ketcher-react 2.18.0-rc.2 → 2.18.0-rc.3

package/dist/index.modern.js

@@ -24,7 +24,7 @@ import _asyncToGenerator from '@babel/runtime/helpers/asyncToGenerator';
 import _regeneratorRuntime from '@babel/runtime/regenerator';
 import _classCallCheck$2 from '@babel/runtime/helpers/classCallCheck';
 import _createClass$2 from '@babel/runtime/helpers/createClass';
-import { KetSerializer, MolSerializer, KetcherLogger, Ketcher, defaultBondThickness, FormatterFactory, notifyRequestCompleted, isControlKey, StereLabelStyleType, StereoColoringType, ShowHydrogenLabels, ShowHydrogenLabelNames, SettingsManager, SdfSerializer, KETCHER_SAVED_OPTIONS_KEY, Bond as Bond$2, Elements, AtomList, getAtomType, StereoLabel, isAttachmentBond, Atom as Atom$2, findStereoAtoms, RxnArrowMode, SimpleObjectMode, SGroup as SGroup$1, Pile, getStereoAtomsMap, identifyStructFormat, SupportedFormat, ChemicalMimeType, RenderStruct, Struct, MonomerMicromolecule, FunctionalGroupsProvider, SaltsAndSolventsProvider, KetcherAsyncEvents, ElementColor, Vec2, Scale, fromMultipleMove, FunctionalGroup, fromSgroupDeletion, fromFragmentDeletion, mergeMapOfItemsToSet, vectorUtils, fromBondAddition, Action, fromAtomAddition, fromAtomsAttrs, checkOverlapping, fromSeveralSgroupAddition, expandSGroupWithMultipleAttachmentPoint, SgContexts, fromSgroupAction, fromItemsFuse, ReBond, setExpandSGroup, fromBondsAttrs, OperationType, ReStruct, fromSimpleObjectResizing, fromArrowResizing, getItemsToFuse, getHoverToFuse, fromTextDeletion, fromTextUpdating, CoordinateTransformation, formatProperties, ketcherProvider, runAsyncAction, getStructure, initHotKeys, keyNorm, Fragment as Fragment$1, fromRGroupAttachmentPointUpdate, fromOneBondDeletion, bondChangingAction, fromChain, fromStereoFlagUpdate, fromOneAtomDeletion, fromArrowDeletion, fromPlusDeletion, fromSimpleObjectDeletion, fromRGroupAttachmentPointDeletion, fromPaste, fromTemplateOnAtom, RGroup as RGroup$2, fromRGroupFragment, fromUpdateIfThen, fromRGroupAttrs, fromArrowAddition, fromPlusAddition, fromRotate, fromFlip, fromSimpleObjectAddition, fromTemplateOnCanvas, fromTemplateOnBondAction, BondAttr, AtomAttr, fromTextCreation, fromHighlightCreate, fromHighlightClear, fromNewCanvas, Render, fromDescriptorsAlign, atomGetAttr, genericsList, getAtomCustomQuery, getFormatMimeTypeByFileName, getPropertiesByFormat, StereoFlag, getPropertiesByImgFormat, b64toBlob, Generics, TextCommand, DefaultStructServiceOptions } from 'ketcher-core';
+import { KetSerializer, MolSerializer, KetcherLogger, Ketcher, defaultBondThickness, FormatterFactory, notifyRequestCompleted, isControlKey, StereLabelStyleType, StereoColoringType, ShowHydrogenLabels, ShowHydrogenLabelNames, SettingsManager, SdfSerializer, KETCHER_SAVED_OPTIONS_KEY, Bond as Bond$2, Elements, AtomList, getAtomType, StereoLabel, isAttachmentBond, Atom as Atom$2, findStereoAtoms, RxnArrowMode, SimpleObjectMode, SGroup as SGroup$1, Pile, getStereoAtomsMap, identifyStructFormat, SupportedFormat, ChemicalMimeType, RenderStruct, Struct, shortcutStr, MonomerMicromolecule, FunctionalGroupsProvider, SaltsAndSolventsProvider, KetcherAsyncEvents, ElementColor, generateMenuShortcuts, Vec2, Scale, fromMultipleMove, FunctionalGroup, fromSgroupDeletion, fromFragmentDeletion, mergeMapOfItemsToSet, vectorUtils, fromBondAddition, Action, fromAtomAddition, fromAtomsAttrs, checkOverlapping, fromSeveralSgroupAddition, expandSGroupWithMultipleAttachmentPoint, SgContexts, fromSgroupAction, fromItemsFuse, ReBond, setExpandSGroup, fromBondsAttrs, OperationType, ReStruct, fromSimpleObjectResizing, fromArrowResizing, getItemsToFuse, getHoverToFuse, fromTextDeletion, fromTextUpdating, CoordinateTransformation, formatProperties, ketcherProvider, runAsyncAction, getStructure, initHotKeys, keyNorm, Fragment as Fragment$1, fromRGroupAttachmentPointUpdate, fromOneBondDeletion, bondChangingAction, fromChain, fromStereoFlagUpdate, fromOneAtomDeletion, fromArrowDeletion, fromPlusDeletion, fromSimpleObjectDeletion, fromRGroupAttachmentPointDeletion, fromPaste, fromTemplateOnAtom, RGroup as RGroup$2, fromRGroupFragment, fromUpdateIfThen, fromRGroupAttrs, fromArrowAddition, fromPlusAddition, fromRotate, fromFlip, fromSimpleObjectAddition, fromTemplateOnCanvas, fromTemplateOnBondAction, BondAttr, AtomAttr, fromTextCreation, fromHighlightCreate, fromHighlightClear, fromNewCanvas, Render, fromDescriptorsAlign, atomGetAttr, genericsList, getAtomCustomQuery, getFormatMimeTypeByFileName, getPropertiesByFormat, StereoFlag, getPropertiesByImgFormat, b64toBlob, Generics, TextCommand, DefaultStructServiceOptions } from 'ketcher-core';
 import * as React from 'react';
 import React__default, { createRef, Component, useRef, useEffect, useLayoutEffect, useState, useMemo, createElement, forwardRef, useCallback, Fragment as Fragment$2, PureComponent, lazy, Suspense } from 'react';
 import _objectWithoutProperties from '@babel/runtime/helpers/objectWithoutProperties';
@@ -36,7 +36,6 @@ import _typeof$3 from '@babel/runtime/helpers/typeof';
 import Ajv from 'ajv';
 import { pick, range, capitalize, without, omit, findLastIndex, findIndex, isEmpty, pickBy, isEqual, escapeRegExp, flow, filter, reduce, throttle, xor, debounce, upperFirst } from 'lodash/fp';
 import _toConsumableArray from '@babel/runtime/helpers/toConsumableArray';
-import { isMacOs, isIE } from 'react-device-detect';
 import styled from '@emotion/styled';
 import _taggedTemplateLiteral from '@babel/runtime/helpers/taggedTemplateLiteral';
 import * as KN from 'w3c-keyname';
@@ -45,13 +44,15 @@ import ReactDOM from 'react-dom';
 import { connect, useDispatch, useSelector, Provider } from 'react-redux';
 import { combineReducers, createStore as createStore$1, applyMiddleware } from 'redux';
 import _, { throttle as throttle$1, intersection, difference, debounce as debounce$1, cloneDeep, isEqual as isEqual$1, capitalize as capitalize$1, range as range$1, isEmpty as isEmpty$1, uniqBy } from 'lodash';
+import * as CFB from 'cfb';
 import require$$0$2 from 'util';
 import 'redux-logger';
 import thunk from 'redux-thunk';
 import useResizeObserver from 'use-resize-observer/polyfilled';
 import { useInView } from 'react-intersection-observer';
-import { IconButton as IconButton$1, Collapse, ClickAwayListener, Button as Button$1, Popover, ToggleButtonGroup, ToggleButton, createTheme, ThemeProvider } from '@mui/material';
+import { IconButton as IconButton$1, Collapse, ClickAwayListener, Button as Button$1, Popover, ToggleButtonGroup, ToggleButton, MenuList, createTheme, ThemeProvider } from '@mui/material';
 import { createSelector } from 'reselect';
+import { isIE } from 'react-device-detect';
 import _classPrivateFieldGet from '@babel/runtime/helpers/classPrivateFieldGet';
 import _classPrivateFieldSet from '@babel/runtime/helpers/classPrivateFieldSet';
 import _assertThisInitialized$2 from '@babel/runtime/helpers/assertThisInitialized';
@@ -271,8 +272,8 @@ var debugObj = {
 var classes$R = {"cliparea":"cliparea-module_cliparea__GdPrN"};
 
 function isClipboardAPIAvailable() {
-  var _navigator;
-  return typeof ((_navigator = navigator) === null || _navigator === void 0 || (_navigator = _navigator.clipboard) === null || _navigator === void 0 ? void 0 : _navigator.writeText) === 'function';
+  var _navigator, _navigator2;
+  return typeof ((_navigator = navigator) === null || _navigator === void 0 || (_navigator = _navigator.clipboard) === null || _navigator === void 0 ? void 0 : _navigator.writeText) === 'function' && typeof ((_navigator2 = navigator) === null || _navigator2 === void 0 || (_navigator2 = _navigator2.clipboard) === null || _navigator2 === void 0 ? void 0 : _navigator2.read) === 'function';
 }
 function notifyCopyCut() {
   var event = new Event('copyOrCutComplete');
@@ -286,6 +287,7 @@ function _callSuper$b(t, o, e) { return o = _getPrototypeOf$2(o), _possibleConst
 function _isNativeReflectConstruct$d() { try { var t = !Boolean.prototype.valueOf.call(Reflect.construct(Boolean, [], function () {})); } catch (t) {} return (_isNativeReflectConstruct$d = function _isNativeReflectConstruct() { return !!t; })(); }
 var ieCb = window.clipboardData;
 var CLIP_AREA_BASE_CLASS = 'cliparea';
+var needSkipCopyEvent = false;
 var ClipArea = function (_Component) {
   _inherits$2(ClipArea, _Component);
   function ClipArea(props) {
@@ -325,10 +327,20 @@ var ClipArea = function (_Component) {
               });
             });
           } else {
-            var data = _this2.props.onLegacyCopy();
-            if (data) {
-              legacyCopy(event.clipboardData, data);
+            if (needSkipCopyEvent) {
+              needSkipCopyEvent = false;
+              return;
             }
+            needSkipCopyEvent = true;
+            _this2.props.onCopy().then(function (data) {
+              addEventListener('copy', function (evt) {
+                legacyCopy(evt.clipboardData, data);
+                evt.preventDefault();
+              }, {
+                once: true
+              });
+              document.execCommand('copy');
+            });
             event.preventDefault();
           }
         },
@@ -617,8 +629,8 @@ function exec(action) {
   return enabled;
 }
 
-function ownKeys$1m(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$1m(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1m(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1m(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$1n(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$1n(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1n(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1n(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var editor = {
   resetToSelect: {
     title: 'Reset to Select Tool',
@@ -873,7 +885,7 @@ var optionsSchema = {
   title: 'Settings',
   type: 'object',
   required: [],
-  properties: _objectSpread$1m(_objectSpread$1m(_objectSpread$1m(_objectSpread$1m(_objectSpread$1m({}, editor), render), server), debug), miew)
+  properties: _objectSpread$1n(_objectSpread$1n(_objectSpread$1n(_objectSpread$1n(_objectSpread$1n({}, editor), render), server), debug), miew)
 };
 function getDefaultOptions() {
   if (!optionsSchema.properties) return {};
@@ -937,7 +949,7 @@ var storage = {
   }
 };
 
