aldehyde 0.2.32 → 0.2.33

package/dist/bundle.7fe4c9d6d1fad1b785b4.js

@@ -0,0 +1 @@
+"use strict";(self.webpackChunkaldehyde=self.webpackChunkaldehyde||[]).push([[836],{57836:function(n,e,t){t.d(e,{M:function(){return Aw}});var r=t(4942),o=t(85893),i=(t(66337),t(10232),t(35666),t(35449),t(83581),t(15861)),a=t(64687),l=t.n(a),c=t(15671),s=t(43144),u=t(50700),d=t(67294),p=t(45987),h=t(60136),f=t(82963),m=t(61120),v=t(86010),g=t(71002),b=t(1581),C=t.n(b),y=t(78230),O=t(29439),w=t(73935),S=t(28216),M=t(14890),x=t(93433),j=(t(94500),t(53894)),E=t(96486),D=t(8107),A=t.n(D),$=t(70131),N=t(10932),P=t(30168),k=t(6867),I=t(12981),T=t(23926),B=t(76914),L=t(42733),_=t(24345),V=t(25974),z=t(42116),G=t(85518),F=t(84506),H=t(86033),R=t(13092),Z=t(31738),K=t(99622),Y=t(11491),U=t(44347),J=t(55651),q=t(93162),W=t(84474),X=t.n(W),Q=t(48287),nn=t(14265),en=t(97326),tn=t(70917),rn=t(1820),on=t(47425),an=t(85092),ln=t(20573),cn=t(44656),sn=t(62640),un=t(9041),dn=t(23106),pn=t(87462);function hn(n,e){var t=n.createStructService(e),r=t.info();return Object.assign(r,{info:t.info.bind(t),convert:t.convert.bind(t),layout:t.layout.bind(t),clean:t.clean.bind(t),aromatize:t.aromatize.bind(t),dearomatize:t.dearomatize.bind(t),calculateCip:t.calculateCip.bind(t),automap:t.automap.bind(t),check:t.check.bind(t),calculate:t.calculate.bind(t),recognize:t.recognize.bind(t),generateImageAsBase64:t.generateImageAsBase64.bind(t),generateInchIKey:t.generateInchIKey.bind(t)})}var fn=d.createContext({}),mn=d.createContext({}),vn=d.createContext({}),gn=d.createContext(null),bn=["H","C","N","O","S","P","F","Cl","Br","I"],Cn={H:"h",C:"c",N:"n",O:"o",S:"s",P:"p",F:"f",Cl:"Shift+c",Br:"b",I:"i",A:"a",Q:"q",R:"r",K:"k",M:"m",Si:"Shift+s",Na:"Shift+n",X:"x",D:"d",B:"Shift+b"},yn=Object.keys(Cn).reduce((function(n,e){return n["atom-".concat(e.toLowerCase())]={title:"Atom ".concat(e),shortcut:Cn[e],action:{tool:"atom",opts:{label:e}}},n}),{});function On(n){var e,r=t.g.currentState.editor,o=r.structSelected(),i=r.errorHandler;try{if(e="mol"===n?new u.jWx:new u.F_l,Boolean(o.simpleObjects.size||o.texts.size)&&e instanceof u.jWx)return i("This feature is not available for Simple objects and Text objects"),null;var a=e.serialize(o);window.clipboardData?window.clipboardData.setData("text",a):navigator.clipboard.writeText(a)}catch(n){i("This feature is not available in your browser")}}function wn(){return wn=(0,i.Z)(l().mark((function n(){var e,o,i,a,c,s,d,p,h,f,m,v;return l().wrap((function(n){for(;;)switch(n.prev=n.next){case 0:return e=t.g.currentState,o=e.editor,i=e.server,a=e.options,c=o.structSelected(),s=o.errorHandler,n.prev=6,d=new u.Yyn(i),p=d.create("ket",a),n.next=11,p.getStructureFromStructAsync(c);case 11:return h=n.sent,f=new u.VA(o,i,{},d),n.next=15,f.generateImage(h,{outputFormat:"png",backgroundColor:"255, 255, 255"});case 15:return m=n.sent,v=new ClipboardItem((0,r.Z)({},m.type,m)),n.next=19,navigator.clipboard.write([v]);case 19:n.next=24;break;case 21:n.prev=21,n.t0=n.catch(6),s("This feature is not available in your browser");case 24:case"end":return n.stop()}}),n,null,[[6,21]])}))),wn.apply(this,arguments)}function Sn(n,e){var t,r;return Boolean(null===(t=n.buttons)||void 0===t||null===(r=t[e])||void 0===r?void 0:r.hidden)}var Mn={"force-update":{shortcut:"Ctrl+Shift+r",action:function(n){n.update(!0)},hidden:function(n){return Sn(n,"force-update")}},"qs-serialize":{shortcut:"Alt+Shift+r",action:function(n){var e=(new u.jWx).serialize(n.struct()),t="mol="+encodeURIComponent(e).replace(/%20/g,"+"),r=document.location.search;document.location.search=r?-1===r.search("mol=")?r+"&"+t:r.replace(/mol=[^&$]*/,t):"?"+t}},hidden:function(n){return Sn(n,"qs-serialize")}};var xn=window.clipboardData,jn=function(n){(0,h.Z)(i,n);var e,t,r=(e=i,t=function(){if("undefined"==typeof Reflect||!Reflect.construct)return!1;if(Reflect.construct.sham)return!1;if("function"==typeof Proxy)return!0;try{return Boolean.prototype.valueOf.call(Reflect.construct(Boolean,[],(function(){}))),!0}catch(n){return!1}}(),function(){var n,r=(0,m.Z)(e);if(t){var o=(0,m.Z)(this).constructor;n=Reflect.construct(r,arguments,o)}else n=r.apply(this,arguments);return(0,f.Z)(this,n)});function i(n){var e;return(0,c.Z)(this,i),(e=r.call(this,n)).textAreaRef=(0,d.createRef)(),e}return(0,s.Z)(i,[{key:"componentDidMount",value:function(){var n=this,e=this.textAreaRef.current;this.target=this.props.target||e.parentNode,this.listeners={mouseup:function(t){var r;(e===t.target||!En(t.target)&&n.props.focused())&&((r=e).value=" ",r.select())},mousedown:function(n){n.shiftKey&&!En(n.target)&&n.preventDefault()},copy:function(e){if(n.props.focused()&&n.props.onCopy){var t=n.props.onCopy();t&&Dn(e.clipboardData,t),e.preventDefault()}},cut:function(e){if(n.props.focused()&&n.props.onCut){var t=n.props.onCut();t&&Dn(e.clipboardData,t),e.preventDefault()}},paste:function(e){if(n.props.focused()&&n.props.onPaste){var t=function(n,e){var t={};return!n&&xn?t["text/plain"]=xn.getData("text"):(t["text/plain"]=n.getData("text/plain"),t=e.reduce((function(e,t){var r=n.getData(t);return r&&(e[t]=r),e}),t)),t}(e.clipboardData,n.props.formats);t&&n.props.onPaste(t),e.preventDefault()}}},Object.keys(this.listeners).forEach((function(e){n.target.addEventListener(e,n.listeners[e])}))}},{key:"shouldComponentUpdate",value:function(){return!1}},{key:"componentWillUnmount",value:function(){var n=this;Object.keys(this.listeners).forEach((function(e){n.target.removeEventListener(e,n.listeners[e])}))}},{key:"render",value:function(){return(0,o.jsx)("textarea",{ref:this.textAreaRef,className:(0,v.Z)("cliparea","cliparea-module_cliparea__GdPrN"),contentEditable:!0,autoFocus:!0,suppressContentEditableWarning:!0})}}]),i}(d.Component);function En(n){return("INPUT"!==n.tagName||"button"!==n.type)&&["INPUT","SELECT","TEXTAREA","OPTION","LABEL"].includes(n.tagName)}function Dn(n,e){if(!n&&xn)xn.setData("text",e["text/plain"]);else{n.setData("text/plain",e["text/plain"]);try{Object.keys(e).forEach((function(t){n.setData(t,e[t])}))}catch(n){}}}var An=["cut","copy","paste"];function $n(n){var e=document.queryCommandSupported(n);if(e)try{e=document.execCommand(n)||window.ClipboardEvent||xn}catch(n){e=!1}return e}function Nn(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Pn(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Nn(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Nn(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var kn={showValenceWarnings:{title:"Show valence warnings",type:"boolean",description:"slider",default:!0},atomColoring:{title:"Atom coloring",type:"boolean",description:"slider",default:!0},showStereoFlags:{title:"Show the Stereo flags",type:"boolean",description:"slider",default:!0},stereoLabelStyle:{title:"Label display at stereogenic centers",enum:[u.xKj.IUPAC,u.xKj.Classic,u.xKj.On,u.xKj.Off],enumNames:["IUPAC style","Classic","On","Off"],default:u.xKj.IUPAC},colorOfAbsoluteCenters:{title:" Absolute Center color",type:"string",default:"#ff0000"},colorOfAndCenters:{title:"AND Centers color",type:"string",default:"#0000cd"},colorOfOrCenters:{title:"OR Centers color",type:"string",default:"#228b22"},colorStereogenicCenters:{title:"Color stereogenic centers",enum:[u.SZr.LabelsOnly,u.SZr.BondsOnly,u.SZr.LabelsAndBonds,u.SZr.Off],enumNames:["Labels Only","Bonds Only","Labels And Bonds","Off"],default:u.SZr.LabelsOnly},autoFadeOfStereoLabels:{title:"Auto fade And/Or center labels",type:"boolean",description:"slider",default:!0},absFlagLabel:{title:"Text of Absolute flag",type:"string",default:"ABS (Chiral)"},andFlagLabel:{title:"Text of AND flag",type:"string",default:"AND Enantiomer"},mixedFlagLabel:{title:"Text of Mixed flag",type:"string",default:"Mixed"},orFlagLabel:{title:"Text of OR flag",type:"string",default:"OR Enantiomer"},font:{title:"Font",type:"string",default:"30px Arial"},fontsz:{title:"Font size",type:"integer",default:13,minimum:1,maximum:96},fontszsub:{title:"Sub font size",type:"integer",default:13,minimum:1,maximum:96},carbonExplicitly:{title:"Display carbon explicitly",type:"boolean",description:"slider",default:!1},showCharge:{title:"Display charge",type:"boolean",description:"slider",default:!0},showValence:{title:"Display valence",type:"boolean",description:"slider",default:!0},showHydrogenLabels:{title:"Show hydrogen labels",enum:["off","Hetero","Terminal","Terminal and Hetero","on"],default:"on"},aromaticCircle:{title:"Aromatic Bonds as circle",type:"boolean",description:"slider",default:!0},doubleBondWidth:{title:"Double bond width",type:"integer",default:6,minimum:1,maximum:96},bondThickness:{title:"Bond thickness",type:"integer",default:2,minimum:1,maximum:96},stereoBondWidth:{title:"Stereo (Wedge) bond width",type:"integer",default:6,minimum:1,maximum:96}},In={"dearomatize-on-load":{title:"dearomatize-on-load",type:"boolean",description:"slider",default:!1},"smart-layout":{title:"Smart-layout",type:"boolean",description:"slider",default:!0},"ignore-stereochemistry-errors":{title:"Ignore stereochemistry errors",type:"boolean",description:"slider",default:!0},"mass-skip-error-on-pseudoatoms":{title:"Ignore pseudoatoms at mass",type:"boolean",description:"slider",default:!1},"gross-formula-add-rsites":{title:"Add Rsites at mass calculation",type:"boolean",description:"slider",default:!0},"gross-formula-add-isotopes":{title:"Add Isotopes at mass calculation",type:"boolean",description:"slider",default:!0}},Tn=Object.keys(In),Bn={miewMode:{title:"Display mode",enum:["LN","BS","LC"],enumNames:["Lines","Balls and Sticks","Licorice"],default:"LN"},miewTheme:{title:"Background color",enum:["light","dark"],enumNames:["Light","Dark"],default:"light"},miewAtomLabel:{title:"Label coloring",enum:["no","bright","blackAndWhite","black"],enumNames:["No","Bright","Black and White","Black"],default:"bright"}},Ln=Object.keys(Bn),_n={title:"Settings",type:"object",required:[],properties:Pn(Pn(Pn(Pn(Pn({},{resetToSelect:{title:"Reset to Select Tool",enum:[!0,"paste",!1],enumNames:["on","After Paste","off"],default:"paste"},rotationStep:{title:"Rotation Step, º",type:"integer",minimum:1,maximum:90,default:15}}),kn),In),{showAtomIds:{title:"Show atom Ids",type:"boolean",description:"slider",default:!1},showBondIds:{title:"Show bonds Ids",type:"boolean",description:"slider",default:!1},showHalfBondIds:{title:"Show half bonds Ids",type:"boolean",description:"slider",default:!1},showLoopIds:{title:"Show loop Ids",type:"boolean",description:"slider",default:!1}}),Bn)};function Vn(){return _n.properties?Object.keys(_n.properties).reduce((function(n,e){return n[e]=_n.properties[e].default,n}),{}):{}}var zn={warningMessage:"Your changes will be lost after the tab closing. See Help (Note 2).",isAvailable:function(){try{return t.g.localStorage}catch(n){return!1}},getItem:function(n){var e=null;try{e=JSON.parse(localStorage.getItem(n))}catch(n){}return e},setItem:function(n,e){var t=null;try{localStorage.setItem(n,JSON.stringify(e)),t=!0}catch(n){t=!1}return t}};function Gn(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Fn(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Gn(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Gn(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Hn={app:{server:!1,templates:!1,functionalGroups:!1,saltsAndSolvents:!1},analyse:{values:null,roundWeight:3,roundMass:3,roundElAnalysis:1},check:{checkOptions:["valence","radicals","pseudoatoms","stereo","query","overlapping_atoms","overlapping_bonds","rgroups","chiral","3d","chiral_flag"]},recognize:{file:null,structStr:null,fragment:!1,version:null},settings:Object.assign(Vn(),function(n){if("object"!==(0,g.Z)(n)||null===n)return null;var e=new(C())({allErrors:!0,keywords:[{keyword:"enumNames",schemaType:"array"}]}).compile(_n);e(n);var t=(e.errors||[]).map((function(n){return n.instancePath.slice(1)}));return Object.keys(n).reduce((function(e,r){return _n.properties?(_n.properties[r]&&-1===t.indexOf(r)&&(e[r]=n[r]),e):e}),{})}(zn.getItem("ketcher-opts"))),getServerSettings:function(){return(0,y.pick)(Tn,this.settings)}};function Rn(n){return function(e){e({type:"APP_OPTIONS",data:n}),e({type:"UPDATE"})}}var Zn=["SET_RECOGNIZE_STRUCT","CHANGE_RECOGNIZE_FILE","CHANGE_IMAGO_VERSION","IS_FRAGMENT_RECOGNIZE"];function Kn(n){return{type:"SET_RECOGNIZE_STRUCT",data:{structStr:n}}}function Yn(n){return{type:"CHANGE_RECOGNIZE_FILE",data:{file:n,structStr:null}}}function Un(n,e){return n.oneOf.reduce((function(n,t){return n[function(n,e){var t=n.properties[e];return t.constant||t.enum[0]}(t,e)]=t,n}),{})}var Jn={enum:["Absolute","Relative","Attached"],default:"Absolute"},qn={title:"Context",enum:["Fragment","Multifragment","Bond","Atom","Group"],default:"Fragment"},Wn={Fragment:{title:"Fragment",type:"Object",oneOf:[{key:"FRG_STR",title:"MDLBG_FRAGMENT_STEREO",type:"object",properties:{type:{enum:["DAT"]},fieldName:{title:"Field name",enum:["MDLBG_FRAGMENT_STEREO"],default:"MDLBG_FRAGMENT_STEREO"},fieldValue:{title:"Field value",enum:["abs","(+)-enantiomer","(-)-enantiomer","racemate","steric","rel","R(a)","S(a)","R(p)","S(p)"],default:"abs"},radiobuttons:Jn},required:["fieldName","fieldValue","radiobuttons"]},{key:"FRG_COEFF",title:"MDLBG_FRAGMENT_COEFFICIENT",type:"object",properties:{type:{enum:["DAT"]},fieldName:{title:"Field name",enum:["MDLBG_FRAGMENT_COEFFICIENT"],default:"MDLBG_FRAGMENT_COEFFICIENT"},fieldValue:{title:"Field value",type:"string",default:"",minLength:1,invalidMessage:"Please, specify field value"},radiobuttons:Jn},required:["fieldName","fieldValue","radiobuttons"]},{key:"FRG_CHRG",title:"MDLBG_FRAGMENT_CHARGE",type:"object",properties:{type:{enum:["DAT"]},fieldName:{title:"Field name",enum:["MDLBG_FRAGMENT_CHARGE"],default:"MDLBG_FRAGMENT_CHARGE"},fieldValue:{title:"Field value",type:"string",default:"",minLength:1,invalidMessage:"Please, specify field value"},radiobuttons:Jn},required:["fieldName","fieldValue","radiobuttons"]},{key:"FRG_RAD",title:"MDLBG_FRAGMENT_RADICALS",type:"object",properties:{type:{enum:["DAT"]},fieldName:{title:"Field name",enum:["MDLBG_FRAGMENT_RADICALS"],default:"MDLBG_FRAGMENT_RADICALS"},fieldValue:{title:"Field value",type:"string",default:"",minLength:1,invalidMessage:"Please, specify field value"},radiobuttons:Jn},required:["fieldName","fieldValue","radiobuttons"]}]},Multifragment:{title:"Multifragment",type:"Object",oneOf:[{key:"MLT_FRG",title:"KETCHER_MULTIPLE_FRAGMENT",type:"object",properties:{type:{enum:["DAT"]},fieldName:{title:"Field name",enum:["KETCHER_MULTIPLE_FRAGMENT"],default:"KETCHER_MULTIPLE_FRAGMENT"},fieldValue:{title:"Field value",enum:["aerosol","alloy","catenane","complex","composite","co-polymer","emulsion","host-guest complex","mixture","rotaxane","suspension"],default:"aerosol"},radiobuttons:Jn},required:["fieldName","fieldValue","radiobuttons"]}]},Bond:{title:"Bond",type:"Object",oneOf:[{key:"SB_STR",title:"MDLBG_STEREO_KEY",type:"object",properties:{type:{enum:["DAT"]},fieldName:{title:"Field name",enum:["MDLBG_STEREO_KEY"],default:"MDLBG_STEREO_KEY"},fieldValue:{title:"Field value",enum:["erythro","threo","alpha","beta","endo","exo","anti","syn","ECL","STG"],default:"erythro"},radiobuttons:Jn},required:["fieldName","fieldValue","radiobuttons"]},{key:"SB_BND",title:"MDLBG_BOND_KEY",type:"object",properties:{type:{enum:["DAT"]},fieldName:{title:"Field name",enum:["MDLBG_BOND_KEY"],default:"MDLBG_BOND_KEY"},fieldValue:{title:"Field value",enum:["Value=4"],default:"Value=4"},radiobuttons:Jn},required:["fieldName","fieldValue","radiobuttons"]}]},Atom:{title:"Atom",type:"Object",oneOf:[{key:"AT_STR",title:"MDLBG_STEREO_KEY",type:"object",properties:{type:{enum:["DAT"]},fieldName:{title:"Field name",enum:["MDLBG_STEREO_KEY"],default:"MDLBG_STEREO_KEY"},fieldValue:{title:"Field value",enum:["RS","SR","P-3","P-3-PI","SP-4","SP-4-PI","T-4","T-4-PI","SP-5","SP-5-PI","TB-5","TB-5-PI","OC-6","TP-6","PB-7","CU-8","SA-8","DD-8","HB-9","TPS-9"],default:"RS"},radiobuttons:Jn},required:["fieldName","fieldValue","radiobuttons"]}]},Group:{title:"Group",type:"Object",oneOf:[{key:"GRP_STR",title:"MDLBG_STEREO_KEY",type:"object",properties:{type:{enum:["DAT"]},fieldName:{title:"Field name",enum:["MDLBG_STEREO_KEY"],default:"MDLBG_STEREO_KEY"},fieldValue:{title:"Field value",enum:["cis","trans"],default:"cis"},radiobuttons:Jn},required:["fieldName","fieldValue","radiobuttons"]}]}},Xn={key:"Custom",type:"object",properties:{type:{enum:["DAT"]},context:{title:"Context",enum:["Atom","Bond","Fragment","Group","Multifragment"],default:"Fragment"},fieldName:{title:"Field name",type:"string",default:"",minLength:1,invalidMessage:"Please, specify field name"},fieldValue:{title:"Field value",type:"string",default:"",minLength:1,invalidMessage:"Please, specify field value"},radiobuttons:{enum:["Absolute","Relative","Attached"],default:"Absolute"}},required:["context","fieldName","fieldValue","radiobuttons"]},Qn=Object.keys(Wn).reduce((function(n,e){return n[e]=Un(Wn[e],"fieldName"),Object.keys(n[e]).forEach((function(t){n[e][t].properties.context=qn})),n}),{});function ne(n){return Object.keys(n)[0]}function ee(){var n,e=arguments.length>0&&void 0!==arguments[0]?arguments[0]:Qn,t=arguments.length>1?arguments[1]:void 0,r=arguments.length>2?arguments[2]:void 0;return"Custom"===e.key?null===(n=e.properties[t])||void 0===n?void 0:n.default:t||r?r?e[t][r]?e[t][r].properties.fieldValue.default:"":ne(e[t]):ne(e)}function te(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function re(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?te(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):te(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var oe,ie,ae,le,ce=function(n,e){var t=e.valid,r=e.errors,o=n.result,i=o.fieldName,a=o.fieldValue;return{result:n.result,valid:t&&!!i&&!!a,errors:r}},se={atomProps:{errors:{},valid:!0,result:{label:"",charge:0,explicitValence:-1,hCount:0,invRet:0,isotope:0,radical:0,ringBondCount:0,substitutionCount:0}},attachmentPoints:{errors:{},valid:!0,result:{primary:!1,secondary:!1}},automap:{errors:{},valid:!0,result:{mode:"discard"}},bondProps:{errors:{},valid:!0,result:{type:"single",topology:0,center:0}},check:{errors:{},moleculeErrors:{}},labelEdit:{errors:{},valid:!0,result:{label:""}},rgroup:{errors:{},valid:!0,result:{values:[]}},rgroupLogic:{errors:{},valid:!0,result:{ifthen:0,range:">0",resth:!1}},save:{errors:{},valid:!0,result:{filename:"ketcher",format:"mol"}},settings:{errors:{},valid:!0,result:Vn()},sgroup:{errors:{},valid:!0,result:{type:"GEN"}},text:{errors:{},valid:!0,result:{}},attach:{errors:{},valid:!0,result:{}},sdata:(oe=Xn,ie="Custom"===oe.key,ae=ie?ee(Xn,"context"):ee(Qn),le=ie?ee(Xn,"fieldName"):ee(Qn,ae),{errors:{},valid:!0,result:{context:ae,fieldName:le,fieldValue:ie?ee(Xn,"fieldValue"):ee(Qn,ae,le),radiobuttons:"Absolute",type:"DAT"}})};function ue(n){return{type:"UPDATE_FORM",data:n}}function de(n,e,t){return"sdata"===t?function(n,e){if(e.data.result.init)return ce(re(re({},n),{},{result:Object.assign({},n.result,e.data.result)}),e.data);var t=e.data.result.context,r=e.data.result.fieldName,o=null;return t!==n.result.context?o=function(n,e){var t=e.context,r=e.fieldValue,o=ee(Xn,"fieldName"),i=r;return i===n.result.fieldValue&&(i=ee(Xn,"fieldValue")),{result:re(re({},e),{},{context:t,fieldName:o,fieldValue:i})}}(n,e.data.result):r!==n.result.fieldName&&(o=function(n,e){var t=e.fieldName,r=n.result.context,o=e.fieldValue;return Qn[r][t]&&(o=ee(Qn,r,t)),o===n.result.fieldValue&&Qn[r][n.result.fieldName]&&(o=""),{result:re(re({},e),{},{fieldName:t,fieldValue:o})}}(n,e.data.result)),o=o||re(re({},n),{},{result:Object.assign({},n.result,e.data.result)}),ce(o,e.data)}(n,e):Object.assign({},n,e.data)}var pe="INDIGO_VERIFICATION",he="ANALYZING_FILE";function fe(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function me(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?fe(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):fe(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function ve(n){return{type:pe,data:n}}function ge(n){return{type:he,data:n}}var be={indigoVerification:!1,isAnalyzingFile:!1},Ce={MUL:"MUL",SRU:"SRU",SUP:"SUP",DAT:"DAT",GEN:"GEN"},ye={title:"Atom",type:"object",required:["label"],properties:{label:{title:"Label",type:"string",maxLength:3,invalidMessage:"Wrong label"},alias:{title:"Alias",type:"string",invalidMessage:"Leading and trailing spaces are not allowed"},charge:{title:"Charge",type:"string",pattern:"^([+-]?)([0-9]{1,3}|1000)([+-]?)$",maxLength:5,default:"0",invalidMessage:"Invalid charge value"},explicitValence:{title:"Valence",enum:[-1,0,1,2,3,4,5,6,7,8],enumNames:["","0","I","II","III","IV","V","VI","VII","VIII"],default:-1},isotope:{title:"Isotope",type:"integer",minimum:0,default:0,invalidMessage:"There must be integer"},radical:{title:"Radical",enum:[0,2,1,3],enumNames:["","Monoradical","Diradical (singlet)","Diradical (triplet)"],default:0},ringBondCount:{title:"Ring bond count",enum:[0,-2,-1,2,3,4],enumNames:["","As drawn","0","2","3","4"],default:0},hCount:{title:"H count",enum:[0,1,2,3,4,5],enumNames:["","0","1","2","3","4"],default:0},substitutionCount:{title:"Substitution count",enum:[0,-2,-1,1,2,3,4,5,6],enumNames:["","As drawn","0","1","2","3","4","5","6"],default:0},unsaturatedAtom:{title:"Unsaturated",type:"boolean",default:!1},invRet:{title:"Inversion",enum:[0,1,2],enumNames:["","Inverts","Retains"],default:0},exactChangeFlag:{title:"Exact change",type:"boolean",default:!1}}},Oe={title:"R-group",type:"object",properties:{values:{type:"array",items:{type:"string",enum:(0,y.range)(1,33),enumNames:(0,y.range)(1,33).map((function(n){return"R"+n}))}}}},we={title:"Label Edit",type:"object",required:["label"],properties:{label:{title:"Atom",default:"",invalidMessage:"Wrong atom symbol",type:"string"}}},Se={title:"Attachment Points",type:"object",properties:{primary:{title:"Primary attachment point",type:"boolean"},secondary:{title:"Secondary attachment point",type:"boolean"}}},Me={title:"Bond",type:"object",required:["type"],properties:{type:{title:"Type",enum:["single","up","down","updown","double","crossed","triple","aromatic","any","hydrogen","singledouble","singlearomatic","doublearomatic","dative"],enumNames:["Single","Single Up","Single Down","Single Up/Down","Double","Double Cis/Trans","Triple","Aromatic","Any","Hydrogen","Single/Double","Single/Aromatic","Double/Aromatic","Dative"],default:"single"},topology:{title:"Topology",enum:[0,1,2],enumNames:["Either","Ring","Chain"],default:0},center:{title:"Reacting Center",enum:[0,-1,1,2,4,8,12],enumNames:["Unmarked","Not center","Center","No change","Made/broken","Order changes","Made/broken and changes"],default:0}}},xe=Un({title:"SGroup",type:"object",required:["type"],oneOf:[{key:"GEN",title:"Generic",type:"object",properties:{type:{enum:["GEN"]}}},{key:"MUL",title:"Multiple group",type:"object",properties:{type:{enum:["MUL"]},mul:{title:"Repeat count",type:"integer",default:1,minimum:1}},required:["mul"]},{key:"SRU",title:"SRU polymer",type:"object",properties:{type:{enum:["SRU"]},subscript:{title:"Polymer label",type:"string",default:"n",pattern:"^[a-zA-Z]$",invalidMessage:"SRU subscript should consist of a single letter"},connectivity:{title:"Repeat Pattern",enum:["ht","hh","eu"],enumNames:["Head-to-tail","Head-to-head","Either unknown"],default:"ht"}},required:["subscript","connectivity"]},{key:"SUP",title:"Superatom",type:"object",properties:{type:{enum:["SUP"]},name:{title:"Name",type:"string",default:"",minLength:1,invalidMessage:"Please, provide a name for the superatom"}},required:["name"]}]},"type"),je={title:"R-Group",type:"object",properties:{range:{title:"Occurrence",type:"string",maxLength:50,invalidMessage:"Wrong value"},resth:{title:"RestH",type:"boolean"},ifthen:{title:"Condition",type:"integer",minium:0}}},Ee={title:"Template edit",type:"object",required:["name"],properties:{name:{title:"Molecule name",type:"string",minLength:1,maxLength:128,invalidMessage:"Template must have a unique name and no more than 128 symbols in length"}}},De=["type","radiobuttons"];function Ae(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function $e(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Ae(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Ae(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function Ne(n){return"R#"===n.label?$e({type:"rlabel",values:Ie(n.rglabel)},n):"L#"===n.label?{type:(e=n).atomList.notList?"not-list":"list",values:e.atomList.ids.map((function(n){return u.eKO.get(n).label}))}:u.eKO.get(n.label)?function(n){var e=n.alias||"",t=n.charge.toString();return{alias:e,label:n.label,charge:t,isotope:n.isotope,explicitValence:n.explicitValence,radical:n.radical,invRet:n.invRet,exactChangeFlag:!!n.exactChangeFlag,ringBondCount:n.ringBondCount,substitutionCount:n.substitutionCount,unsaturatedAtom:!!n.unsaturatedAtom,hCount:n.hCount,stereoParity:n.stereoParity}}(n):!n.label&&"attpnt"in n?{ap:(t=n.attpnt,{primary:(1&(t||0))>0,secondary:(2&(t||0))>0})}:n;var e,t}function Pe(n){return"rlabel"===n.type?{label:n.values.length?"R#":"C",rglabel:0===n.values.length?null:(e=n.values,t=0,e.forEach((function(n){t|=1<<n-1})),t)}:"list"===n.type||"not-list"===n.type?function(n){return{pseudo:null,label:"L#",atomList:new u.Ilx({notList:"not-list"===n.type,ids:n.values.map((function(n){return u.eKO.get(n).number}))})}}(n):!n.label&&"ap"in n?{attpnt:(r=n.ap,(r.primary&&1)+(r.secondary&&2))}:u.eKO.get((0,y.capitalize)(n.label))?ke(n):"A"===n.label||"*"===n.label||"Q"===n.label||"X"===n.label||"R"===n.label?(n.pseudo=n.label,ke(n)):n;var e,t,r}function ke(n){var e,t,r=new RegExp(ye.properties.charge.pattern).exec(n.charge),o=r?parseInt(r[1]+r[3]+r[2]):n.charge,i=Object.assign({},n,{label:(0,y.capitalize)(n.label),alias:n.alias||null,exactChangeFlag:+(null!==(e=n.exactChangeFlag)&&void 0!==e&&e),unsaturatedAtom:+(null!==(t=n.unsaturatedAtom)&&void 0!==t&&t)});return void 0!==o&&(i.charge=o),i}function Ie(n){var e,t,r=[];for(e=0;e<32;e++)n&1<<e&&(t=e+1,r.push(t));return r}function Te(n){return $e({topology:n.topology,reactingCenterStatus:n.center},Be(n.type))}function Be(n){return Object.assign({},_e[n])}function Le(n,e){for(var t in _e)if(_e[t].type===n&&_e[t].stereo===e)return t;throw Error("No such bond caption")}var _e={single:{type:u.fYe.PATTERN.TYPE.SINGLE,stereo:u.fYe.PATTERN.STEREO.NONE},up:{type:u.fYe.PATTERN.TYPE.SINGLE,stereo:u.fYe.PATTERN.STEREO.UP},down:{type:u.fYe.PATTERN.TYPE.SINGLE,stereo:u.fYe.PATTERN.STEREO.DOWN},updown:{type:u.fYe.PATTERN.TYPE.SINGLE,stereo:u.fYe.PATTERN.STEREO.EITHER},double:{type:u.fYe.PATTERN.TYPE.DOUBLE,stereo:u.fYe.PATTERN.STEREO.NONE},crossed:{type:u.fYe.PATTERN.TYPE.DOUBLE,stereo:u.fYe.PATTERN.STEREO.CIS_TRANS},triple:{type:u.fYe.PATTERN.TYPE.TRIPLE,stereo:u.fYe.PATTERN.STEREO.NONE},aromatic:{type:u.fYe.PATTERN.TYPE.AROMATIC,stereo:u.fYe.PATTERN.STEREO.NONE},singledouble:{type:u.fYe.PATTERN.TYPE.SINGLE_OR_DOUBLE,stereo:u.fYe.PATTERN.STEREO.NONE},singlearomatic:{type:u.fYe.PATTERN.TYPE.SINGLE_OR_AROMATIC,stereo:u.fYe.PATTERN.STEREO.NONE},doublearomatic:{type:u.fYe.PATTERN.TYPE.DOUBLE_OR_AROMATIC,stereo:u.fYe.PATTERN.STEREO.NONE},any:{type:u.fYe.PATTERN.TYPE.ANY,stereo:u.fYe.PATTERN.STEREO.NONE},hydrogen:{type:u.fYe.PATTERN.TYPE.HYDROGEN,stereo:u.fYe.PATTERN.STEREO.NONE},dative:{type:u.fYe.PATTERN.TYPE.DATIVE,stereo:u.fYe.PATTERN.STEREO.NONE}};function Ve(n){var e=n.type||"GEN",t=n.attrs,r=t.context,o=t.fieldName,i=t.fieldValue,a=t.absolute,l=t.attached;return n.attrs.radiobuttons=!1===a&&!1===l?"Relative":l?"Attached":"Absolute",Qn[r][o]&&Qn[r][o].properties.fieldValue.items&&(n.attrs.fieldValue=i.split("\n")),Object.assign({type:e},n.attrs)}function ze(n){var e=n.type,t=n.radiobuttons,r=$e({},(0,p.Z)(n,De)),o="absolute",i="attached";switch(t){case"Absolute":r[o]=!0,r[i]=!1;break;case"Attached":r[o]=!1,r[i]=!0;break;case"Relative":r[o]=!1,r[i]=!1}return r.fieldName&&(r.fieldName=r.fieldName.trim()),r.fieldValue&&(r.fieldValue="string"==typeof r.fieldValue?r.fieldValue.trim():r.fieldValue),{type:e,attrs:r}}var Ge={hand:{title:"Hand tool",shortcut:"Mod+Alt+h",action:{tool:"hand"},hidden:function(n){return Sn(n,"hand")}},"select-lasso":{title:"Lasso Selection",shortcut:"Escape",action:{tool:"select",opts:"lasso"}},"select-rectangle":{title:"Rectangle Selection",shortcut:"Escape",action:{tool:"select",opts:"rectangle"},hidden:function(n){return Sn(n,"select-rectangle")}},"select-fragment":{title:"Fragment Selection",shortcut:"Escape",action:{tool:"select",opts:"fragment"},hidden:function(n){return Sn(n,"select-fragment")}},erase:{title:"Erase",shortcut:["Delete","Backspace"],action:{tool:"eraser",opts:1},hidden:function(n){return Sn(n,"erase")}},chain:{title:"Chain",action:{tool:"chain"},hidden:function(n){return Sn(n,"chain")}},"enhanced-stereo":{shortcut:"Alt+e",title:"Stereochemistry",action:{tool:"enhancedStereo"},disabled:function(n){return 0===(0,u.f0f)(null==n?void 0:n.struct(),Array.from(null==n?void 0:n.struct().atoms.keys())).length},hidden:function(n){return Sn(n,"enhanced-stereo")}},"charge-plus":{shortcut:"5",title:"Charge Plus",action:{tool:"charge",opts:1},hidden:function(n){return Sn(n,"charge-plus")}},"charge-minus":{shortcut:"5",title:"Charge Minus",action:{tool:"charge",opts:-1},hidden:function(n){return Sn(n,"charge-minus")}},transforms:{hidden:function(n){return Sn(n,"transforms")}},"transform-rotate":{shortcut:"Alt+r",title:"Rotate Tool",action:{tool:"rotate"},hidden:function(n){return Sn(n,"transform-rotate")}},"transform-flip-h":{shortcut:"Alt+h",title:"Horizontal Flip",action:{tool:"rotate",opts:"horizontal"},hidden:function(n){return Sn(n,"transform-flip-h")}},"transform-flip-v":{shortcut:"Alt+v",title:"Vertical Flip",action:{tool:"rotate",opts:"vertical"},hidden:function(n){return Sn(n,"transform-flip-v")}},sgroup:{shortcut:"Mod+g",title:"S-Group",action:{tool:"sgroup"},hidden:function(n){return Sn(n,"sgroup")}},"sgroup-data":{shortcut:"Mod+g",title:"Data S-Group",action:{tool:"sgroup",opts:"DAT"},hidden:function(n){return Sn(n,"sgroup-data")}},arrows:{hidden:function(n){return Sn(n,"arrows")}},"reaction-arrow-open-angle":{title:"Arrow Open Angle Tool",action:{tool:"reactionarrow",opts:u.mWk.OpenAngle},hidden:function(n){return Sn(n,"reaction-arrow-open-angle")}},"reaction-arrow-filled-triangle":{title:"Arrow Filled Triangle",action:{tool:"reactionarrow",opts:u.mWk.FilledTriangle},hidden:function(n){return Sn(n,"reaction-arrow-filled-triangle")}},"reaction-arrow-filled-bow":{title:"Arrow Filled Bow Tool",action:{tool:"reactionarrow",opts:u.mWk.FilledBow},hidden:function(n){return Sn(n,"reaction-arrow-filled-bow")}},"reaction-arrow-dashed-open-angle":{title:"Arrow Dashed Open Angle Tool",action:{tool:"reactionarrow",opts:u.mWk.DashedOpenAngle},hidden:function(n){return Sn(n,"reaction-arrow-dashed-open-angle")}},"reaction-arrow-failed":{title:"Failed Arrow Tool",action:{tool:"reactionarrow",opts:u.mWk.Failed},hidden:function(n){return Sn(n,"reaction-arrow-failed")}},"reaction-arrow-both-ends-filled-triangle":{title:"Arrow Both Ends Filled Triangle Tool",action:{tool:"reactionarrow",opts:u.mWk.BothEndsFilledTriangle},hidden:function(n){return Sn(n,"reaction-arrow-both-ends-filled-triangle")}},"reaction-arrow-equilibrium-filled-half-bow":{title:"Arrow Equilibrium Filled Half Bow Tool",action:{tool:"reactionarrow",opts:u.mWk.EquilibriumFilledHalfBow},hidden:function(n){return Sn(n,"reaction-arrow-equilibrium-filled-half-bow")}},"reaction-arrow-equilibrium-filled-triangle":{title:"Arrow Equilibrium Filled Triangle Tool",action:{tool:"reactionarrow",opts:u.mWk.EquilibriumFilledTriangle},hidden:function(n){return Sn(n,"reaction-arrow-equilibrium-filled-triangle")}},"reaction-arrow-equilibrium-open-angle":{title:"Arrow Equilibrium Open Angle Tool",action:{tool:"reactionarrow",opts:u.mWk.EquilibriumOpenAngle},hidden:function(n){return Sn(n,"reaction-arrow-equilibrium-open-angle")}},"reaction-arrow-unbalanced-equilibrium-filled-half-bow":{title:"Arrow Unbalanced Equilibrium Filled Half Bow Tool",action:{tool:"reactionarrow",opts:u.mWk.UnbalancedEquilibriumFilledHalfBow},hidden:function(n){return Sn(n,"reaction-arrow-unbalanced-equilibrium-filled-half-bow")}},"reaction-arrow-unbalanced-equilibrium-open-half-angle":{title:"Arrow Unbalanced Equilibrium Open Half Angle Tool",action:{tool:"reactionarrow",opts:u.mWk.UnbalancedEquilibriumOpenHalfAngle},hidden:function(n){return Sn(n,"reaction-arrow-unbalanced-equilibrium-open-half-angle")}},"reaction-arrow-unbalanced-equilibrium-large-filled-half-bow":{title:"Arrow Unbalanced Equilibrium Large Filled Half Bow Tool",action:{tool:"reactionarrow",opts:u.mWk.UnbalancedEquilibriumLargeFilledHalfBow},hidden:function(n){return Sn(n,"reaction-arrow-unbalanced-equilibrium-large-filled-half-bow")}},"reaction-arrow-unbalanced-equilibrium-filled-half-triangle":{title:"Arrow Unbalanced Equilibrium Filled Half Triangle Tool",action:{tool:"reactionarrow",opts:u.mWk.UnbalancedEquilibriumFilledHalfTriangle},hidden:function(n){return Sn(n,"reaction-arrow-unbalanced-equilibrium-filled-half-triangle")}},"reaction-arrow-elliptical-arc-arrow-filled-bow":{title:"Arrow Elliptical Arc Filled Bow Tool",action:{tool:"reactionarrow",opts:u.mWk.EllipticalArcFilledBow},hidden:function(n){return Sn(n,"reaction-arrow-elliptical-arc-arrow-filled-bow")}},"reaction-arrow-elliptical-arc-arrow-filled-triangle":{title:"Arrow Elliptical Arc Filled Triangle Tool",action:{tool:"reactionarrow",opts:u.mWk.EllipticalArcFilledTriangle},hidden:function(n){return Sn(n,"reaction-arrow-elliptical-arc-arrow-filled-triangle")}},"reaction-arrow-elliptical-arc-arrow-open-angle":{title:"Arrow Elliptical Arc Open Angle Tool",action:{tool:"reactionarrow",opts:u.mWk.EllipticalArcOpenAngle},hidden:function(n){return Sn(n,"reaction-arrow-elliptical-arc-arrow-open-angle")}},"reaction-arrow-elliptical-arc-arrow-open-half-angle":{title:"Arrow Elliptical Arc Open Half Angle Tool",action:{tool:"reactionarrow",opts:u.mWk.EllipticalArcOpenHalfAngle},hidden:function(n){return Sn(n,"reaction-arrow-elliptical-arc-arrow-open-half-angle")}},"reaction-plus":{title:"Reaction Plus Tool",action:{tool:"reactionplus"},hidden:function(n){return Sn(n,"reaction-plus")}},"reaction-mapping-tools":{hidden:function(n){return Sn(n,"reaction-mapping-tools")}},"reaction-map":{title:"Reaction Mapping Tool",action:{tool:"reactionmap"},hidden:function(n){return Sn(n,"reaction-map")}},"reaction-unmap":{title:"Reaction Unmapping Tool",action:{tool:"reactionunmap"},hidden:function(n){return Sn(n,"reaction-unmap")}},rgroup:{hidden:function(n){return Sn(n,"rgroup")}},"rgroup-label":{shortcut:"Mod+r",title:"R-Group Label Tool",action:{tool:"rgroupatom"},hidden:function(n){return Sn(n,"rgroup-label")}},"rgroup-fragment":{shortcut:["Mod+Shift+r","Mod+r"],title:"R-Group Fragment Tool",action:{tool:"rgroupfragment"},hidden:function(n){return Sn(n,"rgroup-fragment")}},"rgroup-attpoints":{shortcut:"Mod+r",title:"Attachment Point Tool",action:{tool:"apoint"},hidden:function(n){return Sn(n,"rgroup-attpoints")}},shapes:{hidden:function(n){return Sn(n,"shapes")}},"shape-ellipse":{title:"Shape Ellipse",action:{tool:"simpleobject",opts:u.gN2.ellipse},hidden:function(n){return Sn(n,"shape-ellipse")}},"shape-rectangle":{title:"Shape Rectangle",action:{tool:"simpleobject",opts:u.gN2.rectangle},hidden:function(n){return Sn(n,"shape-rectangle")}},"shape-line":{title:"Shape Line",action:{tool:"simpleobject",opts:u.gN2.line},hidden:function(n){return Sn(n,"shape-line")}},text:{title:"Add text",action:{tool:"text"},hidden:function(n){return Sn(n,"text")}},bonds:{hidden:function(n){return Sn(n,"bonds")}}},Fe={single:"1",double:"2",triple:"3",up:"1",down:"1",updown:"1",crossed:"2",any:"0",aromatic:"4"},He=Me.properties.type,Re=He.enum.reduce((function(n,e,t){return n["bond-".concat(e)]={title:"".concat(He.enumNames[t]," Bond"),shortcut:Fe[e],action:{tool:"bond",opts:Be(e)},hidden:function(n){return Sn(n,"bond-".concat(e))}},n}),Ge),Ze=["rescale","fragment"];function Ke(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Ye(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Ke(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Ke(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function Ue(n){return n&&n.dialog?{type:"MODAL_OPEN",data:{name:n.dialog,prop:n.prop}}:n&&n.thunk?n.thunk:{type:"ACTION",action:n}}function Je(n,e,t){if("string"==typeof n){var r=t=t||{};r.rescale,r.fragment;var o=(0,p.Z)(r,Ze),i=(0,u.lv1)(n);return i===u.D34.cdx&&(n=n.replace(/\s/g,"")),new u.Yyn(e).create(i,o).getStructureFromStringAsync(n)}return Promise.resolve(n)}function qe(n,e){return t=(0,i.Z)(l().mark((function t(r,o){var i,a,c,s,d,p,h,f;return l().wrap((function(t){for(;;)switch(t.prev=t.next){case 0:return i=o(),a=i.editor,c=i.server,s=a.errorHandler,e=Ye(Ye({},e=e||{}),{},{"dearomatize-on-load":a.options()["dearomatize-on-load"]}),r(ge(!0)),t.prev=7,t.next=10,Je(n,c,e);case 10:if(d=t.sent,p=e.fragment,!d.sgroups.some((function(n){return!Ce[n.type]}))){t.next=17;break}return t.next=16,a.event.confirm.dispatch();case 16:d.sgroups=d.sgroups.filter((function(n,e){return Ce[e.type]}));case 17:d.rescale(),a.struct().atoms.size&&(h=a.struct().clone(),d.sgroups.forEach((function(n,e){var t=u.j1n.getOffset(h.sgroups.get(e)),r=new u.UE_(n.atoms),o=u.j1n.getCrossBonds(d,r);u.j1n.bracketPos(n,d,o),t&&n.updateOffset(t)}))),d.findConnectedComponents(),d.setImplicitHydrogen(),f=(0,u.jnZ)(d,Array.from(d.bonds.values())),d.atoms.forEach((function(n,e){var t;if(0===(null==d||null===(t=d.atomGetNeighbors(e))||void 0===t?void 0:t.length))n.stereoLabel=null,n.stereoParity=0;else{var r=f.get(e);r&&(n.stereoLabel=r.stereoLabel,n.stereoParity=r.stereoParity)}})),d.markFragments(),p?d.isBlank()?r({type:"ACTION",action:Re["select-rectangle"].action}):r(Ue({tool:"paste",opts:d})):a.struct(d),r(ge(!1)),r({type:"MODAL_CLOSE"}),t.next=33;break;case 29:t.prev=29,t.t0=t.catch(7),r(ge(!1)),t.t0&&s(t.t0.message);case 33:case"end":return t.stop()}}),t,null,[[7,29]])}))),function(n,e){return t.apply(this,arguments)};var t}function We(n){return function(e,t){var r=t(),o=r.editor,i=r.server,a=function(n,e){var t={};if(e.includes("chiral_flag")&&Array.from(n.frags.values()).some((function(n){return!!n&&"abs"===n.enhancedStereoFlag}))&&(t.chiral_flag="Chiral flag is present on the canvas"),e.includes("valence")){var r=0;n.atoms.forEach((function(n){return n.badConn&&r++})),r>0&&(t.valence="Structure contains ".concat(r," atom").concat(1!==r?"s":""," with bad valence"))}return t}(o.struct(),n),l=t().options.getServerSettings();return l.data={types:(0,y.without)(["valence","chiral_flag"],n)},Qe(o,i,"check",l).then((function(n){n=Object.assign(n,a),e({type:"UPDATE_FORM",data:{moleculeErrors:n}})})).catch((function(n){o.errorHandler(n)}))}}function Xe(n,e,t){return function(r,o){var i=o(),a=i.options.getServerSettings();a.data=e,r(ve(!0)),Qe(i.editor,i.server,n,a,t).then((function(e){var t=(new u.F_l).deserialize(e.struct);return r(qe(t,{rescale:"layout"===n,reactionRelayout:"clean"===n}))})).catch((function(n){i.editor.errorHandler(n)})).finally((function(){r(ve(!1))}))}}function Qe(n,e,t,r,o){var i=n.selection(),a=[],l=new Map,c=(o||n.struct()).clone(null,null,!1,l);i&&(a=(i.atoms?i.atoms:n.explicitSelected().atoms).map((function(n){return l.get(n)})));var s=new u.F_l;return e.then((function(){return e[t](Object.assign({struct:s.serialize(c)},"calculate"!==t&&"check"!==t?{output_format:u.hxV.KET}:null,a&&a.length>0?{selected:a}:null,r.data),(0,y.omit)("data",r))}))}var nt={layout:{shortcut:"Mod+l",title:"Layout",action:{thunk:Xe("layout")},disabled:function(n,e,t){return!t.app.server},hidden:function(n){return Sn(n,"layout")}},clean:{shortcut:"Mod+Shift+l",title:"Clean Up",action:{thunk:Xe("clean")},disabled:function(n,e,t){return!t.app.server},hidden:function(n){return Sn(n,"clean")}},arom:{title:"Aromatize",action:{thunk:Xe("aromatize")},disabled:function(n,e,t){return!t.app.server},hidden:function(n){return Sn(n,"arom")}},dearom:{title:"Dearomatize",action:{thunk:Xe("dearomatize")},disabled:function(n,e,t){return!t.app.server},hidden:function(n){return Sn(n,"dearom")}},cip:{shortcut:"Mod+p",title:"Calculate CIP",action:{thunk:Xe("calculateCip")},disabled:function(n,e,t){return!t.app.server},hidden:function(n){return Sn(n,"cip")}},check:{title:"Check Structure",action:{dialog:"check"},disabled:function(n,e,t){return!t.app.server},hidden:function(n){return Sn(n,"check")}},analyse:{title:"Calculated Values",action:{dialog:"analyse"},disabled:function(n,e,t){return!t.app.server},hidden:function(n){return Sn(n,"analyse")}},recognize:{title:"Recognize Molecule",action:{dialog:"recognize"},disabled:function(n,e,t){var r;return!t.app.server||!(null!==(r=t.app.imagoVersions)&&void 0!==r&&r.length)>0},hidden:function(n){return Sn(n,"recognize")}},miew:{title:"3D Viewer",action:{dialog:"miew"},hidden:function(n){return Sn(n,"miew")}}},et=new u.jWx,tt=["Benzene\n  Ketcher  5112215552D 1   1.00000     0.00000     0\n\n  6  6  0  0  0  0            999 V2000\n    0.6548    2.2452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0813    2.2456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3694    2.6575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0813    1.4204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.6548    1.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3712    1.0086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END","Cyclopentadiene\n  Ketcher  5112215552D 1   1.00000     0.00000     0\n\n  5  5  0  0  0  0            999 V2000\n    3.8091    8.2444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3091    6.7055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6181    7.6510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3091    6.7055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    7.6510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  5  1  0     0  0\n  2  3  2  0     0  0\n  3  1  1  0     0  0\n  4  2  1  0     0  0\n  5  4  2  0     0  0\nM  END","Cyclohexane\n  Ketcher  5112215552D 1   1.00000     0.00000     0\n\n  6  6  0  0  0  0            999 V2000\n    2.5500    3.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5500    2.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4160    2.1722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2820    2.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2820    3.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4160    4.1722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  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\nM  END","Cyclopentane\n  Ketcher 11161218352D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    0.8090    1.5389    0.0000 C   0  0  0  0  0  0        0  0  0\n    1.6180    0.9511    0.0000 C   0  0  0  0  0  0        0  0  0\n    1.3090    0.0000    0.0000 C   0  0  0  0  0  0        0  0  0\n    0.3090    0.0000    0.0000 C   0  0  0  0  0  0        0  0  0\n    0.0000    0.9511    0.0000 C   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  1  1  0     0  0\nM  END","Cyclopropane\n  Ketcher  5112215552D 1   1.00000     0.00000     0\n\n  3  3  0  0  0  0            999 V2000\n    2.6123    1.5663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6098    1.5663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1111    2.4280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  3  1  0     0  0\nM  END","Cyclobutane\n  Ketcher  5112215552D 1   1.00000     0.00000     0\n\n  4  4  0  0  0  0            999 V2000\n    3.4956    1.8862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4919    2.8804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4846    1.8991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4821    2.8804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  4  1  0     0  0\nM  END","Cycloheptane\n  Ketcher  5112215552D 1   1.00000     0.00000     0\n\n  7  7  0  0  0  0            999 V2000\n   21.4111    6.3389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.1938    6.9555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.1653    6.7333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.5987    5.8389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   21.4166    5.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.1660    4.9333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.1938    4.7111    0.0000 C   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  6  1  0     0  0\n  1  5  1  0     0  0\n  5  7  1  0     0  0\n  6  7  1  0     0  0\nM  END","Cyclooctane\n  Ketcher  5112215552D 1   1.00000     0.00000     0\n\n  8  8  0  0  0  0            999 V2000\n    2.9268    2.2122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9270    3.2099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6288    3.9118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6290    1.5102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6266    1.5102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3286    2.2122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3285    3.2099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6266    3.9119    0.0000 C   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  1  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  8  3  1  0     0  0\nM  END"].map((function(n){return et.deserialize(n)})),rt={"template-lib":{shortcut:"Shift+t",title:"Custom Templates",action:{dialog:"templates"},selected:function(n){return"classic"===n._tool.mode},disabled:function(n,e,t){return!t.app.templates},hidden:function(n){return Sn(n,"template-lib")}}},ot=tt.reduce((function(n,e,t){return n["template-".concat(t)]={title:"".concat(e.name),shortcut:"t",action:{tool:"template",opts:{struct:e}}},n}),rt),it=[.2,.3,.4,.5,.6,.7,.8,.9,1,1.1,1.2,1.3,1.4,1.5,1.7,2,2.5,3,3.5,4],at={zoom:{selected:function(n){return n.zoom()},hidden:function(n){return Sn(n,"zoom")}},"zoom-out":{shortcut:["-","_","Shift+-"],title:"Zoom Out",disabled:function(n){return n.zoom()<=it[0]},action:function(n){var e=n.zoom(),t=(0,y.findLastIndex)((function(n){return n<=e}),it);n.zoom(it[it[t]===e&&t>0?t-1:t])},hidden:function(n){return Sn(n,"zoom-out")}},"zoom-in":{shortcut:["+","=","Shift+="],title:"Zoom In",disabled:function(n){return it[it.length-1]<=n.zoom()},action:function(n){var e=n.zoom(),t=(0,y.findIndex)((function(n){return n>=e}),it);n.zoom(it[it[t]===e&&t<it.length-1?t+1:t])},hidden:function(n){return Sn(n,"zoom-in")}},"zoom-list":{hidden:function(n){return Sn(n,"zoom-list")}}},lt={help:{shortcut:["?","&","Shift+/"],action:function(){return null===(n=window.open("https://github.com/epam/ketcher/blob/".concat("v2.7.2\n","/documentation/help.md#ketcher-overview")))||void 0===n?void 0:n.focus();var n},hidden:function(n){return Sn(n,"help")}}},ct={"functional-groups":{shortcut:"Shift+f",title:"Functional Groups",action:{dialog:"templates",prop:{tab:1}},selected:function(n){return"fg"===n._tool.mode},disabled:function(n,e,t){return!t.app.functionalGroups},hidden:function(n){return Sn(n,"functional-groups")}}},st={fullscreen:{title:"Fullscreen mode",action:function(){return e=document.querySelector(".Ketcher-root")||document.documentElement,void(document.fullscreenElement||document.mozFullScreenElement||document.webkitFullscreenElement||document.msFullscreenElement?document.exitFullscreen&&document.exitFullscreen()||document.msExitFullscreen&&document.msExitFullscreen()||document.mozCancelFullScreen&&document.mozCancelFullScreen()||document.webkitExitFullscreen&&document.webkitExitFullscreen():(n=e).requestFullscreen&&n.requestFullscreen()||n.msRequestFullscreen&&n.msRequestFullscreen()||n.mozRequestFullScreen&&n.mozRequestFullScreen()||n.webkitRequestFullscreen&&n.webkitRequestFullscreen());var n,e},hidden:function(n){return Sn(n,"fullscreen")}}};function ut(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function dt(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?ut(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):ut(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var pt,ht,ft,mt,vt,gt,bt,Ct,yt,Ot,wt,St,Mt,xt,jt,Et,Dt,At,$t,Nt,Pt,kt,It,Tt,Bt,Lt,_t,Vt,zt,Gt,Ft,Ht,Rt,Zt,Kt,Yt,Ut,Jt,qt,Wt,Xt,Qt,nr,er,tr,rr,or,ir,ar,lr,cr,sr,ur,dr,pr,hr,fr,mr,vr,gr,br,Cr,yr,Or,wr,Sr,Mr,xr,jr,Er,Dr,Ar,$r,Nr,Pr,kr,Ir,Tr,Br,Lr,_r,Vr,zr,Gr,Fr,Hr,Rr,Zr,Kr,Yr,Ur,Jr,qr,Wr,Xr,Qr,no,eo,to,ro,oo,io,ao,lo,co,so,uo,po,ho,fo,mo,vo,go,bo,Co,yo,Oo,wo,So,Mo,xo,jo,Eo,Do,Ao,$o,No,Po,ko,Io,To,Bo,Lo,_o,Vo,zo,Go,Fo,Ho,Ro,Zo,Ko,Yo,Uo,Jo,qo,Wo,Xo,Qo,ni,ei,ti,ri,oi,ii,ai,li,ci,si,ui,di,pi,hi,fi,mi,vi,gi,bi,Ci,yi,Oi,wi,Si,Mi,xi,ji,Ei,Di,Ai,$i,Ni,Pi,ki,Ii,Ti,Bi,Li,_i,Vi,zi,Gi,Fi,Hi,Ri,Zi,Ki,Yi,Ui,Ji,qi,Wi,Xi,Qi,na,ea,ta,ra,oa,ia,aa,la,ca,sa,ua,da,pa,ha,fa,ma,va,ga,ba,Ca,ya,Oa,wa,Sa,Ma,xa,ja,Ea,Da,Aa,$a,Na,Pa,ka,Ia,Ta,Ba,La,_a,Va,za,Ga,Fa,Ha,Ra,Za,Ka,Ya,Ua,Ja=dt(dt(dt(dt(dt(dt(dt(dt(dt({clear:{shortcut:"Mod+Delete",title:"Clear Canvas",action:{thunk:function(n,e){var t=e().editor;t.struct().isBlank()||t.struct(null),n({type:"ACTION",action:Re["select-rectangle"].action})}},hidden:function(n){return Sn(n,"clear")}},open:{shortcut:"Mod+o",title:"Open…",action:{dialog:"open"},hidden:function(n){return Sn(n,"open")}},save:{shortcut:"Mod+s",title:"Save As…",action:{dialog:"save"},hidden:function(n){return Sn(n,"save")}},undo:{shortcut:"Mod+z",title:"Undo",action:function(n){n.undo()},disabled:function(n){return 0===n.historySize().undo},hidden:function(n){return Sn(n,"undo")}},redo:{shortcut:["Mod+Shift+z","Mod+y"],title:"Redo",action:function(n){n.redo()},disabled:function(n){return 0===n.historySize().redo},hidden:function(n){return Sn(n,"redo")}},cut:{shortcut:"Mod+x",title:"Cut",action:function(n){$n("cut")||Wa("Cut",n.errorHandler)},disabled:function(n){return!qa(n)},hidden:function(n){return Sn(n,"cut")}},copies:{disabled:function(n){return!qa(n)},hidden:function(n){return Sn(n,"copies")}},copy:{shortcut:"Mod+c",title:"Copy",action:function(n){$n("copy")||Wa("Copy",n.errorHandler)},disabled:function(n){return!qa(n)},hidden:function(n){return Sn(n,"copy")}},"copy-image":{shortcut:"Mod+Shift+f",title:"Copy Image",action:function(){!function(){wn.apply(this,arguments)}()},disabled:function(n){return!qa(n)},hidden:function(n){return Sn(n,"copy-image")}},"copy-mol":{shortcut:"Mod+m",title:"Copy as MOL",action:function(){On("mol")},disabled:function(n){return!qa(n)},hidden:function(n){return Sn(n,"copy-mol")}},"copy-ket":{shortcut:"Mod+Shift+k",title:"Copy as KET",action:function(){On("ket")},disabled:function(n){return!qa(n)},hidden:function(n){return Sn(n,"copy-ket")}},paste:{shortcut:"Mod+v",title:"Paste",action:function(n){$n("paste")||Wa("Paste",n.errorHandler)},selected:function(n){var e=n.actions;return e&&e.active&&"paste"===e.active.tool},hidden:function(n){return Sn(n,"paste")}},settings:{title:"Settings",action:{dialog:"settings"},hidden:function(n){return Sn(n,"settings")}},about:{title:"About",action:{dialog:"about"},hidden:function(n){return Sn(n,"about")}},"reaction-automap":{title:"Reaction Auto-Mapping Tool",action:{dialog:"automap"},hidden:function(n){return Sn(n,"reaction-automap")},disabled:function(n,e,t){return!t.app.server||!n.struct().hasRxnArrow()}},"period-table":{title:"Periodic Table",action:{dialog:"period-table"},hidden:function(n){return Sn(n,"period-table")}},"extended-table":{title:"Extended Table",action:{dialog:"extended-table"},hidden:function(n){return Sn(n,"extended-table")}},"select-all":{title:"Select All",shortcut:"Mod+a",action:{thunk:function(n,e){e().editor.selection("all");var t=e().toolbar.visibleTools.select;n({type:"ACTION",action:Re[t].action})}},hidden:function(n){return Sn(n,"select-all")}},"deselect-all":{title:"Deselect All",shortcut:"Mod+Shift+a",action:function(n){n.selection(null)},hidden:function(n){return Sn(n,"deselect-all")}},"select-descriptors":{title:"Select descriptors",shortcut:"Mod+d",action:{thunk:function(n,e){var t=e().toolbar.visibleTools.select,r=e().editor;r.alignDescriptors(),r.selection("descriptors"),n({type:"ACTION",action:Re[t].action})}},hidden:function(n){return Sn(n,"select-descriptors")}},"any-atom":{title:"Any atom",action:{tool:"atom",opts:{label:"A",pseudo:"A",type:"gen"}},hidden:function(n){return Sn(n,"any-atom")}}},nt),Mn),Re),yn),at),ot),ct),st),lt);function qa(n){var e=n.selection();return e&&Object.keys(e).filter((function(n){return!["sgroupData"].includes(n)})).length>0}function Wa(n,e){e("This action is unavailable via menu.\nInstead, use shortcut to "+n+".")}function Xa(){return Xa=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Xa.apply(this,arguments)}function Qa(){return Qa=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Qa.apply(this,arguments)}function nl(){return nl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},nl.apply(this,arguments)}function el(){return el=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},el.apply(this,arguments)}function tl(){return tl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},tl.apply(this,arguments)}function rl(){return rl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},rl.apply(this,arguments)}function ol(){return ol=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ol.apply(this,arguments)}function il(){return il=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},il.apply(this,arguments)}function al(){return al=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},al.apply(this,arguments)}function ll(){return ll=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ll.apply(this,arguments)}function cl(){return cl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},cl.apply(this,arguments)}function sl(){return sl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},sl.apply(this,arguments)}function ul(){return ul=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ul.apply(this,arguments)}function dl(){return dl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},dl.apply(this,arguments)}function pl(){return pl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},pl.apply(this,arguments)}function hl(){return hl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},hl.apply(this,arguments)}function fl(){return fl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},fl.apply(this,arguments)}function ml(){return ml=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ml.apply(this,arguments)}function vl(){return vl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},vl.apply(this,arguments)}function gl(){return gl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},gl.apply(this,arguments)}function bl(){return bl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},bl.apply(this,arguments)}function Cl(){return Cl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Cl.apply(this,arguments)}function yl(){return yl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},yl.apply(this,arguments)}function Ol(){return Ol=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ol.apply(this,arguments)}function wl(){return wl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},wl.apply(this,arguments)}function Sl(){return Sl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Sl.apply(this,arguments)}function Ml(){return Ml=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ml.apply(this,arguments)}function xl(n){return d.createElement("svg",Ml({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Jt||(Jt=d.createElement("path",{d:"M17.25 18.75H9V8.25h8.25v10.5zm0-12H9a1.5 1.5 0 00-1.5 1.5v10.5a1.5 1.5 0 001.5 1.5h8.25a1.5 1.5 0 001.5-1.5V8.25a1.5 1.5 0 00-1.5-1.5zm-2.25-3H6a1.5 1.5 0 00-1.5 1.5v10.5H6V5.25h9v-1.5z",fill:"currentcolor"})))}function jl(){return jl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},jl.apply(this,arguments)}function El(){return El=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},El.apply(this,arguments)}function Dl(){return Dl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Dl.apply(this,arguments)}function Al(){return Al=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Al.apply(this,arguments)}function $l(){return $l=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},$l.apply(this,arguments)}function Nl(){return Nl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Nl.apply(this,arguments)}function Pl(){return Pl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Pl.apply(this,arguments)}function kl(){return kl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},kl.apply(this,arguments)}function Il(){return Il=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Il.apply(this,arguments)}function Tl(){return Tl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Tl.apply(this,arguments)}function Bl(){return Bl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Bl.apply(this,arguments)}function Ll(){return Ll=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ll.apply(this,arguments)}function _l(){return _l=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},_l.apply(this,arguments)}function Vl(){return Vl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Vl.apply(this,arguments)}function zl(){return zl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},zl.apply(this,arguments)}function Gl(n){return d.createElement("svg",zl({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Cr||(Cr=d.createElement("path",{d:"M20.434 7.673c-.1-.6-.713-1.731-2.32-1.731-.126 0-.252.007-.377.023v-.79a1.01 1.01 0 00-.045-.3c-.177-.564-.876-1.631-2.262-1.631a2.599 2.599 0 00-.676.086 2.394 2.394 0 00-.146-.23c-.453-.645-1.186-1-2.063-1-.877 0-1.584.36-2.025 1.017a2.461 2.461 0 00-.361.85 2.663 2.663 0 00-.408-.03c-1.474 0-2.124 1.15-2.262 1.757a1.034 1.034 0 00-.024.222V11.1l-.13-.1c-.588-.5-2.034-1.121-3.391.029-1.357 1.15-1.015 2.664-.431 3.452.453.773 4.512 7.425 10.223 7.425 3.25 0 4.91-1.512 5.729-2.781a6.291 6.291 0 00.98-2.8V7.838c.001-.056-.003-.11-.011-.165zm-1.986 8.542a4.474 4.474 0 01-.7 1.887c-.805 1.2-2.153 1.8-4.008 1.8-4.768 0-8.484-6.412-8.52-6.476a.669.669 0 00-.09-.126c-.294-.408 0-.655.107-.748.267-.227.54-.237.81-.031l1.77 1.452a1 1 0 001.644-.763V6.08a.287.287 0 01.29-.148.44.44 0 01.372.16v4.7a1 1 0 102 0v-6.45c.068-.248.3-.248.422-.248.2 0 .414.032.482.255v6.44a1 1 0 102 0v-5.2a.75.75 0 01.074-.19c.049-.081.108-.15.325-.15a.35.35 0 01.307.15v5.39a1 1 0 102 0V8.047a.583.583 0 01.377-.1c.065 0 .258.006.334.078l.004 8.19z",fill:"currentcolor"})))}function Fl(){return Fl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Fl.apply(this,arguments)}function Hl(n){return d.createElement("svg",Fl({width:24,height:24,viewBox:"0 0 30 30",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),yr||(yr=d.createElement("path",{d:"M10.744 3C8.89 3 7.384 4.525 7.384 6.4v.22h-.012c-1.997 0-3.622 1.602-3.622 3.568l.001 7.02c0 1.77 1.512 3.515 3.112 5.361.72.83 1.919 2.216 2.034 2.731v1.522h13.442v-1.554c0-.59.618-1.77 1.163-2.81.938-1.789 1.998-3.815 1.998-5.991 0-3.258-.01-6.248-.01-6.248 0-1.696-1.39-3.08-3.1-3.08-.203 0-.4.02-.592.057a3.65 3.65 0 00-3.033-1.607c-.367 0-.72.053-1.055.153a3.636 3.636 0 00-3.09-1.705c-.444 0-.87.08-1.264.225A3.345 3.345 0 0010.744 3z",fill:"#fff"})),Or||(Or=d.createElement("path",{d:"M10.744 4.554c1 0 1.808.826 1.808 1.845v1.197c0-1.109.927-2.008 2.068-2.008 1.143 0 2.068.9 2.068 2.008v1.552c0-1.11.93-2.008 2.077-2.008 1.147 0 2.076.899 2.076 2.008v1.068A1.54 1.54 0 0122.39 8.69c.856 0 1.548.684 1.548 1.53 0 0 .01 2.988.01 6.244 0 3.257-3.161 6.636-3.161 8.802H10.45c0-1.94-5.146-5.773-5.146-8.061v-7.02c0-1.112.926-2.014 2.07-2.015v4.051c0 .342.35.62.781.62.432 0 .782-.278.782-.62V6.4c0-1.02.809-1.845 1.807-1.845zm0-1.554C8.89 3 7.384 4.525 7.384 6.4v.22h-.012c-1.997 0-3.622 1.602-3.622 3.568l.001 7.02c0 1.77 1.512 3.515 3.112 5.361.72.83 1.919 2.216 2.034 2.731v1.522h13.442v-1.554c0-.59.618-1.77 1.163-2.81.938-1.789 1.998-3.815 1.998-5.991 0-3.258-.01-6.248-.01-6.248 0-1.696-1.39-3.08-3.1-3.08-.203 0-.4.02-.592.057a3.65 3.65 0 00-3.033-1.607c-.367 0-.72.053-1.055.153a3.636 3.636 0 00-3.09-1.705c-.444 0-.87.08-1.264.225A3.345 3.345 0 0010.744 3z",fill:"#000"})))}function Rl(){return Rl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Rl.apply(this,arguments)}function Zl(){return Zl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Zl.apply(this,arguments)}function Kl(){return Kl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Kl.apply(this,arguments)}function Yl(){return Yl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Yl.apply(this,arguments)}function Ul(){return Ul=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ul.apply(this,arguments)}function Jl(){return Jl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Jl.apply(this,arguments)}function ql(){return ql=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ql.apply(this,arguments)}function Wl(){return Wl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Wl.apply(this,arguments)}function Xl(){return Xl=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Xl.apply(this,arguments)}function Ql(){return Ql=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ql.apply(this,arguments)}function nc(){return nc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},nc.apply(this,arguments)}function ec(){return ec=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ec.apply(this,arguments)}function tc(){return tc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},tc.apply(this,arguments)}function rc(){return rc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},rc.apply(this,arguments)}function oc(){return oc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},oc.apply(this,arguments)}function ic(){return ic=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ic.apply(this,arguments)}function ac(){return ac=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ac.apply(this,arguments)}function lc(){return lc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},lc.apply(this,arguments)}function cc(){return cc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},cc.apply(this,arguments)}function sc(){return sc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},sc.apply(this,arguments)}function uc(){return uc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},uc.apply(this,arguments)}function dc(){return dc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},dc.apply(this,arguments)}function pc(){return pc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},pc.apply(this,arguments)}function hc(){return hc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},hc.apply(this,arguments)}function fc(){return fc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},fc.apply(this,arguments)}function mc(){return mc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},mc.apply(this,arguments)}function vc(){return vc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},vc.apply(this,arguments)}function gc(){return gc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},gc.apply(this,arguments)}function bc(){return bc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},bc.apply(this,arguments)}function Cc(){return Cc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Cc.apply(this,arguments)}function yc(){return yc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},yc.apply(this,arguments)}function Oc(){return Oc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Oc.apply(this,arguments)}function wc(){return wc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},wc.apply(this,arguments)}function Sc(){return Sc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Sc.apply(this,arguments)}function Mc(){return Mc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Mc.apply(this,arguments)}function xc(){return xc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},xc.apply(this,arguments)}function jc(){return jc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},jc.apply(this,arguments)}function Ec(){return Ec=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ec.apply(this,arguments)}function Dc(){return Dc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Dc.apply(this,arguments)}function Ac(){return Ac=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ac.apply(this,arguments)}function $c(){return $c=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},$c.apply(this,arguments)}function Nc(){return Nc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Nc.apply(this,arguments)}function Pc(){return Pc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Pc.apply(this,arguments)}function kc(){return kc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},kc.apply(this,arguments)}function Ic(){return Ic=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ic.apply(this,arguments)}function Tc(){return Tc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Tc.apply(this,arguments)}function Bc(){return Bc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Bc.apply(this,arguments)}function Lc(){return Lc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Lc.apply(this,arguments)}function _c(){return _c=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},_c.apply(this,arguments)}function Vc(){return Vc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Vc.apply(this,arguments)}function zc(){return zc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},zc.apply(this,arguments)}function Gc(){return Gc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Gc.apply(this,arguments)}function Fc(){return Fc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Fc.apply(this,arguments)}function Hc(){return Hc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Hc.apply(this,arguments)}function Rc(){return Rc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Rc.apply(this,arguments)}function Zc(){return Zc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Zc.apply(this,arguments)}function Kc(){return Kc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Kc.apply(this,arguments)}function Yc(){return Yc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Yc.apply(this,arguments)}function Uc(){return Uc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Uc.apply(this,arguments)}function Jc(){return Jc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Jc.apply(this,arguments)}function qc(){return qc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},qc.apply(this,arguments)}function Wc(){return Wc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Wc.apply(this,arguments)}function Xc(){return Xc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Xc.apply(this,arguments)}function Qc(){return Qc=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Qc.apply(this,arguments)}function ns(){return ns=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ns.apply(this,arguments)}function es(){return es=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},es.apply(this,arguments)}function ts(){return ts=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ts.apply(this,arguments)}function rs(){return rs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},rs.apply(this,arguments)}function os(){return os=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},os.apply(this,arguments)}function is(){return is=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},is.apply(this,arguments)}function as(){return as=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},as.apply(this,arguments)}function ls(){return ls=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ls.apply(this,arguments)}function cs(){return cs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},cs.apply(this,arguments)}function ss(){return ss=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ss.apply(this,arguments)}function us(){return us=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},us.apply(this,arguments)}function ds(){return ds=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ds.apply(this,arguments)}function ps(){return ps=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ps.apply(this,arguments)}function hs(){return hs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},hs.apply(this,arguments)}function fs(){return fs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},fs.apply(this,arguments)}function ms(){return ms=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ms.apply(this,arguments)}function vs(){return vs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},vs.apply(this,arguments)}function gs(){return gs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},gs.apply(this,arguments)}function bs(){return bs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},bs.apply(this,arguments)}function Cs(){return Cs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Cs.apply(this,arguments)}function ys(){return ys=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ys.apply(this,arguments)}function Os(){return Os=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Os.apply(this,arguments)}function ws(){return ws=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ws.apply(this,arguments)}function Ss(){return Ss=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ss.apply(this,arguments)}function Ms(){return Ms=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ms.apply(this,arguments)}function xs(){return xs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},xs.apply(this,arguments)}function js(){return js=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},js.apply(this,arguments)}function Es(){return Es=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Es.apply(this,arguments)}function Ds(){return Ds=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ds.apply(this,arguments)}function As(){return As=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},As.apply(this,arguments)}function $s(){return $s=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},$s.apply(this,arguments)}function Ns(){return Ns=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ns.apply(this,arguments)}function Ps(){return Ps=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ps.apply(this,arguments)}function ks(){return ks=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ks.apply(this,arguments)}function Is(){return Is=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Is.apply(this,arguments)}function Ts(){return Ts=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ts.apply(this,arguments)}function Bs(){return Bs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Bs.apply(this,arguments)}function Ls(){return Ls=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ls.apply(this,arguments)}function _s(){return _s=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},_s.apply(this,arguments)}function Vs(){return Vs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Vs.apply(this,arguments)}function zs(){return zs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},zs.apply(this,arguments)}function Gs(){return Gs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Gs.apply(this,arguments)}function Fs(){return Fs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Fs.apply(this,arguments)}function Hs(){return Hs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Hs.apply(this,arguments)}function Rs(){return Rs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Rs.apply(this,arguments)}function Zs(){return Zs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Zs.apply(this,arguments)}function Ks(){return Ks=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ks.apply(this,arguments)}function Ys(){return Ys=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ys.apply(this,arguments)}function Us(){return Us=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Us.apply(this,arguments)}function Js(){return Js=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Js.apply(this,arguments)}function qs(){return qs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},qs.apply(this,arguments)}function Ws(){return Ws=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ws.apply(this,arguments)}function Xs(){return Xs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Xs.apply(this,arguments)}function Qs(){return Qs=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Qs.apply(this,arguments)}function nu(){return nu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},nu.apply(this,arguments)}function eu(){return eu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},eu.apply(this,arguments)}function tu(){return tu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},tu.apply(this,arguments)}function ru(){return ru=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ru.apply(this,arguments)}function ou(){return ou=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},ou.apply(this,arguments)}function iu(){return iu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},iu.apply(this,arguments)}function au(){return au=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},au.apply(this,arguments)}function lu(){return lu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},lu.apply(this,arguments)}function cu(){return cu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},cu.apply(this,arguments)}function su(){return su=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},su.apply(this,arguments)}function uu(){return uu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},uu.apply(this,arguments)}function du(){return du=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},du.apply(this,arguments)}function pu(){return pu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},pu.apply(this,arguments)}function hu(){return hu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},hu.apply(this,arguments)}function fu(){return fu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},fu.apply(this,arguments)}function mu(){return mu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},mu.apply(this,arguments)}function vu(){return vu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},vu.apply(this,arguments)}function gu(){return gu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},gu.apply(this,arguments)}function bu(){return bu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},bu.apply(this,arguments)}function Cu(){return Cu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Cu.apply(this,arguments)}function yu(){return yu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},yu.apply(this,arguments)}function Ou(){return Ou=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ou.apply(this,arguments)}function wu(){return wu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},wu.apply(this,arguments)}function Su(){return Su=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Su.apply(this,arguments)}function Mu(){return Mu=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Mu.apply(this,arguments)}var xu={"α":function(n){return d.createElement("svg",Ns({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Xi||(Xi=d.createElement("path",{d:"M7.744 11.136a2.48 2.48 0 01-1.436-.443c-.412-.29-.733-.69-.963-1.202C5.115 8.98 5 8.391 5 7.727c0-.659.12-1.24.362-1.743A2.9 2.9 0 016.355 4.8c.423-.287.905-.43 1.445-.43.383 0 .72.072 1.01.216.29.143.537.341.741.597.208.256.378.553.511.89h.444l.251 1.637.835 3.29h-1.09l-.785-3.29a6.215 6.215 0 00-.191-.703 3.787 3.787 0 00-.337-.742 1.898 1.898 0 00-.528-.583 1.259 1.259 0 00-.763-.23c-.327 0-.614.098-.861.294a1.868 1.868 0 00-.575.805 3.195 3.195 0 00-.205 1.185c0 .437.065.83.196 1.18.134.35.318.625.554.827.236.199.511.298.827.298.287 0 .538-.078.754-.234.216-.157.4-.355.55-.597.15-.241.273-.493.366-.754.097-.264.168-.502.213-.712l.704-3.29h1.086l-.75 3.29-.251 1.658H10.1c-.137.338-.313.639-.529.903a2.268 2.268 0 01-.775.614c-.301.148-.652.22-1.053.217z"})))},"β":function(n){return d.createElement("svg",Ps({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Qi||(Qi=d.createElement("path",{d:"M7.237 6.954h.84c.6 0 1.093.124 1.483.371.392.245.683.561.873.95.19.387.286.795.286 1.223 0 .498-.117.944-.35 1.339a2.53 2.53 0 01-.954.933c-.404.227-.862.34-1.377.34a2.75 2.75 0 01-.912-.157c-.298-.108-.568-.308-.81-.6l-.063.029V9.507c0 .264.064.508.192.733.127.224.31.403.545.537.236.133.517.2.844.2.338 0 .628-.07.87-.209.243-.142.432-.328.566-.558.133-.233.2-.487.2-.763 0-.272-.064-.522-.192-.75a1.44 1.44 0 00-1.3-.759h-.74v-.984zm.465-3.8c.397 0 .758.062 1.082.187.324.122.602.291.835.507.233.213.412.459.537.737.125.279.188.573.188.882 0 .375-.095.745-.286 1.108a2.313 2.313 0 01-.852.904c-.378.238-.852.358-1.423.358h-.546v-.96h.443c.316 0 .579-.063.789-.191.21-.13.368-.295.473-.494.105-.202.157-.41.157-.627a1.16 1.16 0 00-.4-.903c-.264-.239-.597-.358-.997-.358-.267 0-.51.055-.729.166-.219.11-.393.269-.524.473-.13.202-.196.438-.196.707v8.804H5V5.617c0-.483.118-.909.354-1.278.235-.372.557-.662.963-.87.409-.21.87-.315 1.385-.315z"})))},"γ":function(n){return d.createElement("svg",ks({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),na||(na=d.createElement("path",{d:"M5 4h1.338l1.573 4.828L9.44 4h1.337L8.52 10.435V13H7.276v-2.565L5 4z"})))},"δ":function(n){return d.createElement("svg",Is({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),ea||(ea=d.createElement("path",{d:"M6.271 4.585a1.474 1.474 0 01.614-1.244c.415-.313.983-.469 1.704-.469.299 0 .57.026.814.077.245.048.502.12.772.217v1.12a5.532 5.532 0 00-.678-.208 3.45 3.45 0 00-.848-.107c-.332 0-.585.057-.758.171a.517.517 0 00-.162.746c.062.105.177.214.345.328.167.11.41.223.729.336.897.313 1.555.745 1.973 1.296.417.551.626 1.223.626 2.016v.119c0 .6-.118 1.136-.354 1.61a2.693 2.693 0 01-1.005 1.117c-.435.273-.954.41-1.556.41-.616 0-1.145-.136-1.585-.406a2.67 2.67 0 01-1.006-1.108c-.233-.468-.35-.998-.35-1.589v-.12c0-.443.086-.85.257-1.222.17-.373.399-.686.686-.942.29-.256.609-.426.958-.511l-.004-.035a2.157 2.157 0 01-.86-.647 1.533 1.533 0 01-.312-.955zm.652 4.253v.11c0 .384.056.732.166 1.045.114.312.286.562.516.75.233.184.527.277.882.277.35 0 .638-.092.865-.277a1.67 1.67 0 00.507-.75c.111-.313.167-.66.167-1.044v-.111c0-.307-.064-.607-.192-.9a2.221 2.221 0 00-.541-.758 1.648 1.648 0 00-.806-.413c-.355 0-.648.095-.878.285-.23.188-.402.438-.515.75a3.01 3.01 0 00-.17 1.036z"})))},"ε":function(n){return d.createElement("svg",Ts({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),ta||(ta=d.createElement("path",{d:"M8.06 8.582h1.027v.55h-.831c-.276 0-.52.043-.733.128-.21.085-.377.203-.499.353a.802.802 0 00-.179.52c0 .27.135.493.405.67.27.173.635.26 1.095.26.452 0 .797-.08 1.036-.24.238-.158.392-.4.46-.724h1.283a1.955 1.955 0 01-.269.844c-.148.25-.345.463-.592.64-.245.172-.53.306-.857.4-.324.09-.679.136-1.065.136a4.065 4.065 0 01-1.423-.234c-.418-.156-.749-.377-.993-.66a1.498 1.498 0 01-.362-1.002c0-.193.038-.387.115-.58.08-.193.211-.369.396-.528.187-.16.442-.287.763-.384.324-.1.731-.149 1.223-.149zm1.027.269H8.06c-.472 0-.863-.047-1.172-.141-.31-.094-.553-.216-.729-.366a1.332 1.332 0 01-.375-.508 1.557 1.557 0 01-.106-.554c0-.403.112-.747.336-1.03.225-.288.536-.506.933-.657.398-.15.858-.226 1.381-.226.503 0 .948.077 1.334.23.39.15.7.37.933.656.233.285.37.627.413 1.027H9.723a.957.957 0 00-.456-.634c-.245-.157-.567-.235-.968-.235-.42 0-.751.087-.993.26-.241.173-.363.392-.366.656.003.248.115.446.337.597.221.148.548.222.98.222h.83v.703z"})))},"ζ":function(n){return d.createElement("svg",Bs({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),ra||(ra=d.createElement("path",{d:"M10.04 3.273h.711v.835L8.69 6.746c-.299.386-.556.726-.772 1.018a3.98 3.98 0 00-.494.87c-.114.29-.17.628-.17 1.014 0 .281.085.526.255.733.17.204.408.35.712.439l.677.204c.515.154.914.354 1.198.601.284.245.426.514.426.81 0 .295-.105.604-.315.925-.21.32-.499.622-.865.903l-.712-.58c.176-.19.31-.374.4-.553.094-.18.143-.333.145-.46.003-.114-.068-.225-.213-.333a1.833 1.833 0 00-.596-.264l-.499-.141c-.6-.165-1.065-.439-1.398-.822a2.003 2.003 0 01-.498-1.356c0-.366.037-.7.11-1 .077-.305.187-.595.329-.87.142-.276.315-.55.52-.823.204-.275.437-.568.698-.878l2.412-2.91zm-4.505 0h4.709v1.13H5.535v-1.13z"})))},"η":function(n){return d.createElement("svg",Ls({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),oa||(oa=d.createElement("path",{d:"M6.13 7.113V11H4.855V4.454h1.223V5.52h.081c.154-.35.391-.628.712-.836.321-.21.727-.315 1.219-.315.449 0 .84.094 1.172.281.335.185.595.46.78.827.184.367.277.82.277 1.36v6.617H9.043V6.99c0-.475-.123-.845-.37-1.112-.245-.27-.584-.405-1.019-.405-.292 0-.554.064-.784.192a1.37 1.37 0 00-.545.562c-.131.244-.196.54-.196.886z"})))},"θ":function(n){return d.createElement("svg",_s({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),ia||(ia=d.createElement("path",{d:"M10.611 7.172v1.082H6.388V7.172h4.223zm.66-.09v1.193c0 .878-.116 1.601-.349 2.17-.23.568-.554.99-.971 1.265-.418.273-.907.41-1.466.41-.56 0-1.051-.137-1.475-.41-.423-.276-.753-.697-.988-1.266-.236-.568-.354-1.29-.354-2.169V7.082c0-.87.116-1.584.35-2.143.232-.56.56-.975.98-1.245.42-.27.91-.404 1.47-.404.565 0 1.056.134 1.474.404.42.27.747.685.98 1.245.233.56.35 1.274.35 2.143zm-1.27 1.398V6.873c0-.55-.063-1.011-.191-1.38-.128-.372-.307-.65-.537-.836a1.237 1.237 0 00-.805-.28c-.46 0-.833.212-1.117.638-.284.427-.426 1.046-.426 1.858V8.48c0 .818.144 1.447.43 1.888.29.44.667.66 1.13.66.307 0 .572-.096.797-.29.227-.193.403-.478.528-.856.128-.38.192-.848.192-1.402z"})))},"ι":function(n){return d.createElement("svg",Vs({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),aa||(aa=d.createElement("path",{d:"M6.875 5.455h1.257l-.008 4.78c.002.293.076.484.221.572.148.085.318.128.512.128.093 0 .187-.009.28-.026a4.19 4.19 0 00.218-.043v1.079a3.083 3.083 0 01-.925.136c-.457 0-.83-.133-1.12-.4-.29-.268-.435-.725-.435-1.373V5.455z"})))},"κ":function(n){return d.createElement("svg",zs({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),la||(la=d.createElement("path",{d:"M6.354 5.455V12H4.969V5.455h1.385zm4.423 0L7.611 9.324H5.987l-.196-1.24h1.16l2.121-2.63h1.705zM9.009 12L6.805 9.226l1.002-.86L10.76 12H9.009z"})))},"λ":function(n){return d.createElement("svg",Gs({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),ca||(ca=d.createElement("path",{d:"M10.18 12.094c-.35 0-.657-.097-.921-.29-.261-.196-.465-.492-.61-.886L7.236 6.873 6.792 5.8l-.252-.648c-.11-.281-.227-.492-.35-.63a.698.698 0 00-.447-.244c-.176-.022-.4.002-.673.073L4.763 3.29a2.02 2.02 0 01.337-.094c.142-.028.3-.043.477-.043.492 0 .908.128 1.249.384.34.253.606.632.797 1.138l2.151 5.774c.06.156.124.288.192.396.068.108.186.162.354.162.031 0 .07-.001.115-.004l.102-.013.205 1.035c-.083.023-.175.04-.277.052-.1.014-.195.02-.286.017zM4.37 12l2.57-6.916.652 2.267h-.265L5.722 12h-1.35z"})))},"μ":function(n){return d.createElement("svg",Fs({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),sa||(sa=d.createElement("path",{d:"M4.855 14.429V5.455H6.13v3.83c0 .324.07.61.208.857.142.247.34.44.593.58.255.136.552.204.89.204.338 0 .634-.07.887-.209.255-.139.453-.33.592-.575.142-.247.213-.533.213-.856V5.455h1.274V12H9.534v-.959h-.05c-.16.324-.388.573-.687.746-.298.17-.623.256-.976.256-.352 0-.677-.086-.975-.256a1.774 1.774 0 01-.69-.746h-.052v3.388H4.855z"})))},"ν":function(n){return d.createElement("svg",Hs({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),ua||(ua=d.createElement("path",{d:"M6.804 12L4.371 5.455h1.355l1.794 5.237h.068c.33-.529.6-1.013.81-1.453a8.19 8.19 0 00.494-1.27c.12-.406.205-.813.256-1.219.054-.406.09-.838.107-1.295h1.257a9.816 9.816 0 01-.631 3.34C9.471 9.913 8.867 10.98 8.066 12H6.804z"})))},"ξ":function(n){return d.createElement("svg",Rs({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),da||(da=d.createElement("path",{d:"M10.635 3.418l-.204 1.073c-.517-.147-.969-.221-1.355-.221-.324 0-.601.041-.831.123-.23.083-.407.205-.529.367a.945.945 0 00-.179.584c0 .36.147.636.44.826.292.19.707.286 1.244.286h.86v.805h-.89c-.628 0-1.17-.08-1.624-.238-.452-.162-.8-.392-1.044-.69a1.664 1.664 0 01-.366-1.083c0-.42.119-.787.358-1.1.241-.315.576-.56 1.005-.732.432-.177.933-.265 1.505-.265.3 0 .59.023.869.068.281.046.528.111.741.197zM9.203 6.784h.878v.793h-.843c-.458 0-.846.065-1.164.196-.315.127-.554.32-.716.575-.162.253-.243.57-.243.954 0 .42.127.77.38 1.049.255.278.633.476 1.133.592l.678.154c.568.13.974.298 1.219.502a.982.982 0 01.366.789c-.006.21-.058.429-.158.656a2.838 2.838 0 01-.405.665c-.173.219-.375.42-.605.605l-.758-.567c.238-.253.395-.459.469-.618a.963.963 0 00.11-.392.462.462 0 00-.183-.388c-.122-.093-.33-.173-.622-.238l-.575-.167c-.841-.193-1.458-.49-1.85-.89-.389-.4-.584-.938-.584-1.61 0-.873.297-1.534.891-1.982.597-.452 1.457-.678 2.582-.678z"})))},"ο":function(n){return d.createElement("svg",Zs({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),pa||(pa=d.createElement("path",{d:"M7.614 12.132c-.614 0-1.15-.14-1.607-.422a2.845 2.845 0 01-1.065-1.18c-.253-.506-.38-1.097-.38-1.773 0-.68.127-1.273.38-1.781A2.84 2.84 0 016.007 5.79c.457-.281.993-.422 1.607-.422.613 0 1.149.14 1.606.422.458.281.813.676 1.066 1.185.252.508.379 1.102.379 1.78 0 .677-.127 1.268-.38 1.774-.252.505-.607.899-1.065 1.18-.457.281-.993.422-1.606.422zm.004-1.07c.398 0 .727-.105.989-.315.26-.21.454-.49.58-.84.127-.349.19-.734.19-1.154 0-.418-.063-.801-.19-1.15a1.874 1.874 0 00-.58-.849c-.262-.213-.591-.32-.99-.32-.4 0-.732.107-.996.32a1.904 1.904 0 00-.584.848c-.125.35-.188.733-.188 1.15 0 .421.063.806.188 1.155.128.35.322.63.584.84.264.21.596.315.997.315z"})))},"π":function(n){return d.createElement("svg",Ks({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),ha||(ha=d.createElement("path",{d:"M11.251 5.455v1.07H4.535v-1.07h6.716zm-4.457 0V12H5.537V5.455h1.257zm2.224 0h1.257v4.78c0 .197.033.345.098.444.068.1.157.168.264.205.111.034.23.05.358.05.094 0 .188-.008.282-.025.096-.017.173-.031.23-.043v1.07c-.108.031-.24.063-.397.094a2.579 2.579 0 01-.545.051c-.457 0-.83-.133-1.116-.4-.285-.268-.428-.725-.43-1.373V5.455z"})))},"ρ":function(n){return d.createElement("svg",Ys({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),fa||(fa=d.createElement("path",{d:"M5.805 14.437v-5.83c0-.715.116-1.313.35-1.793.235-.48.56-.841.975-1.083.415-.241.89-.362 1.423-.362.469 0 .878.087 1.228.26.349.17.642.413.877.729.236.315.412.689.529 1.12.12.43.179.902.179 1.42v.119c0 .608-.107 1.145-.32 1.61-.213.467-.517.832-.912 1.096-.392.264-.86.396-1.406.396-.466 0-.852-.1-1.16-.298a2.274 2.274 0 01-.75-.84 6.241 6.241 0 01-.498-1.274l.716-.66c0 .204.024.422.073.652.048.23.13.446.247.647.116.202.273.368.469.499.198.128.447.192.745.192.358 0 .648-.095.87-.286.224-.19.387-.439.49-.745.102-.307.153-.637.153-.99v-.118c0-.45-.054-.856-.162-1.22-.105-.363-.271-.651-.498-.864-.228-.213-.523-.32-.887-.32-.358 0-.649.107-.873.32-.222.21-.382.48-.482.81-.1.329-.148.671-.145 1.026l.026 5.787H5.805z"})))},"σ":function(n){return d.createElement("svg",Us({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),ma||(ma=d.createElement("path",{d:"M4.715 8.898V8.76c0-.585.115-1.112.345-1.58.23-.47.563-.84.997-1.113.435-.272.959-.409 1.573-.409a.659.659 0 01.315.18c.1.09.214.19.345.302.13.108.301.2.511.277.336.13.633.32.891.57.261.25.466.549.614.896.148.343.221.721.221 1.133v.12a3.25 3.25 0 01-.34 1.474 2.737 2.737 0 01-.98 1.095c-.43.276-.95.413-1.56.413-.62 0-1.148-.142-1.586-.426a2.79 2.79 0 01-1.001-1.155 3.786 3.786 0 01-.345-1.64zM6.1 8.76v.137c0 .383.05.736.153 1.057.105.32.271.58.499.775.227.193.525.29.895.29.355 0 .642-.097.86-.29.222-.196.383-.454.482-.775.102-.321.153-.674.153-1.057V8.76c0-.357-.05-.688-.153-.992a1.546 1.546 0 00-.486-.733c-.221-.185-.513-.277-.873-.277-.361 0-.654.092-.878.277-.225.184-.39.429-.495.733a3.02 3.02 0 00-.157.992zm4.913-3.102v1.1H7.63v-1.1h3.383z"})))},"τ":function(n){return d.createElement("svg",Js({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),va||(va=d.createElement("path",{d:"M10.769 5.455v1.099H5.246v-1.1h5.523zm-3.456 0H8.57v4.828c0 .224.031.388.094.49.062.1.14.163.234.191.097.026.195.039.294.039a.868.868 0 00.307-.051c.09-.034.172-.068.243-.102l.243.98c-.193.122-.378.2-.554.234a2.7 2.7 0 01-.563.055c-.503 0-.888-.147-1.155-.443-.267-.295-.4-.773-.4-1.432v-4.79z"})))},"υ":function(n){return d.createElement("svg",qs({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),ga||(ga=d.createElement("path",{d:"M4.855 5.455h1.258V9.51c0 .378.054.678.161.9.108.221.25.38.422.477.177.096.363.145.559.145.335 0 .629-.108.882-.324.253-.216.45-.502.592-.857.142-.358.213-.75.213-1.176a6.797 6.797 0 00-.106-1.057 11.837 11.837 0 00-.6-2.165h1.26c.122.24.234.536.337.891a8.5 8.5 0 01.345 2.331c0 .458-.056.894-.166 1.308a3.254 3.254 0 01-.512 1.104c-.233.318-.532.57-.899.754-.363.185-.798.277-1.304.277-.727 0-1.317-.21-1.768-.63-.45-.42-.674-1.086-.674-1.995v-4.04z"})))},"φ":function(n){return d.createElement("svg",Ws({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),ba||(ba=d.createElement("path",{d:"M6.945 13.454V5.861c0-.503.143-.877.43-1.121.29-.247.693-.37 1.21-.37.56 0 1.063.141 1.509.425.449.284.804.675 1.065 1.172.261.497.392 1.065.392 1.705 0 .451-.07.885-.213 1.3-.14.411-.364.78-.673 1.103-.31.324-.718.58-1.223.767-.506.185-1.124.277-1.854.277-.724 0-1.337-.095-1.837-.285-.5-.194-.903-.456-1.21-.789a3.037 3.037 0 01-.665-1.155 4.572 4.572 0 01-.204-1.376c0-.457.055-.884.166-1.278.114-.398.277-.755.49-1.07.216-.315.476-.581.78-.797l.805.814c-.207.196-.383.41-.528.644a2.99 2.99 0 00-.328.767c-.077.278-.12.585-.128.92 0 .438.087.848.26 1.232.173.38.454.688.844.924.389.233.907.35 1.555.35.642 0 1.162-.11 1.56-.328.397-.222.689-.512.873-.87.188-.358.282-.741.282-1.15a3.215 3.215 0 00-.222-1.121 1.906 1.906 0 00-.571-.805 1.352 1.352 0 00-.882-.303c-.15 0-.263.047-.337.14a.523.523 0 00-.11.342v7.53H6.944z"})))},"χ":function(n){return d.createElement("svg",Xs({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Ca||(Ca=d.createElement("path",{d:"M4.697 13.454L7.518 8.17h.533l1.841 3.584c.097.19.18.328.252.413.073.086.16.14.26.162.099.023.24.034.421.034h.294v1.091h-.294c-.352 0-.643-.03-.873-.093a1.3 1.3 0 01-.597-.35c-.165-.17-.33-.419-.498-.746l-1.083-2.143-1.76 3.332H4.697zM7.4 9.436L5.67 6.159a3.734 3.734 0 00-.277-.46.424.424 0 00-.243-.175 1.87 1.87 0 00-.417-.034h-.295V4.399h.295c.352 0 .64.034.865.102.227.066.423.19.588.37.167.18.34.438.52.777l1.082 2.08L9.55 4.453h1.317L8.166 9.436H7.4z"})))},"ψ":function(n){return d.createElement("svg",Qs({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),ya||(ya=d.createElement("path",{d:"M3.855 4.455h1.249v3.072c0 .61.115 1.1.345 1.466.233.364.543.626.93.788.386.16.809.239 1.27.239.644 0 1.167-.115 1.567-.345.4-.233.693-.533.878-.9.188-.369.281-.758.281-1.167a6.924 6.924 0 00-.064-.784 9.256 9.256 0 00-.37-1.62 9.22 9.22 0 00-.269-.75h1.244c.091.177.18.381.265.614.085.23.16.483.226.759.065.272.116.56.153.86.04.299.06.606.06.921 0 .46-.068.9-.205 1.321-.136.42-.356.795-.66 1.125-.302.33-.704.59-1.206.78-.5.19-1.115.285-1.846.285-.78 0-1.46-.125-2.036-.375a2.85 2.85 0 01-1.339-1.172c-.315-.53-.473-1.215-.473-2.053V4.455zm3.248 0h1.244v9.34H7.103v-9.34z"})))},"ω":function(n){return d.createElement("svg",nu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Oa||(Oa=d.createElement("path",{d:"M4.7 5.455h1.325A9.026 9.026 0 005.42 6.69a5.55 5.55 0 00-.298 1.053c-.054.332-.081.67-.081 1.014 0 .71.109 1.264.328 1.662.218.398.522.597.912.597.34 0 .613-.155.818-.465.204-.312.307-.765.307-1.36V7.113h.975v2.02c0 .625-.083 1.16-.251 1.607-.165.446-.412.788-.741 1.027-.327.236-.73.353-1.21.353-.506 0-.941-.132-1.305-.396-.36-.267-.637-.655-.83-1.163-.194-.509-.289-1.128-.286-1.858 0-.594.078-1.162.234-1.705.16-.542.395-1.057.708-1.542zm5.505 0h1.326c.31.485.544 1 .703 1.542.159.543.238 1.111.238 1.705.003.73-.093 1.35-.29 1.858-.193.508-.471.896-.835 1.163-.36.264-.794.396-1.3.396-.477 0-.88-.117-1.21-.353-.326-.239-.573-.581-.741-1.027-.165-.446-.247-.982-.247-1.607v-2.02h.971v2.08c0 .594.104 1.047.311 1.36.208.309.48.464.819.464.258 0 .48-.09.664-.269.185-.179.327-.436.426-.771.1-.338.15-.744.15-1.219a6.01 6.01 0 00-.085-1.014 5.32 5.32 0 00-.295-1.053 9.016 9.016 0 00-.605-1.235z"})))},"Å":function(n){return d.createElement("svg",ru({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Ma||(Ma=d.createElement("path",{d:"M5.415 12H4.25l2.617-7.273h1.268L10.752 12H9.587L7.531 6.048h-.057L5.414 12zm.195-2.848h3.778v.923H5.61v-.923zm1.893-4.897c-.291 0-.54-.102-.746-.305a1.002 1.002 0 01-.305-.736 1.026 1.026 0 01.518-.902c.161-.094.339-.142.533-.142.192 0 .367.048.525.142.161.093.29.218.384.377.095.158.142.334.142.525 0 .192-.047.367-.142.526a1.082 1.082 0 01-.384.376 1.026 1.026 0 01-.525.139zm0-.543a.49.49 0 00.497-.5.485.485 0 00-.142-.353.476.476 0 00-.355-.145.487.487 0 00-.5.5c0 .138.046.256.141.356a.469.469 0 00.359.142z"})))},"°":function(n){return d.createElement("svg",ou({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),xa||(xa=d.createElement("path",{d:"M7.737 8.219c-.37 0-.706-.09-1.01-.269a2.093 2.093 0 01-.724-.728 1.954 1.954 0 01-.269-1.01c0-.37.09-.705.269-1.006.182-.304.423-.545.724-.724a1.93 1.93 0 011.01-.273c.37 0 .706.09 1.01.273.304.179.546.42.725.724.181.301.272.637.272 1.006 0 .37-.09.706-.272 1.01-.18.304-.42.547-.725.728-.304.18-.64.269-1.01.269zm0-.972a1 1 0 00.524-.14 1.042 1.042 0 00.371-1.415 1.009 1.009 0 00-.37-.37 1 1 0 00-.525-.141 1.042 1.042 0 00-.895.511c-.09.156-.136.33-.136.52a1.015 1.015 0 00.511.895c.157.093.33.14.52.14z"})))},"ħ":function(n){return d.createElement("svg",iu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),ja||(ja=d.createElement("path",{d:"M6.13 9.114V13H4.858V4.273h1.257V7.52h.08c.154-.352.388-.632.704-.84.315-.207.727-.31 1.236-.31.448 0 .84.092 1.176.277.338.184.6.46.784.826.187.364.281.818.281 1.364V13H9.101V8.99c0-.48-.124-.852-.37-1.116-.248-.267-.592-.4-1.032-.4-.301 0-.571.063-.81.191a1.383 1.383 0 00-.558.562c-.134.245-.2.54-.2.887zM3.532 5.833V4.95h3.916v.882H3.531z"})))},"±":function(n){return d.createElement("svg",au({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Ea||(Ea=d.createElement("path",{d:"M5.168 12.616V11.5h5.66v1.116h-5.66zm0-3.477V8.035h5.66V9.14h-5.66zm2.254 1.654V6.386H8.57v4.407H7.422z"})))},"‰":function(n){return d.createElement("svg",lu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Da||(Da=d.createElement("path",{d:"M7.397 11.364v-.46c0-.325.074-.618.222-.883.15-.264.362-.476.635-.635.273-.159.595-.238.967-.238.344 0 .64.08.89.238.25.16.443.371.576.635.136.264.205.558.205.882v.46c0 .325-.069.619-.205.883a1.589 1.589 0 01-.575.635c-.25.159-.547.238-.89.238-.373 0-.695-.08-.968-.238a1.703 1.703 0 01-.635-.635 1.776 1.776 0 01-.222-.882zm.976-.46v.46c0 .244.071.46.213.647.142.188.354.282.635.282s.49-.094.627-.282c.136-.187.204-.403.204-.647v-.46c0-.245-.07-.46-.209-.648-.139-.188-.346-.282-.622-.282-.281 0-.493.094-.635.282a1.044 1.044 0 00-.213.647zm1.85.46v-.46c0-.325.068-.618.204-.883.14-.264.334-.476.584-.635.253-.159.551-.238.895-.238.375 0 .699.08.971.238.273.16.483.371.631.635.148.264.222.558.222.882v.46c0 .325-.074.619-.222.883a1.64 1.64 0 01-.626.635c-.27.159-.59.238-.96.238-.346 0-.647-.08-.902-.238a1.642 1.642 0 01-.588-.635 1.931 1.931 0 01-.21-.882zm.835-.46v.46c0 .244.074.46.222.647.147.188.362.282.643.282.275 0 .483-.094.622-.282.14-.187.209-.403.209-.647v-.46c0-.245-.071-.46-.213-.648-.14-.188-.351-.282-.635-.282-.273 0-.482.094-.627.282a1.05 1.05 0 00-.221.647zM3.004 6.368v-.46c0-.33.068-.632.204-.908.14-.275.341-.495.606-.66.267-.165.59-.247.967-.247.386 0 .71.082.971.247.262.165.46.385.593.66.133.276.2.579.2.908v.46c0 .33-.068.632-.204.908a1.608 1.608 0 01-.597.66c-.261.165-.582.248-.963.248-.386 0-.712-.083-.976-.248a1.648 1.648 0 01-.597-.66 2.018 2.018 0 01-.204-.908zM4 5.91v.46c0 .245.057.466.17.665.117.199.32.298.61.298.284 0 .483-.1.596-.298.117-.199.175-.42.175-.665v-.46c0-.244-.055-.466-.166-.665-.11-.199-.312-.298-.605-.298-.284 0-.486.1-.605.298A1.29 1.29 0 004 5.91zM3.426 13l6-8.727h1.018l-6 8.727H3.426z"})))},"√":function(n){return d.createElement("svg",cu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Aa||(Aa=d.createElement("path",{d:"M7.494 11.611l2.484-7.338h1.27L8.201 13h-.89l.183-1.389zM6.65 8.449l1.112 3.196L7.958 13h-.852L5.351 8.45h1.3zM4.566 9.553V8.449h2.025v1.104H4.566z"})))},"←":function(n){return d.createElement("svg",su({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),$a||($a=d.createElement("path",{d:"M7.16 12.158L3.183 8.182l3.975-3.976.767.759-2.663 2.663h6.69v1.108h-6.69l2.663 2.659-.767.763z"})))},"→":function(n){return d.createElement("svg",uu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Na||(Na=d.createElement("path",{d:"M8.294 12.158l-.767-.759 2.663-2.663H3.5V7.628h6.69l-2.663-2.66.767-.762 3.976 3.976-3.976 3.976z"})))},"←/":function(n){return d.createElement("svg",du({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Pa||(Pa=d.createElement("path",{d:"M7.16 12.157L3.183 8.182l3.975-3.976.767.758-2.663 2.664h6.69v1.108h-6.69l2.663 2.659-.767.762z"})),ka||(ka=d.createElement("path",{d:"M11.665 3.102l-5.843 9.46h-.664L11 3.102h.665z"})))},"/→":function(n){return d.createElement("svg",pu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Ia||(Ia=d.createElement("path",{d:"M8.294 12.157l-.767-.758 2.663-2.663H3.5V7.628h6.69l-2.663-2.66.767-.762 3.976 3.976-3.976 3.975z"})),Ta||(Ta=d.createElement("path",{d:"M11.5 3.102l-5.842 9.46h-.665l5.842-9.46h.665z"})))},"↔":function(n){return d.createElement("svg",hu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Ba||(Ba=d.createElement("path",{d:"M5.057 12.055L1.184 8.182l3.873-3.874.767.759-2.56 2.56h9.562l-2.561-2.56.767-.759 3.873 3.874-3.873 3.873-.767-.767 2.56-2.552H3.264l2.561 2.552-.767.767z"})))},"∏":function(n){return d.createElement("svg",fu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),La||(La=d.createElement("path",{d:"M10.413 3.727v8.377H9.255V4.636H6.123v7.468H4.969V3.727h5.444z"})))},"∑":function(n){return d.createElement("svg",mu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),_a||(_a=d.createElement("path",{d:"M11.184 11.405v.916H5.978v-.916h5.206zm-.309-7.678v.92H5.889v-.92h4.986zM9.678 7.875v.295l-3.434 4.15h-.72v-.738L8.527 8.02 5.523 4.476v-.749h.721l3.434 4.148z"})))},"∞":function(n){return d.createElement("svg",vu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Va||(Va=d.createElement("path",{d:"M5.042 5.842c.324 0 .62.047.886.14.27.095.513.217.729.367.219.148.41.302.575.46.091.086.174.17.247.252.074.082.145.165.213.247.063-.082.127-.162.192-.238.068-.08.154-.167.256-.26.247-.242.554-.463.92-.665.37-.202.797-.303 1.283-.303.455 0 .868.111 1.24.333.375.218.672.512.89.882.222.37.333.778.333 1.227 0 .341-.064.66-.192.959a2.49 2.49 0 01-.528.78 2.455 2.455 0 01-1.743.712c-.324 0-.622-.046-.895-.137a3.256 3.256 0 01-.733-.358 4.588 4.588 0 01-.57-.447 6.736 6.736 0 01-.252-.265 7.034 7.034 0 01-.2-.251l-.218.251a5.09 5.09 0 01-.247.265 4.203 4.203 0 01-.571.447 3.27 3.27 0 01-.729.354 2.66 2.66 0 01-.886.14c-.46 0-.877-.109-1.249-.328a2.5 2.5 0 01-.89-.882 2.378 2.378 0 01-.333-1.24c0-.338.063-.653.188-.946.128-.295.304-.555.528-.78.227-.224.49-.399.789-.524a2.45 2.45 0 01.967-.192zM3.746 8.284c0 .236.059.45.175.644a1.3 1.3 0 001.12.63c.268 0 .514-.06.738-.179.225-.12.433-.27.627-.451a3.717 3.717 0 00.545-.644 6.678 6.678 0 00-.243-.303 2.94 2.94 0 00-.302-.323 2.64 2.64 0 00-.618-.452 1.538 1.538 0 00-.746-.188c-.239 0-.456.059-.652.175a1.3 1.3 0 00-.469.46c-.116.19-.175.4-.175.631zm7.875 0c0-.23-.058-.44-.174-.63a1.276 1.276 0 00-.46-.46 1.222 1.222 0 00-.644-.176c-.182 0-.355.029-.52.086-.165.056-.32.133-.464.23a2.7 2.7 0 00-.392.324c-.128.119-.24.241-.337.366-.097.122-.166.209-.209.26.071.1.15.203.239.311.088.105.19.216.307.333.19.181.397.332.622.451.227.12.479.18.754.18a1.276 1.276 0 001.104-.63c.116-.195.174-.41.174-.645z"})))},"∂":function(n){return d.createElement("svg",gu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),za||(za=d.createElement("path",{d:"M7.723 6.983c.335 0 .655.064.959.192.304.127.567.31.788.545-.07-.508-.209-.943-.413-1.304a2.336 2.336 0 00-.754-.83 1.746 1.746 0 00-.968-.29c-.278 0-.544.026-.797.08-.25.054-.507.13-.771.226l-.158-1.048c.256-.11.522-.205.797-.281.276-.08.63-.12 1.061-.12.739 0 1.354.196 1.846.588.494.392.863.946 1.107 1.662.248.713.371 1.55.371 2.51v.341c.003.744-.113 1.408-.35 1.99-.232.583-.569 1.041-1.01 1.377-.437.332-.964.498-1.58.498-.602 0-1.12-.135-1.556-.405a2.69 2.69 0 01-.997-1.108c-.23-.468-.345-.998-.345-1.589v-.136c0-.56.11-1.057.328-1.492.219-.437.534-.781.946-1.031.415-.25.914-.375 1.496-.375zm.17 1.1c-.366 0-.666.082-.899.246-.23.165-.4.387-.511.665a2.504 2.504 0 00-.162.92v.129c0 .363.054.694.162.992.11.299.278.537.503.716.227.18.518.269.873.269.358 0 .65-.104.878-.311.23-.21.4-.497.512-.861a4.22 4.22 0 00.166-1.232v-.494a1.371 1.371 0 00-.218-.426 1.443 1.443 0 00-.485-.426c-.213-.125-.486-.188-.819-.188z"})))},"∆":function(n){return d.createElement("svg",bu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Ga||(Ga=d.createElement("path",{d:"M4.297 13l3.14-8.727H8.96L12.099 13H4.297zm1.79-1.133h4.227l-2.08-6.009h-.068l-2.08 6.009z"})))},"∫":function(n){return d.createElement("svg",Cu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Fa||(Fa=d.createElement("path",{d:"M8.35 12.473c0 .673-.171 1.189-.512 1.547-.341.358-.833.537-1.475.537a2.815 2.815 0 01-.75-.098l.098-1.07c.066.017.16.033.282.047.122.014.221.021.298.021.278 0 .483-.078.613-.234.131-.154.197-.392.197-.716V5.114c0-.722.178-1.276.536-1.662.361-.387.88-.58 1.556-.58.145 0 .29.011.434.034.148.023.3.053.457.09L9.943 4.03a2.127 2.127 0 00-.328-.038 6.799 6.799 0 00-.397-.013c-.298 0-.518.087-.66.26-.14.17-.209.439-.209.805v7.428z"})))},"≈":function(n){return d.createElement("svg",yu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Ha||(Ha=d.createElement("path",{d:"M4.965 8.178c-.003-.495.074-.894.23-1.198.16-.307.37-.531.635-.673.267-.142.558-.213.874-.213.29 0 .55.06.784.183.235.12.505.305.81.558.204.17.369.291.494.362a.814.814 0 00.409.107c.236 0 .42-.085.554-.256.136-.17.201-.42.196-.75h1.078c.008.489-.068.888-.23 1.198-.16.307-.374.534-.644.682-.267.144-.56.217-.878.217-.28 0-.54-.058-.78-.175-.238-.116-.512-.308-.822-.575a3.4 3.4 0 00-.477-.358.793.793 0 00-.4-.102.709.709 0 00-.55.234c-.142.153-.21.406-.205.759H4.965zm0 2.642c-.003-.495.074-.894.23-1.198.16-.307.37-.531.635-.673.267-.142.558-.213.874-.213.29 0 .55.06.784.183.235.12.505.305.81.558.204.17.369.291.494.362a.814.814 0 00.409.107c.236 0 .42-.085.554-.256.136-.17.201-.42.196-.75h1.078c.008.489-.068.888-.23 1.198-.16.307-.374.534-.644.682-.267.144-.56.217-.878.217-.28 0-.54-.058-.78-.175-.238-.116-.512-.308-.822-.575a3.405 3.405 0 00-.477-.358.793.793 0 00-.4-.102.709.709 0 00-.55.234c-.142.153-.21.406-.205.759H4.965z"})))},"=/":function(n){return d.createElement("svg",Ou({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Ra||(Ra=d.createElement("path",{d:"M8.67 5.399h1.164l-2.502 6.328H6.17L8.67 5.4zM5.266 7.81V6.69h5.458v1.12H5.266zm0 2.625v-1.12h5.458v1.12H5.266z"})))},"≤":function(n){return d.createElement("svg",wu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Za||(Za=d.createElement("path",{d:"M10.827 11.616H5.168V10.5h5.66v1.116zm-5.659-3.57V7.09l5.66-1.858v1.159l-3.879 1.16.043-.078v.188l-.043-.077 3.878 1.16v1.158L5.168 8.045z"})))},"≥":function(n){return d.createElement("svg",Su({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Ka||(Ka=d.createElement("path",{d:"M5.168 11.616V10.5h5.66v1.116h-5.66zm5.66-3.57l-5.66 1.857V8.744l3.874-1.159-.039.077v-.188l.039.077-3.874-1.159v-1.16l5.66 1.859v.954z"})))},"℉":function(n){return d.createElement("svg",tu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),Sa||(Sa=d.createElement("path",{d:"M5.278 8.015c-.307 0-.588-.074-.841-.223a1.744 1.744 0 01-.604-.608 1.628 1.628 0 01-.224-.841c0-.308.075-.587.224-.838.152-.254.353-.455.604-.604.253-.151.534-.227.841-.227a1.677 1.677 0 011.445.831c.152.25.228.53.228.838 0 .308-.076.588-.227.841-.15.254-.35.456-.604.608-.253.149-.534.223-.842.223zm0-.81c.161 0 .307-.038.437-.116a.868.868 0 00.31-1.18.84.84 0 00-.31-.308.833.833 0 00-.437-.118.869.869 0 00-.746.426.846.846 0 00-.113.434.846.846 0 00.426.746c.13.078.275.117.433.117zM8.361 12V4.727h4.51v.945H9.458v2.216h3.09v.94h-3.09V12H8.361z"})))},"℃":function(n){return d.createElement("svg",eu({width:16,height:16,viewBox:"0 0 16 16",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),wa||(wa=d.createElement("path",{d:"M4.278 8.016c-.307 0-.588-.075-.841-.224a1.744 1.744 0 01-.604-.607 1.628 1.628 0 01-.224-.842c0-.308.075-.587.224-.838.152-.253.353-.454.604-.604.253-.151.534-.227.841-.227a1.677 1.677 0 011.445.831c.152.251.228.53.228.838 0 .308-.076.588-.227.842-.15.253-.35.455-.604.607-.253.15-.534.224-.842.224zm0-.81c.161 0 .307-.039.437-.117a.869.869 0 00.31-1.18.84.84 0 00-.31-.308.833.833 0 00-.437-.117.869.869 0 00-.746.426.846.846 0 00-.113.433.846.846 0 00.426.746c.13.078.275.117.433.117zm8.985-.114h-1.108a1.694 1.694 0 00-.664-1.083 1.836 1.836 0 00-.565-.284 2.204 2.204 0 00-.657-.096c-.419 0-.794.106-1.126.316-.329.211-.589.52-.78.927-.19.407-.285.905-.285 1.492 0 .592.095 1.091.284 1.498.192.408.454.715.785.924.331.208.704.312 1.119.312.23 0 .447-.03.653-.092.208-.064.397-.158.565-.28a1.718 1.718 0 00.67-1.07l1.109.004c-.06.357-.174.686-.345.987a2.725 2.725 0 01-.65.774 2.94 2.94 0 01-.902.501 3.338 3.338 0 01-1.107.178c-.63 0-1.191-.15-1.684-.448-.492-.3-.88-.73-1.164-1.289-.282-.559-.423-1.225-.423-2 0-.776.142-1.442.426-1.999.284-.558.672-.987 1.165-1.285a3.158 3.158 0 011.68-.451c.385 0 .745.056 1.08.167.335.109.637.27.905.483.267.21.489.469.664.774.175.303.293.65.355 1.04z"})))},about:function(n){return d.createElement("svg",Xa({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),pt||(pt=d.createElement("path",{d:"M12 4.5a7.5 7.5 0 100 15 7.5 7.5 0 000-15zM12 18c-3.307 0-6-2.693-6-6s2.693-6 6-6 6 2.693 6 6-2.693 6-6 6z",fill:"currentcolor"})),ht||(ht=d.createElement("rect",{x:11.25,y:9.5,width:1.5,height:7,rx:.75,fill:"currentcolor"})),ft||(ft=d.createElement("rect",{x:11.25,y:7.25,width:1.5,height:1.5,rx:.75,fill:"currentcolor"})))},analyse:function(n){return d.createElement("svg",Qa({width:24,height:24,viewBox:"0 0 24 24",xmlns:"http://www.w3.org/2000/svg"},n),mt||(mt=d.createElement("path",{d:"M17.56 18.412a2.551 2.551 0 01-2.2 1.242H8.271a2.571 2.571 0 01-2.3-3.724l3.51-7a.99.99 0 00.1-.441V6.337h-.6v-2h5.705v2h-.846v2.1c.002.162.044.32.121.463l.05.094a4.448 4.448 0 00-1.61 1.239l-.214-.4a2.993 2.993 0 01-.343-1.388V6.554h-.26V8.49c-.001.464-.11.922-.317 1.338l-3.51 7a.57.57 0 00.51.827h7.087a.548.548 0 00.424-.19h.062a4.4 4.4 0 002.084-.521 2.558 2.558 0 01-.366 1.467z",fill:"currentcolor"})),vt||(vt=d.createElement("path",{d:"M15.842 17.465a4.436 4.436 0 110-8.872 4.436 4.436 0 010 8.872zm0-7.87a3.436 3.436 0 100 6.872 3.436 3.436 0 000-6.873z",fill:"currentcolor"})),gt||(gt=d.createElement("path",{d:"M16.6 12.089l-1.007.028c-.16 1.472-.162 3.537-1.806 3.29-.38-.056-.218-.634.16-.578.983.147.915-1.35 1.042-2.695l-.76.02c-.386.012-.385-.588 0-.6l.837-.022c.151-.882.494-1.554 1.458-1.394.38.063.218.64-.16.578-.4-.065-.578.275-.683.8l.918-.026c.386-.011.386.589 0 .599z",fill:"currentcolor"})),bt||(bt=d.createElement("path",{d:"M18.16 13.222c-.265.26-.514.537-.76.815.166.264.346.518.541.76.24.3-.182.725-.424.424A8.779 8.779 0 0117 14.5c-.213.244-.429.487-.654.722-.268.279-.692-.146-.424-.424.268-.278.507-.553.753-.835a9.057 9.057 0 01-.46-.963c-.146-.358.434-.513.578-.16.09.22.19.437.3.648.21-.235.424-.467.65-.69.27-.272.693.153.418.424z",fill:"currentcolor"})))},"any-atom":function(n){return d.createElement("svg",Mu({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Ya||(Ya=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M3 22a.997.997 0 01-1-1v-6a1.5 1.5 0 011.5 1.5v4h4A1.5 1.5 0 019 22H3zM2 9a1.5 1.5 0 001.5-1.5v-4h4A1.5 1.5 0 009 2H3a.997.997 0 00-1 1v6zm13-7a1.5 1.5 0 001.5 1.5h4v4A1.5 1.5 0 0022 9V3a.997.997 0 00-1-1h-6zm7 13a1.5 1.5 0 00-1.5 1.5v4h-4A1.5 1.5 0 0015 22h6a.997.997 0 00.383-.076l.015-.006c.232-.101.419-.288.52-.52l.006-.015A.997.997 0 0022 21v-6z",fill:"currentColor"})),Ua||(Ua=d.createElement("path",{d:"M8.988 16.94a.838.838 0 11-1.576-.565l3.373-9.219a1 1 0 01.939-.656h.552a1 1 0 01.94.656l3.372 9.219a.837.837 0 11-1.576.565l-2.951-8.4a.062.062 0 00-.117 0l-2.956 8.4zm.104-3.05c0-.385.312-.698.698-.698h4.415a.698.698 0 110 1.397H9.79a.698.698 0 01-.698-.698z",fill:"#333"})))},arom:function(n){return d.createElement("svg",nl({width:24,height:24,viewBox:"0 0 24 24",xmlns:"http://www.w3.org/2000/svg"},n),Ct||(Ct=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M11.53 3.626a.94.94 0 01.939 0l6.561 3.781c.291.168.47.477.47.812v7.562a.937.937 0 01-.47.812l-6.562 3.781a.94.94 0 01-.938 0l-6.56-3.781a.937.937 0 01-.47-.812V8.219c0-.335.179-.644.47-.812l6.56-3.781zM12 5.52L6.377 8.76v6.48L12 18.48l5.623-3.24V8.76l-5.623-3.24z",fill:"currentcolor"})),yt||(yt=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M12.005 9.7A2.3 2.3 0 009.702 12a2.3 2.3 0 002.303 2.298 2.3 2.3 0 002.302-2.299 2.3 2.3 0 00-2.302-2.298zM7.825 12a4.177 4.177 0 014.18-4.174 4.177 4.177 0 014.18 4.173 4.177 4.177 0 01-4.18 4.174 4.177 4.177 0 01-4.18-4.174z",fill:"currentcolor"})))},"arrow-upward":function(n){return d.createElement("svg",el({width:21,height:27,viewBox:"0 0 21 27",xmlns:"http://www.w3.org/2000/svg"},n),Ot||(Ot=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M.898 8.972L9.54.395a1.365 1.365 0 011.92 0l8.642 8.577c.53.527.53 1.38 0 1.906-.53.527-1.39.527-1.92 0l-6.324-6.276V26.5H9.142V4.602l-6.324 6.276c-.53.527-1.39.527-1.92 0a1.34 1.34 0 010-1.906z"})))},"bond-any":function(n){return d.createElement("svg",tl({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),wt||(wt=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M15.942 32.078a2 2 0 01-.02 2.828l-3.646 3.595a2 2 0 01-2.808-2.85l3.646-3.593a2 2 0 012.828.02zM23.457 24.538a2 2 0 01-.02 2.829l-3.647 3.592a2 2 0 11-2.807-2.85l3.646-3.592a2 2 0 012.828.021zM31.013 17.036a2 2 0 01-.021 2.829l-3.646 3.592a2 2 0 11-2.807-2.85l3.646-3.592a2 2 0 012.828.021zM38.553 9.52a2 2 0 01-.02 2.828l-3.647 3.594a2 2 0 11-2.808-2.848L35.724 9.5a2 2 0 012.829.02z",fill:"#231F20"})))},"bond-aromatic":function(n){return d.createElement("svg",rl({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),St||(St=d.createElement("path",{d:"M15.886 40.04a2 2 0 01-1.4-3.424l19.6-19.324a2 2 0 012.8 2.85l-19.6 19.322a2 2 0 01-1.4.576zM17.456 27.214l-3.544 3.494a1.998 1.998 0 01-2.896.045 2 2 0 01.095-2.895l3.544-3.494a1.998 1.998 0 012.896-.044 2 2 0 01-.095 2.894zM28.568 15.454a2 2 0 01-1.4-3.424l3.546-3.494a2 2 0 012.8 2.848l-3.542 3.494a2 2 0 01-1.404.576zM20.539 23.368a1.999 1.999 0 01-1.4-3.424l3.542-3.494a2.001 2.001 0 013.286 2.203 2 2 0 01-.486.645L21.943 22.8a2 2 0 01-1.404.568z",fill:"#231F20"})))},"bond-crossed":function(n){return d.createElement("svg",ol({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Mt||(Mt=d.createElement("path",{d:"M39.563 18.718l-14.098 6.8-7.25 13.866a2 2 0 01-3.546-1.852l4.762-9.11-9.26 4.464a2.001 2.001 0 11-1.735-3.6l14.098-6.8 7.25-13.87a2 2 0 113.546 1.852l-4.762 9.11 9.26-4.464a2 2 0 111.735 3.6v.004z",fill:"#231F20"})))},"bond-hydrogen":function(n){return d.createElement("svg",sl({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),$t||($t=d.createElement("path",{d:"M14.261 35.726a2 2 0 01-1.4-3.424l1.012-1a2 2 0 112.8 2.848l-1.012 1a2 2 0 01-1.4.576zM18.875 31.108a2 2 0 01-1.4-3.424l1.012-1a2 2 0 012.8 2.85l-1 1a2 2 0 01-1.412.574zM23.486 26.49a2 2 0 01-1.4-3.426l1-1a2 2 0 012.8 2.848l-1 1a2 2 0 01-1.4.578zM28.112 21.886a2 2 0 01-1.4-3.426l1.01-1a2 2 0 112.8 2.848l-1 1a2 2 0 01-1.41.578zM32.726 17.27a2 2 0 01-1.4-3.424l1.012-1a2 2 0 012.8 2.85l-1.012 1a2 2 0 01-1.4.574z",fill:"#231F20"})))},"bond-dative":function(n){return d.createElement("svg",il({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),xt||(xt=d.createElement("path",{d:"M38.2 11.278l-5.554 11.76c-.234.494-.914.558-1.346.126l-1.65-1.65-15.278 15.054a2.001 2.001 0 01-3.468-1.423 2.002 2.002 0 01.668-1.427l15.252-15.032-1.728-1.728c-.432-.434-.368-1.112.126-1.346l11.76-5.554c.708-.338 1.55.504 1.218 1.22z",fill:"#231F20"})))},"bond-double":function(n){return d.createElement("svg",ll({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Et||(Et=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M36.916 17.314a2 2 0 01-.02 2.828L17.29 39.465a2 2 0 01-2.808-2.85l19.606-19.322a2 2 0 012.828.021zM33.538 8.556a2 2 0 01-.02 2.829L13.912 30.706a2 2 0 01-2.808-2.85L30.71 8.536a2 2 0 012.828.021z",fill:"#231F20"})))},"bond-doublearomatic":function(n){return d.createElement("svg",al({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),jt||(jt=d.createElement("path",{d:"M17.572 27.342l-3.544 3.494a2 2 0 11-2.8-2.85l3.544-3.494a1.999 1.999 0 112.8 2.85zM24.427 19.6a1.999 1.999 0 01-1.4-3.424l3.544-3.494a2 2 0 012.8 2.848l-3.54 3.502a2 2 0 01-1.404.568zM32.102 11.96a2 2 0 100-4 2 2 0 000 4zM20.298 23.762a2 2 0 100-4 2 2 0 000 4zM20.888 36.036l-3.544 3.494a2 2 0 11-2.8-2.85l3.536-3.494a1.999 1.999 0 112.8 2.85h.008zM27.744 28.302a2 2 0 01-1.4-3.424l3.544-3.494a2 2 0 112.8 2.848l-3.544 3.494a2 2 0 01-1.4.576zM35.418 20.654a2 2 0 100-4 2 2 0 000 4zM23.614 32.456a2 2 0 100-4 2 2 0 000 4z",fill:"#231F20"})))},"bond-down":function(n){return d.createElement("svg",cl({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Dt||(Dt=d.createElement("path",{d:"M14.531 35.178l-1.132.658a.866.866 0 01-1.183-1.18l.655-1.14 1.66 1.662zM17.896 33.23l-1.79 1.038-2.33-2.33 1.032-1.796 3.088 3.088zM21.146 31.348l-1.79 1.038-3.706-3.706 1.032-1.796 4.464 4.464zM24.398 29.468l-1.793 1.036-5.084-5.082 1.032-1.798 5.845 5.844zM27.648 27.586l-1.793 1.036-6.46-6.46 1.032-1.796 7.22 7.22zM30.897 25.704l-1.792 1.038-7.836-7.838 1.032-1.796 8.596 8.596zM34.147 23.822l-1.792 1.038-9.212-9.214 1.032-1.796 9.972 9.972zM37.394 21.94l-1.79 1.038-10.59-10.59 1.032-1.796L37.394 21.94zM39.42 20.768l-.566.328L26.888 9.13l.324-.566a.866.866 0 011.362-.18L39.6 19.4a.863.863 0 01-.18 1.368z",fill:"#231F20"})),At||(At=d.createElement("path",{d:"M37.394 21.94l-1.79 1.038-10.59-10.59 1.032-1.796L37.394 21.94zM39.42 20.768l-.566.328L26.888 9.13l.324-.566a.866.866 0 011.362-.18L39.6 19.4a.863.863 0 01-.18 1.368zM34.147 23.822l-1.792 1.038-9.212-9.214 1.032-1.796 9.972 9.972zM30.897 25.704l-1.792 1.038-7.836-7.838 1.032-1.796 8.596 8.596zM27.648 27.586l-1.793 1.036-6.46-6.46 1.032-1.796 7.22 7.22zM24.398 29.468l-1.793 1.036-5.084-5.082 1.032-1.798 5.845 5.844zM21.146 31.348l-1.79 1.038-3.706-3.706 1.032-1.796 4.464 4.464zM17.896 33.23l-1.79 1.038-2.33-2.33 1.032-1.796 3.088 3.088zM14.531 35.178l-1.132.658a.866.866 0 01-1.183-1.18l.655-1.14 1.66 1.662z",fill:"#231F20"})))},"bond-single":function(n){return d.createElement("svg",pl({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),kt||(kt=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M35.227 12.934a2 2 0 01-.02 2.829L15.601 35.087a2 2 0 11-2.808-2.85l19.604-19.323a2 2 0 012.829.02z",fill:"#231F20"})))},"bond-singlearomatic":function(n){return d.createElement("svg",ul({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Nt||(Nt=d.createElement("path",{d:"M15.886 40.04a2 2 0 01-1.4-3.424l19.6-19.324a2 2 0 112.8 2.85l-19.6 19.322a2 2 0 01-1.4.576zM17.584 27.342l-3.544 3.494a2 2 0 11-2.8-2.85l3.544-3.494a1.998 1.998 0 012.896-.044 1.998 1.998 0 01-.096 2.894zM24.441 19.6a2 2 0 01-1.4-3.424l3.54-3.486a1.998 1.998 0 013.343.623 2.001 2.001 0 01-.543 2.225l-3.536 3.494a2 2 0 01-1.404.568zM32.113 11.96a2 2 0 100-4 2 2 0 000 4zM20.31 23.762a2 2 0 100-4 2 2 0 000 4z",fill:"#231F20"})))},"bond-singledouble":function(n){return d.createElement("svg",dl({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Pt||(Pt=d.createElement("path",{d:"M19.078 31.6l-3.544 3.488a2 2 0 11-2.8-2.85l3.543-3.494a2 2 0 112.8 2.85v.006zM30.2 19.832a2 2 0 01-1.4-3.424l3.545-3.494a2 2 0 112.8 2.85L31.6 19.258a2 2 0 01-1.4.574zM22.16 27.748a2 2 0 01-1.4-3.426l3.544-3.494a2 2 0 012.8 2.85l-3.544 3.494a2 2 0 01-1.4.576zM22.4 16.352a2 2 0 01-1.4-3.424l3.544-3.494a2 2 0 112.8 2.848L23.8 15.776a2 2 0 01-1.4.576zM14.372 24.266a2 2 0 01-1.4-3.424l3.54-3.494A2.001 2.001 0 1119.32 20.2l-3.544 3.49a2 2 0 01-1.404.576zM29.946 31.228a2 2 0 01-1.4-3.424l3.546-3.494a2 2 0 112.8 2.848l-3.546 3.494a2 2 0 01-1.4.576zM21.916 39.142a2 2 0 01-1.4-3.424l3.547-3.494a2 2 0 112.8 2.848l-3.543 3.494a2 2 0 01-1.404.576z",fill:"#231F20"})))},"bond-triple":function(n){return d.createElement("svg",hl({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),It||(It=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M35.158 12.928a2 2 0 01-.02 2.829L15.532 35.078a2 2 0 11-2.808-2.849L32.33 12.908a2 2 0 012.828.021zM31.306 5.49a2 2 0 01-.02 2.829L11.678 27.64a2 2 0 11-2.807-2.849L28.477 5.47a2 2 0 012.829.02zM39.013 20.366a2 2 0 01-.02 2.829L19.385 42.517a2 2 0 01-2.807-2.85l19.606-19.322a2 2 0 012.828.021z",fill:"#231F20"})))},"bond-up":function(n){return d.createElement("svg",fl({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Tt||(Tt=d.createElement("path",{d:"M19.71 10.384L6.7 17.918a.433.433 0 01-.592-.59l7.5-13.046a.433.433 0 01.68-.09L19.8 9.7a.432.432 0 01-.09.684z",fill:"#333"})))},"bond-updown":function(n){return d.createElement("svg",ml({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Bt||(Bt=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M27.326 8.31a1 1 0 011.264.128l10.728 10.818a1 1 0 01-1.42 1.408l-7.14-7.2 3.81 9.17a1 1 0 01-1.479 1.216l-7.03-4.693 2.959 6.644a1 1 0 01-1.31 1.325l-5.921-2.562 1.467 4.91a1 1 0 01-1.218 1.251l-4.594-1.237-3.369 5.868a1 1 0 11-1.734-.996l3.752-6.536a1 1 0 011.127-.468l3.607.972-1.569-5.248a1 1 0 011.355-1.204l5.537 2.396-3.321-7.46a1 1 0 011.468-1.238l7.16 4.78-4.498-10.829a1 1 0 01.369-1.215z",fill:"#231F20"})))},"capital-t":function(n){return d.createElement("svg",vl({width:22,height:23,viewBox:"0 0 22 23",xmlns:"http://www.w3.org/2000/svg"},n),Lt||(Lt=d.createElement("path",{d:"M.5 0v4.5h8.25v18h4.5v-18h8.25V0H.5z"})))},chain:function(n){return d.createElement("svg",gl({width:32,height:32,viewBox:"0 0 32 32",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),_t||(_t=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M26.323 10.62c.517.525.51 1.369-.014 1.886l-5.414 5.336c-.33.324-.804.455-1.254.345l-6.996-1.715-4.993 4.92a1.333 1.333 0 01-1.872-1.899l5.523-5.443c.33-.324.804-.455 1.253-.345l6.997 1.715 4.885-4.814a1.333 1.333 0 011.885.014z",fill:"#231F20"})))},"charge-minus":function(n){return d.createElement("svg",bl({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Vt||(Vt=d.createElement("path",{d:"M20 4h-8v2h8V4z",fill:"#231F20"})),zt||(zt=d.createElement("path",{d:"M5.82 19.32a1 1 0 01-.948.68h-.45a1 1 0 01-.942-1.338l3.228-9A1 1 0 017.65 9h1.707a1 1 0 01.941.663l3.224 9A1 1 0 0112.58 20h-.451a1 1 0 01-.948-.68l-2.62-7.764a.062.062 0 00-.117 0L5.819 19.32zm-.392-2.736c0-.501.406-.908.907-.908h4.302a.908.908 0 010 1.816H6.335a.908.908 0 01-.907-.908z",fill:"#000"})))},"charge-plus":function(n){return d.createElement("svg",Cl({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Gt||(Gt=d.createElement("path",{d:"M21.5 6.499v2h-4V12.5h-2V8.499h-4v-2h4V2.5h2v3.999h4z",fill:"#231F20"})),Ft||(Ft=d.createElement("path",{d:"M5.82 19.32a1 1 0 01-.948.68h-.45a1 1 0 01-.942-1.338l3.228-9A1 1 0 017.65 9h1.707a1 1 0 01.941.663l3.224 9A1 1 0 0112.58 20h-.451a1 1 0 01-.948-.68l-2.62-7.764a.062.062 0 00-.117 0L5.819 19.32zm-.392-2.736c0-.501.406-.908.907-.908h4.302a.908.908 0 010 1.816H6.335a.908.908 0 01-.907-.908z",fill:"#000"})))},check:function(n){return d.createElement("svg",yl({width:24,height:24,viewBox:"0 0 24 24",xmlns:"http://www.w3.org/2000/svg"},n),Ht||(Ht=d.createElement("path",{d:"M12 