 R# 0 0\n -1.1873 1.4079 0.0000 O 0 0\n -1.3378 2.9003 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 6\n 4 8 1 1\n 3 9 1 0\n 6 10 1 6\n 9 11 1 1\n 3 1 1 0\n 5 2 1 1\n 8 12 1 0\n 9 13 1 0\n 13 14 1 0\nM RGP 3 10 3 12 2 14 1\nM END\n> <Name>\n(5S)-5-methyl-LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSm5lna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(5S)-Methyl-2O-MOE\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -1.9392 -0.7878 0.0000 C 0 0 2 0 0 0\n -0.6075 -0.0976 0.0000 C 0 0 2 0 0 0\n 0.4605 -1.1509 0.0000 C 0 0 2 0 0 0\n -0.2112 -2.4921 0.0000 C 0 0 1 0 0 0\n -1.6944 -2.2677 0.0000 O 0 0\n -3.2775 -0.1141 0.0000 C 0 0 1 0 0 0\n -0.3864 1.3842 0.0000 O 0 0\n 1.0087 1.9352 0.0000 R# 0 0\n 0.4790 -3.8239 0.0000 R# 0 0\n -3.3642 1.3842 0.0000 O 0 0\n -4.7040 2.0587 0.0000 R# 0 0\n 1.9381 -0.9033 0.0000 O 0 0\n 2.4643 0.5023 0.0000 C 0 0\n 3.9445 0.7504 0.0000 C 0 0\n 4.4706 2.1560 0.0000 O 0 0\n 5.9499 2.4039 0.0000 C 0 0\n -4.5312 -0.9375 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 6\n 1 6 1 0\n 2 7 1 1\n 7 8 1 0\n 3 12 1 1\n 4 9 1 6\n 6 10 1 0\n 10 11 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 6 17 1 6\nM RGP 3 8 2 9 3 11 1\nM END\n> <Name>\n(5S)-Methyl-2O-MOE\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSm5moe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(6S)-6-methyl-FHNA\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -1.4996 -1.1158 0.0000 O 0 0\n -0.7503 0.1837 0.0000 C 0 0 1 0 0 0\n 0.7497 0.1845 0.0000 C 0 0 2 0 0 0\n 1.5004 -1.1142 0.0000 C 0 0 2 0 0 0\n 0.7511 -2.4136 0.0000 C 0 0 1 0 0 0\n -0.7489 -2.4144 0.0000 C 0 0\n 1.5018 -3.7122 0.0000 R# 0 0\n 1.4967 1.4862 0.0000 O 0 0\n -1.4997 1.4840 0.0000 C 0 0 2 0 0 0\n -0.7482 2.7822 0.0000 C 0 0\n 2.9967 1.4910 0.0000 R# 0 0\n 3.0004 -1.1133 0.0000 F 0 0\n -3.0005 1.4862 0.0000 O 0 0\n -3.7495 2.7858 0.0000 R# 0 0\n 2 1 1 6\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 6\n 4 12 1 1\n 3 8 1 1\n 2 9 1 0\n 9 10 1 1\n 8 11 1 0\n 9 13 1 0\n 13 14 1 0\nM RGP 3 7 3 11 2 14 1\nM END\n> <Name>\n(6S)-6-methyl-FHNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSm6fhn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(6S)-6-methyl-alpha-L-LNA\n SciTegic09012117322D\n\n 14 15 0 0 1 0 999 V2000\n 1.1233 0.2604 0.0000 C 0 0 2 0 0 0\n -1.0323 -0.6397 0.0000 C 0 0 1 0 0 0\n -1.8879 0.4463 0.0000 C 0 0 1 0 0 0\n -0.5108 0.2643 0.0000 O 0 0\n 0.3584 -0.9107 0.0000 C 0 0 2 0 0 0\n -3.1915 1.1882 0.0000 R# 0 0\n 0.5071 -2.1734 0.0000 C 0 0 1 0 0 0\n -0.8617 -2.0116 0.0000 O 0 0\n 0.2821 0.5988 0.0000 C 0 0\n 2.1947 1.2825 0.0000 O 0 0\n -1.0539 1.2825 0.0000 O 0 0\n 1.5675 -3.2343 0.0000 C 0 0\n -1.1307 2.7806 0.0000 R# 0 0\n 3.6357 0.8661 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 0\n 3 6 1 6\n 5 7 1 0\n 7 8 1 0\n 2 8 1 6\n 5 9 1 6\n 1 10 1 1\n 9 11 1 0\n 7 12 1 6\n 11 13 1 0\n 10 14 1 0\nM RGP 3 6 3 13 1 14 2\nM END\n> <Name>\n(6S)-6-methyl-alpha-L-LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSm6ALl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(Aminoethyl)amino\n SciTegic07272112182D\n\n 6 5 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\n(Aminoethyl)amino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnen\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n(D)-2-O-(2,3-Isopropylidene glycer-1-yl)ribose\n SciTegic07272112182D\n\n 20 21 0 0 1 0 999 V2000\n 2.4610 0.4907 0.0000 C 0 0 2 0 0 0\n 0.9835 0.2422 0.0000 C 0 0\n 3.1320 1.8323 0.0000 O 0 0\n 3.5296 -0.5620 0.0000 C 0 0\n 4.8610 0.1290 0.0000 O 0 0\n 4.6153 1.6088 0.0000 C 0 0\n 4.1946 3.0485 0.0000 C 0 0\n 6.0612 1.2099 0.0000 C 0 0\n -3.4002 -1.0473 0.0000 C 0 0 2 0 0 0\n -2.0689 -0.3563 0.0000 C 0 0 2 0 0 0\n -1.0218 -1.4126 0.0000 C 0 0 2 0 0 0\n -1.6712 -2.7506 0.0000 C 0 0 1 0 0 0\n -3.1544 -2.5271 0.0000 O 0 0\n -1.8373 1.1239 0.0000 O 0 0\n -4.7388 -0.3744 0.0000 C 0 0\n -0.9723 -4.0778 0.0000 R# 0 0\n -4.8265 1.1239 0.0000 O 0 0\n -6.1667 1.7976 0.0000 R# 0 0\n -0.4384 1.6650 0.0000 R# 0 0\n 0.4582 -1.1637 0.0000 O 0 0\n 1 2 1 6\n 20 2 1 0\n 3 1 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 6 7 1 0\n 6 8 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 9 1 0\n 10 14 1 1\n 11 20 1 1\n 9 15 1 6\n 12 16 1 6\n 15 17 1 0\n 17 18 1 0\n 14 19 1 0\nM RGP 3 16 3 18 1 19 2\nM END\n> <Name>\n(D)-2-O-(2,3-Isopropylidene glycer-1-yl)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nDiprgl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(Dimethylaminoethyl)amino\n SciTegic07272112182D\n\n 8 7 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.2000 0.0000 0.0000 N 0 0\n 6.4992 0.7496 0.0000 C 0 0\n 5.2000 -1.5000 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 6 8 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\n(Dimethylaminoethyl)amino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2nen\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n(L)-2-O-(2,3-Isopropylidene glycer-1-yl)ribose\n SciTegic07272112182D\n\n 20 21 0 0 1 0 999 V2000\n 2.4610 0.4907 0.0000 C 0 0 1 0 0 0\n 0.9835 0.2422 0.0000 C 0 0\n 3.1320 1.8323 0.0000 O 0 0\n 3.5296 -0.5620 0.0000 C 0 0\n 4.8610 0.1290 0.0000 O 0 0\n 4.6153 1.6088 0.0000 C 0 0\n 4.1946 3.0485 0.0000 C 0 0\n 6.0612 1.2099 0.0000 C 0 0\n -3.4002 -1.0473 0.0000 C 0 0 2 0 0 0\n -2.0689 -0.3563 0.0000 C 0 0 2 0 0 0\n -1.0218 -1.4126 0.0000 C 0 0 2 0 0 0\n -1.6712 -2.7506 0.0000 C 0 0 1 0 0 0\n -3.1544 -2.5271 0.0000 O 0 0\n -1.8373 1.1239 0.0000 O 0 0\n -4.7388 -0.3744 0.0000 C 0 0\n -0.9723 -4.0778 0.0000 R# 0 0\n -4.8265 1.1239 0.0000 O 0 0\n -6.1667 1.7976 0.0000 R# 0 0\n -0.4384 1.6650 0.0000 R# 0 0\n 0.4582 -1.1637 0.0000 O 0 0\n 1 2 1 1\n 20 2 1 0\n 3 1 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 6 7 1 0\n 6 8 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 9 1 0\n 10 14 1 1\n 11 20 1 1\n 9 15 1 6\n 12 16 1 6\n 15 17 1 0\n 17 18 1 0\n 14 19 1 0\nM RGP 3 16 3 18 1 19 2\nM END\n> <Name>\n(L)-2-O-(2,3-Isopropylidene glycer-1-yl)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nLiprgl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(R)-4,5,6-Trihydrouracil\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0 1 0 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.5981 -1.5000 0.0000 R# 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 0\n 6 8 2 0\n 2 9 1 1\nM RGP 1 7 1\nM END\n> <Name>\n(R)-4,5,6-Trihydrouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nh456UR\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(R)-2-Fluoro-5-methylribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.4000 -1.8204 0.0000 O 0 0\n -0.6449 -0.3405 0.0000 C 0 0 1 0 0 0\n 1.0831 -2.0448 0.0000 C 0 0 2 0 0 0\n 0.6869 0.3497 0.0000 C 0 0 2 0 0 0\n 1.7549 -0.7036 0.0000 C 0 0 1 0 0 0\n 0.9080 1.8316 0.0000 O 0 0\n 3.2348 -0.4587 0.0000 F 0 0\n -1.9831 0.3332 0.0000 C 0 0 2 0 0 0\n 1.7734 -3.3766 0.0000 R# 0 0\n -2.0698 1.8316 0.0000 O 0 0\n 2.3031 2.3826 0.0000 R# 0 0\n -3.4096 2.5061 0.0000 R# 0 0\n -3.2369 -0.4902 0.0000 C 0 0\n 2 1 1 6\n 1 3 1 0\n 2 4 1 0\n 2 8 1 0\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 11 1 0\n 8 10 1 0\n 10 12 1 0\n 8 13 1 1\nM RGP 3 9 3 11 2 12 1\nM END\n> <Name>\n(R)-2-Fluoro-5-methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRm5fl2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(R)-5-Methyldeoxyribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.3753 -0.3787 0.0000 C 0 0 2 0 0 0\n 0.9565 0.3115 0.0000 C 0 0 2 0 0 0\n 2.0244 -0.7418 0.0000 C 0 0\n 1.3527 -2.0830 0.0000 C 0 0 1 0 0 0\n -0.1304 -1.8586 0.0000 O 0 0\n 1.1776 1.7933 0.0000 O 0 0\n -1.7135 0.2950 0.0000 C 0 0 2 0 0 0\n 2.0429 -3.4148 0.0000 R# 0 0\n 2.5727 2.3443 0.0000 R# 0 0\n -1.8003 1.7933 0.0000 O 0 0\n -3.1400 2.4679 0.0000 R# 0 0\n -2.9673 -0.5284 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 6\n 2 6 1 1\n 1 7 1 0\n 4 8 1 6\n 6 9 1 0\n 7 10 1 0\n 10 11 1 0\n 7 12 1 1\nM RGP 3 8 3 9 2 11 1\nM END\n> <Name>\n(R)-5-Methyldeoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRm5d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(R)-5-hydroxyethyl 2-deoxyribose\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n 1.2991 -0.5282 0.0000 C 0 0 1 0 0 0\n 1.7163 -1.9690 0.0000 C 0 0\n 0.4749 -2.8110 0.0000 C 0 0 1 0 0 0\n -0.7095 -1.8906 0.0000 O 0 0\n -0.2001 -0.4797 0.0000 C 0 0 2 0 0 0\n 0.4264 -4.3102 0.0000 R# 0 0\n -1.0386 0.7620 0.0000 C 0 0 1 0 0 0\n -0.3822 2.1117 0.0000 C 0 0\n -2.5355 0.6530 0.0000 O 0 0\n 2.2209 0.6530 0.0000 O 0 0\n -1.2221 3.3555 0.0000 C 0 0\n -0.5661 4.7044 0.0000 O 0 0\n -3.1900 -0.6967 0.0000 R# 0 0\n 3.7065 0.4459 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 6\n 5 1 1 0\n 3 6 1 6\n 5 7 1 0\n 7 8 1 6\n 7 9 1 0\n 1 10 1 1\n 8 11 1 0\n 11 12 1 0\n 9 13 1 0\n 10 14 1 0\nM RGP 3 6 3 13 1 14 2\nM END\n> <Name>\n(R)-5-hydroxyethyl 2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRhe5d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(R)-F-cLNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -1.7573 0.3923 0.0000 C 0 0\n -0.3792 0.2175 0.0000 C 0 0 2 0 0 0\n -0.8961 -0.6891 0.0000 C 0 0 1 0 0 0\n 1.2548 0.2221 0.0000 C 0 0 2 0 0 0\n 0.4960 -0.9529 0.0000 C 0 0 2 0 0 0\n 0.6513 -2.2149 0.0000 C 0 0 1 0 0 0\n -0.7183 -2.0601 0.0000 O 0 0\n -1.2216 0.7840 0.0000 C 0 0\n 1.7172 -3.2702 0.0000 R# 0 0\n 2.3209 1.2498 0.0000 O 0 0\n 3.7640 0.8408 0.0000 R# 0 0\n 0.3758 1.5136 0.0000 F 0 0\n -2.6483 1.2498 0.0000 O 0 0\n -2.9590 2.7173 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 5 4 1 6\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 6\n 6 9 1 6\n 3 1 1 0\n 5 2 1 0\n 4 10 1 1\n 10 11 1 0\n 2 12 1 1\n 8 13 1 0\n 13 14 1 0\nM RGP 3 9 3 11 2 14 1\nM END\n> <Name>\n(R)-F-cLNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRflcln\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(R)-Sulfoxide BNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -1.7573 0.3923 0.0000 C 0 0\n -0.3792 0.2175 0.0000 S 0 0\n -0.8961 -0.6891 0.0000 C 0 0 1 0 0 0\n 1.2548 0.2221 0.0000 C 0 0 2 0 0 0\n 0.4960 -0.9529 0.0000 C 0 0 2 0 0 0\n 0.6513 -2.2149 0.0000 C 0 0 1 0 0 0\n -0.7183 -2.0601 0.0000 O 0 0\n -1.2216 0.7840 0.0000 C 0 0\n 1.7172 -3.2702 0.0000 R# 0 0\n 2.3209 1.2498 0.0000 O 0 0\n 3.7640 0.8408 0.0000 R# 0 0\n 0.3758 1.5136 0.0000 O 0 0\n -2.6483 1.2498 0.0000 O 0 0\n -2.9590 2.7173 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 6\n 6 9 1 6\n 3 1 1 0\n 5 2 1 6\n 4 10 1 1\n 10 11 1 0\n 2 12 2 0\n 8 13 1 0\n 13 14 1 0\nM RGP 3 9 3 11 2 14 1\nM END\n> <Name>\n(R)-Sulfoxide BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRso2ln\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(R)-cEt BNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n 0.3212 -2.3936 0.0000 C 0 0 1 0 0 0\n 0.5197 -1.0187 0.0000 O 0 0\n -0.4918 -1.2754 0.0000 C 0 0 1 0 0 0\n 0.9595 0.5550 0.0000 C 0 0 2 0 0 0\n -0.3752 0.1366 0.0000 C 0 0 2 0 0 0\n -1.5502 0.6224 0.0000 C 0 0 1 0 0 0\n -1.7659 -0.7389 0.0000 O 0 0\n -1.0347 0.1321 0.0000 C 0 0\n -2.2835 1.9310 0.0000 R# 0 0\n 0.6815 -3.8497 0.0000 C 0 0\n 2.2340 1.3089 0.0000 O 0 0\n 3.5438 0.5778 0.0000 R# 0 0\n -0.1032 1.3089 0.0000 O 0 0\n -0.6554 2.7036 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 1\n 3 1 1 0\n 5 2 1 1\n 1 10 1 6\n 4 11 1 6\n 11 12 1 0\n 8 13 1 0\n 13 14 1 0\nM RGP 3 9 3 12 2 14 1\nM END\n> <Name>\n(R)-cEt BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRcet\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(R)-cMOE BNA\n SciTegic07272112182D\n\n 16 17 0 0 1 0 999 V2000\n 0.0326 -1.7717 0.0000 C 0 0 1 0 0 0\n 0.2312 -0.3968 0.0000 O 0 0\n -0.7803 -0.6535 0.0000 C 0 0 1 0 0 0\n 0.6709 1.1769 0.0000 C 0 0 2 0 0 0\n -0.6638 0.7585 0.0000 C 0 0 2 0 0 0\n -1.8388 1.2444 0.0000 C 0 0 1 0 0 0\n -2.0544 -0.1170 0.0000 O 0 0\n -1.3232 0.7540 0.0000 C 0 0\n -2.5721 2.5529 0.0000 R# 0 0\n 0.3944 -3.2175 0.0000 C 0 0\n 1.9455 1.9308 0.0000 O 0 0\n 3.2552 1.1997 0.0000 R# 0 0\n 1.8372 -3.6309 0.0000 O 0 0\n 2.2012 -5.0861 0.0000 C 0 0\n -0.3917 1.9308 0.0000 O 0 0\n -0.9439 3.3255 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 1\n 3 1 1 0\n 5 2 1 1\n 1 10 1 6\n 4 11 1 6\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 8 15 1 0\n 15 16 1 0\nM RGP 3 9 3 12 2 16 1\nM END\n> <Name>\n(R)-cMOE BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRcmoe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(RC5,SP)-a,b-CNA\n SciTegic07272112182D\n\n 16 17 0 0 1 0 999 V2000\n -1.3284 -2.5753 0.0000 R# 0 0\n -2.4643 -1.5956 0.0000 P 0 0 2 0 0 0\n -3.5768 -0.5894 0.0000 O 0 0\n -3.2616 0.8771 0.0000 C 0 0\n -1.8340 1.3374 0.0000 C 0 0\n -0.7215 0.3312 0.0000 C 0 0 1 0 0 0\n -1.0367 -1.1353 0.0000 O 0 0\n 1.8990 -0.0975 0.0000 C 0 0 1 0 0 0\n 3.1131 0.7834 0.0000 C 0 0\n 2.6505 2.2103 0.0000 C 0 0 1 0 0 0\n 1.1505 2.2113 0.0000 O 0 0\n 0.7068 0.7917 0.0000 C 0 0 2 0 0 0\n -3.9024 -2.0223 0.0000 O 0 0\n 1.8896 -1.5956 0.0000 O 0 0\n 3.5330 3.4232 0.0000 R# 0 0\n 3.1834 -2.3546 0.0000 R# 0 0\n 2 1 1 6\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 6 5 1 6\n 6 7 1 0\n 7 2 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 12 11 1 1\n 12 8 1 0\n 12 6 1 0\n 2 13 2 0\n 8 14 1 6\n 10 15 1 1\n 14 16 1 0\nM RGP 3 1 1 15 3 16 2\nM END\n> <Name>\n(RC5,SP)-a,b-CNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRSpabC\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(Rp)-Methylphosphonate\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n -0.8998 -1.0391 0.0000 R# 0 0\n -0.1499 0.2600 0.0000 P 0 0 2 0 0 0\n 0.6000 -1.0391 0.0000 R# 0 0\n 1.3501 0.2596 0.0000 C 0 0\n -0.9004 1.5587 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 2 4 1 0\n 2 5 2 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\n(Rp)-Methylphosphonate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRmp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\n(Rp)-Phosphorothioate\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n -0.8998 -1.0391 0.0000 R# 0 0\n -0.1499 0.2600 0.0000 P 0 0 2 0 0 0\n 0.6000 -1.0391 0.0000 R# 0 0\n 1.3501 0.2596 0.0000 O 0 0\n -0.9004 1.5587 0.0000 S 0 0\n 2 1 1 1\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\n(Rp)-Phosphorothioate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRsp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\n(S)-5-Hydroxyethyl-2-deoxyribose\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n 1.2991 -0.5282 0.0000 C 0 0 1 0 0 0\n 1.7163 -1.9690 0.0000 C 0 0\n 0.4749 -2.8110 0.0000 C 0 0 1 0 0 0\n -0.7095 -1.8906 0.0000 O 0 0\n -0.2001 -0.4797 0.0000 C 0 0 2 0 0 0\n 0.4264 -4.3102 0.0000 R# 0 0\n -1.0386 0.7620 0.0000 C 0 0 2 0 0 0\n -0.3822 2.1117 0.0000 C 0 0\n -2.5355 0.6530 0.0000 O 0 0\n 2.2209 0.6530 0.0000 O 0 0\n -1.2221 3.3555 0.0000 C 0 0\n -0.5661 4.7044 0.0000 O 0 0\n -3.1900 -0.6967 0.0000 R# 0 0\n 3.7065 0.4459 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 6\n 5 1 1 0\n 3 6 1 6\n 5 7 1 0\n 7 8 1 1\n 7 9 1 0\n 1 10 1 1\n 8 11 1 0\n 11 12 1 0\n 9 13 1 0\n 10 14 1 0\nM RGP 3 6 3 13 1 14 2\nM END\n> <Name>\n(S)-5-Hydroxyethyl-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nShe5d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(S)-5-Methyldeoxyribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.3753 -0.3787 0.0000 C 0 0 2 0 0 0\n 0.9565 0.3115 0.0000 C 0 0 2 0 0 0\n 2.0244 -0.7418 0.0000 C 0 0\n 1.3527 -2.0830 0.0000 C 0 0 1 0 0 0\n -0.1304 -1.8586 0.0000 O 0 0\n 1.1776 1.7933 0.0000 O 0 0\n -1.7135 0.2950 0.0000 C 0 0 1 0 0 0\n 2.0429 -3.4148 0.0000 R# 0 0\n 2.5727 2.3443 0.0000 R# 0 0\n -1.8003 1.7933 0.0000 O 0 0\n -3.1400 2.4679 0.0000 R# 0 0\n -2.9673 -0.5284 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 6\n 2 6 1 1\n 1 7 1 0\n 4 8 1 6\n 6 9 1 0\n 7 10 1 0\n 10 11 1 0\n 7 12 1 6\nM RGP 3 8 3 9 2 11 1\nM END\n> <Name>\n(S)-5-Methyldeoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSm5d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(S)-cEt BNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n 0.3212 -2.3936 0.0000 C 0 0 2 0 0 0\n 0.5197 -1.0187 0.0000 O 0 0\n -0.4918 -1.2754 0.0000 C 0 0 1 0 0 0\n 0.9595 0.5550 0.0000 C 0 0 2 0 0 0\n -0.3752 0.1366 0.0000 C 0 0 2 0 0 0\n -1.5502 0.6224 0.0000 C 0 0 1 0 0 0\n -1.7659 -0.7389 0.0000 O 0 0\n -1.0347 0.1321 0.0000 C 0 0\n -2.2835 1.9310 0.0000 R# 0 0\n 0.6815 -3.8497 0.0000 C 0 0\n 2.2340 1.3089 0.0000 O 0 0\n 3.5438 0.5778 0.0000 R# 0 0\n -0.1032 1.3089 0.0000 O 0 0\n -0.6554 2.7036 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 1\n 3 1 1 0\n 5 2 1 1\n 1 10 1 1\n 4 11 1 6\n 11 12 1 0\n 8 13 1 0\n 13 14 1 0\nM RGP 3 9 3 12 2 14 1\nM END\n> <Name>\n(S)-cEt BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncet\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(S)-cMOE BNA\n SciTegic07272112182D\n\n 16 17 0 0 1 0 999 V2000\n 0.0326 -1.7717 0.0000 C 0 0 2 0 0 0\n 0.2312 -0.3968 0.0000 O 0 0\n -0.7803 -0.6535 0.0000 C 0 0 1 0 0 0\n 0.6709 1.1769 0.0000 C 0 0 2 0 0 0\n -0.6638 0.7585 0.0000 C 0 0 2 0 0 0\n -1.8388 1.2444 0.0000 C 0 0 1 0 0 0\n -2.0544 -0.1170 0.0000 O 0 0\n -1.3232 0.7540 0.0000 C 0 0\n -2.5721 2.5529 0.0000 R# 0 0\n 0.3944 -3.2175 0.0000 C 0 0\n 1.9455 1.9308 0.0000 O 0 0\n 3.2552 1.1997 0.0000 R# 0 0\n 1.8372 -3.6309 0.0000 O 0 0\n 2.2012 -5.0861 0.0000 C 0 0\n -0.3917 1.9308 0.0000 O 0 0\n -0.9439 3.3255 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 1\n 3 1 1 0\n 5 2 1 1\n 1 10 1 1\n 4 11 1 6\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 8 15 1 0\n 15 16 1 0\nM RGP 3 9 3 12 2 16 1\nM END\n> <Name>\n(S)-cMOE BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nScmoe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(S)-cPr-BNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 0.1794 -2.1108 0.0000 C 0 0 2 0 0 0\n 0.3780 -0.7359 0.0000 O 0 0\n -0.6335 -0.9926 0.0000 C 0 0 1 0 0 0\n 0.8177 0.8378 0.0000 C 0 0 2 0 0 0\n -0.5170 0.4194 0.0000 C 0 0 2 0 0 0\n -1.6920 0.9053 0.0000 C 0 0 1 0 0 0\n -1.9076 -0.4561 0.0000 O 0 0\n -1.1764 0.4149 0.0000 C 0 0\n -2.4253 2.2138 0.0000 R# 0 0\n 2.0923 1.5917 0.0000 O 0 0\n 3.4020 0.8606 0.0000 R# 0 0\n 0.5412 -3.5566 0.0000 C 0 0\n 1.9832 -3.9698 0.0000 C 0 0\n -0.2449 1.5917 0.0000 O 0 0\n -0.7971 2.9864 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 1\n 3 1 1 0\n 5 2 1 1\n 4 10 1 6\n 10 11 1 0\n 1 12 1 1\n 12 13 1 0\n 8 14 1 0\n 14 15 1 0\nM RGP 3 9 3 11 2 15 1\nM END\n> <Name>\n(S)-cPr-BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nScPr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(SC5,RP)-a,b-CNA\n SciTegic07272112182D\n\n 16 17 0 0 1 0 999 V2000\n -1.3284 -2.5753 0.0000 R# 0 0\n -2.4643 -1.5956 0.0000 P 0 0 1 0 0 0\n -3.5768 -0.5894 0.0000 O 0 0\n -3.2616 0.8771 0.0000 C 0 0\n -1.8340 1.3374 0.0000 C 0 0\n -0.7215 0.3312 0.0000 C 0 0 2 0 0 0\n -1.0367 -1.1353 0.0000 O 0 0\n 1.8990 -0.0975 0.0000 C 0 0 1 0 0 0\n 3.1131 0.7834 0.0000 C 0 0\n 2.6505 2.2103 0.0000 C 0 0 1 0 0 0\n 1.1505 2.2113 0.0000 O 0 0\n 0.7068 0.7917 0.0000 C 0 0 2 0 0 0\n -3.9024 -2.0223 0.0000 O 0 0\n 1.8896 -1.5956 0.0000 O 0 0\n 3.5330 3.4232 0.0000 R# 0 0\n 3.1834 -2.3546 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 6 5 1 1\n 6 7 1 0\n 7 2 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 12 11 1 1\n 12 8 1 0\n 12 6 1 0\n 2 13 2 0\n 8 14 1 6\n 10 15 1 1\n 14 16 1 0\nM RGP 3 1 1 15 3 16 2\nM END\n> <Name>\n(SC5,RP)-a,b-CNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSRpabC\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(Sp)-Methylphosphonate\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n -0.8998 -1.0391 0.0000 R# 0 0\n -0.1499 0.2600 0.0000 P 0 0 1 0 0 0\n 0.6000 -1.0391 0.0000 R# 0 0\n 1.3501 0.2596 0.0000 C 0 0\n -0.9004 1.5587 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 2 4 1 0\n 2 5 2 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\n(Sp)-Methylphosphonate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSmp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\n(Sp)-Phosphorothioate\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n -0.8998 -1.0391 0.0000 R# 0 0\n -0.1499 0.2600 0.0000 P 0 0 1 0 0 0\n 0.6000 -1.0391 0.0000 R# 0 0\n 1.3501 0.2596 0.0000 O 0 0\n -0.9004 1.5587 0.0000 S 0 0\n 2 1 1 6\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\n(Sp)-Phosphorothioate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSsp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nANA\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.5573 -0.8976 0.0000 O 0 0\n -0.8058 0.4006 0.0000 C 0 0 1 0 0 0\n 0.6942 0.3989 0.0000 C 0 0 2 0 0 0\n 1.4427 -0.9010 0.0000 C 0 0 2 0 0 0\n 0.6912 -2.1992 0.0000 C 0 0 1 0 0 0\n -0.8088 -2.1975 0.0000 C 0 0\n 1.4396 -3.4991 0.0000 R# 0 0\n 2.9427 -0.9028 0.0000 O 0 0\n 1.4434 1.6993 0.0000 O 0 0\n -1.5574 1.6997 0.0000 C 0 0\n 2.9434 1.7016 0.0000 R# 0 0\n -3.0582 1.6993 0.0000 O 0 0\n -3.8094 2.9977 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 6\n 4 8 1 1\n 3 9 1 1\n 2 10 1 6\n 9 11 1 0\n 10 12 1 0\n 12 13 1 0\nM RGP 3 7 3 11 2 13 1\nM END\n> <Name>\nANA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nana\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nAmino\n SciTegic07272112182D\n\n 3 2 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 2.5993 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nAmino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nhn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nAmino(S)-cEt (N-methyl)\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 0.1898 -2.3512 0.0000 C 0 0 2 0 0 0\n 0.3884 -0.9763 0.0000 N 0 0\n -0.6231 -1.2330 0.0000 C 0 0 1 0 0 0\n 0.8281 0.5974 0.0000 C 0 0 2 0 0 0\n -0.5066 0.1790 0.0000 C 0 0 2 0 0 0\n -1.6816 0.6649 0.0000 C 0 0 1 0 0 0\n -1.8972 -0.6965 0.0000 O 0 0\n -1.1660 0.1745 0.0000 C 0 0\n -2.4149 1.9734 0.0000 R# 0 0\n 0.5502 -3.8073 0.0000 C 0 0\n 2.1027 1.3513 0.0000 O 0 0\n 3.4125 0.6202 0.0000 R# 0 0\n -0.2345 1.3513 0.0000 O 0 0\n -0.7867 2.7460 0.0000 R# 0 0\n 1.8388 -0.5938 0.0000 C 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 1\n 3 1 1 0\n 5 2 1 1\n 1 10 1 1\n 4 11 1 6\n 11 12 1 0\n 8 13 1 0\n 13 14 1 0\n 2 15 1 0\nM RGP 3 9 3 12 2 14 1\nM END\n> <Name>\nAmino(S)-cEt (N-methyl)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSmn2ce\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nAmino(R)-cEt (N-methyl)\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 0.1898 -2.3512 0.0000 C 0 0 1 0 0 0\n 0.3884 -0.9763 0.0000 N 0 0\n -0.6231 -1.2330 0.0000 C 0 0 1 0 0 0\n 0.8281 0.5974 0.0000 C 0 0 2 0 0 0\n -0.5066 0.1790 0.0000 C 0 0 2 0 0 0\n -1.6816 0.6649 0.0000 C 0 0 1 0 0 0\n -1.8972 -0.6965 0.0000 O 0 0\n -1.1660 0.1745 0.0000 C 0 0\n -2.4149 1.9734 0.0000 R# 0 0\n 0.5502 -3.8073 0.0000 C 0 0\n 2.1027 1.3513 0.0000 O 0 0\n 3.4125 0.6202 0.0000 R# 0 0\n -0.2345 1.3513 0.0000 O 0 0\n -0.7867 2.7460 0.0000 R# 0 0\n 1.8388 -0.5938 0.0000 C 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 1\n 3 1 1 0\n 5 2 1 1\n 1 10 1 6\n 4 11 1 6\n 11 12 1 0\n 8 13 1 0\n 13 14 1 0\n 2 15 1 0\nM RGP 3 9 3 12 2 14 1\nM END\n> <Name>\nAmino(R)-cEt (N-methyl)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRmn2ce\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nAmino-Modier C6 dT\n SciTegic09012117322D\n\n 23 23 0 0 0 0 999 V2000\n 2.0219 0.3424 0.0000 C 0 0\n 3.1566 -0.6398 0.0000 C 0 0\n 4.5750 -0.1491 0.0000 C 0 0\n 5.7097 -1.1313 0.0000 C 0 0\n 7.1281 -0.6406 0.0000 C 0 0\n 8.2628 -1.6228 0.0000 C 0 0\n 9.6812 -1.1321 0.0000 N 0 0\n 10.8153 -2.1138 0.0000 R# 0 0\n 9.9647 0.3408 0.0000 R# 0 0\n -4.7837 -0.6388 0.0000 C 0 0\n -4.5027 0.8347 0.0000 C 0 0\n -5.6382 1.8148 0.0000 C 0 0\n -7.0548 1.3214 0.0000 N 0 0\n -7.3358 -0.1520 0.0000 C 0 0\n -8.7523 -0.6454 0.0000 O 0 0\n -5.3572 3.2882 0.0000 O 0 0\n -6.2002 -1.1321 0.0000 N 0 0\n -3.0843 1.3254 0.0000 C 0 0\n -6.4812 -2.6056 0.0000 R# 0 0\n -1.9496 0.3432 0.0000 C 0 0\n -0.5312 0.8339 0.0000 C 0 0\n 0.6035 -0.1483 0.0000 N 0 0\n -0.2477 2.3069 0.0000 O 0 0\n 22 1 1 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 7 9 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 2 0\n 12 16 2 0\n 17 10 1 0\n 17 14 1 0\n 11 18 1 0\n 17 19 1 0\n 18 20 2 0\n 20 21 1 0\n 21 22 1 0\n 21 23 2 0\nM RGP 3 8 2 9 3 19 1\nM END\n> <Name>\nAmino-Modier C6 dT\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnC6n5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]H\n\n$$$$\nAmino-Modier C6 dC\n SciTegic09012117322D\n\n 23 23 0 0 0 0 999 V2000\n 2.0219 0.3424 0.0000 C 0 0\n 3.1566 -0.6398 0.0000 C 0 0\n 4.5750 -0.1491 0.0000 C 0 0\n 5.7097 -1.1313 0.0000 C 0 0\n 7.1281 -0.6406 0.0000 C 0 0\n 8.2628 -1.6228 0.0000 C 0 0\n 9.6812 -1.1321 0.0000 N 0 0\n 10.8153 -2.1138 0.0000 R# 0 0\n 9.9647 0.3408 0.0000 R# 0 0\n -4.7837 -0.6388 0.0000 C 0 0\n -4.5027 0.8347 0.0000 C 0 0\n -5.6382 1.8148 0.0000 C 0 0\n -7.0548 1.3214 0.0000 N 0 0\n -7.3358 -0.1520 0.0000 C 0 0\n -8.7523 -0.6454 0.0000 O 0 0\n -5.3572 3.2882 0.0000 N 0 0\n -6.2002 -1.1321 0.0000 N 0 0\n -3.0843 1.3254 0.0000 C 0 0\n -6.4812 -2.6056 0.0000 R# 0 0\n -1.9496 0.3432 0.0000 C 0 0\n -0.5312 0.8339 0.0000 C 0 0\n 0.6035 -0.1483 0.0000 N 0 0\n -0.2477 2.3069 0.0000 O 0 0\n 22 1 1 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 7 9 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 15 2 0\n 12 16 1 0\n 17 10 1 0\n 17 14 1 0\n 11 18 1 0\n 17 19 1 0\n 18 20 2 0\n 20 21 1 0\n 21 22 1 0\n 21 23 2 0\nM RGP 3 8 2 9 3 19 1\nM END\n> <Name>\nAmino-Modier C6 dC\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnC6n5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]H\n\n$$$$\nAzidoadenine\n SciTegic07272112182D\n\n 14 15 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -2.5496 -4.4224 0.0000 N 0 0\n -1.7974 -5.7210 0.0000 N 0 3\n -1.0455 -7.0190 0.0000 N 0 5\n -3.8805 -1.4410 0.0000 R# 0 0\n 2.5981 -1.5000 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 4 1 0\n 8 10 1 0\n 10 11 2 0\n 11 12 2 0\n 7 13 1 0\n 1 14 1 0\nM CHG 2 11 1 12 -1\nM RGP 1 13 1\nM END\n> <Name>\nAzidoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\naz8A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nBenzylamino\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n -2.8595 2.5496 0.0000 R# 0 0\n -1.5606 1.7994 0.0000 N 0 0\n -0.2616 2.5496 0.0000 R# 0 0\n -1.5598 0.2986 0.0000 C 0 0\n -0.2602 -0.4520 0.0000 C 0 0\n -0.2574 -1.9520 0.0000 C 0 0\n 1.0374 0.3004 0.0000 C 0 0\n 1.0431 -2.6995 0.0000 C 0 0\n 2.3407 -1.9471 0.0000 C 0 0\n 2.3379 -0.4471 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 2 0\n 5 7 1 0\n 6 8 1 0\n 8 9 2 0\n 9 10 1 0\n 10 7 2 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nBenzylamino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbnn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nBicycloDNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n 0.6645 1.0853 0.0000 C 0 0 1 0 0 0\n 2.0572 0.5281 0.0000 C 0 0\n 1.9576 -0.9686 0.0000 C 0 0 1 0 0 0\n 0.5034 -1.3364 0.0000 O 0 0\n -0.2958 -0.0670 0.0000 C 0 0 2 0 0 0\n 3.1099 -1.9289 0.0000 R# 0 0\n 1.1757 -0.3289 0.0000 O 0 0\n -1.6736 0.4777 0.0000 C 0 0 2 0 0 0\n -1.5740 1.9744 0.0000 C 0 0\n -0.1198 2.3423 0.0000 C 0 0\n -1.2538 -1.2213 0.0000 H 0 0\n -2.9362 -0.3289 0.0000 O 0 0\n -4.2680 0.3612 0.0000 R# 0 0\n 2.6530 -0.5889 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 3 6 1 6\n 1 7 1 1\n 5 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 1 1 0\n 5 11 1 1\n 8 12 1 1\n 12 13 1 0\n 7 14 1 0\nM RGP 3 6 3 13 1 14 2\nM END\n> <Name>\nBicycloDNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbcdna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nCarbocyclic-2-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6450 -0.4268 0.0000 C 0 0 2 0 0 0\n 0.6867 0.2634 0.0000 C 0 0 2 0 0 0\n 1.7547 -0.7899 0.0000 C 0 0\n 1.0830 -2.1310 0.0000 C 0 0 1 0 0 0\n -0.4002 -1.9066 0.0000 C 0 0\n -1.9833 0.2470 0.0000 C 0 0\n 0.9078 1.7453 0.0000 O 0 0\n 2.3029 2.2963 0.0000 R# 0 0\n 1.7731 -3.4628 0.0000 R# 0 0\n -2.0700 1.7453 0.0000 O 0 0\n -3.4098 2.4198 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 6 10 1 0\n 10 11 1 0\nM RGP 3 8 2 9 3 11 1\nM END\n> <Name>\nCarbocyclic-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc4d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nCarbonyl\n SciTegic07272112182D\n\n 4 3 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 2.5993 0.0004 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nCarbonyl\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nco\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nCarbonylmethyl\n SciTegic09012117322D\n\n 5 4 0 0 0 0 999 V2000\n -1.2000 1.0394 0.0000 R# 0 0\n -0.4504 -0.2599 0.0000 C 0 0\n -1.2013 -1.5584 0.0000 O 0 0\n 1.0504 -0.2599 0.0000 C 0 0\n 1.8013 1.0387 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\nM RGP 2 1 1 5 2\nM END\n> <Name>\nCarbonylmethyl\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncm\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nCeNA\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.3121 -0.9728 0.0000 C 0 0\n -0.5606 0.3254 0.0000 C 0 0 1 0 0 0\n 0.9394 0.3236 0.0000 C 0 0 2 0 0 0\n 1.6879 -0.9763 0.0000 C 0 0\n 0.9364 -2.2744 0.0000 C 0 0 1 0 0 0\n -0.5636 -2.2727 0.0000 C 0 0\n 1.6849 -3.5743 0.0000 R# 0 0\n 1.6886 1.6241 0.0000 O 0 0\n -1.3122 1.6245 0.0000 C 0 0\n 3.1886 1.6264 0.0000 R# 0 0\n -2.8130 1.6241 0.0000 O 0 0\n -3.5642 2.9224 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 2 0\n 5 7 1 6\n 3 8 1 1\n 2 9 1 6\n 8 10 1 0\n 9 11 1 0\n 11 12 1 0\nM RGP 3 7 3 10 2 12 1\nM END\n> <Name>\nCeNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncena\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nDifluoromethylene\n SciTegic07272112182D\n\n 5 4 0 0 0 0 999 V2000\n -1.7998 0.0000 0.0000 R# 0 0\n -0.2998 0.0000 0.0000 C 0 0\n 1.2002 0.0000 0.0000 R# 0 0\n 0.4498 -1.2993 0.0000 F 0 0\n 0.4498 1.2993 0.0000 F 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nDifluoromethylene\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfl2me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nDihydrouracil\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 2.5981 1.5000 0.0000 O 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n -2.5981 -1.5000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 2 7 2 0\n 6 8 2 0\n 5 9 1 0\nM RGP 1 9 1\nM END\n> <Name>\nDihydrouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nhU\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nEthylamino\n SciTegic07272112182D\n\n 5 4 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.8993 0.7496 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nEthylamino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nen\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nEthylphosphate\n SciTegic07272112182D\n\n 7 6 0 0 0 0 999 V2000\n -0.1063 -1.6704 0.0000 R# 0 0\n 0.6436 -0.3713 0.0000 P 0 0\n 1.3935 -1.6704 0.0000 R# 0 0\n 2.1436 -0.3717 0.0000 O 0 0\n -0.1074 0.9281 0.0000 O 0 0\n -1.6082 0.9285 0.0000 C 0 0\n -2.3587 2.2272 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\n 5 6 1 0\n 6 7 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nEthylphosphate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\neop\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nFluoro-CeNA\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.5573 -0.8976 0.0000 C 0 0\n -0.8058 0.4006 0.0000 C 0 0 1 0 0 0\n 0.6942 0.3989 0.0000 C 0 0 2 0 0 0\n 1.4427 -0.9010 0.0000 C 0 0 2 0 0 0\n 0.6912 -2.1992 0.0000 C 0 0 1 0 0 0\n -0.8088 -2.1975 0.0000 C 0 0\n 1.4396 -3.4991 0.0000 R# 0 0\n 1.4434 1.6993 0.0000 O 0 0\n -1.5574 1.6997 0.0000 C 0 0\n 2.9434 1.7016 0.0000 R# 0 0\n 2.9427 -0.9028 0.0000 F 0 0\n -3.0582 1.6993 0.0000 O 0 0\n -3.8094 2.9977 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 2 0\n 5 7 1 6\n 3 8 1 1\n 2 9 1 6\n 8 10 1 0\n 4 11 1 1\n 9 12 1 0\n 12 13 1 0\nM RGP 3 7 3 10 2 13 1\nM END\n> <Name>\nFluoro-CeNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfcena\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nG-clamp (9-(aminoethoxy)phenoxazine)\n SciTegic07272112182D\n\n 20 22 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 N 0 0\n -2.5981 -1.5000 0.0000 O 0 0\n 2.5981 -1.5000 0.0000 N 0 0\n 3.8971 -0.7500 0.0000 C 0 0\n 3.8971 0.7500 0.0000 C 0 0\n 2.5981 1.5000 0.0000 O 0 0\n 5.1962 -1.5000 0.0000 C 0 0\n 6.4952 -0.7500 0.0000 C 0 0\n 6.4952 0.7500 0.0000 C 0 0\n 5.1961 1.5000 0.0000 C 0 0\n 5.1993 -3.0008 0.0000 O 0 0\n 6.5001 -3.7494 0.0000 C 0 0\n 6.5032 -5.2502 0.0000 C 0 0\n 7.8033 -5.9983 0.0000 N 0 0\n -2.5981 1.5000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 1 6 2 0\n 5 7 2 0\n 1 8 1 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 2 11 1 0\n 9 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 15 2 0\n 10 15 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 12 16 1 0\n 4 20 1 0\nM RGP 1 20 1\nM END\n> <Name>\nG-clamp (9-(aminoethoxy)phenoxazine)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ngclamp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nG-clamp (9-(guanylethoxy)phenoxazine)\n SciTegic07272112182D\n\n 23 25 0 0 0 0 999 V2000\n 0.0000 3.0000 0.0000 R# 0 0\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 6.0000 3.0000 0.0000 N 0 0\n 6.7500 1.7010 0.0000 C 0 0\n 6.0000 0.4019 0.0000 C 0 0\n 4.5000 0.4019 0.0000 O 0 0\n 8.2500 1.7010 0.0000 C 0 0\n 9.0000 0.4019 0.0000 C 0 0\n 8.2500 -0.8971 0.0000 C 0 0\n 6.7500 -0.8971 0.0000 C 0 0\n 9.0031 2.9992 0.0000 O 0 0\n 10.5039 2.9970 0.0000 C 0 0\n 11.2570 4.2952 0.0000 C 0 0\n 12.7578 4.2931 0.0000 N 0 0\n 13.5109 5.5913 0.0000 C 0 0\n 12.7632 6.8916 0.0000 N 0 0\n 15.0109 5.5891 0.0000 N 0 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 2 7 2 0\n 3 8 2 0\n 1 4 1 0\n 7 9 1 0\n 9 10 1 0\n 10 11 2 0\n 11 12 1 0\n 6 12 1 0\n 10 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 11 16 1 0\n 13 17 1 0\n 17 18 1 0\n 18 19 1 0\n 19 20 1 0\n 20 21 1 0\n 21 22 1 0\n 21 23 2 0\nM RGP 1 1 1\nM END\n> <Name>\nG-clamp (9-(guanylethoxy)phenoxazine)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nggclam\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nOrotic Acid\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -2.5981 1.5000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 O 0 0\n -2.5981 -1.5000 0.0000 R# 0 0\n 0.0031 -3.0008 0.0000 C 0 0\n -1.2946 -3.7531 0.0000 O 0 0\n 1.3032 -3.7490 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 6 7 2 0\n 2 8 2 0\n 5 9 1 0\n 4 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 1 9 1\nM END\n> <Name>\nOrotic Acid\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nOro\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nIsobutylamino\n SciTegic07272112182D\n\n 7 6 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 C 0 0\n 3.9000 2.2500 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 5 7 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nIsobutylamino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nibun\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nIsoguanine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 N 0 0\n 3.5643 -9.2321 0.0000 O 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 3 1 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 2 11 2 0\n 9 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\nIsoguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nisoG\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nL-2-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.8896 -1.1996 0.0000 O 0 0\n -0.3776 0.2103 0.0000 C 0 0 2 0 0 0\n 0.2930 -2.1222 0.0000 C 0 0 1 0 0 0\n 1.1215 0.1590 0.0000 C 0 0 1 0 0 0\n 1.5360 -1.2826 0.0000 C 0 0\n 2.0407 1.3422 0.0000 O 0 0\n -1.2188 1.4501 0.0000 C 0 0\n -2.7158 1.3422 0.0000 O 0 0\n -3.5580 2.5834 0.0000 R# 0 0\n 0.2417 -3.6214 0.0000 R# 0 0\n 3.5268 1.1385 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 1\n 3 5 1 0\n 4 5 1 0\n 4 6 1 6\n 7 8 1 0\n 8 9 1 0\n 3 10 1 1\n 6 11 1 0\nM RGP 3 9 1 10 3 11 2\nM END\n> <Name>\nL-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nLd\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nMethylamino\n SciTegic07272112182D\n\n 4 3 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 2.5993 0.0004 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nMethylamino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nMethylene\n SciTegic07272112182D\n\n 3 2 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 2.5993 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nMethylene\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nme\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nMethylene cLNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -1.7573 0.3923 0.0000 C 0 0\n -0.3792 0.2175 0.0000 C 0 0\n -0.8961 -0.6891 0.0000 C 0 0 1 0 0 0\n 1.2548 0.2221 0.0000 C 0 0 2 0 0 0\n 0.4960 -0.9529 0.0000 C 0 0 2 0 0 0\n 0.6513 -2.2149 0.0000 C 0 0 1 0 0 0\n -0.7183 -2.0601 0.0000 O 0 0\n -1.2216 0.7840 0.0000 C 0 0\n 1.7172 -3.2702 0.0000 R# 0 0\n 2.3209 1.2498 0.0000 O 0 0\n 3.7640 0.8408 0.0000 R# 0 0\n 0.3758 1.5136 0.0000 C 0 0\n -2.6483 1.2498 0.0000 O 0 0\n -2.9590 2.7173 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 6\n 6 9 1 6\n 3 1 1 0\n 5 2 1 6\n 4 10 1 1\n 10 11 1 0\n 2 12 2 0\n 8 13 1 0\n 13 14 1 0\nM RGP 3 9 3 11 2 14 1\nM END\n> <Name>\nMethylene cLNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmeclna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nMethylenephosphonate\n SciTegic07272112182D\n\n 6 5 0 0 0 0 999 V2000\n -1.3755 0.2167 0.0000 C 0 0\n 0.1253 0.2167 0.0000 P 0 0\n 0.8749 -1.0826 0.0000 R# 0 0\n 0.8762 1.5152 0.0000 O 0 0\n 1.6253 0.2160 0.0000 O 0 0\n -2.1263 -1.0819 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\n 1 6 1 0\nM RGP 2 3 2 6 1\nM END\n> <Name>\nMethylenephosphonate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmepo2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nMethylphosphonate\n SciTegic07272112182D\n\n 5 4 0 0 0 0 999 V2000\n -1.7998 0.0000 0.0000 R# 0 0\n -0.2998 0.0000 0.0000 P 0 0\n 1.2002 0.0000 0.0000 R# 0 0\n 0.4498 -1.2993 0.0000 O 0 0\n 0.4498 1.2993 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nMethylphosphonate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nMethylthiophosphonate\n SciTegic07272112182D\n\n 5 4 0 0 0 0 999 V2000\n -1.7998 0.0000 0.0000 R# 0 0\n -0.2998 0.0000 0.0000 P 0 0\n 1.2002 0.0000 0.0000 R# 0 0\n 0.4498 -1.2993 0.0000 S 0 0\n 0.4498 1.2993 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nMethylthiophosphonate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmsp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nN2-(2-Amino)ethyl guanine\n SciTegic07272112182D\n\n 15 16 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5972 1.5031 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2570 0.0000 N 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 7 8 2 0\n 5 8 1 0\n 6 9 2 0\n 2 10 1 0\n 4 11 1 0\n 7 11 1 0\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 14 15 1 0\nM RGP 1 12 1\nM END\n> <Name>\nN2-(2-Amino)ethyl guanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnen2G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN2-(3-Aminopropyl) guanine\n SciTegic07272112182D\n\n 16 17 0 0 0 0 999 V2000\n 6.9961 1.8908 0.0000 C 0 0\n 5.5695 1.4274 0.0000 C 0 0\n 5.2575 -0.0398 0.0000 N 0 0\n 6.3721 -1.0436 0.0000 C 0 0\n 7.7987 -0.5802 0.0000 N 0 0\n 8.1107 0.8870 0.0000 C 0 0\n 9.5374 1.3504 0.0000 O 0 0\n 6.0630 -2.5123 0.0000 N 0 0\n 7.1796 -3.5150 0.0000 C 0 0\n 6.8705 -4.9837 0.0000 C 0 0\n 7.9872 -5.9864 0.0000 C 0 0\n 7.6782 -7.4543 0.0000 N 0 0\n 6.9965 3.3900 0.0000 N 0 0\n 5.5700 3.8536 0.0000 C 0 0\n 4.6882 2.6402 0.0000 N 0 0\n 3.1882 2.6402 0.0000 R# 0 0\n 2 1 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 4 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 1 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 2 1 0\n 15 16 1 0\nM RGP 1 16 1\nM END\n> <Name>\nN2-(3-Aminopropyl) guanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnpr2G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN2-(Aminoethyl)aminoadenine\n SciTegic07272112182D\n\n 15 16 0 0 0 0 999 V2000\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2570 0.0000 N 0 0\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n 2.5972 1.5031 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 4 9 2 0\n 7 10 1 0\n 10 11 1 0\n 11 12 2 0\n 8 12 1 0\n 9 13 1 0\n 5 14 1 0\n 10 15 1 0\n 1 14 1 0\nM RGP 1 15 1\nM END\n> <Name>\nN2-(Aminoethyl)aminoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnen2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN2-(Methoxypropylamino)adenine\n SciTegic07272112182D\n\n 17 18 0 0 0 0 999 V2000\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2578 0.0000 C 0 0\n 5.1894 6.0109 0.0000 O 0 0\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n 2.5972 1.5031 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 5.1872 7.5109 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 5 10 2 0\n 8 11 1 0\n 11 12 1 0\n 12 13 2 0\n 9 13 1 0\n 10 14 1 0\n 6 15 1 0\n 11 16 1 0\n 1 15 1 0\n 4 17 1 0\nM RGP 1 16 1\nM END\n> <Name>\nN2-(Methoxypropylamino)adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmoprn2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN2-Imidazoylpropylguanine\n SciTegic07272112182D\n\n 20 22 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5972 1.5031 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 5.1894 6.0109 0.0000 N 0 0\n 5.3272 7.4918 0.0000 C 0 0\n 6.7944 7.8037 0.0000 N 0 0\n 7.5444 6.5046 0.0000 C 0 0\n 6.5408 5.3899 0.0000 C 0 0\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2578 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 7 8 2 0\n 5 8 1 0\n 6 9 2 0\n 2 10 1 0\n 4 11 1 0\n 7 11 1 0\n 11 12 1 0\n 13 14 1 0\n 14 15 2 0\n 15 16 1 0\n 16 17 2 0\n 13 17 1 0\n 10 18 1 0\n 18 19 1 0\n 19 20 1 0\n 13 20 1 0\nM RGP 1 12 1\nM END\n> <Name>\nN2-Imidazoylpropylguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nimpr2G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN2-Phenethylaminoadenine\n SciTegic07272112182D\n\n 20 22 0 0 0 0 999 V2000\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2578 0.0000 C 0 0\n 5.1876 6.0124 0.0000 C 0 0\n 5.1824 7.5124 0.0000 C 0 0\n 3.8807 8.2579 0.0000 C 0 0\n 2.5843 7.5034 0.0000 C 0 0\n 2.5895 6.0034 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n 2.5972 1.5031 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 3 8 1 0\n 9 10 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 9 14 2 0\n 12 15 1 0\n 15 16 1 0\n 16 17 2 0\n 13 17 1 0\n 14 18 1 0\n 10 19 1 0\n 15 20 1 0\n 1 19 1 0\nM RGP 1 20 1\nM END\n> <Name>\nN2-Phenethylaminoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nphen2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN2-[(Imidazo-2-yl)ethylamino]adenine\n SciTegic07272112182D\n\n 19 21 0 0 0 0 999 V2000\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2578 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n 2.5972 1.5031 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 5.1017 6.1219 0.0000 N 0 0\n 4.6332 7.5469 0.0000 C 0 0\n 3.1332 7.5416 0.0000 C 0 0\n 2.6746 6.1134 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 4 9 2 0\n 7 10 1 0\n 10 11 1 0\n 11 12 2 0\n 8 12 1 0\n 9 13 1 0\n 5 14 1 0\n 10 15 1 0\n 1 14 1 0\n 3 16 1 0\n 16 17 1 0\n 17 18 2 0\n 18 19 1 0\n 3 19 2 0\nM RGP 1 15 1\nM END\n> <Name>\nN2-[(Imidazo-2-yl)ethylamino]adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n2imen2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN2-[(Imidazol-4-yl)ethyl]guanine\n SciTegic07272112182D\n\n 19 21 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5972 1.5031 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2578 0.0000 C 0 0\n 5.1017 6.1219 0.0000 N 0 0\n 4.6332 7.5469 0.0000 C 0 0\n 3.1332 7.5416 0.0000 N 0 0\n 2.6746 6.1134 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 7 8 2 0\n 5 8 1 0\n 6 9 2 0\n 2 10 1 0\n 4 11 1 0\n 7 11 1 0\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 15 16 1 0\n 16 17 2 0\n 17 18 1 0\n 15 19 2 0\n 14 15 1 0\n 18 19 1 0\nM RGP 1 12 1\nM END\n> <Name>\nN2-[(Imidazol-4-yl)ethyl]guanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n4imen2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN3-(2-Cyanoethyl)thymine\n SciTegic07272112182D\n\n 14 14 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 C 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 N 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 1.5000 0.4019 0.0000 O 0 0\n 4.5000 5.5981 0.0000 C 0 0\n 4.5031 0.4027 0.0000 C 0 0\n 6.0039 0.4049 0.0000 C 0 0\n 6.7570 -0.8933 0.0000 C 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 7.5096 -2.1908 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 4 8 2 0\n 1 9 1 0\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\n 3 13 1 0\n 12 14 3 0\nM RGP 1 13 1\nM END\n> <Name>\nN3-(2-Cyanoethyl)thymine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncneT\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN6-[2-(4-Imidazoyl)ethyl]adenine\n SciTegic07272112182D\n\n 18 20 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0031 -3.0008 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 1.3039 -3.7494 0.0000 C 0 0\n 1.3070 -5.2502 0.0000 C 0 0\n 2.6078 -5.9988 0.0000 C 0 0\n 2.7509 -7.4791 0.0000 N 0 0\n 4.2192 -7.7859 0.0000 C 0 0\n 4.9646 -6.4842 0.0000 N 0 0\n 3.9571 -5.3730 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 7 8 2 0\n 5 8 1 0\n 6 9 1 0\n 4 10 1 0\n 7 10 1 0\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 2 0\n 16 17 1 0\n 14 18 2 0\n 17 18 1 0\nM RGP 1 11 1\nM END\n> <Name>\nN6-[2-(4-Imidazoyl)ethyl]adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n4ime6A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN-(Aminopropyl)imidazoleadenine\n SciTegic07272112182D\n\n 20 22 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 2.5972 1.5031 0.0000 N 0 0\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2578 0.0000 C 0 0\n 5.1894 6.0109 0.0000 N 0 0\n 5.3272 7.4918 0.0000 C 0 0\n 6.7944 7.8037 0.0000 N 0 0\n 7.5444 6.5046 0.0000 C 0 0\n 6.5408 5.3899 0.0000 C 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 1 6 1 0\n 4 8 1 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 8 11 1 0\n 2 12 1 0\n 12 13 1 0\n 13 14 1 0\n 15 14 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 2 0\n 18 19 1 0\n 19 20 2 0\n 20 16 1 0\nM RGP 1 11 1\nM END\n> <Name>\nN-(Aminopropyl)imidazoleadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nimprn2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN-(Methyl)aminooxy BNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n -0.9534 0.5285 0.0000 C 0 0\n -1.7483 -0.7444 0.0000 O 0 0\n 0.1233 2.0603 0.0000 C 0 0\n 0.5491 0.4739 0.0000 C 0 0 1 0 0 0\n 0.1543 -0.5160 0.0000 C 0 0 1 0 0 0\n -0.8527 -1.8179 0.0000 C 0 0 1 0 0 0\n -0.5098 -0.5201 0.0000 O 0 0\n 3.0796 -0.7444 0.0000 O 0 0\n -1.5163 -3.1632 0.0000 R# 0 0\n -1.3844 1.8855 0.0000 O 0 0\n 1.6444 -0.3463 0.0000 C 0 0 2 0 0 0\n 4.1498 0.3066 0.0000 R# 0 0\n -0.3476 1.2002 0.0000 N 0 0\n 0.8594 2.0907 0.0000 C 0 0\n -3.2475 -0.6935 0.0000 R# 0 0\n 13 10 1 0\n 4 1 1 6\n 1 2 1 0\n 4 11 1 0\n 11 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 4 1 0\n 6 9 1 6\n 4 3 1 0\n 5 13 1 6\n 10 3 1 0\n 11 8 1 1\n 8 12 1 0\n 13 14 1 0\n 2 15 1 0\nM RGP 3 9 3 12 2 15 1\nM END\n> <Name>\nN-(Methyl)aminooxy BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmnobna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nN-Hydroxyglycine\n SciTegic07272112182D\n\n 6 5 0 0 0 0 999 V2000\n 2.6000 0.0000 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 0.0007 0.0004 0.0000 O 0 0\n 3.9000 0.7500 0.0000 N 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 5.1992 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 1 4 1 0\n 2 5 1 0\n 4 6 1 0\nM RGP 2 5 1 6 2\nM END\n> <Name>\nN-Hydroxyglycine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ngly\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nN-Methylamino LNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -1.7573 0.3923 0.0000 C 0 0\n -0.3792 0.2175 0.0000 N 0 0\n -0.8961 -0.6891 0.0000 C 0 0 1 0 0 0\n 1.2548 0.2221 0.0000 C 0 0 2 0 0 0\n 0.4960 -0.9529 0.0000 C 0 0 2 0 0 0\n 0.6513 -2.2149 0.0000 C 0 0 1 0 0 0\n -0.7183 -2.0601 0.0000 O 0 0\n -1.2216 0.7840 0.0000 C 0 0\n 1.7172 -3.2702 0.0000 R# 0 0\n 2.3209 1.2498 0.0000 O 0 0\n 3.7640 0.8408 0.0000 R# 0 0\n 0.3758 1.5136 0.0000 C 0 0\n -2.6483 1.2498 0.0000 O 0 0\n -2.9590 2.7173 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 6\n 6 9 1 6\n 3 1 1 0\n 5 2 1 6\n 4 10 1 1\n 10 11 1 0\n 2 12 1 0\n 8 13 1 0\n 13 14 1 0\nM RGP 3 9 3 11 2 14 1\nM END\n> <Name>\nN-Methylamino LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmn2lna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nNPOM-caged thymine\n SciTegic07272112182D\n\n 26 28 0 0 0 0 999 V2000\n 10.3988 -1.4774 0.0000 R# 0 0\n 14.1488 -0.1783 0.0000 N 0 0\n 12.6488 -0.1783 0.0000 C 0 0\n 11.8988 -1.4774 0.0000 N 0 0\n 12.6488 -2.7764 0.0000 C 0 0\n 14.1488 -2.7764 0.0000 C 0 0\n 14.8988 -1.4774 0.0000 C 0 0\n 16.3988 -1.4774 0.0000 O 0 0\n 11.8987 1.1207 0.0000 O 0 0\n 14.8988 -4.0755 0.0000 C 0 0\n 14.9018 1.1200 0.0000 C 0 0\n 16.4027 1.1179 0.0000 O 0 0\n 17.1557 2.4161 0.0000 C 0 0\n 16.4080 3.7164 0.0000 C 0 0\n 18.6566 2.4140 0.0000 C 0 0\n 19.4021 1.1123 0.0000 C 0 0\n 20.9021 1.1072 0.0000 C 0 0\n 21.6565 2.4036 0.0000 C 0 0\n 20.9110 3.7052 0.0000 C 0 0\n 19.4111 3.7104 0.0000 C 0 0\n 21.9012 -0.0106 0.0000 O 0 0\n 23.2736 0.5948 0.0000 C 0 0\n 23.1220 2.0871 0.0000 O 0 0\n 18.6678 5.0143 0.0000 N 0 3\n 19.4242 6.3097 0.0000 O 0 0\n 17.1678 5.0221 0.0000 O 0 5\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 2 7 1 0\n 7 8 2 0\n 3 9 2 0\n 1 4 1 0\n 6 10 1 0\n 2 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 13 15 1 0\n 15 16 2 0\n 16 17 1 0\n 17 18 2 0\n 18 19 1 0\n 19 20 2 0\n 20 15 1 0\n 17 21 1 0\n 21 22 1 0\n 22 23 1 0\n 23 18 1 0\n 20 24 1 0\n 24 25 2 0\n 24 26 1 0\nM CHG 2 24 1 26 -1\nM RGP 1 1 1\nM END\n> <Name>\nNPOM-caged thymine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnpomT\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nNorth-2-ara-fluoro-methanocarbocycle\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n -0.9485 -0.7830 0.0000 C 0 0 2 0 0 0\n 0.1086 0.2813 0.0000 C 0 0 2 0 0 0\n 1.4474 -0.3952 0.0000 C 0 0 1 0 0 0\n 1.2178 -1.8775 0.0000 C 0 0 1 0 0 0\n -0.2630 -2.1172 0.0000 C 0 0 1 0 0 0\n -0.1339 1.7598 0.0000 O 0 0\n -1.9138 0.3450 0.0000 C 0 0\n 2.2820 -2.9346 0.0000 R# 0 0\n 1.0261 2.7108 0.0000 R# 0 0\n -1.8053 -1.9405 0.0000 C 0 0\n 2.7816 0.2903 0.0000 F 0 0\n -1.4128 1.7598 0.0000 O 0 0\n -2.3862 2.9010 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 1 10 1 0\n 5 10 1 1\n 3 11 1 6\n 7 12 1 0\n 12 13 1 0\nM RGP 3 8 3 9 2 13 1\nM END\n> <Name>\nNorth-2-ara-fluoro-methanocarbocycle\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nafl2Nm\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nNorth-2-fluoro-methanocarbocycle\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n -0.9485 -0.7830 0.0000 C 0 0 2 0 0 0\n 0.1086 0.2813 0.0000 C 0 0 2 0 0 0\n 1.4474 -0.3952 0.0000 C 0 0 2 0 0 0\n 1.2178 -1.8775 0.0000 C 0 0 1 0 0 0\n -0.2630 -2.1172 0.0000 C 0 0 1 0 0 0\n -0.1339 1.7598 0.0000 O 0 0\n -1.9138 0.3450 0.0000 C 0 0\n 2.2820 -2.9346 0.0000 R# 0 0\n 1.0261 2.7108 0.0000 R# 0 0\n -1.8053 -1.9405 0.0000 C 0 0\n 2.7816 0.2903 0.0000 F 0 0\n -1.4128 1.7598 0.0000 O 0 0\n -2.3862 2.9010 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 1 10 1 0\n 5 10 1 1\n 3 11 1 1\n 7 12 1 0\n 12 13 1 0\nM RGP 3 8 3 9 2 13 1\nM END\n> <Name>\nNorth-2-fluoro-methanocarbocycle\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfl2Nmc\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nNorth-methanocarbocycle\n SciTegic07272112182D\n\n 12 13 0 0 1 0 999 V2000\n -0.7167 -0.7588 0.0000 C 0 0 2 0 0 0\n 0.3404 0.3055 0.0000 C 0 0 2 0 0 0\n 1.6792 -0.3710 0.0000 C 0 0\n 1.4496 -1.8533 0.0000 C 0 0 1 0 0 0\n -0.0312 -2.0930 0.0000 C 0 0 1 0 0 0\n 0.0979 1.7840 0.0000 O 0 0\n -1.6820 0.3692 0.0000 C 0 0\n 2.5138 -2.9104 0.0000 R# 0 0\n 1.2579 2.7350 0.0000 R# 0 0\n -1.5736 -1.9163 0.0000 C 0 0\n -1.1810 1.7840 0.0000 O 0 0\n -2.1544 2.9252 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 1 10 1 0\n 5 10 1 1\n 7 11 1 0\n 11 12 1 0\nM RGP 3 8 3 9 2 12 1\nM END\n> <Name>\nNorth-methanocarbocycle\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nNmc\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nOxy (ether)\n SciTegic07272112182D\n\n 3 2 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 O 0 0\n 2.5993 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nOxy (ether)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noxy\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nPEG/HEG 18 atom spacer\n SciTegic07272112182D\n\n 21 20 0 0 0 0 999 V2000\n -9.0999 -0.3928 0.0000 C 0 0\n -7.7999 0.3572 0.0000 O 0 0\n -6.5000 -0.3928 0.0000 C 0 0\n -5.2000 0.3572 0.0000 C 0 0\n -3.9000 -0.3928 0.0000 O 0 0\n -2.6000 0.3572 0.0000 C 0 0\n -1.3000 -0.3928 0.0000 C 0 0\n 0.0000 0.3572 0.0000 O 0 0\n 1.3000 -0.3928 0.0000 C 0 0\n 2.6000 0.3572 0.0000 C 0 0\n 3.9000 -0.3928 0.0000 O 0 0\n 5.2000 0.3572 0.0000 C 0 0\n 6.4999 -0.3928 0.0000 C 0 0\n 7.7999 0.3572 0.0000 O 0 0\n 9.0999 -0.3928 0.0000 C 0 0\n 10.3999 0.3572 0.0000 C 0 0\n 11.6999 -0.3928 0.0000 O 0 0\n 12.9992 0.3568 0.0000 R# 0 0\n -10.3999 0.3572 0.0000 C 0 0\n -11.6999 -0.3928 0.0000 O 0 0\n -12.9992 0.3568 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 19 1 1 0\n 19 20 1 0\n 20 21 1 0\nM RGP 2 18 2 21 1\nM END\n> <Name>\nPEG/HEG 18 atom spacer\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSp18\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nPNA (peptide nucleic acid)\n SciTegic09012117322D\n\n 13 12 0 0 0 0 999 V2000\n -1.3523 1.2380 0.0000 C 0 0\n 0.0251 0.6419 0.0000 N 0 0\n 0.2001 -0.8486 0.0000 C 0 0\n 1.5783 -1.4432 0.0000 C 0 0\n 1.2306 1.5360 0.0000 C 0 0\n -2.5577 0.3439 0.0000 C 0 0\n 1.7533 -2.9329 0.0000 R# 0 0\n -3.9351 0.9400 0.0000 N 0 0\n 2.6079 0.9400 0.0000 C 0 0\n 2.7798 -0.5502 0.0000 R# 0 0\n -5.1399 0.0464 0.0000 R# 0 0\n -1.0028 -1.7447 0.0000 O 0 0\n 3.8127 1.8335 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 2 5 1 0\n 1 6 1 0\n 4 7 1 0\n 6 8 1 0\n 5 9 1 0\n 9 10 1 0\n 8 11 1 0\n 3 12 2 0\n 9 13 2 0\nM RGP 3 7 3 10 2 11 1\nM END\n> <Name>\nPNA (peptide nucleic acid)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\npna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\nPNA D-Lysine (peptide nucleic acid)\n SciTegic09012117322D\n\n 18 17 0 0 1 0 999 V2000\n -1.9775 1.2208 0.0000 C 0 0\n -0.9363 0.1399 0.0000 N 0 0\n -1.3552 -1.3012 0.0000 C 0 0\n -2.8126 -1.6600 0.0000 C 0 0\n -3.4345 0.8605 0.0000 C 0 0\n -3.2313 -3.1004 0.0000 R# 0 0\n -4.4757 1.9414 0.0000 N 0 0\n 0.9395 1.9414 0.0000 C 0 0\n -0.0989 3.0239 0.0000 R# 0 0\n -5.9318 1.5813 0.0000 R# 0 0\n -0.3169 -2.3837 0.0000 O 0 0\n 2.3960 2.3000 0.0000 O 0 0\n 0.5206 0.5003 0.0000 C 0 0 1 0 0 0\n 1.5617 -0.5806 0.0000 C 0 0\n 3.0187 -0.2203 0.0000 C 0 0\n 4.0599 -1.3012 0.0000 C 0 0\n 5.5168 -0.9409 0.0000 C 0 0\n 6.5575 -2.0212 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 2 13 1 0\n 1 5 1 0\n 4 6 1 0\n 5 7 1 0\n 13 8 1 0\n 8 9 1 0\n 7 10 1 0\n 3 11 2 0\n 8 12 2 0\n 13 14 1 1\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\nM RGP 3 6 3 9 2 10 1\nM END\n> <Name>\nPNA D-Lysine (peptide nucleic acid)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nDlyspn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\nPNA L-Lysine (peptide nucleic acid)\n SciTegic09012117322D\n\n 18 17 0 0 1 0 999 V2000\n -1.9775 1.2208 0.0000 C 0 0\n -0.9363 0.1399 0.0000 N 0 0\n -1.3552 -1.3012 0.0000 C 0 0\n -2.8126 -1.6600 0.0000 C 0 0\n -3.4345 0.8605 0.0000 C 0 0\n -3.2313 -3.1004 0.0000 R# 0 0\n -4.4757 1.9414 0.0000 N 0 0\n 0.9395 1.9414 0.0000 C 0 0\n -0.0989 3.0239 0.0000 R# 0 0\n -5.9318 1.5813 0.0000 R# 0 0\n -0.3169 -2.3837 0.0000 O 0 0\n 2.3960 2.3000 0.0000 O 0 0\n 0.5206 0.5003 0.0000 C 0 0 2 0 0 0\n 1.5617 -0.5806 0.0000 C 0 0\n 3.0187 -0.2203 0.0000 C 0 0\n 4.0599 -1.3012 0.0000 C 0 0\n 5.5168 -0.9409 0.0000 C 0 0\n 6.5575 -2.0212 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 2 13 1 0\n 1 5 1 0\n 4 6 1 0\n 5 7 1 0\n 13 8 1 0\n 8 9 1 0\n 7 10 1 0\n 3 11 2 0\n 8 12 2 0\n 13 14 1 6\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\nM RGP 3 6 3 9 2 10 1\nM END\n> <Name>\nPNA L-Lysine (peptide nucleic acid)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nLlyspn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\nPhosphonoacetate\n SciTegic07272112182D\n\n 8 7 0 0 0 0 999 V2000\n 0.1884 -1.6241 0.0000 R# 0 0\n 0.9383 -0.3250 0.0000 P 0 0\n 1.6882 -1.6241 0.0000 R# 0 0\n 0.1874 0.9745 0.0000 C 0 0\n 2.4383 -0.3254 0.0000 O 0 0\n -1.3134 0.9748 0.0000 C 0 0\n -2.0633 -0.3243 0.0000 O 0 0\n -2.0639 2.2736 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 2 0\n 4 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nPhosphonoacetate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncmp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nPhosphorodiamidate\n SciTegic09012117322D\n\n 8 7 0 0 0 0 999 V2000\n -0.8449 1.1367 0.0000 N 0 0\n -0.0936 -0.1625 0.0000 C 0 0\n -0.8432 -1.4618 0.0000 C 0 0\n 0.6566 -1.4615 0.0000 R# 0 0\n 1.4072 -0.1625 0.0000 N 0 0\n -2.3449 1.1367 0.0000 C 0 0\n -0.0953 2.4360 0.0000 C 0 0\n 2.1580 -1.4611 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 1 0\n 1 6 1 0\n 1 7 1 0\n 5 8 1 0\nM RGP 2 4 1 8 2\nM END\n> <Name>\nPhosphorodiamidate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2np\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]H\n\n$$$$\nPhosphorodithioate\n SciTegic07272112182D\n\n 5 4 0 0 0 0 999 V2000\n -1.7998 0.0000 0.0000 R# 0 0\n -0.2998 0.0000 0.0000 P 0 0\n 1.2002 0.0000 0.0000 R# 0 0\n 0.4498 -1.2993 0.0000 S 0 0\n 0.4498 1.2993 0.0000 S 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nPhosphorodithioate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns2p\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nPropylamino\n SciTegic07272112182D\n\n 6 5 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nPropylamino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nprn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nPseudouracil\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 2.5981 1.5000 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\nM RGP 1 8 1\nM END\n> <Name>\nPseudouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\npsiU\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nPurine\n SciTegic07272112182D\n\n 10 11 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 4 7 1 0\n 7 8 1 0\n 8 9 2 0\n 5 9 1 0\n 7 10 1 0\nM RGP 1 10 1\nM END\n> <Name>\nPurine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\npurine\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nSouth-methanocarbacycle\n SciTegic07272112182D\n\n 12 13 0 0 1 0 999 V2000\n -0.4943 -0.2124 0.0000 C 0 0 2 0 0 0\n 0.8375 0.4778 0.0000 C 0 0 2 0 0 0\n 1.9055 -0.5755 0.0000 C 0 0\n 1.2337 -1.9167 0.0000 C 0 0 1 0 0 0\n -0.2494 -1.6923 0.0000 C 0 0 1 0 0 0\n 1.0586 1.9597 0.0000 O 0 0\n -1.8325 0.4614 0.0000 C 0 0\n -0.1445 -2.5087 0.0000 R# 0 0\n 2.4537 2.5107 0.0000 R# 0 0\n 0.4098 -3.0978 0.0000 C 0 0\n -1.9192 1.9597 0.0000 O 0 0\n -3.2590 2.6342 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 5 10 1 1\n 4 10 1 0\n 7 11 1 0\n 11 12 1 0\nM RGP 3 8 3 9 2 12 1\nM END\n> <Name>\nSouth-methanocarbacycle\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSmc\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nTricyclic Nucleoside (TriNA1)\n SciTegic07272112182D\n\n 16 18 0 0 1 0 999 V2000\n 2.6530 -0.4520 0.0000 C 0 0 1 0 0 0\n 1.3983 0.2080 0.0000 C 0 0 2 0 0 0\n 0.6593 -1.0047 0.0000 C 0 0 1 0 0 0\n -0.7503 -0.9712 0.0000 O 0 0\n -0.0313 0.2420 0.0000 C 0 0 1 0 0 0\n -0.6920 1.4781 0.0000 C 0 0 1 0 0 0\n 0.7176 1.4446 0.0000 O 0 0\n -1.4309 0.2754 0.0000 C 0 0 1 0 0 0\n -2.6739 1.0051 0.0000 C 0 0\n -3.3546 2.2417 0.0000 C 0 0\n -1.9450 2.2081 0.0000 C 0 0\n 1.3782 -2.3212 0.0000 R# 0 0\n -1.8206 -1.1820 0.0000 O 0 0\n 3.9351 -1.1820 0.0000 O 0 0\n 5.2263 -0.4185 0.0000 R# 0 0\n -3.2691 -1.5715 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 1\n 5 1 1 0\n 5 6 1 0\n 2 7 1 6\n 6 7 1 6\n 5 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 6 11 1 0\n 3 12 1 6\n 8 13 1 6\n 1 14 1 6\n 14 15 1 0\n 13 16 1 0\nM RGP 3 12 3 15 2 16 1\nM END\n> <Name>\nTricyclic Nucleoside (TriNA1)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ntrina1\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nTricyclic Nucleoside (TriNA2)\n SciTegic07272112182D\n\n 16 18 0 0 1 0 999 V2000\n 2.6530 -0.4520 0.0000 C 0 0 1 0 0 0\n 1.3983 0.2080 0.0000 C 0 0 2 0 0 0\n 0.6593 -1.0047 0.0000 C 0 0 1 0 0 0\n -0.7503 -0.9712 0.0000 O 0 0\n -0.0313 0.2420 0.0000 C 0 0 1 0 0 0\n -0.6920 1.4781 0.0000 C 0 0 2 0 0 0\n 0.7176 1.4446 0.0000 O 0 0\n -1.4309 0.2754 0.0000 C 0 0 2 0 0 0\n -2.6739 1.0051 0.0000 C 0 0\n -3.3546 2.2417 0.0000 C 0 0\n -1.9450 2.2081 0.0000 C 0 0\n 1.3782 -2.3212 0.0000 R# 0 0\n -1.8206 -1.1820 0.0000 O 0 0\n 3.9351 -1.1820 0.0000 O 0 0\n 5.2263 -0.4185 0.0000 R# 0 0\n -3.2691 -1.5715 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 1\n 5 1 1 0\n 5 6 1 0\n 2 7 1 6\n 6 7 1 1\n 5 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 6 11 1 0\n 3 12 1 6\n 8 13 1 1\n 1 14 1 6\n 14 15 1 0\n 13 16 1 0\nM RGP 3 12 3 15 2 16 1\nM END\n> <Name>\nTricyclic Nucleoside (TriNA2)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ntrina2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nTricycloDNA\n SciTegic07272112182D\n\n 15 17 0 0 1 0 999 V2000\n 0.9564 0.9968 0.0000 C 0 0 1 0 0 0\n 2.2238 0.1944 0.0000 C 0 0\n 1.8523 -1.2589 0.0000 C 0 0 1 0 0 0\n 0.3553 -1.3546 0.0000 O 0 0\n -0.1983 0.0395 0.0000 C 0 0 2 0 0 0\n 2.8096 -2.4136 0.0000 R# 0 0\n 1.2005 -0.4870 0.0000 O 0 0\n -1.4533 0.8270 0.0000 C 0 0 1 0 0 0\n -1.0818 2.2802 0.0000 C 0 0 2 0 0 0\n 0.4151 2.3760 0.0000 C 0 0\n -1.3512 -0.9202 0.0000 H 0 0\n -2.1444 -0.4870 0.0000 O 0 0\n 2.6054 -1.0127 0.0000 R# 0 0\n -2.5462 1.7647 0.0000 C 0 0\n -3.6433 -0.5444 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 3 6 1 6\n 1 7 1 1\n 5 8 1 0\n 8 9 1 0\n 9 10 1 1\n 10 1 1 0\n 5 11 1 1\n 8 12 1 6\n 7 13 1 0\n 8 14 1 0\n 9 14 1 0\n 12 15 1 0\nM RGP 3 6 3 13 2 15 1\nM END\n> <Name>\nTricycloDNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ntcdna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nXanthine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n 0.0000 3.0000 0.0000 O 0 0\n 2.5981 -1.5000 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 1 0\n 5 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 4 1 0\n 7 10 1 0\n 3 11 2 0\n 1 12 2 0\nM RGP 1 10 1\nM END\n> <Name>\nXanthine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nXan\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nalpha-L-Methylene cLNA\n SciTegic09012117322D\n\n 14 15 0 0 1 0 999 V2000\n 1.3724 0.2490 0.0000 C 0 0 2 0 0 0\n -0.7833 -0.6510 0.0000 C 0 0 1 0 0 0\n -1.6389 0.4349 0.0000 C 0 0 1 0 0 0\n -0.2617 0.2529 0.0000 O 0 0\n 0.6074 -0.9220 0.0000 C 0 0 2 0 0 0\n -2.9425 1.1768 0.0000 R# 0 0\n 0.7561 -2.1847 0.0000 C 0 0\n -0.6126 -2.0229 0.0000 C 0 0\n 0.5311 0.5874 0.0000 C 0 0\n 2.4438 1.2711 0.0000 O 0 0\n -0.8049 1.2711 0.0000 O 0 0\n -1.6701 -3.0867 0.0000 C 0 0\n 3.8848 0.8548 0.0000 R# 0 0\n -0.8816 2.7692 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 0\n 3 6 1 6\n 5 7 1 0\n 7 8 1 0\n 2 8 1 6\n 5 9 1 6\n 1 10 1 1\n 9 11 1 0\n 8 12 2 0\n 10 13 1 0\n 11 14 1 0\nM RGP 3 6 3 13 2 14 1\nM END\n> <Name>\nalpha-L-Methylene cLNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nALmecl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nalpha-L-TriNA1\n SciTegic07272112182D\n\n 16 18 0 0 1 0 999 V2000\n 2.6539 -0.4518 0.0000 C 0 0 2 0 0 0\n 1.3991 0.2079 0.0000 C 0 0 1 0 0 0\n 0.6603 -1.0051 0.0000 C 0 0 1 0 0 0\n -0.7493 -0.9719 0.0000 O 0 0\n -0.0305 0.2415 0.0000 C 0 0 2 0 0 0\n -0.6916 1.4774 0.0000 C 0 0 2 0 0 0\n 0.7180 1.4442 0.0000 O 0 0\n 1.3796 -2.3214 0.0000 R# 0 0\n -1.9448 2.2071 0.0000 C 0 0\n -3.3544 2.2403 0.0000 C 0 0\n -2.6733 1.0039 0.0000 C 0 0\n -1.4301 0.2745 0.0000 C 0 0 1 0 0 0\n 3.9363 -1.1814 0.0000 O 0 0\n -1.8252 -1.1814 0.0000 O 0 0\n -3.2751 -1.5662 0.0000 R# 0 0\n 5.2272 -0.4176 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 6\n 5 1 1 0\n 5 6 1 0\n 2 7 1 1\n 3 8 1 6\n 6 9 1 1\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 5 1 0\n 1 13 1 1\n 12 14 1 6\n 14 15 1 0\n 13 16 1 0\n 6 7 1 0\nM RGP 3 8 3 15 1 16 2\nM END\n> <Name>\nalpha-L-TriNA1\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nALtri1\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nalpha-L-TriNA2\n SciTegic07272112182D\n\n 16 18 0 0 1 0 999 V2000\n 0.3688 0.2749 0.0000 C 0 0 2 0 0 0\n 1.1556 -0.9189 0.0000 C 0 0 1 0 0 0\n 2.5699 -1.0016 0.0000 C 0 0 1 0 0 0\n -0.0102 -1.5217 0.0000 O 0 0\n -1.0095 -0.0878 0.0000 C 0 0 2 0 0 0\n -1.0850 -1.5233 0.0000 C 0 0\n 0.2451 -2.0446 0.0000 O 0 0\n 4.0662 -0.8963 0.0000 R# 0 0\n 1.8404 0.5584 0.0000 O 0 0\n -2.0505 0.9501 0.0000 C 0 0 2 0 0 0\n -1.6991 2.3365 0.0000 C 0 0\n -0.2571 2.7206 0.0000 C 0 0\n 0.7556 1.6827 0.0000 C 0 0\n -3.5000 0.5584 0.0000 O 0 0\n -3.8863 -0.8910 0.0000 R# 0 0\n 2.4962 -0.1965 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 1\n 5 1 1 0\n 5 6 1 0\n 2 7 1 1\n 7 6 1 0\n 3 8 1 6\n 1 9 1 6\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 1 1 0\n 10 14 1 1\n 14 15 1 0\n 9 16 1 0\nM RGP 3 8 3 15 1 16 2\nM END\n> <Name>\nalpha-L-TriNA2\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nALtri2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nciPr BNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 0.2991 -2.2311 0.0000 C 0 0\n 0.4976 -0.8562 0.0000 O 0 0\n -0.5139 -1.1129 0.0000 C 0 0 1 0 0 0\n 0.9374 0.7175 0.0000 C 0 0 2 0 0 0\n -0.3973 0.2991 0.0000 C 0 0 2 0 0 0\n -1.5723 0.7850 0.0000 C 0 0 1 0 0 0\n -1.7880 -0.5764 0.0000 O 0 0\n -1.0568 0.2946 0.0000 C 0 0\n -2.3057 2.0935 0.0000 R# 0 0\n 2.2119 1.4714 0.0000 O 0 0\n 3.5217 0.7403 0.0000 R# 0 0\n -0.7634 -3.2899 0.0000 C 0 0\n 1.7326 -2.6726 0.0000 C 0 0\n -0.1253 1.4714 0.0000 O 0 0\n -0.6775 2.8661 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 1\n 3 1 1 0\n 5 2 1 1\n 4 10 1 6\n 10 11 1 0\n 1 12 1 0\n 1 13 1 0\n 8 14 1 0\n 14 15 1 0\nM RGP 3 9 3 11 2 15 1\nM END\n> <Name>\nciPr BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nciPr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-O-Methylribose (2,5 connectivity)\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.3321 0.5967 0.0000 C 0 0 1 0 0 0\n -1.3928 -0.4639 0.0000 C 0 0 2 0 0 0\n -0.7119 -1.8004 0.0000 C 0 0 1 0 0 0\n 0.7696 -1.5659 0.0000 O 0 0\n 1.0044 -0.0844 0.0000 C 0 0 2 0 0 0\n 2.3408 0.5930 0.0000 C 0 0\n -1.3930 -3.1369 0.0000 R# 0 0\n -0.5694 2.0761 0.0000 O 0 0\n -2.8721 -0.2263 0.0000 O 0 0\n 3.5983 -0.2263 0.0000 O 0 0\n -1.9705 2.6117 0.0000 C 0 0\n 4.9362 0.4518 0.0000 R# 0 0\n -3.4075 1.1749 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 5 6 1 1\n 3 7 1 1\n 1 8 1 6\n 2 9 1 6\n 6 10 1 0\n 8 11 1 0\n 10 12 1 0\n 9 13 1 0\nM RGP 3 7 3 12 2 13 1\nM END\n> <Name>\n3-O-Methylribose (2,5 connectivity)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n25mo3r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]H\n[R3]O\n\n$$$$\n";
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47