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<prerender>\nlibrary.svg#tmpl5\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Galactopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.5577    2.5236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.5577    1.0270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8542    0.2785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1466    1.0269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8543    2.5236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7171    2.0395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2039    2.1495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2039    1.4011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8543    1.0269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5004    1.4010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5004    2.1494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1466    2.5235  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 0  0  0  0  0  0  0\n   -2.8206    1.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4709    1.3185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1170    1.6927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1170    2.4410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7632    2.8152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  6     0  0\n  9  3  1  1     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl7\n\n$$$$\nalpha-D-Gulopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -2.1119    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1119    1.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4083    0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7007    1.3602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4084    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2712    2.3728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7581    2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7581    1.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4084    1.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0545    1.7344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0545    2.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7007    2.8569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  6     0  0\n  9  3  1  6     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl8\n\n$$$$\nalpha-D-Idopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.9244    2.7736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9244    1.2770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2208    0.5285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5132    1.2769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2209    2.7736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0837    2.2895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5706    2.3995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5706    1.6511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2209    1.2769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8670    1.6510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8670    2.3994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5132    2.7735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  1     0  0\n  9  3  1  6     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl9\n\n$$$$\nalpha-D-Lyxofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.1148    2.9334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6088    1.3976    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2406    1.3947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4419    3.1538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2054    2.3397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8260    2.7012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0531    2.0007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8102    2.0007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0483    2.7122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7589    2.9371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  1     0  0\n  8  3  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl10\n\n$$$$\nalpha-D-Lyxopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.4513    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4513    1.3186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7520    0.5702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0444    1.3185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7521    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1017    2.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1017    1.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7521    1.3185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3940    1.6927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3940    2.4410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 10  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  1     0  0\n  8  3  1  1     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl11\n\n$$$$\nalpha-D-Mannopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -2.1577    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1577    1.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4542    0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7466    1.3602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4543    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3171    2.3728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8039    2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8039    1.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4543    1.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1004    1.7344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1004    2.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7466    2.8569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  1     0  0\n  9  3  1  1     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl12\n\n$$$$\nalpha-D-Psicofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   15.0740   -8.2784    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3759   -8.9026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7463  -10.3149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5700  -10.3189    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6353   -7.9706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2665   -9.0586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1656   -7.8559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4589   -8.5718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1574   -9.5078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.1460   -9.5078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8298   -8.5571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8731   -8.2544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  1     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  6     0  0\n  9  3  1  6     0  0\n  8  2  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl13\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Ribofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -1.8940    2.7251    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3879    1.1893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0198    1.1863    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2211    2.9455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9845    2.1313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6051    2.4928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8322    1.7924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5894    1.7924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8274    2.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5381    2.7288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  6     0  0\n  8  3  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl14\n\n$$$$\nalpha-D-Ribopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.1138    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1138    1.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4145    0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7069    1.3602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4146    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7642    2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7642    1.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4146    1.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0565    1.7344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0565    2.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 10  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  6     0  0\n  8  3  1  6     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl15\n\n$$$$\nalpha-D-Sorbofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.6290    2.6125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1517    2.1450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6232    1.0874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2529    1.0845    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4552    2.8429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2290    2.0282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3092    2.9289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8384    2.3927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0642    1.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8216    1.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0626    2.4037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7789    2.6304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  0     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  1     0  0\n  9  3  1  6     0  0\n  8  2  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl16\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Tagatofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.3790    2.4875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9017    2.0200    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3732    0.9624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0029    0.9595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2052    2.7179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9790    1.9032    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.0592    2.8039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5884    2.2677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8142    1.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5716    1.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8126    2.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5289    2.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  0     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  1     0  0\n  9  3  1  1     0  0\n  8  2  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl17\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Talopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.9910    2.9403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9910    1.4436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2875    0.6952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5799    1.4435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2834    2.9403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1462    2.4562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6372    2.5661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6372    1.8178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2834    1.4435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9337    1.8177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9337    2.5660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5799    2.9402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  1     0  0\n  9  3  1  1     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl18\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Threofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     1  0            999 V2000\n   -2.8117    2.6835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3057    1.1476    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9335    1.1447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1388    2.9039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5229    2.4513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7458    1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5029    1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7410    2.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  8  4  1  0     0  0\n  8  7  1  0     0  0\n  4  5  1  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  1  1  6     0  0\n  6  2  1  1     0  0\n  7  3  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl19\n\n$$$$\nalpha-D-Xylofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.1648    2.8084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6588    1.2726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2948    1.2697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4919    3.0288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2554    2.2147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8760    2.5762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0989    1.8757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8560    1.8757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0983    2.5872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8048    2.8121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  6     0  0\n  8  3  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl20\n\n$$$$\nalpha-D-Xylopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.5429    3.0236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5429    1.5270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8396    0.7785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1360    1.5270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8396    3.0236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1934    2.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1934    1.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8396    1.5270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4899    1.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4899    2.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  5 10  1  0     0  0\n 10  9  1  0     0  0\n  9  8  1  0     0  0\n  8  7  1  0     0  0\n  7  6  1  0     0  0\n  6  5  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  6     0  0\n  8  3  1  1     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl21\n\n$$$$\nCyclopenta-1,3-diene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    9.6696   -5.8045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6696   -4.9328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4243   -4.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1804   -4.9328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1804   -5.8045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  1  5  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl22\n\n>  <atomid>\n2\n\n>  <bondid>\n1\n\n$$$$\n1H-indene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    7.1899   -4.2253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1899   -5.2247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0555   -5.7254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9228   -5.2247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9228   -4.2253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0555   -3.7246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8731   -5.5332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4601   -4.7242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8731   -3.9149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  6  1  0     0  0\n  1  6  2  0     0  0\n  4  7  1  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  5  9  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl23\n\n>  <atomid>\n6\n\n>  <bondid>\n7\n\n$$$$\nNaphtalene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n   11.0090   -4.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1429   -5.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1429   -6.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0090   -6.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8751   -6.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8751   -5.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7410   -4.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7410   -6.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6071   -6.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6071   -5.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  6  2  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  8  1  0     0  0\n  7 10  2  0     0  0\n  8  9  2  0     0  0\n  9 10  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl24\n\n>  <atomid>\n6\n\n>  <bondid>\n10\n\n$$$$\nAzulene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n   12.4941   -7.5235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2759   -5.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4941   -5.2765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5192   -5.4990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0853   -6.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5192   -7.3010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2270   -5.5909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2759   -6.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2270   -7.2090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8147   -6.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  8  2  0     0  0\n  1  6  1  0     0  0\n  2  3  1  0     0  0\n  3  4  2  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  7  2  2  0     0  0\n  7 10  1  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n  2  8  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl25\n\n>  <atomid>\n4\n\n>  <bondid>\n4\n\n$$$$\nE-Stilbene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 15  0     0  0            999 V2000\n   10.8250   -2.9010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8250   -2.9010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3250   -3.7670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8249   -4.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8249   -4.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3250   -3.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3250   -3.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8250   -4.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8250   -4.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3250   -5.4990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3250   -5.4990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8250   -4.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3250   -3.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3250   -3.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  6  2  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n 14  9  1  0     0  0\n 10  9  2  0     0  0\n 10 11  1  0     0  0\n 11 12  2  0     0  0\n 12 13  1  0     0  0\n 13 14  2  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl26\n\n>  <atomid>\n2\n\n>  <bondid>\n3\n\n$$$$\nZ-Stilbene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 15  0     0  0            999 V2000\n   12.3750   -3.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3750   -3.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8750   -4.7581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3749   -5.6240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3749   -5.6240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8750   -4.7580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8750   -3.0260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8750   -3.0260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3750   -3.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8750   -4.7580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3750   -5.6240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3750   -5.6240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8750   -4.7581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3750   -3.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  6  2  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  6  1  0     0  0\n  1  7  1  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  9 14  2  0     0  0\n 10 11  2  0     0  0\n 11 12  1  0     0  0\n 12 13  2  0     0  0\n 13 14  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl27\n\n>  <atomid>\n3\n\n>  <bondid>\n3\n\n$$$$\nAnthracene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 16  0     0  0            999 V2000\n    8.0930   -3.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2269   -3.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2269   -4.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0930   -5.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9591   -4.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9591   -3.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8250   -3.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8250   -5.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6911   -4.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6911   -3.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5571   -3.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5571   -5.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4231   -4.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4231   -3.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  6  2  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  8  1  0     0  0\n  7 10  2  0     0  0\n  8  9  2  0     0  0\n 11 10  1  0     0  0\n  9 10  1  0     0  0\n  9 12  1  0     0  0\n 11 14  2  0     0  0\n 12 13  2  0     0  0\n 13 14  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl28\n\n>  <atomid>\n10\n\n>  <bondid>\n15\n\n$$$$\nPhenantrene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 16  0     0  0            999 V2000\n   10.7760   -1.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9099   -2.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9099   -3.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7760   -3.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6420   -3.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6420   -2.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5080   -1.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5080   -3.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3740   -3.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3740   -2.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5080   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3740   -5.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2401   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2401   -3.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  6  2  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  8  1  0     0  0\n  7 10  2  0     0  0\n  9 10  1  0     0  0\n  8 11  2  0     0  0\n  8  9  1  0     0  0\n  9 14  2  0     0  0\n 11 12  1  0     0  0\n 12 13  2  0     0  0\n 13 14  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl29\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nPyrene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 16 19  0     0  0            999 V2000\n   13.2084   -1.8748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2084   -2.8736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0732   -3.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.9399   -2.8736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.9399   -1.8748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0732   -1.3745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0732   -4.3744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.9399   -4.8747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8066   -4.3744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8066   -3.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3434   -3.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3434   -4.3726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2084   -4.8729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2065   -5.8752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0732   -6.3755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.9399   -5.8752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  6  1  0     0  0\n  3  7  2  0     0  0\n  7  8  1  0     0  0\n  8  9  2  0     0  0\n  9 10  1  0     0  0\n  4 10  2  0     0  0\n  2 11  1  0     0  0\n 11 12  2  0     0  0\n 12 13  1  0     0  0\n  7 13  1  0     0  0\n 13 14  2  0     0  0\n 14 15  1  0     0  0\n 15 16  2  0     0  0\n  8 16  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl30\n\n>  <atomid>\n10\n\n>  <bondid>\n12\n\n$$$$\nTriphenylene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 21  0     0  0            999 V2000\n   10.5140   -3.4503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5140   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3807   -4.9503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2474   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2474   -3.4503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3807   -2.9497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6491   -2.9516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7859   -3.4503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7859   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6491   -4.9467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1141   -2.9497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1141   -1.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2474   -1.4481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3807   -1.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3807   -5.9514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2474   -6.4519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1141   -5.9514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1141   -4.9503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  2  3  1  0     0  0\n  3  4  2  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  6  1  0     0  0\n  1  7  1  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n  2 10  1  0     0  0\n  5 11  1  0     0  0\n 11 12  2  0     0  0\n 12 13  1  0     0  0\n 13 14  2  0     0  0\n  6 14  1  0     0  0\n  3 15  1  0     0  0\n 15 16  2  0     0  0\n 16 17  1  0     0  0\n 17 18  2  0     0  0\n  4 18  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl31\n\n>  <atomid>\n7\n\n>  <bondid>\n8\n\n$$$$\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   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 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$$$$\nALA-D-Alanine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  5  0     1  0            999 V2000\n   13.6701   -6.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6701   -5.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8003   -5.3251    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5335   -5.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5335   -4.3254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3999   -5.8240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  1     0  0\n  2  4  1  0     0  0\n  4  5  2  0     0  0\n  4  6  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl117\n\n>  <atomid>\n2\n\n>  <bondid>\n0\n\n$$$$\nARG-D-Arginine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   12.0694   -4.2443    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7765   -4.9514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5148   -5.9202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5506   -6.1773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2934   -7.1415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3248   -7.4032    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0676   -8.3674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1033   -8.6246    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7747   -9.0745    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7407   -4.6943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0024   -3.7255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4467   -5.4025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2 10  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  7  9  2  0     0  0\n 10 11  2  0     0  0\n 10 12  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl118\n\n>  <atomid>\n0\n\n>  <bondid>\n7\n\n$$$$\nASN-D-Asparagine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   10.8319   -5.4762    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6977   -5.9761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6989   -6.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8342   -7.4719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8321   -8.4753    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9683   -6.9719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5657   -5.4726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5645   -4.4747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4317   -5.9725    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  7  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  4  6  2  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl119\n\n>  <atomid>\n0\n\n>  <bondid>\n4\n\n$$$$\nASP-D-Aspartic acid\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   10.7814   -5.6761    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6474   -6.1761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6486   -7.1739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7839   -7.6718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7818   -8.6752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9179   -7.1719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5154   -5.6726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5142   -4.6748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3821   -6.1711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  7  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  4  6  2  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl120\n\n>  <atomid>\n0\n\n>  <bondid>\n4\n\n$$$$\nCYS-D-Cysteine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  6  0     1  0            999 V2000\n    6.9511   -4.7004    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8205   -5.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8205   -6.1991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9511   -6.6987    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6834   -4.7004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6834   -3.7013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5489   -5.1995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  5  1  0     0  0\n  3  4  1  0     0  0\n  5  6  2  0     0  0\n  5  7  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl121\n\n>  <atomid>\n0\n\n>  <bondid>\n3\n\n$$$$\nGLN-D-Glutamine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   11.1341   -5.3758    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0002   -5.8759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0015   -6.8739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1332   -7.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1344   -8.3757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2695   -8.8736    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0006   -8.8757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8652   -5.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8673   -4.3743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7305   -5.8794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  5  7  2  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl122\n\n>  <atomid>\n0\n\n>  <bondid>\n5\n\n$$$$\nGLU-D-Glutamic acid\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   11.4591   -5.3259    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3252   -5.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3265   -6.8240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4582   -7.3276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4594   -8.3256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5945   -8.8236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3256   -8.8257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1902   -5.3279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1923   -4.3243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0555   -5.8295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  5  7  2  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl123\n\n>  <atomid>\n0\n\n>  <bondid>\n5\n\n$$$$\nGLY-Glycine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  4  0     0  0            999 V2000\n   10.6670   -7.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5331   -6.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8010   -6.8750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3990   -7.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5331   -5.8750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  2  5  2  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl124\n\n>  <atomid>\n2\n\n>  <bondid>\n1\n\n$$$$\nHIS-D-Histidine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 11  0     1  0            999 V2000\n   11.4910   -6.5739    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3584   -7.0771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3572   -8.0742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4919   -8.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3861   -9.5713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4100   -9.7753    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9104   -8.9099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5750   -8.1667    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2237   -6.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2217   -5.5747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0896   -7.0762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  9  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4  8  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  2  0     0  0\n  9 10  2  0     0  0\n  9 11  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl125\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nILE-D-Isoleucine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   11.8001   -9.8252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8020   -8.8218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6668   -8.3239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5327   -8.8239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6656   -7.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7997   -6.8261    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5336   -6.8225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5324   -5.8248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4003   -7.3211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  6     0  0\n  3  5  1  0     0  0\n  5  6  1  1     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl126\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nLEU-D-Leucine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   12.2568   -9.3502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2588   -8.3468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3929   -7.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1235   -7.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1224   -6.8511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2564   -6.3511    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9903   -6.3475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9891   -5.3498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8571   -6.8461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  2  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  1     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl127\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nLYS-D-Lysine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   10.6692   -9.3254    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6712   -8.3221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5358   -7.8243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5346   -6.8266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4025   -6.3233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4013   -5.3256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5355   -4.8257    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2659   -4.8278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2679   -3.8246    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1308   -5.3291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  1     0  0\n  6  8  1  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl128\n\n>  <atomid>\n6\n\n>  <bondid>\n0\n\n$$$$\nMET-D-Methionine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   11.6195   -9.8247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4844   -9.3267    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4832   -8.3287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3515   -7.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3502   -6.8270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4841   -6.3270    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2152   -6.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2173   -5.3253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0805   -6.8304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  1     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl129\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nPHE-D-Phenylalanine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 11  0     1  0            999 V2000\n   12.5510   -6.0250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -6.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -6.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -5.0250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.1490   -6.5249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -7.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5510   -8.0249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5510   -9.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -9.5250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -9.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -8.0249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  6  1  0     0  0\n  3  4  2  0     0  0\n  3  5  1  0     0  0\n  6  7  1  0     0  0\n  6 11  2  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n 10 11  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl130\n\n>  <atomid>\n0\n\n>  <bondid>\n4\n\n$$$$\nPRO-D-Proline\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     1  0            999 V2000\n   10.6969   -1.7001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6956   -2.6978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8298   -3.1977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7240   -4.1958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7473   -4.3999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2474   -3.5340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9124   -2.7903    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4026   -3.4047    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  3  2  1  1     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  3  7  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl131\n\n>  <atomid>\n6\n\n>  <bondid>\n2\n\n$$$$\nSER-D-Serine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  6  0     1  0            999 V2000\n   10.3261   -6.8754    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1955   -7.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1955   -8.3741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3261   -8.8737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0584   -6.8754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0584   -5.8763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9239   -7.3745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  5  1  0     0  0\n  3  4  1  0     0  0\n  5  6  2  0     0  0\n  5  7  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl132\n\n>  <atomid>\n0\n\n>  <bondid>\n3\n\n$$$$\nTHR-D-Threonine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   11.5255   -8.1243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3953   -7.6246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -8.1243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3953   -6.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5255   -6.1252    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -6.1252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -5.1257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1245   -6.6245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  1     0  0\n  2  4  1  0     0  0\n  4  5  1  1     0  0\n  4  6  1  0     0  0\n  6  7  2  0     0  0\n  6  8  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl133\n\n>  <atomid>\n4\n\n>  <bondid>\n0\n\n$$$$\nTRP-D-Tryptophan\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 15 16  0     1  0            999 V2000\n   11.9929   -5.3065    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8877   -5.7594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9408   -6.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0974   -7.3028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1680   -6.9465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5350   -7.7214    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0834   -8.5631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0497   -8.3041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7565   -9.0092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4968   -9.9732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5306  -10.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8239   -9.5270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7230   -5.2128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6717   -4.2179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6150   -5.6658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2 13  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4  8  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  2  0     0  0\n  7 12  1  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n 10 11  1  0     0  0\n 11 12  2  0     0  0\n 13 14  2  0     0  0\n 13 15  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl134\n\n>  <atomid>\n0\n\n>  <bondid>\n15\n\n$$$$\nTYR-D-Tyrosine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 13 13  0     1  0            999 V2000\n   12.5019   -5.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3670   -6.3231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3658   -7.3212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4995   -7.8214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5016   -8.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6354   -9.3253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7671   -8.8216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9008   -9.3217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7683   -7.8234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6344   -7.3233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2333   -5.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2344   -4.8247    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0992   -6.3235    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2 11  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4 10  1  0     0  0\n  5  6  1  0     0  0\n  6  7  2  0     0  0\n  7  8  1  0     0  0\n  7  9  1  0     0  0\n  9 10  2  0     0  0\n 11 12  2  0     0  0\n 11 13  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl135\n\n>  <atomid>\n0\n\n>  <bondid>\n8\n\n$$$$\nVAL-D-Valine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   10.8255   -8.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6953   -8.4496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -8.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6953   -7.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8255   -6.9502    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -6.9502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -5.9506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4245   -7.4494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  2  4  1  0     0  0\n  4  5  1  1     0  0\n  4  6  1  0     0  0\n  6  7  2  0     0  0\n  6  8  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl136\n\n>  <atomid>\n4\n\n>  <bondid>\n0\n\n$$$$\nD-Allose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.4194   -1.6883    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9924   -1.0905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4387   -0.4664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0204    0.1639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4629    0.7656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0221    1.3609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4407    1.9808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1127    2.6517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2718    1.3426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2093    0.7656    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2702    0.1833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1849   -0.4782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  6     0  0\n  5 10  1  1     0  0\n  4 11  1  6     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl137\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Altrose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.4516   -1.2975    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0245   -0.6997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4709   -0.0714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0525    0.5547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4950    1.1564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0501    1.7518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4729    2.3717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1448    3.0442    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3040    1.7335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2414    1.1564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3024    0.5742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2171   -0.0873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  1     0  0\n  5 10  1  1     0  0\n  4 11  1  6     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl138\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Arabinose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -3.8949   -0.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4593    0.4968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8995    1.1253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4675    1.7484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9005    2.3460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4667    2.9613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4723   -0.7154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7192    1.7520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6437    1.1253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7111    0.4839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  7  1  0     0  0\n  4  8  1  1     0  0\n  3  9  1  1     0  0\n  2 10  1  6     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl139\n\n>  <atomid>\n6\n\n>  <bondid>\n5\n\n$$$$\nD-Erythrose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   -4.1906    0.0133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7523    0.6006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1844    1.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7532    1.8545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1786    2.4581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7458    3.0700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0034    1.8545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9299    1.2384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  4  7  1  6     0  0\n  3  8  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl140\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Erythrulose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   -4.1896    2.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7907    1.5002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2449    0.8939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8481    0.2611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7539    2.6818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0537    1.4794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9812    0.9226    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3557   -0.3786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  1  5  1  0     0  0\n  2  6  2  0     0  0\n  3  7  1  1     0  0\n  8  4  1  0     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl141\n\n>  <atomid>\n4\n\n>  <bondid>\n3\n\n$$$$\nD-Fructose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.1480    1.9843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5728    1.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1297    0.7648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5540    0.1353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1105   -0.4649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5532   -1.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1339   -1.6816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5796    2.5934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3170    1.3875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3814    0.7735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2979    0.1190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3622   -0.4638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  1  8  1  0     0  0\n  2  9  2  0     0  0\n  3 10  1  1     0  0\n  4 11  1  1     0  0\n  5 12  1  6     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl142\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\nD-Galactose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.8880   -0.9644    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4609   -0.3663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9072    0.2619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4890    0.8881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9315    1.4898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4907    2.0852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9093    2.7051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5812    3.3773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7403    2.0668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6779    1.4898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7387    0.9075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6535    0.2459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  6     0  0\n  5 10  1  6     0  0\n  4 11  1  1     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl143\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Glucose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.5186   -1.2143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9457   -0.6164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4995    0.0120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9178    0.6380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4754    1.2399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9163    1.8351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4978    2.4551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8217    3.1274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6624    1.8167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7249    1.2399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6639    0.6573    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7491   -0.0039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  1     0  0\n  5 10  1  1     0  0\n  4 11  1  1     0  0\n  3 12  1  6     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl144\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Gulose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -4.3047   -1.0894    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8775   -0.4913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3239    0.1369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9056    0.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3481    1.3648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9073    1.9602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3260    2.5801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9978    3.2523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1570    1.9418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0945    1.3648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1554    0.7825    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0702    0.1209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  6     0  0\n  5 10  1  1     0  0\n  4 11  1  1     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl145\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Idose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.7380   -1.2977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3109   -0.6997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7572   -0.0715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3390    0.5547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7815    1.1564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3407    1.7519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7593    2.3718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4312    3.0440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5903    1.7335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5279    1.1564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5887    0.5742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5035   -0.0874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  1     0  0\n  5 10  1  1     0  0\n  4 11  1  1     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl146\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Lyxose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -3.9033    0.3647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3348    0.9551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8987    1.5836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3307    2.2068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8977    2.8043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3273    3.4196    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3259   -0.2571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0749    2.2103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1504    1.5836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0829    0.9422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  7  1  0     0  0\n  4  8  1  6     0  0\n  3  9  1  1     0  0\n  2 10  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl147\n\n>  <atomid>\n6\n\n>  <bondid>\n5\n\n$$$$\nD-Mannose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.9005   -1.2560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4734   -0.6580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9197   -0.0298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5015    0.5964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9440    1.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5032    1.7935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9218    2.4134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5937    3.0856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7528    1.7751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6904    1.1981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7512    0.6158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6660   -0.0458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  1     0  0\n  5 10  1  6     0  0\n  4 11  1  6     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl148\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Psicose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -4.1455    2.7364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7122    2.1393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1459    1.5125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7164    0.8867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1511    0.2825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6999   -0.3115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1099   -0.9416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7230    3.3500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9598    2.1522    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8942    1.5125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9639    0.8833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8992    0.2707    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  1  8  1  0     0  0\n  2  9  2  0     0  0\n  3 10  1  1     0  0\n  4 11  1  6     0  0\n  5 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl149\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\nD-Ribose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -3.4471   -0.1770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8828    0.4134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4426    1.0421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8747    1.6651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4417    2.2627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8713    2.8780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8696   -0.7989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6188    1.6686    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6943    1.0421    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6268    0.4006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  7  1  0     0  0\n  4  8  1  1     0  0\n  3  9  1  6     0  0\n  2 10  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl150\n\n>  <atomid>\n6\n\n>  <bondid>\n5\n\n$$$$\nD-Ribulose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -3.1689   -0.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6004    0.0509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1643    0.6794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5963    1.3026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1633    1.9001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5929    2.5154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4160    0.6794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5914   -1.1613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3485    0.0380    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3252    1.2997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  3  7  1  6     0  0\n  1  8  1  0     0  0\n  2  9  1  1     0  0\n  4 10  2  0     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl151\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\nD-Sorbose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.8077    2.3989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3743    1.8060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8123    1.1791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3785    0.5576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8133   -0.0508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3620   -0.6406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7721   -1.2667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3851    3.0166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6219    1.8147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5564    1.1791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6301    0.5499    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5573   -0.0626    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  1  8  1  0     0  0\n  2  9  2  0     0  0\n  3 10  1  1     0  0\n  4 11  1  1     0  0\n  5 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl152\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\nD-Tagatose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -5.3565    3.2050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7786    2.4087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3570    1.5726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7842    0.7381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3640   -0.0678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7622   -0.8600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3090   -1.7005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7930    4.0234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7752    2.4259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3552    1.5726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7806    0.7334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3619   -0.0835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  1  8  1  0     0  0\n  2  9  2  0     0  0\n  3 10  1  6     0  0\n  4 11  1  1     0  0\n  5 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl153\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\nD-Talose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -4.0547   -0.8394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6275   -0.2413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0739    0.3869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6556    1.0131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0981    1.6148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6573    2.2102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0760    2.8301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7478    3.5023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9070    2.1918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8445    1.6148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9054    1.0325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8202    0.3709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  1     0  0\n  5 10  1  6     0  0\n  4 11  1  1     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl154\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Threose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   -4.7339    0.2599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3006    0.8540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7343    1.4815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3045    2.1079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7353    2.7047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3079    3.3192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5548    2.1114    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.4800    1.4815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  4  7  1  1     0  0\n  3  8  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl155\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Xylose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -3.7801   -0.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2157    0.4968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7755    1.1253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2075    1.7484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7745    2.3460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2083    2.9613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2027   -0.7154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9517    1.7520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0272    1.1253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9597    0.4839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  7  1  0     0  0\n  4  8  1  1     0  0\n  3  9  1  1     0  0\n  2 10  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl156\n\n>  <atomid>\n6\n\n>  <bondid>\n5\n\n$$$$\nD-Xylulose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -2.9398   -0.2937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3754    0.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9352    0.9336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3672    1.5568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9342    2.1584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3638    2.7737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1827    0.9336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3623   -0.9196    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1235    0.2880    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1002    1.5539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  3  7  1  1     0  0\n  1  8  1  0     0  0\n  2  9  1  1     0  0\n  4 10  2  0     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <prerender>\nlibrary.svg#tmpl157\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\n1_2_3-Oxadiazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl158\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nDioxane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    4.2090   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2090   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -4.7018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -3.0482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl159\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nFuran\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl160\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nImidazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl161\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nIndole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    6.3344   -5.9612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7641   -5.9608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0506   -5.5480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7641   -6.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3344   -6.7915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0524   -7.2005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4800   -7.2028    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1974   -6.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1974   -5.9608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\n  8  9  2  0     0  0\n  7  8  1  0     0  0\n  2  9  1  0     0  0\n  4  7  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl162\n\n>  <atomid>\n6\n\n>  <bondid>\n6\n\n$$$$\nIsoquinoline\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    7.2094   -5.7112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6391   -5.7108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9256   -5.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6391   -6.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2094   -6.5415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9274   -6.9505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3533   -5.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0698   -5.7124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3584   -6.9529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0717   -6.5353    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  2  4  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\n  8  7  2  0     0  0\n  9 10  2  0     0  0\n 10  8  1  0     0  0\n  4  9  1  0     0  0\n  2  7  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl163\n\n>  <atomid>\n8\n\n>  <bondid>\n0\n\n$$$$\nIsoxazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl164\n\n>  <atomid>\n2\n\n>  <bondid>\n0\n\n$$$$\nMorpholine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    4.2090   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2090   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -4.7018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -3.0482    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl165\n\n>  <atomid>\n5\n\n>  <bondid>\n1\n\n$$$$\nOxazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl166\n\n>  <atomid>\n4\n\n>  <bondid>\n0\n\n$$$$\nPiperazine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    4.2090   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2090   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -4.7018    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -3.0482    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl167\n\n>  <atomid>\n5\n\n>  <bondid>\n1\n\n$$$$\nPiperidine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    3.0000   -9.5098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000  -10.3366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7160  -10.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4320  -10.3366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4320   -9.5098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7160   -9.0964    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl168\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nPurine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    6.3344   -5.9612    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7641   -5.9608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0506   -5.5480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7641   -6.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3344   -6.7915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0524   -7.2005    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4800   -7.2028    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1974   -6.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1974   -5.9608    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\n  8  9  2  0     0  0\n  7  8  1  0     0  0\n  2  9  1  0     0  0\n  4  7  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl169\n\n>  <atomid>\n6\n\n>  <bondid>\n7\n\n$$$$\nPyran\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    4.2090   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2090   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -4.7018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -3.0482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl170\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nPyrazine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    6.4094   -4.0362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1256   -3.6230    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.8628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4094   -4.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1274   -5.2755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl171\n\n>  <atomid>\n0\n\n>  <bondid>\n2\n\n$$$$\nPyrazol\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl172\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nPyridazine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    6.4094   -4.0362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1256   -3.6230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.8628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4094   -4.8665    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1274   -5.2755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl173\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nPyridine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    6.4094   -4.0362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1256   -3.6230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.8628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4094   -4.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1274   -5.2755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl174\n\n>  <atomid>\n3\n\n>  <bondid>\n1\n\n$$$$\nPyridone\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  7  0     0  0            999 V2000\n    5.2590   -5.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2590   -5.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9750   -6.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6910   -5.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6910   -5.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9750   -4.5982    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5430   -4.5982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  6  1  0     0  0\n  1  7  2  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl175\n\n>  <atomid>\n5\n\n>  <bondid>\n5\n\n$$$$\nPyrimidine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    6.4094   -4.0362    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1256   -3.6230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.8628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4094   -4.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1274   -5.2755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl176\n\n>  <atomid>\n4\n\n>  <bondid>\n1\n\n$$$$\nPyrole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    3.6685  -10.0843    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -9.5986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2553   -8.8126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0817   -8.8126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3370   -9.5986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl177\n\n$$$$\nPyrone\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  7  0     0  0            999 V2000\n    5.2590   -5.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2590   -5.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9750   -6.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6910   -5.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6910   -5.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9750   -4.5982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5430   -4.5982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  6  1  0     0  0\n  1  7  2  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl178\n\n>  <atomid>\n4\n\n>  <bondid>\n4\n\n$$$$\nPyrrolidine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    3.7210   -3.9181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3632   -3.3980    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0779   -3.8107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8532   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0171   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl179\n\n>  <atomid>\n1\n\n>  <bondid>\n2\n\n$$$$\nQuinoline\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    7.2094   -5.7112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6391   -5.7108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9256   -5.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6391   -6.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2094   -6.5415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9274   -6.9505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3533   -5.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0698   -5.7124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3584   -6.9529    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0717   -6.5353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  2  4  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\n  8  7  2  0     0  0\n  9 10  2  0     0  0\n 10  8  1  0     0  0\n  4  9  1  0     0  0\n  2  7  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl180\n\n>  <atomid>\n9\n\n>  <bondid>\n8\n\n$$$$\nTetrahydrofuran\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    3.7210   -3.9181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3632   -3.3980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0779   -3.8107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8532   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0171   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl181\n\n>  <atomid>\n2\n\n>  <bondid>\n2\n\n$$$$\nTetrahydrothiophene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    3.7210   -3.9181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3632   -3.3980    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0779   -3.8107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8532   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0171   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl182\n\n>  <atomid>\n2\n\n>  <bondid>\n2\n\n$$$$\nTetrazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl183\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nThiophene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl184\n\n>  <atomid>\n4\n\n>  <bondid>\n3\n\n$$$$\nTriazine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    6.4094   -4.0362    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.0358    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1256   -3.6230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.8628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4094   -4.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1274   -5.2755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl185\n\n>  <atomid>\n3\n\n>  <bondid>\n1\n\n$$$$\nTriazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <prerender>\nlibrary.svg#tmpl186\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nALA-L-Alanine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  5  0     1  0            999 V2000\n   13.6700   -6.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6700   -5.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8002   -5.3251    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5334   -5.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5334   -4.3254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3998   -5.8240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  6     0  0\n  2  4  1  0     0  0\n  4  5  2  0     0  0\n  4  6  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl187\n\n>  <atomid>\n2\n\n>  <bondid>\n0\n\n$$$$\nARG-L-Arginine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   12.0694   -4.2443    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7765   -4.9514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5148   -5.9202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5506   -6.1773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2934   -7.1415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3248   -7.4032    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0676   -8.3674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1033   -8.6246    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7747   -9.0745    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7407   -4.6943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0024   -3.7255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4467   -5.4025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2 10  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  7  9  2  0     0  0\n 10 11  2  0     0  0\n 10 12  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl188\n\n>  <atomid>\n0\n\n>  <bondid>\n7\n\n$$$$\nASN-L-Asparagine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   10.8319   -5.4762    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6977   -5.9761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6989   -6.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8342   -7.4719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8321   -8.4753    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9683   -6.9719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5657   -5.4726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5645   -4.4747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4317   -5.9725    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  7  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  4  6  2  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl189\n\n>  <atomid>\n0\n\n>  <bondid>\n4\n\n$$$$\nASP-L-Aspartic acid\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   10.7814   -5.6761    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6474   -6.1761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6486   -7.1739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7839   -7.6718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7818   -8.6752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9179   -7.1719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5154   -5.6726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5142   -4.6748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3821   -6.1711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  7  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  4  6  2  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl190\n\n>  <atomid>\n0\n\n>  <bondid>\n4\n\n$$$$\nCYS-L-Cysteine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  6  0     1  0            999 V2000\n    6.9511   -4.7004    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8205   -5.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8205   -6.1991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9511   -6.6987    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6834   -4.7004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6834   -3.7013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5489   -5.1995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  5  1  0     0  0\n  3  4  1  0     0  0\n  5  6  2  0     0  0\n  5  7  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl191\n\n>  <atomid>\n0\n\n>  <bondid>\n3\n\n$$$$\nGLN-L-Glutamine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   11.1341   -5.3758    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0002   -5.8759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0015   -6.8739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1332   -7.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1344   -8.3757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2695   -8.8736    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0006   -8.8757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8652   -5.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8673   -4.3743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7305   -5.8794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  5  7  2  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl192\n\n>  <atomid>\n0\n\n>  <bondid>\n5\n\n$$$$\nGLU-L-Glutamic acid\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   11.4591   -5.3259    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3252   -5.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3265   -6.8240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4582   -7.3276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4594   -8.3256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5945   -8.8236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3256   -8.8257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1902   -5.3279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1923   -4.3243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0555   -5.8295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  5  7  2  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl193\n\n>  <atomid>\n0\n\n>  <bondid>\n5\n\n$$$$\nGLY-Glycine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  4  0     0  0            999 V2000\n   10.6670   -7.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5331   -6.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8010   -6.8750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3990   -7.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5331   -5.8750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  2  5  2  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl194\n\n>  <atomid>\n2\n\n>  <bondid>\n1\n\n$$$$\nHIS-L-Histidine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 11  0     1  0            999 V2000\n   11.4910   -6.5739    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3584   -7.0771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3572   -8.0742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4919   -8.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3861   -9.5713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4100   -9.7753    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9104   -8.9099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5750   -8.1667    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2237   -6.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2217   -5.5747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0896   -7.0762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  9  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4  8  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  2  0     0  0\n  9 10  2  0     0  0\n  9 11  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl195\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nILE-L-Isoleucine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   11.8001   -9.8252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8020   -8.8218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6668   -8.3239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5327   -8.8239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6656   -7.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7997   -6.8261    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5336   -6.8225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5324   -5.8248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4003   -7.3211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  1     0  0\n  3  5  1  0     0  0\n  5  6  1  6     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl196\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nLEU-L-Leucine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   12.2568   -9.3502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2588   -8.3468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3929   -7.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1235   -7.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1224   -6.8511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2564   -6.3511    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9903   -6.3475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9891   -5.3498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8571   -6.8461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  2  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  6     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl197\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nLYS-L-Lysine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   10.6692   -9.3254    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6712   -8.3221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5358   -7.8243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5346   -6.8266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4025   -6.3233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4013   -5.3256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5355   -4.8257    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2659   -4.8278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2679   -3.8246    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1308   -5.3291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  6     0  0\n  6  8  1  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl198\n\n>  <atomid>\n6\n\n>  <bondid>\n0\n\n$$$$\nMET-L-Methionine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   11.6195   -9.8247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4844   -9.3267    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4832   -8.3287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3515   -7.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3502   -6.8270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4841   -6.3270    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2152   -6.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2173   -5.3253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0805   -6.8304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  6     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl199\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nPHE-L-Phenylalanine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 11  0     1  0            999 V2000\n   12.5510   -6.0250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -6.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -6.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -5.0250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.1490   -6.5249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -7.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5510   -8.0249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5510   -9.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -9.5250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -9.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -8.0249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  6  1  0     0  0\n  3  4  2  0     0  0\n  3  5  1  0     0  0\n  6  7  1  0     0  0\n  6 11  2  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n 10 11  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl200\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nPRO-L-Proline\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     1  0            999 V2000\n   10.6969   -1.7001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6956   -2.6978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8298   -3.1977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7240   -4.1958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7473   -4.3999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2474   -3.5340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9124   -2.7903    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4026   -3.4047    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  3  2  1  6     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  3  7  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl201\n\n>  <atomid>\n6\n\n>  <bondid>\n2\n\n$$$$\nSER-L-Serine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  6  0     1  0            999 V2000\n   10.3261   -6.8754    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1955   -7.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1955   -8.3741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3261   -8.8737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0584   -6.8754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0584   -5.8763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9239   -7.3745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  5  1  0     0  0\n  3  4  1  0     0  0\n  5  6  2  0     0  0\n  5  7  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl202\n\n>  <atomid>\n0\n\n>  <bondid>\n3\n\n$$$$\nTHR-L-Threonine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   11.5255   -8.1243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3953   -7.6246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -8.1243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3953   -6.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5255   -6.1252    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -6.1252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -5.1257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1245   -6.6245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  6     0  0\n  2  4  1  0     0  0\n  4  5  1  6     0  0\n  4  6  1  0     0  0\n  6  7  2  0     0  0\n  6  8  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl203\n\n>  <atomid>\n4\n\n>  <bondid>\n0\n\n$$$$\nTRP-L-Tryptophan\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 15 16  0     1  0            999 V2000\n   11.9929   -5.3065    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8877   -5.7594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9408   -6.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0974   -7.3028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1680   -6.9465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5350   -7.7214    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0834   -8.5631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0497   -8.3041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7565   -9.0092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4968   -9.9732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5306  -10.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8239   -9.5270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7230   -5.2128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6717   -4.2179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6150   -5.6658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2 13  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4  8  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  2  0     0  0\n  7 12  1  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n 10 11  1  0     0  0\n 11 12  2  0     0  0\n 13 14  2  0     0  0\n 13 15  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl204\n\n>  <atomid>\n0\n\n>  <bondid>\n15\n\n$$$$\nTYR-L-Tyrosine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 13 13  0     1  0            999 V2000\n   12.5019   -5.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3670   -6.3231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3658   -7.3212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4995   -7.8214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5016   -8.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6354   -9.3253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7671   -8.8216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9008   -9.3217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7683   -7.8234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6344   -7.3233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2333   -5.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2344   -4.8247    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0992   -6.3235    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2 11  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4 10  1  0     0  0\n  5  6  1  0     0  0\n  6  7  2  0     0  0\n  7  8  1  0     0  0\n  7  9  1  0     0  0\n  9 10  2  0     0  0\n 11 12  2  0     0  0\n 11 13  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl205\n\n>  <atomid>\n0\n\n>  <bondid>\n8\n\n$$$$\nVAL-L-Valine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   10.8255   -8.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6953   -8.4496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -8.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6953   -7.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8255   -6.9502    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -6.9502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -5.9506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4245   -7.4494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  2  4  1  0     0  0\n  4  5  1  6     0  0\n  4  6  1  0     0  0\n  6  7  2  0     0  0\n  6  8  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <prerender>\nlibrary.svg#tmpl206\n\n>  <atomid>\n4\n\n>  <bondid>\n0\n\n$$$$\nAdenine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    3.4903   -2.0759    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.1974   -1.8369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -1.3637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.1974   -0.9421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9070   -2.2584    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4956   -0.6934    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8834   -0.5386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6333   -1.8449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6333   -0.9769    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8834    0.2478    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  2  0     0  0\n  2  5  1  0     0  0\n  3  6  2  0     0  0\n  4  7  1  0     0  0\n  5  8  2  0     0  0\n  7  9  2  0     0  0\n  7 10  1  0     0  0\n  4  6  1  0     0  0\n  8  9  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl207\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nCytosine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     0  0            999 V2000\n    3.7084   -1.9709    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4211   -1.5561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -1.5602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4211   -0.7296    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1335   -1.9667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -0.7338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7050   -0.3230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7050    0.4994    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  2  5  2  0     0  0\n  3  6  2  0     0  0\n  4  7  2  0     0  0\n  7  8  1  0     0  0\n  6  7  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl208\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nGuanine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    3.4897    0.3839    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.1974    0.6221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    1.0969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.1974    1.5215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9066    0.2000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5004    1.7668    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8887    1.9244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6377    0.6171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6377    1.4853    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8887    2.7154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3288    0.2133    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  2  0     0  0\n  2  5  1  0     0  0\n  3  6  2  0     0  0\n  4  7  1  0     0  0\n  5  8  2  0     0  0\n  7  9  1  0     0  0\n  7 10  2  0     0  0\n  4  6  1  0     0  0\n  8  9  1  0     0  0\n  8 11  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl209\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nThymine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  9  0     0  0            999 V2000\n    2.4396   -1.5954    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1523   -1.1809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7188   -1.1806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1523   -0.3502    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8646   -1.5913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7189   -0.3543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4364    0.0565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4364    0.8829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0104    0.0579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  2  5  2  0     0  0\n  3  6  2  0     0  0\n  4  7  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl210\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nUracil\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     0  0            999 V2000\n    3.7124   -0.5250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4252   -0.1064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -0.1145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4252    0.7243    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1458   -0.5209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    0.7202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7092    1.1310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7092    1.9576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  2  5  2  0     0  0\n  3  6  2  0     0  0\n  4  7  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl211\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nRibose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 14  0     1  0            999 V2000\n    3.6483   -1.5101    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6483   -2.8768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6030   -2.5039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5685   -2.8768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9582   -3.4695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2479   -3.4695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2479   -2.2377    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2479   -4.2134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9582   -2.2333    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9582   -4.2134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5685   -2.0518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.7706   -2.0564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5685   -3.8042    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6483   -3.6834    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  1     0  0\n  5  6  1  1     0  0\n  2  6  1  1     0  0\n  6  7  1  0     0  0\n  6  8  1  0     0  0\n  5  9  1  0     0  0\n  5 10  1  0     0  0\n  4 11  1  0     0  0\n 11 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl212\n\n>  <atomid>\n0\n\n>  <bondid>\n11\n\n$$$$\nDeoxyribose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 14  0     0  0            999 V2000\n   11.5961   -4.0092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5961   -5.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -6.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -6.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -5.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4831   -5.0674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -4.5860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5320   -4.5909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -6.4519    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -4.7792    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -6.8876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -4.7839    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -6.8876    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5961   -6.3232    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  2  6  1  0     0  0\n  6  5  1  0     0  0\n  5  4  1  0     0  0\n  4  3  1  0     0  0\n  2  3  1  0     0  0\n  2  1  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  5  9  1  0     0  0\n  4 10  1  0     0  0\n  4 11  1  0     0  0\n  3 12  1  0     0  0\n  3 13  1  0     0  0\n  2 14  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl213\n\n>  <atomid>\n0\n\n>  <bondid>\n7\n\n$$$$\nRibose monophosphate\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 18  0     1  0            999 V2000\n   14.4831   -3.7504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4831   -5.1570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4073   -4.7732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3426   -5.1570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7437   -5.7670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0710   -5.7670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0710   -4.4993    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0710   -6.5326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7437   -4.4947    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7437   -6.5326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3426   -4.3079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3426   -6.1115    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4831   -5.9871    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2261   -4.3001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3520   -4.3001    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4739   -4.3001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3520   -3.4183    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3520   -5.1818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  1     0  0\n  5  6  1  1     0  0\n  2  6  1  1     0  0\n  6  7  1  0     0  0\n  6  8  1  0     0  0\n  5  9  1  0     0  0\n  5 10  1  0     0  0\n  4 11  1  0     0  0\n  4 12  1  0     0  0\n  2 13  1  0     0  0\n 14 15  1  0     0  0\n 15 16  1  0     0  0\n 15 17  2  0     0  0\n 15 18  1  0     0  0\n 11 14  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl214\n\n>  <atomid>\n0\n\n>  <bondid>\n14\n\n$$$$\nDeoxyribose monophosphate\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n   11.5961   -4.0092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5961   -5.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -6.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -6.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -5.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4831   -5.0674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -4.5860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5320   -4.5909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6579   -4.5909    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7798   -4.5909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6579   -3.7091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6579   -5.4726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -6.4519    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -4.7792    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -6.8876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -4.7839    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -6.8876    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5961   -6.3232    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  2  6  1  0     0  0\n  6  5  1  0     0  0\n  5  4  1  0     0  0\n  4  3  1  0     0  0\n  2  3  1  0     0  0\n  2  1  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  9 11  2  0     0  0\n  9 12  1  0     0  0\n  5 13  1  0     0  0\n  4 14  1  0     0  0\n  4 15  1  0     0  0\n  3 16  1  0     0  0\n  3 17  1  0     0  0\n  2 18  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <prerender>\nlibrary.svg#tmpl215\n\n>  <atomid>\n0\n\n>  <bondid>\n9\n\n$$$$\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 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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$$$$\nalpha-D-Allopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -4.1124    6.2007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.6076    4.1259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5974    5.2058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4025    4.8658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5974    6.0607    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3373    4.7808    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9974    3.2709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2076    5.2058    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7775    5.3207    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.6076    3.2709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1476    3.8958    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4025    4.0109    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1124    5.3507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7577    4.3259    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7775    4.4658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9974    4.1259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8224    4.3259    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  8  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n  8  4  1  0     0  0\n  3  5  1  0     0  0\n  3  6  1  0     0  0\n  7 16  1  0     0  0\n 17 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <prerender>\nlibrary.svg#tmpl246\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Altropyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -6.8433    4.3051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3385    2.2303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.3283    3.3102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.1334    2.9703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.3283    4.1651    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -8.0682    2.8852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.7283    1.3754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9384    3.3102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.5084    3.4252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3385    1.3754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8784    2.0003    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.1334    2.1154    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.8433    3.4551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4886    2.4303    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.5084    2.5702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.7283    2.2303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.5532    2.4303    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  8  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n  8  4  1  0     0  0\n  3  5  1  0     0  0\n  3  6  1  0     0  0\n  7 16  1  0     0  0\n 17 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <prerender>\nlibrary.svg#tmpl247\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Galactopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -6.4899    2.6666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9851    0.5918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.9748    1.6717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.7800    1.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.9748    2.5266    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.7148    1.2467    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3749   -0.2631    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.1998    0.7918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1550    1.7866    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9851   -0.2631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5250    0.3618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.7800    0.4768    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.4899    1.8166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1352    0.7918    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1550    0.9317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3749    0.5918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5850    1.6717    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n 17  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n 17  4  1  0     0  0\n  3  5  1  0     0  0\n  3  6  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <prerender>\nlibrary.svg#tmpl248\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Glucopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -7.7107   -0.2570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2094   -2.3086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -8.1903   -1.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.0088   -1.5769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -8.1903   -0.3955    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.8273   -1.2408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.5674   -3.1539    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -8.3831   -2.1108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3908   -1.1271    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2094   -3.1539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.7680   -2.5360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.0088   -2.4222    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.7107   -1.0975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3937   -2.1108    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3908   -1.9725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.5674   -2.3086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -8.8923   -1.6610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  6  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n  6  4  1  0     0  0\n  3  5  1  0     0  0\n  3 17  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <prerender>\nlibrary.svg#tmpl249\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Gulopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -5.8152    3.8232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2901    1.7531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.2952    2.8332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1052    2.4882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.2952    3.6832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9101    2.8332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.6702    0.9031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.5202    1.9532    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4801    2.9432    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2901    0.9031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8551    1.5281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1052    1.6382    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.8152    2.9732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4651    1.9532    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4801    2.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.6702    1.7531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.0302    2.4032    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  6  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n  6  4  1  0     0  0\n  3  5  1  0     0  0\n  3 17  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <prerender>\nlibrary.svg#tmpl250\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Idopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -6.0079    2.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4782    0.6560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.4929    1.7359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2981    1.3960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.4929    2.5909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1031    1.7359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.8630   -0.1989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.6879    0.8561    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6731    1.8509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4782   -0.1989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0431    0.4260    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2981    0.5411    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.0079    1.8809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6533    0.8561    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6731    0.9960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.8630    0.6560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.2329    1.3109    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  6  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n  6  4  1  0     0  0\n  3  5  1  0     0  0\n  3 17  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <prerender>\nlibrary.svg#tmpl251\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Mannopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -5.5581    1.8634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0527   -0.1676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.0375    0.8751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8565    0.5342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.0375    1.7202    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.7441    0.4501    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.4199   -1.0126    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.2352    0.0005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2339    1.0134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0527   -1.0126    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6161   -0.4246    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8565   -0.3109    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.5581    1.0134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2325    0.0301    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2339    0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.4199   -0.1676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6705    0.8751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n 17  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n 17  4  1  0     0  0\n  3  5  1  0     0  0\n  3  6  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <prerender>\nlibrary.svg#tmpl252\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Talopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -6.3613    0.1928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8363   -1.8473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.8414   -0.7673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.6514   -1.1373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.8414    0.0827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.5764   -1.2223    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.2164   -2.6973    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.0414   -1.6773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0263   -0.6572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8363   -2.6973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4013   -2.0723    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.6514   -1.9874    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3613   -0.6572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0113   -1.6473    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0263   -1.5074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.2164   -1.8473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4562   -0.7673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n 17  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n 17  4  1  0     0  0\n  3  5  1  0     0  0\n  3  6  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <prerender>\nlibrary.svg#tmpl253\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nfullerene C60\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 60 90  0     0  0            999 V2000\n    8.1533  -10.1609   -0.1552 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5120   -9.2753    0.7287 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7211   -9.6737   -1.3649 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4284   -7.8924    0.4121 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6441   -6.9280    1.4115 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8106   -9.6782    2.0415 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0295   -8.7030    3.0509 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9469   -7.3351    2.7388 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6766  -11.1024   -1.0190 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1155  -11.5835    0.1778 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9755  -10.1416   -1.7961 C   0  0  0  0  0  0  0  0  0  0  0  0\n    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-8.3653   -1.4688 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2260   -8.3597   -1.0520 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9985   -8.7537    0.9805 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5364   -8.7481    1.4094 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3614   -7.8158    0.4528 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  7  1  0  0  0  0\n  3 16  1  0  0  0  0\n  4 16  1  0  0  0  0\n  5 14  1  0  0  0  0\n  6 14  1  0  0  0  0\n  7 14  1  0  0  0  0\n  7 16  1  0  0  0  0\n  8 18  1  0  0  0  0\n  9 18  1  0  0  0  0\n 10 15  1  0  0  0  0\n 11 15  1  0  0  0  0\n 12 17  1  0  0  0  0\n 13 17  1  0  0  0  0\n 14 15  1  0  0  0  0\n 15 18  1  0  0  0  0\n 16 17  1  0  0  0  0\n 17 18  1  0  0  0  0\n  1  7  1  0  0  0  0\nM  END\n>  <atomid>\n0\n\n>  <bondid>\n17\n\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl257\n\n$$$$\nring 6 chair\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n    6.4738   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-4.7668   -0.6787 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2658   -6.7684   -2.2180 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8611   -6.2475   -1.4612 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9719   -5.6379   -0.3097 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2 18  1  0  0  0  0\n  3 12  1  0  0  0  0\n  4 12  1  0  0  0  0\n  5 17  1  0  0  0  0\n  6 17  1  0  0  0  0\n  7 14  1  0  0  0  0\n  8 14  1  0  0  0  0\n  9 10  1  0  0  0  0\n  9 11  1  0  0  0  0\n  9 12  1  0  0  0  0\n  9 14  1  0  0  0  0\n 12 18  1  0  0  0  0\n 13 14  1  0  0  0  0\n 13 15  1  0  0  0  0\n 13 16  1  0  0  0  0\n 13 17  1  0  0  0  0\n 17 18  1  0  0  0  0\n  1 18  1  0  0  0  0\nM  END\n>  <atomid>\n0\n\n>  <bondid>\n17\n\n>  <group>\n3D Templates\n\n>  <prerender>\nlibrary.svg#tmpl258\n\n$$$$\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 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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>  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<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  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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$$$$\nPhenylalanine mustard\n  Ketcher  8252313372D 1   1.00000     0.00000     0\n\n 19 19  0  0  0  0  0  0  0  0999 V2000\n   18.7500   -9.0090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.7500   -9.0090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   20.2500   -9.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.7500  -10.7410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.7500  -10.7410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.2500   -9.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.2500   -9.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.7500  -10.7410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.7500  -10.7410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2500   -9.8750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2500  -11.6071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   17.2500  -11.6071    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   21.2500   -9.8750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   21.7500   -9.0090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.7500   -9.0090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2500   -8.1429    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n   21.7500  -10.7410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.7500  -10.7410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2500  -11.6071    0.0000 Cl  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  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  2  0     0  0\n  9 11  1  0     0  0\n  8 12  1  1     0  0\n  3 13  1  0     0  0\n  13 14  1  0     0  0\n  14 15  1  0     0  0\n  15 16  1  0     0  0\n  13 17  1  0     0  0\n  17 18  1  0     0  0\n  18 19  1  0     0  0\nM  END\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n>  <group>\nAromatics\n\n>  <prerender>\nlibrary.svg#tmpl269\n\n$$$$";
+var templatesRawData$2 = "alpha-D-Allopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -2.4110    3.5743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4110    1.6992    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2304    0.7587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.0499    1.6991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2360    3.5743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.8478    2.9800    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3208    3.1152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3208    2.1638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2360    1.6991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1456    2.1636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1456    3.1151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.0499    3.5741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  6     0  0\n  9  3  1  6     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Altropyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -0.9910    2.2903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.9910    0.7936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2875    0.0452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5799    0.7935    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2834    2.2903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1462    1.8062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.6372    1.9161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.6372    1.1678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2834    0.7935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9337    1.1677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9337    1.9160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5799    2.2902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  1     0  0\n  9  3  1  6     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Arabinofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -1.9332    3.1927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5926    1.1426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7765    1.1387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7048    3.4871    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.0588    2.4002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8825    2.8828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1801    1.9478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1909    1.9478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5142    2.8976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.4573    3.1978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  1     0  0\n  8  3  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Arabinopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   15.5611   -5.2999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.5611   -7.3001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8228   -8.3002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0958   -7.3001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8228   -5.2999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6920   -5.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6920   -6.7999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8228   -7.3001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9648   -6.7999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9648   -5.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  5 10  1  0     0  0\n 10  9  1  0     0  0\n  9  8  1  0     0  0\n  8  7  1  0     0  0\n  7  6  1  0     0  0\n  6  5  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  1     0  0\n  8  3  1  6     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n$$$$\nalpha-D-Erythrofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     1  0            999 V2000\n   -2.3742    2.6418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8682    1.1059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4960    1.1030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7013    2.8623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0854    2.4096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3125    1.7091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0613    1.7091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3035    2.4207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  8  4  1  0     0  0\n  8  7  1  0     0  0\n  4  5  1  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  1  1  6     0  0\n  6  2  1  6     0  0\n  7  3  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Galactopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.5577    2.5236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.5577    1.0270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8542    0.2785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1466    1.0269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8543    2.5236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7171    2.0395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2039    2.1495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2039    1.4011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8543    1.0269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5004    1.4010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5004    2.1494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1466    2.5235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  6     0  0\n  9  3  1  1     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n$$$$\nalpha-D-Glucopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -2.1744    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1744    1.3186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4708    0.5702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7632    1.3185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4709    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3337    2.3312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8206    2.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8206    1.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4709    1.3185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1170    1.6927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1170    2.4410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7632    2.8152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  6     0  0\n  9  3  1  1     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n$$$$\nalpha-D-Gulopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -2.1119    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1119    1.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4083    0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7007    1.3602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4084    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2712    2.3728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7581    2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7581    1.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4084    1.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0545    1.7344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0545    2.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7007    2.8569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  6     0  0\n  9  3  1  6     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n$$$$\nalpha-D-Idopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.9244    2.7736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9244    1.2770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2208    0.5285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5132    1.2769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2209    2.7736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0837    2.2895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5706    2.3995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5706    1.6511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2209    1.2769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8670    1.6510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8670    2.3994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5132    2.7735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  1     0  0\n  9  3  1  6     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n$$$$\nalpha-D-Lyxofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.1148    2.9334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6088    1.3976    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2406    1.3947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4419    3.1538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2054    2.3397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8260    2.7012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0531    2.0007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8102    2.0007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0483    2.7122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7589    2.9371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  1     0  0\n  8  3  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n$$$$\nalpha-D-Lyxopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.4513    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4513    1.3186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7520    0.5702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0444    1.3185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7521    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1017    2.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1017    1.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7521    1.3185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3940    1.6927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3940    2.4410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 10  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  1     0  0\n  8  3  1  1     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n$$$$\nalpha-D-Mannopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -2.1577    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1577    1.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4542    0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7466    1.3602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4543    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3171    2.3728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8039    2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8039    1.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4543    1.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1004    1.7344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1004    2.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7466    2.8569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  1     0  0\n  9  3  1  1     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n$$$$\nalpha-D-Psicofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   15.0740   -8.2784    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3759   -8.9026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7463  -10.3149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5700  -10.3189    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6353   -7.9706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2665   -9.0586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1656   -7.8559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4589   -8.5718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1574   -9.5078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.1460   -9.5078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8298   -8.5571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8731   -8.2544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  1     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  6     0  0\n  9  3  1  6     0  0\n  8  2  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Ribofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -1.8940    2.7251    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3879    1.1893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0198    1.1863    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2211    2.9455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9845    2.1313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6051    2.4928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8322    1.7924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5894    1.7924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8274    2.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5381    2.7288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  6     0  0\n  8  3  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n$$$$\nalpha-D-Ribopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.1138    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1138    1.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4145    0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7069    1.3602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4146    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7642    2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7642    1.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4146    1.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0565    1.7344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0565    2.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 10  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  6     0  0\n  8  3  1  6     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n$$$$\nalpha-D-Sorbofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.6290    2.6125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1517    2.1450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6232    1.0874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2529    1.0845    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4552    2.8429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2290    2.0282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3092    2.9289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8384    2.3927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0642    1.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8216    1.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0626    2.4037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7789    2.6304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  0     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  1     0  0\n  9  3  1  6     0  0\n  8  2  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Tagatofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.3790    2.4875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9017    2.0200    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3732    0.9624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0029    0.9595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2052    2.7179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9790    1.9032    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.0592    2.8039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5884    2.2677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8142    1.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5716    1.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8126    2.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5289    2.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  0     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  1     0  0\n  9  3  1  1     0  0\n  8  2  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Talopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.9910    2.9403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9910    1.4436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2875    0.6952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5799    1.4435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2834    2.9403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1462    2.4562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6372    2.5661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6372    1.8178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2834    1.4435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9337    1.8177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9337    2.5660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5799    2.9402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  6     0  0\n  8  2  1  1     0  0\n  9  3  1  1     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Threofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     1  0            999 V2000\n   -2.8117    2.6835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3057    1.1476    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9335    1.1447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1388    2.9039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5229    2.4513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7458    1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5029    1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7410    2.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  8  4  1  0     0  0\n  8  7  1  0     0  0\n  4  5  1  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  1  1  6     0  0\n  6  2  1  1     0  0\n  7  3  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n$$$$\nalpha-D-Xylofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.1648    2.8084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6588    1.2726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2948    1.2697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4919    3.0288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2554    2.2147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8760    2.5762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0989    1.8757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8560    1.8757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0983    2.5872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8048    2.8121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  6     0  0\n  8  3  1  1     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n$$$$\nalpha-D-Xylopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.5429    3.0236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5429    1.5270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8396    0.7785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1360    1.5270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8396    3.0236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1934    2.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1934    1.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8396    1.5270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4899    1.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4899    2.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  5 10  1  0     0  0\n 10  9  1  0     0  0\n  9  8  1  0     0  0\n  8  7  1  0     0  0\n  7  6  1  0     0  0\n  6  5  1  0     0  0\n  6  1  1  6     0  0\n  7  2  1  6     0  0\n  8  3  1  1     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nalpha-D-Sugars\n\n$$$$\nCyclopenta-1,3-diene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    9.6696   -5.8045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6696   -4.9328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4243   -4.4955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1804   -4.9328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1804   -5.8045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  1  5  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <atomid>\n2\n\n>  <bondid>\n1\n\n$$$$\n1H-indene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    7.1899   -4.2253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1899   -5.2247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0555   -5.7254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9228   -5.2247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9228   -4.2253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0555   -3.7246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8731   -5.5332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4601   -4.7242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8731   -3.9149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  6  1  0     0  0\n  1  6  2  0     0  0\n  4  7  1  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  5  9  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <atomid>\n6\n\n>  <bondid>\n7\n\n$$$$\nNaphtalene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n   11.0090   -4.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1429   -5.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1429   -6.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0090   -6.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8751   -6.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8751   -5.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7410   -4.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7410   -6.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6071   -6.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6071   -5.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  6  2  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  8  1  0     0  0\n  7 10  2  0     0  0\n  8  9  2  0     0  0\n  9 10  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <atomid>\n6\n\n>  <bondid>\n10\n\n$$$$\nAzulene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n   12.4941   -7.5235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2759   -5.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4941   -5.2765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5192   -5.4990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0853   -6.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5192   -7.3010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2270   -5.5909    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2759   -6.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2270   -7.2090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8147   -6.4000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  8  2  0     0  0\n  1  6  1  0     0  0\n  2  3  1  0     0  0\n  3  4  2  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  7  2  2  0     0  0\n  7 10  1  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n  2  8  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <atomid>\n4\n\n>  <bondid>\n4\n\n$$$$\nE-Stilbene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 15  0     0  0            999 V2000\n   10.8250   -2.9010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8250   -2.9010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3250   -3.7670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8249   -4.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8249   -4.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3250   -3.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3250   -3.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8250   -4.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8250   -4.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3250   -5.4990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3250   -5.4990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8250   -4.6330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3250   -3.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3250   -3.7669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  6  2  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n 14  9  1  0     0  0\n 10  9  2  0     0  0\n 10 11  1  0     0  0\n 11 12  2  0     0  0\n 12 13  1  0     0  0\n 13 14  2  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <atomid>\n2\n\n>  <bondid>\n3\n\n$$$$\nZ-Stilbene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 15  0     0  0            999 V2000\n   12.3750   -3.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3750   -3.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8750   -4.7581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3749   -5.6240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3749   -5.6240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8750   -4.7580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8750   -3.0260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8750   -3.0260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3750   -3.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8750   -4.7580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.3750   -5.6240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3750   -5.6240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8750   -4.7581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3750   -3.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  6  2  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  6  1  0     0  0\n  1  7  1  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  9 14  2  0     0  0\n 10 11  2  0     0  0\n 11 12  1  0     0  0\n 12 13  2  0     0  0\n 13 14  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <atomid>\n3\n\n>  <bondid>\n3\n\n$$$$\nAnthracene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 16  0     0  0            999 V2000\n    8.0930   -3.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2269   -3.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2269   -4.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0930   -5.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9591   -4.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9591   -3.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8250   -3.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8250   -5.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6911   -4.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6911   -3.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5571   -3.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5571   -5.2750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4231   -4.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4231   -3.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  6  2  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  8  1  0     0  0\n  7 10  2  0     0  0\n  8  9  2  0     0  0\n 11 10  1  0     0  0\n  9 10  1  0     0  0\n  9 12  1  0     0  0\n 11 14  2  0     0  0\n 12 13  2  0     0  0\n 13 14  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <atomid>\n10\n\n>  <bondid>\n15\n\n$$$$\nPhenantrene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 16  0     0  0            999 V2000\n   10.7760   -1.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9099   -2.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9099   -3.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7760   -3.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6420   -3.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6420   -2.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5080   -1.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5080   -3.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3740   -3.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3740   -2.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5080   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3740   -5.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2401   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2401   -3.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  6  2  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  8  1  0     0  0\n  7 10  2  0     0  0\n  9 10  1  0     0  0\n  8 11  2  0     0  0\n  8  9  1  0     0  0\n  9 14  2  0     0  0\n 11 12  1  0     0  0\n 12 13  2  0     0  0\n 13 14  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nPyrene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 16 19  0     0  0            999 V2000\n   13.2084   -1.8748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2084   -2.8736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0732   -3.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.9399   -2.8736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.9399   -1.8748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0732   -1.3745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0732   -4.3744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.9399   -4.8747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8066   -4.3744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8066   -3.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3434   -3.3739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3434   -4.3726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2084   -4.8729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2065   -5.8752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0732   -6.3755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.9399   -5.8752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  6  1  0     0  0\n  3  7  2  0     0  0\n  7  8  1  0     0  0\n  8  9  2  0     0  0\n  9 10  1  0     0  0\n  4 10  2  0     0  0\n  2 11  1  0     0  0\n 11 12  2  0     0  0\n 12 13  1  0     0  0\n  7 13  1  0     0  0\n 13 14  2  0     0  0\n 14 15  1  0     0  0\n 15 16  2  0     0  0\n  8 16  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <atomid>\n10\n\n>  <bondid>\n12\n\n$$$$\nTriphenylene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 21  0     0  0            999 V2000\n   10.5140   -3.4503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5140   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3807   -4.9503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2474   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2474   -3.4503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3807   -2.9497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6491   -2.9516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7859   -3.4503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7859   -4.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6491   -4.9467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1141   -2.9497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1141   -1.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2474   -1.4481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3807   -1.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3807   -5.9514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2474   -6.4519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1141   -5.9514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1141   -4.9503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  2  3  1  0     0  0\n  3  4  2  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  6  1  0     0  0\n  1  7  1  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n  2 10  1  0     0  0\n  5 11  1  0     0  0\n 11 12  2  0     0  0\n 12 13  1  0     0  0\n 13 14  2  0     0  0\n  6 14  1  0     0  0\n  3 15  1  0     0  0\n 15 16  2  0     0  0\n 16 17  1  0     0  0\n 17 18  2  0     0  0\n  4 18  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <atomid>\n7\n\n>  <bondid>\n8\n\n$$$$\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>  <atomid>\n18\n\n>  <bondid>\n21\n\n$$$$\n14-Annulene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 14  0     0  0            999 V2000\n   12.0122   -0.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1483   -1.2548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1861   -2.2524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8762   -2.2524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8762   -1.2548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3221   -2.7512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3221   -3.7488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1861   -4.2476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9139   -4.2476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7779   -3.7488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7779   -2.7512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1861   -5.2452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0500   -5.7440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9139   -5.2452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  5  2  0     0  0\n  2  3  2  0     0  0\n  4  5  1  0     0  0\n  3  6  1  0     0  0\n  6  7  2  0     0  0\n  7  8  1  0     0  0\n  4 11  2  0     0  0\n  9 10  2  0     0  0\n 10 11  1  0     0  0\n 14  9  1  0     0  0\n  8 12  2  0     0  0\n 12 13  1  0     0  0\n 13 14  2  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\n18-Annulene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n    9.2590    6.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3930    5.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3930    4.7249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1250    5.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9910    6.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8570    4.7249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8570    5.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8570    2.7249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7230    3.2249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7230    4.2249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5270    4.2249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5270    3.2249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3930    2.7249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3930    1.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2590    1.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1250    1.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9910    1.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8570    1.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  1  4  1  0     0  0\n  2  3  1  0     0  0\n  5  4  2  0     0  0\n  5  7  1  0     0  0\n  6  7  2  0     0  0\n  6 10  1  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n  3 11  2  0     0  0\n 11 12  1  0     0  0\n 12 13  2  0     0  0\n 13 14  1  0     0  0\n 14 15  2  0     0  0\n 15 16  1  0     0  0\n 16 17  2  0     0  0\n 18  8  2  0     0  0\n 17 18  1  0     0  0\nM  END\n>  <group>\nAromatics\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\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>  <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>  <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$$$$\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$$$$\nbeta-D-Allopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.8119    2.6861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.8119    1.2770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1792    0.5702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5466    1.2769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1834    2.6861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1462    2.2395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4956    2.3411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4956    1.6261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1834    1.2769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8670    1.6260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8670    2.3410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5466    2.6860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  1     0  0\n  8  2  1  6     0  0\n  9  3  1  6     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Altropyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -0.9910    2.2903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.9910    0.7936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2875    0.0452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5799    0.7935    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2834    2.2903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1462    1.8062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.6372    1.9161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.6372    1.1678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2834    0.7935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9337    1.1677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9337    1.9160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5799    2.2902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  1     0  0\n  8  2  1  1     0  0\n  9  3  1  6     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Arabinofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -1.4482    2.3917    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9421    0.8559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5781    0.8530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7753    2.6122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5387    1.7980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1593    2.1595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3822    1.4591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1394    1.4591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3816    2.1706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0881    2.3955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  1     0  0\n  7  2  1  1     0  0\n  8  3  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Arabinopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   15.5611   -5.2999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.5611   -7.3001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8228   -8.3002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0958   -7.3001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8228   -5.2999    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6920   -5.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6920   -6.7999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.8228   -7.3001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9648   -6.7999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9648   -5.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  5 10  1  0     0  0\n 10  9  1  0     0  0\n  9  8  1  0     0  0\n  8  7  1  0     0  0\n  7  6  1  0     0  0\n  6  5  1  0     0  0\n  6  1  1  1     0  0\n  7  2  1  1     0  0\n  8  3  1  6     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Erythrofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     1  0            999 V2000\n   -2.3742    2.6418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8682    1.1059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4960    1.1030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7013    2.8623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0854    2.4096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3125    1.7091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0613    1.7091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3035    2.4207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  8  4  1  0     0  0\n  8  7  1  0     0  0\n  4  5  1  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  1  1  1     0  0\n  6  2  1  6     0  0\n  7  3  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Fructofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.6256    2.7205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1524    2.2530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6198    1.1954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2536    1.1925    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4559    2.9509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2256    2.1362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3100    3.0369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8350    2.5007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0608    1.8040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8182    1.8040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0592    2.5117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7755    2.7384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  0     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  6     0  0\n  9  3  1  1     0  0\n  8  2  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Galactopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.5577    2.5236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.5577    1.0270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8542    0.2785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1466    1.0269    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8543    2.5236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7171    2.0395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2039    2.1495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2039    1.4011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8543    1.0269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5004    1.4010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5004    2.1494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1466    2.5235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  1     0  0\n  8  2  1  6     0  0\n  9  3  1  1     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Glucopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -2.1744    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1744    1.3186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4708    0.5702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7632    1.3185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4709    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3337    2.3312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8206    2.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8206    1.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4709    1.3185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1170    1.6927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1170    2.4410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7632    2.8152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  1     0  0\n  8  2  1  6     0  0\n  9  3  1  1     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Gulopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -2.1119    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1119    1.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4083    0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7007    1.3602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4084    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2712    2.3728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7581    2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7581    1.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4084    1.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0545    1.7344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0545    2.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7007    2.8569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  1     0  0\n  8  2  1  6     0  0\n  9  3  1  6     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Idopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.9244    2.7736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9244    1.2770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2208    0.5285    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5132    1.2769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2209    2.7736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0837    2.2895    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5706    2.3995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5706    1.6511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2209    1.2769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8670    1.6510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8670    2.3994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5132    2.7735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  1     0  0\n  8  2  1  1     0  0\n  9  3  1  6     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Lyxofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.1148    2.9334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6088    1.3976    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2406    1.3947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4419    3.1538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2054    2.3397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8260    2.7012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0531    2.0007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8102    2.0007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0483    2.7122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7589    2.9371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  1     0  0\n  7  2  1  1     0  0\n  8  3  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Lyxopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.4513    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4513    1.3186    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7520    0.5702    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0444    1.3185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7521    2.8153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1017    2.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1017    1.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7521    1.3185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3940    1.6927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3940    2.4410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 10  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  6  1  1  1     0  0\n  7  2  1  1     0  0\n  8  3  1  1     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Mannopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -2.1577    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1577    1.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4542    0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7466    1.3602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4543    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3171    2.3728    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8039    2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8039    1.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4543    1.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1004    1.7344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1004    2.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7466    2.8569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  1     0  0\n  8  2  1  1     0  0\n  9  3  1  1     0  0\n 10  4  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Psicofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   14.8241   -7.1535    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1260   -7.7777    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4964   -9.1900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3201   -9.1940    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3854   -6.8457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0166   -7.9337    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9157   -6.7310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2090   -7.4469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9075   -8.3829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8961   -8.3829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5799   -7.4322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6232   -7.1295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  6     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  6     0  0\n  9  3  1  6     0  0\n  8  2  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Ribofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -1.8940    2.7251    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3879    1.1893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0198    1.1863    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2211    2.9455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9845    2.1313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6051    2.4928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8322    1.7924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5894    1.7924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8274    2.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5381    2.7288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  1     0  0\n  7  2  1  6     0  0\n  8  3  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Ribopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.1138    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1138    1.3603    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4145    0.6119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7069    1.3602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4146    2.8570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7642    2.4828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7642    1.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4146    1.3602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0565    1.7344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0565    2.4827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 10  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  6  1  1  1     0  0\n  7  2  1  6     0  0\n  8  3  1  6     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Sorbofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.6290    2.6125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1517    2.1450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6232    1.0874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2529    1.0845    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4552    2.8429    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2290    2.0282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3092    2.9289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8384    2.3927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0642    1.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8216    1.6918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0626    2.4037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7789    2.6304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  0     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  1     0  0\n  9  3  1  6     0  0\n  8  2  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Tagatofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.3790    2.4875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9017    2.0200    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3732    0.9624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0029    0.9595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2052    2.7179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9790    1.9032    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.0592    2.8039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5884    2.2677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8142    1.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5716    1.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8126    2.2787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5289    2.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n 11  5  1  0     0  0\n 11 10  1  0     0  0\n  5  8  1  0     0  0\n 10  9  1  0     0  0\n  8  9  1  0     0  0\n  8  7  1  0     0  0\n  7  1  1  0     0  0\n 11 12  1  1     0  0\n 12  6  1  0     0  0\n 10  4  1  1     0  0\n  9  3  1  1     0  0\n  8  2  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Talopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     1  0            999 V2000\n   -1.9910    2.9403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9910    1.4436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2875    0.6952    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5799    1.4435    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2834    2.9403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1462    2.4562    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6372    2.5661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6372    1.8178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2834    1.4435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9337    1.8177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9337    2.5660    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5799    2.9402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  6 12  1  0     0  0\n 11  5  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  1     0  0\n  7  1  1  1     0  0\n  8  2  1  1     0  0\n  9  3  1  1     0  0\n 10  4  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Threofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     1  0            999 V2000\n   -2.8117    2.6835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3057    1.1476    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9335    1.1447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1388    2.9039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5229    2.4513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7458    1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5029    1.7507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7410    2.