5a7 7 0 11-7 7 7.008 7.008 0 017-7zm0-2a9 9 0 100 18 9 9 0 000-18z",fill:"currentcolor"})),Rt||(Rt=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M16.73 9.555l-5.838 5.837-3.314-3.54 1.46-1.367 1.902 2.031 4.376-4.375 1.414 1.414z",fill:"currentcolor"})))},"chiral-flag":function(n){return d.createElement("svg",Ol({"data-name":"Layer 1",xmlns:"http://www.w3.org/2000/svg",viewBox:"0 -5 70 35"},n),Zt||(Zt=d.createElement("path",{d:"M0 25h69V0H0zM68 1v23H1V1z"})),Kt||(Kt=d.createElement("path",{d:"M21 18.14a3.85 3.85 0 002.71-.93 3.07 3.07 0 001-2.43H23.1a2.09 2.09 0 01-.53 1.54 2.09 2.09 0 01-1.55.53 1.94 1.94 0 01-1.64-.8 3.31 3.31 0 01-.6-2v-1.98a3.33 3.33 0 01.59-2 1.89 1.89 0 011.6-.8 2.18 2.18 0 011.59.53 2 2 0 01.54 1.53h1.61a3 3 0 00-1-2.45A4 4 0 0021 7.9a3.58 3.58 0 00-2.78 1.18 4.3 4.3 0 00-1.07 3V14a4.25 4.25 0 001.08 3A3.65 3.65 0 0021 18.14zM27.77 12.54a1.67 1.67 0 01.64-.52 2.09 2.09 0 01.92-.19 1.26 1.26 0 011 .39 1.91 1.91 0 01.34 1.26V18h1.66v-4.51a3.36 3.36 0 00-.66-2.29 2.33 2.33 0 00-1.84-.74 2.42 2.42 0 00-1.17.29 2.63 2.63 0 00-.9.81V7.34h-1.65V18h1.66zM34.16 7.34h1.66V8.8h-1.66zM34.16 10.6h1.66V18h-1.66zM39.32 12.86a1.35 1.35 0 01.5-.58 1.49 1.49 0 01.81-.21h.71l.2-1.55-.24-.06h-.28a1.68 1.68 0 00-1 .32 2.38 2.38 0 00-.72.89l-.11-1.07h-1.53V18h1.66zM45.49 13.65a4.08 4.08 0 00-2.39.6 1.93 1.93 0 00-.85 1.67 2.16 2.16 0 00.62 1.63 2.46 2.46 0 001.77.59 2.3 2.3 0 001.25-.35 2.85 2.85 0 00.9-.87 4 4 0 00.08.53q.06.27.15.55h1.68a4.59 4.59 0 01-.2-.82 6 6 0 01-.06-.88V13a2.31 2.31 0 00-.79-1.89 3.17 3.17 0 00-2.08-.66 3.32 3.32 0 00-2.16.68 1.83 1.83 0 00-.78 1.55h1.6a.86.86 0 01.33-.7 1.39 1.39 0 01.9-.27 1.35 1.35 0 011 .33 1.21 1.21 0 01.34.91v.65zm1.29 2.13a1.59 1.59 0 01-.67.72 2.07 2.07 0 01-1.12.31 1.15 1.15 0 01-.8-.25.86.86 0 01-.28-.67 1.09 1.09 0 01.41-.84 1.67 1.67 0 011.13-.36h1.32zM50.27 7.34h1.66V18h-1.66z"})))},cip:function(n){return d.createElement("svg",wl({width:24,height:24,viewBox:"0 0 24 24",xmlns:"http://www.w3.org/2000/svg"},n),Yt||(Yt=d.createElement("path",{d:"M11.998 19.27L4.607 7.949a.7.7 0 01.347-1.042L9.447 5.27a.7.7 0 01.934.574l1.617 13.426zM5.65 7.718l4.848 7.419-1.06-8.8-3.788 1.38zM19.392 7.947L12 19.27l1.617-13.426a.7.7 0 01.935-.574l4.493 1.635a.7.7 0 01.347 1.041z",fill:"currentcolor"})))},clean:function(n){return d.createElement("svg",Sl({width:24,height:24,viewBox:"0 0 24 24",xmlns:"http://www.w3.org/2000/svg"},n),Ut||(Ut=d.createElement("path",{d:"M19.848 16.312a2.437 2.437 0 11-4.843-.386l-1.987-1.147-1-.578-1 .577-1.687.974a2.437 2.437 0 11-1.234-1.596l1.922-1.109 1-.578V9.16a2.437 2.437 0 112 0v3.31l1 .577 2.09 1.207a2.436 2.436 0 013.741 2.058h-.002z",fill:"currentcolor"})))},copies:xl,copy:xl,"copy-image":function(n){return d.createElement("svg",jl({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),qt||(qt=d.createElement("path",{d:"M17.25 18.75H9V8.25h8.25v10.5zm0-12H9a1.5 1.5 0 00-1.5 1.5v10.5a1.5 1.5 0 001.5 1.5h8.25a1.5 1.5 0 001.5-1.5V8.25a1.5 1.5 0 00-1.5-1.5zm-2.25-3H6a1.5 1.5 0 00-1.5 1.5v10.5H6V5.25h9v-1.5z",fill:"currentColor"})),Wt||(Wt=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M10.2 10a.5.5 0 01.5-.5h5a.5.5 0 01.5.5v2.469c0 .298-.26.527-.559.531a4.497 4.497 0 00-4.124 2.84 4.496 4.496 0 00-.29 1.161c-.03.274-.252.499-.528.499a.5.5 0 01-.5-.5v-7zm3 1.5a1 1 0 11-2 0 1 1 0 012 0z",fill:"currentColor"})),Xt||(Xt=d.createElement("path",{d:"M11.855 17.001c-.035.274.192.499.468.499H15.7a.5.5 0 00.5-.5v-2.905c0-.25-.186-.467-.438-.47a3.88 3.88 0 00-3.664 2.445c-.12.3-.2.613-.242.931z",fill:"currentColor"})))},"copy-mol":function(n){return d.createElement("svg",Dl({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),er||(er=d.createElement("path",{d:"M17.25 18.75H9V8.25h8.25v10.5zm0-12H9a1.5 1.5 0 00-1.5 1.5v10.5a1.5 1.5 0 001.5 1.5h8.25a1.5 1.5 0 001.5-1.5V8.25a1.5 1.5 0 00-1.5-1.5zm-2.25-3H6a1.5 1.5 0 00-1.5 1.5v10.5H6V5.25h9v-1.5z",fill:"currentColor"})),tr||(tr=d.createElement("path",{d:"M10 11a.5.5 0 01.5-.5h.682a.5.5 0 01.462.31l1.462 3.567a.05.05 0 00.094 0l1.463-3.567a.5.5 0 01.462-.31h.682a.5.5 0 01.5.5v4.818a.5.5 0 01-.5.5h-.193a.5.5 0 01-.5-.5V12.56a.029.029 0 00-.03-.029.029.029 0 00-.026.018l-1.373 3.427a.5.5 0 01-.464.314h-.135a.5.5 0 01-.464-.315l-1.373-3.44a.029.029 0 00-.056.01v3.273a.5.5 0 01-.5.5H10.5a.5.5 0 01-.5-.5V11z",fill:"currentColor"})))},"copy-ket":function(n){return d.createElement("svg",El({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Qt||(Qt=d.createElement("path",{d:"M17.25 18.75H9V8.25h8.25v10.5zm0-12H9a1.5 1.5 0 00-1.5 1.5v10.5a1.5 1.5 0 001.5 1.5h8.25a1.5 1.5 0 001.5-1.5V8.25a1.5 1.5 0 00-1.5-1.5zm-2.25-3H6a1.5 1.5 0 00-1.5 1.5v10.5H6V5.25h9v-1.5z",fill:"currentColor"})),nr||(nr=d.createElement("path",{d:"M11.3 16.318a.3.3 0 01-.3-.3V10.8a.3.3 0 01.3-.3h.63a.3.3 0 01.3.3v2.213a.052.052 0 00.092.033l1.989-2.436a.3.3 0 01.232-.11h.694a.3.3 0 01.23.491l-1.607 1.94a.3.3 0 00-.017.36l1.739 2.559a.3.3 0 01-.248.468h-.744a.3.3 0 01-.25-.134l-1.28-1.92a.3.3 0 00-.482-.024l-.28.342a.3.3 0 00-.068.19v1.246a.3.3 0 01-.3.3h-.63z",fill:"currentColor"})))},cut:function(n){return d.createElement("svg",Al({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),rr||(rr=d.createElement("path",{d:"M17.25 5.25l-4.5 4.5 1.5 1.5L19.5 6v-.75h-2.25zM12 12.375a.375.375 0 110-.75.375.375 0 010 .75zM7.5 18a1.5 1.5 0 110-3 1.5 1.5 0 010 3zm0-9a1.5 1.5 0 110-3 1.5 1.5 0 010 3zm2.73-.27c.172-.375.27-.788.27-1.23a3 3 0 10-3 3c.442 0 .855-.098 1.23-.27L10.5 12l-1.77 1.77a2.923 2.923 0 00-1.23-.27 3 3 0 103 3c0-.442-.098-.855-.27-1.23L12 13.5l5.25 5.25h2.25V18l-9.27-9.27z",fill:"currentcolor"})))},dearom:function(n){return d.createElement("svg",$l({width:24,height:24,viewBox:"0 0 24 24",xmlns:"http://www.w3.org/2000/svg"},n),or||(or=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M11.53 3.626a.94.94 0 01.94 0l6.56 3.781c.291.168.47.477.47.812v7.562a.937.937 0 01-.47.812l-6.56 3.781a.94.94 0 01-.94 0l-6.56-3.781a.937.937 0 01-.47-.812V8.219c0-.335.179-.644.47-.812l6.56-3.781zM6.378 8.76v6.48L12 18.48l5.622-3.24V8.76L12 5.52 6.378 8.76z",fill:"currentcolor"})),ir||(ir=d.createElement("path",{d:"M15.565 9.812v4.363l.935.569V9.243l-.935.569zM11.998 6.5C10.5 7.412 9.001 8.325 7.5 9.241l.934.57 3.564-2.173V6.5zM7.5 14.751l4.498 2.749v-1.138L8.434 14.17l-.934.58z",fill:"currentcolor"})))},delete:function(n){return d.createElement("svg",Nl({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),ar||(ar=d.createElement("path",{d:"M15.813 20.483h-7.63a1.8 1.8 0 01-1.8-1.8V7.357h11.23v11.326a1.8 1.8 0 01-1.8 1.8zm-7.43-2h7.23V9.357h-7.23v9.126zM19.305 4.613v2H4.695v-2h3.433l1.034-1.13h5.676l1.034 1.13h3.433z",fill:"currentColor"})))},dropdown:function(n){return d.createElement("svg",Pl({xmlns:"http://www.w3.org/2000/svg",width:1e3,height:1e3,viewBox:"0 0 1000 1000"},n),lr||(lr=d.createElement("path",{d:"M876.337 751.055c0 70.936-57.736 128.672-128.672 128.672H201.297c-70.936 0-128.557-57.736-128.557-128.672L747.55 76.36c70.936 0 128.672 57.506 128.672 128.557v546.138z"})))},"enhanced-stereo":function(n){return d.createElement("svg",kl({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),cr||(cr=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M14 4.5c0 1.138-.76 2.098-1.8 2.4v2.963a2.53 2.53 0 011.54 1.333l1.766-.758A1.501 1.501 0 1118.5 10.3a1.5 1.5 0 01-2.417 1.187l-2.084.894c-.003.301-.057.59-.152.858l1.476 1.273a3 3 0 11-.988 1.108l-1.367-1.18a2.433 2.433 0 01-2.656.184l-2.35 1.442a2.5 2.5 0 11-.683-1.322l1.993-1.223A2.649 2.649 0 019 12.347c0-1.14.711-2.107 1.7-2.452V6.87A2.501 2.501 0 1114 4.5zm-3.635 0a1.134 1.134 0 102.27 0 1.134 1.134 0 00-2.27 0zm1.135 8.955c-.592 0-1.071-.496-1.071-1.108 0-.612.48-1.108 1.07-1.108.592 0 1.072.496 1.072 1.108 0 .612-.48 1.108-1.071 1.108zM4.298 16.5a1.201 1.201 0 102.403 0 1.201 1.201 0 00-2.403 0zM17 18.513a1.513 1.513 0 110-3.026 1.513 1.513 0 010 3.026zM17 11a.7.7 0 110-1.398.7.7 0 010 1.398z",fill:"currentColor"})))},edit:function(n){return d.createElement("svg",Il({width:18,height:18,viewBox:"0 0 18 18",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),sr||(sr=d.createElement("path",{d:"M11.796 7.265l-1.06-1.06L3.75 13.19v1.06h1.06l6.986-6.985zm1.06-1.06l1.061-1.061-1.06-1.06-1.061 1.06 1.06 1.06zM5.432 15.75H2.25v-3.182L12.326 2.492a.75.75 0 011.06 0l2.123 2.121a.75.75 0 010 1.06L5.431 15.75z",fill:"currentColor"})))},"elements-group":function(n){return d.createElement("svg",Tl({width:18,height:15,viewBox:"0 0 18 15",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),ur||(ur=d.createElement("path",{d:"M16.2 2.579H8.705L7.026.899H.768A.768.768 0 000 1.669v11.207a1.8 1.8 0 001.8 1.8h14.4a1.8 1.8 0 001.8-1.8v-8.5a1.8 1.8 0 00-1.8-1.796zm-.2 10.1H2v-8.1h14v8.1z",fill:"currentcolor"})))},"extended-table":function(n){return d.createElement("svg",Ll({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),pr||(pr=d.createElement("path",{d:"M7.445 15.5H4.146c-.357 0-.646.269-.646.6v3.062c0 .331.29.6.646.6h3.299c.357 0 .646-.269.646-.6V16.1c0-.331-.29-.6-.646-.6zM13.652 15.5h-3.299c-.357 0-.646.269-.646.6v3.062c0 .331.29.6.646.6h3.299c.357 0 .646-.269.646-.6V16.1c0-.331-.29-.6-.646-.6zM19.855 15.5h-3.299c-.357 0-.646.269-.646.6v3.062c0 .331.29.6.646.6h3.299c.357 0 .646-.269.646-.6V16.1c0-.331-.29-.6-.646-.6zM5 13.5a.5.5 0 01-.5-.5V5a.5.5 0 01.5-.5h5.296a.5.5 0 01.5.5v.767a.5.5 0 01-.5.5H7.183a.5.5 0 00-.5.5v.845a.5.5 0 00.5.5h2.791a.5.5 0 01.5.5v.771a.5.5 0 01-.5.5H7.183a.5.5 0 00-.5.5v.85a.5.5 0 00.5.5h3.113a.5.5 0 01.5.5V13a.5.5 0 01-.5.5H5zM12.368 6.267a.5.5 0 01-.5-.5V5a.5.5 0 01.5-.5H19a.5.5 0 01.5.5v.767a.5.5 0 01-.5.5h-1.738a.5.5 0 00-.5.5V13a.5.5 0 01-.5.5H15.11a.5.5 0 01-.5-.5V6.767a.5.5 0 00-.5-.5h-1.742z",fill:"#333"})))},erase:function(n){return d.createElement("svg",Bl({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),dr||(dr=d.createElement("path",{d:"M40.284 18.458L30.37 8.546a2 2 0 00-2.828 0L7.716 28.372a2 2 0 000 2.828l7.084 7.082a6.001 6.001 0 008.488 0l17-17a2 2 0 000-2.828l-.004.004zm-19.824 17a2 2 0 01-2.832 0l-5.67-5.672 7.824-7.824 7.084 7.086-6.406 6.41z",fill:"#231F20"})))},"file-thumbnail":function(n){return d.createElement("svg",_l({width:29,height:37,viewBox:"0 0 29 37",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),hr||(hr=d.createElement("path",{d:"M19.872.583H3.747A3.594 3.594 0 00.164 4.167v28.666a3.594 3.594 0 003.583 3.584h21.5a3.594 3.594 0 003.584-3.584V9.543L19.872.583zM3.747 32.833V4.168h14.334v7.167h7.166v21.5h-21.5z",fill:"#005662"})),fr||(fr=d.createElement("path",{d:"M12.21 10.723l-3.66 9.15 10.065 6.404",stroke:"#005662",strokeWidth:1.483})),mr||(mr=d.createElement("circle",{cx:12.213,cy:10.723,r:1.83,fill:"#005662"})),vr||(vr=d.createElement("circle",{cx:8.552,cy:19.872,fill:"#005662",r:1.83})),gr||(gr=d.createElement("circle",{cx:18.619,cy:26.277,r:1.83,fill:"#005662"})))},"fullscreen-enter":function(n){return d.createElement("svg",As({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),qi||(qi=d.createElement("path",{d:"M8.75 3.75h-5v5h1.5V6.312L9 10.063l1-1.124L6.312 5.25H8.75v-1.5zM15.25 3.75h5v5h-1.5V6.312L15 10.063l-1-1.124 3.688-3.688H15.25v-1.5zM15.25 20.25h5v-5h-1.5v2.438L15 13.938l-1 1.124 3.688 3.688H15.25v1.5zM8.75 20.25h-5v-5h1.5v2.438L9 13.938l1 1.124-3.688 3.688H8.75v1.5z",fill:"currentColor"})))},"fullscreen-exit":function(n){return d.createElement("svg",$s({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Wi||(Wi=d.createElement("path",{d:"M19.25 14.25h-5v5h1.5v-2.438l3.75 3.75 1-1.125-3.688-3.687h2.438v-1.5zM5 14.25h5v5H8.5v-2.438l-3.75 3.75-1-1.125 3.688-3.687H5v-1.5zM5 10.063h5v-5H8.5V7.5L4.75 3.75l-1 1.125 3.688 3.688H5v1.5zM19.25 10.063h-5v-5h1.5V7.5l3.75-3.75 1 1.125-3.688 3.688h2.438v1.5z",fill:"currentColor"})))},"generic-groups":function(n){return d.createElement("svg",Vl({xmlns:"http://www.w3.org/2000/svg",viewBox:"0 0 750 750",height:1e3,width:1e3},n),br||(br=d.createElement("path",{d:"M73.129 209.914v403.543h403.226v73.371H62.133c-34.418 0-62.317-27.922-62.317-62.367V209.914zM304.07 343.45l103.004-103.086-48.754-49.89c-10.734-10.73-28.12-10.73-38.855 0l-63.05 64.199c-10.72 10.742-10.72 28.144 0 38.887zm132.696-73.37L334.859 373.53l311.95 313.297 103.375-103.086zm186.218 123.265V136.543c0-53.195-19.43-73.371-73.316-73.371H183.102c-56.454 0-73.317 16.875-73.317 73.371v366.855c0 54.297 16.863 73.372 73.317 73.372h293.253l-73.312-73.372H183.102V136.543h366.566v183.43zm0 0"})))},hand:Gl,compressedhand:Hl,help:function(n){return d.createElement("svg",Rl({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),wr||(wr=d.createElement("path",{d:"M11.25 16.5h1.5V15h-1.5v1.5zm.75-12a7.5 7.5 0 100 15 7.5 7.5 0 000-15zM12 18c-3.307 0-6-2.693-6-6s2.693-6 6-6 6 2.693 6 6-2.693 6-6 6zm0-10.5a3 3 0 00-3 3h1.5a1.5 1.5 0 113 0c0 1.5-2.25 1.313-2.25 3.75h1.5c0-1.688 2.25-1.875 2.25-3.75a3 3 0 00-3-3z",fill:"currentcolor"})))},history:function(n){return d.createElement("svg",Zl({width:24,height:24,viewBox:"0 0 24 24",xmlns:"http://www.w3.org/2000/svg"},n),Sr||(Sr=d.createElement("path",{d:"M17.814 16.537a3.452 3.452 0 00.416-1.649 3.492 3.492 0 00-5.13-3.078 3.48 3.48 0 00-1.422 1.406 3.457 3.457 0 00-.428 1.672 3.492 3.492 0 003.488 3.488c.58.001 1.15-.144 1.66-.422l2.328 2.337 1.417-1.412-2.329-2.342zm-1.586-1.592a1.487 1.487 0 01-1.4 1.427h-.085a1.49 1.49 0 01-1.488-1.488v-.09a1.49 1.49 0 011.432-1.4h.053a1.49 1.49 0 011.488 1.551z",fill:"currentcolor"})),Mr||(Mr=d.createElement("path",{d:"M11.047 20H5.8A1.8 1.8 0 014 18.2V5.8A1.8 1.8 0 015.8 4h12.4A1.8 1.8 0 0120 5.8v5.6h-2V6H6v12h5.047v2z",fill:"currentcolor"})),xr||(xr=d.createElement("path",{d:"M16.798 8.01H7.207v2h9.591v-2zM10.654 11.772H7.207v2h3.447v-2z",fill:"currentcolor"})))},"image-frame":function(n){return d.createElement("svg",Kl({width:47,height:38,viewBox:"0 0 47 38",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),jr||(jr=d.createElement("path",{d:"M0 33.778A4.228 4.228 0 004.222 38h38c2.333 0 4.222-1.9 4.222-4.222V4.222A4.228 4.228 0 0042.222 0h-38A4.228 4.228 0 000 4.222v29.555z",fill:"#EFF2F5"})),Er||(Er=d.createElement("path",{d:"M42.227 4.222h-38v29.556h38V4.222z",fill:"#AFDADF"})),Dr||(Dr=d.createElement("path",{d:"M32.986 11.875L11.148 33.778h31.074V21.11l-9.236-9.236z",fill:"#3498A4"})),Ar||(Ar=d.createElement("path",{d:"M21.114 14.778a7.389 7.389 0 11-14.778 0 7.389 7.389 0 0114.778 0z",fill:"#39BBCA"})),$r||($r=d.createElement("path",{d:"M14.98 17.087L4.227 27.841v5.937H31.67l-16.69-16.69z",fill:"#167782"})))},layout:function(n){return d.createElement("svg",Yl({width:24,height:24,viewBox:"0 0 24 24",xmlns:"http://www.w3.org/2000/svg"},n),Nr||(Nr=d.createElement("path",{d:"M20.055 15.057a2.153 2.153 0 11-4.307 0c0-.115.009-.229.028-.341L14.02 13.7l-.884-.511-.883.51-1.491.86a2.151 2.151 0 11-1.091-1.406l1.7-.98.884-.51V8.739a2.154 2.154 0 111.767 0v2.925l.883.509 1.847 1.067a2.152 2.152 0 013.3 1.818h.003z",fill:"currentcolor"})),Pr||(Pr=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M4 3a1 1 0 011 1v15h15a1 1 0 110 2H4a1 1 0 01-1-1V4a1 1 0 011-1z",fill:"currentcolor"})))},logo:function(n){return d.createElement("svg",Ul({xmlns:"http://www.w3.org/2000/svg",width:1e3,height:1e3},n),kr||(kr=d.createElement("path",{d:"M26.773 102.744h181.755c-.074 123.9-8.793 247.613-8.866 371.514 89.984-124.193 181.422-247.321 271.406-371.514H692.64C590.987 240.298 444.471 342.58 363.684 495.732c77.74 155.676 224.317 259.543 320.493 402.076h-215.4c-70.105-101.553-117.732-223.956-219.713-299.423-39.122-14.846-40.087 60.14-46.238 87.253-5.736 70.546-2.166 141.45-3.164 212.17H25c.007-265.023 1.766-530.041 1.773-795.064zm424.242 392.988c102.855-141.27 241.813-251.718 344.669-392.988 59.768-.743 119.55-1.267 179.316 0C872.393 239.74 719.748 333.773 632.325 482.93c-7.765 45.896 45.968 88.282 71.47 126.581 86.444 99.165 194.622 178.714 269.432 288.074-63.035-.013-126.069.437-189.104.437-100.95-142.27-232.05-260.11-333.108-402.29z"})))},miew:function(n){return d.createElement("svg",Jl({width:24,height:24,viewBox:"0 0 24 24",xmlns:"http://www.w3.org/2000/svg"},n),Ir||(Ir=d.createElement("path",{d:"M19.702 7.246l-.464-.268-.268-.155-6.234-3.6-.464-.268a.535.535 0 00-.536 0l-.464.268-6.234 3.6-.268.155-.468.268a.537.537 0 00-.267.464v8.58a.537.537 0 00.267.464l.465.268 6.234 3.6.268.155.464.268a.535.535 0 00.536 0l.464-.268.268-.155 6.234-3.6.465-.268a.538.538 0 00.267-.464V7.71a.538.538 0 00-.265-.464zm-8.7 11.066l-4.966-2.867V9.71l4.966 2.867v5.735zm1-7.467L7.036 7.978l4.966-2.867 4.966 2.867-4.966 2.867zm1 1.732l4.966-2.867v5.735l-4.966 2.867v-5.735z",fill:"currentcolor"})))},clear:function(n){return d.createElement("svg",ql({width:24,height:24,viewBox:"0 0 24 24",xmlns:"http://www.w3.org/2000/svg"},n),Tr||(Tr=d.createElement("path",{d:"M18.655 7.529L15.02 3.893a1 1 0 00-.707-.293H6.398a1 1 0 00-1 1v14.548a1 1 0 001 1h11.55a.999.999 0 001-1V8.236a1 1 0 00-.293-.707zm-1.707 10.615h-9.55V5.596h5.952v3.6h3.6l-.002 8.948z",fill:"currentcolor"})),Br||(Br=d.createElement("path",{d:"M10.922 14.55h-2v2h2v-2zM10.922 7.92h-2v5.502h2V7.92z",fill:"currentcolor"})))},open:function(n){return d.createElement("svg",Xl({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Vr||(Vr=d.createElement("path",{d:"M7.575 10.5L6 16.5V9h12.75a1.5 1.5 0 00-1.5-1.5H12L10.5 6H6a1.5 1.5 0 00-1.5 1.5v9A1.5 1.5 0 006 18h11.25c.675 0 1.275-.45 1.425-1.125L20.4 10.5H7.575zm9.675 6H7.5L8.7 12h9.75l-1.2 4.5z",fill:"currentcolor"})))},paste:function(n){return d.createElement("svg",Ql({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),zr||(zr=d.createElement("path",{d:"M17.25 18H6.75V6h1.5v2.25h7.5V6h1.5v12zM12 4.5A.75.75 0 1112 6a.75.75 0 010-1.5zm5.25 0h-3.135A2.258 2.258 0 0012 3c-.975 0-1.8.63-2.115 1.5H6.75A1.5 1.5 0 005.25 6v12a1.5 1.5 0 001.5 1.5h10.5a1.5 1.5 0 001.5-1.5V6a1.5 1.5 0 00-1.5-1.5z",fill:"currentcolor"})))},"period-table":function(n){return d.createElement("svg",tc({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Kr||(Kr=d.createElement("path",{d:"M7.445 15.5H4.146c-.357 0-.646.269-.646.6v3.062c0 .331.29.6.646.6h3.299c.357 0 .646-.269.646-.6V16.1c0-.331-.29-.6-.646-.6zM13.652 15.5h-3.299c-.357 0-.646.269-.646.6v3.062c0 .331.29.6.646.6h3.299c.357 0 .646-.269.646-.6V16.1c0-.331-.29-.6-.646-.6zM19.855 15.5h-3.299c-.357 0-.646.269-.646.6v3.062c0 .331.29.6.646.6h3.299c.357 0 .646-.269.646-.6V16.1c0-.331-.29-.6-.646-.6zM5 13.5a.5.5 0 01-.5-.5V5a.5.5 0 01.5-.5h3.125c.657 0 1.224.132 1.7.396.48.26.85.625 1.11 1.094.26.466.39 1.008.39 1.626 0 .62-.133 1.164-.398 1.63A2.7 2.7 0 019.8 10.323c-.489.255-1.068.382-1.74.382H6.324a.5.5 0 01-.5-.5v-.714a.5.5 0 01.5-.5h1.342c.32 0 .587-.057.801-.171a1.16 1.16 0 00.493-.48c.112-.207.167-.449.167-.724 0-.279-.055-.519-.167-.721a1.134 1.134 0 00-.493-.475c-.217-.11-.484-.167-.8-.167H7.12a.5.5 0 00-.5.5V13a.5.5 0 01-.5.5H5zM12.584 6.267a.5.5 0 01-.5-.5V5a.5.5 0 01.5-.5H19a.5.5 0 01.5.5v.767a.5.5 0 01-.5.5h-1.66a.5.5 0 00-.5.5V13a.5.5 0 01-.5.5h-1.091a.5.5 0 01-.5-.5V6.767a.5.5 0 00-.5-.5h-1.665z",fill:"#333"})))},"reaction-arrow-elliptical-arc-arrow-filled-bow":function(n){return d.createElement("svg",ic({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),qr||(qr=d.createElement("path",{d:"M39.6 26.298l-5.735 8.8-3.336-1.4c-.098-4.894-1.702-18.814-7.568-18.814h-.066c-1.948.034-4.67 1.614-6.572 8.95a52.695 52.695 0 00-1.464 9.894l-4-.142c.178-3.63.71-7.232 1.588-10.758C13.855 17.452 16.8 11 22.833 10.898c6.116-.11 8.966 6.388 10.286 11.856.4 1.656.688 3.306.894 4.8l2.24-3.44 3.346 2.184z",fill:"#231F20"})))},"reaction-arrow-elliptical-arc-arrow-filled-triangle":function(n){return d.createElement("svg",ac({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Wr||(Wr=d.createElement("path",{d:"M35.867 26.424l-3.332 7.248-4.612-6.51 1.958-.182c-.716-4.42-2.582-12.084-6.914-12.084h-.066c-1.948.034-4.67 1.614-6.572 8.95a52.71 52.71 0 00-1.464 9.894l-4-.142c.178-3.629.71-7.232 1.588-10.758C13.855 17.452 16.8 11 22.833 10.898h.144c3.934 0 8.906 2.8 10.896 15.714l1.994-.188z",fill:"#231F20"})))},"reaction-arrow-elliptical-arc-arrow-open-angle":function(n){return d.createElement("svg",lc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Xr||(Xr=d.createElement("path",{d:"M37.54 25.236l-4.329 12-7.136-10.356 1.646-1.134 2.484 3.6C29.491 23.314 27.503 15 22.967 15h-.066c-6 .104-7.858 14-8.036 18.846l-4-.144c.178-3.629.71-7.231 1.588-10.756 1.4-5.4 4.334-11.84 10.376-11.946 6.116-.106 8.966 6.388 10.286 11.856a50.963 50.963 0 011.032 5.88l1.506-4.172 1.886.672z",fill:"#231F20"})))},"reaction-arrow-elliptical-arc-arrow-open-half-angle":function(n){return d.createElement("svg",cc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Qr||(Qr=d.createElement("path",{d:"M39.764 27.682l-5.252 5.252-.4.4-.312.312-1.128 1.128-1.472-1.076-.156-.114-.512-.372-6.014-4.366 1.174-1.618 4.666 3.386c-.564-6.054-2.492-15.718-7.38-15.718h-.066c-1.948.034-4.67 1.614-6.572 8.95a52.695 52.695 0 00-1.464 9.894l-4-.142c.178-3.63.71-7.232 1.588-10.758C13.856 17.452 16.8 11 22.834 10.898c6.116-.11 8.966 6.388 10.286 11.856.578 2.48.979 4.999 1.2 7.536l4.022-4.022 1.422 1.414z",fill:"#231F20"})))},"reaction-arrow-open-angle":function(n){return d.createElement("svg",mc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),ao||(ao=d.createElement("path",{d:"M35.967 24l-.67.67-1.33 1.33-10.94 10.94-2.828-2.828 2.828-2.828 3.212-3.214L28.31 26H10.197v-4H28.31l-4.162-4.162-1.12-1.12L20.2 13.89l2.828-2.83L35.967 24z",fill:"#231F20"})))},"reaction-arrow-filled-triangle":function(n){return d.createElement("svg",fc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),io||(io=d.createElement("path",{d:"M34.941 23.986l-1.244 1.244-.784.784L21.947 36.98V26.014h-11.75v-4h11.75V11.048l.028-.028L32.97 22.014l.728.728 1.244 1.244z",fill:"#231F20"})))},"reaction-arrow-filled-bow":function(n){return d.createElement("svg",hc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),oo||(oo=d.createElement("path",{d:"M25.14 28.774c.37-.895.653-1.824.844-2.774H10.2v-4h15.876a18.504 18.504 0 00-1.102-3.982l-3-7 12.98 12.98-12.98 12.98 3.166-8.204z",fill:"#231F20"})))},"reaction-arrow-dashed-open-angle":function(n){return d.createElement("svg",oc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Ur||(Ur=d.createElement("path",{d:"M15.32 22h-4.6v4h4.6v-4zM22.045 22h-4.6v4h4.6v-4zM28.77 22h-4.6v4h4.6v-4z",fill:"#231F20"})),Jr||(Jr=d.createElement("path",{d:"M27.006 12.43L38.576 24l-11.57 11.57-2.83-2.828L32.92 24l-8.744-8.742 2.83-2.828z",fill:"#231F20"})))},"reaction-arrow-failed":function(n){return d.createElement("svg",pc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),ro||(ro=d.createElement("path",{d:"M27.471 28.774c.37-.895.653-1.824.844-2.774H24.43l2.022 2.022-1.414 1.414L21.6 26h-1.172L17 29.436l-1.414-1.414L17.6 26h-5.07v-4h5.07l-2.02-2.022L17 18.564 20.43 22h1.17l3.436-3.436 1.414 1.414L24.43 22h3.97a18.504 18.504 0 00-1.102-3.982l-3.01-7 12.98 12.98-12.98 12.98 3.184-8.204z",fill:"#231F20"})))},"reaction-arrow-both-ends-filled-triangle":function(n){return d.createElement("svg",rc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Yr||(Yr=d.createElement("path",{d:"M29.876 32.824v-6.81H18.124v6.81L9.3 24l8.824-8.822v6.838h11.752v-6.838L38.7 24l-8.824 8.824z",fill:"#231F20"})))},"reaction-arrow-equilibrium-filled-half-bow":function(n){return d.createElement("svg",sc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),no||(no=d.createElement("path",{d:"M36.915 21.6H11.083v-4l17.882.086a8.487 8.487 0 00-.866-3.774l-1.3-2.66L36.915 21.6zM11.083 26.4h25.832v4l-17.882-.086c-.006 1.308.29 2.6.866 3.774l1.3 2.66L11.083 26.4z",fill:"#231F20"})))},"reaction-arrow-equilibrium-filled-triangle":function(n){return d.createElement("svg",uc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),eo||(eo=d.createElement("path",{d:"M11.667 17.028v4h15.788v3.146l9.762-5.146-9.762-5.148v3.148H11.667zM36.334 27.012v4H20.546v3.146l-9.762-5.146 9.762-5.148v3.148h15.788z",fill:"#231F20"})))},"reaction-arrow-equilibrium-open-angle":function(n){return d.createElement("svg",dc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),to||(to=d.createElement("path",{d:"M36.478 21.6H11.522v-4h17.279l-5.042-3.39 2.23-3.32 10.49 7.05v3.66zM22.012 37.11l-10.49-7.05V26.4h24.956v4H19.201l5.041 3.39-2.23 3.32z",fill:"#231F20"})))},"reaction-arrow-unbalanced-equilibrium-filled-half-bow":function(n){return d.createElement("svg",vc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),lo||(lo=d.createElement("path",{d:"M36.289 21.6H12.513v-4l15.826.086a8.487 8.487 0 00-.866-3.774l-1.3-2.66L36.289 21.6zM31.368 30.4L23 30.236c.066.944.325 1.864.76 2.704l1.17 2.26-9.1-8.8h15.536l.002 4z",fill:"#231F20"})))},"reaction-arrow-unbalanced-equilibrium-open-half-angle":function(n){return d.createElement("svg",Cc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),uo||(uo=d.createElement("path",{d:"M36.478 21.6H11.522v-4h17.279l-5.042-3.39 2.23-3.32 10.49 7.05v3.66zM22.012 37.11l-10.49-7.05V26.4h24.956v4H19.201l5.041 3.39-2.23 3.32z",fill:"#231F20"})))},"reaction-arrow-unbalanced-equilibrium-large-filled-half-bow":function(n){return d.createElement("svg",bc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),so||(so=d.createElement("path",{d:"M39.234 21.6H9.2v-4l22.084.086a8.487 8.487 0 00-.866-3.774l-1.3-2.66L39.234 21.6zM33.022 30.4l-12.074-.164a6.94 6.94 0 00.762 2.704l1.168 2.26-9.1-8.8h19.244v4z",fill:"#231F20"})))},"reaction-arrow-unbalanced-equilibrium-filled-half-triangle":function(n){return d.createElement("svg",gc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),co||(co=d.createElement("path",{d:"M32.928 26.4v4H22.644v4.024l-8.06-8.024h18.344zM36.313 21.6H11.688v-4h15.176v-5.41l9.448 9.41z",fill:"#231F20"})))},"reaction-automap":function(n){return d.createElement("svg",yc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),po||(po=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M27.405 23.2v-2.86l4.858 4.86-4.858 4.86V27.2h-9.543v-4h9.543zM11.233 18.122H7.62v-4h7.614v20.156h-4V18.122zM35.874 18.122h-3.612v-4h7.612v20.156h-4V18.122z",fill:"#231F20"})))},"reaction-map":function(n){return d.createElement("svg",Oc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),ho||(ho=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M22.236 16.21h-5.154v-4h9.154v25.14h-4V16.21z",fill:"#231F20"})),fo||(fo=d.createElement("path",{d:"M18.312 27.086h-7.034v4h7.034v-4zM37.076 27.086h-7.034v4h7.034v-4z",fill:"#231F20"})))},"reaction-plus":function(n){return d.createElement("svg",wc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),mo||(mo=d.createElement("path",{d:"M22 12h4v10h10v4H26v10h-4V26H12v-4h10V12z",fill:"#231F20"})))},"reaction-unmap":function(n){return d.createElement("svg",Sc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),vo||(vo=d.createElement("path",{d:"M26.236 12.21v10.084l-4-3.998V16.21H20.15l-3.068-3.068v-.932h9.154zM18.312 27.086h-7.034v4h7.034v-4zM37.311 27.086v4h-2.284l-4-4h6.284z",fill:"#231F20"})),go||(go=d.createElement("path",{d:"M35.402 33.686l-2.828 2.828-6.338-6.338v7.174h-4V26.178L12.212 16.154l1.112-1.114 1.716-1.716 20.362 20.362z",fill:"#231F20"})))},recognize:function(n){return d.createElement("svg",Mc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),bo||(bo=d.createElement("path",{d:"M34.742 18.918L12.364 41.294H6.708v-5.656L29.084 13.26l5.658 5.658zM36.767 7.842l3.394 3.394a1.6 1.6 0 010 2.262l-3.648 3.65-5.657-5.658 3.648-3.648a1.6 1.6 0 012.263 0zM22.828 8.702l2.702 1.476-2.702 1.478-1.476 2.702-1.478-2.702-2.702-1.478 2.702-1.476L21.352 6l1.476 2.702zM11.318 17.126l1.13-3.866 1.132 3.866 3.864 1.13-3.864 1.13-1.132 3.866-1.13-3.866-3.864-1.13 3.864-1.13z",fill:"#231F20"})))},redo:function(n){return d.createElement("svg",xc({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Co||(Co=d.createElement("path",{d:"M16.801 10.95C15.414 9.75 13.614 9 11.626 9c-3.487 0-6.435 2.273-7.47 5.415l1.77.585a6.002 6.002 0 015.7-4.125 5.98 5.98 0 013.84 1.41L12.751 15h6.75V8.25l-2.7 2.7z",fill:"currentcolor"})))},"rgroup-attpoints":function(n){return d.createElement("svg",jc({width:32,height:32,viewBox:"0 0 32 32",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),yo||(yo=d.createElement("path",{d:"M24.963 13.335h-1.6v-4.26h-.764V7.473h2.364v5.862zM21.467 10.979a1.793 1.793 0 00.914-1.556c0-.934-.694-1.95-2.217-1.95h-2.43v5.867h1.6v-2.007h.542l.944 2h1.77l-1.123-2.354zm-2.134-1.246v-.666h.84c.144 0 .618.025.618.349 0 .203-.374.303-.639.31-.179.007-.51.007-.819.007z",fill:"#231F20"})),Oo||(Oo=d.createElement("path",{d:"M18.259 17.119h-1.694a1.619 1.619 0 01-1.616-1.616V5.959a1.617 1.617 0 011.616-1.615h1.694v2h-1.31v8.775h1.31v2zM26.196 17.119h-1.693v-2h1.31V6.344h-1.31v-2h1.693a1.617 1.617 0 011.616 1.615v9.544a1.619 1.619 0 01-1.616 1.616zM13.88 16.756L7.855 22.78l1.415 1.415 6.024-6.025-1.414-1.414z",fill:"#231F20"})),wo||(wo=d.createElement("path",{d:"M11.48 25.085l-6.165 1.652 1.651-6.165 4.513 4.513z",fill:"#231F20"})))},"rgroup-fragment":function(n){return d.createElement("svg",Ec({width:32,height:32,viewBox:"0 0 32 32",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),So||(So=d.createElement("path",{d:"M24.267 19.801h-2v-6.389h-1.284v-2h3.284v8.39zM19.115 16.292c.852-.457 1.386-1.253 1.386-2.203a2.466 2.466 0 00-1.29-2.232 3.435 3.435 0 00-1.044-.373 3.977 3.977 0 00-.736-.072h-3.393v8.39h2v-3.085h1.067l1.458 3.086h2.211l-1.659-3.511zm-3.077-1.576v-1.304h1.393c.278-.002.552.062.8.187a.48.48 0 01.274.49c0 .435-.656.61-1.096.622-.287.008-.86.008-1.37.005zM5.17 19.515l-1.885-1.886 1.947-1.948-1.947-1.948 1.885-1.885 3.834 3.833-3.834 3.834z",fill:"#231F20"})),Mo||(Mo=d.createElement("path",{d:"M14.645 25.2h-2.472a2.236 2.236 0 01-2.232-2.233V9.033A2.235 2.235 0 0112.173 6.8h2.472v2.667h-2.037v13.066h2.037V25.2zM26.235 25.2h-2.472v-2.667H25.8V9.467h-2.037V6.8h2.472a2.234 2.234 0 012.232 2.233v13.934a2.236 2.236 0 01-2.232 2.233z",fill:"#231F20"})))},"rgroup-label":function(n){return d.createElement("svg",Dc({width:32,height:32,viewBox:"0 0 32 32",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),xo||(xo=d.createElement("path",{d:"M27.927 22.052h-2.666v-10.77h-2.409V8.614h5.075v13.437zM19.396 16.176c1.458-.667 2.362-1.923 2.362-3.481 0-1.467-.696-2.678-1.958-3.391-1.1-.621-2.301-.688-2.765-.688H11.78v13.436h2.667v-5.359h2.244l2.533 5.362h2.95l-2.778-5.879zm-4.95-2.15v-2.743h2.589a3.163 3.163 0 011.452.342c.43.243.604.552.604 1.067 0 1.003-1.368 1.304-2.092 1.323a92.9 92.9 0 01-2.552.012zM6.35 19.137l-1.886-1.886 1.948-1.947-1.948-1.948 1.885-1.887 3.833 3.835-3.833 3.833z",fill:"#231F20"})))},save:function(n){return d.createElement("svg",Ac({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),jo||(jo=d.createElement("path",{d:"M17.25 17.625h.375V8.717l-.11-.11-2.122-2.122-.11-.11H6.375v11.25H17.25zm-10.5-12h8.845l2.78 2.78v8.845a1.13 1.13 0 01-1.125 1.125H6.75a1.125 1.125 0 01-1.125-1.125V6.75c0-.62.5-1.125 1.125-1.125zm1.5 2.625h5.25v1.5H8.25v-1.5zm4.875 6a1.125 1.125 0 11-2.25 0 1.125 1.125 0 012.25 0z",fill:"currentcolor",stroke:"currentcolor",strokeWidth:.75})))},search:function(n){return d.createElement("svg",$c({width:28,height:28,viewBox:"0 0 28 28",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Eo||(Eo=d.createElement("path",{d:"M22.697 21.492l-5.68-5.68a6.503 6.503 0 001.358-4c0-1.754-.685-3.399-1.923-4.64a6.514 6.514 0 00-4.64-1.922 6.523 6.523 0 00-4.64 1.923 6.51 6.51 0 00-1.922 4.64c0 1.752.685 3.401 1.923 4.64a6.51 6.51 0 004.64 1.922 6.509 6.509 0 003.996-1.356l5.68 5.678a.18.18 0 00.255 0l.953-.951a.18.18 0 000-.254zm-7.42-6.215a4.874 4.874 0 01-3.464 1.435 4.874 4.874 0 01-3.466-1.434 4.874 4.874 0 01-1.435-3.466c0-1.308.51-2.54 1.435-3.465a4.874 4.874 0 013.466-1.435c1.308 0 2.54.508 3.464 1.435a4.874 4.874 0 011.435 3.466 4.87 4.87 0 01-1.434 3.464z",fill:"currentColor"})))},"select-fragment":function(n){return d.createElement("svg",Nc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Do||(Do=d.createElement("path",{d:"M36.085 41.896a.85.85 0 01-1.182-.458l-1.938-4.6-2.232 1.962a.8.8 0 01-.55.214.85.85 0 01-.628-.284 1.02 1.02 0 01-.262-.688V23.464c-.002-.254.092-.5.262-.688a.85.85 0 01.628-.284.86.86 0 01.568.224h.01l10.212 9.366a1.038 1.038 0 01.116 1.37.867.867 0 01-.508.33l-2.8.6 1.956 4.6a.978.978 0 01-.428 1.284l-3.224 1.63z",fill:"#231F20"})),Ao||(Ao=d.createElement("path",{d:"M34.37 14.838l-13.303-6.6a2 2 0 00-2.319.4l-10.4 10.614a2 2 0 00-.342 2.326l6.883 13.164A2 2 0 0017 35.772l10.29-1.742v-4.054l-9.523 1.612L12.23 21l8.358-8.536 10.703 5.312-.343 2.312 3.563 3.266.95-6.432a2 2 0 00-1.09-2.084z",fill:"#231F20"})))},"select-lasso":function(n){return d.createElement("svg",Pc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),$o||($o=d.createElement("path",{d:"M36.209 42.244a.85.85 0 01-1.182-.456l-1.938-4.6-2.23 1.962a.81.81 0 01-.552.214.849.849 0 01-.628-.284 1.023 1.023 0 01-.26-.688v-14.58a1.028 1.028 0 01.26-.688.851.851 0 01.628-.284c.21.003.414.082.57.224l10.212 9.366a1.036 1.036 0 01.116 1.37.87.87 0 01-.506.33l-2.8.6 1.956 4.6a.976.976 0 01-.426 1.282l-3.22 1.632zM30.673 8.504a2 2 0 00-1.174-.982 22.044 22.044 0 00-4.96-.942 2.012 2.012 0 00-2.14 1.848v.154a2 2 0 001.854 1.988 17.996 17.996 0 014.058.77 2 2 0 002.372-2.836h-.01zm-12.08.4a2 2 0 00-1.878-1.314c-.234 0-.466.042-.686.124a16.25 16.25 0 00-4.568 2.522 2 2 0 002.492 3.128 12.261 12.261 0 013.446-1.9 1.997 1.997 0 001.2-2.566l-.006.006zm21.51 7.252a14.249 14.249 0 00-3.118-4.306 2.001 2.001 0 10-2.77 2.884c.939.881 1.703 1.93 2.254 3.094a2 2 0 003.634-1.672zm-28.74 5.964a7.384 7.384 0 01-.546-2.748c0-.263.015-.526.044-.788a2 2 0 10-3.972-.456c-.048.413-.072.828-.072 1.244.005 1.45.288 2.885.834 4.228a2 2 0 003.712-1.488v.008zm27.866.6a2 2 0 00-2.634 1.032 7.638 7.638 0 01-.922 1.564l2.956 2.712a11.663 11.663 0 001.632-2.676 2 2 0 00-1.032-2.632zm-21.756 5.4a14.372 14.372 0 01-3.36-2.214 2 2 0 10-2.664 2.982 18.365 18.365 0 004.292 2.838 1.966 1.966 0 001.927-.11 2.01 2.01 0 00.937-1.692 2.014 2.014 0 00-1.132-1.806v.002z",fill:"#231F20"})),No||(No=d.createElement("path",{d:"M27.691 29.61v7.244c-1.33 1.234-3.494 2.026-5.69 1.888-1.088-.068-2.292-.458-3.564-.87-1.272-.412-2.726-.886-3.572-.818-1.5.116-3.054 1.366-3.524 1.836a2 2 0 01-2.83-2.828c.282-.28 2.834-2.748 6.046-3 1.634-.126 3.4.446 5.112 1 .982.318 2 .648 2.582.684 1.372.086 2.426-.51 2.762-.854 0-.026 0-.054-.014-.084-.318 0-.644-.01-.968-.026a2 2 0 01.098-3.998h.096c.288.012.574.02.85.02a16.92 16.92 0 002.616-.194z",fill:"#231F20"})))},"select-rectangle":function(n){return d.createElement("svg",kc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Po||(Po=d.createElement("path",{d:"M36.21 42.244a.85.85 0 01-1.181-.456l-1.938-4.6-2.23 1.962a.81.81 0 01-.552.214.851.851 0 01-.628-.284 1.024 1.024 0 01-.26-.688v-14.58a1.028 1.028 0 01.26-.688.85.85 0 01.628-.284.866.866 0 01.57.224L41.09 32.43a1.036 1.036 0 01.116 1.37.87.87 0 01-.506.33l-2.8.6 1.956 4.6a.977.977 0 01-.426 1.282l-3.22 1.632zM8.56 20.102v5.478h4v-5.478h-4zm11.38 12.86v4h5.48v-4h-5.48zM31.526 8.72h-2.105v4h2.105A1.277 1.277 0 0132.8 14v2.102h4V14a5.282 5.282 0 00-5.273-5.28zm-17.69 0A5.282 5.282 0 008.562 14v2.102h4V14a1.276 1.276 0 011.275-1.276h2.104v-4l-2.104-.004zm6.104 0v4h5.48v-4h-5.48zM32.8 20.102V21.8l4 3.668v-5.366h-4zm-18.963 12.86a1.276 1.276 0 01-1.277-1.276V29.58h-4v2.106a5.282 5.282 0 005.276 5.276h2.104v-4h-2.104z",fill:"#231F20"})))},settings:function(n){return d.createElement("svg",Ic({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),ko||(ko=d.createElement("path",{d:"M12 9a3 3 0 110 6 3 3 0 010-6zm0 1.5a1.5 1.5 0 100 3 1.5 1.5 0 000-3zm-1.5 9a.38.38 0 01-.375-.315l-.277-1.987a5.209 5.209 0 01-1.268-.743l-1.867.758a.377.377 0 01-.458-.166l-1.5-2.595a.37.37 0 01.09-.48l1.583-1.245L6.375 12l.053-.75-1.583-1.223a.37.37 0 01-.09-.48l1.5-2.595c.09-.165.293-.232.458-.165l1.867.75c.39-.292.795-.547 1.268-.734l.277-1.988A.38.38 0 0110.5 4.5h3a.38.38 0 01.375.315l.278 1.987c.472.188.877.443 1.267.736l1.868-.75a.369.369 0 01.457.164l1.5 2.595a.37.37 0 01-.09.48l-1.582 1.223.052.75-.052.75 1.582 1.223a.37.37 0 01.09.48l-1.5 2.595a.369.369 0 01-.457.165l-1.868-.75c-.39.292-.795.547-1.267.735l-.278 1.987a.38.38 0 01-.375.315h-3zM11.438 6l-.278 1.957a4.12 4.12 0 00-2.272 1.336l-1.808-.78-.562.975L8.1 10.65c-.3.877-.3 1.83 0 2.7l-1.59 1.17.563.975 1.822-.78a4.083 4.083 0 002.258 1.32L11.43 18h1.14l.278-1.957a4.138 4.138 0 002.257-1.328l1.823.78.562-.975-1.59-1.162c.3-.878.3-1.83 0-2.708l1.583-1.162-.563-.976-1.807.78a4.065 4.065 0 00-2.273-1.327L12.563 6h-1.125z",fill:"currentcolor"})))},"sgroup-data":function(n){return d.createElement("svg",Tc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Io||(Io=d.createElement("path",{d:"M42.844 33.5v4h-4.818v4.818h-4V37.5h-4.818v-4h4.818v-4.818h4V33.5h4.818zM16 40h-4.4A3.6 3.6 0 018 36.4V11.6A3.6 3.6 0 0111.6 8H16v4h-4v24h4v4zM40 25.882h-4V12h-4V8h4.4a3.6 3.6 0 013.6 3.6v14.282zM24.134 32.276a7.671 7.671 0 01-5.918-2.818l3.068-2.566c1.4 1.678 3.528 1.616 4.458.93.256-.2.644-.476.066-1.37-.148-.222-.882-.776-1.876-1.24-.084-.038-.328-.124-.524-.2-1.182-.42-3.162-1.124-4.17-2.736-1.32-2.11-.6-4.77.812-6.306a5.73 5.73 0 014.15-1.816h.052c1.814.018 3.814.898 5.08 1.718l-2.168 3.358c-.964-.63-2.18-1.07-2.948-1.076A1.674 1.674 0 0023 18.68c-.386.422-.572 1.158-.37 1.48.27.432 1.566.892 2.12 1.088.332.118.618.22.872.34.966.448 2.708 1.4 3.546 2.692 1.568 2.424 1.146 5.142-1.05 6.762a6.756 6.756 0 01-3.984 1.234z",fill:"#231F20"})))},sgroup:function(n){return d.createElement("svg",Bc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),To||(To=d.createElement("path",{d:"M16 40h-4.4A3.6 3.6 0 018 36.4V11.6A3.6 3.6 0 0111.6 8H16v4h-4v24h4v4zM36.627 40h-4.4v-4h4V12h-4V8h4.4a3.6 3.6 0 013.6 3.6v24.8a3.6 3.6 0 01-3.6 3.6zM24.134 32.276a7.671 7.671 0 01-5.918-2.818l3.068-2.566c1.4 1.678 3.528 1.616 4.458.93.256-.2.644-.476.066-1.37-.148-.222-.882-.776-1.876-1.24-.084-.038-.328-.124-.524-.2-1.182-.42-3.162-1.124-4.17-2.736-1.32-2.11-.6-4.77.812-6.306a5.73 5.73 0 014.15-1.816h.052c1.814.018 3.814.898 5.08 1.718l-2.168 3.358c-.964-.63-2.18-1.07-2.948-1.076A1.674 1.674 0 0023 18.68c-.386.422-.572 1.158-.37 1.48.27.432 1.566.892 2.12 1.088.332.118.618.22.872.34.966.448 2.708 1.4 3.546 2.692 1.568 2.424 1.146 5.142-1.05 6.762a6.756 6.756 0 01-3.984 1.234z",fill:"#231F20"})))},"template-0":function(n){return d.createElement("svg",Gc({width:32,height:32,viewBox:"0 0 32 32",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Fo||(Fo=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M15.333 4.536c.412-.238.92-.238 1.333 0l8.928 5.155c.413.238.667.678.667 1.154v10.31c0 .476-.254.916-.667 1.154l-8.928 5.155c-.412.238-.92.238-1.333 0L6.405 22.31a1.333 1.333 0 01-.667-1.155v-10.31c0-.476.254-.916.667-1.154l8.928-5.155zm-6.928 7.08v8.769L16 24.77l7.594-4.385v-8.77L16 7.23l-7.595 4.385z",fill:"#231F20"})),Ho||(Ho=d.createElement("path",{d:"M21.084 13.067v5.866l1.333.77v-7.41l-1.333.774zM16 8.587L9.58 12.294l1.333.77L16 10.133V8.588zM9.58 19.705L16 23.409v-1.542l-5.086-2.934-1.333.77z",fill:"#231F20"})))},"template-1":function(n){return d.createElement("svg",Fc({width:32,height:32,viewBox:"0 0 32 32",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Ro||(Ro=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M15.216 5.416c.467-.34 1.1-.34 1.567 0l9.153 6.65c.468.34.663.942.485 1.491l-3.496 10.76c-.179.55-.69.922-1.268.922H10.342c-.578 0-1.09-.372-1.268-.922l-3.496-10.76a1.333 1.333 0 01.484-1.49l9.154-6.651zm-6.802 8.239l2.897 8.917h9.377l2.897-8.917L16 8.143l-7.585 5.512z",fill:"#231F20"})),Zo||(Zo=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M22.35 14.61l-2.184 6.717-1.268-.412 2.183-6.717 1.268.412zM11.834 21.327L9.651 14.61l1.268-.412 2.183 6.717-1.268.412z",fill:"#231F20"})))},"template-2":function(n){return d.createElement("svg",Hc({width:32,height:32,viewBox:"0 0 32 32",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Ko||(Ko=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M15.333 4.536c.412-.238.92-.238 1.333 0l8.928 5.155c.413.238.667.678.667 1.154v10.31c0 .476-.254.916-.667 1.154l-8.928 5.155c-.412.238-.92.238-1.333 0L6.405 22.31a1.333 1.333 0 01-.667-1.155v-10.31c0-.476.254-.916.667-1.154l8.928-5.155zm-6.928 7.08v8.769L16 24.77l7.594-4.385v-8.77L16 7.23l-7.595 4.385z",fill:"#231F20"})))},"template-3":function(n){return d.createElement("svg",Rc({width:32,height:32,viewBox:"0 0 32 32",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Yo||(Yo=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M15.216 6.216c.467-.34 1.1-.34 1.567 0l9.153 6.65c.468.34.663.942.485 1.491l-3.496 10.76c-.179.55-.69.922-1.268.922H10.342c-.578 0-1.09-.372-1.268-.922l-3.496-10.76a1.333 1.333 0 01.484-1.49l9.154-6.651zm-6.802 8.239l2.897 8.917h9.377l2.897-8.917L16 8.943l-7.585 5.512z",fill:"#231F20"})))},"template-4":function(n){return d.createElement("svg",Zc({width:32,height:32,viewBox:"0 0 32 32",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Uo||(Uo=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M16 6.71c.476 0 .916.255 1.154.667l8.662 15.003a1.333 1.333 0 01-1.155 2H7.338a1.333 1.333 0 01-1.154-2l8.66-15.003A1.333 1.333 0 0116 6.711zm0 4L9.647 21.714h12.704l-6.353-11.002z",fill:"#231F20"})))},"template-5":function(n){return d.createElement("svg",Kc({width:32,height:32,viewBox:"0 0 32 32",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Jo||(Jo=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M5.328 6.661c0-.736.597-1.333 1.333-1.333h18.68c.735 0 1.332.597 1.332 1.333V25.34c0 .736-.596 1.333-1.333 1.333H6.661a1.333 1.333 0 01-1.333-1.333V6.66zm2.667 1.334v16.012h16.012V7.995H7.995z",fill:"#231F20"})))},"template-6":function(n){return d.createElement("svg",Yc({width:32,height:32,viewBox:"0 0 32 32",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),qo||(qo=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M15.422 5.625a1.333 1.333 0 011.157 0l7.436 3.58c.365.176.63.51.721.905l1.837 8.048c.09.395-.004.81-.257 1.128l-5.147 6.453a1.333 1.333 0 01-1.042.502h-8.253c-.406 0-.79-.184-1.043-.502l-5.147-6.453a1.333 1.333 0 01-.257-1.128l1.837-8.048c.09-.396.356-.729.722-.905l7.436-3.58zm-5.7 5.704L8.17 18.125l4.346 5.45h6.969l4.346-5.45-1.552-6.796L16 8.306 9.721 11.33z",fill:"#231F20"})))},"template-7":function(n){return d.createElement("svg",Uc({width:32,height:32,viewBox:"0 0 32 32",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Wo||(Wo=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M11.357 6.125c.25-.25.59-.39.943-.39h7.4c.353 0 .692.14.942.39l5.233 5.232c.25.25.39.59.39.943v7.4c0 .354-.14.693-.39.943l-5.233 5.232c-.25.25-.589.39-.942.39h-7.4c-.354 0-.693-.14-.943-.39l-5.232-5.232c-.25-.25-.39-.59-.39-.943v-7.4c0-.354.14-.693.39-.943l5.232-5.232zm1.495 2.276l-4.451 4.451v6.296l4.451 4.45h6.295l4.451-4.45v-6.296l-4.45-4.45h-6.296z",fill:"#231F20"})))},"template-dialog":function(n){return d.createElement("svg",Jc({width:18,height:18,viewBox:"0 0 18 18",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Xo||(Xo=d.createElement("path",{d:"M3.675 12.101l5.345 3.086.004-.002v-.794l-.004.003-4.658-2.69-.687.397zM13.69 11.69V6.31l.688-.397v6.174l-.687-.397zM9.024 2.815l-.004-.002-5.358 3.093.687.397 4.67-2.697.005.003v-.794z",fill:"currentColor"})),Qo||(Qo=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M9.02.75l7.144 4.125v8.25L9.02 17.25l-7.145-4.125v-8.25L9.02.75zM2.563 5.272L9.02 1.544l6.457 3.728v7.456L9.02 16.456l-6.457-3.728V5.272z",fill:"currentColor"})))},"template-lib":function(n){return d.createElement("svg",qc({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),ni||(ni=d.createElement("path",{d:"M7.445 15.5H4.146c-.357 0-.646.269-.646.6v3.062c0 .331.29.6.646.6h3.299c.357 0 .646-.269.646-.6V16.1c0-.331-.29-.6-.646-.6zM13.652 15.5h-3.299c-.357 0-.646.269-.646.6v3.062c0 .331.29.6.646.6h3.299c.357 0 .646-.269.646-.6V16.1c0-.331-.29-.6-.646-.6zM19.855 15.5h-3.299c-.357 0-.646.269-.646.6v3.062c0 .331.29.6.646.6h3.299c.357 0 .646-.269.646-.6V16.1c0-.331-.29-.6-.646-.6zM5 6.267a.5.5 0 01-.5-.5V5a.5.5 0 01.5-.5h6.282a.5.5 0 01.5.5v.767a.5.5 0 01-.5.5H9.669a.5.5 0 00-.5.5V13a.5.5 0 01-.5.5H7.617a.5.5 0 01-.5-.5V6.767a.5.5 0 00-.5-.5H5zM13.299 13.5a.5.5 0 01-.5-.5V5a.5.5 0 01.5-.5h3.059c.645 0 1.201.132 1.67.396.47.26.834.625 1.09 1.094.254.466.382 1.008.382 1.626 0 .62-.13 1.164-.391 1.63a2.674 2.674 0 01-1.107 1.077c-.48.255-1.048.382-1.707.382h-1.696a.5.5 0 01-.5-.5v-.714a.5.5 0 01.5-.5h1.309c.314 0 .576-.057.786-.171.213-.114.375-.274.484-.48.11-.207.164-.449.164-.724 0-.279-.055-.519-.164-.721a1.123 1.123 0 00-.484-.475c-.213-.11-.475-.167-.786-.167h-.527a.5.5 0 00-.5.5V13a.5.5 0 01-.5.5H13.3z",fill:"#333"})))},text:function(n){return d.createElement("svg",Xc({width:32,height:32,viewBox:"0 0 32 32",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),ti||(ti=d.createElement("path",{d:"M23.957 7.205v2.667h-6.624v14.923h-2.667V9.872H8.042V7.205h15.915z",fill:"#231F20"})))},"text-bold":function(n){return d.createElement("svg",Wc({width:24,height:24,viewBox:"0 0 24 24",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),ei||(ei=d.createElement("path",{d:"M9 18.87a1 1 0 01-1-1V6a1 1 0 011-1h3.465c1.406 0 2.527.323 3.363.969.836.633 1.254 1.495 1.254 2.584 0 .608-.146 1.14-.437 1.596-.279.456-.659.81-1.14 1.064-.469.253-.982.38-1.539.38v.057a3.71 3.71 0 011.691.342c.52.24.937.602 1.254 1.083.317.481.475 1.077.475 1.786 0 .81-.196 1.52-.589 2.128-.38.595-.925 1.058-1.634 1.387-.71.33-1.552.494-2.527.494H9zm1.755-2.299h1.767c.62 0 1.108-.165 1.463-.494.355-.33.532-.785.532-1.368 0-.583-.177-1.039-.532-1.368-.355-.342-.842-.513-1.463-.513h-1.767v3.743zm0-5.985h1.672c.557 0 .994-.146 1.311-.437.317-.304.475-.71.475-1.216 0-.52-.158-.918-.475-1.197-.317-.291-.754-.437-1.311-.437h-1.672v3.287z"})))},"text-italic":function(n){return d.createElement("svg",Qc({width:24,height:24,viewBox:"0 0 24 24",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),ri||(ri=d.createElement("path",{d:"M8.066 18.87a.912.912 0 010-1.824h2.031l1.615-10.222H9.977a.912.912 0 110-1.824h5.837a.912.912 0 010 1.824h-2.031l-1.615 10.222h1.735a.912.912 0 110 1.824H8.066z"})))},"text-subscript":function(n){return d.createElement("svg",ns({width:24,height:24,viewBox:"0 0 24 24",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),oi||(oi=d.createElement("path",{d:"M16.65 20.735c-.061 0-.118-.091-.17-.274a1.927 1.927 0 01-.074-.493c0-.055.008-.099.025-.132l2.197-2.685c.221-.277.332-.555.332-.835 0-.225-.075-.397-.225-.518-.15-.123-.345-.185-.586-.185-.16 0-.3.024-.424.073-.12.049-.245.114-.372.195a1 1 0 01-.122.074.23.23 0 01-.097.029.378.378 0 01-.244-.098.739.739 0 01-.181-.239.602.602 0 01-.068-.259c0-.163.084-.304.254-.425a1.78 1.78 0 01.649-.278 3.47 3.47 0 01.825-.098c.397 0 .737.074 1.02.22.287.143.504.344.65.6.146.255.22.548.22.88 0 .267-.047.519-.142.757-.091.237-.22.457-.386.659l-1.63 2.016h2.002c.09 0 .157.036.2.108.042.068.063.177.063.327v.146c0 .15-.02.26-.063.332-.043.069-.11.103-.2.103H16.65zM7.03 17.615c-.687 0-1.03-.105-1.03-.315 0-.105.053-.241.158-.408l3.404-5.326-3.024-4.833c-.105-.192-.158-.331-.158-.418 0-.092.087-.167.26-.222C6.82 6.03 7.082 6 7.43 6h.677c.532 0 .86.105.983.315l1.884 3.071 1.976-3.07a.68.68 0 01.37-.251c.162-.043.375-.065.641-.065h.64c.693 0 1.04.105 1.04.315 0 .118-.053.257-.159.418l-3.117 4.87 3.294 5.289c.099.154.148.29.148.408 0 .21-.346.315-1.039.315h-.64c-.266 0-.48-.021-.64-.065a.524.524 0 01-.343-.25l-2.2-3.544L8.664 17.3a.563.563 0 01-.353.269 3.317 3.317 0 01-.65.046h-.63z"})))},"text-superscript":function(n){return d.createElement("svg",es({width:24,height:24,viewBox:"0 0 24 24",fill:"currentColor",xmlns:"http://www.w3.org/2000/svg"},n),ii||(ii=d.createElement("path",{d:"M7.03 17.615c-.687 0-1.03-.105-1.03-.315 0-.105.053-.241.158-.408l3.404-5.326-3.024-4.833c-.105-.192-.158-.331-.158-.418 0-.092.087-.167.26-.222C6.82 6.03 7.082 6 7.43 6h.677c.532 0 .86.105.983.315l1.884 3.071 1.976-3.07a.68.68 0 01.37-.251c.162-.043.375-.065.641-.065h.64c.693 0 1.04.105 1.04.315 0 .118-.053.257-.159.418l-3.117 4.87 3.294 5.289c.099.154.148.29.148.408 0 .21-.346.315-1.039.315h-.64c-.266 0-.48-.021-.64-.065a.524.524 0 01-.343-.25l-2.2-3.544L8.664 17.3a.563.563 0 01-.353.269 3.317 3.317 0 01-.65.046h-.63zM16.65 9.147c-.061 0-.118-.09-.17-.273a1.927 1.927 0 01-.074-.493c0-.055.008-.1.025-.132l2.197-2.686c.221-.276.332-.555.332-.834 0-.225-.075-.398-.225-.518-.15-.124-.345-.186-.586-.186-.16 0-.3.025-.424.074a2.28 2.28 0 00-.372.195c-.042.03-.083.054-.122.073a.23.23 0 01-.097.03.378.378 0 01-.244-.098.739.739 0 01-.181-.24.602.602 0 01-.068-.258c0-.163.084-.305.254-.425a1.78 1.78 0 01.649-.278A3.47 3.47 0 0118.369 3c.397 0 .737.073 1.02.22.287.143.504.343.65.6.146.254.22.547.22.88 0 .266-.047.518-.142.756-.091.238-.22.457-.386.66l-1.63 2.016h2.002c.09 0 .157.036.2.107.042.069.063.178.063.327v.147c0 .15-.02.26-.063.332-.043.068-.11.102-.2.102H16.65z"})))},"transform-flip-h":function(n){return d.createElement("svg",rs({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),li||(li=d.createElement("path",{d:"M22.001 6v36h4V6h-4zM18.271 40h-6.67a3.6 3.6 0 01-3.6-3.6V11.6a3.6 3.6 0 013.6-3.6h6.67v4h-6.27v24h6.27v4zM36.001 8h.4a3.6 3.6 0 013.6 3.6v.4h-4V8zM40.001 36v.4a3.6 3.6 0 01-3.6 3.6h-.4v-4h4zM34.535 36h-4.534v4h4.534v-4zM34.535 8h-4.534v4h4.534V8zM36.001 14.598v4.534h4v-4.534h-4zM36.001 21.732v4.534h4v-4.534h-4zM36.001 28.866V33.4h4v-4.534h-4z",fill:"#231F20"})))},"transform-flip-v":function(n){return d.createElement("svg",os({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),ci||(ci=d.createElement("path",{d:"M42 22H6v4h36v-4zM40 18.27h-4V12H12v6.27H8V11.6A3.6 3.6 0 0111.6 8h24.8a3.6 3.6 0 013.6 3.6v6.67zM40 36.016v.4a3.6 3.6 0 01-3.6 3.6H36v-4h4zM12 40.016h-.4a3.6 3.6 0 01-3.6-3.6v-.4h4v4zM12 34.55v-4.534H8v4.534h4zM40 34.55v-4.534h-4v4.534h4zM33.4 36.016h-4.535v4H33.4v-4zM26.267 36.016h-4.534v4h4.534v-4zM19.135 36.016H14.6v4h4.534v-4z",fill:"#231F20"})))},"transform-rotate":function(n){return d.createElement("svg",ts({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),ai||(ai=d.createElement("path",{d:"M30.49 35.566l-7.938 6.727-.623-3.439A15 15 0 0110.92 16.66l3.031 1.704a11.523 11.523 0 007.315 16.828l-.569-3.13 9.793 3.504zM37.082 31.341l-3.031-1.704a11.523 11.523 0 00-7.315-16.828l.569 3.14-9.793-3.514 7.937-6.727.623 3.439a15 15 0 0111.01 22.194z",fill:"#231F20"})))},undo:function(n){return d.createElement("svg",is({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),si||(si=d.createElement("path",{d:"M12.375 9c-1.988 0-3.787.75-5.175 1.95l-2.7-2.7V15h6.75l-2.715-2.715a5.965 5.965 0 013.84-1.41 6.009 6.009 0 015.7 4.125l1.777-.585C18.81 11.273 15.862 9 12.375 9z",fill:"currentcolor"})))},"zoom-in":function(n){return d.createElement("svg",as({width:16,height:16,viewBox:"0 0 16 16",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),ui||(ui=d.createElement("path",{d:"M12.665 8.667h-4v4H7.332v-4h-4V7.334h4v-4h1.333v4h4v1.333z",fill:"currentcolor"})))},"zoom-out":function(n){return d.createElement("svg",ls({width:16,height:16,viewBox:"0 0 16 16",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),di||(di=d.createElement("path",{d:"M12.665 8.667H3.332V7.334h9.333v1.333z",fill:"currentcolor"})))},"shape-ellipse":function(n){return d.createElement("svg",Lc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Bo||(Bo=d.createElement("path",{d:"M40.718 13.822v4H35.9v4.818h-4v-4.818h-4.818v-4H31.9V9.004h4v4.818h4.818z",fill:"#231F20"})),Lo||(Lo=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M14.074 17.898C11.609 19.62 10.342 21.81 10.342 24c0 2.191 1.266 4.38 3.728 6.102 2.457 1.719 5.96 2.846 9.93 2.846 3.97 0 7.472-1.127 9.93-2.846 2.462-1.723 3.728-3.911 3.728-6.102h4c0 3.855-2.235 7.14-5.436 9.38-3.208 2.244-7.534 3.568-12.222 3.568s-9.015-1.324-12.222-3.568C8.576 31.14 6.342 27.854 6.342 24c0-3.856 2.238-7.142 5.44-9.38 3.208-2.244 7.534-3.568 12.218-3.568v4c-3.965 0-7.468 1.127-9.926 2.846z",fill:"#231F20"})))},"shape-rectangle":function(n){return d.createElement("svg",zc({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Go||(Go=d.createElement("path",{d:"M43.961 12.61v4h-4.818v4.818h-4V16.61h-4.818v-4h4.818V7.792h4v4.818h4.818zM35.14 25.43v5.97H12.86V16.61h13.462v-4H8.86V35.4h30.28v-9.96l-4-.01z",fill:"#231F20"})))},"shape-polyline":function(n){return d.createElement("svg",Vc({xmlns:"http://www.w3.org/2000/svg",width:1e3,height:1e3,viewBox:"0 0 1000 1000"},n),zo||(zo=d.createElement("path",{d:"M200 210l100 590 80-600 140 600h180l150-650",fill:"#fff",stroke:"#000",strokeWidth:40})))},"shape-line":function(n){return d.createElement("svg",_c({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),_o||(_o=d.createElement("path",{d:"M41.9 12.916v4h-4.818v4.818h-4v-4.818h-4.818v-4h4.818V8.098h4v4.818H41.9z",fill:"#231F20"})),Vo||(Vo=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M10.292 12.756a2 2 0 012.828 0l23.376 23.376a2 2 0 11-2.828 2.828L10.292 15.584a2 2 0 010-2.828z",fill:"#231F20"})))},"not-found":function(n){return d.createElement("svg",Wl({width:85,height:85,viewBox:"0 0 85 85",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Lr||(Lr=d.createElement("path",{d:"M33.494 0a33 33 0 0125.362 54.12l24.762 24.757a3 3 0 01-3.828 4.59l-.42-.342-24.756-24.762A33 33 0 1133.494 0zm0 6a27 27 0 100 54 27 27 0 000-54z",fill:"#525252",fillOpacity:.4})),_r||(_r=d.createElement("path",{stroke:"#005662",strokeWidth:6,strokeLinecap:"round",d:"M22.243 22.558L44.355 44.67M45.191 22.243L23.079 44.355"})))},"save-1":function(n){return d.createElement("svg",ss({width:10,height:12,viewBox:"0 0 10 12",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),hi||(hi=d.createElement("path",{d:"M9.667 4H7.001V0H3v4H.334l4.667 4.667L9.667 4zM.334 10v1.333h9.333V10H.334z",fill:"currentcolor"})))},"open-1":function(n){return d.createElement("svg",us({width:14,height:12,viewBox:"0 0 14 12",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),fi||(fi=d.createElement("path",{d:"M13.665 2H7L5.665.667H.332v10.666h13.333V2zm-1.333 8H1.665V3.333h10.667V10z",fill:"currentcolor"})))},reset:function(n){return d.createElement("svg",ds({width:15,height:12,viewBox:"0 0 15 12",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),mi||(mi=d.createElement("path",{d:"M8.666 0a6 6 0 00-6 6h-2l2.667 2.66L5.999 6H4a4.663 4.663 0 014.667-4.667A4.663 4.663 0 0113.333 6a4.663 4.663 0 01-4.667 4.667 4.63 4.63 0 01-3.293-1.374l-.947.947A5.97 5.97 0 008.666 12a6 6 0 000-12zm-.667 3.333v3.334l2.834 1.68.513-.854L8.999 6.1V3.333H8z",fill:"currentcolor"})))},close:function(n){return d.createElement("svg",ps({width:24,height:24,viewBox:"0 0 24 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),vi||(vi=d.createElement("path",{d:"M13.462 12.046l6.37 6.37-1.413 1.415-6.371-6.371-6.327 6.326-1.414-1.414 6.327-6.326-6.372-6.372L5.676 4.26l6.372 6.372 6.417-6.418 1.414 1.414-6.417 6.418z",fill:"#333"})))},general:function(n){return d.createElement("svg",hs({width:16,height:16,viewBox:"0 0 16 16",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),gi||(gi=d.createElement("path",{d:"M4.5 6.25H2a.5.5 0 00-.5.5v2.5a.5.5 0 00.5.5h2.5a.5.5 0 00.5-.5v-2.5a.5.5 0 00-.5-.5zM13.5 2.5h-3a.5.5 0 00-.5.5v3a.5.5 0 00.5.5h3A.5.5 0 0014 6V3a.5.5 0 00-.5-.5zM13.5 9.5h-3a.5.5 0 00-.5.5v3a.5.5 0 00.5.5h3a.5.5 0 00.5-.5v-3a.5.5 0 00-.5-.5zM5 8h2.5M10 11.5H9A1.5 1.5 0 017.5 10V6A1.5 1.5 0 019 4.5h1",stroke:"#5B6077",strokeLinecap:"round",strokeLinejoin:"round"})))},"general-white":function(n){return d.createElement("svg",fs({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),bi||(bi=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M32.57 11.839v5.466h5.466v-5.466H32.57zm-4-1.2a2.8 2.8 0 012.8-2.8h7.866a2.8 2.8 0 012.8 2.8v7.866a2.8 2.8 0 01-2.8 2.8H31.37a2.8 2.8 0 01-2.8-2.8V16.57H26V26h-.009l-.023 5.422h2.602v-1.926a2.8 2.8 0 012.8-2.8h7.866a2.8 2.8 0 012.8 2.8v7.866a2.8 2.8 0 01-2.8 2.8H31.37a2.8 2.8 0 01-2.8-2.8v-1.94h-3.004a3.6 3.6 0 01-3.6-3.6v-.005l.025-5.817h-2.569v1.932a2.8 2.8 0 01-2.8 2.8H8.756a2.8 2.8 0 01-2.8-2.8v-7.866a2.8 2.8 0 012.8-2.8h7.866a2.8 2.8 0 012.8 2.8V22h2.579v-5.83a3.6 3.6 0 013.6-3.6h2.969v-1.932zM9.956 21.267v5.466h5.466v-5.466H9.956zM32.57 36.163v-5.466h5.466v5.466H32.57z",fill:"#FFF"})))},stereo:function(n){return d.createElement("svg",ms({width:16,height:16,viewBox:"0 0 16 16",fill:"none",xmlns:"http://www.w3.org/2000/svg",xmlnsXlink:"http://www.w3.org/1999/xlink"},n),Ci||(Ci=d.createElement("path",{fill:"url(#stereo_svg__pattern0)",d:"M0 0h16v16H0z"})),yi||(yi=d.createElement("defs",null,d.createElement("pattern",{id:"stereo_svg__pattern0",patternContentUnits:"objectBoundingBox",width:1,height:1},d.createElement("use",{xlinkHref:"#stereo_svg__image0_2343_3998",transform:"scale(.00195)"})),d.createElement("image",{id:"stereo_svg__image0_2343_3998",width:512,height:512,xlinkHref:"data:image/png;base64,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"}))))},"stereo-white":function(n){return d.createElement("svg",vs({width:16,height:16,viewBox:"0 0 16 16",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Oi||(Oi=d.createElement("path",{d:"M6.269 3.233l1.733 1m0 0l1.767-1m-1.767 1v1.234M2.97 9.433l1.533.867m0 0l1.067-.633m-1.067.633v1.767",stroke:"#fff",strokeWidth:.667,strokeLinecap:"round",strokeLinejoin:"round"})),wi||(wi=d.createElement("path",{d:"M8.001 6.385l1.63.94v1.883l-1.63.94-1.63-.94V7.326l1.63-.941z",stroke:"#fff",strokeWidth:.667,strokeLinejoin:"round"})),Si||(Si=d.createElement("path",{d:"M9.6 9.185l1.63.94v1.883l-1.63.94-1.629-.94v-1.882l1.63-.941z",stroke:"#fff",strokeWidth:.667,strokeLinejoin:"round"})),Mi||(Mi=d.createElement("path",{d:"M8.135 7.467l.666.383v.817M9.8 10.267l.667.383v.817M11.232 10.167l1.734-1.034",stroke:"#fff",strokeWidth:.667,strokeLinecap:"round",strokeLinejoin:"round"})),xi||(xi=d.createElement("circle",{cx:5.268,cy:2.6,r:.6,fill:"#fff"})),ji||(ji=d.createElement("circle",{cx:10.735,cy:2.6,r:.6,fill:"#fff"})),Ei||(Ei=d.createElement("circle",{cx:1.934,cy:8.8,r:.6,fill:"#fff"})),Di||(Di=d.createElement("circle",{cx:4.467,cy:13.333,r:.6,fill:"#fff"})),Ai||(Ai=d.createElement("circle",{cx:14.067,cy:8.533,r:.6,fill:"#fff"})))},atoms:function(n){return d.createElement("svg",gs({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),$i||($i=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M10.082 24c-1.306-1.944-2.363-3.86-3.132-5.673-.885-2.086-1.432-4.132-1.474-5.986-.042-1.86.428-3.71 1.791-5.073 1.364-1.363 3.213-1.833 5.073-1.79 1.854.042 3.9.588 5.986 1.473 1.813.77 3.729 1.826 5.673 3.132 1.944-1.306 3.86-2.363 5.673-3.132 2.085-.885 4.132-1.431 5.985-1.474 1.86-.042 3.71.428 5.073 1.791 1.364 1.364 1.834 3.213 1.791 5.073-.042 1.854-.588 3.9-1.473 5.986-.77 1.813-1.826 3.729-3.132 5.673 1.306 1.944 2.363 3.86 3.132 5.673.885 2.086 1.431 4.132 1.473 5.986.043 1.86-.427 3.71-1.79 5.073-1.364 1.363-3.213 1.833-5.074 1.79-1.853-.042-3.9-.588-5.985-1.473-1.813-.77-3.729-1.826-5.673-3.132-1.944 1.306-3.86 2.363-5.673 3.132-2.086.885-4.133 1.431-5.986 1.474-1.86.042-3.71-.428-5.073-1.791-1.363-1.364-1.833-3.213-1.79-5.073.041-1.854.588-3.9 1.473-5.986.769-1.813 1.826-3.729 3.132-5.673zm2.545-3.433a28.55 28.55 0 01-1.995-3.802c-.767-1.807-1.13-3.337-1.157-4.515-.026-1.17.275-1.807.62-2.153.347-.346.983-.647 2.154-.62 1.178.026 2.708.39 4.514 1.156 1.2.51 2.48 1.178 3.803 1.995a54.476 54.476 0 00-4.171 3.768 54.458 54.458 0 00-3.768 4.171zm7.939 14.805a28.557 28.557 0 01-3.802 1.995c-1.807.767-3.337 1.13-4.515 1.157-1.171.026-1.807-.275-2.153-.62-.346-.347-.647-.983-.62-2.154.026-1.178.39-2.708 1.156-4.515.51-1.2 1.178-2.479 1.995-3.802a54.457 54.457 0 003.768 4.171 54.457 54.457 0 004.17 3.768zm3.433-2.384a49.694 49.694 0 01-4.776-4.212A49.694 49.694 0 0115.011 24a49.694 49.694 0 014.212-4.776 49.708 49.708 0 014.776-4.212 49.708 49.708 0 014.776 4.212A49.708 49.708 0 0132.987 24a49.708 49.708 0 01-4.212 4.776 49.694 49.694 0 01-4.776 4.212zm3.433 2.384a28.55 28.55 0 003.802 1.995c1.806.767 3.337 1.13 4.514 1.157 1.172.026 1.808-.275 2.154-.62.346-.347.647-.983.62-2.154-.026-1.178-.39-2.708-1.156-4.515a28.556 28.556 0 00-1.995-3.802 54.5 54.5 0 01-3.768 4.171 54.458 54.458 0 01-4.171 3.768zm7.939-14.805a28.563 28.563 0 001.995-3.802c.766-1.807 1.13-3.337 1.156-4.515.027-1.17-.274-1.807-.62-2.153-.346-.346-.983-.647-2.154-.62-1.177.026-2.708.39-4.514 1.156-1.2.51-2.479 1.178-3.802 1.995a54.457 54.457 0 014.171 3.768 54.5 54.5 0 013.767 4.171z",fill:"#231F20"})),Ni||(Ni=d.createElement("path",{d:"M23.998 25.998a2 2 0 100-4 2 2 0 000 4z",fill:"#231F20"})))},"atoms-white":function(n){return d.createElement("svg",bs({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Pi||(Pi=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M10.082 24c-1.306-1.944-2.363-3.86-3.132-5.673-.885-2.086-1.432-4.132-1.474-5.986-.042-1.86.428-3.71 1.791-5.073 1.364-1.363 3.213-1.833 5.073-1.79 1.854.042 3.9.588 5.986 1.473 1.813.77 3.729 1.826 5.673 3.132 1.944-1.306 3.86-2.363 5.673-3.132 2.085-.885 4.132-1.431 5.985-1.474 1.86-.042 3.71.428 5.073 1.791 1.364 1.364 1.834 3.213 1.791 5.073-.042 1.854-.588 3.9-1.473 5.986-.77 1.813-1.826 3.729-3.132 5.673 1.306 1.944 2.363 3.86 3.132 5.673.885 2.086 1.431 4.132 1.473 5.986.043 1.86-.427 3.71-1.79 5.073-1.364 1.363-3.213 1.833-5.074 1.79-1.853-.042-3.9-.588-5.985-1.473-1.813-.77-3.729-1.826-5.673-3.132-1.944 1.306-3.86 2.363-5.673 3.132-2.086.885-4.133 1.431-5.986 1.474-1.86.042-3.71-.428-5.073-1.791-1.363-1.364-1.833-3.213-1.79-5.073.041-1.854.588-3.9 1.473-5.986.769-1.813 1.826-3.729 3.132-5.673zm2.545-3.433a28.55 28.55 0 01-1.995-3.802c-.767-1.807-1.13-3.337-1.157-4.515-.026-1.17.275-1.807.62-2.153.347-.346.983-.647 2.154-.62 1.178.026 2.708.39 4.514 1.156 1.2.51 2.48 1.178 3.803 1.995a54.476 54.476 0 00-4.171 3.768 54.458 54.458 0 00-3.768 4.171zm7.939 14.805a28.557 28.557 0 01-3.802 1.995c-1.807.767-3.337 1.13-4.515 1.157-1.171.026-1.807-.275-2.153-.62-.346-.347-.647-.983-.62-2.154.026-1.178.39-2.708 1.156-4.515.51-1.2 1.178-2.479 1.995-3.802a54.457 54.457 0 003.768 4.171 54.457 54.457 0 004.17 3.768zm3.433-2.384a49.694 49.694 0 01-4.776-4.212A49.694 49.694 0 0115.011 24a49.694 49.694 0 014.212-4.776 49.708 49.708 0 014.776-4.212 49.708 49.708 0 014.776 4.212A49.708 49.708 0 0132.987 24a49.708 49.708 0 01-4.212 4.776 49.694 49.694 0 01-4.776 4.212zm3.433 2.384a28.55 28.55 0 003.802 1.995c1.806.767 3.337 1.13 4.514 1.157 1.172.026 1.808-.275 2.154-.62.346-.347.647-.983.62-2.154-.026-1.178-.39-2.708-1.156-4.515a28.556 28.556 0 00-1.995-3.802 54.5 54.5 0 01-3.768 4.171 54.458 54.458 0 01-4.171 3.768zm7.939-14.805a28.563 28.563 0 001.995-3.802c.766-1.807 1.13-3.337 1.156-4.515.027-1.17-.274-1.807-.62-2.153-.346-.346-.983-.647-2.154-.62-1.177.026-2.708.39-4.514 1.156-1.2.51-2.479 1.178-3.802 1.995a54.457 54.457 0 014.171 3.768 54.5 54.5 0 013.767 4.171z",fill:"#FFF"})),ki||(ki=d.createElement("path",{d:"M23.998 25.998a2 2 0 100-4 2 2 0 000 4z",fill:"#FFF"})))},bonds:function(n){return d.createElement("svg",Cs({width:16,height:16,viewBox:"0 0 16 16",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Ii||(Ii=d.createElement("path",{d:"M8 2.5v11M3.238 5.25l9.527 5.5M3.238 10.75l9.527-5.5",stroke:"#5B6077",strokeLinecap:"round",strokeLinejoin:"round"})))},"bonds-white":function(n){return d.createElement("svg",ys({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Ti||(Ti=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M24 6.044a2 2 0 012 2v12.492l10.818-6.246a2 2 0 112 3.464L28 24l10.818 6.246a2 2 0 01-2 3.464L26 27.464v12.492a2 2 0 01-4 0V27.464L11.182 33.71a2 2 0 01-2-3.464L20 24 9.182 17.754a2 2 0 012-3.464L22 20.536V8.044a2 2 0 012-2z",fill:"#FFF"})))},server:function(n){return d.createElement("svg",Os({width:16,height:16,viewBox:"0 0 16 16",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Bi||(Bi=d.createElement("path",{d:"M8 8c3.038 0 5.5-1.343 5.5-3S11.038 2 8 2 2.5 3.343 2.5 5 4.962 8 8 8z",stroke:"#5B6077",strokeLinecap:"round",strokeLinejoin:"round"})),Li||(Li=d.createElement("path",{d:"M2.5 5v3c0 1.657 2.462 3 5.5 3s5.5-1.343 5.5-3V5",stroke:"#5B6077",strokeLinecap:"round",strokeLinejoin:"round"})),_i||(_i=d.createElement("path",{d:"M2.5 8v3c0 1.657 2.462 3 5.5 3s5.5-1.343 5.5-3V8",stroke:"#5B6077",strokeLinecap:"round",strokeLinejoin:"round"})))},"server-white":function(n){return d.createElement("svg",ws({width:16,height:16,viewBox:"0 0 16 16",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Vi||(Vi=d.createElement("path",{d:"M8 8c3.038 0 5.5-1.343 5.5-3S11.038 2 8 2 2.5 3.343 2.5 5 4.962 8 8 8z",stroke:"#fff",strokeWidth:.667,strokeLinecap:"round",strokeLinejoin:"round"})),zi||(zi=d.createElement("path",{d:"M2.5 5v3c0 1.657 2.462 3 5.5 3s5.5-1.343 5.5-3V5",stroke:"#fff",strokeWidth:.667,strokeLinecap:"round",strokeLinejoin:"round"})),Gi||(Gi=d.createElement("path",{d:"M2.5 8v3c0 1.657 2.462 3 5.5 3s5.5-1.343 5.5-3V8",stroke:"#fff",strokeWidth:.667,strokeLinecap:"round",strokeLinejoin:"round"})))},"3dviewer":function(n){return d.createElement("svg",Ss({width:16,height:16,viewBox:"0 0 16 16",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Fi||(Fi=d.createElement("path",{d:"M14 11.081V4.916a.5.5 0 00-.255-.436l-5.5-3.094a.5.5 0 00-.49 0l-5.5 3.094A.5.5 0 002 4.916v6.165a.5.5 0 00.255.436l5.5 3.094a.5.5 0 00.49 0l5.5-3.094a.5.5 0 00.255-.436z",stroke:"#5B6077",strokeLinecap:"round",strokeLinejoin:"round"})),Hi||(Hi=d.createElement("path",{d:"M13.932 4.665L8.06 8.001 2.07 4.664M8.059 8L8 14.676",stroke:"#5B6077",strokeLinecap:"round",strokeLinejoin:"round"})))},"3dviewer-white":function(n){return d.createElement("svg",Ms({width:16,height:16,viewBox:"0 0 16 16",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Ri||(Ri=d.createElement("path",{d:"M14 11.081V4.916a.5.5 0 00-.255-.436l-5.5-3.094a.5.5 0 00-.49 0l-5.5 3.094A.5.5 0 002 4.916v6.165a.5.5 0 00.255.436l5.5 3.094a.5.5 0 00.49 0l5.5-3.094a.5.5 0 00.255-.436z",stroke:"#fff",strokeLinecap:"round",strokeLinejoin:"round"})),Zi||(Zi=d.createElement("path",{d:"M13.932 4.665L8.06 8.001 2.07 4.665M8.059 8L8 14.676",stroke:"#fff",strokeLinecap:"round",strokeLinejoin:"round"})))},debugging:function(n){return d.createElement("svg",xs({width:16,height:16,viewBox:"0 0 16 16",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Ki||(Ki=d.createElement("path",{d:"M8 2h0a4.5 4.5 0 00-4.5 4.5v3A4.5 4.5 0 008 14h0a4.5 4.5 0 004.5-4.5v-3A4.5 4.5 0 008 2zM12.5 8.5H14M2 8.5h1.5M2 10.5h1.612M2 6.5h12M8 8.5V14M12.389 10.5H14M3.496 1.75l1.485 1.413M12.495 1.75l-1.481 1.409",stroke:"#5B6077",strokeLinecap:"round",strokeLinejoin:"round"})))},"debugging-white":function(n){return d.createElement("svg",js({width:16,height:16,viewBox:"0 0 16 16",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Yi||(Yi=d.createElement("path",{d:"M8 2h0a4.5 4.5 0 00-4.5 4.5v3A4.5 4.5 0 008 14h0a4.5 4.5 0 004.5-4.5v-3A4.5 4.5 0 008 2zM12.5 8.5H14M2 8.5h1.5M2 10.5h1.612M2 6.5h12M8 8.5V14M12.389 10.5H14M3.496 1.75l1.485 1.413M12.495 1.75l-1.481 1.409",stroke:"#fff",strokeLinecap:"round",strokeLinejoin:"round"})))},"dropdown-indicator":function(n){return d.createElement("svg",Es({width:16,height:16,viewBox:"0 0 16 16",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Ui||(Ui=d.createElement("path",{d:"M4.94 5.727L8 8.78l3.06-3.053.94.94-4 4-4-4 .94-.94z",fill:"#5B6077"})))},"text-special-symbols":function(n){return d.createElement("svg",cs({xmlns:"http://www.w3.org/2000/svg",width:24,height:24,viewBox:"0 0 24 24"},n),pi||(pi=d.createElement("path",{d:"M19.15 19h-5.76v-2.13c2.11-1.62 3.2-3.63 3.2-6.03 0-1.5-.43-2.68-1.27-3.55C14.47 6.42 13.37 6 12.03 6c-1.35 0-2.46.42-3.32 1.3-.87.87-1.3 2.07-1.3 3.58 0 2.38 1.09 4.38 3.2 5.99V19H4.85v-2.13h3.56c-2.37-1.55-3.56-3.64-3.56-6.27 0-2.1.65-3.74 1.96-4.94 1.31-1.21 3.03-1.81 5.16-1.81 2.18 0 3.92.6 5.22 1.79 1.31 1.19 1.96 2.86 1.96 4.94 0 2.63-1.2 4.73-3.6 6.29h3.6V19z"})))},chevron:function(n){return d.createElement("svg",Ds({width:48,height:48,viewBox:"0 0 48 48",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Ji||(Ji=d.createElement("path",{d:"M24 33.23L9.782 19.012l2.828-2.828L24 27.574l11.388-11.39 2.83 2.828L24 33.23z",fill:"#231F20"})))},"open-window-paste-icon":function(n){return d.createElement("svg",nc({width:40,height:40,viewBox:"0 0 40 40",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Gr||(Gr=d.createElement("path",{d:"M33.973 40H6.027A6.027 6.027 0 010 33.973V6.027A6.027 6.027 0 016.027 0h27.946A6.027 6.027 0 0140 6.027v27.946A6.027 6.027 0 0133.973 40z",fill:"#EFF2F5"})),Fr||(Fr=d.createElement("path",{d:"M28.556 30.636H11.444V11.727h2.445v3.546H26.11v-3.546h2.445v18.91zM20 9.364c.324 0 .635.124.864.346.23.221.358.522.358.835 0 .314-.129.614-.358.836-.229.222-.54.346-.864.346-.324 0-.635-.124-.864-.346a1.162 1.162 0 01-.358-.835c0-.314.129-.615.358-.836.229-.222.54-.346.864-.346zm8.556 0h-5.11A3.673 3.673 0 0020 7a3.673 3.673 0 00-3.447 2.364h-5.109c-.648 0-1.27.249-1.728.692A2.325 2.325 0 009 11.727v18.91c0 .626.258 1.227.716 1.67.458.444 1.08.693 1.728.693h17.112c.648 0 1.27-.249 1.728-.692A2.325 2.325 0 0031 30.636V11.727c0-.627-.258-1.228-.716-1.671a2.487 2.487 0 00-1.728-.692z",fill:"#167782"})),Hr||(Hr=d.createElement("path",{fillRule:"evenodd",clipRule:"evenodd",d:"M15 20h10c.55 0 1-.45 1-1s-.45-1-1-1H15c-.55 0-1 .45-1 1s.45 1 1 1zm10 4H15c-.55 0-1-.45-1-1s.45-1 1-1h10c.55 0 1 .45 1 1s-.45 1-1 1zm0 4H15c-.55 0-1-.45-1-1s.45-1 1-1h10c.55 0 1 .45 1 1s-.45 1-1 1z",fill:"#167782"})))},"open-window-upload-icon":function(n){return d.createElement("svg",ec({width:40,height:40,viewBox:"0 0 40 40",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),Rr||(Rr=d.createElement("path",{d:"M33.973 40H6.027A6.027 6.027 0 010 33.973V6.027A6.027 6.027 0 016.027 0h27.946A6.027 6.027 0 0140 6.027v27.946A6.027 6.027 0 0133.973 40z",fill:"#EFF2F5"})),Zr||(Zr=d.createElement("path",{d:"M12.835 18.125l-2.477 9.5V15.75h20.048c0-.63-.249-1.234-.691-1.68a2.35 2.35 0 00-1.668-.695h-8.255L17.434 11h-7.076a2.35 2.35 0 00-1.667.696A2.383 2.383 0 008 13.375v14.25c0 .63.248 1.234.69 1.68a2.35 2.35 0 001.668.695h17.69a2.276 2.276 0 002.24-1.781L33 18.125H12.835zm15.212 9.5h-15.33l1.887-7.125h15.33l-1.887 7.125z",fill:"#167782"})))}};function ju(){return null}var Eu=["name"];function Du(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Au(n){var e=n.name,t=(0,p.Z)(n,Eu),i=function(n){return n&&xu.hasOwnProperty(n)?xu[n]:ju}(e);return(0,o.jsx)(i,function(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Du(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Du(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}({},t))}var $u={Escape:"Esc",Delete:"Del",Mod:/Mac/.test(navigator.platform)?"⌘":"Ctrl"};function Nu(n){return n?(Array.isArray(n)?n[0]:n).replace(/(\b[a-z]\b$|Mod|Escape|Delete)/g,(function(n){return $u[n]||n.toUpperCase()})):""}var Pu=function(n){var e=n.name,t=n.action,i=n.status,a=void 0===i?{}:i,l=n.selected,c=void 0!==l&&l,s=n.disableableButtons,u=n.indigoVerification,d=n.className,p=n.onAction;if(a.hidden)return null;var h=Nu(null==t?void 0:t.shortcut),f=a.disabled||u&&s.includes(e);return(0,o.jsxs)("button",{disabled:f,onClick:function(n){null!=t&&t.action&&p(t.action),n.stopPropagation()},title:h?"".concat(null==t?void 0:t.title," (").concat(h,")"):null==t?void 0:t.title,className:(0,v.Z)("ActionButton-module_button__nfoWQ",(0,r.Z)({},"ActionButton-module_selected__kPCxA",c),d),children:[(0,o.jsx)(Au,{name:e}),(0,o.jsx)("kbd",{children:h})]})};var ku=function(n){(0,h.Z)(o,n);var e,t,r=(e=o,t=function(){if("undefined"==typeof Reflect||!Reflect.construct)return!1;if(Reflect.construct.sham)return!1;if("function"==typeof Proxy)return!0;try{return Boolean.prototype.valueOf.call(Reflect.construct(Boolean,[],(function(){}))),!0}catch(n){return!1}}(),function(){var n,r=(0,m.Z)(e);if(t){var o=(0,m.Z)(this).constructor;n=Reflect.construct(r,arguments,o)}else n=r.apply(this,arguments);return(0,f.Z)(this,n)});function o(n){var e;return(0,c.Z)(this,o),(e=r.call(this,n)).element=document.createElement("div"),e.isElementInDom=!1,e}return(0,s.Z)(o,[{key:"componentDidMount",value:function(){!this.isElementInDom&&this.props.isOpen&&this.addElementInDOM();var n=this.props,e=n.className,t=n.style;e&&this.addClassName(e),t&&this.updateStyle(t)}},{key:"componentWillUnmount",value:function(){this.isElementInDom&&this.removeElementFromDOM()}},{key:"componentDidUpdate",value:function(n){var e=this.props,t=e.isOpen,r=e.className,o=e.style;r!==n.className&&(this.removeClassNames(n.className),this.addClassName(r)),o!==n.style&&this.updateStyle(o,n.style),t!==n.isOpen&&(t&&!this.isElementInDom?this.addElementInDOM():this.isElementInDom&&this.removeElementFromDOM())}},{key:"addElementInDOM",value:function(){var n;null===(n=document.querySelector(".Ketcher-root"))||void 0===n||n.appendChild(this.element),this.isElementInDom=!0}},{key:"removeElementFromDOM",value:function(){var n;null===(n=document.querySelector(".Ketcher-root"))||void 0===n||n.removeChild(this.element),this.isElementInDom=!1}},{key:"removeClassNames",value:function(n){var e=this;n&&n.split(" ").forEach((function(n){e.element.classList.remove(n)}))}},{key:"addClassName",value:function(n){var e=this;n&&n.split(" ").forEach((function(n){e.element.classList.add(n)}))}},{key:"updateStyle",value:function(n,e){var t=this;e&&Object.keys(e).forEach((function(n){t.element.style[n]=""}),this),n&&Object.keys(n).forEach((function(e){t.element.style[e]=n[e]}),this)}},{key:"render",value:function(){var n=this.props.children;return w.createPortal(n,this.element)}}]),o}(d.Component),Iu=function(n){var e=n.options,t=n.status,r=n.disableableButtons,i=n.indigoVerification,a=n.onAction;return(0,o.jsx)(o.Fragment,{children:e.map((function(n){var e=t[n.id];return(0,o.jsx)(Pu,{name:n.id,action:Ja[n.id],status:e,selected:!(null==e||!e.selected),disableableButtons:r,indigoVerification:i,onAction:a},n.id)}))})},Tu=function(n){var e=n.groups,t=n.options,r=n.status,i=n.disableableButtons,a=n.indigoVerification,l=n.onAction;return e?(0,o.jsx)(o.Fragment,{children:e.map((function(n){return(0,o.jsx)("div",{className:"GroupedMultiTool-module_group__BJQAU",children:t.slice(n.start,n.end).map((function(n){var e=r[n.id];return(0,o.jsx)(Pu,{name:n.id,action:Ja[n.id],status:e,selected:!(null==e||!e.selected),disableableButtons:i,indigoVerification:a,onAction:l},n.id)}))},n.start)}))}):null},Bu={"button-common-styles":"ToolbarMultiToolItem-module_button-common-styles__Fuxbo",scrollbar:"ToolbarMultiToolItem-module_scrollbar__XTmfz",icon:"ToolbarMultiToolItem-module_icon__-HQal",iconSelected:"ToolbarMultiToolItem-module_iconSelected__hlO0J",portal:"ToolbarMultiToolItem-module_portal__2XJgz","portal-vertical":"ToolbarMultiToolItem-module_portal-vertical__A0DVe"};function Lu(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function _u(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Lu(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Lu(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Vu=function(n){var e=n.id,t=n.options,r=n.groups,i=n.variant,a=n.status,l=n.opened,c=n.indigoVerification,s=n.disableableButtons,u=n.className,p=n.vertical,h=n.onAction,f=n.onOpen,m=(0,d.useRef)(null),g=function(n){var e=(0,O.Z)(n,3),t=e[0],r=e[1],o=e[2],i=(0,d.useState)(!1),a=(0,O.Z)(i,2),l=a[0],c=a[1];return(0,d.useEffect)((function(){var n=o.length&&o[0].id||"";c(r===t||r===n)}),[r,o]),[l]}([e,l,t]),b=(0,O.Z)(g,1)[0],C=function(n){var e=(0,O.Z)(n,2),t=e[0],r=e[1],o=(0,d.useState)({}),i=(0,O.Z)(o,2),a=i[0],l=i[1];return(0,d.useEffect)((function(){var n;if(t.current){var e=(null===(n=document.querySelector(".Ketcher-root"))||void 0===n?void 0:n.getBoundingClientRect())||{top:0,left:0},r=t.current.getBoundingClientRect(),o=r.top-e.top,i=r.left-e.left+r.width+4;l({top:"".concat(o,"px"),left:"".concat(i,"px")})}}),[t,r]),[a]}([m,b]),y=(0,O.Z)(C,1)[0],w=!1,S=e,M=t.find((function(n){var e;return null===(e=a[n.id])||void 0===e?void 0:e.selected}));M&&(S=M.id,w=!0);var x=a[S];w=w||Boolean(null==x?void 0:x.selected);var j,E=!(t.every((function(n){var e;return null===(e=a[n.id])||void 0===e?void 0:e.hidden}))||null!=x&&x.hidden);!x&&t.length&&(S=(null===(j=t.filter((function(n){var e;return!(null!==(e=a[n.id])&&void 0!==e&&e.hidden)}))[0])||void 0===j?void 0:j.id)||t[0].id);var D={disableableButtons:s,indigoVerification:c,onAction:w?function(){return A()}:h},A=function(){f(e,Boolean(null==x?void 0:x.selected))},$=function(){var n=arguments.length>0&&void 0!==arguments[0]?arguments[0]:"default";switch(n){case"default":return[Iu,"DefaultMultiTool-module_default__zNTMe"];case"grouped":return[Tu];default:throw new Error("Unsupported variant ".concat(n))}}(i),N=(0,O.Z)($,2),P=N[0],k=N[1];return E?(0,o.jsxs)("div",{ref:m,className:Bu.root,children:[(0,o.jsx)(Pu,_u(_u({},D),{},{className:u,name:S,action:Ja[S],status:x,selected:w})),!b&&(0,o.jsx)(Au,{className:"".concat(Bu.icon," ").concat((null==x?void 0:x.selected)&&Bu.iconSelected),name:"dropdown",onClick:A}),b?(0,o.jsx)(ku,{isOpen:b,className:(0,v.Z)(Bu.portal,p&&Bu["portal-vertical"],k),style:y,children:(0,o.jsx)(P,{options:t,groups:r,status:a,disableableButtons:s,indigoVerification:c,onAction:h})}):null]}):null},zu=function(n){var e,t=n.id,r=n.options,i=n.status,a=n.className,l=n.opened,c=n.indigoVerification,s=n.disableableButtons,u=n.vertical,d=n.onAction,p=n.onOpen;return null!=r&&r.length?(0,o.jsx)(Vu,{className:a,id:t,options:r,status:i,opened:l,disableableButtons:s,indigoVerification:c,onAction:d,onOpen:p,vertical:u}):(0,o.jsx)(Pu,{className:a,name:t,action:Ja[t],status:i[t],selected:!(null===(e=i[t])||void 0===e||!e.selected),indigoVerification:c,disableableButtons:s,onAction:d})},Gu=function(n){var e=n.active,t=n.disableableButtons,r=n.indigoVerification,i=n.onAction,a=e&&"template"===e.tool,l=function(n,e){return{shortcut:Ja["template-".concat(e)].shortcut,action:{tool:"template",opts:{struct:n}},title:n.name}};return(0,o.jsx)(o.Fragment,{children:tt.map((function(n,c){return(0,o.jsx)(Pu,{name:"template-".concat(c),action:l(n,c),onAction:i,selected:a&&e&&e.opts.struct===n,status:Ja["template-".concat(c)],disableableButtons:t,indigoVerification:r},"template-".concat(c))}))})},Fu=["className"];function Hu(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Ru(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Hu(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Hu(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Zu=function(n){var e=n.children,t=n.className;return(0,o.jsx)("div",{className:(0,v.Z)("BottomToolbar-module_group__b-pGt",t),children:e})};function Ku(n){return{type:"TMPL_INIT",data:{lib:n}}}var Yu=function(n,e,t){var r=(new u.Ruh).deserialize("alpha-D-Allopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -2.4110    3.5743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4110    1.6992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2304    0.7587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.0499    1.6991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2360    3.5743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.8478    2.9800    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3208    3.1152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3208    2.1638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2360    1.6991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1456    2.1636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1456    3.1151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.0499    3.5741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  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 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  6     0  0\n  9  3  1  6     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl1\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Altropyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -0.9910    2.2903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.9910    0.7936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2875    0.0452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5799    0.7935    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2834    2.2903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1462    1.8062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.6372    1.9161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.6372    1.1678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2834    0.7935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9337    1.1677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9337    1.9160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5799    2.2902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  1     0  0\n  9  3  1  6     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl2\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Arabinofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -1.9332    3.1927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5926    1.1426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7765    1.1387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7048    3.4871    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.0588    2.4002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8825    2.8828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1801    1.9478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1909    1.9478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5142    2.8976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.4573    3.1978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  1     0  0\n  8  3  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl3\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Arabinopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   15.5611   -5.2999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.5611   -7.3001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8228   -8.3002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0958   -7.3001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8228   -5.2999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6920   -5.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6920   -6.7999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8228   -7.3001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9648   -6.7999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9648   -5.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  5 10  1  0     0  0\n 10  9  1  0     0  0\n  9  8  1  0     0  0\n  8  7  1  0     0  0\n  7  6  1  0     0  0\n  6  5  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  1     0  0\n  8  3  1  6     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl4\n\n$$$$\nalpha-D-Erythrofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     1  0            999 V2000\n   -2.3742    2.6418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8682    1.1059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4960    1.1030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7013    2.8623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0854    2.4096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3125    1.7091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0613    1.7091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3035    2.4207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  8  4  1  0     0  0\n  8  7  1  0     0  0\n  4  5  1  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  1  1  6     0  0\n  6  2  1  6     0  0\n  7  3  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl5\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Galactopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.5577    2.5236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.5577    1.0270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8542    0.2785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1466    1.0269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8543    2.5236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7171    2.0395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2039    2.1495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2039    1.4011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8543    1.0269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5004    1.4010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5004    2.1494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1466    2.5235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  6     0  0\n  9  3  1  1     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl6\n\n$$$$\nalpha-D-Glucopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -2.1744    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1744    1.3186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4708    0.5702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7632    1.3185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4709    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3337    2.3312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8206    2.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8206    1.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4709    1.3185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1170    1.6927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1170    2.4410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7632    2.8152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  6     0  0\n  9  3  1  1     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl7\n\n$$$$\nalpha-D-Gulopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -2.1119    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1119    1.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4083    0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7007    1.3602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4084    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2712    2.3728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7581    2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7581    1.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4084    1.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0545    1.7344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0545    2.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7007    2.8569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  6     0  0\n  9  3  1  6     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl8\n\n$$$$\nalpha-D-Idopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.9244    2.7736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9244    1.2770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2208    0.5285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5132    1.2769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2209    2.7736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0837    2.2895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5706    2.3995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5706    1.6511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2209    1.2769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8670    1.6510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8670    2.3994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5132    2.7735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  1     0  0\n  9  3  1  6     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl9\n\n$$$$\nalpha-D-Lyxofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.1148    2.9334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6088    1.3976    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2406    1.3947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4419    3.1538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2054    2.3397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8260    2.7012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0531    2.0007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8102    2.0007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0483    2.7122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7589    2.9371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  1     0  0\n  8  3  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl10\n\n$$$$\nalpha-D-Lyxopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.4513    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4513    1.3186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7520    0.5702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0444    1.3185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7521    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1017    2.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1017    1.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7521    1.3185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3940    1.6927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3940    2.4410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 10  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  1     0  0\n  8  3  1  1     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl11\n\n$$$$\nalpha-D-Mannopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -2.1577    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1577    1.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4542    0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7466    1.3602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4543    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3171    2.3728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8039    2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8039    1.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4543    1.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1004    1.7344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1004    2.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7466    2.8569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  1     0  0\n  9  3  1  1     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl12\n\n$$$$\nalpha-D-Psicofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   15.0740   -8.2784    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3759   -8.9026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7463  -10.3149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5700  -10.3189    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6353   -7.9706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2665   -9.0586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1656   -7.8559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4589   -8.5718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1574   -9.5078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.1460   -9.5078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8298   -8.5571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8731   -8.2544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  1     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  6     0  0\n  9  3  1  6     0  0\n  8  2  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl13\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Ribofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -1.8940    2.7251    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3879    1.1893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0198    1.1863    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2211    2.9455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9845    2.1313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6051    2.4928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8322    1.7924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5894    1.7924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8274    2.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5381    2.7288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  6     0  0\n  8  3  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl14\n\n$$$$\nalpha-D-Ribopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.1138    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1138    1.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4145    0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7069    1.3602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4146    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7642    2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7642    1.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4146    1.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0565    1.7344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0565    2.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 10  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  6     0  0\n  8  3  1  6     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl15\n\n$$$$\nalpha-D-Sorbofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.6290    2.6125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1517    2.1450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6232    1.0874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2529    1.0845    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4552    2.8429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2290    2.0282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3092    2.9289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8384    2.3927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0642    1.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8216    1.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0626    2.4037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7789    2.6304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  0     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  1     0  0\n  9  3  1  6     0  0\n  8  2  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl16\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Tagatofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.3790    2.4875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9017    2.0200    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3732    0.9624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0029    0.9595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2052    2.7179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9790    1.9032    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.0592    2.8039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5884    2.2677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8142    1.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5716    1.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8126    2.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5289    2.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  0     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  1     0  0\n  9  3  1  1     0  0\n  8  2  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl17\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Talopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.9910    2.9403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9910    1.4436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2875    0.6952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5799    1.4435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2834    2.9403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1462    2.4562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6372    2.5661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6372    1.8178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2834    1.4435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9337    1.8177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9337    2.5660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5799    2.9402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  1     0  0\n  9  3  1  1     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl18\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Threofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     1  0            999 V2000\n   -2.8117    2.6835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3057    1.1476    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9335    1.1447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1388    2.9039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5229    2.4513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7458    1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5029    1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7410    2.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  8  4  1  0     0  0\n  8  7  1  0     0  0\n  4  5  1  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  1  1  6     0  0\n  6  2  1  1     0  0\n  7  3  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl19\n\n$$$$\nalpha-D-Xylofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.1648    2.8084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6588    1.2726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2948    1.2697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4919    3.0288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2554    2.2147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8760    2.5762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0989    1.8757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8560    1.8757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0983    2.5872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8048    2.8121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  6     0  0\n  8  3  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl20\n\n$$$$\nalpha-D-Xylopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.5429    3.0236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5429    1.5270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8396    0.7785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1360    1.5270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8396    3.0236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1934    2.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1934    1.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8396    1.5270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4899    1.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4899    2.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  5 10  1  0     0  0\n 10  9  1  0     0  0\n  9  8  1  0     0  0\n  8  7  1  0     0  0\n  7  6  1  0     0  0\n  6  5  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  6     0  0\n  8  3  1  1     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl21\n\n$$$$\nCyclopenta-1,3-diene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    9.6696   -5.8045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6696   -4.9328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4243   -4.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1804   -4.9328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1804   -5.8045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  1  5  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl22\n\n>  <atomid>\n2\n\n>  <bondid>\n1\n\n$$$$\n1H-indene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    7.1899   -4.2253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1899   -5.2247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0555   -5.7254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9228   -5.2247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9228   -4.2253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0555   -3.7246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8731   -5.5332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4601   -4.7242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8731   -3.9149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  6  1  0     0  0\n  1  6  2  0     0  0\n  4  7  1  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  5  9  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl23\n\n>  <atomid>\n6\n\n>  <bondid>\n7\n\n$$$$\nNaphtalene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n   11.0090   -4.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1429   -5.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1429   -6.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0090   -6.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8751   -6.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8751   -5.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7410   -4.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7410   -6.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6071   -6.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6071   -5.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  6  2  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  8  1  0     0  0\n  7 10  2  0     0  0\n  8  9  2  0     0  0\n  9 10  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl24\n\n>  <atomid>\n6\n\n>  <bondid>\n10\n\n$$$$\nAzulene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n   12.4941   -7.5235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2759   -5.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4941   -5.2765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5192   -5.4990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0853   -6.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5192   -7.3010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2270   -5.5909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2759   -6.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2270   -7.2090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8147   -6.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  8  2  0     0  0\n  1  6  1  0     0  0\n  2  3  1  0     0  0\n  3  4  2  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  7  2  2  0     0  0\n  7 10  1  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n  2  8  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl25\n\n>  <atomid>\n4\n\n>  <bondid>\n4\n\n$$$$\nE-Stilbene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 15  0     0  0            999 V2000\n   10.8250   -2.9010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8250   -2.9010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3250   -3.7670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8249   -4.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8249   -4.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3250   -3.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3250   -3.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8250   -4.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8250   -4.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3250   -5.4990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3250   -5.4990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8250   -4.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3250   -3.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3250   -3.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  6  2  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n 14  9  1  0     0  0\n 10  9  2  0     0  0\n 10 11  1  0     0  0\n 11 12  2  0     0  0\n 12 13  1  0     0  0\n 13 14  2  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl26\n\n>  <atomid>\n2\n\n>  <bondid>\n3\n\n$$$$\nZ-Stilbene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 15  0     0  0            999 V2000\n   12.3750   -3.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3750   -3.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8750   -4.7581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3749   -5.6240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3749   -5.6240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8750   -4.7580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8750   -3.0260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8750   -3.0260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3750   -3.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8750   -4.7580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3750   -5.6240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3750   -5.6240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8750   -4.7581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3750   -3.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  6  2  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  6  1  0     0  0\n  1  7  1  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  9 14  2  0     0  0\n 10 11  2  0     0  0\n 11 12  1  0     0  0\n 12 13  2  0     0  0\n 13 14  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl27\n\n>  <atomid>\n3\n\n>  <bondid>\n3\n\n$$$$\nAnthracene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 16  0     0  0            999 V2000\n    8.0930   -3.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2269   -3.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2269   -4.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0930   -5.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9591   -4.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9591   -3.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8250   -3.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8250   -5.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6911   -4.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6911   -3.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5571   -3.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5571   -5.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4231   -4.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4231   -3.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  6  2  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  8  1  0     0  0\n  7 10  2  0     0  0\n  8  9  2  0     0  0\n 11 10  1  0     0  0\n  9 10  1  0     0  0\n  9 12  1  0     0  0\n 11 14  2  0     0  0\n 12 13  2  0     0  0\n 13 14  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl28\n\n>  <atomid>\n10\n\n>  <bondid>\n15\n\n$$$$\nPhenantrene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 16  0     0  0            999 V2000\n   10.7760   -1.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9099   -2.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9099   -3.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7760   -3.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6420   -3.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6420   -2.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5080   -1.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5080   -3.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3740   -3.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3740   -2.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5080   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3740   -5.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2401   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2401   -3.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  6  2  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  8  1  0     0  0\n  7 10  2  0     0  0\n  9 10  1  0     0  0\n  8 11  2  0     0  0\n  8  9  1  0     0  0\n  9 14  2  0     0  0\n 11 12  1  0     0  0\n 12 13  2  0     0  0\n 13 14  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl29\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nPyrene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 16 19  0     0  0            999 V2000\n   13.2084   -1.8748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2084   -2.8736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0732   -3.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.9399   -2.8736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.9399   -1.8748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0732   -1.3745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0732   -4.3744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.9399   -4.8747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8066   -4.3744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8066   -3.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3434   -3.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3434   -4.3726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2084   -4.8729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2065   -5.8752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0732   -6.3755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.9399   -5.8752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  6  1  0     0  0\n  3  7  2  0     0  0\n  7  8  1  0     0  0\n  8  9  2  0     0  0\n  9 10  1  0     0  0\n  4 10  2  0     0  0\n  2 11  1  0     0  0\n 11 12  2  0     0  0\n 12 13  1  0     0  0\n  7 13  1  0     0  0\n 13 14  2  0     0  0\n 14 15  1  0     0  0\n 15 16  2  0     0  0\n  8 16  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl30\n\n>  <atomid>\n10\n\n>  <bondid>\n12\n\n$$$$\nTriphenylene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 21  0     0  0            999 V2000\n   10.5140   -3.4503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5140   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3807   -4.9503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2474   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2474   -3.4503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3807   -2.9497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6491   -2.9516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7859   -3.4503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7859   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6491   -4.9467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1141   -2.9497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1141   -1.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2474   -1.4481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3807   -1.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3807   -5.9514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2474   -6.4519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1141   -5.9514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1141   -4.9503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  2  3  1  0     0  0\n  3  4  2  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  6  1  0     0  0\n  1  7  1  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n  2 10  1  0     0  0\n  5 11  1  0     0  0\n 11 12  2  0     0  0\n 12 13  1  0     0  0\n 13 14  2  0     0  0\n  6 14  1  0     0  0\n  3 15  1  0     0  0\n 15 16  2  0     0  0\n 16 17  1  0     0  0\n 17 18  2  0     0  0\n  4 18  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl31\n\n>  <atomid>\n7\n\n>  <bondid>\n8\n\n$$$$\nTriptycene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 20 24  0     0  0            999 V2000\n    9.9580   -4.2298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9460   -4.5458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4637   -3.7684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5123   -3.3051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9580   -2.9407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5123   -2.2079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3265   -3.7665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8129   -4.6117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5262   -5.0982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3987   -5.0982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9317   -4.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3151   -3.7665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4284   -3.6463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6530   -3.9370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1683   -4.6117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0407   -4.9044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5412   -1.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7350   -0.7404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4524   -0.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7528   -1.0796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  1  5  1  0     0  0\n  5  6  2  0     0  0\n  4  6  1  0     0  0\n  4  7  1  0     0  0\n  1  8  1  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n 10 11  1  0     0  0\n 11 12  2  0     0  0\n  7 12  1  0     0  0\n  3 13  1  0     0  0\n 13 14  2  0     0  0\n 14 15  1  0     0  0\n 15 16  2  0     0  0\n  2 16  1  0     0  0\n  5 17  1  0     0  0\n 17 18  2  0     0  0\n 18 19  1  0     0  0\n 19 20  2  0     0  0\n  6 20  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl32\n\n>  <atomid>\n18\n\n>  <bondid>\n21\n\n$$$$\n14-Annulene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 14  0     0  0            999 V2000\n   12.0122   -0.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1483   -1.2548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1861   -2.2524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8762   -2.2524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8762   -1.2548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3221   -2.7512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3221   -3.7488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1861   -4.2476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9139   -4.2476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7779   -3.7488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7779   -2.7512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1861   -5.2452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0500   -5.7440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9139   -5.2452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  5  2  0     0  0\n  2  3  2  0     0  0\n  4  5  1  0     0  0\n  3  6  1  0     0  0\n  6  7  2  0     0  0\n  7  8  1  0     0  0\n  4 11  2  0     0  0\n  9 10  2  0     0  0\n 10 11  1  0     0  0\n 14  9  1  0     0  0\n  8 12  2  0     0  0\n 12 13  1  0     0  0\n 13 14  2  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl33\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\n18-Annulene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n    9.2590    6.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3930    5.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3930    4.7249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1250    5.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9910    6.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8570    4.7249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8570    5.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8570    2.7249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7230    3.2249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7230    4.2249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5270    4.2249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5270    3.2249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3930    2.7249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3930    1.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2590    1.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1250    1.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9910    1.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8570    1.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  1  4  1  0     0  0\n  2  3  1  0     0  0\n  5  4  2  0     0  0\n  5  7  1  0     0  0\n  6  7  2  0     0  0\n  6 10  1  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n  3 11  2  0     0  0\n 11 12  1  0     0  0\n 12 13  2  0     0  0\n 13 14  1  0     0  0\n 14 15  2  0     0  0\n 15 16  1  0     0  0\n 16 17  2  0     0  0\n 18  8  2  0     0  0\n 17 18  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl34\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nPorphyrin\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 24 28  0     0  0            999 V2000\n    6.4862   -8.7407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1697   -9.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0926   -8.9051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9419   -7.9790    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9418   -7.8094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1979   -4.4543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4907   -5.1739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9262   -6.0260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8876   -5.8394    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0931   -4.8745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4706   -6.9575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4476   -5.0593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7641   -4.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8408   -4.8592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0279   -5.8563    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9564   -5.9910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9807   -4.4031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8077   -9.3808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4794   -8.6971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0074   -7.7383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0106   -7.9610    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8407   -8.9255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9886   -9.3966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4636   -6.8782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  2  3  1  0     0  0\n  3  4  2  0     0  0\n  4  5  1  0     0  0\n  1  5  1  0     0  0\n  5 11  2  0     0  0\n  3 23  1  0     0  0\n  6  7  1  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  6 10  2  0     0  0\n 10 17  1  0     0  0\n  8 11  1  0     0  0\n 12 13  2  0     0  0\n 13 14  1  0     0  0\n 14 15  1  0     0  0\n 15 16  2  0     0  0\n 12 16  1  0     0  0\n 16 24  1  0     0  0\n 14 17  2  0     0  0\n 18 19  2  0     0  0\n 19 20  1  0     0  0\n 20 21  1  0     0  0\n 21 22  1  0     0  0\n 18 22  1  0     0  0\n 22 23  2  0     0  0\n 20 24  2  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl35\n\n>  <atomid>\n10\n\n>  <bondid>\n0\n\n$$$$\nPhthalocyanine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 40 48  0     0  0            999 V2000\n   13.9159   -3.5449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8818   -3.2862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.5888   -3.9932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3301   -4.9591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3641   -5.2179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9102   -6.1090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3641   -7.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9102   -7.8910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3641   -8.7821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3301   -9.0409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.5888  -10.0068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8818  -10.7138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9159  -10.4551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6571   -9.4891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7660   -9.0352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9224   -8.0474    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8750   -9.4891    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9840   -9.0352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0929   -9.4891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8341  -10.4551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8682  -10.7138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1612  -10.0068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4199   -9.0409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3859   -8.7821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8398   -7.8910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8276   -8.0474    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3859   -7.