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var monomersData = "1',2'-Di-Deoxy-Ribose\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n -0.8526 1.5410 0.0000 O 0 0\n -0.3405 0.1310 0.0000 C 0 0 1 0 0 0\n 0.3301 2.4636 0.0000 C 0 0\n 1.1586 0.1823 0.0000 C 0 0 2 0 0 0\n 1.5731 1.6239 0.0000 C 0 0\n 2.0777 -1.0008 0.0000 O 0 0\n -1.1818 -1.1087 0.0000 C 0 0\n -2.6787 -1.0008 0.0000 O 0 0\n -3.3525 -1.9937 0.0000 R# 0 0\n 3.2666 -0.8378 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 1\n 3 5 1 0\n 4 5 1 0\n 4 6 1 6\n 6 10 1 0\n 7 8 1 0\n 8 9 1 0\nM RGP 2 9 1 10 2\nM END\n> <Name>\n1',2'-Di-Deoxy-Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n12ddR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n2,5-Ribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.6295 -1.1398 0.0000 O 0 0\n -0.8657 0.3416 0.0000 C 0 0 1 0 0 0\n 0.8523 -1.3729 0.0000 C 0 0 2 0 0 0\n 0.4701 1.0240 0.0000 C 0 0 2 0 0 0\n 1.5319 -0.0356 0.0000 C 0 0 1 0 0 0\n 0.6566 2.2094 0.0000 O 0 0\n 3.0119 0.1971 0.0000 O 0 0\n -2.2027 1.0176 0.0000 C 0 0\n 1.3982 -2.4414 0.0000 R# 0 0\n -3.4595 0.1971 0.0000 O 0 0\n -4.5303 0.7385 0.0000 R# 0 0\n 3.7667 -0.7357 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 8 10 1 0\n 10 11 1 0\n 7 12 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\n2,5-Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n25R\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n6-amino-hexanol (3' end)\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n -3.6321 -0.5320 0.0000 C 0 0\n -2.3982 0.3223 0.0000 C 0 0\n -1.0410 -0.3184 0.0000 C 0 0\n 0.1930 0.5359 0.0000 C 0 0\n 1.5502 -0.1048 0.0000 C 0 0\n 2.7842 0.7494 0.0000 C 0 0\n 4.1414 0.1087 0.0000 N 0 0\n 5.1280 0.7918 0.0000 R# 0 0\n -4.9894 0.1087 0.0000 O 0 0\n -5.9760 -0.5743 0.0000 R# 0 0\n 4.2400 -1.0872 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 1 9 1 0\n 9 10 1 0\n 7 11 1 0\nM RGP 3 8 2 10 1 11 3\nM END\n> <Name>\n6-amino-hexanol (3' end)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n3A6\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]H\n\n$$$$\n3-FAM\n SciTegic07272112182D\n\n 38 42 0 0 1 0 999 V2000\n -11.6944 -6.1247 0.0000 R# 0 0\n -10.4944 -6.1250 0.0000 O 0 0\n -9.7428 -4.8259 0.0000 C 0 0\n -8.2420 -4.8264 0.0000 C 0 0\n -7.4897 -6.1250 0.0000 O 0 0\n -7.4904 -3.5273 0.0000 C 0 0\n -6.2897 -6.1240 0.0000 R# 0 0\n -5.9896 -3.5276 0.0000 C 0 0\n -5.2380 -2.2286 0.0000 C 0 0\n -3.7372 -2.2289 0.0000 C 0 0\n -2.9856 -0.9298 0.0000 N 0 0\n -1.4848 -0.9303 0.0000 C 0 0\n -0.7333 0.3689 0.0000 C 0 0\n -0.8854 -1.9698 0.0000 O 0 0\n 1.5152 1.6705 0.0000 C 0 0\n 0.7667 0.3706 0.0000 C 0 0\n -1.4848 1.6670 0.0000 C 0 0\n -0.7363 2.9669 0.0000 C 0 0\n 0.7637 2.9686 0.0000 C 0 0\n 3.1364 3.4756 0.0000 O 0 0\n 2.9814 1.9837 0.0000 C 0 0\n 1.7654 4.0841 0.0000 C 0 0\n 1.5144 5.2576 0.0000 O 0 0\n 6.0184 1.4243 0.0000 O 0 0\n 5.0455 0.2826 0.0000 C 0 0\n 3.5703 0.5543 0.0000 C 0 0\n 4.0410 3.1094 0.0000 C 0 0\n 5.5162 2.8377 0.0000 C 0 0\n 6.4886 3.9794 0.0000 C 0 0\n 3.5383 4.5229 0.0000 C 0 0\n 4.5112 5.6646 0.0000 C 0 0\n 5.9864 5.3928 0.0000 C 0 0\n 5.5474 -1.1307 0.0000 C 0 0\n 4.5745 -2.2724 0.0000 C 0 0\n 3.0993 -2.0007 0.0000 C 0 0\n 2.5971 -0.5873 0.0000 C 0 0\n 6.7647 6.3061 0.0000 O 0 0\n 4.9763 -3.4032 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 4 6 1 0\n 5 7 1 0\n 6 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 12 14 2 0\n 16 13 2 0\n 13 17 1 0\n 15 16 1 0\n 17 18 2 0\n 18 19 1 0\n 19 22 1 0\n 15 19 2 0\n 21 15 1 0\n 20 21 1 0\n 20 22 1 0\n 22 23 2 0\n 26 21 1 0\n 21 27 1 0\n 24 25 1 0\n 24 28 1 0\n 27 30 2 0\n 28 27 1 0\n 29 28 2 0\n 30 31 1 0\n 31 32 2 0\n 29 32 1 0\n 33 25 2 0\n 26 25 1 0\n 36 26 2 0\n 33 34 1 0\n 34 35 2 0\n 35 36 1 0\n 32 37 1 0\n 34 38 1 0\nM RGP 2 1 1 7 2\nM END\n> <Name>\n3-FAM\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n3FAM\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n3'-Thiol-Modifier 6 S-S from Glen Research\n SciTegic07272112182D\n\n 18 17 0 0 1 0 999 V2000\n -8.4293 -0.6995 0.0000 C 0 0\n -7.1591 0.0999 0.0000 C 0 0\n -9.7571 0.0000 0.0000 O 0 0\n -5.8312 -0.5996 0.0000 O 0 0\n -4.5610 0.1999 0.0000 C 0 0\n -3.2332 -0.4996 0.0000 C 0 0\n -1.9630 0.2998 0.0000 C 0 0\n -0.6351 -0.3997 0.0000 S 0 0\n 0.6351 0.3997 0.0000 S 0 0\n 1.9629 -0.2998 0.0000 C 0 0\n 3.2332 0.4996 0.0000 C 0 0\n 4.5610 -0.1999 0.0000 C 0 0\n 5.8312 0.5996 0.0000 O 0 0\n 7.1591 -0.0999 0.0000 C 0 0\n 8.4292 0.6995 0.0000 C 0 0\n 9.7571 0.0000 0.0000 O 0 0\n -10.7727 -0.6392 0.0000 R# 0 0\n 10.7728 0.6392 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 3 17 1 0\n 16 18 1 0\nM RGP 2 17 1 18 2\nM END\n> <Name>\n3'-Thiol-Modifier 6 S-S from Glen Research\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n3SS6\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n4-Thio-Ribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.1017 -1.0663 0.0000 S 0 0\n -0.5897 0.3436 0.0000 C 0 0 1 0 0 0\n 0.0809 -1.9889 0.0000 C 0 0 2 0 0 0\n 0.9095 0.2924 0.0000 C 0 0 2 0 0 0\n 1.3239 -1.1493 0.0000 C 0 0 1 0 0 0\n 1.8285 1.4755 0.0000 O 0 0\n 2.4518 -1.5589 0.0000 O 0 0\n -1.4310 1.5834 0.0000 C 0 0\n 0.0399 -3.1881 0.0000 R# 0 0\n -2.9279 1.4755 0.0000 O 0 0\n -3.6017 2.4684 0.0000 R# 0 0\n 3.0174 1.3125 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 12 1 0\n 8 10 1 0\n 10 11 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\n4-Thio-Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n4sR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n6-amino-hexanol (5' end)\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 3.6322 -0.5320 0.0000 C 0 0\n 2.3981 0.3223 0.0000 C 0 0\n 1.0410 -0.3184 0.0000 C 0 0\n -0.1930 0.5358 0.0000 C 0 0\n -1.5502 -0.1048 0.0000 C 0 0\n -2.7842 0.7494 0.0000 C 0 0\n -4.1414 0.1087 0.0000 N 0 0\n -5.1280 0.7918 0.0000 R# 0 0\n 4.9894 0.1087 0.0000 O 0 0\n 5.9760 -0.5743 0.0000 R# 0 0\n -4.2400 -1.0872 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 1 9 1 0\n 9 10 1 0\n 7 11 1 0\nM RGP 3 8 1 10 2 11 3\nM END\n> <Name>\n6-amino-hexanol (5' end)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5A6\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]H\n\n$$$$\n5'-6FAM (6-carboxyfluorescein)\n SciTegic07272112182D\n\n 36 39 0 0 1 0 999 V2000\n -23.5563 -25.6056 0.0000 C 0 0\n -24.3065 -26.9045 0.0000 C 0 0\n -23.5568 -28.2037 0.0000 C 0 0\n -22.0569 -28.2039 0.0000 C 0 0\n -21.3066 -26.9050 0.0000 C 0 0\n -22.0563 -25.6059 0.0000 C 0 0\n -21.3061 -24.3070 0.0000 C 0 0\n -22.0558 -23.0078 0.0000 C 0 0\n -23.5558 -23.0075 0.0000 C 0 0\n -24.3061 -24.3064 0.0000 O 0 0\n -21.3056 -21.7089 0.0000 C 0 0\n -22.0553 -20.4097 0.0000 C 0 0\n -23.5553 -20.4094 0.0000 C 0 0\n -24.3055 -21.7083 0.0000 C 0 0\n -24.1570 -29.2428 0.0000 O 0 0\n -24.1551 -19.3701 0.0000 O 0 0\n -19.8053 -24.3073 0.0000 C 0 0\n -19.0570 -23.0072 0.0000 C 0 0\n -17.5570 -23.0051 0.0000 C 0 0\n -16.8052 -24.3031 0.0000 C 0 0\n -17.5533 -25.6032 0.0000 C 0 0\n -19.0534 -25.6053 0.0000 C 0 0\n -16.8057 -21.7059 0.0000 C 0 0\n -15.3049 -21.7059 0.0000 N 0 0\n -17.4054 -20.6664 0.0000 O 0 0\n -14.5536 -20.4067 0.0000 C 0 0\n -13.0528 -20.4067 0.0000 C 0 0\n -12.3015 -19.1075 0.0000 C 0 0\n -10.8006 -19.1075 0.0000 C 0 0\n -10.0494 -17.8083 0.0000 C 0 0\n -8.5486 -17.8083 0.0000 C 0 0\n -7.7973 -16.5091 0.0000 O 0 0\n -6.5973 -16.5091 0.0000 R# 0 0\n -19.7993 -26.9076 0.0000 C 0 0\n -20.7993 -26.9108 0.0000 O 0 0\n -19.1963 -27.9451 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 2 0\n 9 10 1 0\n 1 6 2 0\n 1 10 1 0\n 6 7 1 0\n 8 11 1 0\n 8 9 1 0\n 9 14 2 0\n 11 12 2 0\n 12 13 1 0\n 13 14 1 0\n 3 15 1 0\n 13 16 2 0\n 7 17 1 0\n 17 18 2 0\n 17 22 1 0\n 18 19 1 0\n 19 20 2 0\n 20 21 1 0\n 21 22 2 0\n 19 23 1 0\n 23 24 1 0\n 23 25 2 0\n 24 26 1 0\n 26 27 1 0\n 27 28 1 0\n 28 29 1 0\n 29 30 1 0\n 30 31 1 0\n 31 32 1 0\n 32 33 1 0\n 22 34 1 0\n 34 35 1 0\n 34 36 2 0\nM RGP 1 33 2\nM END\n> <Name>\n5'-6FAM (6-carboxyfluorescein)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5FAM\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]H\n\n$$$$\n4-Formylbenzamidehexanol (5' end)\n SciTegic07272112182D\n\n 20 20 0 0 1 0 999 V2000\n -26.0016 11.8824 0.0000 H 0 0\n -25.0016 11.8792 0.0000 C 0 0\n -24.2557 10.5767 0.0000 C 0 0\n -25.0076 9.2788 0.0000 C 0 0\n -24.2595 7.9786 0.0000 C 0 0\n -22.7596 7.9765 0.0000 C 0 0\n -22.0084 6.6772 0.0000 C 0 0\n -20.5076 6.6770 0.0000 N 0 0\n -19.7564 5.3778 0.0000 C 0 0\n -18.2555 5.3777 0.0000 C 0 0\n -17.5044 4.0783 0.0000 C 0 0\n -16.0035 4.0783 0.0000 C 0 0\n -15.2523 2.7790 0.0000 C 0 0\n -13.7514 2.7790 0.0000 C 0 0\n -13.0003 1.4796 0.0000 O 0 0\n -22.6081 5.6378 0.0000 O 0 0\n -22.0077 9.2744 0.0000 C 0 0\n -22.7557 10.5745 0.0000 C 0 0\n -24.3986 12.9166 0.0000 O 0 0\n -11.8004 1.4796 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 7 16 2 0\n 6 17 1 0\n 17 18 2 0\n 3 18 1 0\n 2 19 2 0\n 15 20 1 0\nM RGP 1 20 2\nM END\n> <Name>\n4-Formylbenzamidehexanol (5' end)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5FBC6\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]H\n\n$$$$\n2-(methylamino)acetamide (GeneTools 5'-cap for PMO)\n SciTegic07272112182D\n\n 7 6 0 0 1 0 999 V2000\n 3.3003 4.3894 0.0000 O 0 0\n 3.9000 3.3500 0.0000 C 0 0\n 3.1500 2.0500 0.0000 C 0 0\n 3.9000 0.7500 0.0000 N 0 0\n 3.3003 -0.2894 0.0000 C 0 0\n 5.1000 3.3500 0.0000 N 0 0\n 5.1000 0.7500 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 2 6 1 0\n 4 7 1 0\nM RGP 1 7 2\nM END\n> <Name>\n2-(methylamino)acetamide (GeneTools 5'-cap for PMO)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5cGT\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]H\n\n$$$$\n5-ethynyl-uracil\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.8621 -1.2489 0.0000 C 0 0\n 2.4620 -2.2881 0.0000 C 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\n 2 10 1 0\n 10 11 3 0\nM RGP 1 9 1\nM END\n> <Name>\n5-ethynyl-uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5eU\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-fluoro-uracil\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.7117 -0.9884 0.0000 F 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\n 2 10 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-fluoro-uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5fU\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-iodo-uracil\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.7117 -0.9884 0.0000 I 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\n 2 10 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-iodo-uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5iU\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-methyl-cytidine\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 2.6489 0.0000 C 0 0\n -0.3882 2.6490 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3883 0.0509 0.0000 C 0 0\n 1.1117 0.0509 0.0000 N 0 0\n 3.0618 1.3499 0.0000 N 0 0\n -0.9884 -0.9883 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.7118 3.6882 0.0000 C 0 0\n 1 2 1 0\n 1 6 2 0\n 1 7 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 6 1 0\n 5 8 2 0\n 2 10 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-methyl-cytidine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5meC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-tris-propynyl-uracil\n SciTegic07272112182D\n\n 19 19 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.8621 -1.2489 0.0000 C 0 0\n 2.6125 -2.5487 0.0000 C 0 0\n 3.3628 -3.8485 0.0000 C 0 0\n 4.8637 -3.8494 0.0000 N 0 0\n 5.6140 -5.1492 0.0000 C 0 0\n 5.6172 -2.5515 0.0000 C 0 0\n 7.1149 -5.1502 0.0000 C 0 0\n 7.1180 -2.5541 0.0000 C 0 0\n 8.3148 -5.1510 0.0000 C 0 0\n 8.3181 -2.5563 0.0000 C 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\n 2 10 1 0\n 10 11 3 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 13 15 1 0\n 14 16 1 0\n 15 17 1 0\n 16 18 3 0\n 17 19 3 0\nM RGP 1 9 1\nM END\n> <Name>\n5-tris-propynyl-uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5tpU\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nAdenine\n SciTegic07272112182D\n\n 11 12 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 C 0 0\n -0.0787 -2.2532 0.0000 N 0 0\n 2.1768 -0.1209 0.0000 N 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n 1 10 1 0\n 1 6 2 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 1 0\n 7 11 1 0\n 8 9 2 0\nM RGP 1 11 1\nM END\n> <Name>\nAdenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nA\n\n> <MonomerCode>\nA\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nCytosine\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 2.6489 0.0000 C 0 0\n -0.3882 2.6490 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3883 0.0509 0.0000 C 0 0\n 1.1117 0.0509 0.0000 N 0 0\n 3.0618 1.3499 0.0000 N 0 0\n -0.9884 -0.9883 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1 2 1 0\n 1 6 2 0\n 1 7 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 6 1 0\n 5 8 2 0\nM RGP 1 9 1\nM END\n> <Name>\nCytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nC\n\n> <MonomerCode>\nC\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2'-O-Tris-trifluoromethoxyethyl ribose\n SciTegic07272112182D\n\n 28 28 0 0 1 0 999 V2000\n -4.4125 2.2734 0.0000 O 0 0\n -3.9005 3.6833 0.0000 C 0 0 1 0 0 0\n -3.2299 1.3508 0.0000 C 0 0 2 0 0 0\n -2.4014 3.6321 0.0000 C 0 0 2 0 0 0\n -1.9869 2.1905 0.0000 C 0 0 1 0 0 0\n -1.4822 4.8152 0.0000 O 0 0\n -0.5797 1.6761 0.0000 O 0 0\n -4.7418 4.9231 0.0000 C 0 0\n -3.2709 0.1515 0.0000 R# 0 0\n -6.2387 4.8152 0.0000 O 0 0\n -6.9125 5.8082 0.0000 R# 0 0\n -0.2934 4.6522 0.0000 R# 0 0\n -0.3201 0.1978 0.0000 C 0 0\n 1.0894 -0.3174 0.0000 C 0 0\n 1.3489 -1.7956 0.0000 O 0 0\n 2.7585 -2.3109 0.0000 C 0 0\n 3.0181 -3.7891 0.0000 C 0 0\n 3.9091 -1.3475 0.0000 C 0 0\n 1.5836 -3.2910 0.0000 C 0 0\n 4.1451 -4.2011 0.0000 F 0 0\n 2.2514 -4.4311 0.0000 F 0 0\n 3.2249 -4.9711 0.0000 F 0 0\n 5.0367 -1.7584 0.0000 F 0 0\n 3.7017 -0.1655 0.0000 F 0 0\n 4.8289 -0.5766 0.0000 F 0 0\n 0.4570 -2.8778 0.0000 F 0 0\n 0.6625 -4.0600 0.0000 F 0 0\n 1.7547 -4.2762 0.0000 F 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 12 1 0\n 8 10 1 0\n 10 11 1 0\n 7 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 16 18 1 0\n 16 19 1 0\n 17 20 1 0\n 17 21 1 0\n 17 22 1 0\n 18 23 1 0\n 18 24 1 0\n 18 25 1 0\n 19 26 1 0\n 19 27 1 0\n 19 28 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\n2'-O-Tris-trifluoromethoxyethyl ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nFMOE\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nGuanine\n SciTegic07272112182D\n\n 12 13 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 C 0 0\n -0.0787 -2.2532 0.0000 N 0 0\n 2.1768 -0.1209 0.0000 O 0 0\n -0.9527 3.3542 0.0000 N 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n 1 10 2 0\n 1 6 1 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 5 11 1 0\n 7 8 1 0\n 7 12 1 0\n 8 9 2 0\nM RGP 1 12 1\nM END\n> <Name>\nGuanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nG\n\n> <MonomerCode>\nG\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nInosine\n SciTegic07272112182D\n\n 11 12 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 C 0 0\n -0.0787 -2.2532 0.0000 N 0 0\n 2.1768 -0.1209 0.0000 O 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n 1 10 2 0\n 1 6 1 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 1 0\n 7 11 1 0\n 8 9 2 0\nM RGP 1 11 1\nM END\n> <Name>\nInosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nIn\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2,'4'-locked-Ribose\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n -0.9702 0.0384 0.0000 O 0 0\n 0.5413 -0.5559 0.0000 C 0 0 1 0 0 0\n -1.5602 -1.0669 0.0000 C 0 0 2 0 0 0\n 1.9236 0.0726 0.0000 C 0 0 2 0 0 0\n -0.2063 -1.7187 0.0000 C 0 0 1 0 0 0\n 1.5616 1.5445 0.0000 O 0 0\n 0.3744 0.9413 0.0000 C 0 0\n -2.6751 -0.6231 0.0000 R# 0 0\n -0.9999 1.5445 0.0000 O 0 0\n -1.1323 2.7372 0.0000 R# 0 0\n 2.4387 2.3633 0.0000 R# 0 0\n 0.6245 -2.0152 0.0000 C 0 0\n 0.0798 -3.2622 0.0000 O 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 1\n 3 5 1 0\n 3 8 1 6\n 4 5 1 0\n 6 11 1 0\n 7 9 1 0\n 9 10 1 0\n 2 12 1 6\n 12 13 1 0\n 5 13 1 1\n 4 6 1 1\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n2,'4'-locked-Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nLR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2'-O-Methoxyethyl ribose\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2340 0.0328 0.0000 O 0 0\n -1.7220 1.4427 0.0000 C 0 0 1 0 0 0\n -1.0514 -0.8898 0.0000 C 0 0 2 0 0 0\n -0.2229 1.3915 0.0000 C 0 0 2 0 0 0\n 0.1916 -0.0500 0.0000 C 0 0 1 0 0 0\n 0.6962 2.5746 0.0000 O 0 0\n 1.5988 -0.5644 0.0000 O 0 0\n -2.5633 2.6825 0.0000 C 0 0\n -1.0923 -2.0891 0.0000 R# 0 0\n -4.0602 2.5746 0.0000 O 0 0\n -4.7341 3.5674 0.0000 R# 0 0\n 1.8851 2.4118 0.0000 R# 0 0\n 1.8584 -2.0426 0.0000 C 0 0\n 3.2680 -2.5578 0.0000 C 0 0\n 3.5275 -4.0361 0.0000 O 0 0\n 4.6546 -4.4481 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 12 1 0\n 8 10 1 0\n 10 11 1 0\n 7 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\n2'-O-Methoxyethyl ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nMOE\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nTest-6-AP-Phosphate\n Ketcher 9272311252D 1 1.00000 0.00000 0\n\n 13 12 0 0 0 0 0 0 0 0999 V2000\n 8.5250 -7.0500 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0\n 9.0248 -7.9162 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 9.5250 -7.0500 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 9.0248 -6.1838 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 7.5250 -7.0500 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0\n 6.5250 -7.0500 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0\n 5.5250 -7.0500 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0\n 4.5250 -7.0500 0.0000 P 0 0 0 0 0 0 0 0 0 0 0 0\n 7.7838 -8.0159 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 6.5250 -8.0500 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 5.5250 -8.0500 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 4.2662 -8.0159 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 3.6590 -6.5500 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 1 2 2 0 0 0\n 1 3 1 0 0 0\n 1 4 1 0 0 0\n 1 5 1 0 0 0\n 5 6 1 0 0 0\n 6 7 1 0 0 0\n 7 8 1 0 0 0\n 5 9 1 0 0 0\n 6 10 1 0 0 0\n 7 11 1 0 0 0\n 8 12 1 0 0 0\n 8 13 1 0 0 0\nM RGP 6 3 2 9 6 10 5 11 4 12 3 13 1\nM END\n> <Name>\nTest-6-AP-Phosphate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nTest-6-Ph\n\n> <MonomerCode>\nP\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]Cl\n[R3]H\n[R4]O\n[R5]H\n[R6]O\n\n$$$$\nPhosphate\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n -0.2399 0.0000 0.0000 P 0 0\n -1.4399 0.0000 0.0000 R# 0 0\n 0.3598 -1.0394 0.0000 O 0 0\n 0.9601 0.0000 0.0000 R# 0 0\n 0.3598 1.0394 0.0000 O 0 0\n 1 2 1 0\n 1 3 2 0\n 1 4 1 0\n 1 5 1 0\nM RGP 2 2 1 4 2\nM END\n> <Name>\nPhosphate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nP\n\n> <MonomerCode>\nP\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\n2-(methylamino)ethanol (PHONA sugar)\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 1.1375 -0.1688 0.0000 N 0 0\n 2.4375 0.5812 0.0000 C 0 0\n 3.4769 -0.0185 0.0000 R# 0 0\n -0.1625 0.5812 0.0000 C 0 0\n -1.4625 -0.1688 0.0000 C 0 0\n -2.7625 0.5812 0.0000 O 0 0\n -3.8019 -0.0185 0.0000 R# 0 0\n 1.1375 -1.3688 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 1 8 1 0\nM RGP 3 3 2 7 1 8 3\nM END\n> <Name>\n2-(methylamino)ethanol (PHONA sugar)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nPONA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]H\n\n$$$$\nRibose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.1017 -1.0663 0.0000 O 0 0\n -0.5897 0.3436 0.0000 C 0 0 1 0 0 0\n 0.0809 -1.9889 0.0000 C 0 0 2 0 0 0\n 0.9095 0.2924 0.0000 C 0 0 2 0 0 0\n 1.3239 -1.1493 0.0000 C 0 0 1 0 0 0\n 1.8285 1.4755 0.0000 O 0 0\n 2.4518 -1.5589 0.0000 O 0 0\n -1.4310 1.5834 0.0000 C 0 0\n 0.0399 -3.1881 0.0000 R# 0 0\n -2.9279 1.4755 0.0000 O 0 0\n -3.6017 2.4684 0.0000 R# 0 0\n 3.0174 1.3125 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 12 1 0\n 8 10 1 0\n 10 11 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\nRibose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nR\n\n> <MonomerCode>\nR\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nR Propanetriol (GNA sugar)\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 0.2258 -0.3260 0.0000 C 0 0 1 0 0 0\n 0.9760 -1.6259 0.0000 C 0 0\n 2.1760 -1.6267 0.0000 R# 0 0\n 0.9740 0.9749 0.0000 O 0 0\n 2.1741 0.9778 0.0000 R# 0 0\n -1.2751 -0.3249 0.0000 C 0 0\n -2.0254 0.9749 0.0000 O 0 0\n -3.2253 0.9758 0.0000 R# 0 0\n 1 2 1 6\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 1 6 1 0\n 6 7 1 0\n 7 8 1 0\nM RGP 3 3 3 5 2 8 1\nM END\n> <Name>\nR Propanetriol (GNA sugar)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRGNA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nS Propanetriol (GNA sugar)\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 0.2258 -0.3260 0.0000 C 0 0 2 0 0 0\n 0.9760 -1.6259 0.0000 C 0 0\n 2.1760 -1.6267 0.0000 R# 0 0\n 0.9740 0.9749 0.0000 O 0 0\n 2.1741 0.9778 0.0000 R# 0 0\n -1.2751 -0.3249 0.0000 C 0 0\n -2.0254 0.9749 0.0000 O 0 0\n -3.2253 0.9758 0.0000 R# 0 0\n 1 2 1 1\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 1 6 1 0\n 6 7 1 0\n 7 8 1 0\nM RGP 3 3 3 5 2 8 1\nM END\n> <Name>\nS Propanetriol (GNA sugar)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSGNA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nThymine\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.7117 -0.9884 0.0000 C 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\n 2 10 1 0\nM RGP 1 9 1\nM END\n> <Name>\nThymine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nT\n\n> <MonomerCode>\nT\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nUracil\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\nM RGP 1 9 1\nM END\n> <Name>\nUracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nU\n\n> <MonomerCode>\nU\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2'-3'-Unlocked-ribose\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 0.6066 -1.3510 0.0000 O 0 0\n -0.6923 -2.1029 0.0000 C 0 0 2 0 0 0\n 0.6057 0.1499 0.0000 C 0 0 1 0 0 0\n 1.9045 0.9019 0.0000 C 0 0\n -0.6915 -3.6037 0.0000 C 0 0\n -1.7320 -1.5039 0.0000 R# 0 0\n -0.6932 0.9018 0.0000 C 0 0\n -0.6925 2.4027 0.0000 O 0 0\n -1.7310 3.0037 0.0000 R# 0 0\n 1.9036 2.4027 0.0000 O 0 0\n -1.7299 -4.2050 0.0000 O 0 0\n 2.9422 3.0039 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 3 4 1 6\n 2 5 1 6\n 2 6 1 0\n 3 7 1 0\n 7 8 1 0\n 8 9 1 0\n 4 10 1 0\n 5 11 1 0\n 10 12 1 0\nM RGP 3 6 3 9 1 12 2\nM END\n> <Name>\n2'-3'-Unlocked-ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nUNA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nalpha-FANA\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.1017 -1.0663 0.0000 O 0 0\n -0.5897 0.3436 0.0000 C 0 0 1 0 0 0\n 0.0809 -1.9889 0.0000 C 0 0 2 0 0 0\n 0.9095 0.2924 0.0000 C 0 0 2 0 0 0\n 1.3239 -1.1493 0.0000 C 0 0 2 0 0 0\n 1.8285 1.4755 0.0000 O 0 0\n -1.4310 1.5834 0.0000 C 0 0\n 0.0399 -3.1881 0.0000 R# 0 0\n -2.9279 1.4755 0.0000 O 0 0\n -3.6017 2.4684 0.0000 R# 0 0\n 3.0174 1.3125 0.0000 R# 0 0\n 2.4518 -1.5589 0.0000 F 0 0\n 1 2 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 3 8 1 6\n 4 5 1 0\n 4 6 1 1\n 6 11 1 0\n 7 9 1 0\n 9 10 1 0\n 5 12 1 6\n 1 3 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\nalpha-FANA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\naFR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Amino-Ribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.1017 -1.0663 0.0000 O 0 0\n -0.5897 0.3436 0.0000 C 0 0 1 0 0 0\n 0.0809 -1.9889 0.0000 C 0 0 2 0 0 0\n 0.9095 0.2924 0.0000 C 0 0 2 0 0 0\n 1.3239 -1.1493 0.0000 C 0 0 1 0 0 0\n 1.8285 1.4755 0.0000 N 0 0\n 2.4518 -1.5589 0.0000 O 0 0\n -1.4310 1.5834 0.0000 C 0 0\n 0.0399 -3.1881 0.0000 R# 0 0\n -2.9279 1.4755 0.0000 O 0 0\n -3.6017 2.4684 0.0000 R# 0 0\n 3.0174 1.3125 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 12 1 0\n 8 10 1 0\n 10 11 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\n3-Amino-Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\naR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5'-12-amino-dodecanol\n SciTegic07272112182D\n\n 16 15 0 0 1 0 999 V2000\n -8.4583 0.0000 0.0000 N 0 0\n -7.1263 -0.6916 0.0000 C 0 0\n -5.8608 0.1153 0.0000 C 0 0\n -4.5288 -0.5764 0.0000 C 0 0\n -3.2634 0.2305 0.0000 C 0 0\n -1.9315 -0.4611 0.0000 C 0 0\n -0.6660 0.3458 0.0000 C 0 0\n 0.6659 -0.3458 0.0000 C 0 0\n -9.4700 -0.6452 0.0000 R# 0 0\n 1.9314 0.4611 0.0000 C 0 0\n 3.2634 -0.2305 0.0000 C 0 0\n 4.5289 0.5764 0.0000 C 0 0\n 5.8608 -0.1153 0.0000 C 0 0\n 7.1263 0.6916 0.0000 C 0 0\n 8.4583 0.0000 0.0000 O 0 0\n 9.4701 0.6452 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 1 9 1 0\n 8 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\nM RGP 2 9 1 16 2\nM END\n> <Name>\n5'-12-amino-dodecanol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nam12\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n5'-6-amino-hexanol\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n -4.5654 0.0000 0.0000 N 0 0\n -3.2082 -0.6407 0.0000 C 0 0\n -5.5520 -0.6831 0.0000 R# 0 0\n -1.9742 0.2136 0.0000 C 0 0\n -0.6170 -0.4271 0.0000 C 0 0\n 0.6170 0.4271 0.0000 C 0 0\n 1.9742 -0.2136 0.0000 C 0 0\n 3.2082 0.6407 0.0000 C 0 0\n 4.5654 0.0000 0.0000 O 0 0\n 5.5520 0.6830 0.0000 R# 0 0\n 1 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 2 1 1 0\nM RGP 2 3 1 10 2\nM END\n> <Name>\n5'-6-amino-hexanol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nam6\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nBoranophosphate\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n -0.2399 0.0000 0.0000 P 0 0\n -1.4399 0.0000 0.0000 R# 0 0\n 0.3598 -1.0394 0.0000 O 0 0\n 0.9601 0.0000 0.0000 R# 0 0\n 0.3598 1.0394 0.0000 B 0 0\n 1 2 1 0\n 1 3 2 0\n 1 4 1 0\n 1 5 1 0\nM RGP 2 2 1 4 2\nM END\n> <Name>\nBoranophosphate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbP\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nN-benzyl-adenine\n SciTegic07272112182D\n\n 18 20 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 C 0 0\n -0.0787 -2.2532 0.0000 N 0 0\n 2.4638 -0.2109 0.0000 N 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n 3.5776 0.7950 0.0000 C 0 0\n 5.0060 0.3343 0.0000 C 0 0\n 7.8594 -0.5925 0.0000 C 0 0\n 7.5474 0.8747 0.0000 C 0 0\n 6.1207 1.3381 0.0000 C 0 0\n 5.3181 -1.1330 0.0000 C 0 0\n 6.7448 -1.5963 0.0000 C 0 0\n 1 10 1 0\n 1 6 2 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 1 0\n 7 11 1 0\n 8 9 2 0\n 10 12 1 0\n 12 13 1 0\n 16 13 2 0\n 13 17 1 0\n 14 15 2 0\n 15 16 1 0\n 17 18 2 0\n 14 18 1 0\nM RGP 1 11 1\nM END\n> <Name>\nN-benzyl-adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbaA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-cyclopropyl-4-dimethylamino-cytosine\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 2.6489 0.0000 C 0 0\n -0.3882 2.6490 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3883 0.0509 0.0000 C 0 0\n 1.1117 0.0509 0.0000 N 0 0\n 3.3626 1.3468 0.0000 N 0 0\n -0.9884 -0.9883 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.8621 3.9486 0.0000 C 0 0\n 3.1144 4.6215 0.0000 C 0 0\n 1.8143 5.3694 0.0000 C 0 0\n 3.9611 0.3067 0.0000 C 0 0\n 3.9644 2.3849 0.0000 C 0 0\n 1 2 1 0\n 1 6 2 0\n 1 7 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 6 1 0\n 5 8 2 0\n 2 10 1 0\n 10 11 1 0\n 10 12 1 0\n 12 11 1 0\n 7 13 1 0\n 7 14 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-cyclopropyl-4-dimethylamino-cytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncdaC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nT-clamp OMe\n SciTegic07272112182D\n\n 20 23 0 0 1 0 999 V2000\n 6.0065 0.0000 0.0000 N 0 0\n 4.8065 0.0000 0.0000 R# 0 0\n 6.8882 -1.2135 0.0000 C 0 0\n 6.8882 1.2135 0.0000 C 0 0\n 8.3140 0.7500 0.0000 C 0 0\n 8.3140 -0.7500 0.0000 C 0 0\n 9.6130 -1.5000 0.0000 C 0 0\n 9.3808 -3.0307 0.0000 N 0 0\n 8.0105 -3.6408 0.0000 C 0 0\n 6.7969 -2.7592 0.0000 N 0 0\n 10.9120 -0.7500 0.0000 N 0 0\n 9.6130 1.5000 0.0000 C 0 0\n 10.9120 0.7500 0.0000 C 0 0\n 12.2111 1.5000 0.0000 C 0 0\n 12.2111 3.0000 0.0000 C 0 0\n 10.9120 3.7500 0.0000 C 0 0\n 9.6130 3.0000 0.0000 C 0 0\n 13.5124 0.7523 0.0000 O 0 0\n 14.5508 1.3538 0.0000 C 0 0\n 7.8851 -4.8343 0.0000 N 0 0\n 1 2 1 0\n 1 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 3 1 0\n 7 11 1 0\n 5 12 1 0\n 12 13 1 0\n 13 11 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 16 17 1 0\n 17 12 2 0\n 14 18 1 0\n 18 19 1 0\n 9 20 1 0\nM RGP 1 2 1\nM END\n> <Name>\nT-clamp OMe\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nclA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-cyclopropyl-cytosine\n SciTegic07272112182D\n\n 12 13 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 2.6489 0.0000 C 0 0\n -0.3882 2.6490 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3883 0.0509 0.0000 C 0 0\n 1.1117 0.0509 0.0000 N 0 0\n 3.0618 1.3499 0.0000 N 0 0\n -0.9884 -0.9883 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.8621 3.9486 0.0000 C 0 0\n 3.1144 4.6215 0.0000 C 0 0\n 1.8143 5.3694 0.0000 C 0 0\n 1 2 1 0\n 1 6 2 0\n 1 7 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 6 1 0\n 5 8 2 0\n 2 10 1 0\n 10 11 1 0\n 10 12 1 0\n 12 11 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-cyclopropyl-cytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncpC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-cyclopropyl-uracil\n SciTegic07272112182D\n\n 12 13 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.8621 -1.2489 0.0000 C 0 0\n 1.8185 -2.6698 0.0000 C 0 0\n 3.1164 -1.9177 0.0000 C 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\n 2 10 1 0\n 10 11 1 0\n 10 12 1 0\n 12 11 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-cyclopropyl-uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncpU\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN-cyclopropylmethyl-adenine\n SciTegic07272112182D\n\n 15 17 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 C 0 0\n -0.0787 -2.2532 0.0000 N 0 0\n 2.4638 -0.2109 0.0000 N 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n 3.5776 0.7950 0.0000 C 0 0\n 5.0060 0.3343 0.0000 C 0 0\n 6.3863 0.6744 0.0000 C 0 0\n 5.9228 -0.7522 0.0000 C 0 0\n 1 10 1 0\n 1 6 2 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 1 0\n 7 11 1 0\n 8 9 2 0\n 10 12 1 0\n 12 13 1 0\n 13 14 1 0\n 13 15 1 0\n 15 14 1 0\nM RGP 1 11 1\nM END\n> <Name>\nN-cyclopropylmethyl-adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncpmA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nDeoxy-Ribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.8788 -1.2080 0.0000 O 0 0\n -0.3668 0.2019 0.0000 C 0 0 1 0 0 0\n 0.3038 -2.1307 0.0000 C 0 0 2 0 0 0\n 1.1323 0.1506 0.0000 C 0 0 2 0 0 0\n 1.5468 -1.2910 0.0000 C 0 0\n 2.0515 1.3338 0.0000 O 0 0\n -1.2081 1.4417 0.0000 C 0 0\n 0.2628 -3.3299 0.0000 R# 0 0\n -2.7050 1.3338 0.0000 O 0 0\n -3.3788 2.3267 0.0000 R# 0 0\n 3.2403 1.1709 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 3 8 1 6\n 4 5 1 0\n 4 6 1 1\n 6 11 1 0\n 7 9 1 0\n 9 10 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\nDeoxy-Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nN,N-dimethyl-Adenine\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 C 0 0\n -0.0787 -2.2532 0.0000 N 0 0\n 2.4638 -0.2109 0.0000 N 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n 3.3544 0.5933 0.0000 C 0 0\n 2.7154 -1.3842 0.0000 C 0 0\n 1 10 1 0\n 1 6 2 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 1 0\n 7 11 1 0\n 8 9 2 0\n 10 12 1 0\n 10 13 1 0\nM RGP 1 11 1\nM END\n> <Name>\nN,N-dimethyl-Adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndaA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-deaza-8-aza-7-bromo-2-amino-Adenine\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 N 0 0\n -0.0787 -2.2532 0.0000 C 0 0\n 2.1768 -0.1209 0.0000 N 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n -0.9527 3.3542 0.0000 N 0 0\n 0.8922 -2.9584 0.0000 Br 0 0\n 1 10 1 0\n 1 6 2 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 1 0\n 7 11 1 0\n 8 9 2 0\n 5 12 1 0\n 9 13 1 0\nM RGP 1 11 1\nM END\n> <Name>\n7-deaza-8-aza-7-bromo-2-amino-Adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndabA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2,4-Difluoro-Benzene\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 2.6489 0.0000 C 0 0\n -0.3882 2.6490 0.0000 C 0 0\n -1.1382 1.3500 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n 3.0618 1.3499 0.0000 F 0 0\n -0.9884 -0.9883 0.0000 F 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 1 7 1 0\n 5 8 1 0\n 4 9 1 0\nM RGP 1 9 1\nM END\n> <Name>\n2,4-Difluoro-Benzene\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndfB\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5- 1,2-Dierucyl-rac-glycerol (Genzyme)\n SciTegic07272112182D\n\n 51 50 0 0 1 0 999 V2000\n 29.4991 -4.8473 0.0000 C 0 0\n 30.2517 -3.5488 0.0000 C 0 0\n 30.2465 -6.1488 0.0000 O 0 0\n 29.5043 -2.2473 0.0000 O 0 0\n 31.7525 -3.5488 0.0000 C 0 0\n 32.5037 -2.2494 0.0000 O 0 0\n 33.7037 -2.2494 0.0000 R# 0 0\n 30.2569 -0.9489 0.0000 C 0 0\n 29.5095 0.3526 0.0000 C 0 0\n 30.2621 1.6511 0.0000 C 0 0\n 29.5147 2.9526 0.0000 C 0 0\n 30.2673 4.2511 0.0000 C 0 0\n 29.5199 5.5526 0.0000 C 0 0\n 30.2725 6.8511 0.0000 C 0 0\n 29.5251 8.1526 0.0000 C 0 0\n 30.2777 9.4511 0.0000 C 0 0\n 29.5303 10.7526 0.0000 C 0 0\n 30.2829 12.0510 0.0000 C 0 0\n 29.5355 13.3525 0.0000 C 0 0\n 30.2881 14.6510 0.0000 C 0 0\n 29.4939 -7.4473 0.0000 C 0 0\n 30.2413 -8.7488 0.0000 C 0 0\n 29.4887 -10.0473 0.0000 C 0 0\n 30.2361 -11.3488 0.0000 C 0 0\n 29.4835 -12.6473 0.0000 C 0 0\n 30.2309 -13.9488 0.0000 C 0 0\n 29.4783 -15.2473 0.0000 C 0 0\n 30.2257 -16.5487 0.0000 C 0 0\n 29.4731 -17.8472 0.0000 C 0 0\n 30.2205 -19.1487 0.0000 C 0 0\n 29.4679 -20.4472 0.0000 C 0 0\n 30.2153 -21.7487 0.0000 C 0 0\n 29.4627 -23.0472 0.0000 C 0 0\n 30.2101 -24.3487 0.0000 C 0 0\n 31.7109 -24.3531 0.0000 C 0 0\n 29.5407 15.9525 0.0000 C 0 0\n 28.0399 15.9569 0.0000 C 0 0\n 32.4583 -25.6546 0.0000 C 0 0\n 33.9591 -25.6590 0.0000 C 0 0\n 34.7065 -26.9605 0.0000 C 0 0\n 36.2074 -26.9649 0.0000 C 0 0\n 36.9548 -28.2664 0.0000 C 0 0\n 38.4556 -28.2709 0.0000 C 0 0\n 39.0532 -29.3115 0.0000 C 0 0\n 27.2925 17.2584 0.0000 C 0 0\n 25.7917 17.2629 0.0000 C 0 0\n 25.0443 18.5643 0.0000 C 0 0\n 23.5434 18.5688 0.0000 C 0 0\n 22.7960 19.8703 0.0000 C 0 0\n 21.2952 19.8747 0.0000 C 0 0\n 20.6976 20.9153 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 5 1 0\n 5 6 1 0\n 6 7 1 0\n 4 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 19 20 1 0\n 3 21 1 0\n 21 22 1 0\n 22 23 1 0\n 23 24 1 0\n 24 25 1 0\n 25 26 1 0\n 26 27 1 0\n 27 28 1 0\n 28 29 1 0\n 29 30 1 0\n 30 31 1 0\n 31 32 1 0\n 32 33 1 0\n 33 34 2 0\n 34 35 1 0\n 20 36 2 0\n 36 37 1 0\n 35 38 1 0\n 38 39 1 0\n 39 40 1 0\n 40 41 1 0\n 41 42 1 0\n 42 43 1 0\n 43 44 1 0\n 37 45 1 0\n 45 46 1 0\n 46 47 1 0\n 47 48 1 0\n 48 49 1 0\n 49 50 1 0\n 50 51 1 0\nM RGP 1 7 2\nM END\n> <Name>\n5- 1,2-Dierucyl-rac-glycerol (Genzyme)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndier\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]H\n\n$$$$\n2'-O,4'-ethylene bridged Ribose\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -1.7962 0.2830 0.0000 O 0 0\n -0.2126 -0.1654 0.0000 C 0 0 1 0 0 0\n -0.7491 -0.5569 0.0000 C 0 0 2 0 0 0\n 1.0867 0.5840 0.0000 C 0 0 2 0 0 0\n 0.6934 -0.7266 0.0000 C 0 0 1 0 0 0\n 1.9988 1.7614 0.0000 O 0 0\n -0.5224 1.2978 0.0000 C 0 0\n -1.2125 -1.6638 0.0000 R# 0 0\n -1.9499 1.7614 0.0000 O 0 0\n -2.2001 2.9350 0.0000 R# 0 0\n 3.1880 1.6005 0.0000 R# 0 0\n 1.2940 -2.2554 0.0000 O 0 0\n 0.4041 -1.8438 0.0000 C 0 0\n -0.0222 -3.0111 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 1\n 3 5 1 0\n 3 8 1 6\n 4 5 1 0\n 6 11 1 0\n 7 9 1 0\n 9 10 1 0\n 4 6 1 1\n 5 12 1 1\n 2 13 1 6\n 13 14 1 0\n 14 12 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n2'-O,4'-ethylene bridged Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\neR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nN-ethyl-adenine\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 C 0 0\n -0.0787 -2.2532 0.0000 N 0 0\n 2.4638 -0.2109 0.0000 N 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n 3.5776 0.7950 0.0000 C 0 0\n 4.7197 0.4267 0.0000 C 0 0\n 1 10 1 0\n 1 6 2 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 1 0\n 7 11 1 0\n 8 9 2 0\n 10 12 1 0\n 12 13 1 0\nM RGP 1 11 1\nM END\n> <Name>\nN-ethyl-adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\neaA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2'-Flu0ro-Ribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.1017 -1.0663 0.0000 O 0 0\n -0.5897 0.3436 0.0000 C 0 0 1 0 0 0\n 0.0809 -1.9889 0.0000 C 0 0 2 0 0 0\n 0.9095 0.2924 0.0000 C 0 0 2 0 0 0\n 1.3239 -1.1493 0.0000 C 0 0 1 0 0 0\n 1.8285 1.4755 0.0000 O 0 0\n 2.4518 -1.5589 0.0000 F 0 0\n -1.4310 1.5834 0.0000 C 0 0\n 0.0399 -3.1881 0.0000 R# 0 0\n -2.9279 1.4755 0.0000 O 0 0\n -3.6017 2.4684 0.0000 R# 0 0\n 3.0174 1.3125 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 12 1 0\n 8 10 1 0\n 10 11 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\n2'-Flu0ro-Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nhexitol\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.2871 -0.9728 0.0000 O 0 0\n -0.5356 0.3254 0.0000 C 0 0 1 0 0 0\n 0.9644 0.3237 0.0000 C 0 0 2 0 0 0\n 1.7128 -0.9762 0.0000 C 0 0\n 0.9613 -2.2744 0.0000 C 0 0 1 0 0 0\n -0.5387 -2.2726 0.0000 C 0 0\n -1.2872 1.6245 0.0000 C 0 0\n -2.7880 1.6241 0.0000 O 0 0\n -3.3890 2.6628 0.0000 R# 0 0\n 1.7136 1.6241 0.0000 O 0 0\n 1.5602 -3.3144 0.0000 R# 0 0\n 2.9136 1.6260 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 1 6 1 0\n 2 7 1 6\n 7 8 1 0\n 8 9 1 0\n 3 10 1 1\n 5 11 1 6\n 10 12 1 0\nM RGP 3 9 1 11 3 12 2\nM END\n> <Name>\nhexitol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nhx\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2,'4'-locked-Ribose (alpha-L-LNA)\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n -0.9702 0.0384 0.0000 O 0 0\n 0.5413 -0.5559 0.0000 C 0 0 1 0 0 0\n -1.5602 -1.0669 0.0000 C 0 0 2 0 0 0\n 1.9236 0.0726 0.0000 C 0 0 1 0 0 0\n -0.2063 -1.7187 0.0000 C 0 0 2 0 0 0\n 1.5616 1.5445 0.0000 O 0 0\n 0.6245 -2.0152 0.0000 C 0 0\n -2.6751 -0.6231 0.0000 R# 0 0\n 2.4387 2.3633 0.0000 R# 0 0\n 0.3744 0.9413 0.0000 C 0 0\n 0.0798 -3.2622 0.0000 O 0 0\n -0.9999 1.5445 0.0000 O 0 0\n -1.1323 2.7372 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 3 8 1 6\n 4 5 1 0\n 6 9 1 0\n 2 10 1 0\n 5 11 1 6\n 4 6 1 6\n 10 12 1 0\n 7 11 1 0\n 12 13 1 0\nM RGP 3 8 3 9 2 13 1\nM END\n> <Name>\n2,'4'-locked-Ribose (alpha-L-LNA)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nlLR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2'-O-Methyl-Ribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.3493 -0.8393 0.0000 O 0 0\n -0.8372 0.5706 0.0000 C 0 0 1 0 0 0\n -0.1666 -1.7620 0.0000 C 0 0 2 0 0 0\n 0.6619 0.5193 0.0000 C 0 0 2 0 0 0\n 1.0764 -0.9223 0.0000 C 0 0 1 0 0 0\n 1.5811 1.7025 0.0000 O 0 0\n 2.4836 -1.4367 0.0000 O 0 0\n -1.6785 1.8103 0.0000 C 0 0\n -0.2077 -2.9612 0.0000 R# 0 0\n -3.1754 1.7025 0.0000 O 0 0\n -3.8492 2.6954 0.0000 R# 0 0\n 2.7699 1.5395 0.0000 R# 0 0\n 2.6911 -2.6186 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 12 1 0\n 8 10 1 0\n 10 11 1 0\n 7 13 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\n2'-O-Methyl-Ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nN-Methyl-Adenine\n SciTegic07272112182D\n\n 12 13 0 0 1 0 999 V2000\n 1.0354 0.2498 0.0000 C 0 0\n -0.0792 -0.7540 0.0000 C 0 0\n -1.5057 -0.2906 0.0000 C 0 0\n -1.8177 1.1766 0.0000 N 0 0\n -0.7031 2.1804 0.0000 C 0 0\n 0.7235 1.7170 0.0000 N 0 0\n -2.3871 -1.5034 0.0000 N 0 0\n -1.5053 -2.7168 0.0000 C 0 0\n -0.0787 -2.2532 0.0000 N 0 0\n 2.4638 -0.2109 0.0000 N 0 0\n -3.5871 -1.5034 0.0000 R# 0 0\n 3.3544 0.5933 0.0000 C 0 0\n 1 10 1 0\n 1 6 2 0\n 1 2 1 0\n 9 2 1 0\n 2 3 2 0\n 7 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 8 1 0\n 7 11 1 0\n 8 9 2 0\n 10 12 1 0\nM RGP 1 11 1\nM END\n> <Name>\nN-Methyl-Adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmeA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nmorpholino\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.4725 -0.9529 0.0000 O 0 0\n -0.4712 0.5471 0.0000 C 0 0 1 0 0 0\n 0.8284 1.2959 0.0000 C 0 0\n 2.1268 0.5448 0.0000 N 0 0\n 2.1255 -0.9552 0.0000 C 0 0\n 0.8258 -1.7041 0.0000 C 0 0 2 0 0 0\n -1.7719 1.2960 0.0000 C 0 0\n 0.8248 -2.9041 0.0000 R# 0 0\n -3.0712 0.5448 0.0000 O 0 0\n -4.1112 1.1437 0.0000 R# 0 0\n 3.1666 1.1439 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 1 6 1 0\n 2 7 1 6\n 6 8 1 6\n 7 9 1 0\n 9 10 1 0\n 4 11 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\nmorpholino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmph\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nSodium Phosphate\n SciTegic07272112182D\n\n 6 4 0 0 1 0 999 V2000\n -0.1999 -0.6333 0.0000 P 0 0\n -1.3999 -0.6333 0.0000 R# 0 0\n 0.3998 -1.6727 0.0000 O 0 0\n 1.0001 -0.6333 0.0000 R# 0 0\n 0.3998 0.4061 0.0000 O 0 5\n -0.1999 3.1667 0.0000 Na 0 3\n 1 2 1 0\n 1 3 2 0\n 1 4 1 0\n 1 5 1 0\nM CHG 2 5 -1 6 1\nM RGP 2 2 1 4 2\nM END\n> <Name>\nSodium Phosphate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnaP\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nSodium Phosporothioate\n SciTegic07272112182D\n\n 6 4 0 0 1 0 999 V2000\n -0.1999 -0.6333 0.0000 P 0 0\n -1.3999 -0.6333 0.0000 R# 0 0\n 0.3998 -1.6727 0.0000 O 0 0\n 1.0001 -0.6333 0.0000 R# 0 0\n 0.3998 0.4061 0.0000 S 0 5\n -0.1999 3.1667 0.0000 Na 0 3\n 1 2 1 0\n 1 3 2 0\n 1 4 1 0\n 1 5 1 0\nM CHG 2 5 -1 6 1\nM RGP 2 2 1 4 2\nM END\n> <Name>\nSodium Phosporothioate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnasP\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\n5-Propynyl-Cytosine\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 2.6489 0.0000 C 0 0\n -0.3882 2.6490 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3883 0.0509 0.0000 C 0 0\n 1.1117 0.0509 0.0000 N 0 0\n 3.0618 1.3499 0.0000 N 0 0\n -0.9884 -0.9883 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.8622 3.9487 0.0000 C 0 0\n 2.6126 5.2484 0.0000 C 0 0\n 3.2127 6.2877 0.0000 C 0 0\n 1 2 1 0\n 1 6 2 0\n 1 7 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 6 1 0\n 5 8 2 0\n 2 10 1 0\n 10 11 3 0\n 11 12 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-Propynyl-Cytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nprpC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-propynyl Uracil\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.8621 -1.2489 0.0000 C 0 0\n 2.6125 -2.5487 0.0000 C 0 0\n 3.2124 -3.5880 0.0000 C 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\n 2 10 1 0\n 10 11 3 0\n 11 12 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-propynyl Uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nprpU\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-O-beta-hydroxy-ethoxy-methyl Ribose (Qiagen)\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.5533 0.3762 0.0000 O 0 0\n -2.0412 1.7861 0.0000 C 0 0 1 0 0 0\n -1.3706 -0.5464 0.0000 C 0 0 2 0 0 0\n -0.5421 1.7349 0.0000 C 0 0 2 0 0 0\n -0.1276 0.2932 0.0000 C 0 0 1 0 0 0\n 0.3770 2.9180 0.0000 O 0 0\n 1.2795 -0.2212 0.0000 O 0 0\n -2.8825 3.0258 0.0000 C 0 0\n -1.4117 -1.7458 0.0000 R# 0 0\n -4.3794 2.9180 0.0000 O 0 0\n -5.0532 3.9109 0.0000 R# 0 0\n 1.5659 2.7550 0.0000 R# 0 0\n 1.5391 -1.6994 0.0000 C 0 0\n 2.9487 -2.2146 0.0000 O 0 0\n 3.2082 -3.6929 0.0000 C 0 0\n 4.6177 -4.2081 0.0000 C 0 0\n 4.8253 -5.3900 0.0000 O 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 8 1 6\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 12 1 0\n 8 10 1 0\n 10 11 1 0\n 7 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\nM RGP 3 9 3 11 1 12 2\nM END\n> <Name>\n2-O-beta-hydroxy-ethoxy-methyl Ribose (Qiagen)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nqR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nPhosporothioate\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n -0.2399 0.0000 0.0000 P 0 0\n -1.4399 0.0000 0.0000 R# 0 0\n 0.3598 -1.0394 0.0000 O 0 0\n 0.9601 0.0000 0.0000 R# 0 0\n 0.3598 1.0394 0.0000 S 0 0\n 1 2 1 0\n 1 3 2 0\n 1 4 1 0\n 1 5 1 0\nM RGP 2 2 1 4 2\nM END\n> <Name>\nPhosporothioate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nsP\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nRibose\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n -0.2355 -2.0711 0.0000 O 0 0\n -1.4490 -1.1894 0.0000 C 0 0\n 0.9781 -1.1894 0.0000 C 0 0 2 0 0 0\n -0.9855 0.2372 0.0000 C 0 0 1 0 0 0\n 0.5145 0.2372 0.0000 C 0 0 1 0 0 0\n -1.8686 1.4475 0.0000 O 0 0\n 1.3977 1.4475 0.0000 O 0 0\n 2.1193 -1.5602 0.0000 R# 0 0\n -3.0619 1.3203 0.0000 R# 0 0\n 2.5909 1.3203 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 3 5 1 0\n 3 8 1 6\n 4 5 1 0\n 4 6 1 6\n 5 7 1 1\n 6 9 1 0\n 7 10 1 0\nM RGP 3 8 3 9 1 10 2\nM END\n> <Name>\nRibose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ntR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-trifluoromethyl-uracil\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n 1.8617 1.3499 0.0000 C 0 0\n 1.1117 0.0509 0.0000 C 0 0\n -0.3883 0.0509 0.0000 C 0 0\n -1.1382 1.3500 0.0000 N 0 0\n -0.3882 2.6490 0.0000 C 0 0\n 1.1117 2.6489 0.0000 N 0 0\n 3.0618 1.3499 0.0000 O 0 0\n -0.9882 3.6882 0.0000 O 0 0\n -2.3383 1.3500 0.0000 R# 0 0\n 1.8621 -1.2489 0.0000 C 0 0\n 3.0621 -1.2497 0.0000 F 0 0\n 1.2617 -2.2879 0.0000 F 0 0\n 2.4615 -2.2884 0.0000 F 0 0\n 1 7 2 0\n 1 6 1 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 9 1 0\n 5 8 2 0\n 5 6 1 0\n 2 10 1 0\n 10 11 1 0\n 10 12 1 0\n 10 13 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-trifluoromethyl-uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ntfU\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nAlanine\n SciTegic07272112182D\n\n 7 6 0 0 1 0 999 V2000\n -1.2549 -0.3920 0.0000 N 0 0\n -0.2720 0.2633 0.0000 C 0 0 1 0 0 0\n -0.3103 1.7393 0.0000 C 0 0\n 1.0523 -0.3920 0.0000 C 0 0\n 1.0829 -1.5722 0.0000 O 0 0\n 2.0353 0.2633 0.0000 R# 0 0\n -2.3334 0.0905 0.0000 R# 0 0\n 2 1 1 0\n 2 3 1 1\n 2 4 1 0\n 4 5 2 0\n 4 6 1 0\n 1 7 1 0\nM RGP 2 6 2 7 1\nM END\n> <Name>\nAlanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nA\n\n> <MonomerCode>\nA\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nTest-6-AP-Peptide\n Ketcher 9272310562D 1 1.00000 0.00000 0\n\n 23 22 0 0 1 0 0 0 0 0999 V2000\n 12.7761 -7.9506 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 12.7754 -9.0509 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.7276 -9.6021 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.7271 -10.4818 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 14.4899 -9.1629 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 11.8233 -9.6021 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0\n 11.8239 -7.3994 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 11.8245 -6.2991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 10.8724 -5.7479 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 10.1101 -6.1871 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 10.8728 -4.8682 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 11.0606 -9.1637 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 12.7904 -5.7903 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.7564 -6.2991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 14.7564 -6.2991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 15.2564 -5.4331 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 12.7904 -4.7903 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 15.6224 -6.7991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 15.6224 -7.7991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 16.4884 -8.2991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 14.7564 -8.2991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 16.4884 -9.2991 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 17.3544 -9.7991 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 2 1 1 1 0 0\n 2 3 1 0 0 0\n 3 4 2 0 0 0\n 3 5 1 0 0 0\n 2 6 1 0 0 0\n 1 7 1 0 0 0\n 7 8 1 0 0 0\n 8 9 1 0 0 0\n 9 10 1 0 0 0\n 9 11 2 0 0 0\n 6 12 1 0 0 0\n 8 13 1 0 0 0\n 13 14 1 0 0 0\n 14 15 1 0 0 0\n 15 16 1 0 0 0\n 13 17 1 0 0 0\n 15 18 1 0 0 0\n 18 19 1 0 0 0\n 19 20 1 0 0 0\n 19 21 1 0 0 0\n 20 22 1 0 0 0\n 22 23 1 0 0 0\nM RGP 6 5 2 10 3 12 1 16 5 17 4 23 6\nM END\n\n> <Name>\nTest-6-AP-Peptide\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTest-6-P\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]N\n[R4]Cl\n[R5]F\n[R6]Br\n\n$$$$\n2-aminoadipic acid\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 0.8445 0.0123 0.0000 C 0 0\n 0.8436 -1.4885 0.0000 C 0 0 1 0 0 0\n 2.1425 -2.2405 0.0000 C 0 0\n 2.1418 -3.4405 0.0000 O 0 0\n 3.1823 -1.6414 0.0000 R# 0 0\n -0.4552 -2.2405 0.0000 N 0 0\n -0.4543 0.7643 0.0000 C 0 0\n -0.4535 2.2651 0.0000 C 0 0\n -1.7523 3.0170 0.0000 C 0 0\n -2.7921 2.4179 0.0000 R# 0 0\n -1.7517 4.2171 0.0000 O 0 0\n -1.4956 -1.6424 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 1 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 9 11 2 0\n 6 12 1 0\nM RGP 3 5 2 10 3 12 1\nM END\n> <Name>\n2-aminoadipic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAad\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\n2-aminobutanoic acid\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n -0.0318 1.5208 0.0000 C 0 0\n -0.0326 0.0200 0.0000 C 0 0 1 0 0 0\n 1.2663 -0.7320 0.0000 C 0 0\n 1.2656 -1.9320 0.0000 O 0 0\n 2.3061 -0.1329 0.0000 R# 0 0\n -1.3315 -0.7320 0.0000 N 0 0\n -1.0703 2.1220 0.0000 C 0 0\n -2.3718 -0.1339 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 1 7 1 0\n 6 8 1 0\nM RGP 2 5 2 8 1\nM END\n> <Name>\n2-aminobutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAbu\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-aminocapric acid\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n 1.3727 -1.2230 0.0000 C 0 0\n 1.3719 -2.7239 0.0000 C 0 0 1 0 0 0\n 2.6708 -3.4758 0.0000 C 0 0\n 2.6701 -4.6759 0.0000 O 0 0\n 3.7105 -2.8768 0.0000 R# 0 0\n 0.0730 -3.4758 0.0000 N 0 0\n -0.9674 -2.8778 0.0000 R# 0 0\n 0.0739 -0.4711 0.0000 C 0 0\n 0.0748 1.0298 0.0000 C 0 0\n -1.2240 1.7816 0.0000 C 0 0\n -1.2232 3.2825 0.0000 C 0 0\n -2.5221 4.0344 0.0000 C 0 0\n -2.5213 5.5353 0.0000 C 0 0\n -3.5597 6.1366 0.0000 C 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 6 7 1 0\n 1 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\nM RGP 2 5 2 7 1\nM END\n> <Name>\n2-aminocapric acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAca\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nalpha-aminoisobutyric acid (2-aminoalanine)\n SciTegic07272112182D\n\n 8 7 0 0 0 0 999 V2000\n -0.7185 1.1362 0.0000 C 0 0\n -0.1279 0.1134 0.0000 C 0 0\n -1.1506 -0.4772 0.0000 N 0 0\n -2.1736 0.1133 0.0000 R# 0 0\n 0.8950 -0.4772 0.0000 C 0 0\n 0.8951 -1.6582 0.0000 O 0 0\n 1.9179 0.1135 0.0000 R# 0 0\n 0.4626 1.1363 0.0000 C 0 0\n 2 1 1 0\n 3 2 1 0\n 3 4 1 0\n 2 5 1 0\n 5 6 2 0\n 5 7 1 0\n 8 2 1 0\nM RGP 2 4 1 7 2\nM END\n> <Name>\nalpha-aminoisobutyric acid (2-aminoalanine)\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAib\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-aminopimelic acid\n SciTegic07272112182D\n\n 13 12 0 0 1 0 999 V2000\n 0.8990 -0.6122 0.0000 C 0 0\n 0.8982 -2.1130 0.0000 C 0 0 1 0 0 0\n 2.1971 -2.8650 0.0000 C 0 0\n 2.1964 -4.0650 0.0000 O 0 0\n 3.2369 -2.2659 0.0000 R# 0 0\n -0.4007 -2.8650 0.0000 N 0 0\n -0.3998 0.1398 0.0000 C 0 0\n -0.3989 1.6406 0.0000 C 0 0\n -1.6977 2.3925 0.0000 C 0 0\n -1.6969 3.8933 0.0000 C 0 0\n -1.4410 -2.2669 0.0000 R# 0 0\n -0.6571 4.4924 0.0000 R# 0 0\n -2.7355 4.4946 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 1 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 6 11 1 0\n 10 12 1 0\n 10 13 2 0\nM RGP 3 5 2 11 1 12 3\nM END\n> <Name>\n2-aminopimelic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nApm\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\ngamma-amino-beta-hydroxybenzenepentanoic acid\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n 0.7404 -1.8505 0.0000 C 0 0\n 0.1498 -0.8277 0.0000 C 0 0 1 0 0 0\n 0.7404 0.1952 0.0000 O 0 0\n -1.0313 -0.8277 0.0000 C 0 0 2 0 0 0\n -1.6218 0.1952 0.0000 C 0 0\n -1.0313 1.2181 0.0000 C 0 0\n 0.1498 1.2181 0.0000 C 0 0\n 0.7404 2.2410 0.0000 C 0 0\n 0.1499 3.2638 0.0000 C 0 0\n -1.0312 3.2638 0.0000 C 0 0\n -1.6218 2.2410 0.0000 C 0 0\n -1.6218 -1.8505 0.0000 N 0 0\n -1.6570 -2.9283 0.0000 R# 0 0\n 1.9214 -1.8505 0.0000 C 0 0\n 2.5121 -0.8277 0.0000 R# 0 0\n 2.5120 -2.8734 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 6\n 2 4 1 0\n 4 5 1 1\n 6 5 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 6 2 0\n 4 12 1 0\n 12 13 1 0\n 1 14 1 0\n 14 15 1 0\n 14 16 2 0\nM RGP 2 13 1 15 2\nM END\n> <Name>\ngamma-amino-beta-hydroxybenzenepentanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nApp\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-aminosuberic acid\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n 1.3729 -1.0086 0.0000 C 0 0\n 1.3720 -2.5095 0.0000 C 0 0 1 0 0 0\n 2.6709 -3.2614 0.0000 C 0 0\n 2.6702 -4.4614 0.0000 O 0 0\n 3.7107 -2.6624 0.0000 R# 0 0\n 0.0732 -3.2614 0.0000 N 0 0\n 0.0741 -0.2566 0.0000 C 0 0\n 0.0749 1.2442 0.0000 C 0 0\n -1.2239 1.9961 0.0000 C 0 0\n -1.2230 3.4969 0.0000 C 0 0\n -0.9672 -2.6634 0.0000 R# 0 0\n -2.5219 4.2489 0.0000 C 0 0\n -3.5617 3.6498 0.0000 R# 0 0\n -2.5212 5.4489 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 1 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 6 11 1 0\n 12 10 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 3 5 2 11 1 13 3\nM END\n> <Name>\n2-aminosuberic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAsu\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\n2-carboxyazetidine\n SciTegic07272112182D\n\n 8 8 0 0 1 0 999 V2000\n 0.0331 0.2591 0.0000 C 0 0 2 0 0 0\n -0.4189 1.3503 0.0000 C 0 0\n -1.5101 0.8983 0.0000 C 0 0\n -1.0581 -0.1929 0.0000 N 0 0\n -1.5101 -1.2841 0.0000 R# 0 0\n 1.1243 -0.1929 0.0000 C 0 0\n 2.0613 0.5261 0.0000 R# 0 0\n 1.2785 -1.3639 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 4 3 1 0\n 1 4 1 1\n 4 5 1 0\n 1 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 2 5 1 7 2\nM END\n> <Name>\n2-carboxyazetidine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAze\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nbeta-Alanine\n SciTegic07272112182D\n\n 7 6 0 0 0 0 999 V2000\n 0.1914 0.5523 0.0000 C 0 0\n 1.3074 0.1657 0.0000 C 0 0\n 1.5305 -0.9942 0.0000 O 0 0\n 2.2002 0.9389 0.0000 R# 0 0\n -0.7015 -0.2209 0.0000 C 0 0\n -1.8176 0.1657 0.0000 N 0 0\n -2.7104 -0.6075 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 5 6 1 0\n 6 7 1 0\nM RGP 2 4 2 7 1\nM END\n> <Name>\nbeta-Alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBal\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nbutanoic acid\n SciTegic07272112182D\n\n 6 5 0 0 1 0 999 V2000\n 3.3003 4.3894 0.0000 C 0 0\n 3.9000 3.3500 0.0000 C 0 0\n 3.1500 2.0500 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1000 0.7500 0.0000 R# 0 0\n 3.3003 -0.2894 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\nM RGP 1 5 2\nM END\n> <Name>\nbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBua\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n4-amino-3-hydroxybutanoic acid\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n -1.2501 0.5906 0.0000 C 0 0\n -2.2731 0.0000 0.0000 N 0 0\n -3.2959 0.5906 0.0000 R# 0 0\n -0.2273 0.0000 0.0000 C 0 0 1 0 0 0\n -0.2273 -1.1812 0.0000 O 0 0\n 0.7955 0.5906 0.0000 C 0 0\n 1.8184 0.0000 0.0000 C 0 0\n 1.8184 -1.1811 0.0000 O 0 0\n 2.8413 0.5906 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 6\n 4 6 1 0\n 6 7 1 0\n 7 8 2 0\n 7 9 1 0\nM RGP 2 3 1 9 2\nM END\n> <Name>\n4-amino-3-hydroxybutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBux\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nCysteine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.4457 -1.1333 0.0000 C 0 0\n 0.1453 -0.3840 0.0000 C 0 0 2 0 0 0\n 0.1430 1.1168 0.0000 C 0 0\n -1.1573 1.8661 0.0000 S 0 0\n -1.1551 -1.1333 0.0000 N 0 0\n 1.4475 -2.3333 0.0000 O 0 0\n 2.4842 -0.5320 0.0000 R# 0 0\n -2.1942 -0.5331 0.0000 R# 0 0\n -1.1591 3.0661 0.0000 R# 0 0\n 6 1 2 0\n 1 2 1 0\n 1 7 1 0\n 2 5 1 0\n 2 3 1 1\n 3 4 1 0\n 5 8 1 0\n 4 9 1 0\nM RGP 3 7 2 8 1 9 3\nM END\n> <Name>\nCysteine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nC\n\n> <MonomerCode>\nC\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\ngamma-amino-beta-hydroxycyclohexanepentanoic acid\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -0.2371 -1.5700 0.0000 C 0 0 1 0 0 0\n 0.6555 -2.3431 0.0000 C 0 0 2 0 0 0\n 1.7711 -1.9566 0.0000 C 0 0\n 1.9943 -0.7972 0.0000 R# 0 0\n 2.6637 -2.7297 0.0000 O 0 0\n 0.4323 -3.5026 0.0000 O 0 0\n -1.3528 -1.9566 0.0000 N 0 0\n -2.2454 -1.1835 0.0000 R# 0 0\n -0.0140 -0.4106 0.0000 C 0 0\n -0.9066 0.3624 0.0000 C 0 0\n -0.6834 1.5218 0.0000 C 0 0\n -1.5759 2.2948 0.0000 C 0 0\n -1.3527 3.4542 0.0000 C 0 0\n -0.2370 3.8408 0.0000 C 0 0\n 0.6555 3.0677 0.0000 C 0 0\n 0.4324 1.9082 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 3 5 2 0\n 2 6 1 6\n 1 7 1 0\n 7 8 1 0\n 1 9 1 1\n 9 10 1 0\n 10 11 1 0\n 12 11 1 0\n 13 12 1 0\n 14 13 1 0\n 15 14 1 0\n 15 16 1 0\n 11 16 1 0\nM RGP 2 4 2 8 1\nM END\n> <Name>\ngamma-amino-beta-hydroxycyclohexanepentanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nCap\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-cyclohexylalanine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n 1.0999 0.2895 0.0000 C 0 0\n 1.0990 -1.2114 0.0000 C 0 0 1 0 0 0\n 2.3979 -1.9634 0.0000 C 0 0\n 2.3972 -3.1634 0.0000 O 0 0\n 3.4377 -1.3643 0.0000 R# 0 0\n -0.1999 -1.9634 0.0000 N 0 0\n -0.1990 1.0414 0.0000 C 0 0\n -1.2401 -1.3653 0.0000 R# 0 0\n -1.5000 3.2903 0.0000 C 0 0\n -0.2003 2.5413 0.0000 C 0 0\n -1.4973 0.2903 0.0000 C 0 0\n -2.7970 1.0391 0.0000 C 0 0\n -2.7982 2.5391 0.0000 C 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 1 7 1 0\n 6 8 1 0\n 10 7 1 0\n 7 11 1 0\n 9 10 1 0\n 11 12 1 0\n 12 13 1 0\n 9 13 1 0\nM RGP 2 5 2 8 1\nM END\n> <Name>\n3-cyclohexylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nCha\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\ncitrullin\n SciTegic07272112182D\n\n 13 12 0 0 1 0 999 V2000\n 0.8990 -0.6122 0.0000 C 0 0\n 0.8982 -2.1130 0.0000 C 0 0 1 0 0 0\n 2.1971 -2.8650 0.0000 C 0 0\n 2.1964 -4.0650 0.0000 O 0 0\n 3.2369 -2.2659 0.0000 R# 0 0\n -0.4007 -2.8650 0.0000 N 0 0\n -0.3998 0.1398 0.0000 C 0 0\n -1.4410 -2.2669 0.0000 R# 0 0\n -0.3989 1.6406 0.0000 C 0 0\n -1.6977 2.3925 0.0000 N 0 0\n -1.6969 3.8933 0.0000 C 0 0\n -0.6571 4.4924 0.0000 N 0 0\n -2.7355 4.4946 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 1 7 1 0\n 6 8 1 0\n 9 7 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 5 2 8 1\nM END\n> <Name>\ncitrullin\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nCit\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-sulfoalanine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 0.5437 0.7780 0.0000 C 0 0\n 0.5429 -0.7228 0.0000 C 0 0 1 0 0 0\n 1.8417 -1.4748 0.0000 C 0 0\n 1.8410 -2.6748 0.0000 O 0 0\n 2.8815 -0.8757 0.0000 R# 0 0\n -0.7560 -1.4748 0.0000 N 0 0\n -1.7964 -0.8767 0.0000 R# 0 0\n -0.7551 1.5300 0.0000 S 0 0\n -0.7544 2.7300 0.0000 O 0 0\n -1.7949 0.9309 0.0000 O 0 0\n -1.7940 2.1307 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 6 7 1 0\n 1 8 1 0\n 8 9 2 0\n 8 10 2 0\n 8 11 1 0\nM RGP 2 5 2 7 1\nM END\n> <Name>\n3-sulfoalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nCya\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nAspartic acid\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.6310 -1.5578 0.0000 C 0 0\n 1.6327 -2.7392 0.0000 O 0 0\n 0.3507 -0.8201 0.0000 C 0 0 1 0 0 0\n -0.9295 -1.5578 0.0000 N 0 0\n -1.9525 -0.9669 0.0000 R# 0 0\n 0.3485 0.6575 0.0000 C 0 0\n -0.9317 1.3952 0.0000 C 0 0\n -1.9542 0.8032 0.0000 O 0 0\n -0.9335 2.5766 0.0000 O 0 0\n 2.6534 -0.9658 0.0000 R# 0 0\n 0.0851 3.1751 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 7 8 2 0\n 7 9 1 0\n 1 10 1 0\n 9 11 1 0\nM RGP 3 5 1 10 2 11 3\nM END\n> <Name>\nAspartic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD\n\n> <MonomerCode>\nD\n\n> <MonomerNaturalAnalogCode>\nD\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nAspartic acid (OH)\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.6310 -1.5578 0.0000 C 0 0\n 1.6327 -2.7392 0.0000 O 0 0\n 0.3507 -0.8201 0.0000 C 0 0 1 0 0 0\n -0.9295 -1.5578 0.0000 N 0 0\n -1.9525 -0.9669 0.0000 R# 0 0\n 0.3485 0.6575 0.0000 C 0 0\n -0.9317 1.3952 0.0000 C 0 0\n -1.9542 0.8032 0.0000 O 0 0\n -0.9335 2.5766 0.0000 R# 0 0\n 2.6534 -0.9658 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 7 8 2 0\n 7 9 1 0\n 1 10 1 0\nM RGP 3 5 1 10 2 9 3\nM END\n> <Name>\nAspartic acid (OH)\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAspOH\n\n> <MonomerCode>\nAspOH\n\n> <MonomerNaturalAnalogCode>\nD\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\nPyrrolidine\n Ketcher 4232413472D 1 1.00000 0.00000 0\n\n 6 6 0 0 0 0 0 0 0 0999 V2000\n 14.0000 -8.6056 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0\n 14.8090 -9.1934 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 14.5000 -10.1444 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.5000 -10.1444 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 13.1910 -9.1934 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 14.0000 -7.6056 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 1 5 1 0 0 0\n 5 4 1 0 0 0\n 4 3 1 0 0 0\n 3 2 1 0 0 0\n 2 1 1 0 0 0\n 1 6 1 0 0 0\nM RGP 1 6 1\nM END\n> <Name>\nPyrrolidine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPyrro\n\n> <MonomerCode>\nPyrro\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2,4-diaminobutanoic acid\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 0.3641 0.6909 0.0000 C 0 0\n 0.3632 -0.8099 0.0000 C 0 0 1 0 0 0\n 1.6621 -1.5619 0.0000 C 0 0\n 1.6614 -2.7619 0.0000 O 0 0\n 2.7019 -0.9628 0.0000 R# 0 0\n -0.9356 -1.5619 0.0000 N 0 0\n -1.9760 -0.9638 0.0000 R# 0 0\n -0.9347 1.4429 0.0000 C 0 0\n -0.9339 2.9437 0.0000 N 0 0\n -1.9725 3.5449 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 6 7 1 0\n 1 8 1 0\n 8 9 1 0\n 9 10 1 0\nM RGP 3 5 2 7 1 10 3\nM END\n> <Name>\n2,4-diaminobutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDab\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\ndiaminopimelic acid\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n 0.8356 -0.3752 0.0000 C 0 0\n 0.8363 -1.8760 0.0000 C 0 0\n 2.1360 -2.6267 0.0000 C 0 0\n 2.1366 -3.8266 0.0000 O 0 0\n 3.1751 -2.0264 0.0000 R# 0 0\n -0.4632 -2.6267 0.0000 N 0 0\n -0.4641 0.3753 0.0000 C 0 0\n -0.4649 1.8761 0.0000 C 0 0\n -1.7646 2.6267 0.0000 C 0 0\n -1.7653 4.1275 0.0000 C 0 0\n -0.4637 -3.8268 0.0000 R# 0 0\n -0.7262 4.7276 0.0000 O 0 0\n -2.8045 4.7277 0.0000 O 0 0\n -0.2031 -1.2765 0.0000 N 0 0\n 2 1 1 0\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 1 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 6 11 1 0\n 10 12 1 0\n 10 13 2 0\n 2 14 1 0\nM RGP 2 5 2 11 1\nM END\n> <Name>\ndiaminopimelic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDpm\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2,3-diaminopropanoic acid\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 0.1449 1.1182 0.0000 C 0 0\n 0.1441 -0.3826 0.0000 C 0 0 1 0 0 0\n 1.4430 -1.1346 0.0000 C 0 0\n 1.4423 -2.3346 0.0000 O 0 0\n 2.4827 -0.5355 0.0000 R# 0 0\n -1.1548 -1.1346 0.0000 N 0 0\n -2.1952 -0.5365 0.0000 R# 0 0\n -1.1539 1.8702 0.0000 N 0 0\n -1.1532 3.0702 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 2 6 1 0\n 6 7 1 0\n 1 8 1 0\n 8 9 1 0\nM RGP 3 5 2 7 1 9 3\nM END\n> <Name>\n2,3-diaminopropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDpr\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\n2,7-diaminosuberic acid (2,7-diaminooctanedioic acid)\n SciTegic07272112182D\n\n 15 14 0 0 1 0 999 V2000\n 1.3903 -2.7806 0.0000 C 0 0 1 0 0 0\n 2.6907 -3.5299 0.0000 C 0 0\n 2.6925 -4.7299 0.0000 O 0 0\n 3.7292 -2.9286 0.0000 R# 0 0\n 0.0899 -3.5299 0.0000 N 0 0\n -0.9492 -2.9297 0.0000 R# 0 0\n 1.3880 -1.2798 0.0000 C 0 0\n 0.0877 -0.5305 0.0000 C 0 0\n 0.0854 0.9703 0.0000 C 0 0\n -1.2150 1.7195 0.0000 C 0 0\n -1.2173 3.2203 0.0000 C 0 0\n -2.5178 3.9696 0.0000 C 0 0\n -3.5562 3.3684 0.0000 O 0 0\n -2.5194 5.1696 0.0000 O 0 0\n -0.1788 3.8216 0.0000 N 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 5 6 1 0\n 1 7 1 1\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 12 14 2 0\n 11 15 1 0\nM RGP 2 4 2 6 1\nM END\n> <Name>\n2,7-diaminosuberic acid (2,7-diaminooctanedioic acid)\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDsu\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nGlutamic acid\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 0.3442 -1.4777 0.0000 C 0 0 1 0 0 0\n 1.6244 -2.2154 0.0000 C 0 0\n 1.6261 -3.3968 0.0000 O 0 0\n 2.6469 -1.6234 0.0000 R# 0 0\n -0.9361 -2.2154 0.0000 N 0 0\n -1.9591 -1.6245 0.0000 R# 0 0\n 0.3419 -0.0001 0.0000 C 0 0\n -0.9383 0.7375 0.0000 C 0 0\n -0.9406 2.2151 0.0000 C 0 0\n -1.9642 2.8049 0.0000 O 0 0\n 0.0819 2.8071 0.0000 O 0 0\n 0.0729 3.9885 0.0000 R# 0 0\n 2 1 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 5 6 1 0\n 1 7 1 1\n 7 8 1 0\n 8 9 1 0\n 9 10 2 0\n 9 11 1 0\n 11 12 1 0\nM RGP 3 4 2 6 1 12 3\nM END\n> <Name>\nGlutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nE\n\n> <MonomerCode>\nE\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nS-ethylthiocysteine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.8932 -2.0181 0.0000 C 0 0\n 0.5928 -1.2688 0.0000 C 0 0 2 0 0 0\n 0.5905 0.2320 0.0000 C 0 0\n -0.7098 0.9813 0.0000 S 0 0\n -0.7076 -2.0181 0.0000 N 0 0\n 1.8950 -3.2181 0.0000 O 0 0\n 2.9317 -1.4168 0.0000 R# 0 0\n -1.7467 -1.4179 0.0000 R# 0 0\n -0.7121 2.4821 0.0000 S 0 0\n -2.0125 3.2313 0.0000 C 0 0\n -2.0144 4.4314 0.0000 C 0 0\n 6 1 2 0\n 1 2 1 0\n 1 7 1 0\n 2 5 1 0\n 2 3 1 1\n 3 4 1 0\n 5 8 1 0\n 4 9 1 0\n 9 10 1 0\n 10 11 1 0\nM RGP 2 7 2 8 1\nM END\n> <Name>\nS-ethylthiocysteine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nEdc\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nPhenylalanine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.2052 2.5398 0.0000 C 0 0\n -1.5064 3.2860 0.0000 C 0 0\n -2.8032 2.5322 0.0000 C 0 0\n -2.7988 1.0322 0.0000 C 0 0\n -1.4976 0.2861 0.0000 C 0 0\n -0.2008 1.0398 0.0000 C 0 0\n 1.0995 0.2905 0.0000 C 0 0\n 1.1018 -1.2103 0.0000 C 0 0 2 0 0 0\n -0.1986 -1.9596 0.0000 N 0 0\n 2.4022 -1.9596 0.0000 C 0 0\n 2.4040 -3.1596 0.0000 O 0 0\n 3.4407 -1.3583 0.0000 R# 0 0\n -1.2376 -1.3593 0.0000 R# 0 0\n 1 2 1 0\n 1 6 2 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 1\n 8 9 1 0\n 8 10 1 0\n 10 11 2 0\n 10 12 1 0\n 9 13 1 0\nM RGP 2 12 2 13 1\nM END\n> <Name>\nPhenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nF\n\n> <MonomerCode>\nF\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nGlycine\n SciTegic07272112182D\n\n 6 5 0 0 1 0 999 V2000\n -0.3363 0.5346 0.0000 C 0 0\n 0.9929 -0.1107 0.0000 C 0 0\n 1.0782 -1.2890 0.0000 O 0 0\n 1.9709 0.5520 0.0000 R# 0 0\n -1.3260 -0.1107 0.0000 N 0 0\n -2.3797 0.4238 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 5 6 1 0\nM RGP 2 4 2 6 1\nM END\n> <Name>\nGlycine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nG\n\n> <MonomerCode>\nG\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\ngamma-glutamic acid\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 3.1627 -0.1074 0.0000 R# 0 0\n 2.1394 -1.8796 0.0000 O 0 0\n 2.1394 -0.6982 0.0000 C 0 0\n 1.1162 -0.1074 0.0000 C 0 0\n 0.0931 -0.6982 0.0000 C 0 0\n -2.9765 -0.1074 0.0000 R# 0 0\n -1.9534 -0.6982 0.0000 N 0 0\n 0.0929 1.6649 0.0000 R# 0 0\n -1.9534 1.6648 0.0000 O 0 0\n -0.9302 1.0741 0.0000 C 0 0\n -0.9302 -0.1075 0.0000 C 0 0 2 0 0 0\n 3 1 1 0\n 3 2 2 0\n 4 3 1 0\n 5 4 1 0\n 11 5 1 0\n 7 6 1 0\n 11 7 1 0\n 10 8 1 0\n 10 9 2 0\n 11 10 1 6\nM RGP 3 1 2 6 1 8 3\nM END\n> <Name>\ngamma-glutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nGgu\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\ngamma-carboxyglutamic acid\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n -2.0450 1.9399 0.0000 O 0 0\n -3.0677 0.1688 0.0000 R# 0 0\n -2.0451 0.7591 0.0000 C 0 0\n -2.0452 -1.6023 0.0000 R# 0 0\n -1.0226 -1.0121 0.0000 N 0 0\n -0.0001 -1.6024 0.0000 O 0 0\n 2.0450 -1.6025 0.0000 R# 0 0\n 1.0225 -1.0121 0.0000 C 0 0\n 3.0678 0.1686 0.0000 O 0 0\n 2.0452 1.9396 0.0000 O 0 0\n 2.0452 0.7590 0.0000 C 0 0\n 1.0226 0.1687 0.0000 C 0 0\n 0.0000 0.7591 0.0000 C 0 0\n -1.0226 0.1687 0.0000 C 0 0 1 0 0 0\n 3 1 2 0\n 3 2 1 0\n 14 3 1 6\n 5 4 1 0\n 14 5 1 0\n 8 6 2 0\n 8 7 1 0\n 12 8 1 0\n 11 9 1 0\n 11 10 2 0\n 12 11 1 0\n 13 12 1 0\n 14 13 1 0\nM RGP 3 2 3 4 1 7 2\nM END\n> <Name>\ngamma-carboxyglutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nGla\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\nglycolic acid\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n 0.5500 -0.5500 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 0.7003 1.7894 0.0000 O 0 0\n 2.5000 0.7500 0.0000 R# 0 0\n 1.1497 -1.5894 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\nM RGP 1 4 2\nM END\n> <Name>\nglycolic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nGlc\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\npyroglutamic acid\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n 9.1574 -4.5963 0.0000 C 0 0 1 0 0 0\n 7.6654 -4.4422 0.0000 C 0 0\n 7.3510 -2.9755 0.0000 C 0 0\n 8.6486 -2.2231 0.0000 C 0 0\n 9.9062 -5.8940 0.0000 C 0 0\n 8.7719 -1.0295 0.0000 O 0 0\n 9.3065 -6.9335 0.0000 O 0 0\n 9.7651 -3.2249 0.0000 N 0 0\n 11.1062 -5.8940 0.0000 R# 0 0\n 5 1 1 0\n 1 8 1 0\n 1 2 1 6\n 2 3 1 0\n 3 4 1 0\n 4 6 2 0\n 5 7 2 0\n 5 9 1 0\n 4 8 1 0\nM RGP 1 9 2\nM END\n> <Name>\npyroglutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nGlp\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nHistidine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n 1.8978 -1.6508 0.0000 C 0 0\n 1.8993 -2.5957 0.0000 O 0 0\n 0.8739 -1.0609 0.0000 C 0 0 1 0 0 0\n -0.1500 -1.6508 0.0000 N 0 0\n -0.9683 -1.1782 0.0000 R# 0 0\n 0.8720 0.1209 0.0000 C 0 0\n -0.1501 0.7098 0.0000 C 0 0\n -0.2771 1.8841 0.0000 C 0 0\n -1.4330 2.1263 0.0000 N 0 0\n -2.0205 1.1016 0.0000 C 0 0\n -1.2277 0.2263 0.0000 N 0 0\n 2.7155 -1.1774 0.0000 R# 0 0\n -2.0317 3.1449 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 8 7 2 0\n 9 8 1 0\n 10 9 1 0\n 11 7 1 0\n 11 10 2 0\n 1 12 1 0\n 9 13 1 0\nM RGP 3 5 1 12 2 13 3\nM END\n> <Name>\nHistidine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nH\n\n> <MonomerCode>\nH\n\n> <MonomerNaturalAnalogCode>\nH\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nhomoarginine\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n 2.6779 -3.2569 0.0000 C 0 0\n 1.3775 -2.5077 0.0000 C 0 0 2 0 0 0\n 1.3753 -1.0068 0.0000 C 0 0\n 0.0749 -0.2576 0.0000 C 0 0\n 0.0771 -3.2569 0.0000 N 0 0\n 2.6797 -4.4570 0.0000 O 0 0\n -1.2301 3.4933 0.0000 N 0 0\n -2.5305 4.2425 0.0000 C 0 0\n -3.5690 3.6414 0.0000 N 0 0\n -2.5322 5.4425 0.0000 N 0 0\n 3.7164 -2.6557 0.0000 R# 0 0\n -0.9620 -2.6568 0.0000 R# 0 0\n 0.0726 1.2433 0.0000 C 0 0\n -1.2278 1.9924 0.0000 C 0 0\n 6 1 2 0\n 1 2 1 0\n 1 11 1 0\n 2 5 1 0\n 2 3 1 1\n 3 4 1 0\n 7 8 1 0\n 8 10 2 0\n 8 9 1 0\n 5 12 1 0\n 4 13 1 0\n 13 14 1 0\n 7 14 1 0\nM RGP 2 11 2 12 1\nM END\n> <Name>\nhomoarginine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHar\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nhomocysteine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.6657 -1.5600 0.0000 C 0 0\n 0.3653 -0.8107 0.0000 C 0 0 2 0 0 0\n 0.3630 0.6901 0.0000 C 0 0\n -0.9396 2.9402 0.0000 S 0 0\n -0.9351 -1.5600 0.0000 N 0 0\n 1.6675 -2.7600 0.0000 O 0 0\n 2.7042 -0.9587 0.0000 R# 0 0\n -1.9742 -0.9598 0.0000 R# 0 0\n -1.9794 3.5393 0.0000 R# 0 0\n -0.9373 1.4394 0.0000 C 0 0\n 6 1 2 0\n 1 2 1 0\n 1 7 1 0\n 2 5 1 0\n 2 3 1 1\n 5 8 1 0\n 4 9 1 0\n 3 10 1 0\n 4 10 1 0\nM RGP 3 7 2 8 1 9 3\nM END\n> <Name>\nhomocysteine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHcy\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nhomohistidine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n 1.8022 -2.6822 0.0000 C 0 0\n 0.5019 -1.9329 0.0000 C 0 0 2 0 0 0\n 0.4996 -0.4321 0.0000 C 0 0\n -0.8031 1.8154 0.0000 C 0 0\n -0.0518 4.1233 0.0000 C 0 0\n -2.0160 2.6978 0.0000 C 0 0\n 0.4109 2.6965 0.0000 N 0 0\n -1.5517 4.1242 0.0000 N 0 0\n -0.7985 -2.6822 0.0000 N 0 0\n 1.8041 -3.8822 0.0000 O 0 0\n 2.8409 -2.0810 0.0000 R# 0 0\n -1.8377 -2.0820 0.0000 R# 0 0\n -0.8008 0.3172 0.0000 C 0 0\n 10 1 2 0\n 1 2 1 0\n 1 11 1 0\n 2 9 1 0\n 2 3 1 1\n 6 4 2 0\n 7 4 1 0\n 7 5 2 0\n 5 8 1 0\n 8 6 1 0\n 9 12 1 0\n 3 13 1 0\n 4 13 1 0\nM RGP 2 11 2 12 1\nM END\n> <Name>\nhomohistidine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHhs\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nH\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-hydroxyisovaleric acid\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 9.4238 -6.6063 0.0000 C 0 0\n 8.8334 -7.6296 0.0000 O 0 0\n 8.6853 -5.3265 0.0000 C 0 0 1 0 0 0\n 7.2077 -5.3296 0.0000 N 0 0\n 9.4237 -4.0465 0.0000 C 0 0\n 8.8333 -3.0233 0.0000 C 0 0\n 10.6051 -4.0465 0.0000 C 0 0\n 10.6052 -6.6063 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 3 5 1 1\n 5 6 1 0\n 5 7 1 0\n 1 8 1 0\nM RGP 1 8 2\nM END\n> <Name>\n2-hydroxyisovaleric acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHiv\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nhomoserine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.4457 -1.1333 0.0000 C 0 0\n 1.4475 -2.3333 0.0000 O 0 0\n -1.1551 -1.1333 0.0000 N 0 0\n 0.1453 -0.3840 0.0000 C 0 0 1 0 0 0\n 0.1430 1.1168 0.0000 C 0 0\n -1.1573 1.8661 0.0000 C 0 0\n 2.4842 -0.5320 0.0000 R# 0 0\n -2.1942 -0.5331 0.0000 R# 0 0\n -1.1591 3.0661 0.0000 O 0 0\n 2 1 2 0\n 1 4 1 0\n 1 7 1 0\n 4 3 1 0\n 4 5 1 1\n 5 6 1 0\n 3 8 1 0\n 6 9 1 0\nM RGP 2 7 2 8 1\nM END\n> <Name>\nhomoserine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHse\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-hydroxypentanoic acid\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 1.3000 0.7500 0.0000 C 0 0\n 0.7003 1.7894 0.0000 O 0 0\n -0.6500 -0.5500 0.0000 O 0 0\n 0.5500 -0.5500 0.0000 C 0 0 1 0 0 0\n 1.3000 -1.8500 0.0000 C 0 0\n 0.5500 -3.1500 0.0000 C 0 0\n 2.5000 0.7500 0.0000 R# 0 0\n 1.1497 -4.1894 0.0000 C 0 0\n 2 1 2 0\n 1 4 1 0\n 1 7 1 0\n 4 3 1 0\n 4 5 1 6\n 5 6 1 0\n 6 8 1 0\nM RGP 1 7 2\nM END\n> <Name>\n2-hydroxypentanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHva\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n5-hydroxylysine\n SciTegic07272112182D\n\n 13 12 0 0 1 0 999 V2000\n 2.1031 -2.6885 0.0000 C 0 0\n 0.8027 -1.9392 0.0000 C 0 0 2 0 0 0\n 0.8004 -0.4384 0.0000 C 0 0\n -0.5000 0.3109 0.0000 C 0 0\n -0.5022 1.8117 0.0000 C 0 0\n -1.8026 2.5609 0.0000 C 0 0\n -1.8049 4.0617 0.0000 N 0 0\n -0.4977 -2.6885 0.0000 N 0 0\n 2.1049 -3.8885 0.0000 O 0 0\n 3.1416 -2.0873 0.0000 R# 0 0\n -1.5368 -2.0884 0.0000 R# 0 0\n -2.8447 4.6608 0.0000 R# 0 0\n 0.5363 2.4129 0.0000 O 0 0\n 9 1 2 0\n 1 2 1 0\n 1 10 1 0\n 2 8 1 0\n 2 3 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 8 11 1 0\n 7 12 1 0\n 5 13 1 0\nM RGP 3 10 2 11 1 12 3\nM END\n> <Name>\n5-hydroxylysine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHyl\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\n4-hydroxyproline\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n 0.2044 1.3597 0.0000 C 0 0\n -1.2773 1.5932 0.0000 C 0 0 2 0 0 0\n -1.9573 0.2561 0.0000 C 0 0\n -0.8958 -0.8036 0.0000 N 0 0\n 0.4401 -0.1216 0.0000 C 0 0 2 0 0 0\n 1.7742 -0.8036 0.0000 C 0 0\n 1.8362 -2.0021 0.0000 O 0 0\n 2.7813 -0.1510 0.0000 R# 0 0\n -1.0827 -1.9890 0.0000 R# 0 0\n -1.8230 2.6620 0.0000 O 0 0\n 1 2 1 0\n 5 1 1 1\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 6 8 1 0\n 4 9 1 0\n 2 10 1 6\nM RGP 2 8 2 9 1\nM END\n> <Name>\n4-hydroxyproline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHyp\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nIsoleucine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n -1.2557 1.6681 0.0000 C 0 0\n 0.0245 0.9304 0.0000 C 0 0 1 0 0 0\n 0.0268 -0.5472 0.0000 C 0 0 2 0 0 0\n -1.2536 -1.2849 0.0000 N 0 0\n -2.2766 -0.6940 0.0000 R# 0 0\n 1.3069 -1.2849 0.0000 C 0 0\n 1.3086 -2.4664 0.0000 O 0 0\n 2.3294 -0.6930 0.0000 R# 0 0\n 1.0470 1.5223 0.0000 C 0 0\n -1.2574 2.8495 0.0000 C 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 3 6 1 0\n 6 7 2 0\n 6 8 1 0\n 2 9 1 6\n 1 10 1 0\nM RGP 2 5 1 8 2\nM END\n> <Name>\nIsoleucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nI\n\n> <MonomerCode>\nI\n\n> <MonomerNaturalAnalogCode>\nI\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nisovaline\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n -0.2631 1.6583 0.0000 C 0 0\n -0.2625 0.1806 0.0000 C 0 0 2 0 0 0\n -1.5417 -0.5583 0.0000 N 0 0\n -1.5423 -1.7399 0.0000 R# 0 0\n 1.0172 -0.5583 0.0000 C 0 0\n 1.0177 -1.7397 0.0000 O 0 0\n 2.0402 0.0326 0.0000 R# 0 0\n 0.8209 0.4757 0.0000 C 0 0\n -1.2863 2.2491 0.0000 C 0 0\n 2 1 1 1\n 3 2 1 0\n 3 4 1 0\n 2 5 1 0\n 5 6 2 0\n 5 7 1 0\n 2 8 1 0\n 1 9 1 0\nM RGP 2 4 1 7 2\nM END\n> <Name>\nisovaline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nIva\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nLysine\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 2.1478 -2.4874 0.0000 C 0 0\n 0.8474 -1.7382 0.0000 C 0 0 2 0 0 0\n 0.8451 -0.2373 0.0000 C 0 0\n -0.4553 0.5119 0.0000 C 0 0\n -0.4575 2.0128 0.0000 C 0 0\n -1.7579 2.7619 0.0000 C 0 0\n -1.7602 4.2628 0.0000 N 0 0\n -0.4530 -2.4874 0.0000 N 0 0\n 2.1495 -3.6875 0.0000 O 0 0\n 3.1863 -1.8862 0.0000 R# 0 0\n -1.4921 -1.8873 0.0000 R# 0 0\n -2.8000 4.8619 0.0000 R# 0 0\n 9 1 2 0\n 1 2 1 0\n 1 10 1 0\n 2 8 1 0\n 2 3 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 8 11 1 0\n 7 12 1 0\nM RGP 3 10 2 11 1 12 3\nM END\n> <Name>\nLysine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nK\n\n> <MonomerCode>\nK\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nLeucine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 0.3626 0.9903 0.0000 C 0 0\n -0.9395 2.9396 0.0000 C 0 0\n -0.9377 1.7396 0.0000 C 0 0\n -1.9763 1.1383 0.0000 C 0 0\n 0.3649 -0.5105 0.0000 C 0 0 1 0 0 0\n 1.6653 -1.2598 0.0000 C 0 0\n 1.6671 -2.4598 0.0000 O 0 0\n -0.9355 -1.2598 0.0000 N 0 0\n 2.7038 -0.6585 0.0000 R# 0 0\n -1.9746 -0.6596 0.0000 R# 0 0\n 3 1 1 0\n 5 1 1 1\n 3 2 1 0\n 3 4 1 0\n 5 8 1 0\n 5 6 1 0\n 6 7 2 0\n 6 9 1 0\n 8 10 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\nLeucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nL\n\n> <MonomerCode>\nL\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nlactic acid\n SciTegic07272112182D\n\n 6 5 0 0 1 0 999 V2000\n 0.5500 -0.5500 0.0000 C 0 0 1 0 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 0.7003 1.7894 0.0000 O 0 0\n 2.5000 0.7500 0.0000 R# 0 0\n 1.1497 -1.5894 0.0000 O 0 0\n -0.6500 -0.5500 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 1 6 1 1\nM RGP 1 4 2\nM END\n> <Name>\nlactic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLac\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nMethionine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.6657 -1.5600 0.0000 C 0 0\n -0.9351 -1.5600 0.0000 N 0 0\n 1.6675 -2.7600 0.0000 O 0 0\n 0.3653 -0.8107 0.0000 C 0 0 1 0 0 0\n 0.3630 0.6901 0.0000 C 0 0\n -0.9373 1.4394 0.0000 C 0 0\n -1.9794 3.5393 0.0000 C 0 0\n -0.9396 2.9402 0.0000 S 0 0\n 2.7042 -0.9587 0.0000 R# 0 0\n -1.9742 -0.9598 0.0000 R# 0 0\n 3 1 2 0\n 1 4 1 0\n 1 9 1 0\n 4 2 1 0\n 4 5 1 1\n 5 6 1 0\n 6 