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  8  4  1  0     0  0\n  8  7  1  0     0  0\n  4  5  1  0     0  0\n  7  6  1  0     0  0\n  5  6  1  0     0  0\n  5  1  1  1     0  0\n  6  2  1  1     0  0\n  7  3  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Xylofuranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.1648    2.8084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6588    1.2726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2948    1.2697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4919    3.0288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2554    2.2147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8760    2.5762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0989    1.8757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8560    1.8757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0983    2.5872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8048    2.8121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  4  1  0     0  0\n  9  8  1  0     0  0\n  4  6  1  0     0  0\n  8  7  1  0     0  0\n  6  7  1  0     0  0\n  9 10  1  1     0  0\n 10  5  1  0     0  0\n  6  1  1  1     0  0\n  7  2  1  6     0  0\n  8  3  1  1     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nbeta-D-Xylopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     1  0            999 V2000\n   -2.5429    3.0236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5429    1.5270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8396    0.7785    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1360    1.5270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8396    3.0236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1934    2.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1934    1.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8396    1.5270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4899    1.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4899    2.6495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  5 10  1  0     0  0\n 10  9  1  0     0  0\n  9  8  1  0     0  0\n  8  7  1  0     0  0\n  7  6  1  0     0  0\n  6  5  1  0     0  0\n  6  1  1  1     0  0\n  7  2  1  6     0  0\n  8  3  1  1     0  0\n  9  4  1  6     0  0\nM  END\n>  <group>\nbeta-D-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nBicyclo[1-1-1]pentane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  6  0     0  0            999 V2000\n    9.8610   -7.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4888   -6.4956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5708   -7.8431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8036   -8.0042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9790   -7.8371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  4  5  1  0     0  0\n  1  5  1  0     0  0\n  4  3  1  0     0  0\n  2  4  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n2\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[2-1-1]hexane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  7  0     0  0            999 V2000\n    9.7097   -6.3707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3181   -5.6035    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4180   -6.7620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6494   -7.1903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7820   -7.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4069   -7.5965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  3  6  1  0     0  0\n  4  5  1  0     0  0\n  4  6  1  0     0  0\n  1  5  1  0     0  0\n  2  4  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n5\n\n>  <bondid>\n2\n\n$$$$\nBicyclo[2-2-1]heptane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  8  0     0  0            999 V2000\n    8.4502   -7.5691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8558   -6.8358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5667   -6.3361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3112   -7.1358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3890   -5.4309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4498   -6.8526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1221   -7.5469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  1  4  1  0     0  0\n  4  5  1  0     0  0\n  5  3  1  0     0  0\n  3  6  1  0     0  0\n  6  7  1  0     0  0\n  7  4  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n6\n\n>  <bondid>\n6\n\n$$$$\nBicyclo[3-1-1]heptane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  8  0     0  0            999 V2000\n    8.2782   -1.8550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5291   -2.7952    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9238   -2.2925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7847   -2.2925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6209   -1.3393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3670   -1.8368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6898   -3.1107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  4  5  1  0     0  0\n  5  1  1  0     0  0\n  1  6  1  0     0  0\n  6  2  1  0     0  0\n  1  7  1  0     0  0\n  7  4  1  0     0  0\n  4  3  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nBicyclo[2-2-2]octane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  9  0     0  0            999 V2000\n   10.8583   -6.6275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9678   -6.2148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6767   -5.7197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9692   -6.6418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1340   -4.9791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7980   -5.3243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8417   -5.7430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8429   -4.2582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  6  1  0     0  0\n  4  7  1  0     0  0\n  5  8  1  0     0  0\n  6  7  1  0     0  0\n  6  8  1  0     0  0\n  5  2  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n1\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[3-2-1]octane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  9  0     0  0            999 V2000\n    9.0974   -5.5533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4087   -6.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7744   -6.0120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5802   -6.0120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4086   -5.0127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2389   -5.5343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9413   -6.8873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7036   -6.4241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  4  5  1  0     0  0\n  5  1  1  0     0  0\n  1  6  1  0     0  0\n  6  2  1  0     0  0\n  4  7  1  0     0  0\n  1  8  1  0     0  0\n  7  8  1  0     0  0\n  4  3  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n1\n\n>  <bondid>\n7\n\n$$$$\nBicyclo[4-1-1]octane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  9  0     0  0            999 V2000\n    9.6925   -6.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0458   -6.6931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3397   -7.0141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2905   -6.8428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9462   -6.3329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7017   -6.0039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0038   -6.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8230   -5.2859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  1  1  0     0  0\n  7  2  1  0     0  0\n  8  1  1  0     0  0\n  1  7  1  0     0  0\n  8  2  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n6\n\n>  <bondid>\n2\n\n$$$$\nBicyclo[4-1-1]octane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  9  0     0  0            999 V2000\n   10.2044   -7.1593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5546   -7.6794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4884   -7.4862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8148   -7.8278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4736   -7.3223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2224   -6.9962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3764   -8.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3337   -6.2846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  1  1  0     0  0\n  7  2  1  0     0  0\n  8  1  1  0     0  0\n  1  7  1  0     0  0\n  8  2  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n6\n\n>  <bondid>\n2\n\n$$$$\nBicyclo[3-2-2]nonane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    8.9873   -5.7688    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9396   -4.7775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9753   -6.2042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0774   -6.2609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5071   -5.5836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2317   -7.2365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8683   -7.2725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5608   -6.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5275   -6.7292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  1  4  1  0     0  0\n  2  5  1  0     0  0\n  3  6  1  0     0  0\n  4  7  1  0     0  0\n  5  8  1  0     0  0\n  6  9  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n5\n\n>  <bondid>\n5\n\n$$$$\nBicyclo[3-3-1]nonane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    8.9718   -5.4180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8721   -5.4189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4727   -5.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5289   -7.0388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5522   -7.2536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0453   -6.5586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7203   -6.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3240   -5.8707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6297   -4.8964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  1  6  1  0     0  0\n  7  8  1  0     0  0\n  8  3  1  0     0  0\n  3  9  1  0     0  0\n  9  1  1  0     0  0\n  1  2  1  0     0  0\n  2  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n4\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-2-1]nonane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    9.1712   -6.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1464   -6.2056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8839   -5.6171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6571   -5.2966    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6761   -5.5501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9410   -6.1453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9661   -6.6742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7138   -6.0100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9410   -4.5758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  6  9  1  0     0  0\n  9  5  1  0     0  0\n  8  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n6\n\n>  <bondid>\n9\n\n$$$$\nBicyclo[4-2-1]nonane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    9.8115   -5.9359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9067   -6.2317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8460   -5.6949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6107   -5.3780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6184   -5.6284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8802   -6.2172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7040   -6.8849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6444   -6.0834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8802   -4.6651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  6  9  1  0     0  0\n  9  5  1  0     0  0\n  8  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n6\n\n>  <bondid>\n9\n\n$$$$\nBicyclo[4-2-1]nonane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    7.9553   -6.4806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1245   -6.2042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8626   -5.6172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8073   -5.9269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6505   -5.5501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9147   -6.1439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9374   -6.6716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6857   -6.0091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8236   -4.5784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  9  5  1  0     0  0\n  8  7  1  0     0  0\n  9  6  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n6\n\n>  <bondid>\n8\n\n$$$$\nBicyclo[5-1-1]nonane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    7.7834   -6.8950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6536   -6.5515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4441   -5.9761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1897   -5.5634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3360   -5.6252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0166   -6.1147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7177   -6.6607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6682   -6.8540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6683   -5.1050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  3  1  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  2  1  0     0  0\n  3  9  1  0     0  0\n  2  9  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n5\n\n>  <bondid>\n4\n\n$$$$\nBicyclo[3-3-2]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    9.6949   -6.5741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6532   -5.5821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6838   -7.0051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8949   -7.0566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2198   -6.3853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9375   -8.0267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5821   -8.0679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2787   -7.5720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2352   -7.5305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0125   -6.9260    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  1  4  1  0     0  0\n  2  5  1  0     0  0\n  3  6  1  0     0  0\n  5  8  1  0     0  0\n  6  9  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  4 10  1  0     0  0\n 10  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n5\n\n>  <bondid>\n4\n\n$$$$\nBicyclo[4-2-2]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    8.8472   -8.1683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7259   -7.8853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4386   -7.2412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2848   -6.8907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3998   -7.1679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6896   -7.8192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8114   -8.3980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5351   -7.6712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5895   -6.1020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8736   -6.6884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  9  5  1  0     0  0\n  8  7  1  0     0  0\n 10  6  1  0     0  0\n  9 10  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n6\n\n>  <bondid>\n8\n\n$$$$\nBicyclo[4-2-2]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    8.7142   -6.3595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8068   -6.0576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5207   -5.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5526   -5.7547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4737   -5.3433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7622   -5.9919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8793   -6.5683    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6043   -5.8445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6627   -4.2817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9456   -4.8658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  9  5  1  0     0  0\n  8  7  1  0     0  0\n 10  6  1  0     0  0\n  9 10  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n6\n\n>  <bondid>\n8\n\n$$$$\nBicyclo[4-2-2]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    8.8948   -6.4814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1410   -7.3322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0133   -6.5553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6416   -5.8316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5699   -5.6380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8608   -6.2916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9867   -6.8724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7095   -6.1431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7603   -4.5678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0456   -5.1566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  9  5  1  0     0  0\n  8  7  1  0     0  0\n 10  6  1  0     0  0\n  9 10  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n6\n\n>  <bondid>\n8\n\n$$$$\nBicyclo[4-3-1]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    9.3349   -6.7026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2468   -6.4279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9681   -5.8030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7891   -5.4627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8711   -5.7318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1522   -6.3637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1339   -6.4496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6912   -5.5405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0551   -4.6974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6319   -5.8781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  9  5  1  0     0  0\n  9  6  1  0     0  0\n 10  8  1  0     0  0\n 10  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n9\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-3-1]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    8.8223   -6.3064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1166   -6.7735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8745   -6.1531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5558   -5.6824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5492   -5.6698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8328   -6.3073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6175   -6.7466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4940   -5.9863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7350   -4.6265    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3255   -5.8175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  9  5  1  0     0  0\n  9  6  1  0     0  0\n 10  8  1  0     0  0\n 10  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n9\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-3-1]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    9.4787   -5.2376    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3279   -5.2384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0029   -5.6980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0617   -6.9339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0396   -7.1585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5557   -6.4312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1589   -6.2125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8008   -5.7113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1673   -4.6915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6327   -5.7965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  1  6  1  0     0  0\n  7  8  1  0     0  0\n  8  3  1  0     0  0\n  3  9  1  0     0  0\n  9  1  1  0     0  0\n  1  2  1  0     0  0\n 10  2  1  0     0  0\n 10  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n4\n\n>  <bondid>\n10\n\n$$$$\nBicyclo[4-3-1]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    8.5704   -6.7776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0229   -7.5710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0468   -6.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2626   -6.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4354   -7.2985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7455   -6.7578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6855   -7.0209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7071   -7.2278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1753   -5.8290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0646   -7.3398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  1  0     0  0\n  8  3  1  0     0  0\n  3  9  1  0     0  0\n  9  1  1  0     0  0\n  1  2  1  0     0  0\n 10  2  1  0     0  0\n 10  7  1  0     0  0\n  1  6  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n4\n\n>  <bondid>\n9\n\n$$$$\nBicyclo[5-2-1]decane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    8.3634   -6.6141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5495   -7.2830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5102   -6.9328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2905   -6.3299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0719   -5.8974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2732   -5.9622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.9866   -6.4753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6733   -7.0474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5735   -7.2501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5254   -5.4170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  4  1  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9  3  1  0     0  0\n  4 10  1  0     0  0\n  3 10  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n6\n\n>  <bondid>\n0\n\n$$$$\nBicyclo[3-3-3]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    9.9074   -6.3316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8681   -5.3101    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8403   -6.7380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1527   -6.7867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4592   -6.1534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0797   -7.7018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8576   -7.7405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5146   -7.2729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4171   -7.2337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3203   -6.6634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7496   -5.1095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  1  4  1  0     0  0\n  3  6  1  0     0  0\n  5  8  1  0     0  0\n  6  9  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  4 10  1  0     0  0\n 10  7  1  0     0  0\n 11  5  1  0     0  0\n 11  2  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n5\n\n>  <bondid>\n3\n\n$$$$\nBicyclo[4-3-2]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    7.6205   -6.7375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4403   -6.4395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1378   -5.7617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0284   -5.3926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2020   -5.6845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5071   -6.3700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5718   -6.4630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0916   -5.4770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2122   -4.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1122   -5.8433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5429   -5.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  9  5  1  0     0  0\n 10  8  1  0     0  0\n 10  7  1  0     0  0\n 11  6  1  0     0  0\n 11  9  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n9\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-3-2]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    7.3641   -7.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6057   -7.8800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3457   -7.2133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0778   -6.7076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1454   -6.6940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4502   -7.3791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2932   -7.8510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1606   -7.0339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1660   -5.5200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0543   -6.8526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5281   -6.1896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  5  1  0     0  0\n  9  5  1  0     0  0\n 10  8  1  0     0  0\n 10  7  1  0     0  0\n 11  6  1  0     0  0\n 11  9  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n9\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-3-2]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    9.7033   -5.4113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5086   -5.4122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2474   -5.8892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3085   -7.1720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2474   -7.4055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7831   -6.6503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3333   -6.4233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9996   -5.9031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4180   -4.8445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7872   -5.9914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9628   -5.2289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  1  6  1  0     0  0\n  7  8  1  0     0  0\n  8  3  1  0     0  0\n  9  1  1  0     0  0\n  1  2  1  0     0  0\n 10  2  1  0     0  0\n 10  7  1  0     0  0\n 11  3  1  0     0  0\n 11  9  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n4\n\n>  <bondid>\n9\n\n$$$$\nBicyclo[4-3-2]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    9.5890   -6.0668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0222   -6.8881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0821   -5.5563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3408   -5.5563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5198   -6.6060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8056   -6.0463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6729   -6.3187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7305   -6.5329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4155   -4.9619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0302   -6.6489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7926   -5.3863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  1  0     0  0\n  8  3  1  0     0  0\n  3  9  1  0     0  0\n  1  2  1  0     0  0\n 10  2  1  0     0  0\n 10  7  1  0     0  0\n 11  1  1  0     0  0\n 11  9  1  0     0  0\n  1  6  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n4\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-4-1]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    7.3728   -6.4270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5265   -6.7662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7360   -7.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7807   -7.5455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6269   -7.2115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4231   -6.6523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6410   -5.5045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3196   -6.5383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5235   -7.0976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6773   -7.4316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2693   -6.3129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  9  1  0     0  0\n  8 11  1  0     0  0\n 10  9  1  0     0  0\n  5 10  1  0     0  0\n 11  6  1  0     0  0\n  7  5  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n1\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-4-1]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    7.9403   -6.9988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8374   -6.7539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0510   -7.3243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1162   -7.5484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9789   -7.2079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7711   -6.6377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9934   -5.5016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5477   -6.6231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9126   -7.0916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0498   -7.4322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8001   -6.9010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  9  1  0     0  0\n  8 11  1  0     0  0\n 10  9  1  0     0  0\n  5 10  1  0     0  0\n 11  6  1  0     0  0\n  7  5  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n1\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-4-1]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    8.3680   -5.6420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7511   -6.3356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9725   -6.9747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5503   -6.2118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4446   -5.8588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2291   -5.2677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4595   -4.1253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0708   -5.2525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4489   -5.7383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5546   -6.0914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2957   -5.5407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  9  1  0     0  0\n  8 11  1  0     0  0\n 10  9  1  0     0  0\n  5 10  1  0     0  0\n 11  6  1  0     0  0\n  7  5  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n1\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[5-3-1]undecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    7.4699   -5.4930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9044   -6.1137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8921   -6.6506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7678   -6.3049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5569   -5.7261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3072   -5.3108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4607   -5.3728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1456   -5.8656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8448   -6.4150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7887   -6.6095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7825   -4.8494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  5  1  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10  4  1  0     0  0\n  5 11  1  0     0  0\n  4 11  1  0     0  0\n  2  1  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nBicyclo[4-4-2]dodecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 13  0     0  0            999 V2000\n    7.9693   -5.3924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0472   -5.7621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2754   -6.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4140   -6.6115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3360   -6.2475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1138   -5.6380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1109   -4.4385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1806   -5.5138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4028   -6.1232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4808   -6.4871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0361   -5.2682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3405   -4.9653    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  9  1  0     0  0\n  8 11  1  0     0  0\n 10  9  1  0     0  0\n  5 10  1  0     0  0\n 11  6  1  0     0  0\n 12  5  1  0     0  0\n 12  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n1\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-4-2]dodecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 13  0     0  0            999 V2000\n    6.8935   -6.1590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6766   -5.8888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9121   -6.5182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0877   -6.7655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0396   -6.3898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8103   -5.7606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8078   -4.6345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7709   -5.7444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1734   -6.2617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2215   -6.6373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9457   -6.0513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0429   -5.3648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  9  1  0     0  0\n  8 11  1  0     0  0\n 10  9  1  0     0  0\n  5 10  1  0     0  0\n 11  6  1  0     0  0\n 12  5  1  0     0  0\n 12  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n1\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[4-4-2]dodecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 13  0     0  0            999 V2000\n    6.5042   -6.4951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8305   -7.2527    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0721   -7.9506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7035   -7.1174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6802   -6.7317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4449   -6.0862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4449   -4.8994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4564   -6.0697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8695   -6.6002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8927   -6.9858    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6100   -6.3844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6889   -5.6246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  8  9  1  0     0  0\n  8 11  1  0     0  0\n 10  9  1  0     0  0\n  5 10  1  0     0  0\n 11  6  1  0     0  0\n 12  5  1  0     0  0\n 12  7  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n1\n\n>  <bondid>\n1\n\n$$$$\nBicyclo[5-3-2]dodecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 13  0     0  0            999 V2000\n    7.9640   -5.7259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3691   -6.3791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4082   -6.9439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3295   -6.5803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0216   -5.8860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8969   -5.5343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1103   -5.5997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8309   -6.1180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5145   -6.6960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4035   -6.9006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0255   -4.8061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3287   -5.4888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  5  1  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10  4  1  0     0  0\n  2  1  1  0     0  0\n 11  5  1  0     0  0\n 12  4  1  0     0  0\n 11 12  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nBicyclo[5-4-1]dodecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 13  0     0  0            999 V2000\n    7.7173   -5.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8210   -5.4961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0428   -6.0887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1495   -6.3216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0457   -5.9679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8297   -5.3755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5976   -4.9504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7781   -5.0140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4790   -5.5181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1712   -6.0804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0905   -6.2796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0605   -4.4784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11  5  1  0     0  0\n  6 12  1  0     0  0\n  5 12  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n8\n\n>  <bondid>\n7\n\n$$$$\nBicyclo[5-3-3]tridecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 13 14  0     0  0            999 V2000\n    8.4981   -5.1011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2280   -4.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0887   -4.6187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2012   -4.3405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4418   -5.7633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8730   -6.4031    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7468   -5.6806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9461   -5.7884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4646   -4.7690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5590   -4.7986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1539   -5.4010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8112   -6.0270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5669   -6.2486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0     0  0\n  4  3  1  0     0  0\n  2  4  1  0     0  0\n  5  6  1  0     0  0\n  7  1  1  0     0  0\n  8  7  1  0     0  0\n  8  6  1  0     0  0\n  1  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  0     0  0\n 12 13  1  0     0  0\n 13  5  1  0     0  0\n  3  5  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n10\n\n>  <bondid>\n9\n\n$$$$\nBicyclo[5-4-2]tridecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 13 14  0     0  0            999 V2000\n    7.4687   -5.4926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5107   -5.8766    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7478   -6.5099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9306   -6.7589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8885   -6.3808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6576   -5.7476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4784   -5.2933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7402   -5.3611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4893   -5.9002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1604   -6.5011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0052   -6.7140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6549   -4.7411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8882   -5.3775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11  5  1  0     0  0\n 12  6  1  0     0  0\n 13  5  1  0     0  0\n 13 12  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n8\n\n>  <bondid>\n7\n\n$$$$\nBicyclo[5-5-1]tridecane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 13 14  0     0  0            999 V2000\n    7.5850   -5.9774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5169   -6.0690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6632   -7.0919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8369   -7.2880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7693   -6.8637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5517   -6.2665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3258   -5.8379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5160   -5.9020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2226   -6.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9123   -6.9772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8227   -7.1780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7845   -5.3620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0774   -6.6776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11  5  1  0     0  0\n  6 12  1  0     0  0\n  5 12  1  0     0  0\n 13  3  1  0     0  0\n 13  2  1  0     0  0\nM  END\n>  <group>\nBicycles\n\n>  <atomid>\n8\n\n>  <bondid>\n6\n\n$$$$\nAdamantane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 12  0     0  0            999 V2000\n    7.5634   -6.5061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4530   -6.0540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4530   -5.1499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9968   -4.1939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1070   -4.6459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1070   -5.5501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9968   -6.0022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8866   -5.5501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3428   -6.5061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8866   -4.6459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  4 10  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  2  9  1  0     0  0\n  1  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  5  6  1  0     0  0\n  8 10  1  0     0  0\n  2  3  1  0     0  0\nM  END\n>  <group>\nBridged Polycyclics\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nCubane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8 12  0     0  0            999 V2000\n    7.9520   -5.0848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6899   -4.7860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6650   -6.0748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9597   -6.7640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9872   -5.4743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2488   -5.7725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4012   -5.7782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6964   -6.4666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0     0  0\n  3  1  1  0     0  0\n  1  6  1  0     0  0\n  2  5  1  0     0  0\n  7  2  1  0     0  0\n  3  4  1  0     0  0\n  7  3  1  0     0  0\n  4  6  1  0     0  0\n  8  4  1  0     0  0\n  5  6  1  0     0  0\n  8  5  1  0     0  0\n  8  7  1  0     0  0\nM  END\n>  <group>\nBridged Polycyclics\n\n>  <atomid>\n7\n\n>  <bondid>\n11\n\n$$$$\nPrismane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  9  0     0  0            999 V2000\n    7.7612   -4.0397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0907   -4.0333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1698   -4.4963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1678   -5.5167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0887   -5.0413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7593   -5.0602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0     0  0\n  3  1  1  0     0  0\n  3  2  1  0     0  0\n  4  5  1  0     0  0\n  4  6  1  0     0  0\n  5  6  1  0     0  0\n  1  6  1  0     0  0\n  3  4  1  0     0  0\n  2  5  1  0     0  0\nM  END\n>  <group>\nBridged Polycyclics\n\n>  <atomid>\n3\n\n>  <bondid>\n7\n\n$$$$\nTwistane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 12  0     0  0            999 V2000\n   10.9227   -5.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6642   -4.6208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5688   -5.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8274   -4.6208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7871   -7.2292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5284   -6.4333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6238   -7.2292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8825   -6.4333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7835   -5.8799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6165   -5.9203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0     0  0\n  2  4  1  0     0  0\n  3  4  1  0     0  0\n  5  6  1  0     0  0\n  7  5  1  0     0  0\n  8  7  1  0     0  0\n  9  3  1  0     0  0\n  9  6  1  0     0  0\n 10  1  1  0     0  0\n 10  8  1  0     0  0\n  1  6  1  0     0  0\n  3  8  1  0     0  0\nM  END\n>  <group>\nBridged Polycyclics\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\n12-Crown-4\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     0  0            999 V2000\n    9.6950   -4.9978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6961   -3.9955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7230   -3.7807    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4895   -2.8165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4888   -2.8252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2724   -3.7946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3039   -4.0292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3039   -5.0370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2718   -5.2624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.4935   -6.2335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4934   -6.2191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7126   -5.2320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  0     0  0\n 12  1  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\n13-Crown-4\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 13 13  0     0  0            999 V2000\n    6.2108   -5.8522    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2098   -4.8784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1789   -6.0710    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1735   -4.6689    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3479   -7.0179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3527   -3.7257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3428   -7.0999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.3459   -3.6501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7617   -6.1569    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7571   -4.5979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7493   -6.2607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7528   -4.4917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2902   -5.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  6  1  0     0  0\n  5  7  1  0     0  0\n  6  8  1  0     0  0\n  7  9  1  0     0  0\n  8 10  1  0     0  0\n  9 11  1  0     0  0\n 10 12  1  0     0  0\n 11 13  1  0     0  0\n 12 13  1  0     0  0\n  1  2  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\n14-Crown-4\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 14  0     0  0            999 V2000\n   11.4453   -5.1251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9013   -4.2723    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.9150   -5.9676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9132   -4.4080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9274   -5.8351    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5059   -3.4886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5286   -6.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4978   -3.4979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5308   -6.7614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1114   -4.4181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1336   -5.8403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1388   -4.2937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1473   -5.9857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6047   -5.1430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  6  1  0     0  0\n  5  7  1  0     0  0\n  6  8  1  0     0  0\n  7  9  1  0     0  0\n  8 10  1  0     0  0\n  9 11  1  0     0  0\n 10 12  1  0     0  0\n 11 13  1  0     0  0\n 12 14  1  0     0  0\n 13 14  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n$$$$\n15-Crown-5\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 15 15  0     0  0            999 V2000\n    9.3051   -3.6194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1168   -4.1865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4997   -4.1934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8472   -5.1345    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6861   -3.6269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6483   -5.7210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8859   -4.1972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3419   -6.6998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1594   -5.1457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3292   -6.7279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3517   -5.7489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0217   -7.6806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6728   -6.7074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0073   -7.6806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6647   -6.7239    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  6  1  0     0  0\n  5  7  1  0     0  0\n  6  8  1  0     0  0\n  7  9  1  0     0  0\n  8 10  1  0     0  0\n  9 11  1  0     0  0\n 10 12  1  0     0  0\n 11 13  1  0     0  0\n 12 14  1  0     0  0\n 13 15  1  0     0  0\n 14 15  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n$$$$\n16-Crown-5\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 16 16  0     0  0            999 V2000\n   10.1579   -7.9802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3604   -8.5644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8558   -7.0304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5517   -7.9928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6502   -6.4638    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7522   -8.5665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4079   -5.4912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9519   -7.9997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3921   -5.2815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2224   -7.0336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3715   -4.2847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3998   -6.4989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4688   -3.7835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5949   -5.5179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5786   -4.2984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5857   -5.2815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  6  1  0     0  0\n  5  7  1  0     0  0\n  6  8  1  0     0  0\n  7  9  1  0     0  0\n  8 10  1  0     0  0\n  9 11  1  0     0  0\n 10 12  1  0     0  0\n 11 13  1  0     0  0\n 12 14  1  0     0  0\n 13 15  1  0     0  0\n 14 16  1  0     0  0\n 15 16  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\n17-Crown-5\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     0  0            999 V2000\n   11.0779   -6.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1260   -6.4972    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2569   -7.9159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4815   -7.2799    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7011   -7.8978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8165   -7.4802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8151   -6.4943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8549   -6.2786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6443   -5.3223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4333   -4.6975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3911   -5.0835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9204   -4.2341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9543   -4.2341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4969   -5.0788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4504   -4.6735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2557   -5.2828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1487   -7.4881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  6  7  1  0     0  0\n 11 12  1  0     0  0\n 12 13  1  0     0  0\n 13 14  1  0     0  0\n 10 11  1  0     0  0\n 15 16  1  0     0  0\n 14 15  1  0     0  0\n 16  1  1  0     0  0\n  2 17  1  0     0  0\n 17  3  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n$$$$\n18-Crown-6\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n   12.0989   -6.5157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0984   -7.5223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1742   -7.8983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2561   -8.8885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3671   -9.3684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5542   -8.7612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7470   -9.3729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8655   -8.8820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9673   -7.9010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0511   -7.5248    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0591   -6.5276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9807   -6.1495    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8891   -5.1717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7538   -4.6802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5585   -5.2838    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3625   -4.6771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2539   -5.1612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1740   -6.1413    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  3  4  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n  7  8  1  0     0  0\n 12 13  1  0     0  0\n 13 14  1  0     0  0\n 14 15  1  0     0  0\n 11 12  1  0     0  0\n 16 17  1  0     0  0\n 17 18  1  0     0  0\n 15 16  1  0     0  0\n  1 18  1  0     0  0\nM  END\n>  <group>\nCrown Ethers\n\n$$$$\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$$$$\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>  <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$$$$\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$$$$\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>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nALA-D-Alanine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  5  0     1  0            999 V2000\n   13.6701   -6.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6701   -5.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8003   -5.3251    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5335   -5.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5335   -4.3254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3999   -5.8240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  1     0  0\n  2  4  1  0     0  0\n  4  5  2  0     0  0\n  4  6  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n2\n\n>  <bondid>\n0\n\n$$$$\nARG-D-Arginine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   12.0694   -4.2443    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7765   -4.9514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5148   -5.9202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5506   -6.1773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2934   -7.1415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3248   -7.4032    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0676   -8.3674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1033   -8.6246    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7747   -9.0745    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7407   -4.6943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0024   -3.7255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4467   -5.4025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2 10  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  7  9  2  0     0  0\n 10 11  2  0     0  0\n 10 12  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n7\n\n$$$$\nASN-D-Asparagine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   10.8319   -5.4762    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6977   -5.9761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6989   -6.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8342   -7.4719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8321   -8.4753    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9683   -6.9719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5657   -5.4726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5645   -4.4747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4317   -5.9725    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  7  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  4  6  2  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n4\n\n$$$$\nASP-D-Aspartic acid\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   10.7814   -5.6761    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6474   -6.1761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6486   -7.1739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7839   -7.6718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7818   -8.6752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9179   -7.1719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5154   -5.6726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5142   -4.6748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3821   -6.1711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  7  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  4  6  2  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n4\n\n$$$$\nCYS-D-Cysteine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  6  0     1  0            999 V2000\n    6.9511   -4.7004    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8205   -5.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8205   -6.1991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9511   -6.6987    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6834   -4.7004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6834   -3.7013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5489   -5.1995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  5  1  0     0  0\n  3  4  1  0     0  0\n  5  6  2  0     0  0\n  5  7  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n3\n\n$$$$\nGLN-D-Glutamine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   11.1341   -5.3758    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0002   -5.8759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0015   -6.8739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1332   -7.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1344   -8.3757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2695   -8.8736    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0006   -8.8757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8652   -5.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8673   -4.3743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7305   -5.8794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  5  7  2  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n5\n\n$$$$\nGLU-D-Glutamic acid\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   11.4591   -5.3259    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3252   -5.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3265   -6.8240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4582   -7.3276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4594   -8.3256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5945   -8.8236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3256   -8.8257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1902   -5.3279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1923   -4.3243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0555   -5.8295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  5  7  2  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n5\n\n$$$$\nGLY-Glycine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  4  0     0  0            999 V2000\n   10.6670   -7.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5331   -6.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8010   -6.8750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3990   -7.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5331   -5.8750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  2  5  2  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n2\n\n>  <bondid>\n1\n\n$$$$\nHIS-D-Histidine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 11  0     1  0            999 V2000\n   11.4910   -6.5739    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3584   -7.0771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3572   -8.0742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4919   -8.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3861   -9.5713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4100   -9.7753    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9104   -8.9099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5750   -8.1667    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2237   -6.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2217   -5.5747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0896   -7.0762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  9  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4  8  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  2  0     0  0\n  9 10  2  0     0  0\n  9 11  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nILE-D-Isoleucine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   11.8001   -9.8252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8020   -8.8218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6668   -8.3239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5327   -8.8239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6656   -7.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7997   -6.8261    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5336   -6.8225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5324   -5.8248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4003   -7.3211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  6     0  0\n  3  5  1  0     0  0\n  5  6  1  1     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nLEU-D-Leucine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   12.2568   -9.3502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2588   -8.3468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3929   -7.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1235   -7.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1224   -6.8511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2564   -6.3511    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9903   -6.3475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9891   -5.3498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8571   -6.8461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  2  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  1     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nLYS-D-Lysine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   10.6692   -9.3254    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6712   -8.3221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5358   -7.8243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5346   -6.8266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4025   -6.3233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4013   -5.3256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5355   -4.8257    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2659   -4.8278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2679   -3.8246    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1308   -5.3291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  1     0  0\n  6  8  1  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n6\n\n>  <bondid>\n0\n\n$$$$\nMET-D-Methionine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   11.6195   -9.8247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4844   -9.3267    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4832   -8.3287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3515   -7.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3502   -6.8270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4841   -6.3270    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2152   -6.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2173   -5.3253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0805   -6.8304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  1     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nPHE-D-Phenylalanine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 11  0     1  0            999 V2000\n   12.5510   -6.0250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -6.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -6.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -5.0250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.1490   -6.5249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -7.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5510   -8.0249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5510   -9.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -9.5250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -9.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -8.0249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  6  1  0     0  0\n  3  4  2  0     0  0\n  3  5  1  0     0  0\n  6  7  1  0     0  0\n  6 11  2  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n 10 11  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n4\n\n$$$$\nPRO-D-Proline\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     1  0            999 V2000\n   10.6969   -1.7001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6956   -2.6978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8298   -3.1977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7240   -4.1958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7473   -4.3999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2474   -3.5340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9124   -2.7903    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4026   -3.4047    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  3  2  1  1     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  3  7  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n6\n\n>  <bondid>\n2\n\n$$$$\nSER-D-Serine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  6  0     1  0            999 V2000\n   10.3261   -6.8754    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1955   -7.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1955   -8.3741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3261   -8.8737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0584   -6.8754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0584   -5.8763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9239   -7.3745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2  5  1  0     0  0\n  3  4  1  0     0  0\n  5  6  2  0     0  0\n  5  7  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n3\n\n$$$$\nTHR-D-Threonine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   11.5255   -8.1243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3953   -7.6246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -8.1243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3953   -6.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5255   -6.1252    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -6.1252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -5.1257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1245   -6.6245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  1     0  0\n  2  4  1  0     0  0\n  4  5  1  1     0  0\n  4  6  1  0     0  0\n  6  7  2  0     0  0\n  6  8  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n4\n\n>  <bondid>\n0\n\n$$$$\nTRP-D-Tryptophan\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 15 16  0     1  0            999 V2000\n   11.9929   -5.3065    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8877   -5.7594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9408   -6.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0974   -7.3028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1680   -6.9465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5350   -7.7214    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0834   -8.5631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0497   -8.3041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7565   -9.0092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4968   -9.9732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5306  -10.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8239   -9.5270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7230   -5.2128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6717   -4.2179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6150   -5.6658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2 13  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4  8  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  2  0     0  0\n  7 12  1  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n 10 11  1  0     0  0\n 11 12  2  0     0  0\n 13 14  2  0     0  0\n 13 15  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n15\n\n$$$$\nTYR-D-Tyrosine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 13 13  0     1  0            999 V2000\n   12.5019   -5.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3670   -6.3231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3658   -7.3212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4995   -7.8214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5016   -8.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6354   -9.3253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7671   -8.8216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9008   -9.3217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7683   -7.8234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6344   -7.3233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2333   -5.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2344   -4.8247    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0992   -6.3235    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  1     0  0\n  2  3  1  0     0  0\n  2 11  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4 10  1  0     0  0\n  5  6  1  0     0  0\n  6  7  2  0     0  0\n  7  8  1  0     0  0\n  7  9  1  0     0  0\n  9 10  2  0     0  0\n 11 12  2  0     0  0\n 11 13  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n8\n\n$$$$\nVAL-D-Valine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   10.8255   -8.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6953   -8.4496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -8.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6953   -7.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8255   -6.9502    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -6.9502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -5.9506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4245   -7.4494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  2  4  1  0     0  0\n  4  5  1  1     0  0\n  4  6  1  0     0  0\n  6  7  2  0     0  0\n  6  8  1  0     0  0\nM  END\n>  <group>\nD-Amino Acids\n\n>  <atomid>\n4\n\n>  <bondid>\n0\n\n$$$$\nD-Allose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.4194   -1.6883    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9924   -1.0905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4387   -0.4664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0204    0.1639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4629    0.7656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0221    1.3609    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4407    1.9808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1127    2.6517    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2718    1.3426    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2093    0.7656    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2702    0.1833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1849   -0.4782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  6     0  0\n  5 10  1  1     0  0\n  4 11  1  6     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Altrose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.4516   -1.2975    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0245   -0.6997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4709   -0.0714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0525    0.5547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4950    1.1564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0501    1.7518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4729    2.3717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1448    3.0442    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3040    1.7335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2414    1.1564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3024    0.5742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2171   -0.0873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  1     0  0\n  5 10  1  1     0  0\n  4 11  1  6     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Arabinose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -3.8949   -0.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4593    0.4968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8995    1.1253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4675    1.7484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9005    2.3460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4667    2.9613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4723   -0.7154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7192    1.7520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6437    1.1253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7111    0.4839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  7  1  0     0  0\n  4  8  1  1     0  0\n  3  9  1  1     0  0\n  2 10  1  6     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n6\n\n>  <bondid>\n5\n\n$$$$\nD-Erythrose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   -4.1906    0.0133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7523    0.6006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1844    1.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7532    1.8545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1786    2.4581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7458    3.0700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0034    1.8545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9299    1.2384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  4  7  1  6     0  0\n  3  8  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Erythrulose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   -4.1896    2.0954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7907    1.5002    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2449    0.8939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8481    0.2611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7539    2.6818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0537    1.4794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9812    0.9226    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3557   -0.3786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  1  5  1  0     0  0\n  2  6  2  0     0  0\n  3  7  1  1     0  0\n  8  4  1  0     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n4\n\n>  <bondid>\n3\n\n$$$$\nD-Fructose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.1480    1.9843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5728    1.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1297    0.7648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5540    0.1353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1105   -0.4649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5532   -1.0589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1339   -1.6816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5796    2.5934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3170    1.3875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3814    0.7735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2979    0.1190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.3622   -0.4638    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  1  8  1  0     0  0\n  2  9  2  0     0  0\n  3 10  1  1     0  0\n  4 11  1  1     0  0\n  5 12  1  6     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\nD-Galactose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.8880   -0.9644    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4609   -0.3663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9072    0.2619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4890    0.8881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9315    1.4898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4907    2.0852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9093    2.7051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5812    3.3773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7403    2.0668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6779    1.4898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7387    0.9075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6535    0.2459    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  6     0  0\n  5 10  1  6     0  0\n  4 11  1  1     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Glucose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.5186   -1.2143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9457   -0.6164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4995    0.0120    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9178    0.6380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4754    1.2399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9163    1.8351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4978    2.4551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8217    3.1274    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6624    1.8167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7249    1.2399    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6639    0.6573    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7491   -0.0039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  1     0  0\n  5 10  1  1     0  0\n  4 11  1  1     0  0\n  3 12  1  6     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Gulose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -4.3047   -1.0894    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8775   -0.4913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3239    0.1369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9056    0.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3481    1.3648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9073    1.9602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3260    2.5801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9978    3.2523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1570    1.9418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0945    1.3648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1554    0.7825    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0702    0.1209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  6     0  0\n  5 10  1  1     0  0\n  4 11  1  1     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Idose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.7380   -1.2977    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3109   -0.6997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7572   -0.0715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3390    0.5547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7815    1.1564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3407    1.7519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7593    2.3718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4312    3.0440    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5903    1.7335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5279    1.1564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5887    0.5742    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5035   -0.0874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  1     0  0\n  5 10  1  1     0  0\n  4 11  1  1     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Lyxose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -3.9033    0.3647    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3348    0.9551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8987    1.5836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3307    2.2068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8977    2.8043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3273    3.4196    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3259   -0.2571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0749    2.2103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1504    1.5836    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0829    0.9422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  7  1  0     0  0\n  4  8  1  6     0  0\n  3  9  1  1     0  0\n  2 10  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n6\n\n>  <bondid>\n5\n\n$$$$\nD-Mannose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.9005   -1.2560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4734   -0.6580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9197   -0.0298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5015    0.5964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9440    1.1981    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5032    1.7935    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9218    2.4134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5937    3.0856    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7528    1.7751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6904    1.1981    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7512    0.6158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6660   -0.0458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  1     0  0\n  5 10  1  6     0  0\n  4 11  1  6     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Psicose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -4.1455    2.7364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7122    2.1393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1459    1.5125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7164    0.8867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1511    0.2825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6999   -0.3115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1099   -0.9416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7230    3.3500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9598    2.1522    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8942    1.5125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9639    0.8833    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8992    0.2707    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  1  8  1  0     0  0\n  2  9  2  0     0  0\n  3 10  1  1     0  0\n  4 11  1  6     0  0\n  5 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\nD-Ribose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -3.4471   -0.1770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8828    0.4134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4426    1.0421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8747    1.6651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4417    2.2627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8713    2.8780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8696   -0.7989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6188    1.6686    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6943    1.0421    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6268    0.4006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  7  1  0     0  0\n  4  8  1  1     0  0\n  3  9  1  6     0  0\n  2 10  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n6\n\n>  <bondid>\n5\n\n$$$$\nD-Ribulose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -3.1689   -0.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6004    0.0509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1643    0.6794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5963    1.3026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1633    1.9001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5929    2.5154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4160    0.6794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5914   -1.1613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3485    0.0380    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3252    1.2997    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  3  7  1  6     0  0\n  1  8  1  0     0  0\n  2  9  1  1     0  0\n  4 10  2  0     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\nD-Sorbose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -3.8077    2.3989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3743    1.8060    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8123    1.1791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3785    0.5576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8133   -0.0508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3620   -0.6406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7721   -1.2667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3851    3.0166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6219    1.8147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5564    1.1791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6301    0.5499    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5573   -0.0626    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  1  8  1  0     0  0\n  2  9  2  0     0  0\n  3 10  1  1     0  0\n  4 11  1  1     0  0\n  5 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\nD-Tagatose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -5.3565    3.2050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7786    2.4087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3570    1.5726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7842    0.7381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3640   -0.0678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7622   -0.8600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3090   -1.7005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7930    4.0234    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7752    2.4259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3552    1.5726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7806    0.7334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3619   -0.0835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  1  8  1  0     0  0\n  2  9  2  0     0  0\n  3 10  1  6     0  0\n  4 11  1  1     0  0\n  5 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\nD-Talose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   -4.0547   -0.8394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6275   -0.2413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0739    0.3869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6556    1.0131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0981    1.6148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6573    2.2102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0760    2.8301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7478    3.5023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9070    2.1918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8445    1.6148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9054    1.0325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8202    0.3709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  1     0  0\n  5 10  1  6     0  0\n  4 11  1  1     0  0\n  3 12  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Threose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   -4.7339    0.2599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3006    0.8540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7343    1.4815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3045    2.1079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.7353    2.7047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3079    3.3192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.5548    2.1114    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.4800    1.4815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  4  7  1  1     0  0\n  3  8  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nD-Xylose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -3.7801   -0.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2157    0.4968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7755    1.1253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2075    1.7484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7745    2.3460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2083    2.9613    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2027   -0.7154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9517    1.7520    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0272    1.1253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9597    0.4839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  1  7  1  0     0  0\n  4  8  1  1     0  0\n  3  9  1  1     0  0\n  2 10  1  1     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n6\n\n>  <bondid>\n5\n\n$$$$\nD-Xylulose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   -2.9398   -0.2937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3754    0.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9352    0.9336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3672    1.5568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.9342    2.1584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3638    2.7737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1827    0.9336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3623   -0.9196    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1235    0.2880    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1002    1.5539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  3  7  1  1     0  0\n  1  8  1  0     0  0\n  2  9  1  1     0  0\n  4 10  2  0     0  0\nM  END\n>  <group>\nD-Sugars\n\n>  <atomid>\n7\n\n>  <bondid>\n6\n\n$$$$\n1_2_3-Oxadiazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nDioxane\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    4.2090   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2090   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -4.7018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -3.0482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nFuran\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n\n$$$$\nImidazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nIndole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    6.3344   -5.9612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7641   -5.9608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0506   -5.5480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7641   -6.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3344   -6.7915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0524   -7.2005    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4800   -7.2028    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1974   -6.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1974   -5.9608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\n  8  9  2  0     0  0\n  7  8  1  0     0  0\n  2  9  1  0     0  0\n  4  7  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n6\n\n>  <bondid>\n6\n\n$$$$\nIsoquinoline\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    7.2094   -5.7112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6391   -5.7108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9256   -5.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6391   -6.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2094   -6.5415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9274   -6.9505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3533   -5.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0698   -5.7124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3584   -6.9529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0717   -6.5353    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  2  4  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\n  8  7  2  0     0  0\n  9 10  2  0     0  0\n 10  8  1  0     0  0\n  4  9  1  0     0  0\n  2  7  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n8\n\n>  <bondid>\n0\n\n$$$$\nIsoxazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n2\n\n>  <bondid>\n0\n\n$$$$\nMorpholine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    4.2090   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2090   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -4.7018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -3.0482    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n5\n\n>  <bondid>\n1\n\n$$$$\nOxazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n4\n\n>  <bondid>\n0\n\n$$$$\nPiperazine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    4.2090   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2090   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -4.7018    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -3.0482    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n5\n\n>  <bondid>\n1\n\n$$$$\nPiperidine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    3.0000   -9.5098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000  -10.3366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7160  -10.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4320  -10.3366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4320   -9.5098    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7160   -9.0964    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nPurine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9 10  0     0  0            999 V2000\n    6.3344   -5.9612    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7641   -5.9608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0506   -5.5480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7641   -6.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3344   -6.7915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0524   -7.2005    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4800   -7.2028    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1974   -6.7878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1974   -5.9608    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\n  8  9  2  0     0  0\n  7  8  1  0     0  0\n  2  9  1  0     0  0\n  4  7  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n6\n\n>  <bondid>\n7\n\n$$$$\nPyran\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    4.2090   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2090   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -4.7018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -4.2884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6410   -3.4616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9250   -3.0482    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nPyrazine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    6.4094   -4.0362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1256   -3.6230    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.8628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4094   -4.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1274   -5.2755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n0\n\n>  <bondid>\n2\n\n$$$$\nPyrazol\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nPyridazine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    6.4094   -4.0362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1256   -3.6230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.8628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4094   -4.8665    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1274   -5.2755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nPyridine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    6.4094   -4.0362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1256   -3.6230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.8628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4094   -4.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1274   -5.2755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n3\n\n>  <bondid>\n1\n\n$$$$\nPyridone\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  7  0     0  0            999 V2000\n    5.2590   -5.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2590   -5.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9750   -6.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6910   -5.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6910   -5.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9750   -4.5982    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5430   -4.5982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  6  1  0     0  0\n  1  7  2  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n5\n\n>  <bondid>\n5\n\n$$$$\nPyrimidine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    6.4094   -4.0362    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.0358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1256   -3.6230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.8628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4094   -4.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1274   -5.2755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n4\n\n>  <bondid>\n1\n\n$$$$\nPyrole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    3.6685  -10.0843    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -9.5986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2553   -8.8126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0817   -8.8126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3370   -9.5986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n$$$$\nPyrone\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  7  0     0  0            999 V2000\n    5.2590   -5.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2590   -5.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9750   -6.2518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6910   -5.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6910   -5.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9750   -4.5982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5430   -4.5982    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  2  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  6  1  0     0  0\n  1  7  2  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n4\n\n>  <bondid>\n4\n\n$$$$\nPyrrolidine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    3.7210   -3.9181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3632   -3.3980    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0779   -3.8107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8532   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0171   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n1\n\n>  <bondid>\n2\n\n$$$$\nQuinoline\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    7.2094   -5.7112    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6391   -5.7108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9256   -5.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6391   -6.5378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2094   -6.5415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9274   -6.9505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3533   -5.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0698   -5.7124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3584   -6.9529    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0717   -6.5353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  2  4  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\n  8  7  2  0     0  0\n  9 10  2  0     0  0\n 10  8  1  0     0  0\n  4  9  1  0     0  0\n  2  7  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n9\n\n>  <bondid>\n8\n\n$$$$\nTetrahydrofuran\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    3.7210   -3.9181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3632   -3.3980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0779   -3.8107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8532   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0171   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n2\n\n>  <bondid>\n2\n\n$$$$\nTetrahydrothiophene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    3.7210   -3.9181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3632   -3.3980    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0779   -3.8107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8532   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0171   -4.6492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n2\n\n>  <bondid>\n2\n\n$$$$\nTetrazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nThiophene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n4\n\n>  <bondid>\n3\n\n$$$$\nTriazine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    6.4094   -4.0362    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.0358    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1256   -3.6230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8391   -4.8628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4094   -4.8665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1274   -5.2755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n3\n\n>  <bondid>\n1\n\n$$$$\nTriazole\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    4.9500   -4.1780    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2815   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5368   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3632   -2.9063    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6185   -3.6923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  2  0     0  0\n  1  2  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\nM  END\n>  <group>\nHeterocyclic Rings\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nALA-L-Alanine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  5  0     1  0            999 V2000\n   13.6700   -6.8246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6700   -5.8249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8002   -5.3251    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5334   -5.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5334   -4.3254    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3998   -5.8240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  6     0  0\n  2  4  1  0     0  0\n  4  5  2  0     0  0\n  4  6  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n2\n\n>  <bondid>\n0\n\n$$$$\nARG-L-Arginine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 11  0     1  0            999 V2000\n   12.0694   -4.2443    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7765   -4.9514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5148   -5.9202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5506   -6.1773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2934   -7.1415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3248   -7.4032    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0676   -8.3674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1033   -8.6246    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7747   -9.0745    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7407   -4.6943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0024   -3.7255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4467   -5.4025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2 10  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  7  9  2  0     0  0\n 10 11  2  0     0  0\n 10 12  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n7\n\n$$$$\nASN-L-Asparagine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   10.8319   -5.4762    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6977   -5.9761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6989   -6.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8342   -7.4719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8321   -8.4753    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9683   -6.9719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5657   -5.4726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5645   -4.4747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4317   -5.9725    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  7  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  4  6  2  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n4\n\n$$$$\nASP-L-Aspartic acid\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   10.7814   -5.6761    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6474   -6.1761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6486   -7.1739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7839   -7.6718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7818   -8.6752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9179   -7.1719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5154   -5.6726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5142   -4.6748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3821   -6.1711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  7  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  4  6  2  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n4\n\n$$$$\nCYS-L-Cysteine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  6  0     1  0            999 V2000\n    6.9511   -4.7004    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8205   -5.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8205   -6.1991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9511   -6.6987    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6834   -4.7004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6834   -3.7013    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5489   -5.1995    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  5  1  0     0  0\n  3  4  1  0     0  0\n  5  6  2  0     0  0\n  5  7  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n3\n\n$$$$\nGLN-L-Glutamine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   11.1341   -5.3758    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0002   -5.8759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0015   -6.8739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1332   -7.3776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1344   -8.3757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2695   -8.8736    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0006   -8.8757    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8652   -5.3779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8673   -4.3743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7305   -5.8794    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  5  7  2  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n5\n\n$$$$\nGLU-L-Glutamic acid\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   11.4591   -5.3259    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3252   -5.8259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3265   -6.8240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4582   -7.3276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4594   -8.3256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5945   -8.8236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3256   -8.8257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1902   -5.3279    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1923   -4.3243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0555   -5.8295    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  5  7  2  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n5\n\n$$$$\nGLY-Glycine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  4  0     0  0            999 V2000\n   10.6670   -7.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5331   -6.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8010   -6.8750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3990   -7.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5331   -5.8750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  2  5  2  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n2\n\n>  <bondid>\n1\n\n$$$$\nHIS-L-Histidine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 11  0     1  0            999 V2000\n   11.4910   -6.5739    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3584   -7.0771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3572   -8.0742    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4919   -8.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3861   -9.5713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4100   -9.7753    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9104   -8.9099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5750   -8.1667    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2237   -6.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2217   -5.5747    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0896   -7.0762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  9  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4  8  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  2  0     0  0\n  9 10  2  0     0  0\n  9 11  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nILE-L-Isoleucine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   11.8001   -9.8252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.8020   -8.8218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6668   -8.3239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5327   -8.8239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.6656   -7.3261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7997   -6.8261    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5336   -6.8225    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5324   -5.8248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4003   -7.3211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  1     0  0\n  3  5  1  0     0  0\n  5  6  1  6     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nLEU-L-Leucine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   12.2568   -9.3502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2588   -8.3468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3929   -7.8469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1235   -7.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.1224   -6.8511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2564   -6.3511    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9903   -6.3475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9891   -5.3498    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8571   -6.8461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  2  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  6     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nLYS-L-Lysine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10  9  0     1  0            999 V2000\n   10.6692   -9.3254    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6712   -8.3221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5358   -7.8243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5346   -6.8266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4025   -6.3233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4013   -5.3256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5355   -4.8257    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2659   -4.8278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2679   -3.8246    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1308   -5.3291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  6     0  0\n  6  8  1  0     0  0\n  8  9  2  0     0  0\n  8 10  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n6\n\n>  <bondid>\n0\n\n$$$$\nMET-L-Methionine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  8  0     1  0            999 V2000\n   11.6195   -9.8247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4844   -9.3267    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4832   -8.3287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3515   -7.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3502   -6.8270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4841   -6.3270    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2152   -6.3290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2173   -5.3253    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0805   -6.8304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  6     0  0\n  5  7  1  0     0  0\n  7  8  2  0     0  0\n  7  9  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n5\n\n>  <bondid>\n0\n\n$$$$\nPHE-L-Phenylalanine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 11  0     1  0            999 V2000\n   12.5510   -6.0250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -6.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -6.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -5.0250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.1490   -6.5249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -7.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5510   -8.0249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5510   -9.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4169   -9.5250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -9.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2830   -8.0249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  6  1  0     0  0\n  3  4  2  0     0  0\n  3  5  1  0     0  0\n  6  7  1  0     0  0\n  6 11  2  0     0  0\n  7  8  2  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n 10 11  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nPRO-L-Proline\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     1  0            999 V2000\n   10.6969   -1.7001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6956   -2.6978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8298   -3.1977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7240   -4.1958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7473   -4.3999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.2474   -3.5340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9124   -2.7903    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4026   -3.4047    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  3  2  1  6     0  0\n  2  8  1  0     0  0\n  3  4  1  0     0  0\n  3  7  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n6\n\n>  <bondid>\n2\n\n$$$$\nSER-L-Serine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  6  0     1  0            999 V2000\n   10.3261   -6.8754    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1955   -7.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1955   -8.3741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3261   -8.8737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0584   -6.8754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0584   -5.8763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9239   -7.3745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2  5  1  0     0  0\n  3  4  1  0     0  0\n  5  6  2  0     0  0\n  5  7  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n3\n\n$$$$\nTHR-L-Threonine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   11.5255   -8.1243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3953   -7.6246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -8.1243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3953   -6.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5255   -6.1252    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -6.1252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2586   -5.1257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1245   -6.6245    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  6     0  0\n  2  4  1  0     0  0\n  4  5  1  6     0  0\n  4  6  1  0     0  0\n  6  7  2  0     0  0\n  6  8  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n4\n\n>  <bondid>\n0\n\n$$$$\nTRP-L-Tryptophan\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 15 16  0     1  0            999 V2000\n   11.9929   -5.3065    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8877   -5.7594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9408   -6.7608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0974   -7.3028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1680   -6.9465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5350   -7.7214    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0834   -8.5631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0497   -8.3041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7565   -9.0092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4968   -9.9732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5306  -10.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8239   -9.5270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.7230   -5.2128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6717   -4.2179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6150   -5.6658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2 13  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4  8  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  2  0     0  0\n  7 12  1  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n 10 11  1  0     0  0\n 11 12  2  0     0  0\n 13 14  2  0     0  0\n 13 15  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n15\n\n$$$$\nTYR-L-Tyrosine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 13 13  0     1  0            999 V2000\n   12.5019   -5.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3670   -6.3231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.3658   -7.3212    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4995   -7.8214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5016   -8.8251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6354   -9.3253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7671   -8.8216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9008   -9.3217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7683   -7.8234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6344   -7.3233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2333   -5.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.2344   -4.8247    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0992   -6.3235    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  6     0  0\n  2  3  1  0     0  0\n  2 11  1  0     0  0\n  3  4  1  0     0  0\n  4  5  2  0     0  0\n  4 10  1  0     0  0\n  5  6  1  0     0  0\n  6  7  2  0     0  0\n  7  8  1  0     0  0\n  7  9  1  0     0  0\n  9 10  2  0     0  0\n 11 12  2  0     0  0\n 11 13  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n0\n\n>  <bondid>\n8\n\n$$$$\nVAL-L-Valine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  7  0     1  0            999 V2000\n   10.8255   -8.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6953   -8.4496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -8.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.6953   -7.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8255   -6.9502    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -6.9502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5586   -5.9506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4245   -7.4494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  2  4  1  0     0  0\n  4  5  1  6     0  0\n  4  6  1  0     0  0\n  6  7  2  0     0  0\n  6  8  1  0     0  0\nM  END\n>  <group>\nL-Amino Acids\n\n>  <atomid>\n4\n\n>  <bondid>\n0\n\n$$$$\nAdenine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 11  0     0  0            999 V2000\n    3.4903   -2.0759    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.1974   -1.8369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -1.3637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.1974   -0.9421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9070   -2.2584    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4956   -0.6934    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8834   -0.5386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6333   -1.8449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6333   -0.9769    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8834    0.2478    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  2  0     0  0\n  2  5  1  0     0  0\n  3  6  2  0     0  0\n  4  7  1  0     0  0\n  5  8  2  0     0  0\n  7  9  2  0     0  0\n  7 10  1  0     0  0\n  4  6  1  0     0  0\n  8  9  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nCytosine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     0  0            999 V2000\n    3.7084   -1.9709    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4211   -1.5561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -1.5602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4211   -0.7296    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1335   -1.9667    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -0.7338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7050   -0.3230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7050    0.4994    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  2  5  2  0     0  0\n  3  6  2  0     0  0\n  4  7  2  0     0  0\n  7  8  1  0     0  0\n  6  7  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nGuanine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 12  0     0  0            999 V2000\n    3.4897    0.3839    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.1974    0.6221    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    1.0969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.1974    1.5215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9066    0.2000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5004    1.7668    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8887    1.9244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6377    0.6171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6377    1.4853    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8887    2.7154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3288    0.2133    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  2  0     0  0\n  2  5  1  0     0  0\n  3  6  2  0     0  0\n  4  7  1  0     0  0\n  5  8  2  0     0  0\n  7  9  1  0     0  0\n  7 10  2  0     0  0\n  4  6  1  0     0  0\n  8  9  1  0     0  0\n  8 11  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nThymine\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  9  0     0  0            999 V2000\n    2.4396   -1.5954    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1523   -1.1809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7188   -1.1806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1523   -0.3502    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8646   -1.5913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7189   -0.3543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4364    0.0565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4364    0.8829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0104    0.0579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  2  5  2  0     0  0\n  3  6  2  0     0  0\n  4  7  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\n  6  9  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nUracil\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     0  0            999 V2000\n    3.7124   -0.5250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4252   -0.1064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -0.1145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4252    0.7243    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1458   -0.5209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    0.7202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7092    1.1310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7092    1.9576    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  2  5  2  0     0  0\n  3  6  2  0     0  0\n  4  7  1  0     0  0\n  7  8  2  0     0  0\n  6  7  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nRibose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 14  0     1  0            999 V2000\n    3.6483   -1.5101    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6483   -2.8768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6030   -2.5039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5685   -2.8768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9582   -3.4695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2479   -3.4695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2479   -2.2377    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2479   -4.2134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9582   -2.2333    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9582   -4.2134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5685   -2.0518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.7706   -2.0564    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5685   -3.8042    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6483   -3.6834    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  1     0  0\n  5  6  1  1     0  0\n  2  6  1  1     0  0\n  6  7  1  0     0  0\n  6  8  1  0     0  0\n  5  9  1  0     0  0\n  5 10  1  0     0  0\n  4 11  1  0     0  0\n 11 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <atomid>\n0\n\n>  <bondid>\n11\n\n$$$$\nDeoxyribose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 14  0     0  0            999 V2000\n   11.5961   -4.0092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5961   -5.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -6.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -6.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -5.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4831   -5.0674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -4.5860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5320   -4.5909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -6.4519    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -4.7792    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -6.8876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -4.7839    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -6.8876    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5961   -6.3232    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  2  6  1  0     0  0\n  6  5  1  0     0  0\n  5  4  1  0     0  0\n  4  3  1  0     0  0\n  2  3  1  0     0  0\n  2  1  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  5  9  1  0     0  0\n  4 10  1  0     0  0\n  4 11  1  0     0  0\n  3 12  1  0     0  0\n  3 13  1  0     0  0\n  2 14  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <atomid>\n0\n\n>  <bondid>\n7\n\n$$$$\nRibose monophosphate\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 18  0     1  0            999 V2000\n   14.4831   -3.7504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4831   -5.1570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4073   -4.7732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3426   -5.1570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7437   -5.7670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0710   -5.7670    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0710   -4.4993    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   14.0710   -6.5326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7437   -4.4947    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7437   -6.5326    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3426   -4.3079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.3426   -6.1115    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4831   -5.9871    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2261   -4.3001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3520   -4.3001    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4739   -4.3001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3520   -3.4183    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3520   -5.1818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  1     0  0\n  5  6  1  1     0  0\n  2  6  1  1     0  0\n  6  7  1  0     0  0\n  6  8  1  0     0  0\n  5  9  1  0     0  0\n  5 10  1  0     0  0\n  4 11  1  0     0  0\n  4 12  1  0     0  0\n  2 13  1  0     0  0\n 14 15  1  0     0  0\n 15 16  1  0     0  0\n 15 17  2  0     0  0\n 15 18  1  0     0  0\n 11 14  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <atomid>\n0\n\n>  <bondid>\n14\n\n$$$$\nDeoxyribose monophosphate\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n   11.5961   -4.0092    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5961   -5.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -6.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -6.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -5.4644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4831   -5.0674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -4.5860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5320   -4.5909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6579   -4.5909    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7798   -4.5909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6579   -3.7091    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6579   -5.4726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3815   -6.4519    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -4.7792    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7965   -6.8876    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -4.7839    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1697   -6.8876    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5961   -6.3232    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  2  6  1  0     0  0\n  6  5  1  0     0  0\n  5  4  1  0     0  0\n  4  3  1  0     0  0\n  2  3  1  0     0  0\n  2  1  1  0     0  0\n  5  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n  9 11  2  0     0  0\n  9 12  1  0     0  0\n  5 13  1  0     0  0\n  4 14  1  0     0  0\n  4 15  1  0     0  0\n  3 16  1  0     0  0\n  3 17  1  0     0  0\n  2 18  1  0     0  0\nM  END\n>  <group>\nNucleobases\n\n>  <atomid>\n0\n\n>  <bondid>\n9\n\n$$$$\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>  <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>  <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>  <atomid>\n30\n\n>  <bondid>\n32\n\n$$$$\nBenzene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    0.6548    2.2452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0813    2.2456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3694    2.6575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0813    1.4204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.6548    1.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3712    1.0086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  1  2  0     0  0\n  4  2  2  0     0  0\n  1  5  1  0     0  0\n  2  3  1  0     0  0\n  5  6  2  0     0  0\n  6  4  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nBoat\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    5.8944    2.4444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4777    2.4444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4166    3.9499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9277    3.9666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2722    3.2222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0277    3.2222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  1  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  3  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <atomid>\n3\n\n>  <bondid>\n2\n\n$$$$\nChair\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    8.5333    5.5888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.1166    6.6110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9111    6.0833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2555    6.0833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0277    5.5888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6166    6.6222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  1  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  3  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nChair1\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    4.9944    2.4555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7388    3.0777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2777    2.1666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4055    4.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5333    3.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1166    4.4555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  1  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nChair2\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n   10.4055    2.4555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6611    3.0777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1222    2.1666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9944    4.1610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8666    3.5388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2833    4.4555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  1  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nChair3\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n    5.0777    4.5777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4888    9.8610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2000   10.1555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8222    8.7777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3611    4.2888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3277    7.0332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0777    6.3666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4888    8.0721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2388    7.4055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6166    5.6610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8666    7.8666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2000    8.3666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3611    6.0777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7777    6.6610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8222    6.9888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0333    5.6610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4055    8.7777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6166    7.4499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  7 15  1  0     0  0\n 15 13  1  0     0  0\n 13  8  1  0     0  0\n  8 18  1  0     0  0\n 18 12  1  0     0  0\n 12  7  1  0     0  0\n  1  7  1  0     0  0\n  8  2  1  0     0  0\n 12  3  1  0     0  0\n 15  4  1  0     0  0\n  5 13  1  0     0  0\n  6  7  1  0     0  0\n  8  9  1  0     0  0\n 10 18  1  0     0  0\n 11 12  1  0     0  0\n 13 14  1  0     0  0\n 15 16  1  0     0  0\n 17 18  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <atomid>\n0\n\n>  <bondid>\n5\n\n$$$$\nChair4\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n   10.4888    4.5777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0777    9.8610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3666   10.1555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7444    8.7777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2055    4.2888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.2388    7.0332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.4888    6.3666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0777    8.0721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3277    7.4055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9500    5.6610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.7000    7.8666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3666    8.3666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2055    6.0777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.7888    6.6610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7444    6.9888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.5333    5.6610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1611    8.7777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.9500    7.4499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  7 15  1  0     0  0\n 15 13  1  0     0  0\n 13  8  1  0     0  0\n  8 18  1  0     0  0\n 18 12  1  0     0  0\n 12  7  1  0     0  0\n  1  7  1  0     0  0\n  8  2  1  0     0  0\n 12  3  1  0     0  0\n 15  4  1  0     0  0\n  5 13  1  0     0  0\n  6  7  1  0     0  0\n  8  9  1  0     0  0\n 10 18  1  0     0  0\n 11 12  1  0     0  0\n 13 14  1  0     0  0\n 15 16  1  0     0  0\n 17 18  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <atomid>\n0\n\n>  <bondid>\n5\n\n$$$$\nCyclopentadiene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    3.8091    8.2444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3091    6.7055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6181    7.6510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3091    6.7055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    7.6510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  5  1  0     0  0\n  2  3  2  0     0  0\n  3  1  1  0     0  0\n  4  2  1  0     0  0\n  5  4  2  0     0  0\nM  END\n>  <group>\nRings\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nCyclopentadiene\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n   14.3500   -2.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2160   -3.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2160   -4.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4840   -4.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.4840   -3.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  2  0     0  0\n  4  5  2  0     0  0\n  5  1  1  0     0  0\n  4  3  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nRing3\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  3  3  0     0  0            999 V2000\n    2.6123    1.5663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6098    1.5663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1111    2.4280    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  3  1  0     0  0\nM  END\n>  <group>\nRings\n\n$$$$\nRing4\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  4  4  0     0  0            999 V2000\n    3.4956    1.8862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4919    2.8804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4846    1.8991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4821    2.8804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  4  1  0     0  0\nM  END\n>  <group>\nRings\n\n$$$$\nRing5\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    3.3632    3.2710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.3649    3.2710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0647    2.3206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6686    2.2948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8751    1.7233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  5  1  0     0  0\nM  END\n>  <group>\nRings\n\n$$$$\nRing5\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  5  5  0     0  0            999 V2000\n    2.2500    1.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1160    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1160   -0.1750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3840   -0.1750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3840    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  4  5  1  0     0  0\n  5  1  1  0     0  0\n  4  3  1  0     0  0\nM  END\n>  <group>\nRings\n\n$$$$\nRing6\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  6  6  0     0  0            999 V2000\n    2.5500    3.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5500    2.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4160    2.1722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2820    2.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2820    3.6722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4160    4.1722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0     0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\nM  END\n>  <group>\nRings\n\n$$$$\nRing7\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  7  7  0     0  0            999 V2000\n   21.4111    6.3389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.1938    6.9555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.1653    6.7333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.5987    5.8389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   21.4166    5.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.1660    4.9333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.1938    4.7111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  6  1  0     0  0\n  1  5  1  0     0  0\n  5  7  1  0     0  0\n  6  7  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nRing8\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  8  8  0     0  0            999 V2000\n    2.9268    2.2122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9270    3.2099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6288    3.9118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6290    1.5102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6266    1.5102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3286    2.2122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3285    3.2099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6266    3.9119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  1  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  3  1  0     0  0\nM  END\n>  <group>\nRings\n\n$$$$\nRing9\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n  9  9  0     0  0            999 V2000\n    2.7667    2.2210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5972    3.2097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0962    4.0662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5313    1.5810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5375    1.5810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2993    2.2169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.4693    3.1987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0364    4.4023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9746    4.0565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  1  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  8  3  1  0     0  0\n  8  9  1  0     0  0\n  9  7  1  0     0  0\nM  END\n>  <group>\nRings\n\n$$$$\nRing10\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 10 10  0     0  0            999 V2000\n    3.5215    2.9499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3132    2.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3132    1.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0493    2.9499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7854    2.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7854    1.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5215    1.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2575    1.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2575    2.5249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0493    1.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  8  9  1  0     0  0\n  3 10  1  0     0  0\n 10  6  1  0     0  0\n  5  4  1  0     0  0\n  4  2  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  2  3  1  0     0  0\n  9  1  1  0     0  0\n  1  5  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nRing11\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 11 11  0     0  0            999 V2000\n    3.7115    0.9202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6673    0.9202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8179    1.8392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.7664    2.5772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8179    3.2138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6382    4.1686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6721    4.1677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4599    3.2440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5335    3.0226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5480    2.0636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4840    1.8574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11  1  1  0     0  0\n  4  5  1  0     0  0\nM  END\n>  <group>\nRings\n\n$$$$\nRing12\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 12 12  0     0  0            999 V2000\n    3.7276    1.1285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.7247    1.1285    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9441    2.1019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9082    2.3309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9040    3.3264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9232    3.5474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6929    4.5158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6906    4.5147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4660    3.5463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5063    3.3181    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5162    2.3234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4980    2.1108    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  3  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n 11 12  1  0     0  0\n 12  1  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nRing13\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 13 13  0     0  0            999 V2000\n    3.2666    4.9710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4574    4.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9755    4.0189    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.7213    3.9768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0441    3.6774    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6650    3.7016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0441    2.6968    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.7099    2.6175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9763    2.4069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6652    2.4096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0491    1.4518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6845    1.4484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9051    1.1289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  6  1  0     0  0\n  5  7  1  0     0  0\n  6  8  1  0     0  0\n  7  9  1  0     0  0\n  8 10  1  0     0  0\n  9 11  1  0     0  0\n 10 12  1  0     0  0\n 11 13  1  0     0  0\n 12 13  1  0     0  0\n  1  2  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <atomid>\n0\n\n>  <bondid>\n12\n\n$$$$\nRing14\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 14 14  0     0  0            999 V2000\n    6.8995    3.2081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3539    4.0579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3678    2.3687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3685    3.9274    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3883    2.5015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9655    4.8438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9885    1.5835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9602    4.8347    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9932    1.5783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5727    3.9117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5892    2.4908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5971    4.0366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6111    2.3505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0671    3.1903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  1  3  1  0     0  0\n  2  4  1  0     0  0\n  3  5  1  0     0  0\n  4  6  1  0     0  0\n  5  7  1  0     0  0\n  6  8  1  0     0  0\n  7  9  1  0     0  0\n  8 10  1  0     0  0\n  9 11  1  0     0  0\n 10 12  1  0     0  0\n 11 13  1  0     0  0\n 12 14  1  0     0  0\n 13 14  1  0     0  0\nM  END\n>  <group>\nRings\n\n$$$$\nRing15\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 15 15  0     0  0            999 V2000\n    6.3839    2.8393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0478    1.8979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0286    1.8979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6750    0.9634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6672    0.9934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3752    1.9525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.3912    2.0190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.1293    2.9718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9384    3.5389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6710    4.4863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4746    5.0532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2796    4.4781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1008    5.0326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9121    4.4093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5968    3.4606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  3  4  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n  7  8  1  0     0  0\n 12 13  1  0     0  0\n 13 14  1  0     0  0\n 14 15  1  0     0  0\n 11 12  1  0     0  0\n  1 15  1  0     0  0\nM  END\n>  <group>\nRings\n\n$$$$\nRing16\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 16 16  0     0  0            999 V2000\n    5.3307    1.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8666    2.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4647    0.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8666    4.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0006    3.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0006    2.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8666    1.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7326    0.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5987    1.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7326    3.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5987    4.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4647    3.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3307    2.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1967    2.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1967    3.9944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3307    4.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  9  3  1  0     0  0\n  3  1  1  0     0  0\n  1 13  1  0     0  0\n 10  4  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  2  1  0     0  0\n  2  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n 12 11  1  0     0  0\n 11 10  1  0     0  0\n 13 14  1  0     0  0\n 14 15  1  0     0  0\n 15 16  1  0     0  0\n 16 12  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <atomid>\n0\n\n>  <bondid>\n1\n\n$$$$\nRing18\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n    6.7675    4.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7675    3.0235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8338    2.6634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9136    1.6865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0241    1.2306    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2362    1.8639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4295    1.2651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5501    1.7405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6379    2.7240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7034    3.0885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7024    4.0770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6366    4.4288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5561    5.4110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4362    5.8637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2239    5.2349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0336    5.8456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9184    5.3645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8307    4.3812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0     0  0\n  2  3  1  0     0  0\n  4  5  1  0     0  0\n  5  6  1  0     0  0\n  6  7  1  0     0  0\n  3  4  1  0     0  0\n  8  9  1  0     0  0\n  9 10  1  0     0  0\n 10 11  1  0     0  0\n  7  8  1  0     0  0\n 12 13  1  0     0  0\n 13 14  1  0     0  0\n 14 15  1  0     0  0\n 11 12  1  0     0  0\n 16 17  1  0     0  0\n 17 18  1  0     0  0\n 15 16  1  0     0  0\n  1 18  1  0     0  0\nM  END\n>  <group>\nRings\n\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\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>  <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>  <atomid>\n0\n\n>  <bondid>\n0\n\n$$$$\nalpha-D-Allopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -4.1124    6.2007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.6076    4.1259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5974    5.2058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4025    4.8658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5974    6.0607    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.3373    4.7808    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9974    3.2709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2076    5.2058    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7775    5.3207    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.6076    3.2709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1476    3.8958    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4025    4.0109    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1124    5.3507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7577    4.3259    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7775    4.4658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9974    4.1259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8224    4.3259    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  8  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n  8  4  1  0     0  0\n  3  5  1  0     0  0\n  3  6  1  0     0  0\n  7 16  1  0     0  0\n 17 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Altropyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -6.8433    4.3051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3385    2.2303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.3283    3.3102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.1334    2.9703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.3283    4.1651    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -8.0682    2.8852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.7283    1.3754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.9384    3.3102    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.5084    3.4252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3385    1.3754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8784    2.0003    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.1334    2.1154    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.8433    3.4551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4886    2.4303    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.5084    2.5702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.7283    2.2303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.5532    2.4303    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  8  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n  8  4  1  0     0  0\n  3  5  1  0     0  0\n  3  6  1  0     0  0\n  7 16  1  0     0  0\n 17 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Galactopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -6.4899    2.6666    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9851    0.5918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.9748    1.6717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.7800    1.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.9748    2.5266    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.7148    1.2467    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3749   -0.2631    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.1998    0.7918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1550    1.7866    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9851   -0.2631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5250    0.3618    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.7800    0.4768    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.4899    1.8166    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1352    0.7918    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1550    0.9317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3749    0.5918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.5850    1.6717    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n 17  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n 17  4  1  0     0  0\n  3  5  1  0     0  0\n  3  6  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Glucopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -7.7107   -0.2570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2094   -2.3086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -8.1903   -1.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.0088   -1.5769    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -8.1903   -0.3955    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.8273   -1.2408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.5674   -3.1539    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -8.3831   -2.1108    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3908   -1.1271    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2094   -3.1539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.7680   -2.5360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.0088   -2.4222    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.7107   -1.0975    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.3937   -2.1108    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3908   -1.9725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.5674   -2.3086    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -8.8923   -1.6610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  6  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n  6  4  1  0     0  0\n  3  5  1  0     0  0\n  3 17  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Gulopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -5.8152    3.8232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2901    1.7531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.2952    2.8332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1052    2.4882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.2952    3.6832    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9101    2.8332    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.6702    0.9031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.5202    1.9532    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4801    2.9432    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.2901    0.9031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8551    1.5281    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.1052    1.6382    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.8152    2.9732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4651    1.9532    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4801    2.0931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.6702    1.7531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.0302    2.4032    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  6  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n  6  4  1  0     0  0\n  3  5  1  0     0  0\n  3 17  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Idopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -6.0079    2.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4782    0.6560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.4929    1.7359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2981    1.3960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.4929    2.5909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1031    1.7359    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.8630   -0.1989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.6879    0.8561    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6731    1.8509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4782   -0.1989    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.0431    0.4260    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2981    0.5411    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.0079    1.8809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6533    0.8561    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6731    0.9960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.8630    0.6560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.2329    1.3109    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  6  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n  6  4  1  0     0  0\n  3  5  1  0     0  0\n  3 17  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Mannopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -5.5581    1.8634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0527   -0.1676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.0375    0.8751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8565    0.5342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.0375    1.7202    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.7441    0.4501    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.4199   -1.0126    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.2352    0.0005    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2339    1.0134    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0527   -1.0126    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6161   -0.4246    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.8565   -0.3109    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.5581    1.0134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2325    0.0301    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.2339    0.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.4199   -0.1676    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.6705    0.8751    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n 17  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n 17  4  1  0     0  0\n  3  5  1  0     0  0\n  3  6  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\nalpha-D-Talopyranose\n  Ketcher 11161713142D 1   1.00000     0.00000     0\n\n 17 17  0     1  0            999 V2000\n   -6.3613    0.1928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8363   -1.8473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.8414   -0.7673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.6514   -1.1373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.8414    0.0827    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.5764   -1.2223    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.2164   -2.6973    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -7.0414   -1.6773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0263   -0.6572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8363   -2.6973    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4013   -2.0723    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.6514   -1.9874    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.3613   -0.6572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.0113   -1.6473    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.0263   -1.5074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.2164   -1.8473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.4562   -0.7673    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n 17  2  1  0     0  0\n  2 15  1  1     0  0\n  3 16  1  1     0  0\n  3  4  1  0     0  0\n 17  4  1  0     0  0\n  3  5  1  0     0  0\n  3  6  1  0     0  0\n  7 16  1  0     0  0\n  8 16  1  0     0  0\n  9 15  1  0     0  0\n  2 10  1  0     0  0\n 11 15  1  0     0  0\n  4 12  1  0     0  0\n  4 13  1  0     0  0\n  2 14  1  0     0  0\n 15 16  1  1     0  0\n 13  1  1  0     0  0\nM  END\n>  <group>\nSugars\n\n>  <atomid>\n9\n\n>  <bondid>\n16\n\n$$$$\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>  <atomid>\n18\n\n>  <bondid>\n34\n\n$$$$\nadamantane\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 10 12  0     0  0            999 V2000\n   15.2172   -8.1314    1.0220 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.4398   -7.4133   -0.1292 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2919   -8.3429   -0.6392 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.9004   -9.6792   -1.1737 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6785  -10.3958   -0.0237 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8276   -9.4680    0.4869 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.8081   -9.1570   -0.6894 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.0325   -8.4390   -1.8401 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.4215   -7.1042   -1.3049 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.8828   -9.3683   -2.3500 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  4 10  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  2  9  1  0  0  0  0\n  1  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  5  6  1  0  0  0  0\n  8 10  1  0  0  0  0\n  2  3  1  0  0  0  0\nM  END\n>  <group>\n3D Templates\n\n>  <atomid>\n1\n\n>  <bondid>\n0\n$$$$\ncubane\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n  8 12  0     0  0            999 V2000\n   10.5569   -9.9029    4.2925 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2017   -9.5628    4.9812 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5825   -8.4868    3.6463 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3483   -7.9339    4.8851 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9705   -9.0155    6.2193 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.3256   -9.3519    5.5298 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.2296   -8.1444    4.3386 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.9966   -7.5972    5.5784 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  3  1  1  0  0  0  0\n  1  6  1  0  0  0  0\n  2  5  1  0  0  0  0\n  7  2  1  0  0  0  0\n  3  4  1  0  0  0  0\n  7  3  1  0  0  0  0\n  4  6  1  0  0  0  0\n  8  4  1  0  0  0  0\n  5  6  1  0  0  0  0\n  8  5  1  0  0  0  0\n  8  7  1  0  0  0  0\nM  END\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n>  <group>\n3D Templates\n\n$$$$\nring 6 boat\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n   11.2934   -7.8385   -0.6482 H   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2480   -6.3919    0.1251 H   0  0  0  0  0  0  0  0  0  0  0  0\n   12.1209   -8.2282    2.2065 H   0  0  0  0  0  0  0  0  0  0  0  0\n   12.5795  -10.2283    0.6541 H   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2777   -9.8706   -1.8252 H   0  0  0  0  0  0  0  0  0  0  0  0\n   13.5448   -7.5081   -2.7767 H   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7930   -7.7993   -0.2998 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.8567   -7.8369    0.7935 H   0  0  0  0  0  0  0  0  0  0  0  0\n   14.7961   -6.3928    0.4449 H   0  0  0  0  0  0  0  0  0  0  0  0\n   16.0357   -7.4556   -2.0500 H   0  0  0  0  0  0  0  0  0  0  0  0\n   15.7535   -9.8351   -1.1468 H   0  0  0  0  0  0  0  0  0  0  0  0\n   15.0584  -10.2582    1.3110 H   0  0  0  0  0  0  0  0  0  0  0  0\n   14.6187   -8.3063    2.8894 H   0  0  0  0  0  0  0  0  0  0  0  0\n   13.6881   -8.3653   -1.4688 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2260   -8.3597   -1.0520 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.9985   -8.7537    0.9805 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5364   -8.7481    1.4094 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.3614   -7.8158    0.4528 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  7  1  0  0  0  0\n  3 16  1  0  0  0  0\n  4 16  1  0  0  0  0\n  5 14  1  0  0  0  0\n  6 14  1  0  0  0  0\n  7 14  1  0  0  0  0\n  7 16  1  0  0  0  0\n  8 18  1  0  0  0  0\n  9 18  1  0  0  0  0\n 10 15  1  0  0  0  0\n 11 15  1  0  0  0  0\n 12 17  1  0  0  0  0\n 13 17  1  0  0  0  0\n 14 15  1  0  0  0  0\n 15 18  1  0  0  0  0\n 16 17  1  0  0  0  0\n 17 18  1  0  0  0  0\n  1  7  1  0  0  0  0\nM  END\n>  <atomid>\n0\n\n>  <bondid>\n17\n\n>  <group>\n3D Templates\n\n$$$$\nring 6 chair\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 18 18  0     0  0            999 V2000\n    6.4738   -5.6532   -0.6660 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4541   -4.2314    0.0877 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2774   -5.9986    2.2013 H   0  0  0  0  0  0  0  0  0  0  0  0\n    7.7022   -8.0409    0.6946 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4210   -7.7512   -1.7876 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.7429   -5.4159   -2.7877 H   0  0  0  0  0  0  0  0  0  0  0  0\n   12.0262   -7.2017    0.7693 H   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0549   -8.6186   -0.0171 H   0  0  0  0  0  0  0  0  0  0  0  0\n    9.6856   -6.5861    1.4297 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7917   -7.4939    2.7473 H   0  0  0  0  0  0  0  0  0  0  0  0\n   10.0968   -5.1271    1.7849 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1503   -6.5687    0.9919 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3966   -6.2651   -1.0354 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.5752   -7.1963    0.2541 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8371   -4.7668   -0.6787 H   0  0  0  0  0  0  0  0  0  0  0  0\n   11.2658   -6.7684   -2.2180 H   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8611   -6.2475   -1.4612 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.9719   -5.6379   -0.3097 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2 18  1  0  0  0  0\n  3 12  1  0  0  0  0\n  4 12  1  0  0  0  0\n  5 17  1  0  0  0  0\n  6 17  1  0  0  0  0\n  7 14  1  0  0  0  0\n  8 14  1  0  0  0  0\n  9 10  1  0  0  0  0\n  9 11  1  0  0  0  0\n  9 12  1  0  0  0  0\n  9 14  1  0  0  0  0\n 12 18  1  0  0  0  0\n 13 14  1  0  0  0  0\n 13 15  1  0  0  0  0\n 13 16  1  0  0  0  0\n 13 17  1  0  0  0  0\n 17 18  1  0  0  0  0\n  1 18  1  0  0  0  0\nM  END\n>  <atomid>\n0\n\n>  <bondid>\n17\n\n>  <group>\n3D Templates\n\n$$$$\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$$$$\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$$$$\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$$$$\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$$$$\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$$$$\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$$$$\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$$$$\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$$$$\nFeCO5\n  Ketcher  3131814142D 1   1.00000     0.00000     0\n\n 11 10  0     0  0            999 V2000\n   10.8202   -7.3426    0.0023 Fe  0  0  0  0  0  0  0  0  0  0  0  0\n    8.9246   -7.3587    0.0087 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7011   -7.0667   -1.5928 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.7827   -7.6197    1.5703 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8213   -5.0591    0.3328 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.8193   -9.6084   -0.3284 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4397   -6.8395   -2.8953 O   0  0  0  0  0  3  0  0  0  0  0  0\n   12.5339   -7.8271    2.8412 O   0  0  0  0  0  3  0  0  0  0  0  0\n    7.4162   -7.3784    0.0570 O   0  0  0  0  0  3  0  0  0  0  0  0\n   10.8213   -3.5367    0.5648 O   0  0  0  0  0  3  0  0  0  0  0  0\n   10.8194  -11.1133   -0.5606 O   0  0  0  0  0  3  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  1  5  1  0  0  0  0\n  1  6  1  0  0  0  0\n  2  9  3  0  0  0  0\n  3  7  3  0  0  0  0\n  4  8  3  0  0  0  0\n  6 11  3  0  0  0  0\n  5 10  3  0  0  0  0\nM  END\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n>  <group>\n3D Templates\n\n$$$$\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$$$$\nPhenylalanine mustard\n  Ketcher  8252313372D 1   1.00000     0.00000     0\n\n 19 19  0  0  0  0  0  0  0  0999 V2000\n   18.7500   -9.0090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.7500   -9.0090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   20.2500   -9.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.7500  -10.7410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.7500  -10.7410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.2500   -9.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.2500   -9.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.7500  -10.7410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.7500  -10.7410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2500   -9.8750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   15.2500  -11.6071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   17.2500  -11.6071    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   21.2500   -9.8750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   21.7500   -9.0090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.7500   -9.0090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2500   -8.1429    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n   21.7500  -10.7410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   22.7500  -10.7410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   23.2500  -11.6071    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0     0  0\n  2  3  1  0     0  0\n  3  4  2  0     0  0\n  4  5  1  0     0  0\n  5  6  2  0     0  0\n  6  1  1  0     0  0\n  6  7  1  0     0  0\n  7  8  1  0     0  0\n  8  9  1  0     0  0\n  9 10  2  0     0  0\n  9 11  1  0     0  0\n  8 12  1  1     0  0\n  3 13  1  0     0  0\n  13 14  1  0     0  0\n  14 15  1  0     0  0\n  15 16  1  0     0  0\n  13 17  1  0     0  0\n  17 18  1  0     0  0\n  18 19  1  0     0  0\nM  END\n>  <atomid>\n0\n\n>  <bondid>\n0\n\n>  <group>\nAromatics\n\n$$$$";
 