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8398   -6.1090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3859   -5.2179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4199   -4.9591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1612   -3.9932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8682   -3.2862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8341   -3.5449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0929   -4.5109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9840   -4.9648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8276   -5.9526    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8750   -4.5109    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7660   -4.9648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9224   -5.9526    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6571   -4.5109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  2  3  1  0     0  0\n  3  4  2  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  2  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n 10 11  1  0     0  0\n 11 12  2  0     0  0\n 12 13  1  0     0  0\n 13 14  2  0     0  0\n  9 14  1  0     0  0\n 14 15  1  0     0  0\n 15 16  1  0     0  0\n  8 16  2  0     0  0\n 15 17  2  0     0  0\n 17 18  1  0     0  0\n 18 19  2  0     0  0\n 19 20  1  0     0  0\n 20 21  2  0     0  0\n 21 22  1  0     0  0\n 22 23  2  0     0  0\n 23 24  1  0     0  0\n 19 24  1  0     0  0\n 24 25  2  0     0  0\n 25 26  1  0     0  0\n 18 26  1  0     0  0\n 25 27  1  0     0  0\n 27 28  2  0     0  0\n 28 29  1  0     0  0\n 29 30  2  0     0  0\n 30 31  1  0     0  0\n 31 32  2  0     0  0\n 32 33  1  0     0  0\n 33 34  2  0     0  0\n 29 34  1  0     0  0\n 34 35  1  0     0  0\n 35 36  2  0     0  0\n 28 36  1  0     0  0\n 35 37  1  0     0  0\n 37 38  2  0     0  0\n 38 39  1  0     0  0\n  6 39  1  0     0  0\n 38 40  1  0     0  0\n  1 40  1  0     0  0\n  5 40  2  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl36\n\n>  <atomid>\n1\n\n>  <bondid>\n1\n\n$$$$\nC60\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 60 90  0     0  0            999 V2000\n   10.6305   -3.5766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4365   -3.9614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8444   -4.3823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4219   -5.1354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5101   -5.4043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5398   -3.0034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6243   -3.2605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6091   -4.4876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2501   -2.8842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0714   -2.0421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6279   -4.0284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2354   -2.3806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7973   -2.0263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4171   -1.3344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9548   -0.9954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1712   -1.3489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7491   -4.8573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3544   -3.6615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8607   -5.0368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0881   -2.6967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1915   -1.7391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6908   -3.7124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.7895   -2.7961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5564   -1.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2017   -6.7691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0400   -6.5817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6031   -6.0138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3296   -5.6469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6757   -4.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1284   -6.8511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5026   -6.1740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.7601   -5.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6003   -5.9775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1810   -6.7670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8290   -5.6093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0080   -7.1540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3450   -7.2046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7432   -6.4127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1088   -6.4611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8830   -6.8658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6700   -4.6243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0651   -5.8201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2290   -6.1582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4556   -3.8184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6990   -2.2230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8777   -3.0652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8635   -4.2395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4704   -2.5910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0974   -1.4308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2911   -1.0460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1183   -1.4334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6963   -2.1861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5507   -3.3420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9700   -2.5526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2594   -1.6179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4391   -3.1629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0504   -5.3159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2122   -5.5032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9459   -4.5380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6724   -4.1718    0.0000 C   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 12  1  0     0  0\n  2  4  1  0     0  0\n  2  6  1  0     0  0\n  3 11  2  0     0  0\n  3 35  1  0     0  0\n  4  5  2  0     0  0\n  4 33  1  0     0  0\n  5  8  1  0     0  0\n  5 38  1  0     0  0\n  6  7  2  0     0  0\n  6 13  1  0     0  0\n  7  8  1  0     0  0\n  7 54  1  0     0  0\n  8 59  2  0     0  0\n  9 10  2  0     0  0\n  9 11  1  0     0  0\n  9 20  1  0     0  0\n 10 12  1  0     0  0\n 10 14  1  0     0  0\n 11 19  1  0     0  0\n 12 13  2  0     0  0\n 13 16  1  0     0  0\n 14 15  2  0     0  0\n 14 21  1  0     0  0\n 15 16  1  0     0  0\n 15 50  1  0     0  0\n 16 55  2  0     0  0\n 17 18  1  0     0  0\n 17 19  2  0     0  0\n 17 28  1  0     0  0\n 18 20  2  0     0  0\n 18 22  1  0     0  0\n 19 27  1  0     0  0\n 20 21  1  0     0  0\n 21 24  2  0     0  0\n 22 23  2  0     0  0\n 22 29  1  0     0  0\n 23 24  1  0     0  0\n 23 46  1  0     0  0\n 24 51  1  0     0  0\n 25 26  1  0     0  0\n 25 27  2  0     0  0\n 25 36  1  0     0  0\n 26 28  2  0     0  0\n 26 30  1  0     0  0\n 27 35  1  0     0  0\n 28 29  1  0     0  0\n 29 32  2  0     0  0\n 30 31  2  0     0  0\n 30 37  1  0     0  0\n 31 32  1  0     0  0\n 31 42  1  0     0  0\n 32 47  1  0     0  0\n 33 34  1  0     0  0\n 33 35  2  0     0  0\n 34 36  2  0     0  0\n 34 38  1  0     0  0\n 36 37  1  0     0  0\n 37 40  2  0     0  0\n 38 39  2  0     0  0\n 39 40  1  0     0  0\n 39 58  1  0     0  0\n 40 43  1  0     0  0\n 41 42  1  0     0  0\n 41 44  2  0     0  0\n 41 47  1  0     0  0\n 42 43  2  0     0  0\n 43 57  1  0     0  0\n 44 48  1  0     0  0\n 44 60  1  0     0  0\n 45 46  1  0     0  0\n 45 48  2  0     0  0\n 45 51  1  0     0  0\n 46 47  2  0     0  0\n 48 52  1  0     0  0\n 49 50  1  0     0  0\n 49 52  2  0     0  0\n 49 55  1  0     0  0\n 50 51  2  0     0  0\n 52 56  1  0     0  0\n 53 54  2  0     0  0\n 53 56  1  0     0  0\n 53 59  1  0     0  0\n 54 55  1  0     0  0\n 56 60  2  0     0  0\n 57 58  2  0     0  0\n 57 60  1  0     0  0\n 58 59  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl37\n\n$$$$\nC80\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 80120  0     0  0            999 V2000\n   11.8140   -5.2993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5730   -4.2259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3980   -3.2721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3673   -3.9462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8724   -5.9964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8224   -5.9256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6539   -5.6501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4150   -4.6554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9660   -2.7352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7771   -1.7740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0084   -2.0576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3368   -0.7391    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7715   -2.6933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5128   -1.9058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3575   -1.6935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1355   -0.7057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8558   -5.1625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6671   -4.0943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4256   -3.8831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1773   -3.0904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0790   -0.0605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2783   -0.3987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7476   -1.3746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7551   -0.1728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3396    0.4001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9755    0.3491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7881    0.5260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0200    0.2821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5229   -1.1994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3638   -0.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1415   -0.0029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7930   -0.0365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6051   -0.9634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0017   -1.9995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6029   -2.1723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2792   -3.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3934   -0.9879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8243   -2.2661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5823   -2.0565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0719   -3.0611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3761   -0.1533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5941   -0.4991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4269   -0.2243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8338   -1.4933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0674   -4.1953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5676   -4.3667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3874   -3.3401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7983   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7257   -4.9518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.1077   -6.1472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8850   -5.8828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4555   -6.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4785   -3.4557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8925   -4.4562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7361   -4.2450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.1144   -5.4440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9102   -6.5496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4615   -6.6760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2725   -6.4989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2295   -6.4327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1717   -6.0891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5034   -4.7749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9729   -5.7514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4956   -5.9777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2845   -3.4130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2423   -4.0913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4737   -4.3745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9139   -5.4101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4340   -0.8503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8516   -2.8767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6760   -1.9226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8824   -2.2021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1818   -1.9562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8621   -2.8099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6814   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4502   -0.7879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6453   -5.1876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6473   -3.9782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2489   -4.1516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9708   -3.1150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  1  5  1  0     0  0\n  1 48  1  0     0  0\n  2  3  1  0     0  0\n  2  4  1  0     0  0\n  3 11  2  0     0  0\n  3 47  1  0     0  0\n  4  8  2  0     0  0\n  4  9  1  0     0  0\n  5  7  2  0     0  0\n  5 59  1  0     0  0\n  6  7  1  0     0  0\n  6 17  2  0     0  0\n  6 60  1  0     0  0\n  7  8  1  0     0  0\n  8 19  1  0     0  0\n  9 10  2  0     0  0\n  9 13  1  0     0  0\n 10 11  1  0     0  0\n 10 12  1  0     0  0\n 11 23  1  0     0  0\n 12 16  2  0     0  0\n 12 21  1  0     0  0\n 13 15  2  0     0  0\n 13 19  1  0     0  0\n 14 15  1  0     0  0\n 14 20  2  0     0  0\n 14 29  1  0     0  0\n 15 16  1  0     0  0\n 16 31  1  0     0  0\n 17 18  1  0     0  0\n 17 77  1  0     0  0\n 18 19  2  0     0  0\n 18 20  1  0     0  0\n 20 80  1  0     0  0\n 21 22  2  0     0  0\n 21 25  1  0     0  0\n 22 23  1  0     0  0\n 22 24  1  0     0  0\n 23 35  2  0     0  0\n 24 28  2  0     0  0\n 24 33  1  0     0  0\n 25 27  1  0     0  0\n 25 31  2  0     0  0\n 26 27  2  0     0  0\n 26 32  1  0     0  0\n 26 41  1  0     0  0\n 27 28  1  0     0  0\n 28 43  1  0     0  0\n 29 30  2  0     0  0\n 29 73  1  0     0  0\n 30 31  1  0     0  0\n 30 32  1  0     0  0\n 32 76  2  0     0  0\n 33 34  2  0     0  0\n 33 37  1  0     0  0\n 34 35  1  0     0  0\n 34 36  1  0     0  0\n 35 47  1  0     0  0\n 36 40  1  0     0  0\n 36 45  2  0     0  0\n 37 39  2  0     0  0\n 37 43  1  0     0  0\n 38 39  1  0     0  0\n 38 44  2  0     0  0\n 38 53  1  0     0  0\n 39 40  1  0     0  0\n 40 55  2  0     0  0\n 41 42  1  0     0  0\n 41 69  2  0     0  0\n 42 43  2  0     0  0\n 42 44  1  0     0  0\n 44 72  1  0     0  0\n 45 46  1  0     0  0\n 45 49  1  0     0  0\n 46 47  2  0     0  0\n 46 48  1  0     0  0\n 48 52  2  0     0  0\n 49 51  2  0     0  0\n 49 55  1  0     0  0\n 50 51  1  0     0  0\n 50 56  1  0     0  0\n 50 57  2  0     0  0\n 51 52  1  0     0  0\n 52 59  1  0     0  0\n 53 54  2  0     0  0\n 53 65  1  0     0  0\n 54 55  1  0     0  0\n 54 56  1  0     0  0\n 56 68  2  0     0  0\n 57 58  1  0     0  0\n 57 61  1  0     0  0\n 58 59  2  0     0  0\n 58 60  1  0     0  0\n 60 64  2  0     0  0\n 61 63  2  0     0  0\n 61 68  1  0     0  0\n 62 63  1  0     0  0\n 62 66  1  0     0  0\n 62 78  2  0     0  0\n 63 64  1  0     0  0\n 64 77  1  0     0  0\n 65 67  2  0     0  0\n 65 72  1  0     0  0\n 66 67  1  0     0  0\n 66 70  2  0     0  0\n 67 68  1  0     0  0\n 69 71  1  0     0  0\n 69 76  1  0     0  0\n 70 71  1  0     0  0\n 70 74  1  0     0  0\n 71 72  2  0     0  0\n 73 75  1  0     0  0\n 73 80  2  0     0  0\n 74 75  2  0     0  0\n 74 78  1  0     0  0\n 75 76  1  0     0  0\n 77 79  2  0     0  0\n 78 79  1  0     0  0\n 79 80  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl38\n\n$$$$\nbeta-D-Allopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.8119    2.6861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.8119    1.2770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1792    0.5702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5466    1.2769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1834    2.6861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1462    2.2395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4956    2.3411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4956    1.6261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1834    1.2769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8670    1.6260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8670    2.3410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5466    2.6860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  1     0  0\n  8  2  1  6     0  0\n  9  3  1  6     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl39\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Altropyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -0.9910    2.2903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.9910    0.7936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2875    0.0452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5799    0.7935    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2834    2.2903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1462    1.8062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.6372    1.9161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.6372    1.1678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2834    0.7935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9337    1.1677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9337    1.9160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5799    2.2902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  1     0  0\n  8  2  1  1     0  0\n  9  3  1  6     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl40\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Arabinofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -1.4482    2.3917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9421    0.8559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5781    0.8530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7753    2.6122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5387    1.7980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1593    2.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3822    1.4591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1394    1.4591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3816    2.1706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0881    2.3955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  1     0  0\n  7  2  1  1     0  0\n  8  3  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl41\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Arabinopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   15.5611   -5.2999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.5611   -7.3001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8228   -8.3002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0958   -7.3001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8228   -5.2999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6920   -5.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6920   -6.7999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8228   -7.3001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9648   -6.7999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9648   -5.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  5 10  1  0     0  0\n 10  9  1  0     0  0\n  9  8  1  0     0  0\n  8  7  1  0     0  0\n  7  6  1  0     0  0\n  6  5  1  0     0  0\n  6  1  1  1     0  0\n  7  2  1  1     0  0\n  8  3  1  6     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl42\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Erythrofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     1  0            999 V2000\n   -2.3742    2.6418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8682    1.1059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4960    1.1030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7013    2.8623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0854    2.4096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3125    1.7091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0613    1.7091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3035    2.4207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  8  4  1  0     0  0\n  8  7  1  0     0  0\n  4  5  1  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  1  1  1     0  0\n  6  2  1  6     0  0\n  7  3  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl43\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Fructofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.6256    2.7205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1524    2.2530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6198    1.1954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2536    1.1925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4559    2.9509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2256    2.1362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3100    3.0369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8350    2.5007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0608    1.8040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8182    1.8040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0592    2.5117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7755    2.7384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  0     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  6     0  0\n  9  3  1  1     0  0\n  8  2  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl44\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Galactopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.5577    2.5236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.5577    1.0270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8542    0.2785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1466    1.0269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8543    2.5236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7171    2.0395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2039    2.1495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2039    1.4011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8543    1.0269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5004    1.4010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5004    2.1494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1466    2.5235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  1     0  0\n  8  2  1  6     0  0\n  9  3  1  1     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl45\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Glucopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -2.1744    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1744    1.3186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4708    0.5702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7632    1.3185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4709    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3337    2.3312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8206    2.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8206    1.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4709    1.3185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1170    1.6927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1170    2.4410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7632    2.8152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  1     0  0\n  8  2  1  6     0  0\n  9  3  1  1     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl46\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Gulopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -2.1119    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1119    1.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4083    0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7007    1.3602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4084    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2712    2.3728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7581    2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7581    1.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4084    1.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0545    1.7344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0545    2.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7007    2.8569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  1     0  0\n  8  2  1  6     0  0\n  9  3  1  6     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl47\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Idopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.9244    2.7736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9244    1.2770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2208    0.5285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5132    1.2769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2209    2.7736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0837    2.2895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5706    2.3995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5706    1.6511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2209    1.2769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8670    1.6510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8670    2.3994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5132    2.7735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  1     0  0\n  8  2  1  1     0  0\n  9  3  1  6     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl48\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Lyxofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.1148    2.9334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6088    1.3976    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2406    1.3947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4419    3.1538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2054    2.3397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8260    2.7012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0531    2.0007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8102    2.0007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0483    2.7122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7589    2.9371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  1     0  0\n  7  2  1  1     0  0\n  8  3  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl49\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Lyxopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.4513    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4513    1.3186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7520    0.5702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0444    1.3185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7521    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1017    2.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1017    1.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7521    1.3185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3940    1.6927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3940    2.4410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 10  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  6  1  1  1     0  0\n  7  2  1  1     0  0\n  8  3  1  1     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl50\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Mannopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -2.1577    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1577    1.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4542    0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7466    1.3602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4543    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3171    2.3728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8039    2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8039    1.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4543    1.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1004    1.7344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1004    2.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7466    2.8569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  1     0  0\n  8  2  1  1     0  0\n  9  3  1  1     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl51\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Psicofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   14.8241   -7.1535    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1260   -7.7777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4964   -9.1900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3201   -9.1940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3854   -6.8457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0166   -7.9337    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9157   -6.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2090   -7.4469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9075   -8.3829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8961   -8.3829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5799   -7.4322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6232   -7.1295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  6     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  6     0  0\n  9  3  1  6     0  0\n  8  2  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl52\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Ribofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -1.8940    2.7251    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3879    1.1893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0198    1.1863    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2211    2.9455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9845    2.1313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6051    2.4928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8322    1.7924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5894    1.7924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8274    2.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5381    2.7288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  1     0  0\n  7  2  1  6     0  0\n  8  3  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl53\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Ribopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.1138    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1138    1.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4145    0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7069    1.3602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4146    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7642    2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7642    1.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4146    1.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0565    1.7344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0565    2.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 10  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  6  1  1  1     0  0\n  7  2  1  6     0  0\n  8  3  1  6     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl54\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Sorbofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.6290    2.6125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1517    2.1450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6232    1.0874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2529    1.0845    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4552    2.8429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2290    2.0282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3092    2.9289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8384    2.3927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0642    1.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8216    1.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0626    2.4037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7789    2.6304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  0     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  1     0  0\n  9  3  1  6     0  0\n  8  2  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl55\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Tagatofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.3790    2.4875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9017    2.0200    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3732    0.9624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0029    0.9595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2052    2.7179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9790    1.9032    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.0592    2.8039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5884    2.2677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8142    1.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5716    1.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8126    2.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5289    2.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  0     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  1     0  0\n  9  3  1  1     0  0\n  8  2  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl56\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Talopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.9910    2.9403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9910    1.4436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2875    0.6952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5799    1.4435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2834    2.9403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1462    2.4562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6372    2.5661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6372    1.8178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2834    1.4435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9337    1.8177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9337    2.5660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5799    2.9402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  1     0  0\n  8  2  1  1     0  0\n  9  3  1  1     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl57\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Threofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     1  0            999 V2000\n   -2.8117    2.6835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3057    1.1476    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9335    1.1447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1388    2.9039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5229    2.4513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7458    1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5029    1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7410    2.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  8  4  1  0     0  0\n  8  7  1  0     0  0\n  4  5  1  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  1  1  1     0  0\n  6  2  1  1     0  0\n  7  3  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl58\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Xylofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.1648    2.8084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6588    1.2726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2948    1.2697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4919    3.0288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2554    2.2147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8760    2.5762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0989    1.8757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8560    1.8757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0983    2.5872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8048    2.8121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  1     0  0\n  7  2  1  6     0  0\n  8  3  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl59\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Xylopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.5429    3.0236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5429    1.5270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8396    0.7785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1360    1.5270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8396    3.0236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1934    2.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1934    1.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8396    1.5270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4899    1.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4899    2.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  5 10  1  0     0  0\n 10  9  1  0     0  0\n  9  8  1  0     0  0\n  8  7  1  0     0  0\n  7  6  1  0     0  0\n  6  5  1  0     0  0\n  6  1  1  1     0  0\n  7  2  1  6     0  0\n  8  3  1  1     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl60\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nBicyclo[1-1-1]pentane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  6  0     0  0            999 V2000\n    9.8610   -7.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4888   -6.4956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5708   -7.8431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8036   -8.0042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9790   -7.8371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  4  5  1  0     0  0\n  1  5  1  0     0  0\n  4  3  1  0     0  0\n  2  4  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl61\n\n>  <atomid>\n2\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[2-1-1]hexane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  7  0     0  0            999 V2000\n    9.7097   -6.3707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3181   -5.6035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4180   -6.7620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6494   -7.1903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7820   -7.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4069   -7.5965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  3  6  1  0     0  0\n  4  5  1  0     0  0\n  4  6  1  0     0  0\n  1  5  1  0     0  0\n  2  4  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl62\n\n>  <atomid>\n5\n\n>  <bondid>\n2\n\n$$$$\nBicyclo[2-2-1]heptane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  8  0     0  0            999 V2000\n    8.4502   -7.5691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8558   -6.8358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5667   -6.3361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3112   -7.1358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3890   -5.4309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4498   -6.8526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1221   -7.5469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  1  4  1  0     0  0\n  4  5  1  0     0  0\n  5  3  1  0     0  0\n  3  6  1  0     0  0\n  6  7  1  0     0  0\n  7  4  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl63\n\n>  <atomid>\n6\n\n>  <bondid>\n6\n\n$$$$\nBicyclo[3-1-1]heptane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  8  0     0  0            999 V2000\n    8.2782   -1.8550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5291   -2.7952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9238   -2.2925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7847   -2.2925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6209   -1.3393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3670   -1.8368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6898   -3.1107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  4  5  1  0     0  0\n  5  1  1  0     0  0\n  1  6  1  0     0  0\n  6  2  1  0     0  0\n  1  7  1  0     0  0\n  7  4  1  0     0  0\n  4  3  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl64\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nBicyclo[2-2-2]octane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  9  0     0  0            999 V2000\n   10.8583   -6.6275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9678   -6.2148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6767   -5.7197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9692   -6.6418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1340   -4.9791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7980   -5.3243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8417   -5.7430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8429   -4.2582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  6  1  0     0  0\n  4  7  1  0     0  0\n  5  8  1  0     0  0\n  6  7  1  0     0  0\n  6  8  1  0     0  0\n  5  2  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl65\n\n>  <atomid>\n1\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[3-2-1]octane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  9  0     0  0            999 V2000\n    9.0974   -5.5533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4087   -6.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7744   -6.0120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5802   -6.0120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4086   -5.0127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2389   -5.5343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9413   -6.8873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7036   -6.4241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  4  5  1  0     0  0\n  5  1  1  0     0  0\n  1  6  1  0     0  0\n  6  2  1  0     0  0\n  4  7  1  0     0  0\n  1  8  1  0     0  0\n  7  8  1  0     0  0\n  4  3  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl66\n\n>  <atomid>\n1\n\n>  <bondid>\n7\n\n$$$$\nBicyclo[4-1-1]octane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  9  0     0  0            999 V2000\n    9.6925   -6.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0458   -6.6931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3397   -7.0141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2905   -6.8428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9462   -6.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7017   -6.0039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0038   -6.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8230   -5.2859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  1  1  0     0  0\n  7  2  1  0     0  0\n  8  1  1  0     0  0\n  1  7  1  0     0  0\n  8  2  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl67\n\n>  <atomid>\n6\n\n>  <bondid>\n2\n\n$$$$\nBicyclo[4-1-1]octane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  9  0     0  0            999 V2000\n   10.2044   -7.1593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5546   -7.6794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4884   -7.4862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8148   -7.8278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4736   -7.3223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2224   -6.9962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3764   -8.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3337   -6.2846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  1  1  0     0  0\n  7  2  1  0     0  0\n  8  1  1  0     0  0\n  1  7  1  0     0  0\n  8  2  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl68\n\n>  <atomid>\n6\n\n>  <bondid>\n2\n\n$$$$\nBicyclo[3-2-2]nonane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    8.9873   -5.7688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9396   -4.7775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9753   -6.2042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0774   -6.2609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5071   -5.5836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2317   -7.2365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8683   -7.2725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5608   -6.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5275   -6.7292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  1  4  1  0     0  0\n  2  5  1  0     0  0\n  3  6  1  0     0  0\n  4  7  1  0     0  0\n  5  8  1  0     0  0\n  6  9  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl69\n\n>  <atomid>\n5\n\n>  <bondid>\n5\n\n$$$$\nBicyclo[3-3-1]nonane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    8.9718   -5.4180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8721   -5.4189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4727   -5.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5289   -7.0388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5522   -7.2536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0453   -6.5586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7203   -6.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3240   -5.8707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6297   -4.8964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  1  6  1  0     0  0\n  7  8  1  0     0  0\n  8  3  1  0     0  0\n  3  9  1  0     0  0\n  9  1  1  0     0  0\n  1  2  1  0     0  0\n  2  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl70\n\n>  <atomid>\n4\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-2-1]nonane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    9.1712   -6.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1464   -6.2056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8839   -5.6171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6571   -5.2966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6761   -5.5501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9410   -6.1453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9661   -6.6742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7138   -6.0100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9410   -4.5758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  6  9  1  0     0  0\n  9  5  1  0     0  0\n  8  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl71\n\n>  <atomid>\n6\n\n>  <bondid>\n9\n\n$$$$\nBicyclo[4-2-1]nonane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    9.8115   -5.9359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9067   -6.2317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8460   -5.6949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6107   -5.3780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6184   -5.6284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8802   -6.2172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7040   -6.8849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6444   -6.0834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8802   -4.6651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  6  9  1  0     0  0\n  9  5  1  0     0  0\n  8  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl72\n\n>  <atomid>\n6\n\n>  <bondid>\n9\n\n$$$$\nBicyclo[4-2-1]nonane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    7.9553   -6.4806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1245   -6.2042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8626   -5.6172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8073   -5.9269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6505   -5.5501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9147   -6.1439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9374   -6.6716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6857   -6.0091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8236   -4.5784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  9  5  1  0     0  0\n  8  7  1  0     0  0\n  9  6  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl73\n\n>  <atomid>\n6\n\n>  <bondid>\n8\n\n$$$$\nBicyclo[5-1-1]nonane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    7.7834   -6.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6536   -6.5515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4441   -5.9761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1897   -5.5634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3360   -5.6252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0166   -6.1147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7177   -6.6607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6682   -6.8540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6683   -5.1050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  3  1  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  2  1  0     0  0\n  3  9  1  0     0  0\n  2  9  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl74\n\n>  <atomid>\n5\n\n>  <bondid>\n4\n\n$$$$\nBicyclo[3-3-2]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    9.6949   -6.5741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6532   -5.5821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6838   -7.0051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8949   -7.0566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2198   -6.3853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9375   -8.0267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5821   -8.0679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2787   -7.5720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2352   -7.5305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0125   -6.9260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  1  4  1  0     0  0\n  2  5  1  0     0  0\n  3  6  1  0     0  0\n  5  8  1  0     0  0\n  6  9  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  4 10  1  0     0  0\n 10  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl75\n\n>  <atomid>\n5\n\n>  <bondid>\n4\n\n$$$$\nBicyclo[4-2-2]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    8.8472   -8.1683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7259   -7.8853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4386   -7.2412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2848   -6.8907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3998   -7.1679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6896   -7.8192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8114   -8.3980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5351   -7.6712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5895   -6.1020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8736   -6.6884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  9  5  1  0     0  0\n  8  7  1  0     0  0\n 10  6  1  0     0  0\n  9 10  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl76\n\n>  <atomid>\n6\n\n>  <bondid>\n8\n\n$$$$\nBicyclo[4-2-2]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    8.7142   -6.3595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8068   -6.0576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5207   -5.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5526   -5.7547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4737   -5.3433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7622   -5.9919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8793   -6.5683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6043   -5.8445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6627   -4.2817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9456   -4.8658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  9  5  1  0     0  0\n  8  7  1  0     0  0\n 10  6  1  0     0  0\n  9 10  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl77\n\n>  <atomid>\n6\n\n>  <bondid>\n8\n\n$$$$\nBicyclo[4-2-2]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    8.8948   -6.4814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1410   -7.3322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0133   -6.5553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6416   -5.8316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5699   -5.6380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8608   -6.2916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9867   -6.8724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7095   -6.1431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7603   -4.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0456   -5.1566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  9  5  1  0     0  0\n  8  7  1  0     0  0\n 10  6  1  0     0  0\n  9 10  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl78\n\n>  <atomid>\n6\n\n>  <bondid>\n8\n\n$$$$\nBicyclo[4-3-1]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    9.3349   -6.7026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2468   -6.4279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9681   -5.8030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7891   -5.4627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8711   -5.7318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1522   -6.3637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1339   -6.4496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6912   -5.5405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0551   -4.6974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6319   -5.8781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  9  5  1  0     0  0\n  9  6  1  0     0  0\n 10  8  1  0     0  0\n 10  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl79\n\n>  <atomid>\n9\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-3-1]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    8.8223   -6.3064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1166   -6.7735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8745   -6.1531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5558   -5.6824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5492   -5.6698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8328   -6.3073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6175   -6.7466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4940   -5.9863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7350   -4.6265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3255   -5.8175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  9  5  1  0     0  0\n  9  6  1  0     0  0\n 10  8  1  0     0  0\n 10  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl80\n\n>  <atomid>\n9\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-3-1]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    9.4787   -5.2376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3279   -5.2384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0029   -5.6980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0617   -6.9339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0396   -7.1585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5557   -6.4312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1589   -6.2125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8008   -5.7113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1673   -4.6915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6327   -5.7965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  1  6  1  0     0  0\n  7  8  1  0     0  0\n  8  3  1  0     0  0\n  3  9  1  0     0  0\n  9  1  1  0     0  0\n  1  2  1  0     0  0\n 10  2  1  0     0  0\n 10  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl81\n\n>  <atomid>\n4\n\n>  <bondid>\n10\n\n$$$$\nBicyclo[4-3-1]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    8.5704   -6.7776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0229   -7.5710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0468   -6.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2626   -6.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4354   -7.2985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7455   -6.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6855   -7.0209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7071   -7.2278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1753   -5.8290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0646   -7.3398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  1  0     0  0\n  8  3  1  0     0  0\n  3  9  1  0     0  0\n  9  1  1  0     0  0\n  1  2  1  0     0  0\n 10  2  1  0     0  0\n 10  7  1  0     0  0\n  1  6  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl82\n\n>  <atomid>\n4\n\n>  <bondid>\n9\n\n$$$$\nBicyclo[5-2-1]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    8.3634   -6.6141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5495   -7.2830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5102   -6.9328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2905   -6.3299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0719   -5.8974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2732   -5.9622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.9866   -6.4753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6733   -7.0474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5735   -7.2501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5254   -5.4170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  4  1  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9  3  1  0     0  0\n  4 10  1  0     0  0\n  3 10  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl83\n\n>  <atomid>\n6\n\n>  <bondid>\n0\n\n$$$$\nBicyclo[3-3-3]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    9.9074   -6.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8681   -5.3101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8403   -6.7380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1527   -6.7867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4592   -6.1534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0797   -7.7018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8576   -7.7405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5146   -7.2729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4171   -7.2337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3203   -6.6634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7496   -5.1095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  1  4  1  0     0  0\n  3  6  1  0     0  0\n  5  8  1  0     0  0\n  6  9  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  4 10  1  0     0  0\n 10  7  1  0     0  0\n 11  5  1  0     0  0\n 11  2  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl84\n\n>  <atomid>\n5\n\n>  <bondid>\n3\n\n$$$$\nBicyclo[4-3-2]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    7.6205   -6.7375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4403   -6.4395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1378   -5.7617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0284   -5.3926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2020   -5.6845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5071   -6.3700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5718   -6.4630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0916   -5.4770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2122   -4.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1122   -5.8433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5429   -5.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  9  5  1  0     0  0\n 10  8  1  0     0  0\n 10  7  1  0     0  0\n 11  6  1  0     0  0\n 11  9  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl85\n\n>  <atomid>\n9\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-3-2]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    7.3641   -7.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6057   -7.8800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3457   -7.2133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0778   -6.7076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1454   -6.6940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4502   -7.3791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2932   -7.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1606   -7.0339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1660   -5.5200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0543   -6.8526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5281   -6.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  9  5  1  0     0  0\n 10  8  1  0     0  0\n 10  7  1  0     0  0\n 11  6  1  0     0  0\n 11  9  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl86\n\n>  <atomid>\n9\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-3-2]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    9.7033   -5.4113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5086   -5.4122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2474   -5.8892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3085   -7.1720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2474   -7.4055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7831   -6.6503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3333   -6.4233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9996   -5.9031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4180   -4.8445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7872   -5.9914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9628   -5.2289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  1  6  1  0     0  0\n  7  8  1  0     0  0\n  8  3  1  0     0  0\n  9  1  1  0     0  0\n  1  2  1  0     0  0\n 10  2  1  0     0  0\n 10  7  1  0     0  0\n 11  3  1  0     0  0\n 11  9  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl87\n\n>  <atomid>\n4\n\n>  <bondid>\n9\n\n$$$$\nBicyclo[4-3-2]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    9.5890   -6.0668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0222   -6.8881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0821   -5.5563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3408   -5.5563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5198   -6.6060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8056   -6.0463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6729   -6.3187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7305   -6.5329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4155   -4.9619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0302   -6.6489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7926   -5.3863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  1  0     0  0\n  8  3  1  0     0  0\n  3  9  1  0     0  0\n  1  2  1  0     0  0\n 10  2  1  0     0  0\n 10  7  1  0     0  0\n 11  1  1  0     0  0\n 11  9  1  0     0  0\n  1  6  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl88\n\n>  <atomid>\n4\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-4-1]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    7.3728   -6.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5265   -6.7662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7360   -7.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7807   -7.5455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6269   -7.2115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4231   -6.6523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6410   -5.5045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3196   -6.5383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5235   -7.0976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6773   -7.4316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2693   -6.3129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  9  1  0     0  0\n  8 11  1  0     0  0\n 10  9  1  0     0  0\n  5 10  1  0     0  0\n 11  6  1  0     0  0\n  7  5  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl89\n\n>  <atomid>\n1\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-4-1]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    7.9403   -6.9988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8374   -6.7539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0510   -7.3243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1162   -7.5484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9789   -7.2079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7711   -6.6377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9934   -5.5016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5477   -6.6231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9126   -7.0916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0498   -7.4322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8001   -6.9010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  9  1  0     0  0\n  8 11  1  0     0  0\n 10  9  1  0     0  0\n  5 10  1  0     0  0\n 11  6  1  0     0  0\n  7  5  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl90\n\n>  <atomid>\n1\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-4-1]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    8.3680   -5.6420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7511   -6.3356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9725   -6.9747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5503   -6.2118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4446   -5.8588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2291   -5.2677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4595   -4.1253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0708   -5.2525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4489   -5.7383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5546   -6.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2957   -5.5407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  9  1  0     0  0\n  8 11  1  0     0  0\n 10  9  1  0     0  0\n  5 10  1  0     0  0\n 11  6  1  0     0  0\n  7  5  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl91\n\n>  <atomid>\n1\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[5-3-1]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    7.4699   -5.4930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9044   -6.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8921   -6.6506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7678   -6.3049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5569   -5.7261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3072   -5.3108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4607   -5.3728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1456   -5.8656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8448   -6.4150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7887   -6.6095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7825   -4.8494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  5  1  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10  4  1  0     0  0\n  5 11  1  0     0  0\n  4 11  1  0     0  0\n  2  1  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl92\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nBicyclo[4-4-2]dodecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 13  0     0  0            999 V2000\n    7.9693   -5.3924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0472   -5.7621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2754   -6.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4140   -6.6115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3360   -6.2475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1138   -5.6380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1109   -4.4385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1806   -5.5138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4028   -6.1232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4808   -6.4871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0361   -5.2682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3405   -4.9653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  9  1  0     0  0\n  8 11  1  0     0  0\n 10  9  1  0     0  0\n  5 10  1  0     0  0\n 11  6  1  0     0  0\n 12  5  1  0     0  0\n 12  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl93\n\n>  <atomid>\n1\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-4-2]dodecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 13  0     0  0            999 V2000\n    6.8935   -6.1590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6766   -5.8888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9121   -6.5182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0877   -6.7655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0396   -6.3898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8103   -5.7606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8078   -4.6345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7709   -5.7444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1734   -6.2617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2215   -6.6373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9457   -6.0513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0429   -5.3648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  9  1  0     0  0\n  8 11  1  0     0  0\n 10  9  1  0     0  0\n  5 10  1  0     0  0\n 11  6  1  0     0  0\n 12  5  1  0     0  0\n 12  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl94\n\n>  <atomid>\n1\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-4-2]dodecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 13  0     0  0            999 V2000\n    6.5042   -6.4951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8305   -7.2527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0721   -7.9506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7035   -7.1174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6802   -6.7317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4449   -6.0862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4449   -4.8994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4564   -6.0697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8695   -6.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8927   -6.9858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6100   -6.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6889   -5.6246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  9  1  0     0  0\n  8 11  1  0     0  0\n 10  9  1  0     0  0\n  5 10  1  0     0  0\n 11  6  1  0     0  0\n 12  5  1  0     0  0\n 12  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl95\n\n>  <atomid>\n1\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[5-3-2]dodecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 13  0     0  0            999 V2000\n    7.9640   -5.7259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3691   -6.3791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4082   -6.9439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3295   -6.5803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0216   -5.8860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8969   -5.5343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1103   -5.5997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8309   -6.1180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5145   -6.6960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4035   -6.9006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0255   -4.8061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3287   -5.4888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  5  1  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10  4  1  0     0  0\n  2  1  1  0     0  0\n 11  5  1  0     0  0\n 12  4  1  0     0  0\n 11 12  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl96\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nBicyclo[5-4-1]dodecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 13  0     0  0            999 V2000\n    7.7173   -5.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8210   -5.4961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0428   -6.0887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1495   -6.3216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0457   -5.9679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8297   -5.3755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5976   -4.9504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7781   -5.0140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4790   -5.5181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1712   -6.0804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0905   -6.2796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0605   -4.4784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11  5  1  0     0  0\n  6 12  1  0     0  0\n  5 12  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl97\n\n>  <atomid>\n8\n\n>  <bondid>\n7\n\n$$$$\nBicyclo[5-3-3]tridecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 13 14  0     0  0            999 V2000\n    8.4981   -5.1011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2280   -4.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0887   -4.6187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2012   -4.3405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4418   -5.7633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8730   -6.4031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7468   -5.6806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9461   -5.7884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4646   -4.7690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5590   -4.7986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1539   -5.4010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8112   -6.0270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5669   -6.2486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0     0  0\n  4  3  1  0     0  0\n  2  4  1  0     0  0\n  5  6  1  0     0  0\n  7  1  1  0     0  0\n  8  7  1  0     0  0\n  8  6  1  0     0  0\n  1  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  0     0  0\n 12 13  1  0     0  0\n 13  5  1  0     0  0\n  3  5  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl98\n\n>  <atomid>\n10\n\n>  <bondid>\n9\n\n$$$$\nBicyclo[5-4-2]tridecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 13 14  0     0  0            999 V2000\n    7.4687   -5.4926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5107   -5.8766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7478   -6.5099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9306   -6.7589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8885   -6.3808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6576   -5.7476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4784   -5.2933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7402   -5.3611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4893   -5.9002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1604   -6.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0052   -6.7140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6549   -4.7411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8882   -5.3775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11  5  1  0     0  0\n 12  6  1  0     0  0\n 13  5  1  0     0  0\n 13 12  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl99\n\n>  <atomid>\n8\n\n>  <bondid>\n7\n\n$$$$\nBicyclo[5-5-1]tridecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 13 14  0     0  0            999 V2000\n    7.5850   -5.9774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5169   -6.0690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6632   -7.0919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8369   -7.2880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7693   -6.8637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5517   -6.2665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3258   -5.8379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5160   -5.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2226   -6.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9123   -6.9772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8227   -7.1780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7845   -5.3620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0774   -6.6776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11  5  1  0     0  0\n  6 12  1  0     0  0\n  5 12  1  0     0  0\n 13  3  1  0     0  0\n 13  2  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <prerender>\nlibrary.svg#tmpl100\n\n>  <atomid>\n8\n\n>  <bondid>\n6\n\n$$$$\nAdamantane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 12  0     0  0            999 V2000\n    7.5634   -6.5061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4530   -6.0540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4530   -5.1499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9968   -4.1939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1070   -4.6459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1070   -5.5501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9968   -6.0022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8866   -5.5501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3428   -6.5061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8866   -4.6459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  4 10  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  2  9  1  0     0  0\n  1  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  5  6  1  0     0  0\n  8 10  1  0     0  0\n  2  3  1  0     0  0\nM  END\n>  <group>\nBridged Polycyclics\n\n>  <prerender>\nlibrary.svg#tmpl101\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nCubane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8 12  0     0  0            999 V2000\n    7.9520   -5.0848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6899   -4.7860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6650   -6.0748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9597   -6.7640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9872   -5.4743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2488   -5.7725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4012   -5.7782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6964   -6.4666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0     0  0\n  3  1  1  0     0  0\n  1  6  1  0     0  0\n  2  5  1  0     0  0\n  7  2  1  0     0  0\n  3  4  1  0     0  0\n  7  3  1  0     0  0\n  4  6  1  0     0  0\n  8  4  1  0     0  0\n  5  6  1  0     0  0\n  8  5  1  0     0  0\n  8  7  1  0     0  0\nM  END\n>  <group>\nBridged Polycyclics\n\n>  <prerender>\nlibrary.svg#tmpl102\n\n>  <atomid>\n7\n\n>  <bondid>\n11\n\n$$$$\nPrismane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  9  0     0  0            999 V2000\n    7.7612   -4.0397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0907   -4.0333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1698   -4.4963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1678   -5.5167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0887   -5.0413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7593   -5.0602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0     0  0\n  3  1  1  0     0  0\n  3  2  1  0     0  0\n  4  5  1  0     0  0\n  4  6  1  0     0  0\n  5  6  1  0     0  0\n  1  6  1  0     0  0\n  3  4  1  0     0  0\n  2  5  1  0     0  0\nM  END\n>  <group>\nBridged Polycyclics\n\n>  <prerender>\nlibrary.svg#tmpl103\n\n>  <atomid>\n3\n\n>  <bondid>\n7\n\n$$$$\nTwistane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 12  0     0  0            999 V2000\n   10.9227   -5.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6642   -4.6208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5688   -5.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8274   -4.6208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7871   -7.2292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5284   -6.4333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6238   -7.2292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8825   -6.4333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7835   -5.8799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6165   -5.9203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0     0  0\n  2  4  1  0     0  0\n  3  4  1  0     0  0\n  5  6  1  0     0  0\n  7  5  1  0     0  0\n  8  7  1  0     0  0\n  9  3  1  0     0  0\n  9  6  1  0     0  0\n 10  1  1  0     0  0\n 10  8  1  0     0  0\n  1  6  1  0     0  0\n  3  8  1  0     0  0\nM  END\n>  <group>\nBridged Polycyclics\n\n>  <prerender>\nlibrary.svg#tmpl104\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\n12-Crown-4\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     0  0            999 V2000\n    9.6950   -4.9978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6961   -3.9955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7230   -3.7807    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4895   -2.8165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4888   -2.8252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2724   -3.7946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3039   -4.0292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3039   -5.0370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2718   -5.2624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4935   -6.2335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4934   -6.2191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7126   -5.2320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  0     0  0\n 12  1  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n>  <prerender>\nlibrary.svg#tmpl105\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\n13-Crown-4\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 13 13  0     0  0            999 V2000\n    6.2108   -5.8522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2098   -4.8784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1789   -6.0710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1735   -4.6689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3479   -7.0179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3527   -3.7257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3428   -7.0999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3459   -3.6501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7617   -6.1569    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7571   -4.5979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7493   -6.2607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7528   -4.4917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2902   -5.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  6  1  0     0  0\n  5  7  1  0     0  0\n  6  8  1  0     0  0\n  7  9  1  0     0  0\n  8 10  1  0     0  0\n  9 11  1  0     0  0\n 10 12  1  0     0  0\n 11 13  1  0     0  0\n 12 13  1  0     0  0\n  1  2  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n>  <prerender>\nlibrary.svg#tmpl106\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\n14-Crown-4\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 14  0     0  0            999 V2000\n   11.4453   -5.1251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9013   -4.2723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9150   -5.9676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9132   -4.4080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9274   -5.8351    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5059   -3.4886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5286   -6.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4978   -3.4979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5308   -6.7614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1114   -4.4181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1336   -5.8403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1388   -4.2937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1473   -5.9857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6047   -5.1430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  6  1  0     0  0\n  5  7  1  0     0  0\n  6  8  1  0     0  0\n  7  9  1  0     0  0\n  8 10  1  0     0  0\n  9 11  1  0     0  0\n 10 12  1  0     0  0\n 11 13  1  0     0  0\n 12 14  1  0     0  0\n 13 14  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n>  <prerender>\nlibrary.svg#tmpl107\n\n$$$$\n15-Crown-5\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 15 15  0     0  0            999 V2000\n    9.3051   -3.6194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1168   -4.1865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4997   -4.1934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8472   -5.1345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6861   -3.6269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6483   -5.7210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8859   -4.1972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3419   -6.6998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1594   -5.1457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3292   -6.7279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3517   -5.7489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0217   -7.6806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6728   -6.7074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0073   -7.6806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6647   -6.7239    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  6  1  0     0  0\n  5  7  1  0     0  0\n  6  8  1  0     0  0\n  7  9  1  0     0  0\n  8 10  1  0     0  0\n  9 11  1  0     0  0\n 10 12  1  0     0  0\n 11 13  1  0     0  0\n 12 14  1  0     0  0\n 13 15  1  0     0  0\n 14 15  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n>  <prerender>\nlibrary.svg#tmpl108\n\n$$$$\n16-Crown-5\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 16 16  0     0  0            999 V2000\n   10.1579   -7.9802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3604   -8.5644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8558   -7.0304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5517   -7.9928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6502   -6.4638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7522   -8.5665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4079   -5.4912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9519   -7.9997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3921   -5.2815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2224   -7.0336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3715   -4.2847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3998   -6.4989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4688   -3.7835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5949   -5.5179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5786   -4.2984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5857   -5.2815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  6  1  0     0  0\n  5  7  1  0     0  0\n  6  8  1  0     0  0\n  7  9  1  0     0  0\n  8 10  1  0     0  0\n  9 11  1  0     0  0\n 10 12  1  0     0  0\n 11 13  1  0     0  0\n 12 14  1  0     0  0\n 13 15  1  0     0  0\n 14 16  1  0     0  0\n 15 16  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n>  <prerender>\nlibrary.svg#tmpl109\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\n17-Crown-5\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     0  0            999 V2000\n   11.0779   -6.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1260   -6.4972    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2569   -7.9159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4815   -7.2799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7011   -7.8978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8165   -7.4802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8151   -6.4943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8549   -6.2786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6443   -5.3223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4333   -4.6975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3911   -5.0835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9204   -4.2341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9543   -4.2341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4969   -5.0788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4504   -4.6735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2557   -5.2828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1487   -7.4881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  6  7  1  0     0  0\n 11 12  1  0     0  0\n 12 13  1  0     0  0\n 13 14  1  0     0  0\n 10 11  1  0     0  0\n 15 16  1  0     0  0\n 14 15  1  0     0  0\n 16  1  1  0     0  0\n  2 17  1  0     0  0\n 17  3  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n>  <prerender>\nlibrary.svg#tmpl110\n\n$$$$\n18-Crown-6\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n   12.0989   -6.5157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0984   -7.5223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1742   -7.8983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2561   -8.8885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3671   -9.3684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5542   -8.7612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7470   -9.3729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8655   -8.8820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9673   -7.9010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0511   -7.5248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0591   -6.5276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9807   -6.1495    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8891   -5.1717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7538   -4.6802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5585   -5.2838    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3625   -4.6771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2539   -5.1612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1740   -6.1413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  3  4  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n  7  8  1  0     0  0\n 12 13  1  0     0  0\n 13 14  1  0     0  0\n 14 15  1  0     0  0\n 11 12  1  0     0  0\n 16 17  1  0     0  0\n 17 18  1  0     0  0\n 15 16  1  0     0  0\n  1 18  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n>  <prerender>\nlibrary.svg#tmpl111\n\n$$$$\n20-Crown-6\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 20 20  0     0  0            999 V2000\n   12.9696   -6.7231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4562   -7.5685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4568   -5.8692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4567   -7.5264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4506   -5.9049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2686   -8.5088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2545   -4.9333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3166   -8.8267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3019   -4.6233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5590   -8.1616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5486   -5.2850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7892   -4.6263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8656   -8.5059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8443   -4.9441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6577   -7.5325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6557   -5.9166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6451   -7.5828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6382   -5.8785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1304   -6.7355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8033   -8.8212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  6  1  0     0  0\n  5  7  1  0     0  0\n  6  8  1  0     0  0\n  7  9  1  0     0  0\n  8 10  1  0     0  0\n  9 11  1  0     0  0\n 11 12  1  0     0  0\n 13 15  1  0     0  0\n 14 16  1  0     0  0\n 15 17  1  0     0  0\n 16 18  1  0     0  0\n 17 19  1  0     0  0\n 18 19  1  0     0  0\n 12 14  1  0     0  0\n 13 20  1  0     0  0\n 10 20  1  0     0  0\n  3  1  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n>  <prerender>\nlibrary.svg#tmpl112\n\n$$$$\n21-Crown-7\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 21 21  0     0  0            999 V2000\n    9.2476   -4.0933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3448   -4.5154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3272   -5.5163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3374   -5.7205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0975   -6.6848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8706   -7.3222    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4253   -8.2201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0491   -8.9972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0215   -8.7675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4631   -9.6613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4605   -9.6613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8988   -8.7577    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8812   -8.9945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5114   -8.2256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7121   -4.5149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8084   -4.0887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0256   -4.7163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.1044   -7.3150    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7139   -5.5116    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9025   -6.7100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6937   -5.7379    0.0000 C   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  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  3  4  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n  7  8  1  0     0  0\n 12 13  1  0     0  0\n 13 14  1  0     0  0\n 11 12  1  0     0  0\n 15 16  1  0     0  0\n 16 17  1  0     0  0\n  1 17  1  0     0  0\n 14 18  1  0     0  0\n 19 15  1  0     0  0\n 18 20  1  0     0  0\n 19 21  1  0     0  0\n 20 21  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n>  <prerender>\nlibrary.svg#tmpl113\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\n24-Crown-8\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 24 24  0     0  0            999 V2000\n    9.0714   -9.5538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5688   -8.6839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0589   -9.5538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5317   -9.0088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5767   -8.6753    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2612   -8.3147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6218   -8.9758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9970   -7.3518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9000   -8.2659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8824   -6.8882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1947   -7.2962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8855   -5.8841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3145   -6.8085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0044   -5.4160    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3384   -5.8124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2885   -4.4573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2280   -5.3744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5636   -3.7853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9695   -4.4189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6083   -4.1102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7013   -3.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1273   -3.2484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6397   -4.1023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1264   -3.2462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  6  1  0     0  0\n  5  7  1  0     0  0\n  6  8  1  0     0  0\n  7  9  1  0     0  0\n  8 10  1  0     0  0\n  9 11  1  0     0  0\n 10 12  1  0     0  0\n 11 13  1  0     0  0\n 12 14  1  0     0  0\n 13 15  1  0     0  0\n 14 16  1  0     0  0\n 15 17  1  0     0  0\n 16 18  1  0     0  0\n 17 19  1  0     0  0\n 18 20  1  0     0  0\n 19 21  1  0     0  0\n 20 22  1  0     0  0\n 21 23  1  0     0  0\n 22 24  1  0     0  0\n 23 24  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n>  <prerender>\nlibrary.svg#tmpl114\n\n$$$$\n27-Crown-9\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 27 27  0     0  0            999 V2000\n   12.8715   -5.4793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4227   -6.3542    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3172   -4.6439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2176   -6.9623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3116   -4.7071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.0558   -7.9420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0873   -3.7356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.1143   -8.2518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2476   -9.2356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3689   -4.0852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6009   -3.4377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1290   -3.4254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5183   -9.4192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6486   -3.7570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9884  -10.2746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4426   -9.8295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4301   -4.7338    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9807  -10.2746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4253   -4.6828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4473   -9.4221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8996   -5.5250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5287   -9.8321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3912   -6.3772    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7155   -9.2528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6324   -7.0243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8191   -8.2642    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8489   -7.9911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  6  1  0     0  0\n  5  7  1  0     0  0\n  6  8  1  0     0  0\n  8  9  1  0     0  0\n 10 11  1  0     0  0\n 10 12  1  0     0  0\n 11 14  1  0     0  0\n 13 15  1  0     0  0\n 13 16  1  0     0  0\n 14 17  1  0     0  0\n 15 18  1  0     0  0\n 17 19  1  0     0  0\n 18 20  1  0     0  0\n 19 21  1  0     0  0\n 20 22  1  0     0  0\n 21 23  1  0     0  0\n 22 24  1  0     0  0\n 23 25  1  0     0  0\n 24 26  1  0     0  0\n 26 27  1  0     0  0\n 12  7  1  0     0  0\n  9 16  1  0     0  0\n 27 25  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n>  <prerender>\nlibrary.svg#tmpl115\n\n$$$$\n30-Crown-10\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 30 30  0     0  0            999 V2000\n   10.5968   -3.4933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5443   -3.8013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8344   -4.1370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7938   -4.7628    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1029   -3.4529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7946   -4.6212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1487   -3.7257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4230   -5.3890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8987   -4.6893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.0643   -6.3145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9078   -4.5662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9365   -6.8065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3013   -5.3520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9385   -7.7974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6787   -6.2795    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.0639   -8.2936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8115   -6.7735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4322   -9.2202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8115   -7.7678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8108  -10.0124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6722   -8.2700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8119   -9.8780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2940   -9.1976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5637  -10.8535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8989   -9.9918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5955  -11.1458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9003   -9.8692    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1417  -10.8495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0967  -11.1471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8494  -10.4845    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  4  6  1  0     0  0\n  6  8  1  0     0  0\n  7  9  1  0     0  0\n  8 10  1  0     0  0\n  9 11  1  0     0  0\n 10 12  1  0     0  0\n 11 13  1  0     0  0\n 12 14  1  0     0  0\n 14 16  1  0     0  0\n 15 17  1  0     0  0\n 16 18  1  0     0  0\n 17 19  1  0     0  0\n 19 21  1  0     0  0\n 20 22  1  0     0  0\n 21 23  1  0     0  0\n 22 24  1  0     0  0\n 23 25  1  0     0  0\n 24 26  1  0     0  0\n 27 28  1  0     0  0\n 29 30  1  0     0  0\n  5  7  1  0     0  0\n 18 20  1  0     0  0\n 25 27  1  0     0  0\n 28 29  1  0     0  0\n 26 30  1  0     0  0\n 15 13  1  0     0  0\n  5  3  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n>  <prerender>\nlibrary.svg#tmpl116\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nALA-D-Alanine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  5  0     0  0            999 V2000\n   13.6701   -6.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6701   -5.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8003   -5.3251    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5335   -5.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5335   -4.3254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3999   -5.8240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  1     0  0\n  2  4  1  0     0  0\n  4  5  2  0     0  0\n  4  6  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl117\n\n>  <atomid>\n2\n\n>  <bondid>\n0\n\n$$$$\nARG-D-Arginine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     0  0            999 V2000\n   12.0694   -4.2443    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7765   -4.9514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5148   -5.9202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5506   -6.1773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2934   -7.1415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3248   -7.4032    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0676   -8.3674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1033   -8.6246    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7747   -9.0745    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7407   -4.6943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0024   -3.7255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4467   -5.4025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2 10  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  7  9  2  0     0  0\n 10 11  2  0     0  0\n 10 12  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl118\n\n>  <atomid>\n0\n\n>  <bondid>\n7\n\n$$$$\nASN-D-Asparagine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     0  0            999 V2000\n   10.8319   -5.4762    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6977   -5.9761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6989   -6.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8342   -7.4719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8321   -8.4753    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9683   -6.9719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5657   -5.4726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5645   -4.4747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4317   -5.9725    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  7  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  4  6  2  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl119\n\n>  <atomid>\n0\n\n>  <bondid>\n4\n\n$$$$\nASP-D-Aspartic acid\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     0  0            999 V2000\n   10.7814   -5.6761    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6474   -6.1761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6486   -7.1739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7839   -7.6718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7818   -8.6752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9179   -7.1719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5154   -5.6726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5142   -4.6748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3821   -6.1711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  7  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  4  6  2  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl120\n\n>  <atomid>\n0\n\n>  <bondid>\n4\n\n$$$$\nCYS-D-Cysteine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  6  0     0  0            999 V2000\n    6.9511   -4.7004    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8205   -5.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8205   -6.1991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9511   -6.6987    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6834   -4.7004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6834   -3.7013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5489   -5.1995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  5  1  0     0  0\n  3  4  1  0     0  0\n  5  6  2  0     0  0\n  5  7  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl121\n\n>  <atomid>\n0\n\n>  <bondid>\n3\n\n$$$$\nGLN-D-Glutamine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     0  0            999 V2000\n   11.1341   -5.3758    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0002   -5.8759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0015   -6.8739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1332   -7.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1344   -8.3757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2695   -8.8736    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0006   -8.8757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8652   -5.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8673   -4.3743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7305   -5.8794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  5  7  2  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl122\n\n>  <atomid>\n0\n\n>  <bondid>\n5\n\n$$$$\nGLU-D-Glutamic acid\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     0  0            999 V2000\n   11.4591   -5.3259    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3252   -5.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3265   -6.8240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4582   -7.3276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4594   -8.3256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5945   -8.8236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3256   -8.8257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1902   -5.3279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1923   -4.3243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0555   -5.8295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  5  7  2  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl123\n\n>  <atomid>\n0\n\n>  <bondid>\n5\n\n$$$$\nGLY-Glycine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  4  0     0  0            999 V2000\n   10.6670   -7.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5331   -6.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8010   -6.8750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3990   -7.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5331   -5.8750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  2  5  2  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl124\n\n>  <atomid>\n2\n\n>  <bondid>\n1\n\n$$$$\nHIS-D-Histidine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 11  0     0  0            999 V2000\n   11.4910   -6.5739    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3584   -7.0771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3572   -8.0742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4919   -8.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3861   -9.5713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4100   -9.7753    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9104   -8.9099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5750   -8.1667    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2237   -6.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2217   -5.5747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0896   -7.0762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  9  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4  8  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  2  0     0  0\n  9 10  2  0     0  0\n  9 11  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl125\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nILE-D-Isoleucine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     0  0            999 V2000\n   11.8001   -9.8252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8020   -8.8218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6668   -8.3239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5327   -8.8239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6656   -7.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7997   -6.8261    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5336   -6.8225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5324   -5.8248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4003   -7.3211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  6     0  0\n  3  5  1  0     0  0\n  5  6  1  1     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl126\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nLEU-D-Leucine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     0  0            999 V2000\n   12.2568   -9.3502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2588   -8.3468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3929   -7.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1235   -7.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1224   -6.8511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2564   -6.3511    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9903   -6.3475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9891   -5.3498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8571   -6.8461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  2  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  1     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl127\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nLYS-D-Lysine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     0  0            999 V2000\n   10.6692   -9.3254    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6712   -8.3221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5358   -7.8243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5346   -6.8266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4025   -6.3233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4013   -5.3256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5355   -4.8257    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2659   -4.8278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2679   -3.8246    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1308   -5.3291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  1     0  0\n  6  8  1  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl128\n\n>  <atomid>\n6\n\n>  <bondid>\n0\n\n$$$$\nMET-D-Methionine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     0  0            999 V2000\n   11.6195   -9.8247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4844   -9.3267    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4832   -8.3287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3515   -7.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3502   -6.8270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4841   -6.3270    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2152   -6.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2173   -5.3253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0805   -6.8304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  1     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl129\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nPHE-D-Phenylalanine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 11  0     0  0            999 V2000\n   12.5510   -6.0250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -6.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -6.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -5.0250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.1490   -6.5249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -7.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5510   -8.0249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5510   -9.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -9.5250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -9.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -8.0249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  6  1  0     0  0\n  3  4  2  0     0  0\n  3  5  1  0     0  0\n  6  7  1  0     0  0\n  6 11  2  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n 10 11  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl130\n\n>  <atomid>\n0\n\n>  <bondid>\n4\n\n$$$$\nPRO-D-Proline\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     0  0            999 V2000\n   10.6969   -1.7001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6956   -2.6978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8298   -3.1977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7240   -4.1958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7473   -4.3999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2474   -3.5340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9124   -2.7903    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4026   -3.4047    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  3  2  1  1     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  3  7  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl131\n\n>  <atomid>\n6\n\n>  <bondid>\n2\n\n$$$$\nSER-D-Serine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  6  0     0  0            999 V2000\n   10.3261   -6.8754    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1955   -7.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1955   -8.3741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3261   -8.8737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0584   -6.8754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0584   -5.8763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9239   -7.3745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  5  1  0     0  0\n  3  4  1  0     0  0\n  5  6  2  0     0  0\n  5  7  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl132\n\n>  <atomid>\n0\n\n>  <bondid>\n3\n\n$$$$\nTHR-D-Threonine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     0  0            999 V2000\n   11.5255   -8.1243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3953   -7.6246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -8.1243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3953   -6.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5255   -6.1252    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -6.1252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -5.1257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1245   -6.6245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  1     0  0\n  2  4  1  0     0  0\n  4  5  1  1     0  0\n  4  6  1  0     0  0\n  6  7  2  0     0  0\n  6  8  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl133\n\n>  <atomid>\n4\n\n>  <bondid>\n0\n\n$$$$\nTRP-D-Tryptophan\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 15 16  0     0  0            999 V2000\n   11.9929   -5.3065    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8877   -5.7594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9408   -6.