8 1 0\n 8 7 1 0\n 2 10 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\nMethionine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nM\n\n> <MonomerCode>\nM\n\n> <MonomerNaturalAnalogCode>\nM\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nmercaptoacetic acid\n SciTegic07272112182D\n\n 6 5 0 0 1 0 999 V2000\n 0.5500 1.3000 0.0000 C 0 0\n 1.3000 0.0000 0.0000 C 0 0\n 0.7003 -1.0394 0.0000 O 0 0\n 2.5000 0.0000 0.0000 R# 0 0\n 1.3000 2.6000 0.0000 S 0 0\n 0.7003 3.6394 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 5 6 1 0\nM RGP 2 4 2 6 3\nM END\n> <Name>\nmercaptoacetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nMaa\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n[R3]H\n\n$$$$\nmercaptobutanoic acid (GMBA)\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 0.5500 1.3000 0.0000 C 0 0 1 0 0 0\n 1.3000 0.0000 0.0000 C 0 0\n 0.7003 -1.0394 0.0000 O 0 0\n 2.5000 0.0000 0.0000 R# 0 0\n -0.9508 1.3031 0.0000 S 0 0\n -1.5494 2.3432 0.0000 R# 0 0\n 1.3000 2.6000 0.0000 C 0 0\n 0.7003 3.6394 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 5 6 1 0\n 1 7 1 1\n 7 8 1 0\nM RGP 2 4 2 6 3\nM END\n> <Name>\nmercaptobutanoic acid (GMBA)\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nMba\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n[R3]H\n\n$$$$\n4-methyl-3-hydroxyproline\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n 0.0644 0.9085 0.0000 C 0 0\n 0.8995 1.7437 0.0000 O 0 0\n 0.2491 -0.2580 0.0000 C 0 0 1 0 0 0\n 1.3016 -0.7942 0.0000 C 0 0\n 2.2921 -0.1510 0.0000 R# 0 0\n 1.3634 -1.9737 0.0000 O 0 0\n -0.8032 -0.7942 0.0000 N 0 0\n -0.9879 -1.9608 0.0000 R# 0 0\n -1.6383 0.0409 0.0000 C 0 0\n -1.1022 1.0932 0.0000 C 0 0\n -1.6384 2.1456 0.0000 C 0 0\n 1 2 1 0\n 3 1 1 1\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\n 7 3 1 0\n 7 8 1 0\n 9 7 1 0\n 10 9 1 0\n 1 10 1 0\n 10 11 1 0\nM RGP 2 5 2 8 1\nM END\n> <Name>\n4-methyl-3-hydroxyproline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nMhp\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nmercaptopropanoic acid\n SciTegic07272112182D\n\n 7 6 0 0 1 0 999 V2000\n 0.5500 1.3000 0.0000 C 0 0 1 0 0 0\n 1.3000 0.0000 0.0000 C 0 0\n 0.7003 -1.0394 0.0000 O 0 0\n 2.5000 0.0000 0.0000 R# 0 0\n 1.3000 2.6000 0.0000 S 0 0\n 0.7003 3.6394 0.0000 R# 0 0\n -0.6500 1.3000 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 5 6 1 0\n 1 7 1 6\nM RGP 2 4 2 6 3\nM END\n> <Name>\nmercaptopropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nMpa\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n[R3]H\n\n$$$$\nAsparagine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.8929 -1.4175 0.0000 C 0 0\n 1.8947 -2.5989 0.0000 O 0 0\n 0.6127 -0.6799 0.0000 C 0 0 1 0 0 0\n -0.6676 -1.4175 0.0000 N 0 0\n -1.6907 -0.8266 0.0000 R# 0 0\n 0.6104 0.7978 0.0000 C 0 0\n -0.6698 1.5354 0.0000 C 0 0\n -1.6922 0.9434 0.0000 N 0 0\n -0.6716 2.7168 0.0000 O 0 0\n 2.9153 -0.8255 0.0000 R# 0 0\n -2.5341 1.7724 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 7 8 1 0\n 7 9 2 0\n 1 10 1 0\n 8 11 1 0\nM RGP 3 5 1 10 2 11 3\nM END\n> <Name>\nAsparagine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nN\n\n> <MonomerCode>\nN\n\n> <MonomerNaturalAnalogCode>\nN\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\n3-naphthylalanine\n SciTegic07272112182D\n\n 17 18 0 0 1 0 999 V2000\n 1.8370 -0.7903 0.0000 C 0 0\n 1.8392 -2.2912 0.0000 C 0 0 1 0 0 0\n 3.1396 -3.0405 0.0000 C 0 0\n 0.5388 -3.0405 0.0000 N 0 0\n 3.1415 -4.2404 0.0000 O 0 0\n 4.1781 -2.4393 0.0000 R# 0 0\n -0.5003 -2.4402 0.0000 R# 0 0\n -2.0658 1.4514 0.0000 C 0 0\n -3.3671 2.1976 0.0000 C 0 0\n -3.3714 3.6975 0.0000 C 0 0\n -2.0746 4.4513 0.0000 C 0 0\n -0.7734 3.7051 0.0000 C 0 0\n -0.7689 2.2052 0.0000 C 0 0\n 0.5322 1.4589 0.0000 C 0 0\n 0.5367 -0.0410 0.0000 C 0 0\n -0.7602 -0.7949 0.0000 C 0 0\n -2.0614 -0.0487 0.0000 C 0 0\n 2 1 1 1\n 4 2 1 0\n 2 3 1 0\n 3 5 2 0\n 3 6 1 0\n 4 7 1 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 14 15 2 0\n 15 16 1 0\n 16 17 2 0\n 8 13 2 0\n 8 17 1 0\n 13 14 1 0\n 15 1 1 0\nM RGP 2 6 2 7 1\nM END\n> <Name>\n3-naphthylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNal\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nnorleucine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 0.3630 0.6901 0.0000 C 0 0\n -0.9373 1.4394 0.0000 C 0 0\n -0.9396 2.9402 0.0000 C 0 0\n 0.3653 -0.8107 0.0000 C 0 0 1 0 0 0\n 1.6657 -1.5600 0.0000 C 0 0\n 1.6675 -2.7600 0.0000 O 0 0\n -0.9351 -1.5600 0.0000 N 0 0\n 2.7042 -0.9587 0.0000 R# 0 0\n -1.9742 -0.9598 0.0000 R# 0 0\n -1.9794 3.5393 0.0000 C 0 0\n 2 1 1 0\n 4 1 1 1\n 2 3 1 0\n 4 7 1 0\n 4 5 1 0\n 5 6 2 0\n 5 8 1 0\n 7 9 1 0\n 3 10 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\nnorleucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNle\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nnitrotyrosine\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n 0.3609 -1.4586 0.0000 C 0 0\n 1.3835 -0.8682 0.0000 R# 0 0\n -0.6616 -0.8683 0.0000 C 0 0 2 0 0 0\n -0.6616 0.3125 0.0000 C 0 0\n 0.3609 0.9029 0.0000 C 0 0\n 0.3608 2.0837 0.0000 C 0 0\n 1.3834 2.6741 0.0000 C 0 0\n 2.4059 2.0838 0.0000 C 0 0\n 3.4285 2.6742 0.0000 O 0 0\n 2.4060 0.9030 0.0000 C 0 0\n 1.3835 0.3126 0.0000 C 0 0\n -1.6842 -1.4586 0.0000 N 0 0\n -2.7068 -0.8684 0.0000 N 0 0\n -2.7068 0.3124 0.0000 O 0 0\n -3.7293 -1.4588 0.0000 O 0 0\n -1.6841 -2.6394 0.0000 R# 0 0\n 0.3610 -2.6393 0.0000 O 0 0\n 1 2 1 0\n 1 3 1 0\n 3 4 1 1\n 4 5 1 0\n 6 5 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 8 10 1 0\n 10 11 2 0\n 11 5 1 0\n 3 12 1 0\n 12 13 1 0\n 13 14 2 0\n 13 15 2 0\n 12 16 1 0\n 17 1 2 0\nM RGP 2 2 2 16 1\nM END\n> <Name>\nnitrotyrosine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNty\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nnorvaline\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.4457 -1.1333 0.0000 C 0 0\n 0.1453 -0.3840 0.0000 C 0 0 2 0 0 0\n 0.1430 1.1168 0.0000 C 0 0\n -1.1573 1.8661 0.0000 C 0 0\n 1.4475 -2.3333 0.0000 O 0 0\n -1.1551 -1.1333 0.0000 N 0 0\n 2.4842 -0.5320 0.0000 R# 0 0\n -2.1942 -0.5331 0.0000 R# 0 0\n -1.1591 3.0661 0.0000 C 0 0\n 5 1 2 0\n 1 2 1 0\n 1 7 1 0\n 2 6 1 0\n 2 3 1 1\n 3 4 1 0\n 6 8 1 0\n 4 9 1 0\nM RGP 2 7 2 8 1\nM END\n> <Name>\nnorvaline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNva\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-carboxyocthydroindole\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n 2.0870 -0.8839 0.0000 C 0 0\n 3.0775 -0.2406 0.0000 R# 0 0\n 1.0346 -0.3477 0.0000 C 0 0 2 0 0 0\n 0.8498 0.8189 0.0000 C 0 0\n -0.3168 1.0037 0.0000 C 0 0\n -0.8529 -0.0487 0.0000 C 0 0\n -2.0324 -0.1106 0.0000 C 0 0\n -2.6757 0.8800 0.0000 C 0 0\n -2.1395 1.9323 0.0000 C 0 0\n -0.9601 1.9942 0.0000 C 0 0\n -0.0178 -0.8839 0.0000 N 0 0\n -0.2025 -2.0504 0.0000 R# 0 0\n 2.1488 -2.0633 0.0000 O 0 0\n 1 2 1 0\n 1 3 1 0\n 3 4 1 1\n 4 5 1 0\n 6 5 1 0\n 7 6 1 0\n 8 7 1 0\n 9 8 1 0\n 10 5 1 0\n 10 9 1 0\n 6 11 1 0\n 3 11 1 0\n 11 12 1 0\n 13 1 2 0\nM RGP 2 2 2 12 1\nM END\n> <Name>\n2-carboxyocthydroindole\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOic\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nL-ornithine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.8932 -2.0181 0.0000 C 0 0\n 0.5928 -1.2688 0.0000 C 0 0 2 0 0 0\n 0.5905 0.2320 0.0000 C 0 0\n -0.7098 0.9813 0.0000 C 0 0\n -2.0125 3.2313 0.0000 N 0 0\n -0.7076 -2.0181 0.0000 N 0 0\n 1.8950 -3.2181 0.0000 O 0 0\n 2.9317 -1.4168 0.0000 R# 0 0\n -1.7467 -1.4179 0.0000 R# 0 0\n -2.0144 4.4314 0.0000 R# 0 0\n -0.7121 2.4821 0.0000 C 0 0\n 7 1 2 0\n 1 2 1 0\n 1 8 1 0\n 2 6 1 0\n 2 3 1 1\n 3 4 1 0\n 6 9 1 0\n 5 10 1 0\n 4 11 1 0\n 11 5 1 0\nM RGP 3 8 2 9 1 10 3\nM END\n> <Name>\nL-ornithine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOrn\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nProline\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n 0.0018 1.6555 0.0000 C 0 0\n -1.4799 1.8890 0.0000 C 0 0\n -2.1599 0.5519 0.0000 C 0 0\n -1.0984 -0.5079 0.0000 N 0 0\n 0.2376 0.1741 0.0000 C 0 0 2 0 0 0\n 1.5717 -0.5079 0.0000 C 0 0\n 1.6336 -1.7063 0.0000 O 0 0\n 2.5787 0.1448 0.0000 R# 0 0\n -1.2852 -1.6933 0.0000 R# 0 0\n 1 2 1 0\n 5 1 1 1\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 6 8 1 0\n 4 9 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\nProline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nP\n\n> <MonomerCode>\nP\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\npenicillamine (3-mercaptovaline)\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.3220 -1.5015 0.0000 C 0 0\n 0.0231 -0.7495 0.0000 C 0 0 2 0 0 0\n 1.0637 1.3504 0.0000 C 0 0\n 0.0239 0.7513 0.0000 C 0 0\n 0.0252 1.9513 0.0000 C 0 0\n 1.3213 -2.7015 0.0000 O 0 0\n -1.2758 -1.5015 0.0000 N 0 0\n 2.3618 -0.9024 0.0000 R# 0 0\n -2.3162 -0.9034 0.0000 R# 0 0\n -1.2749 1.5033 0.0000 S 0 0\n -1.2742 2.7033 0.0000 R# 0 0\n 6 1 2 0\n 1 2 1 0\n 1 8 1 0\n 2 7 1 0\n 2 4 1 1\n 4 3 1 0\n 4 5 1 0\n 7 9 1 0\n 4 10 1 0\n 10 11 1 0\nM RGP 3 8 2 9 1 11 3\nM END\n> <Name>\npenicillamine (3-mercaptovaline)\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPen\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\n2-phenylglycine\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.1105 -1.1869 0.0000 C 0 0 1 0 0 0\n 1.1883 -1.9388 0.0000 C 0 0\n 1.1876 -3.1389 0.0000 O 0 0\n -1.4095 -1.9388 0.0000 N 0 0\n 2.2281 -1.3398 0.0000 R# 0 0\n -2.4498 -1.3407 0.0000 R# 0 0\n 1.1953 2.5605 0.0000 C 0 0\n -0.1018 3.3139 0.0000 C 0 0\n -1.4027 2.5674 0.0000 C 0 0\n -1.4067 1.0675 0.0000 C 0 0\n -0.1097 0.3140 0.0000 C 0 0\n 1.1914 1.0606 0.0000 C 0 0\n 4 1 1 0\n 1 2 1 0\n 2 3 2 0\n 2 5 1 0\n 4 6 1 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 10 11 2 0\n 11 12 1 0\n 7 12 2 0\n 1 11 1 1\nM RGP 2 5 2 6 1\nM END\n> <Name>\n2-phenylglycine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhg\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nPiperazine quinazolinone acetic acid, 2-(4-oxo-6-piperazin-1-yl-quinazolin-3-yl)acetic acid\n SciTegic07272112182D\n\n 22 24 0 0 1 0 999 V2000\n 1.0933 1.6152 0.0000 C 0 0\n -0.0398 2.5980 0.0000 C 0 0\n -1.4576 2.1082 0.0000 C 0 0\n -1.7421 0.6354 0.0000 C 0 0\n -0.6090 -0.3475 0.0000 C 0 0\n 0.8087 0.1425 0.0000 C 0 0\n 1.9419 -0.8404 0.0000 C 0 0\n 3.3596 -0.3504 0.0000 N 0 0\n 3.6442 1.1223 0.0000 C 0 0\n 2.5111 2.1052 0.0000 C 0 0\n -3.4430 -1.3280 0.0000 C 0 0\n -4.8599 -1.8203 0.0000 C 0 0\n -5.9946 -0.8392 0.0000 N 0 0\n -5.7124 0.6340 0.0000 C 0 0\n -4.2954 1.1262 0.0000 C 0 0\n -3.1606 0.1453 0.0000 N 0 0\n -7.1282 -1.2330 0.0000 R# 0 0\n 4.4954 -1.3315 0.0000 C 0 0\n 5.9133 -0.8392 0.0000 C 0 0\n 1.7143 -2.0185 0.0000 O 0 0\n 6.1389 0.3393 0.0000 R# 0 0\n 6.8214 -1.6237 0.0000 O 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 7 8 1 0\n 8 9 1 0\n 9 10 2 0\n 1 6 1 0\n 1 10 1 0\n 6 7 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 11 16 1 0\n 4 16 1 0\n 13 17 1 0\n 8 18 1 0\n 18 19 1 0\n 7 20 2 0\n 19 21 1 0\n 19 22 2 0\nM RGP 2 17 1 21 2\nM END\n> <Name>\nPiperazine quinazolinone acetic acid, 2-(4-oxo-6-piperazin-1-yl-quinazolin-3-yl)acetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPqa\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nGlutamine\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 1.6237 -2.2154 0.0000 C 0 0\n 1.6254 -3.3969 0.0000 O 0 0\n 0.3435 -1.4777 0.0000 C 0 0 1 0 0 0\n -0.9368 -2.2154 0.0000 N 0 0\n -1.9598 -1.6245 0.0000 R# 0 0\n 0.3413 -0.0001 0.0000 C 0 0\n -0.9389 0.7376 0.0000 C 0 0\n -0.9411 2.2152 0.0000 C 0 0\n 0.0813 2.8071 0.0000 N 0 0\n -1.9648 2.8050 0.0000 O 0 0\n 2.6462 -1.6235 0.0000 R# 0 0\n 0.0799 3.9885 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 8 10 2 0\n 1 11 1 0\n 9 12 1 0\nM RGP 3 5 1 11 2 12 3\nM END\n> <Name>\nGlutamine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nQ\n\n> <MonomerCode>\nQ\n\n> <MonomerNaturalAnalogCode>\nQ\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nArginine\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n 1.7718 -2.5891 0.0000 C 0 0\n 1.7732 -3.5337 0.0000 O 0 0\n 0.7483 -1.9994 0.0000 C 0 0 1 0 0 0\n -0.2752 -2.5891 0.0000 N 0 0\n -1.0932 -2.1168 0.0000 R# 0 0\n 0.7464 -0.8182 0.0000 C 0 0\n -0.2771 -0.2284 0.0000 C 0 0\n -0.2789 0.9529 0.0000 C 0 0\n -1.3024 1.5426 0.0000 N 0 0\n -1.3042 2.7238 0.0000 C 0 0\n -0.4868 3.1971 0.0000 N 0 0\n -2.1227 3.1955 0.0000 N 0 0\n 2.5892 -2.1159 0.0000 R# 0 0\n -0.4883 4.3786 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 10 12 2 0\n 1 13 1 0\n 11 14 1 0\nM RGP 3 5 1 13 2 14 3\nM END\n> <Name>\nArginine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nR\n\n> <MonomerCode>\nR\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nSerine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.3671 -1.0829 0.0000 C 0 0\n 1.3689 -2.2643 0.0000 O 0 0\n 0.0869 -0.3452 0.0000 C 0 0 1 0 0 0\n -1.1934 -1.0829 0.0000 N 0 0\n -2.2165 -0.4920 0.0000 R# 0 0\n 0.0847 1.1324 0.0000 C 0 0\n -0.9391 1.7222 0.0000 O 0 0\n 2.3896 -0.4909 0.0000 R# 0 0\n -0.9481 2.9036 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 1 8 1 0\n 7 9 1 0\nM RGP 3 5 1 8 2 9 3\nM END\n> <Name>\nSerine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nS\n\n> <MonomerCode>\nS\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nsarcosine (N-methylglycine)\n SciTegic07272112182D\n\n 7 6 0 0 0 0 999 V2000\n 0.0000 0.6750 0.0000 C 0 0\n 1.0229 0.0844 0.0000 C 0 0\n 2.0458 0.6749 0.0000 R# 0 0\n 1.0228 -1.0968 0.0000 O 0 0\n -1.0229 0.0844 0.0000 N 0 0\n -2.0457 0.6750 0.0000 C 0 0\n -1.0229 -1.0967 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\n 5 1 1 0\n 5 6 1 0\n 5 7 1 0\nM RGP 2 3 2 7 1\nM END\n> <Name>\nsarcosine (N-methylglycine)\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nSar\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n1-amino-1-carboxycyclopentane\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n 1.0834 0.6054 0.0000 C 0 0\n -0.1301 -0.2763 0.0000 C 0 0 1 0 0 0\n -1.3437 0.6051 0.0000 C 0 0\n -0.8803 2.0318 0.0000 C 0 0\n 0.6197 2.0320 0.0000 C 0 0\n -1.4300 -0.9996 0.0000 N 0 0\n 1.1702 -0.9996 0.0000 C 0 0\n 1.1712 -2.1996 0.0000 O 0 0\n 2.2090 -0.3991 0.0000 R# 0 0\n -2.4695 -0.4001 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 1\n 3 4 1 0\n 4 5 1 0\n 1 5 1 0\n 2 6 1 0\n 2 7 1 0\n 7 8 2 0\n 7 9 1 0\n 6 10 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\n1-amino-1-carboxycyclopentane\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nSpg\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nstatin (4-amino-3-hydroxy-6-methylheptanoic acid)\n SciTegic07272112182D\n\n 13 12 0 0 1 0 999 V2000\n -1.6523 -1.7716 0.0000 R# 0 0\n -1.6523 -0.5905 0.0000 N 0 0\n -0.6295 0.0000 0.0000 C 0 0 1 0 0 0\n -0.6295 1.1811 0.0000 C 0 0\n -1.6524 1.7717 0.0000 C 0 0\n -2.6752 1.1811 0.0000 C 0 0\n -1.6523 2.9528 0.0000 C 0 0\n 0.3934 -0.5906 0.0000 C 0 0 1 0 0 0\n 0.3934 -1.7717 0.0000 O 0 0\n 1.4162 -0.0001 0.0000 C 0 0\n 2.4391 -0.5905 0.0000 C 0 0\n 2.4391 -1.7716 0.0000 O 0 0\n 3.4620 0.0000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 1\n 4 5 1 0\n 5 6 1 0\n 5 7 1 0\n 3 8 1 0\n 8 9 1 6\n 8 10 1 0\n 10 11 1 0\n 11 12 2 0\n 11 13 1 0\nM RGP 2 1 1 13 2\nM END\n> <Name>\nstatin (4-amino-3-hydroxy-6-methylheptanoic acid)\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nSta\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nThreonine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.0488 -1.2558 0.0000 C 0 0\n 1.0481 -2.4369 0.0000 O 0 0\n -0.2297 -0.5156 0.0000 C 0 0 1 0 0 0\n -1.5081 -1.2558 0.0000 N 0 0\n -2.5321 -0.6672 0.0000 R# 0 0\n -0.2289 0.9614 0.0000 C 0 0 2 0 0 0\n 0.7944 1.5510 0.0000 O 0 0\n -1.2510 1.5531 0.0000 C 0 0\n 2.0720 -0.6661 0.0000 R# 0 0\n 0.7866 2.7318 0.0000 R# 0 0\n 2 1 2 0\n 3 1 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 1\n 6 8 1 0\n 1 9 1 0\n 7 10 1 0\nM RGP 3 5 1 9 2 10 3\nM END\n> <Name>\nThreonine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nT\n\n> <MonomerCode>\nT\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\n3-thienylalanine\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n 0.8925 0.4864 0.0000 C 0 0\n 0.8948 -1.0144 0.0000 C 0 0 1 0 0 0\n 2.1952 -1.7637 0.0000 C 0 0\n -0.4056 -1.7637 0.0000 N 0 0\n 2.1969 -2.9637 0.0000 O 0 0\n 3.2337 -1.1625 0.0000 R# 0 0\n -1.4447 -1.1635 0.0000 R# 0 0\n -2.7811 1.7319 0.0000 C 0 0\n -2.0350 3.0332 0.0000 C 0 0\n -0.5669 2.7257 0.0000 S 0 0\n -0.4056 1.2344 0.0000 C 0 0\n -1.7742 0.6202 0.0000 C 0 0\n 2 1 1 1\n 4 2 1 0\n 2 3 1 0\n 3 5 2 0\n 3 6 1 0\n 4 7 1 0\n 8 9 2 0\n 9 10 1 0\n 10 11 1 0\n 11 12 2 0\n 8 12 1 0\n 11 1 1 0\nM RGP 2 6 2 7 1\nM END\n> <Name>\n3-thienylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nThi\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -1.4700 3.5026 0.0000 C 0 0\n -2.7681 2.7511 0.0000 C 0 0\n -2.7664 1.2510 0.0000 C 0 0\n -1.4665 0.5026 0.0000 C 0 0\n -0.1683 1.2542 0.0000 C 0 0\n -0.1701 2.7542 0.0000 C 0 0\n -1.4646 -0.9974 0.0000 C 0 0\n -0.1647 -1.7458 0.0000 N 0 0\n 1.1334 -0.9943 0.0000 C 0 0 1 0 0 0\n 1.1317 0.5057 0.0000 C 0 0\n 2.4326 -1.7458 0.0000 C 0 0\n 3.4721 -1.1463 0.0000 R# 0 0\n 2.4323 -2.9458 0.0000 O 0 0\n -0.1633 -2.9459 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 5 6 1 0\n 1 6 2 0\n 5 10 1 0\n 4 5 2 0\n 4 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 1\n 9 11 1 0\n 11 12 1 0\n 11 13 2 0\n 8 14 1 0\nM RGP 2 12 2 14 1\nM END\n> <Name>\n1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTic\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-methylvaline\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.1685 -1.2160 0.0000 C 0 0\n -0.1303 -0.4641 0.0000 C 0 0 2 0 0 0\n -1.1680 1.6379 0.0000 C 0 0\n -0.1295 1.0368 0.0000 C 0 0\n 0.9103 1.6358 0.0000 C 0 0\n 1.1678 -2.4161 0.0000 O 0 0\n -1.4292 -1.2160 0.0000 N 0 0\n 2.2083 -0.6170 0.0000 R# 0 0\n -2.4696 -0.6180 0.0000 R# 0 0\n -0.1282 2.2367 0.0000 C 0 0\n 6 1 2 0\n 1 2 1 0\n 1 8 1 0\n 2 7 1 0\n 2 4 1 1\n 4 3 1 0\n 4 5 1 0\n 7 9 1 0\n 4 10 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\n3-methylvaline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTle\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nepsilon-N-trimethyllysine\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n 2.3251 -3.2251 0.0000 C 0 0\n 1.0248 -2.4758 0.0000 C 0 0 2 0 0 0\n 1.0225 -0.9750 0.0000 C 0 0\n -0.2779 -0.2257 0.0000 C 0 0\n -0.2802 1.2751 0.0000 C 0 0\n -1.5805 2.0243 0.0000 C 0 0\n -1.5828 3.5251 0.0000 N 0 3\n -0.2756 -3.2251 0.0000 N 0 0\n 2.3269 -4.4251 0.0000 O 0 0\n 3.3637 -2.6238 0.0000 R# 0 0\n -1.3148 -2.6249 0.0000 R# 0 0\n -2.6226 4.1243 0.0000 C 0 0\n -0.5443 4.1264 0.0000 C 0 0\n -1.5841 4.7252 0.0000 C 0 0\n 9 1 2 0\n 1 2 1 0\n 1 10 1 0\n 2 8 1 0\n 2 3 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 8 11 1 0\n 7 12 1 0\n 7 13 1 0\n 7 14 1 0\nM CHG 1 7 1\nM RGP 2 10 2 11 1\nM END\n> <Name>\nepsilon-N-trimethyllysine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTml\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-thiazolylalanine\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n 0.8925 0.4863 0.0000 C 0 0\n 0.8948 -1.0144 0.0000 C 0 0 1 0 0 0\n 2.1952 -1.7637 0.0000 C 0 0\n -0.4056 -1.7637 0.0000 N 0 0\n 2.1970 -2.9637 0.0000 O 0 0\n 3.2337 -1.1625 0.0000 R# 0 0\n -1.4447 -1.1635 0.0000 R# 0 0\n -0.5669 2.7257 0.0000 N 0 0\n -0.4057 1.2344 0.0000 C 0 0\n -1.7742 0.6202 0.0000 C 0 0\n -2.7811 1.7319 0.0000 S 0 0\n -2.0350 3.0333 0.0000 C 0 0\n 2 1 1 1\n 4 2 1 0\n 2 3 1 0\n 3 5 2 0\n 3 6 1 0\n 4 7 1 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 1 0\n 8 12 2 0\n 9 1 1 0\nM RGP 2 6 2 7 1\nM END\n> <Name>\n3-thiazolylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTza\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nValine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.1543 -0.9675 0.0000 C 0 0\n -0.1446 -0.2156 0.0000 C 0 0 2 0 0 0\n -1.1823 1.8865 0.0000 C 0 0\n -0.1438 1.2853 0.0000 C 0 0\n 0.8960 1.8843 0.0000 C 0 0\n 1.1536 -2.1676 0.0000 O 0 0\n -1.4435 -0.9675 0.0000 N 0 0\n 2.1941 -0.3685 0.0000 R# 0 0\n -2.4838 -0.3695 0.0000 R# 0 0\n 6 1 2 0\n 1 2 1 0\n 1 8 1 0\n 2 7 1 0\n 2 4 1 1\n 4 3 1 0\n 4 5 1 0\n 7 9 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\nValine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nV\n\n> <MonomerCode>\nV\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nTryptophan\n SciTegic07272112182D\n\n 17 18 0 0 1 0 999 V2000\n 2.0938 -2.3551 0.0000 C 0 0\n 2.0952 -3.3000 0.0000 O 0 0\n 1.0698 -1.7652 0.0000 C 0 0 1 0 0 0\n 0.0459 -2.3551 0.0000 N 0 0\n -0.7723 -1.8826 0.0000 R# 0 0\n 1.0680 -0.5835 0.0000 C 0 0\n 0.0458 0.0055 0.0000 C 0 0\n -1.0319 -0.4779 0.0000 C 0 0\n -1.8246 0.3978 0.0000 N 0 0\n -1.2370 1.4216 0.0000 C 0 0\n -0.0810 1.1793 0.0000 C 0 0\n 0.7068 2.0591 0.0000 C 0 0\n 0.3387 3.1814 0.0000 C 0 0\n -0.8173 3.4238 0.0000 C 0 0\n -1.6051 2.5438 0.0000 C 0 0\n 2.9114 -1.8818 0.0000 R# 0 0\n -3.0061 0.3887 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 8 7 2 0\n 9 8 1 0\n 10 9 1 0\n 11 7 1 0\n 11 10 2 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 15 10 1 0\n 14 15 2 0\n 1 16 1 0\n 9 17 1 0\nM RGP 3 5 1 16 2 17 3\nM END\n> <Name>\nTryptophan\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nW\n\n> <MonomerCode>\nW\n\n> <MonomerNaturalAnalogCode>\nW\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nalpha-amino-2,4-dioxopyrimidinepropanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n 1.3004 -0.1276 0.0000 C 0 0\n 1.3027 -1.6284 0.0000 C 0 0 1 0 0 0\n 2.6030 -2.3777 0.0000 C 0 0\n 0.0023 -2.3777 0.0000 N 0 0\n 2.6048 -3.5777 0.0000 O 0 0\n 3.6416 -1.7764 0.0000 R# 0 0\n -1.0369 -1.7774 0.0000 R# 0 0\n -1.3056 2.8679 0.0000 N 0 0\n -0.0044 2.1216 0.0000 C 0 0\n 0.0000 0.6217 0.0000 N 0 0\n -1.2969 -0.1321 0.0000 C 0 0\n -2.5980 0.6141 0.0000 C 0 0\n -2.6025 2.1140 0.0000 C 0 0\n -3.6435 2.7110 0.0000 O 0 0\n 1.0330 2.7248 0.0000 O 0 0\n 2 1 1 1\n 4 2 1 0\n 2 3 1 0\n 3 5 2 0\n 3 6 1 0\n 4 7 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 8 13 1 0\n 13 14 2 0\n 9 15 2 0\n 10 1 1 0\nM RGP 2 6 2 7 1\nM END\n> <Name>\nalpha-amino-2,4-dioxopyrimidinepropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nWil\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nTyrosine\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n 2.2957 -1.9502 0.0000 C 0 0\n 2.2972 -2.8951 0.0000 O 0 0\n 1.2718 -1.3602 0.0000 C 0 0 1 0 0 0\n 0.2479 -1.9502 0.0000 N 0 0\n -0.5703 -1.4776 0.0000 R# 0 0\n 1.2701 -0.1785 0.0000 C 0 0\n 0.2461 0.4114 0.0000 C 0 0\n 0.2426 1.5925 0.0000 C 0 0\n -0.7820 2.1801 0.0000 C 0 0\n -1.8031 1.5866 0.0000 C 0 0\n -1.7996 0.4055 0.0000 C 0 0\n -0.7751 -0.1820 0.0000 C 0 0\n -2.6228 2.0566 0.0000 O 0 0\n 3.1134 -1.4768 0.0000 R# 0 0\n -2.6319 3.2381 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 1\n 6 7 1 0\n 8 7 1 0\n 9 8 2 0\n 10 9 1 0\n 11 10 2 0\n 12 7 2 0\n 12 11 1 0\n 10 13 1 0\n 1 14 1 0\n 13 15 1 0\nM RGP 3 5 1 14 2 15 3\nM END\n> <Name>\nTyrosine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nY\n\n> <MonomerCode>\nY\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nN-Terminal Acetic Acid\n SciTegic07272112182D\n\n 4 3 0 0 1 0 999 V2000\n 0.7003 1.7894 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 0.7003 -0.2894 0.0000 O 0 0\n 2.5000 0.7500 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\nM RGP 1 4 2\nM END\n> <Name>\nN-Terminal Acetic Acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nac\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nC-Terminal amine\n SciTegic07272112182D\n\n 2 1 0 0 1 0 999 V2000\n 2.5000 0.7500 0.0000 N 0 0\n 1.3000 0.7500 0.0000 R# 0 0\n 1 2 1 0\nM RGP 1 2 1\nM END\n> <Name>\nC-Terminal amine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nam\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nD-Alanine\n SciTegic07272112182D\n\n 7 6 0 0 1 0 999 V2000\n -1.2546 -0.3919 0.0000 N 0 0\n -0.2719 0.2632 0.0000 C 0 0 2 0 0 0\n -0.3102 1.7388 0.0000 C 0 0\n 1.0520 -0.3919 0.0000 C 0 0\n 1.0826 -1.5717 0.0000 O 0 0\n 2.0347 0.2632 0.0000 R# 0 0\n -2.3327 0.0905 0.0000 R# 0 0\n 2 1 1 0\n 2 3 1 6\n 2 4 1 0\n 4 5 2 0\n 4 6 1 0\n 1 7 1 0\nM RGP 2 6 2 7 1\nM END\n> <Name>\nD-Alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Cysteine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.4457 -1.1333 0.0000 C 0 0\n 0.1453 -0.3840 0.0000 C 0 0 1 0 0 0\n 0.1430 1.1168 0.0000 C 0 0\n -1.1573 1.8661 0.0000 S 0 0\n -1.1551 -1.1333 0.0000 N 0 0\n 1.4475 -2.3333 0.0000 O 0 0\n 2.4842 -0.5320 0.0000 R# 0 0\n -2.1942 -0.5331 0.0000 R# 0 0\n -1.1591 3.0661 0.0000 R# 0 0\n 6 1 2 0\n 1 2 1 0\n 1 7 1 0\n 2 5 1 0\n 2 3 1 6\n 3 4 1 0\n 5 8 1 0\n 4 9 1 0\nM RGP 3 7 2 8 1 9 3\nM END\n> <Name>\nD-Cysteine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Aspartic acid\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.6248 -1.5501 0.0000 C 0 0\n 1.6266 -2.7315 0.0000 O 0 0\n 0.3445 -0.8123 0.0000 C 0 0 2 0 0 0\n -0.9357 -1.5501 0.0000 N 0 0\n -1.9587 -0.9592 0.0000 R# 0 0\n 0.3423 0.6652 0.0000 C 0 0\n -0.9379 1.4029 0.0000 C 0 0\n -1.9604 0.8110 0.0000 O 0 0\n -0.9397 2.5843 0.0000 O 0 0\n 2.6472 -0.9581 0.0000 R# 0 0\n 0.1468 3.0978 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 7 8 2 0\n 7 9 1 0\n 1 10 1 0\n 9 11 1 0\nM RGP 3 5 1 10 2 11 3\nM END\n> <Name>\nD-Aspartic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndD\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nD\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Glutamic acid\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 0.3441 -1.4777 0.0000 C 0 0 2 0 0 0\n 1.6244 -2.2154 0.0000 C 0 0\n 1.6261 -3.3969 0.0000 O 0 0\n 2.6468 -1.6235 0.0000 R# 0 0\n -0.9362 -2.2154 0.0000 N 0 0\n -1.9591 -1.6245 0.0000 R# 0 0\n 0.3420 -0.0001 0.0000 C 0 0\n -0.9383 0.7376 0.0000 C 0 0\n -0.9404 2.2152 0.0000 C 0 0\n -1.9642 2.8050 0.0000 O 0 0\n 0.0820 2.8071 0.0000 O 0 0\n 0.0730 3.9885 0.0000 R# 0 0\n 2 1 1 0\n 2 3 2 0\n 2 4 1 0\n 1 5 1 0\n 5 6 1 0\n 1 7 1 6\n 7 8 1 0\n 8 9 1 0\n 9 10 2 0\n 9 11 1 0\n 11 12 1 0\nM RGP 3 4 2 6 1 12 3\nM END\n> <Name>\nD-Glutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndE\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Phenylalanine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.2052 2.5398 0.0000 C 0 0\n -1.5064 3.2860 0.0000 C 0 0\n -2.8032 2.5322 0.0000 C 0 0\n -2.7988 1.0322 0.0000 C 0 0\n -1.4976 0.2861 0.0000 C 0 0\n -0.2008 1.0398 0.0000 C 0 0\n 1.0995 0.2905 0.0000 C 0 0\n 1.1018 -1.2103 0.0000 C 0 0 1 0 0 0\n -0.1986 -1.9596 0.0000 N 0 0\n 2.4022 -1.9596 0.0000 C 0 0\n 2.4040 -3.1596 0.0000 O 0 0\n 3.4407 -1.3583 0.0000 R# 0 0\n -1.2376 -1.3593 0.0000 R# 0 0\n 1 2 1 0\n 1 6 2 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 6\n 8 9 1 0\n 8 10 1 0\n 10 11 2 0\n 10 12 1 0\n 9 13 1 0\nM RGP 2 12 2 13 1\nM END\n> <Name>\nD-Phenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndF\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Histidine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n 1.8978 -1.6509 0.0000 C 0 0\n 1.8993 -2.5957 0.0000 O 0 0\n 0.8738 -1.0609 0.0000 C 0 0 2 0 0 0\n -0.1501 -1.6509 0.0000 N 0 0\n -0.9683 -1.1782 0.0000 R# 0 0\n 0.8720 0.1209 0.0000 C 0 0\n -0.1501 0.7098 0.0000 C 0 0\n -0.2770 1.8841 0.0000 C 0 0\n -1.4331 2.1263 0.0000 N 0 0\n -2.0206 1.1017 0.0000 C 0 0\n -1.2276 0.2263 0.0000 N 0 0\n 2.7155 -1.1775 0.0000 R# 0 0\n -2.0316 3.1449 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 8 7 2 0\n 9 8 1 0\n 10 9 1 0\n 11 7 1 0\n 11 10 2 0\n 1 12 1 0\n 9 13 1 0\nM RGP 3 5 1 12 2 13 3\nM END\n> <Name>\nD-Histidine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndH\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nH\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Lysine\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 1.7076 -1.9282 0.0000 C 0 0\n 1.7090 -2.8727 0.0000 O 0 0\n 0.6840 -1.3385 0.0000 C 0 0 2 0 0 0\n -0.3395 -1.9282 0.0000 N 0 0\n -1.1574 -1.4558 0.0000 R# 0 0\n 0.6823 -0.1571 0.0000 C 0 0\n -0.3413 0.4325 0.0000 C 0 0\n -0.3430 1.6139 0.0000 C 0 0\n -1.3666 2.2036 0.0000 C 0 0\n -1.3680 3.1481 0.0000 N 0 0\n 2.5250 -1.4549 0.0000 R# 0 0\n -2.3921 3.7373 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 1 11 1 0\n 10 12 1 0\nM RGP 3 5 1 11 2 12 3\nM END\n> <Name>\nD-Lysine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndK\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Leucine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 0.3626 0.9903 0.0000 C 0 0\n -0.9395 2.9396 0.0000 C 0 0\n -0.9377 1.7396 0.0000 C 0 0\n -1.9763 1.1383 0.0000 C 0 0\n 0.3649 -0.5105 0.0000 C 0 0 2 0 0 0\n 1.6653 -1.2598 0.0000 C 0 0\n 1.6671 -2.4598 0.0000 O 0 0\n -0.9355 -1.2598 0.0000 N 0 0\n 2.7038 -0.6585 0.0000 R# 0 0\n -1.9746 -0.6596 0.0000 R# 0 0\n 3 1 1 0\n 5 1 1 6\n 3 2 1 0\n 3 4 1 0\n 5 8 1 0\n 5 6 1 0\n 6 7 2 0\n 6 9 1 0\n 8 10 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\nD-Leucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndL\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Methionine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.6657 -1.5600 0.0000 C 0 0\n -0.9351 -1.5600 0.0000 N 0 0\n 1.6675 -2.7600 0.0000 O 0 0\n 0.3653 -0.8107 0.0000 C 0 0 2 0 0 0\n 0.3630 0.6901 0.0000 C 0 0\n -0.9373 1.4394 0.0000 C 0 0\n -1.9794 3.5393 0.0000 C 0 0\n -0.9396 2.9402 0.0000 S 0 0\n 2.7042 -0.9587 0.0000 R# 0 0\n -1.9742 -0.9598 0.0000 R# 0 0\n 3 1 2 0\n 1 4 1 0\n 1 9 1 0\n 4 2 1 0\n 4 5 1 6\n 5 6 1 0\n 6 8 1 0\n 8 7 1 0\n 2 10 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\nD-Methionine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndM\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nM\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Asparagine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.9098 -1.3951 0.0000 C 0 0\n 1.9116 -2.5765 0.0000 O 0 0\n 0.6296 -0.6575 0.0000 C 0 0 2 0 0 0\n -0.6507 -1.3951 0.0000 N 0 0\n -1.6738 -0.8042 0.0000 R# 0 0\n 0.6273 0.8201 0.0000 C 0 0\n -0.6529 1.5578 0.0000 C 0 0\n -1.6753 0.9658 0.0000 N 0 0\n -0.6547 2.7392 0.0000 O 0 0\n 2.9322 -0.8032 0.0000 R# 0 0\n -2.7030 1.5487 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 7 8 1 0\n 7 9 2 0\n 1 10 1 0\n 8 11 1 0\nM RGP 3 5 1 10 2 11 3\nM END\n> <Name>\nD-Asparagine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndN\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nN\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Proline\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n 0.0018 1.6555 0.0000 C 0 0\n -1.4799 1.8890 0.0000 C 0 0\n -2.1599 0.5519 0.0000 C 0 0\n -1.0984 -0.5079 0.0000 N 0 0\n 0.2376 0.1741 0.0000 C 0 0 1 0 0 0\n 1.5717 -0.5079 0.0000 C 0 0\n 1.6336 -1.7063 0.0000 O 0 0\n 2.5787 0.1448 0.0000 R# 0 0\n -1.2852 -1.6933 0.0000 R# 0 0\n 1 2 1 0\n 5 1 1 6\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 6 8 1 0\n 4 9 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\nD-Proline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndP\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Glutamine\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 1.6243 -2.2154 0.0000 C 0 0\n 1.6260 -3.3969 0.0000 O 0 0\n 0.3442 -1.4777 0.0000 C 0 0 2 0 0 0\n -0.9362 -2.2154 0.0000 N 0 0\n -1.9592 -1.6245 0.0000 R# 0 0\n 0.3419 -0.0001 0.0000 C 0 0\n -0.9383 0.7376 0.0000 C 0 0\n -0.9405 2.2152 0.0000 C 0 0\n 0.0820 2.8071 0.0000 N 0 0\n -1.9641 2.8050 0.0000 O 0 0\n 2.6468 -1.6235 0.0000 R# 0 0\n 0.0730 3.9885 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 8 10 2 0\n 1 11 1 0\n 9 12 1 0\nM RGP 3 5 1 11 2 12 3\nM END\n> <Name>\nD-Glutamine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndQ\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nQ\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Arginine\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n 1.7724 -2.5892 0.0000 C 0 0\n 1.7737 -3.5337 0.0000 O 0 0\n 0.7488 -1.9994 0.0000 C 0 0 2 0 0 0\n -0.2747 -2.5892 0.0000 N 0 0\n -1.0926 -2.1168 0.0000 R# 0 0\n 0.7470 -0.8181 0.0000 C 0 0\n -0.2766 -0.2284 0.0000 C 0 0\n -0.2784 0.9529 0.0000 C 0 0\n -1.3019 1.5426 0.0000 N 0 0\n -1.3037 2.7239 0.0000 C 0 0\n -0.4863 3.1972 0.0000 N 0 0\n -2.1222 3.1954 0.0000 N 0 0\n 2.5898 -2.1159 0.0000 R# 0 0\n -0.4953 4.3786 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 10 12 2 0\n 1 13 1 0\n 11 14 1 0\nM RGP 3 5 1 13 2 14 3\nM END\n> <Name>\nD-Arginine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Serine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.3671 -1.0829 0.0000 C 0 0\n 1.3689 -2.2643 0.0000 O 0 0\n 0.0868 -0.3452 0.0000 C 0 0 2 0 0 0\n -1.1933 -1.0829 0.0000 N 0 0\n -2.2164 -0.4920 0.0000 R# 0 0\n 0.0846 1.1324 0.0000 C 0 0\n -0.9391 1.7221 0.0000 O 0 0\n 2.3895 -0.4908 0.0000 R# 0 0\n -0.9482 2.9036 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 1 8 1 0\n 7 9 1 0\nM RGP 3 5 1 8 2 9 3\nM END\n> <Name>\nD-Serine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndS\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Valine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.1543 -0.9675 0.0000 C 0 0\n -0.1446 -0.2156 0.0000 C 0 0 1 0 0 0\n -1.1823 1.8865 0.0000 C 0 0\n -0.1438 1.2853 0.0000 C 0 0\n 0.8960 1.8843 0.0000 C 0 0\n 1.1536 -2.1676 0.0000 O 0 0\n -1.4435 -0.9675 0.0000 N 0 0\n 2.1941 -0.3685 0.0000 R# 0 0\n -2.4838 -0.3695 0.0000 R# 0 0\n 6 1 2 0\n 1 2 1 0\n 1 8 1 0\n 2 7 1 0\n 2 4 1 6\n 4 3 1 0\n 4 5 1 0\n 7 9 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\nD-Valine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndV\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Isoleucine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n -1.2557 1.6681 0.0000 C 0 0\n 0.0245 0.9304 0.0000 C 0 0 2 0 0 0\n 0.0268 -0.5472 0.0000 C 0 0 1 0 0 0\n -1.2536 -1.2849 0.0000 N 0 0\n -2.2766 -0.6940 0.0000 R# 0 0\n 1.3069 -1.2849 0.0000 C 0 0\n 1.3086 -2.4664 0.0000 O 0 0\n 2.3294 -0.6930 0.0000 R# 0 0\n 1.0470 1.5223 0.0000 C 0 0\n -1.2574 2.8495 0.0000 C 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 3 6 1 0\n 6 7 2 0\n 6 8 1 0\n 2 9 1 1\n 1 10 1 0\nM RGP 2 5 1 8 2\nM END\n> <Name>\nD-Isoleucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndI\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nI\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Threonine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.0488 -1.2558 0.0000 C 0 0\n 1.0481 -2.4369 0.0000 O 0 0\n -0.2297 -0.5156 0.0000 C 0 0 2 0 0 0\n -1.5081 -1.2558 0.0000 N 0 0\n -2.5321 -0.6672 0.0000 R# 0 0\n -0.2289 0.9614 0.0000 C 0 0 1 0 0 0\n 0.7944 1.5510 0.0000 O 0 0\n -1.2510 1.5531 0.0000 C 0 0\n 2.0720 -0.6661 0.0000 R# 0 0\n 0.7866 2.7318 0.0000 R# 0 0\n 2 1 2 0\n 3 1 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 6\n 6 8 1 0\n 1 9 1 0\n 7 10 1 0\nM RGP 3 5 1 9 2 10 3\nM END\n> <Name>\nD-Threonine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndT\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Tryptophan\n SciTegic07272112182D\n\n 17 18 0 0 1 0 999 V2000\n 2.0938 -2.3551 0.0000 C 0 0\n 2.0951 -3.3000 0.0000 O 0 0\n 1.0698 -1.7651 0.0000 C 0 0 2 0 0 0\n 0.0458 -2.3551 0.0000 N 0 0\n -0.7723 -1.8826 0.0000 R# 0 0\n 1.0680 -0.5835 0.0000 C 0 0\n 0.0458 0.0056 0.0000 C 0 0\n -1.0319 -0.4778 0.0000 C 0 0\n -1.8247 0.3977 0.0000 N 0 0\n -1.2370 1.4216 0.0000 C 0 0\n -0.0810 1.1792 0.0000 C 0 0\n 0.7068 2.0591 0.0000 C 0 0\n 0.3388 3.1814 0.0000 C 0 0\n -0.8172 3.4238 0.0000 C 0 0\n -1.6051 2.5439 0.0000 C 0 0\n 2.9114 -1.8817 0.0000 R# 0 0\n -3.0060 0.3887 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 8 7 2 0\n 9 8 1 0\n 10 9 1 0\n 11 7 1 0\n 11 10 2 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 15 10 1 0\n 14 15 2 0\n 1 16 1 0\n 9 17 1 0\nM RGP 3 5 1 16 2 17 3\nM END\n> <Name>\nD-Tryptophan\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndW\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nW\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Tyrosine\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n 2.2956 -1.9503 0.0000 C 0 0\n 2.2970 -2.8952 0.0000 O 0 0\n 1.2717 -1.3603 0.0000 C 0 0 2 0 0 0\n 0.2478 -1.9503 0.0000 N 0 0\n -0.5703 -1.4776 0.0000 R# 0 0\n 1.2701 -0.1786 0.0000 C 0 0\n 0.2461 0.4115 0.0000 C 0 0\n 0.2427 1.5926 0.0000 C 0 0\n -0.7819 2.1801 0.0000 C 0 0\n -1.8030 1.5867 0.0000 C 0 0\n -1.7996 0.4056 0.0000 C 0 0\n -0.7751 -0.1820 0.0000 C 0 0\n -2.6227 2.0568 0.0000 O 0 0\n 3.1134 -1.4770 0.0000 R# 0 0\n -2.6317 3.2381 0.0000 R# 0 0\n 2 1 2 0\n 1 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 6\n 6 7 1 0\n 8 7 1 0\n 9 8 2 0\n 10 9 1 0\n 11 10 2 0\n 12 7 2 0\n 12 11 1 0\n 10 13 1 0\n 1 14 1 0\n 13 15 1 0\nM RGP 3 5 1 14 2 15 3\nM END\n> <Name>\nD-Tyrosine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndY\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nfmoc N-Terminal Protection Group\n SciTegic07272112182D\n\n 18 20 0 0 1 0 999 V2000\n 0.0842 -0.3368 0.0000 C 0 0\n 1.3810 -1.0892 0.0000 C 0 0\n 2.4977 -0.0877 0.0000 C 0 0\n 1.8903 1.2838 0.0000 C 0 0\n 0.3989 1.1298 0.0000 C 0 0\n -0.7138 2.1357 0.0000 C 0 0\n -2.1412 1.6749 0.0000 C 0 0\n -2.4560 0.2083 0.0000 C 0 0\n -1.3433 -0.7975 0.0000 C 0 0\n 1.6892 -2.5561 0.0000 C 0 0\n 3.1148 -3.0224 0.0000 C 0 0\n 4.2315 -2.0208 0.0000 C 0 0\n 3.9225 -0.5530 0.0000 C 0 0\n 2.6389 2.5816 0.0000 C 0 0\n 1.8889 3.8816 0.0000 O 0 0\n 2.6389 5.1816 0.0000 C 0 0\n 2.0393 6.2211 0.0000 O 0 0\n 3.8389 5.1816 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 1 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 1 9 1 0\n 2 10 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 2 0\n 3 13 1 0\n 4 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 2 0\n 16 18 1 0\nM RGP 1 18 2\nM END\n> <Name>\nfmoc N-Terminal Protection Group\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nfmoc\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nN-Methyl-Alanine\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n -0.0001 1.6241 0.0000 C 0 0\n -0.0001 0.4428 0.0000 C 0 0 1 0 0 0\n 1.0229 -0.1476 0.0000 C 0 0\n 2.0457 0.4430 0.0000 R# 0 0\n 1.0230 -1.3286 0.0000 O 0 0\n -1.0229 -0.1476 0.0000 N 0 0\n -2.0458 0.4427 0.0000 C 0 0\n -1.0227 -1.3288 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 1 0\n 3 5 2 0\n 6 2 1 0\n 6 7 1 0\n 6 8 1 0\nM RGP 2 4 2 8 1\nM END\n> <Name>\nN-Methyl-Alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Cysteine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.5613 -0.9000 0.0000 C 0 0\n 0.2609 -0.1507 0.0000 C 0 0 2 0 0 0\n 0.2586 1.3501 0.0000 C 0 0\n -1.0418 2.0994 0.0000 S 0 0\n -1.0395 -0.9000 0.0000 N 0 0\n 1.5630 -2.1000 0.0000 O 0 0\n 2.5998 -0.2987 0.0000 R# 0 0\n -1.0401 -2.1000 0.0000 R# 0 0\n -1.0435 3.2994 0.0000 R# 0 0\n -2.0786 -0.2998 0.0000 C 0 0\n 6 1 2 0\n 1 2 1 0\n 1 7 1 0\n 2 5 1 0\n 2 3 1 1\n 3 4 1 0\n 5 8 1 0\n 4 9 1 0\n 5 10 1 0\nM RGP 3 7 2 8 1 9 3\nM END\n> <Name>\nN-Methyl-Cysteine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nN-Methyl-Aspartic acid\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.7504 -1.0361 0.0000 C 0 0\n 0.4500 -0.2869 0.0000 C 0 0 2 0 0 0\n 0.4477 1.2140 0.0000 C 0 0\n -0.8526 1.9632 0.0000 C 0 0\n -0.8544 3.1632 0.0000 O 0 0\n -1.8912 1.3620 0.0000 R# 0 0\n 1.7522 -2.2362 0.0000 O 0 0\n -0.8504 -1.0361 0.0000 N 0 0\n 2.7889 -0.4349 0.0000 R# 0 0\n -0.8510 -2.2362 0.0000 R# 0 0\n -1.8895 -0.4360 0.0000 C 0 0\n 7 1 2 0\n 1 2 1 0\n 1 9 1 0\n 2 8 1 0\n 2 3 1 1\n 3 4 1 0\n 4 6 1 0\n 4 5 2 0\n 8 10 1 0\n 8 11 1 0\nM RGP 3 6 3 9 2 10 1\nM END\n> <Name>\nN-Methyl-Aspartic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeD\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nD\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\nN-Methyl-Glutamic acid\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 0.4350 -0.8758 0.0000 C 0 0 1 0 0 0\n 0.4328 0.6250 0.0000 C 0 0\n -0.8676 1.3743 0.0000 C 0 0\n -0.8699 2.8751 0.0000 C 0 0\n 1.7354 -1.6251 0.0000 C 0 0\n 0.1686 3.4764 0.0000 R# 0 0\n -1.9097 3.4742 0.0000 O 0 0\n 1.7372 -2.8251 0.0000 O 0 0\n -0.8654 -1.6251 0.0000 N 0 0\n 2.7739 -1.0238 0.0000 R# 0 0\n -0.8660 -2.8251 0.0000 R# 0 0\n -1.9045 -1.0249 0.0000 C 0 0\n 5 1 1 0\n 1 9 1 0\n 1 2 1 1\n 2 3 1 0\n 3 4 1 0\n 4 7 2 0\n 4 6 1 0\n 5 8 2 0\n 5 10 1 0\n 9 11 1 0\n 9 12 1 0\nM RGP 3 6 3 10 2 11 1\nM END\n> <Name>\nN-Methyl-Glutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeE\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\nN-Methyl-Phenylalanine\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -0.1860 2.7672 0.0000 C 0 0\n -1.4858 3.5162 0.0000 C 0 0\n -2.7841 2.7651 0.0000 C 0 0\n -2.7828 1.2651 0.0000 C 0 0\n -1.4831 0.5162 0.0000 C 0 0\n -0.1848 1.2673 0.0000 C 0 0\n 1.1140 0.5153 0.0000 C 0 0\n 1.1132 -0.9855 0.0000 C 0 0 2 0 0 0\n -0.1857 -1.7375 0.0000 N 0 0\n 2.4121 -1.7375 0.0000 C 0 0\n 2.4114 -2.9375 0.0000 O 0 0\n 3.4519 -1.1384 0.0000 R# 0 0\n -1.2253 -1.1383 0.0000 R# 0 0\n -0.1850 -2.9375 0.0000 C 0 0\n 1 2 1 0\n 1 6 2 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 1\n 8 9 1 0\n 8 10 1 0\n 10 11 2 0\n 10 12 1 0\n 9 13 1 0\n 9 14 1 0\nM RGP 2 12 2 13 1\nM END\n> <Name>\nN-Methyl-Phenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeF\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Histidine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n 2.2265 -1.5358 0.0000 C 0 0\n 0.9260 -0.7865 0.0000 C 0 0 2 0 0 0\n 0.9237 0.7143 0.0000 C 0 0\n -0.3744 1.4623 0.0000 C 0 0\n -2.7498 1.9600 0.0000 C 0 0\n -0.5355 2.9536 0.0000 C 0 0\n -1.7429 0.8482 0.0000 N 0 0\n -2.0037 3.2612 0.0000 N 0 0\n -0.3744 -1.5358 0.0000 N 0 0\n 2.2283 -2.7358 0.0000 O 0 0\n 3.2649 -0.9346 0.0000 R# 0 0\n -0.3751 -2.7357 0.0000 R# 0 0\n -1.4135 -0.9355 0.0000 C 0 0\n 10 1 2 0\n 1 2 1 0\n 1 11 1 0\n 2 9 1 0\n 2 3 1 1\n 3 4 1 0\n 6 4 2 0\n 7 4 1 0\n 7 5 2 0\n 5 8 1 0\n 8 6 1 0\n 9 12 1 0\n 9 13 1 0\nM RGP 2 11 2 12 1\nM END\n> <Name>\nN-Methyl-Histidine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeH\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nH\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Isoleucine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n -1.1567 1.9262 0.0000 C 0 0\n -1.1560 3.1262 0.0000 C 0 0\n 0.1413 -0.3266 0.0000 C 0 0 1 0 0 0\n 1.4401 -1.0786 0.0000 C 0 0\n 1.4394 -2.2786 0.0000 O 0 0\n -1.1576 -1.0786 0.0000 N 0 0\n 0.1421 1.1742 0.0000 C 0 0 1 0 0 0\n 1.1819 1.7733 0.0000 C 0 0\n 2.4799 -0.4795 0.0000 R# 0 0\n -2.1973 -0.4794 0.0000 R# 0 0\n -1.1570 -2.2785 0.0000 C 0 0\n 1 7 1 0\n 1 2 1 0\n 3 7 1 0\n 3 6 1 0\n 3 4 1 1\n 4 5 2 0\n 4 9 1 0\n 7 8 1 6\n 6 10 1 0\n 6 11 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\nN-Methyl-Isoleucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeI\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nI\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Lysine\n SciTegic07272112182D\n\n 13 12 0 0 1 0 999 V2000\n 2.1827 -2.2038 0.0000 C 0 0\n 0.8823 -1.4545 0.0000 C 0 0 2 0 0 0\n 0.8800 0.0463 0.0000 C 0 0\n -0.4204 0.7956 0.0000 C 0 0\n -0.4227 2.2964 0.0000 C 0 0\n -1.7230 3.0456 0.0000 C 0 0\n -1.7253 4.5464 0.0000 N 0 0\n -0.4181 -2.2038 0.0000 N 0 0\n 2.1844 -3.4038 0.0000 O 0 0\n 3.2212 -1.6025 0.0000 R# 0 0\n -0.4187 -3.4038 0.0000 R# 0 0\n -2.7651 5.1456 0.0000 R# 0 0\n -1.4572 -1.6036 0.0000 C 0 0\n 9 1 2 0\n 1 2 1 0\n 1 10 1 0\n 2 8 1 0\n 2 3 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 8 11 1 0\n 7 12 1 0\n 8 13 1 0\nM RGP 3 10 2 11 1 12 3\nM END\n> <Name>\nN-Methyl-Lysine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeK\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nN-Methyl-Leucine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 0.4492 1.2148 0.0000 C 0 0\n -0.8489 3.1668 0.0000 C 0 0\n -0.8496 1.9667 0.0000 C 0 0\n -1.8894 1.3677 0.0000 C 0 0\n 0.4484 -0.2861 0.0000 C 0 0 1 0 0 0\n 1.7473 -1.0380 0.0000 C 0 0\n 1.7466 -2.2381 0.0000 O 0 0\n -0.8505 -1.0380 0.0000 N 0 0\n 2.7870 -0.4390 0.0000 R# 0 0\n -1.8902 -0.4389 0.0000 R# 0 0\n -0.8499 -2.2380 0.0000 C 0 0\n 3 1 1 0\n 5 1 1 1\n 3 2 1 0\n 3 4 1 0\n 5 8 1 0\n 5 6 1 0\n 6 7 2 0\n 6 9 1 0\n 8 10 1 0\n 8 11 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\nN-Methyl-Leucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeL\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Methionine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.7507 -1.3091 0.0000 C 0 0\n -0.8500 -1.3091 0.0000 N 0 0\n 1.7525 -2.5091 0.0000 O 0 0\n 0.4504 -0.5598 0.0000 C 0 0 1 0 0 0\n 0.4481 0.9410 0.0000 C 0 0\n -0.8523 1.6903 0.0000 C 0 0\n -1.8944 3.7902 0.0000 C 0 0\n -0.8546 3.1911 0.0000 S 0 0\n 2.7893 -0.7078 0.0000 R# 0 0\n -0.8506 -2.5091 0.0000 R# 0 0\n -1.8891 -0.7089 0.0000 C 0 0\n 3 1 2 0\n 1 4 1 0\n 1 9 1 0\n 4 2 1 0\n 4 5 1 1\n 5 6 1 0\n 6 8 1 0\n 8 7 1 0\n 2 10 1 0\n 2 11 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\nN-Methyl-Methionine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeM\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nM\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Asparagine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.7504 -1.0361 0.0000 C 0 0\n 0.4500 -0.2869 0.0000 C 0 0 2 0 0 0\n 0.4477 1.2140 0.0000 C 0 0\n 1.7522 -2.2362 0.0000 O 0 0\n -0.8504 -1.0361 0.0000 N 0 0\n -0.8526 1.9632 0.0000 C 0 0\n -0.8544 3.1632 0.0000 O 0 0\n -1.8912 1.3620 0.0000 N 0 0\n 2.7889 -0.4349 0.0000 R# 0 0\n -0.8510 -2.2362 0.0000 R# 0 0\n -1.8895 -0.4360 0.0000 C 0 0\n 4 1 2 0\n 1 2 1 0\n 1 9 1 0\n 2 5 1 0\n 2 3 1 1\n 3 6 1 0\n 6 8 1 0\n 6 7 2 0\n 5 10 1 0\n 5 11 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\nN-Methyl-Asparagine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeN\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nN\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Glutamine\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 1.7354 -1.6251 0.0000 C 0 0\n 0.4350 -0.8758 0.0000 C 0 0 2 0 0 0\n 0.4328 0.6250 0.0000 C 0 0\n -0.8676 1.3743 0.0000 C 0 0\n 1.7372 -2.8251 0.0000 O 0 0\n 0.1686 3.4764 0.0000 N 0 0\n -0.8654 -1.6251 0.0000 N 0 0\n -1.9097 3.4742 0.0000 O 0 0\n -0.8699 2.8751 0.0000 C 0 0\n 2.7739 -1.0238 0.0000 R# 0 0\n -0.8660 -2.8251 0.0000 R# 0 0\n -1.9045 -1.0249 0.0000 C 0 0\n 5 1 2 0\n 1 2 1 0\n 1 10 1 0\n 2 7 1 0\n 2 3 1 1\n 3 4 1 0\n 4 9 1 0\n 9 6 1 0\n 9 8 2 0\n 7 11 1 0\n 7 12 1 0\nM RGP 2 10 2 11 1\nM END\n> <Name>\nN-Methyl-Glutamine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeQ\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nQ\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Arginine\n SciTegic07272112182D\n\n 14 13 0 0 1 0 999 V2000\n 2.2317 -2.5715 0.0000 C 0 0\n 0.9313 -1.8222 0.0000 C 0 0 2 0 0 0\n 0.9291 -0.3214 0.0000 C 0 0\n -0.3713 0.4279 0.0000 C 0 0\n -0.3736 1.9287 0.0000 C 0 0\n -0.3691 -2.5715 0.0000 N 0 0\n 2.2335 -3.7715 0.0000 O 0 0\n -1.6740 2.6779 0.0000 N 0 0\n -1.6763 4.1787 0.0000 C 0 0\n -2.7161 4.7779 0.0000 N 0 0\n -0.6377 4.7800 0.0000 N 0 0\n 3.2702 -1.9702 0.0000 R# 0 0\n -0.3697 -3.7715 0.0000 R# 0 0\n -1.4082 -1.9713 0.0000 C 0 0\n 7 1 2 0\n 1 2 1 0\n 1 12 1 0\n 2 6 1 0\n 2 3 1 1\n 3 4 1 0\n 4 5 1 0\n 5 8 1 0\n 8 9 1 0\n 9 11 1 0\n 9 10 2 0\n 6 13 1 0\n 6 14 1 0\nM RGP 2 12 2 13 1\nM END\n> <Name>\nN-Methyl-Arginine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeR\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Serine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 1.4164 -0.5167 0.0000 C 0 0\n 1.4181 -1.7167 0.0000 O 0 0\n -1.1844 -0.5167 0.0000 N 0 0\n 0.1160 0.2326 0.0000 C 0 0 1 0 0 0\n 0.1137 1.7334 0.0000 C 0 0\n -0.9261 2.3325 0.0000 O 0 0\n 2.4549 0.0846 0.0000 R# 0 0\n -1.1850 -1.7167 0.0000 R# 0 0\n -2.2235 0.0835 0.0000 C 0 0\n 2 1 2 0\n 1 4 1 0\n 1 7 1 0\n 4 3 1 0\n 4 5 1 1\n 5 6 1 0\n 3 8 1 0\n 3 9 1 0\nM RGP 2 7 2 8 1\nM END\n> <Name>\nN-Methyl-Serine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeS\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Threonine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.3011 -0.7501 0.0000 C 0 0\n -1.2996 -0.7501 0.0000 N 0 0\n 1.3029 -1.9501 0.0000 O 0 0\n 0.0008 -0.0009 0.0000 C 0 0 1 0 0 0\n 1.0370 2.1012 0.0000 C 0 0\n -0.0015 1.5000 0.0000 C 0 0 1 0 0 0\n -1.0413 2.0990 0.0000 O 0 0\n 2.3397 -0.1489 0.0000 R# 0 0\n -1.3003 -1.9502 0.0000 R# 0 0\n -2.3388 -0.1500 0.0000 C 0 0\n 3 1 2 0\n 4 1 1 1\n 1 8 1 0\n 4 2 1 0\n 4 6 1 0\n 6 5 1 0\n 6 7 1 6\n 2 9 1 0\n 2 10 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\nN-Methyl-Threonine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeT\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Valine\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 1.3011 0.7502 0.0000 C 0 0\n 0.0011 0.0002 0.0000 C 0 0 2 0 0 0\n -1.0421 -2.0992 0.0000 C 0 0\n -0.0020 -1.5005 0.0000 C 0 0\n 1.0362 -2.1024 0.0000 C 0 0\n 2.3405 0.1505 0.0000 O 0 0\n -1.2989 0.7502 0.0000 N 0 0\n 1.3011 1.9502 0.0000 R# 0 0\n -1.2989 1.9502 0.0000 R# 0 0\n -2.3382 0.1505 0.0000 C 0 0\n 6 1 2 0\n 1 2 1 0\n 1 8 1 0\n 2 7 1 0\n 2 4 1 6\n 4 3 1 0\n 4 5 1 0\n 7 9 1 0\n 7 10 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\nN-Methyl-Valine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeV\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Tryptophan\n SciTegic07272112182D\n\n 17 18 0 0 1 0 999 V2000\n 2.4311 -2.7154 0.0000 C 0 0\n 2.4328 -3.9155 0.0000 O 0 0\n -0.1698 -2.7154 0.0000 N 0 0\n 1.1306 -1.9662 0.0000 C 0 0 1 0 0 0\n 1.1284 -0.4655 0.0000 C 0 0\n -0.1698 0.2826 0.0000 C 0 0\n -1.5385 -0.3313 0.0000 C 0 0\n -0.3308 1.7733 0.0000 C 0 0\n -1.7989 2.0810 0.0000 C 0 0\n 0.6697 2.8906 0.0000 C 0 0\n 0.2023 4.3159 0.0000 C 0 0\n -1.2658 4.6238 0.0000 C 0 0\n -2.2664 3.5063 0.0000 C 0 0\n -2.5452 0.7808 0.0000 N 0 0\n 3.4695 -2.1143 0.0000 R# 0 0\n -0.1705 -3.9155 0.0000 R# 0 0\n -1.2088 -2.1153 0.0000 C 0 0\n 2 1 2 0\n 1 4 1 0\n 1 15 1 0\n 4 3 1 0\n 4 5 1 1\n 5 6 1 0\n 7 6 2 0\n 8 6 1 0\n 14 7 1 0\n 8 9 2 0\n 8 10 1 0\n 9 14 1 0\n 13 9 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 2 0\n 3 16 1 0\n 3 17 1 0\nM RGP 2 15 2 16 1\nM END\n> <Name>\nN-Methyl-Tryptophan\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeW\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nW\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Methyl-Tyrosine\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n 2.6718 -1.9575 0.0000 C 0 0\n 0.0710 -1.9575 0.0000 N 0 0\n 2.6736 -3.1576 0.0000 O 0 0\n 1.3714 -1.2083 0.0000 C 0 0 1 0 0 0\n 1.3692 0.2926 0.0000 C 0 0\n 0.0688 1.0418 0.0000 C 0 0\n -1.2281 0.2881 0.0000 C 0 0\n -2.5293 1.0343 0.0000 C 0 0\n -1.2369 3.2880 0.0000 C 0 0\n 0.0644 2.5418 0.0000 C 0 0\n -2.5336 2.5343 0.0000 C 0 0\n -3.5747 3.1312 0.0000 O 0 0\n 3.7103 -1.3564 0.0000 R# 0 0\n 0.0703 -3.1576 0.0000 R# 0 0\n -0.9680 -1.3573 0.0000 C 0 0\n 3 1 2 0\n 1 4 1 0\n 1 13 1 0\n 4 2 1 0\n 4 5 1 1\n 5 6 1 0\n 10 6 1 0\n 7 6 2 0\n 7 8 1 0\n 8 11 2 0\n 11 9 1 0\n 9 10 2 0\n 11 12 1 0\n 2 14 1 0\n 2 15 1 0\nM RGP 2 13 2 14 1\nM END\n> <Name>\nN-Methyl-Tyrosine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nmeY\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nPNA Adenine\n SciTegic07272112182D\n\n 22 23 0 0 0 0 999 V2000\n -4.0177 -3.1348 0.0000 R# 0 0\n -2.8711 -3.4186 0.0000 N 0 0\n -2.0522 -2.5674 0.0000 C 0 0\n -0.9056 -2.8511 0.0000 C 0 0\n -0.0867 -2.0001 0.0000 N 0 0\n -0.4142 -0.8653 0.0000 C 0 0\n -1.5608 -0.5816 0.0000 O 0 0\n 0.4047 -0.0142 0.0000 C 0 0\n 0.0771 1.1205 0.0000 N 0 0\n -1.0335 1.5226 0.0000 C 0 0\n -0.9944 2.7030 0.0000 N 0 0\n 0.1404 3.0305 0.0000 C 0 0\n 0.8026 2.0526 0.0000 C 0 0\n 1.9807 2.1371 0.0000 N 0 0\n 2.4966 3.1995 0.0000 C 0 0\n 1.8343 4.1775 0.0000 N 0 0\n 0.6562 4.0930 0.0000 C 0 0\n -0.0059 5.0710 0.0000 N 0 0\n 1.0598 -2.2838 0.0000 C 0 0\n 1.3874 -3.4186 0.0000 C 0 0\n 0.5685 -4.2696 0.0000 O 0 0\n 2.5340 -3.7022 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 6 8 1 0\n 8 9 1 0\n 9 10 1 0\n 11 10 2 0\n 12 11 1 0\n 13 12 2 0\n 9 13 1 0\n 13 14 1 0\n 15 14 2 0\n 16 15 1 0\n 12 17 1 0\n 17 16 2 0\n 17 18 1 0\n 5 19 1 0\n 19 20 1 0\n 20 21 2 0\n 20 22 1 0\nM RGP 2 1 1 22 2\nM END\n> <Name>\nPNA Adenine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\npnA\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nPNA Cytosine\n SciTegic07272112182D\n\n 20 20 0 0 0 0 999 V2000\n -3.3034 -4.1754 0.0000 R# 0 0\n -3.0802 -3.0156 0.0000 N 0 0\n -1.9642 -2.6289 0.0000 C 0 0\n -1.7410 -1.4691 0.0000 C 0 0\n -0.6250 -1.0825 0.0000 N 0 0\n -0.4018 0.0773 0.0000 C 0 0\n -1.2946 0.8505 0.0000 O 0 0\n 0.7143 0.4640 0.0000 C 0 0\n 0.9374 1.6238 0.0000 N 0 0\n 2.0535 2.0104 0.0000 C 0 0\n 2.9463 1.2372 0.0000 O 0 0\n 2.2767 3.1702 0.0000 N 0 0\n 1.3838 3.9434 0.0000 C 0 0\n 1.6070 5.1032 0.0000 N 0 0\n 0.2678 3.5568 0.0000 C 0 0\n 0.0446 2.3969 0.0000 C 0 0\n 0.2679 -1.8557 0.0000 C 0 0\n 0.0447 -3.0156 0.0000 C 0 0\n -1.0713 -3.4022 0.0000 O 0 0\n 0.9375 -3.7887 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 6 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 2 0\n 12 10 1 0\n 13 12 2 0\n 13 14 1 0\n 15 13 1 0\n 16 15 2 0\n 9 16 1 0\n 5 17 1 0\n 17 18 1 0\n 18 19 2 0\n 18 20 1 0\nM RGP 2 1 1 20 2\nM END\n> <Name>\nPNA Cytosine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\npnC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nPNA Guanine\n SciTegic07272112182D\n\n 23 24 0 0 0 0 999 V2000\n -3.9874 -4.5541 0.0000 R# 0 0\n -3.7641 -3.3943 0.0000 N 0 0\n -2.6481 -3.0076 0.0000 C 0 0\n -2.4249 -1.8478 0.0000 C 0 0\n -1.3088 -1.4613 0.0000 N 0 0\n -1.0856 -0.3015 0.0000 C 0 0\n -1.9783 0.4718 0.0000 O 0 0\n 0.0305 0.0851 0.0000 C 0 0\n 0.2537 1.2449 0.0000 N 0 0\n -0.5533 2.1072 0.0000 C 0 0\n 0.0174 3.1413 0.0000 N 0 0\n 1.1772 2.9181 0.0000 C 0 0\n 1.3232 1.7460 0.0000 C 0 0\n 2.4113 1.2865 0.0000 N 0 0\n 3.3532 1.9990 0.0000 C 0 0\n 4.4414 1.5396 0.0000 N 0 0\n 3.2072 3.1711 0.0000 N 0 0\n 2.1191 3.6306 0.0000 C 0 0\n 1.9731 4.8026 0.0000 O 0 0\n -0.4160 -2.2345 0.0000 C 0 0\n -0.6393 -3.3943 0.0000 C 0 0\n -1.7553 -3.7809 0.0000 O 0 0\n 0.2536 -4.1676 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 6 8 1 0\n 8 9 1 0\n 9 10 1 0\n 11 10 2 0\n 12 11 1 0\n 13 12 2 0\n 9 13 1 0\n 13 14 1 0\n 15 14 2 0\n 15 16 1 0\n 17 15 1 0\n 12 18 1 0\n 18 17 1 0\n 18 19 2 0\n 5 20 1 0\n 20 21 1 0\n 21 22 2 0\n 21 23 1 0\nM RGP 2 1 1 23 2\nM END\n> <Name>\nPNA Guanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\npnG\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nPNA Thymine\n SciTegic07272112182D\n\n 21 21 0 0 0 0 999 V2000\n -3.2737 -4.3815 0.0000 R# 0 0\n -3.0505 -3.2217 0.0000 N 0 0\n -1.9345 -2.8351 0.0000 C 0 0\n -1.7113 -1.6753 0.0000 C 0 0\n -0.5952 -1.2887 0.0000 N 0 0\n -0.3720 -0.1288 0.0000 C 0 0\n -1.2649 0.6444 0.0000 O 0 0\n 0.7440 0.2577 0.0000 C 0 0\n 0.9672 1.4176 0.0000 N 0 0\n 2.0833 1.8041 0.0000 C 0 0\n 2.9761 1.0309 0.0000 O 0 0\n 2.3065 2.9639 0.0000 N 0 0\n 1.4137 3.7372 0.0000 C 0 0\n 1.6369 4.8970 0.0000 O 0 0\n 0.2977 3.3506 0.0000 C 0 0\n -0.5952 4.1238 0.0000 C 0 0\n 0.0745 2.1908 0.0000 C 0 0\n 0.2976 -2.0619 0.0000 C 0 0\n 0.0743 -3.2217 0.0000 C 0 0\n -1.0417 -3.6084 0.0000 O 0 0\n 0.9672 -3.9949 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 6 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 2 0\n 12 10 1 0\n 13 12 1 0\n 13 14 2 0\n 15 13 1 0\n 15 16 1 0\n 17 15 2 0\n 9 17 1 0\n 5 18 1 0\n 18 19 1 0\n 19 20 2 0\n 19 21 1 0\nM RGP 2 1 1 21 2\nM END\n> <Name>\nPNA Thymine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\npnT\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nSelenoCysteine\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 1.2682 -0.7312 0.0000 C 0 0\n -0.0321 0.0180 0.0000 C 0 0 2 0 0 0\n -0.0344 1.5189 0.0000 C 0 0\n -1.0742 2.1179 0.0000 Se 0 0\n -1.3325 -0.7312 0.0000 N 0 0\n 1.2700 -1.9313 0.0000 O 0 0\n 2.3068 -0.1300 0.0000 R# 0 0\n -2.3717 -0.1311 0.0000 R# 0 0\n 6 1 2 0\n 1 2 1 0\n 1 7 1 0\n 2 5 1 0\n 2 3 1 1\n 3 4 1 0\n 5 8 1 0\nM RGP 2 7 2 8 1\nM END\n> <Name>\nSelenoCysteine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nseC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nTest-6-AP-Chem\nKetcher 9272311162D 1 1.00000 0.00000 0\n\n 22 21 0 0 0 0 0 0 0 0999 V2000\n 12.0838 -6.5500 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0\n 11.1373 -6.1032 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 10.2767 -6.6989 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 9.3303 -6.2522 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 8.4697 -6.8478 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.5233 -6.4011 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.6627 -6.9968 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.7162 -6.5500 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\n 12.7718 -6.0736 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 5.0282 -7.0264 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 7.0233 -5.5351 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.0233 -4.5351 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.3162 -3.8280 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 6.5750 -2.8621 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.6091 -2.6032 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 5.8679 -1.6373 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 4.8679 -1.6373 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 10.2767 -7.6989 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 7.5750 -2.8621 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 8.4697 -7.8478 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.9697 -8.7139 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\n 7.9697 -9.7139 0.0000 R# 0 0 0 0 0 0 0 0 0 0 0 0\n 1 2 1 0 0 0\n 2 3 1 0 0 0\n 3 4 1 0 0 0\n 4 5 1 0 0 0\n 5 6 1 0 0 0\n 6 7 1 0 0 0\n 7 8 1 0 0 0\n 1 9 1 0 0 0\n 8 10 1 0 0 0\n 6 11 1 0 0 0\n 11 12 1 0 0 0\n 12 13 1 0 0 0\n 13 14 1 0 0 0\n 14 15 1 0 0 0\n 15 16 1 0 0 0\n 16 17 1 0 0 0\n 3 18 1 0 0 0\n 14 19 1 0 0 0\n 5 20 1 0 0 0\n 20 21 1 0 0 0\n 21 22 1 0 0 0\nM RGP 6 9 2 10 1 17 3 18 5 19 4 22 6\nM END\n> <Name>\nTest-6-AP-Chem\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nTest-6-Ch\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]I\n[R3]Br\n[R4]Cl\n[R5]O\n[R6]H\n\n$$$$\n6-amino-hexanol\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 4.5654 0.0000 0.0000 N 0 0\n 3.2082 0.6407 0.0000 C 0 0\n 1.9742 -0.2135 0.0000 C 0 0\n 0.6170 0.4271 0.0000 C 0 0\n -0.6170 -0.4271 0.0000 C 0 0\n -1.9741 0.2135 0.0000 C 0 0\n -3.2082 -0.6407 0.0000 C 0 0\n -4.5654 0.0000 0.0000 O 0 0\n 5.5520 0.6831 0.0000 R# 0 0\n -5.5520 -0.6831 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 1 9 1 0\n 8 10 1 0\nM RGP 2 9 2 10 1\nM END\n> <Name>\n6-amino-hexanol\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nA6OH\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nAzide\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 3.0997 0.9106 0.0000 O 0 0\n 2.5000 1.9500 0.0000 C 0 0\n 3.2500 3.2500 0.0000 C 0 0\n 2.5000 4.5500 0.0000 C 0 0\n 3.2500 5.8500 0.0000 C 0 0\n 2.5000 7.1500 0.0000 N 0 0\n 3.2500 8.4499 0.0000 N 0 3\n 3.8497 9.4894 0.0000 N 0 5\n 1.3000 1.9500 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 2 0\n 2 9 1 0\nM CHG 2 7 1 8 -1\nM RGP 1 9 1\nM END\n> <Name>\nAzide\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nAz\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n\n$$$$\nEthylene Glycol\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n -1.3000 0.3899 0.0000 O 0 0\n 0.0000 -0.3601 0.0000 C 0 0\n -2.3394 -0.2098 0.0000 R# 0 0\n 1.3000 0.3899 0.0000 C 0 0\n 2.3394 -0.2098 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 4 5 1 0\nM RGP 2 3 1 5 2\nM END\n> <Name>\nEthylene Glycol\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nEG\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n4-(N-maleimidomethyl)cyclohexane-1-carboxylate\n SciTegic07272112182D\n\n 17 18 0 0 1 0 999 V2000\n 4.8398 3.5052 0.0000 C 0 0\n 5.5875 2.2049 0.0000 C 0 0\n 7.0875 2.2023 0.0000 C 0 0\n 7.8397 3.5000 0.0000 C 0 0\n 7.0920 4.8003 0.0000 C 0 0\n 5.5920 4.8030 0.0000 C 0 0\n 4.8375 0.9049 0.0000 C 0 0\n 5.4372 -0.1345 0.0000 O 0 0\n 3.6375 0.9049 0.0000 R# 0 0\n 7.8420 6.1003 0.0000 C 0 0\n 7.0920 7.4003 0.0000 N 0 0\n 7.7107 8.7528 0.0000 C 0 0\n 5.6109 7.5356 0.0000 C 0 0\n 5.2965 9.0023 0.0000 C 0 0\n 6.5942 9.7545 0.0000 C 0 0\n 8.8856 8.9973 0.0000 O 0 0\n 4.8148 6.6378 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 1 6 1 0\n 2 7 1 0\n 7 8 2 0\n 7 9 1 0\n 5 10 1 0\n 10 11 1 0\n 12 11 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 2 0\n 12 15 1 0\n 12 16 2 0\n 13 17 2 0\nM RGP 1 9 1\nM END\n> <Name>\n4-(N-maleimidomethyl)cyclohexane-1-carboxylate\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nMCC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n\n$$$$\nDiethylene Glycol\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n -3.8999 -0.3833 0.0000 O 0 0\n -2.5999 0.3667 0.0000 C 0 0\n -1.3000 -0.3833 0.0000 C 0 0\n 0.0000 0.3667 0.0000 O 0 0\n 1.3000 -0.3833 0.0000 C 0 0\n 2.6000 0.3667 0.0000 C 0 0\n 3.9000 -0.3833 0.0000 O 0 0\n 4.9394 0.2164 0.0000 R# 0 0\n -4.9394 0.2164 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 1 9 1 0\nM RGP 2 8 2 9 1\nM END\n> <Name>\nDiethylene Glycol\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nPEG2\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nSMCC linker from Pierce\n SciTegic07272112182D\n\n 18 19 0 0 1 0 999 V2000\n 0.4966 -1.0108 0.0000 C 0 0\n -0.8438 -1.6860 0.0000 C 0 0\n -2.0992 -0.8637 0.0000 N 0 0\n -4.4215 -0.2334 0.0000 C 0 0\n -3.4845 -1.4048 0.0000 C 0 0\n -2.1504 0.6228 0.0000 C 0 0\n -3.5970 1.0196 0.0000 C 0 0\n -1.2090 1.3667 0.0000 O 0 0\n -3.7953 -2.5638 0.0000 O 0 0\n -4.0204 2.1426 0.0000 R# 0 0\n 1.9171 1.1645 0.0000 C 0 0\n 3.1730 0.3443 0.0000 C 0 0\n 3.0908 -1.1534 0.0000 C 0 0\n 1.7526 -1.8310 0.0000 C 0 0\n 0.5789 0.4870 0.0000 C 0 0\n 4.5135 1.0196 0.0000 C 0 0\n 5.5173 0.3621 0.0000 O 0 0\n 4.5813 2.2177 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 5 3 1 0\n 3 6 1 0\n 4 5 1 0\n 6 7 1 0\n 4 7 1 0\n 6 8 2 0\n 5 9 2 0\n 7 10 1 0\n 14 1 1 0\n 1 15 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 11 15 1 0\n 12 16 1 0\n 16 17 2 0\n 16 18 1 0\nM RGP 2 10 1 18 2\nM END\n> <Name>\nSMCC linker from Pierce\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nSMCC\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nSM(PEG)2 linker from Pierce\n SciTegic07272112182D\n\n 24 24 0 0 1 0 999 V2000\n 0.9955 -0.0240 0.0000 N 0 0\n 2.1808 -0.9447 0.0000 C 0 0\n 3.5711 -0.3794 0.0000 C 0 0\n 4.7564 -1.3000 0.0000 C 0 0\n 6.1443 -0.7358 0.0000 N 0 0\n 8.5647 -0.5561 0.0000 C 0 0\n 7.4197 -1.5251 0.0000 C 0 0\n 6.5009 0.7213 0.0000 C 0 0\n 7.9968 0.8323 0.0000 C 0 0\n 5.7256 1.6372 0.0000 O 0 0\n 7.5086 -2.7219 0.0000 O 0 0\n 8.6283 1.8526 0.0000 R# 0 0\n 2.0167 -2.1334 0.0000 O 0 0\n -0.3947 -0.5893 0.0000 C 0 0\n -1.5801 0.3313 0.0000 C 0 0\n -2.9705 -0.2339 0.0000 O 0 0\n -4.1556 0.6867 0.0000 C 0 0\n -5.5460 0.1214 0.0000 C 0 0\n -6.7313 1.0422 0.0000 O 0 0\n -8.1216 0.4769 0.0000 C 0 0\n -9.3068 1.3976 0.0000 C 0 0\n -10.6971 0.8323 0.0000 C 0 0\n -10.8610 -0.3565 0.0000 R# 0 0\n -11.6448 1.5683 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 7 5 1 0\n 5 8 1 0\n 6 7 1 0\n 8 9 1 0\n 6 9 1 0\n 8 10 2 0\n 7 11 2 0\n 9 12 1 0\n 2 13 2 0\n 1 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 19 20 1 0\n 20 21 1 0\n 21 22 1 0\n 22 23 1 0\n 22 24 2 0\nM RGP 2 12 2 23 1\nM END\n> <Name>\nSM(PEG)2 linker from Pierce\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nSMPEG2\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]H\n\n$$$$\nDipropanol-disulfide\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n -6.8609 -0.6650 0.0000 R# 0 0\n -5.8620 0.0000 0.0000 O 0 0\n -4.5166 -0.6653 0.0000 C 0 0\n -3.2673 0.1663 0.0000 C 0 0\n -1.9220 -0.4990 0.0000 C 0 0\n -0.6726 0.3327 0.0000 S 0 0\n 0.6726 -0.3327 0.0000 S 0 0\n 1.9220 0.4990 0.0000 C 0 0\n 3.2673 -0.1663 0.0000 C 0 0\n 4.5166 0.6653 0.0000 C 0 0\n 5.8620 0.0000 0.0000 O 0 0\n 6.8609 0.6650 0.0000 R# 0 0\n 6 7 1 0\n 2 3 1 0\n 7 8 1 0\n 8 9 1 0\n 3 4 1 0\n 9 10 1 0\n 10 11 1 0\n 4 5 1 0\n 11 12 1 0\n 1 2 1 0\n 5 6 1 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\nDipropanol-disulfide\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nSS3\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nHexynyl alcohol\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 1.4606 0.1503 0.0000 O 0 0\n 2.2118 -1.1490 0.0000 C 0 0\n 0.2606 0.1503 0.0000 R# 0 0\n 3.7126 -1.1491 0.0000 C 0 0\n 4.4638 -2.4484 0.0000 C 0 0\n 5.9647 -2.4484 0.0000 C 0 0\n 6.7158 -3.7477 0.0000 C 0 0\n 7.3165 -4.7866 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 3 0\nM RGP 1 3 1\nM END\n> <Name>\nHexynyl alcohol\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nhxy\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nSymmetric Doubler\n SciTegic07272112182D\n\n 23 22 0 0 1 0 999 V2000\n 5.1451 -1.0717 0.0000 C 0 0\n 3.9656 -0.1437 0.0000 C 0 0\n 2.5718 -0.7004 0.0000 N 0 0\n 1.3922 0.2275 0.0000 C 0 0\n -0.0015 -0.3292 0.0000 C 0 0\n -1.1811 0.5987 0.0000 C 0 0\n -2.5749 0.0420 0.0000 N 0 0\n -3.7544 0.9700 0.0000 C 0 0\n -5.1483 0.4133 0.0000 C 0 0\n -0.2189 -1.8141 0.0000 O 0 0\n -6.3278 1.3412 0.0000 C 0 0\n -7.7215 0.7845 0.0000 C 0 0\n -8.9011 1.7124 0.0000 C 0 0\n -10.2948 1.1557 0.0000 O 0 0\n 6.5389 -0.5150 0.0000 C 0 0\n 7.7185 -1.4429 0.0000 C 0 0\n 9.1122 -0.8862 0.0000 C 0 0\n 10.2918 -1.8141 0.0000 O 0 0\n -3.5831 2.1577 0.0000 O 0 0\n 4.1370 1.0440 0.0000 O 0 0\n -1.3338 -2.2581 0.0000 R# 0 0\n 11.4062 -1.3690 0.0000 R# 0 0\n -11.2381 1.8977 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 5 10 1 0\n 9 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 1 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 8 19 2 0\n 2 20 2 0\n 10 21 1 0\n 18 22 1 0\n 14 23 1 0\nM RGP 3 21 1 22 2 23 3\nM END\n> <Name>\nSymmetric Doubler\n\n> <MonomerType>\nCHEM\n\n> <MonomerName>\nsDBL\n\n> <MonomerCode>\n\n> <MonomerNaturalAnalogCode>\n.