 var cachedInitData;
 var needReinitializeTemplateLibrary = false;
@@ -1056,8 +1068,8 @@ function prefetchRender(tmpls, baseUrl, cacheEl) {
   });
 }
 
-function ownKeys$1l(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$1l(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1l(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1l(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$1m(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$1m(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1m(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1m(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var initOptionsState = {
   app: {
     server: false,
@@ -1155,29 +1167,29 @@ function optionsReducer() {
   var action = arguments.length > 1 ? arguments[1] : undefined;
   var type = action.type,
     data = action.data;
-  if (type === 'APP_OPTIONS') return _objectSpread$1l(_objectSpread$1l({}, state), {}, {
-    app: _objectSpread$1l(_objectSpread$1l({}, state.app), data)
+  if (type === 'APP_OPTIONS') return _objectSpread$1m(_objectSpread$1m({}, state), {}, {
+    app: _objectSpread$1m(_objectSpread$1m({}, state.app), data)
   });
   if (type === 'SAVE_SETTINGS') {
-    return _objectSpread$1l(_objectSpread$1l({}, state), {}, {
-      settings: _objectSpread$1l(_objectSpread$1l({}, state.settings), data)
+    return _objectSpread$1m(_objectSpread$1m({}, state), {}, {
+      settings: _objectSpread$1m(_objectSpread$1m({}, state.settings), data)
     });
   }
-  if (type === 'SAVE_CHECK_OPTS') return _objectSpread$1l(_objectSpread$1l({}, state), {}, {
+  if (type === 'SAVE_CHECK_OPTS') return _objectSpread$1m(_objectSpread$1m({}, state), {}, {
     check: data
   });
-  if (type === 'CHANGE_ANALYSE') return _objectSpread$1l(_objectSpread$1l({}, state), {}, {
-    analyse: _objectSpread$1l(_objectSpread$1l(_objectSpread$1l({}, state.analyse), data), {}, {
+  if (type === 'CHANGE_ANALYSE') return _objectSpread$1m(_objectSpread$1m({}, state), {}, {
+    analyse: _objectSpread$1m(_objectSpread$1m(_objectSpread$1m({}, state.analyse), data), {}, {
       loading: false
     })
   });
-  if (type === 'ANALYSE_LOADING') return _objectSpread$1l(_objectSpread$1l({}, state), {}, {
-    analyse: _objectSpread$1l(_objectSpread$1l({}, state.analyse), {}, {
+  if (type === 'ANALYSE_LOADING') return _objectSpread$1m(_objectSpread$1m({}, state), {}, {
+    analyse: _objectSpread$1m(_objectSpread$1m({}, state.analyse), {}, {
       loading: true
     })
   });
-  if (recognizeActions.includes(type)) return _objectSpread$1l(_objectSpread$1l({}, state), {}, {
-    recognize: _objectSpread$1l(_objectSpread$1l({}, state.recognize), data)
+  if (recognizeActions.includes(type)) return _objectSpread$1m(_objectSpread$1m({}, state), {}, {
+    recognize: _objectSpread$1m(_objectSpread$1m({}, state.recognize), data)
   });
   return state;
 }
@@ -1481,8 +1493,8 @@ function getSdataDefault() {
   return schema[context][fieldName] ? schema[context][fieldName].properties.fieldValue["default"] : '';
 }
 