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0974   -7.3028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1680   -6.9465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5350   -7.7214    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0834   -8.5631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0497   -8.3041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7565   -9.0092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4968   -9.9732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5306  -10.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8239   -9.5270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7230   -5.2128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6717   -4.2179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6150   -5.6658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2 13  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4  8  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  2  0     0  0\n  7 12  1  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n 10 11  1  0     0  0\n 11 12  2  0     0  0\n 13 14  2  0     0  0\n 13 15  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl134\n\n>  <atomid>\n0\n\n>  <bondid>\n15\n\n$$$$\nTYR-D-Tyrosine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 13 13  0     0  0            999 V2000\n   12.5019   -5.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3670   -6.3231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3658   -7.3212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4995   -7.8214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5016   -8.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6354   -9.3253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7671   -8.8216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9008   -9.3217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7683   -7.8234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6344   -7.3233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2333   -5.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2344   -4.8247    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0992   -6.3235    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2 11  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4 10  1  0     0  0\n  5  6  1  0     0  0\n  6  7  2  0     0  0\n  7  8  1  0     0  0\n  7  9  1  0     0  0\n  9 10  2  0     0  0\n 11 12  2  0     0  0\n 11 13  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl135\n\n>  <atomid>\n0\n\n>  <bondid>\n8\n\n$$$$\nVAL-D-Valine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     0  0            999 V2000\n   10.8255   -8.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6953   -8.4496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -8.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6953   -7.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8255   -6.9502    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -6.9502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -5.9506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4245   -7.4494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  2  4  1  0     0  0\n  4  5  1  1     0  0\n  4  6  1  0     0  0\n  6  7  2  0     0  0\n  6  8  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl136\n\n>  <atomid>\n4\n\n>  <bondid>\n0\n\n$$$$\nD-Allose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.4194   -1.6883    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9924   -1.0905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4387   -0.4664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0204    0.1639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4629    0.7656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0221    1.3609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4407    1.9808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1127    2.6517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2718    1.3426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2093    0.7656    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2702    0.1833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1849   -0.4782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  6     0  0\n  5 10  1  1     0  0\n  4 11  1  6     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl137\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Altrose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.4516   -1.2975    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0245   -0.6997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4709   -0.0714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0525    0.5547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4950    1.1564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0501    1.7518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4729    2.3717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1448    3.0442    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3040    1.7335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2414    1.1564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3024    0.5742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2171   -0.0873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  1     0  0\n  5 10  1  1     0  0\n  4 11  1  6     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl138\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Arabinose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -3.8949   -0.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4593    0.4968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8995    1.1253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4675    1.7484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9005    2.3460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4667    2.9613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4723   -0.7154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7192    1.7520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6437    1.1253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7111    0.4839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  7  1  0     0  0\n  4  8  1  1     0  0\n  3  9  1  1     0  0\n  2 10  1  6     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl139\n\n>  <atomid>\n6\n\n>  <bondid>\n5\n\n$$$$\nD-Erythrose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   -4.1906    0.0133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7523    0.6006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1844    1.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7532    1.8545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1786    2.4581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7458    3.0700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0034    1.8545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9299    1.2384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  4  7  1  6     0  0\n  3  8  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl140\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Erythrulose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   -4.1896    2.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7907    1.5002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2449    0.8939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8481    0.2611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7539    2.6818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0537    1.4794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9812    0.9226    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3557   -0.3786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  1  5  1  0     0  0\n  2  6  2  0     0  0\n  3  7  1  1     0  0\n  8  4  1  0     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl141\n\n>  <atomid>\n4\n\n>  <bondid>\n3\n\n$$$$\nD-Fructose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.1480    1.9843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5728    1.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1297    0.7648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5540    0.1353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1105   -0.4649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5532   -1.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1339   -1.6816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5796    2.5934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3170    1.3875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3814    0.7735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2979    0.1190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3622   -0.4638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  1  8  1  0     0  0\n  2  9  2  0     0  0\n  3 10  1  1     0  0\n  4 11  1  1     0  0\n  5 12  1  6     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl142\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\nD-Galactose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.8880   -0.9644    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4609   -0.3663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9072    0.2619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4890    0.8881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9315    1.4898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4907    2.0852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9093    2.7051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5812    3.3773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7403    2.0668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6779    1.4898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7387    0.9075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6535    0.2459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  6     0  0\n  5 10  1  6     0  0\n  4 11  1  1     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl143\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Glucose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.5186   -1.2143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9457   -0.6164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4995    0.0120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9178    0.6380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4754    1.2399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9163    1.8351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4978    2.4551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8217    3.1274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6624    1.8167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7249    1.2399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6639    0.6573    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7491   -0.0039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  1     0  0\n  5 10  1  1     0  0\n  4 11  1  1     0  0\n  3 12  1  6     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl144\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Gulose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -4.3047   -1.0894    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8775   -0.4913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3239    0.1369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9056    0.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3481    1.3648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9073    1.9602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3260    2.5801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9978    3.2523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1570    1.9418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0945    1.3648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1554    0.7825    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0702    0.1209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  6     0  0\n  5 10  1  1     0  0\n  4 11  1  1     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl145\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Idose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.7380   -1.2977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3109   -0.6997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7572   -0.0715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3390    0.5547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7815    1.1564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3407    1.7519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7593    2.3718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4312    3.0440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5903    1.7335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5279    1.1564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5887    0.5742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5035   -0.0874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  1     0  0\n  5 10  1  1     0  0\n  4 11  1  1     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl146\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Lyxose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -3.9033    0.3647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3348    0.9551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8987    1.5836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3307    2.2068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8977    2.8043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3273    3.4196    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3259   -0.2571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0749    2.2103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1504    1.5836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0829    0.9422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  7  1  0     0  0\n  4  8  1  6     0  0\n  3  9  1  1     0  0\n  2 10  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl147\n\n>  <atomid>\n6\n\n>  <bondid>\n5\n\n$$$$\nD-Mannose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.9005   -1.2560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4734   -0.6580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9197   -0.0298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5015    0.5964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9440    1.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5032    1.7935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9218    2.4134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5937    3.0856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7528    1.7751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6904    1.1981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7512    0.6158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6660   -0.0458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  1     0  0\n  5 10  1  6     0  0\n  4 11  1  6     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl148\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Psicose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -4.1455    2.7364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7122    2.1393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1459    1.5125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7164    0.8867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1511    0.2825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6999   -0.3115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1099   -0.9416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7230    3.3500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9598    2.1522    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8942    1.5125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9639    0.8833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8992    0.2707    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  1  8  1  0     0  0\n  2  9  2  0     0  0\n  3 10  1  1     0  0\n  4 11  1  6     0  0\n  5 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl149\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\nD-Ribose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -3.4471   -0.1770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8828    0.4134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4426    1.0421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8747    1.6651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4417    2.2627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8713    2.8780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8696   -0.7989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6188    1.6686    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6943    1.0421    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6268    0.4006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  7  1  0     0  0\n  4  8  1  1     0  0\n  3  9  1  6     0  0\n  2 10  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl150\n\n>  <atomid>\n6\n\n>  <bondid>\n5\n\n$$$$\nD-Ribulose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -3.1689   -0.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6004    0.0509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1643    0.6794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5963    1.3026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1633    1.9001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5929    2.5154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4160    0.6794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5914   -1.1613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3485    0.0380    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3252    1.2997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  3  7  1  6     0  0\n  1  8  1  0     0  0\n  2  9  1  1     0  0\n  4 10  2  0     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl151\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\nD-Sorbose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.8077    2.3989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3743    1.8060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8123    1.1791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3785    0.5576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8133   -0.0508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3620   -0.6406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7721   -1.2667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3851    3.0166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6219    1.8147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5564    1.1791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6301    0.5499    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5573   -0.0626    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  1  8  1  0     0  0\n  2  9  2  0     0  0\n  3 10  1  1     0  0\n  4 11  1  1     0  0\n  5 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl152\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\nD-Tagatose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -5.3565    3.2050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7786    2.4087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3570    1.5726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7842    0.7381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3640   -0.0678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7622   -0.8600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3090   -1.7005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7930    4.0234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7752    2.4259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3552    1.5726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7806    0.7334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3619   -0.0835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  1  8  1  0     0  0\n  2  9  2  0     0  0\n  3 10  1  6     0  0\n  4 11  1  1     0  0\n  5 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl153\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\nD-Talose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -4.0547   -0.8394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6275   -0.2413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0739    0.3869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6556    1.0131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0981    1.6148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6573    2.2102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0760    2.8301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7478    3.5023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9070    2.1918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8445    1.6148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9054    1.0325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8202    0.3709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  1     0  0\n  5 10  1  6     0  0\n  4 11  1  1     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl154\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Threose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   -4.7339    0.2599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3006    0.8540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7343    1.4815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3045    2.1079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7353    2.7047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3079    3.3192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5548    2.1114    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.4800    1.4815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  4  7  1  1     0  0\n  3  8  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl155\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Xylose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -3.7801   -0.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2157    0.4968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7755    1.1253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2075    1.7484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7745    2.3460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2083    2.9613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2027   -0.7154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9517    1.7520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0272    1.1253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9597    0.4839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  7  1  0     0  0\n  4  8  1  1     0  0\n  3  9  1  1     0  0\n  2 10  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl156\n\n>  <atomid>\n6\n\n>  <bondid>\n5\n\n$$$$\nD-Xylulose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -2.9398   -0.2937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3754    0.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9352    0.9336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3672    1.5568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9342    2.1584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3638    2.7737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1827    0.9336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3623   -0.9196    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1235    0.2880    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1002    1.5539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  3  7  1  1     0  0\n  1  8  1  0     0  0\n  2  9  1  1     0  0\n  4 10  2  0     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl157\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\n1_2_3-Oxadiazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl158\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nDioxane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    4.2090   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2090   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -4.7018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -3.0482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl159\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nFuran\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl160\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nImidazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl161\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nIndole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    6.3344   -5.9612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7641   -5.9608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0506   -5.5480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7641   -6.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3344   -6.7915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0524   -7.2005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4800   -7.2028    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1974   -6.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1974   -5.9608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\n  8  9  2  0     0  0\n  7  8  1  0     0  0\n  2  9  1  0     0  0\n  4  7  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl162\n\n>  <atomid>\n6\n\n>  <bondid>\n6\n\n$$$$\nIsoquinoline\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    7.2094   -5.7112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6391   -5.7108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9256   -5.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6391   -6.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2094   -6.5415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9274   -6.9505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3533   -5.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0698   -5.7124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3584   -6.9529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0717   -6.5353    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  2  4  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\n  8  7  2  0     0  0\n  9 10  2  0     0  0\n 10  8  1  0     0  0\n  4  9  1  0     0  0\n  2  7  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl163\n\n>  <atomid>\n8\n\n>  <bondid>\n0\n\n$$$$\nIsoxazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl164\n\n>  <atomid>\n2\n\n>  <bondid>\n0\n\n$$$$\nMorpholine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    4.2090   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2090   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -4.7018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -3.0482    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl165\n\n>  <atomid>\n5\n\n>  <bondid>\n1\n\n$$$$\nOxazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl166\n\n>  <atomid>\n4\n\n>  <bondid>\n0\n\n$$$$\nPiperazine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    4.2090   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2090   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -4.7018    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -3.0482    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl167\n\n>  <atomid>\n5\n\n>  <bondid>\n1\n\n$$$$\nPiperidine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    3.0000   -9.5098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000  -10.3366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7160  -10.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4320  -10.3366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4320   -9.5098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7160   -9.0964    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl168\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nPurine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    6.3344   -5.9612    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7641   -5.9608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0506   -5.5480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7641   -6.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3344   -6.7915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0524   -7.2005    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4800   -7.2028    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1974   -6.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1974   -5.9608    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\n  8  9  2  0     0  0\n  7  8  1  0     0  0\n  2  9  1  0     0  0\n  4  7  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl169\n\n>  <atomid>\n6\n\n>  <bondid>\n7\n\n$$$$\nPyran\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    4.2090   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2090   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -4.7018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -3.0482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl170\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nPyrazine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    6.4094   -4.0362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1256   -3.6230    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.8628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4094   -4.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1274   -5.2755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl171\n\n>  <atomid>\n0\n\n>  <bondid>\n2\n\n$$$$\nPyrazol\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl172\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nPyridazine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    6.4094   -4.0362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1256   -3.6230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.8628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4094   -4.8665    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1274   -5.2755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl173\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nPyridine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    6.4094   -4.0362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1256   -3.6230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.8628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4094   -4.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1274   -5.2755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl174\n\n>  <atomid>\n3\n\n>  <bondid>\n1\n\n$$$$\nPyridone\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  7  0     0  0            999 V2000\n    5.2590   -5.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2590   -5.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9750   -6.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6910   -5.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6910   -5.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9750   -4.5982    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5430   -4.5982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  6  1  0     0  0\n  1  7  2  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl175\n\n>  <atomid>\n5\n\n>  <bondid>\n5\n\n$$$$\nPyrimidine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    6.4094   -4.0362    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1256   -3.6230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.8628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4094   -4.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1274   -5.2755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl176\n\n>  <atomid>\n4\n\n>  <bondid>\n1\n\n$$$$\nPyrole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    3.6685  -10.0843    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -9.5986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2553   -8.8126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0817   -8.8126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3370   -9.5986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl177\n\n$$$$\nPyrone\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  7  0     0  0            999 V2000\n    5.2590   -5.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2590   -5.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9750   -6.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6910   -5.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6910   -5.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9750   -4.5982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5430   -4.5982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  6  1  0     0  0\n  1  7  2  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl178\n\n>  <atomid>\n4\n\n>  <bondid>\n4\n\n$$$$\nPyrrolidine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    3.7210   -3.9181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3632   -3.3980    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0779   -3.8107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8532   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0171   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl179\n\n>  <atomid>\n1\n\n>  <bondid>\n2\n\n$$$$\nQuinoline\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    7.2094   -5.7112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6391   -5.7108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9256   -5.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6391   -6.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2094   -6.5415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9274   -6.9505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3533   -5.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0698   -5.7124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3584   -6.9529    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0717   -6.5353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  2  4  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\n  8  7  2  0     0  0\n  9 10  2  0     0  0\n 10  8  1  0     0  0\n  4  9  1  0     0  0\n  2  7  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl180\n\n>  <atomid>\n9\n\n>  <bondid>\n8\n\n$$$$\nTetrahydrofuran\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    3.7210   -3.9181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3632   -3.3980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0779   -3.8107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8532   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0171   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl181\n\n>  <atomid>\n2\n\n>  <bondid>\n2\n\n$$$$\nTetrahydrothiophene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    3.7210   -3.9181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3632   -3.3980    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0779   -3.8107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8532   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0171   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl182\n\n>  <atomid>\n2\n\n>  <bondid>\n2\n\n$$$$\nTetrazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl183\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nThiophene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl184\n\n>  <atomid>\n4\n\n>  <bondid>\n3\n\n$$$$\nTriazine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    6.4094   -4.0362    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.0358    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1256   -3.6230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.8628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4094   -4.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1274   -5.2755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl185\n\n>  <atomid>\n3\n\n>  <bondid>\n1\n\n$$$$\nTriazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl186\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nALA-L-Alanine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  5  0     0  0            999 V2000\n   13.6700   -6.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6700   -5.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8002   -5.3251    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5334   -5.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5334   -4.3254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3998   -5.8240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  6     0  0\n  2  4  1  0     0  0\n  4  5  2  0     0  0\n  4  6  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl187\n\n>  <atomid>\n2\n\n>  <bondid>\n0\n\n$$$$\nARG-L-Arginine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     0  0            999 V2000\n   12.0694   -4.2443    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7765   -4.9514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5148   -5.9202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5506   -6.1773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2934   -7.1415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3248   -7.4032    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0676   -8.3674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1033   -8.6246    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7747   -9.0745    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7407   -4.6943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0024   -3.7255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4467   -5.4025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2 10  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  7  9  2  0     0  0\n 10 11  2  0     0  0\n 10 12  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl188\n\n>  <atomid>\n0\n\n>  <bondid>\n7\n\n$$$$\nASN-L-Asparagine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     0  0            999 V2000\n   10.8319   -5.4762    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6977   -5.9761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6989   -6.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8342   -7.4719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8321   -8.4753    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9683   -6.9719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5657   -5.4726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5645   -4.4747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4317   -5.9725    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  7  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  4  6  2  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl189\n\n>  <atomid>\n0\n\n>  <bondid>\n4\n\n$$$$\nASP-L-Aspartic acid\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     0  0            999 V2000\n   10.7814   -5.6761    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6474   -6.1761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6486   -7.1739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7839   -7.6718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7818   -8.6752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9179   -7.1719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5154   -5.6726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5142   -4.6748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3821   -6.1711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  7  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  4  6  2  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl190\n\n>  <atomid>\n0\n\n>  <bondid>\n4\n\n$$$$\nCYS-L-Cysteine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  6  0     0  0            999 V2000\n    6.9511   -4.7004    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8205   -5.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8205   -6.1991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9511   -6.6987    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6834   -4.7004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6834   -3.7013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5489   -5.1995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  5  1  0     0  0\n  3  4  1  0     0  0\n  5  6  2  0     0  0\n  5  7  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl191\n\n>  <atomid>\n0\n\n>  <bondid>\n3\n\n$$$$\nGLN-L-Glutamine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     0  0            999 V2000\n   11.1341   -5.3758    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0002   -5.8759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0015   -6.8739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1332   -7.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1344   -8.3757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2695   -8.8736    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0006   -8.8757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8652   -5.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8673   -4.3743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7305   -5.8794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  5  7  2  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl192\n\n>  <atomid>\n0\n\n>  <bondid>\n5\n\n$$$$\nGLU-L-Glutamic acid\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     0  0            999 V2000\n   11.4591   -5.3259    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3252   -5.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3265   -6.8240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4582   -7.3276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4594   -8.3256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5945   -8.8236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3256   -8.8257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1902   -5.3279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1923   -4.3243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0555   -5.8295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  5  7  2  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl193\n\n>  <atomid>\n0\n\n>  <bondid>\n5\n\n$$$$\nGLY-Glycine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  4  0     0  0            999 V2000\n   10.6670   -7.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5331   -6.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8010   -6.8750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3990   -7.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5331   -5.8750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  2  5  2  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl194\n\n>  <atomid>\n2\n\n>  <bondid>\n1\n\n$$$$\nHIS-L-Histidine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 11  0     0  0            999 V2000\n   11.4910   -6.5739    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3584   -7.0771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3572   -8.0742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4919   -8.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3861   -9.5713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4100   -9.7753    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9104   -8.9099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5750   -8.1667    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2237   -6.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2217   -5.5747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0896   -7.0762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  9  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4  8  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  2  0     0  0\n  9 10  2  0     0  0\n  9 11  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl195\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nILE-L-Isoleucine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     0  0            999 V2000\n   11.8001   -9.8252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8020   -8.8218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6668   -8.3239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5327   -8.8239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6656   -7.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7997   -6.8261    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5336   -6.8225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5324   -5.8248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4003   -7.3211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  1     0  0\n  3  5  1  0     0  0\n  5  6  1  6     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl196\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nLEU-L-Leucine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     0  0            999 V2000\n   12.2568   -9.3502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2588   -8.3468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3929   -7.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1235   -7.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1224   -6.8511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2564   -6.3511    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9903   -6.3475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9891   -5.3498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8571   -6.8461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  2  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  6     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl197\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nLYS-L-Lysine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     0  0            999 V2000\n   10.6692   -9.3254    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6712   -8.3221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5358   -7.8243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5346   -6.8266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4025   -6.3233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4013   -5.3256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5355   -4.8257    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2659   -4.8278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2679   -3.8246    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1308   -5.3291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  6     0  0\n  6  8  1  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl198\n\n>  <atomid>\n6\n\n>  <bondid>\n0\n\n$$$$\nMET-L-Methionine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     0  0            999 V2000\n   11.6195   -9.8247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4844   -9.3267    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4832   -8.3287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3515   -7.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3502   -6.8270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4841   -6.3270    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2152   -6.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2173   -5.3253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0805   -6.8304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  6     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl199\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nPHE-L-Phenylalanine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 11  0     0  0            999 V2000\n   12.5510   -6.0250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -6.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -6.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -5.0250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.1490   -6.5249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -7.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5510   -8.0249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5510   -9.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -9.5250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -9.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -8.0249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  6  1  0     0  0\n  3  4  2  0     0  0\n  3  5  1  0     0  0\n  6  7  1  0     0  0\n  6 11  2  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n 10 11  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl200\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nPRO-L-Proline\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     0  0            999 V2000\n   10.6969   -1.7001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6956   -2.6978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8298   -3.1977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7240   -4.1958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7473   -4.3999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2474   -3.5340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9124   -2.7903    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4026   -3.4047    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  3  2  1  6     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  3  7  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl201\n\n>  <atomid>\n6\n\n>  <bondid>\n2\n\n$$$$\nSER-L-Serine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  6  0     0  0            999 V2000\n   10.3261   -6.8754    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1955   -7.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1955   -8.3741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3261   -8.8737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0584   -6.8754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0584   -5.8763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9239   -7.3745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  5  1  0     0  0\n  3  4  1  0     0  0\n  5  6  2  0     0  0\n  5  7  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl202\n\n>  <atomid>\n0\n\n>  <bondid>\n3\n\n$$$$\nTHR-L-Threonine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     0  0            999 V2000\n   11.5255   -8.1243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3953   -7.6246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -8.1243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3953   -6.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5255   -6.1252    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -6.1252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -5.1257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1245   -6.6245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  6     0  0\n  2  4  1  0     0  0\n  4  5  1  6     0  0\n  4  6  1  0     0  0\n  6  7  2  0     0  0\n  6  8  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl203\n\n>  <atomid>\n4\n\n>  <bondid>\n0\n\n$$$$\nTRP-L-Tryptophan\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 15 16  0     0  0            999 V2000\n   11.9929   -5.3065    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8877   -5.7594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9408   -6.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0974   -7.3028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1680   -6.9465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5350   -7.7214    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0834   -8.5631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0497   -8.3041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7565   -9.0092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4968   -9.9732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5306  -10.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8239   -9.5270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7230   -5.2128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6717   -4.2179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6150   -5.6658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2 13  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4  8  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  2  0     0  0\n  7 12  1  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n 10 11  1  0     0  0\n 11 12  2  0     0  0\n 13 14  2  0     0  0\n 13 15  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl204\n\n>  <atomid>\n0\n\n>  <bondid>\n15\n\n$$$$\nTYR-L-Tyrosine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 13 13  0     0  0            999 V2000\n   12.5019   -5.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3670   -6.3231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3658   -7.3212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4995   -7.8214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5016   -8.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6354   -9.3253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7671   -8.8216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9008   -9.3217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7683   -7.8234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6344   -7.3233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2333   -5.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2344   -4.8247    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0992   -6.3235    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2 11  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4 10  1  0     0  0\n  5  6  1  0     0  0\n  6  7  2  0     0  0\n  7  8  1  0     0  0\n  7  9  1  0     0  0\n  9 10  2  0     0  0\n 11 12  2  0     0  0\n 11 13  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl205\n\n>  <atomid>\n0\n\n>  <bondid>\n8\n\n$$$$\nVAL-L-Valine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     0  0            999 V2000\n   10.8255   -8.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6953   -8.4496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -8.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6953   -7.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8255   -6.9502    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -6.9502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -5.9506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4245   -7.4494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  2  4  1  0     0  0\n  4  5  1  6     0  0\n  4  6  1  0     0  0\n  6  7  2  0     0  0\n  6  8  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl206\n\n>  <atomid>\n4\n\n>  <bondid>\n0\n\n$$$$\nAdenine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    3.4903   -2.0759    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.1974   -1.8369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -1.3637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.1974   -0.9421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9070   -2.2584    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4956   -0.6934    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8834   -0.5386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6333   -1.8449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6333   -0.9769    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8834    0.2478    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  2  0     0  0\n  2  5  1  0     0  0\n  3  6  2  0     0  0\n  4  7  1  0     0  0\n  5  8  2  0     0  0\n  7  9  2  0     0  0\n  7 10  1  0     0  0\n  4  6  1  0     0  0\n  8  9  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl207\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nCytosine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     0  0            999 V2000\n    3.7084   -1.9709    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4211   -1.5561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -1.5602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4211   -0.7296    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1335   -1.9667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -0.7338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7050   -0.3230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7050    0.4994    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  2  5  2  0     0  0\n  3  6  2  0     0  0\n  4  7  2  0     0  0\n  7  8  1  0     0  0\n  6  7  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl208\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nGuanine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    3.4897    0.3839    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.1974    0.6221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    1.0969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.1974    1.5215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9066    0.2000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5004    1.7668    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8887    1.9244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6377    0.6171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6377    1.4853    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8887    2.7154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3288    0.2133    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  2  0     0  0\n  2  5  1  0     0  0\n  3  6  2  0     0  0\n  4  7  1  0     0  0\n  5  8  2  0     0  0\n  7  9  1  0     0  0\n  7 10  2  0     0  0\n  4  6  1  0     0  0\n  8  9  1  0     0  0\n  8 11  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl209\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nThymine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  9  0     0  0            999 V2000\n    2.4396   -1.5954    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1523   -1.1809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7188   -1.1806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1523   -0.3502    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8646   -1.5913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7189   -0.3543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4364    0.0565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4364    0.8829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0104    0.0579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  2  5  2  0     0  0\n  3  6  2  0     0  0\n  4  7  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl210\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nUracil\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     0  0            999 V2000\n    3.7124   -0.5250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4252   -0.1064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -0.1145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4252    0.7243    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1458   -0.5209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    0.7202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7092    1.1310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7092    1.9576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  2  5  2  0     0  0\n  3  6  2  0     0  0\n  4  7  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl211\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nRibose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 14  0     0  0            999 V2000\n    3.6483   -1.5101    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6483   -2.8768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6030   -2.5039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5685   -2.8768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9582   -3.4695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2479   -3.4695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2479   -2.2377    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2479   -4.2134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9582   -2.2333    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9582   -4.2134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5685   -2.0518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.7706   -2.0564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5685   -3.8042    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6483   -3.6834    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  1     0  0\n  5  6  1  1     0  0\n  2  6  1  1     0  0\n  6  7  1  0     0  0\n  6  8  1  0     0  0\n  5  9  1  0     0  0\n  5 10  1  0     0  0\n  4 11  1  0     0  0\n 11 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl212\n\n>  <atomid>\n0\n\n>  <bondid>\n11\n\n$$$$\nDeoxyribose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 14  0     0  0            999 V2000\n   11.5961   -4.0092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5961   -5.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -6.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -6.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -5.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4831   -5.0674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -4.5860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5320   -4.5909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -6.4519    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -4.7792    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -6.8876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -4.7839    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -6.8876    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5961   -6.3232    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  2  6  1  0     0  0\n  6  5  1  0     0  0\n  5  4  1  0     0  0\n  4  3  1  0     0  0\n  2  3  1  0     0  0\n  2  1  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  5  9  1  0     0  0\n  4 10  1  0     0  0\n  4 11  1  0     0  0\n  3 12  1  0     0  0\n  3 13  1  0     0  0\n  2 14  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl213\n\n>  <atomid>\n0\n\n>  <bondid>\n7\n\n$$$$\nRibose monophosphate\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n   14.4831   -3.7504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4831   -5.1570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4073   -4.7732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3426   -5.1570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7437   -5.7670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0710   -5.7670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0710   -4.4993    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0710   -6.5326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7437   -4.4947    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7437   -6.5326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3426   -4.3079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3426   -6.1115    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4831   -5.9871    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2261   -4.3001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3520   -4.3001    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4739   -4.3001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3520   -3.4183    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3520   -5.1818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  1     0  0\n  5  6  1  1     0  0\n  2  6  1  1     0  0\n  6  7  1  0     0  0\n  6  8  1  0     0  0\n  5  9  1  0     0  0\n  5 10  1  0     0  0\n  4 11  1  0     0  0\n  4 12  1  0     0  0\n  2 13  1  0     0  0\n 14 15  1  0     0  0\n 15 16  1  0     0  0\n 15 17  2  0     0  0\n 15 18  1  0     0  0\n 11 14  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl214\n\n>  <atomid>\n0\n\n>  <bondid>\n14\n\n$$$$\nDeoxyribose monophosphate\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n   11.5961   -4.0092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5961   -5.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -6.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -6.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -5.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4831   -5.0674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -4.5860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5320   -4.5909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6579   -4.5909    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7798   -4.5909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6579   -3.7091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6579   -5.4726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -6.4519    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -4.7792    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -6.8876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -4.7839    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -6.8876    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5961   -6.3232    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  2  6  1  0     0  0\n  6  5  1  0     0  0\n  5  4  1  0     0  0\n  4  3  1  0     0  0\n  2  3  1  0     0  0\n  2  1  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  9 11  2  0     0  0\n  9 12  1  0     0  0\n  5 13  1  0     0  0\n  4 14  1  0     0  0\n  4 15  1  0     0  0\n  3 16  1  0     0  0\n  3 17  1  0     0  0\n  2 18  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl215\n\n>  <atomid>\n0\n\n>  <bondid>\n9\n\n$$$$\nAdenosine monophosphate\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 23 25  0     1  0            999 V2000\n   13.0195  -10.5215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3520  -10.8431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6070  -11.4643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4320  -11.4643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6869  -10.8431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6070  -12.2893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3520  -10.0181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5270  -10.0181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6869  -10.0181    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   15.1983   -8.5670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.9127   -8.9796    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   15.9127   -9.8046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.1983  -10.2171    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4838   -9.8046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7568   -8.6851    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4838   -8.9796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2376   -9.3262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.1983   -7.7420    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4320  -12.2893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7020  -10.0181    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7020   -9.1931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7020  -10.8431    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8770  -10.0181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  5  1  0     0  0\n  2  3  1  1     0  0\n  2  7  1  0     0  0\n  3  4  1  1     0  0\n  3  6  1  0     0  0\n  5  4  1  1     0  0\n  5  9  1  0     0  0\n  7  8  1  0     0  0\n 14  9  1  0     0  0\n  9 17  1  0     0  0\n 10 11  2  0     0  0\n 10 16  1  0     0  0\n 10 18  1  0     0  0\n 11 12  1  0     0  0\n 12 13  2  0     0  0\n 13 14  1  0     0  0\n 16 14  2  0     0  0\n 15 16  1  0     0  0\n 15 17  2  0     0  0\n  4 19  1  0     0  0\n  8 20  1  0     0  0\n 20 21  2  0     0  0\n 20 22  1  0     0  0\n 20 23  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl216\n\n>  <atomid>\n22\n\n>  <bondid>\n24\n\n$$$$\nAdenosine diphosphate\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 27 29  0     1  0            999 V2000\n   11.2820   -9.5684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6145   -9.8900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8695  -10.5112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6945  -10.5112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.9494   -9.8900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8695  -11.3362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6145   -9.0650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7895   -9.0650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.9494   -9.0650    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4608   -7.6139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1752   -8.0265    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1752   -8.8515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4608   -9.2640    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7463   -8.8515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0193   -7.7320    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7463   -8.0265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5001   -8.3731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4608   -6.7889    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6945  -11.3362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9645   -9.0650    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9645   -8.2400    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9645   -9.8900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1395   -9.0650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3145   -9.0650    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3145   -8.2400    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3145   -9.8900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4895   -9.0650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  5  1  0     0  0\n  2  3  1  1     0  0\n  2  7  1  0     0  0\n  3  4  1  1     0  0\n  3  6  1  0     0  0\n  5  4  1  1     0  0\n  5  9  1  0     0  0\n  7  8  1  0     0  0\n 14  9  1  0     0  0\n  9 17  1  0     0  0\n 10 11  2  0     0  0\n 10 16  1  0     0  0\n 10 18  1  0     0  0\n 11 12  1  0     0  0\n 12 13  2  0     0  0\n 13 14  1  0     0  0\n 16 14  2  0     0  0\n 15 16  1  0     0  0\n 15 17  2  0     0  0\n  4 19  1  0     0  0\n  8 20  1  0     0  0\n 20 21  2  0     0  0\n 20 22  1  0     0  0\n 20 23  1  0     0  0\n 23 24  1  0     0  0\n 24 25  2  0     0  0\n 24 26  1  0     0  0\n 24 27  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl217\n\n>  <atomid>\n26\n\n>  <bondid>\n28\n\n$$$$\nAdenosine triphosphate\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 31 33  0     1  0            999 V2000\n   14.6695  -10.5215    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0020  -10.8431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2570  -11.4643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0820  -11.4643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3369  -10.8431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2570  -12.2893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0020  -10.0181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1770  -10.0181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3369  -10.0181    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   16.8483   -8.5670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.5627   -8.9796    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   17.5627   -9.8046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.8483  -10.2171    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   16.1338   -9.8046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.4068   -8.6851    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   16.1338   -8.9796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8876   -9.3262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.8483   -7.7420    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0820  -12.2893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3520  -10.0181    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3520   -9.1931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3520  -10.8431    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5270  -10.0181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7020  -10.0181    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7020   -9.1931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7020  -10.8431    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8770  -10.0181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0520  -10.0181    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0520   -9.1931    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0520  -10.8431    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2270  -10.0181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  5  1  0     0  0\n  2  3  1  1     0  0\n  2  7  1  0     0  0\n  3  4  1  1     0  0\n  3  6  1  0     0  0\n  5  4  1  1     0  0\n  5  9  1  0     0  0\n  7  8  1  0     0  0\n 14  9  1  0     0  0\n  9 17  1  0     0  0\n 10 11  2  0     0  0\n 10 16  1  0     0  0\n 10 18  1  0     0  0\n 11 12  1  0     0  0\n 12 13  2  0     0  0\n 13 14  1  0     0  0\n 16 14  2  0     0  0\n 15 16  1  0     0  0\n 15 17  2  0     0  0\n  4 19  1  0     0  0\n  8 20  1  0     0  0\n 20 21  2  0     0  0\n 20 22  1  0     0  0\n 20 23  1  0     0  0\n 23 24  1  0     0  0\n 24 25  2  0     0  0\n 24 26  1  0     0  0\n 24 27  1  0     0  0\n 27 28  1  0     0  0\n 28 29  2  0     0  0\n 28 30  1  0     0  0\n 28 31  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl218\n\n>  <atomid>\n30\n\n>  <bondid>\n32\n\n$$$$\nBenzene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    0.6548    2.2452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0813    2.2456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3694    2.6575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0813    1.4204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.6548    1.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3712    1.0086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl219\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nBoat\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    5.8944    2.4444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4777    2.4444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4166    3.9499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9277    3.9666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2722    3.2222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0277    3.2222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  1  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  3  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl220\n\n>  <atomid>\n3\n\n>  <bondid>\n2\n\n$$$$\nChair\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    8.5333    5.5888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1166    6.6110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9111    6.0833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2555    6.0833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0277    5.5888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6166    6.6222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  1  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  3  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl221\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nChair1\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    4.9944    2.4555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7388    3.0777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2777    2.1666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4055    4.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5333    3.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1166    4.4555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  1  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl222\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nChair2\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n   10.4055    2.4555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6611    3.0777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1222    2.1666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9944    4.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8666    3.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2833    4.4555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  1  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl223\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nChair3\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n    5.0777    4.5777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4888    9.8610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2000   10.1555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8222    8.7777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3611    4.2888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3277    7.0332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0777    6.3666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4888    8.0721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2388    7.4055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6166    5.6610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8666    7.8666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2000    8.3666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3611    6.0777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7777    6.6610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8222    6.9888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0333    5.6610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4055    8.7777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6166    7.4499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  7 15  1  0     0  0\n 15 13  1  0     0  0\n 13  8  1  0     0  0\n  8 18  1  0     0  0\n 18 12  1  0     0  0\n 12  7  1  0     0  0\n  1  7  1  0     0  0\n  8  2  1  0     0  0\n 12  3  1  0     0  0\n 15  4  1  0     0  0\n  5 13  1  0     0  0\n  6  7  1  0     0  0\n  8  9  1  0     0  0\n 10 18  1  0     0  0\n 11 12  1  0     0  0\n 13 14  1  0     0  0\n 15 16  1  0     0  0\n 17 18  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl224\n\n>  <atomid>\n0\n\n>  <bondid>\n5\n\n$$$$\nChair4\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n   10.4888    4.5777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0777    9.8610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3666   10.1555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7444    8.7777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2055    4.2888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2388    7.0332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4888    6.3666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0777    8.0721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3277    7.4055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9500    5.6610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7000    7.8666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3666    8.3666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2055    6.0777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.7888    6.6610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7444    6.9888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5333    5.6610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1611    8.7777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9500    7.4499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  7 15  1  0     0  0\n 15 13  1  0     0  0\n 13  8  1  0     0  0\n  8 18  1  0     0  0\n 18 12  1  0     0  0\n 12  7  1  0     0  0\n  1  7  1  0     0  0\n  8  2  1  0     0  0\n 12  3  1  0     0  0\n 15  4  1  0     0  0\n  5 13  1  0     0  0\n  6  7  1  0     0  0\n  8  9  1  0     0  0\n 10 18  1  0     0  0\n 11 12  1  0     0  0\n 13 14  1  0     0  0\n 15 16  1  0     0  0\n 17 18  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl225\n\n>  <atomid>\n0\n\n>  <bondid>\n5\n\n$$$$\nCyclopentadiene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    3.8091    8.2444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3091    6.7055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6181    7.6510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3091    6.7055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    7.6510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  5  1  0     0  0\n  2  3  2  0     0  0\n  3  1  1  0     0  0\n  4  2  1  0     0  0\n  5  4  2  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl226\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nCyclopentadiene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n   14.3500   -2.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2160   -3.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2160   -4.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4840   -4.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4840   -3.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  2  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\n  4  3  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl227\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nRing3\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  3  3  0     0  0            999 V2000\n    2.6123    1.5663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6098    1.5663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1111    2.4280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  3  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl228\n\n$$$$\nRing4\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  4  4  0     0  0            999 V2000\n    3.4956    1.8862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4919    2.8804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4846    1.8991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4821    2.8804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  4  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl229\n\n$$$$\nRing5\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    3.3632    3.2710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3649    3.2710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0647    2.3206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6686    2.2948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8751    1.7233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  5  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl230\n\n$$$$\nRing5\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    2.2500    1.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1160    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1160   -0.1750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3840   -0.1750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3840    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  4  5  1  0     0  0\n  5  1  1  0     0  0\n  4  3  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl231\n\n$$$$\nRing6\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    2.5500    3.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5500    2.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4160    2.1722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2820    2.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2820    3.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4160    4.1722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl232\n\n$$$$\nRing7\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  7  0     0  0            999 V2000\n   21.4111    6.3389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.1938    6.9555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.1653    6.7333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.5987    5.8389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   21.4166    5.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.1660    4.9333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.1938    4.7111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  6  1  0     0  0\n  1  5  1  0     0  0\n  5  7  1  0     0  0\n  6  7  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl233\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nRing8\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     0  0            999 V2000\n    2.9268    2.2122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9270    3.2099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6288    3.9118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6290    1.5102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6266    1.5102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3286    2.2122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3285    3.2099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6266    3.9119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  1  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  3  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl234\n\n$$$$\nRing9\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  9  0     0  0            999 V2000\n    2.7667    2.2210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5972    3.2097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0962    4.0662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5313    1.5810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5375    1.5810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2993    2.2169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.4693    3.1987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0364    4.4023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9746    4.0565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  1  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  8  3  1  0     0  0\n  8  9  1  0     0  0\n  9  7  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl235\n\n$$$$\nRing10\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     0  0            999 V2000\n    3.5215    2.9499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3132    2.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3132    1.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0493    2.9499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7854    2.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7854    1.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5215    1.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2575    1.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2575    2.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0493    1.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  8  9  1  0     0  0\n  3 10  1  0     0  0\n 10  6  1  0     0  0\n  5  4  1  0     0  0\n  4  2  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  2  3  1  0     0  0\n  9  1  1  0     0  0\n  1  5  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl236\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nRing11\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 11  0     0  0            999 V2000\n    3.7115    0.9202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6673    0.9202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8179    1.8392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.7664    2.5772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8179    3.2138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6382    4.1686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6721    4.1677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4599    3.2440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5335    3.0226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5480    2.0636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4840    1.8574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11  1  1  0     0  0\n  4  5  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl237\n\n$$$$\nRing12\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     0  0            999 V2000\n    3.7276    1.1285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.7247    1.1285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9441    2.1019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9082    2.3309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9040    3.3264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9232    3.5474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6929    4.5158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6906    4.5147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4660    3.5463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5063    3.3181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5162    2.3234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4980    2.1108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  0     0  0\n 12  1  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl238\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nRing13\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 13 13  0     0  0            999 V2000\n    3.2666    4.9710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4574    4.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9755    4.0189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.7213    3.9768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0441    3.6774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6650    3.7016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0441    2.6968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.7099    2.6175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9763    2.4069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6652    2.4096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0491    1.4518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6845    1.4484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9051    1.1289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  6  1  0     0  0\n  5  7  1  0     0  0\n  6  8  1  0     0  0\n  7  9  1  0     0  0\n  8 10  1  0     0  0\n  9 11  1  0     0  0\n 10 12  1  0     0  0\n 11 13  1  0     0  0\n 12 13  1  0     0  0\n  1  2  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl239\n\n>  <atomid>\n0\n\n>  <bondid>\n12\n\n$$$$\nRing14\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 14  0     0  0            999 V2000\n    6.8995    3.2081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3539    4.0579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3678    2.3687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3685    3.9274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3883    2.5015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9655    4.8438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9885    1.5835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9602    4.8347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9932    1.5783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5727    3.9117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5892    2.4908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5971    4.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6111    2.3505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0671    3.1903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  6  1  0     0  0\n  5  7  1  0     0  0\n  6  8  1  0     0  0\n  7  9  1  0     0  0\n  8 10  1  0     0  0\n  9 11  1  0     0  0\n 10 12  1  0     0  0\n 11 13  1  0     0  0\n 12 14  1  0     0  0\n 13 14  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl240\n\n$$$$\nRing15\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 15 15  0     0  0            999 V2000\n    6.3839    2.8393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0478    1.8979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0286    1.8979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6750    0.9634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6672    0.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3752    1.9525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.3912    2.0190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.1293    2.9718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9384    3.5389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6710    4.4863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4746    5.0532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2796    4.4781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1008    5.0326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9121    4.4093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5968    3.4606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  3  4  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n  7  8  1  0     0  0\n 12 13  1  0     0  0\n 13 14  1  0     0  0\n 14 15  1  0     0  0\n 11 12  1  0     0  0\n  1 15  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl241\n\n$$$$\nRing16\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 16 16  0     0  0            999 V2000\n    5.3307    1.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8666    2.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4647    0.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8666    4.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0006    3.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0006    2.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8666    1.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7326    0.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5987    1.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7326    3.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5987    4.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4647    3.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3307    2.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1967    2.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1967    3.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3307    4.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  3  1  0     0  0\n  3  1  1  0     0  0\n  1 13  1  0     0  0\n 10  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  2  1  0     0  0\n  2  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n 12 11  1  0     0  0\n 11 10  1  0     0  0\n 13 14  1  0     0  0\n 14 15  1  0     0  0\n 15 16  1  0     0  0\n 16 12  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl242\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nRing18\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n    6.7675    4.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7675    3.0235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8338    2.6634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9136    1.6865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0241    1.2306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2362    1.8639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4295    1.2651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5501    1.7405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6379    2.7240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7034    3.0885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7024    4.0770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6366    4.4288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5561    5.4110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4362    5.8637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2239    5.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0336    5.8456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9184    5.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8307    4.3812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  3  4  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n  7  8  1  0     0  0\n 12 13  1  0     0  0\n 13 14  1  0     0  0\n 14 15  1  0     0  0\n 11 12  1  0     0  0\n 16 17  1  0     0  0\n 17 18  1  0     0  0\n 15 16  1  0     0  0\n  1 18  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl243\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nRing20\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 20 20  0     0  0            999 V2000\n    5.1641    6.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7000    5.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7000    6.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5660    7.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4320    6.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2980    7.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1641    5.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0301    4.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0301    5.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1641    3.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1641    2.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2980    2.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5660    1.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4320    0.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2980    1.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.8339    5.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.8339    4.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7000    3.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.6999    2.8777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5660    2.3777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  2  1  0     0  0\n  5  4  1  0     0  0\n  4  3  1  0     0  0\n  7  1  1  0     0  0\n  1  6  1  0     0  0\n  6  5  1  0     0  0\n 10  8  1  0     0  0\n  8  9  1  0     0  0\n  9  7  1  0     0  0\n 12 11  1  0     0  0\n 11 10  1  0     0  0\n 20 13  1  0     0  0\n 13 14  1  0     0  0\n 14 15  1  0     0  0\n 15 12  1  0     0  0\n  2 16  1  0     0  0\n 16 17  1  0     0  0\n 17 18  1  0     0  0\n 18 19  1  0     0  0\n 19 20  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl244\n\n>  <atomid>\n13\n\n>  <bondid>\n13\n\n$$$$\nRing21\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 21 21  0     0  0            999 V2000\n   13.0927    4.9401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.7000    5.4856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.7000    4.3856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4537    6.0258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4631    7.1298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5095    7.6878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5428    7.1369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5875    7.6838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6370    7.1269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6419    6.0230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6614    3.8372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6675    2.7393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6235    2.1978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5583    2.7574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5110    2.2085    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4619    2.7621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4601    3.8647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4049    5.4888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4047    4.3920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4478    4.0529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4480    5.8274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  2 10  1  0     0  0\n  3 11  1  0     0  0\n 17 19  1  0     0  0\n 18  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  8  9  1  0     0  0\n  9 10  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 19 20  1  0     0  0\n 20  1  1  0     0  0\n  1 21  1  0     0  0\n 21 18  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <prerender>\nlibrary.svg#tmpl245\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Allopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -4.1124    6.2007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.6076    4.1259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5974    5.2058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4025    4.8658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5974    6.0607    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3373    4.7808    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9974    3.2709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2076    5.2058    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7775    5.3207    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.6076    3.2709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1476    3.8958    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4025    4.0109    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1124    5.3507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7577    4.3259    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7775    4.4658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9974    4.1259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8224    4.3259    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  8  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n  8  4  1  0     0  0\n  3  5  1  0     0  0\n  3  6  1  0     0  0\n  7 16  1  0     0  0\n 17 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <prerender>\nlibrary.svg#tmpl246\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Altropyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -6.8433    4.3051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3385    2.2303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.3283    3.3102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.1334    2.9703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.3283    4.1651    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -8.0682    2.8852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.7283    1.3754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9384    3.3102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.5084    3.4252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3385    1.3754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8784    2.0003    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.1334    2.1154    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.8433    3.4551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4886    2.4303    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.5084    2.5702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.7283    2.2303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.5532    2.4303    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  8  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n  8  4  1  0     0  0\n  3  5  1  0     0  0\n  3  6  1  0     0  0\n  7 16  1  0     0  0\n 17 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <prerender>\nlibrary.svg#tmpl247\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Galactopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -6.4899    2.6666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9851    0.5918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.9748    1.6717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.7800    1.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.9748    2.5266    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.7148    1.2467    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3749   -0.2631    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.1998    0.7918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1550    1.7866    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9851   -0.2631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5250    0.3618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.7800    0.4768    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.4899    1.8166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1352    0.7918    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1550    0.9317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3749    0.5918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5850    1.6717    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n 17  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n 17  4  1  0     0  0\n  3  5  1  0     0  0\n  3  6  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <prerender>\nlibrary.svg#tmpl248\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Glucopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -7.7107   -0.2570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2094   -2.3086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -8.1903   -1.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.0088   -1.5769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -8.1903   -0.3955    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.8273   -1.2408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.5674   -3.1539    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -8.3831   -2.1108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3908   -1.1271    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2094   -3.1539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.7680   -2.5360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.0088   -2.4222    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.7107   -1.0975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3937   -2.1108    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3908   -1.9725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.5674   -2.3086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -8.8923   -1.6610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  6  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n  6  4  1  0     0  0\n  3  5  1  0     0  0\n  3 17  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <prerender>\nlibrary.svg#tmpl249\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Gulopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -5.8152    3.8232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2901    1.7531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.2952    2.8332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1052    2.4882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.2952    3.6832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9101    2.8332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.6702    0.9031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.5202    1.9532    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4801    2.9432    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2901    0.9031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8551    1.5281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1052    1.6382    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.8152    2.9732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4651    1.9532    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4801    2.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.6702    1.7531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.0302    2.4032    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  6  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n  6  4  1  0     0  0\n  3  5  1  0     0  0\n  3 17  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <prerender>\nlibrary.svg#tmpl250\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Idopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -6.0079    2.