\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]H\n\n$$$$\nD-Pyl\n SciTegic07272112182D\n\n 19 19 0 0 1 0 999 V2000\n -2.0487 -3.8600 0.0000 R# 0 0\n -1.0256 -4.4508 0.0000 N 0 0\n -0.0024 -3.8600 0.0000 C 0 0 1 0 0 0\n 1.0208 -4.4508 0.0000 C 0 0\n 2.0439 -3.8600 0.0000 R# 0 0\n 1.0208 -5.6322 0.0000 O 0 0\n -0.0024 -2.6786 0.0000 C 0 0\n 0.5883 -1.6554 0.0000 C 0 0\n -0.0024 -0.6322 0.0000 C 0 0\n 0.5883 0.3909 0.0000 C 0 0\n -0.0024 1.4141 0.0000 N 0 0\n 0.5883 2.4373 0.0000 C 0 0\n -0.0024 3.4604 0.0000 C 0 0 1 0 0 0\n 1.7698 2.4373 0.0000 O 0 0\n -1.1768 3.5839 0.0000 C 0 0\n -1.4223 4.7390 0.0000 C 0 0\n -0.3997 5.3294 0.0000 C 0 0\n 0.4779 4.5392 0.0000 N 0 0\n -2.0122 2.7484 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\n 3 7 1 6\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 12 14 2 0\n 17 18 2 0\n 16 17 1 0\n 15 16 1 0\n 13 15 1 1\n 18 13 1 0\n 15 19 1 0\nM RGP 2 1 1 5 2\nM END\n> <Name>\nD-Pyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndPyl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-SelenoCysteine\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n -1.9326 -0.3282 0.0000 R# 0 0\n -0.9095 -0.9190 0.0000 N 0 0\n 0.1137 -0.3282 0.0000 C 0 0 1 0 0 0\n 1.1369 -0.9190 0.0000 C 0 0\n 2.1600 -0.3282 0.0000 R# 0 0\n 1.1369 -2.1004 0.0000 O 0 0\n 0.1137 0.8532 0.0000 C 0 0\n -0.9095 1.4440 0.0000 Se 0 0\n -0.9095 2.6254 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\n 3 7 1 6\n 7 8 1 0\n 8 9 1 0\nM RGP 3 1 1 5 2 9 3\nM END\n> <Name>\nD-SelenoCysteine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\ndSec\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nPyl\n SciTegic07272112182D\n\n 19 19 0 0 1 0 999 V2000\n -2.0487 -3.8600 0.0000 R# 0 0\n -1.0256 -4.4508 0.0000 N 0 0\n -0.0024 -3.8600 0.0000 C 0 0 2 0 0 0\n 1.0208 -4.4508 0.0000 C 0 0\n 2.0439 -3.8600 0.0000 R# 0 0\n 1.0208 -5.6322 0.0000 O 0 0\n -0.0024 -2.6786 0.0000 C 0 0\n 0.5883 -1.6554 0.0000 C 0 0\n -0.0024 -0.6322 0.0000 C 0 0\n 0.5883 0.3909 0.0000 C 0 0\n -0.0024 1.4141 0.0000 N 0 0\n 0.5883 2.4373 0.0000 C 0 0\n -0.0024 3.4604 0.0000 C 0 0 1 0 0 0\n 1.7698 2.4373 0.0000 O 0 0\n -1.1768 3.5839 0.0000 C 0 0\n -1.4223 4.7390 0.0000 C 0 0\n -0.3997 5.3294 0.0000 C 0 0\n 0.4779 4.5392 0.0000 N 0 0\n -2.0122 2.7484 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\n 3 7 1 1\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 12 14 2 0\n 17 18 2 0\n 16 17 1 0\n 15 16 1 0\n 13 15 1 1\n 18 13 1 0\n 15 19 1 0\nM RGP 2 1 1 5 2\nM END\n> <Name>\nPyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPyl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nC-Terminal NMe\n SciTegic07272112182D\n\n 3 2 0 0 0 0 999 V2000\n 8.3795 -8.3427 0.0000 N 0 0\n 8.8579 -7.5142 0.0000 C 0 0\n 7.4230 -8.3427 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\nM RGP 1 3 1\nM END\n> <Name>\nC-Terminal NMe\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNMe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nC-Terminal OMe\n SciTegic07272112182D\n\n 3 2 0 0 0 0 999 V2000\n 8.4509 -11.5165 0.0000 O 0 0\n 8.9293 -10.6879 0.0000 C 0 0\n 7.4944 -11.5165 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\nM RGP 1 3 1\nM END\n> <Name>\nC-Terminal OMe\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOMe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nC-Terminal OtBu\n SciTegic07272112182D\n\n 6 5 0 0 0 0 999 V2000\n 7.7323 -15.8067 0.0000 O 0 0\n 6.7756 -15.8067 0.0000 R# 0 0\n 8.2105 -14.9781 0.0000 C 0 0\n 7.7322 -14.1496 0.0000 C 0 0\n 8.6888 -14.1496 0.0000 C 0 0\n 9.1673 -14.9780 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 3 4 1 0\n 3 5 1 0\n 3 6 1 0\nM RGP 1 2 1\nM END\n> <Name>\nC-Terminal OtBu\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOtBu\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nC-Terminal Oxa\n SciTegic07272112182D\n\n 6 6 0 0 0 0 999 V2000\n 16.7858 -10.6257 0.0000 C 0 0\n 17.3477 -9.8523 0.0000 C 0 0\n 18.2570 -10.1478 0.0000 N 0 0\n 18.2569 -11.1038 0.0000 C 0 0\n 17.3476 -11.3992 0.0000 O 0 0\n 15.8290 -10.6257 0.0000 R# 0 0\n 2 1 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 0\nM RGP 1 6 1\nM END\n> <Name>\nC-Terminal Oxa\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOxa\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nC-Terminal OBz\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 15.2550 -7.2049 0.0000 C 0 0\n 16.2116 -7.2049 0.0000 C 0 0\n 14.7767 -6.3766 0.0000 O 0 0\n 16.6900 -6.3764 0.0000 C 0 0\n 17.6438 -6.3774 0.0000 C 0 0\n 18.1239 -7.2070 0.0000 C 0 0\n 17.6479 -8.0312 0.0000 C 0 0\n 16.6920 -8.0368 0.0000 C 0 0\n 13.8202 -6.3766 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 4 2 2 0\n 5 4 1 0\n 6 5 2 0\n 7 6 1 0\n 8 7 2 0\n 2 8 1 0\n 3 9 1 0\nM RGP 1 9 1\nM END\n> <Name>\nC-Terminal OBz\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOBz\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nC-Terminal methyl\n SciTegic07272112182D\n\n 2 1 0 0 0 0 999 V2000\n 2.8000 0.7500 0.0000 C 0 0\n 1.3000 0.7500 0.0000 R# 0 0\n 1 2 1 0\nM RGP 1 2 1\nM END\n> <Name>\nC-Terminal methyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n-Me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nL-allo-Isoleucine\n SciTegic09012117322D\n\n 10 9 0 0 1 0 999 V2000\n -1.3038 -3.1492 0.0000 C 0 0\n -1.3015 -1.6492 0.0000 C 0 0\n -0.0011 -0.8999 0.0000 C 0 0 1 0 0 0\n 1.2971 -1.6515 0.0000 C 0 0\n 0.0012 0.6009 0.0000 C 0 0 2 0 0 0\n -1.2992 1.3502 0.0000 N 0 0\n -2.5981 0.5999 0.0000 R# 0 0\n 1.3016 1.3502 0.0000 C 0 0\n 2.5998 0.5986 0.0000 R# 0 0\n 1.3039 2.8501 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 0\n 3 4 1 6\n 3 5 1 0\n 5 6 1 6\n 6 7 1 0\n 5 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 2 7 1 9 2\nM END\n> <Name>\nL-allo-Isoleucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\naIle\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nI\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Gamma glutamic acid\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n -3.2036 -1.0674 0.0000 R# 0 0\n -1.7036 -1.0637 0.0000 N 0 0\n -0.9556 0.2375 0.0000 C 0 0 2 0 0 0\n 0.5452 0.2367 0.0000 C 0 0\n 1.2958 -1.0629 0.0000 C 0 0\n 2.7966 -1.0637 0.0000 C 0 0\n 3.5468 0.2352 0.0000 R# 0 0\n 3.5468 -2.3626 0.0000 O 0 0\n -1.7062 1.5371 0.0000 C 0 0\n -0.9560 2.8360 0.0000 R# 0 0\n -3.2062 1.5379 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 6 8 2 0\n 3 9 1 0\n 9 10 1 0\n 9 11 2 0\nM RGP 3 1 1 7 2 10 3\nM END\n> <Name>\nD-Gamma glutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-gGlu\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\nD-Norleucine\n SciTegic09012117322D\n\n 10 9 0 0 1 0 999 V2000\n -2.2134 3.6741 0.0000 C 0 0\n -0.9137 2.9252 0.0000 C 0 0\n -0.9114 1.4244 0.0000 C 0 0\n 0.3890 0.6751 0.0000 C 0 0\n 0.3913 -0.8257 0.0000 C 0 0 1 0 0 0\n -0.9091 -1.5750 0.0000 N 0 0\n -2.2080 -0.8247 0.0000 R# 0 0\n 1.6917 -1.5750 0.0000 C 0 0\n 2.9898 -0.8234 0.0000 R# 0 0\n 1.6939 -3.0749 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 6\n 5 6 1 0\n 6 7 1 0\n 5 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 2 7 1 9 2\nM END\n> <Name>\nD-Norleucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Nle\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Homophenylalanine\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -2.0402 2.2498 0.0000 R# 0 0\n -0.7413 3.0001 0.0000 N 0 0\n 0.5591 2.2509 0.0000 C 0 0 2 0 0 0\n 0.5568 0.7500 0.0000 C 0 0\n -0.7436 0.0008 0.0000 C 0 0\n -0.7458 -1.5001 0.0000 C 0 0\n -2.0444 -2.2508 0.0000 C 0 0\n -2.0436 -3.7508 0.0000 C 0 0\n -0.7441 -4.5001 0.0000 C 0 0\n 0.5545 -3.7494 0.0000 C 0 0\n 0.5536 -2.2494 0.0000 C 0 0\n 1.8595 3.0001 0.0000 C 0 0\n 3.1577 2.2486 0.0000 R# 0 0\n 1.8618 4.5001 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 10 11 2 0\n 6 11 1 0\n 3 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 1 1 13 2\nM END\n> <Name>\nD-Homophenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-hPhe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-4-Hydroxyproline\n SciTegic09012117322D\n\n 10 10 0 0 1 0 999 V2000\n -1.9677 -2.9458 0.0000 O 0 0\n -1.2857 -1.6098 0.0000 C 0 0 1 0 0 0\n 0.1960 -1.3762 0.0000 C 0 0\n 0.4318 0.1051 0.0000 C 0 0 1 0 0 0\n -0.9043 0.7871 0.0000 N 0 0\n -1.1378 2.2688 0.0000 R# 0 0\n -1.9657 -0.2728 0.0000 C 0 0\n 1.7658 0.7871 0.0000 C 0 0\n 3.0246 -0.0286 0.0000 R# 0 0\n 1.8432 2.2851 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 4 3 1 0\n 4 5 1 0\n 5 6 1 0\n 5 7 1 0\n 2 7 1 0\n 4 8 1 1\n 8 9 1 0\n 8 10 2 0\nM RGP 2 6 1 9 2\nM END\n> <Name>\nD-4-Hydroxyproline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Hyp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Norvaline\n SciTegic09012117322D\n\n 9 8 0 0 1 0 999 V2000\n -1.1596 -3.3327 0.0000 C 0 0\n -1.1574 -1.8327 0.0000 C 0 0\n 0.1431 -1.0834 0.0000 C 0 0\n 0.1453 0.4174 0.0000 C 0 0 1 0 0 0\n -1.1550 1.1667 0.0000 N 0 0\n -2.4540 0.4164 0.0000 R# 0 0\n 1.4458 1.1667 0.0000 C 0 0\n 2.7439 0.4151 0.0000 R# 0 0\n 1.4480 2.6666 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 4 3 1 1\n 4 5 1 0\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 2 6 1 8 2\nM END\n> <Name>\nD-Norvaline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Nva\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Ornithine\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n -2.0065 -1.2951 0.0000 R# 0 0\n -0.7076 -2.0454 0.0000 N 0 0\n 0.5928 -1.2962 0.0000 C 0 0 2 0 0 0\n 0.5905 0.2047 0.0000 C 0 0\n -0.7099 0.9540 0.0000 C 0 0\n -0.7121 2.4548 0.0000 C 0 0\n -2.0125 3.2041 0.0000 N 0 0\n -2.0148 4.7041 0.0000 R# 0 0\n 1.8932 -2.0454 0.0000 C 0 0\n 3.1913 -1.2939 0.0000 R# 0 0\n 1.8955 -3.5454 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 3 9 1 0\n 9 10 1 0\n 9 11 2 0\nM RGP 3 1 1 8 3 10 2\nM END\n> <Name>\nD-Ornithine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Orn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nPyroglutamic acid\n SciTegic09012117322D\n\n 10 10 0 0 1 0 999 V2000\n -0.9899 -1.9779 0.0000 R# 0 0\n -0.7563 -0.4962 0.0000 N 0 0\n 0.5796 0.1858 0.0000 C 0 0 1 0 0 0\n 0.3439 1.6671 0.0000 C 0 0\n -1.1378 1.9007 0.0000 C 0 0\n -1.8178 0.5636 0.0000 C 0 0\n -3.2992 0.3279 0.0000 O 0 0\n 1.9137 -0.4962 0.0000 C 0 0\n 3.1725 0.3195 0.0000 R# 0 0\n 1.9912 -1.9942 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 2 6 1 0\n 6 7 2 0\n 3 8 1 1\n 8 9 1 0\n 8 10 2 0\nM RGP 2 1 1 9 2\nM END\n> <Name>\nPyroglutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPyr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Pyroglutamic acid\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n 3.1202 -2.0921 0.0000 R# 0 0\n 1.6281 -2.2462 0.0000 C 0 0\n 1.0161 -3.6157 0.0000 O 0 0\n 0.7500 -1.0323 0.0000 C 0 0 1 0 0 0\n 1.2135 0.3943 0.0000 C 0 0\n 0.0000 1.2760 0.0000 C 0 0\n -1.2135 0.3943 0.0000 C 0 0\n -2.6401 0.8578 0.0000 O 0 0\n -0.7500 -1.0323 0.0000 N 0 0\n 1 2 1 0\n 2 3 2 0\n 4 2 1 6\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 2 0\n 7 9 1 0\n 4 9 1 0\nM RGP 1 1 2\nM END\n> <Name>\nD-Pyroglutamic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Pyr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nE\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n3-Chloro-L-phenylalanine\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8032 -0.2585 0.0000 Cl 0 0\n -2.5064 -1.0123 0.0000 C 0 0\n -2.5107 -2.5123 0.0000 C 0 0\n -1.2139 -3.2661 0.0000 C 0 0\n 0.0873 -2.5199 0.0000 C 0 0\n 0.0917 -1.0199 0.0000 C 0 0\n 1.3921 -0.2706 0.0000 C 0 0\n 1.3944 1.2302 0.0000 C 0 0 2 0 0 0\n 0.0940 1.9795 0.0000 N 0 0\n -1.2049 1.2292 0.0000 R# 0 0\n 2.6948 1.9795 0.0000 C 0 0\n 3.9929 1.2279 0.0000 R# 0 0\n 2.6970 3.4795 0.0000 O 0 0\n -1.2051 -0.2661 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 6\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\n 6 14 2 0\n 2 14 1 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n3-Chloro-L-phenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe3Cl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n4-Chloro-L-phenylalanine\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8113 -3.0442 0.0000 Cl 0 0\n -2.5101 -2.2980 0.0000 C 0 0\n -1.2133 -3.0518 0.0000 C 0 0\n 0.0879 -2.3056 0.0000 C 0 0\n 0.0923 -0.8056 0.0000 C 0 0\n 1.3927 -0.0563 0.0000 C 0 0\n 1.3950 1.4445 0.0000 C 0 0 2 0 0 0\n 0.0946 2.1938 0.0000 N 0 0\n -1.2043 1.4435 0.0000 R# 0 0\n 2.6954 2.1938 0.0000 C 0 0\n 3.9936 1.4422 0.0000 R# 0 0\n 2.6977 3.6938 0.0000 O 0 0\n -1.2045 -0.0518 0.0000 C 0 0\n -2.5057 -0.7980 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n4-Chloro-L-phenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe4Cl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\np-Aminophenylalanine\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8113 -3.0442 0.0000 N 0 0\n -2.5101 -2.2980 0.0000 C 0 0\n -1.2133 -3.0518 0.0000 C 0 0\n 0.0879 -2.3056 0.0000 C 0 0\n 0.0923 -0.8056 0.0000 C 0 0\n 1.3927 -0.0563 0.0000 C 0 0\n 1.3950 1.4445 0.0000 C 0 0 2 0 0 0\n 0.0946 2.1938 0.0000 N 0 0\n -1.2043 1.4435 0.0000 R# 0 0\n 2.6954 2.1938 0.0000 C 0 0\n 3.9936 1.4422 0.0000 R# 0 0\n 2.6977 3.6938 0.0000 O 0 0\n -1.2045 -0.0518 0.0000 C 0 0\n -2.5057 -0.7980 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\np-Aminophenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe4NH\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nO-tert-Butyl-L-serine\n SciTegic09012117322D\n\n 12 11 0 0 1 0 999 V2000\n -2.1692 2.9989 0.0000 C 0 0\n -0.8695 2.2501 0.0000 C 0 0\n 0.4287 3.0016 0.0000 C 0 0\n -0.8710 3.7500 0.0000 C 0 0\n -0.8672 0.7492 0.0000 O 0 0\n 0.4332 -0.0001 0.0000 C 0 0\n 0.4355 -1.5009 0.0000 C 0 0 2 0 0 0\n -0.8649 -2.2502 0.0000 N 0 0\n -2.1638 -1.4999 0.0000 R# 0 0\n 1.7359 -2.2502 0.0000 C 0 0\n 3.0341 -1.4986 0.0000 R# 0 0\n 1.7382 -3.7501 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 1 0\n 5 6 1 0\n 7 6 1 1\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\nO-tert-Butyl-L-serine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nSertBu\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nO-Benzyl-L-tyrosine\n SciTegic07272112182D\n\n 21 22 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 1 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -2.6003 1.4977 0.0000 O 0 0\n -3.8990 0.7455 0.0000 C 0 0\n -5.2003 1.4932 0.0000 C 0 0\n -6.4994 0.7432 0.0000 C 0 0\n -7.7985 1.4932 0.0000 C 0 0\n -7.7985 2.9932 0.0000 C 0 0\n -6.4995 3.7432 0.0000 C 0 0\n -5.2004 2.9933 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 11 16 1 0\n 8 17 1 0\n 17 18 2 0\n 5 18 1 0\n 3 19 1 0\n 19 20 1 0\n 19 21 2 0\nM RGP 2 1 1 20 2\nM END\n> <Name>\nO-Benzyl-L-tyrosine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyr_Bn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-(1-naphthyl)-alanine\n SciTegic09012117322D\n\n 17 18 0 0 1 0 999 V2000\n -1.5241 2.2924 0.0000 R# 0 0\n -0.2254 3.0427 0.0000 N 0 0\n 1.0751 2.2934 0.0000 C 0 0 1 0 0 0\n 1.0728 0.7926 0.0000 C 0 0\n -0.2276 0.0433 0.0000 C 0 0\n -1.5244 0.7971 0.0000 C 0 0\n -2.8256 0.0509 0.0000 C 0 0\n -2.8300 -1.4491 0.0000 C 0 0\n -1.5331 -2.2028 0.0000 C 0 0\n -1.5375 -3.7029 0.0000 C 0 0\n -0.2407 -4.4567 0.0000 C 0 0\n 1.0606 -3.7104 0.0000 C 0 0\n 1.0649 -2.2105 0.0000 C 0 0\n -0.2319 -1.4567 0.0000 C 0 0\n 2.3755 3.0427 0.0000 C 0 0\n 3.6736 2.2912 0.0000 R# 0 0\n 2.3778 4.5427 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 5 14 1 0\n 9 14 1 0\n 3 15 1 0\n 15 16 1 0\n 15 17 2 0\nM RGP 2 1 1 16 2\nM END\n> <Name>\n3-(1-naphthyl)-alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n1Nal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-epsilon-tert-Boc-L-lysine\n SciTegic09012117322D\n\n 18 17 0 0 1 0 999 V2000\n -2.8247 -6.4583 0.0000 C 0 0\n -2.8225 -4.9583 0.0000 C 0 0\n -4.1206 -4.2068 0.0000 C 0 0\n -4.1225 -5.7065 0.0000 C 0 0\n -1.5221 -4.2090 0.0000 O 0 0\n -1.5198 -2.7082 0.0000 C 0 0\n -2.8179 -1.9567 0.0000 O 0 0\n -0.2194 -1.9589 0.0000 N 0 0\n -0.2171 -0.4581 0.0000 C 0 0\n 1.0833 0.2911 0.0000 C 0 0\n 1.0856 1.7919 0.0000 C 0 0\n 2.3860 2.5412 0.0000 C 0 0\n 2.3883 4.0420 0.0000 C 0 0 2 0 0 0\n 1.0879 4.7913 0.0000 N 0 0\n -0.2110 4.0410 0.0000 R# 0 0\n 3.6887 4.7913 0.0000 C 0 0\n 4.9868 4.0397 0.0000 R# 0 0\n 3.6910 6.2913 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 1 0\n 5 6 1 0\n 6 7 2 0\n 6 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 13 12 1 6\n 13 14 1 0\n 14 15 1 0\n 13 16 1 0\n 16 17 1 0\n 16 18 2 0\nM RGP 2 15 1 17 2\nM END\n> <Name>\nN-epsilon-tert-Boc-L-lysine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLysBoc\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nL-allo-Threonine\n SciTegic09012117322D\n\n 9 8 0 0 1 0 999 V2000\n 1.1521 2.0015 0.0000 C 0 0\n -0.1460 1.2499 0.0000 C 0 0 2 0 0 0\n -1.4457 1.9988 0.0000 O 0 0\n -0.1437 -0.2509 0.0000 C 0 0 2 0 0 0\n -1.4441 -1.0002 0.0000 N 0 0\n -2.7430 -0.2499 0.0000 R# 0 0\n 1.1567 -1.0002 0.0000 C 0 0\n 2.4548 -0.2487 0.0000 R# 0 0\n 1.1589 -2.5001 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 2 4 1 0\n 4 5 1 1\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 2 6 1 8 2\nM END\n> <Name>\nL-allo-Threonine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\naThr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-3-naphthylalanine\n SciTegic07272112182D\n\n 17 18 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 2 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -2.5981 1.5000 0.0000 C 0 0\n -3.8971 0.7500 0.0000 C 0 0\n -3.8971 -0.7500 0.0000 C 0 0\n -2.5981 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 8 13 1 0\n 13 14 2 0\n 5 14 1 0\n 3 15 1 0\n 15 16 1 0\n 15 17 2 0\nM RGP 2 1 1 16 2\nM END\n> <Name>\nD-3-naphthylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-2Nal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-3-thienylalanine\n SciTegic09012117322D\n\n 12 12 0 0 1 0 999 V2000\n -1.7045 -1.0135 0.0000 R# 0 0\n -0.4057 -1.7638 0.0000 N 0 0\n 0.8947 -1.0145 0.0000 C 0 0 2 0 0 0\n 0.8925 0.4863 0.0000 C 0 0\n -0.4056 1.2343 0.0000 C 0 0\n -0.5668 2.7256 0.0000 C 0 0\n -2.0349 3.0333 0.0000 C 0 0\n -2.7811 1.7320 0.0000 C 0 0\n -1.7742 0.6202 0.0000 S 0 0\n 2.1951 -1.7638 0.0000 C 0 0\n 3.4933 -1.0124 0.0000 R# 0 0\n 2.1974 -3.2638 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 5 9 1 0\n 3 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 1 1 11 2\nM END\n> <Name>\nD-3-thienylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-2Thi\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-allo-4-hydroxyproline\n SciTegic09012117322D\n\n 10 10 0 0 1 0 999 V2000\n -1.9677 -2.9458 0.0000 O 0 0\n -1.2857 -1.6098 0.0000 C 0 0 2 0 0 0\n 0.1960 -1.3762 0.0000 C 0 0\n 0.4318 0.1051 0.0000 C 0 0 1 0 0 0\n -0.9043 0.7871 0.0000 N 0 0\n -1.1378 2.2688 0.0000 R# 0 0\n -1.9657 -0.2728 0.0000 C 0 0\n 1.7658 0.7871 0.0000 C 0 0\n 3.0246 -0.0286 0.0000 R# 0 0\n 1.8432 2.2851 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 4 3 1 0\n 4 5 1 0\n 5 6 1 0\n 5 7 1 0\n 2 7 1 0\n 4 8 1 1\n 8 9 1 0\n 8 10 2 0\nM RGP 2 6 1 9 2\nM END\n> <Name>\nD-allo-4-hydroxyproline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-aHyp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-allo-Isoleucine\n SciTegic09012117322D\n\n 10 9 0 0 1 0 999 V2000\n -1.3038 -3.1492 0.0000 C 0 0\n -1.3015 -1.6492 0.0000 C 0 0\n -0.0011 -0.8999 0.0000 C 0 0 2 0 0 0\n 1.2971 -1.6515 0.0000 C 0 0\n 0.0012 0.6009 0.0000 C 0 0 1 0 0 0\n -1.2992 1.3502 0.0000 N 0 0\n -2.5981 0.5999 0.0000 R# 0 0\n 1.3016 1.3502 0.0000 C 0 0\n 2.5998 0.5986 0.0000 R# 0 0\n 1.3039 2.8501 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 0\n 3 4 1 1\n 3 5 1 0\n 5 6 1 1\n 6 7 1 0\n 5 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 2 7 1 9 2\nM END\n> <Name>\nD-allo-Isoleucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-aIle\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nI\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-2-phenylglycine\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -2.7098 1.1911 0.0000 R# 0 0\n -1.4094 1.9388 0.0000 N 0 0\n -0.1105 1.1868 0.0000 C 0 0 1 0 0 0\n 1.1884 1.9388 0.0000 C 0 0\n 2.4881 1.1899 0.0000 R# 0 0\n 1.1875 3.4388 0.0000 O 0 0\n -0.1097 -0.3140 0.0000 C 0 0\n -1.4067 -1.0674 0.0000 C 0 0\n -1.4028 -2.5674 0.0000 C 0 0\n -0.1018 -3.3140 0.0000 C 0 0\n 1.1953 -2.5606 0.0000 C 0 0\n 1.1913 -1.0606 0.0000 C 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\n 3 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 7 12 1 0\nM RGP 2 1 1 5 2\nM END\n> <Name>\nD-2-phenylglycine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Phg\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nO-tert-Butyl-D-serine\n SciTegic09012117322D\n\n 12 11 0 0 1 0 999 V2000\n -2.1692 2.9989 0.0000 C 0 0\n -0.8695 2.2501 0.0000 C 0 0\n 0.4287 3.0016 0.0000 C 0 0\n -0.8710 3.7500 0.0000 C 0 0\n -0.8672 0.7492 0.0000 O 0 0\n 0.4332 -0.0001 0.0000 C 0 0\n 0.4355 -1.5009 0.0000 C 0 0 1 0 0 0\n -0.8649 -2.2502 0.0000 N 0 0\n -2.1638 -1.4999 0.0000 R# 0 0\n 1.7359 -2.2502 0.0000 C 0 0\n 3.0341 -1.4986 0.0000 R# 0 0\n 1.7382 -3.7501 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 1 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\nO-tert-Butyl-D-serine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDSertB\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\np-Methylphenylalanine\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8113 -3.0442 0.0000 C 0 0\n -2.5101 -2.2980 0.0000 C 0 0\n -1.2133 -3.0518 0.0000 C 0 0\n 0.0879 -2.3056 0.0000 C 0 0\n 0.0923 -0.8056 0.0000 C 0 0\n 1.3927 -0.0563 0.0000 C 0 0\n 1.3950 1.4445 0.0000 C 0 0 2 0 0 0\n 0.0946 2.1938 0.0000 N 0 0\n -1.2043 1.4435 0.0000 R# 0 0\n 2.6954 2.1938 0.0000 C 0 0\n 3.9936 1.4422 0.0000 R# 0 0\n 2.6977 3.6938 0.0000 O 0 0\n -1.2045 -0.0518 0.0000 C 0 0\n -2.5057 -0.7980 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\np-Methylphenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe4Me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nO-Benzyl-L-serine\n SciTegic09012117322D\n\n 15 15 0 0 1 0 999 V2000\n 1.2919 -5.2492 0.0000 R# 0 0\n 2.5886 -6.0033 0.0000 N 0 0\n 3.8912 -5.2578 0.0000 C 0 0 1 0 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 2.5951 -3.0039 0.0000 O 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 5.1894 -6.0109 0.0000 C 0 0\n 6.4897 -5.2632 0.0000 R# 0 0\n 5.1873 -7.5109 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 7 12 1 0\n 3 13 1 0\n 13 14 1 0\n 13 15 2 0\nM RGP 2 1 1 14 2\nM END\n> <Name>\nO-Benzyl-L-serine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nSer_Bn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nO-tert-Butyl-L-tyrosine\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -5.1332 -2.6056 0.0000 C 0 0\n -3.8304 -1.8621 0.0000 C 0 0\n -3.8234 -0.3621 0.0000 C 0 0\n -5.1258 -1.1058 0.0000 C 0 0\n -2.5340 -2.6181 0.0000 O 0 0\n -1.2305 -1.8742 0.0000 C 0 0\n 0.0664 -2.6280 0.0000 C 0 0\n 1.3676 -1.8818 0.0000 C 0 0\n 1.3720 -0.3818 0.0000 C 0 0\n 2.6724 0.3675 0.0000 C 0 0\n 2.6747 1.8683 0.0000 C 0 0 2 0 0 0\n 1.3742 2.6176 0.0000 N 0 0\n 0.0754 1.8673 0.0000 R# 0 0\n 3.9751 2.6176 0.0000 C 0 0\n 5.2732 1.8660 0.0000 R# 0 0\n 3.9773 4.1176 0.0000 O 0 0\n 0.0752 0.3720 0.0000 C 0 0\n -1.2261 -0.3742 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 11 10 1 6\n 11 12 1 0\n 12 13 1 0\n 11 14 1 0\n 14 15 1 0\n 14 16 2 0\n 9 17 1 0\n 17 18 2 0\n 6 18 1 0\nM RGP 2 13 1 15 2\nM END\n> <Name>\nO-tert-Butyl-L-tyrosine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyrtBu\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nL-allo-4-hydroxyproline\n SciTegic09012117322D\n\n 10 10 0 0 1 0 999 V2000\n -1.9677 -2.9458 0.0000 O 0 0\n -1.2857 -1.6098 0.0000 C 0 0 1 0 0 0\n 0.1960 -1.3762 0.0000 C 0 0\n 0.4318 0.1051 0.0000 C 0 0 2 0 0 0\n -0.9043 0.7871 0.0000 N 0 0\n -1.1378 2.2688 0.0000 R# 0 0\n -1.9657 -0.2728 0.0000 C 0 0\n 1.7658 0.7871 0.0000 C 0 0\n 3.0246 -0.0286 0.0000 R# 0 0\n 1.8432 2.2851 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 4 3 1 0\n 4 5 1 0\n 5 6 1 0\n 5 7 1 0\n 2 7 1 0\n 4 8 1 6\n 8 9 1 0\n 8 10 2 0\nM RGP 2 6 1 9 2\nM END\n> <Name>\nL-allo-4-hydroxyproline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\naHyp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nHomophenylalanine\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -2.0402 2.2498 0.0000 R# 0 0\n -0.7413 3.0001 0.0000 N 0 0\n 0.5591 2.2509 0.0000 C 0 0 1 0 0 0\n 0.5568 0.7500 0.0000 C 0 0\n -0.7436 0.0008 0.0000 C 0 0\n -0.7458 -1.5001 0.0000 C 0 0\n -2.0444 -2.2508 0.0000 C 0 0\n -2.0436 -3.7508 0.0000 C 0 0\n -0.7441 -4.5001 0.0000 C 0 0\n 0.5545 -3.7494 0.0000 C 0 0\n 0.5536 -2.2494 0.0000 C 0 0\n 1.8595 3.0001 0.0000 C 0 0\n 3.1577 2.2486 0.0000 R# 0 0\n 1.8618 4.5001 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 10 11 2 0\n 6 11 1 0\n 3 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 1 1 13 2\nM END\n> <Name>\nHomophenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nhPhe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-3-(1-naphthyl)-alanine\n SciTegic09012117322D\n\n 17 18 0 0 1 0 999 V2000\n -1.5241 2.2924 0.0000 R# 0 0\n -0.2254 3.0427 0.0000 N 0 0\n 1.0751 2.2934 0.0000 C 0 0 2 0 0 0\n 1.0728 0.7926 0.0000 C 0 0\n -0.2276 0.0433 0.0000 C 0 0\n -1.5244 0.7971 0.0000 C 0 0\n -2.8256 0.0509 0.0000 C 0 0\n -2.8300 -1.4491 0.0000 C 0 0\n -1.5331 -2.2028 0.0000 C 0 0\n -1.5375 -3.7029 0.0000 C 0 0\n -0.2407 -4.4567 0.0000 C 0 0\n 1.0606 -3.7104 0.0000 C 0 0\n 1.0649 -2.2105 0.0000 C 0 0\n -0.2319 -1.4567 0.0000 C 0 0\n 2.3755 3.0427 0.0000 C 0 0\n 3.6736 2.2912 0.0000 R# 0 0\n 2.3778 4.5427 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 5 14 1 0\n 9 14 1 0\n 3 15 1 0\n 15 16 1 0\n 15 17 2 0\nM RGP 2 1 1 16 2\nM END\n> <Name>\nD-3-(1-naphthyl)-alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-1Nal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-allo-Threonine\n SciTegic09012117322D\n\n 9 8 0 0 1 0 999 V2000\n 1.1521 2.0015 0.0000 C 0 0\n -0.1460 1.2499 0.0000 C 0 0 1 0 0 0\n -1.4457 1.9988 0.0000 O 0 0\n -0.1437 -0.2509 0.0000 C 0 0 1 0 0 0\n -1.4441 -1.0002 0.0000 N 0 0\n -2.7430 -0.2499 0.0000 R# 0 0\n 1.1567 -1.0002 0.0000 C 0 0\n 2.4548 -0.2487 0.0000 R# 0 0\n 1.1589 -2.5001 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 2 4 1 0\n 4 5 1 6\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 2 6 1 8 2\nM END\n> <Name>\nD-allo-Threonine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-aThr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-2-Amino-3-cyclohexyl-propionic acid\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 2 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 5 10 1 0\n 3 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\nD-2-Amino-3-cyclohexyl-propionic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Cha\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-penicillamine (3-mercaptovaline)\n SciTegic07272112182D\n\n 11 10 0 0 1 0 999 V2000\n 1.2973 1.4333 0.0000 C 0 0\n -0.0008 0.6818 0.0000 C 0 0\n -0.0024 2.1818 0.0000 C 0 0\n -1.3012 1.4310 0.0000 S 0 0\n -1.3035 2.9310 0.0000 R# 0 0\n 0.0014 -0.8191 0.0000 C 0 0 1 0 0 0\n -1.2990 -1.5683 0.0000 N 0 0\n -2.5978 -0.8180 0.0000 R# 0 0\n 1.3018 -1.5683 0.0000 C 0 0\n 2.6000 -0.8168 0.0000 R# 0 0\n 1.3041 -3.0683 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 6 2 1 0\n 6 7 1 6\n 7 8 1 0\n 6 9 1 0\n 9 10 1 0\n 9 11 2 0\nM RGP 3 5 3 8 1 10 2\nM END\n> <Name>\nD-penicillamine (3-mercaptovaline)\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Pen\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\n4-Chloro-D-phenylalanine\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8113 -3.0442 0.0000 Cl 0 0\n -2.5101 -2.2980 0.0000 C 0 0\n -1.2133 -3.0518 0.0000 C 0 0\n 0.0879 -2.3056 0.0000 C 0 0\n 0.0923 -0.8056 0.0000 C 0 0\n 1.3927 -0.0563 0.0000 C 0 0\n 1.3950 1.4445 0.0000 C 0 0 1 0 0 0\n 0.0946 2.1938 0.0000 N 0 0\n -1.2043 1.4435 0.0000 R# 0 0\n 2.6954 2.1938 0.0000 C 0 0\n 3.9936 1.4422 0.0000 R# 0 0\n 2.6977 3.6938 0.0000 O 0 0\n -1.2045 -0.0518 0.0000 C 0 0\n -2.5057 -0.7980 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 1\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n4-Chloro-D-phenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDPhe4C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nO-Benzyl-D-serine\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n 1.2919 -5.2492 0.0000 R# 0 0\n 2.5886 -6.0033 0.0000 N 0 0\n 3.8912 -5.2578 0.0000 C 0 0 2 0 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 2.5951 -3.0039 0.0000 O 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 5.1894 -6.0109 0.0000 C 0 0\n 6.4897 -5.2632 0.0000 R# 0 0\n 5.1873 -7.5109 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 7 12 1 0\n 3 13 1 0\n 13 14 1 0\n 13 15 2 0\nM RGP 2 1 1 14 2\nM END\n> <Name>\nO-Benzyl-D-serine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDSerBn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nMesylate\n SciTegic07272112182D\n\n 5 4 0 0 0 0 999 V2000\n -0.2000 0.7500 0.0000 C 0 0\n 1.3000 0.7500 0.0000 S 0 0\n 2.8000 0.7500 0.0000 R# 0 0\n 2.0496 -0.5493 0.0000 O 0 0\n 2.0496 2.0493 0.0000 O 0 0\n 1 2 1 0\n 2 4 2 0\n 2 5 2 0\n 2 3 1 0\nM RGP 1 3 2\nM END\n> <Name>\nMesylate\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nMsO\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nPerhydroindolic acid\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n -0.2550 2.6034 0.0000 R# 0 0\n -0.0213 1.1217 0.0000 N 0 0\n -1.0820 0.0623 0.0000 C 0 0 1 0 0 0\n -2.5799 0.1419 0.0000 C 0 0\n -3.3978 -1.1155 0.0000 C 0 0\n -2.7178 -2.4526 0.0000 C 0 0\n -1.2199 -2.5322 0.0000 C 0 0\n -0.4020 -1.2748 0.0000 C 0 0 1 0 0 0\n 1.0789 -1.0416 0.0000 C 0 0\n 1.3147 0.4398 0.0000 C 0 0 1 0 0 0\n 2.6487 1.1217 0.0000 C 0 0\n 3.9075 0.3061 0.0000 R# 0 0\n 2.7262 2.6197 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 0\n 3 4 1 6\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 6\n 3 8 1 0\n 8 9 1 0\n 10 9 1 0\n 10 2 1 0\n 10 11 1 6\n 11 12 1 0\n 11 13 2 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\nPerhydroindolic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOic3aS\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nPipecolic acid\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n -0.9064 2.1749 0.0000 R# 0 0\n -0.9082 0.6749 0.0000 N 0 0\n -2.2081 -0.0735 0.0000 C 0 0\n -2.2099 -1.5735 0.0000 C 0 0\n -0.9118 -2.3251 0.0000 C 0 0\n 0.3882 -1.5766 0.0000 C 0 0\n 0.3900 -0.0766 0.0000 C 0 0 1 0 0 0\n 1.6891 0.6749 0.0000 C 0 0\n 2.9885 -0.0744 0.0000 R# 0 0\n 1.6887 2.1749 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 7 6 1 0\n 7 2 1 0\n 7 8 1 6\n 8 9 1 0\n 8 10 2 0\nM RGP 2 1 1 9 2\nM END\n> <Name>\nPipecolic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPip\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-(2-pyridyl)-alanine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 1 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 3 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\n3-(2-pyridyl)-alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n3Pal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-(4-Pyridyl)-alanine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 1 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 3 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\n3-(4-Pyridyl)-alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n4Pal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nAlpha-cyclohexylglycine\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -2.7098 1.1911 0.0000 R# 0 0\n -1.4094 1.9388 0.0000 N 0 0\n -0.1105 1.1868 0.0000 C 0 0 1 0 0 0\n -0.1097 -0.3140 0.0000 C 0 0\n -1.4067 -1.0674 0.0000 C 0 0\n -1.4028 -2.5674 0.0000 C 0 0\n -0.1018 -3.3140 0.0000 C 0 0\n 1.1953 -2.5606 0.0000 C 0 0\n 1.1913 -1.0606 0.0000 C 0 0\n 1.1884 1.9388 0.0000 C 0 0\n 2.4881 1.1899 0.0000 R# 0 0\n 1.1875 3.4388 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 4 9 1 0\n 3 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 1 1 11 2\nM END\n> <Name>\nAlpha-cyclohexylglycine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nChg\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-3-(2-pyridyl)-alanine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 2 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 3 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\nD-3-(2-pyridyl)-alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-3Pal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Isovaline\n SciTegic09012117322D\n\n 9 8 0 0 1 0 999 V2000\n -2.0770 1.3017 0.0000 C 0 0\n -0.5770 1.3004 0.0000 C 0 0\n 0.1731 0.0004 0.0000 C 0 0 1 0 0 0\n -0.5777 -1.2982 0.0000 C 0 0\n -1.3569 -0.0009 0.0000 N 0 0\n -2.1066 -1.3001 0.0000 R# 0 0\n 1.6739 -0.0009 0.0000 C 0 0\n 2.4247 1.2977 0.0000 R# 0 0\n 2.4235 -1.3001 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 0\n 3 4 1 1\n 3 5 1 0\n 5 6 1 0\n 3 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 2 6 1 8 2\nM END\n> <Name>\nD-Isovaline\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDaMeAb\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Alpha-cyclohexylglycine\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -2.7098 1.1911 0.0000 R# 0 0\n -1.4094 1.9388 0.0000 N 0 0\n -0.1105 1.1868 0.0000 C 0 0 2 0 0 0\n -0.1097 -0.3140 0.0000 C 0 0\n -1.4067 -1.0674 0.0000 C 0 0\n -1.4028 -2.5674 0.0000 C 0 0\n -0.1018 -3.3140 0.0000 C 0 0\n 1.1953 -2.5606 0.0000 C 0 0\n 1.1913 -1.0606 0.0000 C 0 0\n 1.1884 1.9388 0.0000 C 0 0\n 2.4881 1.1899 0.0000 R# 0 0\n 1.1875 3.4388 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 4 9 1 0\n 3 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 1 1 11 2\nM END\n> <Name>\nD-Alpha-cyclohexylglycine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Chg\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-Citrullin\n SciTegic09012117322D\n\n 13 12 0 0 1 0 999 V2000\n -0.4064 4.6171 0.0000 N 0 0\n -1.7046 3.8656 0.0000 C 0 0\n -3.0043 4.6145 0.0000 O 0 0\n -1.7024 2.3648 0.0000 N 0 0\n -0.4020 1.6155 0.0000 C 0 0\n -0.3998 0.1146 0.0000 C 0 0\n 0.9006 -0.6347 0.0000 C 0 0\n 0.9028 -2.1354 0.0000 C 0 0 1 0 0 0\n -0.3975 -2.8848 0.0000 N 0 0\n -1.6965 -2.1344 0.0000 R# 0 0\n 2.2032 -2.8848 0.0000 C 0 0\n 3.5014 -2.1332 0.0000 R# 0 0\n 2.2054 -4.3848 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 6\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\nD-Citrullin\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Cit\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-2,4-diaminobutanoic acid\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n -2.2080 -0.8247 0.0000 R# 0 0\n -0.9092 -1.5750 0.0000 N 0 0\n 0.3913 -0.8257 0.0000 C 0 0 2 0 0 0\n 0.3890 0.6751 0.0000 C 0 0\n -0.9114 1.4244 0.0000 C 0 0\n -0.9137 2.9252 0.0000 N 0 0\n -2.2133 3.6741 0.0000 R# 0 0\n 1.6917 -1.5750 0.0000 C 0 0\n 2.9898 -0.8235 0.0000 R# 0 0\n 1.6939 -3.0750 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 3 1 1 7 3 9 2\nM END\n> <Name>\nD-2,4-diaminobutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Dab\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nD-Pipecolic acid\n SciTegic07272112182D\n\n 10 10 0 0 1 0 999 V2000\n -0.9064 2.1749 0.0000 R# 0 0\n -0.9082 0.6749 0.0000 N 0 0\n -2.2081 -0.0735 0.0000 C 0 0\n -2.2099 -1.5735 0.0000 C 0 0\n -0.9118 -2.3251 0.0000 C 0 0\n 0.3882 -1.5766 0.0000 C 0 0\n 0.3900 -0.0766 0.0000 C 0 0 2 0 0 0\n 1.6891 0.6749 0.0000 C 0 0\n 2.9885 -0.0744 0.0000 R# 0 0\n 1.6887 2.1749 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 7 6 1 0\n 7 2 1 0\n 7 8 1 1\n 8 9 1 0\n 8 10 2 0\nM RGP 2 1 1 9 2\nM END\n> <Name>\nD-Pipecolic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Pip\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -0.1815 3.2137 0.0000 R# 0 0\n -0.1833 1.7137 0.0000 N 0 0\n -1.4832 0.9652 0.0000 C 0 0\n -1.4850 -0.5348 0.0000 C 0 0\n -2.7849 -1.2832 0.0000 C 0 0\n -2.7867 -2.7832 0.0000 C 0 0\n -1.4886 -3.5348 0.0000 C 0 0\n -0.1886 -2.7863 0.0000 C 0 0\n -0.1869 -1.2863 0.0000 C 0 0\n 1.1131 -0.5379 0.0000 C 0 0\n 1.1148 0.9621 0.0000 C 0 0 2 0 0 0\n 2.4140 1.7137 0.0000 C 0 0\n 3.7134 0.9644 0.0000 R# 0 0\n 2.4136 3.2137 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\n 9 10 1 0\n 11 10 1 0\n 11 2 1 0\n 11 12 1 1\n 12 13 1 0\n 12 14 2 0\nM RGP 2 1 1 13 2\nM END\n> <Name>\nD-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Tic\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-3-(2-Pyridyl)-alanine\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 2 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 N 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 3 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\nD-3-(2-Pyridyl)-alanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-2Pal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-2-aminobutanoic acid\n SciTegic09012117322D\n\n 8 7 0 0 1 0 999 V2000\n -1.3017 2.2489 0.0000 C 0 0\n -0.0020 1.5001 0.0000 C 0 0\n 0.0003 -0.0008 0.0000 C 0 0 1 0 0 0\n -1.3001 -0.7500 0.0000 N 0 0\n -2.5990 0.0002 0.0000 R# 0 0\n 1.3007 -0.7500 0.0000 C 0 0\n 2.5988 0.0015 0.0000 R# 0 0\n 1.3029 -2.2500 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 3 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 2 5 1 7 2\nM END\n> <Name>\nD-2-aminobutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Abu\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nD-2,3-diaminopropanoic acid\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n -2.4540 -0.4164 0.0000 R# 0 0\n -1.1551 -1.1667 0.0000 N 0 0\n 0.1453 -0.4174 0.0000 C 0 0 2 0 0 0\n 0.1431 1.0834 0.0000 C 0 0\n -1.1573 1.8327 0.0000 N 0 0\n -1.1596 3.3327 0.0000 R# 0 0\n 1.4457 -1.1667 0.0000 C 0 0\n 2.7439 -0.4151 0.0000 R# 0 0\n 1.4480 -2.6667 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 3 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 3 1 1 6 3 8 2\nM END\n> <Name>\nD-2,3-diaminopropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Dap\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]H\n\n$$$$\nCarboxybenzyl\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 2.5951 -3.0039 0.0000 O 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 10 11 2 0\n 6 11 1 0\nM RGP 1 1 2\nM END\n> <Name>\nCarboxybenzyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nCbz\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nC-Terminal ethyl\n SciTegic07272112182D\n\n 3 2 0 0 0 0 999 V2000\n 4.8501 1.2990 0.0000 C 0 0\n 4.0993 0.0004 0.0000 C 0 0\n 2.5993 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\nM RGP 1 3 1\nM END\n> <Name>\nC-Terminal ethyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n-Et\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nEthanamine\n SciTegic07272112182D\n\n 4 3 0 0 0 0 999 V2000\n 7.6505 -0.5497 0.0000 C 0 0\n 6.1505 -0.5497 0.0000 C 0 0\n 5.3993 0.7496 0.0000 N 0 0\n 3.8993 0.7496 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\nM RGP 1 4 1\nM END\n> <Name>\nEthanamine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNHEt\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nEthanol\n SciTegic07272112182D\n\n 4 3 0 0 0 0 999 V2000\n 7.6505 -0.5497 0.0000 C 0 0\n 6.1505 -0.5497 0.0000 C 0 0\n 5.3993 0.7496 0.0000 O 0 0\n 3.8993 0.7496 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\nM RGP 1 4 1\nM END\n> <Name>\nEthanol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOEt\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nTosyl\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n -5.5976 6.6982 0.0000 C 0 0\n -4.8480 5.3989 0.0000 C 0 0\n -5.5984 4.1001 0.0000 C 0 0\n -4.8488 2.8009 0.0000 C 0 0\n -3.3488 2.8004 0.0000 C 0 0\n -2.5984 4.0992 0.0000 C 0 0\n -3.3480 5.3985 0.0000 C 0 0\n -2.5988 1.5004 0.0000 S 0 0\n -1.0988 1.5004 0.0000 R# 0 0\n -3.3484 0.2011 0.0000 O 0 0\n -1.8486 0.2015 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 2 7 1 0\n 5 8 1 0\n 8 9 1 0\n 8 10 2 0\n 8 11 2 0\nM RGP 1 9 2\nM END\n> <Name>\nTosyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTos\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n(4S)-1,3-thiazolidine-4-carboxylic acid\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n -1.3565 1.9415 0.0000 R# 0 0\n -1.1229 0.4598 0.0000 N 0 0\n -2.1844 -0.6001 0.0000 C 0 0\n -1.5044 -1.9371 0.0000 S 0 0\n -0.0227 -1.7036 0.0000 C 0 0\n 0.2131 -0.2222 0.0000 C 0 0 2 0 0 0\n 1.5471 0.4598 0.0000 C 0 0\n 2.8060 -0.3559 0.0000 R# 0 0\n 1.6246 1.9578 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 6 5 1 0\n 6 2 1 0\n 6 7 1 1\n 7 8 1 0\n 7 9 2 0\nM RGP 2 1 1 8 2\nM END\n> <Name>\n(4S)-1,3-thiazolidine-4-carboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Thz\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nDeamino-Cysteine\n SciTegic07272112182D\n\n 6 5 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 S 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 3.9000 2.2500 0.0000 R# 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\nM RGP 1 5 2\nM END\n> <Name>\nDeamino-Cysteine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDACys\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n4-aminobutanoic acid\n SciTegic07272112182D\n\n 8 7 0 0 0 0 999 V2000\n 14.5529 1.2997 0.0000 O 0 0\n 13.8033 2.5990 0.0000 C 0 0\n 14.5542 3.8975 0.0000 O 0 0\n 12.3025 2.5990 0.0000 C 0 0\n 11.5513 1.2997 0.0000 C 0 0\n 10.0505 1.2997 0.0000 C 0 0\n 9.2992 0.0004 0.0000 N 0 0\n 7.7992 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\nM RGP 1 8 1\nM END\n> <Name>\n4-aminobutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDADab\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-cyanoacetic acid\n SciTegic07272112182D\n\n 6 5 0 0 0 0 999 V2000\n 2.8000 0.7500 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 0.5504 2.0493 0.0000 O 0 0\n 0.5500 -0.5500 0.0000 C 0 0\n 1.3000 -1.8500 0.0000 C 0 0\n 2.0496 -3.1493 0.0000 N 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 3 0\nM RGP 1 1 2\nM END\n> <Name>\n2-cyanoacetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAGlyC\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-cyclopentylacetic acid\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 2.5157 -3.6164 0.0000 R# 0 0\n 1.0157 -3.6164 0.0000 C 0 0\n 0.2661 -2.3171 0.0000 O 0 0\n 0.2657 -4.9164 0.0000 C 0 0\n 1.0144 -6.2142 0.0000 C 0 0\n 0.4067 -7.5856 0.0000 C 0 0\n 1.5232 -8.5873 0.0000 C 0 0\n 2.8209 -7.8350 0.0000 C 0 0\n 2.5065 -6.3683 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 5 9 1 0\nM RGP 1 1 2\nM END\n> <Name>\n2-cyclopentylacetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAGlyP\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-hydroxyacetic acid\n SciTegic07272112182D\n\n 6 5 0 0 0 0 999 V2000\n 9.7009 0.0004 0.0000 O 0 0\n 8.9513 1.2997 0.0000 C 0 0\n 9.7021 2.5983 0.0000 O 0 0\n 7.4505 1.2997 0.0000 C 0 0\n 6.6992 0.0004 0.0000 O 0 0\n 5.1992 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\nM RGP 1 6 1\nM END\n> <Name>\n2-hydroxyacetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAGlyO\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-(thiophen-2-yl)acetic acid\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 2.5157 -3.6164 0.0000 R# 0 0\n 1.0157 -3.6164 0.0000 C 0 0\n 0.2661 -2.3171 0.0000 O 0 0\n 0.2657 -4.9164 0.0000 C 0 0\n 1.0144 -6.2142 0.0000 C 0 0\n 0.4067 -7.5856 0.0000 C 0 0\n 1.5232 -8.5873 0.0000 C 0 0\n 2.8209 -7.8350 0.0000 C 0 0\n 2.5065 -6.3683 0.0000 S 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 5 9 1 0\nM RGP 1 1 2\nM END\n> <Name>\n2-(thiophen-2-yl)acetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAGlyT\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n(2R)-2-amino-3-(1-formyl-1H-indol-3-yl)propanoic acid\n SciTegic07272112182D\n\n 18 19 0 0 1 0 999 V2000\n -0.9963 2.1750 0.0000 R# 0 0\n 0.3026 2.9253 0.0000 N 0 0\n 1.6030 2.1761 0.0000 C 0 0 2 0 0 0\n 1.6007 0.6752 0.0000 C 0 0\n 0.3026 -0.0728 0.0000 C 0 0\n -1.0661 0.5411 0.0000 C 0 0\n -2.0728 -0.5709 0.0000 N 0 0\n -3.5621 -0.4074 0.0000 C 0 0\n -4.1668 0.9654 0.0000 O 0 0\n -1.3266 -1.8711 0.0000 C 0 0\n -1.7940 -3.2964 0.0000 C 0 0\n -0.7933 -4.4139 0.0000 C 0 0\n 0.6747 -4.1061 0.0000 C 0 0\n 1.1422 -2.6808 0.0000 C 0 0\n 0.1415 -1.5633 0.0000 C 0 0\n 2.9034 2.9253 0.0000 C 0 0\n 4.2016 2.1738 0.0000 R# 0 0\n 2.9057 4.4253 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 1 0\n 8 9 2 0\n 7 10 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 15 2 0\n 5 15 1 0\n 10 15 1 0\n 3 16 1 0\n 16 17 1 0\n 16 18 2 0\nM RGP 2 1 1 17 2\nM END\n> <Name>\n(2R)-2-amino-3-(1-formyl-1H-indol-3-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDTrpFo\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nW\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-sulfanylacetic acid\n SciTegic07272112182D\n\n 5 4 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 S 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 2.6000 -1.5000 0.0000 R# 0 0\n 3.8993 0.7496 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 3 5 2 0\nM RGP 1 4 2\nM END\n> <Name>\n2-sulfanylacetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDANcy\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nDeamino-Phenylalanine\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 0.3451 -1.7039 0.0000 O 0 0\n 1.8451 -1.7039 0.0000 C 0 0\n 2.5947 -0.4046 0.0000 O 0 0\n 2.5951 -3.0039 0.0000 C 0 0\n 4.0951 -3.0039 0.0000 R# 0 0\n 1.8451 -4.3039 0.0000 C 0 0\n 2.5951 -5.6039 0.0000 C 0 0\n 1.8474 -6.9042 0.0000 C 0 0\n 2.5997 -8.2020 0.0000 C 0 0\n 4.0997 -8.1994 0.0000 C 0 0\n 4.8474 -6.8990 0.0000 C 0 0\n 4.0951 -5.6013 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 4 6 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 7 12 1 0\nM RGP 1 5 2\nM END\n> <Name>\nDeamino-Phenylalanine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAPhe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-(3,5-dimethylphenyl)acetic acid\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 1.1572 0.8886 0.0000 C 0 0\n -0.3428 0.8912 0.0000 C 0 0\n -1.0906 2.1915 0.0000 C 0 0\n -2.5906 2.1941 0.0000 C 0 0\n -3.3383 3.4945 0.0000 C 0 0\n -3.3428 0.8964 0.0000 C 0 0\n -2.5951 -0.4039 0.0000 C 0 0\n -3.3451 -1.7039 0.0000 C 0 0\n -2.5951 -3.0039 0.0000 C 0 0\n -1.0951 -3.0039 0.0000 R# 0 0\n -3.3447 -4.3032 0.0000 O 0 0\n -1.0951 -0.4065 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 9 11 2 0\n 7 12 2 0\n 2 12 1 0\nM RGP 1 10 2\nM END\n> <Name>\n2-(3,5-dimethylphenyl)acetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAPhg3\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nDeamino-Leucine\n SciTegic07272112182D\n\n 8 7 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 1.3000 2.2500 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.2000 0.0000 0.0000 C 0 0\n 5.2000 -1.5000 0.0000 R# 0 0\n 6.4992 0.7496 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 1 7 2\nM END\n> <Name>\nDeamino-Leucine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDALeu\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n(2R)-2-hydroxypropanoic acid\n SciTegic07272112182D\n\n 6 5 0 0 1 0 999 V2000\n 1.3000 2.2500 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0 1 0 0 0\n 0.0007 0.0004 0.0000 O 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 2.6000 -1.5000 0.0000 R# 0 0\n 3.8993 0.7496 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 4 6 2 0\nM RGP 1 5 2\nM END\n> <Name>\n(2R)-2-hydroxypropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-OAla\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n(2S)-2-hydroxy-3-methylbutanoic acid\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 1.3000 2.2500 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0 2 0 0 0\n 2.6000 -1.5000 0.0000 O 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 3.9000 2.2500 0.0000 R# 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 4 2 1 0\n 4 5 1 1\n 4 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 1 7 2\nM END\n> <Name>\n(2S)-2-hydroxy-3-methylbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nL-OVal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nN-Terminal 1-phenylmethanamine\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 3.8926 -3.7566 0.0000 R# 0 0\n 2.5951 -3.0039 0.0000 N 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\nM RGP 1 1 2\nM END\n> <Name>\nN-Terminal 1-phenylmethanamine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNHBn-\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nBenzaldehyde\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 3.8976 -0.7553 0.0000 R# 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 2.5951 -3.0031 0.0000 O 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\nM RGP 1 1 2\nM END\n> <Name>\nBenzaldehyde\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBz\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nN-Terminal ethyl\n SciTegic07272112182D\n\n 3 2 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 2.5993 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\nM RGP 1 3 2\nM END\n> <Name>\nN-Terminal ethyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nEt-\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nN-Terminal methyl\n SciTegic07272112182D\n\n 2 1 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 R# 0 0\n 1 2 1 0\nM RGP 1 2 2\nM END\n> <Name>\nN-Terminal methyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nMe-\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n(2R)-2-amino-3-(4-ethoxyphenyl)propanoic acid\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -5.6925 -2.6973 0.0000 C 0 0\n -4.3898 -1.9538 0.0000 C 0 0\n -3.0933 -2.7099 0.0000 O 0 0\n -1.7898 -1.9660 0.0000 C 0 0\n -0.4930 -2.7198 0.0000 C 0 0\n 0.8083 -1.9736 0.0000 C 0 0\n 0.8127 -0.4736 0.0000 C 0 0\n 2.1131 0.2757 0.0000 C 0 0\n 2.1153 1.7765 0.0000 C 0 0 1 0 0 0\n 0.8149 2.5258 0.0000 N 0 0\n -0.4839 1.7755 0.0000 R# 0 0\n 3.4157 2.5258 0.0000 C 0 0\n 4.7139 1.7743 0.0000 R# 0 0\n 3.4180 4.0258 0.0000 O 0 0\n -0.4842 0.2802 0.0000 C 0 0\n -1.7854 -0.4660 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 9 8 1 1\n 9 10 1 0\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\n 7 15 1 0\n 15 16 2 0\n 4 16 1 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2R)-2-amino-3-(4-ethoxyphenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDTyrEt\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-6-acetamidohexanoic acid\n SciTegic09012117322D\n\n 14 13 0 0 1 0 999 V2000\n -3.8101 -3.4803 0.0000 C 0 0\n -2.5119 -4.2318 0.0000 C 0 0\n -2.5142 -5.7319 0.0000 O 0 0\n -1.2115 -3.4826 0.0000 N 0 0\n -1.2092 -1.9817 0.0000 C 0 0\n 0.0912 -1.2325 0.0000 C 0 0\n 0.0935 0.2684 0.0000 C 0 0\n 1.3938 1.0176 0.0000 C 0 0\n 1.3961 2.5184 0.0000 C 0 0 2 0 0 0\n 0.0957 3.2677 0.0000 N 0 0\n -1.2032 2.5174 0.0000 R# 0 0\n 2.6965 3.2677 0.0000 C 0 0\n 3.9947 2.5161 0.0000 R# 0 0\n 2.6988 4.7677 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 9 8 1 6\n 9 10 1 0\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2S)-2-amino-6-acetamidohexanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLys_Ac\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nN-Terminal methanol\n SciTegic07272112182D\n\n 3 2 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 O 0 0\n 2.5993 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\nM RGP 1 3 2\nM END\n> <Name>\nN-Terminal methanol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOMe-\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n(2S)-2-amino-4-methoxy-4-oxobutanoic acid\n SciTegic09012117322D\n\n 11 10 0 0 1 0 999 V2000\n -2.0126 3.6129 0.0000 C 0 0\n -0.7128 2.8641 0.0000 O 0 0\n -0.7106 1.3632 0.0000 C 0 0\n -2.0087 0.6117 0.0000 O 0 0\n 0.5899 0.6139 0.0000 C 0 0\n 0.5921 -0.8869 0.0000 C 0 0 2 0 0 0\n -0.7082 -1.6362 0.0000 N 0 0\n -2.0072 -0.8859 0.0000 R# 0 0\n 1.8926 -1.6362 0.0000 C 0 0\n 3.1907 -0.8846 0.0000 R# 0 0\n 1.8948 -3.1361 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 6 5 1 1\n 6 7 1 0\n 7 8 1 0\n 6 9 1 0\n 9 10 1 0\n 9 11 2 0\nM RGP 2 8 1 10 2\nM END\n> <Name>\n(2S)-2-amino-4-methoxy-4-oxobutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAspOMe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nD\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-(dimethylamino)benzoic acid\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n -7.8462 -2.7911 0.0000 C 0 0\n -7.1003 -4.0925 0.0000 N 0 0\n -7.8549 -5.3889 0.0000 C 0 0\n -5.5995 -4.0982 0.0000 C 0 0\n -4.8518 -5.3986 0.0000 C 0 0\n -3.3518 -5.4012 0.0000 C 0 0\n -2.5995 -4.1034 0.0000 C 0 0\n -3.3473 -2.8031 0.0000 C 0 0\n -4.8473 -2.8005 0.0000 C 0 0\n -2.5972 -1.5031 0.0000 C 0 0\n -1.0972 -1.5031 0.0000 R# 0 0\n -3.3468 -0.2038 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\n 8 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 1 11 2\nM END\n> <Name>\n3-(dimethylamino)benzoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNMe23A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-amino-3-phenylprop-2-enoic acid\n SciTegic07272112182D\n\n 13 13 0 0 0 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 2 1 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 3 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\n2-amino-3-phenylprop-2-enoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPheaDH\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n4-amino-3-hydroxy-6-methylheptanoic acid\n SciTegic09012117322D\n\n 13 12 0 0 0 0 999 V2000\n -3.5226 -2.6969 0.0000 C 0 0\n -2.7715 -1.3985 0.0000 C 0 0\n -3.5208 -0.0990 0.0000 C 0 0\n -1.2707 -1.3987 0.0000 C 0 0\n -0.5192 -0.0996 0.0000 C 0 0\n -1.2716 1.1990 0.0000 N 0 0\n -2.7716 1.1976 0.0000 R# 0 0\n 0.9817 -0.0999 0.0000 C 0 0\n 1.7310 -1.3993 0.0000 O 0 0\n 1.7331 1.1993 0.0000 C 0 0\n 3.2339 1.1990 0.0000 C 0 0\n 3.9832 -0.1004 0.0000 R# 0 0\n 3.9850 2.4974 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 5 8 1 0\n 8 9 1 0\n 8 10 1 0\n 10 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 7 1 12 2\nM END\n> <Name>\n4-amino-3-hydroxy-6-methylheptanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nSta3xi\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-amino-3-(4-methoxyphenyl)prop-2-enoic acid\n SciTegic07272112182D\n\n 15 15 0 0 0 0 999 V2000\n -4.7686 -2.1340 0.0000 C 0 0\n -3.4728 -2.8897 0.0000 O 0 0\n -2.1693 -2.1457 0.0000 C 0 0\n -0.8725 -2.8995 0.0000 C 0 0\n 0.4287 -2.1534 0.0000 C 0 0\n 0.4331 -0.6534 0.0000 C 0 0\n 1.7335 0.0959 0.0000 C 0 0\n 1.7358 1.5968 0.0000 C 0 0\n 0.4354 2.3460 0.0000 N 0 0\n -0.8635 1.5957 0.0000 R# 0 0\n 3.0362 2.3460 0.0000 C 0 0\n 4.3343 1.5945 0.0000 R# 0 0\n 3.0384 3.8460 0.0000 O 0 0\n -0.8637 0.1004 0.0000 C 0 0\n -2.1650 -0.6458 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 7 6 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\n 6 14 1 0\n 14 15 2 0\n 3 15 1 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n2-amino-3-(4-methoxyphenyl)prop-2-enoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyrabD\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-aminopropan-1-ol\n SciTegic07272112182D\n\n 6 5 0 0 1 0 999 V2000\n 2.6000 -1.5000 0.0000 N 0 0\n 2.6000 0.0000 0.0000 C 0 0 1 0 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 0.0007 0.0004 0.0000 O 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 1 0\n 2 5 1 0\n 5 6 1 0\nM RGP 1 6 2\nM END\n> <Name>\n(2R)-2-aminopropan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAlaol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-amino-2-methylpropan-1-ol\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 5.1965 -1.5117 0.0000 R# 0 0\n 6.6965 -1.5117 0.0000 N 0 0\n 7.4478 -0.2124 0.0000 C 0 0\n 6.6951 1.0860 0.0000 C 0 0\n 5.1951 1.0844 0.0000 O 0 0\n 8.9486 -0.2108 0.0000 C 0 0\n 9.7027 -1.5074 0.0000 C 0 0\n 11.2027 -1.5027 0.0000 C 0 0\n 11.9486 -0.2013 0.0000 C 0 0\n 11.1945 1.0954 0.0000 C 0 0\n 9.6945 1.0906 0.0000 C 0 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 10 11 2 0\n 11 6 1 0\n 1 2 1 0\nM RGP 1 1 1\nM END\n> <Name>\n2-amino-2-methylpropan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDPhgol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2R,3R)-2-aminobutane-1,3-diol\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 1.3000 2.2500 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0 1 0 0 0\n 0.0007 0.0004 0.0000 O 0 0\n 2.6000 0.0000 0.0000 C 0 0 1 0 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 2.5969 -1.5008 0.0000 N 0 0\n 1.2968 -2.2490 0.0000 R# 0 0\n 2 1 1 6\n 2 3 1 0\n 2 4 1 0\n 4 5 1 1\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\nM RGP 1 8 1\nM END\n> <Name>\n(2R,3R)-2-aminobutane-1,3-diol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDThrol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\naminomethanol\n SciTegic07272112182D\n\n 4 3 0 0 0 0 999 V2000\n 7.6505 -0.5497 0.0000 O 0 0\n 6.1505 -0.5497 0.0000 C 0 0\n 5.3993 0.7496 0.0000 N 0 0\n 3.8993 0.7496 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\nM RGP 1 4 1\nM END\n> <Name>\naminomethanol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nGly-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-aminopropan-1-ol\n SciTegic07272112182D\n\n 6 5 0 0 1 0 999 V2000\n 6.7009 2.5990 0.0000 C 0 0\n 7.4505 1.2997 0.0000 C 0 0 1 0 0 0\n 8.9513 1.2997 0.0000 C 0 0\n 9.7021 2.5983 0.0000 O 0 0\n 6.6992 0.0004 0.0000 N 0 0\n 5.1992 0.0004 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 1 0\n 2 5 1 0\n 5 6 1 0\nM RGP 1 6 1\nM END\n> <Name>\n(2S)-2-aminopropan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAla-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2,6-diaminohexan-1-ol\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 16.0614 1.7064 0.0000 N 0 0\n 14.5614 1.7047 0.0000 C 0 0\n 13.8087 3.0031 0.0000 C 0 0\n 12.3079 3.0015 0.0000 C 0 0\n 11.5552 4.2999 0.0000 C 0 0\n 10.0544 4.2983 0.0000 C 0 0 1 0 0 0\n 9.3017 5.5967 0.0000 C 0 0\n 7.8017 5.5951 0.0000 O 0 0\n 9.3031 2.9990 0.0000 N 0 0\n 7.8031 2.9990 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 6 5 1 6\n 6 7 1 0\n 7 8 1 0\n 6 9 1 0\n 9 10 1 0\nM RGP 1 10 1\nM END\n> <Name>\n(2S)-2,6-diaminohexan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLys-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-2-phenylethan-1-ol\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n 5.1951 1.0844 0.0000 O 0 0\n 6.6951 1.0860 0.0000 C 0 0\n 7.4478 -0.2124 0.0000 C 0 0 1 0 0 0\n 6.6965 -1.5117 0.0000 N 0 0\n 5.1965 -1.5117 0.0000 R# 0 0\n 8.9486 -0.2108 0.0000 C 0 0\n 9.7027 -1.5074 0.0000 C 0 0\n 11.2027 -1.5027 0.0000 C 0 0\n 11.9486 -0.2013 0.0000 C 0 0\n 11.1945 1.0954 0.0000 C 0 0\n 9.6945 1.0906 0.0000 C 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 3 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 10 11 2 0\n 6 11 1 0\nM RGP 1 5 1\nM END\n> <Name>\n(2S)-2-amino-2-phenylethan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhg-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n[(2S)-pyrrolidin-2-yl]methanol\n SciTegic07272112182D\n\n 8 8 0 0 1 0 999 V2000\n 3.1247 -2.0836 0.0000 O 0 0\n 1.6332 -2.2426 0.0000 C 0 0\n 0.7500 -1.0323 0.0000 C 0 0 2 0 0 0\n 1.2135 0.3943 0.0000 C 0 0\n 0.0000 1.2760 0.0000 C 0 0\n -1.2135 0.3943 0.0000 C 0 0\n -0.7500 -1.0323 0.0000 N 0 0\n -1.6317 -2.2458 0.0000 R# 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 7 8 1 0\nM RGP 1 8 1\nM END\n> <Name>\n[(2S)-pyrrolidin-2-yl]methanol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPro-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-3-methylbutan-1-ol\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 1.3000 2.2500 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0 1 0 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 2.5969 -1.5008 0.0000 N 0 0\n 1.2968 -2.2490 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 4 2 1 0\n 4 5 1 1\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\nM RGP 1 8 1\nM END\n> <Name>\n(2S)-2-amino-3-methylbutan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nVal-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-aminopropanal\n SciTegic07272112182D\n\n 6 5 0 0 1 0 999 V2000\n 2.6000 -1.5000 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0 2 0 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 0.0007 0.0004 0.0000 R# 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 3 4 1 0\n 2 5 1 0\n 5 6 2 0\nM RGP 1 4 1\nM END\n> <Name>\n(2S)-2-aminopropanal\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAla-al\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN''-[(4S)-4-amino-5-oxopentyl]guanidine\n SciTegic07272112182D\n\n 12 11 0 0 1 0 999 V2000\n 18.1103 -2.2565 0.0000 N 0 0\n 17.3622 -0.9564 0.0000 C 0 0\n 18.1145 0.3414 0.0000 N 0 0\n 15.8614 -0.9547 0.0000 N 0 0\n 15.1087 -2.2531 0.0000 C 0 0\n 13.6079 -2.2515 0.0000 C 0 0\n 12.8552 -3.5499 0.0000 C 0 0\n 11.3544 -3.5483 0.0000 C 0 0 2 0 0 0\n 10.6031 -2.2490 0.0000 N 0 0\n 9.1031 -2.2490 0.0000 R# 0 0\n 10.6017 -4.8467 0.0000 C 0 0\n 9.1017 -4.8451 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 1\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 2 0\nM RGP 1 10 1\nM END\n> <Name>\nN''-[(4S)-4-amino-5-oxopentyl]guanidine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nArg-al\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(3S)-3-amino-4-oxobutanoic acid\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 8.9597 1.7014 0.0000 O 0 0\n 9.7079 3.0015 0.0000 C 0 0\n 11.2079 3.0031 0.0000 O 0 0\n 8.9552 4.2999 0.0000 C 0 0\n 7.4544 4.2983 0.0000 C 0 0 2 0 0 0\n 6.7032 2.9990 0.0000 N 0 0\n 5.2032 2.9990 0.0000 R# 0 0\n 6.7017 5.5967 0.0000 C 0 0\n 5.2017 5.5951 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 5 4 1 6\n 5 6 1 0\n 6 7 1 0\n 5 8 1 0\n 8 9 2 0\nM RGP 1 7 1\nM END\n> <Name>\n(3S)-3-amino-4-oxobutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAsp-al\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nN\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2,6-diaminohexanal\n SciTegic07272112182D\n\n 10 9 0 0 1 0 999 V2000\n 16.0614 1.7064 0.0000 N 0 0\n 14.5614 1.7047 0.0000 C 0 0\n 13.8087 3.0031 0.0000 C 0 0\n 12.3079 3.0015 0.0000 C 0 0\n 11.5552 4.2999 0.0000 C 0 0\n 10.0544 4.2983 0.0000 C 0 0 2 0 0 0\n 9.3031 2.9990 0.0000 N 0 0\n 7.8031 2.9990 0.0000 R# 0 0\n 9.3017 5.5967 0.0000 C 0 0\n 7.8017 5.5951 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 6 5 1 6\n 6 7 1 0\n 7 8 1 0\n 6 9 1 0\n 9 10 2 0\nM RGP 1 8 1\nM END\n> <Name>\n(2S)-2,6-diaminohexanal\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLys-al\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-pyrrolidine-2-carbaldehyde\n SciTegic07272112182D\n\n 8 8 0 0 1 0 999 V2000\n 1.6317 -2.2458 0.0000 R# 0 0\n 3.1317 -2.2458 0.0000 N 0 0\n 4.0134 -3.4593 0.0000 C 0 0\n 5.4400 -2.9958 0.0000 C 0 0\n 5.4399 -1.4958 0.0000 C 0 0\n 4.0134 -1.0323 0.0000 C 0 0 1 0 0 0\n 3.5533 0.3936 0.0000 C 0 0\n 4.5586 1.5069 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 6 5 1 0\n 6 2 1 0\n 6 7 1 6\n 7 8 2 0\nM RGP 1 1 1\nM END\n> <Name>\n(2S)-pyrrolidine-2-carbaldehyde\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPro-al\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nC-Terminal 1-phenylmethanamine\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 3.8926 -3.7566 0.0000 R# 0 0\n 5.3926 -3.7566 0.0000 N 0 0\n 6.1439 -5.0559 0.0000 C 0 0\n 7.6447 -5.0559 0.0000 C 0 0\n 8.3974 -6.3533 0.0000 C 0 0\n 9.8974 -6.3503 0.0000 C 0 0\n 10.6447 -5.0497 0.0000 C 0 0\n 9.8920 -3.7522 0.0000 C 0 0\n 8.3920 -3.7553 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\nM RGP 1 1 1\nM END\n> <Name>\nC-Terminal 1-phenylmethanamine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n-NHBn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-4-methanesulfonylbutanoic acid\n SciTegic09012117322D\n\n 12 11 0 0 1 0 999 V2000\n 0.4287 3.0016 0.0000 C 0 0\n -0.8695 2.2501 0.0000 S 0 0\n -2.1692 2.9989 0.0000 O 0 0\n -0.8710 3.7500 0.0000 O 0 0\n -0.8672 0.7492 0.0000 C 0 0\n 0.4332 -0.0001 0.0000 C 0 0\n 0.4355 -1.5009 0.0000 C 0 0 2 0 0 0\n -0.8649 -2.2502 0.0000 N 0 0\n -2.1638 -1.4999 0.0000 R# 0 0\n 1.7359 -2.2502 0.0000 C 0 0\n 3.0341 -1.4986 0.0000 R# 0 0\n 1.7382 -3.7501 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 2 0\n 2 5 1 0\n 5 6 1 0\n 7 6 1 1\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-4-methanesulfonylbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nMet_O2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nM\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(2-methylphenyl)propanoic acid\n SciTegic09012117322D\n\n 14 14 0 0 1 0 999 V2000\n 1.0137 3.0583 0.0000 C 0 0\n -0.2832 2.3045 0.0000 C 0 0\n -1.5844 3.0507 0.0000 C 0 0\n -2.8813 2.2970 0.0000 C 0 0\n -2.8769 0.7970 0.0000 C 0 0\n -1.5756 0.0508 0.0000 C 0 0\n -0.2788 0.8045 0.0000 C 0 0\n 1.0216 0.0552 0.0000 C 0 0\n 1.0238 -1.4456 0.0000 C 0 0 2 0 0 0\n -0.2765 -2.1949 0.0000 N 0 0\n -1.5754 -1.4446 0.0000 R# 0 0\n 2.3242 -2.1949 0.0000 C 0 0\n 3.6224 -1.4433 0.0000 R# 0 0\n 2.3265 -3.6949 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 2 7 1 0\n 7 8 1 0\n 9 8 1 1\n 9 10 1 0\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2S)-2-amino-3-(2-methylphenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe2Me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(3,4-dichlorophenyl)propanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -3.5578 -3.0413 0.0000 Cl 0 0\n -2.2566 -2.2951 0.0000 C 0 0\n -0.9598 -3.0489 0.0000 C 0 0\n 0.3415 -2.3027 0.0000 C 0 0\n 0.3458 -0.8027 0.0000 C 0 0\n 1.6463 -0.0534 0.0000 C 0 0\n 1.6485 1.4474 0.0000 C 0 0 2 0 0 0\n 0.3481 2.1967 0.0000 N 0 0\n -0.9508 1.4464 0.0000 R# 0 0\n 2.9489 2.1967 0.0000 C 0 0\n 4.2471 1.4452 0.0000 R# 0 0\n 2.9512 3.6967 0.0000 O 0 0\n -0.9510 -0.0489 0.0000 C 0 0\n -2.2522 -0.7951 0.0000 C 0 0\n -3.5491 -0.0413 0.0000 Cl 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\n 14 15 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(3,4-dichlorophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe34d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-bromophenyl)propanoic acid\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8113 -3.0442 0.0000 Br 0 0\n -2.5101 -2.2980 0.0000 C 0 0\n -1.2133 -3.0518 0.0000 C 0 0\n 0.0879 -2.3056 0.0000 C 0 0\n 0.0923 -0.8056 0.0000 C 0 0\n 1.3927 -0.0563 0.0000 C 0 0\n 1.3950 1.4445 0.0000 C 0 0 2 0 0 0\n 0.0946 2.1938 0.0000 N 0 0\n -1.2043 1.4435 0.0000 R# 0 0\n 2.6954 2.1938 0.0000 C 0 0\n 3.9936 1.4422 0.0000 R# 0 0\n 2.6977 3.6938 0.0000 O 0 0\n -1.2045 -0.0518 0.0000 C 0 0\n -2.5057 -0.7980 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-bromophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe4Br\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-iodophenyl)propanoic acid\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8113 -3.0442 0.0000 I 0 0\n -2.5101 -2.2980 0.0000 C 0 0\n -1.2133 -3.0518 0.0000 C 0 0\n 0.0879 -2.3056 0.0000 C 0 0\n 0.0923 -0.8056 0.0000 C 0 0\n 1.3927 -0.0563 0.0000 C 0 0\n 1.3950 1.4445 0.0000 C 0 0 2 0 0 0\n 0.0946 2.1938 0.0000 N 0 0\n -1.2043 1.4435 0.0000 R# 0 0\n 2.6954 2.1938 0.0000 C 0 0\n 3.9936 1.4422 0.0000 R# 0 0\n 2.6977 3.6938 0.0000 O 0 0\n -1.2045 -0.0518 0.0000 C 0 0\n -2.5057 -0.7980 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-iodophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe_4I\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-{4-[(4S)-2,6-dioxo-1,3-diazinane-4-amido]phenyl}propanoic acid\n SciTegic07272112182D\n\n 24 25 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 1 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -2.6003 1.4977 0.0000 N 0 0\n -3.8990 0.7455 0.0000 C 0 0\n -3.8964 -0.7545 0.0000 O 0 0\n -5.2003 1.4932 0.0000 C 0 0 2 0 0 0\n -6.4994 0.7432 0.0000 C 0 0\n -7.7985 1.4932 0.0000 C 0 0\n -9.0975 0.7432 0.0000 O 0 0\n -7.7985 2.9932 0.0000 N 0 0\n -6.4995 3.7432 0.0000 C 0 0\n -6.4995 5.2432 0.0000 O 0 0\n -5.2004 2.9933 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 1 0\n 10 11 2 0\n 12 10 1 6\n 12 13 1 0\n 13 14 1 0\n 14 15 2 0\n 14 16 1 0\n 16 17 1 0\n 17 18 2 0\n 17 19 1 0\n 12 19 1 0\n 8 20 1 0\n 20 21 2 0\n 5 21 1 0\n 3 22 1 0\n 22 23 1 0\n 22 24 2 0\nM RGP 2 1 1 23 2\nM END\n> <Name>\n(2S)-2-amino-3-{4-[(4S)-2,6-dioxo-1,3-diazinane-4-amido]phenyl}propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe4SD\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(phosphonooxy)propanoic acid\n SciTegic09012117322D\n\n 12 11 0 0 1 0 999 V2000\n 0.4287 3.0016 0.0000 O 0 0\n -0.8695 2.2501 0.0000 P 0 0\n -0.8710 3.7500 0.0000 O 0 0\n -2.1692 2.9989 0.0000 O 0 0\n -0.8672 0.7492 0.0000 O 0 0\n 0.4332 -0.0001 0.0000 C 0 0\n 0.4355 -1.5009 0.0000 C 0 0 2 0 0 0\n -0.8649 -2.2502 0.0000 N 0 0\n -2.1638 -1.4999 0.0000 R# 0 0\n 1.7359 -2.2502 0.0000 C 0 0\n 3.0341 -1.4986 0.0000 R# 0 0\n 1.7382 -3.7501 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\n 5 6 1 0\n 7 6 1 1\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(phosphonooxy)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nSerPO3\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nS\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S,3R)-2-amino-3-(phosphonooxy)butanoic acid\n SciTegic09012117322D\n\n 13 12 0 0 1 0 999 V2000\n 1.5982 0.6937 0.0000 C 0 0\n 0.3000 -0.0579 0.0000 C 0 0 1 0 0 0\n -1.0004 0.6914 0.0000 O 0 0\n -1.0027 2.1922 0.0000 P 0 0\n -1.0042 3.6922 0.0000 O 0 0\n 0.2955 2.9438 0.0000 O 0 0\n -2.3024 2.9411 0.0000 O 0 0\n 0.3023 -1.5587 0.0000 C 0 0 2 0 0 0\n -0.9981 -2.3080 0.0000 N 0 0\n -2.2970 -1.5577 0.0000 R# 0 0\n 1.6027 -2.3080 0.0000 C 0 0\n 2.9009 -1.5564 0.0000 R# 0 0\n 1.6050 -3.8079 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 4 6 1 0\n 4 7 2 0\n 2 8 1 0\n 8 9 1 1\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n(2S,3R)-2-amino-3-(phosphonooxy)butanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nThrPO3\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(4R)-1,3-thiazolidine-4-carboxylic acid\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n -1.3565 1.9415 0.0000 R# 0 0\n -1.1229 0.4598 0.0000 N 0 0\n -2.1844 -0.6001 0.0000 C 0 0\n -1.5044 -1.9371 0.0000 S 0 0\n -0.0227 -1.7036 0.0000 C 0 0\n 0.2131 -0.2222 0.0000 C 0 0 1 0 0 0\n 1.5471 0.4598 0.0000 C 0 0\n 2.8060 -0.3559 0.0000 R# 0 0\n 1.6246 1.9578 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 6 5 1 0\n 6 2 1 0\n 6 7 1 6\n 7 8 1 0\n 7 9 2 0\nM RGP 2 1 1 8 2\nM END\n> <Name>\n(4R)-1,3-thiazolidine-4-carboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nThz\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(1-methyl-1H-indol-3-yl)propanoic acid\n SciTegic09012117322D\n\n 17 18 0 0 1 0 999 V2000\n -3.8091 0.3532 0.0000 C 0 0\n -2.3178 0.5140 0.0000 N 0 0\n -1.3111 -0.5980 0.0000 C 0 0\n 0.0575 0.0158 0.0000 C 0 0\n 1.3557 -0.7322 0.0000 C 0 0\n 1.3580 -2.2330 0.0000 C 0 0 2 0 0 0\n 0.0576 -2.9823 0.0000 N 0 0\n -1.2413 -2.2320 0.0000 R# 0 0\n 2.6584 -2.9823 0.0000 C 0 0\n 3.9566 -2.2308 0.0000 R# 0 0\n 2.6606 -4.4823 0.0000 O 0 0\n -0.1035 1.5064 0.0000 C 0 0\n 0.8972 2.6238 0.0000 C 0 0\n 0.4298 4.0491 0.0000 C 0 0\n -1.0382 4.3570 0.0000 C 0 0\n -2.0389 3.2395 0.0000 C 0 0\n -1.5715 1.8142 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 6 5 1 1\n 6 7 1 0\n 7 8 1 0\n 6 9 1 0\n 9 10 1 0\n 9 11 2 0\n 4 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 15 2 0\n 15 16 1 0\n 16 17 2 0\n 2 17 1 0\n 12 17 1 0\nM RGP 2 8 1 10 2\nM END\n> <Name>\n(2S)-2-amino-3-(1-methyl-1H-indol-3-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTrp_Me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nW\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-hydroxy-2,6-dimethylphenyl)propanoic acid\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -1.2401 1.0645 0.0000 C 0 0\n -1.2430 0.0645 0.0000 C 0 0\n -2.5442 -0.6817 0.0000 C 0 0\n -2.5486 -2.1817 0.0000 C 0 0\n -3.8499 -2.9279 0.0000 O 0 0\n -1.2518 -2.9355 0.0000 C 0 0\n 0.0494 -2.1893 0.0000 C 0 0\n 1.3463 -2.9431 0.0000 C 0 0\n 0.0538 -0.6893 0.0000 C 0 0\n 1.3542 0.0600 0.0000 C 0 0\n 1.3565 1.5608 0.0000 C 0 0 2 0 0 0\n 0.0561 2.3101 0.0000 N 0 0\n -0.8098 1.8099 0.0000 R# 0 0\n 2.6569 2.3101 0.0000 C 0 0\n 3.9550 1.5586 0.0000 R# 0 0\n 2.6591 3.8101 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 4 6 2 0\n 6 7 1 0\n 7 8 1 0\n 7 9 2 0\n 2 9 1 0\n 9 10 1 0\n 11 10 1 6\n 11 12 1 0\n 12 13 1 0\n 11 14 1 0\n 14 15 1 0\n 14 16 2 0\nM RGP 2 13 1 15 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-hydroxy-2,6-dimethylphenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyr26d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-hydroxy-3-iodophenyl)propanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -3.5578 -3.0413 0.0000 O 0 0\n -2.2566 -2.2951 0.0000 C 0 0\n -0.9598 -3.0489 0.0000 C 0 0\n 0.3415 -2.3027 0.0000 C 0 0\n 0.3458 -0.8027 0.0000 C 0 0\n 1.6463 -0.0534 0.0000 C 0 0\n 1.6485 1.4474 0.0000 C 0 0 2 0 0 0\n 0.3481 2.1967 0.0000 N 0 0\n -0.9508 1.4464 0.0000 R# 0 0\n 2.9489 2.1967 0.0000 C 0 0\n 4.2471 1.4452 0.0000 R# 0 0\n 2.9512 3.6967 0.0000 O 0 0\n -0.9510 -0.0489 0.0000 C 0 0\n -2.2522 -0.7951 0.0000 C 0 0\n -3.5491 -0.0413 0.0000 I 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\n 14 15 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-hydroxy-3-iodophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyr_3I\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-hydroxy-3-nitrophenyl)propanoic acid\n SciTegic09012117322D\n\n 17 17 0 0 1 0 999 V2000\n -1.0001 -3.6609 0.0000 N 0 3\n -2.3000 -4.4094 0.0000 O 0 5\n 0.2977 -4.4129 0.0000 O 0 0\n -0.9989 -2.1601 0.0000 C 0 0\n 0.3024 -1.4139 0.0000 C 0 0\n -2.2957 -1.4063 0.0000 C 0 0\n 0.3068 0.0860 0.0000 C 0 0\n -3.5969 -2.1525 0.0000 O 0 0\n -2.2913 0.0936 0.0000 C 0 0\n -0.9900 0.8398 0.0000 C 0 0\n 1.6072 0.8353 0.0000 C 0 0\n 1.6095 2.3361 0.0000 C 0 0 2 0 0 0\n 0.3090 3.0854 0.0000 N 0 0\n 2.9099 3.0854 0.0000 C 0 0\n -0.9899 2.3351 0.0000 R# 0 0\n 4.2080 2.3339 0.0000 R# 0 0\n 2.9122 4.5854 0.0000 O 0 0\n 2 1 1 0\n 1 3 2 0\n 4 1 1 0\n 5 4 2 0\n 6 4 1 0\n 7 5 1 0\n 8 6 1 0\n 6 9 2 0\n 10 7 2 0\n 7 11 1 0\n 9 10 1 0\n 12 11 1 6\n 12 13 1 0\n 12 14 1 0\n 13 15 1 0\n 14 16 1 0\n 14 17 2 0\nM CHG 2 1 1 2 -1\nM RGP 2 15 1 16 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-hydroxy-3-nitrophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyr3NO\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-[4-(4-hydroxyphenoxy)phenyl]propanoic acid\n SciTegic07272112182D\n\n 21 22 0 0 1 0 999 V2000\n -6.7347 0.4258 0.0000 O 0 0\n -5.4404 -0.3325 0.0000 C 0 0\n -5.4500 -1.8325 0.0000 C 0 0\n -4.1558 -2.5908 0.0000 C 0 0\n -2.8520 -1.8491 0.0000 C 0 0\n -1.5555 -2.6051 0.0000 O 0 0\n -0.2520 -1.8612 0.0000 C 0 0\n 1.0449 -2.6149 0.0000 C 0 0\n 2.3461 -1.8687 0.0000 C 0 0\n 2.3505 -0.3687 0.0000 C 0 0\n 3.6509 0.3806 0.0000 C 0 0\n 3.6532 1.8814 0.0000 C 0 0 2 0 0 0\n 2.3528 2.6307 0.0000 N 0 0\n 1.0539 1.8804 0.0000 R# 0 0\n 4.9536 2.6307 0.0000 C 0 0\n 6.2517 1.8792 0.0000 R# 0 0\n 4.9558 4.1307 0.0000 O 0 0\n 1.0537 0.3851 0.0000 C 0 0\n -0.2476 -0.3611 0.0000 C 0 0\n -2.8424 -0.3491 0.0000 C 0 0\n -4.1366 0.4092 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 12 11 1 6\n 12 13 1 0\n 13 14 1 0\n 12 15 1 0\n 15 16 1 0\n 15 17 2 0\n 10 18 1 0\n 18 19 2 0\n 7 19 1 0\n 5 20 1 0\n 20 21 2 0\n 2 21 1 0\nM RGP 2 14 1 16 2\nM END\n> <Name>\n(2S)-2-amino-3-[4-(4-hydroxyphenoxy)phenyl]propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyrPh4\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-[4-(sulfooxy)phenyl]propanoic acid\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -3.8234 -0.3621 0.0000 O 0 0\n -3.8304 -1.8621 0.0000 S 0 0\n -5.1332 -2.6056 0.0000 O 0 0\n -5.1258 -1.1058 0.0000 O 0 0\n -2.5340 -2.6181 0.0000 O 0 0\n -1.2305 -1.8742 0.0000 C 0 0\n 0.0664 -2.6280 0.0000 C 0 0\n 1.3676 -1.8818 0.0000 C 0 0\n 1.3720 -0.3818 0.0000 C 0 0\n 2.6724 0.3675 0.0000 C 0 0\n 2.6747 1.8683 0.0000 C 0 0 2 0 0 0\n 1.3742 2.6176 0.0000 N 0 0\n 0.0754 1.8673 0.0000 R# 0 0\n 3.9751 2.6176 0.0000 C 0 0\n 5.2732 1.8660 0.0000 R# 0 0\n 3.9773 4.1176 0.0000 O 0 0\n 0.0752 0.3720 0.0000 C 0 0\n -1.2261 -0.3742 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 2 0\n 2 5 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 11 10 1 6\n 11 12 1 0\n 12 13 1 0\n 11 14 1 0\n 14 15 1 0\n 14 16 2 0\n 9 17 1 0\n 17 18 2 0\n 6 18 1 0\nM RGP 2 13 1 15 2\nM END\n> <Name>\n(2S)-2-amino-3-[4-(sulfooxy)phenyl]propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyrSO3\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-hydroxy-3-methylbutanoic acid\n SciTegic09012117322D\n\n 10 9 0 0 1 0 999 V2000\n 1.1669 1.7265 0.0000 C 0 0\n -0.1312 0.9749 0.0000 C 0 0\n -0.1328 2.4749 0.0000 C 0 0\n -1.4310 1.7238 0.0000 O 0 0\n -0.1290 -0.5259 0.0000 C 0 0 2 0 0 0\n -1.4294 -1.2752 0.0000 N 0 0\n -2.7283 -0.5249 0.0000 R# 0 0\n 1.1715 -1.2752 0.0000 C 0 0\n 2.4696 -0.5236 0.0000 R# 0 0\n 1.1737 -2.7751 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 5 2 1 0\n 5 6 1 1\n 6 7 1 0\n 5 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 2 7 1 9 2\nM END\n> <Name>\n(2S)-2-amino-3-hydroxy-3-methylbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nVal3OH\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-methylpentanoic acid\n SciTegic09012117322D\n\n 10 9 0 0 1 0 999 V2000\n -1.3038 -3.1492 0.0000 C 0 0\n -1.3015 -1.6492 0.0000 C 0 0\n -0.0011 -0.8999 0.0000 C 0 0\n 1.2971 -1.6515 0.0000 C 0 0\n 0.0012 0.6009 0.0000 C 0 0 2 0 0 0\n -1.2992 1.3502 0.0000 N 0 0\n -2.5981 0.5999 0.0000 R# 0 0\n 1.3016 1.3502 0.0000 C 0 0\n 2.5998 0.5986 0.0000 R# 0 0\n 1.3039 2.8501 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 3 1 0\n 5 6 1 6\n 6 7 1 0\n 5 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 2 7 1 9 2\nM END\n> <Name>\n(2S)-2-amino-3-methylpentanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nxiIle\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nI\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-(methylamino)benzoic acid\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n -3.0031 1.0801 0.0000 C 0 0\n -1.5031 1.0823 0.0000 N 0 0\n -0.7554 2.3826 0.0000 R# 0 0\n -0.7500 -0.2160 0.0000 C 0 0\n -1.5000 -1.5150 0.0000 C 0 0\n -0.7500 -2.8140 0.0000 C 0 0\n 0.7500 -2.8140 0.0000 C 0 0\n 1.5000 -1.5150 0.0000 C 0 0\n 0.7500 -0.2160 0.0000 C 0 0\n 1.5031 1.0823 0.0000 C 0 0\n 0.7554 2.3826 0.0000 R# 0 0\n 3.0031 1.0801 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\n 9 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 3 1 11 2\nM END\n> <Name>\n2-(methylamino)benzoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNMe2Ab\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-(methylamino)propanoic acid\n SciTegic09012117322D\n\n 8 7 0 0 0 0 999 V2000\n -3.1201 -0.9815 0.0000 C 0 0\n -1.9857 0.0000 0.0000 N 0 0\n -2.2690 1.4730 0.0000 R# 0 0\n -0.5675 -0.4910 0.0000 C 0 0\n 0.5675 0.4910 0.0000 C 0 0\n 1.9857 0.0000 0.0000 C 0 0\n 2.2690 -1.4730 0.0000 R# 0 0\n 3.1200 0.9815 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 2 3 1 7 2\nM END\n> <Name>\n3-(methylamino)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNMebAl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-2-methyl-3-phenylpropanoic acid\n SciTegic09012117322D\n\n 14 14 0 0 1 0 999 V2000\n -1.1169 -3.0644 0.0000 C 0 0\n -0.3686 -1.7645 0.0000 C 0 0 1 0 0 0\n -1.1211 -0.4659 0.0000 C 0 0\n -0.3737 0.8355 0.0000 C 0 0\n -1.1239 2.1344 0.0000 C 0 0\n -0.3742 3.4336 0.0000 C 0 0\n 1.1257 3.4339 0.0000 C 0 0\n 1.8761 2.1350 0.0000 C 0 0\n 1.1263 0.8358 0.0000 C 0 0\n -1.8986 -1.7630 0.0000 N 0 0\n -2.6481 -0.4636 0.0000 R# 0 0\n 1.1322 -1.7630 0.0000 C 0 0\n 1.8805 -0.4630 0.0000 R# 0 0\n 1.8843 -3.0608 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\n 2 10 1 0\n 10 11 1 0\n 2 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2S)-2-amino-2-methyl-3-phenylpropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\naMePhe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-methylpyrrolidine-2-carboxylic acid\n SciTegic09012117322D\n\n 10 10 0 0 1 0 999 V2000\n -0.6481 -1.6527 0.0000 C 0 0\n 0.0642 -0.3326 0.0000 C 0 0 1 0 0 0\n 0.6126 1.0636 0.0000 C 0 0\n -0.5457 2.0166 0.0000 C 0 0\n -1.8100 1.2094 0.0000 C 0 0\n -1.4330 -0.2425 0.0000 N 0 0\n -2.3861 -1.4008 0.0000 R# 0 0\n 1.5490 -0.2425 0.0000 C 0 0\n 2.3560 -1.5069 0.0000 R# 0 0\n 2.2409 1.0884 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 2 6 1 0\n 6 7 1 0\n 2 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 2 7 1 9 2\nM END\n> <Name>\n(2S)-2-methylpyrrolidine-2-carboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\naMePro\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(3,4-dihydroxyphenyl)-2-methylpropanoic acid\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -1.4451 3.4938 0.0000 C 0 0\n -0.6968 2.1938 0.0000 C 0 0 1 0 0 0\n -1.4494 0.8952 0.0000 C 0 0\n -0.7019 -0.4062 0.0000 C 0 0\n -1.4522 -1.7051 0.0000 C 0 0\n -0.7025 -3.0043 0.0000 C 0 0\n 0.7975 -3.0046 0.0000 C 0 0\n 1.5472 -4.3038 0.0000 O 0 0\n 1.5478 -1.7058 0.0000 C 0 0\n 3.0478 -1.7061 0.0000 O 0 0\n 0.7981 -0.4066 0.0000 C 0 0\n -2.2268 2.1922 0.0000 N 0 0\n -2.9763 0.8929 0.0000 R# 0 0\n 0.8040 2.1922 0.0000 C 0 0\n 1.5523 0.8922 0.0000 R# 0 0\n 1.5561 3.4901 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 7 9 1 0\n 9 10 1 0\n 9 11 2 0\n 4 11 1 0\n 2 12 1 0\n 12 13 1 0\n 2 14 1 0\n 14 15 1 0\n 14 16 2 0\nM RGP 2 13 1 15 2\nM