-function ownKeys$1k(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$1k(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1k(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1k(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$1l(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$1l(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1l(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1l(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var initSdata = function initSdata(schema) {
   var isCustomShema = schema.key === 'Custom';
   var context = isCustomShema ? getSdataDefault(sdataCustomSchema, 'context') : getSdataDefault(sdataSchema);
@@ -1520,7 +1532,7 @@ var onContextChange = function onContextChange(state, payload) {
   var fValue = fieldValue;
   if (fValue === state.result.fieldValue) fValue = getSdataDefault(sdataCustomSchema, 'fieldValue');
   return {
-    result: _objectSpread$1k(_objectSpread$1k({}, payload), {}, {
+    result: _objectSpread$1l(_objectSpread$1l({}, payload), {}, {
       context: context,
       fieldName: fieldName,
       fieldValue: fValue
@@ -1534,7 +1546,7 @@ var onFieldNameChange = function onFieldNameChange(state, payload) {
   if (sdataSchema[context][fieldName]) fieldValue = getSdataDefault(sdataSchema, context, fieldName);
   if (fieldValue === state.result.fieldValue && sdataSchema[context][state.result.fieldName]) fieldValue = '';
   return {
-    result: _objectSpread$1k(_objectSpread$1k({}, payload), {}, {
+    result: _objectSpread$1l(_objectSpread$1l({}, payload), {}, {
       fieldName: fieldName,
       fieldValue: fieldValue
     })
@@ -1542,7 +1554,7 @@ var onFieldNameChange = function onFieldNameChange(state, payload) {
 };
 function sdataReducer(state, action) {
   if (action.data.result.init) {
-    return correctErrors(_objectSpread$1k(_objectSpread$1k({}, state), {}, {
+    return correctErrors(_objectSpread$1l(_objectSpread$1l({}, state), {}, {
       result: Object.assign({}, state.result, action.data.result)
     }), action.data);
   }
@@ -1550,7 +1562,7 @@ function sdataReducer(state, action) {
   var actionFieldName = action.data.result.fieldName;
   var newstate = null;
   if (actionContext !== state.result.context) newstate = onContextChange(state, action.data.result);else if (actionFieldName !== state.result.fieldName) newstate = onFieldNameChange(state, action.data.result);
-  newstate = newstate || _objectSpread$1k(_objectSpread$1k({}, state), {}, {
+  newstate = newstate || _objectSpread$1l(_objectSpread$1l({}, state), {}, {
     result: Object.assign({}, state.result, action.data.result)
   });
   return correctErrors(newstate, action.data);
@@ -1690,8 +1702,8 @@ function formReducer(state, action) {
 var INDIGO_VERIFICATION = 'INDIGO_VERIFICATION';
 var ANALYZING_FILE = 'ANALYZING_FILE';
 