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4782    0.6560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.4929    1.7359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2981    1.3960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.4929    2.5909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1031    1.7359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.8630   -0.1989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.6879    0.8561    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6731    1.8509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4782   -0.1989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0431    0.4260    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2981    0.5411    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.0079    1.8809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6533    0.8561    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6731    0.9960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.8630    0.6560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.2329    1.3109    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  6  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n  6  4  1  0     0  0\n  3  5  1  0     0  0\n  3 17  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <prerender>\nlibrary.svg#tmpl251\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Mannopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -5.5581    1.8634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0527   -0.1676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.0375    0.8751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8565    0.5342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.0375    1.7202    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.7441    0.4501    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.4199   -1.0126    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.2352    0.0005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2339    1.0134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0527   -1.0126    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6161   -0.4246    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8565   -0.3109    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.5581    1.0134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2325    0.0301    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2339    0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.4199   -0.1676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6705    0.8751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n 17  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n 17  4  1  0     0  0\n  3  5  1  0     0  0\n  3  6  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <prerender>\nlibrary.svg#tmpl252\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Talopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -6.3613    0.1928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8363   -1.8473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.8414   -0.7673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.6514   -1.1373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.8414    0.0827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.5764   -1.2223    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.2164   -2.6973    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.0414   -1.6773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0263   -0.6572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8363   -2.6973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4013   -2.0723    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.6514   -1.9874    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3613   -0.6572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0113   -1.6473    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0263   -1.5074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.2164   -1.8473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4562   -0.7673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n 17  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n 17  4  1  0     0  0\n  3  5  1  0     0  0\n  3  6  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <prerender>\nlibrary.svg#tmpl253\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nfullerene C60\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 60 90  0     0  0            999 V2000\n    8.1533  -10.1609   -0.1552 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5120   -9.2753    0.7287 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7211   -9.6737   -1.3649 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4284   -7.8924    0.4121 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6441   -6.9280    1.4115 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8106   -9.6782    2.0415 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0295   -8.7030    3.0509 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9469   -7.3351    2.7388 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6766  -11.1024   -1.0190 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1155  -11.5835    0.1778 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9755  -10.1416   -1.7961 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8475  -11.1110    0.6132 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6349  -10.8139    1.9708 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1564  -11.7548    1.1061 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9409  -11.4548    2.4787 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6874  -10.9874    2.9088 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0739   -8.9381   -2.1897 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7682   -9.8885   -1.4198 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6696   -9.0654   -2.3772 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0644  -10.9756   -0.8317 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3595  -11.3790    0.4827 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7598   -9.2142   -0.6853 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0558   -9.6210    0.6448 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3611  -10.6974    1.2254 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4123   -6.6547   -2.0401 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8008   -6.5277   -1.8552 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8430   -7.9304   -2.3022 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6373   -7.6755   -1.9309 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6791   -7.8462   -1.0006 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0147   -5.5656   -0.8513 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.0674   -5.7391    0.0877 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8951   -6.8726    0.0134 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9892   -7.4108   -0.7846 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5523   -6.1489   -0.5256 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6396   -8.3057   -1.6776 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7701   -5.7695   -1.1557 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7608   -5.0959   -0.4209 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3383   -5.8515    0.8323 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3403   -5.1700    1.5751 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5444   -4.7952    0.9518 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5476   -6.3919    2.2132 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8535   -5.4411    1.4456 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5858   -4.9664    1.8803 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9810   -6.8781    3.4234 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7114   -9.1401    2.8425 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2717   -8.6582    1.6457 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1904   -7.2758    1.3282 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.0632   -8.2456    3.7369 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2924   -9.8955    4.0975 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.9320  -10.7811    3.2133 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1480  -10.4012    2.5830 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8614   -8.6206    4.3621 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6340   -7.6127    4.2389 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0720   -8.8741    3.9774 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9055  -10.0226    3.9070 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0361   -7.4850    4.4331 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0254   -5.4466    3.0771 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6379   -5.5719    2.8889 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9380   -6.6611    3.4734 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7278   -6.4079    3.8535 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1 12  1  0  0  0  0\n  2  4  1  0  0  0  0\n  2  6  1  0  0  0  0\n  3 11  2  0  0  0  0\n  3 35  1  0  0  0  0\n  4  5  2  0  0  0  0\n  4 33  1  0  0  0  0\n  5  8  1  0  0  0  0\n  5 38  1  0  0  0  0\n  6  7  2  0  0  0  0\n  6 13  1  0  0  0  0\n  7  8  1  0  0  0  0\n  7 54  1  0  0  0  0\n  8 59  2  0  0  0  0\n  9 10  2  0  0  0  0\n  9 11  1  0  0  0  0\n  9 20  1  0  0  0  0\n 10 12  1  0  0  0  0\n 10 14  1  0  0  0  0\n 11 19  1  0  0  0  0\n 12 13  2  0  0  0  0\n 13 16  1  0  0  0  0\n 14 15  2  0  0  0  0\n 14 21  1  0  0  0  0\n 15 16  1  0  0  0  0\n 15 50  1  0  0  0  0\n 16 55  2  0  0  0  0\n 17 18  1  0  0  0  0\n 17 19  2  0  0  0  0\n 17 28  1  0  0  0  0\n 18 20  2  0  0  0  0\n 18 22  1  0  0  0  0\n 19 27  1  0  0  0  0\n 20 21  1  0  0  0  0\n 21 24  2  0  0  0  0\n 22 23  2  0  0  0  0\n 22 29  1  0  0  0  0\n 23 24  1  0  0  0  0\n 23 46  1  0  0  0  0\n 24 51  1  0  0  0  0\n 25 26  1  0  0  0  0\n 25 27  2  0  0  0  0\n 25 36  1  0  0  0  0\n 26 28  2  0  0  0  0\n 26 30  1  0  0  0  0\n 27 35  1  0  0  0  0\n 28 29  1  0  0  0  0\n 29 32  2  0  0  0  0\n 30 31  2  0  0  0  0\n 30 37  1  0  0  0  0\n 31 32  1  0  0  0  0\n 31 42  1  0  0  0  0\n 32 47  1  0  0  0  0\n 33 34  1  0  0  0  0\n 33 35  2  0  0  0  0\n 34 36  2  0  0  0  0\n 34 38  1  0  0  0  0\n 36 37  1  0  0  0  0\n 37 40  2  0  0  0  0\n 38 39  2  0  0  0  0\n 39 40  1  0  0  0  0\n 39 58  1  0  0  0  0\n 40 43  1  0  0  0  0\n 41 42  1  0  0  0  0\n 41 44  2  0  0  0  0\n 41 47  1  0  0  0  0\n 42 43  2  0  0  0  0\n 43 57  1  0  0  0  0\n 44 48  1  0  0  0  0\n 44 60  1  0  0  0  0\n 45 46  1  0  0  0  0\n 45 48  2  0  0  0  0\n 45 51  1  0  0  0  0\n 46 47  2  0  0  0  0\n 48 52  1  0  0  0  0\n 49 50  1  0  0  0  0\n 49 52  2  0  0  0  0\n 49 55  1  0  0  0  0\n 50 51  2  0  0  0  0\n 52 56  1  0  0  0  0\n 53 54  2  0  0  0  0\n 53 56  1  0  0  0  0\n 53 59  1  0  0  0  0\n 54 55  1  0  0  0  0\n 56 60  2  0  0  0  0\n 57 58  2  0  0  0  0\n 57 60  1  0  0  0  0\n 58 59  1  0  0  0  0\nM  END\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl254\n\n>  <atomid>\n18\n\n>  <bondid>\n34\n\n$$$$\nadamantane\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 10 12  0     0  0            999 V2000\n   15.2172   -8.1314    1.0220 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4398   -7.4133   -0.1292 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2919   -8.3429   -0.6392 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9004   -9.6792   -1.1737 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6785  -10.3958   -0.0237 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8276   -9.4680    0.4869 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.8081   -9.1570   -0.6894 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.0325   -8.4390   -1.8401 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.4215   -7.1042   -1.3049 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8828   -9.3683   -2.3500 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  4 10  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  2  9  1  0  0  0  0\n  1  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  5  6  1  0  0  0  0\n  8 10  1  0  0  0  0\n  2  3  1  0  0  0  0\nM  END\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl255\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n$$$$\ncubane\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n  8 12  0     0  0            999 V2000\n   10.5569   -9.9029    4.2925 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2017   -9.5628    4.9812 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5825   -8.4868    3.6463 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3483   -7.9339    4.8851 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9705   -9.0155    6.2193 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3256   -9.3519    5.5298 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2296   -8.1444    4.3386 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9966   -7.5972    5.5784 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  3  1  1  0  0  0  0\n  1  6  1  0  0  0  0\n  2  5  1  0  0  0  0\n  7  2  1  0  0  0  0\n  3  4  1  0  0  0  0\n  7  3  1  0  0  0  0\n  4  6  1  0  0  0  0\n  8  4  1  0  0  0  0\n  5  6  1  0  0  0  0\n  8  5  1  0  0  0  0\n  8  7  1  0  0  0  0\nM  END\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl256\n\n$$$$\nring 6 boat\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n   11.2934   -7.8385   -0.6482 H   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2480   -6.3919    0.1251 H   0  0  0  0  0  0  0  0  0  0  0  0\n   12.1209   -8.2282    2.2065 H   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5795  -10.2283    0.6541 H   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2777   -9.8706   -1.8252 H   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5448   -7.5081   -2.7767 H   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7930   -7.7993   -0.2998 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.8567   -7.8369    0.7935 H   0  0  0  0  0  0  0  0  0  0  0  0\n   14.7961   -6.3928    0.4449 H   0  0  0  0  0  0  0  0  0  0  0  0\n   16.0357   -7.4556   -2.0500 H   0  0  0  0  0  0  0  0  0  0  0  0\n   15.7535   -9.8351   -1.1468 H   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0584  -10.2582    1.3110 H   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6187   -8.3063    2.8894 H   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6881   -8.3653   -1.4688 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2260   -8.3597   -1.0520 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9985   -8.7537    0.9805 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5364   -8.7481    1.4094 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3614   -7.8158    0.4528 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  7  1  0  0  0  0\n  3 16  1  0  0  0  0\n  4 16  1  0  0  0  0\n  5 14  1  0  0  0  0\n  6 14  1  0  0  0  0\n  7 14  1  0  0  0  0\n  7 16  1  0  0  0  0\n  8 18  1  0  0  0  0\n  9 18  1  0  0  0  0\n 10 15  1  0  0  0  0\n 11 15  1  0  0  0  0\n 12 17  1  0  0  0  0\n 13 17  1  0  0  0  0\n 14 15  1  0  0  0  0\n 15 18  1  0  0  0  0\n 16 17  1  0  0  0  0\n 17 18  1  0  0  0  0\n  1  7  1  0  0  0  0\nM  END\n>  <atomid>\n0\n\n>  <bondid>\n17\n\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl257\n\n$$$$\nring 6 chair\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n    6.4738   -5.6532   -0.6660 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4541   -4.2314    0.0877 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2774   -5.9986    2.2013 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7022   -8.0409    0.6946 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4210   -7.7512   -1.7876 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7429   -5.4159   -2.7877 H   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0262   -7.2017    0.7693 H   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0549   -8.6186   -0.0171 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6856   -6.5861    1.4297 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7917   -7.4939    2.7473 H   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0968   -5.1271    1.7849 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1503   -6.5687    0.9919 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3966   -6.2651   -1.0354 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5752   -7.1963    0.2541 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8371   -4.7668   -0.6787 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2658   -6.7684   -2.2180 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8611   -6.2475   -1.4612 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9719   -5.6379   -0.3097 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2 18  1  0  0  0  0\n  3 12  1  0  0  0  0\n  4 12  1  0  0  0  0\n  5 17  1  0  0  0  0\n  6 17  1  0  0  0  0\n  7 14  1  0  0  0  0\n  8 14  1  0  0  0  0\n  9 10  1  0  0  0  0\n  9 11  1  0  0  0  0\n  9 12  1  0  0  0  0\n  9 14  1  0  0  0  0\n 12 18  1  0  0  0  0\n 13 14  1  0  0  0  0\n 13 15  1  0  0  0  0\n 13 16  1  0  0  0  0\n 13 17  1  0  0  0  0\n 17 18  1  0  0  0  0\n  1 18  1  0  0  0  0\nM  END\n>  <atomid>\n0\n\n>  <bondid>\n17\n\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl258\n\n$$$$\nferrocene\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 21 30  0     0  0            999 V2000\n   10.7433   -4.6065   -1.0460 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1199   -5.2233    1.4626 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8813   -5.4347    2.6717 H   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9893   -4.9432    0.9828 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0583   -4.4230   -1.4256 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8850   -5.0258    0.7924 C   0  0  0  0  0  5  0  0  0  0  0  0\n    8.5484   -4.7171   -0.5593 C   0  0  0  0  0  5  0  0  0  0  0  0\n   10.0737   -4.8235   -0.3755 C   0  0  0  0  0  5  0  0  0  0  0  0\n   10.3426   -5.1926    1.0905 C   0  0  0  0  0  5  0  0  0  0  0  0\n    8.9947   -5.3190    1.8095 C   0  0  0  0  0  4  0  0  0  0  0  0\n    9.0287   -7.2803   -0.0160 Fe  0  0  0  0  0  0  0  0  0  0  0  0\n    6.8301   -9.3252   -1.3831 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4779   -9.9251    1.0385 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9836  -10.0770    1.2682 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0339   -9.5923   -1.0056 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1165   -9.0779   -2.7663 H   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1539   -9.5146   -0.7880 C   0  0  0  0  0  5  0  0  0  0  0  0\n    9.0210   -9.2478   -1.7601 C   0  0  0  0  0  5  0  0  0  0  0  0\n    7.7109   -9.3705   -0.9994 C   0  0  0  0  0  5  0  0  0  0  0  0\n    8.0440   -9.7186    0.4389 C   0  0  0  0  0  5  0  0  0  0  0  0\n    9.5495   -9.8067    0.5699 C   0  0  0  0  0  4  0  0  0  0  0  0\n  1  8  1  0  0  0  0\n  2  9  1  0  0  0  0\n  3 10  1  0  0  0  0\n  4  6  1  0  0  0  0\n  5  7  1  0  0  0  0\n  6  7  2  0  0  0  0\n  6 10  1  0  0  0  0\n  6 11  1  0  0  0  0\n  7 11  1  0  0  0  0\n  8  9  2  0  0  0  0\n  8 11  1  0  0  0  0\n  9 10  1  0  0  0  0\n  9 11  1  0  0  0  0\n 10 11  1  0  0  0  0\n 11 17  1  0  0  0  0\n 11 18  1  0  0  0  0\n 11 19  1  0  0  0  0\n 11 20  1  0  0  0  0\n 11 21  1  0  0  0  0\n 12 19  1  0  0  0  0\n 13 20  1  0  0  0  0\n 14 21  1  0  0  0  0\n 15 17  1  0  0  0  0\n 16 18  1  0  0  0  0\n 17 18  2  0  0  0  0\n 17 21  1  0  0  0  0\n 18 19  1  0  0  0  0\n 19 20  2  0  0  0  0\n 20 21  1  0  0  0  0\n  7  8  1  0  0  0  0\nM  CHG  3  10  -1  11   2  21  -1\nM  END\n>  <atomid>\n0\n\n>  <bondid>\n29\n\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl259\n\n$$$$\nbis(benzene)chromium\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 25 36  0     0  0            999 V2000\n    6.4355   -9.0395   -1.1100 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.9645   -9.0205   -1.1098 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8350   -9.9405    1.0201 H   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6010   -8.0061   -3.3654 H   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5675   -9.9807    1.0831 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6580   -7.9387   -3.4841 H   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7133   -8.9130   -1.0583 C   0  0  0  0  0  5  0  0  0  0  0  0\n    8.4060   -9.4512    0.1516 C   0  0  0  0  0  5  0  0  0  0  0  0\n    9.9460   -9.4512    0.1516 C   0  0  0  0  0  5  0  0  0  0  0  0\n    7.6316   -8.9131   -1.0546 C   0  0  0  0  0  5  0  0  0  0  0  0\n    9.9423   -8.3732   -2.2747 C   0  0  0  0  0  5  0  0  0  0  0  0\n    8.4043   -8.3734   -2.2720 C   0  0  0  0  0  5  0  0  0  0  0  0\n    9.1789   -6.5719    0.0084 Cr  0  0  0  0  0  0  0  0  0  0  0  0\n    6.4896   -4.2075    1.3040 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.9323   -4.0735    0.9147 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6895   -3.2859   -0.8924 H   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7804   -5.1073    3.2258 H   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3721   -3.1694   -1.1492 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8953   -5.2543    3.5528 H   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7017   -4.2171    0.9515 C   0  0  0  0  0  5  0  0  0  0  0  0\n    8.3254   -3.7502   -0.0765 C   0  0  0  0  0  5  0  0  0  0  0  0\n    9.8419   -3.7057   -0.1884 C   0  0  0  0  0  5  0  0  0  0  0  0\n    7.6652   -4.2995    1.1662 C   0  0  0  0  0  5  0  0  0  0  0  0\n   10.0444   -4.7658    2.2003 C   0  0  0  0  0  5  0  0  0  0  0  0\n    8.5286   -4.8076    2.3055 C   0  0  0  0  0  5  0  0  0  0  0  0\n  1 10  1  0  0  0  0\n  2  7  1  0  0  0  0\n  3  8  1  0  0  0  0\n  4 11  1  0  0  0  0\n  5  9  1  0  0  0  0\n  6 12  1  0  0  0  0\n  7  9  1  0  0  0  0\n  7 11  2  0  0  0  0\n  7 13  1  0  0  0  0\n  8 10  1  0  0  0  0\n  8 13  1  0  0  0  0\n  9 13  1  0  0  0  0\n 10 12  2  0  0  0  0\n 10 13  1  0  0  0  0\n 11 12  1  0  0  0  0\n 11 13  1  0  0  0  0\n 12 13  1  0  0  0  0\n 13 20  1  0  0  0  0\n 13 21  1  0  0  0  0\n 13 22  1  0  0  0  0\n 13 23  1  0  0  0  0\n 13 24  1  0  0  0  0\n 13 25  1  0  0  0  0\n 14 23  1  0  0  0  0\n 15 20  1  0  0  0  0\n 16 21  1  0  0  0  0\n 17 24  1  0  0  0  0\n 18 22  1  0  0  0  0\n 19 25  1  0  0  0  0\n 20 22  1  0  0  0  0\n 20 24  2  0  0  0  0\n 21 22  2  0  0  0  0\n 21 23  1  0  0  0  0\n 23 25  2  0  0  0  0\n 24 25  1  0  0  0  0\n  8  9  2  0  0  0  0\nM  END\n>  <atomid>\n13\n\n>  <bondid>\n32\n\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl260\n\n$$$$\nB12H12(2-)\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 24 42  0     0  0            999 V2000\n   12.4312   -3.2376    0.4439 B   0  0  0  0  0  6  0  0  0  0  0  0\n   16.4207   -5.8576   -0.2695 B   0  0  0  0  0  6  0  0  0  0  0  0\n   14.1001   -6.2706    3.8919 B   0  0  0  0  0  6  0  0  0  0  0  0\n    9.3404   -6.0750    2.9813 B   0  0  0  0  0  6  0  0  0  0  0  0\n    8.7969   -5.5378   -1.7981 B   0  0  0  0  0  6  0  0  0  0  0  0\n   13.1757   -5.4213   -3.7933 B   0  0  0  0  0  6  0  0  0  0  0  0\n    8.1864   -9.9878    0.2781 B   0  0  0  0  0  6  0  0  0  0  0  0\n   10.5209   -9.5795   -3.9123 B   0  0  0  0  0  6  0  0  0  0  0  0\n   15.2666   -9.7699   -2.9723 B   0  0  0  0  0  6  0  0  0  0  0  0\n   15.8533  -10.3140    1.7916 B   0  0  0  0  0  6  0  0  0  0  0  0\n   11.4884  -10.4352    3.7578 B   0  0  0  0  0  6  0  0  0  0  0  0\n   12.1760  -12.6074   -0.4354 B   0  0  0  0  0  6  0  0  0  0  0  0\n   12.4749   -1.7046    0.5839 H   0  0  0  0  0  0  0  0  0  0  0  0\n   17.8310   -5.1795   -0.3652 H   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6662   -5.7081    5.2069 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3627   -5.4572    3.9536 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6209   -4.7599   -2.4114 H   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4468   -4.5890   -5.0444 H   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8191  -10.6723    0.3591 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9409  -10.1369   -5.1983 H   0  0  0  0  0  0  0  0  0  0  0  0\n   16.2582  -10.3930   -3.9739 H   0  0  0  0  0  0  0  0  0  0  0  0\n   17.0014  -11.0826    2.4636 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1894  -11.2582    5.0672 H   0  0  0  0  0  0  0  0  0  0  0  0\n   12.1461  -14.1455   -0.6043 H   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  1  5  1  0  0  0  0\n  1  6  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  6  1  0  0  0  0\n  2  9  1  0  0  0  0\n  2 10  1  0  0  0  0\n  2 14  1  0  0  0  0\n  3  4  1  0  0  0  0\n  3 10  1  0  0  0  0\n  3 11  1  0  0  0  0\n  3 15  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  7  1  0  0  0  0\n  4 11  1  0  0  0  0\n  4 16  1  0  0  0  0\n  5  6  1  0  0  0  0\n  5  7  1  0  0  0  0\n  5  8  1  0  0  0  0\n  5 17  1  0  0  0  0\n  6  8  1  0  0  0  0\n  6  9  1  0  0  0  0\n  6 18  1  0  0  0  0\n  7  8  1  0  0  0  0\n  7 11  1  0  0  0  0\n  7 12  1  0  0  0  0\n  7 19  1  0  0  0  0\n  8  9  1  0  0  0  0\n  8 12  1  0  0  0  0\n  8 20  1  0  0  0  0\n  9 10  1  0  0  0  0\n  9 12  1  0  0  0  0\n  9 21  1  0  0  0  0\n 10 11  1  0  0  0  0\n 10 12  1  0  0  0  0\n 10 22  1  0  0  0  0\n 11 12  1  0  0  0  0\n 11 23  1  0  0  0  0\n 12 24  1  0  0  0  0\n  1 13  1  0  0  0  0\nM  CHG  2   1  -1  12  -1\nM  END\n>  <atomid>\n12\n\n>  <bondid>\n0\n\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl261\n\n$$$$\nvitamin B12\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n103114  0     0  0            999 V2000\n   10.0126   -6.0489  -13.5041 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2665   -4.8038  -15.4155 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0719   -4.7946  -16.7187 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8472   -5.1986  -15.5844 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.9546   -4.9961  -16.0533 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.4802   -5.5205  -14.6269 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.3257   -5.3477  -15.0230 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.2452   -5.9492  -13.5110 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.9757   -6.4703  -12.1989 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.5273   -7.2118  -10.3388 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.0197   -7.7946   -8.9278 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.5538   -8.5006   -7.2370 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8115   -8.8424   -6.3353 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3804   -8.3915   -7.4797 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3227   -8.6564   -7.0103 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7712   -8.1015   -8.4087 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5465   -8.2236   -8.2815 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6917   -7.9286  -10.2200 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4134   -6.8953  -11.4432 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6144   -6.7969  -11.5192 Co  0  0  0  0  0  6  0  0  0  0  0  0\n   12.2857   -5.9898  -13.6053 N   0  0  0  0  0  4  0  0  0  0  0  0\n   15.8974   -6.2784  -12.7299 N   0  0  0  0  0  4  0  0  0  0  0  0\n   14.9683   -7.6066   -9.4297 N   0  0  0  0  0  4  0  0  0  0  0  0\n   11.3583   -7.3147  -10.3330 N   0  0  0  0  0  3  0  0  0  0  0  0\n   13.6089   -4.2778  -10.6365 C   0  0  0  0  0  4  0  0  0  0  0  0\n    9.5801   -8.7584  -13.9042 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4453   -2.8614  -14.8927 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4101   -5.8354  -16.5037 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1634   -2.8242  -17.7312 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3864   -5.7747  -18.2208 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.5249   -7.0185  -16.5061 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.7675   -3.5479  -15.3782 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.4569  -10.0661   -7.3817 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.4052   -7.9169   -6.3130 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8156   -7.2528   -4.7450 H   0  0  0  0  0  0  0  0  0  0  0  0\n   15.7237  -10.7118   -5.8515 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9023  -10.1564   -7.4863 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7957   -6.6276   -6.9202 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9087   -6.6565  -10.0941 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0783   -9.8969  -11.0575 H   0  0  0  0  0  0  0  0  0  0  0  0\n   15.5150   -4.2054  -18.0068 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7364   -9.4165   -5.0289 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5533  -10.7271   -8.9073 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9804   -5.8129  -10.9834 H   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6757  -11.3323  -13.1820 N   0  0  0  0  0  4  0  0  0  0  0  0\n   12.8841  -12.0634  -13.1495 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5374  -11.8140  -13.4950 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3354  -12.8901  -13.6165 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2952  -13.0084  -13.3833 N   0  0  0  0  0  0  0  0  0  0  0  0\n   15.5439  -11.4691  -13.6699 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.2732  -12.1354  -13.9651 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.0710  -13.2114  -14.0865 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0926  -13.5594  -13.9132 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.2799  -11.7879  -14.1397 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.7994  -13.8782  -14.3561 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8380  -13.7498  -13.5877 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9307  -14.2220  -12.4729 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5996  -14.2426  -12.2918 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7574  -15.0262  -10.3782 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5040  -14.9970  -10.5281 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2774  -15.6088  -12.6360 H   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7189  -11.9931  -14.1935 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6269  -15.5329  -15.5283 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6856  -17.1207  -10.1971 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3152  -17.1087   -8.3976 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0383  -13.2992   -8.9005 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7202  -15.8056  -13.5771 H   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7327  -12.3458  -12.9365 P   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7235  -12.3118  -12.2754 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.7534  -13.6586  -12.6192 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5577  -13.4895  -11.9328 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4710  -13.0662  -12.5859 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.7849  -11.8224  -15.4096 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.7267  -12.4339  -11.0249 H   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2585  -14.6633  -11.3010 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2011  -14.0490  -11.8767 N   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2182  -12.9593  -10.6096 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3586  -11.2160  -12.3884 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.1340  -13.0039   -9.7572 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5516   -7.1810  -10.1929 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2010   -6.3792  -10.1999 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4260   -8.3234  -10.2821 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6452   -3.0804  -15.0021 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2828   -2.3624  -15.0118 N   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3796   -4.2070  -15.0993 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6112   -4.4140  -18.1337 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5579   -2.8834  -18.0956 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.9350   -1.8793  -18.0952 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5332   -1.9770  -18.0310 O   0  0  0  0  0  0  0  0  0  0  0  0\n   17.6329   -2.8548  -15.4074 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.4644   -3.4580  -15.4721 N   0  0  0  0  0  0  0  0  0  0  0  0\n   16.6644   -2.1519  -15.4294 O   0  0  0  0  0  0  0  0  0  0  0  0\n   20.3112   -4.5349  -12.8385 H   0  0  0  0  0  0  0  0  0  0  0  0\n   20.3404   -7.4169  -13.9250 C   0  0  0  0  0  0  0  0  0  0  0  0\n   20.0913   -8.6322  -13.9674 C   0  0  0  0  0  0  0  0  0  0  0  0\n   20.6425   -9.7675  -13.9743 C   0  0  0  0  0  0  0  0  0  0  0  0\n   21.1661  -10.6445  -13.9755 N   0  0  0  0  0  0  0  0  0  0  0  0\n   19.7050  -10.3118  -14.0278 O   0  0  0  0  0  0  0  0  0  0  0  0\n   17.5025  -11.2248   -5.7907 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.7454  -12.5808   -5.8163 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.1068  -13.4968   -5.8671 N   0  0  0  0  0  0  0  0  0  0  0  0\n   18.9107  -13.2774   -5.7859 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5851   -2.8203  -10.1780 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1 19  1  0  0  0  0\n  1 21  1  0  0  0  0\n  1 26  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2 27  1  0  0  0  0\n  2 28  1  0  0  0  0\n  3  4  1  0  0  0  0\n  3 29  1  0  0  0  0\n  3 30  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4 21  2  0  0  0  0\n  5  6  2  0  0  0  0\n  5 41  1  0  0  0  0\n  6  7  1  0  0  0  0\n  6 22  1  0  0  0  0\n  7  8  1  0  0  0  0\n  7 31  1  0  0  0  0\n  7 32  1  0  0  0  0\n  8  9  1  0  0  0  0\n  8 93  1  0  0  0  0\n  8 94  1  0  0  0  0\n  9 10  1  0  0  0  0\n  9 22  2  0  0  0  0\n 10 11  2  0  0  0  0\n 11 12  1  0  0  0  0\n 11 23  1  0  0  0  0\n 12 13  1  0  0  0  0\n 12 33  1  0  0  0  0\n 12 34  1  0  0  0  0\n 13 14  1  0  0  0  0\n 13 35  1  0  0  0  0\n 13 36  1  0  0  0  0\n 14 15  1  0  0  0  0\n 14 23  2  0  0  0  0\n 15 16  2  0  0  0  0\n 15 42  1  0  0  0  0\n 16 17  1  0  0  0  0\n 16 24  1  0  0  0  0\n 17 18  1  0  0  0  0\n 17 37  1  0  0  0  0\n 17 38  1  0  0  0  0\n 18 19  1  0  0  0  0\n 18 39  1  0  0  0  0\n 18 40  1  0  0  0  0\n 19 24  1  0  0  0  0\n 19 44  1  0  0  0  0\n 20 21  1  0  0  0  0\n 20 22  1  0  0  0  0\n 20 23  1  0  0  0  0\n 20 24  1  0  0  0  0\n 20 25  1  0  0  0  0\n 20 45  1  0  0  0  0\n 25103  3  0  0  0  0\n 27 83  1  0  0  0  0\n 30 86  1  0  0  0  0\n 32 90  1  0  0  0  0\n 36 99  1  0  0  0  0\n 37 43  1  0  0  0  0\n 39 80  1  0  0  0  0\n 43 77  1  0  0  0  0\n 45 46  2  0  0  0  0\n 45 47  1  0  0  0  0\n 46 49  1  0  0  0  0\n 47 48  2  0  0  0  0\n 47 50  1  0  0  0  0\n 48 49  1  0  0  0  0\n 48 53  1  0  0  0  0\n 49 58  1  0  0  0  0\n 50 51  2  0  0  0  0\n 51 52  1  0  0  0  0\n 51 54  1  0  0  0  0\n 52 53  2  0  0  0  0\n 52 55  1  0  0  0  0\n 56 57  1  0  0  0  0\n 56 58  1  0  0  0  0\n 56 62  1  0  0  0  0\n 56 63  1  0  0  0  0\n 57 60  1  0  0  0  0\n 57 67  1  0  0  0  0\n 57 69  1  0  0  0  0\n 58 59  1  0  0  0  0\n 58 61  1  0  0  0  0\n 59 60  1  0  0  0  0\n 60 64  1  0  0  0  0\n 60 66  1  0  0  0  0\n 64 65  1  0  0  0  0\n 68 69  1  0  0  0  0\n 68 70  1  0  0  0  0\n 68 73  2  0  0  0  0\n 68 78  1  0  0  0  0\n 70 71  1  0  0  0  0\n 71 72  1  0  0  0  0\n 71 74  1  0  0  0  0\n 71 75  1  0  0  0  0\n 72 76  1  0  0  0  0\n 76 77  1  0  0  0  0\n 77 79  2  0  0  0  0\n 80 81  1  0  0  0  0\n 80 82  2  0  0  0  0\n 83 85  2  0  0  0  0\n 86 87  1  0  0  0  0\n 87 88  1  0  0  0  0\n 87 89  2  0  0  0  0\n 90 91  1  0  0  0  0\n 90 92  2  0  0  0  0\n 94 95  1  0  0  0  0\n 95 96  1  0  0  0  0\n 96 97  1  0  0  0  0\n 96 98  2  0  0  0  0\n 99100  1  0  0  0  0\n100101  1  0  0  0  0\n100102  2  0  0  0  0\n 83 84  1  0  0  0  0\nM  CHG  4  20   3  24  -1  25  -1  78  -1\nM  END\n>  <atomid>\n83\n\n>  <bondid>\n113\n\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl262\n\n$$$$\nsucrose\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 31 32  0     0  0            999 V2000\n    5.2890   -7.5286   -0.0614 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6624   -5.1211   -0.7785 H   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2941   -5.7056    2.0759 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9494   -7.5048    1.3153 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0481   -8.2707   -1.1553 H   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2890   -4.4624   -0.8035 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3001   -5.0862    0.5701 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1244   -4.8497    1.9163 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5502   -3.7821    0.2011 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2117   -6.2026    0.8774 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3725   -5.8284   -1.8918 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3225   -6.4586   -0.4301 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2839   -6.9390   -1.5749 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5059   -7.2324   -2.8968 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5117   -6.1824   -4.0570 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2609   -5.5788   -0.5948 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9153   -6.8782   -0.1205 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4269   -6.7225    2.4575 H   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3241   -8.0774    2.1099 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.1140   -7.8468   -1.0282 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3110   -9.0856   -0.5158 H   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5240   -8.9610    1.2547 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7799  -10.1548    1.8160 H   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8853   -8.7670    1.9939 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6894   -7.6334    1.4979 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4355   -6.9446    0.0877 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0396   -5.5329    0.1043 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4050   -5.2699   -0.5577 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7885   -9.0951   -0.3085 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.1875  -10.4160   -0.8042 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.0011  -11.7179   -0.6982 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1 12  1  0  0  0  0\n  2 12  1  0  0  0  0\n  3 10  1  0  0  0  0\n  4 10  1  0  0  0  0\n  5 13  1  0  0  0  0\n  6 16  1  0  0  0  0\n  7  8  1  0  0  0  0\n  7  9  1  0  0  0  0\n  7 10  1  0  0  0  0\n  7 16  1  0  0  0  0\n 10 12  1  0  0  0  0\n 11 13  1  0  0  0  0\n 11 16  1  0  0  0  0\n 12 13  1  0  0  0  0\n 13 14  1  0  0  0  0\n 14 15  1  0  0  0  0\n 16 17  1  0  0  0  0\n 17 26  1  0  0  0  0\n 18 25  1  0  0  0  0\n 19 25  1  0  0  0  0\n 20 26  1  0  0  0  0\n 20 29  1  0  0  0  0\n 21 29  1  0  0  0  0\n 22 23  1  0  0  0  0\n 22 24  1  0  0  0  0\n 22 25  1  0  0  0  0\n 22 29  1  0  0  0  0\n 25 26  1  0  0  0  0\n 26 27  1  0  0  0  0\n 29 30  1  0  0  0  0\n 30 31  1  0  0  0  0\n 27 28  1  0  0  0  0\nM  END\n>  <atomid>\n20\n\n>  <bondid>\n22\n\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl263\n\n$$$$\nMo7O24\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 31 42  0     0  0            999 V2000\n    8.3825   -6.6288    0.5307 Mo  0  0  0  0  0  0  0  0  0  0  0  0\n    8.0566   -8.0054    0.0391 O   0  0  0  0  0  2  0  0  0  0  0  0\n    9.6225   -7.1718    1.1905 O   0  0  0  0  0  2  0  0  0  0  0  0\n    7.4634   -4.7037    0.3717 Mo  0  0  0  0  0  0  0  0  0  0  0  0\n    8.7036   -5.2443    1.0328 O   0  0  0  0  0  2  0  0  0  0  0  0\n    6.5457   -2.7785    0.2130 Mo  0  0  0  0  0  0  0  0  0  0  0  0\n    5.3026   -2.2284   -0.4344 O   0  0  0  0  0  2  0  0  0  0  0  0\n    6.8689   -1.3946    0.7160 O   0  0  0  0  0  2  0  0  0  0  0  0\n    7.7859   -3.3192    0.8741 O   0  0  0  0  0  2  0  0  0  0  0  0\n    7.8935   -5.8337   -1.3972 Mo  0  0  0  0  0  0  0  0  0  0  0  0\n    7.5257   -7.2356   -1.8700 O   0  0  0  0  0  2  0  0  0  0  0  0\n    9.1639   -6.3573   -0.7629 O   0  0  0  0  0  2  0  0  0  0  0  0\n    8.6584   -5.5970   -2.7259 O   0  0  0  0  0  2  0  0  0  0  0  0\n    6.9618   -3.8926   -1.5768 Mo  0  0  0  0  0  0  0  0  0  0  0  0\n    5.6757   -3.3420   -2.2214 O   0  0  0  0  0  2  0  0  0  0  0  0\n    6.6072   -5.3104   -2.0267 O   0  0  0  0  0  2  0  0  0  0  0  0\n    7.3276   -2.5064   -1.0793 O   0  0  0  0  0  2  0  0  0  0  0  0\n    8.2454   -4.4322   -0.9197 O   0  0  0  0  0  3  0  0  0  0  0  0\n    7.7257   -3.6594   -2.9288 O   0  0  0  0  0  2  0  0  0  0  0  0\n    6.3294   -6.3423    1.1548 Mo  0  0  0  0  0  0  0  0  0  0  0  0\n    5.9769   -7.6983    0.6446 O   0  0  0  0  0  2  0  0  0  0  0  0\n    7.5984   -6.9043    1.8353 O   0  0  0  0  0  2  0  0  0  0  0  0\n    5.5195   -6.6078    2.4374 O   0  0  0  0  0  2  0  0  0  0  0  0\n    7.1374   -6.0780   -0.1178 O   0  0  0  0  0  4  0  0  0  0  0  0\n    5.4562   -4.4102    0.9865 Mo  0  0  0  0  0  0  0  0  0  0  0  0\n    5.1170   -5.7537    0.4947 O   0  0  0  0  0  2  0  0  0  0  0  0\n    6.6789   -4.9771    1.6760 O   0  0  0  0  0  3  0  0  0  0  0  0\n    4.2276   -3.8981    0.3645 O   0  0  0  0  0  2  0  0  0  0  0  0\n    5.7599   -3.0518    1.5169 O   0  0  0  0  0  2  0  0  0  0  0  0\n    4.6888   -4.6683    2.2585 O   0  0  0  0  0  2  0  0  0  0  0  0\n    6.2191   -4.1522   -0.2765 O   0  0  0  0  0  4  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  2  0  0  0  0\n  1  5  1  0  0  0  0\n  1 12  1  0  0  0  0\n  1 22  1  0  0  0  0\n  1 24  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  9  1  0  0  0  0\n  4 18  1  0  0  0  0\n  4 24  1  0  0  0  0\n  4 27  1  0  0  0  0\n  4 31  1  0  0  0  0\n  6  7  2  0  0  0  0\n  6  8  2  0  0  0  0\n  6  9  1  0  0  0  0\n  6 17  1  0  0  0  0\n  6 29  1  0  0  0  0\n  6 31  1  0  0  0  0\n 10 11  2  0  0  0  0\n 10 12  1  0  0  0  0\n 10 13  2  0  0  0  0\n 10 16  1  0  0  0  0\n 10 18  1  0  0  0  0\n 10 24  1  0  0  0  0\n 14 15  2  0  0  0  0\n 14 16  1  0  0  0  0\n 14 17  1  0  0  0  0\n 14 18  1  0  0  0  0\n 14 19  2  0  0  0  0\n 14 31  1  0  0  0  0\n 20 21  2  0  0  0  0\n 20 22  1  0  0  0  0\n 20 24  1  0  0  0  0\n 20 26  1  0  0  0  0\n 20 27  1  0  0  0  0\n 25 26  1  0  0  0  0\n 25 27  1  0  0  0  0\n 25 28  2  0  0  0  0\n 25 29  1  0  0  0  0\n 25 30  2  0  0  0  0\n 25 31  1  0  0  0  0\n 20 23  2  0  0  0  0\nM  CHG  8   1   6   2  -2   3  -2   4   6   5  -2   6   6   7  -2   8  -2\nM  END\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl264\n\n$$$$\nC20H20\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 40 50  0     0  0            999 V2000\n    7.5483   -7.7451   -3.3419 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3984   -5.8792   -3.4318 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3399   -6.5425   -1.9898 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6820   -3.9425   -1.6474 H   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8163   -7.1034   -1.6635 H   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5722   -4.7343   -0.6304 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1701   -7.2380   -0.8890 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8300   -6.9765   -2.5544 H   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6631   -7.1690   -1.5375 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4077   -9.5239   -2.1472 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.9006  -10.0139    0.4722 H   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6600   -8.8749    0.2914 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5136   -5.9115   -0.4190 H   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5338   -7.8406    1.4379 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6981   -8.8654    3.4177 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4046  -10.6907    1.7143 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3185   -9.3106    0.9700 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4958  -10.8075   -0.1783 H   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5552   -7.8780    2.6983 H   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8522   -9.1147    0.4514 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1601   -8.2997    0.2353 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5774   -7.5989    1.5700 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6577   -4.0099    0.1683 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0808   -6.4894   -0.1982 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9123   -5.4699   -0.9424 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9155   -8.2329    2.0184 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0766   -7.5513    0.9147 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6780   -6.9857    3.3021 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5861   -5.8939   -0.2667 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9973   -5.0597    1.9875 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3193   -5.8429    1.5048 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4740   -4.7173    2.5743 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9809   -7.1457    1.9811 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8270   -6.1245    1.2483 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0023   -5.4308    0.1366 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9125   -8.9385   -1.4737 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2374   -9.3522   -0.1173 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4116   -8.6461   -1.2148 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7726   -9.9758   -2.5047 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2577   -7.6250   -1.9478 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1 40  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  9  1  0  0  0  0\n  3 25  1  0  0  0  0\n  3 40  1  0  0  0  0\n  4 25  1  0  0  0  0\n  5  7  1  0  0  0  0\n  6 29  1  0  0  0  0\n  7 21  1  0  0  0  0\n  7 29  1  0  0  0  0\n  7 40  1  0  0  0  0\n  8  9  1  0  0  0  0\n  9 24  1  0  0  0  0\n  9 38  1  0  0  0  0\n 10 38  1  0  0  0  0\n 11 12  1  0  0  0  0\n 12 17  1  0  0  0  0\n 12 27  1  0  0  0  0\n 12 38  1  0  0  0  0\n 13 24  1  0  0  0  0\n 14 27  1  0  0  0  0\n 15 26  1  0  0  0  0\n 16 17  1  0  0  0  0\n 17 26  1  0  0  0  0\n 17 37  1  0  0  0  0\n 18 37  1  0  0  0  0\n 19 22  1  0  0  0  0\n 20 21  1  0  0  0  0\n 21 22  1  0  0  0  0\n 21 37  1  0  0  0  0\n 22 26  1  0  0  0  0\n 22 34  1  0  0  0  0\n 23 35  1  0  0  0  0\n 24 27  1  0  0  0  0\n 24 35  1  0  0  0  0\n 25 29  1  0  0  0  0\n 25 35  1  0  0  0  0\n 26 33  1  0  0  0  0\n 27 33  1  0  0  0  0\n 28 33  1  0  0  0  0\n 29 34  1  0  0  0  0\n 30 34  1  0  0  0  0\n 31 32  1  0  0  0  0\n 31 33  1  0  0  0  0\n 31 35  1  0  0  0  0\n 36 37  1  0  0  0  0\n 36 38  1  0  0  0  0\n 36 39  1  0  0  0  0\n 36 40  1  0  0  0  0\n 31 34  1  0  0  0  0\nM  END\n>  <atomid>\n19\n\n>  <bondid>\n27\n\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl265\n\n$$$$\nCo4CO12\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 28 33  0     0  0            999 V2000\n   11.5119   -6.3872    0.2843 Co  0  0  0  0  0  0  0  0  0  0  0  0\n   14.2537   -5.1567    0.9962 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1271   -4.1574   -1.8138 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1405   -4.5859    2.5258 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.6477   -4.5559    1.3649 O   0  0  0  0  0  3  0  0  0  0  0  0\n   10.9606   -3.0390   -2.8593 O   0  0  0  0  0  3  0  0  0  0  0  0\n    9.4644   -3.6875    3.6182 O   0  0  0  0  0  3  0  0  0  0  0  0\n   10.6811  -11.2763    3.0909 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1263   -9.1532    3.4762 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6597  -11.9110    3.5304 O   0  0  0  0  0  3  0  0  0  0  0  0\n   11.3435   -8.7342    4.0978 O   0  0  0  0  0  3  0  0  0  0  0  0\n    8.4053   -7.8212   -2.1068 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9144  -10.0973   -2.4249 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1429   -7.1175   -2.4596 O   0  0  0  0  0  3  0  0  0  0  0  0\n    7.4262  -10.5365   -2.9426 O   0  0  0  0  0  3  0  0  0  0  0  0\n   14.0567   -9.1427   -1.5415 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7234  -11.1613   -1.8250 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5969   -8.6889   -1.7190 O   0  0  0  0  0  3  0  0  0  0  0  0\n   14.0925  -11.7138   -2.1238 O   0  0  0  0  0  3  0  0  0  0  0  0\n    7.8227   -9.3450    1.4166 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6523   -9.0552    2.5252 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6963  -10.0134    2.2132 Co  0  0  0  0  0  0  0  0  0  0  0  0\n   13.6352  -10.5336    1.7363 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.6119  -11.0927    3.0899 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9779  -10.0343   -1.2076 Co  0  0  0  0  0  0  0  0  0  0  0  0\n   11.1257   -9.3771   -3.5447 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9140   -9.2088   -1.3937 Co  0  0  0  0  0  0  0  0  0  0  0  0\n   11.3211   -9.1075   -6.0026 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  1 22  1  0  0  0  0\n  1 25  1  0  0  0  0\n  1 27  1  0  0  0  0\n  2  5  3  0  0  0  0\n  4  7  3  0  0  0  0\n  8 10  3  0  0  0  0\n  8 22  1  0  0  0  0\n  9 11  3  0  0  0  0\n  9 22  1  0  0  0  0\n 12 14  3  0  0  0  0\n 12 27  1  0  0  0  0\n 13 15  3  0  0  0  0\n 13 27  1  0  0  0  0\n 16 18  3  0  0  0  0\n 16 25  1  0  0  0  0\n 17 19  3  0  0  0  0\n 17 25  1  0  0  0  0\n 20 21  2  0  0  0  0\n 20 22  1  0  0  0  0\n 20 27  1  0  0  0  0\n 22 23  1  0  0  0  0\n 22 25  1  0  0  0  0\n 22 27  1  0  0  0  0\n 23 24  2  0  0  0  0\n 23 25  1  0  0  0  0\n 25 26  1  0  0  0  0\n 25 27  1  0  0  0  0\n 26 27  1  0  0  0  0\n 26 28  2  0  0  0  0\n  3  6  3  0  0  0  0\nM  END\n>  <atomid>\n0\n\n>  <bondid>\n4\n\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl266\n\n$$$$\nFeCO5\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 11 10  0     0  0            999 V2000\n   10.8202   -7.3426    0.0023 Fe  0  0  0  0  0  0  0  0  0  0  0  0\n    8.9246   -7.3587    0.0087 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7011   -7.0667   -1.5928 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7827   -7.6197    1.5703 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8213   -5.0591    0.3328 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8193   -9.6084   -0.3284 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4397   -6.8395   -2.8953 O   0  0  0  0  0  3  0  0  0  0  0  0\n   12.5339   -7.8271    2.8412 O   0  0  0  0  0  3  0  0  0  0  0  0\n    7.4162   -7.3784    0.0570 O   0  0  0  0  0  3  0  0  0  0  0  0\n   10.8213   -3.5367    0.5648 O   0  0  0  0  0  3  0  0  0  0  0  0\n   10.8194  -11.1133   -0.5606 O   0  0  0  0  0  3  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  1  5  1  0  0  0  0\n  1  6  1  0  0  0  0\n  2  9  3  0  0  0  0\n  3  7  3  0  0  0  0\n  4  8  3  0  0  0  0\n  6 11  3  0  0  0  0\n  5 10  3  0  0  0  0\nM  END\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl267\n\n$$$$\nChlorophyll A\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 71 79  0     0  0            999 V2000\n   11.3221  -15.0514  -29.5828 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2305  -13.9637  -30.5522 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1059  -13.0987  -31.6421 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2769  -12.0678  -31.9997 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0261  -10.6405  -32.9711 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4490   -9.5603  -33.3639 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3289   -8.2505  -34.2571 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7498   -7.5990  -34.3211 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7441   -8.4574  -33.4907 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4825   -8.0571  -33.3382 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.5957   -9.1542  -32.3699 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.1341   -8.8838  -32.1895 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.7396  -10.0405  -31.2878 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.5583  -11.0170  -30.9261 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.7584  -12.4631  -29.9570 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3808  -13.5626  -29.5873 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.5088  -14.8558  -28.7128 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0728  -15.5355  -28.6110 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.0058  -16.8885  -27.9733 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.0886  -14.6273  -29.4323 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7585  -13.1416  -30.2471 N   0  0  0  0  0  3  0  0  0  0  0  0\n   10.9009  -12.4760  -31.3615 N   0  0  0  0  0  4  0  0  0  0  0  0\n   12.0949   -9.9691  -32.6922 N   0  0  0  0  0  3  0  0  0  0  0  0\n   14.9259  -10.6395  -31.5603 N   0  0  0  0  0  4  0  0  0  0  0  0\n   12.9186  -11.5362  -31.4724 Mg  0  0  0  0  0  4  0  0  0  0  0  0\n   13.5390  -18.2856  -26.9337 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3880  -15.6838  -31.4531 H   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9642  -12.3313  -30.8874 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4960  -13.7478  -32.9395 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8210   -7.6311  -35.0395 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.1900   -6.0441  -35.2381 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9034   -5.4078  -35.2032 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.0857   -7.4693  -32.9022 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.4839  -10.2094  -30.7490 C   0  0  0  0  0  0  0  0  0  0  0  0\n   20.7720  -11.1118  -31.7098 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.0404  -15.4632  -27.9161 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1151  -16.6720  -27.3536 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3024  -16.5936  -28.5919 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2137  -18.6651  -30.3987 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6234  -17.6524  -29.6841 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8802  -17.6043  -29.3038 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7110  -18.5710  -29.6384 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6710  -14.2462  -30.7495 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2457  -14.2569  -29.2809 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0077  -15.0783  -28.8478 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.7950  -14.5946  -25.7989 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4992  -15.1614  -27.9790 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.7321  -14.3398  -28.4070 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6748  -12.8007  -28.3915 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2254  -14.4258  -27.5386 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9849  -15.2471  -27.1029 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0404  -16.7958  -27.1222 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.5187  -15.3305  -26.2394 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.7162  -14.5115  -26.6702 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.6570  -12.9703  -26.6494 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1160  -12.3347  -25.3476 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4772  -12.8605  -23.6798 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.8305  -13.0506  -25.7933 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4219  -12.9260  -26.1739 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1490  -10.7913  -25.3419 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.8590  -10.0255  -25.6682 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.5716   -7.7185  -25.9970 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0884   -8.2829  -27.4995 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.8731   -8.4769  -25.6698 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.6206   -8.2171  -24.8809 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.5885   -6.1725  -25.9962 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.7089   -5.4213  -26.3218 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.7165   -3.8688  -26.3280 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0177   -1.5849  -26.6649 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0177   -3.1249  -26.6649 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3102   -3.9011  -26.9784 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1 20  2  0  0  0  0\n  1 38  1  0  0  0  0\n  2 22  2  0  0  0  0\n  2 43  1  0  0  0  0\n  3  4  1  0  0  0  0\n  3 28  1  0  0  0  0\n  3 29  1  0  0  0  0\n  3 43  1  0  0  0  0\n  4  5  2  0  0  0  0\n  4 22  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  2  0  0  0  0\n  6 23  1  0  0  0  0\n  7  8  1  0  0  0  0\n  7 30  1  0  0  0  0\n  8  9  2  0  0  0  0\n  8 31  1  0  0  0  0\n  9 10  1  0  0  0  0\n  9 23  1  0  0  0  0\n 10 11  2  0  0  0  0\n 11 12  1  0  0  0  0\n 11 24  1  0  0  0  0\n 12 13  2  0  0  0  0\n 12 33  1  0  0  0  0\n 13 14  1  0  0  0  0\n 13 34  1  0  0  0  0\n 14 15  1  0  0  0  0\n 14 24  2  0  0  0  0\n 15 16  2  0  0  0  0\n 16 17  1  0  0  0  0\n 16 21  1  0  0  0  0\n 17 18  2  0  0  0  0\n 17 36  1  0  0  0  0\n 18 19  1  0  0  0  0\n 18 20  1  0  0  0  0\n 19 26  2  0  0  0  0\n 19 38  1  0  0  0  0\n 20 21  1  0  0  0  0\n 21 25  1  0  0  0  0\n 22 25  1  0  0  0  0\n 23 25  1  0  0  0  0\n 24 25  1  0  0  0  0\n 27 43  1  0  0  0  0\n 31 32  2  0  0  0  0\n 34 35  1  0  0  0  0\n 37 38  1  0  0  0  0\n 38 41  1  0  0  0  0\n 39 40  1  0  0  0  0\n 40 41  1  0  0  0  0\n 41 42  2  0  0  0  0\n 43 44  1  0  0  0  0\n 44 45  1  0  0  0  0\n 45 48  1  0  0  0  0\n 46 53  1  0  0  0  0\n 46 58  1  0  0  0  0\n 47 48  1  0  0  0  0\n 47 50  1  0  0  0  0\n 48 49  2  0  0  0  0\n 50 51  1  0  0  0  0\n 51 52  1  0  0  0  0\n 51 54  2  0  0  0  0\n 53 54  1  0  0  0  0\n 54 55  1  0  0  0  0\n 56 57  1  0  0  0  0\n 56 58  1  0  0  0  0\n 56 59  1  0  0  0  0\n 56 60  1  0  0  0  0\n 60 61  1  0  0  0  0\n 61 64  1  0  0  0  0\n 62 63  1  0  0  0  0\n 62 64  1  0  0  0  0\n 62 65  1  0  0  0  0\n 62 66  1  0  0  0  0\n 66 67  1  0  0  0  0\n 67 68  1  0  0  0  0\n 68 70  1  0  0  0  0\n 70 71  1  0  0  0  0\n 69 70  1  0  0  0  0\nM  CHG  3  21  -1  23  -1  25   2\nM  END\n>  <atomid>\n31\n\n>  <bondid>\n44\n\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl268\n\n$$$$\n"),o=function(n,e,t){var r=n.reduce((function(n,e){var t=Ju(e).file;return t&&-1===n.indexOf(t)&&n.push(t),n}),[]);return Promise.all(r.map((function(n){return Uu(e+n).catch((function(){return null}))}))).then((function(n){return n.forEach((function(n){n&&(t.innerHTML+=n)})),r.filter((function(e,t){return!!n[t]}))}))}(r,n+"/templates/",e);return o.then((function(n){return r.map((function(e){var t=Ju(e);return t.file&&(e.props.prerender=-1!==n.indexOf(t.file)?"#".concat(t.id):""),e}))}))};function Uu(n){return fetch(n,{credentials:"same-origin"}).then((function(e){if(e.ok)return e.text();throw Error("Could not fetch "+n)}))}function Ju(n){var e=n.props.prerender,t=e&&e.split("#",2);return{file:e&&t[0],id:e&&t[1]}}function qu(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Wu(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?qu(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):qu(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function Xu(n,e,t){return new Promise((function(r,o){n({type:"MODAL_OPEN",data:{name:e,prop:Wu(Wu({},t),{},{onResult:r,onCancel:o})}})}))}function Qu(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function nd(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Qu(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Qu(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function ed(n){return{type:"TMPL_SELECT",data:{selected:n}}}function td(n){var e=new u.F_l,t=n.filter((function(n){return"User Templates"===n.props.group})).map((function(n){return{struct:e.serialize(n.struct),props:Object.assign({},(0,y.omit)(["group"],n.props))}}));zn.setItem("ketcher-tmpls",t)}var rd={lib:[],selected:null,filter:"",group:null,attach:{},mode:"classic"},od=["TMPL_INIT","TMPL_SELECT","TMPL_CHANGE_GROUP","TMPL_CHANGE_FILTER"],id=["INIT_ATTACH","SET_ATTACH_POINTS","SET_TMPL_NAME"],ad=["type","action"];function ld(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function cd(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?ld(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):ld(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function sd(n,e,t){var r=t.editor,o=t.server;return"function"==typeof n.selected?n.selected(r,o):!(!n.action||!n.action.tool)&&(0,y.isEqual)(e,n.action)}function ud(n,e){var t=e.editor,r=e.server,o=e.options;return"function"==typeof n.disabled&&n.disabled(t,r,o)}function dd(n,e){var t=e.options;return"function"==typeof n.hidden&&n.hidden(t)}function pd(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function hd(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?pd(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):pd(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var fd={lib:[],functionalGroupInfo:null,mode:"fg"},md=function(n){return{type:"FG_HIGHLIGHT",payload:n}};function vd(n,e){n(md(e))}function gd(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}var bd=new Map,Cd=function(){function n(){(0,c.Z)(this,n)}return(0,s.Z)(n,null,[{key:"prepareStruct",value:function(n){if(n.sgroups.size>0){var e=n.clone();return e.sgroups.delete(0),e}return n}},{key:"render",value:function(n,e){var t=arguments.length>2&&void 0!==arguments[2]?arguments[2]:{};if(n&&e){var o=t.cachePrefix,i="".concat(void 0===o?"":o).concat(e.name);if(bd.has(i))return void(n.innerHTML=bd.get(i));var a=this.prepareStruct(e);a.initHalfBonds(),a.initNeighbors(),a.setImplicitHydrogen(),a.markFragments();var l=new u.Hrh(n,function(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?gd(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):gd(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}({autoScale:!0},t));l.setMolecule(a),l.update(!0,t.viewSz),bd.set(i,l.clientArea.innerHTML)}}}]),n}();function yd(n){return new Promise((function(e,r){if(t.g.FileReader)e(Od);else if(t.g.ActiveXObject)try{var o=new ActiveXObject("Scripting.FileSystemObject");e((function(n){return Promise.resolve(function(n,e){var t=n.OpenTextFile(e.name,1),r=t.ReadAll();return t.Close(),r}(o,n))}))}catch(n){r(n)}else n?e(n.then((function(){throw Error("Server doesn't still support echo method")}))):r(new Error("Your browser does not support opening files locally"))}))}function Od(n){var e=n.name.endsWith("cdx");return new Promise((function(t,r){var o=new FileReader;o.onload=function(){var r=e?o.result.slice(37):o.result;n.msClose&&n.msClose(),t(r)},o.onerror=function(n){r(n)},e?o.readAsDataURL(n):o.readAsText(n,"UTF-8")}))}var wd={Alpha:"A",alpha:"α",Beta:"B",beta:"β",Gamma:"Г",gamma:"γ"},Sd=new RegExp("\\b"+Object.keys(wd).join("\\b|\\b")+"\\b","g");function Md(n){return n.replace(Sd,(function(n){return wd[n]}))}function xd(n,e){var t=e.trim(),r=new RegExp((0,y.escapeRegExp)(Md(t)),"i");return(0,y.flow)((0,y.filter)((function(n){return!t||function(n){return[n.struct.name,n.props.abbreviation,n.props.name].filter(Boolean).some((function(n){return r.test(Md(n))}))}(n)})),(0,y.reduce)((function(n,e){return n[e.props.group]?n[e.props.group].push(e):n[e.props.group]=[e],n}),{}))(n)}var jd=function(n){return n.enum.reduce((function(e,t,r){var o,i;return e.push({value:t,label:null!==(o=null==n||null===(i=n.enumNames)||void 0===i?void 0:i[r])&&void 0!==o?o:t}),e}),[])};function Ed(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Dd(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Ed(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Ed(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Ad={lib:[],mode:"fg"},$d=function(n,e){n.slice(0,50).forEach((function(n){var t=document.createElement("div");t.style.width="100px",t.style.height="100px",t.style.display="none",document.body.appendChild(t),Cd.render(t,n,Dd(Dd({},e),{},{autoScaleMargin:15})),t.remove()}))};function Nd(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Pd(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Nd(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Nd(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var kd={freqAtoms:[],currentAtom:0,opened:null,visibleTools:{select:"select-rectangle"}};function Id(n){var e=Object.keys(Re).find((function(e){return(0,y.isEqual)(n,Re[e].action)})),t=document.getElementById(e),o=t&&function(n,e){e=e||document.body;for(var t=n;t&&"hidden"!==window.getComputedStyle(t).overflow&&!t.classList.contains("opened");){if(t===e)return null;t=t.parentNode}return t}(t);return o&&""!==o.id?(0,r.Z)({},o.id,t.id):null}var Td=["type"],Bd=["buttons"];function Ld(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function _d(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Ld(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Ld(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Vd=(0,M.UY)({actionState:function(){var n,e=arguments.length>0&&void 0!==arguments[0]?arguments[0]:null,t=arguments.length>1?arguments[1]:void 0,r=t.type,o=t.action,i=(0,p.Z)(t,ad);switch(r){case"INIT":o=Ja["select-rectangle"].action;case"ACTION":n=function(n,e){var t=e.action,r=e.editor,o=e.server,i=e.options;if(t.tool){if(r.tool(t.tool,t.opts))return t}else"function"==typeof t&&t(r,o,i);return n}(e&&e.activeTool,cd(cd({},i),{},{action:o}));case"UPDATE":return Object.keys(Ja).reduce((function(n,e){var t=function(n,e,t){var r=Ja[n];return(0,y.pickBy)((function(n){return n}),{selected:sd(r,e,t),disabled:ud(r,t),hidden:dd(r,t)})}(e,n.activeTool,i);return(0,y.isEmpty)(t)||(n[e]=t),n}),{activeTool:n||e.activeTool});default:return e}},toolbar:function(){var n,e,t,r=arguments.length>0&&void 0!==arguments[0]?arguments[0]:kd,o=arguments.length>1?arguments[1]:void 0,i=o.type,a=o.data;switch(i){case"ACTION":var l=Id(o.action);return Pd(Pd({},r),{},l?{opened:null,visibleTools:Pd(Pd({},r.visibleTools),l)}:{opened:null});case"ADD_ATOMS":var c=(n=a,e=r.freqAtoms,t=r.currentAtom,n=(0,y.capitalize)(n),bn.indexOf(n)>-1||-1!==e.indexOf(n)?{freqAtoms:e}:(e[t]=n,{freqAtoms:e,currentAtom:t=(t+1)%7}));return Pd(Pd({},r),c);case"CLEAR_VISIBLE":var s=Id(o.data),u=function(n,e){var t=/(bond)(-)(common|stereo|query)/,r=window.innerHeight;return Object.keys(n).reduce((function(e,o){return"bond"===o&&r>700||"transform"===o&&r>800||"rgroup"===o&&r>850||"shape"===o&&r>900||(!o.match(t)||r>700)&&(e[o]=n[o]),e}),Pd({},e))}(r.visibleTools,s);return Pd(Pd({},r),{},{opened:null,visibleTools:Pd({},u)});case"OPENED":return a.isSelected&&r.opened?Pd(Pd({},r),{},{opened:null}):Pd(Pd({},r),{},{opened:a.menuName});case"UPDATE":case"MODAL_OPEN":return Pd(Pd({},r),{},{opened:null});default:return r}},modal:function(){var n=arguments.length>0&&void 0!==arguments[0]?arguments[0]:null,e=arguments.length>1?arguments[1]:void 0,t=e.type,r=e.data;if("UPDATE_FORM"===t){if(!n)return null;var o=de(n.form,e,n.name);return Wu(Wu({},n),{},{form:o})}switch(t){case"MODAL_CLOSE":return null;case"MODAL_OPEN":return{name:r.name,form:se[r.name]||null,prop:r.prop||null};default:return n}},server:function(){return arguments.length>0&&void 0!==arguments[0]?arguments[0]:null},editor:function(){return arguments.length>0&&void 0!==arguments[0]?arguments[0]:null},options:function(){var n=arguments.length>0&&void 0!==arguments[0]?arguments[0]:{},e=arguments.length>1?arguments[1]:void 0,t=e.type,r=e.data;return"APP_OPTIONS"===t?Fn(Fn({},n),{},{app:Fn(Fn({},n.app),r)}):"SAVE_SETTINGS"===t?Fn(Fn({},n),{},{settings:r}):"SAVE_CHECK_OPTS"===t?Fn(Fn({},n),{},{check:r}):"CHANGE_ANALYSE"===t?Fn(Fn({},n),{},{analyse:Fn(Fn(Fn({},n.analyse),r),{},{loading:!1})}):"ANALYSE_LOADING"===t?Fn(Fn({},n),{},{analyse:Fn(Fn({},n.analyse),{},{loading:!0})}):Zn.includes(t)?Fn(Fn({},n),{},{recognize:Fn(Fn({},n.recognize),r)}):n},templates:function(){var n=arguments.length>0&&void 0!==arguments[0]?arguments[0]:rd,e=arguments.length>1?arguments[1]:void 0;if(od.includes(e.type))return Object.assign({},n,e.data);if(id.includes(e.type)){var t=Object.assign({},n.attach,e.data);return nd(nd({},n),{},{attach:t})}if("TMPL_DELETE"===e.type){var r=Object.assign({},n),o=r.lib.filter((function(n){return n!==e.data.tmpl}));return nd(nd({},r),{},{lib:o})}return n},functionalGroups:function(){var n=arguments.length>0&&void 0!==arguments[0]?arguments[0]:fd,e=arguments.length>1?arguments[1]:void 0,t=e.type,r=e.payload;switch(t){case"FG_INIT":return hd(hd({},n),r);case"FG_HIGHLIGHT":return hd(hd({},n),{},{functionalGroupInfo:r});default:return n}},saltsAndSolvents:function(){var n=arguments.length>0&&void 0!==arguments[0]?arguments[0]:Ad,e=arguments.length>1?arguments[1]:void 0,t=e.type,r=e.payload;return"SALTS_AND_SOLVENTS_INIT"===t?Dd(Dd({},n),r):n},requestsStatuses:function(){var n=arguments.length>0&&void 0!==arguments[0]?arguments[0]:be,e=arguments.length>1?arguments[1]:void 0,t=e.type,r=e.data;switch(t){case pe:return me(me({},n),{},{indigoVerification:r});case he:return me(me({},n),{},{isAnalyzingFile:r});default:return n}}});var zd=(0,S.$j)((function(n){return{active:n.actionState&&n.actionState.activeTool,status:n.actionState||{},opened:n.toolbar.opened,indigoVerification:n.requestsStatuses.indigoVerification,disableableButtons:[]}}),(function(n){return{onAction:function(e){return n(Ue(e))},onOpen:function(e,t){return n({type:"OPENED",data:{menuName:e,isSelected:t}})}}}))((function(n){var e=n.className,t=(0,p.Z)(n,Fu),r=t.active,i=t.disableableButtons,a=t.indigoVerification,l=t.onAction;return(0,o.jsxs)("div",{className:(0,v.Z)("BottomToolbar-module_root__kjkSm",e),children:[(0,o.jsx)(Zu,{children:(0,o.jsx)(Gu,{active:r,indigoVerification:a,disableableButtons:i,onAction:l})}),(0,o.jsx)(Zu,{children:(0,o.jsx)(zu,Ru({id:"template-lib"},t))})]})}));function Gd(n){return n.map((function(n){return{id:n}}))}var Fd=Gd(["bond-single","bond-double","bond-triple"]),Hd=Gd(["bond-up","bond-down","bond-updown","bond-crossed"]),Rd=Gd(["bond-any","bond-aromatic","bond-singledouble","bond-singlearomatic","bond-doublearomatic"]),Zd=Gd(["bond-dative","bond-hydrogen"]),Kd=[Fd,Hd,Rd,Zd],Yd=Kd.flat(),Ud=Kd.reduce((function(n,e,t){var r,o=(null===(r=n[t-1])||void 0===r?void 0:r.end)||0;return n.push({start:o,end:o+e.length}),n}),[]),Jd=Gd(["rgroup-label","rgroup-fragment","rgroup-attpoints"]),qd=Gd(["shape-ellipse","shape-rectangle","shape-line"]),Wd=Gd(["transform-rotate","transform-flip-h","transform-flip-v"]),Xd=Gd(["select-rectangle","select-lasso","select-fragment"]),Qd=Gd(["reaction-arrow-open-angle","reaction-arrow-filled-triangle","reaction-arrow-filled-bow","reaction-arrow-dashed-open-angle","reaction-arrow-failed","reaction-arrow-both-ends-filled-triangle","reaction-arrow-equilibrium-filled-half-bow","reaction-arrow-equilibrium-filled-triangle","reaction-arrow-equilibrium-open-angle","reaction-arrow-unbalanced-equilibrium-filled-half-bow","reaction-arrow-unbalanced-equilibrium-open-half-angle","reaction-arrow-unbalanced-equilibrium-large-filled-half-bow","reaction-arrow-unbalanced-equilibrium-filled-half-triangle","reaction-arrow-elliptical-arc-arrow-filled-bow","reaction-arrow-elliptical-arc-arrow-filled-triangle","reaction-arrow-elliptical-arc-arrow-open-angle","reaction-arrow-elliptical-arc-arrow-open-half-angle"]),np=Gd(["reaction-map","reaction-unmap","reaction-automap"]),ep="ArrowScroll-module_button__ygMgL";function tp(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function rp(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?tp(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):tp(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var op=100;function ip(){var n=arguments.length>0&&void 0!==arguments[0]?arguments[0]:{},e=(0,d.useState)({height:void 0,width:void 0}),t=(0,O.Z)(e,2),r=t[0],o=t[1],i=(0,d.useMemo)((function(){return(0,E.throttle)(o,op)}),[]),a=A()(rp({onResize:i},n));return rp({ref:a.ref},r)}function ap(){return d.useContext(gn)}var lp=function(){return d.useContext(fn)},cp=function(n,e){var t=(0,d.useRef)(n);(0,d.useEffect)((function(){t.current=n}),[n]),(0,d.useEffect)((function(){if(null!==e){var n=setInterval((function(){return t.current()}),e);return function(){return clearInterval(n)}}}),[e])},sp="ketcher-init",up=function(){var n=(0,S.I0)(),e=lp().getKetcherInstance,t=function(){n(ve(!0))},r=function(){n(ve(!1))};(0,d.useEffect)((function(){var n=function(){var n;(n=e()).eventBus.addListener(u.DEm.LOADING,t),n.eventBus.addListener(u.DEm.SUCCESS,r),n.eventBus.addListener(u.DEm.FAILURE,r)};return window.addEventListener(sp,(function(){n()})),function(){var o;(o=e()).eventBus.removeListener(u.DEm.LOADING,t),o.eventBus.removeListener(u.DEm.SUCCESS,r),o.eventBus.removeListener(u.DEm.FAILURE,r),window.removeEventListener(sp,n)}}),[])},dp=function(n){var e=n.startInView,t=n.endInView,r=n.scrollUp,i=n.scrollDown,a=(0,d.useState)(!1),l=(0,O.Z)(a,2),c=l[0],s=l[1],u=(0,d.useState)(!1),p=(0,O.Z)(u,2),h=p[0],f=p[1];return cp(i,c?100:null),cp(r,h?100:null),(0,d.useEffect)((function(){return function(){f(!1)}}),[e]),(0,d.useEffect)((function(){return function(){s(!1)}}),[t]),(0,o.jsxs)("div",{className:"ArrowScroll-module_scroll__h9kCx",children:[t?(0,o.jsx)(o.Fragment,{}):(0,o.jsx)("button",{onClick:function(){return i()},onMouseUp:function(){return s(!1)},onMouseDown:function(){return s(!0)},className:(0,v.Z)(ep,"ArrowScroll-module_down__yDzZX"),children:"▼"}),e?(0,o.jsx)(o.Fragment,{}):(0,o.jsx)("button",{onClick:function(){return r()},onMouseUp:function(){return f(!1)},onMouseDown:function(){return f(!0)},className:(0,v.Z)(ep,"ArrowScroll-module_up__Q1ubd"),children:"▲"})]})},pp=["height"];function hp(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function fp(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?hp(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):hp(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var mp=function(n){var e=n.height,t=(0,p.Z)(n,pp);return e&&e<=770?(0,o.jsx)(Vu,fp({id:"bonds",options:Yd,variant:"grouped",groups:Ud},t)):(0,o.jsxs)(o.Fragment,{children:[(0,o.jsx)(Vu,fp({id:"bond-common",options:Fd},t)),(0,o.jsx)(Vu,fp({id:"bond-stereo",options:Hd},t)),(0,o.jsx)(Vu,fp({id:"bond-query",options:Rd},t)),(0,o.jsx)(Vu,fp({id:"bond-special",options:Zd},t))]})};function vp(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}var gp=function(n){return(0,o.jsx)(zu,function(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?vp(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):vp(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}({id:"rgroup",options:Jd},n))};function bp(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}var Cp=function(n){return(0,o.jsx)(zu,function(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?bp(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):bp(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}({id:"shapes",options:qd},n))},yp=["height"];function Op(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function wp(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Op(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Op(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Sp=function(n){var e=n.height,t=(0,p.Z)(n,yp);return e&&e<=870?(0,o.jsx)(zu,wp({id:"transforms",options:Wd},t)):(0,o.jsxs)(o.Fragment,{children:[(0,o.jsx)(zu,wp({id:"transform-rotate"},t)),(0,o.jsx)(zu,wp({id:"transform-flip-h"},t)),(0,o.jsx)(zu,wp({id:"transform-flip-v"},t))]})},Mp={"button-common-styles":"LeftToolbar-module_button-common-styles__WgnON",scrollbar:"LeftToolbar-module_scrollbar__OBwid",group:"LeftToolbar-module_group__0s41t",root:"LeftToolbar-module_root__yhhZm",buttons:"LeftToolbar-module_buttons__lnIjn",borderOff:"LeftToolbar-module_borderOff__om425",groupItem:"LeftToolbar-module_groupItem__OqQu0"},xp=["className"];function jp(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Ep(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?jp(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):jp(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Dp=(0,S.$j)((function(n){return{status:n.actionState||{},opened:n.toolbar.opened,indigoVerification:n.requestsStatuses.indigoVerification,disableableButtons:[]}}),(function(n){return{onAction:function(e){return n(Ue(e))},onOpen:function(e,t){return n({type:"OPENED",data:{menuName:e,isSelected:t}})}}}))((function(n){var e=n.className,t=(0,p.Z)(n,xp),r=ip(),i=r.ref,a=r.height,l=(0,d.useRef)(),c=(0,$.YD)({threshold:.8}),s=(0,O.Z)(c,2),u=s[0],h=s[1],f=(0,$.YD)({threshold:.8}),m=(0,O.Z)(f,2),g=m[0],b=m[1],C=(0,d.useRef)(),y=function(n){var e=n.id,r=n.options;return zu(Ep({id:e,options:r},t))},w=t.status,S=function(n){var e=n.items,r=n.className,i=[];return e&&e.forEach((function(n){var e,t,r=!0;(null!==(e=w[n.id])&&void 0!==e&&e.hidden||null!==(t=n.options)&&void 0!==t&&t.every((function(n){var e;return null===(e=w[n.id])||void 0===e?void 0:e.hidden})))&&(r=!1),r&&i.push(n)})),i.length?(0,o.jsx)("div",{className:(0,v.Z)(Mp.group,r),children:i.map((function(n){switch(n.id){case"bond-common":return(0,d.createElement)(mp,Ep(Ep({},t),{},{height:a,key:n.id}));case"transform-rotate":return(0,d.createElement)(Sp,Ep(Ep({},t),{},{height:a,key:n.id}));case"rgroup":return(0,d.createElement)(gp,Ep(Ep({},t),{},{key:n.id}));case"shapes":return(0,d.createElement)(Cp,Ep(Ep({},t),{},{key:n.id}));default:return(0,o.jsx)(y,{id:n.id,options:n.options},n.id)}}))}):null};return(0,o.jsxs)("div",{className:(0,v.Z)(Mp.root,e),ref:i,children:[(0,o.jsxs)("div",{className:Mp.buttons,ref:l,children:[(0,o.jsx)("div",{className:Mp.listener,ref:u,children:(0,o.jsx)(S,{className:Mp.groupItem,items:[{id:"hand"},{id:"select",options:Xd},{id:"erase"}]})}),(0,o.jsx)(S,{className:Mp.groupItem,items:[{id:"bonds",options:[].concat((0,x.Z)(Fd),(0,x.Z)(Rd),(0,x.Z)(Zd),(0,x.Z)(Hd))},{id:"chain"}]}),(0,o.jsx)(S,{className:Mp.groupItem,items:[{id:"charge-plus"},{id:"charge-minus"}]}),(0,o.jsx)(S,{className:Mp.groupItem,items:[{id:"transforms",options:Wd}]}),(0,o.jsx)(S,{className:Mp.groupItem,items:[{id:"sgroup"},{id:"sgroup-data"}]}),(0,o.jsx)(S,{className:Mp.groupItem,items:[{id:"reaction-plus"},{id:"arrows",options:Qd},{id:"reaction-mapping-tools",options:np}]}),(0,o.jsx)("div",{className:Mp.listener,ref:C,children:(0,o.jsx)(S,{className:Mp.groupItem,items:[{id:"rgroup",options:Jd}]})}),(0,o.jsx)(S,{className:Mp.groupItem,items:[{id:"shapes",options:qd}]}),(0,o.jsx)("div",{ref:g,children:(0,o.jsx)(S,{className:Mp.groupItem,items:[{id:"text"}]})})]}),(0,o.jsx)(dp,{startInView:h,endInView:b,scrollUp:function(){l.current.scrollTop-=C.current.offsetHeight},scrollDown:function(){l.current.scrollTop+=C.current.offsetHeight}})]})})),Ap={"button-common-styles":"Atom-module_button-common-styles__j3EUJ",scrollbar:"Atom-module_scrollbar__iO-Ni",atom:"Atom-module_atom__g2RUu"},$p=["el","shortcut","selected"];function Np(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Pp(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Np(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Np(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function kp(n){var e=n.el,t=n.shortcut,r=n.selected,i=(0,p.Z)(n,$p);return(0,o.jsx)("button",Pp(Pp({title:t?"".concat(e.title," (").concat(t,")"):e.title,className:(0,v.Z)(Ap.atom,{selected:r}),value:e.number},i),{},{children:(0,o.jsx)("span",{children:e.label})}))}var Ip={aliceblue:[240,248,255],antiquewhite:[250,235,215],aqua:[0,255,255],aquamarine:[127,255,212],azure:[240,255,255],beige:[245,245,220],bisque:[255,228,196],black:[0,0,0],blanchedalmond:[255,235,205],blue:[0,0,255],blueviolet:[138,43,226],brown:[165,42,42],burlywood:[222,184,135],cadetblue:[95,158,160],chartreuse:[127,255,0],chocolate:[210,105,30],coral:[255,127,80],cornflowerblue:[100,149,237],cornsilk:[255,248,220],crimson:[220,20,60],cyan:[0,255,255],darkblue:[0,0,139],darkcyan:[0,139,139],darkgoldenrod:[184,134,11],darkgray:[169,169,169],darkgreen:[0,100,0],darkgrey:[169,169,169],darkkhaki:[189,183,107],darkmagenta:[139,0,139],darkolivegreen:[85,107,47],darkorange:[255,140,0],darkorchid:[153,50,204],darkred:[139,0,0],darksalmon:[233,150,122],darkseagreen:[143,188,143],darkslateblue:[72,61,139],darkslategray:[47,79,79],darkslategrey:[47,79,79],darkturquoise:[0,206,209],darkviolet:[148,0,211],deeppink:[255,20,147],deepskyblue:[0,191,255],dimgray:[105,105,105],dimgrey:[105,105,105],dodgerblue:[30,144,255],firebrick:[178,34,34],floralwhite:[255,250,240],forestgreen:[34,139,34],fuchsia:[255,0,255],gainsboro:[220,220,220],ghostwhite:[248,248,255],gold:[255,215,0],goldenrod:[218,165,32],gray:[128,128,128],green:[0,128,0],greenyellow:[173,255,47],grey:[128,128,128],honeydew:[240,255,240],hotpink:[255,105,180],indianred:[205,92,92],indigo:[75,0,130],ivory:[255,255,240],khaki:[240,230,140],lavender:[230,230,250],lavenderblush:[255,240,245],lawngreen:[124,252,0],lemonchiffon:[255,250,205],lightblue:[173,216,230],lightcoral:[240,128,128],lightcyan:[224,255,255],lightgoldenrodyellow:[250,250,210],lightgray:[211,211,211],lightgreen:[144,238,144],lightgrey:[211,211,211],lightpink:[255,182,193],lightsalmon:[255,160,122],lightseagreen:[32,178,170],lightskyblue:[135,206,250],lightslategray:[119,136,153],lightslategrey:[119,136,153],lightsteelblue:[176,196,222],lightyellow:[255,255,224],lime:[0,255,0],limegreen:[50,205,50],linen:[250,240,230],magenta:[255,0,255],maroon:[128,0,0],mediumaquamarine:[102,205,170],mediumblue:[0,0,205],mediumorchid:[186,85,211],mediumpurple:[147,112,219],mediumseagreen:[60,179,113],mediumslateblue:[123,104,238],mediumspringgreen:[0,250,154],mediumturquoise:[72,209,204],mediumvioletred:[199,21,133],midnightblue:[25,25,112],mintcream:[245,255,250],mistyrose:[255,228,225],moccasin:[255,228,181],navajowhite:[255,222,173],navy:[0,0,128],oldlace:[253,245,230],olive:[128,128,0],olivedrab:[107,142,35],orange:[255,165,0],orangered:[255,69,0],orchid:[218,112,214],palegoldenrod:[238,232,170],palegreen:[152,251,152],paleturquoise:[175,238,238],palevioletred:[219,112,147],papayawhip:[255,239,213],peachpuff:[255,218,185],peru:[205,133,63],pink:[255,192,203],plum:[221,160,221],powderblue:[176,224,230],purple:[128,0,128],rebeccapurple:[102,51,153],red:[255,0,0],rosybrown:[188,143,143],royalblue:[65,105,225],saddlebrown:[139,69,19],salmon:[250,128,114],sandybrown:[244,164,96],seagreen:[46,139,87],seashell:[255,245,238],sienna:[160,82,45],silver:[192,192,192],skyblue:[135,206,235],slateblue:[106,90,205],slategray:[112,128,144],slategrey:[112,128,144],snow:[255,250,250],springgreen:[0,255,127],steelblue:[70,130,180],tan:[210,180,140],teal:[0,128,128],thistle:[216,191,216],tomato:[255,99,71],turquoise:[64,224,208],violet:[238,130,238],wheat:[245,222,179],white:[255,255,255],whitesmoke:[245,245,245],yellow:[255,255,0],yellowgreen:[154,205,50]},Tp={red:0,orange:60,yellow:120,green:180,blue:240,purple:300};function Bp(n,e){var t=function(n){var e,t,r=[],o=1;if("string"==typeof n)if(Ip[n])r=Ip[n].slice(),t="rgb";else if("transparent"===n)o=0,t="rgb",r=[0,0,0];else if(/^#[A-Fa-f0-9]+$/.test(n)){var i=n.slice(1);o=1,(c=i.length)<=4?(r=[parseInt(i[0]+i[0],16),parseInt(i[1]+i[1],16),parseInt(i[2]+i[2],16)],4===c&&(o=parseInt(i[3]+i[3],16)/255)):(r=[parseInt(i[0]+i[1],16),parseInt(i[2]+i[3],16),parseInt(i[4]+i[5],16)],8===c&&(o=parseInt(i[6]+i[7],16)/255)),r[0]||(r[0]=0),r[1]||(r[1]=0),r[2]||(r[2]=0),t="rgb"}else if(e=/^((?:rgb|hs[lvb]|hwb|cmyk?|xy[zy]|gray|lab|lchu?v?|[ly]uv|lms)a?)\s*\(([^\)]*)\)/.exec(n)){var a=e[1],l="rgb"===a;t=i=a.replace(/a$/,"");var c="cmyk"===i?4:"gray"===i?1:3;r=e[2].trim().split(/\s*[,\/]\s*|\s+/).map((function(n,e){if(/%$/.test(n))return e===c?parseFloat(n)/100:"rgb"===i?255*parseFloat(n)/100:parseFloat(n);if("h"===i[e]){if(/deg$/.test(n))return parseFloat(n);if(void 0!==Tp[n])return Tp[n]}return parseFloat(n)})),a===i&&r.push(1),o=l||void 0===r[c]?1:r[c],r=r.slice(0,c)}else n.length>10&&/[0-9](?:\s|\/)/.test(n)&&(r=n.match(/([0-9]+)/g).map((function(n){return parseFloat(n)})),t=n.match(/([a-z])/gi).join("").toLowerCase());else isNaN(n)?Array.isArray(n)||n.length?(r=[n[0],n[1],n[2]],t="rgb",o=4===n.length?n[3]:1):n instanceof Object&&(null!=n.r||null!=n.red||null!=n.R?(t="rgb",r=[n.r||n.red||n.R||0,n.g||n.green||n.G||0,n.b||n.blue||n.B||0]):(t="hsl",r=[n.h||n.hue||n.H||0,n.s||n.saturation||n.S||0,n.l||n.lightness||n.L||n.b||n.brightness]),o=n.a||n.alpha||n.opacity||1,null!=n.opacity&&(o/=100)):(t="rgb",r=[n>>>16,(65280&n)>>>8,255&n]);return{space:t,values:r,alpha:o}}(n);return null==e&&(e=t.alpha),"h"===t.space[0]?t.space+["a(",t.values[0],",",t.values[1],"%,",t.values[2],"%,",e,")"].join(""):t.space+["a(",t.values,",",e,")"].join("")}var Lp=(0,N.Z)(kp)((function(n){var e,t=null!=n&&null!==(e=n.el)&&void 0!==e&&e.label?u.wql[n.el.label]:"#000";return"\n       color: ".concat(t,";\n       border: 1px solid ").concat(t,";\n       background-color: transparent;\n       cursor: pointer;\n       &:hover {\n         background-color: ").concat(Bp(t,.2),";\n       }\n       &:active {\n         color: #fff;\n         background-color: ").concat(Bp(t,.8),";\n       }\n       &.selected {\n         color: #fff;\n         background-color: ").concat(Bp(t,.8),";\n         &:hover {\n           background-color: ").concat(t,";\n         }\n       }\n   ")})),_p=(0,d.forwardRef)((function(n,e){var t=n.atoms,r=n.active,i=n.onAction,a=r&&"atom"===r.tool;return(0,o.jsx)("div",{ref:e,children:t.map((function(n){var e=u.eKO.get(n),l=t.indexOf(n)>-1?Nu(Cn[n]):null,c=a&&r&&r.opts.label===n;return(0,o.jsx)(Lp,{el:e,shortcut:l,className:c?"selected":"",selected:c,onClick:function(){return i({tool:"atom",opts:{label:n}})}},n)}))})})),Vp=["className"];function zp(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Gp(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?zp(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):zp(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Fp,Hp,Rp,Zp,Kp,Yp,Up,Jp,qp,Wp,Xp,Qp,nh,eh,th,rh,oh=function(n){var e=n.children,t=n.className;return(0,o.jsx)("div",{className:(0,v.Z)("RightToolbar-module_group__3mhUx",t),children:e})},ih=(0,S.$j)((function(n){return{active:n.actionState&&n.actionState.activeTool,status:n.actionState||{},freqAtoms:n.toolbar.freqAtoms,opened:n.toolbar.opened,indigoVerification:n.requestsStatuses.indigoVerification,disableableButtons:[]}}),(function(n){return{onAction:function(e){return n(Ue(e))},onOpen:function(e,t){return n({type:"OPENED",data:{menuName:e,isSelected:t}})}}}))((function(n){var e=n.className,t=(0,p.Z)(n,Vp),r=t.active,i=t.onAction,a=t.freqAtoms,l=(0,$.YD)({threshold:.95}),c=(0,O.Z)(l,2),s=c[0],u=c[1],h=(0,$.YD)({threshold:.8}),f=(0,O.Z)(h,2),m=f[0],g=f[1],b=(0,d.useRef)(),C=(0,d.useRef)();return(0,o.jsxs)("div",{className:(0,v.Z)("RightToolbar-module_root__1D5hp",e),children:[(0,o.jsxs)("div",{className:"RightToolbar-module_buttons__YxRHI",ref:C,children:[(0,o.jsxs)(oh,{className:"RightToolbar-module_atomsList__ar08-",children:[(0,o.jsx)(_p,{ref:s,atoms:bn,active:r,onAction:i}),(0,o.jsx)(_p,{atoms:a,active:r,onAction:i}),(0,o.jsx)(zu,Gp({id:"period-table"},t))]}),(0,o.jsx)(oh,{children:(0,o.jsxs)("div",{ref:b,children:[(0,o.jsx)(zu,Gp({id:"any-atom"},t)),(0,o.jsx)(zu,Gp({id:"extended-table"},t))]})}),(0,o.jsx)("div",{ref:m})]}),(0,o.jsx)(dp,{startInView:u,endInView:g,scrollUp:function(){C.current.scrollTop-=b.current.offsetHeight},scrollDown:function(){C.current.scrollTop+=b.current.offsetHeight}})]})})),ah=(0,N.Z)(k.Z)(Fp||(Fp=(0,P.Z)(["\n  display: block;\n  color: #333;\n  border: 0;\n  position: relative;\n  background: inherit;\n\n  flex-shrink: 0;\n\n  border-radius: 4px;\n  margin: 0px;\n  padding: 2px;\n  height: 28px;\n  width: 28px;\n\n  &:hover {\n    color: #006775;\n    transform: none;\n    box-shadow: none;\n    transition: none;\n    background: none;\n  }\n\n  &:active {\n    background-color: #006775;\n    color: white;\n    &:hover {\n      background-color: #188794;\n    }\n  }\n\n  & svg {\n    width: 100%;\n    height: 100%;\n  }\n\n  &.Mui-disabled {\n    cursor: not-allowed;\n    opacity: 0.5;\n    background-color: initial;\n    color: #333;\n    pointer-events: auto;\n  }\n\n  @media only screen and (min-width: 1024px) {\n    height: 32px;\n    width: 32px;\n    padding: 4px;\n  }\n\n  @media only screen and (min-width: 1920px) {\n    height: 40px;\n    width: 40px;\n    padding: 5px;\n  }\n"]))),lh=function(n){var e=n.onClick,t=n.iconName,r=n.title,i=n.shortcut,a=n.isHidden,l=void 0!==a&&a,c=n.disabled,s=void 0!==c&&c,u=i?"".concat(r," (").concat(i,")"):r;return l?null:(0,o.jsx)(ah,{title:u,onClick:e,disabled:s,children:(0,o.jsx)(Au,{name:t})})},ch=function(n){var e=n.onFileOpen,t=n.onSave,r=n.shortcuts,i=n.hiddenButtons;return(0,o.jsxs)(o.Fragment,{children:[(0,o.jsx)(lh,{title:"Open...",onClick:e,iconName:"open",shortcut:r.open,isHidden:i.includes("open")}),(0,o.jsx)(lh,{title:"Save as...",onClick:t,iconName:"save",shortcut:r.save,isHidden:i.includes("save")})]})},sh=(0,N.Z)("div")(Hp||(Hp=(0,P.Z)(["\n  position: relative;\n"]))),uh=(0,N.Z)("div")(Rp||(Rp=(0,P.Z)(["\n  display: flex;\n  position: absolute;\n  left: 5px;\n  border-radius: 2px;\n  flex-direction: column;\n  z-index: 20;\n  white-space: nowrap;\n  word-break: keep-all;\n  padding: 2px;\n  background: white; // TODO use variable\n  border: 1px solid #cad3dd; // TODO use variable\n  border-radius: 5px;\n  box-shadow: 0 6px 12px rgb(0 0 0 / 18%);\n"]))),dh=(0,N.Z)(k.Z)(Zp||(Zp=(0,P.Z)(["\n  position: absolute;\n  padding: 0;\n  right: 0;\n  bottom: 0;\n\n  &.disabled {\n    cursor: not-allowed;\n    opacity: 0.5;\n    background-color: initial;\n    color: #333;\n    pointer-events: auto;\n  }\n"]))),ph=(0,N.Z)(Au)(Kp||(Kp=(0,P.Z)(["\n  display: block;\n  width: 7px;\n  height: 7px;\n  margin: 1px;\n\n  &:hover {\n    fill: #005662;\n    transform: none;\n    box-shadow: none;\n    transition: none;\n    background: none;\n  }\n\n  &svg {\n    width: 100%;\n    height: 100%;\n  }\n\n  &svg path {\n    fill: inherit;\n  }\n"]))),hh=(0,S.$j)(null,(function(n){return{onToolOpen:function(){return n({type:"OPENED",data:{menuName:null,isSelected:null}})}}}))((function(n){var e=n.topElement,t=n.dropDownElements,r=n.onToolOpen,i=(0,d.useState)(!1),a=(0,O.Z)(i,2),l=a[0],c=a[1],s=function(){c(!1)};return(0,o.jsxs)(sh,{children:[e&&e,0!==t.filter((function(n){return!n.props.isHidden})).length&&(0,o.jsx)(dh,{onClick:function(){r(),c(!0)},className:"expanded ".concat(null!=e&&e.props.disabled?"disabled":""),children:!l&&(0,o.jsx)(ph,{name:"dropdown"})}),(0,o.jsx)(I.Z,{in:l,timeout:"auto",onClick:s,unmountOnExit:!0,children:(0,o.jsx)(T.Z,{onClickAway:s,children:(0,o.jsx)(uh,{children:t})})})]})})),fh=function(n){var e=n.onCopy,t=n.onCopyMol,r=n.onCopyKet,i=n.onCopyImage,a=n.onPaste,l=n.onCut,c=n.shortcuts,s=n.disabledButtons,u=n.hiddenButtons,d=[{name:"copy",title:"Copy",handler:e},{name:"copy-mol",title:"Copy as MOL",handler:t},{name:"copy-ket",title:"Copy as KET",handler:r},{name:"copy-image",title:"Copy Image",handler:i}],p=function(n){return(0,o.jsx)(lh,{title:n.title,onClick:n.handler,iconName:n.name,shortcut:c[n.name],disabled:s.includes(n.name),isHidden:u.includes(n.name)},n.name)},h=d.find((function(n){return!u.includes(n.name)})),f=d.filter((function(n){return n!==h})).map((function(n){return p(n)}));return(0,o.jsxs)(o.Fragment,{children:[!u.includes("copies")&&(0,o.jsx)(hh,{topElement:p(h),dropDownElements:f}),(0,o.jsx)(lh,{title:"Paste",onClick:a,iconName:"paste",shortcut:c.paste,disabled:s.includes("paste"),isHidden:u.includes("paste")}),(0,o.jsx)(lh,{title:"Cut",onClick:l,iconName:"cut",shortcut:c.cut,disabled:s.includes("cut"),isHidden:u.includes("cut")})]})},mh=(0,N.Z)("hr")(Yp||(Yp=(0,P.Z)(["\n  margin: 0px 3px;\n  flex-shrink: 0;\n  height: 45%;\n  align-self: center;\n  border-width: 0px thin 0px 0px;\n  border-style: solid;\n  border-color: #b4b9d6; // TODO: use variable\n"]))),vh=function(){return(0,o.jsx)(mh,{})},gh=function(n){var e=n.onUndo,t=n.onRedo,r=n.disabledButtons,i=n.hiddenButtons,a=n.shortcuts;return(0,o.jsxs)(o.Fragment,{children:[(0,o.jsx)(vh,{}),(0,o.jsx)(lh,{title:"Undo",onClick:e,iconName:"undo",disabled:r.includes("undo"),isHidden:i.includes("undo"),shortcut:a.undo}),(0,o.jsx)(lh,{title:"Redo",onClick:t,iconName:"redo",disabled:r.includes("redo"),isHidden:i.includes("redo"),shortcut:a.redo}),(0,o.jsx)(vh,{})]})},bh=(0,N.Z)("input")(Up||(Up=(0,P.Z)(["\n  border: 1px solid #cad3dd;\n  border-radius: 4px;\n  padding: 3px 8px;\n  color: #585858;\n  font-size: 14px;\n  line-height: 16px;\n  caret-color: #43b5c0;\n  margin-bottom: 8px;\n\n  &:hover {\n    border-color: #43b5c0;\n  }\n\n  &:active,\n  &:focus {\n    border-color: #167782;\n    outline: none;\n  }\n\n  &::after,\n  &::before {\n    display: none;\n  }\n"]))),Ch=function(n){n.target.select()},yh=function(n,e){e&&(e.value="".concat(n,"%"))},Oh=function(n){var e=n.onZoomSubmit,t=n.currentZoom,r=n.inputRef,i=n.shortcuts;(0,d.useEffect)((function(){var n=r.current;yh(t,n),document.activeElement===n&&(null==n||n.select())}),[t,r]);var a=(0,d.useCallback)((function(n){var t=r.current;t&&([i["zoom-out"],i["zoom-in"]].includes(n.key)||n.nativeEvent.stopImmediatePropagation(),"Enter"===n.key&&(e(),t.select()))}),[e,r,i]);return(0,d.useEffect)((function(){var n=r.current;null==n||n.focus(),null==n||n.select()}),[r]),(0,o.jsx)(bh,{ref:r,onFocus:Ch,onKeyDown:a})},wh=(0,N.Z)("div")(Jp||(Jp=(0,P.Z)(["\n  position: relative;\n"]))),Sh=(0,N.Z)(B.Z)(qp||(qp=(0,P.Z)(["\n  display: flex;\n  color: #000000;\n  padding-right: 0;\n  padding-left: 0;\n\n  & svg {\n    margin-left: 2px;\n    width: 16px;\n    height: 16px;\n  }\n"]))),Mh=(0,N.Z)("span")(Wp||(Wp=(0,P.Z)(["\n  width: 35px;\n"]))),xh=(0,N.Z)(L.ZP)(Xp||(Xp=(0,P.Z)(["\n  & .MuiPopover-paper {\n    padding: 8px;\n    width: 135px;\n    border: none;\n    border-radius: 0px 0px 4px 4px;\n    box-shadow: 0px 30px 48px -17px rgba(160, 165, 174, 0.3);\n    box-sizing: border-box;\n  }\n"]))),jh=(0,N.Z)("div")(Qp||(Qp=(0,P.Z)(["\n  display: flex;\n  flex-direction: column;\n  white-space: nowrap;\n  word-break: keep-all;\n  background: white;\n"]))),Eh=(0,N.Z)(B.Z)(nh||(nh=(0,P.Z)(["\n  display: flex;\n  justify-content: space-between;\n  font-weight: 400;\n  font-size: 12px;\n  line-height: 14px;\n  padding: 7px 8px;\n  text-transform: none;\n  color: #333333;\n"]))),Dh=(0,N.Z)("span")(eh||(eh=(0,P.Z)(["\n  color: #cad3dd;\n"]))),Ah=function(n){var e=n.currentZoom,t=n.onZoom,r=n.onZoomIn,i=n.onZoomOut,a=n.disabledButtons,l=n.hiddenButtons,c=n.shortcuts,s=(0,d.useState)(!1),u=(0,O.Z)(s,2),p=u[0],h=u[1],f=(0,d.useRef)(null),m=(0,d.useRef)(null),v=(0,d.useCallback)((function(){var n=m.current;if(n){var r,o,i=(r=n.value,o=parseInt(r||""),isNaN(o)?0:o);if(i&&i!==e){var a=function(n,e){if(0===n)return e;var t=100*Math.min.apply(Math,(0,x.Z)(it)),r=100*Math.max.apply(Math,(0,x.Z)(it));return n<t?t:n>r?r:n}(i,e);yh(a,n),t(a)}else yh(e,n)}}),[t,e]);return(0,o.jsxs)(wh,{ref:f,children:[(0,o.jsxs)(Sh,{onClick:function(){h(!0)},children:[(0,o.jsxs)(Mh,{children:[Math.round(e),"%"]}),(0,o.jsx)(Au,{name:"chevron"})]}),(0,o.jsx)(xh,{open:p,onClose:function(n,e){"backdropClick"===e&&v(),h(!1)},anchorEl:f.current,container:f.current,anchorOrigin:{vertical:"bottom",horizontal:"left"},children:(0,o.jsxs)(jh,{children:[(0,o.jsx)(Oh,{onZoomSubmit:v,inputRef:m,currentZoom:e,shortcuts:c}),!l.includes("zoom-out")&&(0,o.jsxs)(Eh,{title:"Zoom Out",onClick:i,disabled:a.includes("zoom-out"),children:[(0,o.jsx)("span",{children:"Zoom out"}),(0,o.jsx)(Dh,{children:c["zoom-out"]})]}),!l.includes("zoom-in")&&(0,o.jsxs)(Eh,{title:"Zoom In",onClick:r,disabled:a.includes("zoom-in"),children:[(0,o.jsx)("span",{children:"Zoom in"}),(0,o.jsx)(Dh,{children:c["zoom-in"]})]}),(0,o.jsx)(Eh,{onClick:function(){t(100)},children:(0,o.jsx)("span",{children:"Zoom 100%"})})]})})]})},$h=(0,N.Z)("div")(th||(th=(0,P.Z)(["\n  display: flex;\n  align-items: center;\n  flex-grow: 1;\n  justify-content: flex-end;\n"]))),Nh=function(n){var e=n.disabledButtons,t=n.hiddenButtons,r=n.onSettingsOpen,i=n.onFullscreen,a=n.onHelp,l=n.onAboutOpen,c=n.className;return(0,o.jsxs)($h,{className:c,children:[(0,o.jsx)(lh,{title:"Settings",onClick:r,iconName:"settings",disabled:e.includes("settings"),isHidden:t.includes("settings")}),(0,o.jsx)(lh,{title:"Help (".concat(Nu(["?","&","Shift+/"]),")"),onClick:a,iconName:"help",disabled:e.includes("help"),isHidden:t.includes("help")}),(0,o.jsx)(lh,{title:"About",onClick:l,iconName:"about",disabled:e.includes("about"),isHidden:t.includes("about")}),(0,o.jsx)(lh,{title:"Fullscreen mode",onClick:i,iconName:document.fullscreenElement||document.mozFullScreenElement||document.webkitFullscreenElement||document.msFullscreenElement?"fullscreen-exit":"fullscreen-enter",disabled:e.includes("fullscreen"),isHidden:t.includes("fullscreen")})]})},Ph=function(n){var e=n.isCollapsed,t=n.onLayout,r=n.onClean,i=n.onAromatize,a=n.onDearomatize,l=n.onCalculate,c=n.onCheck,s=n.onAnalyse,u=n.onStereo,d=n.onMiew,p=n.disabledButtons,h=n.indigoVerification,f=n.hiddenButtons,m=n.shortcuts,v=[{name:"arom",title:"Aromatize",handler:i},{name:"dearom",title:"Dearomatize",handler:a},{name:"layout",title:"Layout",handler:t},{name:"clean",title:"Clean Up",handler:r},{name:"cip",title:"Calculate CIP",handler:l},{name:"check",title:"Check Structure",handler:c},{name:"analyse",title:"Calculated Values",handler:s},{name:"enhanced-stereo",title:"Stereochemistry",handler:u},{name:"miew",title:"3D Viewer",handler:d}],g=function(n){return(0,o.jsx)(lh,{title:n.title,onClick:n.handler,iconName:n.name,shortcut:m[n.name],disabled:h||p.includes(n.name),isHidden:f.includes(n.name)},n.name)},b=v.find((function(n){return!f.includes(n.name)})),C=v.filter((function(n){return n!==b})).map((function(n){return g(n)}));return e?(0,o.jsx)(hh,{topElement:g(b),dropDownElements:C}):(0,o.jsxs)(o.Fragment,{children:[b&&g(b),(0,o.jsx)(o.Fragment,{children:C})]})},kh=(0,N.Z)("div")(rh||(rh=(0,P.Z)(["\n  display: flex;\n  flex-direction: row;\n  align-items: center;\n  gap: 0px;\n  height: 36px;\n  padding: 0px 8px;\n\n  .group {\n    display: flex;\n    flex-direction: row;\n    gap: 0px;\n  }\n\n  & * {\n    box-sizing: border-box;\n  }\n\n  @media only screen and (min-width: 1024px) {\n    height: 40px;\n    gap: 4px;\n\n    .group {\n      gap: 4px;\n    }\n  }\n\n  @media only screen and (min-width: 1920px) {\n    height: 64px;\n    gap: 12px;\n  }\n"]))),Ih=Object.keys(Ja).reduce((function(n,e){var t;if(null!==(t=Ja[e])&&void 0!==t&&t.shortcut){var r=Nu(Ja[e].shortcut);n[e]=r}return n}),{}),Th=(0,S.$j)((function(n){var e,t,r=n.actionState||{},o=Object.keys(r).reduce((function(n,e){var t;return null!==(t=r[e])&&void 0!==t&&t.disabled&&n.push(e),n}),[]),i=Object.keys(r).reduce((function(n,e){var t;return null!==(t=r[e])&&void 0!==t&&t.hidden&&n.push(e),n}),[]);return{currentZoom:Math.round(100*(null===(e=n.actionState)||void 0===e||null===(t=e.zoom)||void 0===t?void 0:t.selected)),disabledButtons:o,hiddenButtons:i,shortcuts:Ih,status:n.actionState||{},opened:n.toolbar.opened,indigoVerification:n.requestsStatuses.indigoVerification,disableableButtons:["layout","clean","arom","dearom","cip","enhanced-stereo"]}}),(function(n){var e=function(e){n(Ue(Ja[e].action))};return{onClear:function(){return e("clear")},onFileOpen:function(){return e("open")},onSave:function(){return e("save")},onUndo:function(){return e("undo")},onRedo:function(){return e("redo")},onCopy:function(){return e("copy")},onCopyMol:function(){return e("copy-mol")},onCopyKet:function(){return e("copy-ket")},onCopyImage:function(){return e("copy-image")},onCut:function(){return e("cut")},onPaste:function(){return e("paste")},onZoomIn:function(){return e("zoom-in")},onZoomOut:function(){return e("zoom-out")},onZoom:function(e){return n(Ue((function(n){return n.zoom(e/100)})))},onSettingsOpen:function(){return e("settings")},onLayout:function(){return e("layout")},onClean:function(){return e("clean")},onAromatize:function(){return e("arom")},onDearomatize:function(){return e("dearom")},onCalculate:function(){return e("cip")},onCheck:function(){return e("check")},onAnalyse:function(){return e("analyse")},onStereo:function(){return e("enhanced-stereo")},onMiew:function(){return e("miew")},onAction:function(e){return n(Ue(e))},onOpen:function(e,t){return n({type:"OPENED",data:{menuName:e,isSelected:t}})},onFullscreen:function(){return e("fullscreen")},onHelp:function(){return e("help")},onAbout:function(){return e("about")}}}))((function(n){var e=n.className,t=n.disabledButtons,r=n.indigoVerification,i=n.hiddenButtons,a=n.shortcuts,l=n.onClear,c=n.onFileOpen,s=n.onSave,u=n.onUndo,d=n.onRedo,p=n.onCopy,h=n.onCopyMol,f=n.onCopyKet,m=n.onCopyImage,v=n.onCut,g=n.onPaste,b=n.currentZoom,C=n.onZoom,y=n.onZoomIn,O=n.onZoomOut,w=n.onSettingsOpen,S=n.onLayout,M=n.onClean,x=n.onAromatize,j=n.onDearomatize,E=n.onCalculate,D=n.onCheck,A=n.onAnalyse,$=n.onStereo,N=n.onMiew,P=n.onFullscreen,k=n.onAbout,I=n.onHelp,T=ip(),B=T.ref,L=T.width,_=void 0===L?50:L;return(0,o.jsxs)(kh,{className:e,ref:B,children:[(0,o.jsx)(lh,{title:"Clear Canvas",onClick:l,iconName:"clear",shortcut:a.clear,isHidden:i.includes("clear")}),(0,o.jsx)(ch,{onFileOpen:c,onSave:s,shortcuts:a,hiddenButtons:i}),(0,o.jsx)(fh,{onCopy:p,onCopyMol:h,onCopyKet:f,onCopyImage:m,onPaste:g,onCut:v,shortcuts:a,disabledButtons:t,hiddenButtons:i}),(0,o.jsx)(gh,{onUndo:u,onRedo:d,disabledButtons:t,hiddenButtons:i,shortcuts:a}),(0,o.jsx)(Ph,{onLayout:S,onClean:M,onAromatize:x,onDearomatize:j,onCalculate:E,onCheck:D,onAnalyse:A,onStereo:$,onMiew:N,disabledButtons:t,hiddenButtons:i,shortcuts:a,indigoVerification:r,isCollapsed:_<650}),(0,o.jsx)(Nh,{onHistoryClick:function(){},onSettingsOpen:w,onFullscreen:P,onHelp:I,onAboutOpen:k,disabledButtons:t,hiddenButtons:i}),(0,o.jsx)(vh,{}),!i.includes("zoom-list")&&(0,o.jsx)(Ah,{currentZoom:b||1,onZoomIn:y,onZoomOut:O,onZoom:C,shortcuts:a,disabledButtons:t,hiddenButtons:i})]})})),Bh="undefined"!=typeof navigator&&/Mac/.test(navigator.platform);function Lh(n){var e,t,r,o,i=n.split(/\+(?!$)/),a=i[i.length-1];"Space"===a&&(a=" ");for(var l=0;l<i.length-1;l++){var c=i[l];if(/^(cmd|meta|m)$/i.test(c))o=!0;else if(/^a(lt)?$/i.test(c))e=!0;else if(/^(c|ctrl|control)$/i.test(c))t=!0;else if(/^s(hift)?$/i.test(c))r=!0;else{if(!/^mod$/i.test(c))throw new Error("Unrecognized modifier name: "+c);Bh?o=!0:t=!0}}return e&&(a="Alt+"+a),t&&(a="Ctrl+"+a),o&&(a="Meta+"+a),r&&(a="Shift+"+a),a}function _h(n,e,t){return e.altKey&&(n="Alt+"+n),e.ctrlKey&&(n="Ctrl+"+n),e.metaKey&&(n="Meta+"+n),!1!==t&&e.shiftKey&&(n="Shift+"+n),n}function Vh(n,e){return n.replace(/[а-я]/,z.ue[e.keyCode]).replace(/[А-Я]/,z.uY[e.keyCode])}function zh(n){var e=arguments.length>1&&void 0!==arguments[1]&&arguments[1],t=Vh(z.YG(n),n),r=1===t.length&&" "!==t;return r&&!e?_h(t,n,!r):_h(z.ue[n.keyCode],n,!0)}function Gh(n){return n instanceof KeyboardEvent?zh.apply(void 0,arguments):"object"===(0,g.Z)(n)?(e=n,t=Object.create(null),Object.keys(e).forEach((function(n){t[Lh(n)]=e[n]})),t):Lh(n);var e,t}function Fh(n,e){(null==e||e>n.length)&&(e=n.length);for(var t=0,r=new Array(e);t<e;t++)r[t]=n[t];return r}Gh.lookup=function(n,e){var t=Vh(z.YG(e),e);"Add"===t&&(t="+"),"Subtract"===t&&(t="-");var r,o=1===t.length&&" "!==t,i=n[_h(t,e,!o)];return e.shiftKey&&o&&(r=z.ue[e.keyCode])&&(i=n[_h(r,e,!0)]||i),i};var Hh=function(){function n(e){(0,c.Z)(this,n),this.editor=e,this.editor.selection(null)}return(0,s.Z)(n,[{key:"mousemove",value:function(n){var e=this.editor.render.ctab.molecule,t=this.editor.findItem(n,["atoms"]);if(t){var r=e.atoms.get(t.id);"R#"!==(null==r?void 0:r.label)&&null===(null==r?void 0:r.rglabel)&&this.editor.hover(t)}else this.editor.hover(null)}},{key:"click",value:function(n){var e=this.editor,t=e.render.ctab.molecule,r=t.functionalGroups,o=e.findItem(n,["atoms"]),i=[],a=[];if(o&&r.size&&"atoms"===o.map){var l=u.J41.atomsInFunctionalGroup(r,o.id);null!==l&&i.push(l)}if(!(i.length>0)){if(o&&"atoms"===o.map){this.editor.hover(null);var c=t.atoms.get(o.id);if("R#"===(null==c?void 0:c.label)&&null!==(null==c?void 0:c.rglabel))return;var s=e.event.elementEdit.dispatch({attpnt:null==c?void 0:c.attpnt});return Promise.resolve(s).then((function(n){if((null==c?void 0:c.attpnt)!==n.attpnt){var t=(0,u.dBq)(e.render.ctab,o.id,n,null);e.update(t)}})).catch((function(){return null})),!0}return!0}var d,p=function(n,e){var t="undefined"!=typeof Symbol&&n[Symbol.iterator]||n["@@iterator"];if(!t){if(Array.isArray(n)||(t=function(n,e){if(n){if("string"==typeof n)return Fh(n,e);var t=Object.prototype.toString.call(n).slice(8,-1);return"Object"===t&&n.constructor&&(t=n.constructor.name),"Map"===t||"Set"===t?Array.from(n):"Arguments"===t||/^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(t)?Fh(n,e):void 0}}(n))||e&&n&&"number"==typeof n.length){t&&(n=t);var r=0,o=function(){};return{s:o,n:function(){return r>=n.length?{done:!0}:{done:!1,value:n[r++]}},e:function(n){throw n},f:o}}throw new TypeError("Invalid attempt to iterate non-iterable instance.\nIn order to be iterable, non-array objects must have a [Symbol.iterator]() method.")}var i,a=!0,l=!1;return{s:function(){t=t.call(n)},n:function(){var n=t.next();return a=n.done,n},e:function(n){l=!0,i=n},f:function(){try{a||null==t.return||t.return()}finally{if(l)throw i}}}}(i);try{for(p.s();!(d=p.n()).done;){var h=d.value,f=u.J41.findFunctionalGroupByAtom(r,h);null===f||a.includes(f)||a.push(f)}}catch(n){p.e(n)}finally{p.f()}this.editor.event.removeFG.dispatch({fgIds:a})}}]),n}();function Rh(n,e){var t=u.Sgu.diff(e,n);return Math.atan2(t.y,t.x)}function Zh(n){var e=Math.round(n/Math.PI*180);return e>180?e-=360:e<=-180&&(e+=360),e}var Kh={calcAngle:Rh,fracAngle:u.jD1,calcNewAtomPos:function(n,e,t){var r=new u.Sgu(1,0).rotate(t?Rh(n,e):(0,u.jD1)(n,e));return r.add_(n),r},degrees:Zh,mergeBondsParams:function(n,e,t,r){var o=n.atoms.get(e.begin),i=t.atoms.get(r.begin),a=n.atoms.get(e.end),l=t.atoms.get(r.end),c=Rh(o.pp,a.pp)-Rh(i.pp,l.pp),s=Math.abs(Zh(c)%180),d=u.Sgu.dist(o.pp,a.pp)/u.Sgu.dist(i.pp,l.pp);return{merged:!(0,E.inRange)(s,10,170)&&(0,E.inRange)(d,.8,1.2),angle:c,scale:d,cross:Math.abs(Zh(c))>90}}};function Yh(n,e){var t="undefined"!=typeof Symbol&&n[Symbol.iterator]||n["@@iterator"];if(!t){if(Array.isArray(n)||(t=function(n,e){if(n){if("string"==typeof n)return Uh(n,e);var t=Object.prototype.toString.call(n).slice(8,-1);return"Object"===t&&n.constructor&&(t=n.constructor.name),"Map"===t||"Set"===t?Array.from(n):"Arguments"===t||/^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(t)?Uh(n,e):void 0}}(n))||e&&n&&"number"==typeof n.length){t&&(n=t);var r=0,o=function(){};return{s:o,n:function(){return r>=n.length?{done:!0}:{done:!1,value:n[r++]}},e:function(n){throw n},f:o}}throw new TypeError("Invalid attempt to iterate non-iterable instance.\nIn order to be iterable, non-array objects must have a [Symbol.iterator]() method.")}var i,a=!0,l=!1;return{s:function(){t=t.call(n)},n:function(){var n=t.next();return a=n.done,n},e:function(n){l=!0,i=n},f:function(){try{a||null==t.return||t.return()}finally{if(l)throw i}}}}function Uh(n,e){(null==e||e>n.length)&&(e=n.length);for(var t=0,r=new Array(e);t<e;t++)r[t]=n[t];return r}var Jh=new WeakMap,qh=function(){function n(e,t){if((0,c.Z)(this,n),l={writable:!0,value:void 0},function(n,e){if(e.has(n))throw new TypeError("Cannot initialize the same private elements twice on an object")}(i=this,a=Jh),a.set(i,l),this.editor=e,this.atomProps=t,(0,R.Z)(this,Jh,{type:1,stereo:u.fYe.PATTERN.STEREO.NONE}),this.editor.hoverIcon.show().attr("text","".concat(t.label)).attr("fill","".concat(u.wql[t.label])),this.editor.updateHoverIconPosition(),e.selection()){var r;if(null!==(r=e.selection())&&void 0!==r&&r.atoms){var o=(0,u.dBq)(e.render.ctab,e.selection().atoms,t,!0);e.update(o),e.selection(null)}this.isNotActiveTool=!0}var i,a,l}return(0,s.Z)(n,[{key:"mousedown",value:function(n){var e=this.editor.render.ctab,t=e.sgroups,r=e.molecule,o=r.functionalGroups;this.editor.hover(null),this.editor.selection(null);var i=this.editor.findItem(n,["atoms","functionalGroups"]);if(i&&"functionalGroups"===i.map&&o&&u.J41.isContractedFunctionalGroup(i.id,o)){var a=new u.aUM,l=t.get(i.id),c=u.j1n.getAtoms(r,null==l?void 0:l.item),s=(0,F.Z)(c),d=s[0],p=s.slice(1),h=r.atomGetNeighbors(d),f=null==h?void 0:h.some((function(n){return!c.includes(n.aid)}));if(f)a.mergeWith((0,u.U9$)(e,i.id)),a.mergeWith((0,u.nHA)(e,{atoms:p})),a.mergeWith((0,u.dBq)(e,d,this.atomProps,!0));else{var m,v=null===(m=e.atoms.get(d))||void 0===m?void 0:m.a.pp;a.mergeWith((0,u.nHA)(e,{atoms:u.j1n.getAtoms(r,null==l?void 0:l.item),bonds:u.j1n.getBonds(r,null==l?void 0:l.item)})),a.mergeWith((0,u.f8s)(e,v,this.atomProps))}this.editor.update(a)}var g=[],b=[];if(i&&o.size&&"atoms"===i.map){var C=u.J41.atomsInFunctionalGroup(o,i.id);null!==C&&g.push(C)}if(g.length>0){var y,O=Yh(g);try{for(O.s();!(y=O.n()).done;){var w=y.value,S=u.J41.findFunctionalGroupByAtom(o,w);null===S||b.includes(S)||b.push(S)}}catch(n){O.e(n)}finally{O.f()}this.editor.event.removeFG.dispatch({fgIds:b})}else i?"atoms"===i.map&&(this.dragCtx={item:i}):this.dragCtx={}}},{key:"mouseleave",value:function(){this.editor.hoverIcon.hide()}},{key:"mouseover",value:function(){this.editor.hoverIcon.show(),this.editor.updateHoverIconPosition()}},{key:"mousemove",value:function(n){var e=this.editor.render,t=n.layerX,r=n.layerY;if(!this.dragCtx||!this.dragCtx.item){var o=this.editor.hoverIcon.getBBox(),i=o.height,a=o.width;return this.editor.hoverIcon.attr({x:t-a/2,y:r-i/2}),void this.editor.hover(this.editor.findItem(n,["atoms","functionalGroups"]),null,n)}var l=this.dragCtx,c=this.editor.findItem(n,["atoms"]);if(c&&"atoms"===c.map&&c.id===l.item.id)this.editor.hover(this.editor.findItem(n,["atoms"]));else{var s=e.ctab.molecule.atoms.get(l.item.id),d=Kh.calcAngle(null==s?void 0:s.pp,e.page2obj(n));n.ctrlKey||(d=Kh.fracAngle(d,null));var p=Kh.degrees(d);this.editor.event.message.dispatch({info:p+"º"});var h=Kh.calcNewAtomPos(null==s?void 0:s.pp,e.page2obj(n),n.ctrlKey);l.action&&l.action.perform(e.ctab),l.action=(0,u.QXZ)(e.ctab,(0,H.Z)(this,Jh),l.item.id,Object.assign({},this.atomProps),h,h)[0],this.editor.update(l.action,!0)}}},{key:"mouseup",value:function(n){var e=this.editor.render.ctab.molecule.functionalGroups,t=this.editor.findItem(n,["atoms","bonds"]),r=[],o=[];if(t&&e&&"atoms"===t.map){var i=u.J41.atomsInFunctionalGroup(e,t.id);null!==i&&r.push(i)}if(r.length>0){var a,l=Yh(r);try{for(l.s();!(a=l.n()).done;){var c=a.value,s=u.J41.findFunctionalGroupByAtom(e,c);null===s||o.includes(s)||o.push(s)}}catch(n){l.e(n)}finally{l.f()}this.editor.event.removeFG.dispatch({fgIds:o})}else{if(this.dragCtx){var d=this.dragCtx,p=this.editor.render;this.editor.update(d.action||(d.item?(0,u.dBq)(p.ctab,d.item.id,this.atomProps,!0):(0,u.f8s)(p.ctab,p.page2obj(n),this.atomProps))),delete this.dragCtx}this.editor.event.message.dispatch({info:!1})}}}]),n}();function Wh(n,e){var t,r=n.dragCtx,o=n.editor,i=null===(t=r.item)||void 0===t?void 0:t.id,a=e.ctab.molecule.functionalGroups,l=null!=i?e.ctab.molecule.atoms.get(i):new u.hgN({label:""}),c=u.J41.findFunctionalGroupByAtom(a,i);r.timeout=setTimeout((function(){if(delete n.dragCtx,null==c){o.selection(null);var t=o.event.quickEdit.dispatch(l);Promise.resolve(t).then((function(n){var t=i?(0,u.dBq)(e.ctab,i,n,null):(0,u.f8s)(e.ctab,r.xy0,n);o.update(t)})).catch((function(){return null}))}else o.event.removeFG.dispatch({fgIds:[c]})}),750),r.stopTapping=function(){r.timeout&&(clearTimeout(r.timeout),delete r.timeout)}}function Xh(n,e){var t="undefined"!=typeof Symbol&&n[Symbol.iterator]||n["@@iterator"];if(!t){if(Array.isArray(n)||(t=function(n,e){if(n){if("string"==typeof n)return Qh(n,e);var t=Object.prototype.toString.call(n).slice(8,-1);return"Object"===t&&n.constructor&&(t=n.constructor.name),"Map"===t||"Set"===t?Array.from(n):"Arguments"===t||/^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(t)?Qh(n,e):void 0}}(n))||e&&n&&"number"==typeof n.length){t&&(n=t);var r=0,o=function(){};return{s:o,n:function(){return r>=n.length?{done:!0}:{done:!1,value:n[r++]}},e:function(n){throw n},f:o}}throw new TypeError("Invalid attempt to iterate non-iterable instance.\nIn order to be iterable, non-array objects must have a [Symbol.iterator]() method.")}var i,a=!0,l=!1;return{s:function(){t=t.call(n)},n:function(){var n=t.next();return a=n.done,n},e:function(n){l=!0,i=n},f:function(){try{a||null==t.return||t.return()}finally{if(l)throw i}}}}function Qh(n,e){(null==e||e>n.length)&&(e=n.length);for(var t=0,r=new Array(e);t<e;t++)r[t]=n[t];return r}var nf=function(){function n(e,t){(0,c.Z)(this,n),this.attach={atomid:t.atomid||0,bondid:t.bondid||0},this.editor=e,this.editor.selection({atoms:[this.attach.atomid],bonds:[this.attach.bondid]})}return(0,s.Z)(n,[{key:"mousemove",value:function(n){var e,t=this.editor.render,r=this.editor.findItem(n,["atoms","bonds"]),o=t.ctab.molecule;return r&&("atoms"===r.map&&u.eKO.get(null===(e=o.atoms.get(r.id))||void 0===e?void 0:e.label)||"bonds"===r.map)?this.editor.hover(r):this.editor.hover(null),!0}},{key:"click",value:function(n){var e,t=this.editor,r=t.render.ctab.molecule,o=r.functionalGroups,i=t.findItem(n,["atoms","bonds"]),a=[],l=[],c=[];if(i&&o.size&&"atoms"===i.map){var s=u.J41.atomsInFunctionalGroup(o,i.id);null!==s&&a.push(s)}if(i&&o.size&&"bonds"===i.map){var d=u.J41.bondsInFunctionalGroup(r,o,i.id);null!==d&&l.push(d)}if(a.length>0){var p,h=Xh(a);try{for(h.s();!(p=h.n()).done;){var f=p.value,m=u.J41.findFunctionalGroupByAtom(o,f);null===m||c.includes(m)||c.push(m)}}catch(n){h.e(n)}finally{h.f()}this.editor.event.removeFG.dispatch({fgIds:c})}else{if(!(l.length>0))return i&&("atoms"===i.map&&u.eKO.get(null===(e=r.atoms.get(i.id))||void 0===e?void 0:e.label)||"bonds"===i.map)&&("atoms"===i.map?this.attach.atomid=i.id:this.attach.bondid=i.id,this.editor.selection({atoms:[this.attach.atomid],bonds:[this.attach.bondid]}),this.editor.event.attachEdit.dispatch(this.attach)),!0;var v,g=Xh(l);try{for(g.s();!(v=g.n()).done;){var b=v.value,C=u.J41.findFunctionalGroupByBond(r,o,b);null===C||c.includes(C)||c.push(C)}}catch(n){g.e(n)}finally{g.f()}this.editor.event.removeFG.dispatch({fgIds:c})}}}]),n}();function ef(n,e){var t="undefined"!=typeof Symbol&&n[Symbol.iterator]||n["@@iterator"];if(!t){if(Array.isArray(n)||(t=function(n,e){if(n){if("string"==typeof n)return tf(n,e);var t=Object.prototype.toString.call(n).slice(8,-1);return"Object"===t&&n.constructor&&(t=n.constructor.name),"Map"===t||"Set"===t?Array.from(n):"Arguments"===t||/^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(t)?tf(n,e):void 0}}(n))||e&&n&&"number"==typeof n.length){t&&(n=t);var r=0,o=function(){};return{s:o,n:function(){return r>=n.length?{done:!0}:{done:!1,value:n[r++]}},e:function(n){throw n},f:o}}throw new TypeError("Invalid attempt to iterate non-iterable instance.\nIn order to be iterable, non-array objects must have a [Symbol.iterator]() method.")}var i,a=!0,l=!1;return{s:function(){t=t.call(n)},n:function(){var n=t.next();return a=n.done,n},e:function(n){l=!0,i=n},f:function(){try{a||null==t.return||t.return()}finally{if(l)throw i}}}}function tf(n,e){(null==e||e>n.length)&&(e=n.length);for(var t=0,r=new Array(e);t<e;t++)r[t]=n[t];return r}var rf=function(){function n(e,t){var r;if((0,c.Z)(this,n),this.editor=e,this.atomProps={label:"C"},this.bondProps=t,e.selection()&&null!==(r=e.selection())&&void 0!==r&&r.bonds){var o=(0,u.Wa4)(e.render.ctab,e.selection().bonds,t);e.update(o),e.selection(null),this.isNotActiveTool=!0}}return(0,s.Z)(n,[{key:"mousedown",value:function(n){if(!this.dragCtx){var e=this.editor.render.ctab.molecule,t=e.functionalGroups,r=this.editor.findItem(n,["atoms","bonds"]),o=[],i=[],a=[];if(r&&t.size&&"atoms"===r.map){var l=u.J41.atomsInFunctionalGroup(t,r.id);null!==l&&o.push(l)}if(r&&t.size&&"bonds"===r.map){var c=u.J41.bondsInFunctionalGroup(e,t,r.id);null!==c&&i.push(c)}if(o.length>0){var s,d=ef(o);try{for(d.s();!(s=d.n()).done;){var p=s.value,h=u.J41.findFunctionalGroupByAtom(t,p);null===h||a.includes(h)||a.push(h)}}catch(n){d.e(n)}finally{d.f()}this.editor.event.removeFG.dispatch({fgIds:a})}else{if(!(i.length>0)){var f=this.editor.render;return this.editor.hover(null),this.editor.selection(null),this.dragCtx={xy0:f.page2obj(n),item:this.editor.findItem(n,["atoms","bonds"])},this.dragCtx.item||delete this.dragCtx.item,!0}var m,v=ef(i);try{for(v.s();!(m=v.n()).done;){var g=m.value,b=u.J41.findFunctionalGroupByBond(e,t,g);null===b||a.includes(b)||a.push(b)}}catch(n){v.e(n)}finally{v.f()}this.editor.event.removeFG.dispatch({fgIds:a})}}}},{key:"mousemove",value:function(n){var e=this.editor.render.ctab,t=e.sgroups,r=e.molecule,o=r.functionalGroups,i=this.editor,a=i.render;if("dragCtx"in this){var l=this.dragCtx,c=a.page2obj(n),s=Kh.calcAngle(l.xy0,c);n.ctrlKey||(s=Kh.fracAngle(s,null));var d=Kh.degrees(s);if(this.editor.event.message.dispatch({info:d+"º"}),!("item"in l)||"atoms"===l.item.map){var p,h,f,m;"action"in l&&l.action.perform(a.ctab);var v=[];if("item"in l&&"atoms"===l.item.map){p=l.item.id,h=i.findItem(n,["atoms"],l.item);var g=i.findItem(n,["functionalGroups"]);if(g&&u.J41.isContractedFunctionalGroup(g.id,o)){var b=t.get(g.id);h={id:u.j1n.getAtoms(r,null==b?void 0:b.item)[0],map:"atoms"}}var C=h&&u.J41.findFunctionalGroupByAtom(o,h.id),y="number"==typeof C&&t.get(C),O=y&&u.j1n.getAtoms(r,y.item);if(h&&y&&h.id!==(null==O?void 0:O[0])&&(this.editor.event.removeFG.dispatch({fgIds:[C]}),h=null),h&&y&&h.id===(null==O?void 0:O[0])){var w=r.atomGetNeighbors(h.id);null==w||w.forEach((function(n){(null==O||!O.includes(n.aid))&&!v.includes(n.aid)&&v.push(n.aid)}))}v.length>=1&&(h=null)}else{p=this.atomProps,f=l.xy0;var S=[],M=[];if((h=i.findItem(n,["atoms"]))&&"atoms"===h.map&&o.size&&this.dragCtx){var x=u.J41.atomsInFunctionalGroup(o,h.id);null!==x&&S.push(x)}if(S.length>0){var j,E=ef(S);try{for(E.s();!(j=E.n()).done;){var D=j.value,A=u.J41.findFunctionalGroupByAtom(o,D);null!==A&&!M.includes(A)&&M.push(A)}}catch(n){E.e(n)}finally{E.f()}}if(M.length>0)return this.editor.event.removeFG.dispatch({fgIds:M}),void delete this.dragCtx}var $=Number.MAX_VALUE;if(h&&"atoms"===h.map)h=h.id;else{h=this.atomProps;var N=a.page2obj(n);if($=u.Sgu.dist(l.xy0,N),f)m=Kh.calcNewAtomPos(f,N,n.ctrlKey);else{var P=a.ctab.molecule.atoms.get(p);f=Kh.calcNewAtomPos(null==P?void 0:P.pp.get_xy0(),N,n.ctrlKey)}}return $>.3?l.action=(0,u.QXZ)(a.ctab,this.bondProps,p,h,f,m)[0]:delete l.action,this.editor.update(l.action,!0),!0}}return this.editor.hover(this.editor.findItem(n,["atoms","bonds"]),null,n),!0}},{key:"mouseup",value:function(n){if("dragCtx"in this){var e=this.dragCtx,t=this.editor.render,r=t.ctab.molecule;if("action"in e)this.editor.update(e.action);else if("item"in e){if("atoms"===e.item.map)this.editor.update((0,u.QXZ)(t.ctab,this.bondProps,e.item.id,void 0)[0]);else if("bonds"===e.item.map){var o=Object.assign({},this.bondProps),i=r.bonds.get(e.item.id);this.editor.update((0,u.Mqr)(t.ctab,e.item.id,i,o))}}else{var a=t.page2obj(n),l=new u.Sgu(.5,0).rotate(this.bondProps.type===u.fYe.PATTERN.TYPE.SINGLE?-Math.PI/6:0),c=(0,u.QXZ)(t.ctab,this.bondProps,{label:"C"},{label:"C"},u.Sgu.diff(a,l),u.Sgu.sum(a,l));this.editor.update(c[0])}delete this.dragCtx}return this.editor.event.message.dispatch({info:!1}),!0}}]),n}();function of(n,e){var t="undefined"!=typeof Symbol&&n[Symbol.iterator]||n["@@iterator"];if(!t){if(Array.isArray(n)||(t=function(n,e){if(n){if("string"==typeof n)return af(n,e);var t=Object.prototype.toString.call(n).slice(8,-1);return"Object"===t&&n.constructor&&(t=n.constructor.name),"Map"===t||"Set"===t?Array.from(n):"Arguments"===t||/^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(t)?af(n,e):void 0}}(n))||e&&n&&"number"==typeof n.length){t&&(n=t);var r=0,o=function(){};return{s:o,n:function(){return r>=n.length?{done:!0}:{done:!1,value:n[r++]}},e:function(n){throw n},f:o}}throw new TypeError("Invalid attempt to iterate non-iterable instance.\nIn order to be iterable, non-array objects must have a [Symbol.iterator]() method.")}var i,a=!0,l=!1;return{s:function(){t=t.call(n)},n:function(){var n=t.next();return a=n.done,n},e:function(n){l=!0,i=n},f:function(){try{a||null==t.return||t.return()}finally{if(l)throw i}}}}function af(n,e){(null==e||e>n.length)&&(e=n.length);for(var t=0,r=new Array(e);t<e;t++)r[t]=n[t];return r}var lf=function(){function n(e){(0,c.Z)(this,n),this.editor=e,this.editor.selection(null)}return(0,s.Z)(n,[{key:"mousedown",value:function(n){if(!this.dragCtx){var e=this.editor.render.ctab.molecule,t=e.functionalGroups,r=this.editor.render,o=this.editor.findItem(n,["atoms","bonds"]),i=[],a=[],l=[];if(o&&t.size&&"atoms"===o.map){var c=u.J41.atomsInFunctionalGroup(t,o.id);null!==c&&i.push(c)}if(o&&t.size&&"bonds"===o.map){var s=u.J41.bondsInFunctionalGroup(e,t,o.id);null!==s&&a.push(s)}if(i.length>0){var d,p=of(i);try{for(p.s();!(d=p.n()).done;){var h=d.value,f=u.J41.findFunctionalGroupByAtom(t,h);null===f||l.includes(f)||l.push(f)}}catch(n){p.e(n)}finally{p.f()}this.editor.event.removeFG.dispatch({fgIds:l})}else{if(!(a.length>0))return this.editor.hover(null),this.dragCtx={xy0:r.page2obj(n),item:o},o&&"atoms"===o.map&&(this.editor.selection({atoms:[o.id]}),Wh(this,r)),this.dragCtx.item||delete this.dragCtx.item,!0;var m,v=of(a);try{for(v.s();!(m=v.n()).done;){var g=m.value,b=u.J41.findFunctionalGroupByBond(e,t,g);null===b||l.includes(b)||l.push(b)}}catch(n){v.e(n)}finally{v.f()}this.editor.event.removeFG.dispatch({fgIds:l})}}}},{key:"mousemove",value:function(n){var e=this.editor,t=e.render.ctab,r=this.dragCtx;if(e.hover(this.editor.findItem(n,["atoms","bonds"]),null,n),!r)return!0;if(r&&r.stopTapping&&r.stopTapping(),e.selection(null),!r.item||"atoms"===r.item.map){var o;r.action&&r.action.perform(t);var i=t.molecule.atoms,a=r.item?null===(o=i.get(r.item.id))||void 0===o?void 0:o.pp:r.xy0,l=e.render.page2obj(n),c=Math.ceil(u.Sgu.diff(l,a).length()),s=n.ctrlKey?Kh.calcAngle(a,l):Kh.fracAngle(a,l),d=(0,u.bDx)(t,a,s,c,r.item?r.item.id:null),p=(0,O.Z)(d,2),h=p[0],f=p[1];return e.event.message.dispatch({info:c+" sectors"}),r.action=h,e.update(r.action,!0),r.mergeItems=(0,u.z8H)(e,f),e.hover((0,u.QOv)(r.mergeItems)),!0}return!0}},{key:"mouseup",value:function(){var n,e=this.editor.render.ctab,t=e.molecule,r=t.functionalGroups,o=[],i=[];if(this.dragCtx&&this.dragCtx.mergeItems&&r.size&&(n=this.dragCtx.mergeItems.atoms.values().next().value),n){var a=u.J41.atomsInFunctionalGroup(r,n);null!==a&&o.push(a)}if(!(o.length>0)){var l=this.dragCtx;if(!l)return!0;delete this.dragCtx;var c=this.editor;if(l.stopTapping&&l.stopTapping(),!l.action&&l.item&&"bonds"===l.item.map){var s=t.bonds.get(l.item.id);l.action=(0,u.Mqr)(e,l.item.id,s,{type:u.fYe.PATTERN.TYPE.SINGLE,stereo:u.fYe.PATTERN.STEREO.NONE})}else l.action=l.action?(0,u.ghY)(e,l.mergeItems).mergeWith(l.action):(0,u.ghY)(e,l.mergeItems);return c.selection(null),c.hover(null),l.action&&c.update(l.action),c.event.message.dispatch({info:!1}),!0}var d,p=of(o);try{for(p.s();!(d=p.n()).done;){var h=d.value,f=u.J41.findFunctionalGroupByAtom(r,h);null===f||i.includes(f)||i.push(f)}}catch(n){p.e(n)}finally{p.f()}this.editor.event.removeFG.dispatch({fgIds:i})}},{key:"cancel",value:function(){this.mouseup()}},{key:"mouseleave",value:function(){this.mouseup()}}]),n}();function cf(n,e){(null==e||e>n.length)&&(e=n.length);for(var t=0,r=new Array(e);t<e;t++)r[t]=n[t];return r}var sf=function(){function n(e,t){(0,c.Z)(this,n),this.editor=e,this.editor.selection(null),this.charge=t}return(0,s.Z)(n,[{key:"mousemove",value:function(n){var e,t=this.editor.render.ctab.molecule,r=this.editor.findItem(n,["atoms"]);return r&&"atoms"===r.map&&u.eKO.get(null===(e=t.atoms.get(r.id))||void 0===e?void 0:e.label)?this.editor.hover(r):this.editor.hover(null,null,n),!0}},{key:"click",value:function(n){var e,t,r=this.editor,o=this.editor.render.ctab.molecule,i=o.functionalGroups,a=r.render,l=r.findItem(n,["atoms","bonds"]),c=[],s=[];if(l&&i.size&&"atoms"===l.map){var d=u.J41.atomsInFunctionalGroup(i,l.id);null!==d&&c.push(d)}if(!(c.length>0))return l&&"atoms"===l.map&&u.eKO.get(null===(e=o.atoms.get(l.id))||void 0===e?void 0:e.label)&&(this.editor.hover(null),this.editor.update((0,u.dBq)(a.ctab,l.id,{charge:(null===(t=o.atoms.get(l.id))||void 0===t?void 0:t.charge)+this.charge},null))),!0;var p,h=function(n,e){var t="undefined"!=typeof Symbol&&n[Symbol.iterator]||n["@@iterator"];if(!t){if(Array.isArray(n)||(t=function(n,e){if(n){if("string"==typeof n)return cf(n,e);var t=Object.prototype.toString.call(n).slice(8,-1);return"Object"===t&&n.constructor&&(t=n.constructor.name),"Map"===t||"Set"===t?Array.from(n):"Arguments"===t||/^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(t)?cf(n,e):void 0}}(n))||e&&n&&"number"==typeof n.length){t&&(n=t);var r=0,o=function(){};return{s:o,n:function(){return r>=n.length?{done:!0}:{done:!1,value:n[r++]}},e:function(n){throw n},f:o}}throw new TypeError("Invalid attempt to iterate non-iterable instance.\nIn order to be iterable, non-array objects must have a [Symbol.iterator]() method.")}var i,a=!0,l=!1;return{s:function(){t=t.call(n)},n:function(){var n=t.next();return a=n.done,n},e:function(n){l=!0,i=n},f:function(){try{a||null==t.return||t.return()}finally{if(l)throw i}}}}(c);try{for(h.s();!(p=h.n()).done;){var f=p.value,m=u.J41.findFunctionalGroupByAtom(i,f);null===m||s.includes(m)||s.push(m)}}catch(n){h.e(n)}finally{h.f()}this.editor.event.removeFG.dispatch({fgIds:s})}}]),n}(),uf=function(){function n(e){(0,c.Z)(this,n);var t=e.selection();this.editor=e,this.isNotActiveTool=!0,this.stereoAtoms=(0,u.f0f)(e.struct(),t?t.atoms||[]:Array.from(e.struct().atoms.keys())),0!==this.stereoAtoms.length&&this.changeAtomsStereoAction().then((function(n){return n&&e.update(n)}))}return(0,s.Z)(n,[{key:"changeAtomsStereoAction",value:function(){var n=this,e=this.editor.struct(),t=this.editor.render.ctab,r=this.stereoAtoms.map((function(n){var t=e.atoms.get(n);return t&&t.stereoLabel})),o=r.some((function(n){return n!==r[0]}));return this.editor.event.enhancedStereoEdit.dispatch({stereoLabel:o?null:r[0]}).then((function(r){if(!r)return null;var o=n.stereoAtoms.reduce((function(n,r){var o;return n.mergeWith((0,u.Eps)(t,null===(o=e.atoms.get(r))||void 0===o?void 0:o.fragment))}),(0,u.dBq)(t,n.stereoAtoms,{stereoLabel:r},!1));return o.operations.reverse(),o}))}}]),n}();function df(n,e){for(var t=new u.Sgu(0,1),r=t.rotate(Math.PI/2),o=u.Sgu.diff(n[n.length-1],e),i=u.Sgu.dot(r,o),a=u.Sgu.dot(t,o),l=new u.Sgu(0,0),c=0,s=1e-5,d=!1,p=!1,h=0;h<n.length;++h){var f=u.Sgu.diff(n[h],e),m=u.Sgu.diff(f,o),v=u.Sgu.dot(r,f),g=u.Sgu.dot(t,f);d=!1,v*i<0&&(g*a>-s?a>-s&&(d=!0):(Math.abs(i)*Math.abs(g)-Math.abs(v)*Math.abs(a))*g>0&&(d=!0)),d&&p&&u.Sgu.dot(m,r)*u.Sgu.dot(l,r)>=0&&(d=!1),d&&c++,o=f,i=v,a=g,l=m,p=d}return c%2!=0}var pf=function(n,e,t){var r=[],o=[],i=n.sgroups,a=n.molecule.functionalGroups,l=Math.min(e.x,t.x),c=Math.max(e.x,t.x),s=Math.min(e.y,t.y),d=Math.max(e.y,t.y);n.bonds.forEach((function(e,t){var o=u.Sgu.lc2(n.atoms.get(e.b.begin).a.pp,.5,n.atoms.get(e.b.end).a.pp,.5);o.x>l&&o.x<c&&o.y>s&&o.y<d&&!u.J41.isBondInContractedFunctionalGroup(e.b,i,a,!0)&&r.push(t)})),n.atoms.forEach((function(e,t){var r=u.J41.findFunctionalGroupByAtom(a,t),p=n.sgroups.get(r);e.a.pp.x>l&&e.a.pp.x<c&&e.a.pp.y>s&&e.a.pp.y<d&&(!u.J41.isAtomInContractedFunctionalGroup(e.a,i,a,!0)||t===p.item.atoms[0])&&o.push(t)}));var p=[],h=[],f=[];n.rxnArrows.forEach((function(n,e){n.item.center().x>l&&n.item.center().x<c&&n.item.center().y>s&&n.item.center().y<d&&p.push(e)})),n.rxnPluses.forEach((function(n,e){n.item.pp.x>l&&n.item.pp.x<c&&n.item.pp.y>s&&n.item.pp.y<d&&h.push(e)})),n.simpleObjects.forEach((function(n,e){n.getReferencePoints(!0).find((function(n){return n.x>l&&n.x<c&&n.y>s&&n.y<d}))&&f.push(e)}));var m=[];n.enhancedFlags.forEach((function(n,e){n.pp&&n.pp.x>l&&n.pp.x<c&&n.pp.y>s&&n.pp.y<d&&m.push(e)}));var v=[];n.sgroupData.forEach((function(n,e){n.sgroup.pp.x>l&&n.sgroup.pp.x<c&&n.sgroup.pp.y>s&&n.sgroup.pp.y<d&&v.push(e)}));var g=[];return n.texts.forEach((function(n,e){n.getReferencePoints().find((function(n){return n.x>l&&n.x<c&&n.y>s&&n.y<d}))&&g.push(e)})),{atoms:o,bonds:r,rxnArrows:p,rxnPluses:h,enhancedFlags:m,sgroupData:v,simpleObjects:f,texts:g}},hf=function(n,e){for(var t=[],r=[],o=[],i=n.sgroups,a=n.molecule.functionalGroups,l=0;l<e.length;++l)o[l]=new u.Sgu(e[l].x,e[l].y);n.bonds.forEach((function(e,r){var l=u.Sgu.lc2(n.atoms.get(e.b.begin).a.pp,.5,n.atoms.get(e.b.end).a.pp,.5);df(o,l)&&!u.J41.isBondInContractedFunctionalGroup(e.b,i,a,!0)&&t.push(r)})),n.atoms.forEach((function(e,t){var l=u.J41.findFunctionalGroupByAtom(a,t),c=n.sgroups.get(l);!df(o,e.a.pp)||u.J41.isAtomInContractedFunctionalGroup(e.a,i,a,!0)&&t!