END\n> <Name>\n(2S)-2-amino-3-(3,4-dihydroxyphenyl)-2-methylpropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\naMeTy3\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S,3R,4R)-2-amino-3-hydroxy-4-methyloct-6-enoic acid\n SciTegic09012117322D\n\n 14 13 0 0 1 0 999 V2000\n -3.0691 4.9815 0.0000 C 0 0\n -1.7694 4.2325 0.0000 C 0 0\n -1.7672 2.7317 0.0000 C 0 0\n -0.4668 1.9824 0.0000 C 0 0\n -0.4646 0.4816 0.0000 C 0 0 1 0 0 0\n -1.7627 -0.2700 0.0000 C 0 0\n 0.8358 -0.2678 0.0000 C 0 0 1 0 0 0\n 2.1340 0.4838 0.0000 O 0 0\n 0.8380 -1.7685 0.0000 C 0 0 2 0 0 0\n -0.4623 -2.5178 0.0000 N 0 0\n -1.7613 -1.7674 0.0000 R# 0 0\n 2.1384 -2.5178 0.0000 C 0 0\n 3.4366 -1.7663 0.0000 R# 0 0\n 2.1406 -4.0178 0.0000 O 0 0\n 2 1 1 0\n 2 3 2 0\n 3 4 1 0\n 5 4 1 0\n 5 6 1 6\n 7 5 1 0\n 7 8 1 1\n 7 9 1 0\n 9 10 1 1\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2S,3R,4R)-2-amino-3-hydroxy-4-methyloct-6-enoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBmt\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3-(benzylsulfanyl)propanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n 1.2919 -5.2492 0.0000 R# 0 0\n 2.5886 -6.0033 0.0000 N 0 0\n 3.8912 -5.2578 0.0000 C 0 0 1 0 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 2.5951 -3.0039 0.0000 S 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 5.1894 -6.0109 0.0000 C 0 0\n 6.4897 -5.2632 0.0000 R# 0 0\n 5.1873 -7.5109 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 7 12 1 0\n 3 13 1 0\n 13 14 1 0\n 13 15 2 0\nM RGP 2 1 1 14 2\nM END\n> <Name>\n(2R)-2-amino-3-(benzylsulfanyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nCys_Bn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(1-methyl-1H-imidazol-4-yl)propanoic acid\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -3.9438 -1.4499 0.0000 C 0 0\n -2.4525 -1.6111 0.0000 N 0 0\n -1.7063 -2.9124 0.0000 C 0 0\n -0.2382 -2.6048 0.0000 N 0 0\n -0.0770 -1.1135 0.0000 C 0 0\n 1.2211 -0.3655 0.0000 C 0 0\n 1.2234 1.1353 0.0000 C 0 0 2 0 0 0\n -0.0770 1.8846 0.0000 N 0 0\n -1.3759 1.1343 0.0000 R# 0 0\n 2.5238 1.8846 0.0000 C 0 0\n 3.8220 1.1331 0.0000 R# 0 0\n 2.5261 3.3846 0.0000 O 0 0\n -1.4455 -0.4994 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 2 0\n 2 13 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(1-methyl-1H-imidazol-4-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHis1Me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nH\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-aminopent-4-enoic acid\n SciTegic09012117322D\n\n 9 8 0 0 1 0 999 V2000\n -2.4540 0.4164 0.0000 R# 0 0\n -1.1550 1.1667 0.0000 N 0 0\n 0.1453 0.4174 0.0000 C 0 0 1 0 0 0\n 0.1431 -1.0834 0.0000 C 0 0\n -1.1574 -1.8327 0.0000 C 0 0\n -1.1596 -3.3327 0.0000 C 0 0\n 1.4458 1.1667 0.0000 C 0 0\n 2.7439 0.4151 0.0000 R# 0 0\n 1.4480 2.6666 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 3 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 2 1 1 8 2\nM END\n> <Name>\n(2S)-2-aminopent-4-enoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nGlyall\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-2-cyclopropylacetic acid\n SciTegic09012117322D\n\n 9 9 0 0 1 0 999 V2000\n -2.7445 0.3715 0.0000 R# 0 0\n -1.4441 1.1192 0.0000 N 0 0\n -0.1452 0.3672 0.0000 C 0 0 1 0 0 0\n -0.1444 -1.1228 0.0000 C 0 0\n -0.8909 -2.4239 0.0000 C 0 0\n 0.6090 -2.4198 0.0000 C 0 0\n 1.1537 1.1192 0.0000 C 0 0\n 2.4534 0.3702 0.0000 R# 0 0\n 1.1529 2.6192 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 4 6 1 0\n 3 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 2 1 1 8 2\nM END\n> <Name>\n(2S)-2-amino-2-cyclopropylacetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nGlycPr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(3S)-3-aminooxolan-2-one\n SciTegic07272112182D\n\n 8 8 0 0 1 0 999 V2000\n 3.1247 -2.0836 0.0000 R# 0 0\n 4.6247 -2.0836 0.0000 N 0 0\n 5.3747 -3.3807 0.0000 C 0 0 1 0 0 0\n 4.7626 -4.7501 0.0000 C 0 0\n 5.8759 -5.7554 0.0000 C 0 0\n 7.1760 -5.0073 0.0000 O 0 0\n 6.8662 -3.5396 0.0000 C 0 0\n 7.8715 -2.4263 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 7 8 2 0\nM RGP 1 1 1\nM END\n> <Name>\n(3S)-3-aminooxolan-2-one\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHsl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-4-(2-aminophenyl)-4-oxobutanoic acid\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -3.0073 -1.4547 0.0000 N 0 0\n -1.7078 -2.2040 0.0000 C 0 0\n -1.7070 -3.7040 0.0000 C 0 0\n -0.4075 -4.4533 0.0000 C 0 0\n 0.8911 -3.7025 0.0000 C 0 0\n 0.8902 -2.2025 0.0000 C 0 0\n -0.4092 -1.4533 0.0000 C 0 0\n -0.4070 0.0476 0.0000 C 0 0\n -1.7051 0.7991 0.0000 O 0 0\n 0.8934 0.7969 0.0000 C 0 0\n 0.8957 2.2977 0.0000 C 0 0 2 0 0 0\n -0.4047 3.0470 0.0000 N 0 0\n -1.7036 2.2967 0.0000 R# 0 0\n 2.1961 3.0470 0.0000 C 0 0\n 3.4943 2.2954 0.0000 R# 0 0\n 2.1984 4.5470 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 2 7 1 0\n 7 8 1 0\n 8 9 2 0\n 8 10 1 0\n 11 10 1 6\n 11 12 1 0\n 12 13 1 0\n 11 14 1 0\n 14 15 1 0\n 14 16 2 0\nM RGP 2 13 1 15 2\nM END\n> <Name>\n(2S)-2-amino-4-(2-aminophenyl)-4-oxobutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAspPh2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nD\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-aziridine-2-carboxylic acid\n SciTegic09012117322D\n\n 7 7 0 0 1 0 999 V2000\n -2.6157 1.1160 0.0000 R# 0 0\n -1.5553 0.0552 0.0000 N 0 0\n -1.1673 -1.3938 0.0000 C 0 0\n -0.1065 -0.3333 0.0000 C 0 0 1 0 0 0\n 1.3321 0.0552 0.0000 C 0 0\n 2.3945 -1.0037 0.0000 R# 0 0\n 1.7183 1.5046 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 4 3 1 0\n 4 2 1 0\n 4 5 1 6\n 5 6 1 0\n 5 7 2 0\nM RGP 2 1 1 6 2\nM END\n> <Name>\n(2S)-aziridine-2-carboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAzi\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-Aminobenzoic acid\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n -3.0718 1.2967 0.0000 R# 0 0\n -1.5718 1.2989 0.0000 N 0 0\n -0.8187 0.0006 0.0000 C 0 0\n -1.5687 -1.2984 0.0000 C 0 0\n -0.8187 -2.5974 0.0000 C 0 0\n 0.6813 -2.5974 0.0000 C 0 0\n 1.4313 -1.2984 0.0000 C 0 0\n 0.6813 0.0006 0.0000 C 0 0\n 1.4344 1.2989 0.0000 C 0 0\n 0.6867 2.5992 0.0000 R# 0 0\n 2.9344 1.2967 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 3 8 1 0\n 8 9 1 0\n 9 10 1 0\n 9 11 2 0\nM RGP 2 1 1 10 2\nM END\n> <Name>\n2-Aminobenzoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n2Abz\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n3-Aminobenzoic acid\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n -4.1342 0.0728 0.0000 R# 0 0\n -2.8331 0.8193 0.0000 N 0 0\n -1.5349 0.0663 0.0000 C 0 0\n -1.5349 -1.4338 0.0000 C 0 0\n -0.2359 -2.1837 0.0000 C 0 0\n 1.0632 -1.4337 0.0000 C 0 0\n 1.0632 0.0663 0.0000 C 0 0\n -0.2359 0.8163 0.0000 C 0 0\n 2.3614 0.8193 0.0000 C 0 0\n 3.6617 0.0716 0.0000 R# 0 0\n 2.3593 2.3193 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 3 8 1 0\n 7 9 1 0\n 9 10 1 0\n 9 11 2 0\nM RGP 2 1 1 10 2\nM END\n> <Name>\n3-Aminobenzoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n3Abz\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n4-Aminobenzoic acid\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n -4.0902 1.1834 0.0000 R# 0 0\n -3.3420 -0.1167 0.0000 N 0 0\n -1.8412 -0.1198 0.0000 C 0 0\n -1.0912 -1.4189 0.0000 C 0 0\n 0.4088 -1.4189 0.0000 C 0 0\n 1.1588 -0.1198 0.0000 C 0 0\n 0.4088 1.1792 0.0000 C 0 0\n -1.0912 1.1792 0.0000 C 0 0\n 2.6596 -0.1167 0.0000 C 0 0\n 3.4119 -1.4145 0.0000 R# 0 0\n 3.4078 1.1834 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 3 8 1 0\n 6 9 1 0\n 9 10 1 0\n 9 11 2 0\nM RGP 2 1 1 10 2\nM END\n> <Name>\n4-Aminobenzoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n4Abz\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n1-aminocyclopropane-1-carboxylic acid\n SciTegic07272112182D\n\n 8 8 0 0 0 0 999 V2000\n -2.7619 -0.1359 0.0000 R# 0 0\n -1.4625 0.6134 0.0000 N 0 0\n -0.1626 -0.1562 0.0000 C 0 0\n -0.9129 -1.4551 0.0000 C 0 0\n 0.5871 -1.4554 0.0000 C 0 0\n 1.1376 0.6134 0.0000 C 0 0\n 2.4363 -0.1374 0.0000 R# 0 0\n 1.1389 2.1134 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 3 5 1 0\n 3 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 2 1 1 7 2\nM END\n> <Name>\n1-aminocyclopropane-1-carboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAc3c\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n1-aminocyclohexane-1-carboxylic acid\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n -2.7175 0.4554 0.0000 R# 0 0\n -1.4181 1.2047 0.0000 N 0 0\n -0.1182 0.4961 0.0000 C 0 0\n -1.4174 -0.2537 0.0000 C 0 0\n -1.4175 -1.7537 0.0000 C 0 0\n -0.1186 -2.5039 0.0000 C 0 0\n 1.1805 -1.7541 0.0000 C 0 0\n 1.1807 -0.2541 0.0000 C 0 0\n 1.1820 1.2047 0.0000 C 0 0\n 2.4807 0.4540 0.0000 R# 0 0\n 1.1833 2.7047 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 3 8 1 0\n 3 9 1 0\n 9 10 1 0\n 9 11 2 0\nM RGP 2 1 1 10 2\nM END\n> <Name>\n1-aminocyclohexane-1-carboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAc6c\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R,3S,4S)-2-amino-3-hydroxy-4-methyloct-6-enoic acid\n SciTegic09012117322D\n\n 14 13 0 0 1 0 999 V2000\n -3.0691 4.9815 0.0000 C 0 0\n -1.7694 4.2325 0.0000 C 0 0\n -1.7672 2.7317 0.0000 C 0 0\n -0.4668 1.9824 0.0000 C 0 0\n -0.4646 0.4816 0.0000 C 0 0 2 0 0 0\n -1.7627 -0.2700 0.0000 C 0 0\n 0.8358 -0.2678 0.0000 C 0 0 2 0 0 0\n 2.1340 0.4838 0.0000 O 0 0\n 0.8380 -1.7685 0.0000 C 0 0 1 0 0 0\n -0.4623 -2.5178 0.0000 N 0 0\n -1.7613 -1.7674 0.0000 R# 0 0\n 2.1384 -2.5178 0.0000 C 0 0\n 3.4366 -1.7663 0.0000 R# 0 0\n 2.1406 -4.0178 0.0000 O 0 0\n 2 1 1 0\n 2 3 2 0\n 3 4 1 0\n 5 4 1 0\n 5 6 1 1\n 7 5 1 0\n 7 8 1 6\n 7 9 1 0\n 9 10 1 6\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2R,3S,4S)-2-amino-3-hydroxy-4-methyloct-6-enoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Bmt\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-6-[(diaminomethylidene)amino]hexanoic acid\n SciTegic09012117322D\n\n 14 13 0 0 1 0 999 V2000\n -3.8101 -3.4803 0.0000 N 0 0\n -2.5119 -4.2318 0.0000 C 0 0\n -2.5142 -5.7319 0.0000 N 0 0\n -1.2115 -3.4826 0.0000 N 0 0\n -1.2092 -1.9817 0.0000 C 0 0\n 0.0912 -1.2325 0.0000 C 0 0\n 0.0935 0.2684 0.0000 C 0 0\n 1.3938 1.0176 0.0000 C 0 0\n 1.3961 2.5184 0.0000 C 0 0 1 0 0 0\n 0.0957 3.2677 0.0000 N 0 0\n -1.2032 2.5174 0.0000 R# 0 0\n 2.6965 3.2677 0.0000 C 0 0\n 3.9947 2.5161 0.0000 R# 0 0\n 2.6988 4.7677 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 9 8 1 1\n 9 10 1 0\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2R)-2-amino-6-[(diaminomethylidene)amino]hexanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-hArg\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3-(4-fluorophenyl)propanoic acid\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8113 -3.0442 0.0000 F 0 0\n -2.5101 -2.2980 0.0000 C 0 0\n -1.2133 -3.0518 0.0000 C 0 0\n 0.0879 -2.3056 0.0000 C 0 0\n 0.0923 -0.8056 0.0000 C 0 0\n 1.3927 -0.0563 0.0000 C 0 0\n 1.3950 1.4445 0.0000 C 0 0 1 0 0 0\n 0.0946 2.1938 0.0000 N 0 0\n -1.2043 1.4435 0.0000 R# 0 0\n 2.6954 2.1938 0.0000 C 0 0\n 3.9936 1.4422 0.0000 R# 0 0\n 2.6977 3.6938 0.0000 O 0 0\n -1.2045 -0.0518 0.0000 C 0 0\n -2.5057 -0.7980 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 1\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2R)-2-amino-3-(4-fluorophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDPhe4F\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3-(2-methyl-1H-indol-3-yl)propanoic acid\n SciTegic07272112182D\n\n 17 18 0 0 1 0 999 V2000\n -1.7477 1.9238 0.0000 C 0 0\n -1.4399 0.4557 0.0000 C 0 0\n -2.4466 -0.6562 0.0000 N 0 0\n -1.7004 -1.9565 0.0000 C 0 0\n -2.1678 -3.3818 0.0000 C 0 0\n -1.1672 -4.4993 0.0000 C 0 0\n 0.3009 -4.1914 0.0000 C 0 0\n 0.7683 -2.7661 0.0000 C 0 0\n -0.2323 -1.6487 0.0000 C 0 0\n -0.0712 -0.1581 0.0000 C 0 0\n 1.2269 0.5899 0.0000 C 0 0\n 1.2292 2.0907 0.0000 C 0 0 1 0 0 0\n -0.0712 2.8400 0.0000 N 0 0\n -1.3701 2.0897 0.0000 R# 0 0\n 2.5296 2.8400 0.0000 C 0 0\n 3.8277 2.0884 0.0000 R# 0 0\n 2.5318 4.3400 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\n 9 10 1 0\n 2 10 2 0\n 10 11 1 0\n 12 11 1 1\n 12 13 1 0\n 13 14 1 0\n 12 15 1 0\n 15 16 1 0\n 15 17 2 0\nM RGP 2 14 1 16 2\nM END\n> <Name>\n(2R)-2-amino-3-(2-methyl-1H-indol-3-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDTrp2M\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nW\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n 3.5418 -9.1526 0.0000 O 0 0\n 2.7937 -7.8525 0.0000 C 0 0\n 1.2937 -7.8508 0.0000 O 0 0\n 3.5464 -6.5540 0.0000 C 0 0 1 0 0 0\n 5.0472 -6.5557 0.0000 C 0 0\n 5.7999 -5.2572 0.0000 C 0 0\n 7.2999 -5.2568 0.0000 C 0 0\n 8.0495 -3.9575 0.0000 C 0 0\n 7.2990 -2.6587 0.0000 C 0 0\n 8.0486 -1.3594 0.0000 O 0 0\n 5.7990 -2.6592 0.0000 C 0 0\n 5.0486 -1.3604 0.0000 O 0 0\n 5.0495 -3.9584 0.0000 C 0 0\n 2.7951 -5.2547 0.0000 N 0 0\n 1.2951 -5.2547 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 4 2 1 0\n 4 5 1 6\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 9 11 1 0\n 11 12 1 0\n 11 13 2 0\n 6 13 1 0\n 4 14 1 0\n 14 15 1 0\nM RGP 1 15 1\nM END\n> <Name>\n(2R)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDTyr3O\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2R)-2-amino-3-(4-methoxyphenyl)propanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -4.7686 -2.1340 0.0000 C 0 0\n -3.4728 -2.8897 0.0000 O 0 0\n -2.1693 -2.1457 0.0000 C 0 0\n -0.8725 -2.8995 0.0000 C 0 0\n 0.4287 -2.1534 0.0000 C 0 0\n 0.4331 -0.6534 0.0000 C 0 0\n 1.7335 0.0959 0.0000 C 0 0\n 1.7358 1.5968 0.0000 C 0 0 1 0 0 0\n 0.4354 2.3460 0.0000 N 0 0\n -0.8635 1.5957 0.0000 R# 0 0\n 3.0362 2.3460 0.0000 C 0 0\n 4.3343 1.5945 0.0000 R# 0 0\n 3.0384 3.8460 0.0000 O 0 0\n -0.8637 0.1004 0.0000 C 0 0\n -2.1650 -0.6458 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 8 7 1 1\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\n 6 14 1 0\n 14 15 2 0\n 3 15 1 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n(2R)-2-amino-3-(4-methoxyphenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDTyrMe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3-methylpentanoic acid\n SciTegic09012117322D\n\n 10 9 0 0 1 0 999 V2000\n -1.3038 -3.1492 0.0000 C 0 0\n -1.3015 -1.6492 0.0000 C 0 0\n -0.0011 -0.8999 0.0000 C 0 0\n 1.2971 -1.6515 0.0000 C 0 0\n 0.0012 0.6009 0.0000 C 0 0 1 0 0 0\n -1.2992 1.3502 0.0000 N 0 0\n -2.5981 0.5999 0.0000 R# 0 0\n 1.3016 1.3502 0.0000 C 0 0\n 2.5998 0.5986 0.0000 R# 0 0\n 1.3039 2.8501 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 3 1 0\n 5 6 1 1\n 6 7 1 0\n 5 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 2 7 1 9 2\nM END\n> <Name>\n(2R)-2-amino-3-methylpentanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDxiIle\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nI\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-6-[(propan-2-yl)amino]hexanoic acid\n SciTegic09012117322D\n\n 14 13 0 0 1 0 999 V2000\n -2.5142 -5.7319 0.0000 C 0 0\n -2.5119 -4.2318 0.0000 C 0 0\n -3.8101 -3.4803 0.0000 C 0 0\n -1.2115 -3.4826 0.0000 N 0 0\n -1.2092 -1.9817 0.0000 C 0 0\n 0.0912 -1.2325 0.0000 C 0 0\n 0.0935 0.2684 0.0000 C 0 0\n 1.3938 1.0176 0.0000 C 0 0\n 1.3961 2.5184 0.0000 C 0 0 2 0 0 0\n 0.0957 3.2677 0.0000 N 0 0\n -1.2032 2.5174 0.0000 R# 0 0\n 2.6965 3.2677 0.0000 C 0 0\n 3.9947 2.5161 0.0000 R# 0 0\n 2.6988 4.7677 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 9 8 1 6\n 9 10 1 0\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2S)-2-amino-6-[(propan-2-yl)amino]hexanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLysiPr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\nC-Terminal toluene\n SciTegic07272112182D\n\n 8 8 0 0 0 0 999 V2000\n 2.5951 -3.0031 0.0000 R# 0 0\n 4.0951 -3.0031 0.0000 C 0 0\n 4.8464 -1.7038 0.0000 C 0 0\n 6.3464 -1.7017 0.0000 C 0 0\n 7.0945 -0.4016 0.0000 C 0 0\n 6.3427 0.8964 0.0000 C 0 0\n 4.8427 0.8943 0.0000 C 0 0\n 4.0945 -0.4058 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 3 8 1 0\nM RGP 1 1 1\nM END\n> <Name>\nC-Terminal toluene\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\n-Bn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nPhenyl\n SciTegic07272112182D\n\n 7 7 0 0 0 0 999 V2000\n 2.5981 -1.5000 0.0000 R# 0 0\n 4.0981 -1.5000 0.0000 C 0 0\n 4.8481 -2.7990 0.0000 C 0 0\n 6.3481 -2.7990 0.0000 C 0 0\n 7.0981 -1.5000 0.0000 C 0 0\n 6.3481 -0.2010 0.0000 C 0 0\n 4.8481 -0.2010 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 2 7 1 0\nM RGP 1 1 1\nM END\n> <Name>\nPhenyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPh\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nTert-butyloxycarbonyl\n SciTegic07272112182D\n\n 8 7 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 1.3000 2.2500 0.0000 C 0 0\n 0.0011 1.5002 0.0000 C 0 0\n 2.6000 0.0000 0.0000 O 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 3.9000 2.2500 0.0000 R# 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 1 0\n 5 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 1 7 2\nM END\n> <Name>\nTert-butyloxycarbonyl\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBoc\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-cyclohexylacetic acid\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 1.2948 -3.7516 0.0000 R# 0 0\n 2.5951 -3.0039 0.0000 C 0 0\n 3.8926 -3.7566 0.0000 O 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 5 10 1 0\nM RGP 1 1 2\nM END\n> <Name>\n2-cyclohexylacetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAChg\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n3,3-diphenylpropanoic acid\n SciTegic07272112182D\n\n 17 18 0 0 0 0 999 V2000\n 5.1935 -3.0096 0.0000 R# 0 0\n 3.8934 -3.7577 0.0000 C 0 0\n 3.8917 -5.2577 0.0000 O 0 0\n 2.5949 -3.0050 0.0000 C 0 0\n 2.5966 -1.5042 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8990 -0.7582 0.0000 C 0 0\n 3.9042 0.7419 0.0000 C 0 0\n 5.2058 1.4875 0.0000 C 0 0\n 6.5023 0.7331 0.0000 C 0 0\n 6.4972 -0.7669 0.0000 C 0 0\n 5.1956 -1.5125 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 10 11 2 0\n 6 11 1 0\n 5 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 15 2 0\n 15 16 1 0\n 16 17 2 0\n 12 17 1 0\nM RGP 1 1 2\nM END\n> <Name>\n3,3-diphenylpropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDADip\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n3,3-dimethylbutanoic acid\n SciTegic07272112182D\n\n 8 7 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 1.3000 2.2500 0.0000 C 0 0\n 0.0011 1.5002 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 3.9000 2.2500 0.0000 R# 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 1 0\n 5 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 1 7 2\nM END\n> <Name>\n3,3-dimethylbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAGlyB\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n4-phenylbutanoic acid\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 2.5909 -6.0056 0.0000 R# 0 0\n 3.8912 -5.2578 0.0000 C 0 0\n 5.1887 -6.0105 0.0000 O 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 2.5951 -3.0039 0.0000 C 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 7 12 1 0\nM RGP 1 1 2\nM END\n> <Name>\n4-phenylbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAhPhe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-(4-methoxyphenyl)acetic acid\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n -0.1391 7.2331 0.0000 C 0 0\n -1.6391 7.2378 0.0000 O 0 0\n -2.3945 5.9409 0.0000 C 0 0\n -3.8945 5.9435 0.0000 C 0 0\n -4.6468 4.6458 0.0000 C 0 0\n -3.8990 3.3455 0.0000 C 0 0\n -4.6490 2.0455 0.0000 C 0 0\n -3.8990 0.7455 0.0000 C 0 0\n -2.3990 0.7455 0.0000 R# 0 0\n -4.6486 -0.5538 0.0000 O 0 0\n -2.3990 3.3428 0.0000 C 0 0\n -1.6468 4.6406 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 8 10 2 0\n 6 11 1 0\n 11 12 2 0\n 3 12 1 0\nM RGP 1 9 2\nM END\n> <Name>\n2-(4-methoxyphenyl)acetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAnTyr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-(4-chlorophenyl)acetic acid\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n -1.6422 7.2386 0.0000 Cl 0 0\n -2.3945 5.9409 0.0000 C 0 0\n -3.8945 5.9435 0.0000 C 0 0\n -4.6468 4.6458 0.0000 C 0 0\n -3.8990 3.3455 0.0000 C 0 0\n -4.6490 2.0455 0.0000 C 0 0\n -3.8990 0.7455 0.0000 C 0 0\n -2.3990 0.7455 0.0000 R# 0 0\n -4.6486 -0.5538 0.0000 O 0 0\n -2.3990 3.3428 0.0000 C 0 0\n -1.6468 4.6406 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 7 9 2 0\n 5 10 1 0\n 10 11 2 0\n 2 11 1 0\nM RGP 1 8 2\nM END\n> <Name>\n2-(4-chlorophenyl)acetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDAPhg4\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n(2R)-2-hydroxy-3-methylbutanoic acid\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 1.3000 2.2500 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0 1 0 0 0\n 2.6000 -1.5000 0.0000 O 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 3.9000 2.2500 0.0000 R# 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 4 2 1 0\n 4 5 1 6\n 4 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 1 7 2\nM END\n> <Name>\n(2R)-2-hydroxy-3-methylbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-OVal\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nV\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n(2S)-2-hydroxy-4-methylpentanoic acid\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 0.0007 0.0004 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 1.3000 2.2500 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0 2 0 0 0\n 3.9000 2.2500 0.0000 O 0 0\n 5.2000 0.0000 0.0000 C 0 0\n 5.2000 -1.5000 0.0000 R# 0 0\n 6.4992 0.7496 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 5 4 1 0\n 5 6 1 6\n 5 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 1 8 2\nM END\n> <Name>\n(2S)-2-hydroxy-4-methylpentanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOLeu\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nN-Terminal toluene\n SciTegic07272112182D\n\n 8 8 0 0 0 0 999 V2000\n 2.5951 -3.0031 0.0000 R# 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 3 8 1 0\nM RGP 1 1 2\nM END\n> <Name>\nN-Terminal toluene\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBn-\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nN-Terminal phenylmethanol\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 3.8926 -3.7566 0.0000 R# 0 0\n 2.5951 -3.0039 0.0000 O 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\nM RGP 1 1 2\nM END\n> <Name>\nN-Terminal phenylmethanol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOBn-\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\nDeamino-Lysine\n SciTegic07272112182D\n\n 10 9 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 N 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.2000 0.0000 0.0000 C 0 0\n 6.5000 0.7500 0.0000 C 0 0\n 6.5000 2.2500 0.0000 R# 0 0\n 7.7999 0.0000 0.0000 C 0 0\n 7.7999 -1.5000 0.0000 O 0 0\n 9.0992 0.7496 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 6 8 1 0\n 8 9 1 0\n 8 10 2 0\nM RGP 1 7 2\nM END\n> <Name>\nDeamino-Lysine\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDALys\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n4-(dimethylamino)benzoic acid\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n -7.1102 -3.6899 0.0000 C 0 0\n -5.6102 -3.6946 0.0000 N 0 0\n -4.8648 -4.9963 0.0000 C 0 0\n -4.8549 -2.3977 0.0000 C 0 0\n -3.3549 -2.4003 0.0000 C 0 0\n -2.6026 -1.1026 0.0000 C 0 0\n -3.3504 0.1977 0.0000 C 0 0\n -4.8504 0.2003 0.0000 C 0 0\n -5.6026 -1.0974 0.0000 C 0 0\n -2.6003 1.4977 0.0000 C 0 0\n -1.1003 1.4977 0.0000 R# 0 0\n -3.3499 2.7970 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 1 11 2\nM END\n> <Name>\n4-(dimethylamino)benzoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNMe24A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R2]O\n\n$$$$\n2-amino-3-(3-nitrophenyl)prop-2-enoic acid\n SciTegic07272112182D\n\n 16 16 0 0 0 0 999 V2000\n -4.5486 -1.0149 0.0000 O 0 5\n -3.2461 -0.2709 0.0000 N 0 3\n -3.2396 1.2290 0.0000 O 0 0\n -1.9501 -1.0278 0.0000 C 0 0\n -1.9545 -2.5278 0.0000 C 0 0\n -0.6577 -3.2816 0.0000 C 0 0\n 0.6436 -2.5354 0.0000 C 0 0\n 0.6480 -1.0354 0.0000 C 0 0\n 1.9484 -0.2861 0.0000 C 0 0\n 1.9506 1.2147 0.0000 C 0 0\n 0.6502 1.9640 0.0000 N 0 0\n -0.6487 1.2137 0.0000 R# 0 0\n 3.2510 1.9640 0.0000 C 0 0\n 4.5492 1.2124 0.0000 R# 0 0\n 3.2533 3.4640 0.0000 O 0 0\n -0.6489 -0.2816 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 9 8 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 13 15 2 0\n 8 16 2 0\n 4 16 1 0\nM CHG 2 1 -1 2 1\nM RGP 2 12 1 14 2\nM END\n> <Name>\n2-amino-3-(3-nitrophenyl)prop-2-enoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPheNO2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-amino-2-methylpropan-1-ol\n SciTegic07272112182D\n\n 7 6 0 0 0 0 999 V2000\n 6.7009 2.5990 0.0000 C 0 0\n 7.4505 1.2997 0.0000 C 0 0\n 8.2007 2.5986 0.0000 C 0 0\n 8.9513 1.2997 0.0000 C 0 0\n 9.7021 2.5983 0.0000 O 0 0\n 6.6992 0.0004 0.0000 N 0 0\n 5.1992 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 2 6 1 0\n 6 7 1 0\nM RGP 1 7 1\nM END\n> <Name>\n2-amino-2-methylpropan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAib-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n[(2R)-pyrrolidin-2-yl]methanol\n SciTegic07272112182D\n\n 8 8 0 0 1 0 999 V2000\n 3.1247 -2.0836 0.0000 O 0 0\n 1.6332 -2.2426 0.0000 C 0 0\n 0.7500 -1.0323 0.0000 C 0 0 1 0 0 0\n 1.2135 0.3943 0.0000 C 0 0\n 0.0000 1.2760 0.0000 C 0 0\n -1.2135 0.3943 0.0000 C 0 0\n -0.7500 -1.0323 0.0000 N 0 0\n -1.6317 -2.2458 0.0000 R# 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 7 8 1 0\nM RGP 1 8 1\nM END\n> <Name>\n[(2R)-pyrrolidin-2-yl]methanol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDProol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-4-methylpentan-1-ol\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 11.2079 3.0031 0.0000 C 0 0\n 9.7079 3.0015 0.0000 C 0 0\n 8.9597 1.7014 0.0000 C 0 0\n 8.9552 4.2999 0.0000 C 0 0\n 7.4544 4.2983 0.0000 C 0 0 1 0 0 0\n 6.7017 5.5967 0.0000 C 0 0\n 5.2017 5.5951 0.0000 O 0 0\n 6.7032 2.9990 0.0000 N 0 0\n 5.2032 2.9990 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 5 4 1 6\n 5 6 1 0\n 6 7 1 0\n 5 8 1 0\n 8 9 1 0\nM RGP 1 9 1\nM END\n> <Name>\n(2S)-2-amino-4-methylpentan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLeu-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-3-phenylpropan-1-ol\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n 3.8912 -5.2570 0.0000 O 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 2.5951 -3.0039 0.0000 C 0 0 2 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n -0.0041 -2.9953 0.0000 R# 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 3 11 1 0\n 11 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n(2S)-2-amino-3-phenylpropan-1-ol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S,3S)-2-aminobutane-1,3-diol\n SciTegic07272112182D\n\n 8 7 0 0 1 0 999 V2000\n 1.3000 2.2500 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0 2 0 0 0\n 0.0007 0.0004 0.0000 O 0 0\n 2.6000 0.0000 0.0000 C 0 0 2 0 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 2.5969 -1.5008 0.0000 N 0 0\n 1.2968 -2.2490 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 2 4 1 0\n 4 5 1 6\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\nM RGP 1 8 1\nM END\n> <Name>\n(2S,3S)-2-aminobutane-1,3-diol\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nThr-ol\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-aminoacetaldehyde\n SciTegic07272112182D\n\n 5 4 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\nM RGP 1 1 1\nM END\n> <Name>\n2-aminoacetaldehyde\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nGly-al\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-4-methylpentanal\n SciTegic07272112182D\n\n 9 8 0 0 1 0 999 V2000\n 11.2079 3.0031 0.0000 C 0 0\n 9.7079 3.0015 0.0000 C 0 0\n 8.9597 1.7014 0.0000 C 0 0\n 8.9552 4.2999 0.0000 C 0 0\n 7.4544 4.2983 0.0000 C 0 0 2 0 0 0\n 6.7032 2.9990 0.0000 N 0 0\n 5.2032 2.9990 0.0000 R# 0 0\n 6.7017 5.5967 0.0000 C 0 0\n 5.2017 5.5951 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 5 4 1 6\n 5 6 1 0\n 6 7 1 0\n 5 8 1 0\n 8 9 2 0\nM RGP 1 7 1\nM END\n> <Name>\n(2S)-2-amino-4-methylpentanal\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLeu-al\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nL\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-3-phenylpropanal\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n 1.2951 -5.2547 0.0000 R# 0 0\n 1.2956 -3.7547 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 1 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 3 11 1 0\n 11 12 2 0\nM RGP 1 1 1\nM END\n> <Name>\n(2S)-2-amino-3-phenylpropanal\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe-al\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-2-amino-6-{[bis(ethylamino)methylidene]amino}hexanoic acid\n SciTegic09012117322D\n\n 18 17 0 0 1 0 999 V2000\n -2.8981 -7.0008 0.0000 C 0 0\n -2.8959 -5.5008 0.0000 C 0 0\n -1.5954 -4.7515 0.0000 N 0 0\n -1.5932 -3.2507 0.0000 C 0 0\n -0.2927 -2.5014 0.0000 N 0 0\n -0.2905 -1.0006 0.0000 C 0 0\n 1.0099 -0.2514 0.0000 C 0 0\n 1.0122 1.2494 0.0000 C 0 0\n 2.3126 1.9987 0.0000 C 0 0\n 2.3149 3.4995 0.0000 C 0 0 2 0 0 0\n 1.0145 4.2488 0.0000 N 0 0\n -0.2844 3.4985 0.0000 R# 0 0\n 3.6153 4.2488 0.0000 C 0 0\n 4.9134 3.4972 0.0000 R# 0 0\n 3.6176 5.7488 0.0000 O 0 0\n -2.8904 -2.4961 0.0000 N 0 0\n -2.8865 -0.9953 0.0000 C 0 0\n -4.1831 -0.2410 0.0000 C 0 0\n 1 2 1 0\n 3 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 10 9 1 6\n 10 11 1 0\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 13 15 2 0\n 4 16 2 0\n 16 17 1 0\n 17 18 1 0\nM RGP 2 12 1 14 2\nM END\n> <Name>\n(2S)-2-amino-6-{[bis(ethylamino)methylidene]amino}hexanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nLhArgE\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-4-methanesulfinylbutanoic acid\n SciTegic09012117322D\n\n 11 10 0 0 1 0 999 V2000\n 0.3495 3.3425 0.0000 C 0 0\n -0.9487 2.5910 0.0000 S 0 0\n -2.2484 3.3398 0.0000 O 0 0\n -0.9464 1.0901 0.0000 C 0 0\n 0.3540 0.3409 0.0000 C 0 0\n 0.3563 -1.1600 0.0000 C 0 0 2 0 0 0\n -0.9441 -1.9092 0.0000 N 0 0\n 1.6567 -1.9092 0.0000 C 0 0\n -2.2430 -1.1590 0.0000 R# 0 0\n 2.9549 -1.1577 0.0000 R# 0 0\n 1.6590 -3.4092 0.0000 O 0 0\n 1 2 1 0\n 3 2 2 0\n 2 4 1 0\n 4 5 1 0\n 6 5 1 1\n 6 7 1 0\n 6 8 1 0\n 7 9 1 0\n 8 10 1 0\n 8 11 2 0\nM RGP 2 9 1 10 2\nM END\n> <Name>\n(2S)-2-amino-4-methanesulfinylbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nMet_O\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nM\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-2-(4-hydroxyphenyl)acetic acid\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.0993 4.4423 0.0000 O 0 0\n -0.1001 2.9423 0.0000 C 0 0\n -1.3996 2.1930 0.0000 C 0 0\n -1.4004 0.6930 0.0000 C 0 0\n -0.1018 -0.0577 0.0000 C 0 0\n 1.1977 0.6916 0.0000 C 0 0\n 1.1985 2.1916 0.0000 C 0 0\n -0.0995 -1.5586 0.0000 C 0 0 2 0 0 0\n -1.3999 -2.3078 0.0000 N 0 0\n -2.6988 -1.5575 0.0000 R# 0 0\n 1.2009 -2.3078 0.0000 C 0 0\n 2.4990 -1.5563 0.0000 R# 0 0\n 1.2031 -3.8078 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 2 7 1 0\n 8 5 1 0\n 8 9 1 1\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n(2S)-2-amino-2-(4-hydroxyphenyl)acetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nnTyr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S,3aR,7aS)-octahydro-1H-indole-2-carboxylic acid\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n -0.2550 2.6034 0.0000 R# 0 0\n -0.0213 1.1217 0.0000 N 0 0\n -1.0820 0.0623 0.0000 C 0 0 1 0 0 0\n -2.5799 0.1419 0.0000 C 0 0\n -3.3978 -1.1155 0.0000 C 0 0\n -2.7178 -2.4526 0.0000 C 0 0\n -1.2199 -2.5322 0.0000 C 0 0\n -0.4020 -1.2748 0.0000 C 0 0 2 0 0 0\n 1.0789 -1.0416 0.0000 C 0 0\n 1.3147 0.4398 0.0000 C 0 0 1 0 0 0\n 2.6487 1.1217 0.0000 C 0 0\n 3.9075 0.3061 0.0000 R# 0 0\n 2.7262 2.6197 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 0\n 3 4 1 6\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 1\n 3 8 1 0\n 8 9 1 0\n 10 9 1 0\n 10 2 1 0\n 10 11 1 6\n 11 12 1 0\n 11 13 2 0\nM RGP 2 1 1 12 2\nM END\n> <Name>\n(2S,3aR,7aS)-octahydro-1H-indole-2-carboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nOic3aR\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(2-fluorophenyl)propanoic acid\n SciTegic09012117322D\n\n 14 14 0 0 1 0 999 V2000\n 1.0137 3.0583 0.0000 F 0 0\n -0.2832 2.3045 0.0000 C 0 0\n -1.5844 3.0507 0.0000 C 0 0\n -2.8813 2.2970 0.0000 C 0 0\n -2.8769 0.7970 0.0000 C 0 0\n -1.5756 0.0508 0.0000 C 0 0\n -0.2788 0.8045 0.0000 C 0 0\n 1.0216 0.0552 0.0000 C 0 0\n 1.0238 -1.4456 0.0000 C 0 0 2 0 0 0\n -0.2765 -2.1949 0.0000 N 0 0\n -1.5754 -1.4446 0.0000 R# 0 0\n 2.3242 -2.1949 0.0000 C 0 0\n 3.6224 -1.4433 0.0000 R# 0 0\n 2.3265 -3.6949 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 2 7 1 0\n 7 8 1 0\n 9 8 1 1\n 9 10 1 0\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2S)-2-amino-3-(2-fluorophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe_2F\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(3-fluorophenyl)propanoic acid\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8032 -0.2585 0.0000 F 0 0\n -2.5064 -1.0123 0.0000 C 0 0\n -2.5107 -2.5123 0.0000 C 0 0\n -1.2139 -3.2661 0.0000 C 0 0\n 0.0873 -2.5199 0.0000 C 0 0\n 0.0917 -1.0199 0.0000 C 0 0\n 1.3921 -0.2706 0.0000 C 0 0\n 1.3944 1.2302 0.0000 C 0 0 2 0 0 0\n 0.0940 1.9795 0.0000 N 0 0\n -1.2049 1.2292 0.0000 R# 0 0\n 2.6948 1.9795 0.0000 C 0 0\n 3.9929 1.2279 0.0000 R# 0 0\n 2.6970 3.4795 0.0000 O 0 0\n -1.2051 -0.2661 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 1 0\n 8 7 1 6\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\n 6 14 2 0\n 2 14 1 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n(2S)-2-amino-3-(3-fluorophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe_3F\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-fluorophenyl)propanoic acid\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -3.8113 -3.0442 0.0000 F 0 0\n -2.5101 -2.2980 0.0000 C 0 0\n -1.2133 -3.0518 0.0000 C 0 0\n 0.0879 -2.3056 0.0000 C 0 0\n 0.0923 -0.8056 0.0000 C 0 0\n 1.3927 -0.0563 0.0000 C 0 0\n 1.3950 1.4445 0.0000 C 0 0 2 0 0 0\n 0.0946 2.1938 0.0000 N 0 0\n -1.2043 1.4435 0.0000 R# 0 0\n 2.6954 2.1938 0.0000 C 0 0\n 3.9936 1.4422 0.0000 R# 0 0\n 2.6977 3.6938 0.0000 O 0 0\n -1.2045 -0.0518 0.0000 C 0 0\n -2.5057 -0.7980 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-fluorophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe_4F\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-nitrophenyl)propanoic acid\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -3.2553 -2.6153 0.0000 N 0 3\n -3.2623 -4.1153 0.0000 O 0 5\n -4.5511 -1.8597 0.0000 O 0 0\n -1.9519 -1.8714 0.0000 C 0 0\n -0.6550 -2.6252 0.0000 C 0 0\n -1.9475 -0.3714 0.0000 C 0 0\n 0.6462 -1.8790 0.0000 C 0 0\n -0.6462 0.3748 0.0000 C 0 0\n 0.6506 -0.3790 0.0000 C 0 0\n 1.9510 0.3703 0.0000 C 0 0\n 1.9533 1.8711 0.0000 C 0 0 2 0 0 0\n 0.6529 2.6204 0.0000 N 0 0\n 3.2537 2.6204 0.0000 C 0 0\n -0.6460 1.8701 0.0000 R# 0 0\n 4.5518 1.8689 0.0000 R# 0 0\n 3.2559 4.1204 0.0000 O 0 0\n 2 1 1 0\n 1 3 2 0\n 4 1 1 0\n 5 4 2 0\n 4 6 1 0\n 7 5 1 0\n 6 8 2 0\n 9 7 2 0\n 9 8 1 0\n 10 9 1 0\n 11 10 1 6\n 11 12 1 0\n 11 13 1 0\n 14 12 1 0\n 13 15 1 0\n 13 16 2 0\nM CHG 2 1 1 2 -1\nM RGP 2 14 1 15 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-nitrophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhe4NO\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-methyl-3-phenylbutanoic acid\n SciTegic09012117322D\n\n 15 15 0 0 1 0 999 V2000\n 2.0773 -1.0021 0.0000 C 0 0\n 0.7791 -0.2505 0.0000 C 0 0\n 2.0792 0.4978 0.0000 C 0 0\n 0.7814 1.2503 0.0000 C 0 0 2 0 0 0\n -0.5190 1.9996 0.0000 N 0 0\n -1.8179 1.2493 0.0000 R# 0 0\n 2.0818 1.9996 0.0000 C 0 0\n 3.3799 1.2480 0.0000 R# 0 0\n 2.0841 3.4996 0.0000 O 0 0\n -0.5213 -0.9998 0.0000 C 0 0\n -1.8197 -0.2486 0.0000 C 0 0\n -3.1194 -0.9975 0.0000 C 0 0\n -3.1207 -2.4974 0.0000 C 0 0\n -1.8223 -3.2486 0.0000 C 0 0\n -0.5226 -2.4998 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 4 2 1 0\n 4 5 1 6\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\n 7 9 2 0\n 2 10 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 15 2 0\n 10 15 1 0\nM RGP 2 6 1 8 2\nM END\n> <Name>\n(2S)-2-amino-3-methyl-3-phenylbutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nPhebbd\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid\n SciTegic09012117322D\n\n 17 18 0 0 1 0 999 V2000\n 1.1222 4.8834 0.0000 O 0 0\n 0.1216 3.7659 0.0000 C 0 0\n -1.3465 4.0738 0.0000 C 0 0\n -2.3471 2.9564 0.0000 C 0 0\n -1.8797 1.5311 0.0000 C 0 0\n -2.6260 0.2308 0.0000 N 0 0\n -1.6193 -0.8812 0.0000 C 0 0\n -0.2507 -0.2673 0.0000 C 0 0\n 1.0476 -1.0153 0.0000 C 0 0\n 1.0498 -2.5161 0.0000 C 0 0 2 0 0 0\n -0.2506 -3.2655 0.0000 N 0 0\n -1.5495 -2.5151 0.0000 R# 0 0\n 2.3501 -3.2655 0.0000 C 0 0\n 3.6483 -2.5139 0.0000 R# 0 0\n 2.3524 -4.7655 0.0000 O 0 0\n -0.4117 1.2232 0.0000 C 0 0\n 0.5890 2.3407 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 10 9 1 1\n 10 11 1 0\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 13 15 2 0\n 8 16 1 0\n 5 16 1 0\n 16 17 2 0\n 2 17 1 0\nM RGP 2 12 1 14 2\nM END\n> <Name>\n(2S)-2-amino-3-(5-hydroxy-1H-indol-3-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTrp5OH\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nW\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(1-methoxy-1H-indol-3-yl)propanoic acid\n SciTegic09012117322D\n\n 18 19 0 0 1 0 999 V2000\n -4.1668 -0.9653 0.0000 C 0 0\n -3.5621 0.4074 0.0000 O 0 0\n -2.0728 0.5709 0.0000 N 0 0\n -1.0661 -0.5411 0.0000 C 0 0\n 0.3025 0.0728 0.0000 C 0 0\n 1.6007 -0.6752 0.0000 C 0 0\n 1.6030 -2.1761 0.0000 C 0 0 2 0 0 0\n 0.3026 -2.9254 0.0000 N 0 0\n -0.9963 -2.1750 0.0000 R# 0 0\n 2.9034 -2.9254 0.0000 C 0 0\n 4.2016 -2.1739 0.0000 R# 0 0\n 2.9056 -4.4253 0.0000 O 0 0\n 0.1415 1.5633 0.0000 C 0 0\n 1.1422 2.6808 0.0000 C 0 0\n 0.6748 4.1060 0.0000 C 0 0\n -0.7932 4.4139 0.0000 C 0 0\n -1.7939 3.2964 0.0000 C 0 0\n -1.3265 1.8712 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 1\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 16 17 1 0\n 17 18 2 0\n 3 18 1 0\n 13 18 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(1-methoxy-1H-indol-3-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTrpOme\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nW\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-hydroxy-3,5-diiodophenyl)propanoic acid\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -3.4976 -2.7570 0.0000 O 0 0\n -2.1964 -2.0108 0.0000 C 0 0\n -0.8995 -2.7646 0.0000 C 0 0\n -0.9039 -4.2646 0.0000 I 0 0\n 0.4017 -2.0184 0.0000 C 0 0\n 0.4061 -0.5184 0.0000 C 0 0\n 1.7065 0.2309 0.0000 C 0 0\n 1.7088 1.7317 0.0000 C 0 0 2 0 0 0\n 0.4084 2.4810 0.0000 N 0 0\n -0.8905 1.7307 0.0000 R# 0 0\n 3.0092 2.4810 0.0000 C 0 0\n 4.3073 1.7295 0.0000 R# 0 0\n 3.0114 3.9810 0.0000 O 0 0\n -0.8907 0.2354 0.0000 C 0 0\n -2.1920 -0.5108 0.0000 C 0 0\n -3.4888 0.2430 0.0000 I 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 3 5 1 0\n 5 6 2 0\n 6 7 1 0\n 8 7 1 6\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\n 6 14 1 0\n 14 15 2 0\n 2 15 1 0\n 15 16 1 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-hydroxy-3,5-diiodophenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyr35d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -3.5578 -3.0413 0.0000 O 0 0\n -2.2566 -2.2951 0.0000 C 0 0\n -0.9598 -3.0489 0.0000 C 0 0\n 0.3415 -2.3027 0.0000 C 0 0\n 0.3458 -0.8027 0.0000 C 0 0\n 1.6463 -0.0534 0.0000 C 0 0\n 1.6485 1.4474 0.0000 C 0 0 2 0 0 0\n 0.3481 2.1967 0.0000 N 0 0\n -0.9508 1.4464 0.0000 R# 0 0\n 2.9489 2.1967 0.0000 C 0 0\n 4.2471 1.4452 0.0000 R# 0 0\n 2.9512 3.6967 0.0000 O 0 0\n -0.9510 -0.0489 0.0000 C 0 0\n -2.2522 -0.7951 0.0000 C 0 0\n -3.5491 -0.0413 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\n 5 13 1 0\n 13 14 2 0\n 2 14 1 0\n 14 15 1 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyr3OH\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-methoxyphenyl)propanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -4.7686 -2.1340 0.0000 C 0 0\n -3.4728 -2.8897 0.0000 O 0 0\n -2.1693 -2.1457 0.0000 C 0 0\n -0.8725 -2.8995 0.0000 C 0 0\n 0.4287 -2.1534 0.0000 C 0 0\n 0.4331 -0.6534 0.0000 C 0 0\n 1.7335 0.0959 0.0000 C 0 0\n 1.7358 1.5968 0.0000 C 0 0 2 0 0 0\n 0.4354 2.3460 0.0000 N 0 0\n -0.8635 1.5957 0.0000 R# 0 0\n 3.0362 2.3460 0.0000 C 0 0\n 4.3343 1.5945 0.0000 R# 0 0\n 3.0384 3.8460 0.0000 O 0 0\n -0.8637 0.1004 0.0000 C 0 0\n -2.1650 -0.6458 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 8 7 1 6\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\n 6 14 1 0\n 14 15 2 0\n 3 15 1 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-methoxyphenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyr_Me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-[4-(phosphonooxy)phenyl]propanoic acid\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -3.8234 -0.3621 0.0000 O 0 0\n -3.8304 -1.8621 0.0000 P 0 0\n -5.1258 -1.1058 0.0000 O 0 0\n -5.1332 -2.6056 0.0000 O 0 0\n -2.5340 -2.6181 0.0000 O 0 0\n -1.2305 -1.8742 0.0000 C 0 0\n 0.0664 -2.6280 0.0000 C 0 0\n 1.3676 -1.8818 0.0000 C 0 0\n 1.3720 -0.3818 0.0000 C 0 0\n 2.6724 0.3675 0.0000 C 0 0\n 2.6747 1.8683 0.0000 C 0 0 2 0 0 0\n 1.3742 2.6176 0.0000 N 0 0\n 0.0754 1.8673 0.0000 R# 0 0\n 3.9751 2.6176 0.0000 C 0 0\n 5.2732 1.8660 0.0000 R# 0 0\n 3.9773 4.1176 0.0000 O 0 0\n 0.0752 0.3720 0.0000 C 0 0\n -1.2261 -0.3742 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 11 10 1 6\n 11 12 1 0\n 12 13 1 0\n 11 14 1 0\n 14 15 1 0\n 14 16 2 0\n 9 17 1 0\n 17 18 2 0\n 6 18 1 0\nM RGP 2 13 1 15 2\nM END\n> <Name>\n(2S)-2-amino-3-[4-(phosphonooxy)phenyl]propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nTyrPO3\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-4-hydroxypyrrolidine-2-carboxylic acid\n SciTegic09012117322D\n\n 10 10 0 0 1 0 999 V2000\n -1.9677 -2.9458 0.0000 O 0 0\n -1.2857 -1.6098 0.0000 C 0 0\n 0.1960 -1.3762 0.0000 C 0 0\n 0.4318 0.1051 0.0000 C 0 0 2 0 0 0\n -0.9043 0.7871 0.0000 N 0 0\n -1.1378 2.2688 0.0000 R# 0 0\n -1.9657 -0.2728 0.0000 C 0 0\n 1.7658 0.7871 0.0000 C 0 0\n 3.0246 -0.0286 0.0000 R# 0 0\n 1.8432 2.2851 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 4 3 1 0\n 4 5 1 0\n 5 6 1 0\n 5 7 1 0\n 2 7 1 0\n 4 8 1 6\n 8 9 1 0\n 8 10 2 0\nM RGP 2 6 1 9 2\nM END\n> <Name>\n(2S)-4-hydroxypyrrolidine-2-carboxylic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nxiHyp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-hydroxybutanoic acid\n SciTegic09012117322D\n\n 9 8 0 0 1 0 999 V2000\n 1.1521 2.0015 0.0000 C 0 0\n -0.1460 1.2499 0.0000 C 0 0\n -1.4457 1.9988 0.0000 O 0 0\n -0.1437 -0.2509 0.0000 C 0 0 2 0 0 0\n -1.4441 -1.0002 0.0000 N 0 0\n -2.7430 -0.2499 0.0000 R# 0 0\n 1.1567 -1.0002 0.0000 C 0 0\n 2.4548 -0.2487 0.0000 R# 0 0\n 1.1589 -2.5001 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 4 2 1 0\n 4 5 1 1\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 2 6 1 8 2\nM END\n> <Name>\n(2S)-2-amino-3-hydroxybutanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nxiThr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n4-(methylamino)benzoic acid\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n -3.7490 1.3013 0.0000 C 0 0\n -3.0008 0.0011 0.0000 N 0 0\n -3.7531 -1.2966 0.0000 R# 0 0\n -1.5000 -0.0019 0.0000 C 0 0\n -0.7500 -1.3010 0.0000 C 0 0\n 0.7500 -1.3010 0.0000 C 0 0\n 1.5000 -0.0019 0.0000 C 0 0\n 0.7500 1.2971 0.0000 C 0 0\n -0.7500 1.2971 0.0000 C 0 0\n 3.0008 0.0011 0.0000 C 0 0\n 3.7531 -1.2966 0.0000 R# 0 0\n 3.7490 1.3013 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 3 1 11 2\nM END\n> <Name>\n4-(methylamino)benzoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nNMe4Ab\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-hydroxyphenyl)-2-methylpropanoic acid\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -1.2419 3.3801 0.0000 C 0 0\n -0.4936 2.0800 0.0000 C 0 0 1 0 0 0\n -1.2462 0.7815 0.0000 C 0 0\n -0.4987 -0.5200 0.0000 C 0 0\n -1.2490 -1.8188 0.0000 C 0 0\n -0.4993 -3.1180 0.0000 C 0 0\n 1.0007 -3.1184 0.0000 C 0 0\n 1.7504 -4.4176 0.0000 O 0 0\n 1.7510 -1.8195 0.0000 C 0 0\n 1.0013 -0.5203 0.0000 C 0 0\n -2.0236 2.0785 0.0000 N 0 0\n -2.7731 0.7792 0.0000 R# 0 0\n 1.0072 2.0785 0.0000 C 0 0\n 1.7555 0.7785 0.0000 R# 0 0\n 1.7593 3.3763 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 7 9 1 0\n 9 10 2 0\n 4 10 1 0\n 2 11 1 0\n 11 12 1 0\n 2 13 1 0\n 13 14 1 0\n 13 15 2 0\nM RGP 2 12 1 14 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-hydroxyphenyl)-2-methylpropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\naMeTyr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-8-oxodecanoic acid\n SciTegic09012117322D\n\n 15 14 0 0 1 0 999 V2000\n -3.5597 6.0494 0.0000 C 0 0\n -2.2600 5.3005 0.0000 C 0 0\n -2.2577 3.7997 0.0000 C 0 0\n -3.5558 3.0481 0.0000 O 0 0\n -0.9573 3.0504 0.0000 C 0 0\n -0.9550 1.5496 0.0000 C 0 0\n 0.3454 0.8003 0.0000 C 0 0\n 0.3477 -0.7004 0.0000 C 0 0\n 1.6481 -1.4497 0.0000 C 0 0\n 1.6504 -2.9505 0.0000 C 0 0 2 0 0 0\n 0.3500 -3.6998 0.0000 N 0 0\n -0.9489 -2.9496 0.0000 R# 0 0\n 2.9508 -3.6998 0.0000 C 0 0\n 4.2489 -2.9483 0.0000 R# 0 0\n 2.9531 -5.1998 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 3 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 10 9 1 1\n 10 11 1 0\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 13 15 2 0\nM RGP 2 12 1 14 2\nM END\n> <Name>\n(2S)-2-amino-8-oxodecanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAoda\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(4-benzoylphenyl)propanoic acid\n SciTegic07272112182D\n\n 21 22 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 1 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.6003 1.4977 0.0000 C 0 0\n -2.6030 2.9977 0.0000 O 0 0\n -3.8990 0.7455 0.0000 C 0 0\n -5.2007 1.4909 0.0000 C 0 0\n -6.4972 0.7364 0.0000 C 0 0\n -6.4920 -0.7636 0.0000 C 0 0\n -5.1903 -1.5091 0.0000 C 0 0\n -3.8939 -0.7546 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 8 11 1 0\n 11 12 2 0\n 11 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 16 17 1 0\n 17 18 2 0\n 13 18 1 0\n 3 19 1 0\n 19 20 1 0\n 19 21 2 0\nM RGP 2 1 1 20 2\nM END\n> <Name>\n(2S)-2-amino-3-(4-benzoylphenyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBpa\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3-(methylsulfanyl)propanoic acid\n SciTegic09012117322D\n\n 9 8 0 0 1 0 999 V2000\n -1.1596 -3.3327 0.0000 C 0 0\n -1.1574 -1.8327 0.0000 S 0 0\n 0.1431 -1.0834 0.0000 C 0 0\n 0.1453 0.4174 0.0000 C 0 0 2 0 0 0\n -1.1550 1.1667 0.0000 N 0 0\n -2.4540 0.4164 0.0000 R# 0 0\n 1.4458 1.1667 0.0000 C 0 0\n 2.7439 0.4151 0.0000 R# 0 0\n 1.4480 2.6666 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 4 3 1 6\n 4 5 1 0\n 5 6 1 0\n 4 7 1 0\n 7 8 1 0\n 7 9 2 0\nM RGP 2 6 1 8 2\nM END\n> <Name>\n(2R)-2-amino-3-(methylsulfanyl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nCys_Me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3,3-diphenylpropanoic acid\n SciTegic07272112182D\n\n 19 20 0 0 1 0 999 V2000\n -2.6668 1.7759 0.0000 R# 0 0\n -1.3676 2.5255 0.0000 N 0 0\n -0.0676 1.7755 0.0000 C 0 0 1 0 0 0\n -0.0676 0.2748 0.0000 C 0 0\n 1.2314 -0.4771 0.0000 C 0 0\n 1.2334 -1.9771 0.0000 C 0 0\n 2.5334 -2.7254 0.0000 C 0 0\n 3.8314 -1.9737 0.0000 C 0 0\n 3.8295 -0.4737 0.0000 C 0 0\n 2.5295 0.2746 0.0000 C 0 0\n -1.3686 -0.4736 0.0000 C 0 0\n -1.3718 -1.9737 0.0000 C 0 0\n -2.6724 -2.7210 0.0000 C 0 0\n -3.9699 -1.9684 0.0000 C 0 0\n -3.9668 -0.4684 0.0000 C 0 0\n -2.6662 0.2790 0.0000 C 0 0\n 1.2324 2.5255 0.0000 C 0 0\n 1.2324 4.0255 0.0000 R# 0 0\n 2.5317 1.7759 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 4 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 11 16 1 0\n 3 17 1 0\n 17 18 1 0\n 17 19 2 0\nM RGP 2 1 1 18 2\nM END\n> <Name>\n(2S)-2-amino-3,3-diphenylpropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDip\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-6-[(diaminomethyl)amino]hexanoic acid\n SciTegic09012117322D\n\n 14 13 0 0 1 0 999 V2000\n -2.5142 -5.7319 0.0000 N 0 0\n -2.5119 -4.2318 0.0000 C 0 0\n -3.8101 -3.4803 0.0000 N 0 0\n -1.2115 -3.4826 0.0000 N 0 0\n -1.2092 -1.9817 0.0000 C 0 0\n 0.0912 -1.2325 0.0000 C 0 0\n 0.0935 0.2684 0.0000 C 0 0\n 1.3938 1.0176 0.0000 C 0 0\n 1.3961 2.5184 0.0000 C 0 0 2 0 0 0\n 0.0957 3.2677 0.0000 N 0 0\n -1.2032 2.5174 0.0000 R# 0 0\n 2.6965 3.2677 0.0000 C 0 0\n 3.9947 2.5161 0.0000 R# 0 0\n 2.6988 4.7677 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 9 8 1 6\n 9 10 1 0\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 2 11 1 13 2\nM END\n> <Name>\n(2S)-2-amino-6-[(diaminomethyl)amino]hexanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nhArg\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(1-benzyl-1H-imidazol-4-yl)propanoic acid\n SciTegic09012117322D\n\n 19 20 0 0 1 0 999 V2000\n 0.2119 -2.7206 0.0000 R# 0 0\n 1.5107 -3.4708 0.0000 N 0 0\n 2.8111 -2.7215 0.0000 C 0 0 1 0 0 0\n 2.8089 -1.2207 0.0000 C 0 0\n 1.5107 -0.4727 0.0000 C 0 0\n 1.3494 1.0186 0.0000 C 0 0\n -0.1097 1.3062 0.0000 N 0 0\n -0.7270 2.6742 0.0000 C 0 0\n -2.2203 2.8245 0.0000 C 0 0\n -2.8392 4.1909 0.0000 C 0 0\n -4.3320 4.3381 0.0000 C 0 0\n -5.2058 3.1189 0.0000 C 0 0\n -4.5869 1.7526 0.0000 C 0 0\n -3.0942 1.6053 0.0000 C 0 0\n -0.8648 0.0249 0.0000 C 0 0\n 0.1422 -1.0869 0.0000 N 0 0\n 4.1115 -3.4708 0.0000 C 0 0\n 5.4097 -2.7192 0.0000 R# 0 0\n 4.1138 -4.9708 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 9 14 1 0\n 7 15 1 0\n 15 16 2 0\n 5 16 1 0\n 3 17 1 0\n 17 18 1 0\n 17 19 2 0\nM RGP 2 1 1 18 2\nM END\n> <Name>\n(2S)-2-amino-3-(1-benzyl-1H-imidazol-4-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHis1Bn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nH\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-(1-methyl-1H-imidazol-5-yl)propanoic acid\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n 0.5030 3.4455 0.0000 C 0 0\n -0.6088 2.4385 0.0000 N 0 0\n -2.0769 2.7461 0.0000 C 0 0\n -2.8231 1.4448 0.0000 N 0 0\n -1.8161 0.3331 0.0000 C 0 0\n -0.4476 0.9472 0.0000 C 0 0\n 0.8506 0.1992 0.0000 C 0 0\n 0.8528 -1.3016 0.0000 C 0 0 2 0 0 0\n -0.4476 -2.0509 0.0000 N 0 0\n -1.7464 -1.3006 0.0000 R# 0 0\n 2.1532 -2.0509 0.0000 C 0 0\n 3.4514 -1.2994 0.0000 R# 0 0\n 2.1555 -3.5509 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 2 6 1 0\n 6 7 1 0\n 8 7 1 1\n 8 9 1 0\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n(2S)-2-amino-3-(1-methyl-1H-imidazol-5-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHis3Me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nH\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2,6-diamino-5-hydroxyhexanoic acid\n SciTegic09012117322D\n\n 12 11 0 0 1 0 999 V2000\n -2.0635 -4.4369 0.0000 N 0 0\n -2.0613 -2.9369 0.0000 C 0 0\n -0.7609 -2.1876 0.0000 C 0 0\n 0.5373 -2.9391 0.0000 O 0 0\n -0.7587 -0.6868 0.0000 C 0 0\n 0.5417 0.0626 0.0000 C 0 0\n 0.5440 1.5634 0.0000 C 0 0 2 0 0 0\n -0.7565 2.3126 0.0000 N 0 0\n -2.0553 1.5623 0.0000 R# 0 0\n 1.8443 2.3126 0.0000 C 0 0\n 3.1425 1.5611 0.0000 R# 0 0\n 1.8465 3.8126 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 3 5 1 0\n 5 6 1 0\n 7 6 1 6\n 7 8 1 0\n 8 9 1 0\n 7 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 2 9 1 11 2\nM END\n> <Name>\n(2S)-2,6-diamino-5-hydroxyhexanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nHyl5xi\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nK\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2S)-2-amino-3-{[1,1'-biphenyl]-4-yl}propanoic acid\n SciTegic07272112182D\n\n 19 20 0 0 1 0 999 V2000\n -0.0041 -2.9953 0.0000 R# 0 0\n 1.2925 -3.7494 0.0000 N 0 0\n 2.5951 -3.0039 0.0000 C 0 0 1 0 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.5987 1.5004 0.0000 C 0 0\n -2.6012 3.0004 0.0000 C 0 0\n -3.9015 3.7484 0.0000 C 0 0\n -5.1993 2.9963 0.0000 C 0 0\n -5.1969 1.4963 0.0000 C 0 0\n -3.8967 0.7484 0.0000 C 0 0\n 3.8933 -3.7570 0.0000 C 0 0\n 5.1937 -3.0093 0.0000 R# 0 0\n 3.8912 -5.2570 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 8 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 11 16 1 0\n 3 17 1 0\n 17 18 1 0\n 17 19 2 0\nM RGP 2 1 1 18 2\nM END\n> <Name>\n(2S)-2-amino-3-{[1,1'-biphenyl]-4-yl}propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nBip\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-aminobut-2-enoic acid\n SciTegic09012117322D\n\n 8 7 0 0 0 0 999 V2000\n -1.3017 2.2489 0.0000 C 0 0\n -0.0020 1.5001 0.0000 C 0 0\n 0.0003 -0.0008 0.0000 C 0 0\n -1.3001 -0.7500 0.0000 N 0 0\n -2.5990 0.0002 0.0000 R# 0 0\n 1.3007 -0.7500 0.0000 C 0 0\n 2.5988 0.0015 0.0000 R# 0 0\n 1.3029 -2.2500 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 3 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 2 5 1 7 2\nM END\n> <Name>\n2-aminobut-2-enoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nAbu23D\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3,3-diphenylpropanoic acid\n SciTegic07272112182D\n\n 19 20 0 0 1 0 999 V2000\n -2.6668 1.7759 0.0000 R# 0 0\n -1.3676 2.5255 0.0000 N 0 0\n -0.0676 1.7755 0.0000 C 0 0 2 0 0 0\n -0.0676 0.2748 0.0000 C 0 0\n 1.2314 -0.4771 0.0000 C 0 0\n 1.2334 -1.9771 0.0000 C 0 0\n 2.5334 -2.7254 0.0000 C 0 0\n 3.8314 -1.9737 0.0000 C 0 0\n 3.8295 -0.4737 0.0000 C 0 0\n 2.5295 0.2746 0.0000 C 0 0\n -1.3686 -0.4736 0.0000 C 0 0\n -1.3718 -1.9737 0.0000 C 0 0\n -2.6724 -2.7210 0.0000 C 0 0\n -3.9699 -1.9684 0.0000 C 0 0\n -3.9668 -0.4684 0.0000 C 0 0\n -2.6662 0.2790 0.0000 C 0 0\n 1.2324 2.5255 0.0000 C 0 0\n 1.2324 4.0255 0.0000 R# 0 0\n 2.5317 1.7759 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 1\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 4 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 11 16 1 0\n 3 17 1 0\n 17 18 1 0\n 17 19 2 0\nM RGP 2 1 1 18 2\nM END\n> <Name>\n(2R)-2-amino-3,3-diphenylpropanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-Dip\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n2-aminoprop-2-enoic acid\n SciTegic07272112182D\n\n 7 6 0 0 0 0 999 V2000\n 2.6000 -1.5000 0.0000 C 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 0.0007 0.0004 0.0000 R# 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 3.9000 2.2500 0.0000 R# 0 0\n 5.1992 0.0004 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 2 5 1 0\n 5 6 1 0\n 5 7 2 0\nM RGP 2 4 1 6 2\nM END\n> <Name>\n2-aminoprop-2-enoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDha\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-6-{[bis(ethylamino)methylidene]amino}hexanoic acid\n SciTegic09012117322D\n\n 18 17 0 0 1 0 999 V2000\n -2.8981 -7.0008 0.0000 C 0 0\n -2.8959 -5.5008 0.0000 C 0 0\n -1.5954 -4.7515 0.0000 N 0 0\n -1.5932 -3.2507 0.0000 C 0 0\n -0.2927 -2.5014 0.0000 N 0 0\n -0.2905 -1.0006 0.0000 C 0 0\n 1.0099 -0.2514 0.0000 C 0 0\n 1.0122 1.2494 0.0000 C 0 0\n 2.3126 1.9987 0.0000 C 0 0\n 2.3149 3.4995 0.0000 C 0 0 1 0 0 0\n 1.0145 4.2488 0.0000 N 0 0\n -0.2844 3.4985 0.0000 R# 0 0\n 3.6153 4.2488 0.0000 C 0 0\n 4.9134 3.4972 0.0000 R# 0 0\n 3.6176 5.7488 0.0000 O 0 0\n -2.8904 -2.4961 0.0000 N 0 0\n -2.8865 -0.9953 0.0000 C 0 0\n -4.1831 -0.2410 0.0000 C 0 0\n 1 2 1 0\n 3 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 10 9 1 1\n 10 11 1 0\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 13 15 2 0\n 4 16 2 0\n 16 17 1 0\n 17 18 1 0\nM RGP 2 12 1 14 2\nM END\n> <Name>\n(2R)-2-amino-6-{[bis(ethylamino)methylidene]amino}hexanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDhArgE\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-4-[(S)-methanesulfinyl]butanoic acid\n SciTegic09012117322D\n\n 11 10 0 0 1 0 999 V2000\n 0.3495 3.3425 0.0000 C 0 0\n -0.9487 2.5910 0.0000 S 0 0 2 0 0 0\n -2.2484 3.3398 0.0000 O 0 0\n -0.9464 1.0901 0.0000 C 0 0\n 0.3540 0.3409 0.0000 C 0 0\n 0.3563 -1.1600 0.0000 C 0 0 1 0 0 0\n -0.9441 -1.9092 0.0000 N 0 0\n 1.6567 -1.9092 0.0000 C 0 0\n -2.2430 -1.1590 0.0000 R# 0 0\n 2.9549 -1.1577 0.0000 R# 0 0\n 1.6590 -3.4092 0.0000 O 0 0\n 2 1 1 1\n 3 2 2 0\n 2 4 1 0\n 4 5 1 0\n 6 5 1 6\n 6 7 1 0\n 6 8 1 0\n 7 9 1 0\n 8 10 1 0\n 8 11 2 0\nM RGP 2 9 1 10 2\nM END\n> <Name>\n(2R)-2-amino-4-[(S)-methanesulfinyl]butanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDMetSO\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nM\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3-(1-benzyl-1H-imidazol-4-yl)propanoic acid\n SciTegic09012117322D\n\n 19 20 0 0 1 0 999 V2000\n 0.2119 -2.7206 0.0000 R# 0 0\n 1.5107 -3.4708 0.0000 N 0 0\n 2.8111 -2.7215 0.0000 C 0 0 2 0 0 0\n 2.8089 -1.2207 0.0000 C 0 0\n 1.5107 -0.4727 0.0000 C 0 0\n 1.3494 1.0186 0.0000 C 0 0\n -0.1097 1.3062 0.0000 N 0 0\n -0.7270 2.6742 0.0000 C 0 0\n -2.2203 2.8245 0.0000 C 0 0\n -2.8392 4.1909 0.0000 C 0 0\n -4.3320 4.3381 0.0000 C 0 0\n -5.2058 3.1189 0.0000 C 0 0\n -4.5869 1.7526 0.0000 C 0 0\n -3.0942 1.6053 0.0000 C 0 0\n -0.8648 0.0249 0.0000 C 0 0\n 0.1422 -1.0869 0.0000 N 0 0\n 4.1115 -3.4708 0.0000 C 0 0\n 5.4097 -2.7192 0.0000 R# 0 0\n 4.1138 -4.9708 0.0000 O 0 0\n 1 2 1 0\n 3 2 1 6\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 9 14 1 0\n 7 15 1 0\n 15 16 2 0\n 5 16 1 0\n 3 17 1 0\n 17 18 1 0\n 17 19 2 0\nM RGP 2 1 1 18 2\nM END\n> <Name>\n(2R)-2-amino-3-(1-benzyl-1H-imidazol-4-yl)propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDHis1B\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nH\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-2-(4-hydroxyphenyl)acetic acid\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.0993 4.4423 0.0000 O 0 0\n -0.1001 2.9423 0.0000 C 0 0\n -1.3996 2.1930 0.0000 C 0 0\n -1.4004 0.6930 0.0000 C 0 0\n -0.1018 -0.0577 0.0000 C 0 0\n 1.1977 0.6916 0.0000 C 0 0\n 1.1985 2.1916 0.0000 C 0 0\n -0.0995 -1.5586 0.0000 C 0 0 1 0 0 0\n -1.3999 -2.3078 0.0000 N 0 0\n -2.6988 -1.5575 0.0000 R# 0 0\n 1.2009 -2.3078 0.0000 C 0 0\n 2.4990 -1.5563 0.0000 R# 0 0\n 1.2031 -3.8078 0.0000 O 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 7 2 0\n 2 7 1 0\n 8 5 1 0\n 8 9 1 6\n 9 10 1 0\n 8 11 1 0\n 11 12 1 0\n 11 13 2 0\nM RGP 2 10 1 12 2\nM END\n> <Name>\n(2R)-2-amino-2-(4-hydroxyphenyl)acetic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nD-nTyr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nY\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n(2R)-2-amino-3-[4-(carbamoylamino)phenyl]propanoic acid\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -4.1249 -0.4271 0.0000 N 0 0\n -4.1319 -1.9271 0.0000 C 0 0\n -5.4347 -2.6706 0.0000 O 0 0\n -2.8355 -2.6832 0.0000 N 0 0\n -1.5320 -1.9393 0.0000 C 0 0\n -0.2351 -2.6931 0.0000 C 0 0\n 1.0661 -1.9469 0.0000 C 0 0\n 1.0705 -0.4469 0.0000 C 0 0\n 2.3709 0.3024 0.0000 C 0 0\n 2.3731 1.8032 0.0000 C 0 0 1 0 0 0\n 1.0727 2.5525 0.0000 N 0 0\n -0.2261 1.8022 0.0000 R# 0 0\n 3.6735 2.5525 0.0000 C 0 0\n 4.9717 1.8010 0.0000 R# 0 0\n 3.6758 4.0525 0.0000 O 0 0\n -0.2264 0.3069 0.0000 C 0 0\n -1.5276 -0.4393 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 10 9 1 1\n 10 11 1 0\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 13 15 2 0\n 8 16 1 0\n 16 17 2 0\n 5 17 1 0\nM RGP 2 12 1 14 2\nM END\n> <Name>\n(2R)-2-amino-3-[4-(carbamoylamino)phenyl]propanoic acid\n\n> <MonomerType>\nPEPTIDE\n\n> <MonomerName>\nDPhe4u\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nF\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n\n$$$$\n1,3 Propanediol\n SciTegic07272112182D\n\n 7 6 0 0 0 0 999 V2000\n 1.3000 0.7500 0.0000 O 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.2000 0.0000 0.0000 C 0 0\n 6.5000 0.7500 0.0000 O 0 0\n 0.0007 0.0004 0.0000 R# 0 0\n 7.7992 0.0004 0.0000 R# 0 0\n 3 2 1 0\n 4 3 1 0\n 5 4 1 0\n 1 6 1 0\n 5 7 1 0\n 1 2 1 0\nM RGP 2 6 1 7 2\nM END\n> <Name>\n1,3 Propanediol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noC3o\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n1,3-Diaza-2-oxophenoxazin\n SciTegic07272112182D\n\n 16 18 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5000 0.4019 0.0000 O 0 0\n 6.0000 0.4019 0.0000 C 0 0\n 6.7500 1.7010 0.0000 C 0 0\n 6.7500 -0.8971 0.0000 C 0 0\n 8.2500 -0.8971 0.0000 C 0 0\n 9.0000 0.4019 0.0000 C 0 0\n 8.2500 1.7010 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 6 7 1 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 7 1 0\n 11 13 2 0\n 13 14 1 0\n 14 15 2 0\n 15 16 1 0\n 16 12 2 0\nM RGP 1 8 1\nM END\n> <Name>\n1,3-Diaza-2-oxophenoxazin\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ntCo\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n1,3-Dihydroxy-2-propoxymethyl (ganciclovir sugar)\n SciTegic09012117322D\n\n 10 9 0 0 1 0 999 V2000\n 1.5583 0.3008 0.0000 C 0 0\n -1.0386 -2.7040 0.0000 C 0 0\n 0.2603 -1.9520 0.0000 O 0 0\n 0.2594 -0.4512 0.0000 C 0 0 2 0 0 0\n -1.0394 0.3008 0.0000 C 0 0\n -1.0378 -4.2040 0.0000 R# 0 0\n 1.5575 1.8016 0.0000 O 0 0\n -1.0386 1.8016 0.0000 O 0 0\n 2.8556 2.5531 0.0000 R# 0 0\n -2.3367 2.5532 0.0000 R# 0 0\n 2 3 1 0\n 4 3 1 6\n 4 1 1 0\n 4 5 1 0\n 2 6 1 0\n 1 7 1 0\n 5 8 1 0\n 7 9 1 0\n 8 10 1 0\nM RGP 3 6 3 9 2 10 1\nM END\n> <Name>\n1,3-Dihydroxy-2-propoxymethyl (ganciclovir sugar)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndhp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n1,4 Butanediol\n SciTegic09012117322D\n\n 8 7 0 0 0 0 999 V2000\n -3.2715 0.0000 0.0000 O 0 0\n -1.8941 -0.5960 0.0000 C 0 0\n -0.6887 0.2980 0.0000 C 0 0\n 0.6887 -0.2980 0.0000 C 0 0\n 1.8942 0.5961 0.0000 C 0 0\n 3.2715 0.0000 0.0000 O 0 0\n -4.4764 -0.8936 0.0000 R# 0 0\n 4.4763 0.8936 0.0000 R# 0 0\n 3 2 1 0\n 4 3 1 0\n 5 4 1 0\n 6 5 1 0\n 1 7 1 0\n 6 8 1 0\n 1 2 1 0\nM RGP 2 7 1 8 2\nM END\n> <Name>\n1,4 Butanediol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noC4o\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n1,5 Pentanediol\n SciTegic07272112182D\n\n 9 8 0 0 0 0 999 V2000\n 1.3000 0.7500 0.0000 O 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.2000 0.0000 0.0000 C 0 0\n 6.5000 0.7500 0.0000 C 0 0\n 7.7999 0.0000 0.0000 C 0 0\n 9.0999 0.7500 0.0000 O 0 0\n 0.0007 0.0004 0.0000 R# 0 0\n 10.3992 0.0004 0.0000 R# 0 0\n 3 2 1 0\n 4 3 1 0\n 5 4 1 0\n 6 5 1 0\n 7 6 1 0\n 1 8 1 0\n 7 9 1 0\n 1 2 1 0\nM RGP 2 8 1 9 2\nM END\n> <Name>\n1,5 Pentanediol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noC5o\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n1,6 Hexanediol\n SciTegic07272112182D\n\n 10 9 0 0 0 0 999 V2000\n 1.9742 -0.2136 0.0000 C 0 0\n 3.2082 0.6407 0.0000 C 0 0\n 4.5654 0.0000 0.0000 O 0 0\n 5.7987 0.8538 0.0000 R# 0 0\n -4.5654 0.0000 0.0000 O 0 0\n -3.2082 -0.6407 0.0000 C 0 0\n -5.7987 -0.8538 0.0000 R# 0 0\n -1.9742 0.2136 0.0000 C 0 0\n -0.6170 -0.4271 0.0000 C 0 0\n 0.6170 0.4271 0.0000 C 0 0\n 1 10 1 0\n 2 1 1 0\n 3 2 1 0\n 3 4 1 0\n 5 7 1 0\n 5 6 1 0\n 6 8 1 0\n 8 9 1 0\n 9 10 1 0\nM RGP 2 4 2 7 1\nM END\n> <Name>\n1,6 Hexanediol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noC6o\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n1,7 Heptanediol\n SciTegic07272112182D\n\n 11 10 0 0 0 0 999 V2000\n 1.3000 0.7500 0.0000 O 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.2000 0.0000 0.0000 C 0 0\n 6.5000 0.7500 0.0000 C 0 0\n 7.7999 0.0000 0.0000 C 0 0\n 9.0999 0.7500 0.0000 C 0 0\n 10.3999 0.0000 0.0000 C 0 0\n 11.6999 0.7500 0.0000 O 0 0\n 0.0007 0.0004 0.0000 R# 0 0\n 12.9992 0.0004 0.0000 R# 0 0\n 3 2 1 0\n 4 3 1 0\n 5 4 1 0\n 6 5 1 0\n 7 6 1 0\n 8 7 1 0\n 9 8 1 0\n 1 10 1 0\n 9 11 1 0\n 1 2 1 0\nM RGP 2 10 1 11 2\nM END\n> <Name>\n1,7 Heptanediol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noC7o\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n1,11 Undecanediol\n SciTegic07272112182D\n\n 15 14 0 0 0 0 999 V2000\n 1.3000 0.7500 0.0000 O 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.2000 0.0000 0.0000 C 0 0\n 6.5000 0.7500 0.0000 C 0 0\n 7.7999 0.0000 0.0000 C 0 0\n 9.0999 0.7500 0.0000 C 0 0\n 10.3999 0.0000 0.0000 C 0 0\n 11.6999 0.7500 0.0000 C 0 0\n 12.9999 0.0000 0.0000 C 0 0\n 14.2999 0.7500 0.0000 C 0 0\n 15.5999 0.0000 0.0000 C 0 0\n 16.8999 0.7500 0.0000 O 0 0\n 0.0007 0.0004 0.0000 R# 0 0\n 18.1991 0.0004 0.0000 R# 0 0\n 3 2 1 0\n 4 3 1 0\n 5 4 1 0\n 6 5 1 0\n 7 6 1 0\n 8 7 1 0\n 9 8 1 0\n 10 9 1 0\n 11 10 1 0\n 12 11 1 0\n 13 12 1 0\n 1 14 1 0\n 13 15 1 0\n 1 2 1 0\nM RGP 2 14 1 15 2\nM END\n> <Name>\n1,11 Undecanediol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noC11o\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n1,12 Dodecanediol\n SciTegic09012117322D\n\n 16 15 0 0 0 0 999 V2000\n -8.4582 0.0000 0.0000 O 0 0\n -7.1263 -0.6916 0.0000 C 0 0\n -5.8608 0.1153 0.0000 C 0 0\n -4.5288 -0.5764 0.0000 C 0 0\n -3.2634 0.2305 0.0000 C 0 0\n -1.9315 -0.4611 0.0000 C 0 0\n -0.6660 0.3458 0.0000 C 0 0\n 0.6660 -0.3458 0.0000 C 0 0\n 1.9314 0.4611 0.0000 C 0 0\n 3.2634 -0.2305 0.0000 C 0 0\n 4.5289 0.5764 0.0000 C 0 0\n 5.8608 -0.1153 0.0000 C 0 0\n 7.1263 0.6916 0.0000 C 0 0\n 8.4583 0.0000 0.0000 O 0 0\n -9.7230 -0.8065 0.0000 R# 0 0\n 9.7230 0.8065 0.0000 R# 0 0\n 2 1 1 0\n 3 2 1 0\n 4 3 1 0\n 5 4 1 0\n 6 5 1 0\n 7 6 1 0\n 8 7 1 0\n 9 8 1 0\n 10 9 1 0\n 11 10 1 0\n 12 11 1 0\n 13 12 1 0\n 14 13 1 0\n 1 15 1 0\n 14 16 1 0\nM RGP 2 15 1 16 2\nM END\n> <Name>\n1,12 Dodecanediol\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noC12o\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n1-Methyl-pseudouracil\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 C 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 2.7991 0.0000 N 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 7.0981 4.0981 0.0000 C 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 3 7 2 0\n 5 8 2 0\n 2 9 1 0\n 4 10 1 0\nM RGP 1 9 1\nM END\n> <Name>\n1-Methyl-pseudouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm1Yra\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n1-Methyladenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 N 0 0\n 6.4176 -8.3053 0.0000 C 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 5 1 0\n 4 10 2 0\n 3 11 1 0\n 7 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n1-Methyladenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm1A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n1-Methylguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 6.4176 -8.3053 0.0000 C 0 0\n 3.5643 -9.2321 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 O 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 1 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 9 10 1 0\n 3 11 1 0\n 2 12 1 0\n 6 13 2 0\nM RGP 1 10 1\nM END\n> <Name>\n1-Methylguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm1G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-O-(6-aminohexyl)ribose\n SciTegic07272112182D\n\n 20 20 0 0 1 0 999 V2000\n -2.4816 0.4041 0.0000 C 0 0 1 0 0 0\n -2.0660 -1.0372 0.0000 C 0 0 2 0 0 0\n -3.3083 -1.8779 0.0000 C 0 0 1 0 0 0\n -4.4917 -0.9561 0.0000 O 0 0\n -3.9808 0.4542 0.0000 C 0 0 2 0 0 0\n -4.8230 1.6933 0.0000 C 0 0\n -3.3584 -3.3770 0.0000 R# 0 0\n -1.5585 1.5842 0.0000 O 0 0\n -0.6563 -1.5446 0.0000 O 0 0\n -6.3199 1.5842 0.0000 O 0 0\n -7.1631 2.8247 0.0000 R# 0 0\n -0.0731 1.3755 0.0000 R# 0 0\n 0.4906 -0.5765 0.0000 C 0 0\n 1.9027 -1.0848 0.0000 C 0 0\n 3.0496 -0.1167 0.0000 C 0 0\n 4.4617 -0.6250 0.0000 C 0 0\n 5.6086 0.3431 0.0000 C 0 0\n 7.0207 -0.1652 0.0000 C 0 0\n 8.1676 0.8029 0.0000 N 0 0\n 9.5790 0.2949 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 5 6 1 6\n 3 7 1 6\n 1 8 1 1\n 2 9 1 1\n 6 10 1 0\n 10 11 1 0\n 8 12 1 0\n 9 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 19 20 1 0\nM RGP 4 7 3 11 1 12 2 20 4\nM END\n> <Name>\n2-O-(6-aminohexyl)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnC62r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n[R4]H\n\n$$$$\n2,2-Dimethylguanine\n SciTegic07272112182D\n\n 14 15 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 O 0 0\n 3.5672 -9.2336 0.0000 N 0 0\n 4.6832 -10.2358 0.0000 C 0 0\n 2.1414 -9.6994 0.0000 C 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 5 1 0\n 4 10 2 0\n 2 11 1 0\n 11 12 1 0\n 11 13 1 0\n 7 14 1 0\nM RGP 1 14 1\nM END\n> <Name>\n2,2-Dimethylguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm22G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2,3-Oxetanearabinose\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n -1.1982 -1.2308 0.0000 O 0 0\n -0.5767 0.1344 0.0000 C 0 0 1 0 0 0\n -0.0918 -2.2437 0.0000 C 0 0 2 0 0 0\n 0.9137 -0.0347 0.0000 C 0 0 1 0 0 0\n 1.2134 -1.5045 0.0000 C 0 0 2 0 0 0\n 0.7420 1.4469 0.0000 O 0 0\n -1.3178 1.4366 0.0000 C 0 0\n -2.8186 1.4469 0.0000 O 0 0\n -0.2610 -3.7341 0.0000 R# 0 0\n 1.9462 2.3412 0.0000 R# 0 0\n 2.6674 -1.1365 0.0000 O 0 0\n 2.3418 0.3277 0.0000 C 0 0\n -3.5605 2.7505 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 6\n 7 8 1 0\n 3 9 1 6\n 6 10 1 0\n 5 11 1 6\n 11 12 1 0\n 12 4 1 0\n 8 13 1 0\nM RGP 3 9 3 10 2 13 1\nM END\n> <Name>\n2,3-Oxetanearabinose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nox23ar\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2,4-BNANC (oxyamino-BNA)\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -0.8920 0.6779 0.0000 C 0 0\n -1.6870 -0.5951 0.0000 O 0 0\n 0.1846 2.2096 0.0000 C 0 0\n -0.2862 1.3495 0.0000 O 0 0\n 0.6105 0.6233 0.0000 C 0 0 1 0 0 0\n 0.2157 -0.3666 0.0000 C 0 0 1 0 0 0\n -0.7913 -1.6686 0.0000 C 0 0 1 0 0 0\n -0.4485 -0.3707 0.0000 O 0 0\n 3.1410 -0.5951 0.0000 O 0 0\n -1.4549 -3.0138 0.0000 R# 0 0\n -1.3230 2.0348 0.0000 N 0 0\n 1.7058 -0.1970 0.0000 C 0 0 2 0 0 0\n 4.2112 0.4560 0.0000 R# 0 0\n -3.1861 -0.5441 0.0000 R# 0 0\n 4 11 1 0\n 5 1 1 6\n 1 2 1 0\n 5 12 1 0\n 12 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 5 1 0\n 7 10 1 6\n 5 3 1 0\n 6 4 1 6\n 11 3 1 0\n 12 9 1 1\n 9 13 1 0\n 2 14 1 0\nM RGP 3 10 3 13 2 14 1\nM END\n> <Name>\n2,4-BNANC (oxyamino-BNA)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbnanc\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2,4-BNANCMe (N-Methyl-oxyamino BNA)\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n -0.7065 0.5190 0.0000 C 0 0\n -1.5015 -0.7540 0.0000 O 0 0\n 0.3701 2.0507 0.0000 C 0 0\n -0.1007 1.1907 0.0000 O 0 0\n 0.7960 0.4644 0.0000 C 0 0 1 0 0 0\n 0.4011 -0.5255 0.0000 C 0 0 1 0 0 0\n -0.6058 -1.8275 0.0000 C 0 0 1 0 0 0\n -0.2630 -0.5296 0.0000 O 0 0\n 3.3265 -0.7540 0.0000 O 0 0\n -1.2694 -3.1727 0.0000 R# 0 0\n -1.1376 1.8760 0.0000 N 0 0\n 1.8913 -0.3558 0.0000 C 0 0 2 0 0 0\n 4.3967 0.2971 0.0000 R# 0 0\n -2.5966 2.2242 0.0000 C 0 0\n -3.0006 -0.7030 0.0000 R# 0 0\n 4 11 1 0\n 5 1 1 6\n 1 2 1 0\n 5 12 1 0\n 12 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 5 1 0\n 7 10 1 6\n 5 3 1 0\n 6 4 1 6\n 11 3 1 0\n 12 9 1 1\n 9 13 1 0\n 11 14 1 0\n 2 15 1 0\nM RGP 3 10 3 13 2 15 1\nM END\n> <Name>\n2,4-BNANCMe (N-Methyl-oxyamino BNA)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbnancm\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Aminoadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 3.8763 7.7649 0.0000 C 0 0\n 2.7616 6.7611 0.0000 N 0 0\n 3.0736 5.2939 0.0000 C 0 0\n 4.5003 4.8305 0.0000 C 0 0\n 5.6149 5.8343 0.0000 C 0 0\n 5.3029 7.3015 0.0000 N 0 0\n 2.1923 4.0811 0.0000 N 0 0\n 3.0741 2.8677 0.0000 C 0 0\n 4.5007 3.3313 0.0000 N 0 0\n 7.0415 5.3709 0.0000 N 0 0\n 3.5643 9.2321 0.0000 N 0 0\n 0.6923 4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 1 6 1 0\n 3 7 1 0\n 7 8 1 0\n 8 9 2 0\n 4 9 1 0\n 5 10 1 0\n 1 11 1 0\n 7 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n2-Aminoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-(Methoxy)amino LNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n -1.7278 0.2031 0.0000 C 0 0\n -0.3497 0.0282 0.0000 N 0 0\n -0.8666 -0.8784 0.0000 C 0 0 1 0 0 0\n 1.2843 0.0329 0.0000 C 0 0 2 0 0 0\n 0.5255 -1.1421 0.0000 C 0 0 2 0 0 0\n 0.6808 -2.4041 0.0000 C 0 0 1 0 0 0\n -0.6888 -2.2493 0.0000 O 0 0\n -1.1921 0.5947 0.0000 C 0 0\n 1.7467 -3.4595 0.0000 R# 0 0\n 2.3504 1.0606 0.0000 O 0 0\n 3.7936 0.6516 0.0000 R# 0 0\n 0.3813 1.3433 0.0000 O 0 0\n -0.3892 2.6302 0.0000 C 0 0\n -2.6188 1.0606 0.0000 O 0 0\n -2.9295 2.5281 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 6\n 6 9 1 6\n 3 1 1 0\n 5 2 1 6\n 4 10 1 1\n 10 11 1 0\n 2 12 1 0\n 12 13 1 0\n 8 14 1 0\n 14 15 1 0\nM RGP 3 9 3 11 2 15 1\nM END\n> <Name>\n2-(Methoxy)amino LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmon2ln\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-(Methoxyethoxy)amino LNA (N-MOE)\n SciTegic09012117322D\n\n 18 19 0 0 1 0 999 V2000\n 1.8450 1.6552 0.0000 C 0 0 1 0 0 0\n -0.3106 0.7551 0.0000 C 0 0 2 0 0 0\n -1.1662 1.8411 0.0000 C 0 0 1 0 0 0\n 0.2110 1.6591 0.0000 O 0 0\n 1.0801 0.4842 0.0000 C 0 0 1 0 0 0\n 2.9164 2.6773 0.0000 O 0 0\n -2.4698 2.5830 0.0000 R# 0 0\n 1.2288 -0.7785 0.0000 C 0 0\n -0.1399 -0.6167 0.0000 N 0 0\n 4.3575 2.2610 0.0000 R# 0 0\n -1.1939 -1.6825 0.0000 O 0 0\n -0.7981 -3.1303 0.0000 C 0 0\n -1.8533 -4.1974 0.0000 C 0 0\n -1.4576 -5.6452 0.0000 O 0 0\n -2.5122 -6.7119 0.0000 C 0 0\n 1.0038 1.9936 0.0000 C 0 0\n -0.3322 2.6773 0.0000 O 0 0\n -0.4089 4.1754 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 0\n 5 1 1 0\n 3 7 1 6\n 5 8 1 0\n 2 9 1 1\n 8 9 1 0\n 1 6 1 6\n 9 11 1 0\n 6 10 1 0\n 14 15 1 0\n 13 14 1 0\n 12 13 1 0\n 11 12 1 0\n 5 16 1 1\n 16 17 1 0\n 17 18 1 0\nM RGP 3 7 3 10 2 18 1\nM END\n> <Name>\n2-(Methoxyethoxy)amino LNA (N-MOE)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmoeon2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-(R)-Methyl-cLNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -1.7573 0.3923 0.0000 C 0 0\n -0.3792 0.2175 0.0000 C 0 0 2 0 0 0\n -0.8961 -0.6891 0.0000 C 0 0 1 0 0 0\n 1.2548 0.2221 0.0000 C 0 0 2 0 0 0\n 0.4960 -0.9529 0.0000 C 0 0 2 0 0 0\n 