-function ownKeys$1j(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$1j(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1j(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1j(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$1k(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$1k(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1k(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1k(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function indigoVerification(data) {
   return {
     type: INDIGO_VERIFICATION,
@@ -1716,13 +1728,13 @@ function requestReducer () {
   switch (type) {
     case INDIGO_VERIFICATION:
       {
-        return _objectSpread$1j(_objectSpread$1j({}, state), {}, {
+        return _objectSpread$1k(_objectSpread$1k({}, state), {}, {
           indigoVerification: data
         });
       }
     case ANALYZING_FILE:
       {
-        return _objectSpread$1j(_objectSpread$1j({}, state), {}, {
+        return _objectSpread$1k(_objectSpread$1k({}, state), {}, {
           isAnalyzingFile: data
         });
       }
@@ -1740,8 +1752,8 @@ var supportedSGroupTypes = {
   queryComponent: 'queryComponent'
 };
 
-function ownKeys$1i(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$1i(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1i(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1i(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$1j(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$1j(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1j(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1j(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var atom = {
   title: 'Atom',
   type: 'object',
@@ -1973,7 +1985,7 @@ var sgroup = {
   title: 'SGroup',
   type: 'object',
   required: ['type'],
-  oneOf: [_objectSpread$1i({}, sdataCustomSchema), {
+  oneOf: [_objectSpread$1j({}, sdataCustomSchema), {
     key: 'MUL',
     title: 'Multiple group',
     type: 'object',
@@ -2080,12 +2092,12 @@ var attachSchema = {
 
 var _excluded$z = ["aromaticity", "ringMembership", "ringSize", "connectivity", "chirality", "customQuery"],
   _excluded2$7 = ["type", "radiobuttons"];
-function ownKeys$1h(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$1h(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1h(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1h(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$1i(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$1i(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1i(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1i(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var DefaultStereoGroupNumber = 1;
 function fromElement(selem) {
   if (selem.label === 'R#') {
-    return _objectSpread$1h({
+    return _objectSpread$1i({
       type: 'rlabel',
       values: fromRlabel(selem.rglabel)
     }, selem);
@@ -2342,7 +2354,7 @@ function fromBond(sbond) {
 }
 function toBond(bond) {
   var isCustomQuery = bond.customQuery !== '';
-  return _objectSpread$1h({
+  return _objectSpread$1i({
     topology: bond.topology,
     reactingCenterStatus: bond.center,
     customQuery: !isCustomQuery ? null : bond.customQuery
@@ -2438,7 +2450,7 @@ function toSgroup(sgroup) {
   var type = sgroup.type,
     radiobuttons = sgroup.radiobuttons,
     props = _objectWithoutProperties(sgroup, _excluded2$7);
-  var attrs = _objectSpread$1h({}, props);
+  var attrs = _objectSpread$1i({}, props);
   var absolute = 'absolute';
   var attached = 'attached';
   switch (radiobuttons) {
@@ -2993,8 +3005,8 @@ var tools = typeSchema$1["enum"].reduce(function (res, type, i) {
 
 var _excluded$y = ["rescale", "fragment"],
   _excluded2$6 = ["isPaste", "method"];
-function ownKeys$1g(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$1g(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1g(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1g(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$1h(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$1h(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1h(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1h(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function onAction(action) {
   if (action && action.dialog) {
     return {
@@ -3049,7 +3061,7 @@ function load(struct, options) {
             errorHandler = editor.errorHandler;
             options = options || {};
             _options2 = options, isPaste = _options2.isPaste, method = _options2.method, otherOptions = _objectWithoutProperties(_options2, _excluded2$6);
-            otherOptions = _objectSpread$1g(_objectSpread$1g({}, otherOptions), {}, {
+            otherOptions = _objectSpread$1h(_objectSpread$1h({}, otherOptions), {}, {
               'dearomatize-on-load': editor.options()['dearomatize-on-load'],
               ignoreChiralFlag: editor.options().ignoreChiralFlag
             });
@@ -3552,7 +3564,7 @@ var zoom = {
 
 var openHelpLink = function openHelpLink() {
   var _window$open;
-  return (_window$open = window.open("https://github.com/epam/ketcher/blob/".concat("v2.18.0-rc.2\n", "/documentation/help.md#ketcher-overview"))) === null || _window$open === void 0 ? void 0 : _window$open.focus();
+  return (_window$open = window.open("https://github.com/epam/ketcher/blob/".concat("v2.18.0-rc.3\n", "/documentation/help.md#ketcher-overview"))) === null || _window$open === void 0 ? void 0 : _window$open.focus();
 };
 var help = {
   help: {
@@ -3624,11 +3636,11 @@ var fullscreen = {
   }
 };
 
-function ownKeys$1f(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$1f(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1f(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1f(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
-var config = _objectSpread$1f(_objectSpread$1f(_objectSpread$1f(_objectSpread$1f(_objectSpread$1f(_objectSpread$1f(_objectSpread$1f(_objectSpread$1f(_objectSpread$1f({
+function ownKeys$1g(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$1g(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1g(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1g(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+var config = _objectSpread$1g(_objectSpread$1g(_objectSpread$1g(_objectSpread$1g(_objectSpread$1g(_objectSpread$1g(_objectSpread$1g(_objectSpread$1g(_objectSpread$1g({
   clear: {
-    shortcut: 'Mod+Delete',
+    shortcut: ['Mod+Delete', 'Mod+Backspace'],
     title: 'Clear Canvas',
     action: {
       thunk: function thunk(dispatch, getState) {
@@ -3936,21 +3948,6 @@ function hasSelection(editor) {
 
 var classes$Q = {"button-common-styles":"ActionButton-module_button-common-styles__y-hng","scrollbar":"ActionButton-module_scrollbar__lD3MH","button":"ActionButton-module_button__nfoWQ","selected":"ActionButton-module_selected__kPCxA"};
 
-var shortcutAliasMap = {
-  Escape: 'Esc',
-  Delete: 'Del',
-  Mod: isMacOs ? '⌘' : 'Ctrl'
-};
-function shortcutStr(shortcut) {
-  if (!shortcut) {
-    return '';
-  }
-  var shortcutKey = Array.isArray(shortcut) ? shortcut[0] : shortcut;
-  return shortcutKey.replace(/(\b[a-z]\b$|Mod|Escape|Delete)/g, function (key) {
-    return shortcutAliasMap[key] || key.toUpperCase();
-  });
-}
-
 var _path$37, _rect$4, _rect2$3;
 function _extends$3d() { _extends$3d = Object.assign ? Object.assign.bind() : function (target) { for (var i = 1; i < arguments.length; i++) { var source = arguments[i]; for (var key in source) { if (Object.prototype.hasOwnProperty.call(source, key)) { target[key] = source[key]; } } } return target; }; return _extends$3d.apply(this, arguments); }
 function SvgAbout(props) {
@@ -7788,12 +7785,12 @@ var StyledButton = styled.button({
 });
 
 var _excluded$x = ["children"];
-function ownKeys$1e(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$1e(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1e(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1e(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$1f(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$1f(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1f(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1f(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var Button = function Button(_ref) {
   var children = _ref.children,
     props = _objectWithoutProperties(_ref, _excluded$x);
-  return jsx(StyledButton, _objectSpread$1e(_objectSpread$1e({}, props), {}, {
+  return jsx(StyledButton, _objectSpread$1f(_objectSpread$1f({}, props), {}, {
     children: children
   }));
 };
@@ -7851,10 +7848,10 @@ var StyledInput$1 = styled.input({
   }
 });
 
-function ownKeys$1d(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$1d(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1d(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1d(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$1e(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$1e(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1e(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1e(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var Input$2 = function Input(props) {
-  return jsx(StyledInput$1, _objectSpread$1d({}, props));
+  return jsx(StyledInput$1, _objectSpread$1e({}, props));
 };
 
 var Container = styled.div({
@@ -7905,15 +7902,15 @@ var error$1 = {
   close: 'Close'
 };
 
-var styles$g = {"infoModalOverlay":"InfoModal-module_infoModalOverlay__Ve2pm","infoModalWindow":"InfoModal-module_infoModalWindow__Qd-UI","infoModalBody":"InfoModal-module_infoModalBody__BYoCY","modalHidden":"InfoModal-module_modalHidden__6HnzH","ok":"InfoModal-module_ok__BETvY"};
+var styles$h = {"infoModalOverlay":"InfoModal-module_infoModalOverlay__Ve2pm","infoModalWindow":"InfoModal-module_infoModalWindow__Qd-UI","infoModalBody":"InfoModal-module_infoModalBody__BYoCY","modalHidden":"InfoModal-module_modalHidden__6HnzH","ok":"InfoModal-module_ok__BETvY"};
 
 var InfoModal$1 = function InfoModal(_ref) {
   var message = _ref.message,
     close = _ref.close;
   return jsx("div", {
-    className: styles$g.infoModalOverlay,
+    className: styles$h.infoModalOverlay,
     children: jsxs("div", {
-      className: styles$g.infoModalWindow,
+      className: styles$h.infoModalWindow,
       role: "dialog",
       "aria-modal": "true",
       "aria-labelledby": "dialog-label",
@@ -7923,13 +7920,13 @@ var InfoModal$1 = function InfoModal(_ref) {
         id: "dialog-label",
         children: error$1.message
       }), jsx("div", {
-        className: styles$g.infoModalBody,
+        className: styles$h.infoModalBody,
         id: "dialog-content",
         "data-testid": "info-modal-body",
         children: message
       }), jsx("footer", {
         children: jsx("button", {
-          className: styles$g.ok,
+          className: styles$h.ok,
           onClick: close,
           children: error$1.close
         })
@@ -7938,11 +7935,11 @@ var InfoModal$1 = function InfoModal(_ref) {
   });
 };
 
-var styles$f = {"button-common-styles":"Dialog-module_button-common-styles__Xehyp","scrollbar":"Dialog-module_scrollbar__L8hUr","dialog":"Dialog-module_dialog__hiRBI","hide":"Dialog-module_hide__bbkvB","header":"Dialog-module_header__8QGek","btnContainer":"Dialog-module_btnContainer__ulrFM","buttonTop":"Dialog-module_buttonTop__91ha8","closeButton":"Dialog-module_closeButton__XyaAE","footer":"Dialog-module_footer__PliV0","ok":"Dialog-module_ok__BUQ6q","cancel":"Dialog-module_cancel__8d83c","withDivider":"Dialog-module_withDivider__YBKiQ","body":"Dialog-module_body__EWh4H","withMargin":"Dialog-module_withMargin__-zVS4"};
+var styles$g = {"button-common-styles":"Dialog-module_button-common-styles__Xehyp","scrollbar":"Dialog-module_scrollbar__L8hUr","dialog":"Dialog-module_dialog__hiRBI","hide":"Dialog-module_hide__bbkvB","header":"Dialog-module_header__8QGek","btnContainer":"Dialog-module_btnContainer__ulrFM","buttonTop":"Dialog-module_buttonTop__91ha8","closeButton":"Dialog-module_closeButton__XyaAE","footer":"Dialog-module_footer__PliV0","ok":"Dialog-module_ok__BUQ6q","cancel":"Dialog-module_cancel__8d83c","withDivider":"Dialog-module_withDivider__YBKiQ","body":"Dialog-module_body__EWh4H","withMargin":"Dialog-module_withMargin__-zVS4"};
 
 var _excluded$w = ["children", "title", "params", "result", "valid", "buttons", "headerContent", "footerContent", "className", "buttonsNameMap", "needMargin", "withDivider", "focusable"];
-function ownKeys$1c(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$1c(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1c(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1c(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$1d(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$1d(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1d(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1d(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var Dialog = function Dialog(props) {
   var children = props.children,
     title = props.title,
@@ -7997,7 +7994,7 @@ var Dialog = function Dialog(props) {
       event.stopPropagation();
     }
   };
-  return jsxs("div", _objectSpread$1c(_objectSpread$1c({
+  return jsxs("div", _objectSpread$1d(_objectSpread$1d({
     ref: dialogRef,
     role: "dialog",
     onSubmit: function onSubmit(event) {
@@ -8005,35 +8002,35 @@ var Dialog = function Dialog(props) {
     },
     onKeyDown: keyDown,
     tabIndex: -1,
-    className: clsx(styles$f.dialog, className, params.className)
+    className: clsx(styles$g.dialog, className, params.className)
   }, rest), {}, {
     children: [jsxs("header", {
-      className: clsx(styles$f.header, withDivider && styles$f.withDivider),
+      className: clsx(styles$g.header, withDivider && styles$g.withDivider),
       children: [headerContent || jsx("span", {
         children: title
       }), jsx("div", {
-        className: styles$f.btnContainer,
+        className: styles$g.btnContainer,
         children: jsx("button", {
-          className: styles$f.buttonTop,
+          className: styles$g.buttonTop,
           onClick: function onClick() {
             return exit('Cancel');
           },
           "data-testid": 'close-icon',
           children: jsx(Icon, {
             name: 'close',
-            className: styles$f.closeButton
+            className: styles$g.closeButton
           })
         })
       })]
     }), jsx("div", {
-      className: clsx(styles$f.body, needMargin && styles$f.withMargin),
+      className: clsx(styles$g.body, needMargin && styles$g.withMargin),
       children: children
     }), (footerContent || buttons.length > 0) && jsxs("footer", {
-      className: styles$f.footer,
+      className: styles$g.footer,
       children: [footerContent, buttons.length > 0 && buttons.map(function (button) {
         return typeof button !== 'string' ? button : jsx("input", {
           type: "button",
-          className: clsx(isButtonOk(button) ? styles$f.ok : styles$f.cancel, button === 'Save' && styles$f.save),
+          className: clsx(isButtonOk(button) ? styles$g.ok : styles$g.cancel, button === 'Save' && styles$g.save),
           value: buttonsNameMap && buttonsNameMap[button] ? buttonsNameMap[button] : button,
           disabled: isButtonOk(button) && !valid(),
           onClick: function onClick() {
@@ -8323,8 +8320,8 @@ function usePortalStyle(_ref) {
   return [portalStyle];
 }
 
-function ownKeys$1b(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$1b(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1b(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1b(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$1c(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$1c(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1c(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1c(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var ToolbarMultiToolItem = function ToolbarMultiToolItem(props) {
   var id = props.id,
     options = props.options,
@@ -8398,7 +8395,7 @@ var ToolbarMultiToolItem = function ToolbarMultiToolItem(props) {
     ref: ref,
     className: classes$O.root,
     "data-testid": "".concat(dataTestId || iconName, "-in-toolbar"),
-    children: [jsx(ActionButton, _objectSpread$1b(_objectSpread$1b({}, actionButtonProps), {}, {
+    children: [jsx(ActionButton, _objectSpread$1c(_objectSpread$1c({}, actionButtonProps), {}, {
       className: className,
       name: iconName,
       action: config[currentId],
@@ -8504,8 +8501,8 @@ var TemplatesList = function TemplatesList(props) {
 var classes$N = {"button-common-styles":"BottomToolbar-module_button-common-styles__PbtE9","scrollbar":"BottomToolbar-module_scrollbar__i1f8P","group":"BottomToolbar-module_group__b-pGt","root":"BottomToolbar-module_root__kjkSm"};
 
 var _excluded$v = ["className"];
-function ownKeys$1a(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$1a(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1a(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1a(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$1b(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$1b(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1b(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1b(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var Group$1 = function Group(_ref) {
   var children = _ref.children,
     className = _ref.className;
@@ -8530,22 +8527,22 @@ var BottomToolbar = function BottomToolbar(props) {
         indigoVerification: indigoVerification,
         disableableButtons: disableableButtons,
         onAction: onAction
-      }), jsx(ToolbarGroupItem, _objectSpread$1a({
+      }), jsx(ToolbarGroupItem, _objectSpread$1b({
         id: "template-lib"
       }, rest))]
     })
   });
 };
 
-function ownKeys$19(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$19(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$19(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$19(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$1a(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$1a(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$1a(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$1a(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function openDialog(dispatch, dialogName, props) {
   return new Promise(function (resolve, reject) {
     dispatch({
       type: 'MODAL_OPEN',
       data: {
         name: dialogName,
-        prop: _objectSpread$19(_objectSpread$19({}, props), {}, {
+        prop: _objectSpread$1a(_objectSpread$1a({}, props), {}, {
           onResult: resolve,
           onCancel: reject
         })
@@ -8564,14 +8561,14 @@ function modalReducer() {
       return null;
     }
     var formState = formReducer(state.form, action);
-    return _objectSpread$19(_objectSpread$19({}, state), {}, {
+    return _objectSpread$1a(_objectSpread$1a({}, state), {}, {
       form: formState
     });
   }
   switch (type) {
     case 'MODAL_CLOSE':
       if (state !== null && state !== void 0 && state.parentModal) {
-        state.parentModal.prop = _objectSpread$19(_objectSpread$19(_objectSpread$19({}, state.parentModal.prop), state.parentModal.form.result), {}, {
+        state.parentModal.prop = _objectSpread$1a(_objectSpread$1a(_objectSpread$1a({}, state.parentModal.prop), state.parentModal.form.result), {}, {
           isRestoredModal: true
         });
         return state.parentModal;
@@ -8589,8 +8586,8 @@ function modalReducer() {
   }
 }
 
-function ownKeys$18(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$18(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$18(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$18(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$19(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$19(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$19(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$19(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function selectTmpl(tmpl) {
   return {
     type: 'TMPL_SELECT',
@@ -8698,7 +8695,7 @@ function saveUserTmpl(struct) {
       var name = _ref.name,
         attach = _ref.attach;
       tmpl.struct.name = name.trim();
-      tmpl.props = _objectSpread$18(_objectSpread$18({}, attach), {}, {
+      tmpl.props = _objectSpread$19(_objectSpread$19({}, attach), {}, {
         group: 'User Templates'
       });
       var lib = getState().templates.lib.concat(tmpl);
@@ -8738,7 +8735,7 @@ function templatesReducer() {
   if (tmplActions.includes(action.type)) return Object.assign({}, state, action.data);
   if (attachActions.includes(action.type)) {
     var attach = Object.assign({}, state.attach, action.data);
-    return _objectSpread$18(_objectSpread$18({}, state), {}, {
+    return _objectSpread$19(_objectSpread$19({}, state), {}, {
       attach: attach
     });
   }
@@ -8747,7 +8744,7 @@ function templatesReducer() {
     var lib = currentState.lib.filter(function (value) {
       return value !== action.data.tmpl;
     });
-    return _objectSpread$18(_objectSpread$18({}, currentState), {}, {
+    return _objectSpread$19(_objectSpread$19({}, currentState), {}, {
       lib: lib
     });
   }
@@ -8809,8 +8806,8 @@ function abbreviationLookupReducer() {
   }
 }
 
-function ownKeys$17(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$17(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$17(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$17(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$18(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$18(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$18(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$18(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var initialState$3 = {
   cursorPosition: {
     x: 0,
@@ -8835,7 +8832,7 @@ function commonReducer() {
   switch (action.type) {
     case COMMON_ACTIONS.COMMON_UPDATE_CURSOR_POSITION:
       {
-        return _objectSpread$17(_objectSpread$17({}, state), {}, {
+        return _objectSpread$18(_objectSpread$18({}, state), {}, {
           cursorPosition: {
             x: action.data.x,
             y: action.data.y
@@ -8848,8 +8845,8 @@ function commonReducer() {
 }
 
 var _excluded$u = ["type", "action"];
-function ownKeys$16(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$16(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$16(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$16(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$17(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$17(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$17(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$17(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function execute(activeTool, _ref) {
   var action = _ref.action,
     editor = _ref.editor,
@@ -8907,7 +8904,7 @@ function actionStateReducer () {
       }
     case 'ACTION':
       {
-        activeTool = execute(state && state.activeTool, _objectSpread$16(_objectSpread$16({}, params), {}, {
+        activeTool = execute(state && state.activeTool, _objectSpread$17(_objectSpread$17({}, params), {}, {
           action: action
         }));
         if (activeTool.tool === 'select') {
@@ -8951,17 +8948,54 @@ function fileOpener(server) {
     }
   });
 }
+function arrayBufferToBase64(buffer) {
+  var binary = '';
+  var bytes = new Uint8Array(buffer);
+  var len = bytes.byteLength;
+  for (var i = 0; i < len; i++) {
+    binary += String.fromCharCode(bytes[i]);
+  }
+  return btoa(binary);
+}
 function throughFileReader(file) {
-  var isCDX = file.name.endsWith('cdx') && !file.name.endsWith('b64cdx');
+  var CDX = 'cdx';
+  var PPTX = 'pptx';
+  var fileType;
+  if (file.name.endsWith('cdx') && !file.name.endsWith('b64cdx')) {
+    fileType = CDX;
+  } else if (file.name.endsWith('pptx')) {
+    fileType = PPTX;
+  }
   return new Promise(function (resolve, reject) {
     var rd = new FileReader();
-    rd.onload = function () {
-      var content;
-      if (isCDX) {
-        var base64String = rd.result.split(',').at(-1);
-        content = base64String;
-      } else {
-        content = rd.result;
+    rd.onload = function (e) {
+      var content, structures;
+      var cfb;
+      switch (fileType) {
+        case CDX:
+          content = rd.result.split(',').at(-1);
+          break;
+        case PPTX:
+          cfb = CFB.read(e.target.result, {
+            type: 'binary'
+          });
+          structures = [];
+          cfb.FullPaths.forEach(function (path) {
+            if (path.endsWith('.bin')) {
+              var ole = CFB.find(cfb, path);
+              var sdf = CFB.find(CFB.parse(ole.content), 'CONTENTS');
+              var base64String = arrayBufferToBase64(sdf.content);
+              structures.push(base64String);
+            }
+          });
+          content = {
+            structures: structures,
+            isPPTX: true
+          };
+          break;
+        default:
+          content = rd.result;
+          break;
       }
       if (file.msClose) file.msClose();
       resolve(content);
@@ -8969,7 +9003,17 @@ function throughFileReader(file) {
     rd.onerror = function (event) {
       reject(event);
     };
-    isCDX ? rd.readAsDataURL(file) : rd.readAsText(file, 'UTF-8');
+    switch (fileType) {
+      case CDX:
+        rd.readAsDataURL(file);
+        break;
+      case PPTX:
+        rd.readAsBinaryString(file);
+        break;
+      default:
+        rd.readAsText(file, 'UTF-8');
+        break;
+    }
   });
 }
 function throughFileSystemObject(fso, file) {
@@ -11404,8 +11448,8 @@ var errors = {
 	codes: codes_1
 };
 