==c.item.atoms[0]||r.push(t)}));var c=[],s=[],d=[],p=[];n.rxnArrows.forEach((function(n,e){n.getReferencePoints(!0).find((function(n){return df(o,n)}))&&c.push(e)})),n.rxnPluses.forEach((function(n,e){df(o,n.item.pp)&&s.push(e)})),n.simpleObjects.forEach((function(n,e){n.getReferencePoints(!0).find((function(n){return df(o,n)}))&&d.push(e)})),n.texts.forEach((function(n,e){n.getReferencePoints().find((function(n){return df(o,n)}))&&p.push(e)}));var h=[];n.enhancedFlags.forEach((function(n,e){n.pp&&df(o,n.pp)&&h.push(e)}));var f=[];return n.sgroupData.forEach((function(n,e){df(o,n.sgroup.pp)&&f.push(e)})),{atoms:r,bonds:t,rxnArrows:c,rxnPluses:s,enhancedFlags:h,sgroupData:f,simpleObjects:d,texts:p}},ff=function(){function n(e,t,r){(0,c.Z)(this,n),this.mode=e,this.fragment=r,this.editor=t}return(0,s.Z)(n,[{key:"getSelection",value:function(){var n=this.editor.render;if(0===this.mode)return hf(n.ctab,this.points);if(1===this.mode)return pf(n.ctab,this.points[0],this.points[1]);throw new Error("Selector mode unknown")}},{key:"begin",value:function(n){var e=this.editor.render;this.points=[e.page2obj(n)],1===this.mode&&this.points.push(this.points[0])}},{key:"running",value:function(){return!!this.points}},{key:"addPoint",value:function(n){if(!this.points)return null;var e=this.editor.render;return 0===this.mode?this.points.push(e.page2obj(n)):1===this.mode&&(this.points=[this.points[0],e.page2obj(n)]),this.update(),this.getSelection()}},{key:"update",value:function(){if(this.selection&&(this.selection.remove(),this.selection=null),this.points&&this.points.length>1){var n=this.editor.render,e=this.points.map((function(e){return u.Ciz.obj2scaled(e,n.options).add(n.options.offset)}));this.selection=0===this.mode?n.selectionPolygon(e):n.selectionRectangle(e[0],e[1])}}},{key:"end",value:function(){var n=this.getSelection();return this.points=null,this.update(),n}},{key:"cancel",value:function(){this.points=null,this.update()}}]),n}();function mf(n,e){var t="undefined"!=typeof Symbol&&n[Symbol.iterator]||n["@@iterator"];if(!t){if(Array.isArray(n)||(t=function(n,e){if(n){if("string"==typeof n)return vf(n,e);var t=Object.prototype.toString.call(n).slice(8,-1);return"Object"===t&&n.constructor&&(t=n.constructor.name),"Map"===t||"Set"===t?Array.from(n):"Arguments"===t||/^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(t)?vf(n,e):void 0}}(n))||e&&n&&"number"==typeof n.length){t&&(n=t);var r=0,o=function(){};return{s:o,n:function(){return r>=n.length?{done:!0}:{done:!1,value:n[r++]}},e:function(n){throw n},f:o}}throw new TypeError("Invalid attempt to iterate non-iterable instance.\nIn order to be iterable, non-array objects must have a [Symbol.iterator]() method.")}var i,a=!0,l=!1;return{s:function(){t=t.call(n)},n:function(){var n=t.next();return a=n.done,n},e:function(n){l=!0,i=n},f:function(){try{a||null==t.return||t.return()}finally{if(l)throw i}}}}function vf(n,e){(null==e||e>n.length)&&(e=n.length);for(var t=0,r=new Array(e);t<e;t++)r[t]=n[t];return r}var gf=["atoms","bonds","sgroups","functionalGroups","sgroupData"],bf=function(){function n(e,t){(0,c.Z)(this,n),this.editor=e,this.type=t,this.lassoHelper=new ff(1,e,null),this.checkSelection()}return(0,s.Z)(n,[{key:"checkSelection",value:function(){var e=this.editor.selection()||{};if(e.atoms&&e.bonds){var t,r,o,i=null===(t=this.editor.selection())||void 0===t?void 0:t.atoms,a=this.editor.render.ctab,l=a.molecule,c=l.sgroups,s={atoms:[],bonds:[]},d=[],p=l.functionalGroups,h=[],f=c.find((function(n,e){return(0,y.isEqual)(e.atoms,i)}));if(i&&p.size){var m,v=mf(i);try{for(v.s();!(m=v.n()).done;){var g,b=m.value,C=u.J41.atomsInFunctionalGroup(p,b);null==C&&(o=!0);var O=null!==C&&(null===(g=a.atoms.get(C))||void 0===g?void 0:g.a);if(O){var w,S=mf(O.sgs.values());try{for(S.s();!(w=S.n()).done;)r=w.value}catch(n){S.e(n)}finally{S.f()}}if(O&&u.J41.isAtomInContractedFunctionalGroup(O,c,p,!1)){var M,j,E=void 0!==r&&u.j1n.getAtoms(l,c.get(r)),D=void 0!==r&&u.j1n.getBonds(l,c.get(r));b===E[0]&&(M=s.atoms).push.apply(M,(0,x.Z)(E))&&(j=s.bonds).push.apply(j,(0,x.Z)(D))}O&&d.push(C)}}catch(n){v.e(n)}finally{v.f()}}if(o&&(d=[]),d&&d.length>0){var A,$=mf(d);try{for($.s();!(A=$.n()).done;){var N=A.value,P=u.J41.findFunctionalGroupByAtom(p,N);null===P||h.includes(P)||h.push(P)}}catch(n){$.e(n)}finally{$.f()}}if(h.length)return this.editor.selection(null),void this.editor.event.removeFG.dispatch({fgIds:h});n.sgroupDialog(this.editor,null!=f?f:null,this.type),this.isNotActiveTool=!0}}},{key:"mousedown",value:function(n){var e=this.editor.findItem(n,gf),t=this.editor.render.ctab,r=t.sgroups,o=t.molecule,i=o.functionalGroups,a=[],l=[],c=[];if(e&&i.size&&"atoms"===e.map){var s,d=u.J41.atomsInFunctionalGroup(i,e.id),p=null!==d&&(null===(s=t.atoms.get(d))||void 0===s?void 0:s.a);p&&!u.J41.isAtomInContractedFunctionalGroup(p,r,i,!0)&&a.push(d)}if(e&&i.size&&"bonds"===e.map){var h,f=u.J41.bondsInFunctionalGroup(o,i,e.id),m=null!==f&&(null===(h=t.bonds.get(f))||void 0===h?void 0:h.b);m&&!u.J41.isBondInContractedFunctionalGroup(m,r,i,!0)&&l.push(f)}if(e&&i.size&&"functionalGroups"===e.map){var v=r.get(e.id);if(u.J41.isFunctionalGroup(null==v?void 0:v.item))return void this.editor.event.removeFG.dispatch({fgIds:[e.id]})}if(a.length>0){var g,b=mf(a);try{for(b.s();!(g=b.n()).done;){var C=g.value,y=u.J41.findFunctionalGroupByAtom(i,C);null===y||c.includes(y)||c.push(y)}}catch(n){b.e(n)}finally{b.f()}this.editor.event.removeFG.dispatch({fgIds:c})}else if(l.length>0){var O,w=mf(l);try{for(w.s();!(O=w.n()).done;){var S=O.value,M=u.J41.findFunctionalGroupByBond(o,i,S);null===M||c.includes(M)||c.push(M)}}catch(n){w.e(n)}finally{w.f()}this.editor.event.removeFG.dispatch({fgIds:c})}else e||this.lassoHelper.begin(n)}},{key:"mousemove",value:function(n){this.lassoHelper.running(n)?this.editor.selection(this.lassoHelper.addPoint(n)):this.editor.hover(this.editor.findItem(n,gf))}},{key:"mouseleave",value:function(n){this.lassoHelper.running(n)&&this.lassoHelper.end(n)}},{key:"mouseup",value:function(e){var t,r,o,i=this.editor.render.ctab,a=i.sgroups,l=i.molecule,c=l.functionalGroups,s=this.editor.findItem(e,gf),d=this.editor.selection(),p={atoms:[],bonds:[]},h=[],f=[],m=[];if(!(s&&"functionalGroups"===s.map&&c.size&&u.J41.isContractedFunctionalGroup(s.id,c))){if(d&&c.size&&d.atoms){var v,g=mf(d.atoms);try{for(g.s();!(v=g.n()).done;){var b,C=v.value,y=u.J41.atomsInFunctionalGroup(c,C);null==y&&(r=!0);var O=null!==y&&(null===(b=i.atoms.get(y))||void 0===b?void 0:b.a);if(O){var w,S=mf(O.sgs.values());try{for(S.s();!(w=S.n()).done;)t=w.value}catch(n){S.e(n)}finally{S.f()}}if(O&&u.J41.isAtomInContractedFunctionalGroup(O,a,c,!0)){var M,j,E,D,A=void 0!==t&&u.j1n.getAtoms(l,null===(M=i.sgroups.get(t))||void 0===M?void 0:M.item),$=void 0!==t&&u.j1n.getBonds(l,null===(j=i.sgroups.get(t))||void 0===j?void 0:j.item);C===A[0]&&(E=p.atoms).push.apply(E,(0,x.Z)(A))&&(D=p.bonds).push.apply(D,(0,x.Z)($))}O&&h.push(y)}}catch(n){g.e(n)}finally{g.f()}}if(d&&c.size&&d.bonds){var N,P=mf(d.bonds);try{for(P.s();!(N=P.n()).done;){var k,I=N.value,T=u.J41.bondsInFunctionalGroup(l,c,I);null===T&&(o=!0),null!==T&&(null===(k=i.bonds.get(T))||void 0===k?void 0:k.b)&&f.push(T)}}catch(n){P.e(n)}finally{P.f()}}if(h.length&&h.forEach((function(n){var e,t,r=u.J41.findFunctionalGroupByAtom(c,n),o=u.j1n.getAtoms(l,null===(e=i.sgroups.get(r))||void 0===e?void 0:e.item);(t=p.atoms).push.apply(t,(0,x.Z)(o))})),f.length&&f.forEach((function(n){var e,t,r=u.J41.findFunctionalGroupByBond(l,c,n),o=u.j1n.getBonds(l,null===(e=i.sgroups.get(r))||void 0===e?void 0:e.item);(t=p.bonds).push.apply(t,(0,x.Z)(o))})),(r||o)&&(h=null,f=null),h&&h.length>0){var B,L=mf(h);try{for(L.s();!(B=L.n()).done;){var _=B.value,V=u.J41.findFunctionalGroupByAtom(c,_);null===V||m.includes(V)||m.push(V)}}catch(n){L.e(n)}finally{L.f()}}if(f&&f.length>0){var z,G=mf(f);try{for(G.s();!(z=G.n()).done;){var F=z.value,H=u.J41.findFunctionalGroupByBond(l,c,F);null===H||m.includes(H)||m.push(H)}}catch(n){G.e(n)}finally{G.f()}}if(1===m.length)return this.editor.selection(null),this.lassoHelper.cancel(),void this.editor.event.removeFG.dispatch({fgIds:m});var R=null,Z=null;if(this.lassoHelper.running(e))Z=p.atoms.length>0?kf(this.lassoHelper.end(e),p,!1):this.lassoHelper.end(e),this.editor.selection(Z);else{if(!s)return;if(this.editor.hover(null),"atoms"===s.map)Z={atoms:[s.id]};else if("bonds"===s.map){var K=this.editor.render.ctab.bonds.get(s.id);Z={atoms:[null==K?void 0:K.b.begin,null==K?void 0:K.b.end]}}else{if("sgroups"!==s.map&&"sgroupData"!==s.map)return;R=s.id}}(null!==R||Z&&Z.atoms)&&n.sgroupDialog(this.editor,R,this.type)}}},{key:"cancel",value:function(){this.lassoHelper.running()&&this.lassoHelper.end(),this.editor.selection(null)}}],[{key:"sgroupDialog",value:function(n,e,t){var r=n.render.ctab,o=r.molecule,i=n.selection()||{},a=null!==e?o.sgroups.get(e):null,l=a?a.type:t,c="DAT"===l?"sdataEdit":"sgroupEdit";if(i.atoms||i.bonds||a){var s;a?(s=a.getAttrs()).context||(s.context=function(n,e){var t=n.molecule;if(1===e.length)return u.I6H.Atom;if(wf(n,e))return u.I6H.Multifragment;if(Of(n,e))return u.I6H.Fragment;var r=new u.UE_(e),o=Array.from(t.bonds.values()).filter((function(n){return r.has(n.begin)&&r.has(n.end)}));return yf(o)?u.I6H.Group:u.I6H.Bond}(r,a.atoms)):s={context:Cf(r,i)};var d=n.event[c].dispatch({type:l,attrs:s});Promise.resolve(d).then((function(t){if("DAT"!==t.type&&(0,u.tIy)(o,i.atoms||[]))n.event.message.dispatch({error:"Partial S-group overlapping is not allowed."});else{if(!(a||"DAT"===t.type||i.atoms&&0!==i.atoms.length))return;if(a&&a.getAttrs().context===t.attrs.context){var l=(0,u.V4S)(r,t.type,a.atoms,t.attrs).mergeWith((0,u.U9$)(r,e));return n.update(l),void n.selection(i)}var c=function(n,e,t,r){var o=e.render.ctab,i=o.molecule.sgroups.get(n),a=i&&i.atoms||r.atoms||[],l=t.attrs.context,c=(0,u.Hwe)(l,o,t,a,r);return c.selection=c.selection||r,null!=n&&(c.action=c.action.mergeWith((0,u.U9$)(o,n))),e.selection(c.selection),c}(e,n,t,i);n.update(c.action),n.selection(null)}})).catch((function(){return null}))}}}]),n}();function Cf(n,e){var t=n.molecule;if(e.atoms&&!e.bonds)return u.I6H.Atom;var r=e.bonds.map((function(n){return t.bonds.get(n)}));if(!yf(r))return u.I6H.Bond;e.atoms=e.atoms||[];var o=new u.UE_(e.atoms),i=r.every((function(n){return o.has(n.begin)&&o.has(n.end)}));return Of(n,e.atoms)&&i?u.I6H.Fragment:wf(n,e.atoms)?u.I6H.Multifragment:u.I6H.Group}function yf(n){if(0===n.length)return!0;for(var e=0;e<n.length;++e)for(var t=n[e],r=0;r<n.length;++r)if(e!==r){var o=n[r];if(t.end===o.begin||t.end===o.end)return!0}return!1}function Of(n,e){return 1===Sf(n,e)}function wf(n,e){return Sf(n,e)>1}function Sf(n,e){var t=new u.UE_(e);return Array.from(n.connectedComponents.values()).reduce((function(n,e){return n+(t.isSuperset(e)?1:0)}),0)}function Mf(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function xf(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Mf(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Mf(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function jf(n,e){var t="undefined"!=typeof Symbol&&n[Symbol.iterator]||n["@@iterator"];if(!t){if(Array.isArray(n)||(t=function(n,e){if(n){if("string"==typeof n)return Ef(n,e);var t=Object.prototype.toString.call(n).slice(8,-1);return"Object"===t&&n.constructor&&(t=n.constructor.name),"Map"===t||"Set"===t?Array.from(n):"Arguments"===t||/^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(t)?Ef(n,e):void 0}}(n))||e&&n&&"number"==typeof n.length){t&&(n=t);var r=0,o=function(){};return{s:o,n:function(){return r>=n.length?{done:!0}:{done:!1,value:n[r++]}},e:function(n){throw n},f:o}}throw new TypeError("Invalid attempt to iterate non-iterable instance.\nIn order to be iterable, non-array objects must have a [Symbol.iterator]() method.")}var i,a=!0,l=!1;return{s:function(){t=t.call(n)},n:function(){var n=t.next();return a=n.done,n},e:function(n){l=!0,i=n},f:function(){try{a||null==t.return||t.return()}finally{if(l)throw i}}}}function Ef(n,e){(null==e||e>n.length)&&(e=n.length);for(var t=0,r=new Array(e);t<e;t++)r[t]=n[t];return r}function Df(n,e,t){!function(n,e){if(e.has(n))throw new TypeError("Cannot initialize the same private elements twice on an object")}(n,e),e.set(n,t)}var Af=new WeakMap,$f=new WeakMap,Nf=function(){function n(e,t){(0,c.Z)(this,n),Df(this,Af,{writable:!0,value:void 0}),Df(this,$f,{writable:!0,value:void 0}),this.editor=e,(0,R.Z)(this,Af,t),(0,R.Z)(this,$f,new ff("lasso"===(0,H.Z)(this,Af)?0:1,e,"fragment"===(0,H.Z)(this,Af)))}return(0,s.Z)(n,[{key:"mousedown",value:function(n){var e,t=this.editor.render,r=t.ctab,o=r.molecule,i=o.functionalGroups,a=[],l={atoms:[],bonds:[]};this.editor.hover(null);var c=(0,H.Z)(this,$f).fragment||n.ctrlKey,s=this.editor.findItem(n,c?["frags","sgroups","functionalGroups","sgroupData","rgroups","rxnArrows","rxnPluses","enhancedFlags","simpleObjects","texts"]:["atoms","bonds","sgroups","functionalGroups","sgroupData","rgroups","rxnArrows","rxnPluses","enhancedFlags","simpleObjects","texts"],null);if(s&&"atoms"===s.map&&i.size){var d,p=null!==u.J41.atomsInFunctionalGroup(i,s.id)&&(null===(d=r.atoms.get(s.id))||void 0===d?void 0:d.a);if(p){var h,f=jf(p.sgs.values());try{for(f.s();!(h=f.n()).done;)e=h.value}catch(n){f.e(n)}finally{f.f()}}p&&void 0!==e&&!a.includes(e)&&a.push(e)}if(s&&"bonds"===s.map&&i.size){var m=u.J41.bondsInFunctionalGroup(o,i,s.id),v=u.J41.findFunctionalGroupByBond(o,i,m);null===v||a.includes(v)||a.push(v)}if(a.length){var g,b=jf(a);try{for(b.s();!(g=b.n()).done;){var C=g.value,y=r.sgroups.get(C);if(y){var O,w,S=u.j1n.getAtoms(o,y.item),M=u.j1n.getBonds(o,y.item);(O=l.atoms).push.apply(O,(0,x.Z)(S))&&(w=l.bonds).push.apply(w,(0,x.Z)(M))}}}catch(n){b.e(n)}finally{b.f()}this.editor.selection(l)}if(this.dragCtx={item:s,xy0:t.page2obj(n)},s&&"atoms"!==s.map||Wh(this,t),!s)return n.shiftKey||this.editor.selection(null),delete this.dragCtx.item,(0,H.Z)(this,$f).fragment||(0,H.Z)(this,$f).begin(n),!0;var j=Pf(s),E=r.sgroups.get(s.id),D=this.editor.selection();if("frags"===s.map){var A=r.frags.get(s.id);j={atoms:A.fragGetAtoms(r,s.id),bonds:A.fragGetBonds(r,s.id)}}else if("sgroups"!==s.map&&"functionalGroups"!==s.map||!E){if("rgroups"===s.map){var $=r.rgroups.get(s.id);j={atoms:$.getAtoms(t),bonds:$.getBonds(t)}}else if("sgroupData"===s.map&&If(D,s))return!0}else{var N=E.item;j={atoms:u.j1n.getAtoms(o,N),bonds:u.j1n.getBonds(o,N)}}return n.shiftKey?this.editor.selection(kf(j,D,!0)):(this.editor.selection(null),this.editor.selection(If(D,s)?D:j)),!0}},{key:"mousemove",value:function(n){var e=this.editor,t=e.render,r=e.render.ctab,o=this.dragCtx;if(o&&o.stopTapping&&o.stopTapping(),o&&o.item){var i,a,l=r.molecule.atoms,c=e.selection();if("atoms"===o.item.map&&1===(null==l||null===(i=l.get(o.item.id))||void 0===i?void 0:i.neighbors.length)&&1===(null==c||null===(a=c.atoms)||void 0===a?void 0:a.length)&&!c.bonds){var s=t.page2obj(n),d=Kh.calcAngle(o.xy0,s),p=Kh.degrees(d);this.editor.event.message.dispatch({info:p+"º"})}if("simpleObjects"===o.item.map&&o.item.ref){null!=o&&o.action&&o.action.perform(t.ctab);var h=t.page2obj(n),f=h.sub(this.dragCtx.xy0);return o.action=(0,u.cMT)(t.ctab,o.item.id,f,h,o.item.ref,n.shiftKey),e.update(o.action,!0),!0}if("rxnArrows"===o.item.map&&o.item.ref){null!=o&&o.action&&o.action.perform(t.ctab);var m=t.page2obj(n),v=m.sub(o.xy0);return o.previous=m,o.action=(0,u.gHo)(t.ctab,o.item.id,v,m,o.item.ref),e.update(o.action,!0),!0}o.action&&(o.action.perform(r),e.update(o.action,!0));var g=e.explicitSelected();return o.action=(0,u.DYm)(r,g,e.render.page2obj(n).sub(o.xy0)),o.mergeItems=(0,u.z8H)(e,g),e.hover((0,u.QOv)(o.mergeItems)),e.update(o.action,!0),!0}if((0,H.Z)(this,$f).running()){var b=(0,H.Z)(this,$f).addPoint(n);return e.selection(n.shiftKey?kf(b,e.selection(),!1):b),!0}var C=(0,H.Z)(this,$f).fragment||n.ctrlKey?["frags","sgroups","functionalGroups","sgroupData","rgroups","rxnArrows","rxnPluses","enhancedFlags","simpleObjects","texts"]:["atoms","bonds","sgroups","functionalGroups","sgroupData","rgroups","rxnArrows","rxnPluses","enhancedFlags","simpleObjects","texts"];return e.hover(e.findItem(n,C,null),null,n),!0}},{key:"mouseup",value:function(n){var e,t=this.editor,r=t.selection(),o=t.render.ctab,i=o.molecule,a=i.functionalGroups,l=[],c={atoms:[],bonds:[]};if(r&&a.size&&r.atoms){var s,d=jf(r.atoms);try{for(d.s();!(s=d.n()).done;){var p,h=s.value,f=u.J41.atomsInFunctionalGroup(a,h),m=null!==f&&(null===(p=o.atoms.get(f))||void 0===p?void 0:p.a);if(m){var v,g=jf(m.sgs.values());try{for(g.s();!(v=g.n()).done;)e=v.value}catch(n){g.e(n)}finally{g.f()}}m&&void 0!==e&&!l.includes(e)&&l.push(e)}}catch(n){d.e(n)}finally{d.f()}}if(r&&a.size&&r.bonds){var b,C=jf(r.bonds);try{for(C.s();!(b=C.n()).done;){var y=b.value,O=u.J41.bondsInFunctionalGroup(i,a,y),w=u.J41.findFunctionalGroupByBond(i,a,O);null===w||l.includes(w)||l.push(w)}}catch(n){C.e(n)}finally{C.f()}}if(l.length){var S,M=jf(l);try{for(M.s();!(S=M.n()).done;){var j=S.value,E=o.sgroups.get(j);if(E){var D,A,$=u.j1n.getAtoms(i,E.item),N=u.j1n.getBonds(i,E.item);(D=c.atoms).push.apply(D,(0,x.Z)($))&&(A=c.bonds).push.apply(A,(0,x.Z)(N))}}}catch(n){M.e(n)}finally{M.f()}}var P=this.dragCtx;P&&P.stopTapping&&P.stopTapping();var k=o.sgroups.get(e);return(u.j1n.isSaltOrSolvent(null==k?void 0:k.item.data.name)||this.isDraggingStructureOnSaltOrSolvent(P,o.sgroups))&&P?(function(n,e,t){var r=e.action?(0,u.ghY)(n,null).mergeWith(e.action):(0,u.ghY)(n,null);t.hover(null),e.mergeItems&&t.selection(null),t.update(r),t.event.message.dispatch({info:!1})}(o,P,t),delete this.dragCtx,(0,H.Z)(this,$f).running()&&this.selectElementsOnCanvas(c,t,n),!0):(P&&P.item?(P.action=P.action?(0,u.ghY)(o,P.mergeItems).mergeWith(P.action):(0,u.ghY)(o,P.mergeItems),t.hover(null),P.mergeItems&&t.selection(null),0!==P.action.operations.length&&t.update(P.action),delete this.dragCtx):(0,H.Z)(this,$f).running()?this.selectElementsOnCanvas(c,t,n):(0,H.Z)(this,$f).fragment&&(n.shiftKey||t.selection(null)),t.event.message.dispatch({info:!1}),!0)}},{key:"dblclick",value:function(n){var e=this.editor,t=e.render.ctab,r=t.molecule,o=t.sgroups,i=r.functionalGroups,a=e.render,l=e.findItem(n,["atoms","bonds","sgroups","functionalGroups","sgroupData","texts"],null),c=[],s=[],d=[];if(l&&i&&"atoms"===l.map){var p,h=u.J41.atomsInFunctionalGroup(i,l.id),f=null!==h&&(null===(p=t.atoms.get(h))||void 0===p?void 0:p.a);null===h||u.J41.isAtomInContractedFunctionalGroup(f,o,i,!0)||c.push(h)}if(l&&i&&"bonds"===l.map){var m,v=u.J41.bondsInFunctionalGroup(r,i,l.id),g=null!==v&&(null===(m=t.bonds.get(v))||void 0===m?void 0:m.b);null===v||u.J41.isBondInContractedFunctionalGroup(g,o,i,!0)||s.push(v)}if(c.length>0){var b,C=jf(c);try{for(C.s();!(b=C.n()).done;){var y=b.value,O=u.J41.findFunctionalGroupByAtom(i,y);null===O||d.includes(O)||d.push(O)}}catch(n){C.e(n)}finally{C.f()}e.event.removeFG.dispatch({fgIds:d})}else{if(!(s.length>0)){if(!l)return!0;var w=this.editor.selection();if("atoms"===l.map){var S=new u.aUM,M=r.atoms.get(l.id),x=e.event.elementEdit.dispatch(M);if(null!=w&&w.atoms){var j=w.atoms;Promise.resolve(x).then((function(n){j.forEach((function(e){S.mergeWith((0,u.dBq)(t,e,n,!1))})),e.update(S)})).catch((function(){return null}))}}else if("bonds"===l.map){var E,D=null===(E=a.ctab.bonds.get(l.id))||void 0===E?void 0:E.b,A=e.event.bondEdit.dispatch(D);if(null!=w&&w.bonds){var $=new u.aUM,N=w.bonds;Promise.resolve(A).then((function(n){N.forEach((function(e){$.mergeWith((0,u.Wa4)(t,e,n))})),e.update($)})).catch((function(){return null}))}}else if("sgroups"===l.map&&!u.J41.isFunctionalGroup(r.sgroups.get(l.id))||"sgroupData"===l.map)e.selection(Pf(l)),bf.sgroupDialog(e,l.id,null);else if("texts"===l.map){e.selection(Pf(l));var P=r.texts.get(l.id);e.event.elementEdit.dispatch(xf(xf({},P),{},{type:"text"})).then((function(n){var r=n.content;r?r!==(null==P?void 0:P.content)&&e.update((0,u.rzF)(t,l.id,r)):e.update((0,u.NmG)(t,l.id))})).catch((function(){return null}))}return!0}var k,I=jf(s);try{for(I.s();!(k=I.n()).done;){var T=k.value,B=u.J41.findFunctionalGroupByBond(r,i,T);null===B||d.includes(B)||d.push(B)}}catch(n){I.e(n)}finally{I.f()}this.editor.event.removeFG.dispatch({fgIds:d})}}},{key:"mouseleave",value:function(n){if(this.dragCtx&&this.dragCtx.stopTapping&&this.dragCtx.stopTapping(),this.dragCtx&&this.dragCtx.action){var e=this.dragCtx.action;this.editor.update(e)}(0,H.Z)(this,$f).running()&&this.editor.selection((0,H.Z)(this,$f).end()),delete this.dragCtx,this.editor.hover(null)}},{key:"selectElementsOnCanvas",value:function(n,e,t){var r=n.atoms.length>0?kf((0,H.Z)(this,$f).end(),n,!1):(0,H.Z)(this,$f).end();e.selection(t.shiftKey?kf(r,e.selection(),!1):r)}},{key:"isDraggingStructureOnSaltOrSolvent",value:function(n,e){var t,r;if(null!=n&&n.mergeItems){var o=Array.from(n.mergeItems.atoms.values()),i=Array.from(n.mergeItems.bonds.values()),a=Array.from(e.values()).map((function(n){return n.item}));t=o.some((function(n){return u.j1n.isAtomInSaltOrSolvent(n,a)})),r=i.some((function(n){return u.j1n.isBondInSaltOrSolvent(n,a)}))}return t||r}}]),n}();function Pf(n){var e={};return e[n.map]=[n.id],e}function kf(n,e,t){return e&&Object.keys(e).forEach((function(r){n[r]?n[r]=function(n,e,t){return e.reduce((function(e,r){return t?n=(0,y.xor)(n,[r]):n.includes(r)||n.push(r),n}),[])}(n[r],e[r],t):n[r]=e[r].slice()})),n}function If(n,e){return n&&n[e.map]&&n[e.map].includes(e.id)}function Tf(n,e){var t="undefined"!=typeof Symbol&&n[Symbol.iterator]||n["@@iterator"];if(!t){if(Array.isArray(n)||(t=function(n,e){if(n){if("string"==typeof n)return Bf(n,e);var t=Object.prototype.toString.call(n).slice(8,-1);return"Object"===t&&n.constructor&&(t=n.constructor.name),"Map"===t||"Set"===t?Array.from(n):"Arguments"===t||/^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(t)?Bf(n,e):void 0}}(n))||e&&n&&"number"==typeof n.length){t&&(n=t);var r=0,o=function(){};return{s:o,n:function(){return r>=n.length?{done:!0}:{done:!1,value:n[r++]}},e:function(n){throw n},f:o}}throw new TypeError("Invalid attempt to iterate non-iterable instance.\nIn order to be iterable, non-array objects must have a [Symbol.iterator]() method.")}var i,a=!0,l=!1;return{s:function(){t=t.call(n)},n:function(){var n=t.next();return a=n.done,n},e:function(n){l=!0,i=n},f:function(){try{a||null==t.return||t.return()}finally{if(l)throw i}}}}function Bf(n,e){(null==e||e>n.length)&&(e=n.length);for(var t=0,r=new Array(e);t<e;t++)r[t]=n[t];return r}var Lf=function(){function n(e,t){if((0,c.Z)(this,n),this.editor=e,this.maps=["atoms","bonds","rxnArrows","rxnPluses","sgroups","functionalGroups","sgroupData","simpleObjects","texts"],this.lassoHelper=new ff(t||0,e,null),e.selection()){var r=(0,u.nHA)(e.render.ctab,e.selection());e.update(r),e.selection(null),this.isNotActiveTool=!0}}return(0,s.Z)(n,[{key:"mousedown",value:function(n){this.editor.findItem(n,this.maps)||this.lassoHelper.begin(n)}},{key:"mousemove",value:function(n){this.lassoHelper.running()?this.editor.selection(this.lassoHelper.addPoint(n)):this.editor.hover(this.editor.findItem(n,this.maps))}},{key:"mouseup",value:function(){var n,e=this.editor.render.ctab,t=e.sgroups,r=e.molecule,o=r.functionalGroups,i=this.editor.selection(),a={atoms:[],bonds:[]},l=[],c=[],s=[];if(i&&o.size&&i.atoms){var d,p=Tf(i.atoms);try{for(p.s();!(d=p.n()).done;){var h,f=d.value,m=u.J41.atomsInFunctionalGroup(o,f),v=null!==m&&(null===(h=e.atoms.get(m))||void 0===h?void 0:h.a);if(v){var g,b=Tf(v.sgs.values());try{for(b.s();!(g=b.n()).done;)n=g.value}catch(n){b.e(n)}finally{b.f()}}if(v&&u.J41.isAtomInContractedFunctionalGroup(v,t,o,!0)){var C,y,O,w,S=void 0!==n&&u.j1n.getAtoms(r,null===(C=e.sgroups.get(n))||void 0===C?void 0:C.item),M=void 0!==n&&u.j1n.getBonds(r,null===(y=e.sgroups.get(n))||void 0===y?void 0:y.item);f===S[0]&&(O=a.atoms).push.apply(O,(0,x.Z)(S))&&(w=a.bonds).push.apply(w,(0,x.Z)(M))}v&&!u.J41.isAtomInContractedFunctionalGroup(v,t,o,!0)&&l.push(m)}}catch(n){p.e(n)}finally{p.f()}}if(i&&o.size&&i.bonds){var j,E=Tf(i.bonds);try{for(E.s();!(j=E.n()).done;){var D,A=j.value,$=u.J41.bondsInFunctionalGroup(r,o,A),N=null!==$&&(null===(D=e.bonds.get($))||void 0===D?void 0:D.b);N&&!u.J41.isBondInContractedFunctionalGroup(N,t,o,!0)&&c.push($)}}catch(n){E.e(n)}finally{E.f()}}if(l.length>0){var P,k=Tf(l);try{for(k.s();!(P=k.n()).done;){var I=P.value,T=u.J41.findFunctionalGroupByAtom(o,I);null!==T&&!s.includes(T)&&s.push(T)}}catch(n){k.e(n)}finally{k.f()}}if(c.length>0){var B,L=Tf(c);try{for(L.s();!(B=L.n()).done;){var _=B.value,V=u.J41.findFunctionalGroupByBond(r,o,_);null!==V&&!s.includes(V)&&s.push(V)}}catch(n){L.e(n)}finally{L.f()}}if(s.length>0){var z=[];s.forEach((function(n){var e;(null===(e=t.get(n))||void 0===e?void 0:e.item.atoms).forEach((function(e){!l.includes(e)&&!z.includes(n)&&z.push(n)}))})),z.length>0&&(this.editor.selection(null),this.editor.event.removeFG.dispatch({fgIds:z}),this.lassoHelper.cancel())}var G=this.editor.render;if(this.lassoHelper.running()){var F=a.atoms.length>0?kf(this.lassoHelper.end(),a,!1):this.lassoHelper.end();this.editor.update((0,u.nHA)(G.ctab,F)),this.editor.selection(null)}}},{key:"click",value:function(n){var e=this.editor.render,t=e.ctab,r=this.editor.render.ctab,o=r.sgroups,i=r.molecule,a=i.functionalGroups,l=this.editor.findItem(n,this.maps),c=[],s=[],d=[];if(l&&a&&"functionalGroups"===l.map&&!u.J41.isContractedFunctionalGroup(l.id,a)){var p=o.get(l.id);u.J41.isFunctionalGroup(null==p?void 0:p.item)&&d.push(l.id)}else if(l&&a&&"atoms"===l.map){var h,f=u.J41.atomsInFunctionalGroup(a,l.id),m=null!==f&&(null===(h=r.atoms.get(f))||void 0===h?void 0:h.a);m&&!u.J41.isAtomInContractedFunctionalGroup(m,o,a,!0)&&c.push(f)}else if(l&&a&&"bonds"===l.map){var v,g=u.J41.bondsInFunctionalGroup(i,a,l.id),b=null!==g&&(null===(v=r.bonds.get(g))||void 0===v?void 0:v.b);b&&!u.J41.isBondInContractedFunctionalGroup(b,o,a,!0)&&s.push(g)}if(c.length){var C,y=Tf(c);try{for(y.s();!(C=y.n()).done;){var O=C.value,w=u.J41.findFunctionalGroupByAtom(a,O);null===w||d.includes(w)||d.push(w)}}catch(n){y.e(n)}finally{y.f()}}else if(s.length){var S,M=Tf(s);try{for(M.s();!(S=M.n()).done;){var j=S.value,E=u.J41.findFunctionalGroupByBond(i,a,j);null===E||d.includes(E)||d.push(E)}}catch(n){M.e(n)}finally{M.f()}}if(d.length)this.editor.event.removeFG.dispatch({fgIds:d});else if(l){if(this.editor.hover(null),"atoms"===l.map)this.editor.update((0,u.RmL)(t,l.id));else if("bonds"===l.map)this.editor.update((0,u.k_5)(t,l.id));else if("functionalGroups"===l.map&&u.J41.isContractedFunctionalGroup(l.id,a)){var D=o.get(l.id);this.editor.update((0,u.nHA)(e.ctab,{atoms:(0,x.Z)(u.j1n.getAtoms(i,null==D?void 0:D.item)),bonds:(0,x.Z)(u.j1n.getBonds(i,null==D?void 0:D.item))}))}else if("sgroups"===l.map||"sgroupData"===l.map){var A=o.get(l.id);u.J41.isFunctionalGroup(null==A?void 0:A.item)?this.editor.event.removeFG.dispatch({fgIds:[l.id]}):this.editor.update((0,u.U9$)(t,l.id))}else if("rxnArrows"===l.map)this.editor.update((0,u.OAk)(t,l.id));else if("rxnPluses"===l.map)this.editor.update((0,u.QqH)(t,l.id));else if("simpleObjects"===l.map)this.editor.update((0,u.ltA)(t,l.id));else{if("texts"!==l.map)return;this.editor.update((0,u.NmG)(t,l.id))}this.editor.selection(null)}}},{key:"mouseleave",value:function(){this.mouseup()}},{key:"cancel",value:function(){this.lassoHelper.running()&&this.lassoHelper.end(),this.editor.selection(null)}}]),n}(),_f=function(){function n(e){(0,c.Z)(this,n),(0,r.Z)(this,"begPos",null),(0,r.Z)(this,"endPos",null),this.editor=e;var t=this.editor.lastEvent||{clientX:0,clientY:0},o=t.clientX,i=t.clientY;this.editor.event.cursor.dispatch({status:"enable",cursorPosition:{clientX:o,clientY:i}})}return(0,s.Z)(n,[{key:"mousedown",value:function(n){var e=n.clientX,t=n.clientY;this.begPos=new u.Sgu(e,t)}},{key:"mousemove",value:function(n){if(this.editor.event.cursor.dispatch({status:"move"}),null!=this.begPos){var e=n.clientX,t=n.clientY;this.endPos=new u.Sgu(e,t);var r=this.editor.render,o=u.Sgu.diff(this.endPos,this.begPos).scaled(1/this.editor.zoom());this.begPos=this.endPos,r.ctab.translate(o),r.options.offset=r.options.offset.add(o),r.update(!1)}}},{key:"mouseup",value:function(n){if(null!==this.begPos){var e=this.editor.render;this.endPos=e.page2obj(n),this.begPos=null,this.endPos=null,e.update(!1)}}},{key:"mouseover",value:function(){this.editor.event.cursor.dispatch({status:"mouseover"})}},{key:"mouseleave",value:function(){this.begPos=null,this.endPos=null,this.editor.event.cursor.dispatch({status:"leave"})}},{key:"cancel",value:function(){this.editor.event.cursor.dispatch({status:"disable"})}}]),n}();function Vf(n,e){var t="undefined"!=typeof Symbol&&n[Symbol.iterator]||n["@@iterator"];if(!t){if(Array.isArray(n)||(t=function(n,e){if(n){if("string"==typeof n)return zf(n,e);var t=Object.prototype.toString.call(n).slice(8,-1);return"Object"===t&&n.constructor&&(t=n.constructor.name),"Map"===t||"Set"===t?Array.from(n):"Arguments"===t||/^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(t)?zf(n,e):void 0}}(n))||e&&n&&"number"==typeof n.length){t&&(n=t);var r=0,o=function(){};return{s:o,n:function(){return r>=n.length?{done:!0}:{done:!1,value:n[r++]}},e:function(n){throw n},f:o}}throw new TypeError("Invalid attempt to iterate non-iterable instance.\nIn order to be iterable, non-array objects must have a [Symbol.iterator]() method.")}var i,a=!0,l=!1;return{s:function(){t=t.call(n)},n:function(){var n=t.next();return a=n.done,n},e:function(n){l=!0,i=n},f:function(){try{a||null==t.return||t.return()}finally{if(l)throw i}}}}function zf(n,e){(null==e||e>n.length)&&(e=n.length);for(var t=0,r=new Array(e);t<e;t++)r[t]=n[t];return r}var Gf=function(){function n(e,t){(0,c.Z)(this,n),this.editor=e,this.editor.selection(null),this.struct=t;var r=this.editor.render,o=r.clientArea,i=o.clientHeight,a=o.clientWidth,l=this.editor.lastEvent?r.page2obj(this.editor.lastEvent):r.page2obj({pageX:a/2,pageY:i/2}),s=(0,u.lI3)(r.ctab,this.struct,l),d=(0,O.Z)(s,2),p=d[0],h=d[1];this.action=p,this.editor.update(this.action,!0),this.mergeItems=(0,u.z8H)(this.editor,h),this.editor.hover((0,u.QOv)(this.mergeItems),this)}return(0,s.Z)(n,[{key:"mousemove",value:function(n){var e=this.editor.render;this.action&&this.action.perform(e.ctab);var t=(0,u.lI3)(e.ctab,this.struct,e.page2obj(n)),r=(0,O.Z)(t,2),o=r[0],i=r[1];this.action=o,this.editor.update(this.action,!0),this.mergeItems=(0,u.z8H)(this.editor,i),this.editor.hover((0,u.QOv)(this.mergeItems))}},{key:"mouseup",value:function(){var n=this.editor.render.ctab.molecule,e=n.functionalGroups,t=[],r=[],o=[];if(this.mergeItems&&e.size&&this.mergeItems.atoms.size){var i,a=Vf(this.mergeItems.atoms.values());try{for(a.s();!(i=a.n()).done;){var l=i.value,c=u.J41.atomsInFunctionalGroup(e,l);null!==c&&t.push(c)}}catch(n){a.e(n)}finally{a.f()}}if(this.mergeItems&&e.size&&this.mergeItems.bonds.size){var s,d=Vf(this.mergeItems.bonds.values());try{for(d.s();!(s=d.n()).done;){var p=s.value,h=u.J41.atomsInFunctionalGroup(e,p);null!==h&&r.push(h)}}catch(n){d.e(n)}finally{d.f()}}if(t.length>0){var f,m=Vf(t);try{for(m.s();!(f=m.n()).done;){var v=f.value,g=u.J41.findFunctionalGroupByAtom(e,v);null===g||o.includes(g)||o.push(g)}}catch(n){m.e(n)}finally{m.f()}this.editor.event.removeFG.dispatch({fgIds:o})}else if(r.length>0){var b,C=Vf(r);try{for(C.s();!(b=C.n()).done;){var y=b.value,O=u.J41.findFunctionalGroupByBond(n,e,y);null===O||o.includes(O)||o.push(O)}}catch(n){C.e(n)}finally{C.f()}this.editor.event.removeFG.dispatch({fgIds:o})}else{var w=this.editor,S=w.render.ctab;if(w.selection(null),this.action=this.action?(0,u.ghY)(S,this.mergeItems).mergeWith(this.action):(0,u.ghY)(S,this.mergeItems),w.hover(null),this.action){var M=this.action;delete this.action,this.editor.update(M)}}}},{key:"cancel",value:function(){var n=this.editor.render;this.editor.hover(null),this.action&&(this.action.perform(n.ctab),delete this.action,n.update())}},{key:"mouseleave",value:function(){this.cancel()}}]),n}();function Ff(n,e){(null==e||e>n.length)&&(e=n.length);for(var t=0,r=new Array(e);t<e;t++)r[t]=n[t];return r}var Hf=function(){function n(e){(0,c.Z)(this,n),e.selection(null),this.editor=e}return(0,s.Z)(n,[{key:"mousemove",value:function(n){var e=this.editor.render.ctab.molecule,t=this.editor.findItem(n,["atoms"]);if(t){var r=e.atoms.get(t.id);null===(null==r?void 0:r.attpnt)&&this.editor.hover(t)}else this.editor.hover(null)}},{key:"click",value:function(n){var e=this.editor.render.ctab.molecule.functionalGroups,t=this.editor.render,r=this.editor.findItem(n,["atoms"]),o=[],i=[];if(r&&e&&"atoms"===r.map){var a=u.J41.atomsInFunctionalGroup(e,r.id);null!==a&&o.push(a)}if(!(o.length>0)){if(!r)return this.editor.hover(null),Rf(this.editor,null,t.page2obj(n)),!0;if("atoms"===r.map){this.editor.hover(null);var l=this.editor.render.ctab.molecule.atoms.get(r.id);if(null!==(null==l?void 0:l.attpnt))return;return Rf(this.editor,r.id,null),!0}return!0}var c,s=function(n,e){var t="undefined"!=typeof Symbol&&n[Symbol.iterator]||n["@@iterator"];if(!t){if(Array.isArray(n)||(t=function(n,e){if(n){if("string"==typeof n)return Ff(n,e);var t=Object.prototype.toString.call(n).slice(8,-1);return"Object"===t&&n.constructor&&(t=n.constructor.name),"Map"===t||"Set"===t?Array.from(n):"Arguments"===t||/^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(t)?Ff(n,e):void 0}}(n))||e&&n&&"number"==typeof n.length){t&&(n=t);var r=0,o=function(){};return{s:o,n:function(){return r>=n.length?{done:!0}:{done:!1,value:n[r++]}},e:function(n){throw n},f:o}}throw new TypeError("Invalid attempt to iterate non-iterable instance.\nIn order to be iterable, non-array objects must have a [Symbol.iterator]() method.")}var i,a=!0,l=!1;return{s:function(){t=t.call(n)},n:function(){var n=t.next();return a=n.done,n},e:function(n){l=!0,i=n},f:function(){try{a||null==t.return||t.return()}finally{if(l)throw i}}}}(o);try{for(s.s();!(c=s.n()).done;){var d=c.value,p=u.J41.findFunctionalGroupByAtom(e,d);null===p||i.includes(p)||i.push(p)}}catch(n){s.e(n)}finally{s.f()}this.editor.event.removeFG.dispatch({fgIds:i})}}]),n}();function Rf(n,e,t){var r=n.render.ctab.molecule,o=e||0===e?r.atoms.get(e):null,i=o?o.rglabel:0,a=o?o.label:"R#",l=n.event.elementEdit.dispatch({label:"R#",rglabel:i,fragId:o?o.fragment:null});Promise.resolve(l).then((function(r){r=Object.assign({},u.hgN.attrlist,r),!e&&0!==e&&r.rglabel?n.update((0,u.f8s)(n.render.ctab,t,r)):i!==r.rglabel&&(r.aam=o.aam,r.attpnt=o.attpnt,r.rglabel||"R#"===a||(r.label=a),n.update((0,u.dBq)(n.render.ctab,e,r,!1)))})).catch((function(){return null}))}function Zf(n,e){var t="undefined"!=typeof Symbol&&n[Symbol.iterator]||n["@@iterator"];if(!t){if(Array.isArray(n)||(t=function(n,e){if(n){if("string"==typeof n)return Kf(n,e);var t=Object.prototype.toString.call(n).slice(8,-1);return"Object"===t&&n.constructor&&(t=n.constructor.name),"Map"===t||"Set"===t?Array.from(n):"Arguments"===t||/^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(t)?Kf(n,e):void 0}}(n))||e&&n&&"number"==typeof n.length){t&&(n=t);var r=0,o=function(){};return{s:o,n:function(){return r>=n.length?{done:!0}:{done:!1,value:n[r++]}},e:function(n){throw n},f:o}}throw new TypeError("Invalid attempt to iterate non-iterable instance.\nIn order to be iterable, non-array objects must have a [Symbol.iterator]() method.")}var i,a=!0,l=!1;return{s:function(){t=t.call(n)},n:function(){var n=t.next();return a=n.done,n},e:function(n){l=!0,i=n},f:function(){try{a||null==t.return||t.return()}finally{if(l)throw i}}}}function Kf(n,e){(null==e||e>n.length)&&(e=n.length);for(var t=0,r=new Array(e);t<e;t++)r[t]=n[t];return r}var Yf=function(){function n(e){(0,c.Z)(this,n),e.selection(null),this.editor=e}return(0,s.Z)(n,[{key:"mousemove",value:function(n){this.editor.hover(this.editor.findItem(n,["frags","rgroups"]))}},{key:"click",value:function(n){var e=this.editor.render.ctab,t=e.molecule,r=t.functionalGroups,o=this.editor,i=o.findItem(n,["frags","rgroups"]),a=o.findItem(n,["atoms","bonds"]),l=[],c=[],s=[];if(a&&r&&"atoms"===a.map){var d=u.J41.atomsInFunctionalGroup(r,a.id);null!==d&&l.push(d)}if(a&&r&&"bonds"===a.map){var p=u.J41.bondsInFunctionalGroup(t,r,a.id);null!==p&&c.push(p)}if(l.length>0){var h,f=Zf(l);try{for(f.s();!(h=f.n()).done;){var m=h.value,v=u.J41.findFunctionalGroupByAtom(r,m);null===v||s.includes(v)||s.push(v)}}catch(n){f.e(n)}finally{f.f()}this.editor.event.removeFG.dispatch({fgIds:s})}else{if(!(c.length>0)){if(!i)return!0;this.editor.hover(null);var g="rgroups"===i.map?i.id:u.vfe.findRGroupByFragment(t.rgroups,i.id),b=Object.assign({label:g},"frags"===i.map?{fragId:i.id}:t.rgroups.get(i.id)),C=o.event.rgroupEdit.dispatch(b);return Promise.resolve(C).then((function(n){var t;if("rgroups"!==i.map){var r=u.vfe.findRGroupByFragment(e.molecule.rgroups,i.id);t=(0,u.GoV)(e,n.label,i.id).mergeWith((0,u.Dps)(e,n.label,r))}else t=(0,u.dmV)(e,i.id,n);o.update(t)})).catch((function(){return null})),!0}var y,O=Zf(c);try{for(O.s();!(y=O.n()).done;){var w=y.value,S=u.J41.findFunctionalGroupByBond(t,r,w);null===S||s.includes(S)||s.push(S)}}catch(n){O.e(n)}finally{O.f()}this.editor.event.removeFG.dispatch({fgIds:s})}}},{key:"cancel",value:function(){this.editor.hover(null)}}]),n}(),Uf=function(){function n(e,t){(0,c.Z)(this,n),this.mode=t,this.editor=e,this.editor.selection(null)}return(0,s.Z)(n,[{key:"mousedown",value:function(n){var e=this.editor.render.page2obj(n);this.dragCtx={p0:e};var t=this.editor.findItem(n,["rxnArrows"]);t&&"rxnArrows"===t.map?(this.editor.hover(null),this.editor.selection({rxnArrows:[t.id]}),this.dragCtx.ci=t):(this.dragCtx.isNew=!0,this.editor.selection(null))}},{key:"mousemove",value:function(n){var e=this.editor.render;if(this.dragCtx){var t=e.page2obj(n),r=t.sub(this.dragCtx.p0);if(this.dragCtx.previous=t,this.dragCtx.ci)this.dragCtx.action&&this.dragCtx.action.perform(e.ctab),this.dragCtx.ci.ref?this.dragCtx.action=(0,u.gHo)(e.ctab,this.dragCtx.ci.id,r,t,this.dragCtx.ci.ref):this.dragCtx.action=(0,u.DYm)(e.ctab,this.editor.selection()||{},r),this.editor.update(this.dragCtx.action,!0);else{if(this.dragCtx.action)this.dragCtx.action.perform(e.ctab);else{var o=(0,u.OnW)(e.ctab,[this.dragCtx.p0,this.dragCtx.p0],this.mode),i=o.operations[0];this.dragCtx.itemId=i.data.id,this.dragCtx.action=o,this.editor.update(this.dragCtx.action,!0)}this.dragCtx.action=(0,u.gHo)(e.ctab,this.dragCtx.itemId,r,t,null),this.editor.update(this.dragCtx.action,!0)}}else{var a=this.editor.findItem(n,["rxnArrows"]);this.editor.hover(a,null,n)}}},{key:"mouseup",value:function(){if(!this.dragCtx)return!0;var n=this.editor.render,e=this.dragCtx.p0,t=Jf(e,this.dragCtx.previous);return this.dragCtx.action&&(this.dragCtx.isNew&&(this.editor.update((0,u.OAk)(n.ctab,this.dragCtx.itemId),!0),this.dragCtx.action=(0,u.OnW)(n.ctab,[e,t],this.mode)),this.editor.update(this.dragCtx.action)),delete this.dragCtx,!0}},{key:"click",value:function(n){var e=this.editor.render,t=this.editor.findItem(n,["rxnArrows"]),r=e.page2obj(n);if(!t){var o=[r,Jf(r,null)];this.editor.update((0,u.OnW)(e.ctab,o,this.mode))}}}]),n}();function Jf(n,e){if(!e)return new u.Sgu(n.x+2,n.y);var t,r,o,i,a,l,c=(t=n.x,r=n.y,o=e.x,i=e.y,a=Math.sqrt(Math.pow(o-t,2)+Math.pow(i-r,2)),l=function(n,e,t,r){var o=n-t,i=e-r;return o||i?(180+180*Math.atan2(-i,-o)/Math.PI+360)%360:0}(o,i,t,r),{length:a,angle:l});if(c.length<=1.5){var s=new u.Sgu;return s.x=n.x+2*Math.cos(Math.PI*c.angle/180),s.y=n.y+2*Math.sin(Math.PI*c.angle/180),s}return e}var qf=function(){function n(e){(0,c.Z)(this,n),this.editor=e,this.editor.selection(null)}return(0,s.Z)(n,[{key:"mousedown",value:function(n){var e=this.editor.render;this.rcs=e.ctab.molecule.getComponents();var t=this.editor.findItem(n,["atoms"]);t&&"atoms"===t.map&&(this.editor.hover(null),this.dragCtx={item:t,xy0:e.page2obj(n)})}},{key:"mousemove",value:function(n){var e=this.editor,t=e.render;if("dragCtx"in this){var r,o,i,a=this.editor.findItem(n,["atoms"],this.dragCtx.item),l=t.ctab.molecule.atoms;a&&"atoms"===a.map&&Wf(this.rcs,this.dragCtx.item.id,a.id)?(e.hover(a),this.updateLine(null===(r=l.get(this.dragCtx.item.id))||void 0===r?void 0:r.pp,null===(o=l.get(a.id))||void 0===o?void 0:o.pp)):(e.hover(null),this.updateLine(null===(i=l.get(this.dragCtx.item.id))||void 0===i?void 0:i.pp,t.page2obj(n)))}else e.hover(e.findItem(n,["atoms"]))}},{key:"updateLine",value:function(n,e){if(this.line&&(this.line.remove(),this.line=null),n&&e){var t=this.editor.render;this.line=t.selectionLine(u.Ciz.obj2scaled(n,t.options).add(t.options.offset),u.Ciz.obj2scaled(e,t.options).add(t.options.offset))}}},{key:"mouseup",value:function(n){var e=this;if("dragCtx"in this){var t=this.editor.render,r=this.editor.findItem(n,["atoms"],this.dragCtx.item);if(r&&"atoms"===r.map&&Wf(this.rcs,this.dragCtx.item.id,r.id)){var o=new u.aUM,i=t.ctab.molecule.atoms,a=i.get(this.dragCtx.item.id),l=i.get(r.id),c=null==a?void 0:a.aam,s=null==l?void 0:l.aam;if(!c||c!==s){if((c&&c!==s||!c&&s)&&i.forEach((function(n,r){r!==e.dragCtx.item.id&&(c&&n.aam===c||s&&n.aam===s)&&o.mergeWith((0,u.dBq)(t.ctab,r,{aam:0},null))})),c)o.mergeWith((0,u.dBq)(t.ctab,r.id,{aam:c},null));else{var d=0;i.forEach((function(n){d=Math.max(d,n.aam||0)})),o.mergeWith((0,u.dBq)(t.ctab,this.dragCtx.item.id,{aam:d+1},null)),o.mergeWith((0,u.dBq)(t.ctab,r.id,{aam:d+1},null))}this.editor.update(o)}}this.updateLine(null,null),delete this.dragCtx}this.editor.hover(null)}}]),n}();function Wf(n,e,t){for(var r,o,i=0;(!r||!o)&&i<n.reactants.length;i++){var a=Array.from(n.reactants[i]);!r&&a.indexOf(e)>=0&&(r="r"),!o&&a.indexOf(t)>=0&&(o="r")}for(var l=0;(!r||!o)&&l<n.products.length;l++){var c=Array.from(n.products[l]);!r&&c.indexOf(e)>=0&&(r="p"),!o&&c.indexOf(t)>=0&&(o="p")}return r&&o&&r!==o}var Xf=function(){function n(e){(0,c.Z)(this,n),this.editor=e,this.editor.selection(null)}return(0,s.Z)(n,[{key:"mousedown",value:function(n){var e=this.editor.render,t=this.editor.findItem(n,["rxnPluses"]);t&&"rxnPluses"===t.map&&(this.editor.hover(null),this.editor.selection({rxnPluses:[t.id]}),this.dragCtx={xy0:e.page2obj(n)})}},{key:"mousemove",value:function(n){var e=this.editor,t=e.render;"dragCtx"in this?(this.dragCtx.action&&this.dragCtx.action.perform(t.ctab),this.dragCtx.action=(0,u.DYm)(t.ctab,this.editor.selection()||{},t.page2obj(n).sub(this.dragCtx.xy0)),e.update(this.dragCtx.action,!0)):e.hover(e.findItem(n,["rxnPluses"]))}},{key:"mouseup",value:function(){return!this.dragCtx||(this.dragCtx.action&&this.editor.update(this.dragCtx.action),delete this.dragCtx,!0)}},{key:"click",value:function(n){var e=this.editor.render;this.editor.findItem(n,["rxnPluses"])||this.editor.update((0,u.v$W)(e.ctab,e.page2obj(n)))}}]),n}(),Qf=function(){function n(e){(0,c.Z)(this,n),this.editor=e,this.editor.selection(null)}return(0,s.Z)(n,[{key:"mousemove",value:function(n){var e,t=this.editor.findItem(n,["atoms"]);t&&"atoms"===t.map?this.editor.hover(null!==(e=this.editor.render.ctab.molecule.atoms.get(t.id))&&void 0!==e&&e.aam?t:null):this.editor.hover(null)}},{key:"mouseup",value:function(n){var e,t=this,r=this.editor.findItem(n,["atoms"]),o=this.editor.render.ctab.molecule.atoms;if(r&&"atoms"===r.map&&null!==(e=o.get(r.id))&&void 0!==e&&e.aam){var i,a=new u.aUM,l=null===(i=o.get(r.id))||void 0===i?void 0:i.aam;o.forEach((function(n,e){n.aam===l&&a.mergeWith((0,u.dBq)(t.editor.render.ctab,e,{aam:0},null))})),this.editor.update(a)}this.editor.hover(null)}}]),n}(),nm=function(){function n(e,t){var r;if((0,c.Z)(this,n),this.editor=e,t){var o=e.render.ctab,i=e.selection(),a=i&&i.bonds&&1===Object.keys(i).length&&1===i.bonds.length?(0,u.HIi)(o,i.bonds[0],t):(0,u.Hlm)(o,i,t,null);return e.update(a),void(this.isNotActiveTool=!0)}e.selection()&&null!==(r=e.selection())&&void 0!==r&&r.atoms||this.editor.selection(null)}return(0,s.Z)(n,[{key:"mousedown",value:function(n){var e,t=new u.Sgu,r=this.editor.selection(),o=this.editor.render,i=o.ctab.molecule;if(r&&r.atoms){var a,l=null,c=!1;r.atoms.forEach((function(n){var e=i.atoms.get(n);t.add_(null==e?void 0:e.pp),c||null==e||e.neighbors.find((function(e){var t,o=i.halfBonds.get(e);if(o&&-1===(null===(t=r.atoms)||void 0===t?void 0:t.indexOf(o.end))){if(o.loop>=0){var a=i.atoms.get(n);if(null==a||!a.neighbors.find((function(n){var e,t=i.halfBonds.get(n);return(null==t?void 0:t.loop)>=0&&-1!==(null===(e=r.atoms)||void 0===e?void 0:e.indexOf(null==t?void 0:t.end))})))return c=!0,!0}if(null==l)l=n;else if(l!==n)return c=!0,!0}return!1}))})),t=c||null===l?t.scaled(1/r.atoms.length):null===(a=i.atoms.get(l))||void 0===a?void 0:a.pp}else null!==(e=i.atoms)&&void 0!==e&&e.size?(i.atoms.forEach((function(n){t.add_(n.pp)})),t=t.scaled(1/i.atoms.size)):t=o.page2obj(n);return this.dragCtx={xy0:t,angle1:Kh.calcAngle(t,o.page2obj(n))},!0}},{key:"mousemove",value:function(n){if(!this.dragCtx)return!0;var e=this.editor.render,t=this.dragCtx,r=e.page2obj(n),o=Kh.calcAngle(t.xy0,r)-t.angle1;n.ctrlKey||(o=Kh.fracAngle(o,null));var i=Kh.degrees(o);if("angle"in t&&t.angle===i)return!0;"action"in t&&t.action.perform(e.ctab),t.angle=i,t.action=(0,u.TPF)(e.ctab,this.editor.selection(),t.xy0,o),this.editor.event.message.dispatch({info:i+"º"});var a=this.editor.explicitSelected();return t.mergeItems=(0,u.z8H)(this.editor,a),this.editor.hover((0,u.QOv)(t.mergeItems)),this.editor.update(t.action,!0),!0}},{key:"mouseup",value:function(){if(!this.dragCtx)return!0;var n=this.dragCtx,e=this.editor.render.ctab,t=n.action?(0,u.ghY)(e,n.mergeItems).mergeWith(n.action):(0,u.ghY)(e,n.mergeItems);return delete this.dragCtx,this.editor.update(t),this.editor.hover(null),n.mergeItems&&this.editor.selection(null),this.editor.event.message.dispatch({info:!1}),!0}},{key:"cancel",value:function(){this.mouseup()}},{key:"mouseleave",value:function(){this.mouseup()}}]),n}(),em=function(){function n(e,t){(0,c.Z)(this,n),this.mode=t,this.editor=e,this.editor.selection(null)}return(0,s.Z)(n,[{key:"mousedown",value:function(n){var e=this.editor.render.page2obj(n);this.dragCtx={p0:e};var t=this.editor.findItem(n,["simpleObjects"]);t&&"simpleObjects"===t.map?(this.editor.hover(null),this.editor.selection({simpleObjects:[t.id]}),this.dragCtx.ci=t):(this.dragCtx.isNew=!0,this.editor.selection(null))}},{key:"mousemove",value:function(n){var e=this.editor.render;if(this.dragCtx){var t=e.page2obj(n),r=t.sub(this.dragCtx.p0);if(this.dragCtx.previous=t,this.dragCtx.ci)this.dragCtx.action&&this.dragCtx.action.perform(e.ctab),this.dragCtx.ci.ref?this.dragCtx.action=(0,u.cMT)(e.ctab,this.dragCtx.ci.id,r,t,this.dragCtx.ci.ref,n.shiftKey):this.dragCtx.action=(0,u.DYm)(e.ctab,this.editor.selection()||{},r),this.editor.update(this.dragCtx.action,!0);else{if(this.dragCtx.action)this.dragCtx.action.perform(e.ctab);else{var o=(0,u.g5D)(e.ctab,[this.dragCtx.p0,this.dragCtx.p0],this.mode,!1),i=o.operations[0];this.dragCtx.itemId=i.data.id,this.dragCtx.action=o,this.editor.update(this.dragCtx.action,!0)}this.dragCtx.action=(0,u.cMT)(e.ctab,this.dragCtx.itemId,r,t,null,n.shiftKey),this.editor.update(this.dragCtx.action,!0)}}else{var a=this.editor.findItem(n,["simpleObjects"]);this.editor.hover(a)}}},{key:"mouseup",value:function(n){if(!this.dragCtx)return!0;if(this.dragCtx.action){if(this.dragCtx.isNew){var e=this.editor.render;this.editor.update((0,u.ltA)(e.ctab,this.dragCtx.itemId),!0),this.dragCtx.action=(0,u.g5D)(e.ctab,[this.dragCtx.p0,this.dragCtx.previous],this.mode,n.shiftKey)}this.editor.update(this.dragCtx.action)}return delete this.dragCtx,!0}}]),n}();function tm(n,e){var t="undefined"!=typeof Symbol&&n[Symbol.iterator]||n["@@iterator"];if(!t){if(Array.isArray(n)||(t=function(n,e){if(n){if("string"==typeof n)return rm(n,e);var t=Object.prototype.toString.call(n).slice(8,-1);return"Object"===t&&n.constructor&&(t=n.constructor.name),"Map"===t||"Set"===t?Array.from(n):"Arguments"===t||/^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(t)?rm(n,e):void 0}}(n))||e&&n&&"number"==typeof n.length){t&&(n=t);var r=0,o=function(){};return{s:o,n:function(){return r>=n.length?{done:!0}:{done:!1,value:n[r++]}},e:function(n){throw n},f:o}}throw new TypeError("Invalid attempt to iterate non-iterable instance.\nIn order to be iterable, non-array objects must have a [Symbol.iterator]() method.")}var i,a=!0,l=!1;return{s:function(){t=t.call(n)},n:function(){var n=t.next();return a=n.done,n},e:function(n){l=!0,i=n},f:function(){try{a||null==t.return||t.return()}finally{if(l)throw i}}}}function rm(n,e){(null==e||e>n.length)&&(e=n.length);for(var t=0,r=new Array(e);t<e;t++)r[t]=n[t];return r}var om=function(){function n(e,t){(0,c.Z)(this,n),this.editor=e,this.mode=function(n){var e;return n.mode?n.mode:["Functional Groups","Salts and Solvents"].includes(null===(e=n.props)||void 0===e?void 0:e.group)?"fg":null}(t),this.editor.selection(null),this.template={aid:parseInt(t.aid)||0,bid:parseInt(t.bid)||0};var r=t.struct;r.rescale();var o=new u.Sgu;r.atoms.forEach((function(n){o.add_(n.pp)})),this.template.molecule=r,this.findItems=[],this.template.xy0=o.scaled(1/(r.atoms.size||1));var i=r.atoms.get(this.template.aid);i&&(this.template.angle0=Kh.calcAngle(i.pp,this.template.xy0),this.findItems.push("atoms"));var a=r.bonds.get(this.template.bid);a&&"fg"!==this.mode&&(this.template.sign=im(r,a,this.template.xy0),this.findItems.push("bonds")),r.sgroups.size&&this.findItems.push("sgroups")}return(0,s.Z)(n,[{key:"mousedown",value:function(n){var e=this.editor.findItem(n,["atoms","bonds","sgroups","functionalGroups"]),t=this.editor.struct(),r=[],o=[],i=[],a=[],l=this.editor.render.ctab,c=l.molecule,s=c.functionalGroups;if(e&&s.size&&"functionalGroups"===e.map&&u.J41.isContractedFunctionalGroup(e.id,s)&&i.push(e.id),e&&s.size&&"atoms"===e.map){var d=u.J41.atomsInFunctionalGroup(s,e.id);null!==d&&r.push(d)}if(e&&s.size&&"bonds"===e.map){var p=u.J41.bondsInFunctionalGroup(c,s,e.id);null!==p&&o.push(p)}if(i.length>0){var h,f=tm(i);try{for(f.s();!(h=f.n()).done;){var m=h.value;a.includes(m)||a.push(m)}}catch(n){f.e(n)}finally{f.f()}}if(r.length>0){var v,g=tm(r);try{for(g.s();!(v=g.n()).done;){var b=v.value,C=u.J41.findFunctionalGroupByAtom(s,b);null===C||a.includes(C)||a.push(C)}}catch(n){g.e(n)}finally{g.f()}}if(o.length>0){var y,O=tm(o);try{for(O.s();!(y=O.n()).done;){var w=y.value,S=u.J41.findFunctionalGroupByBond(c,t.functionalGroups,w);null===S||a.includes(S)||a.push(S)}}catch(n){O.e(n)}finally{O.f()}}if(!a.length){var M=this.editor;this.editor.hover(null),this.dragCtx={xy0:M.render.page2obj(n),item:M.findItem(n,this.findItems)};var x=this.dragCtx,j=x.item;if(!j)return delete x.item,!0;if("bonds"===j.map&&"fg"!==this.mode){var E,D,A,$=l.molecule,N=new u.Sgu,P=$.bonds.get(j.id),k=null===(E=$.atoms.get(null==P?void 0:P.begin))||void 0===E?void 0:E.fragment,I=$.getFragmentIds(k),T=0,B=null===(D=$.halfBonds.get(null==P?void 0:P.hb1))||void 0===D?void 0:D.loop;if(B&&B<0&&(B=null===(A=$.halfBonds.get(null==P?void 0:P.hb2))||void 0===A?void 0:A.loop),B&&B>=0){var L,_=null===(L=$.loops.get(B))||void 0===L?void 0:L.hbs;null==_||_.forEach((function(n){var e,t=null===(e=$.halfBonds.get(n))||void 0===e?void 0:e.begin;if(t){var r=$.atoms.get(t);r&&(N.add_(r.pp),T++)}}))}else I.forEach((function(n){var e=$.atoms.get(n);e&&(N.add_(e.pp),T++)}));x.v0=N.scaled(1/T);var V=im($,P,x.v0);x.sign1=V||1,x.sign2=this.template.sign}return!0}this.editor.event.removeFG.dispatch({fgIds:a})}},{key:"mousemove",value:function(n){var e=this.editor.render.ctab;if(!this.dragCtx)return this.editor.hover(this.editor.findItem(n,this.findItems),null,n),!0;var t=this.dragCtx,r=t.item,o=null,i=this.editor.render.page2obj(n),a=e.molecule;if(r&&"bonds"===r.map&&"fg"!==this.mode){var l=a.bonds.get(r.id),c=im(a,l,i);if(t.sign1*this.template.sign>0&&(c=-c),c!==t.sign2||!t.action){t.action&&t.action.perform(e),t.sign2=c;var s=(0,u.e9t)(e,this.template,r.id,this.editor.event,t.sign1*t.sign2>0,!1),d=(0,O.Z)(s,2),p=d[0],h=d[1];t.action=p,this.editor.update(t.action,!0),t.mergeItems=(0,u.z8H)(this.editor,h),this.editor.hover((0,u.QOv)(t.mergeItems))}return!0}var f=null;if(r){if("atoms"===r.map){var m;(o=null===(m=a.atoms.get(r.id))||void 0===m?void 0:m.pp)&&(f="fg"===this.mode||u.Sgu.dist(o,i)>1)}}else o=t.xy0;var v=Kh.calcAngle(o,i);n.ctrlKey||(v=Kh.fracAngle(v,null));var g=Kh.degrees(v);if(this.editor.event.message.dispatch({info:g+"º"}),t.hasOwnProperty("angle")&&t.angle===g&&(!t.hasOwnProperty("extra_bond")||t.extra_bond===f))return!0;t.action&&t.action.perform(e),t.angle=g;var b,C=null;if(r){if("atoms"===r.map){var y=(0,u.ksM)(e,this.template,r.id,v,f),w=(0,O.Z)(y,2);C=w[0],b=w[1],t.extra_bond=f}}else{var S=(0,u.m81)(e,this.template,o,v),M=(0,O.Z)(S,2);C=M[0],b=M[1]}return t.action=C,this.editor.update(t.action,!0),"fg"!==this.mode&&(t.mergeItems=(0,u.z8H)(this.editor,b),this.editor.hover((0,u.QOv)(t.mergeItems))),!0}},{key:"mouseup",value:function(n){var e=this,t=this.dragCtx;if(!t)return!0;delete this.dragCtx;var r,o=this.editor.render.ctab,i=o.molecule,a=t.item;if(t.action&&a&&"bonds"===a.map&&"fg"!==this.mode)return t.action.perform(o),(0,u.e9t)(o,this.template,a.id,this.editor.event,t.sign1*t.sign2>0,!0).then((function(n){var t=(0,O.Z)(n,2),r=t[0],i=t[1],a=(0,u.z8H)(e.editor,i);r=(0,u.ghY)(o,a).mergeWith(r),e.editor.update(r)})),!0;var l=null;if(u.j1n.isSaltOrSolvent(this.template.molecule.name))return function(n,e,t,r){var o=(0,u.m81)(n,e,t.xy0,0),i=(0,O.Z)(o,1)[0];r.update(i),r.selection(null),r.hover(null),r.event.message.dispatch({info:!1})}(o,this.template,t,this.editor),!0;if(!t.action)if(a){if("atoms"===a.map){var c,s,d,p=null===(c=o.atoms.get(a.id))||void 0===c?void 0:c.a.neighbors.length;if(p&&p>1)s=null,d=!0;else if(1===p){var h,f=i.atoms.get(a.id),m=f&&(null===(h=i.halfBonds.get(f.neighbors[0]))||void 0===h?void 0:h.end),v=m&&i.atoms.get(m);s=n.ctrlKey?Kh.calcAngle(null==v?void 0:v.pp,null==f?void 0:f.pp):Kh.fracAngle(Kh.calcAngle(v.pp,null==f?void 0:f.pp),null),d=!1}else s=0,d=!1;var g=(0,u.ksM)(o,this.template,a.id,s,d),b=(0,O.Z)(g,2);r=b[0],l=b[1],t.action=r}else if("bonds"===a.map&&"fg"!==this.mode)return(0,u.e9t)(o,this.template,a.id,this.editor.event,t.sign1*t.sign2>0,!0).then((function(n){var t=(0,O.Z)(n,2),r=t[0],i=t[1];if("fg"!==e.mode){var a=(0,u.z8H)(e.editor,i);r=(0,u.ghY)(o,a).mergeWith(r),e.editor.update(r)}})),!0}else{var C=(0,u.m81)(o,this.template,t.xy0,0),y=(0,O.Z)(C,2);r=y[0],l=y[1],t.action=r}this.editor.selection(null),!t.mergeItems&&l&&"fg"!==this.mode&&(t.mergeItems=(0,u.z8H)(this.editor,l)),t.action=t.action?(0,u.ghY)(o,t.mergeItems).mergeWith(t.action):(0,u.ghY)(o,t.mergeItems),this.editor.hover(null);var w=t.action;return w&&!w.isDummy()&&this.editor.update(w),this.editor.event.message.dispatch({info:!1}),!0}},{key:"cancel",value:function(n){this.mouseup(n)}},{key:"mouseleave",value:function(n){this.mouseup(n)}}]),n}();function im(n,e,t){var r=n.atoms.get(e.begin).pp,o=n.atoms.get(e.end).pp,i=u.Sgu.cross(u.Sgu.diff(r,o),u.Sgu.diff(t,o));return i>0?1:i<0?-1:0}var am=function(){function n(e){(0,c.Z)(this,n),this.editor=e,this.editor.selection(null)}return(0,s.Z)(n,[{key:"mousedown",value:function(n){var e=this.editor.render,t=this.editor.findItem(n,["texts"]);this.editor.selection(null),t&&"texts"===t.map&&(this.editor.hover(null),this.editor.selection({texts:[t.id]}),this.dragCtx={xy0:e.page2obj(n),action:new u.aUM})}},{key:"mousemove",value:function(n){var e=this.editor.render;this.dragCtx?(this.dragCtx.action&&this.dragCtx.action.perform(e.ctab),this.dragCtx.action=(0,u.DYm)(e.ctab,this.editor.selection()||{},e.page2obj(n).sub(this.dragCtx.xy0)),this.editor.update(this.dragCtx.action,!0)):this.editor.hover(this.editor.findItem(n,["texts"]),null,n)}},{key:"mouseup",value:function(){return this.dragCtx&&(this.editor.update(this.dragCtx.action),delete this.dragCtx),!0}},{key:"click",value:function(n){var e=this.editor.render,t=this.editor.findItem(n,["texts"]);return this.editor.hover(null),t||lm(this.editor,null,e.page2obj(n),[]),!0}},{key:"dblclick",value:function(n){var e=this.editor.findItem(n,["texts"]);return this.editor.hover(null),"texts"===e.map&&lm(this.editor,e.id,e.position,e.pos),!0}}]),n}();function lm(n,e,t,r){var o=n.render.ctab.molecule,i=e||0===e?o.texts.get(e):null,a=i?i.content:"";n.event.elementEdit.dispatch({content:a,id:e,position:t,pos:r,type:"text"}).then((function(o){var i=o.content;!e&&0!==e&&i?n.update((0,u.$Tq)(n.render.ctab,i,t,r)):i?i!==a&&n.update((0,u.rzF)(n.render.ctab,e,i)):n.update((0,u.NmG)(n.render.ctab,e))})).catch((function(){return null}))}var cm={hand:_f,rgroupatom:Hf,select:Nf,sgroup:bf,eraser:Lf,atom:qh,bond:rf,chain:lf,template:om,charge:sf,rgroupfragment:Yf,apoint:Hh,attach:nf,reactionarrow:Uf,reactionplus:Xf,reactionmap:qf,reactionunmap:Qf,paste:Gf,rotate:nm,enhancedStereo:uf,simpleobject:em,text:am};function sm(n,e){var t="undefined"!=typeof Symbol&&n[Symbol.iterator]||n["@@iterator"];if(!t){if(Array.isArray(n)||(t=function(n,e){if(n){if("string"==typeof n)return um(n,e);var t=Object.prototype.toString.call(n).slice(8,-1);return"Object"===t&&n.constructor&&(t=n.constructor.name),"Map"===t||"Set"===t?Array.from(n):"Arguments"===t||/^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(t)?um(n,e):void 0}}(n))||e&&n&&"number"==typeof n.length){t&&(n=t);var r=0,o=function(){};return{s:o,n:function(){return r>=n.length?{done:!0}:{done:!1,value:n[r++]}},e:function(n){throw n},f:o}}throw new TypeError("Invalid attempt to iterate non-iterable instance.\nIn order to be iterable, non-array objects must have a [Symbol.iterator]() method.")}var i,a=!0,l=!1;return{s:function(){t=t.call(n)},n:function(){var n=t.next();return a=n.done,n},e:function(n){l=!0,i=n},f:function(){try{a||null==t.return||t.return()}finally{if(l)throw i}}}}function um(n,e){(null==e||e>n.length)&&(e=n.length);for(var t=0,r=new Array(e);t<e;t++)r[t]=n[t];return r}function dm(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function pm(){return pm=(0,i.Z)(l().mark((function n(e){var t,r,o,i,a,c,s;return l().wrap((function(n){for(;;)switch(n.prev=n.next){case 0:if(t=e.hoveredItemId,r=e.newAction,o=e.render,i=e.editor,a=e.dispatch,c={atom:function(){return hm({hoveredItemId:t,newAction:r,render:o,editor:i})},bond:function(){return fm({hoveredItemId:t,newAction:r,render:o,editor:i})},eraser:function(){return mm({hoveredItemId:t,newAction:r,render:o,editor:i})},select:function(){return vm({hoveredItemId:t,newAction:r,render:o,editor:i})},charge:function(){return gm({hoveredItemId:t,newAction:r,render:o,editor:i})},rgroupatom:function(){return bm({hoveredItemId:t,newAction:r,render:o,editor:i})},sgroup:function(){cm.sgroup.sgroupDialog(i,t,null)},hand:function(){return a(Ue({tool:"hand"}))}}[r.tool],s="hand"!==r.tool||"select"!==r.tool,!c){n.next=11;break}return n.next=7,ym({hoveredItemId:t,render:o,editor:i,newAction:r});case 7:if(n.sent||!s){n.next=10;break}return n.abrupt("return");case 10:c();case 11:case"end":return n.stop()}}),n)}))),pm.apply(this,arguments)}function hm(n){var e=n.hoveredItemId,t=n.newAction,o=n.render,i=n.editor,a=function(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?dm(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):dm(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}({},t.opts),l=(0,u.dBq)(o.ctab,e,a,!0);i.update(l)}function fm(n){var e=n.hoveredItemId,t=n.newAction,r=n.render,o=n.editor,i=(0,u.QXZ)(r.ctab,t.opts,e,void 0)[0];o.update(i)}function mm(n){var e=n.hoveredItemId,t=n.render;n.editor.update((0,u.RmL)(t.ctab,e))}function vm(n){var e=n.hoveredItemId;n.editor.selection({atoms:[e]})}function gm(n){var e,t=n.hoveredItemId,r=n.newAction,o=n.render,i=n.editor,a=null===(e=o.ctab.atoms.get(t))||void 0===e?void 0:e.a;if(a){var l=(0,u.dBq)(o.ctab,t,{charge:a.charge+r.opts},null);i.update(l)}}function bm(n){return Cm.apply(this,arguments)}function Cm(){return Cm=(0,i.Z)(l().mark((function n(e){var t,r,o,i,a,c,s,d;return l().wrap((function(n){for(;;)switch(n.prev=n.next){case 0:return t=e.hoveredItemId,r=e.render,o=e.editor,i=r.ctab.molecule,a=t||0===t?i.atoms.get(t):null,c=a?a.rglabel:0,s=a?a.label:"R#",n.prev=5,n.next=8,o.event.elementEdit.dispatch({label:"R#",rglabel:c,fragId:a?a.fragment:null});case 8:d=n.sent,d=Object.assign({},u.hgN.attrlist,d),!t&&0!==t&&d.rglabel?o.update((0,u.f8s)(o.render.ctab,null,d)):c!==d.rglabel&&(d.rglabel||"R#"===s||(d.label=s),o.update((0,u.dBq)(o.render.ctab,t,d,!1))),n.next=15;break;case 13:n.prev=13,n.t0=n.catch(5);case 15:case"end":return n.stop()}}),n,null,[[5,13]])}))),Cm.apply(this,arguments)}function ym(n){return Om.apply(this,arguments)}function Om(){return Om=(0,i.Z)(l().mark((function n(e){var t,r,o,i,a,c,s,d,p,h,f,m,v,g,b;return l().wrap((function(n){for(;;)switch(n.prev=n.next){case 0:if(r=e.hoveredItemId,o=e.render,i=e.editor,a=[],c=[],s=null===(t=o.ctab.atoms.get(r))||void 0===t?void 0:t.a,d=o.ctab.molecule,p=d.functionalGroups,h=Array.from(d.sgroups.values()),s&&p&&null!==(f=u.J41.atomsInFunctionalGroup(p,r))&&a.push(f),!(a.length>0)){n.next=17;break}if(!u.j1n.isAtomInSaltOrSolvent(r,h)){n.next=12;break}return n.abrupt("return",!1);case 12:m=sm(a);try{for(m.s();!(v=m.n()).done;)g=v.value,null===(b=u.J41.findFunctionalGroupByAtom(p,g))||c.includes(b)||c.push(b)}catch(n){m.e(n)}finally{m.f()}return n.next=16,i.event.removeFG.dispatch({fgIds:c});case 16:return n.abrupt("return",n.sent);case 17:return n.abrupt("return",!0);case 18:case"end":return n.stop()}}),n)}))),Om.apply(this,arguments)}function wm(n,e){(null==e||e>n.length)&&(e=n.length);for(var t=0,r=new Array(e);t<e;t++)r[t]=n[t];return r}function Sm(n){return function(e,t){var r=function(){var n,e={};return Object.keys(Ja).forEach((function(t){(n=Ja[t]).shortcut&&(Array.isArray(n.shortcut)?n.shortcut.forEach((function(n){Mm(n,t,e)})):Mm(n.shortcut,t,e))})),Gh(e)}();n.addEventListener("keydown",(function(n){return function(n,e,t,r){if(!e.modal){var o=e.editor,i=o.render,a=e.actionState,l=a.activeTool,c=Gh(r),s=o.selection()&&o.selection().atoms,u=null;if(c&&1===c.length&&s&&c.match(/\w/))Xu(n,"labelEdit",{letter:c}).then((function(e){n(Ue({tool:"atom",opts:e}))})).catch((function(){return null})),r.preventDefault();else if(void 0!==(u=Gh.lookup(t,r))){var d=function(n,e){var t=n.indexOf(e.tool);return n.forEach((function(n,r){(0,y.isEqual)(Ja[n].action,e)&&(t=r)})),t}(u,l),p=u[d=(d+1)%(null!==u?u.length:1)];if(a[p]&&!0===a[p].disabled)return void r.preventDefault();if(-1===An.indexOf(p)){var h=Ja[p].action,f=function(n){var e,t=function(n,e){var t="undefined"!=typeof Symbol&&n[Symbol.iterator]||n["@@iterator"];if(!t){if(Array.isArray(n)||(t=function(n,e){if(n){if("string"==typeof n)return wm(n,e);var t=Object.prototype.toString.call(n).slice(8,-1);return"Object"===t&&n.constructor&&(t=n.constructor.name),"Map"===t||"Set"===t?Array.from(n):"Arguments"===t||/^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(t)?wm(n,e):void 0}}(n))||e&&n&&"number"==typeof n.length){t&&(n=t);var r=0,o=function(){};return{s:o,n:function(){return r>=n.length?{done:!0}:{done:!1,value:n[r++]}},e:function(n){throw n},f:o}}throw new TypeError("Invalid attempt to iterate non-iterable instance.\nIn order to be iterable, non-array objects must have a [Symbol.iterator]() method.")}var i,a=!0,l=!1;return{s:function(){t=t.call(n)},n:function(){var n=t.next();return a=n.done,n},e:function(n){l=!0,i=n},f:function(){try{a||null==t.return||t.return()}finally{if(l)throw i}}}}(n.entries());try{for(t.s();!(e=t.n()).done;){var r=(0,O.Z)(e.value,2),o=r[0];if(r[1].hover)return o}}catch(n){t.e(n)}finally{t.f()}return null}(i.ctab.atoms);null!==f?function(n){pm.apply(this,arguments)}({hoveredItemId:f,newAction:h,render:i,editor:o,dispatch:n}):n(Ue(h)),r.preventDefault()}else G.w1&&$n(r)}}}(e,t(),r,n)}))}}function Mm(n,e,t){Array.isArray(t[n])?t[n].push(e):t[n]=[e]}var xm=/\$RXN\n+\s+0\s+0\s+0\n*/;function jm(n){var e=Object.keys(u.xz_).map((function(n){return u.xz_[n].mime})),r=(0,y.debounce)(0,(function(e){return n(Ue(e))})),o=(0,y.debounce)(0,(function(e,t){return n(qe(e,t))}));return{formats:e,focused:function(){return!t.g.currentState.modal},onCut:function(){var n=t.g.currentState.editor,e=Em(n);return e?r({tool:"eraser",opts:1}):n.selection(null),e},onCopy:function(){var n=t.g.currentState.editor,e=Em(n);return n.selection(null),e},onPaste:function(n){var e=n[u.hxV.KET]||n[u.hxV.Mol]||n[u.hxV.Rxn]||n["text/plain"];!e&&xm.test(n["text/plain"])||o(e,{fragment:!0})}}}function Em(n){var e={},t=n.structSelected(),r=n.errorHandler;if(t.isBlank())return null;if(Boolean(t.simpleObjects.size||t.texts.size)&&G.w1)return r('The structure you are trying to copy contains Simple object or/and Text object.To copy Simple object or Text object in Internet Explorer try "Copy as KET" button'),null;var o=new u.jWx;try{var i=(new u.F_l).serialize(t);e[u.hxV.KET]=i;var a=t.isReaction?u.hxV.Mol:u.hxV.Rxn,l=o.serialize(t);return e["text/plain"]=l,e[a]=l,e}catch(n){r(n.message)}return null}var Dm=(0,S.$j)(null,(function(n){return n(jm)}))(jn),Am=(0,S.$j)(null,(function(n){return{onInitTmpls:function(e,t){!function(n,e,t){Yu(e,t).then((function(e){var t=e.concat(function(){var n=zn.getItem("ketcher-tmpls");if(!Array.isArray(n)||0===n.length)return[];var e=new u.F_l;return n.map((function(n){try{return""===n.props&&(n.props={}),n.props.group="User Templates",{struct:e.deserialize(n.struct),props:n.props}}catch(n){return null}})).filter((function(n){return null!==n}))}());n(Ku(t)),n(Rn({templates:!0}))}))}(n,t,e)}}}))((function(n){var e=n.onInitTmpls,t=(0,d.useRef)(null),r=d.useContext(vn).staticResourcesUrl;return(0,d.useEffect)((function(){e(t.current,r)}),[]),(0,o.jsx)("div",{style:{display:"none"},ref:t})})),$m={"button-common-styles":"Select-module_button-common-styles__cgaVz",scrollbar:"Select-module_scrollbar__cA89D",dropdownList:"Select-module_dropdownList__rdcrH",selectContainer:"Select-module_selectContainer__yXT-t"},Nm={"button-common-styles":"Dialog-module_button-common-styles__HcaFV",scrollbar:"Dialog-module_scrollbar__9Iy27",dialog:"Dialog-module_dialog__IafFQ",hide:"Dialog-module_hide__6R16B",header:"Dialog-module_header__T7-24",btnContainer:"Dialog-module_btnContainer__TOLPx",buttonTop:"Dialog-module_buttonTop__ZhwZQ",closeButton:"Dialog-module_closeButton__Ch6UT",footer:"Dialog-module_footer__NTq5o",ok:"Dialog-module_ok__T4j7Z",cancel:"Dialog-module_cancel__RcR-D",withDivider:"Dialog-module_withDivider__8LsbA",body:"Dialog-module_body__YgzDR",withMargin:"Dialog-module_withMargin__SDH61"},Pm=["children","title","params","result","valid","buttons","headerContent","footerContent","className","buttonsNameMap","needMargin","withDivider","focusable"];function km(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Im(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?km(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):km(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Tm=function(n){var e=n.children,t=n.title,r=n.params,i=n.result,a=void 0===i?function(){return null}:i,l=n.valid,c=void 0===l?function(){return!!a()}:l,s=n.buttons,u=void 0===s?["OK"]:s,h=n.headerContent,f=n.footerContent,m=n.className,g=n.buttonsNameMap,b=n.needMargin,C=void 0===b||b,y=n.withDivider,O=void 0!==y&&y,w=n.focusable,S=void 0===w||w,M=(0,p.Z)(n,Pm),x=(0,d.useRef)(null);(0,d.useLayoutEffect)((function(){return S&&x.current.focus(),function(){var n,e;null===(n=x.current)||void 0===n||null===(e=n.closest(".Ketcher-root"))||void 0===e||e.getElementsByClassName("cliparea")[0].focus()}}),[S]);var j=function(n){return"OK"===n||"Save"===n},E=function(n){var e=j(n)?"onOk":"onCancel";r&&e in r&&("onOk"!==e||c())&&r[e](a())};return(0,o.jsxs)("div",Im(Im({ref:x,role:"dialog",onSubmit:function(n){return n.preventDefault()},onKeyDown:function(n){var e=z.YG(n),t=document.activeElement,r=t&&"TEXTAREA"===t.tagName;("Escape"===e||"Enter"===e&&!r)&&(E("Enter"===e?"OK":"Cancel"),n.preventDefault(),n.stopPropagation())},tabIndex:-1,className:(0,v.Z)(Nm.dialog,m,r.className)},M),{},{children:[(0,o.jsxs)("header",{className:(0,v.Z)(Nm.header,O&&Nm.withDivider),children:[h||(0,o.jsx)("span",{children:t}),(0,o.jsx)("div",{className:Nm.btnContainer,children:(0,o.jsx)("button",{className:Nm.buttonTop,onClick:function(){return E("Cancel")},children:(0,o.jsx)(Au,{name:"close",className:Nm.closeButton})})})]}),(0,o.jsx)("div",{className:(0,v.Z)(Nm.body,C&&Nm.withMargin),children:e}),(f||u.length>0)&&(0,o.jsxs)("footer",{className:Nm.footer,children:[f,u.length>0&&u.map((function(n){return"string"!=typeof n?n:(0,o.jsx)("input",{type:"button",className:(0,v.Z)(j(n)?Nm.ok:Nm.cancel,"Save"===n&&Nm.save),value:g&&g[n]?g[n]:n,disabled:j(n)&&!c(),onClick:function(){return E(n)}},n)}))]})]}))},Bm=function(){return(0,o.jsxs)("div",{className:"LoadingCircles-module_container__MPCs0",children:[(0,o.jsx)("span",{}),(0,o.jsx)("span",{}),(0,o.jsx)("span",{})]})},Lm=["id","dist"];function _m(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}var Vm=.4,zm={atoms:Gm,bonds:Fm,enhancedFlags:function(n,e,t,r,o){var i,a=null;return n.enhancedFlags.forEach((function(t,r){var l=n.molecule.frags.get(r);if(l&&l.enhancedStereoFlag&&o.showStereoFlags){var c=l.stereoFlagPosition?new u.Sgu(l.stereoFlagPosition.x,l.stereoFlagPosition.y):u.HYg.getDefaultStereoFlagPosition(n.molecule,r);if(c&&!(Math.abs(e.x-c.x)>=1)){var s=Math.abs(e.y-c.y);s<.3&&(!a||s<i)&&(a={id:r,dist:i=s})}}})),a},sgroupData:function(n,e){var t=null,r=null;return n.sgroupData.forEach((function(n,o){if("DAT"!==n.sgroup.type)throw new Error("Data group expected");if("MRV_IMPLICIT_H"!==n.sgroup.data.fieldName){var i=n.sgroup.dataArea,a=i.p0.y<e.y&&i.p1.y>e.y&&i.p0.x<e.x&&i.p1.x>e.x,l=Math.min(Math.abs(i.p0.x-e.x),Math.abs(i.p1.x-e.x));a&&(null===r||l<t)&&(r={id:o,dist:l},t=l)}})),r},sgroups:function(n,e){var t=null,r=Vm;return n.molecule.sgroups.forEach((function(n,o){if(n.functionalGroup&&!n.expanded&&n.firstSgroupAtom)return null;var i=n.bracketDir,a=i.rotateSC(1,0),l=new u.Sgu(u.Sgu.dot(e,i),u.Sgu.dot(e,a));n.areas.forEach((function(n){var e=n.p0.y<l.y&&n.p1.y>l.y&&n.p0.x<l.x&&n.p1.x>l.x,i=Math.min(Math.abs(n.p0.x-l.x),Math.abs(n.p1.x-l.x));e&&(null===t||i<r)&&(t=o,r=i)}))})),null!==t?{id:t,dist:r}:null},functionalGroups:function(n,e){var t=null,r=Vm;return n.molecule.sgroups.forEach((function(n,o){if(n.functionalGroup&&!n.data.expanded&&n.firstSgroupAtom){var i=n.firstSgroupAtom.pp,a=new u.Sgu(.625,.625),l={p0:u.Sgu.diff(i,a),p1:u.Sgu.sum(i,a)},c=l.p0.y<e.y&&l.p1.y>e.y&&l.p0.x<e.x&&l.p1.x>e.x,s=Math.min(Math.abs(l.p0.x-e.x),Math.abs(l.p0.y-e.y),Math.abs(l.p1.x-e.x),Math.abs(l.p0.y-e.y));c&&(null===t||s<r)&&(t=o,r=s)}})),null!==t?{id:t,dist:r}:null},rxnArrows:function(n,e){var t=null,r=null,o=null;return n.rxnArrows.forEach((function(i,a){var l=i.calcDistance(e,n.render.options.scale);l.minDist<.3&&(!o||l.minDist<t)&&(t=l.minDist,r=l.refPoint,o={id:a,dist:t,ref:r})})),o},rxnPluses:function(n,e){var t=null,r=null;return n.rxnPluses.forEach((function(n,o){var i=n.item.pp,a=Math.max(Math.abs(e.x-i.x),Math.abs(e.y-i.y));a<.3&&(!r||a<t)&&(r={id:o,dist:t=a})})),r},frags:function(n,e,t,r,o){r=Math.min(r||Vm,Vm);var i=n.molecule,a=Gm(n,e,t,r);if(a)return{id:i.atoms.get(a.id).fragment,dist:a.dist};var l=Fm(n,e,t,r,o);if(l){var c=i.bonds.get(l.id).begin;return{id:i.atoms.get(c).fragment,dist:l.dist}}return null},rgroups:function(n,e,t,r){r=Math.min(r||Vm,Vm);var o=null;return n.rgroups.forEach((function(n,i){if(i!==t&&n.labelBox&&n.labelBox.contains(e,.5)){var a=u.Sgu.dist(n.labelBox.centre(),e);(!o||a<r)&&(o={id:i,dist:r=a})}})),o},simpleObjects:function(n,e){var t=null,r=null,o=null;return n.simpleObjects.forEach((function(i,a){var l=i.calcDistance(e,n.render.options.scale);l.minDist<.3&&(!o||l.minDist<t)&&(t=l.minDist,r=l.refPoint,o={id:a,dist:t,ref:r})})),o},texts:function(n,e){var t=null,r=null;return n.texts.forEach((function(o,i){var a=o.getReferencePoints(n),l=a[0].x,c=a[0].y,s=a[2].x,d=a[2].y,p=[];e.x>=l&&e.x<=s&&(e.y<c?p.push(c-e.y):e.y>d?p.push(e.y-d):p.push(e.y-c,d-e.y)),e.x<l&&e.y<c&&p.push(u.Sgu.dist(new u.Sgu(l,c),e)),e.x>s&&e.y>d&&p.push(u.Sgu.dist(new u.Sgu(s,d),e)),e.x<l&&e.y>d&&p.push(u.Sgu.dist(new u.Sgu(l,d),e)),e.x>s&&e.y<c&&p.push(u.Sgu.dist(new u.Sgu(s,c),e)),e.y>=c&&e.y<=d&&(e.x<l?p.push(l-e.x):e.x>s?p.push(e.x-s):p.push(0));var h=Math.min.apply(Math,p);h<Vm&&(!r||h<t)&&(r={id:i,dist:t=h})})),r}};function Gm(n,e,t,r){var o=null,i=Vm,a=t&&"atoms"===t.map?t.id:null,l=n.sgroups,c=n.molecule.functionalGroups;return r=r||i,r=Math.min(r,i),n.atoms.forEach((function(n,t){if(u.J41.isAtomInContractedFunctionalGroup(n.a,l,c,!0))return null;if(t!==a){var i=u.Sgu.dist(e,n.a.pp);i<r&&(o=t,r=i)}})),null!==o?{id:o,dist:r}:null}function Fm(n,e,t,r,o){var i=null,a=null,l=.8*Vm,c=t&&"bonds"===t.map?t.id:null,s=n.sgroups,d=n.molecule.functionalGroups;r=r||l;var p=r=Math.min(r,l);return n.bonds.forEach((function(t,r){if(r!==c){var o=n.atoms.get(t.b.begin).a,i=n.atoms.get(t.b.end).a;if(u.J41.isBondInContractedFunctionalGroup(t.b,s,d,!0))return null;var l=u.Sgu.lc2(o.pp,.5,i.pp,.5),h=u.Sgu.dist(e,l);h<p&&(p=h,a=r)}})),n.bonds.forEach((function(t,o){if(o!==c){if(u.J41.isBondInContractedFunctionalGroup(t.b,s,d,!0))return null;var a=n.molecule.halfBonds.get(t.b.hb1),l=a.dir,p=a.norm,h=n.atoms.get(t.b.begin).a.pp,f=n.atoms.get(t.b.end).a.pp;if(u.Sgu.dot(e.sub(h),l)*u.Sgu.dot(e.sub(f),l)<0){var m=Math.abs(u.Sgu.dot(e.sub(h),p));m<r&&(i=o,r=m)}}})),null!==a?{id:a,dist:p}:null!==i&&r>Vm*o?{id:i,dist:r}:null}var Hm=function(n,e,t,o,i){return(t=t||Object.keys(zm)).reduce((function(t,a){var l=t?t.dist:null,c=zm[a](n,e,o,l,i);return null!==c&&(null===t||c.dist<t.dist)?function(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?_m(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):_m(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}({map:a,id:c.id,dist:c.dist},(0,p.Z)(c,Lm)):t}),null)},Rm=function(n,e){var t=arguments.length>2&&void 0!==arguments[2]?arguments[2]:["atoms","bonds"],r=arguments.length>3?arguments[3]:void 0,o={atoms:new Map,bonds:new Map},i=n.molecule;e.atoms.forEach((function(n){o.atoms.set(n,i.atoms.get(n).pp)})),e.bonds.forEach((function(n){var e=i.bonds.get(n);o.bonds.set(n,u.Sgu.lc2(i.atoms.get(e.begin).pp,.5,i.atoms.get(e.end).pp,.5))}));var a={};return t.forEach((function(t){a[t]=Array.from(o[t].keys()).reduce((function(i,a){var l={map:t,id:a},c=zm[t](n,o[t].get(a),l,null,r);return c&&!e[t].includes(c.id)&&i.set(a,c.id),i}),new Map)})),a},Zm=function(){function n(e){(0,c.Z)(this,n),this.editor=e}return(0,s.Z)(n,[{key:"getAll",value:function(){var n=this.editor.render.ctab.molecule.highlights;return(0,x.Z)(n).map((function(n){var e=(0,O.Z)(n,2);return{id:e[0],highlight:e[1]}}))}},{key:"create",value:function(){for(var n=this,e=[],t=arguments.length,r=new Array(t),o=0;o<t;o++)r[o]=arguments[o];r.forEach((function(t){var r=t.atoms,o=t.bonds,i=t.color;if("string"==typeof i&&(r||o)){var a=function(n,e,t){Array.isArray(e)||(e=[]),Array.isArray(t)||(t=[]);var r=n.atoms,o=n.bonds;return e.length>0&&(e=e.filter((function(n){return r.has(n)}))),t.length>0&&(t=t.filter((function(n){return o.has(n)}))),{validAtoms:e,validBonds:t}}(n.editor.render.ctab.molecule,r,o),l=a.validAtoms,c=a.validBonds;0===l.length&&0===c.length||e.push({atoms:l,bonds:c,color:i})}}));var i=(0,u.atm)(this.editor.render.ctab,e);this.editor.update(i)}},{key:"clear",value:function(){var n=(0,u.Ksv)(this.editor.render.ctab);this.editor.update(n)}}]),n}();var Km=["atoms","bonds","frags","sgroups","sgroupData","rgroups","rxnArrows","rxnPluses","enhancedFlags","simpleObjects","texts"],Ym=["atoms","bonds","rxnArrows","rxnPluses","functionalGroups","frags","merge","rgroups","sgroups","sgroupData","enhancedFlags","simpleObjects","texts"],Um=new WeakMap,Jm=function(){function n(e,t){var r,o,i;(0,c.Z)(this,n),i={writable:!0,value:void 0},function(n,e){if(e.has(n))throw new TypeError("Cannot initialize the same private elements twice on an object")}(r=this,o=Um),o.set(r,i),this.render=new u.Hrh(e,Object.assign({scale:40},t)),this._selection=null,this._tool=null,this.historyStack=[],this.historyPtr=0,this.errorHandler=null,this.highlights=new Zm(this),this.renderAndRecoordinateStruct=this.renderAndRecoordinateStruct.bind(this),this.setOptions=this.setOptions.bind(this),this.lastCursorPosition={x:0,y:0},this.createHoverIcon(),this.event={message:new K.w0,elementEdit:new K.he,bondEdit:new K.he,rgroupEdit:new K.he,sgroupEdit:new K.he,sdataEdit:new K.he,quickEdit:new K.he,attachEdit:new K.he,removeFG:new K.he,change:new K.w0,selectionChange:new K.he,aromatizeStruct:new K.he,dearomatizeStruct:new K.he,enhancedStereoEdit:new K.he,confirm:new K.he,cursor:new K.he,showInfo:new K.he},function(n,e){["click","dblclick","mousedown","mousemove","mouseup","mouseleave","mouseover"].forEach((function(t){n.event[t]=new K.ZN;var r=n.event[t];e.addEventListener(t,r.dispatch.bind(r)),r.add((function(e){if(function(n,e){["mousemove","click","mousedown","mouseup","mouseover"].includes(e.type)&&(n.lastCursorPosition={x:e.layerX,y:e.layerY})}(n,e),"mouseup"!==t&&"mouseleave"!==t&&(function(n){return n.which&&3===n.which||n.button&&2===n.button}(e)||!e.target||"DIV"===e.target.nodeName))return n.hover(null),!0;var r=n.tool();return n.lastEvent=e,r&&t in r?(r[t](e),!0):(function(n,e){"mouseup"===e&&n.selection(null)}(n,t),!0)}),-1)}))}(this,e)}return(0,s.Z)(n,[{key:"isDitrty",value:function(){var n=this.historyPtr;return!(!this.historyStack.length||!(0,H.Z)(this,Um)||(0,y.isEqual)(this.historyStack[n-1],(0,H.Z)(this,Um)))}},{key:"setOrigin",value:function(){var n=this.historyPtr;(0,R.Z)(this,Um,n?this.historyStack[n-1]:null)}},{key:"tool",value:function(n,e){if(0===arguments.length)return this._tool;this._tool&&this._tool.cancel&&this._tool.cancel();var t=new cm[n](this,e);return"atom"===n||this.hoverIcon.hide(),!t||t.isNotActiveTool?null:(this._tool=t,this._tool)}},{key:"updateHoverIconPosition",value:function(){var n=this.lastCursorPosition,e=n.x,t=n.y,r=this.hoverIcon.getBBox(),o=r.height,i=r.width;this.hoverIcon.attr({x:e-i/2,y:t-o/2})}},{key:"createHoverIcon",value:function(){this.hoverIcon=this.render.paper.text(0,0,"").attr("font-size",this.options().fontsz).attr("opacity",.7),this.updateHoverIconPosition()}},{key:"clear",value:function(){this.struct(void 0)}},{key:"renderAndRecoordinateStruct",value:function(n){var e=(0,u.oEw)(this.render.ctab,n);return this.update(e),qm(this,Wm(this.render.ctab)),this.render.ctab.molecule}},{key:"struct",value:function(n){if(0===arguments.length)return this.render.ctab.molecule;this.selection(null);var e=n||new u.AUF,t=this.renderAndRecoordinateStruct(e);return this.createHoverIcon(),t}},{key:"structToAddFragment",value:function(n){var e=n.mergeInto(this.render.ctab.molecule);return this.renderAndRecoordinateStruct(e)}},{key:"setOptions",value:function(n){return this.render.updateOptions(n)}},{key:"options",value:function(n){if(0===arguments.length)return this.render.options;var e=this.render.ctab.molecule,t=this.render.options.zoom;return this.render.clientArea.innerHTML="",this.render=new u.Hrh(this.render.clientArea,Object.assign({scale:40},n)),this.render.setMolecule(e),this.render.setZoom(t),this.render.update(),this.render.options}},{key:"zoom",value:function(n){if(0===arguments.length)return this.render.options.zoom;this.render.setZoom(n);var e=this.selection();return qm(this,Wm(this.render.ctab,e)),this.render.update(),this.render.options.zoom}},{key:"selection",value:function(n){if(0===arguments.length)return this._selection;var e=this.render.ctab;if(this._selection=null,"all"===n&&(n=Km.reduce((function(n,t){return n[t]=Array.from(e[t].keys()),n}),{})),"descriptors"===n&&(e=this.render.ctab,n={sgroupData:Array.from(e.sgroupData.keys())}),n){var t={};Object.keys(n).forEach((function(e){n[e].length>0&&(t[e]=n[e].slice())})),0!==Object.keys(t).length&&(this._selection=t);var r=function(n,e){var t={};n.forEach((function(n,e){t[n.fragment]?t[n.fragment].push(e):t[n.fragment]=[e]}));var r=[];return Object.keys(t).forEach((function(n){var o=!0;t[n].forEach((function(n){e.includes(n)||(o=!1)})),o&&r.push(Number(n))})),r}(this.struct().atoms,this.explicitSelected().atoms);0!==r.length&&(this._selection&&this._selection.enhancedFlags?this._selection.enhancedFlags=Array.from(new Set([].concat((0,x.Z)(this._selection.enhancedFlags),(0,x.Z)(r)))):t.enhancedFlags=r)}return this.render.ctab.setSelection(this._selection),this.event.selectionChange.dispatch(this._selection),this.render.update(),this._selection}},{key:"hover",value:function(n,e,t){var r=e||this._tool,o=null;if(!("ci"in r)||n&&r.ci.map===n.map&&r.ci.id===n.id||(Xm(r.ci,!1,this.render),delete r.ci),n&&Xm(n,!0,this.render)&&(r.ci=n),t){var i=this.findItem(t,["sgroups","functionalGroups"]);if(i){var a,l=null===(a=this.struct())||void 0===a?void 0:a.sgroups.get(i.id);if(l&&!l.data.expanded){var c=l.data.name;o={groupStruct:u.J41.getFunctionalGroupByName(c),event:t,sGroup:l}}}o?this.event.showInfo.dispatch(o):this.event.showInfo.dispatch(null)}}},{key:"update",value:function(n,e){!0===n?this.render.update(!0):(e||n.isDummy()||(this.historyStack.splice(this.historyPtr,33,n),this.historyStack.length>32&&this.historyStack.shift(),this.historyPtr=this.historyStack.length,this.event.change.dispatch(n)),this.render.update())}},{key:"historySize",value:function(){return{undo:this.historyPtr,redo:this.historyStack.length-this.historyPtr}}},{key:"undo",value:function(){if(0===this.historyPtr)throw new Error("Undo stack is empty");if(this.tool()&&this.tool().cancel&&this.tool().cancel(),this.selection(null),this._tool instanceof cm.paste)this.event.change.dispatch();else{this.historyPtr--;var n=this.historyStack[this.historyPtr].perform(this.render.ctab);this.historyStack[this.historyPtr]=n,this.event.change.dispatch(n),this.render.update()}}},{key:"redo",value:function(){if(this.historyPtr===this.historyStack.length)throw new Error("Redo stack is empty");if(this.tool()&&this.tool().cancel&&this.tool().cancel(),this.selection(null),this._tool instanceof cm.paste)this.event.change.dispatch();else{var n=this.historyStack[this.historyPtr].perform(this.render.ctab);this.historyStack[this.historyPtr]=n,this.historyPtr++,this.event.change.dispatch(n),this.render.update()}}},{key:"subscribe",value:function(n,e){var t={handler:e};if("change"===n){var r=function(n){return function(n,e){var t=[];return n.operations.reverse().forEach((function(n){var e=n._inverted;switch(e.type){case u.C8.ATOM_ADD:case u.C8.ATOM_DELETE:t.push({operation:e.type,id:e.data.aid,label:e.data.atom.label?e.data.atom.label:"",position:{x:+e.data.pos.x.toFixed(2),y:+e.data.pos.y.toFixed(2)}});break;case u.C8.ATOM_ATTR:t.push({operation:n.type,id:n.data.aid,attribute:n.data.attribute,from:n.data.value,to:n.data2.value});break;case u.C8.ATOM_MOVE:t.push({operation:e.type,id:e.data.aid,position:{x:+e.data.d.x.toFixed(2),y:+e.data.d.y.toFixed(2)}});break;case u.C8.BOND_ADD:case u.C8.BOND_DELETE:t.push({operation:e.type,id:e.data.bid});break;case u.C8.FRAGMENT_ADD:case u.C8.FRAGMENT_DELETE:t.push({operation:e.type,id:e.frid});break;case u.C8.FRAGMENT_ADD_STEREO_ATOM:case u.C8.FRAGMENT_DELETE_STEREO_ATOM:t.push({operation:e.type,atomId:e.data.aid,fragId:e.data.frid});break;case u.C8.S_GROUP_ATOM_ADD:case u.C8.S_GROUP_ATOM_REMOVE:t.push({operation:e.type,atomId:e.data.aid,sGroupId:e.data.sgid});break;case u.C8.S_GROUP_CREATE:case u.C8.S_GROUP_DELETE:t.push({operation:e.type,type:e.data.type,sGroupId:e.data.sgid});break;case u.C8.RXN_ARROW_ADD:case u.C8.RXN_ARROW_DELETE:t.push({operation:e.type,id:e.data.id,mode:e.data.mode,position:e.data.pos.map((function(n){return{x:+n.x.toFixed(2),y:+n.y.toFixed(2)}}))});break;case u.C8.RXN_ARROW_RESIZE:t.push({operation:e.type,id:e.data.id});break;case u.C8.RXN_ARROW_MOVE:t.push({operation:e.type,id:e.data.id,position:{x:+e.data.d.x.toFixed(2),y:+e.data.d.y.toFixed(2)}});break;case u.C8.R_GROUP_FRAGMENT:t.push({operation:n.type,id:e.frid});break;case u.C8.SIMPLE_OBJECT_ADD:case u.C8.SIMPLE_OBJECT_DELETE:t.push({operation:e.type,id:e.data.id,mode:e.data.mode});break;case u.C8.SIMPLE_OBJECT_RESIZE:t.push({operation:e.type,id:e.data.id});break;case u.C8.SIMPLE_OBJECT_MOVE:t.push({operation:n.type,id:n.data.id,position:{x:+n.data.d.x.toFixed(2),y:+n.data.d.y.toFixed(2)}});break;default:t.push({operation:e.type})}})),e(t)}(n,e)};t.handler=r,this.event[n].add(r)}else this.event[n].add(e);return t}},{key:"unsubscribe",value:function(n,e){this.event[n].remove(e.handler)}},{key:"findItem",value:function(n,e){var t=arguments.length>2&&void 0!==arguments[2]?arguments[2]:null,r=new u.Sgu(this.render.page2obj(n));return Hm(this.render.ctab,r,e,t,this.render.options)}},{key:"findMerge",value:function(n,e){return Rm(this.render.ctab,n,e,this.render.options)}},{key:"explicitSelected",value:function(){var n=this.selection()||{},e=Km.reduce((function(e,t){return e[t]=n[t]?n[t].slice():[],e}),{}),t=this.render.ctab.molecule;return e.bonds&&e.bonds.forEach((function(n){var r=t.bonds.get(n);e.atoms=e.atoms||[],e.atoms.indexOf(r.begin)<0&&e.atoms.push(r.begin),e.atoms.indexOf(r.end)<0&&e.atoms.push(r.end)})),e.atoms&&e.bonds&&t.bonds.forEach((function(n,t){e.bonds.indexOf(t)>=0&&e.atoms.indexOf(n.begin)>=0&&e.atoms.indexOf(n.end)>=0&&(e.bonds=e.bonds||[],e.bonds.push(t))})),e}},{key:"structSelected",value:function(){var n=this.render.ctab.molecule,e=this.explicitSelected(),t=n.clone(new u.UE_(e.atoms),new u.UE_(e.bonds),!0,null,new u.UE_(e.simpleObjects),new u.UE_(e.texts));return n.rxnArrows.forEach((function(n,r){-1!==e.rxnArrows.indexOf(r)&&t.rxnArrows.add(n.clone())})),n.rxnPluses.forEach((function(n,r){-1!==e.rxnPluses.indexOf(r)&&t.rxnPluses.add(n.clone())})),t.isReaction=n.isReaction&&n.isRxn(),t}},{key:"alignDescriptors",value:function(){this.selection(null);var n=(0,u.NZY)(this.render.ctab);this.update(n),this.render.update(!0)}}]),n}();function qm(n,e){e?n.render.setScrollOffset(e.x,e.y):n.render.setScrollOffset(0,0)}function Wm(n,e){var t=n.getVBoxObj(e||{});return u.Sgu.lc2(t.p0,.5,t.p1,.5)}function Xm(n,e,t){if(-1===Ym.indexOf(n.map))return!1;var r=null;if("merge"===n.map)return Object.keys(n.items).forEach((function(o){n.items[o].forEach((function(n){(r=t.ctab[o].get(n))&&r.setHover(e,t)}))})),!0;if("functionalGroups"===n.map&&(n.map="sgroups"),!(r=t.ctab[n.map].get(n.id)))return!0;if("sgroups"===n.map&&"DAT"===r.item.type||"sgroupData"===n.map){var o=t.ctab.sgroups.get(n.id);o&&o.setHover(e,t);var i=t.ctab.sgroupData.get(n.id);i&&i.setHover(e,t)}else r.setHover(e,t);return!0}var Qm=function(){var n=lp().getKetcherInstance,e=(0,S.I0)(),t=(0,d.useState)(!1),i=(0,O.Z)(t,2),a=i[0],l=i[1],c=(0,d.useState)([]),s=(0,O.Z)(c,2),p=s[0],h=s[1];return(0,o.jsxs)(Z.xV,{id:"contextmenu",onShow:function(e){return function(e){var t=n().editor,r=t.struct(),o=t.selection();l(!1),h([]);var i,a=[],c=t.findItem({clientX:e.detail.position.x,clientY:e.detail.position.y},["sgroups","functionalGroups","atoms","bonds"]);if(c)switch(c.map){case"atoms":null!==(i=u.J41.findFunctionalGroupByAtom(r.functionalGroups,c.id))&&r.functionalGroups.forEach((function(n){n.relatedSGroupId===i&&!a.includes(n)&&a.push(n)}));break;case"bonds":null!==(i=u.J41.findFunctionalGroupByBond(r,r.functionalGroups,c.id))&&r.functionalGroups.forEach((function(n){n.relatedSGroupId===i&&!a.includes(n)&&a.push(n)}));break;case"sgroups":var s=r.sgroups.get(c.id);u.J41.isFunctionalGroup(s)&&r.functionalGroups.forEach((function(n){n.relatedSGroupId===(null==s?void 0:s.id)&&!a.includes(n)&&a.push(n)}));break;case"functionalGroups":var d=r.sgroups.get(c.id);u.J41.isFunctionalGroup(d)&&r.functionalGroups.forEach((function(n){n.relatedSGroupId===(null==d?void 0:d.id)&&!a.includes(n)&&a.push(n)}))}o&&o.atoms&&o.atoms.forEach((function(n){var e=u.J41.findFunctionalGroupByAtom(r.functionalGroups,n);null!==e&&r.functionalGroups.forEach((function(n){n.relatedSGroupId===e&&!a.includes(n)&&a.push(n)}))})),a.length&&(h(a),l(!0))}(e)},className:(0,v.Z)((0,r.Z)({},"ContextMenu-module_isHidden__eOjF4",!a)),children:[(0,o.jsxs)(Z.sN,{onClick:function(){var t=n().editor,r=new u.aUM,o=p[0].isExpanded;null==p||p.forEach((function(n){r.mergeWith((0,u.wSe)(t.render.ctab,n.relatedSGroupId,{expanded:!o}))})),t.update(r),l(!1),h([]),vd(e,{group:null,id:null})},children:[p.length&&p[0].isExpanded?"Contract ":"Expand ","Abbreviation"]}),(0,o.jsx)(Z.sN,{divider:!0}),(0,o.jsx)(Z.sN,{onClick:function(){var e=n().editor,t=new u.aUM;null==p||p.forEach((function(n){t.mergeWith((0,u.U9$)(e.render.ctab,n.relatedSGroupId))})),e.update(t),l(!1),h([])},children:"Remove Abbreviation"})]})},nv="StructEditor-module_visible__3eFNB",ev="StructEditor-module_enableCursor__Qla0A",tv=function(n){var e=n.Icon,t=n.PressedIcon,r=n.enableHandTool,i=(0,d.useState)({clientX:50,clientY:50}),a=(0,O.Z)(i,2),l=a[0],c=a[1],s=(0,d.useState)(!1),u=(0,O.Z)(s,2),p=u[0],h=u[1],f=function(n){n.pageX,n.pageY;var e=n.clientX,t=n.clientY;c({clientX:e,clientY:t})},m=function(){h(!0)},v=function(){h(!1)};return(0,d.useEffect)((function(){return document.addEventListener("mousemove",f,!1),document.addEventListener("mouseenter",f,!1),document.addEventListener("mousedown",m,!1),document.addEventListener("mouseup",v,!1),function(){document.removeEventListener("mousedown",m),document.removeEventListener("mouseup",v),document.removeEventListener("mousemove",f),document.removeEventListener("mouseenter",f)}}),[]),r?(0,o.jsx)("div",{style:{position:"fixed",top:0,bottom:0,left:0,right:0,zIndex:9999,pointerEvents:"none"},children:p?(0,o.jsx)(t,{style:{position:"absolute",left:l.clientX,top:l.clientY}}):(0,o.jsx)(e,{style:{position:"absolute",left:l.clientX,top:l.clientY}})}):null},rv=["struct","Tag"];function ov(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function iv(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?ov(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):ov(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var av=function(n){(0,h.Z)(i,n);var e,t,r=(e=i,t=function(){if("undefined"==typeof Reflect||!Reflect.construct)return!1;if(Reflect.construct.sham)return!1;if("function"==typeof Proxy)return!0;try{return Boolean.prototype.valueOf.call(Reflect.construct(Boolean,[],(function(){}))),!0}catch(n){return!1}}(),function(){var n,r=(0,m.Z)(e);if(t){var o=(0,m.Z)(this).constructor;n=Reflect.construct(r,arguments,o)}else n=r.apply(this,arguments);return(0,f.Z)(this,n)});function i(n){var e;return(0,c.Z)(this,i),(e=r.call(this,n)).tagRef=(0,d.createRef)(),e}return(0,s.Z)(i,[{key:"shouldComponentUpdate",value:function(n){return Boolean(this.props.id&&this.props.id!==n.id)}},{key:"update",value:function(){var n,e=this.tagRef.current,t=this.props,r=t.struct,o=t.options;if(r instanceof u.AUF)n=r;else try{n=(new u.jWx).deserialize(r)}catch(e){n=null}null==e||e.childNodes.forEach((function(n){n.remove()})),Cd.render(e,n,o)}},{key:"componentDidMount",value:function(){this.update()}},{key:"componentDidUpdate",value:function(){this.update()}},{key:"render",value:function(){var n=this.props,e=n.struct,t=n.Tag,r=void 0===t?"div":t,i=(0,p.Z)(n,rv);return(0,o.jsx)(r,iv(iv({ref:this.tagRef},i),{},{children:e?null:"No molecule"}))}}]),i}(d.Component),lv=function(n){return n.functionalGroups.functionalGroupInfo};function cv(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function sv(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?cv(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):cv(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var uv=(0,S.$j)((function(n){var e,t,r,o,i,a,l,c,s;return{clientX:(null===(e=lv(n))||void 0===e||null===(t=e.event)||void 0===t?void 0:t.clientX)||0,clientY:(null===(r=lv(n))||void 0===r||null===(o=r.event)||void 0===o?void 0:o.clientY)||0,groupStruct:(null===(i=lv(n))||void 0===i?void 0:i.groupStruct)||null,sGroup:(null===(a=lv(n))||void 0===a?void 0:a.sGroup)||null,render:null===(l=n.editor)||void 0===l||null===(c=l.render)||void 0===c||null===(s=c.ctab)||void 0===s?void 0:s.render}}))((function(n){var e,t,r=n.clientX,i=void 0===r?0:r,a=n.clientY,l=void 0===a?0:a,c=n.render,s=n.className,p=n.groupStruct,h=n.sGroup,f=(0,d.useState)(null),m=(0,O.Z)(f,2),g=m[0],b=m[1],C=(0,d.useRef)(null),y=null==h||null===(e=h.data)||void 0===e?void 0:e.name;(0,d.useEffect)((function(){return p?t=setTimeout((function(){b(p.clone())}),400):b(null),function(){return clearTimeout(t)}}),[y]);var w=function(n,e,t,r){var o=0,i=0,a=0,l=0;if(r){var c,s,d,p,h,f,m,v=r.areas[0],g=u.Ciz.obj2scaled(v.p0,t.options),b=u.Ciz.obj2scaled(v.p1,t.options);o=b.x-g.x,i=b.y-g.y;var C=function(n,e){var t,r,o=n.firstSgroupAtom;if(o)return o.pp;var i=(0,O.Z)(n.atoms,1)[0];return(null===(t=e.ctab.atoms)||void 0===t||null===(r=t.get(i))||void 0===r?void 0:r.a.pp)||new u.Sgu(0,0)}(r,t),y=u.Ciz.obj2scaled(C,{scale:t.options.scale*t.options.zoom});a=y.x-o/2-20,l=y.y+20;var w=(null==t||null===(c=t.clientArea)||void 0===c?void 0:c.clientWidth)-o/2,S=40+o/2,M=(null==t||null===(s=t.clientArea)||void 0===s?void 0:s.clientHeight)-i;n>w?a=y.x-o-20:n<S&&(a=y.x-20),e>M&&(l=y.y-i-60),a+=(null==t||null===(d=t.options.offset)||void 0===d?void 0:d.x)-(null==t||null===(p=t.clientArea)||void 0===p?void 0:p.scrollLeft),l+=(null==t||null===(h=t.options)||void 0===h||null===(f=h.offset)||void 0===f?void 0:f.y)-(null==t||null===(m=t.clientArea)||void 0===m?void 0:m.scrollTop)}return[new u.Sgu(a,l),new u.Sgu(o,i)]}(i,l,c,h),S=(0,O.Z)(w,2),M=S[0],x=S[1],j=M.x,E=M.y,D=x.x,A=x.y;return g&&(0,o.jsx)("div",{style:{left:j+"px",top:E+"px"},className:(0,v.Z)("InfoPanel-module_infoPanel__irvZL",s),children:(0,o.jsx)(av,{struct:g,id:y,ref:C,options:sv(sv({},c.options),{},{autoScale:!0,autoScaleMargin:0,rescaleAmount:1,cachePrefix:"infoPanel",viewSz:new u.Sgu(D,A),width:D,height:A})})})})),dv=["Tag","struct","tool","toolOpts","options","onInit","onSelectionChange","onElementEdit","onEnhancedStereoEdit","onQuickEdit","onBondEdit","onRgroupEdit","onSgroupEdit","onSdataEdit","onRemoveFG","onMessage","onAromatizeStruct","onDearomatizeStruct","onAttachEdit","indigoVerification","onCipChange","className","onConfirm","onShowInfo","showAttachmentPoints"];function pv(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function hv(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?pv(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):pv(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function fv(n,e){var t=arguments.length>2&&void 0!==arguments[2]?arguments[2]:{},r=e.struct,o=e.tool,i=e.toolOpts,a=e.options;r!==t.struct&&n.struct(r),o===t.tool&&i===t.toolOpts||(n.tool(o,i),i!==t.toolOpts&&n.event.message.dispatch({info:JSON.stringify(i)})),t.options&&a!==t.options&&n.options(a),Object.keys(n.event).forEach((function(r){var o="on".concat((0,y.upperFirst)(r));e[o]!==t[o]&&(t[o]&&n.event[r].remove(t[o]),e[o]&&n.event[r].add(e[o]))}))}var mv,vv,gv,bv,Cv,yv=function(n){(0,h.Z)(i,n);var e,t,r=(e=i,t=function(){if("undefined"==typeof Reflect||!Reflect.construct)return!1;if(Reflect.construct.sham)return!1;if("function"==typeof Proxy)return!0;try{return Boolean.prototype.valueOf.call(Reflect.construct(Boolean,[],(function(){}))),!0}catch(n){return!1}}(),function(){var n,r=(0,m.Z)(e);if(t){var o=(0,m.Z)(this).constructor;n=Reflect.construct(r,arguments,o)}else n=r.apply(this,arguments);return(0,f.Z)(this,n)});function i(n){var e;return(0,c.Z)(this,i),(e=r.call(this,n)).state={enableCursor:!1,clientX:0,clientY:0},e.editorRef=(0,d.createRef)(),e.logRef=(0,d.createRef)(),e}return(0,s.Z)(i,[{key:"shouldComponentUpdate",value:function(n,e){return this.props.indigoVerification!==n.indigoVerification||e.enableCursor!==this.state.enableCursor}},{key:"UNSAFE_componentWillReceiveProps",value:function(n){fv(this.editor,n,this.props)}},{key:"componentDidMount",value:function(){var n=this;this.editor=new Jm(this.editorRef.current,hv({},this.props.options)),fv(this.editor,this.props),this.props.onInit&&this.props.onInit(this.editor),this.editor.event.message.add((function(e){var t=n.logRef.current;if(e.info&&n.props.showAttachmentPoints){try{var r=JSON.parse(e.info);t.innerHTML="Atom Id: ".concat(r.atomid,", Bond Id: ").concat(r.bondid)}catch(n){t.innerHTML=e.info}t.classList.add(nv)}else t.classList.remove(nv)})),this.editor.event.cursor.add((function(e){switch(e.status){case"enable":n.editorRef.current.classList.add(ev);var t=n.editorRef.current.getBoundingClientRect(),r=t.left,o=t.top,i=t.right,a=t.bottom,l=e.cursorPosition,c=l.clientX,s=l.clientY,u=c>=r&&c<=i&&s>=o&&c<=a;!n.state.enableCursor&&u&&n.setState({enableCursor:!0});break;case"move":n.editorRef.current.classList.add(ev),n.setState({enableCursor:!0,clientX:c,clientY:s});break;case"disable":case"leave":n.editorRef.current.classList.remove(ev),n.setState({enableCursor:!1});break;case"mouseover":n.editorRef.current.classList.add(ev),n.setState({enableCursor:!0})}})),this.editor.event.message.dispatch({info:JSON.stringify(this.props.toolOpts)})}},{key:"componentWillUnmount",value:function(){var n,e;n=this.editor,e=this.props,Object.keys(n.event).forEach((function(t){var r="on".concat((0,y.upperFirst)(t));e[r]&&n.event[t].remove(e[r])}))}},{key:"render",value:function(){var n=this.props,e=n.Tag,t=void 0===e?"div":e;n.struct,n.tool,n.toolOpts,n.options,n.onInit,n.onSelectionChange,n.onElementEdit,n.onEnhancedStereoEdit,n.onQuickEdit,n.onBondEdit,n.onRgroupEdit,n.onSgroupEdit,n.onSdataEdit,n.onRemoveFG,n.onMessage,n.onAromatizeStruct,n.onDearomatizeStruct,n.onAttachEdit;var r=n.indigoVerification;n.onCipChange;var i=n.className;n.onConfirm,n.onShowInfo,n.showAttachmentPoints;var a=(0,p.Z)(n,dv),l=this.state,c=l.clientX,s=void 0===c?0:c,u=l.clientY,d=void 0===u?0:u;return(0,o.jsxs)(t,hv(hv({className:(0,v.Z)("StructEditor-module_canvas__LLnzh",i),onMouseDown:function(n){return n.preventDefault()}},a),{},{children:[(0,o.jsxs)(Z.W4,{id:"contextmenu",attributes:{onClick:Z.SC},holdToDisplay:-1,children:[(0,o.jsx)("div",{ref:this.editorRef,className:(0,v.Z)("StructEditor-module_intermediateCanvas__fR3ws"),onMouseDown:function(n){return n.preventDefault()}}),(0,o.jsx)(tv,{Icon:Gl,PressedIcon:Hl,enableHandTool:this.state.enableCursor}),(0,o.jsx)("div",{className:"StructEditor-module_measureLog__B2wuy",ref:this.logRef}),r&&(0,o.jsx)("div",{className:"StructEditor-module_spinnerOverlay__5H1IM",children:(0,o.jsx)(Bm,{})})]}),(0,o.jsx)(uv,{clientX:s,clientY:d,render:this.props.render,groupStruct:this.props.groupStruct,sGroup:this.props.sGroup}),(0,o.jsx)(Qm,{})]}))}}]),i}(d.Component);function Ov(){return Ov=Object.assign||function(n){for(var e=1;e<arguments.length;e++){var t=arguments[e];for(var r in t)Object.prototype.hasOwnProperty.call(t,r)&&(n[r]=t[r])}return n},Ov.apply(this,arguments)}function wv(n){return d.createElement("svg",Ov({width:22,height:24,viewBox:"0 0 22 24",fill:"none",xmlns:"http://www.w3.org/2000/svg"},n),mv||(mv=d.createElement("path",{fill:"transparent",d:"M0 0h21.503v24H0z"})),vv||(vv=d.createElement("path",{d:"M13.507 18.936l-2.04-1.92c-.7-.659-1.403-1.317-2.108-1.983v3.097c0 .43.003.86.007 1.289 0 .049-.007.09-.007.126v2.04c0 .834 0 1.557.003 2.02l.278.163c.719.3 1.434.307 2.151.033l4.264-2.469c-.358-.326-1.395-1.31-2.548-2.396zM6.159 19.39v-1.091L6.163 2.23v-.002L1.26 5.059C.421 5.647.002 6.482.002 7.553c0 2.944.006 5.888-.002 8.831-.003 1.08.398 1.913 1.212 2.517l4.946 2.856v-2.318-.05z",fill:"#676767"})),gv||(gv=d.createElement("path",{d:"M18.642 4.137l1.672.966c.785.58 1.187 1.385 1.188 2.41v8.974c0 1-.385 1.79-1.133 2.367l-1.423.822h-.004c-.097-.097-6.384-6.375-6.513-6.386.044-.044.56-.582 1.278-1.33L20.3 5.097l-1.658-.96z",fill:"url(#logo_svg__paint0_linear_5175_84899)"})),bv||(bv=d.createElement("path",{d:"M17.335 3.383L11.849.216c-.718-.29-1.455-.29-2.219.011l-.27.139s0 10.346.041 11.106c.341-.346 7.808-7.96 7.934-8.09z",fill:"url(#logo_svg__paint1_linear_5175_84899)"})),Cv||(Cv=d.createElement("defs",null,d.createElement("linearGradient",{id:"logo_svg__paint0_linear_5175_84899",x1:19.854,y1:4.363,x2:11.579,y2:13.111,gradientUnits:"userSpaceOnUse"},d.createElement("stop",{stopColor:"#3BC2D7"}),d.createElement("stop",{offset:.74,stopColor:"#1D9DB1"})),d.createElement("linearGradient",{id:"logo_svg__paint1_linear_5175_84899",x1:19.854,y1:4.363,x2:11.579,y2:13.111,gradientUnits:"userSpaceOnUse"},d.createElement("stop",{stopColor:"#3BC2D7"}),d.createElement("stop",{offset:.74,stopColor:"#1D9DB1"})))))}var Sv,Mv={"button-common-styles":"About-module_button-common-styles__XmSbT",scrollbar:"About-module_scrollbar__4-AeI",dialog_body:"About-module_dialog_body__ebQu-",about:"About-module_about__ZVesh",body:"About-module_body__8VOc3",versionName:"About-module_versionName__1gqJr",firstline:"About-module_firstline__h5XMW",links:"About-module_links__sMpyx",infoLinks:"About-module_infoLinks__4-Tot",indigoVersion:"About-module_indigoVersion__WKFlu",headerContent:"About-module_headerContent__YclOx",title:"About-module_title__k-6Zg",indigoFirstLine:"About-module_indigoFirstLine__-86rb",okButton:"About-module_okButton__FMcEk"},xv=(0,S.$j)((function(n){return{date:n.options.app.buildDate.replace("T","; "),indigoVersion:n.options.app.indigoVersion,indigoMachine:n.options.app.indigoMachine,feedbackLink:"http://lifescience.opensource.epam.com/ketcher/#feedback",overviewLink:"https://lifescience.opensource.epam.com/ketcher/index.html",lifeScienciesLink:"http://lifescience.opensource.epam.com/",version:n.options.app.version}}),(function(n){return{onOk:function(e){n({type:"MODAL_CLOSE"})}}}))((function(n){var e=n.indigoVersion&&n.indigoVersion.split(".r");return(0,o.jsxs)(Tm,{className:"".concat(Mv.about," ").concat(Mv.dialog_body),params:n,buttons:[(0,o.jsx)("button",{onClick:n.onOk,className:Mv.okButton,children:"Ok"},"ok")],children:[(0,o.jsx)("div",{className:Mv.headerContent,children:(0,o.jsxs)("a",{href:n.overviewLink,target:"_blank",rel:"noopener noreferrer",children:[(0,o.jsx)(wv,{}),(0,o.jsx)("span",{className:Mv.title,children:"Ketcher"})]})}),(0,o.jsx)("div",{className:Mv.body,children:(0,o.jsx)("div",{className:Mv.verionsInfo,children:(0,o.jsxs)("dl",{className:Mv.ketcherVersionInfo,children:[(0,o.jsx)("dt",{children:(0,o.jsxs)("a",{href:n.overviewLink,target:"_blank",rel:"noopener noreferrer",children:["Version ",n.version]})}),(0,o.jsxs)("dd",{children:["Build at ",(0,o.jsx)("time",{children:n.date})]}),(0,o.jsxs)("div",{className:Mv.infoLinks,children:[(0,o.jsx)("dt",{children:(0,o.jsx)("a",{href:n.feedbackLink,target:"_blank",rel:"noopener noreferrer",children:"Feedback"})}),(0,o.jsx)("dt",{children:(0,o.jsx)("a",{href:n.lifeScienciesLink,target:"_blank",rel:"noopener noreferrer",children:"Epam Life Sciencies"})})]}),(0,o.jsx)("br",{}),(0,o.jsxs)("div",{class:Mv.indigoVersion,children:[(0,o.jsxs)("a",{href:"http://lifescience.opensource.epam.com/indigo/",target:"_blank",rel:"noopener noreferrer",children:[" ","Indigo Toolkit"]}),n.indigoMachine&&(0,o.jsx)("div",{children:n.indigoMachine})]}),(0,o.jsx)("div",{children:n.indigoVersion?(0,o.jsxs)(d.Fragment,{children:[(0,o.jsxs)("dd",{children:["Version ",e[0]]}),e[1]&&(0,o.jsxs)("dd",{children:["Build ",e[1]]})]}):(0,o.jsx)("p",{children:"Standalone"})})]})})})]})})),jv=(0,N.Z)(L.ZP)(Sv||(Sv=(0,P.Z)(["\n  & .MuiPopover-paper {\n    padding: 0 8px;\n    box-shadow: 4px 0px, 2px rgba(0, 0, 0, 0.25);\n    font-size: 12px;\n    max-width: 160px;\n  }\n"]))),Ev=function(n){var e=n.error,t=n.anchorEl,r=n.handleClose;return(0,o.jsx)(jv,{id:"form-error",open:!0,anchorEl:t,disableAutoFocus:!0,sx:{pointerEvents:"none"},onClose:r,anchorOrigin:{vertical:"bottom",horizontal:"center"},transformOrigin:{vertical:"top",horizontal:"left"},children:(0,o.jsx)(o.Fragment,{children:(0,o.jsx)("p",{children:e})})})},Dv={fieldSetLabel:"input-module_fieldSetLabel__DxKa5",input:"input-module_input__WzHgL",checkbox:"input-module_checkbox__CowSc",radioButton:"input-module_radioButton__2eHO0",slider:"input-module_slider__-Xsc0",select:"input-module_select__GhgBs",genericInput:"input-module_genericInput__XdZ2R"},Av=["schema","value","onChange","type","isFocused"],$v=["schema","value","onChange"],Nv=["schema","value","onChange"],Pv=["schema","value","selected","onSelect","type","checked"],kv=["value","onChange","name"],Iv=["children","onChange","style"],Tv=["children","onChange"];function Bv(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Lv(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Bv(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Bv(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function _v(n){n.schema;var e=n.value,t=void 0===e?"":e,r=n.onChange,i=n.type,a=void 0===i?"text":i,l=n.isFocused,c=void 0!==l&&l,s=(0,p.Z)(n,Av),u=(0,d.useRef)(null);return(0,d.useEffect)((function(){u.current&&c&&u.current.focus()}),[u,c]),(0,o.jsxs)(o.Fragment,{children:[(0,o.jsx)("input",Lv({type:a,value:t,onInput:r,onChange:r,className:(0,v.Z)(Dv.input,Dv.genericInput),ref:u},s)),"checkbox"===a&&(0,o.jsx)("span",{className:Dv.checkbox}),"radio"===a&&(0,o.jsx)("span",{className:Dv.radioButton})]})}function Vv(n){n.schema;var e=n.value,t=n.onChange,r=(0,p.Z)(n,$v);return(0,o.jsx)("textarea",Lv({value:e,onInput:t},r))}function zv(n){n.schema;var e=n.value,t=void 0===e?"":e,r=n.onChange,i=(0,p.Z)(n,Nv);return(0,o.jsxs)("div",{className:Dv.fieldSetItem,children:[(0,o.jsx)("input",Lv({type:"checkbox",checked:t,onClick:r,onChange:r,className:Dv.input},i)),(0,o.jsx)("span",{className:Dv.checkbox})]})}function Gv(n){var e=n.schema,t=n.value,r=n.name,i=n.onSelect,a=n.className,l=n.multiple,c=void 0!==l&&l;return(0,o.jsx)("select",{onChange:i,value:t,name:r,multiple:c,className:(0,v.Z)(Dv.select,a),children:Rv(e,(function(n,e){return(0,o.jsx)("option",{value:e,children:n},e)}))})}function Fv(n){var e=n.schema,t=n.value,r=n.selected,i=n.onSelect,a=n.type,l=void 0===a?"radio":a,c=n.checked,s=(0,p.Z)(n,Pv);return(0,o.jsx)("fieldset",{onClick:i,children:Rv(e,(function(n,e){return(0,o.jsx)("li",{className:Dv.fieldSetItem,children:(0,o.jsxs)("label",{className:Dv.fieldSetLabel,children:[(0,o.jsx)("input",Lv({type:l,defaultChecked:r(e,"radio"===l?c:t),value:"object"!==(0,g.Z)(e)&&e,className:Dv.input},s)),"checkbox"===l&&(0,o.jsx)("span",{className:Dv.checkbox}),"radio"===l&&(0,o.jsx)("span",{className:Dv.radioButton}),n]})},n)}))})}function Hv(n){var e=n.value,t=n.onChange,r=n.name,i=(0,p.Z)(n,kv);return(0,o.jsxs)("div",{className:Dv.slider,children:[(0,o.jsx)("input",Lv({type:"checkbox",checked:e,onClick:t,onChange:t,name:r},i)),(0,o.jsx)("span",{})]},r)}function Rv(n,e){var t=Array.isArray(n);if(!t&&n.items&&(n=n.items),"function"==typeof e)return(t?n:n.enum).map((function(r,o){var i=t?r.title:n.enumNames&&n.enumNames[o];return e(void 0!==i?i:r,r&&void 0!==r.value?r.value:r)}));if(!t)return n.enum[e];var r=n[e];return void 0!==r.value?r.value:r}_v.val=function(n,e){var t=n.target,r="number"===t.type||"range"===t.type||e&&("number"===e.type||"integer"===e.type),o=r?t.value.replace(/,/g,"."):t.value;return r&&!isNaN(o-0)?o-0:o},Vv.val=function(n){return n.target.value},zv.val=function(n){return n.stopPropagation(),!!n.target.checked},Gv.val=function(n,e){var t=n.target;return t.multiple?[].reduce.call(t.options,(function(n,t,r){return t.selected?[Rv(e,r)].concat((0,x.Z)(n)):n}),[]):Rv(e,t.selectedIndex)},Fv.val=function(n,e){var t=n.target;if("INPUT"===n.target.tagName){var r=t.parentNode.parentNode.parentNode,o=[].reduce.call(r.querySelectorAll("input"),(function(n,t,r){return t.checked?[Rv(e,r)].concat((0,x.Z)(n)):n}),[]);return"radio"===t.type?o[0]:o}n.stopPropagation()},Hv.val=function(n){return n.stopPropagation(),!!n.target.checked};var Zv=function(n){(0,h.Z)(i,n);var e,t,r=(e=i,t=function(){if("undefined"==typeof Reflect||!Reflect.construct)return!1;if(Reflect.construct.sham)return!1;if("function"==typeof Proxy)return!0;try{return Boolean.prototype.valueOf.call(Reflect.construct(Boolean,[],(function(){}))),!0}catch(n){return!1}}(),function(){var n,r=(0,m.Z)(e);if(t){var o=(0,m.Z)(this).constructor;n=Reflect.construct(r,arguments,o)}else n=r.apply(this,arguments);return(0,f.Z)(this,n)});function i(){return(0,c.Z)(this,i),r.apply(this,arguments)}return(0,s.Z)(i,[{key:"shouldComponentUpdate",value:function(n){n.children,n.onChange,n.style;var e=(0,p.Z)(n,Iv);return function(n,e){for(var t in n)if(!(t in e))return!0;for(var r in e)if(n[r]!==e[r])return!0;return!1}((0,y.omit)(this.props,["children","onChange","style"]),e)}},{key:"render",value:function(){var n=this.props.component;this.component=n||function(n){var e=n.schema,t=n.type,r=n.multiple;return"boolean"===(null==e?void 0:e.type)&&"slider"===(null==e?void 0:e.description)?Hv:e&&(e.enum||e.items||Array.isArray(e))?r||"array"===e.type?"checkbox"===t?Fv:Gv:"radio"===t?Fv:Gv:"checkbox"===t||e&&"boolean"===e.type?zv:"textarea"===t?Vv:_v}(this.props),this.ctrl=function(n,e){var t=e.schema,r=e.multiple,o=e.onChange;return t&&(t.enum||t.items||Array.isArray(t))&&"string"!==t.type?r||"array"===t.type?function(n,e,t){return{multiple:!0,selected:function(n,e){return e&&e.indexOf(n)>=0},onSelect:function(r,o){if(n.val){var i=n.val(r,e);void 0!==i&&t(i)}else{var a=o?o.indexOf(r):-1;t(a<0?o?[r].concat((0,x.Z)(o)):[r]:[].concat((0,x.Z)(o.slice(0,a)),(0,x.Z)(o.slice(a+1))))}}}}(n,t,o):function(n,e,t){return{selected:function(n,e){return e===n},onSelect:function(r){var o=n.val?n.val(r,e):r;void 0!==o&&t(o)}}}(n,t,o):function(n,e,t){var r={};return e&&("number"!==e.type&&"integer"!==e.type||(r={type:"text"})),Lv({onChange:function(r){var o=n.val?n.val(r,e):r;t(o)}},r)}(n,t,o)}(this.component,this.props);var e=this.props;e.children,e.onChange;var t=(0,p.Z)(e,Tv),r=this.component;return(0,o.jsx)(r,Lv(Lv({},this.ctrl),t))}}]),i}(d.Component),Kv=function(n){var e=n.className;return(0,o.jsx)(Au,{name:"chevron",className:(0,v.Z)(e,$m.chevronIcon)})},Yv=function(n){var e,t=n.className,r=n.value,i=n.onChange,a=n.multiple,l=void 0!==a&&a,c=n.disabled,s=n.options,u=(0,d.useState)(),p=(0,O.Z)(u,2),h=p[0],f=p[1];return(0,d.useEffect)((function(){var n;return s&&(n=s.find((function(n){return n.value===r}))),f(n)}),[s,r]),(0,o.jsx)(Y.Z,{className:(0,v.Z)($m.selectContainer,t),value:null!==(e=null==h?void 0:h.value)&&void 0!==e?e:"",onChange:function(n){i(n.target.value)},multiple:l,disabled:c,MenuProps:{className:$m.dropdownList},IconComponent:Kv,children:s&&s.map((function(n){return(0,o.jsx)(U.Z,{value:n.value,disableRipple:!0,children:n.label},n.value)}))})},Uv="form-module_dataError__IXK1h",Jv="form-module_inputWrapper__sIDHH",qv=["schema","result","customValid"],Wv=["labelPos","title","children"],Xv=["name","onChange","component","labelPos","className"],Qv=["dataError"],ng=["title","name","schema"];function eg(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function tg(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?eg(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):eg(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var rg=function(n){(0,h.Z)(a,n);var e,t,i=(e=a,t=function(){if("undefined"==typeof Reflect||!Reflect.construct)return!1;if(Reflect.construct.sham)return!1;if("function"==typeof Proxy)return!0;try{return Boolean.prototype.valueOf.call(Reflect.construct(Boolean,[],(function(){}))),!0}catch(n){return!1}}(),function(){var n,r=(0,m.Z)(e);if(t){var o=(0,m.Z)(this).constructor;n=Reflect.construct(r,arguments,o)}else n=r.apply(this,arguments);return(0,f.Z)(this,n)});function a(n){var e;(0,c.Z)(this,a);var t=(e=i.call(this,n)).props,r=t.onUpdate,o=t.schema,l=t.init;if(e.schema=cg(o,n),l){var s=e.schema.serialize(l),u=s.valid,d=ug(s.errors);r(tg(tg({},l),{},{init:!0}),u,d)}return e}return(0,s.Z)(a,[{key:"componentDidUpdate",value:function(n){var e=this.props,t=e.schema,r=e.result;e.customValid;var o=(0,p.Z)(e,qv);t.key&&t.key!==n.schema.key&&(this.schema=cg(t,o),this.schema.serialize(r),this.updateState(r))}},{key:"updateState",value:function(n){var e=this.props.onUpdate,t=this.schema.serialize(n);e(t.instance,t.valid,ug(t.errors))}},{key:"field",value:function(n,e){var t=this,o=this.props,i=o.result,a=o.errors,l=i[n];return{dataError:a&&a[n],value:l,onChange:function(o){var i=Object.assign({},t.props.result,(0,r.Z)({},n,o));t.updateState(i),e&&e(o)}}}},{key:"render",value:function(){var n=this.props,e=n.schema,t=n.children;return(0,o.jsx)("form",{children:(0,o.jsx)(gn.Provider,{value:{schema:e,stateStore:this},children:t})})}}]),a}(d.Component),og=(0,S.$j)(null,(function(n){return{onUpdate:function(e,t,r){n(ue({result:e,valid:t,errors:r}))}}}))(rg);function ig(n){var e=n.labelPos,t=n.title,r=n.children,i=(0,p.Z)(n,Wv);return(0,o.jsxs)("label",tg(tg({},i),{},{children:[t&&"after"!==e?(0,o.jsx)("span",{children:t}):"",r,t&&"after"===e?(0,o.jsx)("span",{children:t}):""]}))}function ag(n){var e=n.name,t=n.onChange,i=n.component,a=n.labelPos,l=n.className,c=(0,p.Z)(n,Xv),s=(0,d.useState)(null),u=(0,O.Z)(s,2),h=u[0],f=u[1],m=(0,d.useCallback)((function(n){f(n.currentTarget)}),[]),g=(0,d.useCallback)((function(){f(null)}),[]),b=ap(),C=b.schema,y=b.stateStore,w=c.schema||C.properties[e],S=y.field(e,t),M=S.dataError,x=(0,p.Z)(S,Qv),j=i,E=i?(0,o.jsx)(j,tg(tg({name:e,schema:w},x),c)):(0,o.jsx)(Zv,tg(tg({name:e,schema:w},x),c));return!1===a?E:(0,o.jsxs)(ig,{className:(0,v.Z)((0,r.Z)({},Uv,M),l),error:M,title:c.title||w.title,labelPos:a,children:[(0,o.jsx)("span",{className:Jv,onMouseEnter:m,onMouseLeave:g,children:E}),M&&h&&(0,o.jsx)(Ev,{anchorEl:h,open:!!h,error:M,onClose:g})]})}var lg=function(n){var e=n.title,t=n.name,r=n.schema,i=(0,p.Z)(n,ng),a={title:e,enum:[],enumNames:[]};return Object.keys(r).forEach((function(n){a.enum.push(n),a.enumNames.push(r[n].title||n)})),(0,o.jsx)(ag,tg(tg({name:t,options:jd(a),title:e},i),{},{component:Yv}))};function cg(n,e){var t=e.customValid,r=e.serialize,o=void 0===r?{}:r,i=(e.deserialize,new(C())({allErrors:!0,verbose:!0,strictSchema:!1}));t&&((n=Object.assign({},n)).properties=Object.keys(t).reduce((function(n,e){return i.addFormat(t[e].name,t[e]),n[e]=tg({format:e},n[e]),n}),n.properties));var a=i.compile(n);return{key:n.key||"",serialize:function(e){return a(e),{instance:sg(o,e,n),valid:a(e),errors:a.errors||[]}},deserialize:function(n){return a(n),n}}}function sg(n,e,t){var r={};return"object"===(0,g.Z)(e)&&t.properties?(Object.keys(t.properties).forEach((function(t){t in e&&(r[t]=e[n[t]]||e[t])})),r):void 0!==e?e:t.default}function ug(n){var e,t={};return n.forEach((function(n){e=n.instancePath.slice(1),t[e]||(t[e]=function(n){return n.parentSchema.invalidMessage?"function"==typeof n.parentSchema.invalidMessage?n.parentSchema.invalidMessage(n.data):n.parentSchema.invalidMessage:n.message}(n))})),t}var dg={colorPickerInput:"ColorPicker-module_colorPickerInput__voi2r",selectedInput:"ColorPicker-module_selectedInput__Ykcjd",colorPickerWrap:"ColorPicker-module_colorPickerWrap__IAQVo",withPalette:"ColorPicker-module_withPalette__gTwNu",colorPicker:"ColorPicker-module_colorPicker__Uz3PM",colorPickerBtn:"ColorPicker-module_colorPickerBtn__nr6ph",colorPickerPreview:"ColorPicker-module_colorPickerPreview__-Rf-i",colorPickerOverlay:"ColorPicker-module_colorPickerOverlay__WzC-w",colorContainer:"ColorPicker-module_colorContainer__ib5up",hex:"ColorPicker-module_hex__mE9my",presetColors:"ColorPicker-module_presetColors__J-ysq",chooseColor:"ColorPicker-module_chooseColor__fdzt8",clicked:"ColorPicker-module_clicked__8BNoN",expandIcon:"ColorPicker-module_expandIcon__oH4ka",turnedIcon:"ColorPicker-module_turnedIcon__-zaq-",colorPickerWrapper:"ColorPicker-module_colorPickerWrapper__GJm87"},pg=["#FF4545","#FFAD31","#68D442","#3ACACC","#4434FF","#9C9C9C","#000000"],hg=function(n){var e,t,i=(0,d.useState)(!1),a=(0,O.Z)(i,2),l=a[0],c=a[1],s=(0,d.useState)(!1),u=(0,O.Z)(s,2),p=u[0],h=u[1],f=n.onChange,m=n.value,g=(0,d.useCallback)((function(n){f(n)}),[f]),b=(0,d.useCallback)((function(n,e){var t;return function(r){t||(n(r),t=!0,setTimeout((function(){return t=!1}),e))}}),[]),C=(0,d.useCallback)(b((function(n){n.preventDefault(),c((function(n){return!n})),h(!1)}),200),[]);return(0,o.jsxs)("div",{className:dg.colorPickerWrapper,"data-testid":"color-picker-field",onClick:function(n){return n.preventDefault()},children:[(0,o.jsxs)("div",{className:(0,v.Z)((e={},(0,r.Z)(e,dg.colorPickerInput,!0),(0,r.Z)(e,dg.selectedInput,l),e)),onClick:C,children:[(0,o.jsx)("div",{className:dg.colorPickerPreview,"data-testid":"color-picker-preview",style:{backgroundColor:m}}),(0,o.jsx)(Au,{className:(0,v.Z)((t={},(0,r.Z)(t,dg.expandIcon,!0),(0,r.Z)(t,dg.turnedIcon,!l),t)),name:"chevron"})]}),l&&(0,o.jsxs)("div",{className:(0,v.Z)(dg.colorPickerWrap,p&&dg.withPalette),onBlur:function(n){n.currentTarget.contains(n.relatedTarget)||C(n)},"data-testid":"color-picker-preset",children:[(0,o.jsxs)("div",{className:dg.presetColors,children:[(0,o.jsx)("button",{className:(0,v.Z)(dg.chooseColor,p&&dg.clicked),onClick:function(){h(!0)},autoFocus:!0,"data-testid":"color-picker-btn"}),pg.map((function(n){return(0,o.jsx)("button",{onClick:function(){return function(n){g(n)}(n)},style:{backgroundColor:n},className:dg.presetColor},n)}))]}),p&&(0,o.jsxs)("div",{className:dg.colorPicker,children:[(0,o.jsx)(J.gW,{color:m,onChange:g}),(0,o.jsxs)("div",{className:dg.colorContainer,children:[(0,o.jsx)("span",{className:dg.hex,children:"HEX"}),(0,o.jsx)(J.ZE,{"data-testid":"color-picker-input",color:m,onChange:g})]})]})]})]})},fg=["schema","value","onChange","name"];function mg(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function vg(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?mg(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):mg(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var gg=jd({enum:["cm","px","pt","inch"]}),bg=function(n){var e=n.schema,t=n.value,r=n.onChange,i=n.name,a=(0,p.Z)(n,fg),l=(0,d.useState)("px"),c=(0,O.Z)(l,2),s=c[0],u=c[1],h=(0,d.useState)(t||e.default),f=(0,O.Z)(h,2),m=f[0],v=f[1];(0,d.useEffect)((function(){"px"===s&&(null==m?void 0:m.toFixed())-0!==t&&(u("px"),v(t))}),[]);var g=function(){var n=yg(t,"px",s);v(n)};(0,d.useEffect)((function(){g()}),[t,s,g]);var b=e||e.properties[i];return(0,o.jsxs)("div",vg(vg({className:"measure-input-module_measureInput__uZQ-j"},a),{},{children:[(0,o.jsx)("span",{children:a.title||b.title}),(0,o.jsxs)("div",{style:{display:"flex"},children:[(0,o.jsx)(Zv,{schema:e,step:"px"===s||"pt"===s?"1":"0.001",value:m,onChange:function(n){var e=yg(n,s,"px");v(n),r(e)}}),(0,o.jsx)(Yv,{onChange:function(n){v((function(e){yg(e,s,n)})),u(n)},options:gg,value:s,className:"measure-input-module_select__1ZFmv"})]})]}))},Cg={px:1,cm:37.795278,pt:1.333333,inch:96};function yg(n,e,t){return!n&&0!==n||isNaN(n)?null:"px"===t||"pt"===t?