0.6513 -2.2149 0.0000 C 0 0 1 0 0 0\n -0.7183 -2.0601 0.0000 O 0 0\n -1.2216 0.7840 0.0000 C 0 0\n 1.7172 -3.2702 0.0000 R# 0 0\n 2.3209 1.2498 0.0000 O 0 0\n 3.7640 0.8408 0.0000 R# 0 0\n 0.3758 1.5136 0.0000 C 0 0\n -2.6483 1.2498 0.0000 O 0 0\n -2.9590 2.7173 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 5 4 1 6\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 6\n 6 9 1 6\n 3 1 1 0\n 5 2 1 0\n 4 10 1 1\n 10 11 1 0\n 2 12 1 1\n 8 13 1 0\n 13 14 1 0\nM RGP 3 9 3 11 2 14 1\nM END\n> <Name>\n2-(R)-Methyl-cLNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRmclna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Amino-N6-imidazoylpropyladenine\n SciTegic07272112182D\n\n 20 22 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0031 -3.0008 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 2.5981 1.5000 0.0000 N 0 0\n 1.3039 -3.7494 0.0000 C 0 0\n 1.3070 -5.2502 0.0000 C 0 0\n 2.6078 -5.9988 0.0000 C 0 0\n 2.6109 -7.4996 0.0000 N 0 0\n 3.8244 -8.3594 0.0000 C 0 0\n 3.3609 -9.7860 0.0000 N 0 0\n 1.8609 -9.7860 0.0000 C 0 0\n 1.3974 -8.3594 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 7 8 2 0\n 5 8 1 0\n 6 9 1 0\n 4 10 1 0\n 7 10 1 0\n 10 11 1 0\n 2 12 1 0\n 9 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 2 0\n 18 19 1 0\n 19 20 2 0\n 16 20 1 0\nM RGP 1 11 1\nM END\n> <Name>\n2-Amino-N6-imidazoylpropyladenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nimpr6n\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Aminoribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.9146 -0.3813 0.0000 C 0 0 2 0 0 0\n 0.4172 0.3089 0.0000 C 0 0 2 0 0 0\n 1.4851 -0.7445 0.0000 C 0 0 2 0 0 0\n 0.8134 -2.0856 0.0000 C 0 0 1 0 0 0\n -0.6697 -1.8612 0.0000 O 0 0\n 0.6383 1.7907 0.0000 O 0 0\n -2.2528 0.2924 0.0000 C 0 0\n 1.5036 -3.4174 0.0000 R# 0 0\n 2.0334 2.3417 0.0000 R# 0 0\n 2.9650 -0.4996 0.0000 N 0 0\n -2.3396 1.7907 0.0000 O 0 0\n -3.6793 2.4652 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 7 11 1 0\n 11 12 1 0\nM RGP 3 8 3 9 2 12 1\nM END\n> <Name>\n2-Aminoribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-C-Methylribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.0259 -0.3236 0.0000 C 0 0 2 0 0 0\n 0.3059 0.3666 0.0000 C 0 0 2 0 0 0\n 1.3739 -0.6867 0.0000 C 0 0 2 0 0 0\n 0.7021 -2.0279 0.0000 C 0 0 1 0 0 0\n -0.7810 -1.8035 0.0000 O 0 0\n 0.5270 1.8485 0.0000 O 0 0\n -2.3641 0.3502 0.0000 C 0 0\n 1.3923 -3.3596 0.0000 R# 0 0\n 1.9221 2.3995 0.0000 R# 0 0\n 2.3084 -1.8600 0.0000 O 0 0\n 1.8808 0.7250 0.0000 C 0 0\n -2.4508 1.8485 0.0000 O 0 0\n -3.7906 2.5230 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 3 11 1 0\n 7 12 1 0\n 12 13 1 0\nM RGP 3 8 3 9 2 13 1\nM END\n> <Name>\n2-C-Methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nBcm2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Chloro-N6-cyclopentyladenine\n SciTegic07272112182D\n\n 17 19 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 7.0433 -5.3736 0.0000 N 0 0\n 3.5643 -9.2321 0.0000 Cl 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 8.1571 -6.3795 0.0000 C 0 0\n 9.6092 -6.0582 0.0000 C 0 0\n 10.3546 -7.3599 0.0000 C 0 0\n 9.3469 -8.4710 0.0000 C 0 0\n 7.9788 -7.8561 0.0000 C 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 5 1 0\n 4 10 1 0\n 2 11 1 0\n 7 12 1 0\n 10 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 13 1 0\nM RGP 1 12 1\nM END\n> <Name>\n2-Chloro-N6-cyclopentyladenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncl2cyp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Chloroadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 6.9961 1.8908 0.0000 C 0 0\n 6.9965 3.3900 0.0000 N 0 0\n 5.5699 3.8536 0.0000 C 0 0\n 4.6882 2.6402 0.0000 N 0 0\n 5.5695 1.4274 0.0000 C 0 0\n 8.1107 0.8870 0.0000 C 0 0\n 5.2575 -0.0398 0.0000 N 0 0\n 6.3721 -1.0436 0.0000 C 0 0\n 7.7987 -0.5802 0.0000 N 0 0\n 3.1882 2.6402 0.0000 R# 0 0\n 9.5374 1.3504 0.0000 N 0 0\n 6.0601 -2.5108 0.0000 Cl 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 5 1 2 0\n 1 6 1 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 6 2 0\n 4 10 1 0\n 6 11 1 0\n 8 12 1 0\nM RGP 1 10 1\nM END\n> <Name>\n2-Chloroadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncl2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Deoxy-2-methoxypropyl\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2590 0.0451 0.0000 O 0 0\n -1.7470 1.4550 0.0000 C 0 0 1 0 0 0\n -1.0764 -0.8776 0.0000 C 0 0 2 0 0 0\n -0.2479 1.4037 0.0000 C 0 0 2 0 0 0\n 0.1666 -0.0379 0.0000 C 0 0 1 0 0 0\n 0.6713 2.5869 0.0000 O 0 0\n -2.5882 2.6948 0.0000 C 0 0\n -4.0852 2.5869 0.0000 O 0 0\n -4.9274 3.8281 0.0000 R# 0 0\n -1.1277 -2.3767 0.0000 R# 0 0\n 1.5738 -0.5523 0.0000 C 0 0\n 2.1574 2.3832 0.0000 R# 0 0\n 1.8333 -2.0305 0.0000 C 0 0\n 3.2429 -2.5458 0.0000 C 0 0\n 3.5024 -4.0240 0.0000 O 0 0\n 4.9112 -4.5390 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-Deoxy-2-methoxypropyl\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmopr2d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Fluoroadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n 0.0000 3.0000 0.0000 F 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n 2.5981 -1.5000 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 4 1 0\n 3 10 1 0\n 7 11 1 0\n 1 12 1 0\nM RGP 1 11 1\nM END\n> <Name>\n2-Fluoroadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfl2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Iodoadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n 0.0000 3.0000 0.0000 I 0 0\n 2.5981 -1.5000 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 4 1 0\n 7 10 1 0\n 3 11 1 0\n 1 12 1 0\nM RGP 1 10 1\nM END\n> <Name>\n2-Iodoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nio2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Methoxyadenine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 7.0416 -5.3709 0.0000 N 0 0\n 3.5672 -9.2336 0.0000 O 0 0\n 4.6832 -10.2358 0.0000 C 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 5 1 0\n 7 10 1 0\n 4 11 1 0\n 2 12 1 0\n 12 13 1 0\nM RGP 1 10 1\nM END\n> <Name>\n2-Methoxyadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmo2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Methoxyethylamino\n SciTegic07272112182D\n\n 7 6 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.2000 0.0000 0.0000 O 0 0\n 6.4992 0.7496 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\n2-Methoxyethylamino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmoen\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n2-Methyladenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 3.5643 -9.2321 0.0000 C 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 9 11 1 0\n 2 12 1 0\nM RGP 1 11 1\nM END\n> <Name>\n2-Methyladenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Methylguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 5.5695 -1.4273 0.0000 C 0 0\n 4.6882 -2.6401 0.0000 N 0 0\n 5.5700 -3.8536 0.0000 C 0 0\n 6.9965 -3.3899 0.0000 N 0 0\n 6.9961 -1.8907 0.0000 C 0 0\n 5.2575 0.0399 0.0000 N 0 0\n 8.1108 -0.8870 0.0000 C 0 0\n 7.7988 0.5802 0.0000 N 0 0\n 6.3722 1.0436 0.0000 C 0 0\n 3.1882 -2.6401 0.0000 R# 0 0\n 9.5374 -1.3504 0.0000 O 0 0\n 6.0570 2.5110 0.0000 N 0 0\n 4.6297 2.9724 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 1 2 0\n 1 6 1 0\n 5 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 6 2 0\n 2 10 1 0\n 7 11 2 0\n 9 12 1 0\n 12 13 1 0\nM RGP 1 10 1\nM END\n> <Name>\n2-Methylguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Methylseleno-2-deoxyribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.1828 -0.4514 0.0000 C 0 0 2 0 0 0\n 0.1490 0.2388 0.0000 C 0 0 2 0 0 0\n 1.2170 -0.8145 0.0000 C 0 0 2 0 0 0\n 0.5452 -2.1557 0.0000 C 0 0 1 0 0 0\n -0.9379 -1.9313 0.0000 O 0 0\n -2.5210 0.2223 0.0000 C 0 0\n 0.3701 1.7207 0.0000 O 0 0\n 1.7652 2.2716 0.0000 R# 0 0\n 1.2354 -3.4875 0.0000 R# 0 0\n 2.6946 -0.5669 0.0000 Se 0 0\n 3.2204 0.8380 0.0000 C 0 0\n -2.6077 1.7207 0.0000 O 0 0\n -3.9475 2.3952 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 3 10 1 1\n 10 11 1 0\n 6 12 1 0\n 12 13 1 0\nM RGP 3 8 2 9 3 13 1\nM END\n> <Name>\n2-Methylseleno-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nse2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Methylthio-2-deoxyribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.1828 -0.4514 0.0000 C 0 0 2 0 0 0\n 0.1490 0.2388 0.0000 C 0 0 2 0 0 0\n 1.2170 -0.8145 0.0000 C 0 0 2 0 0 0\n 0.5452 -2.1557 0.0000 C 0 0 1 0 0 0\n -0.9379 -1.9313 0.0000 O 0 0\n -2.5210 0.2223 0.0000 C 0 0\n 0.3701 1.7207 0.0000 O 0 0\n -2.6077 1.7207 0.0000 O 0 0\n -3.9475 2.3952 0.0000 R# 0 0\n 1.7652 2.2716 0.0000 R# 0 0\n 1.2354 -3.4875 0.0000 R# 0 0\n 2.6946 -0.5669 0.0000 S 0 0\n 3.2204 0.8380 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\n 3 12 1 1\n 12 13 1 0\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n2-Methylthio-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nms2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Methylthioadenine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 3.5672 -9.2336 0.0000 S 0 0\n 4.6832 -10.2358 0.0000 C 0 0\n 7.0416 -5.3709 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 2 10 1 0\n 10 11 1 0\n 6 12 1 0\n 9 13 1 0\nM RGP 1 13 1\nM END\n> <Name>\n2-Methylthioadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nms2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-N-Methylcarbamoylribose\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -1.9948 -0.0515 0.0000 O 0 0\n -1.4827 1.3584 0.0000 C 0 0 1 0 0 0\n -0.8121 -0.9742 0.0000 C 0 0 2 0 0 0\n 0.0164 1.3070 0.0000 C 0 0 2 0 0 0\n 0.4308 -0.1346 0.0000 C 0 0 1 0 0 0\n 0.9355 2.4902 0.0000 O 0 0\n -2.3240 2.5981 0.0000 C 0 0\n -3.8209 2.4902 0.0000 O 0 0\n -4.6632 3.7315 0.0000 R# 0 0\n -0.8634 -2.4733 0.0000 R# 0 0\n 1.8380 -0.6489 0.0000 O 0 0\n 2.4216 2.2866 0.0000 R# 0 0\n 2.0976 -2.1271 0.0000 C 0 0\n 3.5072 -2.6424 0.0000 N 0 0\n 0.9475 -3.0901 0.0000 O 0 0\n 3.7665 -4.1198 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 13 15 2 0\n 14 16 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-N-Methylcarbamoylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmnc2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-4-(Imidazo-1-yl) butylribose\n SciTegic07272112182D\n\n 21 22 0 0 1 0 999 V2000\n -3.8016 -2.0204 0.0000 C 0 0 2 0 0 0\n -2.4699 -1.3302 0.0000 C 0 0 2 0 0 0\n -1.4019 -2.3835 0.0000 C 0 0 2 0 0 0\n -2.0736 -3.7247 0.0000 C 0 0 1 0 0 0\n -3.5568 -3.5003 0.0000 O 0 0\n -5.1399 -1.3466 0.0000 C 0 0\n -2.2488 0.1517 0.0000 O 0 0\n -0.8536 0.7027 0.0000 R# 0 0\n 0.0757 -2.1358 0.0000 O 0 0\n -1.3834 -5.0564 0.0000 R# 0 0\n 0.6019 -0.7302 0.0000 C 0 0\n 2.0821 -0.4822 0.0000 C 0 0\n 2.6082 0.9234 0.0000 C 0 0\n 4.0884 1.1715 0.0000 C 0 0\n 4.6145 2.5771 0.0000 N 0 0\n 6.0516 2.9599 0.0000 C 0 0\n 6.1146 4.4586 0.0000 N 0 0\n 4.7087 4.9815 0.0000 C 0 0\n 3.7769 3.8061 0.0000 C 0 0\n -5.2266 0.1517 0.0000 O 0 0\n -6.5664 0.8262 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 3 9 1 1\n 4 10 1 6\n 9 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 2 0\n 17 18 1 0\n 18 19 2 0\n 19 15 1 0\n 6 20 1 0\n 20 21 1 0\nM RGP 3 8 2 10 3 21 1\nM END\n> <Name>\n2-O-4-(Imidazo-1-yl) butylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nimbu2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(2,2,3,3,3-Pentafluoropropyl)ribose\n SciTegic07272112182D\n\n 20 20 0 0 1 0 999 V2000\n -3.0073 -1.1253 0.0000 C 0 0 2 0 0 0\n -1.6755 -0.4351 0.0000 C 0 0 2 0 0 0\n -0.6076 -1.4885 0.0000 C 0 0 2 0 0 0\n -1.2793 -2.8296 0.0000 C 0 0 1 0 0 0\n -2.7624 -2.6052 0.0000 O 0 0\n -4.3455 -0.4516 0.0000 C 0 0\n -1.4545 1.0467 0.0000 O 0 0\n -0.0593 1.5977 0.0000 R# 0 0\n 0.8701 -1.2408 0.0000 O 0 0\n -0.5891 -4.1614 0.0000 R# 0 0\n 1.3962 0.1648 0.0000 C 0 0\n 2.8764 0.4129 0.0000 C 0 0\n 3.8304 -0.7446 0.0000 F 0 0\n 2.3512 -0.9922 0.0000 F 0 0\n 3.4025 1.8185 0.0000 C 0 0\n 3.9277 3.2235 0.0000 F 0 0\n 2.4485 2.9760 0.0000 F 0 0\n 4.8819 2.0664 0.0000 F 0 0\n -4.4323 1.0467 0.0000 O 0 0\n -5.7721 1.7212 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 3 9 1 1\n 4 10 1 6\n 9 11 1 0\n 11 12 1 0\n 12 15 1 0\n 12 13 1 0\n 12 14 1 0\n 15 18 1 0\n 15 17 1 0\n 15 16 1 0\n 6 19 1 0\n 19 20 1 0\nM RGP 3 8 2 10 3 20 1\nM END\n> <Name>\n2-O-(2,2,3,3,3-Pentafluoropropyl)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfl5pr2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(2-Acetamide)ribose\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.1567 -0.6707 0.0000 C 0 0 2 0 0 0\n -0.8249 0.0195 0.0000 C 0 0 2 0 0 0\n 0.2430 -1.0338 0.0000 C 0 0 2 0 0 0\n -0.4287 -2.3750 0.0000 C 0 0 1 0 0 0\n -1.9118 -2.1506 0.0000 O 0 0\n -0.6039 1.5014 0.0000 O 0 0\n -3.4949 0.0031 0.0000 C 0 0\n 0.2615 -3.7068 0.0000 R# 0 0\n -3.5817 1.5014 0.0000 O 0 0\n -4.9215 2.1759 0.0000 R# 0 0\n 1.7207 -0.7861 0.0000 O 0 0\n 0.7913 2.0524 0.0000 R# 0 0\n 2.2468 0.6194 0.0000 C 0 0\n 3.7270 0.8675 0.0000 C 0 0\n 4.2528 2.2723 0.0000 O 0 0\n 4.6810 -0.2900 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 2 0\n 14 16 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-(2-Acetamide)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnac2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(2-Amino)ethylribose\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -1.9316 -0.2576 0.0000 O 0 0\n -1.4196 1.1523 0.0000 C 0 0 1 0 0 0\n -0.7490 -1.1802 0.0000 C 0 0 2 0 0 0\n 0.0796 1.1010 0.0000 C 0 0 2 0 0 0\n 0.4940 -0.3406 0.0000 C 0 0 1 0 0 0\n 0.9987 2.2842 0.0000 O 0 0\n -2.2608 2.3921 0.0000 C 0 0\n -3.7578 2.2842 0.0000 O 0 0\n -4.6000 3.5255 0.0000 R# 0 0\n -0.8003 -2.6793 0.0000 R# 0 0\n 1.9012 -0.8549 0.0000 O 0 0\n 2.4848 2.0805 0.0000 R# 0 0\n 2.1607 -2.3332 0.0000 C 0 0\n 3.5703 -2.8484 0.0000 C 0 0\n 3.8297 -4.3258 0.0000 N 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-(2-Amino)ethylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nne2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(2-Fluoroethyl)ribose\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -1.8446 -0.6900 0.0000 C 0 0 2 0 0 0\n -0.5129 0.0002 0.0000 C 0 0 2 0 0 0\n 0.5551 -1.0531 0.0000 C 0 0 2 0 0 0\n -0.1166 -2.3943 0.0000 C 0 0 1 0 0 0\n -1.5998 -2.1699 0.0000 O 0 0\n -3.1829 -0.0163 0.0000 C 0 0\n -0.2918 1.4820 0.0000 O 0 0\n 1.1033 2.0330 0.0000 R# 0 0\n 2.0327 -0.8055 0.0000 O 0 0\n 0.5736 -3.7261 0.0000 R# 0 0\n 2.5589 0.6001 0.0000 C 0 0\n 4.0390 0.8482 0.0000 C 0 0\n 4.5649 2.2530 0.0000 F 0 0\n -3.2696 1.4820 0.0000 O 0 0\n -4.6094 2.1566 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 3 9 1 1\n 4 10 1 6\n 9 11 1 0\n 11 12 1 0\n 12 13 1 0\n 6 14 1 0\n 14 15 1 0\nM RGP 3 8 2 10 3 15 1\nM END\n> <Name>\n2-O-(2-Fluoroethyl)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfle2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(2-Formaldoximino)ethylribose\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.5633 0.3990 0.0000 O 0 0\n -2.0512 1.8089 0.0000 C 0 0 1 0 0 0\n -1.3806 -0.5236 0.0000 C 0 0 2 0 0 0\n -0.5521 1.7576 0.0000 C 0 0 2 0 0 0\n -0.1377 0.3160 0.0000 C 0 0 1 0 0 0\n 0.3670 2.9408 0.0000 O 0 0\n -2.8925 3.0487 0.0000 C 0 0\n -4.3894 2.9408 0.0000 O 0 0\n -5.2317 4.1821 0.0000 R# 0 0\n -1.4319 -2.0228 0.0000 R# 0 0\n 1.2695 -0.1984 0.0000 O 0 0\n 1.8531 2.7371 0.0000 R# 0 0\n 1.5290 -1.6766 0.0000 C 0 0\n 2.9387 -2.1918 0.0000 C 0 0\n 3.1982 -3.6700 0.0000 O 0 0\n 4.6078 -4.1853 0.0000 N 0 0\n 4.8671 -5.6627 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 2 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-(2-Formaldoximino)ethylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmenoe2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(2-Phenoxyethyl)ribose\n SciTegic07272112182D\n\n 21 22 0 0 1 0 999 V2000\n -3.9854 -1.4750 0.0000 C 0 0 2 0 0 0\n -2.6541 -0.7840 0.0000 C 0 0 2 0 0 0\n -1.6070 -1.8403 0.0000 C 0 0 2 0 0 0\n -2.2564 -3.1783 0.0000 C 0 0 1 0 0 0\n -3.7397 -2.9548 0.0000 O 0 0\n -2.4225 0.6962 0.0000 O 0 0\n -5.3241 -0.8021 0.0000 C 0 0\n -1.5575 -4.5055 0.0000 R# 0 0\n -1.0236 1.2374 0.0000 R# 0 0\n -0.1270 -1.5913 0.0000 O 0 0\n 1.8783 0.0635 0.0000 C 0 0\n 0.3983 -0.1855 0.0000 C 0 0\n 2.4037 1.4694 0.0000 O 0 0\n 3.8837 1.7183 0.0000 C 0 0\n 4.4108 3.1227 0.0000 C 0 0\n 5.8905 3.3684 0.0000 C 0 0\n 6.8432 2.2098 0.0000 C 0 0\n 6.3161 0.8055 0.0000 C 0 0\n 4.8364 0.5597 0.0000 C 0 0\n -5.4117 0.6962 0.0000 O 0 0\n -6.7519 1.3699 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 11 12 1 0\n 10 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 2 0\n 15 16 1 0\n 16 17 2 0\n 17 18 1 0\n 18 19 2 0\n 19 14 1 0\n 7 20 1 0\n 20 21 1 0\nM RGP 3 8 3 9 2 21 1\nM END\n> <Name>\n2-O-(2-Phenoxyethyl)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nphoe2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(2-Trifluoro)ethylribose\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.4630 -0.7363 0.0000 C 0 0 2 0 0 0\n -1.1312 -0.0461 0.0000 C 0 0 2 0 0 0\n -0.0632 -1.0994 0.0000 C 0 0 2 0 0 0\n -0.7350 -2.4406 0.0000 C 0 0 1 0 0 0\n -2.2181 -2.2161 0.0000 O 0 0\n -0.9101 1.4358 0.0000 O 0 0\n -3.8012 -0.0625 0.0000 C 0 0\n -0.0448 -3.7723 0.0000 R# 0 0\n 0.4850 1.9868 0.0000 R# 0 0\n 1.4144 -0.8517 0.0000 O 0 0\n 1.9405 0.5539 0.0000 C 0 0\n 3.4207 0.8020 0.0000 C 0 0\n 4.9002 1.0492 0.0000 F 0 0\n 4.3748 -0.3555 0.0000 F 0 0\n 3.9466 2.2068 0.0000 F 0 0\n -3.8879 1.4358 0.0000 O 0 0\n -5.2277 2.1103 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 11 10 1 0\n 11 12 1 0\n 12 15 1 0\n 12 14 1 0\n 12 13 1 0\n 7 16 1 0\n 16 17 1 0\nM RGP 3 8 3 9 2 17 1\nM END\n> <Name>\n2-O-(2-Trifluoro)ethylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfl3e2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(3,3,3-Trifluoropropyl)ribose\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -2.6639 -1.2218 0.0000 C 0 0 2 0 0 0\n -1.3321 -0.5316 0.0000 C 0 0 2 0 0 0\n -0.2641 -1.5849 0.0000 C 0 0 2 0 0 0\n -0.9359 -2.9261 0.0000 C 0 0 1 0 0 0\n -2.4190 -2.7017 0.0000 O 0 0\n -1.1110 0.9502 0.0000 O 0 0\n -4.0021 -0.5481 0.0000 C 0 0\n -0.2457 -4.2579 0.0000 R# 0 0\n 0.2841 1.5012 0.0000 R# 0 0\n 1.2135 -1.3373 0.0000 O 0 0\n 3.2198 0.3164 0.0000 C 0 0\n 1.7396 0.0683 0.0000 C 0 0\n 3.7459 1.7220 0.0000 C 0 0\n 5.2253 1.9699 0.0000 F 0 0\n 2.7919 2.8795 0.0000 F 0 0\n 4.2711 3.1270 0.0000 F 0 0\n -4.0888 0.9502 0.0000 O 0 0\n -5.4286 1.6247 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 11 12 1 0\n 10 12 1 0\n 11 13 1 0\n 13 14 1 0\n 13 15 1 0\n 13 16 1 0\n 7 17 1 0\n 17 18 1 0\nM RGP 3 8 3 9 2 18 1\nM END\n> <Name>\n2-O-(3,3,3-Trifluoropropyl)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfl3pr2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(4-Aminobutyl)ribose\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.5868 -1.0670 0.0000 C 0 0 2 0 0 0\n -1.2550 -0.3768 0.0000 C 0 0 2 0 0 0\n -0.1871 -1.4301 0.0000 C 0 0 2 0 0 0\n -0.8588 -2.7713 0.0000 C 0 0 1 0 0 0\n -2.3419 -2.5469 0.0000 O 0 0\n -1.0340 1.1050 0.0000 O 0 0\n -3.9250 -0.3933 0.0000 C 0 0\n -0.1686 -4.1031 0.0000 R# 0 0\n 0.3612 1.6560 0.0000 R# 0 0\n 1.2906 -1.1825 0.0000 O 0 0\n 3.8230 1.8768 0.0000 C 0 0\n 3.2969 0.4712 0.0000 C 0 0\n 1.8167 0.2231 0.0000 C 0 0\n 5.3032 2.1248 0.0000 C 0 0\n 5.8290 3.5297 0.0000 N 0 0\n -4.0118 1.1050 0.0000 O 0 0\n -5.3516 1.7795 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 12 13 1 0\n 11 12 1 0\n 10 13 1 0\n 11 14 1 0\n 14 15 1 0\n 7 16 1 0\n 16 17 1 0\nM RGP 3 8 3 9 2 17 1\nM END\n> <Name>\n2-O-(4-Aminobutyl)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnbu2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(6-(N-glutaryl-GalNAc3)aminohexylribose\n SciTegic09012117322D\n\n124127 0 0 1 0 999 V2000\n 11.7833 -3.3225 0.0000 C 0 0\n 10.8292 -2.1641 0.0000 C 0 0\n 11.3545 -0.7581 0.0000 C 0 0\n 10.4003 0.4003 0.0000 C 0 0\n 8.9198 0.1541 0.0000 C 0 0\n 7.9656 1.3126 0.0000 C 0 0\n 6.4851 1.0664 0.0000 N 0 0\n 5.5310 2.2249 0.0000 C 0 0\n 6.0573 3.6295 0.0000 O 0 0\n -3.7798 3.3088 0.0000 O 0 0\n -3.2532 4.7142 0.0000 C 0 0\n -1.7729 4.9618 0.0000 C 0 0\n -0.8189 3.8033 0.0000 N 0 0\n -1.2464 6.3671 0.0000 C 0 0\n 0.2339 6.6147 0.0000 O 0 0\n -2.3073 3.5281 0.0000 C 0 0\n -1.3523 2.3704 0.0000 O 0 0\n -5.2601 3.0613 0.0000 C 0 0\n -5.7867 1.6558 0.0000 C 0 0\n -1.8764 0.9642 0.0000 C 0 0\n -0.9213 -0.1935 0.0000 C 0 0\n 0.7605 8.0201 0.0000 C 0 0\n 2.2408 8.2677 0.0000 C 0 0\n 2.7674 9.6731 0.0000 C 0 0\n 1.8138 10.8309 0.0000 O 0 0\n 0.8026 -10.4496 0.0000 C 0 0\n 0.2784 -11.8559 0.0000 C 0 0\n 1.2336 -13.0137 0.0000 C 0 0\n 0.7094 -14.4200 0.0000 C 0 0\n -1.4454 -1.5999 0.0000 C 0 0\n -0.4903 -2.7576 0.0000 N 0 0\n -2.9247 -1.8485 0.0000 O 0 0\n -1.0145 -4.1638 0.0000 C 0 0\n -0.0593 -5.3216 0.0000 C 0 0\n -0.5835 -6.7279 0.0000 C 0 0\n 0.3716 -7.8856 0.0000 N 0 0\n -0.1525 -9.2919 0.0000 C 0 0\n -1.6317 -9.5405 0.0000 O 0 0\n -7.2670 1.4083 0.0000 C 0 0\n -8.2207 2.5661 0.0000 O 0 0\n -13.8143 -4.9560 0.0000 C 0 0\n -15.2946 -5.2035 0.0000 C 0 0\n -15.8212 -6.6090 0.0000 C 0 0\n -17.3015 -6.8565 0.0000 C 0 0\n -7.7936 0.0028 0.0000 N 0 0\n -11.8074 -3.3030 0.0000 N 0 0\n -13.2877 -3.5506 0.0000 C 0 0\n -14.2413 -2.3928 0.0000 O 0 0\n 10.2684 14.8795 0.0000 C 0 0\n 10.7950 16.2849 0.0000 C 0 0\n 12.2753 16.5325 0.0000 C 0 0\n 12.8019 17.9379 0.0000 C 0 0\n 4.2477 9.9206 0.0000 N 0 0\n 4.7743 11.3261 0.0000 C 0 0\n 6.2546 11.5736 0.0000 C 0 0\n 6.7812 12.9791 0.0000 C 0 0\n 8.2615 13.2266 0.0000 N 0 0\n 8.7881 14.6319 0.0000 C 0 0\n 7.8345 15.7898 0.0000 O 0 0\n -11.2808 -1.8976 0.0000 C 0 0\n -9.8005 -1.6500 0.0000 C 0 0\n -9.2739 -0.2447 0.0000 C 0 0\n 0.6616 4.0495 0.0000 C 0 0\n 1.1880 5.4542 0.0000 O 0 0\n 1.6158 2.8910 0.0000 C 0 0\n 3.0963 3.1372 0.0000 C 0 0\n 4.0505 1.9787 0.0000 C 0 0\n 7.3996 -4.6122 0.0000 C 0 0 2 0 0 0\n 8.7310 -3.9212 0.0000 C 0 0 2 0 0 0\n 9.7780 -4.9774 0.0000 C 0 0 2 0 0 0\n 9.1286 -6.3155 0.0000 C 0 0 1 0 0 0\n 7.6455 -6.0920 0.0000 O 0 0\n 6.0609 -3.9393 0.0000 C 0 0\n 8.9625 -2.4410 0.0000 O 0 0\n 10.3614 -1.8997 0.0000 R# 0 0\n 11.2580 -4.7284 0.0000 O 0 0\n 9.8276 -7.6427 0.0000 R# 0 0\n 16.8113 21.2461 0.0000 C 0 0 2 0 0 0\n 15.8557 22.4022 0.0000 C 0 0 1 0 0 0\n 14.3766 22.1527 0.0000 C 0 0 1 0 0 0\n 13.8532 20.7471 0.0000 C 0 0 2 0 0 0\n 14.8088 19.5909 0.0000 C 0 0 1 0 0 0\n 16.2879 19.8404 0.0000 O 0 0\n 14.2822 18.1854 0.0000 O 0 0\n 13.4209 23.3089 0.0000 O 0 0\n 16.3792 23.8080 0.0000 O 0 0\n 18.2907 21.4988 0.0000 C 0 0\n 18.8122 22.9052 0.0000 O 0 0\n 1.5665 -19.5470 0.0000 C 0 0 2 0 0 0\n 0.0868 -19.7930 0.0000 C 0 0 1 0 0 0\n -0.8661 -18.6346 0.0000 C 0 0 1 0 0 0\n -0.3394 -17.2302 0.0000 C 0 0 2 0 0 0\n 1.1404 -16.9840 0.0000 C 0 0 1 0 0 0\n 2.0933 -18.1424 0.0000 O 0 0\n 1.6645 -15.5776 0.0000 O 0 0\n -2.3458 -18.8807 0.0000 O 0 0\n -0.4398 -21.1974 0.0000 O 0 0\n 2.5177 -20.7079 0.0000 C 0 0\n 1.9889 -22.1116 0.0000 O 0 0\n -21.3167 -10.1578 0.0000 C 0 0 2 0 0 0\n -22.2684 -8.9983 0.0000 C 0 0 1 0 0 0\n -21.7401 -7.5945 0.0000 C 0 0 1 0 0 0\n -20.2601 -7.3500 0.0000 C 0 0 2 0 0 0\n -19.3084 -8.5094 0.0000 C 0 0 1 0 0 0\n -19.8367 -9.9134 0.0000 O 0 0\n -17.8281 -8.2620 0.0000 O 0 0\n -22.6917 -6.4350 0.0000 O 0 0\n -23.7483 -9.2427 0.0000 O 0 0\n -21.8482 -11.5613 0.0000 C 0 0\n -23.3285 -11.8037 0.0000 O 0 0\n 12.3727 20.5004 0.0000 N 0 0\n 9.9386 21.4121 0.0000 O 0 0\n 11.4182 21.6586 0.0000 C 0 0\n 11.9441 23.0633 0.0000 C 0 0\n -1.2953 -16.0730 0.0000 N 0 0\n -3.7308 -15.1651 0.0000 O 0 0\n -2.7754 -16.3214 0.0000 C 0 0\n -3.2996 -17.7269 0.0000 C 0 0\n -19.7344 -5.9442 0.0000 N 0 0\n -20.1629 -3.3806 0.0000 O 0 0\n -20.6883 -4.7855 0.0000 C 0 0\n -22.1678 -5.0325 0.0000 C 0 0\n 5.9733 -2.4410 0.0000 O 0 0\n 4.6331 -1.7674 0.0000 R# 0 0\n113114 1 0\n112113 2 0\n111113 1 0\n117118 1 0\n116117 2 0\n115117 1 0\n121122 1 0\n120121 2 0\n119121 1 0\n 1 76 1 0\n 2 1 1 0\n 3 2 1 0\n 4 3 1 0\n 5 4 1 0\n 6 5 1 0\n 6 7 1 0\n 8 9 2 0\n 7 8 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 12 14 1 0\n 14 15 1 0\n 12 16 1 0\n 16 17 1 0\n 10 18 1 0\n 18 19 1 0\n 17 20 1 0\n 20 21 1 0\n 15 22 1 0\n 22 23 1 0\n 23 24 1 0\n 24 25 2 0\n 27 26 1 0\n 28 27 1 0\n 29 28 1 0\n 95 29 1 0\n 21 30 1 0\n 30 31 1 0\n 30 32 2 0\n 33 31 1 0\n 34 33 1 0\n 35 34 1 0\n 35 36 1 0\n 37 26 1 0\n 37 38 2 0\n 19 39 1 0\n 39 40 2 0\n 42 41 1 0\n 43 42 1 0\n 44 43 1 0\n106 44 1 0\n 47 41 1 0\n 47 48 2 0\n 45 39 1 0\n 50 49 1 0\n 51 50 1 0\n 52 51 1 0\n 84 52 1 0\n 54 53 1 0\n 55 54 1 0\n 56 55 1 0\n 56 57 1 0\n 57 58 1 0\n 58 49 1 0\n 58 59 2 0\n 53 24 1 0\n 36 37 1 0\n 46 47 1 0\n 46 60 1 0\n 60 61 1 0\n 61 62 1 0\n 62 45 1 0\n 63 64 2 0\n 63 65 1 0\n 65 66 1 0\n 66 67 1 0\n 8 67 1 0\n 68 69 1 0\n 69 70 1 0\n 70 71 1 0\n 71 72 1 0\n 72 68 1 0\n 68 73 1 6\n 69 74 1 1\n 74 75 1 0\n 70 76 1 1\n 71 77 1 6\n 78 79 1 0\n 79 80 1 0\n 80 81 1 0\n 81 82 1 0\n 82 83 1 0\n 83 78 1 0\n 82 84 1 1\n 80 85 1 1\n 79 86 1 1\n 78 87 1 1\n 87 88 1 0\n 81111 1 6\n 89 90 1 0\n 90 91 1 0\n 91 92 1 0\n 92 93 1 0\n 93 94 1 0\n 94 89 1 0\n 93 95 1 6\n 91 96 1 6\n 90 97 1 6\n 89 98 1 6\n 98 99 1 0\n 92115 1 1\n100101 1 0\n101102 1 0\n102103 1 0\n103104 1 0\n104105 1 0\n105100 1 0\n104106 1 6\n102107 1 6\n101108 1 6\n100109 1 6\n109110 1 0\n103119 1 1\n 63 13 1 0\n 73123 1 0\n123124 1 0\nM RGP 3 75 2 77 3 124 1\nM END\n> <Name>\n2-O-(6-(N-glutaryl-GalNAc3)aminohexylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nGalNAc\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(N-Methylacetamide)ribose\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.4939 -0.8190 0.0000 C 0 0 2 0 0 0\n -1.1622 -0.1288 0.0000 C 0 0 2 0 0 0\n -0.0942 -1.1821 0.0000 C 0 0 2 0 0 0\n -0.7659 -2.5233 0.0000 C 0 0 1 0 0 0\n -2.2491 -2.2989 0.0000 O 0 0\n -0.9411 1.3530 0.0000 O 0 0\n -3.8322 -0.1453 0.0000 C 0 0\n -0.0757 -3.8551 0.0000 R# 0 0\n 0.4541 1.9040 0.0000 R# 0 0\n 1.3834 -0.9345 0.0000 O 0 0\n 3.9159 2.1248 0.0000 N 0 0\n 3.3898 0.7192 0.0000 C 0 0\n 1.9096 0.4711 0.0000 C 0 0\n 5.3953 2.3727 0.0000 C 0 0\n 4.3438 -0.4383 0.0000 O 0 0\n -3.9189 1.3530 0.0000 O 0 0\n -5.2587 2.0275 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 12 13 1 0\n 11 12 1 0\n 10 13 1 0\n 11 14 1 0\n 12 15 2 0\n 7 16 1 0\n 16 17 1 0\nM RGP 3 8 3 9 2 17 1\nM END\n> <Name>\n2-O-(N-Methylacetamide)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnma\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(Pyren-1-yl)methylribose\n SciTegic07272112182D\n\n 29 33 0 0 1 0 999 V2000\n -5.0170 -2.3487 0.0000 C 0 0 2 0 0 0\n -3.6856 -1.6577 0.0000 C 0 0 2 0 0 0\n -2.6386 -2.7139 0.0000 C 0 0 2 0 0 0\n -3.2880 -4.0519 0.0000 C 0 0 1 0 0 0\n -4.7712 -3.8284 0.0000 O 0 0\n -3.4541 -0.1775 0.0000 O 0 0\n -6.3556 -1.6757 0.0000 C 0 0\n -2.5891 -5.3791 0.0000 R# 0 0\n -6.4433 -0.1775 0.0000 O 0 0\n -7.7835 0.4962 0.0000 R# 0 0\n -2.0551 0.3637 0.0000 R# 0 0\n -1.1586 -2.4650 0.0000 O 0 0\n 0.8468 -0.8102 0.0000 C 0 0\n -0.6333 -1.0591 0.0000 C 0 0\n 1.7995 -1.9688 0.0000 C 0 0\n 3.2792 -1.7230 0.0000 C 0 0\n 3.8063 -0.3186 0.0000 C 0 0\n 2.8536 0.8400 0.0000 C 0 0\n 1.3738 0.5942 0.0000 C 0 0\n 3.3806 2.2443 0.0000 C 0 0\n 2.4279 3.4029 0.0000 C 0 0\n 0.9481 3.1572 0.0000 C 0 0\n 0.4211 1.7528 0.0000 C 0 0\n 5.2860 -0.0729 0.0000 C 0 0\n 5.8130 1.3315 0.0000 C 0 0\n 4.8603 2.4901 0.0000 C 0 0\n 5.3873 3.8945 0.0000 C 0 0\n 4.4346 5.0531 0.0000 C 0 0\n 2.9549 4.8073 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 12 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 13 14 1 0\n 12 14 1 0\n 13 15 2 0\n 15 16 1 0\n 16 17 2 0\n 17 18 1 0\n 18 19 2 0\n 19 13 1 0\n 18 20 1 0\n 20 21 2 0\n 21 22 1 0\n 22 23 2 0\n 23 19 1 0\n 17 24 1 0\n 24 25 1 0\n 25 26 2 0\n 26 20 1 0\n 26 27 1 0\n 27 28 1 0\n 28 29 2 0\n 29 21 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n2-O-(Pyren-1-yl)methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\npyren1\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-(S)-Methyl MOE\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.4939 -0.8190 0.0000 C 0 0 2 0 0 0\n -1.1622 -0.1288 0.0000 C 0 0 2 0 0 0\n -0.0942 -1.1821 0.0000 C 0 0 2 0 0 0\n -0.7659 -2.5233 0.0000 C 0 0 1 0 0 0\n -2.2491 -2.2989 0.0000 O 0 0\n -0.9411 1.3530 0.0000 O 0 0\n -3.8322 -0.1453 0.0000 C 0 0\n -0.0757 -3.8551 0.0000 R# 0 0\n 1.3834 -0.9345 0.0000 O 0 0\n 0.4541 1.9040 0.0000 R# 0 0\n 1.9096 0.4711 0.0000 C 0 0\n 3.3898 0.7192 0.0000 C 0 0 2 0 0 0\n 4.3438 -0.4383 0.0000 C 0 0\n 3.9159 2.1248 0.0000 O 0 0\n 5.3953 2.3727 0.0000 C 0 0\n -3.9189 1.3530 0.0000 O 0 0\n -5.2587 2.0275 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 9 1 1\n 1 7 1 6\n 4 8 1 6\n 6 10 1 0\n 9 11 1 0\n 11 12 1 0\n 12 13 1 1\n 12 14 1 0\n 14 15 1 0\n 7 16 1 0\n 16 17 1 0\nM RGP 3 8 3 10 2 17 1\nM END\n> <Name>\n2-O-(S)-Methyl MOE\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSm2moe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[(dimethylaminooxy)ethyl]ribose (DMAOE)\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -2.9344 -1.1208 0.0000 C 0 0 2 0 0 0\n -1.6027 -0.4306 0.0000 C 0 0 2 0 0 0\n -0.5347 -1.4839 0.0000 C 0 0 2 0 0 0\n -1.2064 -2.8251 0.0000 C 0 0 1 0 0 0\n -2.6896 -2.6007 0.0000 O 0 0\n -1.3816 1.0513 0.0000 O 0 0\n -4.2727 -0.4470 0.0000 C 0 0\n -0.5162 -4.1568 0.0000 R# 0 0\n 0.0136 1.6023 0.0000 R# 0 0\n 0.9429 -1.2362 0.0000 O 0 0\n 2.9493 0.4174 0.0000 C 0 0\n 1.4691 0.1694 0.0000 C 0 0\n 3.4754 1.8230 0.0000 O 0 0\n 4.9556 2.0711 0.0000 N 0 0\n 5.9096 0.9136 0.0000 C 0 0\n 5.4814 3.4759 0.0000 C 0 0\n -4.3594 1.0513 0.0000 O 0 0\n -5.6992 1.7258 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 11 12 1 0\n 13 11 1 0\n 10 12 1 0\n 14 16 1 0\n 14 15 1 0\n 13 14 1 0\n 7 17 1 0\n 17 18 1 0\nM RGP 3 8 3 9 2 18 1\nM END\n> <Name>\n2-O-[(dimethylaminooxy)ethyl]ribose (DMAOE)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndmaoe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Allylribose\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -1.8446 -0.6900 0.0000 C 0 0 2 0 0 0\n -0.5129 0.0002 0.0000 C 0 0 2 0 0 0\n 0.5551 -1.0531 0.0000 C 0 0 2 0 0 0\n -0.1166 -2.3943 0.0000 C 0 0 1 0 0 0\n -1.5998 -2.1699 0.0000 O 0 0\n -0.2918 1.4820 0.0000 O 0 0\n -3.1829 -0.0163 0.0000 C 0 0\n 0.5736 -3.7261 0.0000 R# 0 0\n -3.2696 1.4820 0.0000 O 0 0\n -4.6094 2.1566 0.0000 R# 0 0\n 1.1033 2.0330 0.0000 R# 0 0\n 2.0327 -0.8055 0.0000 O 0 0\n 4.5649 2.2530 0.0000 C 0 0\n 4.0390 0.8482 0.0000 C 0 0\n 2.5589 0.6001 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 12 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 14 15 1 0\n 13 14 2 0\n 12 15 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n2-O-Allylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nallyl2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Aminooxyethylribose (AOE)\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2224 -0.8464 0.0000 C 0 0 2 0 0 0\n -0.8907 -0.1562 0.0000 C 0 0 2 0 0 0\n 0.1773 -1.2095 0.0000 C 0 0 2 0 0 0\n -0.4944 -2.5507 0.0000 C 0 0 1 0 0 0\n -1.9776 -2.3263 0.0000 O 0 0\n -0.6696 1.3256 0.0000 O 0 0\n -3.5607 -0.1727 0.0000 C 0 0\n 0.1958 -3.8825 0.0000 R# 0 0\n -3.6474 1.3256 0.0000 O 0 0\n -4.9872 2.0002 0.0000 R# 0 0\n 1.6549 -0.9619 0.0000 O 0 0\n 0.7255 1.8766 0.0000 R# 0 0\n 2.1811 0.4437 0.0000 C 0 0\n 3.6612 0.6918 0.0000 C 0 0\n 4.1874 2.0974 0.0000 O 0 0\n 5.6667 2.3453 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-Aminooxyethylribose (AOE)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\naoe2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Aminopentylribose\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -2.9120 0.7423 0.0000 O 0 0\n -2.3999 2.1522 0.0000 C 0 0 1 0 0 0\n -1.7293 -0.1803 0.0000 C 0 0 2 0 0 0\n -0.9008 2.1009 0.0000 C 0 0 2 0 0 0\n -0.4863 0.6593 0.0000 C 0 0 1 0 0 0\n 0.0183 3.2841 0.0000 O 0 0\n -3.2412 3.3920 0.0000 C 0 0\n -4.7381 3.2841 0.0000 O 0 0\n -5.5803 4.5253 0.0000 R# 0 0\n -1.7806 -1.6795 0.0000 R# 0 0\n 0.9209 0.1449 0.0000 O 0 0\n 1.5044 3.0804 0.0000 R# 0 0\n 1.1804 -1.3333 0.0000 C 0 0\n 2.5900 -1.8485 0.0000 C 0 0\n 2.8495 -3.3267 0.0000 C 0 0\n 4.2591 -3.8420 0.0000 C 0 0\n 4.5186 -5.3202 0.0000 C 0 0\n 5.9274 -5.8352 0.0000 N 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-Aminopentylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnC52r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Aminopropylribose\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2224 -0.8464 0.0000 C 0 0 2 0 0 0\n -0.8907 -0.1562 0.0000 C 0 0 2 0 0 0\n 0.1773 -1.2095 0.0000 C 0 0 2 0 0 0\n -0.4944 -2.5507 0.0000 C 0 0 1 0 0 0\n -1.9776 -2.3263 0.0000 O 0 0\n -0.6696 1.3256 0.0000 O 0 0\n -3.5607 -0.1727 0.0000 C 0 0\n 0.1958 -3.8825 0.0000 R# 0 0\n 0.7255 1.8766 0.0000 R# 0 0\n 1.6549 -0.9619 0.0000 O 0 0\n 4.1874 2.0974 0.0000 C 0 0\n 3.6612 0.6918 0.0000 C 0 0\n 2.1811 0.4437 0.0000 C 0 0\n 5.6667 2.3453 0.0000 N 0 0\n -3.6474 1.3256 0.0000 O 0 0\n -4.9872 2.0002 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 12 13 1 0\n 11 12 1 0\n 10 13 1 0\n 11 14 1 0\n 7 15 1 0\n 15 16 1 0\nM RGP 3 8 3 9 2 16 1\nM END\n> <Name>\n2-O-Aminopropylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnpr2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Benzyloxyethylribose\n SciTegic07272112182D\n\n 22 23 0 0 1 0 999 V2000\n -4.0441 -2.2530 0.0000 C 0 0 2 0 0 0\n -2.7127 -1.5620 0.0000 C 0 0 2 0 0 0\n -1.6657 -2.6183 0.0000 C 0 0 2 0 0 0\n -2.3151 -3.9563 0.0000 C 0 0 1 0 0 0\n -3.7983 -3.7328 0.0000 O 0 0\n -5.3827 -1.5801 0.0000 C 0 0\n -2.4812 -0.0818 0.0000 O 0 0\n -5.4704 -0.0818 0.0000 O 0 0\n -6.8105 0.5919 0.0000 R# 0 0\n -1.0822 0.4593 0.0000 R# 0 0\n -0.1856 -2.3694 0.0000 O 0 0\n -1.6162 -5.2835 0.0000 R# 0 0\n 0.3397 -0.9635 0.0000 C 0 0\n 1.8197 -0.7145 0.0000 C 0 0\n 2.3450 0.6913 0.0000 O 0 0\n 3.8251 0.9403 0.0000 C 0 0\n 4.3504 2.3462 0.0000 C 0 0\n 5.8293 2.5971 0.0000 C 0 0\n 6.3514 4.0033 0.0000 C 0 0\n 5.3947 5.1586 0.0000 C 0 0\n 3.9158 4.9077 0.0000 C 0 0\n 3.3937 3.5015 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 3 11 1 1\n 4 12 1 6\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 2 0\n 18 19 1 0\n 19 20 2 0\n 20 21 1 0\n 21 22 2 0\n 22 17 1 0\nM RGP 3 9 1 10 2 12 3\nM END\n> <Name>\n2-O-Benzyloxyethylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbnoe2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Benzylribose\n SciTegic07272112182D\n\n 19 20 0 0 1 0 999 V2000\n -3.1268 -0.8718 0.0000 C 0 0 2 0 0 0\n -1.7954 -0.1808 0.0000 C 0 0 2 0 0 0\n -0.7484 -1.2370 0.0000 C 0 0 2 0 0 0\n -1.3978 -2.5750 0.0000 C 0 0 1 0 0 0\n -2.8810 -2.3515 0.0000 O 0 0\n -1.5639 1.2994 0.0000 O 0 0\n -4.4654 -0.1988 0.0000 C 0 0\n -0.6989 -3.9023 0.0000 R# 0 0\n -0.1649 1.8406 0.0000 R# 0 0\n 0.7316 -0.9881 0.0000 O 0 0\n 2.7370 0.6667 0.0000 C 0 0\n 1.2570 0.4178 0.0000 C 0 0\n 3.2640 2.0711 0.0000 C 0 0\n 4.7438 2.3169 0.0000 C 0 0\n 5.6965 1.1582 0.0000 C 0 0\n 5.1694 -0.2461 0.0000 C 0 0\n 3.6897 -0.4919 0.0000 C 0 0\n -4.5531 1.2994 0.0000 O 0 0\n -5.8933 1.9731 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 11 12 1 0\n 10 12 1 0\n 11 13 2 0\n 13 14 1 0\n 14 15 2 0\n 15 16 1 0\n 16 17 2 0\n 17 11 1 0\n 7 18 1 0\n 18 19 1 0\nM RGP 3 8 3 9 2 19 1\nM END\n> <Name>\n2-O-Benzylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbn2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Butylribose\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2224 -0.8464 0.0000 C 0 0 2 0 0 0\n -0.8907 -0.1562 0.0000 C 0 0 2 0 0 0\n 0.1773 -1.2095 0.0000 C 0 0 2 0 0 0\n -0.4944 -2.5507 0.0000 C 0 0 1 0 0 0\n -1.9776 -2.3263 0.0000 O 0 0\n -0.6696 1.3256 0.0000 O 0 0\n -3.5607 -0.1727 0.0000 C 0 0\n 0.1958 -3.8825 0.0000 R# 0 0\n 0.7255 1.8766 0.0000 R# 0 0\n 1.6549 -0.9619 0.0000 O 0 0\n 4.1874 2.0974 0.0000 C 0 0\n 3.6612 0.6918 0.0000 C 0 0\n 2.1811 0.4437 0.0000 C 0 0\n 5.6667 2.3453 0.0000 C 0 0\n -3.6474 1.3256 0.0000 O 0 0\n -4.9872 2.0002 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 12 13 1 0\n 11 12 1 0\n 10 13 1 0\n 11 14 1 0\n 7 15 1 0\n 15 16 1 0\nM RGP 3 8 3 9 2 16 1\nM END\n> <Name>\n2-O-Butylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbu2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Dimethylaminocarbamoylribose\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.2687 0.0472 0.0000 O 0 0\n -1.7567 1.4571 0.0000 C 0 0 1 0 0 0\n -1.0861 -0.8754 0.0000 C 0 0 2 0 0 0\n -0.2576 1.4058 0.0000 C 0 0 2 0 0 0\n 0.1569 -0.0358 0.0000 C 0 0 1 0 0 0\n 0.6616 2.5890 0.0000 O 0 0\n -2.5979 2.6969 0.0000 C 0 0\n -4.0949 2.5890 0.0000 O 0 0\n -4.9371 3.8303 0.0000 R# 0 0\n -1.1374 -2.3745 0.0000 R# 0 0\n 1.5641 -0.5501 0.0000 O 0 0\n 2.1477 2.3853 0.0000 R# 0 0\n 1.8236 -2.0284 0.0000 C 0 0\n 3.2332 -2.5436 0.0000 N 0 0\n 0.6735 -2.9913 0.0000 O 0 0\n 3.4926 -4.0210 0.0000 C 0 0\n 4.3833 -1.5807 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 13 15 2 0\n 14 16 1 0\n 14 17 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-Dimethylaminocarbamoylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2nc2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Dimethylaminoethylribose\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.4126 -1.0379 0.0000 C 0 0 2 0 0 0\n -1.0809 -0.3477 0.0000 C 0 0 2 0 0 0\n -0.0129 -1.4010 0.0000 C 0 0 2 0 0 0\n -0.6846 -2.7422 0.0000 C 0 0 1 0 0 0\n -2.1678 -2.5178 0.0000 O 0 0\n -0.8598 1.1342 0.0000 O 0 0\n -3.7509 -0.3641 0.0000 C 0 0\n 0.0056 -4.0740 0.0000 R# 0 0\n 0.5354 1.6852 0.0000 R# 0 0\n 1.4647 -1.1533 0.0000 O 0 0\n 3.4711 0.5003 0.0000 C 0 0\n 1.9909 0.2522 0.0000 C 0 0\n 3.9972 1.9059 0.0000 N 0 0\n 3.0431 3.0634 0.0000 C 0 0\n 5.4766 2.1539 0.0000 C 0 0\n -3.8376 1.1342 0.0000 O 0 0\n -5.1774 1.8087 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 11 12 1 0\n 10 12 1 0\n 13 15 1 0\n 13 14 1 0\n 11 13 1 0\n 7 16 1 0\n 16 17 1 0\nM RGP 3 8 3 9 2 17 1\nM END\n> <Name>\n2-O-Dimethylaminoethylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2e2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Ethoxymethylribose\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2590 0.0451 0.0000 O 0 0\n -1.7470 1.4550 0.0000 C 0 0 1 0 0 0\n -1.0764 -0.8776 0.0000 C 0 0 2 0 0 0\n -0.2479 1.4037 0.0000 C 0 0 2 0 0 0\n 0.1666 -0.0379 0.0000 C 0 0 1 0 0 0\n 0.6713 2.5869 0.0000 O 0 0\n -2.5882 2.6948 0.0000 C 0 0\n -4.0852 2.5869 0.0000 O 0 0\n -4.9274 3.8281 0.0000 R# 0 0\n -1.1277 -2.3767 0.0000 R# 0 0\n 1.5738 -0.5523 0.0000 O 0 0\n 2.1574 2.3832 0.0000 R# 0 0\n 1.8333 -2.0305 0.0000 C 0 0\n 3.2429 -2.5458 0.0000 O 0 0\n 3.5024 -4.0240 0.0000 C 0 0\n 4.9112 -4.5390 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-Ethoxymethylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\neom2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Ethylribose\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -1.5185 -0.5291 0.0000 C 0 0 2 0 0 0\n -0.1867 0.1611 0.0000 C 0 0 2 0 0 0\n 0.8812 -0.8922 0.0000 C 0 0 2 0 0 0\n 0.2095 -2.2334 0.0000 C 0 0 1 0 0 0\n -1.2736 -2.0090 0.0000 O 0 0\n 0.0343 1.6430 0.0000 O 0 0\n -2.8567 0.1447 0.0000 C 0 0\n 0.8997 -3.5651 0.0000 R# 0 0\n 2.3589 -0.6445 0.0000 O 0 0\n 1.4295 2.1940 0.0000 R# 0 0\n 2.8850 0.7611 0.0000 C 0 0\n 4.3644 1.0090 0.0000 C 0 0\n -2.9435 1.6430 0.0000 O 0 0\n -4.2833 2.3175 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 9 1 1\n 1 7 1 6\n 4 8 1 6\n 6 10 1 0\n 9 11 1 0\n 11 12 1 0\n 7 13 1 0\n 13 14 1 0\nM RGP 3 8 3 10 2 14 1\nM END\n> <Name>\n2-O-Ethylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ne2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Isopropylribose\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -1.6473 -0.6570 0.0000 C 0 0 2 0 0 0\n -0.3155 0.0332 0.0000 C 0 0 2 0 0 0\n 0.7525 -1.0201 0.0000 C 0 0 2 0 0 0\n 0.0807 -2.3613 0.0000 C 0 0 1 0 0 0\n -1.4024 -2.1369 0.0000 O 0 0\n -0.0944 1.5151 0.0000 O 0 0\n -2.9855 0.0168 0.0000 C 0 0\n 0.7709 -3.6930 0.0000 R# 0 0\n -3.0722 1.5151 0.0000 O 0 0\n -4.4120 2.1896 0.0000 R# 0 0\n 1.3007 2.0661 0.0000 R# 0 0\n 2.2301 -0.7724 0.0000 O 0 0\n 4.2356 0.8811 0.0000 C 0 0\n 2.7563 0.6332 0.0000 C 0 0\n 1.8022 1.7906 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 12 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 13 14 1 0\n 12 14 1 0\n 14 15 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n2-O-Isopropylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nipr2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Methyl carbocyclic ribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.1828 -0.4514 0.0000 C 0 0 2 0 0 0\n 0.1490 0.2388 0.0000 C 0 0 2 0 0 0\n 1.2170 -0.8145 0.0000 C 0 0 2 0 0 0\n 0.5452 -2.1557 0.0000 C 0 0 1 0 0 0\n -0.9379 -1.9313 0.0000 C 0 0\n 0.3701 1.7207 0.0000 O 0 0\n -2.5210 0.2223 0.0000 C 0 0\n 1.2354 -3.4875 0.0000 R# 0 0\n 1.7652 2.2716 0.0000 R# 0 0\n 2.6946 -0.5669 0.0000 O 0 0\n 3.2204 0.8380 0.0000 C 0 0\n -2.6077 1.7207 0.0000 O 0 0\n -3.9475 2.3952 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 10 11 1 0\n 7 12 1 0\n 12 13 1 0\nM RGP 3 8 3 9 2 13 1\nM END\n> <Name>\n2-O-Methyl carbocyclic ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc4m\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Methyl-4-thioribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.1828 -0.4514 0.0000 C 0 0 2 0 0 0\n 0.1490 0.2388 0.0000 C 0 0 2 0 0 0\n 1.2170 -0.8145 0.0000 C 0 0 2 0 0 0\n 0.5452 -2.1557 0.0000 C 0 0 1 0 0 0\n -0.9379 -1.9313 0.0000 S 0 0\n 0.3701 1.7207 0.0000 O 0 0\n -2.5210 0.2223 0.0000 C 0 0\n 1.2354 -3.4875 0.0000 R# 0 0\n -2.6077 1.7207 0.0000 O 0 0\n -3.9475 2.3952 0.0000 R# 0 0\n 2.6946 -0.5669 0.0000 O 0 0\n 1.7652 2.2716 0.0000 R# 0 0\n 3.2204 0.8380 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-Methyl-4-thioribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns4m\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Methylaminoethylribose (MMAE)\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2590 0.0451 0.0000 O 0 0\n -1.7470 1.4550 0.0000 C 0 0 1 0 0 0\n -1.0764 -0.8776 0.0000 C 0 0 2 0 0 0\n -0.2479 1.4037 0.0000 C 0 0 2 0 0 0\n 0.1666 -0.0379 0.0000 C 0 0 1 0 0 0\n 0.6713 2.5869 0.0000 O 0 0\n -2.5882 2.6948 0.0000 C 0 0\n -4.0852 2.5869 0.0000 O 0 0\n -4.9274 3.8281 0.0000 R# 0 0\n -1.1277 -2.3767 0.0000 R# 0 0\n 1.5738 -0.5523 0.0000 O 0 0\n 2.1574 2.3832 0.0000 R# 0 0\n 1.8333 -2.0305 0.0000 C 0 0\n 3.2429 -2.5458 0.0000 C 0 0\n 3.5024 -4.0240 0.0000 N 0 0\n 4.9112 -4.5390 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-Methylaminoethylribose (MMAE)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmne2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-N-[2-(methylsulfanyl)ethyl]acetamidoribose\n SciTegic07272112182D\n\n 20 20 0 0 1 0 999 V2000\n -3.5566 -1.4808 0.0000 C 0 0 2 0 0 0\n -2.2248 -0.7906 0.0000 C 0 0 2 0 0 0\n -1.1569 -1.8440 0.0000 C 0 0 2 0 0 0\n -1.8286 -3.1851 0.0000 C 0 0 1 0 0 0\n -3.3117 -2.9607 0.0000 O 0 0\n -2.0038 0.6912 0.0000 O 0 0\n -4.8948 -0.8071 0.0000 C 0 0\n -1.1384 -4.5169 0.0000 R# 0 0\n -4.9816 0.6912 0.0000 O 0 0\n -6.3214 1.3657 0.0000 R# 0 0\n -0.6086 1.2422 0.0000 R# 0 0\n 0.3208 -1.5963 0.0000 O 0 0\n 2.8532 1.4629 0.0000 N 0 0\n 2.3271 0.0574 0.0000 C 0 0\n 0.8469 -0.1907 0.0000 C 0 0\n 4.3334 1.7110 0.0000 C 0 0\n 3.2811 -1.1001 0.0000 O 0 0\n 4.8595 3.1166 0.0000 C 0 0\n 6.3397 3.3647 0.0000 S 0 0\n 6.8655 4.7695 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 12 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 14 15 1 0\n 13 14 1 0\n 12 15 1 0\n 13 16 1 0\n 14 17 2 0\n 16 18 1 0\n 18 19 1 0\n 19 20 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n2-O-N-[2-(methylsulfanyl)ethyl]acetamidoribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmseac\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Nonylribose\n SciTegic07272112182D\n\n 21 21 0 0 1 0 999 V2000\n -4.2203 -2.0781 0.0000 C 0 0 2 0 0 0\n -2.8885 -1.3879 0.0000 C 0 0 2 0 0 0\n -1.8205 -2.4412 0.0000 C 0 0 2 0 0 0\n -2.4923 -3.7824 0.0000 C 0 0 1 0 0 0\n -3.9754 -3.5580 0.0000 O 0 0\n -2.6674 0.0939 0.0000 O 0 0\n -5.5585 -1.4044 0.0000 C 0 0\n -1.8021 -5.1142 0.0000 R# 0 0\n -5.6452 0.0939 0.0000 O 0 0\n -6.9850 0.7685 0.0000 R# 0 0\n -1.2723 0.6449 0.0000 R# 0 0\n -0.3429 -2.1936 0.0000 O 0 0\n 2.1895 0.8657 0.0000 C 0 0\n 1.6634 -0.5399 0.0000 C 0 0\n 0.1832 -0.7880 0.0000 C 0 0\n 3.6697 1.1138 0.0000 C 0 0\n 4.1959 2.5194 0.0000 C 0 0\n 5.6760 2.7674 0.0000 C 0 0\n 6.2022 4.1730 0.0000 C 0 0\n 7.6823 4.4211 0.0000 C 0 0\n 8.2082 5.8259 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 12 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 14 15 1 0\n 13 14 1 0\n 12 15 1 0\n 13 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 19 20 1 0\n 20 21 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n2-O-Nonylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nC92r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Pentylribose\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.5868 -1.0670 0.0000 C 0 0 2 0 0 0\n -1.2550 -0.3768 0.0000 C 0 0 2 0 0 0\n -0.1871 -1.4301 0.0000 C 0 0 2 0 0 0\n -0.8588 -2.7713 0.0000 C 0 0 1 0 0 0\n -2.3419 -2.5469 0.0000 O 0 0\n -1.0340 1.1050 0.0000 O 0 0\n -3.9250 -0.3933 0.0000 C 0 0\n -0.1686 -4.1031 0.0000 R# 0 0\n 0.3612 1.6560 0.0000 R# 0 0\n 1.2906 -1.1825 0.0000 O 0 0\n 3.8230 1.8768 0.0000 C 0 0\n 3.2969 0.4712 0.0000 C 0 0\n 1.8167 0.2231 0.0000 C 0 0\n 5.3032 2.1248 0.0000 C 0 0\n 5.8290 3.5297 0.0000 C 0 0\n -4.0118 1.1050 0.0000 O 0 0\n -5.3516 1.7795 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 12 13 1 0\n 11 12 1 0\n 10 13 1 0\n 11 14 1 0\n 14 15 1 0\n 7 16 1 0\n 16 17 1 0\nM RGP 3 8 3 9 2 17 1\nM END\n> <Name>\n2-O-Pentylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nC52r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Phenylribose\n SciTegic07272112182D\n\n 18 19 0 0 1 0 999 V2000\n -2.2444 -1.1524 0.0000 C 0 0 2 0 0 0\n -0.9131 -0.4614 0.0000 C 0 0 2 0 0 0\n 0.1340 -1.5177 0.0000 C 0 0 2 0 0 0\n -0.5154 -2.8556 0.0000 C 0 0 1 0 0 0\n -1.9987 -2.6321 0.0000 O 0 0\n -0.6815 1.0188 0.0000 O 0 0\n -3.5831 -0.4795 0.0000 C 0 0\n 0.1835 -4.1829 0.0000 R# 0 0\n -3.6707 1.0188 0.0000 O 0 0\n -5.0109 1.6925 0.0000 R# 0 0\n 1.6140 -1.2687 0.0000 O 0 0\n 0.7174 1.5600 0.0000 R# 0 0\n 2.1393 0.1372 0.0000 C 0 0\n 3.6182 0.3881 0.0000 C 0 0\n 4.1403 1.7943 0.0000 C 0 0\n 3.1836 2.9496 0.0000 C 0 0\n 1.7047 2.6986 0.0000 C 0 0\n 1.1826 1.2925 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 16 17 1 0\n 17 18 2 0\n 18 13 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-Phenylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nph2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Propargylribose\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -2.0488 0.7379 0.0000 C 0 0 2 0 0 0\n -0.5488 0.7379 0.0000 C 0 0 2 0 0 0\n -0.0853 -0.6887 0.0000 C 0 0 2 0 0 0\n -1.2988 -1.5704 0.0000 C 0 0 1 0 0 0\n -2.5123 -0.6887 0.0000 O 0 0\n -2.9270 1.9518 0.0000 C 0 0\n 0.3293 1.9518 0.0000 O 0 0\n 1.8215 1.7991 0.0000 R# 0 0\n 1.3406 -1.1487 0.0000 O 0 0\n -1.2988 -3.0704 0.0000 R# 0 0\n 2.4545 -0.1429 0.0000 C 0 0\n 3.8828 -0.6037 0.0000 C 0 0\n -4.4192 1.7991 0.0000 R# 0 0\n 5.3103 -1.0642 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 3 9 1 1\n 4 10 1 6\n 9 11 1 0\n 11 12 1 0\n 6 13 1 0\n 12 14 3 0\nM RGP 3 8 2 10 3 13 1\nM END\n> <Name>\n2-O-Propargylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nprparg\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-Propylribose\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -1.8446 -0.6900 0.0000 C 0 0 2 0 0 0\n -0.5129 0.0002 0.0000 C 0 0 2 0 0 0\n 0.5551 -1.0531 0.0000 C 0 0 2 0 0 0\n -0.1166 -2.3943 0.0000 C 0 0 1 0 0 0\n -1.5998 -2.1699 0.0000 O 0 0\n -0.2918 1.4820 0.0000 O 0 0\n -3.1829 -0.0163 0.0000 C 0 0\n 0.5736 -3.7261 0.0000 R# 0 0\n 1.1033 2.0330 0.0000 R# 0 0\n 2.0327 -0.8055 0.0000 O 0 0\n 4.5649 2.2530 0.0000 C 0 0\n 4.0390 0.8482 0.0000 C 0 0\n 2.5589 0.6001 0.0000 C 0 0\n -3.2696 1.4820 0.0000 O 0 0\n -4.6094 2.1566 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 12 13 1 0\n 11 12 1 0\n 10 13 1 0\n 7 14 1 0\n 14 15 1 0\nM RGP 3 8 3 9 2 15 1\nM END\n> <Name>\n2-O-Propylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\npr2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[2-(1-Imidizolyl)ethyl] ribose\n SciTegic07272112182D\n\n 19 20 0 0 1 0 999 V2000\n -2.9212 -1.4749 0.0000 C 0 0 2 0 0 0\n -1.5894 -0.7847 0.0000 C 0 0 2 0 0 0\n -0.5215 -1.8381 0.0000 C 0 0 2 0 0 0\n -1.1932 -3.1792 0.0000 C 0 0 1 0 0 0\n -2.6763 -2.9548 0.0000 O 0 0\n -1.3684 0.6971 0.0000 O 0 0\n -4.2594 -0.8012 0.0000 C 0 0\n -0.5030 -4.5110 0.0000 R# 0 0\n -4.3462 0.6971 0.0000 O 0 0\n -5.6860 1.3716 0.0000 R# 0 0\n 0.9562 -1.5904 0.0000 O 0 0\n 0.0268 1.2481 0.0000 R# 0 0\n 1.4823 -0.1848 0.0000 C 0 0\n 2.9625 0.0633 0.0000 C 0 0\n 3.4886 1.4689 0.0000 N 0 0\n 4.9258 1.8517 0.0000 C 0 0\n 4.9887 3.3503 0.0000 C 0 0\n 3.5828 3.8733 0.0000 N 0 0\n 2.6510 2.6978 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 2 0\n 17 18 1 0\n 18 19 2 0\n 19 15 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-[2-(1-Imidizolyl)ethyl] ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nime2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[2-(2-Methoxyethoxy)ethoxy]ethylribose (TriMOE)\n SciTegic07272112182D\n\n 22 22 0 0 1 0 999 V2000\n -4.6607 -2.3543 0.0000 C 0 0 2 0 0 0\n -3.3289 -1.6641 0.0000 C 0 0 2 0 0 0\n -2.2609 -2.7174 0.0000 C 0 0 2 0 0 0\n -2.9327 -4.0586 0.0000 C 0 0 1 0 0 0\n -4.4158 -3.8341 0.0000 O 0 0\n -3.1078 -0.1822 0.0000 O 0 0\n -5.9989 -1.6805 0.0000 C 0 0\n -2.2425 -5.3903 0.0000 R# 0 0\n -1.7127 0.3688 0.0000 R# 0 0\n -0.7833 -2.4697 0.0000 O 0 0\n 1.2230 -0.8160 0.0000 C 0 0\n -0.2571 -1.0641 0.0000 C 0 0\n 1.7492 0.5895 0.0000 O 0 0\n 3.2294 0.8376 0.0000 C 0 0\n 3.7555 2.2432 0.0000 C 0 0\n 5.2357 2.4913 0.0000 O 0 0\n 5.7618 3.8969 0.0000 C 0 0\n 7.2420 4.1449 0.0000 C 0 0\n 7.7681 5.5505 0.0000 O 0 0\n 9.2475 5.7985 0.0000 C 0 0\n -6.0856 -0.1822 0.0000 O 0 0\n -7.4254 0.4923 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 11 12 1 0\n 10 12 1 0\n 13 14 1 0\n 11 13 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 19 20 1 0\n 7 21 1 0\n 21 22 1 0\nM RGP 3 8 3 9 2 22 1\nM END\n> <Name>\n2-O-[2-(2-Methoxyethoxy)ethoxy]ethylribose (TriMOE)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ntrimoe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[2-((N,N-diethyl)aminooxy)ethyl]ribose\n SciTegic07272112182D\n\n 20 20 0 0 1 0 999 V2000\n -3.6522 -1.3653 0.0000 C 0 0 2 0 0 0\n -2.3204 -0.6751 0.0000 C 0 0 2 0 0 0\n -1.2525 -1.7284 0.0000 C 0 0 2 0 0 0\n -1.9242 -3.0696 0.0000 C 0 0 1 0 0 0\n -3.4073 -2.8452 0.0000 O 0 0\n -2.0994 0.8067 0.0000 O 0 0\n -4.9905 -0.6916 0.0000 C 0 0\n -1.2340 -4.4014 0.0000 R# 0 0\n -5.0772 0.8067 0.0000 O 0 0\n -6.4170 1.4812 0.0000 R# 0 0\n 0.2252 -1.4808 0.0000 O 0 0\n -0.7042 1.3577 0.0000 R# 0 0\n 0.7513 -0.0752 0.0000 C 0 0\n 2.2315 0.1729 0.0000 C 0 0\n 2.7576 1.5785 0.0000 O 0 0\n 4.2378 1.8265 0.0000 N 0 0\n 5.1947 0.6704 0.0000 C 0 0\n 4.7639 3.2321 0.0000 C 0 0\n 6.6738 0.9200 0.0000 C 0 0\n 6.2433 3.4801 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 18 1 0\n 16 17 1 0\n 17 19 1 0\n 18 20 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-[2-((N,N-diethyl)aminooxy)ethyl]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ne2noe2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[2-((N-Isopropyl-N-methyl)aminooxy)ethyl]ribose\n SciTegic07272112182D\n\n 20 20 0 0 1 0 999 V2000\n -3.3509 1.2004 0.0000 O 0 0\n -2.8388 2.6103 0.0000 C 0 0 1 0 0 0\n -2.1682 0.2778 0.0000 C 0 0 2 0 0 0\n -1.3397 2.5590 0.0000 C 0 0 2 0 0 0\n -0.9252 1.1174 0.0000 C 0 0 1 0 0 0\n -0.4205 3.7422 0.0000 O 0 0\n -3.6801 3.8501 0.0000 C 0 0\n -5.1770 3.7422 0.0000 O 0 0\n -6.0192 4.9835 0.0000 R# 0 0\n -2.2195 -1.2213 0.0000 R# 0 0\n 0.4820 0.6031 0.0000 O 0 0\n 1.0656 3.5385 0.0000 R# 0 0\n 0.7415 -0.8752 0.0000 C 0 0\n 2.1511 -1.3904 0.0000 C 0 0\n 2.4106 -2.8686 0.0000 O 0 0\n 3.8202 -3.3839 0.0000 N 0 0\n 4.9703 -2.4209 0.0000 C 0 0\n 4.0797 -4.8621 0.0000 C 0 0\n 5.4885 -5.3771 0.0000 C 0 0\n 2.9296 -5.8251 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 16 18 1 0\n 18 19 1 0\n 18 20 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-[2-((N-Isopropyl-N-methyl)aminooxy)ethyl]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\niprmno\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[2-(Guanidinium)ethyl]ribose\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -2.9344 -1.1208 0.0000 C 0 0 2 0 0 0\n -1.6027 -0.4306 0.0000 C 0 0 2 0 0 0\n -0.5347 -1.4839 0.0000 C 0 0 2 0 0 0\n -1.2064 -2.8251 0.0000 C 0 0 1 0 0 0\n -2.6896 -2.6007 0.0000 O 0 0\n -1.3816 1.0513 0.0000 O 0 0\n -4.2727 -0.4470 0.0000 C 0 0\n -0.5162 -4.1568 0.0000 R# 0 0\n -4.3594 1.0513 0.0000 O 0 0\n -5.6992 1.7258 0.0000 R# 0 0\n 0.9429 -1.2362 0.0000 O 0 0\n 0.0136 1.6023 0.0000 R# 0 0\n 1.4691 0.1694 0.0000 C 0 0\n 2.9493 0.4174 0.0000 C 0 0\n 3.4754 1.8230 0.0000 N 0 0\n 4.9556 2.0711 0.0000 C 0 0\n 5.4814 3.4759 0.0000 N 0 0\n 5.9096 0.9136 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 2 0\n 16 18 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-[2-(Guanidinium)ethyl]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nguane2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[2-(Methylthio)ethyl]ribose\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2224 -0.8464 0.0000 C 0 0 2 0 0 0\n -0.8907 -0.1562 0.0000 C 0 0 2 0 0 0\n 0.1773 -1.2095 0.0000 C 0 0 2 0 0 0\n -0.4944 -2.5507 0.0000 C 0 0 1 0 0 0\n -1.9776 -2.3263 0.0000 O 0 0\n -0.6696 1.3256 0.0000 O 0 0\n -3.5607 -0.1727 0.0000 C 0 0\n 0.1958 -3.8825 0.0000 R# 0 0\n -3.6474 1.3256 0.0000 O 0 0\n -4.9872 2.0002 0.0000 R# 0 0\n 1.6549 -0.9619 0.0000 O 0 0\n 0.7255 1.8766 0.0000 R# 0 0\n 2.1811 0.4437 0.0000 C 0 0\n 3.6612 0.6918 0.0000 C 0 0\n 4.1874 2.0974 0.0000 S 0 0\n 5.6667 2.3453 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-[2-(Methylthio)ethyl]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmse2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[2-(methylsulfinyl)ethyl]ribose\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.3974 0.3384 0.0000 O 0 0\n -1.8854 1.7483 0.0000 C 0 0 1 0 0 0\n -1.2148 -0.5842 0.0000 C 0 0 2 0 0 0\n -0.3862 1.6970 0.0000 C 0 0 2 0 0 0\n 0.0282 0.2554 0.0000 C 0 0 1 0 0 0\n 0.5329 2.8802 0.0000 O 0 0\n -2.7266 2.9881 0.0000 C 0 0\n -4.2236 2.8802 0.0000 O 0 0\n -5.0658 4.1215 0.0000 R# 0 0\n -1.2661 -2.0833 0.0000 R# 0 0\n 1.4354 -0.2589 0.0000 O 0 0\n 2.0190 2.6765 0.0000 R# 0 0\n 1.6949 -1.7372 0.0000 C 0 0\n 3.1045 -2.2524 0.0000 C 0 0\n 3.3640 -3.7306 0.0000 S 0 0\n 2.2139 -4.6936 0.0000 C 0 0\n 4.7729 -4.2456 0.0000 O 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 15 17 2 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-[2-(methylsulfinyl)ethyl]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmsoe2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[2-[2-(N,N-dimethyl)aminoethoxy]ethyl]ribose\n SciTegic07272112182D\n\n 20 20 0 0 1 0 999 V2000\n -3.7572 -1.6462 0.0000 C 0 0 2 0 0 0\n -2.4255 -0.9560 0.0000 C 0 0 2 0 0 0\n -1.3575 -2.0093 0.0000 C 0 0 2 0 0 0\n -2.0292 -3.3505 0.0000 C 0 0 1 0 0 0\n -3.5124 -3.1261 0.0000 O 0 0\n -2.2044 0.5258 0.0000 O 0 0\n -5.0955 -0.9725 0.0000 C 0 0\n -1.3390 -4.6823 0.0000 R# 0 0\n -5.1822 0.5258 0.0000 O 0 0\n -6.5220 1.2004 0.0000 R# 0 0\n -0.8093 1.0768 0.0000 R# 0 0\n 0.1201 -1.7617 0.0000 O 0 0\n 2.1264 -0.1080 0.0000 C 0 0\n 0.6463 -0.3561 0.0000 C 0 0\n 2.6526 1.2976 0.0000 O 0 0\n 4.1328 1.5457 0.0000 C 0 0\n 4.6589 2.9512 0.0000 C 0 0\n 6.1391 3.1993 0.0000 N 0 0\n 7.0931 2.0418 0.0000 C 0 0\n 6.6649 4.6041 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 12 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 13 14 1 0\n 15 13 1 0\n 12 14 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 20 1 0\n 18 19 1 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n2-O-[2-[2-(N,N-dimethyl)aminoethoxy]ethyl]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndmaeoe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[3-(N,N-Dimethyl)aminopropyl]ribose\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -2.9344 -1.1208 0.0000 C 0 0 2 0 0 0\n -1.6027 -0.4306 0.0000 C 0 0 2 0 0 0\n -0.5347 -1.4839 0.0000 C 0 0 2 0 0 0\n -1.2064 -2.8251 0.0000 C 0 0 1 0 0 0\n -2.6896 -2.6007 0.0000 O 0 0\n -1.3816 1.0513 0.0000 O 0 0\n -4.2727 -0.4470 0.0000 C 0 0\n -0.5162 -4.1568 0.0000 R# 0 0\n -4.3594 1.0513 0.0000 O 0 0\n -5.6992 1.7258 0.0000 R# 0 0\n 0.9429 -1.2362 0.0000 O 0 0\n 0.0136 1.6023 0.0000 R# 0 0\n 1.4691 0.1694 0.0000 C 0 0\n 2.9493 0.4174 0.0000 C 0 0\n 3.4754 1.8230 0.0000 C 0 0\n 4.9556 2.0711 0.0000 N 0 0\n 5.9096 0.9136 0.0000 C 0 0\n 5.4814 3.4759 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 11 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 18 1 0\n 16 17 1 0\nM RGP 3 8 3 10 1 12 2\nM END\n> <Name>\n2-O-[3-(N,N-Dimethyl)aminopropyl]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2npr2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[(2-Methoxy)ethyl]-4-thioribose\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.2224 -0.8464 0.0000 C 0 0 2 0 0 0\n -0.8907 -0.1562 0.0000 C 0 0 2 0 0 0\n 0.1773 -1.2095 0.0000 C 0 0 2 0 0 0\n -0.4944 -2.5507 0.0000 C 0 0 1 0 0 0\n -1.9776 -2.3263 0.0000 S 0 0\n -0.6696 1.3256 0.0000 O 0 0\n -3.5607 -0.1727 0.0000 C 0 0\n 0.1958 -3.8825 0.0000 R# 0 0\n 1.6549 -0.9619 0.0000 O 0 0\n 0.7255 1.8766 0.0000 R# 0 0\n 2.1811 0.4437 0.0000 C 0 0\n 3.6612 0.6918 0.0000 C 0 0\n 4.1874 2.0974 0.0000 O 0 0\n 5.6667 2.3453 0.0000 C 0 0\n -3.6474 1.3256 0.0000 O 0 0\n -4.9872 2.0002 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 9 1 1\n 1 7 1 6\n 4 8 1 6\n 6 10 1 0\n 9 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 7 15 1 0\n 15 16 1 0\nM RGP 3 8 3 10 2 16 1\nM END\n> <Name>\n2-O-[(2-Methoxy)ethyl]-4-thioribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns4moe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[(Dimethylamino)ethylcarbamoyl]ribose\n SciTegic07272112182D\n\n 20 20 0 0 1 0 999 V2000\n -3.0819 1.1713 0.0000 O 0 0\n -2.5699 2.5812 0.0000 C 0 0 1 0 0 0\n -1.8992 0.2486 0.0000 C 0 0 2 0 0 0\n -1.0707 2.5299 0.0000 C 0 0 2 0 0 0\n -0.6563 1.0883 0.0000 C 0 0 1 0 0 0\n -0.1516 3.7131 0.0000 O 0 0\n -3.4111 3.8210 0.0000 C 0 0\n -4.9081 3.7131 0.0000 O 0 0\n -5.7503 4.9543 0.0000 R# 0 0\n -1.9506 -1.2505 0.0000 R# 0 0\n 0.7509 0.5739 0.0000 O 0 0\n 1.3345 3.5094 0.0000 R# 0 0\n 1.0104 -0.9043 0.0000 C 0 0\n 2.4200 -1.4196 0.0000 N 0 0\n -0.1397 -1.8673 0.0000 O 0 0\n 2.6795 -2.8978 0.0000 C 0 0\n 4.0891 -3.4130 0.0000 C 0 0\n 4.3487 -4.8913 0.0000 N 0 0\n 5.7575 -5.4062 0.0000 C 0 0\n 3.1986 -5.8542 0.0000 C 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\n 11 13 1 0\n 13 14 1 0\n 13 15 2 0\n 14 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 18 20 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-O-[(Dimethylamino)ethylcarbamoyl]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2nenc\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[(N,N-dimethyl)acetamido]ribose\n SciTegic07272112182D\n\n 18 18 0 0 1 0 999 V2000\n -2.6585 -1.0014 0.0000 C 0 0 2 0 0 0\n -1.3267 -0.3112 0.0000 C 0 0 2 0 0 0\n -0.2587 -1.3645 0.0000 C 0 0 2 0 0 0\n -0.9305 -2.7057 0.0000 C 0 0 1 0 0 0\n -2.4136 -2.4813 0.0000 O 0 0\n -3.9967 -0.3276 0.0000 C 0 0\n -1.1056 1.1707 0.0000 O 0 0\n -4.0834 1.1707 0.0000 O 0 0\n -5.4232 1.8452 0.0000 R# 0 0\n 0.2895 1.7217 0.0000 R# 0 0\n 1.2189 -1.1168 0.0000 O 0 0\n -0.2403 -4.0374 0.0000 R# 0 0\n 1.7450 0.2888 0.0000 C 0 0\n 3.2252 0.5368 0.0000 C 0 0\n 3.7513 1.9424 0.0000 N 0 0\n 5.2307 2.1904 0.0000 C 0 0\n 4.1793 -0.6207 0.0000 O 0 0\n 2.7973 3.0999 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 3 11 1 1\n 4 12 1 6\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 14 17 2 0\n 15 18 1 0\nM RGP 3 9 1 10 2 12 3\nM END\n> <Name>\n2-O-[(N,N-dimethyl)acetamido]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndmac\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-O-[N-[2-(Dimethylamino)ethyl]acetamido]ribose\n SciTegic07272112182D\n\n 21 21 0 0 1 0 999 V2000\n -3.9039 -1.5860 0.0000 C 0 0 2 0 0 0\n -2.5722 -0.8958 0.0000 C 0 0 2 0 0 0\n -1.5042 -1.9491 0.0000 C 0 0 2 0 0 0\n -2.1759 -3.2902 0.0000 C 0 0 1 0 0 0\n -3.6591 -3.0658 0.0000 O 0 0\n -5.2422 -0.9122 0.0000 C 0 0\n -2.3511 0.5861 0.0000 O 0 0\n -5.3289 0.5861 0.0000 O 0 0\n -6.6687 1.2606 0.0000 R# 0 0\n -0.9559 1.1371 0.0000 R# 0 0\n -0.0266 -1.7014 0.0000 O 0 0\n -1.4857 -4.6220 0.0000 R# 0 0\n 0.4996 -0.2958 0.0000 C 0 0\n 1.9798 -0.0477 0.0000 C 0 0\n 2.5059 1.3578 0.0000 N 0 0\n 3.9861 1.6059 0.0000 C 0 0\n 2.9338 -1.2052 0.0000 O 0 0\n 4.5122 3.0115 0.0000 C 0 0\n 5.9924 3.2596 0.0000 N 0 0\n 6.9464 2.1021 0.0000 C 0 0\n 6.5182 4.6644 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 3 11 1 1\n 4 12 1 6\n 11 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 14 17 2 0\n 16 18 1 0\n 18 19 1 0\n 19 21 1 0\n 19 20 1 0\nM RGP 3 9 1 10 2 12 3\nM END\n> <Name>\n2-O-[N-[2-(Dimethylamino)ethyl]acetamido]ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ndmaeac\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Phenylthio-2-deoxyribose\n SciTegic07272112182D\n\n 18 19 0 0 1 0 999 V2000\n -2.2444 -1.1524 0.0000 C 0 0 2 0 0 0\n -0.9131 -0.4614 0.0000 C 0 0 2 0 0 0\n 0.1340 -1.5177 0.0000 C 0 0 2 0 0 0\n -0.5154 -2.8556 0.0000 C 0 0 1 0 0 0\n -1.9987 -2.6321 0.0000 O 0 0\n -3.5831 -0.4795 0.0000 C 0 0\n -0.6815 1.0188 0.0000 O 0 0\n 0.7174 1.5600 0.0000 R# 0 0\n 0.1835 -4.1829 0.0000 R# 0 0\n 1.6140 -1.2687 0.0000 S 0 0\n 2.1393 0.1372 0.0000 C 0 0\n 3.6182 0.3881 0.0000 C 0 0\n 4.1403 1.7943 0.0000 C 0 0\n 3.1836 2.9496 0.0000 C 0 0\n 1.7047 2.6986 0.0000 C 0 0\n 1.1826 1.2925 0.0000 C 0 0\n -3.6707 1.0188 0.0000 O 0 0\n -5.0109 1.6925 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 3 10 1 1\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 16 11 1 0\n 6 17 1 0\n 17 18 1 0\nM RGP 3 8 2 9 3 18 1\nM END\n> <Name>\n2-Phenylthio-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nphs2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Thio LNA\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n 0.6312 -2.0624 0.0000 C 0 0\n 0.0863 -3.3094 0.0000 S 0 0\n 0.5482 -0.6031 0.0000 C 0 0 1 0 0 0\n 1.9307 0.0252 0.0000 C 0 0 2 0 0 0\n -0.1994 -1.7658 0.0000 C 0 0 2 0 0 0\n -1.5533 -1.1139 0.0000 C 0 0 1 0 0 0\n -0.9631 -0.0086 0.0000 O 0 0\n 0.3822 0.8942 0.0000 C 0 0\n -2.9468 -0.5588 0.0000 R# 0 0\n 1.5689 1.4971 0.0000 O 0 0\n 2.6655 2.5205 0.0000 R# 0 0\n -0.9922 1.4971 0.0000 O 0 0\n -1.1582 2.9879 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 6\n 3 1 1 0\n 5 2 1 1\n 4 10 1 1\n 10 11 1 0\n 8 12 1 0\n 12 13 1 0\nM RGP 3 9 3 11 2 13 1\nM END\n> <Name>\n2-Thio LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns2lna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Thio-(R)-cEt\n SciTegic09012117322D\n\n 14 15 0 0 1 0 999 V2000\n 1.1233 0.2604 0.0000 C 0 0 1 0 0 0\n -1.0323 -0.6397 0.0000 C 0 0 2 0 0 0\n -1.8879 0.4463 0.0000 C 0 0 1 0 0 0\n -0.5108 0.2643 0.0000 O 0 0\n 0.3584 -0.9107 0.0000 C 0 0 1 0 0 0\n 2.1947 1.2825 0.0000 O 0 0\n -3.1915 1.1882 0.0000 R# 0 0\n 0.5071 -2.1734 0.0000 C 0 0 2 0 0 0\n -0.8617 -2.0116 0.0000 S 0 0\n 1.5675 -3.2343 0.0000 C 0 0\n 3.6357 0.8661 0.0000 R# 0 0\n 0.2821 0.5988 0.0000 C 0 0\n -1.0539 1.2825 0.0000 O 0 0\n -1.1307 2.7806 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 0\n 5 1 1 0\n 3 7 1 6\n 5 8 1 0\n 2 9 1 1\n 8 9 1 0\n 1 6 1 6\n 8 10 1 1\n 6 11 1 0\n 5 12 1 1\n 12 13 1 0\n 13 14 1 0\nM RGP 3 7 3 11 2 14 1\nM END\n> <Name>\n2-Thio-(R)-cEt\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRs2cEt\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Thio-(S)-cEt\n SciTegic09012117322D\n\n 14 15 0 0 1 0 999 V2000\n 1.1233 0.2604 0.0000 C 0 0 1 0 0 0\n -1.0323 -0.6397 0.0000 C 0 0 2 0 0 0\n -1.8879 0.4463 0.0000 C 0 0 1 0 0 0\n -0.5108 0.2643 0.0000 O 0 0\n 0.3584 -0.9107 0.0000 C 0 0 1 0 0 0\n 2.1947 1.2825 0.0000 O 0 0\n -3.1915 1.1882 0.0000 R# 0 0\n 0.5071 -2.1734 0.0000 C 0 0 1 0 0 0\n -0.8617 -2.0116 0.0000 S 0 0\n 1.5675 -3.2343 0.0000 C 0 0\n 3.6357 0.8661 0.0000 R# 0 0\n 0.2821 0.5988 0.0000 C 0 0\n -1.0539 1.2825 0.0000 O 0 0\n -1.1307 2.7806 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 0\n 5 1 1 0\n 3 7 1 6\n 5 8 1 0\n 2 9 1 1\n 8 9 1 0\n 1 6 1 6\n 8 10 1 6\n 6 11 1 0\n 5 12 1 1\n 12 13 1 0\n 13 14 1 0\nM RGP 3 7 3 11 2 14 1\nM END\n> <Name>\n2-Thio-(S)-cEt\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSs2cEt\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-Thiocytosine\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.5981 -1.5000 0.0000 R# 0 0\n 0.0000 -3.0000 0.0000 S 0 0\n 2.5981 1.5000 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 0\n 6 8 2 0\n 2 9 1 0\nM RGP 1 7 1\nM END\n> <Name>\n2-Thiocytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns2C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Thiothymine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 S 0 0\n 4.5000 0.4019 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\nM RGP 1 8 1\nM END\n> <Name>\n2-Thiothymine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns2T\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-Thiouracil\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 2.5981 1.5000 0.0000 S 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\nM RGP 1 8 1\nM END\n> <Name>\n2-Thiouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns2U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n2-alpha-C-Ethyl-2-deoxyribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.1828 -0.4514 0.0000 C 0 0 2 0 0 0\n 0.1490 0.2388 0.0000 C 0 0 2 0 0 0\n 1.2170 -0.8145 0.0000 C 0 0 2 0 0 0\n 0.5452 -2.1557 0.0000 C 0 0 1 0 0 0\n -0.9379 -1.9313 0.0000 O 0 0\n 0.3701 1.7207 0.0000 O 0 0\n -2.5210 0.2223 0.0000 C 0 0\n 1.2354 -3.4875 0.0000 R# 0 0\n 1.7652 2.2716 0.0000 R# 0 0\n 2.6946 -0.5669 0.0000 C 0 0\n 3.2204 0.8380 0.0000 C 0 0\n -2.6077 1.7207 0.0000 O 0 0\n -3.9475 2.3952 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 3 10 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 10 11 1 0\n 7 12 1 0\n 12 13 1 0\nM RGP 3 8 3 9 2 13 1\nM END\n> <Name>\n2-alpha-C-Ethyl-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nAe2d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n2-alpha-C-Methyl-2-deoxyribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.1351 -1.0500 0.0000 O 0 0\n -0.6231 0.3599 0.0000 C 0 0 1 0 0 0\n 0.0475 -1.9727 0.0000 C 0 0 2 0 0 0\n 0.8761 0.3086 0.0000 C 0 0 2 0 0 0\n 1.2905 -1.1330 0.0000 C 0 0 1 0 0 0\n 1.7952 1.4918 0.0000 O 0 0\n -1.4643 1.5997 0.0000 C 0 0\n -2.9613 1.4918 0.0000 O 0 0\n -3.8035 2.7330 0.0000 R# 0 0\n -0.0038 -3.4718 0.0000 R# 0 0\n 2.7004 -1.6451 0.0000 C 0 0\n 3.2813 1.2881 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 6\n 3 5 1 0\n 4 5 1 0\n 4 6 1 1\n 7 8 1 0\n 8 9 1 0\n 3 10 1 6\n 5 11 1 1\n 6 12 1 0\nM RGP 3 9 1 10 3 12 2\nM END\n> <Name>\n2-alpha-C-Methyl-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nAm2d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-(Dimethylamino)propylaminoadenine\n SciTegic07272112182D\n\n 18 19 0 0 0 0 999 V2000\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2578 0.0000 C 0 0\n 5.1894 6.0109 0.0000 N 0 0\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n 2.5972 1.5031 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 5.1872 7.5109 0.0000 C 0 0\n 6.4897 5.2632 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 5 10 2 0\n 8 11 1 0\n 11 12 1 0\n 12 13 2 0\n 9 13 1 0\n 10 14 1 0\n 6 15 1 0\n 11 16 1 0\n 1 15 1 0\n 4 17 1 0\n 4 18 1 0\nM RGP 1 16 1\nM END\n> <Name>\n3-(Dimethylamino)propylaminoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2nprn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n3-Chloro HNA\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.5573 -0.8976 0.0000 O 0 0\n -0.8058 0.4006 0.0000 C 0 0 1 0 0 0\n 0.6942 0.3989 0.0000 C 0 0 2 0 0 0\n 1.4427 -0.9010 0.0000 C 0 0 2 0 0 0\n 0.6912 -2.1992 0.0000 C 0 0 1 0 0 0\n -0.8088 -2.1975 0.0000 C 0 0\n 1.4396 -3.4991 0.0000 R# 0 0\n 2.9427 -0.9028 0.0000 Cl 0 0\n 1.4434 1.6993 0.0000 O 0 0\n -1.5574 1.6997 0.0000 C 0 0\n 2.9434 1.7016 0.0000 R# 0 0\n -3.0582 1.6993 0.0000 O 0 0\n -3.8094 2.9977 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 6\n 4 8 1 1\n 3 9 1 1\n 2 10 1 6\n 9 11 1 0\n 10 12 1 0\n 12 13 1 0\nM RGP 3 7 3 11 2 13 1\nM END\n> <Name>\n3-Chloro HNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nclhna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Deaza-3-allylguanine\n SciTegic07272112182D\n\n 15 16 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 0.0031 3.0008 0.0000 C 0 0\n 1.3039 3.7494 0.0000 C 0 0\n 1.3070 5.2494 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 7 8 2 0\n 5 8 1 0\n 6 9 2 0\n 2 10 1 0\n 4 11 1 0\n 7 11 1 0\n 11 12 1 0\n 3 13 1 0\n 13 14 1 0\n 14 15 2 0\nM RGP 1 12 1\nM END\n> <Name>\n3-Deaza-3-allylguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc3ally\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n3-Deazaadenine\n SciTegic07272112182D\n\n 11 12 0 0 0 0 999 V2000\n 5.9498 4.1210 0.0000 C 0 0\n 6.2618 2.6538 0.0000 C 0 0\n 7.6885 2.1904 0.0000 C 0 0\n 7.0645 5.1248 0.0000 C 0 0\n 8.4911 4.6614 0.0000 N 0 0\n 8.8031 3.1942 0.0000 C 0 0\n 7.6888 0.6912 0.0000 N 0 0\n 6.2623 0.2275 0.0000 C 0 0\n 5.3805 1.4410 0.0000 N 0 0\n 10.2297 2.7308 0.0000 N 0 0\n 3.8805 1.4410 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 3 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 2 1 0\n 6 10 1 0\n 9 11 1 0\nM RGP 1 11 1\nM END\n> <Name>\n3-Deazaadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc3A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n3-Deazaguanine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 7 8 2 0\n 5 8 1 0\n 6 9 2 0\n 2 10 1 0\n 4 11 1 0\n 7 11 1 0\n 11 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n3-Deazaguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc3G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n3-Deoxy-3-amino-2-O-methylribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.1828 -0.4514 0.0000 C 0 0 2 0 0 0\n 0.1490 0.2388 0.0000 C 0 0 2 0 0 0\n 1.2170 -0.8145 0.0000 C 0 0 2 0 0 0\n 0.5452 -2.1557 0.0000 C 0 0 1 0 0 0\n -0.9379 -1.9313 0.0000 O 0 0\n -2.5210 0.2223 0.0000 C 0 0\n 0.3701 1.7207 0.0000 N 0 0\n -2.6077 1.7207 0.0000 O 0 0\n -3.9475 2.3952 0.0000 R# 0 0\n 1.7652 2.2716 0.0000 R# 0 0\n 1.2354 -3.4875 0.0000 R# 0 0\n 2.6946 -0.5669 0.0000 O 0 0\n 3.2204 0.8380 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\n 3 12 1 1\n 12 13 1 0\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n3-Deoxy-3-amino-2-O-methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn3m\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Deoxy-3-amino-2-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6450 -0.4268 0.0000 C 0 0 2 0 0 0\n 0.6867 0.2634 0.0000 C 0 0 2 0 0 0\n 1.7547 -0.7899 0.0000 C 0 0\n 1.0830 -2.1310 0.0000 C 0 0 1 0 0 0\n -0.4002 -1.9066 0.0000 O 0 0\n -1.9833 0.2470 0.0000 C 0 0\n 0.9078 1.7453 0.0000 N 0 0\n 2.3029 2.2963 0.0000 R# 0 0\n 1.7731 -3.4628 0.0000 R# 0 0\n -2.0700 1.7453 0.0000 O 0 0\n -3.4098 2.4198 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 6 10 1 0\n 10 11 1 0\nM RGP 3 8 2 9 3 11 1\nM END\n> <Name>\n3-Deoxy-3-amino-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn3d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Deoxy-3-amino-2-fluororibose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.9146 -0.3813 0.0000 C 0 0 2 0 0 0\n 0.4172 0.3089 0.0000 C 0 0 2 0 0 0\n 1.4851 -0.7445 0.0000 C 0 0 2 0 0 0\n 0.8134 -2.0856 0.0000 C 0 0 1 0 0 0\n -0.6697 -1.8612 0.0000 O 0 0\n -2.2528 0.2924 0.0000 C 0 0\n 0.6383 1.7907 0.0000 N 0 0\n 2.0334 2.3417 0.0000 R# 0 0\n 1.5036 -3.4174 0.0000 R# 0 0\n 2.9650 -0.4996 0.0000 F 0 0\n -2.3396 1.7907 0.0000 O 0 0\n -3.6793 2.4652 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 3 10 1 1\n 6 11 1 0\n 11 12 1 0\nM RGP 3 8 2 9 3 12 1\nM END\n> <Name>\n3-Deoxy-3-amino-2-fluororibose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn3fl2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Deoxy-3-amino-4-carboxyl-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6576 0.1670 0.0000 C 0 0 2 0 0 0\n 0.8424 0.1670 0.0000 C 0 0 2 0 0 0\n 1.3059 -1.2595 0.0000 C 0 0\n 0.0924 -2.1412 0.0000 C 0 0 1 0 0 0\n -1.1212 -1.2595 0.0000 O 0 0\n -1.5358 1.3810 0.0000 C 0 0\n 1.7205 1.3810 0.0000 N 0 0\n -3.0278 1.2268 0.0000 R# 0 0\n 3.2127 1.2282 0.0000 R# 0 0\n 0.0924 -3.6412 0.0000 R# 0 0\n -0.9237 2.7504 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 7 9 1 0\n 4 10 1 6\n 6 11 2 0\nM RGP 3 8 1 9 2 10 3\nM END\n> <Name>\n3-Deoxy-3-amino-4-carboxyl-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn3co4d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Deoxy-3-methylene-2-O-methylribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.1828 -0.4514 0.0000 C 0 0 2 0 0 0\n 0.1490 0.2388 0.0000 C 0 0 2 0 0 0\n 1.2170 -0.8145 0.0000 C 0 0 2 0 0 0\n 0.5452 -2.1557 0.0000 C 0 0 1 0 0 0\n -0.9379 -1.9313 0.0000 O 0 0\n -2.5210 0.2223 0.0000 C 0 0\n 0.3701 1.7207 0.0000 C 0 0\n -2.6077 1.7207 0.0000 O 0 0\n -3.9475 2.3952 0.0000 R# 0 0\n 1.7652 2.2716 0.0000 R# 0 0\n 1.2354 -3.4875 0.0000 R# 0 0\n 2.6946 -0.5669 0.0000 O 0 0\n 3.2204 0.8380 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\n 3 12 1 1\n 12 13 1 0\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n3-Deoxy-3-methylene-2-O-methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nme3m\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\n3-Deoxy-3-methylene-2-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6450 -0.4268 0.0000 C 0 0 2 0 0 0\n 0.6867 0.2634 0.0000 C 0 0 2 0 0 0\n 1.7547 -0.7899 0.0000 C 0 0\n 1.0830 -2.1310 0.0000 C 0 0 1 0 0 0\n -0.4002 -1.9066 0.0000 O 0 0\n -1.9833 0.2470 0.0000 C 0 0\n 0.9078 1.7453 0.0000 C 0 0\n 2.3029 2.2963 0.0000 R# 0 0\n 1.7731 -3.4628 0.0000 R# 0 0\n -2.0700 1.7453 0.0000 O 0 0\n -3.4098 2.4198 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 6 10 1 0\n 10 11 1 0\nM RGP 3 8 2 9 3 11 1\nM END\n> <Name>\n3-Deoxy-3-methylene-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nme3d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\n3-Deoxy-3-methylene-2-fluororibose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.9146 -0.3813 0.0000 C 0 0 2 0 0 0\n 0.4172 0.3089 0.0000 C 0 0 2 0 0 0\n 1.4851 -0.7445 0.0000 C 0 0 2 0 0 0\n 0.8134 -2.0856 0.0000 C 0 0 1 0 0 0\n -0.6697 -1.8612 0.0000 O 0 0\n -2.2528 0.2924 0.0000 C 0 0\n 0.6383 1.7907 0.0000 C 0 0\n -2.3396 1.7907 0.0000 O 0 0\n -3.6793 2.4652 0.0000 R# 0 0\n 2.0334 2.3417 0.0000 R# 0 0\n 1.5036 -3.4174 0.0000 R# 0 0\n 2.9650 -0.4996 0.0000 F 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\n 3 12 1 1\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n3-Deoxy-3-methylene-2-fluororibose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nme3fl2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\n3-Deoxy-3-methyleneribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.9146 -0.3813 0.0000 C 0 0 2 0 0 0\n 0.4172 0.3089 0.0000 C 0 0 2 0 0 0\n 1.4851 -0.7445 0.0000 C 0 0 2 0 0 0\n 0.8134 -2.0856 0.0000 C 0 0 1 0 0 0\n -0.6697 -1.8612 0.0000 O 0 0\n -2.2528 0.2924 0.0000 C 0 0\n 0.6383 1.7907 0.0000 C 0 0\n -2.3396 1.7907 0.0000 O 0 0\n -3.6793 2.4652 0.0000 R# 0 0\n 2.0334 2.3417 0.0000 R# 0 0\n 1.5036 -3.4174 0.0000 R# 0 0\n 2.9650 -0.4996 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\n 3 12 1 1\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n3-Deoxy-3-methyleneribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nme3r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\n3-Deoxy-3-thio-2-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6450 -0.4268 0.0000 C 0 0 2 0 0 0\n 0.6867 0.2634 0.0000 C 0 0 2 0 0 0\n 1.7547 -0.7899 0.0000 C 0 0\n 1.0830 -2.1310 0.0000 C 0 0 1 0 0 0\n -0.4002 -1.9066 0.0000 O 0 0\n -1.9833 0.2470 0.0000 C 0 0\n 0.9078 1.7453 0.0000 S 0 0\n -2.0700 1.7453 0.0000 O 0 0\n -3.4098 2.4198 0.0000 R# 0 0\n 2.3029 2.2963 0.0000 R# 0 0\n 1.7731 -3.4628 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n3-Deoxy-3-thio-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns3d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Deoxyribose (2,5 connectivity)\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -1.0009 -0.2740 0.0000 C 0 0 2 0 0 0\n -0.0525 0.8882 0.0000 C 0 0\n 1.3458 0.3453 0.0000 C 0 0 2 0 0 0\n 1.2616 -1.1523 0.0000 C 0 0 1 0 0 0\n -0.1887 -1.5350 0.0000 O 0 0\n 2.6071 1.1540 0.0000 O 0 0\n -2.4966 -0.1868 0.0000 C 0 0\n 2.4238 -2.1007 0.0000 R# 0 0\n 3.9400 0.4660 0.0000 R# 0 0\n -3.1710 1.1540 0.0000 O 0 0\n -4.6685 1.2412 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 0\n 3 6 1 1\n 1 7 1 6\n 4 8 1 6\n 3 2 1 0\n 6 9 1 0\n 7 10 1 0\n 10 11 1 0\nM RGP 3 8 3 9 2 11 1\nM END\n> <Name>\n3-Deoxyribose (2,5 connectivity)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n25d3r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Fluoro HNA\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.5573 -0.8976 0.0000 O 0 0\n -0.8058 0.4006 0.0000 C 0 0 1 0 0 0\n 0.6942 0.3989 0.0000 C 0 0 2 0 0 0\n 1.4427 -0.9010 0.0000 C 0 0 2 0 0 0\n 0.6912 -2.1992 0.0000 C 0 0 1 0 0 0\n -0.8088 -2.1975 0.0000 C 0 0\n 1.4396 -3.4991 0.0000 R# 0 0\n 2.9427 -0.9028 0.0000 F 0 0\n 1.4434 1.6993 0.0000 O 0 0\n -1.5574 1.6997 0.0000 C 0 0\n 2.9434 1.7016 0.0000 R# 0 0\n -3.0582 1.6993 0.0000 O 0 0\n -3.8094 2.9977 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 6\n 4 8 1 1\n 3 9 1 1\n 2 10 1 6\n 9 11 1 0\n 10 12 1 0\n 12 13 1 0\nM RGP 3 7 3 11 2 13 1\nM END\n> <Name>\n3-Fluoro HNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfhna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Methyl-alpha-L-LNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -0.4476 -0.4896 0.0000 C 0 0 2 0 0 0\n -0.0232 0.8433 0.0000 C 0 0 1 0 0 0\n 0.6412 -1.3962 0.0000 C 0 0 1 0 0 0\n 2.0234 -1.3733 0.0000 C 0 0 1 0 0 0\n 1.0122 -0.4208 0.0000 O 0 0\n 1.2845 1.6145 0.0000 O 0 0\n 3.4222 -1.9149 0.0000 R# 0 0\n 2.5763 0.8521 0.0000 R# 0 0\n -1.5203 -1.1722 0.0000 C 0 0\n -0.5300 -2.1308 0.0000 O 0 0\n -1.8131 0.1227 0.0000 C 0 0\n -1.9766 1.6145 0.0000 O 0 0\n -3.3492 2.2194 0.0000 R# 0 0\n -1.2996 1.6312 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 0\n 4 7 1 1\n 6 8 1 0\n 1 9 1 0\n 3 10 1 1\n 9 10 1 0\n 1 11 1 1\n 11 12 1 0\n 12 13 1 0\n 2 14 1 1\nM RGP 3 7 3 8 2 13 1\nM END\n> <Name>\n3-Methyl-alpha-L-LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm3ALln\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-Methylcytosine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 2.7991 0.0000 N 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 0.2010 0.0000 C 0 0\n 8.5981 1.5000 0.0000 N 0 0\n 7.0981 4.0981 0.0000 C 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 4.0981 4.0981 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 2 0\n 5 7 2 0\n 4 8 1 0\n 2 9 1 0\n 1 10 2 0\nM RGP 1 9 1\nM END\n> <Name>\n3-Methylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm3C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n3-Methyluracil\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 2.2500 -4.2990 0.0000 C 0 0\n 3.7500 -4.2990 0.0000 C 0 0\n 4.5000 -3.0000 0.0000 C 0 0\n 3.7500 -1.7010 0.0000 N 0 0\n 2.2500 -1.7010 0.0000 C 0 0\n 1.5000 -3.0000 0.0000 N 0 0\n 4.5000 -0.4019 0.0000 C 0 0\n 4.5000 -5.5981 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 6.0000 -3.0000 0.0000 O 0 0\n 1.5000 -0.4019 0.0000 O 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 4 7 1 0\n 2 8 1 0\n 6 9 1 0\n 3 10 2 0\n 5 11 2 0\nM RGP 1 9 1\nM END\n> <Name>\n3-Methyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm3U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n3-N-(p-Methoxybenzyl)thymine\n SciTegic07272112182D\n\n 19 20 0 0 0 0 999 V2000\n 0.0000 3.0000 0.0000 R# 0 0\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 O 0 0\n -2.5981 -1.5000 0.0000 C 0 0\n 2.5973 -1.5031 0.0000 C 0 0\n 2.5951 -3.0039 0.0000 C 0 0\n 3.8915 -3.7585 0.0000 C 0 0\n 3.8864 -5.2585 0.0000 C 0 0\n 2.5847 -6.0040 0.0000 C 0 0\n 1.2883 -5.2495 0.0000 C 0 0\n 1.2935 -3.7495 0.0000 C 0 0\n 2.5765 -7.5048 0.0000 O 0 0\n 1.2738 -8.2484 0.0000 C 0 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 2 7 1 0\n 7 8 2 0\n 3 9 2 0\n 6 10 1 0\n 1 4 1 0\n 2 11 1 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 15 2 0\n 15 16 1 0\n 16 17 2 0\n 17 12 1 0\n 15 18 1 0\n 18 19 1 0\nM RGP 1 1 1\nM END\n> <Name>\n3-N-(p-Methoxybenzyl)thymine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmo4bn3\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n3-O-FEt ANA\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -2.4844 -1.0542 0.0000 O 0 0\n -1.7329 0.2440 0.0000 C 0 0 1 0 0 0\n -0.2329 0.2423 0.0000 C 0 0 2 0 0 0\n 0.5156 -1.0576 0.0000 C 0 0 2 0 0 0\n -0.2359 -2.3558 0.0000 C 0 0 1 0 0 0\n -1.7359 -2.3541 0.0000 C 0 0\n 0.5126 -3.6557 0.0000 R# 0 0\n 2.0164 -1.0563 0.0000 O 0 0\n 0.5164 1.5427 0.0000 O 0 0\n -2.4845 1.5431 0.0000 C 0 0\n 2.0164 1.5450 0.0000 R# 0 0\n 2.7665 0.2437 0.0000 C 0 0\n 4.2673 0.2450 0.0000 C 0 0\n 5.0170 1.5442 0.0000 F 0 0\n -3.9853 1.5427 0.0000 O 0 0\n -4.7365 2.8411 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 6\n 4 8 1 1\n 3 9 1 1\n 2 10 1 6\n 9 11 1 0\n 8 12 1 0\n 12 13 1 0\n 13 14 1 0\n 10 15 1 0\n 15 16 1 0\nM RGP 3 7 3 11 2 16 1\nM END\n> <Name>\n3-O-FEt ANA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfleana\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-O-MOE-ANA\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -2.8678 -1.1452 0.0000 O 0 0\n -2.1163 0.1530 0.0000 C 0 0 1 0 0 0\n -0.6163 0.1513 0.0000 C 0 0 2 0 0 0\n 0.1322 -1.1486 0.0000 C 0 0 2 0 0 0\n -0.6193 -2.4468 0.0000 C 0 0 1 0 0 0\n -2.1193 -2.4451 0.0000 C 0 0\n 0.1292 -3.7467 0.0000 R# 0 0\n 0.1330 1.4517 0.0000 O 0 0\n -2.8679 1.4521 0.0000 C 0 0\n 1.6330 1.4540 0.0000 R# 0 0\n 1.6330 -1.1473 0.0000 O 0 0\n 2.3831 0.1527 0.0000 C 0 0\n 3.8839 0.1540 0.0000 C 0 0\n 4.6340 1.4540 0.0000 O 0 0\n 6.1340 1.4553 0.0000 C 0 0\n -4.3687 1.4517 0.0000 O 0 0\n -5.1199 2.7501 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 6\n 4 11 1 1\n 3 8 1 1\n 2 9 1 6\n 8 10 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 9 16 1 0\n 16 17 1 0\nM RGP 3 7 3 10 2 17 1\nM END\n> <Name>\n3-O-MOE-ANA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmoe3an\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-O-Methyl-ANA\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -1.8212 -0.9263 0.0000 O 0 0\n -1.0697 0.3719 0.0000 C 0 0 1 0 0 0\n 0.4303 0.3701 0.0000 C 0 0 2 0 0 0\n 1.1788 -0.9298 0.0000 C 0 0 2 0 0 0\n 0.4273 -2.2280 0.0000 C 0 0 1 0 0 0\n -1.0727 -2.2262 0.0000 C 0 0\n 1.1758 -3.5279 0.0000 R# 0 0\n 2.6796 -0.9284 0.0000 O 0 0\n 1.1796 1.6706 0.0000 O 0 0\n -1.8213 1.6709 0.0000 C 0 0\n 2.6796 1.6728 0.0000 R# 0 0\n 3.4293 0.3708 0.0000 C 0 0\n -3.3221 1.6706 0.0000 O 0 0\n -4.0733 2.9689 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 6\n 4 8 1 1\n 3 9 1 1\n 2 10 1 6\n 9 11 1 0\n 8 12 1 0\n 10 13 1 0\n 13 14 1 0\nM RGP 3 7 3 11 2 14 1\nM END\n> <Name>\n3-O-Methyl-ANA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm3ana\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-O-methoxyethyl ribose (2,5 connectivity)\n SciTegic07272112182D\n\n 16 16 0 0 1 0 999 V2000\n -0.2254 -1.5142 0.0000 C 0 0 2 0 0 0\n 0.7240 -0.3530 0.0000 C 0 0 2 0 0 0\n 2.1218 -0.8971 0.0000 C 0 0 2 0 0 0\n 2.0363 -2.3946 0.0000 C 0 0 1 0 0 0\n 0.5856 -2.7761 0.0000 O 0 0\n -1.7211 -1.4257 0.0000 C 0 0\n 0.3400 1.0952 0.0000 O 0 0\n -1.1084 1.4884 0.0000 C 0 0\n 3.3805 -0.0843 0.0000 O 0 0\n 3.1976 -3.3441 0.0000 R# 0 0\n 4.7156 -0.7679 0.0000 R# 0 0\n -1.4931 2.9391 0.0000 C 0 0\n -2.9415 3.3322 0.0000 O 0 0\n -3.3260 4.7821 0.0000 C 0 0\n -2.3942 -0.0843 0.0000 O 0 0\n -3.8916 0.0043 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 3 9 1 1\n 4 10 1 6\n 9 11 1 0\n 8 12 1 0\n 12 13 1 0\n 13 14 1 0\n 6 15 1 0\n 15 16 1 0\nM RGP 3 10 3 11 2 16 1\nM END\n> <Name>\n3-O-methoxyethyl ribose (2,5 connectivity)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n25moe3\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-ara FHNA\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.5573 -0.8976 0.0000 O 0 0\n -0.8058 0.4006 0.0000 C 0 0 1 0 0 0\n 0.6942 0.3989 0.0000 C 0 0 2 0 0 0\n 1.4427 -0.9010 0.0000 C 0 0 1 0 0 0\n 0.6912 -2.1992 0.0000 C 0 0 1 0 0 0\n -0.8088 -2.1975 0.0000 C 0 0\n 1.4396 -3.4991 0.0000 R# 0 0\n 2.9427 -0.9028 0.0000 F 0 0\n 1.4434 1.6993 0.0000 O 0 0\n -1.5574 1.6997 0.0000 C 0 0\n 2.9434 1.7016 0.0000 R# 0 0\n -3.0582 1.6993 0.0000 O 0 0\n -3.8094 2.9977 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 6\n 4 8 1 6\n 3 9 1 1\n 2 10 1 6\n 9 11 1 0\n 10 12 1 0\n 12 13 1 0\nM RGP 3 7 3 11 2 13 1\nM END\n> <Name>\n3-ara FHNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nafhna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-beta-C-Methyl-2-deoxyribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.3033 -0.5714 0.0000 C 0 0 2 0 0 0\n 0.7136 0.5313 0.0000 C 0 0 2 0 0 0\n 2.0766 -0.0951 0.0000 C 0 0\n 1.9020 -1.5850 0.0000 C 0 0 1 0 0 0\n 0.4312 -1.8793 0.0000 O 0 0\n -0.7029 0.9851 0.0000 O 0 0\n -1.7910 -0.3940 0.0000 C 0 0\n 3.0047 -2.6019 0.0000 R# 0 0\n -0.9309 1.9588 0.0000 R# 0 0\n 1.8558 1.5036 0.0000 C 0 0\n -2.3831 0.9851 0.0000 O 0 0\n -3.8725 1.1628 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 0\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 2 10 1 6\n 7 11 1 0\n 11 12 1 0\nM RGP 3 8 3 9 2 12 1\nM END\n> <Name>\n3-beta-C-Methyl-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nBcm3d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-beta-C-Methylribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.5636 -0.6206 0.0000 C 0 0 2 0 0 0\n 0.4533 0.4821 0.0000 C 0 0 2 0 0 0\n 1.8162 -0.1443 0.0000 C 0 0 2 0 0 0\n 1.6417 -1.6341 0.0000 C 0 0 1 0 0 0\n 0.1708 -1.9285 0.0000 O 0 0\n -0.9633 0.9359 0.0000 O 0 0\n -2.0514 -0.4432 0.0000 C 0 0\n 2.7443 -2.6510 0.0000 R# 0 0\n -2.6434 0.9359 0.0000 O 0 0\n -4.1329 1.1136 0.0000 R# 0 0\n -1.1912 1.9096 0.0000 R# 0 0\n 1.5954 1.4544 0.0000 C 0 0\n 3.1241 0.5901 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 0\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 2 12 1 6\n 3 13 1 1\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n3-beta-C-Methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nBcm3r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n4,5,6-Trihydrouracil\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.5981 -1.5000 0.0000 R# 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 0\n 6 8 2 0\n 2 9 1 0\nM RGP 1 7 1\nM END\n> <Name>\n4,5,6-Trihydrouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nh456U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n4-Acetylamino-2-deoxyribose\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -0.2580 0.2861 0.0000 C 0 0 2 0 0 0\n 1.0738 0.9763 0.0000 C 0 0 2 0 0 0\n 2.1417 -0.0770 0.0000 C 0 0\n 1.4700 -1.4182 0.0000 C 0 0 1 0 0 0\n -0.0131 -1.1938 0.0000 N 0 0\n 1.2949 2.4582 0.0000 O 0 0\n -1.5962 0.9598 0.0000 C 0 0\n 2.1602 -2.7500 0.0000 R# 0 0\n -1.6830 2.4582 0.0000 O 0 0\n -3.0227 3.1327 0.0000 R# 0 0\n 2.6900 3.0092 0.0000 R# 0 0\n -1.0674 -2.2583 0.0000 C 0 0\n -0.6717 -3.7052 0.0000 C 0 0\n -2.5184 -1.8780 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 5 12 1 0\n 12 13 1 0\n 12 14 2 0\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n4-Acetylamino-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nacn4d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n4-Acetylcytosine\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -2.5981 -1.5000 0.0000 R# 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5972 1.5031 0.0000 N 0 0\n 2.5951 3.0039 0.0000 C 0 0\n 1.2948 3.7517 0.0000 C 0 0\n 3.8926 3.7566 0.0000 O 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 4 8 2 0\n 2 9 1 0\n 9 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 1 7 1\nM END\n> <Name>\n4-Acetylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nac4C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n4-Cyanoethylthiothymidine\n SciTegic07272112182D\n\n 14 14 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 C 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 N 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0008 2.9969 0.0000 S 0 0\n 1.5000 0.4019 0.0000 O 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 4.5000 5.5981 0.0000 C 0 0\n 6.7494 1.6961 0.0000 C 0 0\n 8.2502 1.6930 0.0000 C 0 0\n 8.9988 0.3922 0.0000 C 0 0\n 9.7469 -0.9079 0.0000 N 0 0\n 13 14 3 0\n 1 2 2 0\n 3 4 1 0\n 4 5 2 0\n 1 5 1 0\n 5 6 1 0\n 3 7 2 0\n 2 8 1 0\n 3 8 1 0\n 8 9 1 0\n 1 10 1 0\n 6 11 1 0\n 11 12 1 0\n 12 13 1 0\nM RGP 1 9 1\nM END\n> <Name>\n4-Cyanoethylthiothymidine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncnes4T\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n4-Deoxouracil\n SciTegic07272112182D\n\n 8 8 0 0 0 0 999 V2000\n 2.2500 -4.2990 0.0000 C 0 0\n 3.7500 -4.2990 0.0000 C 0 0\n 4.5000 -3.0000 0.0000 C 0 0\n 1.5000 -3.0000 0.0000 N 0 0\n 2.2500 -1.7010 0.0000 C 0 0\n 3.7500 -1.7010 0.0000 N 0 0\n 1.5000 -0.4019 0.0000 O 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 2 0\n 5 7 2 0\n 4 8 1 0\nM RGP 1 8 1\nM END\n> <Name>\n4-Deoxouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nd4U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n4-Hexan-6-ol-5-methylcytosine\n SciTegic07272112182D\n\n 18 18 0 0 0 0 999 V2000\n -4.9930 -0.8266 0.0000 C 0 0\n -3.6174 -1.4246 0.0000 C 0 0\n -2.4117 -0.5323 0.0000 C 0 0\n -2.5816 0.9581 0.0000 N 0 0\n -3.9572 1.5561 0.0000 C 0 0\n -4.1271 3.0464 0.0000 O 0 0\n -1.0340 -1.1278 0.0000 N 0 0\n -5.1629 0.6638 0.0000 N 0 0\n -3.4475 -2.9150 0.0000 C 0 0\n -6.5386 1.2618 0.0000 R# 0 0\n 0.1711 -0.2333 0.0000 C 0 0\n 1.5487 -0.8288 0.0000 C 0 0\n 2.7538 0.0657 0.0000 C 0 0\n 4.1314 -0.5298 0.0000 C 0 0\n 5.3365 0.3647 0.0000 C 0 0\n 6.7141 -0.2308 0.0000 C 0 0\n 7.9193 0.6638 0.0000 O 0 0\n 9.2961 0.0686 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 3 7 1 0\n 8 1 1 0\n 8 5 1 0\n 2 9 1 0\n 8 10 1 0\n 7 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\nM RGP 2 10 1 18 2\nM END\n> <Name>\n4-Hexan-6-ol-5-methylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noC64m5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n4-Methylcytosine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 2.5981 1.5000 0.0000 O 0 0\n -0.0031 -3.0008 0.0000 N 0 0\n -1.3032 -3.7490 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 3 1 0\n 3 7 1 0\n 2 8 2 0\n 4 9 1 0\n 9 10 1 0\nM RGP 1 7 1\nM END\n> <Name>\n4-Methylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm4C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n4-N-Hydroxcytosine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n 2.5981 1.5000 0.0000 O 0 0\n -0.0031 -3.0008 0.0000 N 0 0\n -1.3032 -3.7490 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 3 1 0\n 2 7 2 0\n 4 8 1 0\n 8 9 1 0\n 3 10 1 0\nM RGP 1 10 1\nM END\n> <Name>\n4-N-Hydroxcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noh4C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n4-Thio-2-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6450 -0.4268 0.0000 C 0 0 2 0 0 0\n 0.6867 0.2634 0.0000 C 0 0 2 0 0 0\n 1.7547 -0.7899 0.0000 C 0 0\n 1.0830 -2.1310 0.0000 C 0 0 1 0 0 0\n -0.4002 -1.9066 0.0000 S 0 0\n -1.9833 0.2470 0.0000 C 0 0\n 0.9078 1.7453 0.0000 O 0 0\n 2.3029 2.2963 0.0000 R# 0 0\n 1.7731 -3.4628 0.0000 R# 0 0\n -2.0700 1.7453 0.0000 O 0 0\n -3.4098 2.4198 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 6 10 1 0\n 10 11 1 0\nM RGP 3 8 2 9 3 11 1\nM END\n> <Name>\n4-Thio-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns4d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n4-Thiothymidine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 S 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5000 0.4019 0.0000 C 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 2 8 2 0\n 5 9 1 0\n 3 10 1 0\nM RGP 1 10 1\nM END\n> <Name>\n4-Thiothymidine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns4T\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n4-Thiouracil\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 C 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 N 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 S 0 0\n 1.5000 0.4019 0.0000 O 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1 2 2 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 0\n 5 6 2 0\n 3 7 2 0\n 2 8 1 0\n 3 8 1 0\n 8 9 1 0\nM RGP 1 9 1\nM END\n> <Name>\n4-Thiouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns4U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5,6-Dihydrothymine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 7.0981 4.0981 0.0000 C 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 2 0\n 3 8 2 0\n 6 9 1 0\n 2 10 1 0\nM RGP 1 10 1\nM END\n> <Name>\n5,6-Dihydrothymine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nh56T\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5,6-Dimethyluracil\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 1.5000 0.4019 0.0000 C 0 0\n 4.5000 0.4019 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 4 10 1 0\n 5 11 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5,6-Dimethyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm6T\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5,6-Propylene uracil\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.2135 0.2752 0.0000 C 0 0\n 3.0000 -0.6065 0.0000 C 0 0\n 1.7865 0.2752 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\n 4 12 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5,6-Propylene uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\npr56U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-(2-Bromovinyl)uracil\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 7.0958 4.1004 0.0000 C 0 0\n 6.3436 5.3990 0.0000 C 0 0\n 7.0909 6.6996 0.0000 Br 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 4 7 1 0\n 7 8 2 0\n 8 9 1 0\n 3 10 2 0\n 5 11 2 0\n 2 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n5-(2-Bromovinyl)uracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbrviny\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-(Propargylamine)cytosine\n SciTegic07272112182D\n\n 13 13 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 N 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5004 0.4012 0.0000 C 0 0\n 5.2508 -0.8985 0.0000 C 0 0\n 6.0012 -2.1983 0.0000 C 0 0\n 5.2520 -3.4978 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 6 7 1 0\n 2 8 2 0\n 5 9 1 0\n 9 10 3 0\n 10 11 1 0\n 11 12 1 0\n 3 13 1 0\nM RGP 1 13 1\nM END\n> <Name>\n5-(Propargylamine)cytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnpry5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-(R)-Methyl-(R)-cEt BNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 0.3816 -2.3581 0.0000 C 0 0 1 0 0 0\n 0.7121 -1.0088 0.0000 O 0 0\n -0.3195 -1.1665 0.0000 C 0 0 1 0 0 0\n 1.3019 0.5151 0.0000 C 0 0 2 0 0 0\n -0.0669 0.2276 0.0000 C 0 0 2 0 0 0\n -1.1895 0.8248 0.0000 C 0 0 1 0 0 0\n -1.5357 -0.5094 0.0000 O 0 0\n 2.6434 1.1422 0.0000 O 0 0\n -1.1965 0.0610 0.0000 C 0 0 1 0 0 0\n -1.7929 2.1980 0.0000 R# 0 0\n -2.6880 -0.0977 0.0000 C 0 0\n 3.8764 0.2879 0.0000 R# 0 0\n -0.1556 1.1422 0.0000 O 0 0\n 0.5995 -3.8421 0.0000 C 0 0\n -0.5704 2.5837 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 6\n 4 8 1 6\n 3 9 1 0\n 6 10 1 1\n 9 11 1 1\n 3 1 1 0\n 5 2 1 1\n 8 12 1 0\n 9 13 1 0\n 1 14 1 6\n 13 15 1 0\nM RGP 3 10 3 12 2 15 1\nM END\n> <Name>\n5-(R)-Methyl-(R)-cEt BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5R6Rm5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-(R)-Methyl-(S)-cEt BNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 0.3816 -2.3581 0.0000 C 0 0 2 0 0 0\n 0.7121 -1.0088 0.0000 O 0 0\n -0.3195 -1.1665 0.0000 C 0 0 1 0 0 0\n 1.3019 0.5151 0.0000 C 0 0 2 0 0 0\n -0.0669 0.2276 0.0000 C 0 0 2 0 0 0\n -1.1895 0.8248 0.0000 C 0 0 1 0 0 0\n -1.5357 -0.5094 0.0000 O 0 0\n 2.6434 1.1422 0.0000 O 0 0\n -1.1965 0.0610 0.0000 C 0 0 1 0 0 0\n -1.7929 2.1980 0.0000 R# 0 0\n -2.6880 -0.0977 0.0000 C 0 0\n 3.8764 0.2879 0.0000 R# 0 0\n -0.1556 1.1422 0.0000 O 0 0\n 0.5995 -3.8421 0.0000 C 0 0\n -0.5704 2.5837 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 6\n 4 8 1 6\n 3 9 1 0\n 6 10 1 1\n 9 11 1 1\n 3 1 1 0\n 5 2 1 1\n 8 12 1 0\n 9 13 1 0\n 1 14 1 1\n 13 15 1 0\nM RGP 3 10 3 12 2 15 1\nM END\n> <Name>\n5-(R)-Methyl-(S)-cEt BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5R6Sm5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-(S)-Methyl-(R)-cEt BNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 0.3816 -2.3581 0.0000 C 0 0 1 0 0 0\n 0.7121 -1.0088 0.0000 O 0 0\n -0.3195 -1.1665 0.0000 C 0 0 1 0 0 0\n 1.3019 0.5151 0.0000 C 0 0 2 0 0 0\n -0.0669 0.2276 0.0000 C 0 0 2 0 0 0\n -1.1895 0.8248 0.0000 C 0 0 1 0 0 0\n -1.5357 -0.5094 0.0000 O 0 0\n 2.6434 1.1422 0.0000 O 0 0\n -1.1965 0.0610 0.0000 C 0 0 2 0 0 0\n -1.7929 2.1980 0.0000 R# 0 0\n -2.6880 -0.0977 0.0000 C 0 0\n 3.8764 0.2879 0.0000 R# 0 0\n -0.1556 1.1422 0.0000 O 0 0\n 0.5995 -3.8421 0.0000 C 0 0\n -0.5704 2.5837 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 6\n 4 8 1 6\n 3 9 1 0\n 6 10 1 1\n 9 11 1 6\n 3 1 1 0\n 5 2 1 1\n 8 12 1 0\n 9 13 1 0\n 1 14 1 6\n 13 15 1 0\nM RGP 3 10 3 12 2 15 1\nM END\n> <Name>\n5-(S)-Methyl-(R)-cEt BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5S6Rm5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-(S)-Methyl-(S)-cEt BNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 0.3816 -2.3581 0.0000 C 0 0 2 0 0 0\n 0.7121 -1.0088 0.0000 O 0 0\n -0.3195 -1.1665 0.0000 C 0 0 1 0 0 0\n 1.3019 0.5151 0.0000 C 0 0 2 0 0 0\n -0.0669 0.2276 0.0000 C 0 0 2 0 0 0\n -1.1895 0.8248 0.0000 C 0 0 1 0 0 0\n -1.5357 -0.5094 0.0000 O 0 0\n 2.6434 1.1422 0.0000 O 0 0\n -1.1965 0.0610 0.0000 C 0 0 2 0 0 0\n -1.7929 2.1980 0.0000 R# 0 0\n -2.6880 -0.0977 0.0000 C 0 0\n 3.8764 0.2879 0.0000 R# 0 0\n -0.1556 1.1422 0.0000 O 0 0\n 0.5995 -3.8421 0.0000 C 0 0\n -0.5704 2.5837 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 6\n 4 8 1 6\n 3 9 1 0\n 6 10 1 1\n 9 11 1 6\n 3 1 1 0\n 5 2 1 1\n 8 12 1 0\n 9 13 1 0\n 1 14 1 1\n 13 15 1 0\nM RGP 3 10 3 12 2 15 1\nM END\n> <Name>\n5-(S)-Methyl-(S)-cEt BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5S6Sm5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Allyluracil\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 7.0958 4.1004 0.0000 C 0 0\n 6.3436 5.3990 0.0000 C 0 0\n 7.0909 6.6996 0.0000 C 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 2 7 1 0\n 4 8 1 0\n 8 9 1 0\n 9 10 2 0\n 5 11 2 0\n 3 12 2 0\nM RGP 1 7 1\nM END\n> <Name>\n5-Allyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nallyl5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Aminohexylcytosine\n SciTegic07272112182D\n\n 16 16 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.4977 0.3997 0.0000 C 0 0\n 3.7455 -0.8990 0.0000 C 0 0\n 4.4932 -2.2003 0.0000 C 0 0\n 3.7409 -3.4990 0.0000 C 0 0\n 4.4887 -4.8003 0.0000 C 0 0\n 3.7364 -6.0990 0.0000 C 0 0\n 4.4837 -7.3996 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 6 7 1 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5-Aminohexylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnC65C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Aminohexyluracil\n SciTegic07272112182D\n\n 17 17 0 0 0 0 999 V2000\n -4.2493 1.5455 0.0000 N 0 0\n -4.6630 0.1037 0.0000 C 0 0\n -3.6212 -0.9755 0.0000 N 0 0\n -2.1657 -0.6129 0.0000 C 0 0\n -1.7520 0.8289 0.0000 C 0 0\n -2.7938 1.9081 0.0000 C 0 0\n -2.3801 3.3499 0.0000 O 0 0\n -4.0349 -2.4173 0.0000 R# 0 0\n -6.1185 -0.2590 0.0000 O 0 0\n -0.2949 1.1888 0.0000 C 0 0\n 0.7459 0.1075 0.0000 C 0 0\n 2.2030 0.4673 0.0000 C 0 0\n 3.2438 -0.6139 0.0000 C 0 0\n 4.7009 -0.2541 0.0000 C 0 0\n 5.7417 -1.3354 0.0000 C 0 0\n 7.1988 -0.9755 0.0000 N 0 0\n 8.2390 -2.0562 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\nM RGP 2 8 1 17 2\nM END\n> <Name>\n5-Aminohexyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnC65U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n5-Aminopropyluracil\n SciTegic07272112182D\n\n 13 13 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.4977 0.3997 0.0000 C 0 0\n 3.7455 -0.8990 0.0000 C 0 0\n 4.4932 -2.2003 0.0000 C 0 0\n 3.7413 -3.4983 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5-Aminopropyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnpr5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Bromocytosine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5000 0.4019 0.0000 Br 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 6 7 1 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5-Bromocytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbr5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Bromouracil\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5000 0.4019 0.0000 Br 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5-Bromouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbr5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Chlorocytosine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 2.2500 -4.2990 0.0000 C 0 0\n 3.7500 -4.2990 0.0000 C 0 0\n 4.5000 -3.0000 0.0000 C 0 0\n 1.5000 -3.0000 0.0000 N 0 0\n 2.2500 -1.7010 0.0000 C 0 0\n 3.7500 -1.7010 0.0000 N 0 0\n 1.5000 -0.4019 0.0000 O 0 0\n 6.0000 -3.0000 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 4.5000 -5.5981 0.0000 Cl 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 2 0\n 5 7 2 0\n 3 8 1 0\n 4 9 1 0\n 2 10 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-Chlorocytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncl5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Chlorouracil\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 2.2500 -4.2990 0.0000 C 0 0\n 3.7500 -4.2990 0.0000 C 0 0\n 4.5000 -3.0000 0.0000 C 0 0\n 1.5000 -3.0000 0.0000 N 0 0\n 2.2500 -1.7010 0.0000 C 0 0\n 3.7500 -1.7010 0.0000 N 0 0\n 1.5000 -0.4019 0.0000 O 0 0\n 6.0000 -3.0000 0.0000 O 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 4.5000 -5.5981 0.0000 Cl 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 5 7 2 0\n 3 8 2 0\n 4 9 1 0\n 2 10 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-Chlorouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncl5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Cyanouracil\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n 2.5988 1.5004 0.0000 C 0 0\n 0.0000 3.0000 0.0000 O 0 0\n -2.5981 -1.5000 0.0000 O 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 3.8978 2.2504 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 2 7 1 0\n 3 8 2 0\n 5 9 2 0\n 4 10 1 0\n 7 11 3 0\nM RGP 1 10 1\nM END\n> <Name>\n5-Cyanouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nCN5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-DBCO-U (ethylene carbamoyl hexylamino linker)\n SciTegic07272112182D\n\n 45 48 0 0 0 0 999 V2000\n 21.4447 15.6293 0.0000 R# 0 0\n 25.1948 14.3302 0.0000 C 0 0\n 23.6947 14.3302 0.0000 C 0 0\n 22.9447 15.6293 0.0000 N 0 0\n 23.6947 16.9283 0.0000 C 0 0\n 25.1947 16.9283 0.0000 N 0 0\n 25.9447 15.6293 0.0000 C 0 0\n 27.4447 15.6293 0.0000 O 0 0\n 22.9447 18.2274 0.0000 O 0 0\n 25.9425 13.0289 0.0000 C 0 0\n 25.1903 11.7302 0.0000 C 0 0\n 25.9381 10.4289 0.0000 C 0 0\n 27.4381 10.4264 0.0000 O 0 0\n 25.1859 9.1302 0.0000 N 0 0\n 25.9336 7.8289 0.0000 C 0 0\n 25.1814 6.5302 0.0000 C 0 0\n 25.9292 5.2290 0.0000 C 0 0\n 25.1770 3.9303 0.0000 C 0 0\n 25.9247 2.6290 0.0000 C 0 0\n 25.1725 1.3303 0.0000 C 0 0\n 25.9203 0.0290 0.0000 N 0 0\n 25.1681 -1.2697 0.0000 C 0 0\n 25.9158 -2.5710 0.0000 C 0 0\n 23.6681 -1.2671 0.0000 O 0 0\n 25.1636 -3.8697 0.0000 C 0 0\n 25.9114 -5.1709 0.0000 C 0 0\n 25.1591 -6.4696 0.0000 C 0 0\n 25.9069 -7.7709 0.0000 C 0 0\n 25.1529 -9.0726 0.0000 N 0 0\n 27.4069 -7.7735 0.0000 O 0 0\n 23.6665 -8.8717 0.0000 C 0 0\n 22.4733 -9.7808 0.0000 C 0 0\n 22.2724 -11.2673 0.0000 C 0 0\n 25.8611 -11.7522 0.0000 C 0 0\n 26.0620 -10.2658 0.0000 C 0 0\n 21.2841 -8.8633 0.0000 C 0 0\n 19.8963 -9.4325 0.0000 C 0 0\n 19.6954 -10.9190 0.0000 C 0 0\n 20.8823 -11.8362 0.0000 C 0 0\n 27.0504 -12.6698 0.0000 C 0 0\n 28.4381 -12.1005 0.0000 C 0 0\n 28.6390 -10.6140 0.0000 C 0 0\n 27.4521 -9.6968 0.0000 C 0 0\n 24.6680 -12.6613 0.0000 C 0 0\n 23.1815 -12.4604 0.0000 C 0 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 2 7 1 0\n 7 8 2 0\n 1 4 1 0\n 5 9 2 0\n 2 10 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 2 0\n 12 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 19 20 1 0\n 20 21 1 0\n 21 22 1 0\n 22 23 1 0\n 22 24 2 0\n 23 25 1 0\n 25 26 1 0\n 26 27 1 0\n 27 28 1 0\n 28 29 1 0\n 28 30 2 0\n 29 31 1 0\n 31 32 1 0\n 32 33 2 0\n 34 35 2 0\n 35 29 1 0\n 32 36 1 0\n 36 37 2 0\n 37 38 1 0\n 38 39 2 0\n 39 33 1 0\n 34 40 1 0\n 40 41 2 0\n 41 42 1 0\n 42 43 2 0\n 43 35 1 0\n 34 44 1 0\n 44 45 3 0\n 45 33 1 0\nM RGP 1 1 1\nM END\n> <Name>\n5-DBCO-U (ethylene carbamoyl hexylamino linker)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nDBCOnC\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Deoxy-2-O-methylribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.2827 0.5989 0.0000 C 0 0 2 0 0 0\n 0.2173 0.5989 0.0000 C 0 0 2 0 0 0\n 0.6809 -0.8276 0.0000 C 0 0 2 0 0 0\n -0.5327 -1.7093 0.0000 C 0 0 1 0 0 0\n -1.7462 -0.8276 0.0000 O 0 0\n -2.1608 1.8129 0.0000 C 0 0\n 1.0955 1.8129 0.0000 O 0 0\n 2.5877 1.6601 0.0000 R# 0 0\n -0.5327 -3.2093 0.0000 R# 0 0\n 2.1067 -1.2877 0.0000 O 0 0\n 3.2200 -0.2824 0.0000 C 0 0\n -3.6530 1.6601 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 3 10 1 1\n 10 11 1 0\n 6 12 1 0\nM RGP 3 8 2 9 3 12 1\nM END\n> <Name>\n5-Deoxy-2-O-methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nd5m\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Deoxy-2-O-methyoxyethylribose\n SciTegic07272112182D\n\n 15 15 0 0 1 0 999 V2000\n -2.4562 0.6440 0.0000 C 0 0 2 0 0 0\n -0.9562 0.6440 0.0000 C 0 0 2 0 0 0\n -0.4927 -0.7826 0.0000 C 0 0 2 0 0 0\n -1.7062 -1.6642 0.0000 C 0 0 1 0 0 0\n -2.9197 -0.7826 0.0000 O 0 0\n -3.3343 1.8580 0.0000 C 0 0\n -0.0781 1.8580 0.0000 O 0 0\n 1.4141 1.7052 0.0000 R# 0 0\n 0.9332 -1.2426 0.0000 O 0 0\n -1.7062 -3.1642 0.0000 R# 0 0\n 2.0471 -0.2367 0.0000 C 0 0\n 3.4754 -0.6975 0.0000 C 0 0\n 4.5893 0.3083 0.0000 O 0 0\n 6.0169 -0.1523 0.0000 C 0 0\n -4.8265 1.7052 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 3 9 1 1\n 4 10 1 6\n 9 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 6 15 1 0\nM RGP 3 8 2 10 3 15 1\nM END\n> <Name>\n5-Deoxy-2-O-methyoxyethylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nd5moe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Deoxy-5-amino-2-O-methylribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.1828 -0.4514 0.0000 C 0 0 2 0 0 0\n 0.1490 0.2388 0.0000 C 0 0 2 0 0 0\n 1.2170 -0.8145 0.0000 C 0 0 2 0 0 0\n 0.5452 -2.1557 0.0000 C 0 0 1 0 0 0\n -0.9379 -1.9313 0.0000 O 0 0\n -2.5210 0.2223 0.0000 C 0 0\n 0.3701 1.7207 0.0000 O 0 0\n -2.6077 1.7207 0.0000 N 0 0\n -3.9475 2.3952 0.0000 R# 0 0\n 1.7652 2.2716 0.0000 R# 0 0\n 1.2354 -3.4875 0.0000 R# 0 0\n 2.6946 -0.5669 0.0000 O 0 0\n 3.2204 0.8380 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\n 3 12 1 1\n 12 13 1 0\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n5-Deoxy-5-amino-2-O-methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn5m\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Deoxy-5-amino-2-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6450 -0.4268 0.0000 C 0 0 2 0 0 0\n 0.6867 0.2634 0.0000 C 0 0 2 0 0 0\n 1.7547 -0.7899 0.0000 C 0 0\n 1.0830 -2.1310 0.0000 C 0 0 1 0 0 0\n -0.4002 -1.9066 0.0000 O 0 0\n -1.9833 0.2470 0.0000 C 0 0\n 0.9078 1.7453 0.0000 O 0 0\n 2.3029 2.2963 0.0000 R# 0 0\n 1.7731 -3.4628 0.0000 R# 0 0\n -2.0700 1.7453 0.0000 N 0 0\n -3.4098 2.4198 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 6 10 1 0\n 10 11 1 0\nM RGP 3 8 2 9 3 11 1\nM END\n> <Name>\n5-Deoxy-5-amino-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn5d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Deoxy-5-amino-2-fluororibose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.9146 -0.3813 0.0000 C 0 0 2 0 0 0\n 0.4172 0.3089 0.0000 C 0 0 2 0 0 0\n 1.4851 -0.7445 0.0000 C 0 0 2 0 0 0\n 0.8134 -2.0856 0.0000 C 0 0 1 0 0 0\n -0.6697 -1.8612 0.0000 O 0 0\n -2.2528 0.2924 0.0000 C 0 0\n 0.6383 1.7907 0.0000 O 0 0\n -2.3396 1.7907 0.0000 N 0 0\n -3.6793 2.4652 0.0000 R# 0 0\n 2.0334 2.3417 0.0000 R# 0 0\n 1.5036 -3.4174 0.0000 R# 0 0\n 2.9650 -0.4996 0.0000 F 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\n 3 12 1 1\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n5-Deoxy-5-amino-2-fluororibose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn5fl2r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Deoxy-5-aminoribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.9146 -0.3813 0.0000 C 0 0 2 0 0 0\n 0.4172 0.3089 0.0000 C 0 0 2 0 0 0\n 1.4851 -0.7445 0.0000 C 0 0 2 0 0 0\n 0.8134 -2.0856 0.0000 C 0 0 1 0 0 0\n -0.6697 -1.8612 0.0000 O 0 0\n -2.2528 0.2924 0.0000 C 0 0\n 0.6383 1.7907 0.0000 O 0 0\n -2.3396 1.7907 0.0000 N 0 0\n -3.6793 2.4652 0.0000 R# 0 0\n 2.0334 2.3417 0.0000 R# 0 0\n 1.5036 -3.4174 0.0000 R# 0 0\n 2.9650 -0.4996 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\n 3 12 1 1\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n5-Deoxy-5-aminoribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn5r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Deoxy-5-thioribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6450 -0.4268 0.0000 C 0 0 2 0 0 0\n 0.6867 0.2634 0.0000 C 0 0 2 0 0 0\n 1.7547 -0.7899 0.0000 C 0 0\n 1.0830 -2.1310 0.0000 C 0 0 1 0 0 0\n -0.4002 -1.9066 0.0000 O 0 0\n -1.9833 0.2470 0.0000 C 0 0\n 0.9078 1.7453 0.0000 O 0 0\n -2.0700 1.7453 0.0000 S 0 0\n -3.4098 2.4198 0.0000 R# 0 0\n 2.3029 2.2963 0.0000 R# 0 0\n 1.7731 -3.4628 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 6 8 1 0\n 8 9 1 0\n 7 10 1 0\n 4 11 1 6\nM RGP 3 9 1 10 2 11 3\nM END\n> <Name>\n5-Deoxy-5-thioribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns5d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Ethyluracil\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 7.0958 4.1004 0.0000 C 0 0\n 6.3440 5.3983 0.0000 C 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 2 7 1 0\n 4 8 1 0\n 8 9 1 0\n 3 10 2 0\n 5 11 2 0\nM RGP 1 7 1\nM END\n> <Name>\n5-Ethyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ne5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Ethynylcytosine\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 N 0 0\n -2.5981 -1.5000 0.0000 O 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 0.0000 3.0000 0.0000 N 0 0\n 2.5988 1.5004 0.0000 C 0 0\n 3.8985 2.2508 0.0000 C 0 0\n 5.1976 3.0009 0.0000 C 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 2 0\n 6 8 1 0\n 3 9 1 0\n 2 10 1 0\n 10 11 3 0\n 11 12 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5-Ethynylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nethy5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Fluorocytosine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -2.5981 -1.5000 0.0000 R# 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 F 0 0\n 2.5981 1.5000 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 4 8 2 0\n 3 9 1 0\n 2 10 1 0\nM RGP 1 7 1\nM END\n> <Name>\n5-Fluorocytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfl5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Formyl-2-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6576 0.1670 0.0000 C 0 0 2 0 0 0\n 0.8424 0.1670 0.0000 C 0 0 2 0 0 0\n 1.3059 -1.2595 0.0000 C 0 0\n 0.0924 -2.1412 0.0000 C 0 0 1 0 0 0\n -1.1212 -1.2595 0.0000 O 0 0\n -1.5358 1.3810 0.0000 C 0 0\n 1.7205 1.3810 0.0000 O 0 0\n 3.2127 1.2282 0.0000 R# 0 0\n 0.0924 -3.6412 0.0000 R# 0 0\n -3.0278 1.2268 0.0000 R# 0 0\n -0.9237 2.7504 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 6 10 1 0\n 6 11 2 0\nM RGP 3 8 2 9 3 10 1\nM END\n> <Name>\n5-Formyl-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n5formD\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Formylcytosine\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 8.5981 1.5000 0.0000 N 0 0\n 7.0958 4.1004 0.0000 C 0 0\n 6.3440 5.3983 0.0000 O 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 3 1 0\n 5 7 1 0\n 4 8 1 0\n 8 9 2 0\n 3 10 2 0\n 2 11 1 0\nM RGP 1 11 1\nM END\n> <Name>\n5-Formylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nform5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Formyluracil\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 7.0958 4.1004 0.0000 C 0 0\n 6.3440 5.3983 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 5 7 2 0\n 3 8 2 0\n 2 9 1 0\n 4 10 1 0\n 10 11 2 0\nM RGP 1 9 1\nM END\n> <Name>\n5-Formyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nform5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Hydroxycytosine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 2.2500 -4.2990 0.0000 C 0 0\n 3.7500 -4.2990 0.0000 C 0 0\n 4.5000 -3.0000 0.0000 C 0 0\n 3.7500 -1.7010 0.0000 N 0 0\n 2.2500 -1.7010 0.0000 C 0 0\n 1.5000 -3.0000 0.0000 N 0 0\n 1.5000 -0.4019 0.0000 O 0 0\n 6.0000 -3.0000 0.0000 N 0 0\n 4.5000 -5.5981 0.0000 O 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 2 0\n 3 8 1 0\n 2 9 1 0\n 6 10 1 0\nM RGP 1 10 1\nM END\n> <Name>\n5-Hydroxycytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noh5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Hydroxymethylcytosine\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 8.5981 1.5000 0.0000 N 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 7.0958 4.1004 0.0000 C 0 0\n 6.3440 5.3983 0.0000 O 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 1 2 0\n 5 7 1 0\n 3 8 2 0\n 6 9 1 0\n 9 10 1 0\n 2 11 1 0\nM RGP 1 11 1\nM END\n> <Name>\n5-Hydroxymethylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nhm5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Hydroxyuracil\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 2.2500 -4.2990 0.0000 C 0 0\n 3.7500 -4.2990 0.0000 C 0 0\n 4.5000 -3.0000 0.0000 C 0 0\n 3.7500 -1.7010 0.0000 N 0 0\n 2.2500 -1.7010 0.0000 C 0 0\n 1.5000 -3.0000 0.0000 N 0 0\n 1.5000 -0.4019 0.0000 O 0 0\n 6.0000 -3.0000 0.0000 O 0 0\n 4.5000 -5.5981 0.0000 O 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 2 0\n 3 8 2 0\n 2 9 1 0\n 6 10 1 0\nM RGP 1 10 1\nM END\n> <Name>\n5-Hydroxyuracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noh5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Hyroxymethyluracil\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 7.0958 4.1004 0.0000 C 0 0\n 6.3440 5.3983 0.0000 O 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 2 0\n 5 7 2 0\n 3 8 2 0\n 6 9 1 0\n 9 10 1 0\n 2 11 1 0\nM RGP 1 11 1\nM END\n> <Name>\n5-Hyroxymethyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nohm5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Iodocytosine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5000 0.4019 0.0000 I 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 6 7 1 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5-Iodocytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nio5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Isopropyluracil\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.4977 0.3997 0.0000 C 0 0\n 3.7459 -0.8983 0.0000 C 0 0\n 5.9977 0.3970 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\n 10 11 1 0\n 10 12 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5-Isopropyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nipr5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Methoxyuracil\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 7.0958 4.1004 0.0000 O 0 0\n 6.3440 5.3983 0.0000 C 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 3 7 2 0\n 5 8 2 0\n 6 9 1 0\n 9 10 1 0\n 2 11 1 0\nM RGP 1 11 1\nM END\n> <Name>\n5-Methoxyuracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmo5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Methyl-2-O-methylribose\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -0.9132 -0.4085 0.0000 C 0 0 2 0 0 0\n 0.4186 0.2817 0.0000 C 0 0 2 0 0 0\n 1.4866 -0.7716 0.0000 C 0 0 2 0 0 0\n 0.8148 -2.1128 0.0000 C 0 0 1 0 0 0\n -0.6683 -1.8883 0.0000 O 0 0\n 0.6397 1.7636 0.0000 O 0 0\n -2.2514 0.2653 0.0000 C 0 0\n 1.5050 -3.4445 0.0000 R# 0 0\n 2.0348 2.3146 0.0000 R# 0 0\n -2.3381 1.7636 0.0000 O 0 0\n 2.9642 -0.5239 0.0000 O 0 0\n 3.4901 0.8809 0.0000 C 0 0\n -3.6779 2.4381 0.0000 R# 0 0\n -3.5052 -0.5582 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 0\n 2 6 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 7 10 1 0\n 3 11 1 1\n 11 12 1 0\n 10 13 1 0\n 7 14 1 0\nM RGP 3 8 3 9 2 13 1\nM END\n> <Name>\n5-Methyl-2-O-methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm5m\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Methyldeoxyribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.3753 -0.3787 0.0000 C 0 0 2 0 0 0\n 0.9565 0.3115 0.0000 C 0 0 2 0 0 0\n 2.0244 -0.7418 0.0000 C 0 0\n 1.3527 -2.0830 0.0000 C 0 0 1 0 0 0\n -0.1304 -1.8586 0.0000 O 0 0\n 1.1776 1.7933 0.0000 O 0 0\n -1.7135 0.2950 0.0000 C 0 0\n 2.0429 -3.4148 0.0000 R# 0 0\n 2.5727 2.3443 0.0000 R# 0 0\n -1.8003 1.7933 0.0000 O 0 0\n -3.1400 2.4679 0.0000 R# 0 0\n -2.9673 -0.5284 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 0\n 2 6 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 7 10 1 0\n 10 11 1 0\n 7 12 1 0\nM RGP 3 8 3 9 2 11 1\nM END\n> <Name>\n5-Methyldeoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm5d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n5-Thiazolecytidine\n SciTegic07272112182D\n\n 14 15 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n -2.5981 1.5000 0.0000 O 0 0\n 2.5987 -1.5004 0.0000 C 0 0\n 3.9511 -0.8815 0.0000 N 0 0\n 4.9531 -1.9978 0.0000 C 0 0\n 4.2010 -3.2956 0.0000 C 0 0\n 2.7343 -2.9815 0.0000 S 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 1 6 1 0\n 6 7 1 0\n 4 8 2 0\n 1 9 1 0\n 9 10 2 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 9 1 0\n 3 14 1 0\nM RGP 1 14 1\nM END\n> <Name>\n5-Thiazolecytidine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nthiz5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Thiazoleuridine\n SciTegic07272112182D\n\n 14 15 0 0 0 0 999 V2000\n 2.5981 -1.5000 0.0000 R# 0 0\n 4.0981 -1.5000 0.0000 N 0 0\n 4.8481 -2.7990 0.0000 C 0 0\n 6.3481 -2.7990 0.0000 N 0 0\n 7.0981 -1.5000 0.0000 C 0 0\n 6.3481 -0.2010 0.0000 C 0 0\n 4.8481 -0.2010 0.0000 C 0 0\n 8.5981 -1.5000 0.0000 O 0 0\n 4.0981 -4.0981 0.0000 O 0 0\n 7.0985 1.0987 0.0000 C 0 0\n 8.5791 1.2390 0.0000 S 0 0\n 8.8886 2.7067 0.0000 C 0 0\n 7.5884 3.4546 0.0000 C 0 0\n 6.4753 2.4492 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 2 0\n 2 7 1 0\n 5 8 2 0\n 3 9 2 0\n 6 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 10 2 0\nM RGP 1 1 1\nM END\n> <Name>\n5-Thiazoleuridine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nthiz5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Thienyl-6-azauracil\n SciTegic07272112182D\n\n 14 15 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 N 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 5.9814 0.2657 0.0000 C 0 0\n 6.2956 -1.2010 0.0000 C 0 0\n 4.9978 -1.9531 0.0000 C 0 0\n 3.8815 -0.9511 0.0000 S 0 0\n 4.5004 0.4013 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 10 11 1 0\n 11 12 2 0\n 12 13 1 0\n 13 14 1 0\n 10 14 2 0\n 5 14 1 0\nM RGP 1 8 1\nM END\n> <Name>\n5-Thienyl-6-azauracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nthien5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Trifluoromethylcytosine\n SciTegic07272112182D\n\n 13 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 N 0 0\n -2.5981 -1.5000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 N 0 0\n 2.5988 1.5004 0.0000 C 0 0\n 3.8983 0.7513 0.0000 F 0 0\n 2.5983 3.0004 0.0000 F 0 0\n 3.8975 2.2511 0.0000 F 0 0\n 0.0000 -3.0000 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 2 0\n 3 8 1 0\n 2 9 1 0\n 9 10 1 0\n 9 11 1 0\n 9 12 1 0\n 6 13 1 0\nM RGP 1 13 1\nM END\n> <Name>\n5-Trifluoromethylcytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfl3mC\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-Vinyluracil\n SciTegic07272112182D\n\n 11 11 0 0 0 0 999 V2000\n 4.8481 2.7991 0.0000 C 0 0\n 4.0981 1.5000 0.0000 N 0 0\n 4.8481 0.2010 0.0000 C 0 0\n 6.3481 2.7991 0.0000 C 0 0\n 7.0981 1.5000 0.0000 C 0 0\n 6.3481 0.2010 0.0000 N 0 0\n 2.5981 1.5000 0.0000 R# 0 0\n 4.0981 -1.0981 0.0000 O 0 0\n 8.5981 1.5000 0.0000 O 0 0\n 7.0958 4.1004 0.0000 C 0 0\n 6.3440 5.3983 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 2 7 1 0\n 3 8 2 0\n 5 9 2 0\n 4 10 1 0\n 10 11 2 0\nM RGP 1 7 1\nM END\n> <Name>\n5-Vinyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nvinyl5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n5-[(Methylamino)methyl]uridine\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 4.4977 0.3997 0.0000 C 0 0\n 3.7455 -0.8990 0.0000 N 0 0\n 4.4928 -2.1996 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 2 7 2 0\n 6 8 2 0\n 3 9 1 0\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\nM RGP 1 9 1\nM END\n> <Name>\n5-[(Methylamino)methyl]uridine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmnm5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-(p-Nitrobenzylthio)purine\n SciTegic07272112182D\n\n 21 23 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 7.0433 -5.3736 0.0000 S 0 0\n 8.1571 -6.3795 0.0000 C 0 0\n 9.5855 -5.9188 0.0000 C 0 0\n 10.7002 -6.9226 0.0000 C 0 0\n 12.1268 -6.4592 0.0000 C 0 0\n 9.8976 -4.4516 0.0000 C 0 0\n 11.3242 -3.9882 0.0000 C 0 0\n 12.4388 -4.9920 0.0000 C 0 0\n 13.8672 -4.5313 0.0000 N 0 3\n 14.1818 -3.0647 0.0000 O 0 5\n 14.9804 -5.5367 0.0000 O 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 9 10 1 0\n 6 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 2 0\n 14 15 1 0\n 13 16 1 0\n 16 17 2 0\n 17 18 1 0\n 18 15 2 0\n 18 19 1 0\n 19 20 1 0\n 19 21 2 0\nM CHG 2 19 1 20 -1\nM RGP 1 10 1\nM END\n> <Name>\n6-(p-Nitrobenzylthio)purine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnobn6p\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Aminohexyl-2-aminoguanine\n SciTegic09012117322D\n\n 21 22 0 0 0 0 999 V2000\n -4.6234 -0.1544 0.0000 C 0 0\n -4.5733 1.3448 0.0000 C 0 0\n -5.9828 1.8556 0.0000 N 0 0\n -6.9045 0.6722 0.0000 C 0 0\n -6.0638 -0.5701 0.0000 N 0 0\n -3.3501 -0.9473 0.0000 N 0 0\n -2.0267 -0.2411 0.0000 C 0 0\n -1.9767 1.2581 0.0000 N 0 0\n -3.2500 2.0510 0.0000 C 0 0\n -3.1999 3.5502 0.0000 O 0 0\n -6.5745 -1.9804 0.0000 R# 0 0\n -0.7511 -1.0318 0.0000 N 0 0\n 9.6429 -1.3604 0.0000 R# 0 0\n 8.4154 0.9292 0.0000 R# 0 0\n 0.5719 -0.3233 0.0000 C 0 0\n 1.8476 -1.1141 0.0000 C 0 0\n 3.1706 -0.4056 0.0000 C 0 0\n 4.4462 -1.1963 0.0000 C 0 0\n 5.7693 -0.4878 0.0000 C 0 0\n 7.0449 -1.2786 0.0000 C 0 0\n 8.3680 -0.5701 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 1 0\n 9 2 1 0\n 9 10 2 0\n 5 11 1 0\n 7 12 1 0\n 21 13 1 0\n 21 14 1 0\n 12 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 19 20 1 0\n 20 21 1 0\nM RGP 3 11 1 13 2 14 3\nM END\n> <Name>\n6-Aminohexyl-2-aminoguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnC6n2G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]H\n\n$$$$\n6-Aminohexyl-8-aminoadenine\n SciTegic09012117322D\n\n 21 22 0 0 0 0 999 V2000\n 0.4096 -0.5840 0.0000 C 0 0\n 1.6691 -1.4002 0.0000 C 0 0\n 3.0061 -0.7183 0.0000 C 0 0\n 4.2656 -1.5345 0.0000 C 0 0\n 5.6026 -0.8527 0.0000 C 0 0\n 6.8621 -1.6689 0.0000 C 0 0\n 8.1991 -0.9870 0.0000 N 0 0\n 9.4579 -1.8028 0.0000 R# 0 0\n 8.2766 0.5110 0.0000 R# 0 0\n -4.5277 0.1792 0.0000 C 0 0\n -3.7094 1.4364 0.0000 C 0 0\n -2.2616 1.0470 0.0000 N 0 0\n -2.1847 -0.4510 0.0000 C 0 0\n -3.5857 -0.9870 0.0000 N 0 0\n -6.0256 0.2594 0.0000 N 0 0\n -6.7051 1.5967 0.0000 C 0 0\n -5.8867 2.8538 0.0000 N 0 0\n -4.3889 2.7736 0.0000 C 0 0\n -3.5705 4.0307 0.0000 N 0 0\n -3.9756 -2.4355 0.0000 R# 0 0\n -0.9274 -1.2658 0.0000 N 0 0\n 21 1 1 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 7 9 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 10 1 0\n 10 15 1 0\n 15 16 2 0\n 16 17 1 0\n 17 18 2 0\n 18 11 1 0\n 18 19 1 0\n 14 20 1 0\n 13 21 1 0\nM RGP 3 8 2 9 3 20 1\nM END\n> <Name>\n6-Aminohexyl-8-aminoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnC6n8A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]H\n\n$$$$\n6-Aza-5-propynyluracil\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 N 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5004 0.4012 0.0000 C 0 0\n 5.2508 -0.8985 0.0000 C 0 0\n 6.0008 -2.1976 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\n 10 11 3 0\n 11 12 1 0\nM RGP 1 8 1\nM END\n> <Name>\n6-Aza-5-propynyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nz6pry5\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Azacytosine\n SciTegic09012117322D\n\n 9 9 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 2.5981 1.5000 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 6 7 1 0\n 3 8 1 0\n 2 9 2 0\nM RGP 1 8 1\nM END\n> <Name>\n6-Azacytosine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nz5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Azathymine\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 N 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5000 0.4019 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\nM RGP 1 8 1\nM END\n> <Name>\n6-Azathymine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nz5T\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Azauracil\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 2.5981 1.5000 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\nM RGP 1 8 1\nM END\n> <Name>\n6-Azauracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nz6U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Chloroguanine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 Cl 0 0\n 3.5643 -9.2321 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 2 11 1 0\n 9 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n6-Chloroguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncl6G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Chloropurine\n SciTegic07272112182D\n\n 11 12 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 Cl 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 9 11 1 0\nM RGP 1 11 1\nM END\n> <Name>\n6-Chloropurine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncl6pur\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Cyclohexyladenine\n SciTegic07272112182D\n\n 17 19 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0433 -5.3736 0.0000 N 0 0\n 8.1571 -6.3795 0.0000 C 0 0\n 9.5854 -5.9211 0.0000 C 0 0\n 10.6965 -6.9288 0.0000 C 0 0\n 10.3795 -8.3949 0.0000 C 0 0\n 8.9513 -8.8533 0.0000 C 0 0\n 7.8401 -7.8457 0.0000 C 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 11 1 0\n 9 17 1 0\nM RGP 1 17 1\nM END\n> <Name>\n6-Cyclohexyladenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncyh6A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Cyclopentyladenine\n SciTegic07272112182D\n\n 16 18 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0433 -5.3736 0.0000 N 0 0\n 8.1571 -6.3795 0.0000 C 0 0\n 9.6092 -6.0582 0.0000 C 0 0\n 10.3546 -7.3599 0.0000 C 0 0\n 9.3469 -8.4710 0.0000 C 0 0\n 7.9788 -7.8561 0.0000 C 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 11 1 0\n 9 16 1 0\nM RGP 1 16 1\nM END\n> <Name>\n6-Cyclopentyladenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncyp6A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Ethyladenine\n SciTegic07272112182D\n\n 14 15 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0433 -5.3736 0.0000 O 0 0\n 8.1571 -6.3795 0.0000 C 0 0\n 9.5847 -5.9190 0.0000 C 0 0\n 3.5643 -9.2321 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 10 11 1 0\n 11 12 1 0\n 2 13 1 0\n 9 14 1 0\nM RGP 1 14 1\nM END\n> <Name>\n6-Ethyladenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ne6A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Methoxypurine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0433 -5.3736 0.0000 O 0 0\n 8.1565 -6.3790 0.0000 C 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 10 11 1 0\n 9 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n6-Methoxypurine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmo6pur\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Methylguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0433 -5.3736 0.0000 O 0 0\n 8.1565 -6.3790 0.0000 C 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 3.5643 -9.2321 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 10 11 1 0\n 9 12 1 0\n 2 13 1 0\nM RGP 1 12 1\nM END\n> <Name>\n6-Methylguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm6G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Methylpurine\n SciTegic07272112182D\n\n 11 12 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 C 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 9 11 1 0\nM RGP 1 11 1\nM END\n> <Name>\n6-Methylpurine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm6pur\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Methylthioguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0433 -5.3736 0.0000 S 0 0\n 8.1565 -6.3790 0.0000 C 0 0\n 3.5643 -9.2321 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 10 11 1 0\n 2 12 1 0\n 9 13 1 0\nM RGP 1 13 1\nM END\n> <Name>\n6-Methylthioguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nms6G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Methylthiopurine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0433 -5.3736 0.0000 S 0 0\n 8.1565 -6.3790 0.0000 C 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 10 11 1 0\n 9 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n6-Methylthiopurine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nms6pur\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Methyluracil\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 1.5000 0.4019 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\n 4 10 1 0\nM RGP 1 8 1\nM END\n> <Name>\n6-Methyluracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm6U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Thioguanine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 7.0416 -5.3709 0.0000 S 0 0\n 3.5643 -9.2321 0.0000 N 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 5 1 0\n 7 10 1 0\n 4 11 2 0\n 2 12 1 0\nM RGP 1 10 1\nM END\n> <Name>\n6-Thioguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns6G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-Thiopurine\n SciTegic07272112182D\n\n 11 12 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 7.0416 -5.3709 0.0000 S 0 0\n 1 2 1 0\n 2 3 2 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 1 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 9 10 1 0\n 6 11 2 0\nM RGP 1 10 1\nM END\n> <Name>\n6-Thiopurine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns6puri\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n6-beta-Hydroxycarbo-2-deoxyribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.5239 -0.1789 0.0000 C 0 0 2 0 0 0\n 0.8079 0.5113 0.0000 C 0 0 2 0 0 0\n 1.8758 -0.5420 0.0000 C 0 0\n 1.2041 -1.8832 0.0000 C 0 0 1 0 0 0\n -0.2790 -1.6588 0.0000 C 0 0 2 0 0 0\n 1.0289 1.9932 0.0000 O 0 0\n -1.8621 0.4949 0.0000 C 0 0\n 1.8943 -3.2149 0.0000 R# 0 0\n -1.9489 1.9932 0.0000 O 0 0\n -3.2887 2.6677 0.0000 R# 0 0\n 2.4241 2.5442 0.0000 R# 0 0\n -1.3324 -2.7267 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 1 7 1 6\n 4 8 1 6\n 7 9 1 0\n 9 10 1 0\n 6 11 1 0\n 5 12 1 6\nM RGP 3 8 3 10 1 11 2\nM END\n> <Name>\n6-beta-Hydroxycarbo-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nBcoh4d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n7-Azaguanine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 N 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 O 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 3.5643 -9.2321 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 1 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 2 0\n 9 11 1 0\n 2 12 1 0\nM RGP 1 11 1\nM END\n> <Name>\n7-Azaguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nz7G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Deaza-7-cyanoadenine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n -3.1875 -2.6385 0.0000 C 0 0\n -3.6507 -4.0652 0.0000 N 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 7 8 2 0\n 5 8 1 0\n 6 9 1 0\n 4 10 1 0\n 7 10 1 0\n 10 11 1 0\n 8 12 1 0\n 12 13 3 0\nM RGP 1 11 1\nM END\n> <Name>\n7-Deaza-7-cyanoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc7cn7A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Deaza-7-iodo-2-aminoadenine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n 2.5981 1.5000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n -3.1882 -2.6402 0.0000 I 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 7 8 2 0\n 5 8 1 0\n 6 9 1 0\n 2 10 1 0\n 4 11 1 0\n 7 11 1 0\n 11 12 1 0\n 8 13 1 0\nM RGP 1 12 1\nM END\n> <Name>\n7-Deaza-7-iodo-2-aminoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc7io7n\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Deaza-7-iodoadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n -3.1882 -2.6402 0.0000 I 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 7 8 2 0\n 5 8 1 0\n 6 9 1 0\n 4 10 1 0\n 7 10 1 0\n 10 11 1 0\n 8 12 1 0\nM RGP 1 11 1\nM END\n> <Name>\n7-Deaza-7-iodoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc7io7A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Deaza-7-iodoguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n -3.1882 -2.6402 0.0000 I 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 7 8 2 0\n 5 8 1 0\n 6 9 2 0\n 2 10 1 0\n 4 11 1 0\n 7 11 1 0\n 11 12 1 0\n 8 13 1 0\nM RGP 1 12 1\nM END\n> <Name>\n7-Deaza-7-iodoguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc7io7G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Deaza-7-propyne-2-aminoadenine\n SciTegic07272112182D\n\n 15 16 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n -3.1875 -2.6385 0.0000 C 0 0\n -3.6510 -4.0660 0.0000 C 0 0\n -4.1142 -5.4927 0.0000 C 0 0\n 2.5981 1.5000 0.0000 N 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 7 8 2 0\n 5 8 1 0\n 6 9 1 0\n 4 10 1 0\n 7 10 1 0\n 10 11 1 0\n 8 12 1 0\n 12 13 3 0\n 13 14 1 0\n 2 15 1 0\nM RGP 1 11 1\nM END\n> <Name>\n7-Deaza-7-propyne-2-aminoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc7py7N\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Deaza-7-propynyladenine\n SciTegic07272112182D\n\n 14 15 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n -3.1875 -2.6385 0.0000 C 0 0\n -3.6510 -4.0660 0.0000 C 0 0\n -4.1142 -5.4927 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 7 8 2 0\n 5 8 1 0\n 6 9 1 0\n 4 10 1 0\n 7 10 1 0\n 10 11 1 0\n 8 12 1 0\n 12 13 3 0\n 13 14 1 0\nM RGP 1 11 1\nM END\n> <Name>\n7-Deaza-7-propynyladenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc7py7A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Deazaadenine\n SciTegic07272112182D\n\n 11 12 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 C 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n 2.5981 -1.5000 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 4 1 0\n 7 10 1 0\n 1 11 1 0\nM RGP 1 10 1\nM END\n> <Name>\n7-Deazaadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc7A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Deazaguanine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 5.9498 4.1210 0.0000 N 0 0\n 6.2618 2.6538 0.0000 C 0 0\n 7.6885 2.1904 0.0000 C 0 0\n 7.0645 5.1248 0.0000 C 0 0\n 8.4911 4.6614 0.0000 N 0 0\n 8.8031 3.1942 0.0000 C 0 0\n 7.6888 0.6912 0.0000 C 0 0\n 6.2623 0.2275 0.0000 C 0 0\n 5.3805 1.4410 0.0000 N 0 0\n 10.2297 2.7308 0.0000 O 0 0\n 6.7525 6.5920 0.0000 N 0 0\n 3.8805 1.4410 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 1 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 3 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 2 1 0\n 6 10 2 0\n 4 11 1 0\n 9 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n7-Deazaguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc7G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Methyl 8-dihydroguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n 0.6924 -4.0811 0.0000 C 0 0\n 2.5981 -1.5000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 5 1 0\n 9 10 1 0\n 7 11 1 0\n 1 12 2 0\n 3 13 1 0\nM RGP 1 10 1\nM END\n> <Name>\n7-Methyl 8-dihydroguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm7h8G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Methylguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -2.4133 -1.7530 0.0000 N 0 3\n 0.0000 3.0000 0.0000 N 0 0\n 2.5981 -1.5000 0.0000 O 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n 0.6924 -4.0811 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 5 1 0\n 3 10 1 0\n 1 11 2 0\n 9 12 1 0\n 7 13 1 0\nM CHG 1 9 1\nM RGP 1 12 1\nM END\n> <Name>\n7-Methylguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm7G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n7-Nitro-1,3-diaza-2-oxophenothiazin\n SciTegic07272112182D\n\n 19 21 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 N 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 4.5000 0.4019 0.0000 S 0 0\n 6.0000 0.4019 0.0000 C 0 0\n 6.7500 1.7010 0.0000 C 0 0\n 6.7500 -0.8971 0.0000 C 0 0\n 8.2500 -0.8971 0.0000 C 0 0\n 9.0000 0.4019 0.0000 C 0 0\n 8.2500 1.7010 0.0000 C 0 0\n 9.0031 -2.1953 0.0000 N 0 3\n 8.2553 -3.4957 0.0000 O 0 5\n 10.5031 -2.1932 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 6 7 1 0\n 3 8 1 0\n 2 9 2 0\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 7 1 0\n 11 13 2 0\n 13 14 1 0\n 14 15 2 0\n 15 16 1 0\n 16 12 2 0\n 14 17 1 0\n 17 18 1 0\n 17 19 2 0\nM CHG 2 17 1 18 -1\nM RGP 1 8 1\nM END\n> <Name>\n7-Nitro-1,3-diaza-2-oxophenothiazin\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ntCnitr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Aminoadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n -2.5532 -4.4223 0.0000 N 0 0\n 2.5981 -1.5000 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 5 1 0\n 9 10 1 0\n 8 11 1 0\n 1 12 1 0\nM RGP 1 10 1\nM END\n> <Name>\n8-Aminoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn8A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Aminoguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n 2.5981 -1.5000 0.0000 O 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n -2.5532 -4.4223 0.0000 N 0 0\n 0.0000 3.0000 0.0000 N 0 0\n 1 2 1 0\n 2 3 2 0\n 1 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 3 1 0\n 5 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 4 2 0\n 1 10 2 0\n 7 11 1 0\n 8 12 1 0\n 3 13 1 0\nM RGP 1 11 1\nM END\n> <Name>\n8-Aminoguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nn8G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Aza-3-deazaguanine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 N 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 7 8 2 0\n 5 8 1 0\n 6 9 2 0\n 2 10 1 0\n 4 11 1 0\n 7 11 1 0\n 11 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\n8-Aza-3-deazaguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nz8c3G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Azaadenine\n SciTegic07272112182D\n\n 11 12 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 N 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 N 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 5 1 0\n 4 10 1 0\n 7 11 1 0\nM RGP 1 11 1\nM END\n> <Name>\n8-Azaadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nz8A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Bromoadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n -2.5532 -4.4223 0.0000 Br 0 0\n 2.5981 -1.5000 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 4 1 0\n 7 10 1 0\n 8 11 1 0\n 1 12 1 0\nM RGP 1 10 1\nM END\n> <Name>\n8-Bromoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbr8A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Bromoguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n 0.0000 3.0000 0.0000 N 0 0\n 2.5981 -1.5000 0.0000 O 0 0\n -2.5532 -4.4223 0.0000 Br 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 4 1 0\n 3 10 1 0\n 1 11 2 0\n 8 12 1 0\n 7 13 1 0\nM RGP 1 13 1\nM END\n> <Name>\n8-Bromoguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbr8G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Chloroadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 6.9961 1.8908 0.0000 C 0 0\n 6.9965 3.3900 0.0000 N 0 0\n 5.5699 3.8536 0.0000 C 0 0\n 4.6882 2.6402 0.0000 N 0 0\n 5.5695 1.4274 0.0000 C 0 0\n 8.1107 0.8870 0.0000 C 0 0\n 5.2575 -0.0398 0.0000 N 0 0\n 6.3721 -1.0436 0.0000 C 0 0\n 7.7987 -0.5802 0.0000 N 0 0\n 3.1882 2.6402 0.0000 R# 0 0\n 9.5374 1.3504 0.0000 N 0 0\n 5.1065 5.2802 0.0000 Cl 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 5 1 2 0\n 1 6 1 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 6 2 0\n 4 10 1 0\n 6 11 1 0\n 3 12 1 0\nM RGP 1 10 1\nM END\n> <Name>\n8-Chloroadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncl8A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Oxo-9-thioguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 6.9961 1.8908 0.0000 C 0 0\n 6.9965 3.3900 0.0000 S 0 0\n 5.5699 3.8536 0.0000 C 0 0\n 4.6882 2.6402 0.0000 N 0 0\n 5.5695 1.4274 0.0000 C 0 0\n 8.1107 0.8870 0.0000 C 0 0\n 5.2575 -0.0398 0.0000 N 0 0\n 6.3721 -1.0436 0.0000 C 0 0\n 7.7987 -0.5802 0.0000 N 0 0\n 6.0601 -2.5108 0.0000 N 0 0\n 3.1882 2.6402 0.0000 R# 0 0\n 9.5374 1.3504 0.0000 O 0 0\n 5.1065 5.2802 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 2 0\n 1 6 1 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 6 1 0\n 8 10 1 0\n 4 11 1 0\n 6 12 2 0\n 3 13 2 0\nM RGP 1 11 1\nM END\n> <Name>\n8-Oxo-9-thioguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\no8s9G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Oxoadenine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n -2.5532 -4.4223 0.0000 O 0 0\n 2.5981 -1.5000 0.0000 N 0 0\n 1 2 1 0\n 1 3 2 0\n 3 4 1 0\n 4 5 2 0\n 4 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 3 1 0\n 5 9 1 0\n 9 2 2 0\n 6 10 1 0\n 7 11 2 0\n 1 12 1 0\nM RGP 1 10 1\nM END\n> <Name>\n8-Oxoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\no8A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Oxoguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 6.9961 1.8908 0.0000 C 0 0\n 6.9965 3.3900 0.0000 N 0 0\n 5.5699 3.8536 0.0000 C 0 0\n 4.6882 2.6402 0.0000 N 0 0\n 5.5695 1.4274 0.0000 C 0 0\n 8.1107 0.8870 0.0000 C 0 0\n 5.2575 -0.0398 0.0000 N 0 0\n 6.3721 -1.0436 0.0000 C 0 0\n 7.7987 -0.5802 0.0000 N 0 0\n 9.5374 1.3504 0.0000 O 0 0\n 5.1065 5.2802 0.0000 O 0 0\n 6.0601 -2.5108 0.0000 N 0 0\n 3.1882 2.6402 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 2 0\n 1 6 1 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 6 1 0\n 6 10 2 0\n 3 11 2 0\n 8 12 1 0\n 4 13 1 0\nM RGP 1 13 1\nM END\n> <Name>\n8-Oxoguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\no8G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n8-Thioguanine\n SciTegic07272112182D\n\n 13 14 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n -2.5532 -4.4223 0.0000 S 0 0\n 2.5981 -1.5000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 5 1 0\n 9 10 1 0\n 8 11 2 0\n 1 12 2 0\n 3 13 1 0\nM RGP 1 10 1\nM END\n> <Name>\n8-Thioguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns8G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n9-Allylguanine\n SciTegic07272112182D\n\n 16 17 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n 0.0000 3.0000 0.0000 N 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n -2.5532 -4.4223 0.0000 O 0 0\n 0.6890 -4.0818 0.0000 C 0 0\n 2.5981 -1.5000 0.0000 O 0 0\n 0.2235 -5.5086 0.0000 C 0 0\n 1.2251 -6.6252 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 1 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 5 1 0\n 3 10 1 0\n 9 11 1 0\n 8 12 2 0\n 7 13 1 0\n 1 14 2 0\n 13 15 1 0\n 15 16 2 0\nM RGP 1 11 1\nM END\n> <Name>\n9-Allylguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nallyl9\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(2S)-methyl-cLNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -1.7573 0.3923 0.0000 C 0 0\n -0.3792 0.2175 0.0000 C 0 0 1 0 0 0\n -0.8961 -0.6891 0.0000 C 0 0 1 0 0 0\n 1.2548 0.2221 0.0000 C 0 0 2 0 0 0\n 0.4960 -0.9529 0.0000 C 0 0 2 0 0 0\n 0.6513 -2.2149 0.0000 C 0 0 1 0 0 0\n -0.7183 -2.0601 0.0000 O 0 0\n -1.2216 0.7840 0.0000 C 0 0\n 1.7172 -3.2702 0.0000 R# 0 0\n 2.3209 1.2498 0.0000 O 0 0\n 3.7640 0.8408 0.0000 R# 0 0\n 0.3758 1.5136 0.0000 C 0 0\n -2.6483 1.2498 0.0000 O 0 0\n -2.9590 2.7173 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 5 4 1 6\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 6\n 6 9 1 6\n 3 1 1 0\n 5 2 1 0\n 4 10 1 1\n 10 11 1 0\n 2 12 1 6\n 8 13 1 0\n 13 14 1 0\nM RGP 3 9 3 11 2 14 1\nM END\n> <Name>\n(2S)-methyl-cLNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSmclna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(5R)-5-Methyl-LNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n 0.3972 -2.1683 0.0000 C 0 0\n -0.1631 -3.4084 0.0000 O 0 0\n 0.3322 -0.7081 0.0000 C 0 0 1 0 0 0\n 1.7223 -0.0968 0.0000 C 0 0 2 0 0 0\n -0.4298 -1.8615 0.0000 C 0 0 2 0 0 0\n -1.7755 -1.1928 0.0000 C 0 0 1 0 0 0\n -1.1717 -0.0949 0.0000 O 0 0\n 1.9043 1.4079 0.0000 O 0 0\n 0.1808 0.7908 0.0000 C 0 0 1 0 0 0\n -3.1621 -0.6206 0.0000 R# 0 0\n 1.3983 1.6670 0.0000 C 0 0\n 3.2919 1.9775 0.0000 R# 0 0\n -1.1873 1.4079 0.0000 O 0 0\n -1.3378 2.9003 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 6\n 4 8 1 1\n 3 9 1 0\n 6 10 1 6\n 9 11 1 6\n 3 1 1 0\n 5 2 1 1\n 8 12 1 0\n 9 13 1 0\n 13 14 1 0\nM RGP 3 10 3 12 2 14 1\nM END\n> <Name>\n(5R)-5-Methyl-LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRm5lna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(5R)-5-methyl-alpha-L-LNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n 0.3322 -0.7081 0.0000 C 0 0 2 0 0 0\n 1.7223 -0.0968 0.0000 C 0 0 1 0 0 0\n -0.4298 -1.8615 0.0000 C 0 0 1 0 0 0\n -1.7755 -1.1928 0.0000 C 0 0 1 0 0 0\n -1.1717 -0.0949 0.0000 O 0 0\n 1.9043 1.4079 0.0000 O 0 0\n -3.1621 -0.6206 0.0000 R# 0 0\n 3.2919 1.9775 0.0000 R# 0 0\n 0.3972 -2.1683 0.0000 C 0 0\n -0.1631 -3.4084 0.0000 O 0 0\n 0.1808 0.7908 0.0000 C 0 0 2 0 0 0\n -1.1873 1.4079 0.0000 O 0 0\n -1.3378 2.9003 0.0000 R# 0 0\n 1.3983 1.6670 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 1\n 2 6 1 6\n 4 7 1 6\n 6 8 1 0\n 1 9 1 0\n 3 10 1 6\n 9 10 1 0\n 1 11 1 0\n 11 12 1 0\n 12 13 1 0\n 11 14 1 6\nM RGP 3 7 3 8 2 13 1\nM END\n> <Name>\n(5R)-5-methyl-alpha-L-LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRm5ALl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(5R)-Me-2O-MOE\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -1.9392 -0.7878 0.0000 C 0 0 2 0 0 0\n -0.6075 -0.0976 0.0000 C 0 0 2 0 0 0\n 0.4605 -1.1509 0.0000 C 0 0 2 0 0 0\n -0.2112 -2.4921 0.0000 C 0 0 1 0 0 0\n -1.6944 -2.2677 0.0000 O 0 0\n -3.2775 -0.1141 0.0000 C 0 0 2 0 0 0\n -0.3864 1.3842 0.0000 O 0 0\n 1.0087 1.9352 0.0000 R# 0 0\n 0.4790 -3.8239 0.0000 R# 0 0\n -3.3642 1.3842 0.0000 O 0 0\n -4.7040 2.0587 0.0000 R# 0 0\n 1.9381 -0.9033 0.0000 O 0 0\n 2.4643 0.5023 0.0000 C 0 0\n 3.9445 0.7504 0.0000 C 0 0\n 4.4706 2.1560 0.0000 O 0 0\n 5.9499 2.4039 0.0000 C 0 0\n -4.5312 -0.9375 