-function ownKeys$15(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$15(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$15(Object(t), !0).forEach(function (r) { _defineProperty(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$15(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$16(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$16(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$16(Object(t), !0).forEach(function (r) { _defineProperty(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$16(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function _defineProperty(obj, key, value) { key = _toPropertyKey(key); if (key in obj) { Object.defineProperty(obj, key, { value: value, enumerable: true, configurable: true, writable: true }); } else { obj[key] = value; } return obj; }
 function _classCallCheck(instance, Constructor) { if (!(instance instanceof Constructor)) { throw new TypeError("Cannot call a class as a function"); } }
 function _defineProperties(target, props) { for (var i = 0; i < props.length; i++) { var descriptor = props[i]; descriptor.enumerable = descriptor.enumerable || false; descriptor.configurable = true; if ("value" in descriptor) descriptor.writable = true; Object.defineProperty(target, _toPropertyKey(descriptor.key), descriptor); } }
@@ -11833,7 +11877,7 @@ var AssertionError = /*#__PURE__*/function (_Error, _inspect$custom) {
       // the minimum depth. Otherwise those values would be too verbose compared
       // to the actual error message which contains a combined view of these two
       // input values.
-      return inspect(this, _objectSpread$15(_objectSpread$15({}, ctx), {}, {
+      return inspect(this, _objectSpread$16(_objectSpread$16({}, ctx), {}, {
         customInspect: false,
         depth: 0
       }));
@@ -13453,8 +13497,8 @@ function setFunctionalGroupsTooltip(_ref) {
   showTooltip(editor, infoPanelData);
 }
 
-function ownKeys$14(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$14(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$14(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$14(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$15(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$15(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$15(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$15(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var initialState$2 = {
   lib: [],
   functionalGroupInfo: null,
@@ -13467,9 +13511,9 @@ var functionalGroupsReducer = function functionalGroupsReducer() {
     payload = _ref.payload;
   switch (type) {
     case 'FG_INIT':
-      return _objectSpread$14(_objectSpread$14({}, state), payload);
+      return _objectSpread$15(_objectSpread$15({}, state), payload);
     case 'FG_HIGHLIGHT':
-      return _objectSpread$14(_objectSpread$14({}, state), {}, {
+      return _objectSpread$15(_objectSpread$15({}, state), {}, {
         functionalGroupInfo: payload
       });
     default:
@@ -13527,8 +13571,8 @@ function initFGTemplates() {
 
 var templatesRawData = "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$$$$\nacetic anhydride\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    0.5143    0.5143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7848   -0.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8133   -0.2357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5143    2.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1123    0.5143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1124    2.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4114   -0.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\n  3  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  5  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 acetic anhydride\nM  END\n>  <name>\nacetic anhydride\n\n>  <abbreviation>\nacetic anhydride\n\n>  <group>\nSalts and Solvents\n\n$$$$\nformic acid\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    0.5143    0.5143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7848   -0.2357    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8133   -0.2357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5143    2.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 formic acid\nM  END\n>  <name>\nformic acid\n\n>  <abbreviation>\nformic acid\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethane sulphonic acid\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.5143    0.5143    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5143    2.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5143   -0.9857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.0143    0.5143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.9857    0.5143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  2  0  0  0  0\n  1  4  1  0  0  0  0\n  1  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 methane sulphonic acid\nM  END\n>  <name>\nmethane sulphonic acid\n\n>  <abbreviation>\nmethane sulphonic acid\n\n>  <group>\nSalts and Solvents\n\n$$$$\npropionic acid\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.5143    0.5143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7848   -0.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8133   -0.2357    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5143    2.0143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.0838    0.5143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\n  2  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 propionic acid\nM  END\n>  <name>\npropionic acid\n\n>  <abbreviation>\npropionic acid\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,2-propanediol\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n   -3.3587   -3.5057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.0597   -2.7557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.0596   -1.2558    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7606   -3.5057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5384   -2.7557    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  4  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 1,2-propanediol\nM  END\n>  <name>\n1,2-propanediol\n\n>  <abbreviation>\n1,2-propanediol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,3-propanediol\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n   15.0779   -8.5508    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   16.3769   -9.3007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   17.6759   -8.5507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.9750   -9.3007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   20.2740   -8.5507    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 1,3-propanediol\nM  END\n>  <name>\n1,3-propanediol\n\n>  <abbreviation>\n1,3-propanediol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,4-butanediol\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n   -0.3480    1.2991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.9509    2.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2500    1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5491    2.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8481    1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1472    2.0491    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 1,4-butanediol\nM  END\n>  <name>\n1,4-butanediol\n\n>  <abbreviation>\n1,4-butanediol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1-butanol\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.1714    0.3286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.4705    1.0786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    1.0786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    0.3286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7257    1.0786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 1-butanol\nM  END\n>  <name>\n1-butanol\n\n>  <abbreviation>\n1-butanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1-propanol\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    0.1714    1.2286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7257    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 1-propanol\nM  END\n>  <name>\n1-propanol\n\n>  <abbreviation>\n1-propanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2-butanol\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.1714    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.4705    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.1714    2.7286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  1  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 2-butanol\nM  END\n>  <name>\n2-butanol\n\n>  <abbreviation>\n2-butanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2-ethylhexanol\n  -INDIGO-11302219142D\n\n  9  8  0  0  0  0  0  0  0  0999 V2000\n   10.7337    0.4167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1355    0.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8365   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5375    0.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1355    1.9167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4345   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2384   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.4345    2.6667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9394    0.4167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  6  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  5  1  0  0  0  0\n  2  6  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  7  1  0  0  0  0\n  5  8  1  0  0  0  0\n  7  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 2-ethylhexanol\nM  END\n>  <name>\n2-ethylhexanol\n\n>  <abbreviation>\n2-ethylhexanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nisopropanol\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    0.1714    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.4705    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.1714    2.7286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 2-propanol\nM  END\n>  <name>\nisopropanol\n\n>  <abbreviation>\n2-propanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2-methoxyethanol\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.1714    0.3286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.4705    1.0786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    1.0786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    0.3286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7257    1.0786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 2-methoxyethanol\nM  END\n>  <name>\n2-methoxyethanol\n\n>  <abbreviation>\n2-methoxyethanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2-pentanol\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n   -5.1971   -3.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8980   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5991   -3.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.3000   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.0009   -3.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.3000   -1.2500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 2-pentanol\nM  END\n>  <name>\n2-pentanol\n\n>  <abbreviation>\n2-pentanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nbenzyl alcohol\n  -INDIGO-11302219142D\n\n  8  8  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000    1.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990    2.5000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  2  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  3  1  0  0  0  0\n  1  7  1  0  0  0  0\n  7  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 benzyl alcohol\nM  END\n>  <name>\nbenzyl alcohol\n\n>  <abbreviation>\nbenzyl alcohol\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncyclohexanol\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    4.2990    2.0175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2990    0.5175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -0.2325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981   -0.2325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -1.7325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981   -1.7325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2990   -2.4825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  4  6  1  0  0  0  0\n  5  7  1  0  0  0  0\n  6  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 cyclohexanol\nM  END\n>  <name>\ncyclohexanol\n\n>  <abbreviation>\ncyclohexanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nethanol\n  -INDIGO-11302219142D\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    0.1714    1.2286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 ethyl alcohol\nM  END\n>  <name>\nethanol\n\n>  <abbreviation>\nethyl alcohol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nethylene glycol\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    0.1714    1.2286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7256    0.4786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 ethane-1,2-diol\nM  END\n>  <name>\nethylene glycol\n\n>  <abbreviation>\nethane-1,2-diol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nglycerol\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    0.9915    2.6580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2906    1.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5896    2.6580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5897    4.1580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8887    1.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1878    2.6580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  5  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 glycerol\nM  END\n>  <name>\nglycerol\n\n>  <abbreviation>\nglycerol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nisoamyl alcohol\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    0.1714    0.3286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.4705    1.0786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    1.0786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    0.3286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7257    1.0786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266   -1.1714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 isoamyl alcohol\nM  END\n>  <name>\nisoamyl alcohol\n\n>  <abbreviation>\nisoamyl alcohol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nisobutanol\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.1714    1.2286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1276    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    1.2286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7257    0.4786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.4266    2.7286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  3  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 isobutanol\nM  END\n>  <name>\nisobutanol\n\n>  <abbreviation>\nisobutanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethanol\n  -INDIGO-11302219142D\n\n  2  1  0  0  0  0  0  0  0  0999 V2000\n    0.0709    0.8536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5710    0.8536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  2   1   2\nM  SMT   1 methyl alcohol\nM  END\n>  <name>\nmethanol\n\n>  <abbreviation>\nmethyl alcohol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nt-butanol\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.0709    0.8536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5710    0.8536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.4291    0.8536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0709    2.3536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0709   -0.6464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  1  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 t-butanol\nM  END\n>  <name>\nt-butanol\n\n>  <abbreviation>\nt-butanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\nwater\n  -INDIGO-11302219142D\n\n  1  0  0  0  0  0  0  0  0  0999 V2000\n    0.7500    2.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  1   1\nM  SMT   1 water\nM  END\n>  <name>\nwater\n\n>  <abbreviation>\nwater\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncarbon dioxide\n  -INDIGO-11302219142D\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n   -1.2000    0.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7000    0.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.3000    0.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 carbon dioxide\nM  END\n>  <name>\ncarbon dioxide\n\n>  <abbreviation>\ncarbon dioxide\n\n>  <group>\nSalts and Solvents\n\n$$$$\nbenzene\n  -INDIGO-11302219142D\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  2  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  3  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 benzene\nM  END\n>  <name>\nbenzene\n\n>  <abbreviation>\nbenzene\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncumene\n  -INDIGO-11302219142D\n\n  9  9  0  0  0  0  0  0  0  0999 V2000\n    4.2989    1.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2989    0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981    2.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    2.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981   -0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981   -1.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -1.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2989   -2.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  2  5  2  0  0  0  0\n  2  6  1  0  0  0  0\n  5  7  1  0  0  0  0\n  6  8  2  0  0  0  0\n  7  9  2  0  0  0  0\n  8  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 cumene\nM  END\n>  <name>\ncumene\n\n>  <abbreviation>\ncumene\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmesitylene\n  -INDIGO-11302219142D\n\n  9  9  0  0  0  0  0  0  0  0999 V2000\n    1.2991    3.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2991    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5980    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5980    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8971   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2991   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2991   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  2  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  2  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  7  9  2  0  0  0  0\n  2  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 mesitylene\nM  END\n>  <name>\nmesitylene\n\n>  <abbreviation>\nmesitylene\n\n>  <group>\nSalts and Solvents\n\n$$$$\ntoluene\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000    1.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  2  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  3  1  0  0  0  0\n  1  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 toluene\nM  END\n>  <name>\ntoluene\n\n>  <abbreviation>\ntoluene\n\n>  <group>\nSalts and Solvents\n\n$$$$\nn,n-dimethylaniline\n  -INDIGO-11302219142D\n\n  9  9  0  0  0  0  0  0  0  0999 V2000\n    4.2989    1.8750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2989    0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981   -0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981    2.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    2.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981   -1.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -1.8750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2989   -2.6250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  5  1  0  0  0  0\n  1  6  1  0  0  0  0\n  2  3  2  0  0  0  0\n  2  4  1  0  0  0  0\n  3  7  1  0  0  0  0\n  4  8  2  0  0  0  0\n  7  9  2  0  0  0  0\n  8  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 N,N-dimethylaniline\nM  END\n>  <name>\nn,n-dimethylaniline\n\n>  <abbreviation>\nN,N-dimethylaniline\n\n>  <group>\nSalts and Solvents\n\n$$$$\npyridine\n  -INDIGO-11302219142D\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  2  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  3  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 pyridine\nM  END\n>  <name>\npyridine\n\n>  <abbreviation>\npyridine\n\n>  <group>\nSalts and Solvents\n\n$$$$\ntriethylamine\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    1.5000    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2010   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7990   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7990    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0980    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.0980    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  2  5  1  0  0  0  0\n  4  6  1  0  0  0  0\n  3  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 triethylamine\nM  END\n>  <name>\ntriethylamine\n\n>  <abbreviation>\ntriethylamine\n\n>  <group>\nSalts and Solvents\n\n$$$$\nacetonitrile\n  -INDIGO-11302219142D\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  3  0  0  0  0\n  1  3  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 acetonitrile\nM  END\n>  <name>\nacetonitrile\n\n>  <abbreviation>\nacetonitrile\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndimethyl acetamide\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    2.7990    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7990    1.5000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0980   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000   -0.7500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000   -2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2009    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 dimethyl acetamide\nM  END\n>  <name>\ndimethyl acetamide\n\n>  <abbreviation>\ndimethyl acetamide\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndimethyl formamide\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    2.7990    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7990    1.5000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0980   -0.7500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000   -0.7500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000   -2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2009    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 DMF\nM  END\n>  <name>\ndimethyl formamide\n\n>  <abbreviation>\nDMF\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndimethyl sulfoxide\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    1.5000    0.0000    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2010   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7990   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    1.5000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 DMSO\nM  END\n>  <name>\ndimethyl sulfoxide\n\n>  <abbreviation>\nDMSO\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndimethylpropylene urea\n  -INDIGO-11302219142D\n\n  9  9  0  0  0  0  0  0  0  0999 V2000\n    3.4378    2.0544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.1388    1.3044    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    2.1387   -0.1955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.8397   -0.9455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.4593   -0.1956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.4593    1.3044    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.7584    2.0545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.8397    2.0544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.8397    3.5545    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  6  8  1  0  0  0  0\n  2  8  1  0  0  0  0\n  8  9  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 dimethylpropylene urea\nM  END\n>  <name>\ndimethylpropylene urea\n\n>  <abbreviation>\ndimethylpropylene urea\n\n>  <group>\nSalts and Solvents\n\n$$$$\nformamide\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    0.2485   -6.0342    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5476   -5.2841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5476   -3.7842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.8467   -6.0341    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  2  0  0  0  0\n  2  4  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 formamide\nM  END\n>  <name>\nformamide\n\n>  <abbreviation>\nformamide\n\n>  <group>\nSalts and Solvents\n\n$$$$\nn-methyl-2-pyrrolidone\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    0.7500    2.3100    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.4600    1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9600    1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.7500    3.8100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3860    1.8953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  3  2  1  0  0  0  0\n  2  1  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  3  1  0  0  0  0\n  1  6  1  0  0  0  0\n  4  7  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 N-methyl-2-pyrrolidone\nM  END\n>  <name>\nn-methyl-2-pyrrolidone\n\n>  <abbreviation>\nN-methyl-2-pyrrolidone\n\n>  <group>\nSalts and Solvents\n\n$$$$\nn-methylformamide\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.1009    0.5500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    1.4000    1.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.4000    2.8000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6990    0.5500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1981    1.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  2  0  0  0  0\n  2  4  1  0  0  0  0\n  1  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 N-methylformamide\nM  END\n>  <name>\nn-methylformamide\n\n>  <abbreviation>\nN-methylformamide\n\n>  <group>\nSalts and Solvents\n\n$$$$\npropane nitrile\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    6.8971    0.7500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2990   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5981    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  4  3  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 propane nitrile\nM  END\n>  <name>\npropane nitrile\n\n>  <abbreviation>\npropane nitrile\n\n>  <group>\nSalts and Solvents\n\n$$$$\nsulfolane\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    0.7500    2.3100    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.4600    1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9600    1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    3.6090    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.0673    3.5678    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  3  2  1  0  0  0  0\n  2  1  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  3  1  0  0  0  0\n  1  6  2  0  0  0  0\n  1  7  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 sulfolane\nM  END\n>  <name>\nsulfolane\n\n>  <abbreviation>\nsulfolane\n\n>  <group>\nSalts and Solvents\n\n$$$$\namyl acetate\n  -INDIGO-11302219142D\n\n  9  8  0  0  0  0  0  0  0  0999 V2000\n    5.8307    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1297   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5316   -0.3786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8307    1.8714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2326    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9335   -0.3785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.6345    0.3715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.6646   -0.3785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.9636    0.3715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\n  3  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 amyl acetate\nM  END\n>  <name>\namyl acetate\n\n>  <abbreviation>\namyl acetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nbutyl acetate\n  -INDIGO-11302219142D\n\n  8  7  0  0  0  0  0  0  0  0999 V2000\n    7.5466    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8456    2.2500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9486    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6495    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2476    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.3505    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8456    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1446    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  5  1  0  0  0  0\n  1  7  1  0  0  0  0\n  2  7  2  0  0  0  0\n  3  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  4  6  1  0  0  0  0\n  7  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 butyl acetate\nM  END\n>  <name>\nbutyl acetate\n\n>  <abbreviation>\nbutyl acetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndimethyl carbonate\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    0.5429   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5429    1.1571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7562   -1.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8419   -1.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.0552   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1409   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  4  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 dimethyl carbonate\nM  END\n>  <name>\ndimethyl carbonate\n\n>  <abbreviation>\ndimethyl carbonate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nethyl acetate\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    2.7079   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7079    1.1571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0070   -1.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.4089   -1.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.1099   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.1891   -1.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 ethyl acetate\nM  END\n>  <name>\nethyl acetate\n\n>  <abbreviation>\nethyl acetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nethyl formate\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    5.8087   -2.6404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8087   -1.1506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5094   -3.4018    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2098   -2.6486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9103   -3.4018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.1078   -3.3904    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  2  0  0  0  0\n  3  1  1  0  0  0  0\n  4  3  1  0  0  0  0\n  5  4  1  0  0  0  0\n  1  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 ethyl formate\nM  END\n>  <name>\nethyl formate\n\n>  <abbreviation>\nethyl formate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nethyl lactate\n  -INDIGO-11302219142D\n\n  8  7  0  0  0  0  0  0  0  0999 V2000\n   -0.3480    1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.9509    2.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2500    1.2991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5491    2.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5491    3.5491    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8480    1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1471    2.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8480   -0.2009    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  4  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  6  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 ethyl lactate\nM  END\n>  <name>\nethyl lactate\n\n>  <abbreviation>\nethyl lactate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nethyl propionate\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n   -0.3480    1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.9509    2.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2500    1.2991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5491    2.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5491    3.5491    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8480    1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1471    2.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  4  6  1  0  0  0  0\n  6  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 ethyl propionate\nM  END\n>  <name>\nethyl propionate\n\n>  <abbreviation>\nethyl propionate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nethylene carbonate\n  -INDIGO-11302219142D\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n    1.0323    3.5259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0323    2.0259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2458    1.1443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7823   -0.2824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2824   -0.2824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.1813    1.1443    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  2  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 ethylene carbonate\nM  END\n>  <name>\nethylene carbonate\n\n>  <abbreviation>\nethylene carbonate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nisobutyl acetate\n  -INDIGO-11302219142D\n\n  8  7  0  0  0  0  0  0  0  0999 V2000\n    4.4399   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4399    1.1571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.7390   -1.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1409   -1.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8419   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5429   -1.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5429   -2.5929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7561   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  6  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 isobutyl acetate\nM  END\n>  <name>\nisobutyl acetate\n\n>  <abbreviation>\nisobutyl acetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nisopropyl acetate\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    3.1409   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1409    1.1571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4400   -1.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8419   -1.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5429   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7561   -1.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5429    1.1571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  5  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 isopropyl acetate\nM  END\n>  <name>\nisopropyl acetate\n\n>  <abbreviation>\nisopropyl acetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethyl acetate\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.5429   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5429    1.1571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7562   -1.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.8419   -1.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.1409   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 methyl acetate\nM  END\n>  <name>\nmethyl acetate\n\n>  <abbreviation>\nmethyl acetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethyl formate\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    1.5821   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5821    1.1571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.8812   -1.0929    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2831   -1.0929    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.0159   -0.3429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 methyl formate\nM  END\n>  <name>\nmethyl formate\n\n>  <abbreviation>\nmethyl formate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethyl lactate\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    7.6971   -2.1071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3980   -2.8571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0991   -2.1071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0991   -0.6071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8000   -2.8571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5009   -2.1071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8000   -4.3571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  2  0  0  0  0\n  3  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  5  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 methyl lactate\nM  END\n>  <name>\nmethyl lactate\n\n>  <abbreviation>\nmethyl lactate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nn-octylacetate\n  -INDIGO-11302219142D\n\n 12 11  0  0  0  0  0  0  0  0999 V2000\n    7.7009    4.9462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0000    5.6962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.2991    4.9462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.5980    5.6962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.8971    4.9462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.1962    5.6962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.4953    4.9462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   16.7942    5.6962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   18.0933    4.9462    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   19.3924    5.6962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   20.6913    4.9462    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   19.3924    7.1962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  9 10  1  0  0  0  0\n 10 11  1  0  0  0  0\n 10 12  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  4   9  10  11  12\nM  SMT   1 n-octylacetate\nM  END\n>  <name>\nn-octylacetate\n\n>  <abbreviation>\nn-octylacetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\npropyl acetate\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    6.3403   -0.1607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6395    2.0893    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.7423   -0.1607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0413    0.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4433    0.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6395    0.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.9385   -0.1607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  4  1  0  0  0  0\n  1  6  1  0  0  0  0\n  2  6  2  0  0  0  0\n  3  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  6  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 propyl acetate\nM  END\n>  <name>\npropyl acetate\n\n>  <abbreviation>\npropyl acetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\npropylene carbonate\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    0.5661   -1.8745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.5661   -0.3746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.6474    0.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.1839    1.9338    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3160    1.9338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.1978    3.1472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7797    0.5071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  5  7  1  0  0  0  0\n  2  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 propylene carbonate\nM  END\n>  <name>\npropylene carbonate\n\n>  <abbreviation>\npropylene carbonate\n\n>  <group>\nSalts and Solvents\n\n$$$$\nt-butyl acetate\n  -INDIGO-11302219142D\n\n  8  7  0  0  0  0  0  0  0  0999 V2000\n    6.0125   -7.4927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.7134   -6.7427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.7134   -5.2428    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4144   -7.4928    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.1153   -6.7428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.8163   -5.9928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3653   -8.0418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.8653   -5.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  2  0  0  0  0\n  2  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  5  7  1  0  0  0  0\n  5  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 t-butyl acetate\nM  END\n>  <name>\nt-butyl acetate\n\n>  <abbreviation>\nt-butyl acetate\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,2-dimethoxyethane\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n   -0.0857    0.1714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2133   -0.5786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5124    0.1714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.3848   -0.5786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8114   -0.5786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6838    0.1714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  4  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 1,2-dimethoxyethane\nM  END\n>  <name>\n1,2-dimethoxyethane\n\n>  <abbreviation>\n1,2-dimethoxyethane\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,4-dioxane\n  -INDIGO-11302219142D\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n    3.9490   -2.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6500   -3.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6500   -4.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9490   -5.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2481   -4.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2481   -3.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0  0  0  0\n  2  1  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  1  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 1,4-dioxane\nM  END\n>  <name>\n1,4-dioxane\n\n>  <abbreviation>\n1,4-dioxane\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2-methyl tetrahydrofuran\n  -INDIGO-11302219142D\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n    0.7500    2.3100    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.4600    1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9600    1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.3860    1.8953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  2  1  0  0  0  0\n  2  1  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  3  1  0  0  0  0\n  4  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 2-methyl tetrahydrofuran\nM  END\n>  <name>\n2-methyl tetrahydrofuran\n\n>  <abbreviation>\n2-methyl tetrahydrofuran\n\n>  <group>\nSalts and Solvents\n\n$$$$\nanisole\n  -INDIGO-11302219142D\n\n  8  8  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000    1.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990    2.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  2  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  3  1  0  0  0  0\n  1  7  1  0  0  0  0\n  7  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 anisole\nM  END\n>  <name>\nanisole\n\n>  <abbreviation>\nanisole\n\n>  <group>\nSalts and Solvents\n\n$$$$\nbutyl carbitol\n  -INDIGO-11302219142D\n\n 11 10  0  0  0  0  0  0  0  0999 V2000\n   -0.2227   -3.0342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0742   -3.7829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.3750   -3.0387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6719   -3.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9782   -3.0336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.2751   -3.7823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.5758   -3.0382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.8728   -3.7870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.1792   -3.0330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.4761   -3.7817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.7768   -3.0376    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  9 10  1  0  0  0  0\n 10 11  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  3   9  10  11\nM  SMT   1 butyl carbitol\nM  END\n>  <name>\nbutyl carbitol\n\n>  <abbreviation>\nbutyl carbitol\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncyclopentyl methyl ether\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    6.1000    1.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010    1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990    1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5053    1.7481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.3855    0.7467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.4886   -0.4632    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9950   -0.6239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  5  4  1  0  0  0  0\n  4  2  1  0  0  0  0\n  2  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 cyclopentyl methyl ether\nM  END\n>  <name>\ncyclopentyl methyl ether\n\n>  <abbreviation>\ncyclopentyl methyl ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndibutyl ether\n  -INDIGO-11302219142D\n\n  9  8  0  0  0  0  0  0  0  0999 V2000\n    5.4509    4.6471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7500    3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0491    4.6471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3480    3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6470    4.6471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   11.9461    3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2452    4.6471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5441    3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8432    4.6471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 dibutyl ether\nM  END\n>  <name>\ndibutyl ether\n\n>  <abbreviation>\ndibutyl ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndiethyl ether\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    6.1000    1.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990    2.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010    2.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5019    1.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.6980    1.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  2  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 ether\nM  END\n>  <name>\ndiethyl ether\n\n>  <abbreviation>\nether\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndiethylene glycol\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    7.7875   -1.4835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4896   -2.2328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1892   -1.4790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8854   -2.2317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5884   -1.4840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2906   -2.2333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0845   -2.2313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  7  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 diethylene glycol\nM  END\n>  <name>\ndiethylene glycol\n\n>  <abbreviation>\ndiethylene glycol\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndiglyme\n  -INDIGO-11302219142D\n\n  9  8  0  0  0  0  0  0  0  0999 V2000\n   -0.0857    0.1714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2133   -0.5786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5124    0.1714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.3848   -0.5786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8114   -0.5786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.6838    0.1714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.9828   -0.5786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -5.2818    0.1714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -6.5809   -0.5786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  4  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 diglyme\nM  END\n>  <name>\ndiethylene glycol dimethyl ether\n\n>  <abbreviation>\ndiglyme\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndiisopropyl ether\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    5.5971    2.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2980    3.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2980    5.1000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9991    2.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7000    3.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.4009    2.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7000    5.1000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  5  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 diisopropyl ether\nM  END\n>  <name>\ndiisopropyl ether\n\n>  <abbreviation>\ndiisopropyl ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndimethyl ether\n  -INDIGO-11302219142D\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    4.2989   -0.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5980    0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9999    0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 dimethyl ether\nM  END\n>  <name>\ndimethyl ether\n\n>  <abbreviation>\ndimethyl ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndiphenyl ether\n  -INDIGO-11302219142D\n\n 13 14  0  0  0  0  0  0  0  0999 V2000\n    7.1190    1.0305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8200    0.2805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.8200   -1.2196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5210   -1.9696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2219   -1.2195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2219    0.2805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.5209    1.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4181    0.2804    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7171    1.0304    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0161    0.2805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.0161   -1.2194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.7170   -1.9694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.4180   -1.2195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  2  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  2  0  0  0  0\n  2  7  1  0  0  0  0\n  1  8  1  0  0  0  0\n  8  9  2  0  0  0  0\n  9 10  1  0  0  0  0\n 10 11  2  0  0  0  0\n 11 12  1  0  0  0  0\n 12 13  2  0  0  0  0\n  8 13  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  5   9  10  11  12  13\nM  SMT   1 diphenyl ether\nM  END\n>  <name>\ndiphenyl ether\n\n>  <abbreviation>\ndiphenyl ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\nethoxybenzene\n  -INDIGO-11302219142D\n\n  9  9  0  0  0  0  0  0  0  0999 V2000\n    0.0000    6.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    4.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2991    3.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2991    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5980    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5980    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2991   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  2  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  2  0  0  0  0\n  4  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 ethoxybenzene\nM  END\n>  <name>\nethoxybenzene\n\n>  <abbreviation>\nethoxybenzene\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethyl t-butyl ether\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    6.1000    1.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010    1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990    1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5019    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0510    2.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5510   -0.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  2  5  1  0  0  0  0\n  2  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 methyl t-butyl ether\nM  END\n>  <name>\nmethyl t-butyl ether\n\n>  <abbreviation>\nmethyl t-butyl ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\nt-amyl methyl ether\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    6.8972    0.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5982    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2990   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8482    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3482   -1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1962    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  7  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  2  5  1  0  0  0  0\n  3  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 t-amyl methyl ether\nM  END\n>  <name>\nt-amyl methyl ether\n\n>  <abbreviation>\nt-amyl methyl ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\nt-butylethyl ether\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    2.3688   -7.1130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0698   -7.8630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.2293   -7.1129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.5283   -7.8629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8274   -8.6129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.2783   -6.5639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7783   -9.1620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  1  0  0  0  0\n  4  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 t-butylethyl ether\nM  END\n>  <name>\nt-butylethyl ether\n\n>  <abbreviation>\nt-butylethyl ether\n\n>  <group>\nSalts and Solvents\n\n$$$$\ntetrahydrofuran\n  -INDIGO-11302219142D\n\n  5  5  0  0  0  0  0  0  0  0999 V2000\n    0.7500    2.3100    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.4600    1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.9600    1.4300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  3  2  1  0  0  0  0\n  2  1  1  0  0  0  0\n  1  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  3  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 THF\nM  END\n>  <name>\ntetrahydrofuran\n\n>  <abbreviation>\nTHF\n\n>  <group>\nSalts and Solvents\n\n$$$$\ntriethylene glycol\n  -INDIGO-11302219142D\n\n 10  9  0  0  0  0  0  0  0  0999 V2000\n    4.1520    3.8971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.4509    4.6471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.7500    3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.0491    4.6471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    9.3480    3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   10.6471    4.6471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.9462    3.8971    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   13.2453    4.6471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   14.5442    3.8971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   15.8433    4.6471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  9 10  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  2   9  10\nM  SMT   1 triethylene glycol\nM  END\n>  <name>\ntriethylene glycol\n\n>  <abbreviation>\ntriethylene glycol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,2,4-trichlorobenzene\n  -INDIGO-11302219142D\n\n  9  9  0  0  0  0  0  0  0  0999 V2000\n    2.2506   -3.8983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.9991   -2.5989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2506   -1.2994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.7485   -1.2994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000   -2.5989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.7485   -3.8983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000   -5.1978    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    2.9991    0.0000    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  6  2  0  0  0  0\n  2  3  2  0  0  0  0\n  3  4  1  0  0  0  0\n  3  9  1  0  0  0  0\n  4  5  2  0  0  0  0\n  4  8  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 1,2,4-trichlorobenzene\nM  END\n>  <name>\n1,2,4-trichlorobenzene\n\n>  <abbreviation>\n1,2,4-trichlorobenzene\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,2-dichlorobenzene\n  -INDIGO-11302219142D\n\n  8  8  0  0  0  0  0  0  0  0999 V2000\n    0.9558   -0.8403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4581   -0.8408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.2048    0.4582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.4555    1.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.9571    1.7589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2065    0.4576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2078    3.0567    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    3.2060    3.0573    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  6  2  0  0  0  0\n  2  3  2  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  4  8  1  0  0  0  0\n  5  6  1  0  0  0  0\n  5  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 1,2-dichlorobenzene\nM  END\n>  <name>\n1,2-dichlorobenzene\n\n>  <abbreviation>\n1,2-dichlorobenzene\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,2-dichloroethane\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n   -0.2571    0.8286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0419    1.5786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.3409    0.8286    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n   -1.5562    1.5786    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  1  4  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 DCE\nM  END\n>  <name>\n1,2-dichloroethane\n\n>  <abbreviation>\nDCE\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2,2,2-trifluoroethanol\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    2.3661   -2.2500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0670   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0670    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0670    1.5000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.4330    0.0000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5670    0.0000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  3  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 2,2,2-trifluoroethanol\nM  END\n>  <name>\n2,2,2-trifluoroethanol\n\n>  <abbreviation>\n2,2,2-trifluoroethanol\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2,3,4-trifluorotoluene\n  -INDIGO-11302219142D\n\n 10 10  0  0  0  0  0  0  0  0999 V2000\n    4.0898    1.7173    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0899    1.7173    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5899   -0.8808    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0898   -0.8807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8398    0.4183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8399   -2.1798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3399    0.4182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5898   -0.8807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.3399   -2.1798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0899   -0.8808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  5  1  0  0  0  0\n  2  7  1  0  0  0  0\n  3 10  1  0  0  0  0\n  4  5  2  0  0  0  0\n  4  6  1  0  0  0  0\n  4  8  1  0  0  0  0\n  5  7  1  0  0  0  0\n  6  9  2  0  0  0  0\n  7 10  2  0  0  0  0\n  9 10  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  2   9  10\nM  SMT   1 2,3,4-trifluorotoluene\nM  END\n>  <name>\n2,3,4-trifluorotoluene\n\n>  <abbreviation>\n2,3,4-trifluorotoluene\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncarbon tetrachloride\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000    1.7500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -1.2500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    7.6000    0.2500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    4.6000    0.2500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  1  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 carbon tetrachloride\nM  END\n>  <name>\ncarbon tetrachloride\n\n>  <abbreviation>\ncarbon tetrachloride\n\n>  <group>\nSalts and Solvents\n\n$$$$\nchloroacetic acid\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    9.0626   -7.0246    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.0626   -5.5268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   10.3632   -7.7759    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4658   -7.0246    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    7.7666   -7.7759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  2  0  0  0  0\n  3  1  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  1  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 chloroacetic acid\nM  END\n>  <name>\nchloroacetic acid\n\n>  <abbreviation>\nchloroacetic acid\n\n>  <group>\nSalts and Solvents\n\n$$$$\nchlorobenzene\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000    1.7500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  2  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  3  1  0  0  0  0\n  1  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 chlorobenzene\nM  END\n>  <name>\nchlorobenzene\n\n>  <abbreviation>\nchlorobenzene\n\n>  <group>\nSalts and Solvents\n\n$$$$\nchloroform\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000    1.7500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -1.2500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    7.6000    0.2500    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6000    0.2500    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  1  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 chloroform\nM  END\n>  <name>\nchloroform\n\n>  <abbreviation>\nchloroform\n\n>  <group>\nSalts and Solvents\n\n$$$$\ndichloromethane\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -0.5000    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -0.5000    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    6.8500    1.5490    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    5.3500    1.5490    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  1  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 DCM\nM  END\n>  <name>\ndichloromethane\n\n>  <abbreviation>\nDCM\n\n>  <group>\nSalts and Solvents\n\n$$$$\nfluorobenzene\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    1.2991    3.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2991    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5980    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5980    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2991   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  2  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  2  0  0  0  0\n  2  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 fluorobenzene\nM  END\n>  <name>\nfluorobenzene\n\n>  <abbreviation>\nfluorobenzene\n\n>  <group>\nSalts and Solvents\n\n$$$$\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$$$$\nperfluorotoluene\n  -INDIGO-11302219142D\n\n 15 15  0  0  0  0  0  0  0  0999 V2000\n    3.0000    0.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1962    0.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5982    3.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    7.0982    2.2500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0982    2.2500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    8.1962   -2.2500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -2.2500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5982   -3.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5982    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2990    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8972    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5982    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.8972   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2990   -1.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.5982   -2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1 10  1  0  0  0  0\n  2 11  1  0  0  0  0\n  3 12  1  0  0  0  0\n  4 12  1  0  0  0  0\n  5 12  1  0  0  0  0\n  6 13  1  0  0  0  0\n  7 14  1  0  0  0  0\n  8 15  1  0  0  0  0\n  9 10  2  0  0  0  0\n  9 11  1  0  0  0  0\n  9 12  1  0  0  0  0\n 10 14  1  0  0  0  0\n 11 13  2  0  0  0  0\n 13 15  1  0  0  0  0\n 14 15  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  7   9  10  11  12  13  14  15\nM  SMT   1 perfluorotoluene\nM  END\n>  <name>\nperfluorotoluene\n\n>  <abbreviation>\nperfluorotoluene\n\n>  <group>\nSalts and Solvents\n\n$$$$\ntrichloroacetic acid\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    4.3154   -3.6247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6336   -2.8642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.6336   -1.3688    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0543   -2.8010    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    3.1051   -4.3218    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    4.3090   -5.1835    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    6.9579   -3.6120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  2  1  1  0  0  0  0\n  3  2  2  0  0  0  0\n  4  1  1  0  0  0  0\n  5  1  1  0  0  0  0\n  6  1  1  0  0  0  0\n  7  2  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 trichloroacetic acid\nM  END\n>  <name>\ntrichloroacetic acid\n\n>  <abbreviation>\ntrichloroacetic acid\n\n>  <group>\nSalts and Solvents\n\n$$$$\ntrichloroacetonitrile\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    4.5000    0.0000    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000    1.5000    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    3.0000   -1.5000    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0\n    1.5000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    0.0000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  2  5  1  0  0  0  0\n  5  6  3  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 trichloroacetonitrile\nM  END\n>  <name>\ntrichloroacetonitrile\n\n>  <abbreviation>\ntrichloroacetonitrile\n\n>  <group>\nSalts and Solvents\n\n$$$$\ntrifluoroacetic acid\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    1.0500   -4.9991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    0.3000   -3.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0500   -2.4009    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2000   -3.7000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7000   -3.7000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2000   -2.2000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2000   -5.2000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  2  0  0  0  0\n  2  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  1  0  0  0  0\n  4  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 trifluoroacetic acid\nM  END\n>  <name>\ntrifluoroacetic acid\n\n>  <abbreviation>\ntrifluoroacetic acid\n\n>  <group>\nSalts and Solvents\n\n$$$$\ntrifluoromethylbenzene\n  -INDIGO-11302219142D\n\n 10 10  0  0  0  0  0  0  0  0999 V2000\n    6.1000    0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -0.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8010   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000   -2.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.3990   -2.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000    1.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1000    3.2500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    4.6000    1.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n    7.6000    1.7500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  2  0  0  0  0\n  2  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  3  1  0  0  0  0\n  1  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  7  9  1  0  0  0  0\n  7 10  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  2   9  10\nM  SMT   1 trifluoromethylbenzene\nM  END\n>  <name>\ntrifluoromethylbenzene\n\n>  <abbreviation>\ntrifluoromethylbenzene\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2-methylpentane\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    0.5471   -1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7520   -0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.0509   -1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3500   -0.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.6491   -1.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.3500    1.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 2-methylpentane\nM  END\n>  <name>\n2-methylpentane\n\n>  <abbreviation>\n2-methylpentane\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncis-decalin\n  -INDIGO-11302219142D\n\n 12 13  0  0  1  0  0  0  0  0999 V2000\n    2.6130   -0.7481    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0\n    2.6130   -2.2234    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0\n    1.3195   -3.0026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3195    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8754    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8754   -2.9714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000   -0.7481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1948   -0.7481    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1948   -2.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000   -2.2234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5583    0.8018    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6130   -3.6988    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  4  1  0  0  0  0\n  1  5  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  6  1  0  0  0  0\n  3 10  1  0  0  0  0\n  4  7  1  0  0  0  0\n  5  8  1  0  0  0  0\n  6  9  1  0  0  0  0\n  7 10  1  0  0  0  0\n  8  9  1  0  0  0  0\n  1 11  1  1  0  0  0\n  2 12  1  1  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  4   9  10  11  12\nM  SMT   1 cis-decalin\nM  END\n>  <name>\ncis-decalin\n\n>  <abbreviation>\ncis-decalin\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncyclohexane\n  -INDIGO-11302219142D\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n    3.9490   -2.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6500   -3.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6500   -4.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9490   -5.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2481   -4.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2481   -3.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0  0  0  0\n  2  1  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  1  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 cyclohexane\nM  END\n>  <name>\ncyclohexane\n\n>  <abbreviation>\ncyclohexane\n\n>  <group>\nSalts and Solvents\n\n$$$$\nisooctane\n  -INDIGO-11302219142D\n\n  8  7  0  0  0  0  0  0  0  0999 V2000\n    4.6062   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9052   -1.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2043   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5033   -1.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8023   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1552   -0.4581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.6552   -0.4580    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5033   -0.2571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  2  6  1  0  0  0  0\n  2  7  1  0  0  0  0\n  4  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 isooctane\nM  END\n>  <name>\nisooctane\n\n>  <abbreviation>\nisooctane\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethylcyclohexane\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    3.9490   -2.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6500   -3.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6500   -4.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9490   -5.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2481   -4.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2481   -3.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9490   -0.8000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0  0  0  0\n  2  1  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  1  1  0  0  0  0\n  1  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 methylcyclohexane\nM  END\n>  <name>\nmethylcyclohexane\n\n>  <abbreviation>\nmethylcyclohexane\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethylcyclopentane\n  -INDIGO-11302219142D\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n    4.2136    0.4041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.4271   -0.4776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.0001   -0.4776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.9636   -1.9041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.4636   -1.9041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2136    1.9041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  6  1  0  0  0  0\n  2  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  4  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 methylcyclopentane\nM  END\n>  <name>\nmethylcyclopentane\n\n>  <abbreviation>\nmethylcyclopentane\n\n>  <group>\nSalts and Solvents\n\n$$$$\nheptane\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    4.6062   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9052   -1.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2043   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5033   -1.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8023   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1014   -1.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   12.4004   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 n-heptane\nM  END\n>  <name>\nheptane\n\n>  <abbreviation>\nn-heptane\n\n>  <group>\nSalts and Solvents\n\n$$$$\nhexane\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    4.6062   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.9052   -1.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.2043   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    8.5033   -1.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    9.8023   -2.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   11.1014   -1.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 n-hexane\nM  END\n>  <name>\nhexane\n\n>  <abbreviation>\nn-hexane\n\n>  <group>\nSalts and Solvents\n\n$$$$\npentane\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    2.5624   -4.3230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1578   -4.3230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.8600   -3.5708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.4556   -3.5708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.2647   -3.5708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  2  3  1  0  0  0  0\n  3  1  1  0  0  0  0\n  4  2  1  0  0  0  0\n  5  1  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 pentane\nM  END\n>  <name>\npentane\n\n>  <abbreviation>\npentane\n\n>  <group>\nSalts and Solvents\n\n$$$$\n2-pentanone\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n   -1.5971   -4.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.2980   -3.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0009   -4.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.3000   -3.4500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5991   -4.2000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.3000   -1.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  4  6  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 2-pentanone\nM  END\n>  <name>\n2-pentanone\n\n>  <abbreviation>\n2-pentanone\n\n>  <group>\nSalts and Solvents\n\n$$$$\n3-pentanone\n  -INDIGO-11302219142D\n\n  6  5  0  0  0  0  0  0  0  0999 V2000\n    2.6558    5.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9548    4.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2538    5.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    5.2539    6.9040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    6.5530    4.6539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    7.8520    5.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  2  0  0  0  0\n  3  5  1  0  0  0  0\n  5  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 3-pentanone\nM  END\n>  <name>\n3-pentanone\n\n>  <abbreviation>\n3-pentanone\n\n>  <group>\nSalts and Solvents\n\n$$$$\nacetone\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    0.0571    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2419   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3562   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0571    1.8714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 propanone\nM  END\n>  <name>\nacetone\n\n>  <abbreviation>\npropanone\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncyclohexanone\n  -INDIGO-11302219142D\n\n  7  7  0  0  0  0  0  0  0  0999 V2000\n    0.0571    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2419   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3562   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0571    1.8714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2419   -1.8786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0571   -2.6286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3562   -1.8786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\n  2  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  3  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 cyclohexanone\nM  END\n>  <name>\ncyclohexanone\n\n>  <abbreviation>\ncyclohexanone\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncyclopentanone\n  -INDIGO-11302219142D\n\n  6  6  0  0  0  0  0  0  0  0999 V2000\n    1.0323    3.5259    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0323    2.0259    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.2458    1.1443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.7823   -0.2824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.2824   -0.2824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.1813    1.1443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  2  6  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  6   1   2   3   4   5   6\nM  SMT   1 cyclopentanone\nM  END\n>  <name>\ncyclopentanone\n\n>  <abbreviation>\ncyclopentanone\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethyl ethyl ketone\n  -INDIGO-11302219142D\n\n  5  4  0  0  0  0  0  0  0  0999 V2000\n    0.0571    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2419   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3562   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0571    1.8714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5409    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\n  2  5  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  5   1   2   3   4   5\nM  SMT   1 MEK\nM  END\n>  <name>\nmethyl ethyl ketone\n\n>  <abbreviation>\nMEK\n\n>  <group>\nSalts and Solvents\n\n$$$$\nmethyl isobutyl ketone\n  -INDIGO-11302219142D\n\n  7  6  0  0  0  0  0  0  0  0999 V2000\n    0.0571    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2419   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3562   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0571    1.8714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5409    0.3714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.8399   -0.3786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.5409    1.8714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  2  0  0  0  0\n  2  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  5  7  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  7   1   2   3   4   5   6   7\nM  SMT   1 methyl isobutyl ketone\nM  END\n>  <name>\nmethyl isobutyl ketone\n\n>  <abbreviation>\nmethyl isobutyl ketone\n\n>  <group>\nSalts and Solvents\n\n$$$$\ncarbon disulfide\n  -INDIGO-11302219142D\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    5.7990    0.0000    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    2.7989    0.0000    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0\n    4.2989    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  3  2  0  0  0  0\n  2  3  2  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 carbon disulfide\nM  END\n>  <name>\ncarbon disulfide\n\n>  <abbreviation>\ncarbon disulfide\n\n>  <group>\nSalts and Solvents\n\n$$$$\nnitromethane\n  -INDIGO-11302219142D\n\n  4  3  0  0  0  0  0  0  0  0999 V2000\n    1.5009    0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.8000    1.5000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.0991    0.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.8000    3.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  2  0  0  0  0\nM  CHG  2   2   1   3  -1\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  4   1   2   3   4\nM  SMT   1 nitromethane\nM  END\n>  <name>\nnitromethane\n\n>  <abbreviation>\nnitromethane\n\n>  <group>\nSalts and Solvents\n\n$$$$\no-xylene\n  -INDIGO-11302219142D\n\n  8  8  0  0  0  0  0  0  0  0999 V2000\n   -2.1500    4.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4490    3.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4490    2.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1500    1.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.8510    2.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.8510    3.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1500    5.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.4481    4.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  1  1  0  0  0  0\n  1  7  1  0  0  0  0\n  6  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 o-xylene\nM  END\n>  <name>\no-xylene\n\n>  <abbreviation>\no-xylene\n\n>  <group>\nSalts and Solvents\n\n$$$$\nm-xylene\n  -INDIGO-11302219142D\n\n  8  8  0  0  0  0  0  0  0  0999 V2000\n   -2.1500    4.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4490    3.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4490    2.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1500    1.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.8510    2.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.8510    3.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1500    5.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.4480    1.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  1  1  0  0  0  0\n  1  7  1  0  0  0  0\n  5  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 m-xylene\nM  END\n>  <name>\nm-xylene\n\n>  <abbreviation>\nm-xylene\n\n>  <group>\nSalts and Solvents\n\n$$$$\np-xylene\n  -INDIGO-11302219142D\n\n  8  8  0  0  0  0  0  0  0  0999 V2000\n   -2.1500    4.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4490    3.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.4490    2.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1500    1.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.8510    2.2250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.8510    3.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1500    5.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.1500   -0.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  2  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  2  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  2  0  0  0  0\n  6  1  1  0  0  0  0\n  1  7  1  0  0  0  0\n  4  8  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SMT   1 p-xylene\nM  END\n>  <name>\np-xylene\n\n>  <abbreviation>\np-xylene\n\n>  <group>\nSalts and Solvents\n\n$$$$\nDIPEA\n  -INDIGO-11302219142D\n\n  9  8  0  0  0  0  0  0  0  0999 V2000\n   -1.5490    7.3145    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.5490    8.8145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8481    6.5645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.2500    6.5645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -4.1471    7.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8481    5.0645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0490    7.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.2500    5.0645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.8481    9.5645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  1  3  1  0  0  0  0\n  1  4  1  0  0  0  0\n  3  5  1  0  0  0  0\n  3  6  1  0  0  0  0\n  4  7  1  0  0  0  0\n  4  8  1  0  0  0  0\n  2  9  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  1   9\nM  SMT   1 DIPEA\nM  END\n>  <name>\nn,n-diisopropylethylamine\n\n>  <abbreviation>\nDIPEA\n\n>  <group>\nSalts and Solvents\n\n$$$$\n1,5-diazabicyclo[5.4.0]undec-7-ene\n  -INDIGO-11302219142D\n\n 11 12  0  0  0  0  0  0  0  0999 V2000\n    1.6852   -0.3846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3514    1.0778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.0000    1.7286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.3515    1.0777    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.6852   -0.3847    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.1695   -0.6090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -3.7175   -2.0053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -2.7822   -3.1781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -1.2990   -2.9545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n   -0.7500   -1.5574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    0.7500   -1.5574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  3  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  7  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  9 10  2  3  0  0  0\n 10  5  1  0  0  0  0\n 10 11  1  0  0  0  0\n 11  1  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  3   9  10  11\nM  SMT   1 DBU\nM  END\n>  <name>\n1,5-diazabicyclo[5.4.0]undec-7-ene\n\n>  <abbreviation>\nDBU\n\n>  <group>\nSalts and Solvents\n\n$$$$\nhexamethylphosphoramide\n  -INDIGO-11302219142D\n\n 11 10  0  0  0  0  0  0  0  0999 V2000\n    2.3174   -0.9012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.6235   -1.9903    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    4.8900   -0.9145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5935   -3.2519    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n    3.5935   -4.7619    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    5.0831   -3.2205    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    6.0654   -4.1562    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    6.1687   -1.9999    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.1521   -3.2278    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3934   -4.5570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.0626   -2.3997    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  4  5  2  0  0  0  0\n  4  6  1  0  0  0  0\n  6  7  1  0  0  0  0\n  6  8  1  0  0  0  0\n  4  9  1  0  0  0  0\n  9 10  1  0  0  0  0\n  9 11  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  3   9  10  11\nM  SMT   1 HMPA\nM  END\n>  <name>\nhexamethylphosphoramide\n\n>  <abbreviation>\nHMPA\n\n>  <group>\nSalts and Solvents\n\n$$$$\nhexamethylphosphorous triamide\n  -INDIGO-11302219142D\n\n 10  9  0  0  0  0  0  0  0  0999 V2000\n    0.0007    0.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3000    0.7500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3000    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6000    0.0000    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9000    0.7500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    5.1992    0.0004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9000    2.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    2.6031   -1.5008    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0\n    3.9032   -2.2490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3053   -2.2531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\n  2  4  1  0  0  0  0\n  4  5  1  0  0  0  0\n  5  6  1  0  0  0  0\n  5  7  1  0  0  0  0\n  4  8  1  0  0  0  0\n  8  9  1  0  0  0  0\n  8 10  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  8   1   2   3   4   5   6   7   8\nM  SAL   1  2   9  10\nM  SMT   1 HMPT\nM  END\n>  <name>\nhexamethylphosphorous triamide\n\n>  <abbreviation>\nHMPT\n\n>  <group>\nSalts and Solvents\n\n$$$$\nheavy water\n  -INDIGO-11302219142D\n\n  3  2  0  0  0  0  0  0  0  0999 V2000\n    0.0007    0.0004    0.0000 D   0  0  0  0  0  0  0  0  0  0  0  0\n    1.3000    0.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0\n    2.5993    0.0004    0.0000 D   0  0  0  0  0  0  0  0  0  0  0  0\n  1  2  1  0  0  0  0\n  2  3  1  0  0  0  0\nM  STY  1   1 SUP\nM  SLB  1   1   1\nM  SAL   1  3   1   2   3\nM  SMT   1 D2O\nM  END\n>  <name>\nheavy water\n\n>  <abbreviation>\nD2O\n\n>  <group>\nSalts and Solvents\n\n$$$$\n";
 