(n*Cg[e]/Cg[t]).toFixed()-0:(n*Cg[e]/Cg[t]).toFixed(3)-0}var Og=["children","type","server","className"];function wg(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Sg(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?wg(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):wg(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Mg=function(n){(0,h.Z)(i,n);var e,t,r=(e=i,t=function(){if("undefined"==typeof Reflect||!Reflect.construct)return!1;if(Reflect.construct.sham)return!1;if("function"==typeof Proxy)return!0;try{return Boolean.prototype.valueOf.call(Reflect.construct(Boolean,[],(function(){}))),!0}catch(n){return!1}}(),function(){var n,r=(0,m.Z)(e);if(t){var o=(0,m.Z)(this).constructor;n=Reflect.construct(r,arguments,o)}else n=r.apply(this,arguments);return(0,f.Z)(this,n)});function i(n){var e;return(0,c.Z)(this,i),(e=r.call(this,n)).state={},n.server&&yd(n.server).then((function(n){e.setState({opener:n})})),e}return(0,s.Z)(i,[{key:"open",value:function(n){var e=n.target.files,t=function(){return null},r=this.props,o=r.onLoad,i=void 0===o?t:o,a=r.onError,l=void 0===a?t:a;this.state.opener&&e.length?this.state.opener(e[0]).then(i,l):e.length&&i(e[0]),n.target.value=null,n.preventDefault()}},{key:"render",value:function(){var n=this,e=this.props,t=e.children,r=e.type;e.server;var i=e.className,a=(0,p.Z)(e,Og);return(0,o.jsxs)("button",Sg(Sg({onClick:function(){return n.btn.click()},className:(0,v.Z)("buttons-module_openButton__wErm9",i)},a),{},{children:[(0,o.jsx)("input",{onChange:function(e){return n.open(e)},accept:r,type:"file",ref:function(e){n.btn=e}}),t]}))}}]),i}(d.Component);function xg(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function jg(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?xg(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):xg(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Eg=function(n){var e=function(){return null},t=n.server,r=n.filename,i=void 0===r?"unnamed":r,a=n.outputFormat,l=n.data,c=n.type,s=n.mode,u=void 0===s?"saveFile":s,d=n.onSave,p=void 0===d?e:d,h=n.onError,f=void 0===h?e:h,m=n.className,v=lp().getKetcherInstance;return(0,o.jsx)("button",jg(jg({className:m,onClick:function(n){!function(n){n.preventDefault(),"saveImage"===u?v().generateImage(l,{outputFormat:a}).then((function(n){(0,q.saveAs)(n,"".concat(i,".").concat(a)),p()})).catch((function(n){f(n)})):function(){if(l)try{Dg(t).then((function(n){n(l,i,c),p()}))}catch(n){f(n)}}()}(n)}},n),{},{children:n.children}))},Dg=function(n){return new Promise((function(e,r){t.g.Blob&&q.saveAs?e((function(n,e,t){var r=new Blob([n],{type:t});(0,q.saveAs)(r,e)})):n?e(n.then((function(){throw Error("Server doesn't still support echo method")}))):r(new Error("Your browser does not support opening files locally"))}))},Ag=function(n){var e=n.tabs,t=n.className,i=n.changedGroups,a=(0,d.useState)(["General"]),l=(0,O.Z)(a,2),c=l[0],s=l[1];return(0,o.jsx)("div",{className:(0,v.Z)("Accordion-module_accordionWrapper__RKk00",t),children:e.map((function(n){var e,t,a,l=n.label,u=n.content,d=n.key,p=c.includes(l);return(0,o.jsxs)("div",{children:[(0,o.jsx)("div",{onClick:(a=l,function(){var n=!c.includes(a);s(n?[].concat((0,x.Z)(c),[a]):(0,x.Z)(c).filter((function(n){return n!==a})))}),className:"Accordion-module_accordionSummaryWrapper__roIRd",children:(0,o.jsxs)("div",{className:"Accordion-module_accordionSummary__1Gq0d",children:[(0,o.jsx)(Au,{className:(0,v.Z)((e={},(0,r.Z)(e,"Accordion-module_expandIcon__ncUKv",!0),(0,r.Z)(e,"Accordion-module_turnedIcon__v1sCA",!p),e)),name:"chevron"}),(0,o.jsxs)("div",{className:"Accordion-module_groupLabel__23y4U",children:[(0,o.jsx)(Au,{name:"elements-group",className:"Accordion-module_groupIcon__1g1lx"}),(0,o.jsx)("span",{children:l})]}),i.has(l)&&(0,o.jsx)("span",{className:"Accordion-module_changeMarker__UPtGx"})]})}),(0,o.jsx)("div",{className:(0,v.Z)((t={},(0,r.Z)(t,"Accordion-module_accordionDetailsWrapper__fnSnc",!0),(0,r.Z)(t,"Accordion-module_hiddenAccordion__WZFcJ",!p),t)),children:(0,o.jsx)("div",{className:"Accordion-module_accordionDetails__g2RM0",children:u})})]},d)}))})},$g=["Arial","Arial Black","Comic Sans MS","Courier New","Georgia","Impact","Charcoal","Lucida Console","Monaco","Palatino Linotype","Book Antiqua","Palatino","Tahoma","Geneva","Times New Roman","Times","Verdana","Symbol","MS Serif","MS Sans Serif","New York","Droid Sans","Droid Serif","Droid Sans Mono","Roboto"];function Ng(n){var e=(0,d.useState)(null),t=(0,O.Z)(e,2),r=t[0],i=t[1],a=n.value,l=n.onChange,c=(0,d.useCallback)((function(n){l(n)}),[l]);return(0,d.useEffect)((function(){var n,e=!0;return(n=$g.map((function(n){return new(X())(n).check().then((function(){return n}),(function(){return null}))})),Promise.all(n)).then((function(n){var t=n.filter((function(n){return null!==n})).map((function(n){return{value:"30px ".concat(n),label:n}}));e&&i(t)})),function(){return e=!1}}),[]),(0,o.jsx)(Yv,{onChange:c,value:a,disabled:null===r,options:r})}var Pg={headerContent:"Settings-module_headerContent__wBYFf",title:"Settings-module_title__a6mod",button:"Settings-module_button__VZ2w7",accordion:"Settings-module_accordion__1uSYy",settings:"Settings-module_settings__Z5btc"},kg={resetToSelect:"General",rotationStep:"General",showValenceWarnings:"General",atomColoring:"General",font:"General",fontsz:"General",fontszsub:"General",showStereoFlags:"Stereochemistry",stereoLabelStyle:"Stereochemistry",colorOfAbsoluteCenters:"Stereochemistry",colorOfAndCenters:"Stereochemistry",colorOfOrCenters:"Stereochemistry",colorStereogenicCenters:"Stereochemistry",autoFadeOfStereoLabels:"Stereochemistry",absFlagLabel:"Stereochemistry",andFlagLabel:"Stereochemistry",orFlagLabel:"Stereochemistry",mixedFlagLabel:"Stereochemistry",carbonExplicitly:"Atoms",showCharge:"Atoms",showValence:"Atoms",showHydrogenLabels:"Atoms",aromaticCircle:"Bonds",doubleBondWidth:"Bonds",bondThickness:"Bonds",stereoBondWidth:"Bonds","smart-layout":"Server","ignore-stereochemistry-errors":"Server","mass-skip-error-on-pseudoatoms":"Server","gross-formula-add-rsites":"Server","gross-formula-add-isotopes":"Server",miewMode:"3D Viewer",miewTheme:"3D Viewer",miewAtomLabel:"3D Viewer",showAtomIds:"Options for Debugging",showBondIds:"Options for Debugging",showHalfBondIds:"Options for Debugging",showLoopIds:"Options for Debugging"},Ig=["initState","formState","server","onOpenFile","onReset","appOpts"];function Tg(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Bg(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Tg(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Tg(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Lg=Vn(),_g=function(n){var e=n.server,t=n.onOpenFile,r=n.onReset,i=n.formState,a=n.initState;return(0,o.jsxs)("div",{className:Pg.headerContent,children:[(0,o.jsx)("span",{className:Pg.title,children:" Settings"}),(0,o.jsx)(Mg,{title:"Open from File",server:e,onLoad:t,className:Pg.button,children:(0,o.jsx)(Au,{name:"open-1"})},"settings"),(0,o.jsx)(Eg,{title:"Save to File",data:JSON.stringify(i.result),filename:"ketcher-settings",className:Pg.button,children:(0,o.jsx)(Au,{name:"save-1"})},"ketcher-settings"),(0,o.jsx)("button",{title:"Reset",onClick:r,className:Pg.button,disabled:i.result.init?(0,E.isEqual)(Lg,a):(0,E.isEqual)(Lg,i.result),children:(0,o.jsx)(Au,{name:"reset"})},"settings-button")]})},Vg=_n.properties,zg=(0,S.$j)((function(n){return{server:n.options.app.server?n.server:null,appOpts:n.options.app,initState:n.options.settings,formState:n.modal.form}}),(function(n,e){return{onOpenFile:function(e){try{n(ue({result:JSON.parse(e)}))}catch(n){}},onReset:function(){return n({type:"UPDATE_FORM",data:{result:Vn(),valid:!0,errors:{}}})},onOk:function(t){var r;n((r=t,zn.setItem("ketcher-opts",r),{type:"SAVE_SETTINGS",data:r})),e.onOk(t)}}}))((function(n){var e=n.initState,t=n.formState,r=n.server,i=n.onOpenFile,a=n.onReset,l=n.appOpts,c=(0,p.Z)(n,Ig),s=(0,d.useState)(new Set),u=(0,O.Z)(s,2),h=u[0],f=u[1];(0,d.useEffect)((function(){var n=new Set;for(var r in e)if(e[r]!==t.result[r]){var o=kg[r];n.add(o)}f(n)}),[e,t.result]);var m=[{key:"general",label:"General",content:(0,o.jsxs)("fieldset",{children:[(0,o.jsx)(ag,{name:"resetToSelect",component:Yv,options:jd(null==Vg?void 0:Vg.resetToSelect)}),(0,o.jsx)(ag,{name:"rotationStep"}),(0,o.jsx)(ag,{name:"showValenceWarnings"}),(0,o.jsx)(ag,{name:"atomColoring"}),(0,o.jsx)(ag,{name:"font",component:Ng}),(0,o.jsx)(ag,{name:"fontsz",component:bg,labelPos:!1}),(0,o.jsx)(ag,{name:"fontszsub",component:bg,labelPos:!1})]})},{key:"stereo",label:"Stereochemistry",content:(0,o.jsxs)("fieldset",{children:[(0,o.jsx)(ag,{name:"showStereoFlags"}),(0,o.jsx)(ag,{name:"stereoLabelStyle",component:Yv,options:jd(null==Vg?void 0:Vg.stereoLabelStyle)}),(0,o.jsx)(ag,{name:"colorOfAbsoluteCenters",component:hg}),(0,o.jsx)(ag,{name:"colorOfAndCenters",component:hg}),(0,o.jsx)(ag,{name:"colorOfOrCenters",component:hg}),(0,o.jsx)(ag,{name:"colorStereogenicCenters",component:Yv,options:jd(null==Vg?void 0:Vg.colorStereogenicCenters)}),(0,o.jsx)(ag,{name:"autoFadeOfStereoLabels"}),(0,o.jsx)(ag,{name:"absFlagLabel"}),(0,o.jsx)(ag,{name:"andFlagLabel"}),(0,o.jsx)(ag,{name:"orFlagLabel"}),(0,o.jsx)(ag,{name:"mixedFlagLabel"})]})},{key:"atoms",label:"Atoms",content:(0,o.jsxs)("fieldset",{children:[(0,o.jsx)(ag,{name:"carbonExplicitly"}),(0,o.jsx)(ag,{name:"showCharge"}),(0,o.jsx)(ag,{name:"showValence"}),(0,o.jsx)(ag,{name:"showHydrogenLabels",component:Yv,options:jd(null==Vg?void 0:Vg.showHydrogenLabels)})]})},{key:"bonds",label:"Bonds",content:(0,o.jsxs)("fieldset",{children:[(0,o.jsx)(ag,{name:"aromaticCircle"}),(0,o.jsx)(ag,{name:"doubleBondWidth",component:bg,labelPos:!1}),(0,o.jsx)(ag,{name:"bondThickness",component:bg,labelPos:!1}),(0,o.jsx)(ag,{name:"stereoBondWidth",component:bg,labelPos:!1})]})},{key:"server",label:"Server",content:(0,o.jsxs)("fieldset",{disabled:!l.server,children:[(0,o.jsx)(ag,{name:"smart-layout"}),(0,o.jsx)(ag,{name:"ignore-stereochemistry-errors"}),(0,o.jsx)(ag,{name:"mass-skip-error-on-pseudoatoms"}),(0,o.jsx)(ag,{name:"gross-formula-add-rsites"}),(0,o.jsx)(ag,{name:"gross-formula-add-isotopes"})]})},{key:"3dviewer",label:"3D Viewer",content:(0,o.jsxs)("fieldset",{className:Pg.viewer,children:[(0,o.jsx)(ag,{name:"miewMode",component:Yv,options:jd(null==Vg?void 0:Vg.miewMode)}),(0,o.jsx)(ag,{name:"miewTheme",component:Yv,options:jd(null==Vg?void 0:Vg.miewTheme)}),(0,o.jsx)(ag,{name:"miewAtomLabel",component:Yv,options:jd(null==Vg?void 0:Vg.miewAtomLabel)})]})},{key:"debugging",label:"Options for Debugging",content:(0,o.jsxs)("fieldset",{children:[(0,o.jsx)(ag,{name:"showAtomIds"}),(0,o.jsx)(ag,{name:"showBondIds"}),(0,o.jsx)(ag,{name:"showHalfBondIds"}),(0,o.jsx)(ag,{name:"showLoopIds"})]})}];return(0,o.jsx)(Tm,{className:Pg.settings,result:function(){return t.result},valid:function(){return t.valid},params:c,buttonsNameMap:{OK:"Apply"},buttons:["Cancel","OK"],withDivider:!0,needMargin:!1,headerContent:(0,o.jsx)(_g,{server:r,onOpenFile:i,onReset:a,formState:t,initState:e}),children:(0,o.jsx)(og,Bg(Bg({schema:_n,init:e},t),{},{children:(0,o.jsx)(Ag,{tabs:m,className:Pg.accordion,changedGroups:h})}))})}));function Gg(n){var e=n.moleculeErrors,t=n.checkSchema,r=Object.keys(e);return(0,o.jsx)(o.Fragment,{children:(0,o.jsx)("fieldset",{children:0===r.length?(0,o.jsx)("div",{children:(0,o.jsx)("dd",{children:"No errors detected"})}):r.map((function(n,r){return(0,o.jsxs)("div",{children:[(0,o.jsxs)("dt",{children:[(i=n,a=t.properties.checkOptions.items,l=a.enum.indexOf(i),a.enumNames[l])," warning:"]}),(0,o.jsx)("dd",{children:e[n]})]},r);var i,a,l}))})})}var Fg="Check-module_buttonSecondary__2482r",Hg="Check-module_buttonPrimary__1h5p1",Rg="Check-module_centeredContainer__t61r8",Zg=["formState","checkState","onCheck","onApply","onCancel"];function Kg(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Yg(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Kg(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Kg(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Ug={title:"Check",type:"object",properties:{checkOptions:{title:"Settings",type:"array",items:{type:"string",enum:["valence","radicals","pseudoatoms","stereo","query","overlapping_atoms","overlapping_bonds","rgroups","chiral","3d","chiral_flag"],enumNames:["Valence","Radical","Pseudoatom","Stereochemistry","Query","Overlapping Atoms","Overlapping Bonds","R-Groups","Chirality","3D Structure","Chiral flag"]}}}},Jg=function(n){var e=n.handleCheck,t=n.handleApply,r=n.onCancel,i=n.isStuctureChecking,a=n.isCheckedWithNewSettings;return(0,o.jsxs)("div",{className:"Check-module_buttons__cjuqO",children:[(0,o.jsx)("div",{children:(0,o.jsx)("button",{className:a?Fg:Hg,onClick:e,disabled:!i,children:"Check"})}),(0,o.jsxs)("div",{className:"Check-module_buttonsRight__L1v9A",children:[(0,o.jsx)("button",{className:Fg,onClick:r,children:"Cancel"}),(0,o.jsx)("button",{className:Hg,onClick:t,disabled:!i,children:"Apply"})]})]})},qg=(0,S.$j)((function(n){return{formState:n.modal.form,checkState:n.options.check}}),(function(n,e){return{onCheck:function(t){return n(We(t)).catch(e.onCancel)},onApply:function(t){n({type:"SAVE_CHECK_OPTS",data:t}),e.onOk(t)}}}))((function(n){var e,t,r=n.formState,i=n.checkState,a=n.onCheck,l=n.onApply,c=n.onCancel,s=(0,p.Z)(n,Zg),u=r.result,h=void 0===u?i:u,f=r.moleculeErrors,m=(0,d.useState)(!1),v=(0,O.Z)(m,2),g=v[0],b=v[1],C=(0,d.useState)(null),y=(0,O.Z)(C,2),w=y[0],S=y[1],M=(0,d.useState)(!1),x=(0,O.Z)(M,2),j=x[0],E=x[1],D=function(){b(!1),a(h.checkOptions).then((function(){b(!0),S(new Date),E(!0)}))};return(0,d.useEffect)((function(){D()}),[]),(0,o.jsx)(Tm,{title:"Structure Check",className:"Check-module_dialog_body__wHZMM",params:Yg(Yg({},s),{},{onCancel:c}),buttons:[],footerContent:(0,o.jsx)(Jg,{handleCheck:D,handleApply:function(){return l(h)},onCancel:c,isStuctureChecking:g,isCheckedWithNewSettings:j}),withDivider:!0,children:(0,o.jsx)(og,Yg(Yg({schema:Ug,init:i},r),{},{result:h,children:(0,o.jsxs)("div",{className:"Check-module_wrapper__27SOp",children:[(0,o.jsxs)("div",{className:"Check-module_settings__knuQF",children:[(0,o.jsx)("label",{children:"Settings"}),(0,o.jsx)("div",{className:g?"":"Check-module_checkBoxesDisabled__EAdRo",children:(0,o.jsx)(ag,{name:"checkOptions",labelPos:!1,multiple:!0,type:"checkbox",disabled:!g,onChange:function(){return E(!1)}})})]}),(0,o.jsxs)("div",{className:"Check-module_checkInfo__Iqq6t",children:[(0,o.jsxs)("span",{children:["Last check:"," ",w&&(e=w,t=function(n){return(n+"").padStart(2,0)},"".concat(t(e.getHours()),":").concat(t(e.getMinutes()),":").concat(t(e.getSeconds()),"  ").concat(t(e.getDate()),".").concat(t(e.getMonth()+1),".").concat(t(e.getFullYear())))]}),(0,o.jsx)("div",{className:Object.keys(f).length&&g?"Check-module_warnings__b4ozd":Rg,children:g?(0,o.jsx)("div",{className:Object.keys(f).length?"Check-module_warningsContainer__vSbyK":Rg,children:(0,o.jsx)(Gg,{moleculeErrors:f,checkSchema:Ug})}):(0,o.jsx)(Bm,{})})]})]})}))})})),Wg={"button-common-styles":"FormulaInput-module_button-common-styles__xQ8ZA",scrollbar:"FormulaInput-module_scrollbar__8TUkb",chem_input:"FormulaInput-module_chem_input__oprB3"},Xg=/\b(\d*)([A-Z][a-z]{0,3}#?)(\d*)\s*\b/g,Qg=/error:.*/g;function nb(n){var e=n.content,t=n.contentEditable;return(0,o.jsx)("div",{className:Wg.chem_input,onKeyPress:function(n){return n.preventDefault()},onPaste:function(n){return n.preventDefault()},onKeyDown:function(n){if(8===n.keyCode)return n.preventDefault(),!1},contentEditable:t,suppressContentEditableWarning:!0,children:e})}function eb(n){var e=n.value,t=n.contentEditable;if(Qg.test(e))return nb(e);for(var r,i=[],a=0;null!==(r=Xg.exec(e));)r[1].length>0&&i.push((0,o.jsx)("sup",{children:r[1]},i.length)),i.push(e.substring(a,r.index)+r[2]),r[3].length>0&&i.push((0,o.jsx)("sub",{children:r[3]},i.length)),a=r.index+r[0].length;return 0===a?i.push(e):i.push(e.substring(a,e.length)),nb({content:i,contentEditable:t})}function tb(n){var e=n.value;return(0,o.jsx)("input",{type:"text",spellCheck:!1,value:e,readOnly:!0,onChange:function(n){return n.preventDefault()}})}var rb=["values","round","loading","onAnalyse","onChangeRound"];function ob(n,e){return"number"==typeof n?n.toFixed(e):n.replace(/[0-9]*\.[0-9]+/g,(function(n){return(+n).toFixed(e)}))}var ib=jd({enum:(0,y.range)(0,8)}),ab=function(n){(0,h.Z)(i,n);var e,t,r=(e=i,t=function(){if("undefined"==typeof Reflect||!Reflect.construct)return!1;if(Reflect.construct.sham)return!1;if("function"==typeof Proxy)return!0;try{return Boolean.prototype.valueOf.call(Reflect.construct(Boolean,[],(function(){}))),!0}catch(n){return!1}}(),function(){var n,r=(0,m.Z)(e);if(t){var o=(0,m.Z)(this).constructor;n=Reflect.construct(r,arguments,o)}else n=r.apply(this,arguments);return(0,f.Z)(this,n)});function i(){return(0,c.Z)(this,i),r.apply(this,arguments)}return(0,s.Z)(i,[{key:"componentDidMount",value:function(){this.props.onAnalyse()}},{key:"render",value:function(){var n=this.props,e=n.values,t=n.round,r=n.loading;n.onAnalyse;var i=n.onChangeRound,a=(0,p.Z)(n,rb);return(0,o.jsx)(Tm,{title:"Calculated Values",className:"Analyse-module_analyse__MR-Tu",withDivider:!0,needMargin:!0,valid:function(){return!0},buttons:["OK"],buttonsNameMap:{OK:"Close"},params:a,children:(0,o.jsx)("ul",{children:[{name:"Chemical Formula",key:"gross",withSelector:!1},{name:"Molecular Weight",key:"molecular-weight",round:"roundWeight",withSelector:!0},{name:"Exact Mass",key:"monoisotopic-mass",round:"roundMass",withSelector:!0},{name:"Elemental Analysis",key:"mass-composition",round:"roundElAnalysis",withSelector:!1}].map((function(n){return(0,o.jsxs)("li",{className:"Analyse-module_contentWrapper__B4WCi",children:[(0,o.jsxs)("div",{className:"Analyse-module_inputWrapper__uR995",children:[(0,o.jsxs)("label",{children:[n.name,":"]}),"gross"===n.key?(0,o.jsx)(eb,{value:e&&!r?e[n.key]:"",contentEditable:!1}):"mass-composition"===n.key?(0,o.jsx)("textarea",{readOnly:!0,value:e&&!r?ob(e[n.key],t[n.round]):0}):(0,o.jsx)(tb,{value:e&&!r?ob(e[n.key],t[n.round]):0})]}),n.withSelector?(0,o.jsxs)("div",{className:"Analyse-module_selectWrapper__xEkKL",children:[(0,o.jsx)("span",{children:"Decimal places"}),(0,o.jsx)(Yv,{options:ib,value:t[n.round],onChange:function(e){return i(n.round,e)},className:"Analyse-module_select__c6hFt"})]}):null]},n.key)}))})})}}]),i}(d.Component);(0,r.Z)(ab,"contextType",mn);var lb=(0,S.$j)((function(n){return{values:n.options.analyse.values,loading:n.options.analyse.loading,round:{roundWeight:n.options.analyse.roundWeight,roundMass:n.options.analyse.roundMass,roundElAnalysis:n.options.analyse.roundElAnalysis}}}),(function(n){return{onAnalyse:function(){return n((function(n,e){n({type:"ANALYSE_LOADING"});var t=e(),r=t.editor,o=t.server,i=t.options.getServerSettings();return i.data={properties:["molecular-weight","most-abundant-mass","monoisotopic-mass","gross","mass-composition"]},Qe(r,o,"calculate",i).then((function(e){return n({type:"CHANGE_ANALYSE",data:{values:e}})})).catch((function(n){r.errorHandler(n)}))}))},onChangeRound:function(e,t){return n(function(n,e){return{type:"CHANGE_ANALYSE",data:(0,r.Z)({},n,e)}}(e,t))}}}))(ab),cb={"button-common-styles":"Recognize-module_button-common-styles__B04E6",scrollbar:"Recognize-module_scrollbar__rohcP",recognize:"Recognize-module_recognize__66jG2",footerContent:"Recognize-module_footerContent__0MAC7",imagoVersion:"Recognize-module_imagoVersion__nBIj6",openButton:"Recognize-module_openButton__H-j5I",imagesContainer:"Recognize-module_imagesContainer__rXWWk",topBody:"Recognize-module_topBody__ZCCjN",output:"Recognize-module_output__WgRnP",picture:"Recognize-module_picture__x2Y7S",filename:"Recognize-module_filename__-1HIU",messageContainer:"Recognize-module_messageContainer__tMvyb",primaryButton:"Recognize-module_primaryButton__rzm03",secondaryButton:"Recognize-module_secondaryButton__H1Q28",struct:"Recognize-module_struct__W55TL"},sb=function(n){var e=n.clickHandler,t=n.label,r=n.title,i=n.styles,a=n.disabled;return(0,o.jsx)("input",{type:"button",className:i,value:t,title:r||t,disabled:a,onClick:e},"Open")},ub=["file","structStr","fragment","version","imagoVersions","onOk"],db=["onRecognize","isFragment","onImage","onChangeImago"];function pb(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function hb(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?pb(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):pb(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function fb(n){var e;return null==n||null===(e=n.type)||void 0===e?void 0:e.includes("image")}function mb(n){var e=n.onImage,t=n.structStr,r=n.openHandler,i=n.copyHandler;return(0,o.jsxs)("div",{className:cb.footerContent,children:[(0,o.jsxs)(Mg,{onLoad:e,type:"image/*",className:cb.openButton,children:[(0,o.jsx)(Au,{name:"open"}),(0,o.jsx)("span",{children:"Change image"})]},"choose"),(0,o.jsxs)("div",{children:[(0,o.jsx)(sb,{disabled:!t,clickHandler:r,styles:cb.secondaryButton,label:"Open as new Project"},"openButton"),(0,o.jsx)(sb,{disabled:!t,clickHandler:i,styles:cb.primaryButton,label:"Add to Canvas",title:"Structure will be loaded as fragment and added to Clipboard"},"copyButton")]})]})}function vb(n){if(!n)return null;var e=window.URL||window.webkitURL;return e?e.createObjectURL(n):"No preview"}var gb=(0,S.$j)((function(n){return{imagoVersions:n.options.app.imagoVersions,file:n.options.recognize.file,structStr:n.options.recognize.structStr,fragment:n.options.recognize.fragment,version:n.options.recognize.version||n.options.app.imagoVersions[1]}}),(function(n){return{isFragment:function(e){return n({type:"IS_FRAGMENT_RECOGNIZE",data:{fragment:e}})},onImage:function(e){return n(Yn(e))},onRecognize:function(e,t){return n(function(n,e){return function(t,r){var o=r().server.recognize,i=r().editor,a=o(n,e).then((function(n){t(Kn(n.struct))}),(function(n){t(Kn(null)),i.errorHandler(n)}));t(Kn(a))}}(e,t))},onChangeImago:function(e){return n({type:"CHANGE_IMAGO_VERSION",data:{version:e}})},onOk:function(e){n(qe(e.structStr,{rescale:!0,fragment:e.fragment}))}}}))((function(n){var e=n.file,t=n.structStr,r=n.fragment,i=n.version,a=n.imagoVersions,l=n.onOk,c=(0,p.Z)(n,ub),s=c.onRecognize;c.isFragment;var u=c.onImage,h=c.onChangeImago,f=(0,p.Z)(c,db),m=(0,d.useState)(!0),v=(0,O.Z)(m,2),g=v[0],b=v[1];(0,d.useEffect)((function(){s(e,i)}),[e,i]);var C=(0,d.useCallback)((function(){return u(null),!0}),[u]);return(0,o.jsxs)(Tm,{title:"Import Structure from Image",className:cb.recognize,params:hb(hb({},f),{},{onOk:l}),result:function(){return!t||t instanceof Promise?null:{structStr:t,fragment:r}},withDivider:!0,needMargin:!1,footerContent:(0,o.jsx)(mb,{onImage:u,openHandler:function(){l({structStr:t,fragment:!1})},structStr:t,copyHandler:function(){l({structStr:t,fragment:!0})}}),buttons:[],children:[(0,o.jsxs)("div",{className:cb.topBody,children:[(0,o.jsxs)("label",{className:cb.imagoVersion,children:["Imago version",(0,o.jsx)(Zv,{schema:{enum:a,enumNames:(0,y.range)(1,a.length+1).map((function(n){return"Version ".concat(n)}))},value:i,onChange:h})]}),(0,o.jsx)("span",{children:"Original image"}),(0,o.jsx)("span",{children:"Recognized structure preview"})]}),(0,o.jsxs)("div",{className:cb.imagesContainer,children:[(0,o.jsxs)("div",{className:cb.picture,children:[e&&fb(e)&&g&&(0,o.jsx)("img",{alt:"",id:"pic",src:vb(e)||"",onError:function(){b(!1)}}),(0,o.jsxs)("span",{className:cb.filename,children:[" ",e?e.name:null," "]}),e&&fb(e)&&!g&&(0,o.jsx)("div",{className:cb.messageContainer,children:(0,o.jsxs)("p",{children:["Preview of '",e.type,"' MIME type is not supported by current browser"]})}),(!e||!fb(e)&&C())&&(0,o.jsx)("div",{className:cb.messageContainer,children:(0,o.jsx)("p",{children:"Please choose image"})})]}),(0,o.jsx)("div",{className:cb.output,children:t&&(t instanceof Promise||"string"!=typeof t?(0,o.jsx)("div",{className:cb.messageContainer,children:(0,o.jsx)(Bm,{})}):(0,o.jsx)(av,{className:cb.struct,struct:t}))})]})]})})),bb=["miewOpts","server","struct","onExportCML","miewTheme"],Cb={dark:"0x202020",light:"0xcccccc"},yb={no:null,bright:{colorer:"EL"},blackAndWhite:{colorer:["UN",{color:16777215}],bg:"0x000"},black:{colorer:["UN",{color:0}]}};var Ob=function(){return(0,o.jsx)("div",{className:"Miew-module_warning__IDl5F",children:"Stereocenters can be changed after the strong 3D rotation"})},wb=(0,S.$j)((function(n){return{miewOpts:(e=(0,y.pick)(Ln,n.options.settings),t={settings:{bg:{color:Number(Cb[e.miewTheme])},autoPreset:!1,editing:!0,inversePanning:!0},reps:[{mode:e.miewMode}]},r=function(n){var e=n.miewAtomLabel;return null===yb[e]?null:{colorer:yb[e].colorer,selector:"not elem C",mode:["TX",{bg:yb[e].bg||Cb[n.miewTheme],showBg:!0,template:"{{elem}}"}]}}(e),r&&t.reps.push(r),t),server:n.options.app.server?n.server:null,struct:n.editor.struct(),miewTheme:n.options.settings.miewTheme};var e,t,r}),(function(n){return{onExportCML:function(e){n(qe(e))}}}))((function(n){var e=n.miewOpts,t=n.server,r=n.struct,i=n.onExportCML,a=n.miewTheme,l=void 0===a?"light":a,c=(0,p.Z)(n,bb),s=(0,d.useRef)(),h=(0,d.useCallback)((function(n){s.current=n,new u.Yyn(t).create(u.D34.cml).getStructureFromStructAsync(r).then((function(e){return n.load(e,{sourceType:"immediate",fileType:"cml"})})).then((function(){return n.setOptions(e)})).catch((function(n){}))}),[e,t,r]),f=(0,d.useCallback)((function(){var n,e=null===(n=s.current)||void 0===n?void 0:n.exportCML();e&&i(e)}),[i,s]);return(0,o.jsx)(Tm,{title:"Miew",needMargin:!1,params:c,buttons:["Cancel",(0,o.jsx)("button",{onClick:f,className:"Miew-module_applyButton__ZDE-i",children:"Apply"},"apply")],footerContent:(0,o.jsx)(Ob,{}),className:"Miew-module_miewDialog__gHvYc",children:(0,o.jsx)("div",{children:(0,o.jsx)("div",{className:"".concat("Miew-module_miewContainer__2SNw3"," ").concat("dark"===l?"Miew-module_miewDarkTheme__kMFzc":""),children:(0,o.jsx)(Q.Z,{onInit:h})})})})})),Sb=function(n){var e,t=n.label,r=(null===(e=u.eKO.get((0,y.capitalize)(t)))||void 0===e?void 0:e.number)||"";return(0,o.jsxs)("label",{children:[(0,o.jsx)("span",{children:"Number"}),(0,o.jsx)("input",{type:"text",readOnly:!0,value:r})]})},Mb="Atom-module_checkbox__Vup40",xb=["formState","stereoParity"];function jb(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Eb(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?jb(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):jb(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Db=ye.properties,Ab=(0,S.$j)((function(n){return{formState:n.modal.form}}))((function(n){var e=n.formState;n.stereoParity;var t=(0,p.Z)(n,xb),i=(0,d.useState)(t.label),a=(0,O.Z)(i,2),l=a[0],c=a[1],s=(0,d.useState)(["General"]),h=(0,O.Z)(s,2),f=h[0],m=h[1],g=(0,d.useCallback)((function(n){c(n)}),[]),b=[{groupName:"General",component:(0,o.jsxs)("div",{children:[(0,o.jsx)(ag,{name:"label",onChange:g,autoFocus:!0}),(0,o.jsx)(Sb,{label:l}),(0,o.jsx)(ag,{name:"alias"}),(0,o.jsx)(ag,{name:"charge",maxLength:"5"}),(0,o.jsx)(ag,{name:"isotope"}),(0,o.jsx)(ag,{name:"explicitValence",component:Yv,options:jd(Db.explicitValence)}),(0,o.jsx)(ag,{name:"radical",component:Yv,options:jd(Db.radical)})]})},{groupName:"Query specific",component:(0,o.jsxs)("div",{className:"Atom-module_querySpecific__7XxMr",children:[(0,o.jsx)(ag,{name:"ringBondCount",component:Yv,options:jd(Db.ringBondCount)}),(0,o.jsx)(ag,{name:"hCount",component:Yv,options:jd(Db.hCount)}),(0,o.jsx)(ag,{name:"substitutionCount",component:Yv,options:jd(Db.substitutionCount)}),(0,o.jsx)(ag,{name:"unsaturatedAtom",labelPos:"before",className:Mb})]})},{groupName:"Reaction flags",component:(0,o.jsxs)("div",{className:"Atom-module_reactionFlags__gdNb1",children:[(0,o.jsx)(ag,{name:"invRet",component:Yv,options:jd(Db.invRet)}),(0,o.jsx)(ag,{name:"exactChangeFlag",labelPos:"before",className:Mb})]})}];return(0,o.jsx)(Tm,{title:"Atom Properties",className:"Atom-module_atomProps__pqBjY",result:function(){return e.result},valid:function(){return e.valid},params:t,buttonsNameMap:{OK:"Apply"},buttons:["Cancel","OK"],withDivider:!0,children:(0,o.jsx)(og,Eb(Eb({schema:ye,customValid:{label:function(n){return(e=n)&&!!u.eKO.get((0,y.capitalize)(e));var e},charge:function(n){return e=n,(t=new RegExp(ye.properties.charge.pattern).exec(e))&&(""===t[1]||""===t[3]);var e,t}},init:t},e),{},{children:(0,o.jsx)("div",{className:"Atom-module_accordionWrapper__MSuU7",children:b.map((function(n){var e,t,i,a=n.groupName,l=n.component,c=f.includes(a);return(0,o.jsxs)("div",{children:[(0,o.jsx)("div",{onClick:(i=a,function(){var n=!f.includes(i);m(n?[].concat((0,x.Z)(f),[i]):(0,x.Z)(f).filter((function(n){return n!==i})))}),className:"Atom-module_accordionSummaryWrapper__MGqsq",children:(0,o.jsxs)("div",{className:"Atom-module_accordionSummary__HMKzl",children:[(0,o.jsx)("span",{children:a}),(0,o.jsx)(Au,{className:(0,v.Z)((e={},(0,r.Z)(e,"Atom-module_expandIcon__mPszC",!0),(0,r.Z)(e,"Atom-module_turnedIcon__0Kzwy",!c),e)),name:"chevron"})]})}),(0,o.jsx)("div",{className:(0,v.Z)((t={},(0,r.Z)(t,"Atom-module_accordionDetailsWrapper__p6EI7",!0),(0,r.Z)(t,"Atom-module_hiddenAccordion__pDNdM",!c),t)),children:(0,o.jsx)("div",{className:"Atom-module_accordionDetails__-B3jK",children:l})})]},a)}))})}))})})),$b=["formState"];function Nb(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Pb(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Nb(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Nb(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var kb=(0,S.$j)((function(n){return{formState:n.modal.form}}))((function(n){var e=n.formState,t=(0,p.Z)(n,$b);return(0,o.jsx)(Tm,{title:"Attachment Points",className:"Attach-module_attachPoints__5QEAv",result:function(){return e.result},valid:function(){return e.valid},params:t,buttonsNameMap:{OK:"Apply"},buttons:["Cancel","OK"],withDivider:!0,children:(0,o.jsxs)(og,Pb(Pb({schema:Se,init:t},e),{},{children:[(0,o.jsx)(ag,{name:"primary"}),(0,o.jsx)(ag,{name:"secondary"})]}))})})),Ib=["formState"];function Tb(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Bb(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Tb(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Tb(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Lb={title:"Reaction Auto-Mapping",type:"object",required:["mode"],properties:{mode:{title:"Mode",enum:["discard","keep","alter","clear"],enumNames:["Discard","Keep","Alter","Clear"],default:"discard"}}},_b=(0,S.$j)((function(n){return{formState:n.modal.form}}),(function(n,e){return{onOk:function(t){n(Xe("automap",t)),e.onOk(t)}}}))((function(n){var e=n.formState,t=(0,p.Z)(n,Ib);return(0,o.jsx)(Tm,{title:"Reaction Auto-Mapping",className:"Automap-module_automap__531ko",result:function(){return e.result},valid:function(){return e.valid},params:t,withDivider:!0,buttons:["Cancel","OK"],buttonsNameMap:{OK:"Apply"},children:(0,o.jsx)(og,Bb(Bb({schema:Lb},e),{},{children:(0,o.jsx)(ag,Bb(Bb({name:"mode",options:jd(Lb.properties.mode)},n),{},{component:Yv}))}))})})),Vb=["formState"];function zb(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Gb(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?zb(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):zb(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Fb=(0,S.$j)((function(n){return{formState:n.modal.form}}))((function(n){var e=n.formState,t=(0,p.Z)(n,Vb),r=Me.properties;return(0,o.jsx)(Tm,{title:"Bond Properties",className:"Bond-module_bond__EDfLY",result:function(){return e.result},valid:function(){return e.valid},params:t,buttonsNameMap:{OK:"Apply"},buttons:["Cancel","OK"],withDivider:!0,children:(0,o.jsxs)(og,Gb(Gb({schema:Me,init:t},e),{},{children:[(0,o.jsx)(ag,{name:"type",component:Yv,options:jd(r.type)}),(0,o.jsx)(ag,{name:"topology",component:Yv,options:jd(r.topology)}),(0,o.jsx)(ag,{name:"center",component:Yv,options:jd(r.center)})]}))})}));function Hb(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Rb(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Hb(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Hb(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Zb=function(n){var e=n.rgroupLabels,t=n.label,r=n.name,i={title:ap().schema.properties[r].title,enum:[0],enumNames:["Always"]};return e.forEach((function(n){t!==n&&(i.enum.push(n),i.enumNames.push("IF R".concat(t," THEN R").concat(n)))})),(0,o.jsx)(ag,Rb(Rb({schema:i,className:"IfThenSelect-module_field__9YaPA"},n),{},{component:Yv,options:jd(i)}))},Kb=["formState","label","rgroupLabels"];function Yb(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Ub(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Yb(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Yb(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Jb=(0,S.$j)((function(n){return{formState:n.modal.form}}))((function(n){var e=n.formState,t=n.label,r=n.rgroupLabels,i=(0,p.Z)(n,Kb);return(0,o.jsx)(Tm,{title:"R-Group Logic Condition",className:"RgroupLogic-module_rgroupLogic__q4RTy",result:function(){return e.result},valid:function(){return e.valid},params:i,buttonsNameMap:{OK:"Apply"},buttons:["Cancel","OK"],withDivider:!0,children:(0,o.jsxs)(og,Ub(Ub({schema:je,customValid:{range:function(n){return n.replace(/\s*/g,"").replace(/,+/g,",").replace(/^,/,"").replace(/,$/,"").split(",").every((function(n){return n.match(/^[>,<=]?[0-9]+$/g)||n.match(/^[0-9]+-[0-9]+$/g)}))}},init:i},e),{},{children:[(0,o.jsx)(ag,{name:"range"}),(0,o.jsx)(ag,{name:"resth",labelPos:"after",className:"RgroupLogic-module_resth__RL2qE"}),(0,o.jsx)(Zb,{name:"ifthen",label:t,rgroupLabels:r})]}))})})),qb=function(n){var e=n.fileName;return(0,o.jsxs)("div",{className:"AnalyzingFile-module_analyzingFileWrapper__j0Ltf",children:[e&&(0,o.jsxs)("div",{className:"AnalyzingFile-module_fileBox__ywFIh",children:[(0,o.jsx)(Au,{name:"file-thumbnail"}),(0,o.jsx)("p",{children:e})]}),(0,o.jsx)(Bm,{})]})},Wb="OpenOptions-module_dropContainer__PL6Tg",Xb="OpenOptions-module_buttonLabelWrapper__h2YsI",Qb="OpenOptions-module_buttonLabel__LiY--",nC="OpenOptions-module_textLabelWrapper__Vx8NF",eC="OpenOptions-module_textLabel__TlOfz",tC="OpenOptions-module_dropIconWrapper__ibBQx",rC=["buttonLabel","textLabel","iconName","disabled","disabledText"];function oC(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function iC(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?oC(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):oC(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var aC=function(n){var e=n.buttonLabel,t=n.textLabel,r=n.iconName,i=n.disabled,a=n.disabledText,l=(0,p.Z)(n,rC),c=(0,nn.uI)(iC({multiple:!1,disabled:i},l)),s=c.getRootProps,u=c.getInputProps,h=c.isDragActive,f=c.open,m=(0,d.useMemo)((function(){return[Wb,h?"FileDrop-module_isHovered__c-CDn":null,i?"FileDrop-module_isDisabled__Ejuyq":null].join(" ")}),[h]);return(0,o.jsxs)("div",iC(iC({onKeyDown:f},s({className:m})),{},{children:[(0,o.jsx)("input",iC({},u())),(0,o.jsx)("div",{className:tC,children:(0,o.jsx)(Au,{name:r})}),i?(0,o.jsx)("p",{className:eC,children:a}):(0,o.jsxs)(o.Fragment,{children:[(0,o.jsx)("div",{className:nC,children:(0,o.jsx)("p",{className:eC,children:t})}),(0,o.jsx)("div",{className:Xb,children:(0,o.jsx)("p",{className:Qb,children:e})})]})]}))},lC=function(n){var e=n.selectClipboard,t=n.fileLoadHandler,r=n.imageLoadHandler,i=n.isRecognizeDisabled,a=n.errorHandler;return(0,o.jsxs)("div",{className:"OpenOptions-module_optionsContainer__-WqT8",children:[(0,o.jsxs)("div",{onClick:e,className:Wb,children:[(0,o.jsx)("div",{className:tC,children:(0,o.jsx)(Au,{name:"open-window-paste-icon"})}),(0,o.jsx)("div",{className:nC}),(0,o.jsx)("div",{className:Xb,children:(0,o.jsx)("p",{className:Qb,children:"Paste from clipboard"})})]}),(0,o.jsx)(aC,{onDropAccepted:t,onDropRejected:function(n){return a("Unable to accept file(s). ".concat(n))},buttonLabel:"Open from file",textLabel:"or drag file here",iconName:"open-window-upload-icon"}),(0,o.jsx)(aC,{accept:"image/*",disabled:i,disabledText:"Image Recognition service is not available",onDropAccepted:r,onDropRejected:function(){return a("Unable to accept file(s). Make sure you upload 1 image.")},buttonLabel:"Open from image",textLabel:"or drag file here",iconName:"image-frame"})]})},cC=function(n){var e=n.structStr,t=n.inputHandler,r=n.autoFocus,i=void 0!==r&&r;return(0,o.jsx)(o.Fragment,{children:(0,o.jsx)("textarea",{className:"Open-module_textareaEditor__ZbEVj",value:e,onChange:function(n){return t(n.target.value)},autoFocus:i})})};function sC(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function uC(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?sC(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):sC(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var dC=function(n){if(n.isAnalyzingFile)return(0,o.jsx)(qb,{fileName:n.fileName});switch(n.currentState){case n.states.idle:return(0,o.jsx)(lC,uC({},n));case n.states.textEditor:return(0,o.jsx)(cC,uC({},n));default:return null}},pC=["server","onImageUpload","errorHandler","isAnalyzingFile","isRecognizeDisabled"];function hC(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}var fC={idle:"idle",textEditor:"textEditor",imageRec:"imageRec"},mC=function(n){var e=n.structStr,t=n.openHandler,r=n.copyHandler,i=n.onCancel;return(0,o.jsxs)("div",{className:"Open-module_footerContent__Q0hTw",children:[(0,o.jsx)("button",{onClick:i,className:"Open-module_cancelButton__0TQzA",children:"Cancel"}),(0,o.jsxs)("div",{className:"Open-module_buttonsContainer__L1HqU",children:[(0,o.jsx)(sb,{disabled:!e,clickHandler:t,styles:"Open-module_openButton__cj3oU",label:"Open as New Project"},"openButton"),(0,o.jsx)(sb,{disabled:!e,clickHandler:r,styles:"Open-module_copyButton__KlXKd",label:"Add to Canvas",title:"Structure will be loaded as fragment and added to Clipboard"},"copyButton")]})]})},vC=(0,S.$j)((function(n){var e;return{server:n.server,errorHandler:n.editor.errorHandler,isRecognizeDisabled:null===(e=n.actionState.recognize)||void 0===e?void 0:e.disabled,isAnalyzingFile:n.requestsStatuses.isAnalyzingFile}}),(function(n){return{onOk:function(e){e.fragment&&$n("copy"),n(qe(e.structStr,{badHeaderRecover:!0,fragment:e.fragment}))},onImageUpload:function(e){n(Yn(e))}}}))((function(n){var e=n.server,t=n.onImageUpload,i=n.errorHandler,a=n.isAnalyzingFile,l=n.isRecognizeDisabled,c=(0,p.Z)(n,pC),s=(0,d.useState)(""),u=(0,O.Z)(s,2),h=u[0],f=u[1],m=(0,d.useState)(""),v=(0,O.Z)(m,2),g=v[0],b=v[1],C=(0,d.useState)(),y=(0,O.Z)(C,2),w=y[0],S=y[1],M=(0,d.useState)(fC.idle),x=(0,O.Z)(M,2),j=x[0],E=x[1];(0,d.useEffect)((function(){e&&yd(e).then((function(n){S({chosenOpener:n})}))}),[e]);var D=c.onOk,A=j===fC.textEditor&&!a;return j===fC.imageRec?(0,o.jsx)(gb,function(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?hC(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):hC(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}({},c)):(0,o.jsx)(Tm,{title:"Open structure",className:"Open-module_open__m8V9g",params:c,result:function(){return null},footerContent:A?(0,o.jsx)(mC,{structStr:h,openHandler:function(){D({structStr:h,fragment:!1})},copyHandler:function(){D({structStr:h,fragment:!0})},onCancel:c.onCancel}):void 0,buttons:[],withDivider:!0,children:(0,o.jsx)(dC,{isAnalyzingFile:a,fileName:g,currentState:j,states:fC,selectClipboard:function(){return E(fC.textEditor)},fileLoadHandler:function(n){b(n[0].name),w.chosenOpener(n[0]).then((function(n){f(n),E(fC.textEditor)}),(function(){return i("Error processing file")}))},imageLoadHandler:function(n){t(n[0]),E(fC.imageRec)},errorHandler:i,isRecognizeDisabled:l,structStr:h,inputHandler:f,autoFocus:!0})})}));function gC(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function bC(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?gC(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):gC(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var CC=function(n){(0,h.Z)(a,n);var e,t,i=(e=a,t=function(){if("undefined"==typeof Reflect||!Reflect.construct)return!1;if(Reflect.construct.sham)return!1;if("function"==typeof Proxy)return!0;try{return Boolean.prototype.valueOf.call(Reflect.construct(Boolean,[],(function(){}))),!0}catch(n){return!1}}(),function(){var n,r=(0,m.Z)(e);if(t){var o=(0,m.Z)(this).constructor;n=Reflect.construct(r,arguments,o)}else n=r.apply(this,arguments);return(0,f.Z)(this,n)});function a(n){var e;return(0,c.Z)(this,a),(e=i.call(this,n)).state={},e.state.tabIndex=n.tabIndex||0,e.props.changeTab(e.state.tabIndex),e}return(0,s.Z)(a,[{key:"changeTab",value:function(n,e){this.setState({tabIndex:e}),this.props.changeTab&&this.props.changeTab(e)}},{key:"componentDidUpdate",value:function(n){this.props.tabIndex!==n.tabIndex&&this.setState({tabIndex:this.props.tabIndex})}},{key:"render",value:function(){var n=this,e=this.props,t=e.tabs,i=e.contentClassName,a=e.className,l=e.tabIndex,c=t[this.state.tabIndex],s=null==c?void 0:c.component,u=null==c?void 0:c.props;return(0,o.jsxs)("div",{children:[(0,o.jsx)("ul",{className:a,tabIndex:l,children:(0,o.jsx)("li",{className:"Tabs-module_tabs__PuztJ",children:t.map((function(e,t){return(0,o.jsx)("a",{className:(0,v.Z)((0,r.Z)({},"Tabs-module_active__eeyNd",n.state.tabIndex===t)),onClick:function(e){return n.changeTab(e,t)},children:e.caption},t)}))})}),c&&(0,o.jsx)("div",{className:i,children:(0,o.jsx)(s,bC({},u))})]})}}]),a}(d.Component),yC="Save-module_ok__SgeCM";function OC(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function wC(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?OC(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):OC(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var SC={title:"Save",type:"object",properties:{filename:{title:"File name:",type:"string",maxLength:128,pattern:'^[^.<>:?"*\\\\|\\/][^<>:?"*\\\\|\\/]*$',invalidMessage:function(n){return n?n.length>128?"Filename is too long":"A filename cannot contain characters: \\ / : * ? \" < > | and cannot start with '.'":"Filename should contain at least one character"}},format:{title:"File format:",enum:Object.keys(u.xz_),enumNames:Object.keys(u.xz_).map((function(n){return u.xz_[n].name}))}}},MC=function(n){(0,h.Z)(a,n);var e,t,i=(e=a,t=function(){if("undefined"==typeof Reflect||!Reflect.construct)return!1;if(Reflect.construct.sham)return!1;if("function"==typeof Proxy)return!0;try{return Boolean.prototype.valueOf.call(Reflect.construct(Boolean,[],(function(){}))),!0}catch(n){return!1}}(),function(){var n,r=(0,m.Z)(e);if(t){var o=(0,m.Z)(this).constructor;n=Reflect.construct(r,arguments,o)}else n=r.apply(this,arguments);return(0,f.Z)(this,n)});function a(n){var e;(0,c.Z)(this,a),e=i.call(this,n),(0,r.Z)((0,en.Z)(e),"isImageFormat",(function(n){return!!(0,u.voO)(n)})),(0,r.Z)((0,en.Z)(e),"showStructWarningMessage",(function(n){var t=e.props.formState.errors;return"mol"!==n&&Object.keys(t).length>0})),(0,r.Z)((0,en.Z)(e),"changeType",(function(n){var t=e.props,r=t.struct,o=t.server,i=t.options,a=t.formState,l=e.context.errorHandler;if(e.isImageFormat(n)){var c=(new u.F_l).serialize(r);e.setState({disableControls:!0,tabIndex:0,imageFormat:n,structStr:c,isLoading:!0});var s={};return s.outputFormat=n,o.generateImageAsBase64(c,s).then((function(n){e.setState({disableControls:!1,tabIndex:0,imageSrc:n,isLoading:!1})})).catch((function(n){return l(n),e.props.onResetForm(a),n}))}return e.setState({disableControls:!0,isLoading:!0}),new u.Yyn(o).create(n,i).getStructureFromStructAsync(r).then((function(n){e.setState({tabIndex:0,structStr:n})}),(function(n){return l(n.message),e.props.onResetForm(a),n})).finally((function(){e.setState({disableControls:!1,tabIndex:0,isLoading:!1})}))})),(0,r.Z)((0,en.Z)(e),"changeTab",(function(n){e.setState({tabIndex:n})})),(0,r.Z)((0,en.Z)(e),"getWarnings",(function(n){var t=e.props,r=t.struct,o=t.moleculeErrors,i=[];if(!e.isImageFormat(n)){var a=function(n,e){var t=[],r=(0,u.ymK)(e).name,o=n.rxnArrows.size,i=n.hasRxnArrow();if("smiles"!==e&&"smarts"!==e||t.push("Structure contains query properties of atoms and bonds that are not supported in the ".concat(null==e?void 0:e.toUpperCase(),". Query properties will not be reflected in the file saved.")),"smiles"===e){var a=Array.from(n.atoms.values()).some((function(n){return n.pseudo}));a&&t.push("Structure contains generic atoms. They will be saved as any atom (*).")}if("ket"!==e){if(i){var l=Array.from(n.rxnArrows.values())[0].mode;l!==u.mWk.OpenAngle&&t.push("The ".concat(r," format does not support drawn elements: the reaction ").concat(l," arrow will be replaced with the reaction arrow"))}o>1&&t.push("The ".concat(r," format does not support drawn elements: reaction arrows will be lost."))}if(["inChI","inChIAuxInfo","smiles","smilesExt"].includes(e)){0!==n.rgroups.size&&t.push("In ".concat(r," the structure will be saved without R-group fragments"));var c=(n=n.clone()).atoms.find((function(n,e){return"R#"===e.label}));null!==c&&t.push("In ".concat(r," the structure will be saved without R-group members")),null!==n.sgroups.find((function(n,e){return"MUL"!==e.type&&!/^INDIGO_.+_DESC$/i.test(e.data.fieldName)}))&&t.push("In ".concat(r," the structure will be saved without S-groups"))}if(["smiles","smilesExt","smarts","inChI","inChIAuxInfo","cml"].includes(e)){var s=n.atoms.find((function(n,e){return e.explicitValence>=0}));null!==s&&t.push("In ".concat(r," valence is not supported"))}return["mol","rxn"].includes(e)&&Array.from(n.frags.values()).some((function(n){return!(null==n||!n.enhancedStereoFlag)&&n.enhancedStereoFlag!==u.Jj2.Abs}))&&t.push("Structure contains enhanced stereochemistry features. Information will be partly lost."),["inChI","inChIAuxInfo","smiles","smilesExt"].includes(e)&&0!==n.functionalGroups.size&&t.push("In ".concat(r," the structure will be saved without functional groups.")),["cml"].includes(e)&&0!==n.functionalGroups.size&&t.push("Structure contains functional groups. In ".concat(r," information will be partly lost.")),0!==t.length?t.join("\n"):null}(r,n);e.showStructWarningMessage(n)&&i.push("Structure contains errors, please check the data, otherwise you can lose some properties or the whole structure after saving in this format."),a&&i.push(a)}return o&&i.push.apply(i,(0,x.Z)(Object.values(o))),i})),(0,r.Z)((0,en.Z)(e),"renderForm",(function(){var n=Object.assign({},e.props.formState),t=n.result,r=t.filename,i=t.format,a=0===e.getWarnings(i).length?[{caption:"Preview",component:e.renderSaveFile,tabIndex:0}]:[{caption:"Preview",component:e.renderSaveFile,tabIndex:0},{caption:"Warnings",component:e.renderWarnings,tabIndex:1}];return(0,o.jsxs)("div",{className:"Save-module_formContainer__v1pIq",children:[(0,o.jsxs)(og,wC(wC({schema:e.saveSchema,init:{filename:r,format:e.isRxn?"rxn":"mol"}},n),{},{children:[(0,o.jsx)(ag,{name:"filename"}),(0,o.jsx)(ag,{name:"format",onChange:e.changeType,options:jd(e.saveSchema.properties.format),component:Yv})]})),(0,o.jsx)(CC,{className:"Save-module_tabs__TOB-R",captions:a,tabIndex:e.state.tabIndex,changeTab:e.changeTab,tabs:a})]})})),(0,r.Z)((0,en.Z)(e),"renderSaveFile",(function(){var n=Object.assign({},e.props.formState);delete n.moleculeErrors;var t=n.result;t.filename;var r=t.format,i=e.state,a=i.structStr,l=i.imageSrc,c=i.isLoading,s=e.props.struct.isBlank();return c?(0,o.jsx)("div",{className:"Save-module_loadingCirclesContainer__COUKN",children:(0,o.jsx)(Bm,{})}):e.isImageFormat(r)?(0,o.jsx)("div",{className:"Save-module_imageContainer__gFELk",children:!s&&(0,o.jsx)("img",{src:"data:image/".concat(r,"+xml;base64,").concat(l),alt:"".concat(r," preview")})}):(0,o.jsx)("div",{className:"Save-module_previewBackground__AbaUf",children:(0,o.jsx)("textarea",{value:a,className:"Save-module_previewArea__-0SLb",readOnly:!0,ref:e.textAreaRef})})})),(0,r.Z)((0,en.Z)(e),"renderWarnings",(function(){var n=Object.assign({},e.props.formState).result;n.filename;var t=n.format,r=e.getWarnings(t);return r.length?(0,o.jsx)("div",{className:"Save-module_warnings__1PxJT",children:r.map((function(n){return(0,o.jsx)("div",{className:"Save-module_warningsContainer__-3yVy",children:(0,o.jsx)("span",{className:"Save-module_warningsArr__bKUFY",children:n})})}))}):null})),(0,r.Z)((0,en.Z)(e),"getButtons",(function(){var n=e.state,t=n.disableControls,r=n.imageFormat,i=n.structStr,a=e.props.formState,l=a.result,c=l.filename,s=l.format,d=e.props.struct.isBlank(),p=e.props.struct.atoms.size&&e.props.struct.bonds.size,h=[(0,o.jsx)("button",{className:"Save-module_saveTmpl__O-d0T",disabled:t||d||!p,onClick:function(){return e.props.onTmplSave(e.props.struct)},children:"Save to Templates"},"save-tmpl")];return h.push((0,o.jsx)("button",{mode:"onCancel",className:"Save-module_cancel__SMkEV",onClick:function(){return e.props.onOk({})},type:"button",children:"Cancel"},"cancel")),e.isImageFormat(s)?h.push((0,o.jsx)(Eg,{mode:"saveImage",data:i,filename:c,outputFormat:r,type:"image/".concat(s,"+xml"),onSave:e.props.onOk,disabled:t||!a.valid||d||!e.props.server,className:yC,children:"Save"},"save-image-button")):h.push((0,o.jsx)(Eg,{mode:"saveFile",data:i,filename:c+(0,u.ymK)(s).extensions[0],type:s.mime,server:e.props.server,onSave:e.props.onOk,disabled:t||!a.valid||d,className:yC,children:"Save"},"save-file-button")),h})),e.state={disableControls:!0,imageFormat:"svg",tabIndex:0,isLoading:!0},e.isRxn=e.props.struct.hasRxnArrow(),e.textAreaRef=(0,d.createRef)();var t=[e.isRxn?"rxn":"mol","smiles","ket"];return e.props.server&&t.push(e.isRxn?"rxnV3000":"molV3000","smilesExt","smarts","inChI","inChIAuxInfo","cml","svg","png","cdxml"),e.saveSchema=SC,e.saveSchema.properties.format=Object.assign(e.saveSchema.properties.format,{enum:t,enumNames:t.map((function(n){return((0,u.ymK)(n)||(0,u.voO)(n)).name}))}),e}return(0,s.Z)(a,[{key:"componentDidMount",value:function(){var n=this,e=this.props.checkState.checkOptions;this.props.onCheck(e),this.changeType(this.isRxn?"rxn":"mol").then((function(e){return e instanceof Error&&n.setState({disableControls:!0})}))}},{key:"render",value:function(){return(0,o.jsx)(Tm,{className:"Save-module_dialog__of-0M",title:"Save Structure",params:this.props,buttons:this.getButtons(),needMargin:!1,withDivider:!0,children:this.renderForm()})}}]),a}(d.Component);(0,r.Z)(MC,"contextType",mn);var xC=(0,S.$j)((function(n){return{server:n.options.app.server?n.server:null,struct:n.editor.struct(),options:n.options.getServerSettings(),formState:n.modal.form,moleculeErrors:n.modal.form.moleculeErrors,checkState:n.options.check}}),(function(n){return{onCheck:function(e){return n(We(e))},onTmplSave:function(e){return n(function(n){var e={struct:n.clone(),props:{}};return function(n,t){Xu(n,"attach",{tmpl:e}).then((function(r){var o=r.name,i=r.attach;e.struct.name=o.trim(),e.props=nd(nd({},i),{},{group:"User Templates"});var a=t().templates.lib.concat(e);n(Ku(a)),td(a)})).catch((function(){return null}))}}(e))},onResetForm:function(e){return n(ue(e))}}}))(MC),jC="enhancedStereo-module_labelGroupSelect__K7TYC",EC=["struct","formState","init"];function DC(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function AC(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?DC(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):DC(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var $C=(0,S.$j)((function(n){return{formState:n.modal.form||{result:{},valid:!1},struct:n.editor.struct()}}))((function(n){var e,t=n.struct,r=n.formState,i=n.init,a=(0,p.Z)(n,EC),l=r.result,c=r.valid,s=function(n,e){return e.filter((function(e){return null!==n.atoms.get(e).stereoLabel})).map((function(e){return n.atoms.get(e).stereoLabel}))}(t,Array.from(t.atoms.keys())),d=(e=s.map((function(n){var e;return n.match(/&/)?+(null===(e=n.match(/\d+/))||void 0===e?void 0:e.join()):0})),Math.max.apply(Math,(0,x.Z)(e))),h=function(n){var e=n.map((function(n){var e;return n.match(/or/)?+(null===(e=n.match(/\d+/))||void 0===e?void 0:e.join()):0}));return Math.max.apply(Math,(0,x.Z)(e))}(s);return(0,o.jsx)(Tm,{title:"Enhanced Stereochemistry",className:"enhancedStereo-module_enhancedStereo__8FLSY",params:a,result:function(){return l},valid:function(){return c},withDivider:!0,buttons:["Cancel","OK"],buttonsNameMap:{OK:"Apply"},children:(0,o.jsx)(og,AC(AC({schema:{title:"Enhanced Stereo",type:"object",properties:{type:{type:"string"},andNumber:{type:"integer"},orNumber:{type:"integer"}}},init:i},r),{},{children:(0,o.jsxs)("fieldset",{children:[(0,o.jsxs)("label",{children:[(0,o.jsx)(ag,{name:"type",labelPos:!1,type:"radio",value:u.YkY.Abs,checked:l.type===u.YkY.Abs}),"ABS"]}),0!==d&&(0,o.jsxs)("label",{children:[(0,o.jsx)(ag,{name:"type",labelPos:!1,type:"radio",value:u.YkY.And,checked:l.type===u.YkY.And}),"Add to AND",(0,o.jsx)(ag,{name:"andNumber",schema:(0,E.range)(1,d+1),type:"text",className:jC}),"Group"]}),0!==h&&(0,o.jsxs)("label",{children:[(0,o.jsx)(ag,{name:"type",labelPos:!1,type:"radio",value:u.YkY.Or,checked:l.type===u.YkY.Or}),"Add to OR",(0,o.jsx)(ag,{name:"orNumber",schema:(0,E.range)(1,h+1),type:"text",className:jC}),"Group"]}),(0,o.jsxs)("label",{children:[(0,o.jsx)(ag,{name:"type",labelPos:!1,type:"radio",value:"&".concat(d+1)}),"Create new AND Group"]}),(0,o.jsxs)("label",{children:[(0,o.jsx)(ag,{name:"type",labelPos:!1,type:"radio",value:"or".concat(h+1)}),"Create new OR Group"]})]})}))})})),NC=["formState"];function PC(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function kC(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?PC(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):PC(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function IC(n){var e=n.match(/^(\d+)?([a-z*]{1,3})(\.|:|\^\^)?(\d+[-+]|[-+])?$/i);if(e){var t="*"===e[2]?"A":(0,y.capitalize)(e[2]),r=0,o=0,i=0;if(e[1]&&(o=parseInt(e[1])),e[3]&&(i={":":1,".":2,"^^":3}[e[3]]),e[4]&&(r=parseInt(e[4]),isNaN(r)&&(r=1),e[4].endsWith("-")&&(r=-r)),"A"===t||"Q"===t||"X"===t||"M"===t||u.eKO.get(t))return{label:t,charge:r,isotope:o,radical:i}}return null}var TC=(0,S.$j)((function(n){return{formState:n.modal.form}}))((function(n){var e,t,r,i,a={label:n.letter||(e=n,t=Math.abs(e.charge),r=["",":",".","^^"][e.radical]||"",i="",t&&(i=e.charge<0?"-":"+"),(e.isotope||"")+e.label+r+(t>1?t:"")+i)},l=n.formState,c=(0,p.Z)(n,NC),s=l.result,u=l.valid;return(0,o.jsx)(Tm,{title:"Label Edit",valid:function(){return u},withDivider:!0,needMargin:!1,result:function(){return IC(s.label)},className:"labelEdit-module_labelEdit__9LnIH",buttons:["Cancel","OK"],buttonsNameMap:{OK:"Apply"},focusable:!1,params:c,children:(0,o.jsx)(og,kC(kC({schema:we,customValid:{label:function(n){return IC(n)}},init:a},l),{},{children:(0,o.jsx)(ag,{name:"label",maxLength:"20",size:"10",autoFocus:!0,className:"labelEdit-module_labelEditInputField__tb-J4"})}))})}));function BC(n){var e=n.el,t=n.isInfo,r={color:u.wql[e.label]||"black",fontSize:"12px"},i={color:u.wql[e.label]||"black",fontWeight:"bold",fontSize:"18px"};return(0,o.jsxs)("div",{className:(0,v.Z)("AtomInfo-module_ket_atom_info__GOuZ6",!t&&"AtomInfo-module_none__PRuzx"),children:[(0,o.jsx)("div",{style:r,children:e.number}),(0,o.jsx)("span",{style:i,children:e.label}),(0,o.jsx)("br",{}),e.title,(0,o.jsx)("br",{}),e.mass]})}function LC(){return(0,o.jsx)("tbody",{children:(0,o.jsx)("tr",{children:(0,y.range)(0,19).map((function(n){return(0,o.jsx)("th",{children:n||""},n)}))})})}function _C(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function VC(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?_C(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):_C(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function zC(n){var e=n.row,t=n.caption,r=n.refer,i=n.onAtomSelect,a=n.onDoubleClick,l=n.currentEvents,c=n.atomClassNames,s=n.className;return(0,o.jsx)("tbody",{children:(0,o.jsxs)("tr",{children:[(0,o.jsx)("th",{children:t}),e.map((function(n,e){return"number"!=typeof n?(0,o.jsx)("td",{children:(0,o.jsx)(kp,VC({el:n,className:v.Z.apply(void 0,(0,x.Z)(c(n))),onClick:function(){return i(n.label)},onDoubleClick:function(){return a()}},l(n)))},e):r(n)?(0,o.jsx)("td",{className:s,children:r(n)},e):(0,o.jsx)("td",{colSpan:n},e)}))]})})}function GC(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function FC(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?GC(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):GC(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function HC(n){var e=n.row,t=n.caption,r=n.onAtomSelect,i=n.onDoubleClick,a=n.currentEvents,l=n.atomClassNames,c=n.className;return(0,o.jsx)("tbody",{children:(0,o.jsxs)("tr",{children:[(0,o.jsx)("th",{colSpan:"3",className:c,children:t}),e.map((function(n){return(0,o.jsx)("td",{children:(0,o.jsx)(kp,FC({el:n,className:v.Z.apply(void 0,(0,x.Z)(l(n))),onClick:function(){return r(n.label)},onDoubleClick:function(){return i()}},a(n)))},n.label)})),(0,o.jsx)("td",{})]})})}var RC={"button-common-styles":"ElementsTable-module_button-common-styles__-6eHN",scrollbar:"ElementsTable-module_scrollbar__0R-HA",table:"ElementsTable-module_table__iNPVY",main_row:"ElementsTable-module_main_row__csN5a",outiner_row:"ElementsTable-module_outiner_row__fzfGL",noble:"ElementsTable-module_noble__65B92",alkali:"ElementsTable-module_alkali__sM9z9","alkaline-earth":"ElementsTable-module_alkaline-earth__t2h2s",metalloid:"ElementsTable-module_metalloid__Ui4Y8","other-nonmetal":"ElementsTable-module_other-nonmetal__mbkMN","post-transition":"ElementsTable-module_post-transition__k4C-G",transition:"ElementsTable-module_transition__GCnID",lanthanide:"ElementsTable-module_lanthanide__wVoLa",actinide:"ElementsTable-module_actinide__bVCBg",halogen:"ElementsTable-module_halogen__W6EjM","unknown-props":"ElementsTable-module_unknown-props__d9rq4","unknown-state":"ElementsTable-module_unknown-state__lRBCp",button:"ElementsTable-module_button__xCaL4",selected:"ElementsTable-module_selected__B9LGf"};function ZC(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function KC(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?ZC(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):ZC(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var YC=["alkali","alkaline-earth","transition","post-transition"],UC={He:16,B:10,Al:10,Hf:1,Rf:1},JC="actinide",qC="lanthanide",WC=u.eKO.filter((function(n){return n&&n.type!==JC&&n.type!==qC&&89!==n.number&&57!==n.number})).reduce((function(n,e){var t=n[e.period-1];return t?(UC[e.label]&&t.push(UC[e.label]),t.push(e)):n.push([e]),n}),[]),XC=u.eKO.filter((function(n){return n&&(n.type===qC||57===n.number)})),QC=u.eKO.filter((function(n){return n&&(n.type===JC||89===n.number)})),ny=function(n){(0,h.Z)(a,n);var e,t,i=(e=a,t=function(){if("undefined"==typeof Reflect||!Reflect.construct)return!1;if(Reflect.construct.sham)return!1;if("function"==typeof Proxy)return!0;try{return Boolean.prototype.valueOf.call(Reflect.construct(Boolean,[],(function(){}))),!0}catch(n){return!1}}(),function(){var n,r=(0,m.Z)(e);if(t){var o=(0,m.Z)(this).constructor;n=Reflect.construct(r,arguments,o)}else n=r.apply(this,arguments);return(0,f.Z)(this,n)});function a(){var n;(0,c.Z)(this,a);for(var e=arguments.length,t=new Array(e),o=0;o<e;o++)t[o]=arguments[o];return n=i.call.apply(i,[this].concat(t)),(0,r.Z)((0,en.Z)(n),"getAtomClassNames",(function(e){var t=n.props.selected,r=YC.includes(e.type)?"".concat(e.type," ").concat("metal"):e.type||"unknown-props";return[].concat((0,x.Z)(r.split(" ")),[e.state||"unknown-state",e.origin,"button",t(e.label)&&"selected"]).map((function(n){return RC[n]}))})),n}return(0,s.Z)(a,[{key:"shouldComponentUpdate",value:function(n){return n.value!==this.props.value}},{key:"render",value:function(){var n=this,e=this.props,t={currentEvents:e.currentEvents,onAtomSelect:e.onAtomSelect,onDoubleClick:e.onDoubleClick};return(0,o.jsxs)("table",{className:RC.table,summary:"Periodic table of the chemical elements",children:[(0,o.jsx)(LC,{}),WC.map((function(e,r){return(0,o.jsx)(zC,KC({atomClassNames:n.getAtomClassNames,className:RC.main_row,row:e,caption:r+1,refer:function(n){return 1===n&&(5===r?"*":"**")}},t),r)})),(0,o.jsx)(HC,KC({atomClassNames:this.getAtomClassNames,className:RC.outiner_row,row:XC,caption:"*"},t)),(0,o.jsx)(HC,KC({atomClassNames:this.getAtomClassNames,className:RC.outiner_row,row:QC,caption:"**"},t))]})}}]),a}(d.Component),ey="BoxWithLines-module_upperLines__8pL-R",ty="BoxWithLines-module_lowerLine__tBZJd",ry=function(){return(0,o.jsxs)("div",{className:"BoxWithLines-module_horizintalNodeLines__QO-Su",children:[(0,o.jsx)("div",{className:ey}),(0,o.jsx)("div",{className:ty})]})},oy=function(){return(0,o.jsxs)("div",{className:"BoxWithLines-module_verticalNodeLines__wBgwS",children:[(0,o.jsx)("div",{className:ey}),(0,o.jsx)("div",{className:ty})]})},iy={"button-common-styles":"GenSet-module_button-common-styles__0Ro-U",scrollbar:"GenSet-module_scrollbar__Ev8Uz",genGroupLegendBox:"GenSet-module_genGroupLegendBox__CSTQr",legendBox:"GenSet-module_legendBox__0zIAk",SpecialNodes:"GenSet-module_SpecialNodes__oFKp3",AtomGenerics:"GenSet-module_AtomGenerics__MoQCf",GroupGenerics:"GenSet-module_GroupGenerics__pFPtX",Cyclic:"GenSet-module_Cyclic__VJRtt",Acyclic:"GenSet-module_Acyclic__R97MM",CyclicCarbo:"GenSet-module_CyclicCarbo__Aanb0",AcyclicCarbo:"GenSet-module_AcyclicCarbo__nowGn",CyclicHetero:"GenSet-module_CyclicHetero__bbOnT",AcyclicHetero:"GenSet-module_AcyclicHetero__hnr4G",button:"GenSet-module_button__TCbeM",selected:"GenSet-module_selected__58d2u"},ay=function(n){return["Acyclic","Cyclic","Acyclic Carbo","Cyclic Carbo","Acyclic Hetero","Cyclic Hetero"].includes(n)};function ly(n){var e=n.labels,t=n.selected,i=n.onAtomSelect,a=n.className,l=n.group;return(0,o.jsx)(o.Fragment,{children:e.map((function(n,e){var c,s=n.items,u=n.displayName;return(0,o.jsxs)("fieldset",{className:a,children:[(0,o.jsx)("div",{className:iy[(c=l,c.replaceAll(" ",""))],children:s.map((function(n,e){return(0,o.jsx)("button",{onClick:function(){return i(n.label,!1)},onDoubleClick:function(){return i(n.label,!0)},title:n.description||n.label,className:(0,v.Z)((0,r.Z)({},iy.selected,t(n.label)),iy.button),children:n.label},e)}))}),!ay(l)&&u&&(0,o.jsx)("div",{className:iy.legendBox,children:(0,o.jsx)("legend",{children:u})}),ay(l)&&u&&(0,o.jsx)("div",{className:iy.genGroupLegendBox,children:(0,o.jsx)("legend",{className:iy.genGroupLegend,children:u})})]},e)}))})}var cy={fieldFlexWrapper:"GenGroup-module_fieldFlexWrapper__mBHRt",buttonContainer:"GenGroup-module_buttonContainer__7qTti",genButtonContainer:"GenGroup-module_genButtonContainer__6Bwe1",subGroup:"GenGroup-module_subGroup__afiEU",legendMain:"GenGroup-module_legendMain__h-Wl3",legend:"GenGroup-module_legend__JWafm",fieldset:"GenGroup-module_fieldset__JehYt"},sy=function(n){var e,t=n.group,r=n.onAtomSelect,i=n.selected;return(0,o.jsx)("div",{className:cy.fieldFlexWrapper,children:(0,o.jsxs)("fieldset",{className:cy.fieldset,children:[(0,o.jsx)("legend",{className:cy[(e=t.title,["Atom Generics","Special Nodes","Group Generics","Acyclic","Cyclic"].includes(e)?"legendMain":"legend")],children:t.title}),(0,o.jsx)("div",{className:ay(t.title)?cy.genButtonContainer:cy.buttonContainer,children:t.itemSets&&(0,o.jsx)(ly,{labels:t.itemSets,selected:i,onAtomSelect:r,className:cy.subGroup,group:t.title})})]})})},uy="GenericGroups-module_subgroupContainer__xULxX";function dy(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function py(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?dy(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):dy(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var hy,fy=function(n,e,t){return(0,o.jsx)(sy,{group:my[n],selected:e,onAtomSelect:t})},my=function n(e){for(var t={},r=0,o=Object.keys(e);r<o.length;r++){var i,a=o[r];t[a]=py({},e[a]),null!==(i=t[a])&&void 0!==i&&i.subGroups&&(t=py(py({},t),n(t[a].subGroups)))}return t}(u.X6G);function vy(n){var e=n.selected,t=n.onAtomSelect;return(0,o.jsxs)("div",{className:"GenericGroups-module_genericGroups__z4EaG",children:[(0,o.jsxs)("div",{className:"GenericGroups-module_topGroupsContainer__bMeoG",children:[fy(hy.atomsGen,e,t),fy(hy.specialNodes,e,t)]}),fy(hy.groupGen,e,t),(0,o.jsx)(ry,{}),(0,o.jsxs)("div",{className:"GenericGroups-module_groupGenerics__6UpH6",children:[(0,o.jsxs)("div",{children:[fy(hy.groupAcyclic,e,t),(0,o.jsxs)("div",{className:uy,children:[(0,o.jsx)(oy,{}),(0,o.jsxs)("div",{children:[fy(hy.acyclicCarbo,e,t),fy(hy.acyclicHetero,e,t)]})]})]}),(0,o.jsxs)("div",{children:[fy(hy.groupCyclic,e,t),(0,o.jsxs)("div",{className:uy,children:[(0,o.jsx)(oy,{}),(0,o.jsxs)("div",{children:[fy(hy.cyclicCarbo,e,t),fy(hy.cyclicHetero,e,t)]})]})]})]})]})}!function(n){n.atomsGen="atoms-gen",n.specialNodes="special-nodes",n.groupGen="group-gen",n.groupAcyclic="group-acyclic",n.acyclicCarbo="acyclic-carbo",n.acyclicHetero="acyclic-hetero",n.groupCyclic="group-cyclic",n.cyclicHetero="cyclic-hetero",n.cyclicCarbo="cyclic-carbo"}(hy||(hy={}));var gy=["value","onChange"];function by(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Cy(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?by(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):by(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var yy=[{title:"Single",value:"atom"},{title:"List",value:"list"},{title:"Not List",value:"not-list"}];function Oy(n){var e=n.value,t=n.onChange,r=(0,p.Z)(n,gy);return(0,o.jsx)("fieldset",{className:"TypeChoice-module_fieldset__yJqT7",children:yy.map((function(n){return(0,o.jsxs)("label",{children:[(0,o.jsx)(_v,Cy({type:"radio",value:n.value,checked:n.value===e,onChange:function(){return t(n.value)}},r)),n.title]},n.title)}))})}function wy(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}var Sy=function(n){(0,h.Z)(a,n);var e,t,i=(e=a,t=function(){if("undefined"==typeof Reflect||!Reflect.construct)return!1;if(Reflect.construct.sham)return!1;if("function"==typeof Proxy)return!0;try{return Boolean.prototype.valueOf.call(Reflect.construct(Boolean,[],(function(){}))),!0}catch(n){return!1}}(),function(){var n,r=(0,m.Z)(e);if(t){var o=(0,m.Z)(this).constructor;n=Reflect.construct(r,arguments,o)}else n=r.apply(this,arguments);return(0,f.Z)(this,n)});function a(n){var e;return(0,c.Z)(this,a),e=i.call(this,n),(0,r.Z)((0,en.Z)(e),"changeType",(function(n){"list"!==e.state.type&&"not-list"!==e.state.type||"list"!==n&&"not-list"!==n?e.setState({type:n,value:"atom"===n||"gen"===n?null:[]}):e.setState({type:n})})),(0,r.Z)((0,en.Z)(e),"headerContent",(function(){return(0,o.jsxs)("div",{className:"PeriodTable-module_dialogHeader__-Wgw4",children:[(0,o.jsx)(Au,{name:"period-table"}),(0,o.jsx)("span",{children:"Periodic Table"})]})})),(0,r.Z)((0,en.Z)(e),"selected",(function(n){var t=e.state,r=t.type,o=t.value;return"atom"===r||"gen"===r?o===n:o.includes(n)})),(0,r.Z)((0,en.Z)(e),"onAtomSelect",(function(n){if(arguments.length>1&&void 0!==arguments[1]&&arguments[1]){var t=e.result(),r=e.state.type;t&&"atom"===r&&e.props.onOk(e.result())}else{var o=e.state,i=o.type,a=o.value;e.setState({value:"atom"===i||"gen"===i?n:(0,y.xor)([n],a)})}})),(0,r.Z)((0,en.Z)(e),"result",(function(){var n=e.state,t=n.type,r=n.value;return r&&r.length?"atom"===t?{label:r,pseudo:null}:"gen"===t?{type:t,label:r,pseudo:r}:{type:t,values:r}:null})),(0,r.Z)((0,en.Z)(e),"currentEvents",(function(n){return{onMouseEnter:function(){return e.setState({current:n,isInfo:!0})},onMouseLeave:function(){return e.setState({isInfo:!1})}}})),e.state={type:n.type||"atom",value:n.values||(n.pseudo?null:n.label)||null,current:u.eKO.get(2),isInfo:!1},e}return(0,s.Z)(a,[{key:"render",value:function(){var n=this,e=this.state;e.type;var t=e.value,r=this.headerContent;return(0,o.jsx)(Tm,{headerContent:(0,o.jsx)(r,{}),className:"PeriodTable-module_elementsTable__Vcz12",params:this.props,result:this.result,buttons:["Cancel","OK"],buttonsNameMap:{OK:"Add"},needMargin:!1,footerContent:(0,o.jsx)(Oy,{value:this.state.type,onChange:this.changeType}),children:(0,o.jsxs)("div",{className:"PeriodTable-module_periodTable__l-Uqx",children:[(0,o.jsx)(BC,{el:this.state.current,isInfo:this.state.isInfo}),(0,o.jsx)(ny,{value:t,currentEvents:this.currentEvents,selected:this.selected,onAtomSelect:function(e){return n.onAtomSelect(e)},onDoubleClick:function(e){return n.onAtomSelect(e,!0)}})]})})}}]),a}(d.Component);var My=(0,S.$j)((function(n,e){return e.values||e.label?{}:(t=n.editor,(o=t.selection())&&1===Object.keys(o).length&&o.atoms&&1===Object.keys(o.atoms).length?function(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?wy(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):wy(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}({},Ne(t.struct().atoms.get(o.atoms[0]))):{});var t,o}),(function(n,e){return{onOk:function(t){t.type&&"atom"!==t.type||n({type:"ADD_ATOMS",data:t.label}),n(Ue({tool:"atom",opts:Pe(t)})),e.onOk(t)}}}))(Sy);function xy(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}var jy=(0,S.$j)((function(n,e){return e.values||e.label?{}:(t=n.editor,1===(null==(i=t.selection())||null===(o=i.atoms)||void 0===o?void 0:o.length)?function(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?xy(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):xy(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}({},Ne(t.struct().atoms.get(i.atoms[0]))):{});var t,o,i}),(function(n,e){return{onOk:function(t){n(Ue({tool:"atom",opts:Pe(t)})),e.onOk(t)}}}))((function(n){var e=(0,d.useState)(n.pseudo?n.label:null),t=(0,O.Z)(e,2),r=t[0],i=t[1],a=function(){return r&&r.length?{type:"gen",label:r,pseudo:r}:null};return(0,o.jsx)(Tm,{title:"Extended Table",withDivider:!0,className:"ExtendedTable-module_extendedTable__2-hjV",params:n,result:a,buttons:["Cancel","OK"],buttonsNameMap:{OK:"Add"},needMargin:!1,children:(0,o.jsx)(vy,{selected:function(n){return r===n},onAtomSelect:function(e){var t=arguments.length>1&&void 0!==arguments[1]&&arguments[1];i(e),t&&n.onOk(a())}})})})),Ey="RemoveFG-module_window__6PHH4",Dy="RemoveFG-module_question__J8Qzx",Ay="RemoveFG-module_header__1hBAs",$y="RemoveFG-module_footer__8wImu",Ny="RemoveFG-module_buttonOk__zR5x4",Py="RemoveFG-module_buttonCancel__xCaJt";function ky(n,e){(null==e||e>n.length)&&(e=n.length);for(var t=0,r=new Array(e);t<e;t++)r[t]=n[t];return r}function Iy(n){var e,t=n.value,r=n.onChange,i=n.schema,a=n.disabledIds,l=n.multiple,c=n.classes.selected||"selected";return(0,o.jsx)("ul",{children:i.items.enum.map((function(n,s){return e=t.includes(n)?c:"",(0,o.jsx)("li",{children:(0,o.jsx)("button",{disabled:a.includes(n),type:"button",className:e,onClick:function(){return r(function(n,e,t){return n?(0,y.xor)(e,[t]):(0,y.xor)(e,e.concat([t]))}(l,t,n))},children:i.items.enumNames[s]})},n)}))})}var Ty={"button-common-styles":"rgroup-module_button-common-styles__O66iR",scrollbar:"rgroup-module_scrollbar__GmU8o",rgroup:"rgroup-module_rgroup__Pm-uA",selected:"rgroup-module_selected__hP5cM"},By=["disabledIds","values","formState","type"];function Ly(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function _y(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Ly(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Ly(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Vy=(0,S.$j)((function(n){return{formState:n.modal.form}}))((function(n){var e=n.disabledIds,t=n.values,r=n.formState,i=n.type,a=(0,p.Z)(n,By);return(0,o.jsx)(Tm,{title:"R-Group",className:Ty.rgroup,params:a,result:function(){return r.result},buttonsNameMap:{OK:"Apply"},buttons:["Cancel","OK"],withDivider:!0,children:(0,o.jsx)(og,_y(_y({schema:Oe,init:{values:t}},r),{},{children:(0,o.jsx)(ag,{name:"values",multiple:"atom"===i,labelPos:!1,component:Iy,disabledIds:e,classes:Ty})}))})})),zy={"button-common-styles":"sgroup-module_button-common-styles__MAeEP",scrollbar:"sgroup-module_scrollbar__T3fpf",sgroup:"sgroup-module_sgroup__Kh2Xj"},Gy=["context","fieldName","fieldValue","type","radiobuttons","formState"];function Fy(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Hy(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Fy(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Fy(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Ry=function(n,e,t,r,i){return Object.keys(n.properties).filter((function(n){return"type"!==n&&"context"!==n&&"fieldName"!==n})).map((function(n){return"radiobuttons"===n?(0,o.jsx)(ag,{name:n,checked:i,type:"radio",labelPos:!1},"".concat(e,"-").concat(t,"-").concat(n,"-radio")):"fieldValue"===n?(0,o.jsx)(ag,{name:n,placeholder:"Enter value"},"".concat(e,"-").concat(t,"-").concat(n,"-select")):(0,o.jsx)(ag,{name:n,type:"textarea"},"".concat(e,"-").concat(t,"-").concat(n,"-select"))}))},Zy=(0,S.$j)((function(n){return{formState:n.modal.form}}))((function(n){var e=n.context,t=n.fieldName,r=n.fieldValue,i=n.type,a=n.radiobuttons,l=n.formState,c=(0,p.Z)(n,Gy),s=l.result,u=l.valid,d=Xn,h={context:e||ee(d,"context"),fieldName:t||ee(d,"fieldName"),type:i,radiobuttons:a||ee(d,"radiobuttons")};h.fieldValue=r||ee(d,"fieldValue");var f={context:s.context.trim(),fieldName:s.fieldName.trim(),fieldValue:"string"==typeof s.fieldValue?s.fieldValue.trim():s.fieldValue};return(0,o.jsx)(Tm,{title:"S-Group Properties",className:zy.sgroup,result:function(){return s},valid:function(){return u},buttons:["Cancel","OK"],buttonsNameMap:{OK:"Apply"},withDivider:!0,needMargin:!1,params:c,children:(0,o.jsx)(og,Hy(Hy({serialize:f,schema:d,init:h},l),{},{children:(0,o.jsxs)("fieldset",{className:"sdata",children:[(0,o.jsx)(ag,{name:"context",options:jd(d.properties.context),component:Yv}),(0,o.jsx)(ag,{name:"fieldName",placeholder:"Enter name"}),Ry(d,s.context,s.fieldName,s.fieldValue,a)]})}))})})),Ky=["formState"];function Yy(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Uy(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?Yy(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):Yy(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Jy,qy,Wy,Xy,Qy,nO,eO,tO,rO,oO,iO,aO=function(n){return Object.keys(xe[n].properties).filter((function(n){return"type"!==n})).map((function(e){var t={};return"name"===e&&(t.maxLength=15),"fieldName"===e&&(t.maxLength=30),"fieldValue"===e&&(t.type="textarea"),"radiobuttons"===e&&(t.type="radio"),"connectivity"===e?(0,o.jsx)(ag,Uy(Uy({name:e},t),{},{component:Yv,options:jd(xe[n].properties[e])}),"".concat(n,"-").concat(e)):(0,o.jsx)(ag,Uy({name:e},t),"".concat(n,"-").concat(e))}))},lO=(0,S.$j)((function(n){return{formState:n.modal.form}}))((function(n){var e=n.formState,t=(0,p.Z)(n,Ky),r=e.result,i=e.valid,a=r.type;return(0,o.jsx)(Tm,{title:"S-Group Properties",className:zy.sgroup,result:function(){return r},valid:function(){return i},buttons:["Cancel","OK"],buttonsNameMap:{OK:"Apply"},withDivider:!0,params:t,children:(0,o.jsxs)(og,Uy(Uy({schema:xe[a],init:t},e),{},{children:[(0,o.jsx)(lg,{title:"Type",name:"type",schema:xe}),"GEN"!==a&&(0,o.jsx)("fieldset",{className:"DAT"===a?zy.data:"base",children:aO(a)})]}))})})),cO={"button-common-styles":"template-lib-module_button-common-styles__9adxB",scrollbar:"template-lib-module_scrollbar__ZFwCC",warning:"template-lib-module_warning__UqgEG",dialogHeader:"template-lib-module_dialogHeader__-AmwE",button:"template-lib-module_button__LKf1c",dialog_body:"template-lib-module_dialog_body__QtL0J",inputContainer:"template-lib-module_inputContainer__dxoHA",searchIcon:"template-lib-module_searchIcon__o7cAy",accordionSummary:"template-lib-module_accordionSummary__2hIop",groupIcon:"template-lib-module_groupIcon__LBIRH",expandIcon:"template-lib-module_expandIcon__Fb1EU",tabsContent:"template-lib-module_tabsContent__1QMnN",resultsContainer:"template-lib-module_resultsContainer__KnPBZ",saveButton:"template-lib-module_saveButton__8PE6t",tabs:"template-lib-module_tabs__YkpEG"},sO=["onInit"],uO=["name","onNameEdit","onAttachEdit"];function dO(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function pO(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?dO(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):dO(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var hO=(0,N.Z)(Tm)(Jy||(Jy=(0,P.Z)(["\n  background-color: #fff;\n\n  & header {\n    text-transform: none;\n    border-bottom: 1px solid #e1e5ea;\n    margin: 0;\n    padding: 12px;\n  }\n\n  & form {\n    display: flex;\n\n    & label::after {\n      top: 92px;\n      margin-right: 12px;\n    }\n  }\n"]))),fO=(0,N.Z)("div")(qy||(qy=(0,P.Z)(["\n  border: 1px solid #b4b9d6;\n  background-color: #ffff;\n  border-radius: 5px;\n  position: relative;\n  height: 300px;\n  width: 330px;\n  overflow: hidden;\n\n  & .structEditor {\n    height: 100%;\n    width: 100%;\n    border: none;\n  }\n"]))),mO=(0,N.Z)("div")(Wy||(Wy=(0,P.Z)(["\n  padding: 0 5px;\n"]))),vO=(0,N.Z)("div")(Xy||(Xy=(0,P.Z)(["\n  padding: 12px;\n  border-radius: 0 0 0 8px;\n  background-color: #eff2f5;\n"]))),gO=(0,N.Z)("div")(Qy||(Qy=(0,P.Z)(["\n  width: 40%;\n  min-width: 200px;\n  box-sizing: border-box;\n  padding: 12px;\n  display: flex;\n  flex-direction: column;\n"]))),bO=(0,N.Z)(ag)(nO||(nO=(0,P.Z)(["\n  display: flex;\n  flex-direction: column;\n  margin-bottom: 12px;\n\n  & > input[type='text'] {\n    display: block;\n    width: 100%;\n    box-sizing: border-box;\n    padding: 4px 16px 4px 8px;\n    border: 1px solid #cad3dd;\n    border-radius: 4px;\n    line-height: 16px;\n    font-size: 14px;\n    margin-top: 2px;\n\n    &:hover {\n      border-color: #43b5c0;\n    }\n\n    &:hover,\n    :focus {\n      box-shadow: none;\n    }\n  }\n\n  & span {\n    display: block;\n    width: 100%;\n  }\n"]))),CO=(0,N.Z)("span")(eO||(eO=(0,P.Z)(["\n  display: block;\n  width: 100%;\n  height: 24px;\n  box-sizing: border-box;\n  padding: 4px 8px;\n  border: 1px solid #cad3dd;\n  border-radius: 4px;\n  line-height: 14px;\n  font-size: 14px;\n  background-color: #eff2f5;\n  margin-top: 2px;\n"]))),yO=(0,N.Z)("div")(tO||(tO=(0,P.Z)(["\n  display: flex;\n  flex-direction: row;\n  margin-top: auto;\n  justify-content: flex-end;\n  gap: 8px;\n"]))),OO=(0,tn.iv)(rO||(rO=(0,P.Z)(["\n  width: fit-content;\n  padding: 5px 8px;\n  text-transform: none;\n  font-size: 12px;\n  line-height: 14px;\n  box-shadow: none;\n"]))),wO=(0,N.Z)(B.Z)(oO||(oO=(0,P.Z)(["\n  ","\n  background-color: #167782;\n\n  &:hover {\n    background-color: #43b5c0;\n    box-shadow: none;\n  }\n\n  &:disabled {\n    background-color: #e1e5ea;\n    color: #333333;\n  }\n"])),OO),SO=(0,N.Z)(B.Z)(iO||(iO=(0,P.Z)(["\n  ","\n  border-color: #585858;\n  color: #585858;\n\n  &:hover {\n    border-color: #333333;\n    color: #333333;\n    box-shadow: none;\n  }\n"])),OO),MO={selectionStyle:{fill:"#167782","fill-opacity":"0.28",stroke:"#167782"},hoverStyle:{stroke:"#1a7090","stroke-width":1.2},hoverStyleSimpleObject:{"stroke-opacity":.3}},xO=function(n){(0,h.Z)(i,n);var e,t,r=(e=i,t=function(){if("undefined"==typeof Reflect||!Reflect.construct)return!1;if(Reflect.construct.sham)return!1;if("function"==typeof Proxy)return!0;try{return Boolean.prototype.valueOf.call(Reflect.construct(Boolean,[],(function(){}))),!0}catch(n){return!1}}(),function(){var n,r=(0,m.Z)(e);if(t){var o=(0,m.Z)(this).constructor;n=Reflect.construct(r,arguments,o)}else n=r.apply(this,arguments);return(0,f.Z)(this,n)});function i(n){var e,t,o,a,l,s,u=n.onInit,d=(0,p.Z)(n,sO);return(0,c.Z)(this,i),(e=r.call(this)).tmpl=(t=d.tmpl,(o={struct:(a=t.struct,l=a.clone(),s=l.getCoordBoundingBox(),l.atoms.forEach((function(n){n.pp=n.pp.sub(s.min)})),l.sgroups.forEach((function(n){n.pp=n.pp?n.pp.sub(s.min):s.min})),l.rxnArrows.forEach((function(n){n.pos=n.pos.map((function(n){return n.sub(s.min)}))})),l.rxnPluses.forEach((function(n){n.pp=n.pp.sub(s.min)})),l.simpleObjects.forEach((function(n){n.pos=n.pos.map((function(n){return n.sub(s.min)}))})),l.texts.forEach((function(n){n.position=n.position.sub(s.min)})),l),props:{atomid:+t.props.atomid||0,bondid:+t.props.bondid||0}}).struct.name=t.struct.name,o),u(e.tmpl.struct.name,e.tmpl.props),e.onResult=e.onResult.bind((0,en.Z)(e)),e}return(0,s.Z)(i,[{key:"onResult",value:function(){var n=this.props,e=n.name,t=n.atomid,r=n.bondid;return e&&(e!==this.tmpl.struct.name||t!==this.tmpl.props.atomid||r!==this.tmpl.props.bondid)&&e.trim().length?{name:e,attach:{atomid:t,bondid:r}}:null}},{key:"checkIsValidName",value:function(n){return!!n&&!this.props.templateLib.some((function(e){return e.struct.name===n&&"User Templates"===e.props.group}))&&n.length<=128}},{key:"render",value:function(){var n=this,e=this.props,t=e.name;e.onNameEdit;var r=e.onAttachEdit,i=(0,p.Z)(e,uO),a=this.tmpl.struct,l=a.atoms.get(this.props.atomid)&&a.bonds.get(this.props.bondid)?this.props:this.tmpl.props,c=l.atomid,s=l.bondid,u=Object.assign(MO,this.props.globalSettings,{scale:EO(a)});return(0,o.jsx)(hO,{title:"Template edit",result:this.onResult,valid:function(){return n.props.formState.valid&&t},params:i,buttons:[],needMargin:!1,children:(0,o.jsxs)(og,pO(pO({schema:Ee,customValid:{name:function(e){return n.checkIsValidName(e)}}},this.props.formState),{},{children:[(0,o.jsxs)(vO,{children:[(0,o.jsx)(fO,{children:(0,o.jsx)(yv,{className:"structEditor",struct:a,onAttachEdit:r,tool:"attach",toolOpts:{atomid:c,bondid:s},options:u,showAttachmentPoints:!1})}),zn.isAvailable()?null:(0,o.jsx)(mO,{children:zn.warningMessage})]}),(0,o.jsxs)(gO,{children:[(0,o.jsx)(bO,{name:"name",value:t,onChange:this.props.onNameEdit,placeholder:"template"}),(0,o.jsx)("span",{children:"Selected attachment points"}),(0,o.jsxs)(CO,{children:["Atom ID: ",(0,o.jsx)("strong",{children:c})," Bond ID:"," ",(0,o.jsx)("strong",{children:s})]}),(0,o.jsxs)(yO,{children:[(0,o.jsx)(SO,{variant:"outlined",onClick:this.props.onCancel,className:cO.button,children:"Cancel"}),(0,o.jsx)(wO,{variant:"contained",onClick:function(){return n.props.onOk(n.onResult())},className:cO.button,disabled:!this.checkIsValidName(t),children:"Apply"})]})]})]}))})}}]),i}(d.Component),jO=(0,S.$j)((function(n){return pO(pO({},n.templates.attach),{},{templateLib:n.templates.lib,formState:n.modal.form,globalSettings:n.options.settings})}),(function(n){return{onInit:function(e,t){return n(function(n,e){return{type:"INIT_ATTACH",data:{name:n,atomid:e.atomid,bondid:e.bondid}}}(e,t))},onAttachEdit:function(e){return n({type:"SET_ATTACH_POINTS",data:{atomid:(t=e).atomid,bondid:t.bondid}});var t},onNameEdit:function(e){return n(function(n){return{type:"SET_TMPL_NAME",data:{name:n}}}(e))}}}))(xO);function EO(n){var e=n.getCoordBoundingBox(),t=220/Math.max(e.max.y-e.min.y,e.max.x-e.min.x);return t<35?35:t>50?50:40}var DO="TemplateTable-module_td__6LIhx",AO="TemplateTable-module_button__dpOF0",$O=["tmpl","options"];function NO(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function PO(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?NO(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):NO(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var kO=function(n){return"Salts and Solvents"===n.props.group},IO=function(n){return"Functional Groups"===n.props.group};function TO(n,e){return kO(n)?n.props.abbreviation:n.struct.name||"".concat(n.props.group," template ").concat(e+1)}var BO,LO=function(n){var e=n.tmpl,t=n.options,r=(0,p.Z)(n,$O);return(0,o.jsx)(av,PO({struct:e.struct,options:PO(PO({},t),{},{autoScaleMargin:15})},r))},_O=function(n){var e=n.templates,t=n.selected,r=n.onSelect,i=n.onDelete,a=n.onAttach,l=n.titleRows,c=void 0===l?2:l,s=(0,S.v9)((function(n){return function(n){return n.options.settings}(n)}));return(0,o.jsx)("div",{className:"".concat("TemplateTable-module_tableContent__dnVKg"," ").concat(1===c?"TemplateTable-module_oneRowTitleTable__N8Ibd":"TemplateTable-module_twoRowsTitleTable__ZYwHq"),children:e.map((function(n,e){return(0,o.jsxs)("div",{className:n.struct!==(null==t?void 0:t.struct)?DO:"".concat(DO," ").concat("TemplateTable-module_selected__qZEF9"),title:Md((l=n,c=e,kO(l)?l.props.name:l.struct.name||"".concat(l.props.group," template ").concat(c+1))),onClick:function(){return r(n)},children:[(0,o.jsx)(LO,{tmpl:n,options:s,className:"TemplateTable-module_struct__lOLBI"}),(0,o.jsx)("div",{className:"".concat("TemplateTable-module_structTitle__2XUWI"," ").concat((null==t?void 0:t.struct)===n.struct?"TemplateTable-module_selectedTitle__J-cte":""),children:Md(TO(n,e))}),"User Templates"===n.props.group&&(0,o.jsx)("button",{className:"".concat(AO," ").concat("TemplateTable-module_deleteButton__KfBpW"),onClick:function(){return i(n)},children:(0,o.jsx)(Au,{name:"delete"})}),!IO(n)&&!kO(n)&&(0,o.jsx)("button",{className:"".concat(AO," ").concat("TemplateTable-module_editButton__A0BoE"),onClick:function(){return a(n)},children:(0,o.jsx)(Au,{name:"edit"})})]},n.struct.name!==(null==t?void 0:t.struct.name)?"".concat(n.struct.name,"_").concat(e):"".concat(n.struct.name,"_").concat(e,"_selected"));var l,c}))})},VO=function(n){return n.saltsAndSolvents.lib},zO=function(n){var e=n.textInfo;return(0,o.jsxs)("div",{className:"emptySearchResult-module_emptySearch__aUSew",children:[(0,o.jsx)("p",{children:e}),(0,o.jsx)(Au,{name:"not-found"})]})},GO="Salts and Solvents",FO=["children","value","index"],HO=["filter","onFilter","onChangeGroup","mode","initialTab","functionalGroups","lib","saltsAndSolvents"];function RO(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function ZO(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?RO(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):RO(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function KO(n){var e=n.children,t=n.value,r=n.index,i=(0,p.Z)(n,FO);return(0,o.jsx)("div",ZO(ZO({className:cO.tabPanel,component:"div",role:"tabpanel",id:"scrollable-auto-tabpanel-".concat(r),"aria-labelledby":"scrollable-auto-tab-".concat(r)},i),{},{children:t===r&&e}))}function YO(n){return{id:"scrollable-auto-tab-".concat(n),"aria-controls":"scrollable-auto-tabpanel-".concat(n)}}!function(n){n[n.TemplateLibrary=0]="TemplateLibrary",n[n.FunctionalGroupLibrary=1]="FunctionalGroupLibrary",n[n.SaltsAndSolvents=2]="SaltsAndSolvents"}(BO||(BO={}));var UO=(0,ln.P1)((function(n){return n.lib}),(function(n){return n.filter}),(function(n,e){var t=e.trim(),r=new RegExp((0,y.escapeRegExp)(Md(t)),"i");return(0,y.flow)((0,y.filter)((function(n){return!t||r.test(Md(n.struct.name))||r.test(Md(n.props.group))})),(0,y.reduce)((function(n,e){return n[e.props.group]?n[e.props.group].push(e):n[e.props.group]=[e],n}),{}))(n)})),JO="Functional Groups",qO=function(){return(0,o.jsxs)("div",{className:cO.dialogHeader,children:[(0,o.jsx)(Au,{name:"template-dialog"}),(0,o.jsx)("span",{children:"Templates"})]})},WO=function(n){var e=n.data,t=n.tab,r=(0,o.jsx)("span",{children:"Click to add to canvas"});return t===BO.SaltsAndSolvents?r:(0,o.jsxs)("div",{style:{flexGrow:1,display:"flex",justifyContent:"space-between",alignItems:"center"},children:[(0,o.jsx)(Eg,{data:e,className:cO.saveButton,filename:t===BO.TemplateLibrary?"ketcher-tmpls.sdf":"ketcher-fg-tmpls.sdf",children:"Save to SDF"},"save-to-SDF"),r]})},XO=(0,S.$j)((function(n){var e,t,r;return ZO(ZO({},(0,y.omit)(["attach"],n.templates)),{},{initialTab:null===(e=n.modal)||void 0===e||null===(t=e.prop)||void 0===t?void 0:t.tab,functionalGroups:(r=n,r.functionalGroups.lib),saltsAndSolvents:VO(n)})}),(function(n,e){return{onFilter:function(e){return n(function(n){return{type:"TMPL_CHANGE_FILTER",data:{filter:n,selected:null}}}(e))},onSelect:function(t){return function(n,e,t){t(ed(null)),n&&(t(ed(n)),t(Ue({tool:"template",opts:n})),e.onOk(n))}(t,e,n)},onChangeGroup:function(e){return n(function(n){return{type:"TMPL_CHANGE_GROUP",data:{group:n,selected:null}}}(e))},onAttach:function(e){return n(function(n){return function(e,t){Xu(e,"attach",{tmpl:n}).then((function(e){n.struct.name=e?e.name.trim():n.struct.name,n.props=e?Object.assign({},n.props,e.attach):n.props,"User Templates"===n.props.group&&td(t().templates.lib)}),(function(){return null})).then((function(){return Xu(e,"templates").catch((function(){return null}))}))}}(e))},onDelete:function(e){return n(function(n){return function(e,t){var r=t().templates.lib.filter((function(e){return e!==n}));e(function(n){return{type:"TMPL_DELETE",data:{tmpl:n}}}(n)),td(r)}}(e))}}}))((function(n){var e,t=n.filter,i=n.onFilter,a=n.onChangeGroup;n.mode;var l=n.initialTab,c=n.functionalGroups,s=n.lib,h=n.saltsAndSolvents,f=(0,p.Z)(n,HO),m=(0,d.useState)(null!=l?l:BO.TemplateLibrary),v=(0,O.Z)(m,2),g=v[0],b=v[1],C=(0,d.useState)([n.group]),w=(0,O.Z)(C,2),S=w[0],M=w[1],j=function(n,e){var t=(0,d.useState)(!0),r=(0,O.Z)(t,2),o=r[0],i=r[1],a=(0,d.useRef)(null),l=(0,d.useState)(n[GO]),c=(0,O.Z)(l,2),s=c[0],u=c[1],p=(0,d.useCallback)((function(n){u((function(e){return[].concat((0,x.Z)(null!=e?e:[]),(0,x.Z)(n.splice(0,16)))})),n.length>0&&(a.current=setTimeout((function(){return p(n)}),300))}),[]);return(0,d.useEffect)((function(){var t,r=null!==(t=xd(n,e)[GO])&&void 0!==t?t:[];p(r)}),[n,p]),(0,d.useEffect)((function(){if(o)i(!1);else{clearTimeout(a.current);var t=xd(n,e)[GO];u(t)}}),[n,e]),s}(h,t),E=(0,d.useState)(c[JO]),D=(0,O.Z)(E,2),A=D[0],$=D[1],N=UO(n);(0,d.useEffect)((function(){$(xd(c,t)[JO])}),[c,t]);var P=new u.Ruh,k=(e={},(0,r.Z)(e,BO.TemplateLibrary,s),(0,r.Z)(e,BO.FunctionalGroupLibrary,c),(0,r.Z)(e,BO.SaltsAndSolvents,h),e),I=P.serialize(k[g]),T=function(e){a(e.props.group),n.onSelect(e)};return(0,o.jsxs)(Tm,{headerContent:(0,o.jsx)(qO,{}),footerContent:(0,o.jsx)(WO,{tab:g,data:I}),className:"".concat(cO.dialog_body),params:(0,y.omit)(["group"],f),buttons:[],needMargin:!1,children:[(0,o.jsxs)("div",{className:cO.inputContainer,children:[(0,o.jsx)(Zv,{className:cO.input,type:"search",value:t,onChange:function(n){return i(n)},placeholder:"Search by elements...",isFocused:!0}),(0,o.jsx)(Au,{name:"search",className:cO.searchIcon})]}),(0,o.jsxs)(cn.Z,{value:g,onChange:function(e,t){b(t),n.onSelect(null)},className:cO.tabs,children:[(0,o.jsx)(sn.Z,ZO({label:"Template Library"},YO(BO.TemplateLibrary))),(0,o.jsx)(sn.Z,ZO({label:"Functional Groups"},YO(BO.FunctionalGroupLibrary))),(0,o.jsx)(sn.Z,ZO({label:"Salts and Solvents"},YO(BO.SaltsAndSolvents)))]}),(0,o.jsxs)("div",{className:cO.tabsContent,children:[(0,o.jsx)(KO,{value:g,index:BO.TemplateLibrary,children:(0,o.jsx)("div",{children:Object.keys(N).length?Object.keys(N).map((function(e){var t,r=S.includes(e);return(0,o.jsxs)(rn.Z,{square:!0,onChange:(t=e,function(n,e){M(e?[].concat((0,x.Z)(S),[t]):(0,x.Z)(S).filter((function(n){return n!==t})))}),expanded:r,children:[(0,o.jsxs)(on.Z,{className:cO.accordionSummary,expandIcon:(0,o.jsx)(Au,{className:cO.expandIcon,name:"chevron"}),children:[(0,o.jsx)(Au,{name:"elements-group",className:cO.groupIcon}),"".concat(Md(e)," (").concat(N[e].length,")")]}),(0,o.jsx)(an.Z,{children:(0,o.jsx)(_O,{templates:r?N[e]:[],onSelect:function(n){return T(n)},selected:n.selected,onDelete:n.onDelete,onAttach:n.onAttach})})]},e)})):(0,o.jsx)("div",{className:cO.resultsContainer,children:(0,o.jsx)(zO,{textInfo:"No items found"})})})}),(0,o.jsx)(KO,{value:g,index:BO.FunctionalGroupLibrary,children:null!=A&&A.length?(0,o.jsx)("div",{className:cO.resultsContainer,children:(0,o.jsx)(_O,{titleRows:1,templates:A,onSelect:function(n){return T(n)},selected:n.selected})}):(0,o.jsx)("div",{className:cO.resultsContainer,children:(0,o.jsx)(zO,{textInfo:"No items found"})})}),(0,o.jsx)(KO,{value:g,index:BO.SaltsAndSolvents,children:null!=j&&j.length?(0,o.jsx)("div",{className:cO.resultsContainer,children:(0,o.jsx)(_O,{titleRows:1,templates:j,onSelect:function(n){return T(n)},selected:n.selected})}):(0,o.jsx)("div",{className:cO.resultsContainer,children:(0,o.jsx)(zO,{textInfo:"No items found"})})})]})]})})),QO=function(n){var e=n.editorState,t=n.setEditorState,r=n.styles,i="13px",a=(0,d.useState)(!1),l=(0,O.Z)(a,2),c=l[0],s=l[1],u=(0,d.useState)(i),p=(0,O.Z)(u,2),h=p[0],f=p[1],m=r.fontSize.current(e);(0,d.useEffect)((function(){f(m||i)}),[m]);var v=(0,y.range)(4,145),g=(0,d.useMemo)((function(){return v.map((function(n){return(0,o.jsx)("div",{className:"FontControl-module_fontSizeOption__eGz-q",onMouseDown:function(o){return function(n,o){n.preventDefault(),f(o);var i=r.fontSize.remove(e);t(r.fontSize.add(i,o)),s(!1)}(o,"".concat(n,"px"))},children:n},n)}))}),[c]);return(0,o.jsxs)("div",{children:[(0,o.jsx)("button",{className:"FontControl-module_fontBtn__zGgG3",onMouseDown:function(n){n.preventDefault(),s(!c)},children:parseFloat(h)}),c?(0,o.jsx)("div",{className:"FontControl-module_fontSizeMenu__4RvmP",children:g}):null]})},nw=function(n){var e=n.select;return(0,o.jsx)("div",{className:"SpecialSymbolsList-module_window__4tD1N",children:["α","β","γ","δ","ε","ζ","η","θ","ι","κ","λ","μ","ν","ξ","ο","π","ρ","σ","τ","υ","φ","χ","ψ","ω","℃","℉","Å","°","ħ","±","‰","√","←","→","←/","/→","↔","∏","∑","∞","∂","∆","∫","≈","=/","≤","≥"].map((function(n,t){return(0,o.jsx)("button",{className:"SpecialSymbolsList-module_button__uCp6O",value:n,onMouseDown:function(t){e(t,n)},children:(0,o.jsx)(Au,{name:n})},"symbol-".concat(t))}))})},ew=function(n){var e=n.editorState,t=n.setEditorState,r=n.styles,i=(0,d.useState)(!1),a=(0,O.Z)(i,2),l=a[0],c=a[1];return(0,o.jsxs)("div",{onBlur:function(n){n.currentTarget.contains(n.relatedTarget)||function(n){n.stopPropagation(),n.preventDefault(),c(!1)}(n)},children:[(0,o.jsx)("button",{title:"symbols",onMouseDown:function(n){n.preventDefault(),c(!l)},className:l?"SpecialSymbolsButton-module_activeTextButton__jbgHY":"SpecialSymbolsButton-module_textButton__1gh-c",children:(0,o.jsx)(Au,{name:"text-special-symbols"})}),l&&(0,o.jsx)(nw,{select:function(n,o){n.preventDefault();var i=e.getSelection(),a=e.getCurrentContent(),l=un.Modifier.replaceText(a,i,o,r),s=un.EditorState.push(e,l,"insert-characters");t(s),c(!1)}})]})},tw=function(n){return(0,o.jsx)("button",{className:(0,v.Z)("TextButton-module_textButton__Ocny2",(0,r.Z)({},"TextButton-module_isActive__DQ-xh",n.active)),title:n.button.command.toLowerCase(),onMouseDown:function(e){!function(e,t){e.preventDefault(),n.toggleStyle(t)}(e,n.button.command)},children:(0,o.jsx)(Au,{name:n.button.name})})},rw=(0,dn.ZP)(["font-size"]),ow=rw.styles,iw=rw.customStyleFn,aw=[{command:u.Cv7.Bold,name:"text-bold"},{command:u.Cv7.Italic,name:"text-italic"},{command:u.Cv7.Superscript,name:"text-superscript"},{command:u.Cv7.Subscript,name:"text-subscript"}],lw=(0,S.$j)((function(n){return{formState:n.modal}}))((function(n){var e=n.formState,t=n.position,r=n.id,i=n.content?JSON.parse(n.content):null,a=(0,d.useState)(un.EditorState.moveFocusToEnd(un.EditorState.createWithContent((0,un.convertFromRaw)(i||{blocks:[],entityMap:{}})))),l=(0,O.Z)(a,2),c=l[0],s=l[1],p=c.getCurrentInlineStyle(),h=(0,d.useCallback)((function(n){var e=c;switch(n){case u.Cv7.Subscript:p.has(u.Cv7.Superscript)&&(e=un.RichUtils.toggleInlineStyle(e,u.Cv7.Superscript));break;case u.Cv7.Superscript:p.has(u.Cv7.Subscript)&&(e=un.RichUtils.toggleInlineStyle(e,u.Cv7.Subscript))}e=un.RichUtils.toggleInlineStyle(e,n),s(e)}),[p,c]),f=(0,d.useRef)(),m=(0,d.useCallback)((function(){f.current.focus()}),[f]);return(0,d.useEffect)((function(){m()}),[m]),(0,o.jsxs)(Tm,{className:"Text-module_textEditor__EFR54",title:"Text Editor",params:n,result:function(){var n=c.getCurrentContent();return{content:n.hasText()?JSON.stringify((0,un.convertToRaw)(n)):"",position:t,id:r}},valid:function(){return e.form.valid},buttonsNameMap:{OK:"Apply"},buttons:["Cancel","OK"],withDivider:!0,children:[(0,o.jsxs)("div",{className:"Text-module_controlPanel__agLDc",onClick:m,children:[aw.map((function(n){return(0,o.jsx)(tw,{button:n,active:p.has(n.command),toggleStyle:h},n.name)})),(0,o.jsx)(ew,{editorState:c,setEditorState:s,styles:p}),(0,o.jsx)("span",{children:"Font Size"}),(0,o.jsx)(QO,{editorState:c,setEditorState:s,styles:ow})]}),(0,o.jsx)("span",{children:"Text:"}),(0,o.jsx)(un.Editor,{keyBindingFn:function(n){return"Enter"===n.key&&n.stopPropagation(),(0,un.getDefaultKeyBinding)(n)},editorState:c,onChange:function(n){s(n)},customStyleMap:{SUBSCRIPT:{verticalAlign:"sub",transform:"scale(0.7)",transformOrigin:"left"},SUPERSCRIPT:{verticalAlign:"super",transform:"scale(0.7)",transformOrigin:"left",lineHeight:0}},customStyleFn:iw,ref:f})]})})),cw={open:vC,analyse:lb,recognize:gb,"period-table":My,"extended-table":jy,rgroup:Vy,attach:jO,templates:XO,about:xv,miew:wb,atomProps:Ab,attachmentPoints:kb,automap:_b,bondProps:Fb,check:qg,enhancedStereo:$C,labelEdit:TC,rgroupLogic:Jb,removeFG:function(n){var e=(0,lp().getKetcherInstance)().editor,t=n.fgIds,r=function(e,t){n[e](t)};return(0,o.jsxs)("div",{onSubmit:function(n){return n.preventDefault()},tabIndex:-1,className:Ey,children:[(0,o.jsx)("header",{className:Ay,children:"Edit Abbreviation"}),(0,o.jsx)("div",{className:Dy,children:"A change was detected for the abbreviation. Do you want to remove the abbreviation information from the structure and continue work with separate atoms and bonds?"}),(0,o.jsxs)("footer",{className:$y,children:[(0,o.jsx)("input",{type:"button",value:"Cancel",className:Py,onClick:function(){return r("onOk",!1)}}),(0,o.jsx)("input",{type:"button",value:"Remove Abbreviation",className:Ny,onClick:function(){return r("onOk",function(){if(t.length>0){var n,r=function(n,e){var t="undefined"!=typeof Symbol&&n[Symbol.iterator]||n["@@iterator"];if(!t){if(Array.isArray(n)||(t=function(n,e){if(n){if("string"==typeof n)return ky(n,e);var t=Object.prototype.toString.call(n).slice(8,-1);return"Object"===t&&n.constructor&&(t=n.constructor.name),"Map"===t||"Set"===t?Array.from(n):"Arguments"===t||/^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(t)?ky(n,e):void 0}}(n))||e&&n&&"number"==typeof n.length){t&&(n=t);var r=0,o=function(){};return{s:o,n:function(){return r>=n.length?{done:!0}:{done:!1,value:n[r++]}},e:function(n){throw n},f:o}}throw new TypeError("Invalid attempt to iterate non-iterable instance.\nIn order to be iterable, non-array objects must have a [Symbol.iterator]() method.")}var i,a=!0,l=!1;return{s:function(){t=t.call(n)},n:function(){var n=t.next();return a=n.done,n},e:function(n){l=!0,i=n},f:function(){try{a||null==t.return||t.return()}finally{if(l)throw i}}}}(t);try{for(r.s();!(n=r.n()).done;){var o=n.value;e.update((0,u.U9$)(e.render.ctab,o))}}catch(n){r.e(n)}finally{r.f()}}return!0}())}})]})]})},save:xC,settings:zg,sgroup:lO,sdata:Zy,text:lw,confirm:function(n){var e=n.onOk,t=n.onCancel;return(0,o.jsxs)("div",{className:Ey,children:[(0,o.jsx)("header",{className:Ay,children:"Warning!"}),(0,o.jsx)("div",{className:Dy,children:"Unsupported S-group type found. Would you like to import structure without it?"}),(0,o.jsxs)("footer",{className:$y,children:[(0,o.jsx)("input",{type:"button",value:"Cancel",className:Py,onClick:function(){return t()}}),(0,o.jsx)("input",{type:"button",value:"OK",className:Ny,onClick:function(){return e()}})]})]})}},sw=["modal"];function uw(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function dw(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?uw(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):uw(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function pw(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function hw(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?pw(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):pw(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var fw=(0,S.$j)((function(n){return{modal:n.modal}}),(function(n){return{onOk:function(e){n({type:"MODAL_CLOSE"})},onCancel:function(){n({type:"MODAL_CLOSE"})}}}),(function(n,e){var t=n.modal&&n.modal.prop,r=t?(0,y.omit)(["onResult","onCancel"],t):{};return hw(hw({modal:n.modal},r),{},{onOk:function(n){t&&t.onResult&&t.onResult(n),e.onOk(n)},onCancel:function(){t&&t.onCancel&&t.onCancel(),e.onCancel()}})}))((function(n){var e=n.modal,t=(0,p.Z)(n,sw),i=(0,d.useRef)(null),a=A()({ref:i}),l=a.height,c=a.width;if(!e)return null;var s=cw[e.name];if(!s)throw new Error("There is no modal window named ".concat(e.name));return(0,o.jsx)("div",{className:(0,v.Z)("Modal-module_modalOverlay__AzVeg",$m.selectContainer),ref:i,children:(0,o.jsx)(s,dw({className:(0,v.Z)((0,r.Z)({},"Modal-module_smallScreen__nzt2L",l&&l<=600||c&&c<=600))},t))})}));function mw(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function vw(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?mw(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):mw(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}function gw(n,e){var r=(0,y.debounce)(100,(function(){return n({type:"UPDATE"})})),o=function(n){return new Promise((function(e){return setTimeout(e,n)}))};function i(n){var e=t.g.currentState,o=e.actionState.activeTool.tool;if("select"!==o){var i=e.toolbar.visibleTools.select,a=e.options.settings.resetToSelect;!0===a||a===o?n({type:"ACTION",action:Ja[i].action}):r()}}return{onInit:function(e){n({type:"INIT",editor:e})},onChange:function(e){void 0===e?o(0).then((function(){return n(i)})):n(i)},onSelectionChange:function(){r()},onElementEdit:function(t){var r="text"===t.type?t:Ne(t),o=null;if("text"===r.type)return Xu(n,"text",r);if(u.eKO.get(r.label))o=Xu(n,"atomProps",r);else if(1===Object.keys(r).length&&"ap"in r)o=Xu(n,"attachmentPoints",r.ap).then((function(n){return{ap:n}}));else if("list"===r.type||"not-list"===r.type)o=Xu(n,r.pseudo?"extended-table":"period-table",vw(vw({},r),{},{pseudo:r.pseudo}));else if("rlabel"===r.type){var i=e().editor.struct().rgroups,a={type:"atom",values:r.values,disabledIds:Array.from(i.entries()).reduce((function(n,e){var t=(0,O.Z)(e,2),o=t[0];return t[1].frags.has(r.fragId)&&n.push(o),n}),[])};o=Xu(n,"rgroup",a).then((function(n){return{values:n.values,type:"rlabel"}}))}else o=Xu(n,r.pseudo?"extended-table":"period-table",vw(vw({},r),{},{pseudo:r.pseudo}));return o.then(Pe)},onEnhancedStereoEdit:function(e){var t=(0,pn.Z)({},e);return o(0).then((function(){return t=function(n){if(null===n)return{type:null};var e=n.match(/\D+/g)[0],t=+n.replace(e,"");return e===u.YkY.Abs?{type:n,orNumber:1,andNumber:1}:e===u.YkY.And?{type:e,orNumber:1,andNumber:t}:e===u.YkY.Or?{type:e,orNumber:t,andNumber:1}:void 0}(t.stereoLabel),Xu(n,"enhancedStereo",{init:t}).then((function(n){return function(n){switch(n.type){case u.YkY.And:return"".concat(u.YkY.And).concat(n.andNumber||1);case u.YkY.Or:return"".concat(u.YkY.Or).concat(n.orNumber||1);default:return n.type}}(n)}),(function(){return null}))}))},onQuickEdit:function(e){return Xu(n,"labelEdit",e)},onBondEdit:function(e){return Xu(n,"bondProps",(t=e,{type:Le(t.type,t.stereo),topology:t.topology||0,center:t.reactingCenterStatus||0})).then(Te);var t},onRgroupEdit:function(t){var r=e().editor.struct();if(Object.keys(t).length>2){var o=Array.from(r.rgroups.keys());return t.range||(t.range=">0"),Xu(n,"rgroupLogic",Object.assign({rgroupLabels:o},t))}var i=Array.from(r.atoms.values()).reduce((function(n,e){return e.fragment===t.fragId&&null!==e.rglabel?n.concat(Ne(e).values):n}),[]),a={type:"fragment",values:[t.label],disabledIds:i};return Xu(n,"rgroup",a).then((function(n){return{label:n.values[0]}}))},onSgroupEdit:function(e){return o(0).then((function(){return Xu(n,"sgroup",Ve(e))})).then(ze)},onRemoveFG:function(e){return o(0).then((function(){return Xu(n,"removeFG",e)}))},onSdataEdit:function(e){return o(0).then((function(){return Xu(n,"DAT"===e.type?"sdata":"sgroup",Ve(e))})).then(ze)},onMessage:function(n){n.error},onAromatizeStruct:function(n){var t=e(),r=t.options.getServerSettings();return Qe(t.editor,t.server,"aromatize",r,n).catch((function(n){return t.editor.errorHandler(n)}))},onDearomatizeStruct:function(n){var t=e(),r=t.options.getServerSettings();return Qe(t.editor,t.server,"dearomatize",r,n).catch((function(n){return t.editor.errorHandler(n)}))},onMouseDown:function(){r()},onConfirm:function(){return Xu(n,"confirm")},onShowInfo:function(e){if(e){var t=e.groupStruct,r=e.event,o=e.sGroup;vd(n,{groupStruct:t,event:r,sGroup:o})}else vd(n,{groupStruct:null,event:null,sGroup:null})}}}var bw=(0,S.$j)((function(n){return{options:n.options.settings,indigoVerification:n.requestsStatuses.indigoVerification}}),(function(n){return n(gw)}))(yv),Cw=(0,_.Z)({components:{MuiButtonBase:{defaultProps:{disableRipple:!0}}}}),yw={checkServer:function(){return function(n,e){var t=e(),r=t.editor;t.server.then((function(e){return n(Rn({indigoVersion:null==e?void 0:e.indigoVersion,imagoVersions:null==e?void 0:e.imagoVersions,server:null==e?void 0:e.isAvailable}))}),(function(n){return r.errorHandler(n)}))}}},Ow=(0,S.$j)(null,yw)((function(n){var e=(0,S.I0)(),t=n.checkServer;return up(),(0,d.useEffect)((function(){var n;t(),e((n=(0,i.Z)(l().mark((function n(e){var t,r,o,i;return l().wrap((function(n){for(;;)switch(n.prev=n.next){case 0:t=u.uMq.getInstance(),r=new u.Ruh,o=r.deserialize("Ac\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    3.3951   -3.5754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6785   -3.9891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3951   -2.7480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  1  3  2  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 Ac\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nBn\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    9.2471   -6.8849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2471   -7.7119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5306   -8.1254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5306   -8.9561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2489   -9.3651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9609   -8.9523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9609   -8.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0  0  0  0\n  7  2  1  0  0  0  0\n  6  7  2  0  0  0  0\n  5  6  1  0  0  0  0\n  4  5  2  0  0  0  0\n  3  4  1  0  0  0  0\n  2  1  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 Bn\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nBoc\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  7  6  0  0  1  0  0  0  0  0999 V2000\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2500    1.2990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2500   -1.2990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7500    2.7990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7500   -0.2010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  2  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  1  0  0  0  0\n  4  7  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 Boc\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nBu\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n   12.6135   -8.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3295   -7.9183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0455   -8.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.7615   -7.9183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 Bu\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n$$$$\n\nBz\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0  0  0  0  0  0  0  0999 V2000\n    9.1980   -7.1408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1980   -7.9679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4815   -8.3813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4815   -9.2120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1998   -9.6211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9118   -9.2083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9118   -8.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9143   -6.7272    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  2  3  2  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  2  0  0  0  0\n  7  2  1  0  0  0  0\n  1  8  2  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 Bz\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nCbz\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0  0  1  0  0  0  0  0999 V2000\n    8.5563    4.7294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8554    3.9794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8554    2.4794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5563    1.7294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2573    2.4794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2573    3.9794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9582    4.7294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6592    3.9794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3602    4.7294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3602    6.2294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  1  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  9 10  2  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SMT   1 Cbz\nM  SAL   1 10   1   2   3   4   5   6   7   8   9  10\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nC2H5\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  2  1  0  0  0  0  0  0  0  0999 V2000\n    2.3125   -3.6875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0285   -3.2741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  2   1   2\nM  SMT   1 C2H5\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n$$$$\n\nCCl3\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    3.7449   -7.2954    0.0000 C   0  0  3  0  0  0  0  0  0  0  0  0\n    3.7449   -6.5524    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    4.5875   -7.2954    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    2.9179   -7.2954    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 CCl3\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n$$$$\n\nCF3\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    3.7449   -7.2954    0.0000 C   0  0  3  0  0  0  0  0  0  0  0  0\n    3.7449   -6.5524    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5875   -7.2954    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9179   -7.2954    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 CF3\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nCN\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  2  1  0  0  1  0  0  0  0  0999 V2000\n   -4.4500    5.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9500    5.0500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  3  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SMT   1 CN\nM  SAL   1 2   1   2\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nCO2Et\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    8.1962   -6.9168    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2413   -6.9167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2187   -6.3264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1736   -6.3264    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2641   -6.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\n  3  2  1  0  0  0  0\n  2  5  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   3   2   5   4\nM  SMT   1 CO2Et\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nCO2H\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n   13.6876   -8.3811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4041   -7.9673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9709   -7.9673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 CO2H\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nCO2Me\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    8.4852   -6.1758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2023   -5.7617    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9195   -6.1757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7680   -5.7617    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  1  4  2  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 CO2Me\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nCONH2\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  3  2  0  0  1  0  0  0  0  0999 V2000\n   -7.8000    3.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.0500    4.5490    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.0500    1.9510    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SMT   1 CONH2\nM  SAL   1 3   1   2   3\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nCO2Pr\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    8.2161   -8.0454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2839   -7.4545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2611   -8.0452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2386   -7.4549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3068   -8.0451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1935   -7.4549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  4  1  0  0  0  0\n  1  6  2  0  0  0  0\n  4  3  1  0  0  0  0\n  3  2  1  0  0  0  0\n  2  5  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   4   3   2   5   6\nM  SMT   1 CO2Pr\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nCO2tBu\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n   12.5930   -8.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8080   -7.2933    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1803   -8.6827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9825   -8.4678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1974   -7.6656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.7846   -8.2529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5697   -9.0550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  1  0  0  0  0\n  4  7  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 CO2tBu\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nCp\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0  0  0  0  0  0  0  0999 V2000\n    9.2500   -7.4876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5798   -7.9745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8358   -8.7624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6642   -8.7624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9202   -7.9745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  2  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  5  1  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 Cp\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nCPh3\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n 19 21  0  0  0  0  0  0  0  0999 V2000\n   15.9886   -1.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.9886    0.0188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.7001    0.4303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.7001    1.2533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.9909    1.6684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2735    1.2529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2735    0.4338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.9301   -0.7496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.5932   -1.2407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.3491   -0.9130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.4450   -0.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.7775    0.3981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.0261    0.0699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0133   -0.7081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8526    0.0987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0721    0.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4516   -0.1839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6191   -0.9941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4003   -1.2545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0  0  0  0\n  7  2  2  0  0  0  0\n  6  7  1  0  0  0  0\n  5  6  2  0  0  0  0\n  4  5  1  0  0  0  0\n  3  4  2  0  0  0  0\n  8  9  1  0  0  0  0\n 13  8  2  0  0  0  0\n 12 13  1  0  0  0  0\n 11 12  2  0  0  0  0\n 10 11  1  0  0  0  0\n  9 10  2  0  0  0  0\n 14 15  1  0  0  0  0\n 19 14  2  0  0  0  0\n 18 19  1  0  0  0  0\n 17 18  2  0  0  0  0\n 16 17  1  0  0  0  0\n 15 16  2  0  0  0  0\n  1  2  1  0  0  0  0\n  1  8  1  0  0  0  0\n  1 14  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1 15   1   2   3   4   5   6   7   8   9  10  11  12  13  14  15\nM  SAL   1  4  16  17  18  19\nM  SMT   1 CPh3\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nCy\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0  0  1  0  0  0  0  0999 V2000\n    3.9490   -2.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6500   -3.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6500   -4.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9490   -5.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2481   -4.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2481   -3.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0  0  0  0\n  2  1  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  1  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1 6   1   2   3   4   5   6\nM  SMT   1 Cy\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nEt\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  2  1  0  0  0  0  0  0  0  0999 V2000\n   13.3295   -8.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0455   -7.9183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\nG    1  0\nEt\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  2   1   2\nM  SMT   1 Et\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nFMOC\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n 17 19  0  0  1  0  0  0  0  0999 V2000\n    7.2573    3.9794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9582    4.7294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6592    3.9794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3602    4.7294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3602    6.2294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4141    2.4876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8814    2.1758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6313    3.4748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6276    4.5895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0985    3.7867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5620    5.2133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5583    6.3280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0911    6.0161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4105    1.3729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8740   -0.0537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3412   -0.3655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3449    0.7492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  1  6  1  0  0  0  0\n  6  7  2  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  2  0  0  0  0\n  9  1  1  0  0  0  0\n  8 10  1  0  0  0  0\n 10 11  2  0  0  0  0\n 11 12  1  0  0  0  0\n 12 13  2  0  0  0  0\n 13  9  1  0  0  0  0\n  6 14  1  0  0  0  0\n 14 15  2  0  0  0  0\n 15 16  1  0  0  0  0\n 16 17  2  0  0  0  0\n 17  7  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1 17   1   2   3   4   5   6   7   8   9  10  11  12  13  14  15  16  17\nM  SMT   1 FMOC\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\niBu\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    8.5340   -8.7451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2500   -8.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9660   -8.7451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2500   -7.5049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 iBu\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nIndole\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0  0  0  0  0  0  0  0999 V2000\n    6.0712   -7.3174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5571   -7.9865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0711   -8.6554    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2847   -8.3999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2847   -7.5730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5715   -7.1602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8554   -7.5733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8554   -8.4034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5732   -8.8125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  5  1  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  2  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  2  0  0  0  0\n  9  4  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  9   1   2   3   4   5   6   7   8   9\nM  SMT   1 Indole\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\niPr\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n   16.5000  -12.5433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.7840  -12.9567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.2160  -12.9567    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  1  3  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 iPr\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nMe\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  1  0  0  0  0  0  0  0  0  0999 V2000\n    9.2500   -8.