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 6\n 1 6 1 0\n 2 7 1 1\n 7 8 1 0\n 3 12 1 1\n 4 9 1 6\n 6 10 1 0\n 10 11 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 6 17 1 1\nM RGP 3 8 2 9 3 11 1\nM END\n> <Name>\n(5R)-Me-2O-MOE\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRm5moe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(5S)-2-Fluoro-5-methylribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.4000 -1.8204 0.0000 O 0 0\n -0.6449 -0.3405 0.0000 C 0 0 1 0 0 0\n 1.0831 -2.0448 0.0000 C 0 0 2 0 0 0\n 0.6869 0.3497 0.0000 C 0 0 2 0 0 0\n 1.7549 -0.7036 0.0000 C 0 0 1 0 0 0\n 0.9080 1.8316 0.0000 O 0 0\n 3.2348 -0.4587 0.0000 F 0 0\n -1.9831 0.3332 0.0000 C 0 0 1 0 0 0\n 1.7734 -3.3766 0.0000 R# 0 0\n -2.0698 1.8316 0.0000 O 0 0\n 2.3031 2.3826 0.0000 R# 0 0\n -3.4096 2.5061 0.0000 R# 0 0\n -3.2369 -0.4902 0.0000 C 0 0\n 2 1 1 6\n 1 3 1 0\n 2 4 1 0\n 2 8 1 0\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 11 1 0\n 8 10 1 0\n 10 12 1 0\n 8 13 1 6\nM RGP 3 9 3 11 2 12 1\nM END\n> <Name>\n(5S)-2-Fluoro-5-methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSm5fl2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(5S)-5-Methyl-alpha-L-LNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n 0.3322 -0.7081 0.0000 C 0 0 2 0 0 0\n 1.7223 -0.0968 0.0000 C 0 0 1 0 0 0\n -0.4298 -1.8615 0.0000 C 0 0 1 0 0 0\n -1.7755 -1.1928 0.0000 C 0 0 1 0 0 0\n -1.1717 -0.0949 0.0000 O 0 0\n 1.9043 1.4079 0.0000 O 0 0\n -3.1621 -0.6206 0.0000 R# 0 0\n 3.2919 1.9775 0.0000 R# 0 0\n 0.3972 -2.1683 0.0000 C 0 0\n -0.1631 -3.4084 0.0000 O 0 0\n 0.1808 0.7908 0.0000 C 0 0 1 0 0 0\n -1.1873 1.4079 0.0000 O 0 0\n -1.3378 2.9003 0.0000 R# 0 0\n 1.3983 1.6670 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 1\n 2 6 1 6\n 4 7 1 6\n 6 8 1 0\n 1 9 1 0\n 3 10 1 6\n 9 10 1 0\n 1 11 1 0\n 11 12 1 0\n 12 13 1 0\n 11 14 1 1\nM RGP 3 7 3 8 2 13 1\nM END\n> <Name>\n(5S)-5-Methyl-alpha-L-LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSm5ALl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(5S)-5-Vinyl-BNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 1.8111 -1.6646 0.0000 C 0 0\n 1.9118 -3.0216 0.0000 O 0 0\n 1.0560 -0.4130 0.0000 C 0 0 1 0 0 0\n 1.9848 0.7883 0.0000 C 0 0 2 0 0 0\n 0.9381 -1.7904 0.0000 C 0 0 2 0 0 0\n -0.5636 -1.8463 0.0000 C 0 0 1 0 0 0\n -0.5581 -0.5934 0.0000 O 0 0\n 0.9773 1.9207 0.0000 O 0 0\n -0.1677 0.4656 0.0000 C 0 0 2 0 0 0\n -2.0550 -2.0065 0.0000 R# 0 0\n -1.5358 -0.1515 0.0000 C 0 0\n -2.7542 0.7235 0.0000 C 0 0\n 1.4688 3.3379 0.0000 R# 0 0\n -0.5354 1.9207 0.0000 O 0 0\n -1.9783 2.3306 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 6\n 4 8 1 1\n 3 9 1 0\n 6 10 1 6\n 9 11 1 6\n 3 1 1 0\n 5 2 1 1\n 11 12 2 0\n 8 13 1 0\n 9 14 1 0\n 14 15 1 0\nM RGP 3 10 3 13 2 15 1\nM END\n> <Name>\n(5S)-5-Vinyl-BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSvinyl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(5S)-5-methyl-LNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n 0.3972 -2.1683 0.0000 C 0 0\n -0.1631 -3.4084 0.0000 O 0 0\n 0.3322 -0.7081 0.0000 C 0 0 1 0 0 0\n 1.7223 -0.0968 0.0000 C 0 0 2 0 0 0\n -0.4298 -1.8615 0.0000 C 0 0 2 0 0 0\n -1.7755 -1.1928 0.0000 C 0 0 1 0 0 0\n -1.1717 -0.0949 0.0000 O 0 0\n 1.9043 1.4079 0.0000 O 0 0\n 0.1808 0.7908 0.0000 C 0 0 2 0 0 0\n -3.1621 -0.6206 0.0000 R# 0 0\n 1.3983 1.6670 0.0000 C 0 0\n 3.2919 1.9775 0.0000 R# 0 0\n -1.1873 1.4079 0.0000 O 0 0\n -1.3378 2.9003 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 6\n 4 8 1 1\n 3 9 1 0\n 6 10 1 6\n 9 11 1 1\n 3 1 1 0\n 5 2 1 1\n 8 12 1 0\n 9 13 1 0\n 13 14 1 0\nM RGP 3 10 3 12 2 14 1\nM END\n> <Name>\n(5S)-5-methyl-LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSm5lna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(5S)-Methyl-2O-MOE\n SciTegic07272112182D\n\n 17 17 0 0 1 0 999 V2000\n -1.9392 -0.7878 0.0000 C 0 0 2 0 0 0\n -0.6075 -0.0976 0.0000 C 0 0 2 0 0 0\n 0.4605 -1.1509 0.0000 C 0 0 2 0 0 0\n -0.2112 -2.4921 0.0000 C 0 0 1 0 0 0\n -1.6944 -2.2677 0.0000 O 0 0\n -3.2775 -0.1141 0.0000 C 0 0 1 0 0 0\n -0.3864 1.3842 0.0000 O 0 0\n 1.0087 1.9352 0.0000 R# 0 0\n 0.4790 -3.8239 0.0000 R# 0 0\n -3.3642 1.3842 0.0000 O 0 0\n -4.7040 2.0587 0.0000 R# 0 0\n 1.9381 -0.9033 0.0000 O 0 0\n 2.4643 0.5023 0.0000 C 0 0\n 3.9445 0.7504 0.0000 C 0 0\n 4.4706 2.1560 0.0000 O 0 0\n 5.9499 2.4039 0.0000 C 0 0\n -4.5312 -0.9375 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 6\n 1 6 1 0\n 2 7 1 1\n 7 8 1 0\n 3 12 1 1\n 4 9 1 6\n 6 10 1 0\n 10 11 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 6 17 1 6\nM RGP 3 8 2 9 3 11 1\nM END\n> <Name>\n(5S)-Methyl-2O-MOE\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSm5moe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(6S)-6-methyl-FHNA\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n -1.4996 -1.1158 0.0000 O 0 0\n -0.7503 0.1837 0.0000 C 0 0 1 0 0 0\n 0.7497 0.1845 0.0000 C 0 0 2 0 0 0\n 1.5004 -1.1142 0.0000 C 0 0 2 0 0 0\n 0.7511 -2.4136 0.0000 C 0 0 1 0 0 0\n -0.7489 -2.4144 0.0000 C 0 0\n 1.5018 -3.7122 0.0000 R# 0 0\n 1.4967 1.4862 0.0000 O 0 0\n -1.4997 1.4840 0.0000 C 0 0 2 0 0 0\n -0.7482 2.7822 0.0000 C 0 0\n 2.9967 1.4910 0.0000 R# 0 0\n 3.0004 -1.1133 0.0000 F 0 0\n -3.0005 1.4862 0.0000 O 0 0\n -3.7495 2.7858 0.0000 R# 0 0\n 2 1 1 6\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 6\n 4 12 1 1\n 3 8 1 1\n 2 9 1 0\n 9 10 1 1\n 8 11 1 0\n 9 13 1 0\n 13 14 1 0\nM RGP 3 7 3 11 2 14 1\nM END\n> <Name>\n(6S)-6-methyl-FHNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSm6fhn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(6S)-6-methyl-alpha-L-LNA\n SciTegic09012117322D\n\n 14 15 0 0 1 0 999 V2000\n 1.1233 0.2604 0.0000 C 0 0 2 0 0 0\n -1.0323 -0.6397 0.0000 C 0 0 1 0 0 0\n -1.8879 0.4463 0.0000 C 0 0 1 0 0 0\n -0.5108 0.2643 0.0000 O 0 0\n 0.3584 -0.9107 0.0000 C 0 0 2 0 0 0\n -3.1915 1.1882 0.0000 R# 0 0\n 0.5071 -2.1734 0.0000 C 0 0 1 0 0 0\n -0.8617 -2.0116 0.0000 O 0 0\n 0.2821 0.5988 0.0000 C 0 0\n 2.1947 1.2825 0.0000 O 0 0\n -1.0539 1.2825 0.0000 O 0 0\n 1.5675 -3.2343 0.0000 C 0 0\n -1.1307 2.7806 0.0000 R# 0 0\n 3.6357 0.8661 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 0\n 3 6 1 6\n 5 7 1 0\n 7 8 1 0\n 2 8 1 6\n 5 9 1 6\n 1 10 1 1\n 9 11 1 0\n 7 12 1 6\n 11 13 1 0\n 10 14 1 0\nM RGP 3 6 3 13 1 14 2\nM END\n> <Name>\n(6S)-6-methyl-alpha-L-LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSm6ALl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(Aminoethyl)amino\n SciTegic07272112182D\n\n 6 5 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\n(Aminoethyl)amino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnen\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n(D)-2-O-(2,3-Isopropylidene glycer-1-yl)ribose\n SciTegic07272112182D\n\n 20 21 0 0 1 0 999 V2000\n 2.4610 0.4907 0.0000 C 0 0 2 0 0 0\n 0.9835 0.2422 0.0000 C 0 0\n 3.1320 1.8323 0.0000 O 0 0\n 3.5296 -0.5620 0.0000 C 0 0\n 4.8610 0.1290 0.0000 O 0 0\n 4.6153 1.6088 0.0000 C 0 0\n 4.1946 3.0485 0.0000 C 0 0\n 6.0612 1.2099 0.0000 C 0 0\n -3.4002 -1.0473 0.0000 C 0 0 2 0 0 0\n -2.0689 -0.3563 0.0000 C 0 0 2 0 0 0\n -1.0218 -1.4126 0.0000 C 0 0 2 0 0 0\n -1.6712 -2.7506 0.0000 C 0 0 1 0 0 0\n -3.1544 -2.5271 0.0000 O 0 0\n -1.8373 1.1239 0.0000 O 0 0\n -4.7388 -0.3744 0.0000 C 0 0\n -0.9723 -4.0778 0.0000 R# 0 0\n -4.8265 1.1239 0.0000 O 0 0\n -6.1667 1.7976 0.0000 R# 0 0\n -0.4384 1.6650 0.0000 R# 0 0\n 0.4582 -1.1637 0.0000 O 0 0\n 1 2 1 6\n 20 2 1 0\n 3 1 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 6 7 1 0\n 6 8 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 9 1 0\n 10 14 1 1\n 11 20 1 1\n 9 15 1 6\n 12 16 1 6\n 15 17 1 0\n 17 18 1 0\n 14 19 1 0\nM RGP 3 16 3 18 1 19 2\nM END\n> <Name>\n(D)-2-O-(2,3-Isopropylidene glycer-1-yl)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nDiprgl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(Dimethylaminoethyl)amino\n SciTegic07272112182D\n\n 8 7 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.2000 0.0000 0.0000 N 0 0\n 6.4992 0.7496 0.0000 C 0 0\n 5.2000 -1.5000 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 6 8 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\n(Dimethylaminoethyl)amino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2nen\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\n(L)-2-O-(2,3-Isopropylidene glycer-1-yl)ribose\n SciTegic07272112182D\n\n 20 21 0 0 1 0 999 V2000\n 2.4610 0.4907 0.0000 C 0 0 1 0 0 0\n 0.9835 0.2422 0.0000 C 0 0\n 3.1320 1.8323 0.0000 O 0 0\n 3.5296 -0.5620 0.0000 C 0 0\n 4.8610 0.1290 0.0000 O 0 0\n 4.6153 1.6088 0.0000 C 0 0\n 4.1946 3.0485 0.0000 C 0 0\n 6.0612 1.2099 0.0000 C 0 0\n -3.4002 -1.0473 0.0000 C 0 0 2 0 0 0\n -2.0689 -0.3563 0.0000 C 0 0 2 0 0 0\n -1.0218 -1.4126 0.0000 C 0 0 2 0 0 0\n -1.6712 -2.7506 0.0000 C 0 0 1 0 0 0\n -3.1544 -2.5271 0.0000 O 0 0\n -1.8373 1.1239 0.0000 O 0 0\n -4.7388 -0.3744 0.0000 C 0 0\n -0.9723 -4.0778 0.0000 R# 0 0\n -4.8265 1.1239 0.0000 O 0 0\n -6.1667 1.7976 0.0000 R# 0 0\n -0.4384 1.6650 0.0000 R# 0 0\n 0.4582 -1.1637 0.0000 O 0 0\n 1 2 1 1\n 20 2 1 0\n 3 1 1 0\n 1 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 6 7 1 0\n 6 8 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 9 1 0\n 10 14 1 1\n 11 20 1 1\n 9 15 1 6\n 12 16 1 6\n 15 17 1 0\n 17 18 1 0\n 14 19 1 0\nM RGP 3 16 3 18 1 19 2\nM END\n> <Name>\n(L)-2-O-(2,3-Isopropylidene glycer-1-yl)ribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nLiprgl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(R)-4,5,6-Trihydrouracil\n SciTegic07272112182D\n\n 9 9 0 0 1 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0 1 0 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.5981 -1.5000 0.0000 R# 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 0\n 6 8 2 0\n 2 9 1 1\nM RGP 1 7 1\nM END\n> <Name>\n(R)-4,5,6-Trihydrouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nh456UR\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\n(R)-2-Fluoro-5-methylribose\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.4000 -1.8204 0.0000 O 0 0\n -0.6449 -0.3405 0.0000 C 0 0 1 0 0 0\n 1.0831 -2.0448 0.0000 C 0 0 2 0 0 0\n 0.6869 0.3497 0.0000 C 0 0 2 0 0 0\n 1.7549 -0.7036 0.0000 C 0 0 1 0 0 0\n 0.9080 1.8316 0.0000 O 0 0\n 3.2348 -0.4587 0.0000 F 0 0\n -1.9831 0.3332 0.0000 C 0 0 2 0 0 0\n 1.7734 -3.3766 0.0000 R# 0 0\n -2.0698 1.8316 0.0000 O 0 0\n 2.3031 2.3826 0.0000 R# 0 0\n -3.4096 2.5061 0.0000 R# 0 0\n -3.2369 -0.4902 0.0000 C 0 0\n 2 1 1 6\n 1 3 1 0\n 2 4 1 0\n 2 8 1 0\n 3 5 1 0\n 3 9 1 6\n 4 5 1 0\n 4 6 1 1\n 5 7 1 1\n 6 11 1 0\n 8 10 1 0\n 10 12 1 0\n 8 13 1 1\nM RGP 3 9 3 11 2 12 1\nM END\n> <Name>\n(R)-2-Fluoro-5-methylribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRm5fl2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(R)-5-Methyldeoxyribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.3753 -0.3787 0.0000 C 0 0 2 0 0 0\n 0.9565 0.3115 0.0000 C 0 0 2 0 0 0\n 2.0244 -0.7418 0.0000 C 0 0\n 1.3527 -2.0830 0.0000 C 0 0 1 0 0 0\n -0.1304 -1.8586 0.0000 O 0 0\n 1.1776 1.7933 0.0000 O 0 0\n -1.7135 0.2950 0.0000 C 0 0 2 0 0 0\n 2.0429 -3.4148 0.0000 R# 0 0\n 2.5727 2.3443 0.0000 R# 0 0\n -1.8003 1.7933 0.0000 O 0 0\n -3.1400 2.4679 0.0000 R# 0 0\n -2.9673 -0.5284 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 6\n 2 6 1 1\n 1 7 1 0\n 4 8 1 6\n 6 9 1 0\n 7 10 1 0\n 10 11 1 0\n 7 12 1 1\nM RGP 3 8 3 9 2 11 1\nM END\n> <Name>\n(R)-5-Methyldeoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRm5d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(R)-5-hydroxyethyl 2-deoxyribose\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n 1.2991 -0.5282 0.0000 C 0 0 1 0 0 0\n 1.7163 -1.9690 0.0000 C 0 0\n 0.4749 -2.8110 0.0000 C 0 0 1 0 0 0\n -0.7095 -1.8906 0.0000 O 0 0\n -0.2001 -0.4797 0.0000 C 0 0 2 0 0 0\n 0.4264 -4.3102 0.0000 R# 0 0\n -1.0386 0.7620 0.0000 C 0 0 1 0 0 0\n -0.3822 2.1117 0.0000 C 0 0\n -2.5355 0.6530 0.0000 O 0 0\n 2.2209 0.6530 0.0000 O 0 0\n -1.2221 3.3555 0.0000 C 0 0\n -0.5661 4.7044 0.0000 O 0 0\n -3.1900 -0.6967 0.0000 R# 0 0\n 3.7065 0.4459 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 6\n 5 1 1 0\n 3 6 1 6\n 5 7 1 0\n 7 8 1 6\n 7 9 1 0\n 1 10 1 1\n 8 11 1 0\n 11 12 1 0\n 9 13 1 0\n 10 14 1 0\nM RGP 3 6 3 13 1 14 2\nM END\n> <Name>\n(R)-5-hydroxyethyl 2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRhe5d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(R)-F-cLNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -1.7573 0.3923 0.0000 C 0 0\n -0.3792 0.2175 0.0000 C 0 0 2 0 0 0\n -0.8961 -0.6891 0.0000 C 0 0 1 0 0 0\n 1.2548 0.2221 0.0000 C 0 0 2 0 0 0\n 0.4960 -0.9529 0.0000 C 0 0 2 0 0 0\n 0.6513 -2.2149 0.0000 C 0 0 1 0 0 0\n -0.7183 -2.0601 0.0000 O 0 0\n -1.2216 0.7840 0.0000 C 0 0\n 1.7172 -3.2702 0.0000 R# 0 0\n 2.3209 1.2498 0.0000 O 0 0\n 3.7640 0.8408 0.0000 R# 0 0\n 0.3758 1.5136 0.0000 F 0 0\n -2.6483 1.2498 0.0000 O 0 0\n -2.9590 2.7173 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 5 4 1 6\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 6\n 6 9 1 6\n 3 1 1 0\n 5 2 1 0\n 4 10 1 1\n 10 11 1 0\n 2 12 1 1\n 8 13 1 0\n 13 14 1 0\nM RGP 3 9 3 11 2 14 1\nM END\n> <Name>\n(R)-F-cLNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRflcln\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(R)-Sulfoxide BNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -1.7573 0.3923 0.0000 C 0 0\n -0.3792 0.2175 0.0000 S 0 0\n -0.8961 -0.6891 0.0000 C 0 0 1 0 0 0\n 1.2548 0.2221 0.0000 C 0 0 2 0 0 0\n 0.4960 -0.9529 0.0000 C 0 0 2 0 0 0\n 0.6513 -2.2149 0.0000 C 0 0 1 0 0 0\n -0.7183 -2.0601 0.0000 O 0 0\n -1.2216 0.7840 0.0000 C 0 0\n 1.7172 -3.2702 0.0000 R# 0 0\n 2.3209 1.2498 0.0000 O 0 0\n 3.7640 0.8408 0.0000 R# 0 0\n 0.3758 1.5136 0.0000 O 0 0\n -2.6483 1.2498 0.0000 O 0 0\n -2.9590 2.7173 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 6\n 6 9 1 6\n 3 1 1 0\n 5 2 1 6\n 4 10 1 1\n 10 11 1 0\n 2 12 2 0\n 8 13 1 0\n 13 14 1 0\nM RGP 3 9 3 11 2 14 1\nM END\n> <Name>\n(R)-Sulfoxide BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRso2ln\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(R)-cEt BNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n 0.3212 -2.3936 0.0000 C 0 0 1 0 0 0\n 0.5197 -1.0187 0.0000 O 0 0\n -0.4918 -1.2754 0.0000 C 0 0 1 0 0 0\n 0.9595 0.5550 0.0000 C 0 0 2 0 0 0\n -0.3752 0.1366 0.0000 C 0 0 2 0 0 0\n -1.5502 0.6224 0.0000 C 0 0 1 0 0 0\n -1.7659 -0.7389 0.0000 O 0 0\n -1.0347 0.1321 0.0000 C 0 0\n -2.2835 1.9310 0.0000 R# 0 0\n 0.6815 -3.8497 0.0000 C 0 0\n 2.2340 1.3089 0.0000 O 0 0\n 3.5438 0.5778 0.0000 R# 0 0\n -0.1032 1.3089 0.0000 O 0 0\n -0.6554 2.7036 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 1\n 3 1 1 0\n 5 2 1 1\n 1 10 1 6\n 4 11 1 6\n 11 12 1 0\n 8 13 1 0\n 13 14 1 0\nM RGP 3 9 3 12 2 14 1\nM END\n> <Name>\n(R)-cEt BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRcet\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(R)-cMOE BNA\n SciTegic07272112182D\n\n 16 17 0 0 1 0 999 V2000\n 0.0326 -1.7717 0.0000 C 0 0 1 0 0 0\n 0.2312 -0.3968 0.0000 O 0 0\n -0.7803 -0.6535 0.0000 C 0 0 1 0 0 0\n 0.6709 1.1769 0.0000 C 0 0 2 0 0 0\n -0.6638 0.7585 0.0000 C 0 0 2 0 0 0\n -1.8388 1.2444 0.0000 C 0 0 1 0 0 0\n -2.0544 -0.1170 0.0000 O 0 0\n -1.3232 0.7540 0.0000 C 0 0\n -2.5721 2.5529 0.0000 R# 0 0\n 0.3944 -3.2175 0.0000 C 0 0\n 1.9455 1.9308 0.0000 O 0 0\n 3.2552 1.1997 0.0000 R# 0 0\n 1.8372 -3.6309 0.0000 O 0 0\n 2.2012 -5.0861 0.0000 C 0 0\n -0.3917 1.9308 0.0000 O 0 0\n -0.9439 3.3255 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 1\n 3 1 1 0\n 5 2 1 1\n 1 10 1 6\n 4 11 1 6\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 8 15 1 0\n 15 16 1 0\nM RGP 3 9 3 12 2 16 1\nM END\n> <Name>\n(R)-cMOE BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRcmoe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(RC5,SP)-a,b-CNA\n SciTegic07272112182D\n\n 16 17 0 0 1 0 999 V2000\n -1.3284 -2.5753 0.0000 R# 0 0\n -2.4643 -1.5956 0.0000 P 0 0 2 0 0 0\n -3.5768 -0.5894 0.0000 O 0 0\n -3.2616 0.8771 0.0000 C 0 0\n -1.8340 1.3374 0.0000 C 0 0\n -0.7215 0.3312 0.0000 C 0 0 1 0 0 0\n -1.0367 -1.1353 0.0000 O 0 0\n 1.8990 -0.0975 0.0000 C 0 0 1 0 0 0\n 3.1131 0.7834 0.0000 C 0 0\n 2.6505 2.2103 0.0000 C 0 0 1 0 0 0\n 1.1505 2.2113 0.0000 O 0 0\n 0.7068 0.7917 0.0000 C 0 0 2 0 0 0\n -3.9024 -2.0223 0.0000 O 0 0\n 1.8896 -1.5956 0.0000 O 0 0\n 3.5330 3.4232 0.0000 R# 0 0\n 3.1834 -2.3546 0.0000 R# 0 0\n 2 1 1 6\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 6 5 1 6\n 6 7 1 0\n 7 2 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 12 11 1 1\n 12 8 1 0\n 12 6 1 0\n 2 13 2 0\n 8 14 1 6\n 10 15 1 1\n 14 16 1 0\nM RGP 3 1 1 15 3 16 2\nM END\n> <Name>\n(RC5,SP)-a,b-CNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRSpabC\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(Rp)-Methylphosphonate\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n -0.8998 -1.0391 0.0000 R# 0 0\n -0.1499 0.2600 0.0000 P 0 0 2 0 0 0\n 0.6000 -1.0391 0.0000 R# 0 0\n 1.3501 0.2596 0.0000 C 0 0\n -0.9004 1.5587 0.0000 O 0 0\n 2 1 1 1\n 2 3 1 0\n 2 4 1 0\n 2 5 2 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\n(Rp)-Methylphosphonate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRmp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\n(Rp)-Phosphorothioate\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n -0.8998 -1.0391 0.0000 R# 0 0\n -0.1499 0.2600 0.0000 P 0 0 2 0 0 0\n 0.6000 -1.0391 0.0000 R# 0 0\n 1.3501 0.2596 0.0000 O 0 0\n -0.9004 1.5587 0.0000 S 0 0\n 2 1 1 1\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\n(Rp)-Phosphorothioate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRsp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\n(S)-5-Hydroxyethyl-2-deoxyribose\n SciTegic07272112182D\n\n 14 14 0 0 1 0 999 V2000\n 1.2991 -0.5282 0.0000 C 0 0 1 0 0 0\n 1.7163 -1.9690 0.0000 C 0 0\n 0.4749 -2.8110 0.0000 C 0 0 1 0 0 0\n -0.7095 -1.8906 0.0000 O 0 0\n -0.2001 -0.4797 0.0000 C 0 0 2 0 0 0\n 0.4264 -4.3102 0.0000 R# 0 0\n -1.0386 0.7620 0.0000 C 0 0 2 0 0 0\n -0.3822 2.1117 0.0000 C 0 0\n -2.5355 0.6530 0.0000 O 0 0\n 2.2209 0.6530 0.0000 O 0 0\n -1.2221 3.3555 0.0000 C 0 0\n -0.5661 4.7044 0.0000 O 0 0\n -3.1900 -0.6967 0.0000 R# 0 0\n 3.7065 0.4459 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 6\n 5 1 1 0\n 3 6 1 6\n 5 7 1 0\n 7 8 1 1\n 7 9 1 0\n 1 10 1 1\n 8 11 1 0\n 11 12 1 0\n 9 13 1 0\n 10 14 1 0\nM RGP 3 6 3 13 1 14 2\nM END\n> <Name>\n(S)-5-Hydroxyethyl-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nShe5d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(S)-5-Methyldeoxyribose\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -0.3753 -0.3787 0.0000 C 0 0 2 0 0 0\n 0.9565 0.3115 0.0000 C 0 0 2 0 0 0\n 2.0244 -0.7418 0.0000 C 0 0\n 1.3527 -2.0830 0.0000 C 0 0 1 0 0 0\n -0.1304 -1.8586 0.0000 O 0 0\n 1.1776 1.7933 0.0000 O 0 0\n -1.7135 0.2950 0.0000 C 0 0 1 0 0 0\n 2.0429 -3.4148 0.0000 R# 0 0\n 2.5727 2.3443 0.0000 R# 0 0\n -1.8003 1.7933 0.0000 O 0 0\n -3.1400 2.4679 0.0000 R# 0 0\n -2.9673 -0.5284 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 6\n 2 6 1 1\n 1 7 1 0\n 4 8 1 6\n 6 9 1 0\n 7 10 1 0\n 10 11 1 0\n 7 12 1 6\nM RGP 3 8 3 9 2 11 1\nM END\n> <Name>\n(S)-5-Methyldeoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSm5d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(S)-cEt BNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n 0.3212 -2.3936 0.0000 C 0 0 2 0 0 0\n 0.5197 -1.0187 0.0000 O 0 0\n -0.4918 -1.2754 0.0000 C 0 0 1 0 0 0\n 0.9595 0.5550 0.0000 C 0 0 2 0 0 0\n -0.3752 0.1366 0.0000 C 0 0 2 0 0 0\n -1.5502 0.6224 0.0000 C 0 0 1 0 0 0\n -1.7659 -0.7389 0.0000 O 0 0\n -1.0347 0.1321 0.0000 C 0 0\n -2.2835 1.9310 0.0000 R# 0 0\n 0.6815 -3.8497 0.0000 C 0 0\n 2.2340 1.3089 0.0000 O 0 0\n 3.5438 0.5778 0.0000 R# 0 0\n -0.1032 1.3089 0.0000 O 0 0\n -0.6554 2.7036 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 1\n 3 1 1 0\n 5 2 1 1\n 1 10 1 1\n 4 11 1 6\n 11 12 1 0\n 8 13 1 0\n 13 14 1 0\nM RGP 3 9 3 12 2 14 1\nM END\n> <Name>\n(S)-cEt BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncet\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(S)-cMOE BNA\n SciTegic07272112182D\n\n 16 17 0 0 1 0 999 V2000\n 0.0326 -1.7717 0.0000 C 0 0 2 0 0 0\n 0.2312 -0.3968 0.0000 O 0 0\n -0.7803 -0.6535 0.0000 C 0 0 1 0 0 0\n 0.6709 1.1769 0.0000 C 0 0 2 0 0 0\n -0.6638 0.7585 0.0000 C 0 0 2 0 0 0\n -1.8388 1.2444 0.0000 C 0 0 1 0 0 0\n -2.0544 -0.1170 0.0000 O 0 0\n -1.3232 0.7540 0.0000 C 0 0\n -2.5721 2.5529 0.0000 R# 0 0\n 0.3944 -3.2175 0.0000 C 0 0\n 1.9455 1.9308 0.0000 O 0 0\n 3.2552 1.1997 0.0000 R# 0 0\n 1.8372 -3.6309 0.0000 O 0 0\n 2.2012 -5.0861 0.0000 C 0 0\n -0.3917 1.9308 0.0000 O 0 0\n -0.9439 3.3255 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 1\n 3 1 1 0\n 5 2 1 1\n 1 10 1 1\n 4 11 1 6\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 8 15 1 0\n 15 16 1 0\nM RGP 3 9 3 12 2 16 1\nM END\n> <Name>\n(S)-cMOE BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nScmoe\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(S)-cPr-BNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 0.1794 -2.1108 0.0000 C 0 0 2 0 0 0\n 0.3780 -0.7359 0.0000 O 0 0\n -0.6335 -0.9926 0.0000 C 0 0 1 0 0 0\n 0.8177 0.8378 0.0000 C 0 0 2 0 0 0\n -0.5170 0.4194 0.0000 C 0 0 2 0 0 0\n -1.6920 0.9053 0.0000 C 0 0 1 0 0 0\n -1.9076 -0.4561 0.0000 O 0 0\n -1.1764 0.4149 0.0000 C 0 0\n -2.4253 2.2138 0.0000 R# 0 0\n 2.0923 1.5917 0.0000 O 0 0\n 3.4020 0.8606 0.0000 R# 0 0\n 0.5412 -3.5566 0.0000 C 0 0\n 1.9832 -3.9698 0.0000 C 0 0\n -0.2449 1.5917 0.0000 O 0 0\n -0.7971 2.9864 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 1\n 3 1 1 0\n 5 2 1 1\n 4 10 1 6\n 10 11 1 0\n 1 12 1 1\n 12 13 1 0\n 8 14 1 0\n 14 15 1 0\nM RGP 3 9 3 11 2 15 1\nM END\n> <Name>\n(S)-cPr-BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nScPr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(SC5,RP)-a,b-CNA\n SciTegic07272112182D\n\n 16 17 0 0 1 0 999 V2000\n -1.3284 -2.5753 0.0000 R# 0 0\n -2.4643 -1.5956 0.0000 P 0 0 1 0 0 0\n -3.5768 -0.5894 0.0000 O 0 0\n -3.2616 0.8771 0.0000 C 0 0\n -1.8340 1.3374 0.0000 C 0 0\n -0.7215 0.3312 0.0000 C 0 0 2 0 0 0\n -1.0367 -1.1353 0.0000 O 0 0\n 1.8990 -0.0975 0.0000 C 0 0 1 0 0 0\n 3.1131 0.7834 0.0000 C 0 0\n 2.6505 2.2103 0.0000 C 0 0 1 0 0 0\n 1.1505 2.2113 0.0000 O 0 0\n 0.7068 0.7917 0.0000 C 0 0 2 0 0 0\n -3.9024 -2.0223 0.0000 O 0 0\n 1.8896 -1.5956 0.0000 O 0 0\n 3.5330 3.4232 0.0000 R# 0 0\n 3.1834 -2.3546 0.0000 R# 0 0\n 2 1 1 1\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 6 5 1 1\n 6 7 1 0\n 7 2 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 12 11 1 1\n 12 8 1 0\n 12 6 1 0\n 2 13 2 0\n 8 14 1 6\n 10 15 1 1\n 14 16 1 0\nM RGP 3 1 1 15 3 16 2\nM END\n> <Name>\n(SC5,RP)-a,b-CNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSRpabC\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n(Sp)-Methylphosphonate\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n -0.8998 -1.0391 0.0000 R# 0 0\n -0.1499 0.2600 0.0000 P 0 0 1 0 0 0\n 0.6000 -1.0391 0.0000 R# 0 0\n 1.3501 0.2596 0.0000 C 0 0\n -0.9004 1.5587 0.0000 O 0 0\n 2 1 1 6\n 2 3 1 0\n 2 4 1 0\n 2 5 2 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\n(Sp)-Methylphosphonate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSmp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\n(Sp)-Phosphorothioate\n SciTegic07272112182D\n\n 5 4 0 0 1 0 999 V2000\n -0.8998 -1.0391 0.0000 R# 0 0\n -0.1499 0.2600 0.0000 P 0 0 1 0 0 0\n 0.6000 -1.0391 0.0000 R# 0 0\n 1.3501 0.2596 0.0000 O 0 0\n -0.9004 1.5587 0.0000 S 0 0\n 2 1 1 6\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\n(Sp)-Phosphorothioate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSsp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nANA\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.5573 -0.8976 0.0000 O 0 0\n -0.8058 0.4006 0.0000 C 0 0 1 0 0 0\n 0.6942 0.3989 0.0000 C 0 0 2 0 0 0\n 1.4427 -0.9010 0.0000 C 0 0 2 0 0 0\n 0.6912 -2.1992 0.0000 C 0 0 1 0 0 0\n -0.8088 -2.1975 0.0000 C 0 0\n 1.4396 -3.4991 0.0000 R# 0 0\n 2.9427 -0.9028 0.0000 O 0 0\n 1.4434 1.6993 0.0000 O 0 0\n -1.5574 1.6997 0.0000 C 0 0\n 2.9434 1.7016 0.0000 R# 0 0\n -3.0582 1.6993 0.0000 O 0 0\n -3.8094 2.9977 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 5 7 1 6\n 4 8 1 1\n 3 9 1 1\n 2 10 1 6\n 9 11 1 0\n 10 12 1 0\n 12 13 1 0\nM RGP 3 7 3 11 2 13 1\nM END\n> <Name>\nANA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nana\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nAmino\n SciTegic07272112182D\n\n 3 2 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 2.5993 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nAmino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nhn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nAmino(S)-cEt (N-methyl)\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 0.1898 -2.3512 0.0000 C 0 0 2 0 0 0\n 0.3884 -0.9763 0.0000 N 0 0\n -0.6231 -1.2330 0.0000 C 0 0 1 0 0 0\n 0.8281 0.5974 0.0000 C 0 0 2 0 0 0\n -0.5066 0.1790 0.0000 C 0 0 2 0 0 0\n -1.6816 0.6649 0.0000 C 0 0 1 0 0 0\n -1.8972 -0.6965 0.0000 O 0 0\n -1.1660 0.1745 0.0000 C 0 0\n -2.4149 1.9734 0.0000 R# 0 0\n 0.5502 -3.8073 0.0000 C 0 0\n 2.1027 1.3513 0.0000 O 0 0\n 3.4125 0.6202 0.0000 R# 0 0\n -0.2345 1.3513 0.0000 O 0 0\n -0.7867 2.7460 0.0000 R# 0 0\n 1.8388 -0.5938 0.0000 C 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 1\n 3 1 1 0\n 5 2 1 1\n 1 10 1 1\n 4 11 1 6\n 11 12 1 0\n 8 13 1 0\n 13 14 1 0\n 2 15 1 0\nM RGP 3 9 3 12 2 14 1\nM END\n> <Name>\nAmino(S)-cEt (N-methyl)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSmn2ce\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nAmino(R)-cEt (N-methyl)\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 0.1898 -2.3512 0.0000 C 0 0 1 0 0 0\n 0.3884 -0.9763 0.0000 N 0 0\n -0.6231 -1.2330 0.0000 C 0 0 1 0 0 0\n 0.8281 0.5974 0.0000 C 0 0 2 0 0 0\n -0.5066 0.1790 0.0000 C 0 0 2 0 0 0\n -1.6816 0.6649 0.0000 C 0 0 1 0 0 0\n -1.8972 -0.6965 0.0000 O 0 0\n -1.1660 0.1745 0.0000 C 0 0\n -2.4149 1.9734 0.0000 R# 0 0\n 0.5502 -3.8073 0.0000 C 0 0\n 2.1027 1.3513 0.0000 O 0 0\n 3.4125 0.6202 0.0000 R# 0 0\n -0.2345 1.3513 0.0000 O 0 0\n -0.7867 2.7460 0.0000 R# 0 0\n 1.8388 -0.5938 0.0000 C 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 1\n 3 1 1 0\n 5 2 1 1\n 1 10 1 6\n 4 11 1 6\n 11 12 1 0\n 8 13 1 0\n 13 14 1 0\n 2 15 1 0\nM RGP 3 9 3 12 2 14 1\nM END\n> <Name>\nAmino(R)-cEt (N-methyl)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nRmn2ce\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nAmino-Modier C6 dT\n SciTegic09012117322D\n\n 23 23 0 0 0 0 999 V2000\n 2.0219 0.3424 0.0000 C 0 0\n 3.1566 -0.6398 0.0000 C 0 0\n 4.5750 -0.1491 0.0000 C 0 0\n 5.7097 -1.1313 0.0000 C 0 0\n 7.1281 -0.6406 0.0000 C 0 0\n 8.2628 -1.6228 0.0000 C 0 0\n 9.6812 -1.1321 0.0000 N 0 0\n 10.8153 -2.1138 0.0000 R# 0 0\n 9.9647 0.3408 0.0000 R# 0 0\n -4.7837 -0.6388 0.0000 C 0 0\n -4.5027 0.8347 0.0000 C 0 0\n -5.6382 1.8148 0.0000 C 0 0\n -7.0548 1.3214 0.0000 N 0 0\n -7.3358 -0.1520 0.0000 C 0 0\n -8.7523 -0.6454 0.0000 O 0 0\n -5.3572 3.2882 0.0000 O 0 0\n -6.2002 -1.1321 0.0000 N 0 0\n -3.0843 1.3254 0.0000 C 0 0\n -6.4812 -2.6056 0.0000 R# 0 0\n -1.9496 0.3432 0.0000 C 0 0\n -0.5312 0.8339 0.0000 C 0 0\n 0.6035 -0.1483 0.0000 N 0 0\n -0.2477 2.3069 0.0000 O 0 0\n 22 1 1 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 7 9 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 2 0\n 12 16 2 0\n 17 10 1 0\n 17 14 1 0\n 11 18 1 0\n 17 19 1 0\n 18 20 2 0\n 20 21 1 0\n 21 22 1 0\n 21 23 2 0\nM RGP 3 8 2 9 3 19 1\nM END\n> <Name>\nAmino-Modier C6 dT\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnC6n5U\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]H\n\n$$$$\nAmino-Modier C6 dC\n SciTegic09012117322D\n\n 23 23 0 0 0 0 999 V2000\n 2.0219 0.3424 0.0000 C 0 0\n 3.1566 -0.6398 0.0000 C 0 0\n 4.5750 -0.1491 0.0000 C 0 0\n 5.7097 -1.1313 0.0000 C 0 0\n 7.1281 -0.6406 0.0000 C 0 0\n 8.2628 -1.6228 0.0000 C 0 0\n 9.6812 -1.1321 0.0000 N 0 0\n 10.8153 -2.1138 0.0000 R# 0 0\n 9.9647 0.3408 0.0000 R# 0 0\n -4.7837 -0.6388 0.0000 C 0 0\n -4.5027 0.8347 0.0000 C 0 0\n -5.6382 1.8148 0.0000 C 0 0\n -7.0548 1.3214 0.0000 N 0 0\n -7.3358 -0.1520 0.0000 C 0 0\n -8.7523 -0.6454 0.0000 O 0 0\n -5.3572 3.2882 0.0000 N 0 0\n -6.2002 -1.1321 0.0000 N 0 0\n -3.0843 1.3254 0.0000 C 0 0\n -6.4812 -2.6056 0.0000 R# 0 0\n -1.9496 0.3432 0.0000 C 0 0\n -0.5312 0.8339 0.0000 C 0 0\n 0.6035 -0.1483 0.0000 N 0 0\n -0.2477 2.3069 0.0000 O 0 0\n 22 1 1 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 7 9 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 15 2 0\n 12 16 1 0\n 17 10 1 0\n 17 14 1 0\n 11 18 1 0\n 17 19 1 0\n 18 20 2 0\n 20 21 1 0\n 21 22 1 0\n 21 23 2 0\nM RGP 3 8 2 9 3 19 1\nM END\n> <Name>\nAmino-Modier C6 dC\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnC6n5C\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]H\n\n$$$$\nAzidoadenine\n SciTegic07272112182D\n\n 14 15 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -2.5496 -4.4224 0.0000 N 0 0\n -1.7974 -5.7210 0.0000 N 0 3\n -1.0455 -7.0190 0.0000 N 0 5\n -3.8805 -1.4410 0.0000 R# 0 0\n 2.5981 -1.5000 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 2 0\n 5 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 4 1 0\n 8 10 1 0\n 10 11 2 0\n 11 12 2 0\n 7 13 1 0\n 1 14 1 0\nM CHG 2 11 1 12 -1\nM RGP 1 13 1\nM END\n> <Name>\nAzidoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\naz8A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nBenzylamino\n SciTegic07272112182D\n\n 10 10 0 0 0 0 999 V2000\n -2.8595 2.5496 0.0000 R# 0 0\n -1.5606 1.7994 0.0000 N 0 0\n -0.2616 2.5496 0.0000 R# 0 0\n -1.5598 0.2986 0.0000 C 0 0\n -0.2602 -0.4520 0.0000 C 0 0\n -0.2574 -1.9520 0.0000 C 0 0\n 1.0374 0.3004 0.0000 C 0 0\n 1.0431 -2.6995 0.0000 C 0 0\n 2.3407 -1.9471 0.0000 C 0 0\n 2.3379 -0.4471 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 2 0\n 5 7 1 0\n 6 8 1 0\n 8 9 2 0\n 9 10 1 0\n 10 7 2 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nBenzylamino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbnn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nBicycloDNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n 0.6645 1.0853 0.0000 C 0 0 1 0 0 0\n 2.0572 0.5281 0.0000 C 0 0\n 1.9576 -0.9686 0.0000 C 0 0 1 0 0 0\n 0.5034 -1.3364 0.0000 O 0 0\n -0.2958 -0.0670 0.0000 C 0 0 2 0 0 0\n 3.1099 -1.9289 0.0000 R# 0 0\n 1.1757 -0.3289 0.0000 O 0 0\n -1.6736 0.4777 0.0000 C 0 0 2 0 0 0\n -1.5740 1.9744 0.0000 C 0 0\n -0.1198 2.3423 0.0000 C 0 0\n -1.2538 -1.2213 0.0000 H 0 0\n -2.9362 -0.3289 0.0000 O 0 0\n -4.2680 0.3612 0.0000 R# 0 0\n 2.6530 -0.5889 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 3 6 1 6\n 1 7 1 1\n 5 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 1 1 0\n 5 11 1 1\n 8 12 1 1\n 12 13 1 0\n 7 14 1 0\nM RGP 3 6 3 13 1 14 2\nM END\n> <Name>\nBicycloDNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nbcdna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nCarbocyclic-2-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.6450 -0.4268 0.0000 C 0 0 2 0 0 0\n 0.6867 0.2634 0.0000 C 0 0 2 0 0 0\n 1.7547 -0.7899 0.0000 C 0 0\n 1.0830 -2.1310 0.0000 C 0 0 1 0 0 0\n -0.4002 -1.9066 0.0000 C 0 0\n -1.9833 0.2470 0.0000 C 0 0\n 0.9078 1.7453 0.0000 O 0 0\n 2.3029 2.2963 0.0000 R# 0 0\n 1.7731 -3.4628 0.0000 R# 0 0\n -2.0700 1.7453 0.0000 O 0 0\n -3.4098 2.4198 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 1 6 1 6\n 2 7 1 1\n 7 8 1 0\n 4 9 1 6\n 6 10 1 0\n 10 11 1 0\nM RGP 3 8 2 9 3 11 1\nM END\n> <Name>\nCarbocyclic-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nc4d\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nCarbonyl\n SciTegic07272112182D\n\n 4 3 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 2.5993 0.0004 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nCarbonyl\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nco\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nCarbonylmethyl\n SciTegic09012117322D\n\n 5 4 0 0 0 0 999 V2000\n -1.2000 1.0394 0.0000 R# 0 0\n -0.4504 -0.2599 0.0000 C 0 0\n -1.2013 -1.5584 0.0000 O 0 0\n 1.0504 -0.2599 0.0000 C 0 0\n 1.8013 1.0387 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 2 4 1 0\n 4 5 1 0\nM RGP 2 1 1 5 2\nM END\n> <Name>\nCarbonylmethyl\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncm\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nCeNA\n SciTegic07272112182D\n\n 12 12 0 0 1 0 999 V2000\n -1.3121 -0.9728 0.0000 C 0 0\n -0.5606 0.3254 0.0000 C 0 0 1 0 0 0\n 0.9394 0.3236 0.0000 C 0 0 2 0 0 0\n 1.6879 -0.9763 0.0000 C 0 0\n 0.9364 -2.2744 0.0000 C 0 0 1 0 0 0\n -0.5636 -2.2727 0.0000 C 0 0\n 1.6849 -3.5743 0.0000 R# 0 0\n 1.6886 1.6241 0.0000 O 0 0\n -1.3122 1.6245 0.0000 C 0 0\n 3.1886 1.6264 0.0000 R# 0 0\n -2.8130 1.6241 0.0000 O 0 0\n -3.5642 2.9224 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 2 0\n 5 7 1 6\n 3 8 1 1\n 2 9 1 6\n 8 10 1 0\n 9 11 1 0\n 11 12 1 0\nM RGP 3 7 3 10 2 12 1\nM END\n> <Name>\nCeNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncena\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nDifluoromethylene\n SciTegic07272112182D\n\n 5 4 0 0 0 0 999 V2000\n -1.7998 0.0000 0.0000 R# 0 0\n -0.2998 0.0000 0.0000 C 0 0\n 1.2002 0.0000 0.0000 R# 0 0\n 0.4498 -1.2993 0.0000 F 0 0\n 0.4498 1.2993 0.0000 F 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nDifluoromethylene\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfl2me\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nDihydrouracil\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 2.5981 1.5000 0.0000 O 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n -2.5981 -1.5000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 1 0\n 2 7 2 0\n 6 8 2 0\n 5 9 1 0\nM RGP 1 9 1\nM END\n> <Name>\nDihydrouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nhU\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nEthylamino\n SciTegic07272112182D\n\n 5 4 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.8993 0.7496 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nEthylamino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nen\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nEthylphosphate\n SciTegic07272112182D\n\n 7 6 0 0 0 0 999 V2000\n -0.1063 -1.6704 0.0000 R# 0 0\n 0.6436 -0.3713 0.0000 P 0 0\n 1.3935 -1.6704 0.0000 R# 0 0\n 2.1436 -0.3717 0.0000 O 0 0\n -0.1074 0.9281 0.0000 O 0 0\n -1.6082 0.9285 0.0000 C 0 0\n -2.3587 2.2272 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\n 5 6 1 0\n 6 7 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nEthylphosphate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\neop\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nFluoro-CeNA\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -1.5573 -0.8976 0.0000 C 0 0\n -0.8058 0.4006 0.0000 C 0 0 1 0 0 0\n 0.6942 0.3989 0.0000 C 0 0 2 0 0 0\n 1.4427 -0.9010 0.0000 C 0 0 2 0 0 0\n 0.6912 -2.1992 0.0000 C 0 0 1 0 0 0\n -0.8088 -2.1975 0.0000 C 0 0\n 1.4396 -3.4991 0.0000 R# 0 0\n 1.4434 1.6993 0.0000 O 0 0\n -1.5574 1.6997 0.0000 C 0 0\n 2.9434 1.7016 0.0000 R# 0 0\n 2.9427 -0.9028 0.0000 F 0 0\n -3.0582 1.6993 0.0000 O 0 0\n -3.8094 2.9977 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 1 2 0\n 5 7 1 6\n 3 8 1 1\n 2 9 1 6\n 8 10 1 0\n 4 11 1 1\n 9 12 1 0\n 12 13 1 0\nM RGP 3 7 3 10 2 13 1\nM END\n> <Name>\nFluoro-CeNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfcena\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nG-clamp (9-(aminoethoxy)phenoxazine)\n SciTegic07272112182D\n\n 20 22 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 N 0 0\n -2.5981 -1.5000 0.0000 O 0 0\n 2.5981 -1.5000 0.0000 N 0 0\n 3.8971 -0.7500 0.0000 C 0 0\n 3.8971 0.7500 0.0000 C 0 0\n 2.5981 1.5000 0.0000 O 0 0\n 5.1962 -1.5000 0.0000 C 0 0\n 6.4952 -0.7500 0.0000 C 0 0\n 6.4952 0.7500 0.0000 C 0 0\n 5.1961 1.5000 0.0000 C 0 0\n 5.1993 -3.0008 0.0000 O 0 0\n 6.5001 -3.7494 0.0000 C 0 0\n 6.5032 -5.2502 0.0000 C 0 0\n 7.8033 -5.9983 0.0000 N 0 0\n -2.5981 1.5000 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 1 6 2 0\n 5 7 2 0\n 1 8 1 0\n 8 9 1 0\n 9 10 2 0\n 10 11 1 0\n 2 11 1 0\n 9 12 1 0\n 12 13 2 0\n 13 14 1 0\n 14 15 2 0\n 10 15 1 0\n 16 17 1 0\n 17 18 1 0\n 18 19 1 0\n 12 16 1 0\n 4 20 1 0\nM RGP 1 20 1\nM END\n> <Name>\nG-clamp (9-(aminoethoxy)phenoxazine)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ngclamp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nG-clamp (9-(guanylethoxy)phenoxazine)\n SciTegic07272112182D\n\n 23 25 0 0 0 0 999 V2000\n 0.0000 3.0000 0.0000 R# 0 0\n 3.7500 4.2990 0.0000 N 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 C 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 1.5000 5.5981 0.0000 O 0 0\n 6.0000 3.0000 0.0000 N 0 0\n 6.7500 1.7010 0.0000 C 0 0\n 6.0000 0.4019 0.0000 C 0 0\n 4.5000 0.4019 0.0000 O 0 0\n 8.2500 1.7010 0.0000 C 0 0\n 9.0000 0.4019 0.0000 C 0 0\n 8.2500 -0.8971 0.0000 C 0 0\n 6.7500 -0.8971 0.0000 C 0 0\n 9.0031 2.9992 0.0000 O 0 0\n 10.5039 2.9970 0.0000 C 0 0\n 11.2570 4.2952 0.0000 C 0 0\n 12.7578 4.2931 0.0000 N 0 0\n 13.5109 5.5913 0.0000 C 0 0\n 12.7632 6.8916 0.0000 N 0 0\n 15.0109 5.5891 0.0000 N 0 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 2 7 2 0\n 3 8 2 0\n 1 4 1 0\n 7 9 1 0\n 9 10 1 0\n 10 11 2 0\n 11 12 1 0\n 6 12 1 0\n 10 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 16 2 0\n 11 16 1 0\n 13 17 1 0\n 17 18 1 0\n 18 19 1 0\n 19 20 1 0\n 20 21 1 0\n 21 22 1 0\n 21 23 2 0\nM RGP 1 1 1\nM END\n> <Name>\nG-clamp (9-(guanylethoxy)phenoxazine)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nggclam\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nC\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nOrotic Acid\n SciTegic07272112182D\n\n 12 12 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -2.5981 1.5000 0.0000 O 0 0\n 2.5981 1.5000 0.0000 O 0 0\n -2.5981 -1.5000 0.0000 R# 0 0\n 0.0031 -3.0008 0.0000 C 0 0\n -1.2946 -3.7531 0.0000 O 0 0\n 1.3032 -3.7490 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 1 0\n 6 3 1 0\n 6 7 2 0\n 2 8 2 0\n 5 9 1 0\n 4 10 1 0\n 10 11 1 0\n 10 12 2 0\nM RGP 1 9 1\nM END\n> <Name>\nOrotic Acid\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nOro\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nIsobutylamino\n SciTegic07272112182D\n\n 7 6 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 C 0 0\n 3.9000 2.2500 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\n 5 7 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nIsobutylamino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nibun\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nIsoguanine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 2.7617 -6.7611 0.0000 N 0 0\n 3.8763 -7.7649 0.0000 C 0 0\n 5.3029 -7.3015 0.0000 N 0 0\n 3.0737 -5.2939 0.0000 C 0 0\n 4.5003 -4.8305 0.0000 C 0 0\n 5.6149 -5.8343 0.0000 C 0 0\n 4.5007 -3.3313 0.0000 N 0 0\n 3.0741 -2.8677 0.0000 C 0 0\n 2.1924 -4.0811 0.0000 N 0 0\n 7.0416 -5.3709 0.0000 N 0 0\n 3.5643 -9.2321 0.0000 O 0 0\n 0.6924 -4.0811 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 3 1 0\n 5 7 1 0\n 7 8 2 0\n 8 9 1 0\n 9 4 1 0\n 6 10 1 0\n 2 11 2 0\n 9 12 1 0\nM RGP 1 12 1\nM END\n> <Name>\nIsoguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nisoG\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nL-2-deoxyribose\n SciTegic07272112182D\n\n 11 11 0 0 1 0 999 V2000\n -0.8896 -1.1996 0.0000 O 0 0\n -0.3776 0.2103 0.0000 C 0 0 2 0 0 0\n 0.2930 -2.1222 0.0000 C 0 0 1 0 0 0\n 1.1215 0.1590 0.0000 C 0 0 1 0 0 0\n 1.5360 -1.2826 0.0000 C 0 0\n 2.0407 1.3422 0.0000 O 0 0\n -1.2188 1.4501 0.0000 C 0 0\n -2.7158 1.3422 0.0000 O 0 0\n -3.5580 2.5834 0.0000 R# 0 0\n 0.2417 -3.6214 0.0000 R# 0 0\n 3.5268 1.1385 0.0000 R# 0 0\n 1 2 1 0\n 1 3 1 0\n 2 4 1 0\n 2 7 1 1\n 3 5 1 0\n 4 5 1 0\n 4 6 1 6\n 7 8 1 0\n 8 9 1 0\n 3 10 1 1\n 6 11 1 0\nM RGP 3 9 1 10 3 11 2\nM END\n> <Name>\nL-2-deoxyribose\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nLd\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nMethylamino\n SciTegic07272112182D\n\n 4 3 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 2.5993 0.0004 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nMethylamino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nMethylene\n SciTegic07272112182D\n\n 3 2 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 2.5993 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nMethylene\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nme\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nMethylene cLNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -1.7573 0.3923 0.0000 C 0 0\n -0.3792 0.2175 0.0000 C 0 0\n -0.8961 -0.6891 0.0000 C 0 0 1 0 0 0\n 1.2548 0.2221 0.0000 C 0 0 2 0 0 0\n 0.4960 -0.9529 0.0000 C 0 0 2 0 0 0\n 0.6513 -2.2149 0.0000 C 0 0 1 0 0 0\n -0.7183 -2.0601 0.0000 O 0 0\n -1.2216 0.7840 0.0000 C 0 0\n 1.7172 -3.2702 0.0000 R# 0 0\n 2.3209 1.2498 0.0000 O 0 0\n 3.7640 0.8408 0.0000 R# 0 0\n 0.3758 1.5136 0.0000 C 0 0\n -2.6483 1.2498 0.0000 O 0 0\n -2.9590 2.7173 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 6\n 6 9 1 6\n 3 1 1 0\n 5 2 1 6\n 4 10 1 1\n 10 11 1 0\n 2 12 2 0\n 8 13 1 0\n 13 14 1 0\nM RGP 3 9 3 11 2 14 1\nM END\n> <Name>\nMethylene cLNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmeclna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nMethylenephosphonate\n SciTegic07272112182D\n\n 6 5 0 0 0 0 999 V2000\n -1.3755 0.2167 0.0000 C 0 0\n 0.1253 0.2167 0.0000 P 0 0\n 0.8749 -1.0826 0.0000 R# 0 0\n 0.8762 1.5152 0.0000 O 0 0\n 1.6253 0.2160 0.0000 O 0 0\n -2.1263 -1.0819 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\n 1 6 1 0\nM RGP 2 3 2 6 1\nM END\n> <Name>\nMethylenephosphonate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmepo2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nMethylphosphonate\n SciTegic07272112182D\n\n 5 4 0 0 0 0 999 V2000\n -1.7998 0.0000 0.0000 R# 0 0\n -0.2998 0.0000 0.0000 P 0 0\n 1.2002 0.0000 0.0000 R# 0 0\n 0.4498 -1.2993 0.0000 O 0 0\n 0.4498 1.2993 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nMethylphosphonate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nMethylthiophosphonate\n SciTegic07272112182D\n\n 5 4 0 0 0 0 999 V2000\n -1.7998 0.0000 0.0000 R# 0 0\n -0.2998 0.0000 0.0000 P 0 0\n 1.2002 0.0000 0.0000 R# 0 0\n 0.4498 -1.2993 0.0000 S 0 0\n 0.4498 1.2993 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nMethylthiophosphonate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmsp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nN2-(2-Amino)ethyl guanine\n SciTegic07272112182D\n\n 15 16 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5972 1.5031 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2570 0.0000 N 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 7 8 2 0\n 5 8 1 0\n 6 9 2 0\n 2 10 1 0\n 4 11 1 0\n 7 11 1 0\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 14 15 1 0\nM RGP 1 12 1\nM END\n> <Name>\nN2-(2-Amino)ethyl guanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnen2G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN2-(3-Aminopropyl) guanine\n SciTegic07272112182D\n\n 16 17 0 0 0 0 999 V2000\n 6.9961 1.8908 0.0000 C 0 0\n 5.5695 1.4274 0.0000 C 0 0\n 5.2575 -0.0398 0.0000 N 0 0\n 6.3721 -1.0436 0.0000 C 0 0\n 7.7987 -0.5802 0.0000 N 0 0\n 8.1107 0.8870 0.0000 C 0 0\n 9.5374 1.3504 0.0000 O 0 0\n 6.0630 -2.5123 0.0000 N 0 0\n 7.1796 -3.5150 0.0000 C 0 0\n 6.8705 -4.9837 0.0000 C 0 0\n 7.9872 -5.9864 0.0000 C 0 0\n 7.6782 -7.4543 0.0000 N 0 0\n 6.9965 3.3900 0.0000 N 0 0\n 5.5700 3.8536 0.0000 C 0 0\n 4.6882 2.6402 0.0000 N 0 0\n 3.1882 2.6402 0.0000 R# 0 0\n 2 1 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 4 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 1 13 1 0\n 13 14 2 0\n 14 15 1 0\n 15 2 1 0\n 15 16 1 0\nM RGP 1 16 1\nM END\n> <Name>\nN2-(3-Aminopropyl) guanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnpr2G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN2-(Aminoethyl)aminoadenine\n SciTegic07272112182D\n\n 15 16 0 0 0 0 999 V2000\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2570 0.0000 N 0 0\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n 2.5972 1.5031 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 4 9 2 0\n 7 10 1 0\n 10 11 1 0\n 11 12 2 0\n 8 12 1 0\n 9 13 1 0\n 5 14 1 0\n 10 15 1 0\n 1 14 1 0\nM RGP 1 15 1\nM END\n> <Name>\nN2-(Aminoethyl)aminoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnen2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN2-(Methoxypropylamino)adenine\n SciTegic07272112182D\n\n 17 18 0 0 0 0 999 V2000\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2578 0.0000 C 0 0\n 5.1894 6.0109 0.0000 O 0 0\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n 2.5972 1.5031 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 5.1872 7.5109 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 6 1 0\n 6 7 2 0\n 7 8 1 0\n 8 9 2 0\n 9 10 1 0\n 5 10 2 0\n 8 11 1 0\n 11 12 1 0\n 12 13 2 0\n 9 13 1 0\n 10 14 1 0\n 6 15 1 0\n 11 16 1 0\n 1 15 1 0\n 4 17 1 0\nM RGP 1 16 1\nM END\n> <Name>\nN2-(Methoxypropylamino)adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmoprn2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN2-Imidazoylpropylguanine\n SciTegic07272112182D\n\n 20 22 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5972 1.5031 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 5.1894 6.0109 0.0000 N 0 0\n 5.3272 7.4918 0.0000 C 0 0\n 6.7944 7.8037 0.0000 N 0 0\n 7.5444 6.5046 0.0000 C 0 0\n 6.5408 5.3899 0.0000 C 0 0\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2578 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 7 8 2 0\n 5 8 1 0\n 6 9 2 0\n 2 10 1 0\n 4 11 1 0\n 7 11 1 0\n 11 12 1 0\n 13 14 1 0\n 14 15 2 0\n 15 16 1 0\n 16 17 2 0\n 13 17 1 0\n 10 18 1 0\n 18 19 1 0\n 19 20 1 0\n 13 20 1 0\nM RGP 1 12 1\nM END\n> <Name>\nN2-Imidazoylpropylguanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nimpr2G\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN2-Phenethylaminoadenine\n SciTegic07272112182D\n\n 20 22 0 0 0 0 999 V2000\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2578 0.0000 C 0 0\n 5.1876 6.0124 0.0000 C 0 0\n 5.1824 7.5124 0.0000 C 0 0\n 3.8807 8.2579 0.0000 C 0 0\n 2.5843 7.5034 0.0000 C 0 0\n 2.5895 6.0034 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n 2.5972 1.5031 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 3 8 1 0\n 9 10 1 0\n 10 11 2 0\n 11 12 1 0\n 12 13 2 0\n 13 14 1 0\n 9 14 2 0\n 12 15 1 0\n 15 16 1 0\n 16 17 2 0\n 13 17 1 0\n 14 18 1 0\n 10 19 1 0\n 15 20 1 0\n 1 19 1 0\nM RGP 1 20 1\nM END\n> <Name>\nN2-Phenethylaminoadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nphen2A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN2-[(Imidazo-2-yl)ethylamino]adenine\n SciTegic07272112182D\n\n 19 21 0 0 0 0 999 V2000\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2578 0.0000 C 0 0\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n 2.5972 1.5031 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 5.1017 6.1219 0.0000 N 0 0\n 4.6332 7.5469 0.0000 C 0 0\n 3.1332 7.5416 0.0000 C 0 0\n 2.6746 6.1134 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 7 8 2 0\n 8 9 1 0\n 4 9 2 0\n 7 10 1 0\n 10 11 1 0\n 11 12 2 0\n 8 12 1 0\n 9 13 1 0\n 5 14 1 0\n 10 15 1 0\n 1 14 1 0\n 3 16 1 0\n 16 17 1 0\n 17 18 2 0\n 18 19 1 0\n 3 19 2 0\nM RGP 1 15 1\nM END\n> <Name>\nN2-[(Imidazo-2-yl)ethylamino]adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n2imen2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN2-[(Imidazol-4-yl)ethyl]guanine\n SciTegic07272112182D\n\n 19 21 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 2.5972 1.5031 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2578 0.0000 C 0 0\n 5.1017 6.1219 0.0000 N 0 0\n 4.6332 7.5469 0.0000 C 0 0\n 3.1332 7.5416 0.0000 N 0 0\n 2.6746 6.1134 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 1 0\n 7 8 2 0\n 5 8 1 0\n 6 9 2 0\n 2 10 1 0\n 4 11 1 0\n 7 11 1 0\n 11 12 1 0\n 10 13 1 0\n 13 14 1 0\n 15 16 1 0\n 16 17 2 0\n 17 18 1 0\n 15 19 2 0\n 14 15 1 0\n 18 19 1 0\nM RGP 1 12 1\nM END\n> <Name>\nN2-[(Imidazol-4-yl)ethyl]guanine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n4imen2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nG\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN3-(2-Cyanoethyl)thymine\n SciTegic07272112182D\n\n 14 14 0 0 0 0 999 V2000\n 3.7500 4.2990 0.0000 C 0 0\n 2.2500 4.2990 0.0000 C 0 0\n 1.5000 3.0000 0.0000 N 0 0\n 2.2500 1.7010 0.0000 C 0 0\n 3.7500 1.7010 0.0000 N 0 0\n 4.5000 3.0000 0.0000 C 0 0\n 6.0000 3.0000 0.0000 O 0 0\n 1.5000 0.4019 0.0000 O 0 0\n 4.5000 5.5981 0.0000 C 0 0\n 4.5031 0.4027 0.0000 C 0 0\n 6.0039 0.4049 0.0000 C 0 0\n 6.7570 -0.8933 0.0000 C 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 7.5096 -2.1908 0.0000 N 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 4 8 2 0\n 1 9 1 0\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\n 3 13 1 0\n 12 14 3 0\nM RGP 1 13 1\nM END\n> <Name>\nN3-(2-Cyanoethyl)thymine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncneT\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN6-[2-(4-Imidazoyl)ethyl]adenine\n SciTegic07272112182D\n\n 18 20 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n 0.0031 -3.0008 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 1.3039 -3.7494 0.0000 C 0 0\n 1.3070 -5.2502 0.0000 C 0 0\n 2.6078 -5.9988 0.0000 C 0 0\n 2.7509 -7.4791 0.0000 N 0 0\n 4.2192 -7.7859 0.0000 C 0 0\n 4.9646 -6.4842 0.0000 N 0 0\n 3.9571 -5.3730 0.0000 C 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 7 8 2 0\n 5 8 1 0\n 6 9 1 0\n 4 10 1 0\n 7 10 1 0\n 10 11 1 0\n 9 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 2 0\n 16 17 1 0\n 14 18 2 0\n 17 18 1 0\nM RGP 1 11 1\nM END\n> <Name>\nN6-[2-(4-Imidazoyl)ethyl]adenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n4ime6A\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN-(Aminopropyl)imidazoleadenine\n SciTegic07272112182D\n\n 20 22 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 N 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 2.5972 1.5031 0.0000 N 0 0\n 2.5951 3.0039 0.0000 C 0 0\n 3.8933 3.7570 0.0000 C 0 0\n 3.8912 5.2578 0.0000 C 0 0\n 5.1894 6.0109 0.0000 N 0 0\n 5.3272 7.4918 0.0000 C 0 0\n 6.7944 7.8037 0.0000 N 0 0\n 7.5444 6.5046 0.0000 C 0 0\n 6.5408 5.3899 0.0000 C 0 0\n 1 2 2 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 1 6 1 0\n 4 8 1 0\n 8 9 1 0\n 9 10 2 0\n 5 10 1 0\n 8 11 1 0\n 2 12 1 0\n 12 13 1 0\n 13 14 1 0\n 15 14 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 2 0\n 18 19 1 0\n 19 20 2 0\n 20 16 1 0\nM RGP 1 11 1\nM END\n> <Name>\nN-(Aminopropyl)imidazoleadenine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nimprn2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nA\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nN-(Methyl)aminooxy BNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n -0.9534 0.5285 0.0000 C 0 0\n -1.7483 -0.7444 0.0000 O 0 0\n 0.1233 2.0603 0.0000 C 0 0\n 0.5491 0.4739 0.0000 C 0 0 1 0 0 0\n 0.1543 -0.5160 0.0000 C 0 0 1 0 0 0\n -0.8527 -1.8179 0.0000 C 0 0 1 0 0 0\n -0.5098 -0.5201 0.0000 O 0 0\n 3.0796 -0.7444 0.0000 O 0 0\n -1.5163 -3.1632 0.0000 R# 0 0\n -1.3844 1.8855 0.0000 O 0 0\n 1.6444 -0.3463 0.0000 C 0 0 2 0 0 0\n 4.1498 0.3066 0.0000 R# 0 0\n -0.3476 1.2002 0.0000 N 0 0\n 0.8594 2.0907 0.0000 C 0 0\n -3.2475 -0.6935 0.0000 R# 0 0\n 13 10 1 0\n 4 1 1 6\n 1 2 1 0\n 4 11 1 0\n 11 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 4 1 0\n 6 9 1 6\n 4 3 1 0\n 5 13 1 6\n 10 3 1 0\n 11 8 1 1\n 8 12 1 0\n 13 14 1 0\n 2 15 1 0\nM RGP 3 9 3 12 2 15 1\nM END\n> <Name>\nN-(Methyl)aminooxy BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmnobna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nN-Hydroxyglycine\n SciTegic07272112182D\n\n 6 5 0 0 0 0 999 V2000\n 2.6000 0.0000 0.0000 C 0 0\n 1.3000 0.7500 0.0000 C 0 0\n 0.0007 0.0004 0.0000 O 0 0\n 3.9000 0.7500 0.0000 N 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 5.1992 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 1 4 1 0\n 2 5 1 0\n 4 6 1 0\nM RGP 2 5 1 6 2\nM END\n> <Name>\nN-Hydroxyglycine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ngly\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nN-Methylamino LNA\n SciTegic07272112182D\n\n 14 15 0 0 1 0 999 V2000\n -1.7573 0.3923 0.0000 C 0 0\n -0.3792 0.2175 0.0000 N 0 0\n -0.8961 -0.6891 0.0000 C 0 0 1 0 0 0\n 1.2548 0.2221 0.0000 C 0 0 2 0 0 0\n 0.4960 -0.9529 0.0000 C 0 0 2 0 0 0\n 0.6513 -2.2149 0.0000 C 0 0 1 0 0 0\n -0.7183 -2.0601 0.0000 O 0 0\n -1.2216 0.7840 0.0000 C 0 0\n 1.7172 -3.2702 0.0000 R# 0 0\n 2.3209 1.2498 0.0000 O 0 0\n 3.7640 0.8408 0.0000 R# 0 0\n 0.3758 1.5136 0.0000 C 0 0\n -2.6483 1.2498 0.0000 O 0 0\n -2.9590 2.7173 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 6\n 6 9 1 6\n 3 1 1 0\n 5 2 1 6\n 4 10 1 1\n 10 11 1 0\n 2 12 1 0\n 8 13 1 0\n 13 14 1 0\nM RGP 3 9 3 11 2 14 1\nM END\n> <Name>\nN-Methylamino LNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nmn2lna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nNPOM-caged thymine\n SciTegic07272112182D\n\n 26 28 0 0 0 0 999 V2000\n 10.3988 -1.4774 0.0000 R# 0 0\n 14.1488 -0.1783 0.0000 N 0 0\n 12.6488 -0.1783 0.0000 C 0 0\n 11.8988 -1.4774 0.0000 N 0 0\n 12.6488 -2.7764 0.0000 C 0 0\n 14.1488 -2.7764 0.0000 C 0 0\n 14.8988 -1.4774 0.0000 C 0 0\n 16.3988 -1.4774 0.0000 O 0 0\n 11.8987 1.1207 0.0000 O 0 0\n 14.8988 -4.0755 0.0000 C 0 0\n 14.9018 1.1200 0.0000 C 0 0\n 16.4027 1.1179 0.0000 O 0 0\n 17.1557 2.4161 0.0000 C 0 0\n 16.4080 3.7164 0.0000 C 0 0\n 18.6566 2.4140 0.0000 C 0 0\n 19.4021 1.1123 0.0000 C 0 0\n 20.9021 1.1072 0.0000 C 0 0\n 21.6565 2.4036 0.0000 C 0 0\n 20.9110 3.7052 0.0000 C 0 0\n 19.4111 3.7104 0.0000 C 0 0\n 21.9012 -0.0106 0.0000 O 0 0\n 23.2736 0.5948 0.0000 C 0 0\n 23.1220 2.0871 0.0000 O 0 0\n 18.6678 5.0143 0.0000 N 0 3\n 19.4242 6.3097 0.0000 O 0 0\n 17.1678 5.0221 0.0000 O 0 5\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 2 0\n 6 7 1 0\n 2 7 1 0\n 7 8 2 0\n 3 9 2 0\n 1 4 1 0\n 6 10 1 0\n 2 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 13 15 1 0\n 15 16 2 0\n 16 17 1 0\n 17 18 2 0\n 18 19 1 0\n 19 20 2 0\n 20 15 1 0\n 17 21 1 0\n 21 22 1 0\n 22 23 1 0\n 23 18 1 0\n 20 24 1 0\n 24 25 2 0\n 24 26 1 0\nM CHG 2 24 1 26 -1\nM RGP 1 1 1\nM END\n> <Name>\nNPOM-caged thymine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nnpomT\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nT\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nNorth-2-ara-fluoro-methanocarbocycle\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n -0.9485 -0.7830 0.0000 C 0 0 2 0 0 0\n 0.1086 0.2813 0.0000 C 0 0 2 0 0 0\n 1.4474 -0.3952 0.0000 C 0 0 1 0 0 0\n 1.2178 -1.8775 0.0000 C 0 0 1 0 0 0\n -0.2630 -2.1172 0.0000 C 0 0 1 0 0 0\n -0.1339 1.7598 0.0000 O 0 0\n -1.9138 0.3450 0.0000 C 0 0\n 2.2820 -2.9346 0.0000 R# 0 0\n 1.0261 2.7108 0.0000 R# 0 0\n -1.8053 -1.9405 0.0000 C 0 0\n 2.7816 0.2903 0.0000 F 0 0\n -1.4128 1.7598 0.0000 O 0 0\n -2.3862 2.9010 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 1 10 1 0\n 5 10 1 1\n 3 11 1 6\n 7 12 1 0\n 12 13 1 0\nM RGP 3 8 3 9 2 13 1\nM END\n> <Name>\nNorth-2-ara-fluoro-methanocarbocycle\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nafl2Nm\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nNorth-2-fluoro-methanocarbocycle\n SciTegic07272112182D\n\n 13 14 0 0 1 0 999 V2000\n -0.9485 -0.7830 0.0000 C 0 0 2 0 0 0\n 0.1086 0.2813 0.0000 C 0 0 2 0 0 0\n 1.4474 -0.3952 0.0000 C 0 0 2 0 0 0\n 1.2178 -1.8775 0.0000 C 0 0 1 0 0 0\n -0.2630 -2.1172 0.0000 C 0 0 1 0 0 0\n -0.1339 1.7598 0.0000 O 0 0\n -1.9138 0.3450 0.0000 C 0 0\n 2.2820 -2.9346 0.0000 R# 0 0\n 1.0261 2.7108 0.0000 R# 0 0\n -1.8053 -1.9405 0.0000 C 0 0\n 2.7816 0.2903 0.0000 F 0 0\n -1.4128 1.7598 0.0000 O 0 0\n -2.3862 2.9010 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 1 10 1 0\n 5 10 1 1\n 3 11 1 1\n 7 12 1 0\n 12 13 1 0\nM RGP 3 8 3 9 2 13 1\nM END\n> <Name>\nNorth-2-fluoro-methanocarbocycle\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nfl2Nmc\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nNorth-methanocarbocycle\n SciTegic07272112182D\n\n 12 13 0 0 1 0 999 V2000\n -0.7167 -0.7588 0.0000 C 0 0 2 0 0 0\n 0.3404 0.3055 0.0000 C 0 0 2 0 0 0\n 1.6792 -0.3710 0.0000 C 0 0\n 1.4496 -1.8533 0.0000 C 0 0 1 0 0 0\n -0.0312 -2.0930 0.0000 C 0 0 1 0 0 0\n 0.0979 1.7840 0.0000 O 0 0\n -1.6820 0.3692 0.0000 C 0 0\n 2.5138 -2.9104 0.0000 R# 0 0\n 1.2579 2.7350 0.0000 R# 0 0\n -1.5736 -1.9163 0.0000 C 0 0\n -1.1810 1.7840 0.0000 O 0 0\n -2.1544 2.9252 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 1 10 1 0\n 5 10 1 1\n 7 11 1 0\n 11 12 1 0\nM RGP 3 8 3 9 2 12 1\nM END\n> <Name>\nNorth-methanocarbocycle\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nNmc\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nOxy (ether)\n SciTegic07272112182D\n\n 3 2 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 O 0 0\n 2.5993 0.0004 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nOxy (ether)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\noxy\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nPEG/HEG 18 atom spacer\n SciTegic07272112182D\n\n 21 20 0 0 0 0 999 V2000\n -9.0999 -0.3928 0.0000 C 0 0\n -7.7999 0.3572 0.0000 O 0 0\n -6.5000 -0.3928 0.0000 C 0 0\n -5.2000 0.3572 0.0000 C 0 0\n -3.9000 -0.3928 0.0000 O 0 0\n -2.6000 0.3572 0.0000 C 0 0\n -1.3000 -0.3928 0.0000 C 0 0\n 0.0000 0.3572 0.0000 O 0 0\n 1.3000 -0.3928 0.0000 C 0 0\n 2.6000 0.3572 0.0000 C 0 0\n 3.9000 -0.3928 0.0000 O 0 0\n 5.2000 0.3572 0.0000 C 0 0\n 6.4999 -0.3928 0.0000 C 0 0\n 7.7999 0.3572 0.0000 O 0 0\n 9.0999 -0.3928 0.0000 C 0 0\n 10.3999 0.3572 0.0000 C 0 0\n 11.6999 -0.3928 0.0000 O 0 0\n 12.9992 0.3568 0.0000 R# 0 0\n -10.3999 0.3572 0.0000 C 0 0\n -11.6999 -0.3928 0.0000 O 0 0\n -12.9992 0.3568 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 7 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 14 1 0\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\n 19 1 1 0\n 19 20 1 0\n 20 21 1 0\nM RGP 2 18 2 21 1\nM END\n> <Name>\nPEG/HEG 18 atom spacer\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSp18\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nPNA (peptide nucleic acid)\n SciTegic09012117322D\n\n 13 12 0 0 0 0 999 V2000\n -1.3523 1.2380 0.0000 C 0 0\n 0.0251 0.6419 0.0000 N 0 0\n 0.2001 -0.8486 0.0000 C 0 0\n 1.5783 -1.4432 0.0000 C 0 0\n 1.2306 1.5360 0.0000 C 0 0\n -2.5577 0.3439 0.0000 C 0 0\n 1.7533 -2.9329 0.0000 R# 0 0\n -3.9351 0.9400 0.0000 N 0 0\n 2.6079 0.9400 0.0000 C 0 0\n 2.7798 -0.5502 0.0000 R# 0 0\n -5.1399 0.0464 0.0000 R# 0 0\n -1.0028 -1.7447 0.0000 O 0 0\n 3.8127 1.8335 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 2 5 1 0\n 1 6 1 0\n 4 7 1 0\n 6 8 1 0\n 5 9 1 0\n 9 10 1 0\n 8 11 1 0\n 3 12 2 0\n 9 13 2 0\nM RGP 3 7 3 10 2 11 1\nM END\n> <Name>\nPNA (peptide nucleic acid)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\npna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\nPNA D-Lysine (peptide nucleic acid)\n SciTegic09012117322D\n\n 18 17 0 0 1 0 999 V2000\n -1.9775 1.2208 0.0000 C 0 0\n -0.9363 0.1399 0.0000 N 0 0\n -1.3552 -1.3012 0.0000 C 0 0\n -2.8126 -1.6600 0.0000 C 0 0\n -3.4345 0.8605 0.0000 C 0 0\n -3.2313 -3.1004 0.0000 R# 0 0\n -4.4757 1.9414 0.0000 N 0 0\n 0.9395 1.9414 0.0000 C 0 0\n -0.0989 3.0239 0.0000 R# 0 0\n -5.9318 1.5813 0.0000 R# 0 0\n -0.3169 -2.3837 0.0000 O 0 0\n 2.3960 2.3000 0.0000 O 0 0\n 0.5206 0.5003 0.0000 C 0 0 1 0 0 0\n 1.5617 -0.5806 0.0000 C 0 0\n 3.0187 -0.2203 0.0000 C 0 0\n 4.0599 -1.3012 0.0000 C 0 0\n 5.5168 -0.9409 0.0000 C 0 0\n 6.5575 -2.0212 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 2 13 1 0\n 1 5 1 0\n 4 6 1 0\n 5 7 1 0\n 13 8 1 0\n 8 9 1 0\n 7 10 1 0\n 3 11 2 0\n 8 12 2 0\n 13 14 1 1\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\nM RGP 3 6 3 9 2 10 1\nM END\n> <Name>\nPNA D-Lysine (peptide nucleic acid)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nDlyspn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\nPNA L-Lysine (peptide nucleic acid)\n SciTegic09012117322D\n\n 18 17 0 0 1 0 999 V2000\n -1.9775 1.2208 0.0000 C 0 0\n -0.9363 0.1399 0.0000 N 0 0\n -1.3552 -1.3012 0.0000 C 0 0\n -2.8126 -1.6600 0.0000 C 0 0\n -3.4345 0.8605 0.0000 C 0 0\n -3.2313 -3.1004 0.0000 R# 0 0\n -4.4757 1.9414 0.0000 N 0 0\n 0.9395 1.9414 0.0000 C 0 0\n -0.0989 3.0239 0.0000 R# 0 0\n -5.9318 1.5813 0.0000 R# 0 0\n -0.3169 -2.3837 0.0000 O 0 0\n 2.3960 2.3000 0.0000 O 0 0\n 0.5206 0.5003 0.0000 C 0 0 2 0 0 0\n 1.5617 -0.5806 0.0000 C 0 0\n 3.0187 -0.2203 0.0000 C 0 0\n 4.0599 -1.3012 0.0000 C 0 0\n 5.5168 -0.9409 0.0000 C 0 0\n 6.5575 -2.0212 0.0000 N 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 2 13 1 0\n 1 5 1 0\n 4 6 1 0\n 5 7 1 0\n 13 8 1 0\n 8 9 1 0\n 7 10 1 0\n 3 11 2 0\n 8 12 2 0\n 13 14 1 6\n 14 15 1 0\n 15 16 1 0\n 16 17 1 0\n 17 18 1 0\nM RGP 3 6 3 9 2 10 1\nM END\n> <Name>\nPNA L-Lysine (peptide nucleic acid)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nLlyspn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]O\n[R3]O\n\n$$$$\nPhosphonoacetate\n SciTegic07272112182D\n\n 8 7 0 0 0 0 999 V2000\n 0.1884 -1.6241 0.0000 R# 0 0\n 0.9383 -0.3250 0.0000 P 0 0\n 1.6882 -1.6241 0.0000 R# 0 0\n 0.1874 0.9745 0.0000 C 0 0\n 2.4383 -0.3254 0.0000 O 0 0\n -1.3134 0.9748 0.0000 C 0 0\n -2.0633 -0.3243 0.0000 O 0 0\n -2.0639 2.2736 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 2 0\n 4 6 1 0\n 6 7 1 0\n 6 8 2 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nPhosphonoacetate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ncmp\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nPhosphorodiamidate\n SciTegic09012117322D\n\n 8 7 0 0 0 0 999 V2000\n -0.8449 1.1367 0.0000 N 0 0\n -0.0936 -0.1625 0.0000 C 0 0\n -0.8432 -1.4618 0.0000 C 0 0\n 0.6566 -1.4615 0.0000 R# 0 0\n 1.4072 -0.1625 0.0000 N 0 0\n -2.3449 1.1367 0.0000 C 0 0\n -0.0953 2.4360 0.0000 C 0 0\n 2.1580 -1.4611 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 2 5 1 0\n 1 6 1 0\n 1 7 1 0\n 5 8 1 0\nM RGP 2 4 1 8 2\nM END\n> <Name>\nPhosphorodiamidate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nm2np\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]H\n\n$$$$\nPhosphorodithioate\n SciTegic07272112182D\n\n 5 4 0 0 0 0 999 V2000\n -1.7998 0.0000 0.0000 R# 0 0\n -0.2998 0.0000 0.0000 P 0 0\n 1.2002 0.0000 0.0000 R# 0 0\n 0.4498 -1.2993 0.0000 S 0 0\n 0.4498 1.2993 0.0000 S 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 2 0\n 2 5 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nPhosphorodithioate\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ns2p\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]O\n\n$$$$\nPropylamino\n SciTegic07272112182D\n\n 6 5 0 0 0 0 999 V2000\n 0.0007 0.0004 0.0000 R# 0 0\n 1.3000 0.7500 0.0000 N 0 0\n 1.3000 2.2500 0.0000 R# 0 0\n 2.6000 0.0000 0.0000 C 0 0\n 3.9000 0.7500 0.0000 C 0 0\n 5.1992 0.0004 0.0000 C 0 0\n 1 2 1 0\n 2 3 1 0\n 2 4 1 0\n 4 5 1 0\n 5 6 1 0\nM RGP 2 1 1 3 2\nM END\n> <Name>\nPropylamino\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nprn\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nP\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n\n$$$$\nPseudouracil\n SciTegic07272112182D\n\n 9 9 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 C 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 N 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n 0.0000 -3.0000 0.0000 O 0 0\n 0.0000 3.0000 0.0000 R# 0 0\n 2.5981 1.5000 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 2 0\n 4 5 1 0\n 5 6 1 0\n 1 6 1 0\n 6 7 2 0\n 3 8 1 0\n 2 9 2 0\nM RGP 1 8 1\nM END\n> <Name>\nPseudouracil\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\npsiU\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nU\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nPurine\n SciTegic07272112182D\n\n 10 11 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 N 0 0\n 1.2990 0.7500 0.0000 C 0 0\n 0.0000 1.5000 0.0000 N 0 0\n -1.2990 0.7500 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -2.7248 1.2135 0.0000 N 0 0\n -3.6065 0.0000 0.0000 C 0 0\n -2.7248 -1.2135 0.0000 N 0 0\n -3.1882 2.6401 0.0000 R# 0 0\n 1 2 1 0\n 2 3 2 0\n 3 4 1 0\n 4 5 2 0\n 5 6 1 0\n 1 6 2 0\n 4 7 1 0\n 7 8 1 0\n 8 9 2 0\n 5 9 1 0\n 7 10 1 0\nM RGP 1 10 1\nM END\n> <Name>\nPurine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\npurine\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nSouth-methanocarbacycle\n SciTegic07272112182D\n\n 12 13 0 0 1 0 999 V2000\n -0.4943 -0.2124 0.0000 C 0 0 2 0 0 0\n 0.8375 0.4778 0.0000 C 0 0 2 0 0 0\n 1.9055 -0.5755 0.0000 C 0 0\n 1.2337 -1.9167 0.0000 C 0 0 1 0 0 0\n -0.2494 -1.6923 0.0000 C 0 0 1 0 0 0\n 1.0586 1.9597 0.0000 O 0 0\n -1.8325 0.4614 0.0000 C 0 0\n -0.1445 -2.5087 0.0000 R# 0 0\n 2.4537 2.5107 0.0000 R# 0 0\n 0.4098 -3.0978 0.0000 C 0 0\n -1.9192 1.9597 0.0000 O 0 0\n -3.2590 2.6342 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 2 6 1 1\n 1 7 1 6\n 4 8 1 6\n 6 9 1 0\n 5 10 1 1\n 4 10 1 0\n 7 11 1 0\n 11 12 1 0\nM RGP 3 8 3 9 2 12 1\nM END\n> <Name>\nSouth-methanocarbacycle\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nSmc\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nTricyclic Nucleoside (TriNA1)\n SciTegic07272112182D\n\n 16 18 0 0 1 0 999 V2000\n 2.6530 -0.4520 0.0000 C 0 0 1 0 0 0\n 1.3983 0.2080 0.0000 C 0 0 2 0 0 0\n 0.6593 -1.0047 0.0000 C 0 0 1 0 0 0\n -0.7503 -0.9712 0.0000 O 0 0\n -0.0313 0.2420 0.0000 C 0 0 1 0 0 0\n -0.6920 1.4781 0.0000 C 0 0 1 0 0 0\n 0.7176 1.4446 0.0000 O 0 0\n -1.4309 0.2754 0.0000 C 0 0 1 0 0 0\n -2.6739 1.0051 0.0000 C 0 0\n -3.3546 2.2417 0.0000 C 0 0\n -1.9450 2.2081 0.0000 C 0 0\n 1.3782 -2.3212 0.0000 R# 0 0\n -1.8206 -1.1820 0.0000 O 0 0\n 3.9351 -1.1820 0.0000 O 0 0\n 5.2263 -0.4185 0.0000 R# 0 0\n -3.2691 -1.5715 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 1\n 5 1 1 0\n 5 6 1 0\n 2 7 1 6\n 6 7 1 6\n 5 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 6 11 1 0\n 3 12 1 6\n 8 13 1 6\n 1 14 1 6\n 14 15 1 0\n 13 16 1 0\nM RGP 3 12 3 15 2 16 1\nM END\n> <Name>\nTricyclic Nucleoside (TriNA1)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ntrina1\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nTricyclic Nucleoside (TriNA2)\n SciTegic07272112182D\n\n 16 18 0 0 1 0 999 V2000\n 2.6530 -0.4520 0.0000 C 0 0 1 0 0 0\n 1.3983 0.2080 0.0000 C 0 0 2 0 0 0\n 0.6593 -1.0047 0.0000 C 0 0 1 0 0 0\n -0.7503 -0.9712 0.0000 O 0 0\n -0.0313 0.2420 0.0000 C 0 0 1 0 0 0\n -0.6920 1.4781 0.0000 C 0 0 2 0 0 0\n 0.7176 1.4446 0.0000 O 0 0\n -1.4309 0.2754 0.0000 C 0 0 2 0 0 0\n -2.6739 1.0051 0.0000 C 0 0\n -3.3546 2.2417 0.0000 C 0 0\n -1.9450 2.2081 0.0000 C 0 0\n 1.3782 -2.3212 0.0000 R# 0 0\n -1.8206 -1.1820 0.0000 O 0 0\n 3.9351 -1.1820 0.0000 O 0 0\n 5.2263 -0.4185 0.0000 R# 0 0\n -3.2691 -1.5715 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 1\n 5 1 1 0\n 5 6 1 0\n 2 7 1 6\n 6 7 1 1\n 5 8 1 0\n 8 9 1 0\n 9 10 1 0\n 10 11 1 0\n 6 11 1 0\n 3 12 1 6\n 8 13 1 1\n 1 14 1 6\n 14 15 1 0\n 13 16 1 0\nM RGP 3 12 3 15 2 16 1\nM END\n> <Name>\nTricyclic Nucleoside (TriNA2)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ntrina2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nTricycloDNA\n SciTegic07272112182D\n\n 15 17 0 0 1 0 999 V2000\n 0.9564 0.9968 0.0000 C 0 0 1 0 0 0\n 2.2238 0.1944 0.0000 C 0 0\n 1.8523 -1.2589 0.0000 C 0 0 1 0 0 0\n 0.3553 -1.3546 0.0000 O 0 0\n -0.1983 0.0395 0.0000 C 0 0 2 0 0 0\n 2.8096 -2.4136 0.0000 R# 0 0\n 1.2005 -0.4870 0.0000 O 0 0\n -1.4533 0.8270 0.0000 C 0 0 1 0 0 0\n -1.0818 2.2802 0.0000 C 0 0 2 0 0 0\n 0.4151 2.3760 0.0000 C 0 0\n -1.3512 -0.9202 0.0000 H 0 0\n -2.1444 -0.4870 0.0000 O 0 0\n 2.6054 -1.0127 0.0000 R# 0 0\n -2.5462 1.7647 0.0000 C 0 0\n -3.6433 -0.5444 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 3 6 1 6\n 1 7 1 1\n 5 8 1 0\n 8 9 1 0\n 9 10 1 1\n 10 1 1 0\n 5 11 1 1\n 8 12 1 6\n 7 13 1 0\n 8 14 1 0\n 9 14 1 0\n 12 15 1 0\nM RGP 3 6 3 13 2 15 1\nM END\n> <Name>\nTricycloDNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\ntcdna\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nXanthine\n SciTegic07272112182D\n\n 12 13 0 0 0 0 999 V2000\n 1.2990 -0.7500 0.0000 C 0 0\n 1.2990 0.7500 0.0000 N 0 0\n 0.0000 1.5000 0.0000 C 0 0\n 0.0000 -1.5000 0.0000 C 0 0\n -1.2990 -0.7500 0.0000 C 0 0\n -1.2990 0.7500 0.0000 N 0 0\n -2.4133 -1.7530 0.0000 N 0 0\n -1.8032 -3.1233 0.0000 C 0 0\n -0.3114 -2.9665 0.0000 N 0 0\n -3.8805 -1.4410 0.0000 R# 0 0\n 0.0000 3.0000 0.0000 O 0 0\n 2.5981 -1.5000 0.0000 O 0 0\n 1 2 1 0\n 2 3 1 0\n 1 4 1 0\n 4 5 2 0\n 5 6 1 0\n 6 3 1 0\n 5 7 1 0\n 7 8 1 0\n 8 9 2 0\n 9 4 1 0\n 7 10 1 0\n 3 11 2 0\n 1 12 2 0\nM RGP 1 10 1\nM END\n> <Name>\nXanthine\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nXan\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nX\n\n> <BranchMonomer>\ntrue\n\n> <MonomerCaps>\n[R1]H\n\n$$$$\nalpha-L-Methylene cLNA\n SciTegic09012117322D\n\n 14 15 0 0 1 0 999 V2000\n 1.3724 0.2490 0.0000 C 0 0 2 0 0 0\n -0.7833 -0.6510 0.0000 C 0 0 1 0 0 0\n -1.6389 0.4349 0.0000 C 0 0 1 0 0 0\n -0.2617 0.2529 0.0000 O 0 0\n 0.6074 -0.9220 0.0000 C 0 0 2 0 0 0\n -2.9425 1.1768 0.0000 R# 0 0\n 0.7561 -2.1847 0.0000 C 0 0\n -0.6126 -2.0229 0.0000 C 0 0\n 0.5311 0.5874 0.0000 C 0 0\n 2.4438 1.2711 0.0000 O 0 0\n -0.8049 1.2711 0.0000 O 0 0\n -1.6701 -3.0867 0.0000 C 0 0\n 3.8848 0.8548 0.0000 R# 0 0\n -0.8816 2.7692 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 1 5 1 0\n 3 6 1 6\n 5 7 1 0\n 7 8 1 0\n 2 8 1 6\n 5 9 1 6\n 1 10 1 1\n 9 11 1 0\n 8 12 2 0\n 10 13 1 0\n 11 14 1 0\nM RGP 3 6 3 13 2 14 1\nM END\n> <Name>\nalpha-L-Methylene cLNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nALmecl\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nalpha-L-TriNA1\n SciTegic07272112182D\n\n 16 18 0 0 1 0 999 V2000\n 2.6539 -0.4518 0.0000 C 0 0 2 0 0 0\n 1.3991 0.2079 0.0000 C 0 0 1 0 0 0\n 0.6603 -1.0051 0.0000 C 0 0 1 0 0 0\n -0.7493 -0.9719 0.0000 O 0 0\n -0.0305 0.2415 0.0000 C 0 0 2 0 0 0\n -0.6916 1.4774 0.0000 C 0 0 2 0 0 0\n 0.7180 1.4442 0.0000 O 0 0\n 1.3796 -2.3214 0.0000 R# 0 0\n -1.9448 2.2071 0.0000 C 0 0\n -3.3544 2.2403 0.0000 C 0 0\n -2.6733 1.0039 0.0000 C 0 0\n -1.4301 0.2745 0.0000 C 0 0 1 0 0 0\n 3.9363 -1.1814 0.0000 O 0 0\n -1.8252 -1.1814 0.0000 O 0 0\n -3.2751 -1.5662 0.0000 R# 0 0\n 5.2272 -0.4176 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 6\n 5 1 1 0\n 5 6 1 0\n 2 7 1 1\n 3 8 1 6\n 6 9 1 1\n 9 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 5 1 0\n 1 13 1 1\n 12 14 1 6\n 14 15 1 0\n 13 16 1 0\n 6 7 1 0\nM RGP 3 8 3 15 1 16 2\nM END\n> <Name>\nalpha-L-TriNA1\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nALtri1\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nalpha-L-TriNA2\n SciTegic07272112182D\n\n 16 18 0 0 1 0 999 V2000\n 0.3688 0.2749 0.0000 C 0 0 2 0 0 0\n 1.1556 -0.9189 0.0000 C 0 0 1 0 0 0\n 2.5699 -1.0016 0.0000 C 0 0 1 0 0 0\n -0.0102 -1.5217 0.0000 O 0 0\n -1.0095 -0.0878 0.0000 C 0 0 2 0 0 0\n -1.0850 -1.5233 0.0000 C 0 0\n 0.2451 -2.0446 0.0000 O 0 0\n 4.0662 -0.8963 0.0000 R# 0 0\n 1.8404 0.5584 0.0000 O 0 0\n -2.0505 0.9501 0.0000 C 0 0 2 0 0 0\n -1.6991 2.3365 0.0000 C 0 0\n -0.2571 2.7206 0.0000 C 0 0\n 0.7556 1.6827 0.0000 C 0 0\n -3.5000 0.5584 0.0000 O 0 0\n -3.8863 -0.8910 0.0000 R# 0 0\n 2.4962 -0.1965 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 5 4 1 1\n 5 1 1 0\n 5 6 1 0\n 2 7 1 1\n 7 6 1 0\n 3 8 1 6\n 1 9 1 6\n 5 10 1 0\n 10 11 1 0\n 11 12 1 0\n 12 13 1 0\n 13 1 1 0\n 10 14 1 1\n 14 15 1 0\n 9 16 1 0\nM RGP 3 8 3 15 1 16 2\nM END\n> <Name>\nalpha-L-TriNA2\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nALtri2\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\nciPr BNA\n SciTegic07272112182D\n\n 15 16 0 0 1 0 999 V2000\n 0.2991 -2.2311 0.0000 C 0 0\n 0.4976 -0.8562 0.0000 O 0 0\n -0.5139 -1.1129 0.0000 C 0 0 1 0 0 0\n 0.9374 0.7175 0.0000 C 0 0 2 0 0 0\n -0.3973 0.2991 0.0000 C 0 0 2 0 0 0\n -1.5723 0.7850 0.0000 C 0 0 1 0 0 0\n -1.7880 -0.5764 0.0000 O 0 0\n -1.0568 0.2946 0.0000 C 0 0\n -2.3057 2.0935 0.0000 R# 0 0\n 2.2119 1.4714 0.0000 O 0 0\n 3.5217 0.7403 0.0000 R# 0 0\n -0.7634 -3.2899 0.0000 C 0 0\n 1.7326 -2.6726 0.0000 C 0 0\n -0.1253 1.4714 0.0000 O 0 0\n -0.6775 2.8661 0.0000 R# 0 0\n 1 2 1 0\n 3 4 1 0\n 4 5 1 0\n 5 6 1 0\n 6 7 1 0\n 3 7 1 0\n 3 8 1 1\n 6 9 1 1\n 3 1 1 0\n 5 2 1 1\n 4 10 1 6\n 10 11 1 0\n 1 12 1 0\n 1 13 1 0\n 8 14 1 0\n 14 15 1 0\nM RGP 3 9 3 11 2 15 1\nM END\n> <Name>\nciPr BNA\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\nciPr\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]H\n[R2]H\n[R3]O\n\n$$$$\n3-O-Methylribose (2,5 connectivity)\n SciTegic07272112182D\n\n 13 13 0 0 1 0 999 V2000\n -0.3321 0.5967 0.0000 C 0 0 1 0 0 0\n -1.3928 -0.4639 0.0000 C 0 0 2 0 0 0\n -0.7119 -1.8004 0.0000 C 0 0 1 0 0 0\n 0.7696 -1.5659 0.0000 O 0 0\n 1.0044 -0.0844 0.0000 C 0 0 2 0 0 0\n 2.3408 0.5930 0.0000 C 0 0\n -1.3930 -3.1369 0.0000 R# 0 0\n -0.5694 2.0761 0.0000 O 0 0\n -2.8721 -0.2263 0.0000 O 0 0\n 3.5983 -0.2263 0.0000 O 0 0\n -1.9705 2.6117 0.0000 C 0 0\n 4.9362 0.4518 0.0000 R# 0 0\n -3.4075 1.1749 0.0000 R# 0 0\n 1 2 1 0\n 2 3 1 0\n 3 4 1 0\n 4 5 1 0\n 5 1 1 0\n 5 6 1 1\n 3 7 1 1\n 1 8 1 6\n 2 9 1 6\n 6 10 1 0\n 8 11 1 0\n 10 12 1 0\n 9 13 1 0\nM RGP 3 7 3 12 2 13 1\nM END\n> <Name>\n3-O-Methylribose (2,5 connectivity)\n\n> <MonomerType>\nRNA\n\n> <MonomerName>\n25mo3r\n\n> <MonomerCode>\n.\n\n> <MonomerNaturalAnalogCode>\nR\n\n> <BranchMonomer>\nfalse\n\n> <MonomerCaps>\n[R1]O\n[R2]H\n[R3]O\n\n$$$$\n";
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isReady: null,
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