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  1   1\nM  SMT   1 Me\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nMes\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0  0  1  0  0  0  0  0999 V2000\n   -0.1000    1.6571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.6500    0.3581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.6500    2.9561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.1500    0.3581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9000    1.6571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.1500    2.9561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9000    4.2552    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9000   -0.9409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  2  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  3  1  0  0  0  0\n  6  7  1  0  0  0  0\n  4  8  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1 8   1   2   3   4   5   6   7   8\nM  SMT   1 Mes\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nMs\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n   13.6876   -8.4891    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6876   -7.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5143   -8.4891    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8607   -8.4891    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  1  3  2  0  0  0  0\n  1  4  2  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 Ms\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nNCO\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    6.2976   -9.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1250   -9.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9524   -9.9063    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  2  3  2  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 NCO\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nNCS\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    7.0476   -8.8750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8750   -8.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7024   -8.8750    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  2  3  2  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 NCS\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nNHPh\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    6.5715   -5.1888    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.7479   -5.1888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3322   -4.4689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5051   -4.4689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0946   -5.1877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5086   -5.9047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3338   -5.9047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  4  2  0  0  0  0\n  2  3  1  0  0  0  0\n  7  2  2  0  0  0  0\n  6  7  1  0  0  0  0\n  5  6  2  0  0  0  0\n  4  5  1  0  0  0  0\n  1  2  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 NHPh\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nNO2\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  3  2  0  0  1  0  0  0  0  0999 V2000\n   -6.6000    4.4000    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0\n   -5.8500    5.6990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.8500    3.1010    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\nM  CHG  2   1   1   3  -1\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SMT   1 NO2\nM  SAL   1 3   1   2   3\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nOAc\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  4  3  0  0  1  0  0  0  0  0999 V2000\n   -8.0010    2.5000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.7019    3.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.4029    2.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.7019    4.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  2  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SMT   1 OAc\nM  SAL   1 4   1   2   3   4\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nOCF3\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  5  4  0  0  1  0  0  0  0  0999 V2000\n    0.0000    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    0.0000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000   -1.5000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    1.5000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  2  5  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SMT   1 OCF3\nM  SAL   1 5   1   2   3   4   5\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nOCN\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    6.2976   -8.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1250   -8.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9524   -8.1250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  3  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 OCN\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nOEt\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n   14.3514   -7.9669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6354   -8.3803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9194   -7.9669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  2  3  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 OEt\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nOMe\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  2  1  0  0  0  0  0  0  0  0999 V2000\n   13.9934   -7.9675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2774   -8.3809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  2   1   2\nM  SMT   1 OMe\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nPh\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n   14.3985   -7.7114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3985   -8.5387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6865   -8.9516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9682   -8.5424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9682   -7.7118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6847   -7.2984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  2  0  0  0  0\n  3  2  1  0  0  0  0\n  4  3  2  0  0  0  0\n  5  4  1  0  0  0  0\n  6  5  2  0  0  0  0\n  1  6  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 Ph\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nPhCOOH\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  9  9  0  0  0  0  0  0  0  0999 V2000\n   13.6014   -8.4081    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8849   -7.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.1683   -8.4081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4518   -7.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7352   -8.4081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7352   -9.2355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4518   -9.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.1683   -9.2355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8849   -7.1670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  3  2  1  0  0  0  0\n  4  3  1  0  0  0  0\n  5  4  2  0  0  0  0\n  6  5  1  0  0  0  0\n  7  6  2  0  0  0  0\n  8  7  1  0  0  0  0\n  3  8  2  0  0  0  0\n  2  9  2  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  9   1   2   3   4   5   6   7   8   9\nM  SMT   1 PhCOOH\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nPiv\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  6  5  0  0  1  0  0  0  0  0999 V2000\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2500    1.2990    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -2.5981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5490   -0.5490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.9510   -2.0490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  3  6  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SMT   1 Piv\nM  SAL   1 6   1   2   3   4   5   6\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nPO2\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    9.1697   -8.4569    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5847   -7.7424    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0\n    8.3425   -8.4569    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\nG    1  0\nM  CHG  1   2  -1\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 PO2\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nPO3\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    7.8750   -3.5505    0.0000 P   0  0  3  0  0  0  0  0  0  0  0  0\n    8.7022   -3.5505    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0\n    7.8750   -2.7234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0478   -3.5505    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  1  4  1  0  0  0  0\nG    1  0\nM  CHG  2   2  -1   4  -1\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 PO3\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nPO3H2\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  4  3  0  0  1  0  0  0  0  0999 V2000\n   -1.2500    0.8500    0.0000 P   0  0  0  0  0  5  0  0  0  0  0  0\n   -1.2500    2.3500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2500   -0.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2500    0.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SMT   1 PO3H2\nM  SAL   1 4   1   2   3   4\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nPO4\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    9.6258   -5.7188    0.0000 P   0  0  3  0  0  0  0  0  0  0  0  0\n   10.4530   -5.7188    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0\n    9.6258   -4.8916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7945   -5.7188    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0\n    9.6258   -6.5459    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  1  4  1  0  0  0  0\n  1  5  1  0  0  0  0\nG    1  0\nM  CHG  3   2  -1   4  -1   5  -1\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 PO4\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nPO4H2\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  5  4  0  0  1  0  0  0  0  0999 V2000\n   -2.7500    0.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2500    0.8500    0.0000 P   0  0  0  0  0  5  0  0  0  0  0  0\n   -1.2500    2.3500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2500   -0.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2500    0.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0  0  0  0\n  2  4  1  0  0  0  0\n  2  5  1  0  0  0  0\n  2  1  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SMT   1 PO4H2\nM  SAL   1 5   1   2   3   4   5\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nPr\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n   12.9715   -8.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6875   -7.9183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4035   -8.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 Pr\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nsBu\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    5.6730   -8.0431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9564   -8.4569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3895   -8.4569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1061   -8.0431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  1  3  1  0  0  0  0\n  3  4  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 sBu\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nSCN\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    4.9851   -6.8125    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8125   -6.8125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6399   -6.8125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  3  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 SCN\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nSO2\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    6.9189   -5.7696    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3330   -5.0545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0918   -5.7696    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  2  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 SO2\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nSO2Cl\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    8.8345   -7.9568    0.0000 S   0  0  3  0  0  0  0  0  0  0  0  0\n    9.6659   -7.9568    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    8.8345   -7.1296    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0074   -7.9568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  1  4  2  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 SO2Cl\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nSO2H\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  3  2  0  0  1  0  0  0  0  0999 V2000\n   -1.2500    0.8500    0.0000 S   0  0  0  0  0  5  0  0  0  0  0  0\n   -1.2500    2.3500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2500   -0.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  2  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SMT   1 SO2H\nM  SAL   1 3   1   2   3\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nSO3\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    9.0313   -7.9568    0.0000 S   0  0  3  0  0  0  0  0  0  0  0  0\n    9.8626   -7.9568    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0\n    9.0313   -7.1296    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2042   -7.9568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  1  4  2  0  0  0  0\nG    1  0\nM  CHG  1   2  -1\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 SO3\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nSO3H\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  4  3  0  0  1  0  0  0  0  0999 V2000\n   -1.2500    0.8500    0.0000 S   0  0  0  0  0  6  0  0  0  0  0  0\n   -1.2500    2.3500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2500   -0.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2500    0.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  2  0  0  0  0\n  1  4  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SMT   1 SO3H\nM  SAL   1 4   1   2   3   4\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nSO4\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    7.6894   -6.2813    0.0000 S   0  0  3  0  0  0  0  0  0  0  0  0\n    8.5166   -6.2813    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0\n    7.6894   -5.4541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8582   -6.2813    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6894   -7.1085    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  1  4  2  0  0  0  0\n  1  5  1  0  0  0  0\nG    1  0\nM  CHG  2   2  -1   5  -1\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 SO4\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nSO4H\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  5  4  0  0  1  0  0  0  0  0999 V2000\n   -2.7500    0.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2500    0.8500    0.0000 S   0  0  0  0  0  6  0  0  0  0  0  0\n   -1.2500    2.3500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2500   -0.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2500    0.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0  0  0  0\n  2  4  2  0  0  0  0\n  2  5  1  0  0  0  0\n  2  1  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SMT   1 SO4H\nM  SAL   1 5   1   2   3   4   5\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nster\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n17 20  0  0  0  0  0  0  0  0999 V2000\n   14.0708  -13.7848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0708  -12.9569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.7877  -12.5430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.5046  -12.9569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.5046  -13.7848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.7877  -14.1987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.2215  -14.1987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.9384  -13.7848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.9384  -12.9570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.2215  -12.5431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.2215  -11.7152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.9385  -11.3013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.6553  -11.7153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.6553  -12.5431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.4426  -12.7989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.9292  -12.1293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.4427  -11.4595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  2  3  1  0  0  0  0\n  4  3  1  0  0  0  0\n  5  4  1  0  0  0  0\n  6  5  1  0  0  0  0\n  1  6  1  0  0  0  0\n  5  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  9 10  1  0  0  0  0\n 10  4  1  0  0  0  0\n 11 10  1  0  0  0  0\n 12 11  1  0  0  0  0\n 13 12  1  0  0  0  0\n 14 13  1  0  0  0  0\n  9 14  1  0  0  0  0\n 15 14  1  0  0  0  0\n 16 15  1  0  0  0  0\n 17 16  1  0  0  0  0\n 13 17  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1 17   1   2   3   4   5   6   7   8   9  10  11  12  13  14  15  16  17\nM  SMT   1 ster\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nTBDMS\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  7  6  0  0  1  0  0  0  0  0999 V2000\n    0.0000    0.0000    0.0000 Si  0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  2  5  1  0  0  0  0\n  2  6  1  0  0  0  0\n  2  7  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SMT   1 TBDMS\nM  SAL   1 7   1   2   3   4   5   6   7\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nTBDPS\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n 17 18  0  0  1  0  0  0  0  0999 V2000\n    0.0000    0.0000    0.0000 Si  0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2990    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2990    3.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2990    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2990    3.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    4.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2990   -2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2990   -3.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2990   -2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2990   -3.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000   -4.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  2  5  1  0  0  0  0\n  1  6  1  0  0  0  0\n  7  6  1  0  0  0  0\n  7  8  2  0  0  0  0\n  6  9  2  0  0  0  0\n  9 10  1  0  0  0  0\n 10 11  2  0  0  0  0\n 11  8  1  0  0  0  0\n  1 12  1  0  0  0  0\n 13 12  1  0  0  0  0\n 13 14  2  0  0  0  0\n 12 15  2  0  0  0  0\n 15 16  1  0  0  0  0\n 16 17  2  0  0  0  0\n 17 14  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SMT   1 TBDPS\nM  SAL   1 17   1   2   3   4   5   6   7   8   9  10  11  12  13  14  15  16  17\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\ntBu\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n   13.6875   -8.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9715   -8.7451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4035   -8.7451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6875   -7.5049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\nG    1  0\ntBu\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 tBu\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nTf\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n   10.9688   -5.2936    0.0000 S   0  0  3  0  0  0  0  0  0  0  0  0\n   10.9688   -4.1127    0.0000 C   0  0  3  0  0  0  0  0  0  0  0  0\n    9.9456   -3.5220    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9688   -2.9313    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   11.9919   -3.5220    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   12.1499   -5.2936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7876   -5.2936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  2  5  1  0  0  0  0\n  1  6  2  0  0  0  0\n  1  7  2  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 Tf\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nTMS\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n  4  3  0  0  1  0  0  0  0  0999 V2000\n    1.5000    0.0000    0.0000 Si  0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SMT   1 TMS\nM  SAL   1 4   1   2   3   4\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nTos\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0  0  1  0  0  0  0  0999 V2000\n    0.0000    0.0000    0.0000 S   0  0  0  0  0  6  0  0  0  0  0  0\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    1.5000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000   -1.5000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7500   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2500    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  1  4  2  0  0  0  0\n  2  5  2  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  2  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  2  0  0  0  0\n  9  2  1  0  0  0  0\n  7 10  1  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1 10   1   2   3   4   5   6   7   8   9  10\nM  SMT   1 Tos\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n\nTs\nKetcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0  0  0  0  0  0  0  0999 V2000\n    9.2500   -9.7293    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2500   -8.9027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5318   -8.4935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5318   -7.6629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2483   -7.2495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9619   -7.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9619   -8.4898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2483   -6.4223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0768   -9.7293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4232   -9.7293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  3  2  2  0  0  0  0\n  4  3  1  0  0  0  0\n  5  4  2  0  0  0  0\n  6  5  1  0  0  0  0\n  7  6  2  0  0  0  0\n  2  7  1  0  0  0  0\n  5  8  1  0  0  0  0\n  1  9  2  0  0  0  0\n  1 10  2  0  0  0  0\nG    1  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1 10   1   2   3   4   5   6   7   8   9  10\nM  SMT   1 Ts\nM  END\n\n>  <group>\nFunctional Groups\n\n>  <atomid>\n0\n\n$$$$\n"),i=o.reduce((function(n,e){var t=e.struct;return[].concat((0,x.Z)(n),[t])}),[]),t.setFunctionalGroupsList(i),e({type:"FG_INIT",payload:{lib:o}}),e(Rn({functionalGroups:!0}));case 7:case"end":return n.stop()}}),n)}))),function(e){return n.apply(this,arguments)})),e(function(){return n=(0,i.Z)(l().mark((function n(e,t){var r,o,i,a,c,s;return l().wrap((function(n){for(;;)switch(n.prev=n.next){case 0:r=t().options.settings,o=u.o2T.getInstance(),i=u.uMq.getInstance(),a=new u.Ruh,c=a.deserialize("acetic acid\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    0.5143    0.5143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7848   -0.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8133   -0.2357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5143    2.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 acetic acid\nM  END\n>  <name>\nacetic acid\n\n>  <abbreviation>\nacetic acid\n\n>  <group>\nSalts and Solvents\n\n$$$$\nacetic anhydride\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    0.5143    0.5143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7848   -0.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8133   -0.2357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5143    2.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1123    0.5143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1124    2.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4114   -0.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\n  3  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  5  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 acetic anhydride\nM  END\n>  <name>\nacetic anhydride\n\n>  <abbreviation>\nacetic anhydride\n\n>  <group>\nSalts and Solvents\n\n$$$$\nformic acid\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    0.5143    0.5143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7848   -0.2357    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8133   -0.2357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5143    2.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 formic acid\nM  END\n>  <name>\nformic acid\n\n>  <abbreviation>\nformic acid\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethane sulphonic acid\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.5143    0.5143    0.0000 S   0  0  0  0  0  6  0  0  0  0  0  0\n    0.5143    2.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5143   -0.9857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0143    0.5143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.9857    0.5143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  2  0  0  0  0\n  1  4  1  0  0  0  0\n  1  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 methane sulphonic acid\nM  END\n>  <name>\nmethane sulphonic acid\n\n>  <abbreviation>\nmethane sulphonic acid\n\n>  <group>\nSalts and Solvents\n\n$$$$\npropionic acid\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.5143    0.5143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7848   -0.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8133   -0.2357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5143    2.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.0838    0.5143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\n  2  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 propionic acid\nM  END\n>  <name>\npropionic acid\n\n>  <abbreviation>\npropionic acid\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,2-propanediol\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n   -3.3587   -3.5057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.0597   -2.7557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.0596   -1.2558    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7606   -3.5057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5384   -2.7557    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  4  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 1,2-propanediol\nM  END\n>  <name>\n1,2-propanediol\n\n>  <abbreviation>\n1,2-propanediol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,3-propanediol\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n   15.0779   -8.5508    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   16.3769   -9.3007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.6759   -8.5507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.9750   -9.3007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   20.2740   -8.5507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 1,3-propanediol\nM  END\n>  <name>\n1,3-propanediol\n\n>  <abbreviation>\n1,3-propanediol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,4-butanediol\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n   -0.3480    1.2991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.9509    2.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2500    1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5491    2.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8481    1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1472    2.0491    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 1,4-butanediol\nM  END\n>  <name>\n1,4-butanediol\n\n>  <abbreviation>\n1,4-butanediol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1-butanol\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.1714    0.3286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.4705    1.0786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    1.0786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    0.3286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7257    1.0786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 1-butanol\nM  END\n>  <name>\n1-butanol\n\n>  <abbreviation>\n1-butanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1-propanol\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    0.1714    1.2286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7257    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 1-propanol\nM  END\n>  <name>\n1-propanol\n\n>  <abbreviation>\n1-propanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2-butanol\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.1714    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.4705    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.1714    2.7286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  1  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 2-butanol\nM  END\n>  <name>\n2-butanol\n\n>  <abbreviation>\n2-butanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2-ethylhexanol\n  -INDIGO-11302219142D\n\n  9  8  0  0  0  0  0  0  0  0999 V2000\n   10.7337    0.4167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1355    0.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8365   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5375    0.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1355    1.9167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4345   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2384   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4345    2.6667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9394    0.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  5  1  0  0  0  0\n  2  6  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  7  1  0  0  0  0\n  5  8  1  0  0  0  0\n  7  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 2-ethylhexanol\nM  END\n>  <name>\n2-ethylhexanol\n\n>  <abbreviation>\n2-ethylhexanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nisopropanol\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    0.1714    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.4705    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.1714    2.7286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 2-propanol\nM  END\n>  <name>\nisopropanol\n\n>  <abbreviation>\n2-propanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2-methoxyethanol\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.1714    0.3286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.4705    1.0786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    1.0786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    0.3286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7257    1.0786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 2-methoxyethanol\nM  END\n>  <name>\n2-methoxyethanol\n\n>  <abbreviation>\n2-methoxyethanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2-pentanol\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n   -5.1971   -3.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8980   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5991   -3.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.3000   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.0009   -3.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.3000   -1.2500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 2-pentanol\nM  END\n>  <name>\n2-pentanol\n\n>  <abbreviation>\n2-pentanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nbenzyl alcohol\n  -INDIGO-11302219142D\n\n  8  8  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000    1.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990    2.5000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  2  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  3  1  0  0  0  0\n  1  7  1  0  0  0  0\n  7  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 benzyl alcohol\nM  END\n>  <name>\nbenzyl alcohol\n\n>  <abbreviation>\nbenzyl alcohol\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncyclohexanol\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    4.2990    2.0175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2990    0.5175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -0.2325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981   -0.2325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -1.7325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981   -1.7325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2990   -2.4825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  4  6  1  0  0  0  0\n  5  7  1  0  0  0  0\n  6  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 cyclohexanol\nM  END\n>  <name>\ncyclohexanol\n\n>  <abbreviation>\ncyclohexanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nethanol\n  -INDIGO-11302219142D\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    0.1714    1.2286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 ethyl alcohol\nM  END\n>  <name>\nethanol\n\n>  <abbreviation>\nethyl alcohol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nethylene glycol\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    0.1714    1.2286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7256    0.4786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 ethane-1,2-diol\nM  END\n>  <name>\nethylene glycol\n\n>  <abbreviation>\nethane-1,2-diol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nglycerol\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    0.9915    2.6580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2906    1.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5896    2.6580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5897    4.1580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8887    1.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1878    2.6580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  5  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 glycerol\nM  END\n>  <name>\nglycerol\n\n>  <abbreviation>\nglycerol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nisoamyl alcohol\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    0.1714    0.3286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.4705    1.0786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    1.0786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    0.3286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7257    1.0786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266   -1.1714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 isoamyl alcohol\nM  END\n>  <name>\nisoamyl alcohol\n\n>  <abbreviation>\nisoamyl alcohol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nisobutanol\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.1714    1.2286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7257    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    2.7286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  3  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 isobutanol\nM  END\n>  <name>\nisobutanol\n\n>  <abbreviation>\nisobutanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethanol\n  -INDIGO-11302219142D\n\n  2  1  0  0  0  0  0  0  0  0999 V2000\n    0.0709    0.8536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5710    0.8536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  2   1   2\nM  SMT   1 methyl alcohol\nM  END\n>  <name>\nmethanol\n\n>  <abbreviation>\nmethyl alcohol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nt-butanol\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.0709    0.8536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5710    0.8536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.4291    0.8536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0709    2.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0709   -0.6464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  1  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 t-butanol\nM  END\n>  <name>\nt-butanol\n\n>  <abbreviation>\nt-butanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nwater\n  -INDIGO-11302219142D\n\n  1  0  0  0  0  0  0  0  0  0999 V2000\n    0.7500    2.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  1   1\nM  SMT   1 water\nM  END\n>  <name>\nwater\n\n>  <abbreviation>\nwater\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncarbon dioxide\n  -INDIGO-11302219142D\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n   -1.2000    0.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7000    0.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.3000    0.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 carbon dioxide\nM  END\n>  <name>\ncarbon dioxide\n\n>  <abbreviation>\ncarbon dioxide\n\n>  <group>\nSalts and Solvents\n\n$$$$\nbenzene\n  -INDIGO-11302219142D\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  2  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  3  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 benzene\nM  END\n>  <name>\nbenzene\n\n>  <abbreviation>\nbenzene\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncumene\n  -INDIGO-11302219142D\n\n  9  9  0  0  0  0  0  0  0  0999 V2000\n    4.2989    1.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2989    0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981    2.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    2.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981   -0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981   -1.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -1.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2989   -2.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  2  5  2  0  0  0  0\n  2  6  1  0  0  0  0\n  5  7  1  0  0  0  0\n  6  8  2  0  0  0  0\n  7  9  2  0  0  0  0\n  8  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 cumene\nM  END\n>  <name>\ncumene\n\n>  <abbreviation>\ncumene\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmesitylene\n  -INDIGO-11302219142D\n\n  9  9  0  0  0  0  0  0  0  0999 V2000\n    1.2991    3.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2991    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5980    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5980    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8971   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2991   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2991   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  2  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  2  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  7  9  2  0  0  0  0\n  2  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 mesitylene\nM  END\n>  <name>\nmesitylene\n\n>  <abbreviation>\nmesitylene\n\n>  <group>\nSalts and Solvents\n\n$$$$\ntoluene\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000    1.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  2  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  3  1  0  0  0  0\n  1  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 toluene\nM  END\n>  <name>\ntoluene\n\n>  <abbreviation>\ntoluene\n\n>  <group>\nSalts and Solvents\n\n$$$$\nn,n-dimethylaniline\n  -INDIGO-11302219142D\n\n  9  9  0  0  0  0  0  0  0  0999 V2000\n    4.2989    1.8750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2989    0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981   -0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981    2.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    2.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981   -1.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -1.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2989   -2.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  5  1  0  0  0  0\n  1  6  1  0  0  0  0\n  2  3  2  0  0  0  0\n  2  4  1  0  0  0  0\n  3  7  1  0  0  0  0\n  4  8  2  0  0  0  0\n  7  9  2  0  0  0  0\n  8  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 N,N-dimethylaniline\nM  END\n>  <name>\nn,n-dimethylaniline\n\n>  <abbreviation>\nN,N-dimethylaniline\n\n>  <group>\nSalts and Solvents\n\n$$$$\npyridine\n  -INDIGO-11302219142D\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  2  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  3  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 pyridine\nM  END\n>  <name>\npyridine\n\n>  <abbreviation>\npyridine\n\n>  <group>\nSalts and Solvents\n\n$$$$\ntriethylamine\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    1.5000    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2010   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7990   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7990    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0980    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.0980    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  2  5  1  0  0  0  0\n  4  6  1  0  0  0  0\n  3  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 triethylamine\nM  END\n>  <name>\ntriethylamine\n\n>  <abbreviation>\ntriethylamine\n\n>  <group>\nSalts and Solvents\n\n$$$$\nacetonitrile\n  -INDIGO-11302219142D\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  3  0  0  0  0\n  1  3  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 acetonitrile\nM  END\n>  <name>\nacetonitrile\n\n>  <abbreviation>\nacetonitrile\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndimethyl acetamide\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    2.7990    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7990    1.5000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0980   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000   -0.7500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000   -2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2009    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 dimethyl acetamide\nM  END\n>  <name>\ndimethyl acetamide\n\n>  <abbreviation>\ndimethyl acetamide\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndimethyl formamide\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    2.7990    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7990    1.5000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0980   -0.7500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000   -0.7500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000   -2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2009    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 DMF\nM  END\n>  <name>\ndimethyl formamide\n\n>  <abbreviation>\nDMF\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndimethyl sulfoxide\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    1.5000    0.0000    0.0000 S   0  0  0  0  0  4  0  0  0  0  0  0\n    0.2010   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7990   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    1.5000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 DMSO\nM  END\n>  <name>\ndimethyl sulfoxide\n\n>  <abbreviation>\nDMSO\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndimethylpropylene urea\n  -INDIGO-11302219142D\n\n  9  9  0  0  0  0  0  0  0  0999 V2000\n    3.4378    2.0544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.1388    1.3044    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    2.1387   -0.1955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.8397   -0.9455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.4593   -0.1956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.4593    1.3044    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.7584    2.0545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.8397    2.0544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.8397    3.5545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  6  8  1  0  0  0  0\n  2  8  1  0  0  0  0\n  8  9  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 dimethylpropylene urea\nM  END\n>  <name>\ndimethylpropylene urea\n\n>  <abbreviation>\ndimethylpropylene urea\n\n>  <group>\nSalts and Solvents\n\n$$$$\nformamide\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    0.2485   -6.0342    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5476   -5.2841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5476   -3.7842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.8467   -6.0341    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  2  0  0  0  0\n  2  4  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 formamide\nM  END\n>  <name>\nformamide\n\n>  <abbreviation>\nformamide\n\n>  <group>\nSalts and Solvents\n\n$$$$\nn-methyl-2-pyrrolidone\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    0.7500    2.3100    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.4600    1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9600    1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.7500    3.8100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3860    1.8953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  3  2  1  0  0  0  0\n  2  1  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  3  1  0  0  0  0\n  1  6  1  0  0  0  0\n  4  7  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 N-methyl-2-pyrrolidone\nM  END\n>  <name>\nn-methyl-2-pyrrolidone\n\n>  <abbreviation>\nN-methyl-2-pyrrolidone\n\n>  <group>\nSalts and Solvents\n\n$$$$\nn-methylformamide\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.1009    0.5500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    1.4000    1.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.4000    2.8000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6990    0.5500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1981    1.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  2  0  0  0  0\n  2  4  1  0  0  0  0\n  1  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 N-methylformamide\nM  END\n>  <name>\nn-methylformamide\n\n>  <abbreviation>\nN-methylformamide\n\n>  <group>\nSalts and Solvents\n\n$$$$\npropane nitrile\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    6.8971    0.7500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2990   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  4  3  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 propane nitrile\nM  END\n>  <name>\npropane nitrile\n\n>  <abbreviation>\npropane nitrile\n\n>  <group>\nSalts and Solvents\n\n$$$$\nsulfolane\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    0.7500    2.3100    0.0000 S   0  0  0  0  0  6  0  0  0  0  0  0\n   -0.4600    1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9600    1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    3.6090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.0673    3.5678    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  3  2  1  0  0  0  0\n  2  1  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  3  1  0  0  0  0\n  1  6  2  0  0  0  0\n  1  7  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 sulfolane\nM  END\n>  <name>\nsulfolane\n\n>  <abbreviation>\nsulfolane\n\n>  <group>\nSalts and Solvents\n\n$$$$\namyl acetate\n  -INDIGO-11302219142D\n\n  9  8  0  0  0  0  0  0  0  0999 V2000\n    5.8307    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1297   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5316   -0.3786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8307    1.8714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2326    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9335   -0.3785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.6345    0.3715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.6646   -0.3785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9636    0.3715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\n  3  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 amyl acetate\nM  END\n>  <name>\namyl acetate\n\n>  <abbreviation>\namyl acetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nbutyl acetate\n  -INDIGO-11302219142D\n\n  8  7  0  0  0  0  0  0  0  0999 V2000\n    7.5466    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8456    2.2500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9486    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6495    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2476    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.3505    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8456    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1446    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  5  1  0  0  0  0\n  1  7  1  0  0  0  0\n  2  7  2  0  0  0  0\n  3  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  4  6  1  0  0  0  0\n  7  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 butyl acetate\nM  END\n>  <name>\nbutyl acetate\n\n>  <abbreviation>\nbutyl acetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndimethyl carbonate\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    0.5429   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5429    1.1571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7562   -1.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8419   -1.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.0552   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1409   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  4  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 dimethyl carbonate\nM  END\n>  <name>\ndimethyl carbonate\n\n>  <abbreviation>\ndimethyl carbonate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nethyl acetate\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    2.7079   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7079    1.1571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0070   -1.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.4089   -1.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.1099   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1891   -1.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 ethyl acetate\nM  END\n>  <name>\nethyl acetate\n\n>  <abbreviation>\nethyl acetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nethyl formate\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    5.8087   -2.6404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8087   -1.1506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5094   -3.4018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2098   -2.6486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9103   -3.4018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1078   -3.3904    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  2  0  0  0  0\n  3  1  1  0  0  0  0\n  4  3  1  0  0  0  0\n  5  4  1  0  0  0  0\n  1  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 ethyl formate\nM  END\n>  <name>\nethyl formate\n\n>  <abbreviation>\nethyl formate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nethyl lactate\n  -INDIGO-11302219142D\n\n  8  7  0  0  0  0  0  0  0  0999 V2000\n   -0.3480    1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.9509    2.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2500    1.2991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5491    2.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5491    3.5491    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8480    1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1471    2.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8480   -0.2009    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  4  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  6  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 ethyl lactate\nM  END\n>  <name>\nethyl lactate\n\n>  <abbreviation>\nethyl lactate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nethyl propionate\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n   -0.3480    1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.9509    2.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2500    1.2991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5491    2.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5491    3.5491    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8480    1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1471    2.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  4  6  1  0  0  0  0\n  6  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 ethyl propionate\nM  END\n>  <name>\nethyl propionate\n\n>  <abbreviation>\nethyl propionate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nethylene carbonate\n  -INDIGO-11302219142D\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n    1.0323    3.5259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0323    2.0259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2458    1.1443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7823   -0.2824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2824   -0.2824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.1813    1.1443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  2  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 ethylene carbonate\nM  END\n>  <name>\nethylene carbonate\n\n>  <abbreviation>\nethylene carbonate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nisobutyl acetate\n  -INDIGO-11302219142D\n\n  8  7  0  0  0  0  0  0  0  0999 V2000\n    4.4399   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4399    1.1571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.7390   -1.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1409   -1.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8419   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5429   -1.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5429   -2.5929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7561   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  6  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 isobutyl acetate\nM  END\n>  <name>\nisobutyl acetate\n\n>  <abbreviation>\nisobutyl acetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nisopropyl acetate\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    3.1409   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1409    1.1571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4400   -1.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8419   -1.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5429   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7561   -1.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5429    1.1571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  5  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 isopropyl acetate\nM  END\n>  <name>\nisopropyl acetate\n\n>  <abbreviation>\nisopropyl acetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethyl acetate\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.5429   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5429    1.1571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7562   -1.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8419   -1.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1409   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 methyl acetate\nM  END\n>  <name>\nmethyl acetate\n\n>  <abbreviation>\nmethyl acetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethyl formate\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    1.5821   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5821    1.1571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.8812   -1.0929    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2831   -1.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.0159   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 methyl formate\nM  END\n>  <name>\nmethyl formate\n\n>  <abbreviation>\nmethyl formate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethyl lactate\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    7.6971   -2.1071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3980   -2.8571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0991   -2.1071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0991   -0.6071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8000   -2.8571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5009   -2.1071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8000   -4.3571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  2  0  0  0  0\n  3  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  5  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 methyl lactate\nM  END\n>  <name>\nmethyl lactate\n\n>  <abbreviation>\nmethyl lactate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nn-octylacetate\n  -INDIGO-11302219142D\n\n 12 11  0  0  0  0  0  0  0  0999 V2000\n    7.7009    4.9462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0000    5.6962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2991    4.9462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5980    5.6962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8971    4.9462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1962    5.6962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.4953    4.9462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.7942    5.6962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.0933    4.9462    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   19.3924    5.6962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   20.6913    4.9462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.3924    7.1962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  9 10  1  0  0  0  0\n 10 11  1  0  0  0  0\n 10 12  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  4   9  10  11  12\nM  SMT   1 n-octylacetate\nM  END\n>  <name>\nn-octylacetate\n\n>  <abbreviation>\nn-octylacetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\npropyl acetate\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    6.3403   -0.1607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6395    2.0893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7423   -0.1607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0413    0.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4433    0.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6395    0.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9385   -0.1607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  4  1  0  0  0  0\n  1  6  1  0  0  0  0\n  2  6  2  0  0  0  0\n  3  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  6  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 propyl acetate\nM  END\n>  <name>\npropyl acetate\n\n>  <abbreviation>\npropyl acetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\npropylene carbonate\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    0.5661   -1.8745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5661   -0.3746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.6474    0.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.1839    1.9338    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3160    1.9338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.1978    3.1472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7797    0.5071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  5  7  1  0  0  0  0\n  2  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 propylene carbonate\nM  END\n>  <name>\npropylene carbonate\n\n>  <abbreviation>\npropylene carbonate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nt-butyl acetate\n  -INDIGO-11302219142D\n\n  8  7  0  0  0  0  0  0  0  0999 V2000\n    6.0125   -7.4927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.7134   -6.7427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.7134   -5.2428    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4144   -7.4928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.1153   -6.7428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.8163   -5.9928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3653   -8.0418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.8653   -5.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  2  0  0  0  0\n  2  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  5  7  1  0  0  0  0\n  5  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 t-butyl acetate\nM  END\n>  <name>\nt-butyl acetate\n\n>  <abbreviation>\nt-butyl acetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,2-dimethoxyethane\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n   -0.0857    0.1714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2133   -0.5786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5124    0.1714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.3848   -0.5786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8114   -0.5786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6838    0.1714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  4  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 1,2-dimethoxyethane\nM  END\n>  <name>\n1,2-dimethoxyethane\n\n>  <abbreviation>\n1,2-dimethoxyethane\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,4-dioxane\n  -INDIGO-11302219142D\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n    3.9490   -2.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6500   -3.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6500   -4.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9490   -5.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2481   -4.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2481   -3.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0  0  0  0\n  2  1  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  1  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 1,4-dioxane\nM  END\n>  <name>\n1,4-dioxane\n\n>  <abbreviation>\n1,4-dioxane\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2-methyl tetrahydrofuran\n  -INDIGO-11302219142D\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n    0.7500    2.3100    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.4600    1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9600    1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3860    1.8953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  2  1  0  0  0  0\n  2  1  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  3  1  0  0  0  0\n  4  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 2-methyl tetrahydrofuran\nM  END\n>  <name>\n2-methyl tetrahydrofuran\n\n>  <abbreviation>\n2-methyl tetrahydrofuran\n\n>  <group>\nSalts and Solvents\n\n$$$$\nanisole\n  -INDIGO-11302219142D\n\n  8  8  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000    1.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990    2.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  2  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  3  1  0  0  0  0\n  1  7  1  0  0  0  0\n  7  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 anisole\nM  END\n>  <name>\nanisole\n\n>  <abbreviation>\nanisole\n\n>  <group>\nSalts and Solvents\n\n$$$$\nbutyl carbitol\n  -INDIGO-11302219142D\n\n 11 10  0  0  0  0  0  0  0  0999 V2000\n   -0.2227   -3.0342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0742   -3.7829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.3750   -3.0387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6719   -3.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9782   -3.0336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2751   -3.7823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5758   -3.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8728   -3.7870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1792   -3.0330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4761   -3.7817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7768   -3.0376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  9 10  1  0  0  0  0\n 10 11  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  3   9  10  11\nM  SMT   1 butyl carbitol\nM  END\n>  <name>\nbutyl carbitol\n\n>  <abbreviation>\nbutyl carbitol\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncyclopentyl methyl ether\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    6.1000    1.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010    1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990    1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5053    1.7481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.3855    0.7467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4886   -0.4632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9950   -0.6239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  5  4  1  0  0  0  0\n  4  2  1  0  0  0  0\n  2  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 cyclopentyl methyl ether\nM  END\n>  <name>\ncyclopentyl methyl ether\n\n>  <abbreviation>\ncyclopentyl methyl ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndibutyl ether\n  -INDIGO-11302219142D\n\n  9  8  0  0  0  0  0  0  0  0999 V2000\n    5.4509    4.6471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7500    3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0491    4.6471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3480    3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6470    4.6471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.9461    3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2452    4.6471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5441    3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8432    4.6471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 dibutyl ether\nM  END\n>  <name>\ndibutyl ether\n\n>  <abbreviation>\ndibutyl ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndiethyl ether\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    6.1000    1.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990    2.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010    2.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5019    1.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6980    1.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  2  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 ether\nM  END\n>  <name>\ndiethyl ether\n\n>  <abbreviation>\nether\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndiethylene glycol\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    7.7875   -1.4835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4896   -2.2328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1892   -1.4790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8854   -2.2317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5884   -1.4840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2906   -2.2333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0845   -2.2313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  7  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 diethylene glycol\nM  END\n>  <name>\ndiethylene glycol\n\n>  <abbreviation>\ndiethylene glycol\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndiglyme\n  -INDIGO-11302219142D\n\n  9  8  0  0  0  0  0  0  0  0999 V2000\n   -0.0857    0.1714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2133   -0.5786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5124    0.1714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.3848   -0.5786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8114   -0.5786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6838    0.1714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9828   -0.5786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2818    0.1714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.5809   -0.5786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  4  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 diglyme\nM  END\n>  <name>\ndiethylene glycol dimethyl ether\n\n>  <abbreviation>\ndiglyme\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndiisopropyl ether\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    5.5971    2.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2980    3.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2980    5.1000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9991    2.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7000    3.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.4009    2.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7000    5.1000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  5  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 diisopropyl ether\nM  END\n>  <name>\ndiisopropyl ether\n\n>  <abbreviation>\ndiisopropyl ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndimethyl ether\n  -INDIGO-11302219142D\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    4.2989   -0.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5980    0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9999    0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 dimethyl ether\nM  END\n>  <name>\ndimethyl ether\n\n>  <abbreviation>\ndimethyl ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndiphenyl ether\n  -INDIGO-11302219142D\n\n 13 14  0  0  0  0  0  0  0  0999 V2000\n    7.1190    1.0305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8200    0.2805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8200   -1.2196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5210   -1.9696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2219   -1.2195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2219    0.2805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5209    1.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4181    0.2804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7171    1.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0161    0.2805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0161   -1.2194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7170   -1.9694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4180   -1.2195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  2  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  2  0  0  0  0\n  2  7  1  0  0  0  0\n  1  8  1  0  0  0  0\n  8  9  2  0  0  0  0\n  9 10  1  0  0  0  0\n 10 11  2  0  0  0  0\n 11 12  1  0  0  0  0\n 12 13  2  0  0  0  0\n  8 13  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  5   9  10  11  12  13\nM  SMT   1 diphenyl ether\nM  END\n>  <name>\ndiphenyl ether\n\n>  <abbreviation>\ndiphenyl ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\nethoxybenzene\n  -INDIGO-11302219142D\n\n  9  9  0  0  0  0  0  0  0  0999 V2000\n    0.0000    6.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    4.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2991    3.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2991    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5980    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5980    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2991   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  2  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  2  0  0  0  0\n  4  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 ethoxybenzene\nM  END\n>  <name>\nethoxybenzene\n\n>  <abbreviation>\nethoxybenzene\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethyl t-butyl ether\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    6.1000    1.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010    1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990    1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5019    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0510    2.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5510   -0.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  2  5  1  0  0  0  0\n  2  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 methyl t-butyl ether\nM  END\n>  <name>\nmethyl t-butyl ether\n\n>  <abbreviation>\nmethyl t-butyl ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\nt-amyl methyl ether\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    6.8972    0.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5982    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2990   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8482    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3482   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1962    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  7  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  2  5  1  0  0  0  0\n  3  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 t-amyl methyl ether\nM  END\n>  <name>\nt-amyl methyl ether\n\n>  <abbreviation>\nt-amyl methyl ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\nt-butylethyl ether\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    2.3688   -7.1130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0698   -7.8630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.2293   -7.1129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.5283   -7.8629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8274   -8.6129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2783   -6.5639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7783   -9.1620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  1  0  0  0  0\n  4  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 t-butylethyl ether\nM  END\n>  <name>\nt-butylethyl ether\n\n>  <abbreviation>\nt-butylethyl ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\ntetrahydrofuran\n  -INDIGO-11302219142D\n\n  5  5  0  0  0  0  0  0  0  0999 V2000\n    0.7500    2.3100    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.4600    1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9600    1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  2  1  0  0  0  0\n  2  1  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  3  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 THF\nM  END\n>  <name>\ntetrahydrofuran\n\n>  <abbreviation>\nTHF\n\n>  <group>\nSalts and Solvents\n\n$$$$\ntriethylene glycol\n  -INDIGO-11302219142D\n\n 10  9  0  0  0  0  0  0  0  0999 V2000\n    4.1520    3.8971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.4509    4.6471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7500    3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0491    4.6471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3480    3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6471    4.6471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.9462    3.8971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2453    4.6471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5442    3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8433    4.6471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  9 10  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  2   9  10\nM  SMT   1 triethylene glycol\nM  END\n>  <name>\ntriethylene glycol\n\n>  <abbreviation>\ntriethylene glycol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,2,4-trichlorobenzene\n  -INDIGO-11302219142D\n\n  9  9  0  0  0  0  0  0  0  0999 V2000\n    2.2506   -3.8983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9991   -2.5989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2506   -1.2994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.7485   -1.2994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000   -2.5989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.7485   -3.8983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000   -5.1978    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    2.9991    0.0000    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  6  2  0  0  0  0\n  2  3  2  0  0  0  0\n  3  4  1  0  0  0  0\n  3  9  1  0  0  0  0\n  4  5  2  0  0  0  0\n  4  8  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 1,2,4-trichlorobenzene\nM  END\n>  <name>\n1,2,4-trichlorobenzene\n\n>  <abbreviation>\n1,2,4-trichlorobenzene\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,2-dichlorobenzene\n  -INDIGO-11302219142D\n\n  8  8  0  0  0  0  0  0  0  0999 V2000\n    0.9558   -0.8403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4581   -0.8408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2048    0.4582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4555    1.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.9571    1.7589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2065    0.4576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2078    3.0567    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    3.2060    3.0573    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  6  2  0  0  0  0\n  2  3  2  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  4  8  1  0  0  0  0\n  5  6  1  0  0  0  0\n  5  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 1,2-dichlorobenzene\nM  END\n>  <name>\n1,2-dichlorobenzene\n\n>  <abbreviation>\n1,2-dichlorobenzene\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,2-dichloroethane\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n   -0.2571    0.8286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0419    1.5786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.3409    0.8286    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n   -1.5562    1.5786    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  1  4  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 DCE\nM  END\n>  <name>\n1,2-dichloroethane\n\n>  <abbreviation>\nDCE\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2,2,2-trifluoroethanol\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    2.3661   -2.2500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0670   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0670    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0670    1.5000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.4330    0.0000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5670    0.0000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  3  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 2,2,2-trifluoroethanol\nM  END\n>  <name>\n2,2,2-trifluoroethanol\n\n>  <abbreviation>\n2,2,2-trifluoroethanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2,3,4-trifluorotoluene\n  -INDIGO-11302219142D\n\n 10 10  0  0  0  0  0  0  0  0999 V2000\n    4.0898    1.7173    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0899    1.7173    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5899   -0.8808    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0898   -0.8807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8398    0.4183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8399   -2.1798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3399    0.4182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5898   -0.8807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3399   -2.1798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0899   -0.8808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  5  1  0  0  0  0\n  2  7  1  0  0  0  0\n  3 10  1  0  0  0  0\n  4  5  2  0  0  0  0\n  4  6  1  0  0  0  0\n  4  8  1  0  0  0  0\n  5  7  1  0  0  0  0\n  6  9  2  0  0  0  0\n  7 10  2  0  0  0  0\n  9 10  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  2   9  10\nM  SMT   1 2,3,4-trifluorotoluene\nM  END\n>  <name>\n2,3,4-trifluorotoluene\n\n>  <abbreviation>\n2,3,4-trifluorotoluene\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncarbon tetrachloride\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000    1.7500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -1.2500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    7.6000    0.2500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    4.6000    0.2500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  1  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 carbon tetrachloride\nM  END\n>  <name>\ncarbon tetrachloride\n\n>  <abbreviation>\ncarbon tetrachloride\n\n>  <group>\nSalts and Solvents\n\n$$$$\nchloroacetic acid\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    9.0626   -7.0246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0626   -5.5268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3632   -7.7759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4658   -7.0246    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    7.7666   -7.7759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  2  0  0  0  0\n  3  1  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  1  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 chloroacetic acid\nM  END\n>  <name>\nchloroacetic acid\n\n>  <abbreviation>\nchloroacetic acid\n\n>  <group>\nSalts and Solvents\n\n$$$$\nchlorobenzene\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000    1.7500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  2  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  3  1  0  0  0  0\n  1  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 chlorobenzene\nM  END\n>  <name>\nchlorobenzene\n\n>  <abbreviation>\nchlorobenzene\n\n>  <group>\nSalts and Solvents\n\n$$$$\nchloroform\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000    1.7500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -1.2500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    7.6000    0.2500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6000    0.2500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  1  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 chloroform\nM  END\n>  <name>\nchloroform\n\n>  <abbreviation>\nchloroform\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndichloromethane\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -0.5000    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -0.5000    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    6.8500    1.5490    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3500    1.5490    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  1  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 DCM\nM  END\n>  <name>\ndichloromethane\n\n>  <abbreviation>\nDCM\n\n>  <group>\nSalts and Solvents\n\n$$$$\nfluorobenzene\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    1.2991    3.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2991    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5980    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5980    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2991   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  2  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  2  0  0  0  0\n  2  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 fluorobenzene\nM  END\n>  <name>\nfluorobenzene\n\n>  <abbreviation>\nfluorobenzene\n\n>  <group>\nSalts and Solvents\n\n$$$$\nperfluorocyclic ether\n  -INDIGO-11302219142D\n\n 25 25  0  0  0  0  0  0  0  0999 V2000\n   -1.9038   -6.0746    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9038   -4.5746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4038   -4.5746    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9038   -3.0746    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.4038   -4.5746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.4038   -6.0746    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.4038   -3.0746    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0962   -4.5746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0962   -6.0746    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0962   -3.0746    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5962   -4.5746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5962   -6.0746    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5962   -3.0746    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0962   -4.5746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9395   -6.0662    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9395   -3.0827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3099   -2.4726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5598   -1.1736    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5233   -1.5909    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3135   -3.5873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3173   -2.4726    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5271   -4.4689    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5635   -4.8864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7677   -5.7808    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    5.4224   -6.3797    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  2  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  5  7  1  0  0  0  0\n  5  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  8 10  1  0  0  0  0\n  8 11  1  0  0  0  0\n 11 12  1  0  0  0  0\n 11 13  1  0  0  0  0\n 11 14  1  0  0  0  0\n 14 15  1  0  0  0  0\n 14 16  1  0  0  0  0\n 16 17  1  0  0  0  0\n 17 18  1  0  0  0  0\n 17 19  1  0  0  0  0\n 17 20  1  0  0  0  0\n 20 21  1  0  0  0  0\n 20 22  1  0  0  0  0\n 20 23  1  0  0  0  0\n 14 23  1  0  0  0  0\n 23 24  1  0  0  0  0\n 23 25  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  8   9  10  11  12  13  14  15  16\nM  SAL   1  8  17  18  19  20  21  22  23  24\nM  SAL   1  1  25\nM  SMT   1 perfluorocyclic ether\nM  END\n>  <name>\nperfluorocyclic ether\n\n>  <abbreviation>\nperfluorocyclic ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\nperfluorocyclohexane\n  -INDIGO-11302219142D\n\n 18 18  0  0  0  0  0  0  0  0999 V2000\n    7.8482    2.0490    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5982    0.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5491    2.7990    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0490    2.7990    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5982   -0.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8482   -2.0490    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    0.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7500    2.0490    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0490   -2.7990    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5491   -2.7990    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7500   -2.0490    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -0.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0982    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.7991    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0982   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5000    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.7991   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5000   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1 13  1  0  0  0  0\n  2 13  1  0  0  0  0\n  3 14  1  0  0  0  0\n  4 14  1  0  0  0  0\n  5 15  1  0  0  0  0\n  6 15  1  0  0  0  0\n  7 16  1  0  0  0  0\n  8 16  1  0  0  0  0\n  9 17  1  0  0  0  0\n 10 17  1  0  0  0  0\n 11 18  1  0  0  0  0\n 12 18  1  0  0  0  0\n 13 14  1  0  0  0  0\n 13 15  1  0  0  0  0\n 14 16  1  0  0  0  0\n 15 17  1  0  0  0  0\n 16 18  1  0  0  0  0\n 17 18  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  8   9  10  11  12  13  14  15  16\nM  SAL   1  2  17  18\nM  SMT   1 perfluorocyclohexane\nM  END\n>  <name>\nperfluorocyclohexane\n\n>  <abbreviation>\nperfluorocyclohexane\n\n>  <group>\nSalts and Solvents\n\n$$$$\nperfluorohexane\n  -INDIGO-11302219142D\n\n 20 19  0  0  0  0  0  0  0  0999 V2000\n    6.1472    0.9240    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6472   -1.6740    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9463   -0.9240    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4462    1.6740    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3482   -2.4240    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8482    0.1740    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7453    2.4240    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2453   -0.1740    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0491   -3.1740    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5490   -0.5760    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -2.6250    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0444    3.1740    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5444    0.5760    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0935    2.6250    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8972   -0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1963    0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5982   -1.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4953    1.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2991   -1.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7944    1.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1 15  1  0  0  0  0\n  2 15  1  0  0  0  0\n  3 16  1  0  0  0  0\n  4 16  1  0  0  0  0\n  5 17  1  0  0  0  0\n  6 17  1  0  0  0  0\n  7 18  1  0  0  0  0\n  8 18  1  0  0  0  0\n  9 19  1  0  0  0  0\n 10 19  1  0  0  0  0\n 11 19  1  0  0  0  0\n 12 20  1  0  0  0  0\n 13 20  1  0  0  0  0\n 14 20  1  0  0  0  0\n 15 16  1  0  0  0  0\n 15 17  1  0  0  0  0\n 16 18  1  0  0  0  0\n 17 19  1  0  0  0  0\n 18 20  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  8   9  10  11  12  13  14  15  16\nM  SAL   1  4  17  18  19  20\nM  SMT   1 perfluorohexane\nM  END\n>  <name>\nperfluorohexane\n\n>  <abbreviation>\nperfluorohexane\n\n>  <group>\nSalts and Solvents\n\n$$$$\nperfluorotoluene\n  -INDIGO-11302219142D\n\n 15 15  0  0  0  0  0  0  0  0999 V2000\n    3.0000    0.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1962    0.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5982    3.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0982    2.2500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0982    2.2500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1962   -2.2500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -2.2500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5982   -3.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5982    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2990    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8972    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5982    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8972   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2990   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5982   -2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1 10  1  0  0  0  0\n  2 11  1  0  0  0  0\n  3 12  1  0  0  0  0\n  4 12  1  0  0  0  0\n  5 12  1  0  0  0  0\n  6 13  1  0  0  0  0\n  7 14  1  0  0  0  0\n  8 15  1  0  0  0  0\n  9 10  2  0  0  0  0\n  9 11  1  0  0  0  0\n  9 12  1  0  0  0  0\n 10 14  1  0  0  0  0\n 11 13  2  0  0  0  0\n 13 15  1  0  0  0  0\n 14 15  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  7   9  10  11  12  13  14  15\nM  SMT   1 perfluorotoluene\nM  END\n>  <name>\nperfluorotoluene\n\n>  <abbreviation>\nperfluorotoluene\n\n>  <group>\nSalts and Solvents\n\n$$$$\ntrichloroacetic acid\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    4.3154   -3.6247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6336   -2.8642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6336   -1.3688    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0543   -2.8010    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    3.1051   -4.3218    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    4.3090   -5.1835    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    6.9579   -3.6120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  3  2  2  0  0  0  0\n  4  1  1  0  0  0  0\n  5  1  1  0  0  0  0\n  6  1  1  0  0  0  0\n  7  2  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 trichloroacetic acid\nM  END\n>  <name>\ntrichloroacetic acid\n\n>  <abbreviation>\ntrichloroacetic acid\n\n>  <group>\nSalts and Solvents\n\n$$$$\ntrichloroacetonitrile\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    4.5000    0.0000    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    1.5000    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -1.5000    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  2  5  1  0  0  0  0\n  5  6  3  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 trichloroacetonitrile\nM  END\n>  <name>\ntrichloroacetonitrile\n\n>  <abbreviation>\ntrichloroacetonitrile\n\n>  <group>\nSalts and Solvents\n\n$$$$\ntrifluoroacetic acid\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    1.0500   -4.9991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.3000   -3.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0500   -2.4009    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2000   -3.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7000   -3.7000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2000   -2.2000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2000   -5.2000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  2  0  0  0  0\n  2  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  1  0  0  0  0\n  4  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 trifluoroacetic acid\nM  END\n>  <name>\ntrifluoroacetic acid\n\n>  <abbreviation>\ntrifluoroacetic acid\n\n>  <group>\nSalts and Solvents\n\n$$$$\ntrifluoromethylbenzene\n  -INDIGO-11302219142D\n\n 10 10  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000    1.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000    3.2500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6000    1.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6000    1.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  2  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  3  1  0  0  0  0\n  1  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  7  9  1  0  0  0  0\n  7 10  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  2   9  10\nM  SMT   1 trifluoromethylbenzene\nM  END\n>  <name>\ntrifluoromethylbenzene\n\n>  <abbreviation>\ntrifluoromethylbenzene\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2-methylpentane\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    0.5471   -1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7520   -0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.0509   -1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3500   -0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6491   -1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3500    1.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 2-methylpentane\nM  END\n>  <name>\n2-methylpentane\n\n>  <abbreviation>\n2-methylpentane\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncis-decalin\n  -INDIGO-11302219142D\n\n 12 13  0  0  1  0  0  0  0  0999 V2000\n    2.6130   -0.7481    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0\n    2.6130   -2.2234    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0\n    1.3195   -3.0026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3195    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8754    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8754   -2.9714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000   -0.7481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1948   -0.7481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1948   -2.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000   -2.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5583    0.8018    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6130   -3.6988    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  4  1  0  0  0  0\n  1  5  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  6  1  0  0  0  0\n  3 10  1  0  0  0  0\n  4  7  1  0  0  0  0\n  5  8  1  0  0  0  0\n  6  9  1  0  0  0  0\n  7 10  1  0  0  0  0\n  8  9  1  0  0  0  0\n  1 11  1  1  0  0  0\n  2 12  1  1  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  4   9  10  11  12\nM  SMT   1 cis-decalin\nM  END\n>  <name>\ncis-decalin\n\n>  <abbreviation>\ncis-decalin\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncyclohexane\n  -INDIGO-11302219142D\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n    3.9490   -2.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6500   -3.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6500   -4.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9490   -5.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2481   -4.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2481   -3.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0  0  0  0\n  2  1  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  1  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 cyclohexane\nM  END\n>  <name>\ncyclohexane\n\n>  <abbreviation>\ncyclohexane\n\n>  <group>\nSalts and Solvents\n\n$$$$\nisooctane\n  -INDIGO-11302219142D\n\n  8  7  0  0  0  0  0  0  0  0999 V2000\n    4.6062   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9052   -1.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2043   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5033   -1.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8023   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1552   -0.4581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6552   -0.4580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5033   -0.2571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  2  6  1  0  0  0  0\n  2  7  1  0  0  0  0\n  4  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 isooctane\nM  END\n>  <name>\nisooctane\n\n>  <abbreviation>\nisooctane\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethylcyclohexane\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    3.9490   -2.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6500   -3.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6500   -4.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9490   -5.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2481   -4.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2481   -3.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9490   -0.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0  0  0  0\n  2  1  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  1  1  0  0  0  0\n  1  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 methylcyclohexane\nM  END\n>  <name>\nmethylcyclohexane\n\n>  <abbreviation>\nmethylcyclohexane\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethylcyclopentane\n  -INDIGO-11302219142D\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n    4.2136    0.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.4271   -0.4776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0001   -0.4776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9636   -1.9041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4636   -1.9041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2136    1.9041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  6  1  0  0  0  0\n  2  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  4  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 methylcyclopentane\nM  END\n>  <name>\nmethylcyclopentane\n\n>  <abbreviation>\nmethylcyclopentane\n\n>  <group>\nSalts and Solvents\n\n$$$$\nheptane\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    4.6062   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9052   -1.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2043   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5033   -1.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8023   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1014   -1.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4004   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 n-heptane\nM  END\n>  <name>\nheptane\n\n>  <abbreviation>\nn-heptane\n\n>  <group>\nSalts and Solvents\n\n$$$$\nhexane\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    4.6062   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9052   -1.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2043   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5033   -1.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8023   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1014   -1.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 n-hexane\nM  END\n>  <name>\nhexane\n\n>  <abbreviation>\nn-hexane\n\n>  <group>\nSalts and Solvents\n\n$$$$\npentane\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    2.5624   -4.3230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1578   -4.3230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8600   -3.5708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4556   -3.5708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2647   -3.5708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0  0  0  0\n  3  1  1  0  0  0  0\n  4  2  1  0  0  0  0\n  5  1  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 pentane\nM  END\n>  <name>\npentane\n\n>  <abbreviation>\npentane\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2-pentanone\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n   -1.5971   -4.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.2980   -3.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0009   -4.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.3000   -3.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5991   -4.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.3000   -1.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 2-pentanone\nM  END\n>  <name>\n2-pentanone\n\n>  <abbreviation>\n2-pentanone\n\n>  <group>\nSalts and Solvents\n\n$$$$\n3-pentanone\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    2.6558    5.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9548    4.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2538    5.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2539    6.9040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5530    4.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8520    5.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  2  0  0  0  0\n  3  5  1  0  0  0  0\n  5  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 3-pentanone\nM  END\n>  <name>\n3-pentanone\n\n>  <abbreviation>\n3-pentanone\n\n>  <group>\nSalts and Solvents\n\n$$$$\nacetone\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    0.0571    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2419   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3562   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0571    1.8714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 propanone\nM  END\n>  <name>\nacetone\n\n>  <abbreviation>\npropanone\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncyclohexanone\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    0.0571    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2419   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3562   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0571    1.8714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2419   -1.8786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0571   -2.6286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3562   -1.8786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\n  2  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  3  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 cyclohexanone\nM  END\n>  <name>\ncyclohexanone\n\n>  <abbreviation>\ncyclohexanone\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncyclopentanone\n  -INDIGO-11302219142D\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n    1.0323    3.5259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0323    2.0259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2458    1.1443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7823   -0.2824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2824   -0.2824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.1813    1.1443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  2  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 cyclopentanone\nM  END\n>  <name>\ncyclopentanone\n\n>  <abbreviation>\ncyclopentanone\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethyl ethyl ketone\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.0571    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2419   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3562   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0571    1.8714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5409    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\n  2  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 MEK\nM  END\n>  <name>\nmethyl ethyl ketone\n\n>  <abbreviation>\nMEK\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethyl isobutyl ketone\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    0.0571    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2419   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3562   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0571    1.8714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5409    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8399   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5409    1.8714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\n  2  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  5  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 methyl isobutyl ketone\nM  END\n>  <name>\nmethyl isobutyl ketone\n\n>  <abbreviation>\nmethyl isobutyl ketone\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncarbon disulfide\n  -INDIGO-11302219142D\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    5.7990    0.0000    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7989    0.0000    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2989    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  3  2  0  0  0  0\n  2  3  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 carbon disulfide\nM  END\n>  <name>\ncarbon disulfide\n\n>  <abbreviation>\ncarbon disulfide\n\n>  <group>\nSalts and Solvents\n\n$$$$\nnitromethane\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    1.5009    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.8000    1.5000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0991    0.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.8000    3.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  2  0  0  0  0\nM  CHG  2   2   1   3  -1\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 nitromethane\nM  END\n>  <name>\nnitromethane\n\n>  <abbreviation>\nnitromethane\n\n>  <group>\nSalts and Solvents\n\n$$$$\no-xylene\n  -INDIGO-11302219142D\n\n  8  8  0  0  0  0  0  0  0  0999 V2000\n   -2.1500    4.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4490    3.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4490    2.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1500    1.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.8510    2.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.8510    3.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1500    5.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.4481    4.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  1  1  0  0  0  0\n  1  7  1  0  0  0  0\n  6  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 o-xylene\nM  END\n>  <name>\no-xylene\n\n>  <abbreviation>\no-xylene\n\n>  <group>\nSalts and Solvents\n\n$$$$\nm-xylene\n  -INDIGO-11302219142D\n\n  8  8  0  0  0  0  0  0  0  0999 V2000\n   -2.1500    4.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4490    3.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4490    2.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1500    1.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.8510    2.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.8510    3.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1500    5.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.4480    1.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  1  1  0  0  0  0\n  1  7  1  0  0  0  0\n  5  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 m-xylene\nM  END\n>  <name>\nm-xylene\n\n>  <abbreviation>\nm-xylene\n\n>  <group>\nSalts and Solvents\n\n$$$$\np-xylene\n  -INDIGO-11302219142D\n\n  8  8  0  0  0  0  0  0  0  0999 V2000\n   -2.1500    4.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4490    3.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4490    2.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1500    1.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.8510    2.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.8510    3.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1500    5.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1500   -0.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  1  1  0  0  0  0\n  1  7  1  0  0  0  0\n  4  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 p-xylene\nM  END\n>  <name>\np-xylene\n\n>  <abbreviation>\np-xylene\n\n>  <group>\nSalts and Solvents\n\n$$$$\nDIPEA\n  -INDIGO-11302219142D\n\n  9  8  0  0  0  0  0  0  0  0999 V2000\n   -1.5490    7.3145    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.5490    8.8145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8481    6.5645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.2500    6.5645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1471    7.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8481    5.0645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0490    7.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.2500    5.0645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8481    9.5645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  3  6  1  0  0  0  0\n  4  7  1  0  0  0  0\n  4  8  1  0  0  0  0\n  2  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 DIPEA\nM  END\n>  <name>\nn,n-diisopropylethylamine\n\n>  <abbreviation>\nDIPEA\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,5-diazabicyclo[5.4.0]undec-7-ene\n  -INDIGO-11302219142D\n\n 11 12  0  0  0  0  0  0  0  0999 V2000\n    1.6852   -0.3846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3514    1.0778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    1.7286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.3515    1.0777    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.6852   -0.3847    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1695   -0.6090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7175   -2.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7822   -3.1781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2990   -2.9545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7500   -1.5574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.7500   -1.5574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  9 10  2  3  0  0  0\n 10  5  1  0  0  0  0\n 10 11  1  0  0  0  0\n 11  1  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  3   9  10  11\nM  SMT   1 DBU\nM  END\n>  <name>\n1,5-diazabicyclo[5.4.0]undec-7-ene\n\n>  <abbreviation>\nDBU\n\n>  <group>\nSalts and Solvents\n\n$$$$\nhexamethylphosphoramide\n  -INDIGO-11302219142D\n\n 11 10  0  0  0  0  0  0  0  0999 V2000\n    2.3174   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6235   -1.9903    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8900   -0.9145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5935   -3.2519    0.0000 P   0  0  0  0  0  5  0  0  0  0  0  0\n    3.5935   -4.7619    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0831   -3.2205    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0654   -4.1562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1687   -1.9999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.1521   -3.2278    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3934   -4.5570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0626   -2.3997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  4  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  6  8  1  0  0  0  0\n  4  9  1  0  0  0  0\n  9 10  1  0  0  0  0\n  9 11  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  3   9  10  11\nM  SMT   1 HMPA\nM  END\n>  <name>\nhexamethylphosphoramide\n\n>  <abbreviation>\nHMPA\n\n>  <group>\nSalts and Solvents\n\n$$$$\nhexamethylphosphorous triamide\n  -INDIGO-11302219142D\n\n 10  9  0  0  0  0  0  0  0  0999 V2000\n    0.0007    0.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3000    0.7500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3000    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6000    0.0000    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9000    0.7500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1992    0.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9000    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6031   -1.5008    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9032   -2.2490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3053   -2.2531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  5  7  1  0  0  0  0\n  4  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  8 10  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  2   9  10\nM  SMT   1 HMPT\nM  END\n>  <name>\nhexamethylphosphorous triamide\n\n>  <abbreviation>\nHMPT\n\n>  <group>\nSalts and Solvents\n\n$$$$\nheavy water\n  -INDIGO-11302219142D\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    0.0007    0.0004    0.0000 D   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3000    0.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5993    0.0004    0.0000 D   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 D2O\nM  END\n>  <name>\nheavy water\n\n>  <abbreviation>\nD2O\n\n>  <group>\nSalts and Solvents\n\n$$$$\n"),s=c.reduce((function(n,e){var t=e.struct,r=e.props;return t.abbreviation=String(r.abbreviation),n.push(t),n}),[]),$d(s,r),o.setSaltsAndSolventsList(s),i.addToFunctionalGroupsList(s),e({type:"SALTS_AND_SOLVENTS_INIT",payload:{lib:c}}),e(Rn({saltsAndSolvents:!0}));case 11:case"end":return n.stop()}}),n)}))),function(e,t){return n.apply(this,arguments)};var n}()),window.scrollTo(0,0)}),[]),(0,o.jsx)(V.Z,{theme:Cw,children:(0,o.jsxs)("div",{className:"App-module_app__8cgyF",children:[(0,o.jsx)(Am,{}),(0,o.jsx)(bw,{className:"App-module_canvas__taJxn"}),(0,o.jsx)(Th,{className:"App-module_top__SBeSV"}),(0,o.jsx)(Dp,{className:"App-module_left__2iz-i"}),(0,o.jsx)(zd,{className:"App-module_bottom__tQA2B"}),(0,o.jsx)(ih,{className:"App-module_right__U7A5Q"}),(0,o.jsx)(Dm,{}),(0,o.jsx)(fw,{})]})})}));function ww(n,e,r,i,a){var l=function(n,e,r){var o=n.buttons,i=void 0===o?{}:o,a=(0,p.Z)(n,Bd),l={actionState:null,editor:null,modal:null,options:Object.assign(Hn,{app:a,buttons:i}),server:e||Promise.reject(new Error("Standalone mode!")),templates:rd},c=[j.Z],s=function(n){return function(e,r){switch(r.type){case"INIT":n(r.editor);case"UPDATE":r.type;var o=(0,p.Z)(r,Td);o&&(e=_d(_d({},e),o))}var i=Vd(e,_d(_d({},r),(0,y.pick)(["editor","server","options"],e))),a=i===e.shared?e:_d(_d({},e),i);return t.g.currentState=a,a}}(r);return(0,M.MT)(s,l,M.md.apply(void 0,c))}(r,i,a);l.dispatch(Sm(n)),l.dispatch((function(n,e){var t=(0,y.throttle)(250,(function(){var t=e();t.editor.render.update(),n({type:"CLEAR_VISIBLE",data:t.actionState.activeTool})}));addEventListener("resize",t)})),w.render((0,o.jsx)(S.zt,{store:l,children:(0,o.jsx)(vn.Provider,{value:{staticResourcesUrl:e},children:(0,o.jsx)(mn.Provider,{value:{errorHandler:r.errorHandler},children:(0,o.jsx)(fn.Provider,{value:{getKetcherInstance:function(){return window.ketcher}},children:(0,o.jsx)(Ow,{})})})})}),n)}var Sw=function(){function n(){(0,c.Z)(this,n),this.structService=null,this.editor=null,this.serviceMode=null,this.formatterFactory=null}var e,t;return(0,s.Z)(n,[{key:"appendApiAsync",value:(t=(0,i.Z)(l().mark((function n(e){return l().wrap((function(n){for(;;)switch(n.prev=n.next){case 0:this.structService=hn(e,{"smart-layout":!0,"ignore-stereochemistry-errors":!0,"mass-skip-error-on-pseudoatoms":!1,"gross-formula-add-rsites":!0,"aromatize-skip-superatoms":!0,"dearomatize-on-load":!1});case 1:case"end":return n.stop()}}),n,this)}))),function(n){return t.apply(this,arguments)})},{key:"appendServiceMode",value:function(n){this.serviceMode=n}},{key:"appendUiAsync",value:(e=(0,i.Z)(l().mark((function n(e,t,r,o){var i,a;return l().wrap((function(n){for(;;)switch(n.prev=n.next){case 0:return i=this.structService,n.next=3,new Promise((function(n){ww(e,t,{buttons:o||{},errorHandler:r||null,version:"2.7.2",buildDate:"2023-02-08T19:57:37",buildNumber:""},i,n)}));case 3:a=n.sent,this.editor=a,this.editor.errorHandler=r&&"function"==typeof r?r:function(){},this.formatterFactory=new u.Yyn(i);case 7:case"end":return n.stop()}}),n,this)}))),function(n,t,r,o){return e.apply(this,arguments)})},{key:"build",value:function(){if(!this.serviceMode)throw new Error("You should append ServiceMode before building");if(!this.structService)throw new Error("You should append Api before building");if(!this.formatterFactory)throw new Error("You should append StructureServiceFactory before building");var n=new u.VA(this.editor,this.structService,this.formatterFactory);n[this.serviceMode]=!0;var e=new URLSearchParams(document.location.search).get("moll");return e&&n.setMolecule(e),n}}]),n}();function Mw(){return Mw=(0,i.Z)(l().mark((function n(e){var t,r,o,i,a,c;return l().wrap((function(n){for(;;)switch(n.prev=n.next){case 0:return t=e.element,r=e.staticResourcesUrl,o=e.structServiceProvider,i=e.buttons,a=e.errorHandler,c=new Sw,n.next=4,c.appendApiAsync(o);case 4:return c.appendServiceMode(o.mode),n.next=7,c.appendUiAsync(t,r,a,i);case 7:return n.abrupt("return",c.build());case 8:case"end":return n.stop()}}),n)}))),Mw.apply(this,arguments)}var xw={"button-common-styles":"Editor-module_button-common-styles__h4pal",scrollbar:"Editor-module_scrollbar__yVsY8",small:"Editor-module_small__8cgEX",editor:"Editor-module_editor__o0Gjz","-hidden":"Editor-module_-hidden__aKodt"};function jw(n,e){var t=Object.keys(n);if(Object.getOwnPropertySymbols){var r=Object.getOwnPropertySymbols(n);e&&(r=r.filter((function(e){return Object.getOwnPropertyDescriptor(n,e).enumerable}))),t.push.apply(t,r)}return t}function Ew(n){for(var e=1;e<arguments.length;e++){var t=null!=arguments[e]?arguments[e]:{};e%2?jw(Object(t),!0).forEach((function(e){(0,r.Z)(n,e,t[e])})):Object.getOwnPropertyDescriptors?Object.defineProperties(n,Object.getOwnPropertyDescriptors(t)):jw(Object(t)).forEach((function(e){Object.defineProperty(n,e,Object.getOwnPropertyDescriptor(t,e))}))}return n}var Dw={smallWidth:1040,smallHeight:600};function Aw(n){var e=(0,d.useRef)(null),t=n.onInit,i=ip({ref:e}),a=i.height,l=i.width,c=new Event(sp);return(0,d.useEffect)((function(){(function(n){return Mw.apply(this,arguments)})(Ew(Ew({},n),{},{element:e.current})).then((function(n){"function"==typeof t&&(t(n),window.dispatchEvent(c))}))}),[]),(0,o.jsx)("div",{ref:e,className:(0,v.Z)("Ketcher-root",xw.editor,(0,r.Z)({},xw.small,a&&a<=Dw.smallHeight||l&&l<=Dw.smallWidth))})}}}]);