-function ownKeys$13(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$13(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$13(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$13(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$14(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$14(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$14(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$14(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var initialState$1 = {
   lib: [],
   mode: MODES.FG
@@ -13540,7 +13584,7 @@ var saltsAndSolventsReducer = function saltsAndSolventsReducer() {
     payload = _ref.payload;
   switch (type) {
     case 'SALTS_AND_SOLVENTS_INIT':
-      return _objectSpread$13(_objectSpread$13({}, state), payload);
+      return _objectSpread$14(_objectSpread$14({}, state), payload);
     default:
       return state;
   }
@@ -13589,8 +13633,8 @@ function initSaltsAndSolventsTemplates() {
   }();
 }
 
-function ownKeys$12(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$12(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$12(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$12(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$13(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$13(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$13(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$13(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var initial = {
   freqAtoms: [],
   currentAtom: 0,
@@ -13610,7 +13654,7 @@ function updateVisibleTools(visibleTool, activeTool) {
     if (key === 'shape' && menuHeight > 900) return res;
     if (!key.match(regExp) || menuHeight > 700) res[key] = visibleTool[key];
     return res;
-  }, _objectSpread$12({}, activeTool));
+  }, _objectSpread$13({}, activeTool));
 }
 function initResize() {
   return function (dispatch, getState) {
@@ -13634,41 +13678,41 @@ function toolbarReducer () {
     case 'ACTION':
       {
         var visibleTool = toolInMenu(action.action);
-        return visibleTool ? _objectSpread$12(_objectSpread$12({}, state), {}, {
+        return visibleTool ? _objectSpread$13(_objectSpread$13({}, state), {}, {
           opened: null,
-          visibleTools: _objectSpread$12(_objectSpread$12({}, state.visibleTools), visibleTool)
-        }) : _objectSpread$12(_objectSpread$12({}, state), {}, {
+          visibleTools: _objectSpread$13(_objectSpread$13({}, state.visibleTools), visibleTool)
+        }) : _objectSpread$13(_objectSpread$13({}, state), {}, {
           opened: null
         });
       }
     case 'ADD_ATOMS':
       {
         var newState = addFreqAtom(data, state.freqAtoms, state.currentAtom);
-        return _objectSpread$12(_objectSpread$12({}, state), newState);
+        return _objectSpread$13(_objectSpread$13({}, state), newState);
       }
     case 'CLEAR_VISIBLE':
       {
         var activeTool = toolInMenu(action.data);
         var correctTools = updateVisibleTools(state.visibleTools, activeTool);
-        return _objectSpread$12(_objectSpread$12({}, state), {}, {
+        return _objectSpread$13(_objectSpread$13({}, state), {}, {
           opened: null,
-          visibleTools: _objectSpread$12({}, correctTools)
+          visibleTools: _objectSpread$13({}, correctTools)
         });
       }
     case 'OPENED':
       {
-        return data.isSelected && state.opened ? _objectSpread$12(_objectSpread$12({}, state), {}, {
+        return data.isSelected && state.opened ? _objectSpread$13(_objectSpread$13({}, state), {}, {
           opened: null
-        }) : _objectSpread$12(_objectSpread$12({}, state), {}, {
+        }) : _objectSpread$13(_objectSpread$13({}, state), {}, {
           opened: data.menuName
         });
       }
     case 'UPDATE':
-      return _objectSpread$12(_objectSpread$12({}, state), {}, {
+      return _objectSpread$13(_objectSpread$13({}, state), {}, {
         opened: null
       });
     case 'MODAL_OPEN':
-      return _objectSpread$12(_objectSpread$12({}, state), {}, {
+      return _objectSpread$13(_objectSpread$13({}, state), {}, {
         opened: null
       });
     default:
@@ -13711,8 +13755,8 @@ function hiddenAncestor(el, base) {
   return findEl;
 }
 
-function ownKeys$11(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$11(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$11(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$11(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$12(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$12(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$12(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$12(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var initialState = {
   visible: false,
   rotateHandlePosition: {
@@ -13734,7 +13778,7 @@ var floatingToolsReducer = function floatingToolsReducer() {
     payload = _ref.payload;
   switch (type) {
     case 'UPDATE_FLOATING_TOOLS':
-      return _objectSpread$11(_objectSpread$11({}, state), payload);
+      return _objectSpread$12(_objectSpread$12({}, state), payload);
     default:
       return state;
   }
@@ -13742,8 +13786,8 @@ var floatingToolsReducer = function floatingToolsReducer() {
 
 var _excluded$t = ["type"],
   _excluded2$5 = ["buttons"];
-function ownKeys$10(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$10(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$10(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$10(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$11(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$11(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$11(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$11(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var shared = combineReducers({
   common: commonReducer,
   actionState: actionStateReducer,
@@ -13776,11 +13820,11 @@ function getRootReducer(setEditor) {
         {
           action.type;
             var data = _objectWithoutProperties(action, _excluded$t);
-          if (data) state = _objectSpread$10(_objectSpread$10({}, state), data);
+          if (data) state = _objectSpread$11(_objectSpread$11({}, state), data);
         }
     }
-    var sh = shared(state, _objectSpread$10(_objectSpread$10({}, action), pick(['editor', 'server', 'options'], state)));
-    var finalState = sh === state.shared ? state : _objectSpread$10(_objectSpread$10({}, state), sh);
+    var sh = shared(state, _objectSpread$11(_objectSpread$11({}, action), pick(['editor', 'server', 'options'], state)));
+    var finalState = sh === state.shared ? state : _objectSpread$11(_objectSpread$11({}, state), sh);
     global.currentState = finalState;
     return finalState;
   };
@@ -13869,8 +13913,8 @@ function useSettingsContext() {
   return React__default.useContext(settingsContext);
 }
 
-function ownKeys$$(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$$(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$$(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$$(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$10(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$10(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$10(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$10(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var throttleMilliseconds = 100;
 function useThrottleResizeObserver() {
   var options = arguments.length > 0 && arguments[0] !== undefined ? arguments[0] : {};
@@ -13884,11 +13928,11 @@ function useThrottleResizeObserver() {
   var onResize = useMemo(function () {
     return throttle$1(setSize, throttleMilliseconds);
   }, []);
-  var _useResizeObserver = useResizeObserver(_objectSpread$$({
+  var _useResizeObserver = useResizeObserver(_objectSpread$10({
       onResize: onResize
     }, options)),
     ref = _useResizeObserver.ref;
-  return _objectSpread$$({
+  return _objectSpread$10({
     ref: ref
   }, size);
 }
@@ -14018,13 +14062,13 @@ var mediaSizes$2 = {
 };
 
 var _excluded$s = ["height"];
-function ownKeys$_(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$_(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$_(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$_(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$$(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$$(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$$(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$$(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var Bond$1 = function Bond(props) {
   var height = props.height,
     rest = _objectWithoutProperties(props, _excluded$s);
   if (height && height <= mediaSizes$2.bondCollapsableHeight) {
-    return jsx(ToolbarMultiToolItem, _objectSpread$_({
+    return jsx(ToolbarMultiToolItem, _objectSpread$$({
       id: "bonds",
       options: groupOptions,
       variant: "grouped",
@@ -14032,35 +14076,35 @@ var Bond$1 = function Bond(props) {
     }, rest));
   }
   return jsxs(Fragment, {
-    children: [jsx(ToolbarMultiToolItem, _objectSpread$_({
+    children: [jsx(ToolbarMultiToolItem, _objectSpread$$({
       id: "bond-common",
       options: bondCommon
-    }, rest)), jsx(ToolbarMultiToolItem, _objectSpread$_({
+    }, rest)), jsx(ToolbarMultiToolItem, _objectSpread$$({
       id: "bond-stereo",
       options: bondStereo
-    }, rest)), jsx(ToolbarMultiToolItem, _objectSpread$_({
+    }, rest)), jsx(ToolbarMultiToolItem, _objectSpread$$({
       id: "bond-query",
       options: bondQuery
-    }, rest)), jsx(ToolbarMultiToolItem, _objectSpread$_({
+    }, rest)), jsx(ToolbarMultiToolItem, _objectSpread$$({
       id: "bond-special",
       options: bondSpecial
     }, rest))]
   });
 };
 
-function ownKeys$Z(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$Z(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$Z(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$Z(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$_(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$_(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$_(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$_(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var RGroup$1 = function RGroup(props) {
-  return jsx(ToolbarGroupItem, _objectSpread$Z({
+  return jsx(ToolbarGroupItem, _objectSpread$_({
     id: "rgroup",
     options: rGroupOptions
   }, props));
 };
 
-function ownKeys$Y(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$Y(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$Y(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$Y(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$Z(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$Z(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$Z(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$Z(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var Shape = function Shape(props) {
-  return jsx(ToolbarGroupItem, _objectSpread$Y({
+  return jsx(ToolbarGroupItem, _objectSpread$Z({
     id: "shapes",
     options: shapeOptions
   }, props));
@@ -14069,8 +14113,8 @@ var Shape = function Shape(props) {
 var classes$L = {"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"};
 
 var _excluded$r = ["className"];
-function ownKeys$X(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$X(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$X(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$X(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$Y(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$Y(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$Y(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$Y(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var LeftToolbar = function LeftToolbar(props) {
   var _scrollRef$current;
   var className = props.className,
@@ -14096,7 +14140,7 @@ var LeftToolbar = function LeftToolbar(props) {
     var id = _ref.id,
       options = _ref.options,
       dataTestId = _ref.dataTestId;
-    return ToolbarGroupItem(_objectSpread$X({
+    return ToolbarGroupItem(_objectSpread$Y({
       id: id,
       options: options,
       dataTestId: dataTestId
@@ -14133,16 +14177,16 @@ var LeftToolbar = function LeftToolbar(props) {
       children: visibleItems.map(function (item) {
         switch (item.id) {
           case 'bond-common':
-            return createElement(Bond$1, _objectSpread$X(_objectSpread$X({}, rest), {}, {
+            return createElement(Bond$1, _objectSpread$Y(_objectSpread$Y({}, rest), {}, {
               height: height,
               key: item.id
             }));
           case 'rgroup':
-            return createElement(RGroup$1, _objectSpread$X(_objectSpread$X({}, rest), {}, {
+            return createElement(RGroup$1, _objectSpread$Y(_objectSpread$Y({}, rest), {}, {
               key: item.id
             }));
           case 'shapes':
-            return createElement(Shape, _objectSpread$X(_objectSpread$X({}, rest), {}, {
+            return createElement(Shape, _objectSpread$Y(_objectSpread$Y({}, rest), {}, {
               key: item.id
             }));
           case 'bonds':
@@ -14270,14 +14314,14 @@ var LeftToolbarContainer = connect(mapStateToProps$k, mapDispatchToProps$k)(Left
 var classes$K = {"button-common-styles":"Atom-module_button-common-styles__j3EUJ","scrollbar":"Atom-module_scrollbar__iO-Ni","atom":"Atom-module_atom__g2RUu"};
 
 var _excluded$q = ["el", "shortcut", "selected"];
-function ownKeys$W(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$W(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$W(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$W(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$X(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$X(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$X(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$X(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function Atom$1(_ref) {
   var el = _ref.el,
     shortcut = _ref.shortcut,
     selected = _ref.selected,
     props = _objectWithoutProperties(_ref, _excluded$q);
-  return jsx("button", _objectSpread$W(_objectSpread$W({
+  return jsx("button", _objectSpread$X(_objectSpread$X({
     title: shortcut ? "".concat(el.title, " (").concat(shortcut, ")") : el.title,
     className: clsx(classes$K.atom, {
       selected: selected
@@ -14338,8 +14382,8 @@ var HorizontalDivider = function HorizontalDivider() {
 };
 
 var _excluded$p = ["className"];
-function ownKeys$V(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$V(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$V(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$V(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$W(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$W(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$W(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$W(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var Group = function Group(_ref) {
   var children = _ref.children,
     className = _ref.className;
@@ -14405,7 +14449,7 @@ var RightToolbar = function RightToolbar(props) {
             atoms: freqAtoms,
             active: active,
             onAction: onAction
-          }), jsx(ToolbarGroupItem, _objectSpread$V({
+          }), jsx(ToolbarGroupItem, _objectSpread$W({
             id: "period-table"
           }, rest))]
         })
@@ -14415,11 +14459,11 @@ var RightToolbar = function RightToolbar(props) {
           className: classes$J.groupItem,
           children: jsxs("div", {
             ref: sizeRef,
-            children: [jsx(ToolbarGroupItem, _objectSpread$V({
+            children: [jsx(ToolbarGroupItem, _objectSpread$W({
               id: "any-atom"
             }, rest)), jsx("div", {
               className: classes$J.button,
-              children: jsx(ToolbarGroupItem, _objectSpread$V({
+              children: jsx(ToolbarGroupItem, _objectSpread$W({
                 id: "extended-table"
               }, rest))
             })]
@@ -15087,15 +15131,7 @@ var hiddenButtonsSelector = createSelector([getActionState], function (actionSta
   }, []);
 });
 var disableableButtons = ['layout', 'clean', 'arom', 'dearom', 'cip', 'enhanced-stereo'];
-var shortcuts = Object.keys(config).reduce(function (acc, key) {
-  var _action$key;
-  if ((_action$key = config[key]) !== null && _action$key !== void 0 && _action$key.shortcut) {
-    var shortcut = config[key].shortcut;
-    var processedShortcut = shortcutStr(shortcut);
-    acc[key] = processedShortcut;
-  }
-  return acc;
-}, {});
+var shortcuts = generateMenuShortcuts(config);
 var mapStateToProps$i = function mapStateToProps(state) {
   var _state$actionState;
   return {
@@ -15285,8 +15321,8 @@ var selectAbbreviationLookupValue = function selectAbbreviationLookupValue(state
   return (_state$abbreviationLo = state.abbreviationLookup.lookupValue) !== null && _state$abbreviationLo !== void 0 ? _state$abbreviationLo : '';
 };
 
-function ownKeys$U(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$U(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$U(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$U(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$V(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$V(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$V(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$V(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var destinationVectorMapping = {
   ArrowUp: new Vec2(0, -1),
   ArrowDown: new Vec2(0, 1),
@@ -15311,7 +15347,7 @@ function moveSelectedItems(editor, key, isShiftPressed) {
   if (isClose) {
     var moveStep = isShiftPressed ? getFasterStep(destinationVectorInCanvas) : destinationVectorInCanvas;
     editor.render.setViewBox(function (prev) {
-      return _objectSpread$U(_objectSpread$U({}, prev), {}, {
+      return _objectSpread$V(_objectSpread$V({}, prev), {}, {
         minX: prev.minX + moveStep.x,
         minY: prev.minY + moveStep.y
       });
@@ -16847,8 +16883,8 @@ var handleMovingPosibilityCursor = function handleMovingPosibilityCursor(item, c
 function _createForOfIteratorHelper$b(o, allowArrayLike) { var it = typeof Symbol !== "undefined" && o[Symbol.iterator] || o["@@iterator"]; if (!it) { if (Array.isArray(o) || (it = _unsupportedIterableToArray$b(o)) || allowArrayLike && o && typeof o.length === "number") { if (it) o = it; var i = 0; var F = function F() {}; return { s: F, n: function n() { if (i >= o.length) return { done: true }; return { done: false, value: o[i++] }; }, e: function e(_e) { throw _e; }, f: F }; } 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 normalCompletion = true, didErr = false, err; return { s: function s() { it = it.call(o); }, n: function n() { var step = it.next(); normalCompletion = step.done; return step; }, e: function e(_e2) { didErr = true; err = _e2; }, f: function f() { try { if (!normalCompletion && it["return"] != null) it["return"](); } finally { if (didErr) throw err; } } }; }
 function _unsupportedIterableToArray$b(o, minLen) { if (!o) return; if (typeof o === "string") return _arrayLikeToArray$b(o, minLen); var n = Object.prototype.toString.call(o).slice(8, -1); if (n === "Object" && o.constructor) n = o.constructor.name; if (n === "Map" || n === "Set") return Array.from(o); if (n === "Arguments" || /^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(n)) return _arrayLikeToArray$b(o, minLen); }
 function _arrayLikeToArray$b(arr, len) { if (len == null || len > arr.length) len = arr.length; for (var i = 0, arr2 = new Array(len); i < len; i++) arr2[i] = arr[i]; return arr2; }
-function ownKeys$T(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$T(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$T(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$T(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$U(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$U(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$U(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$U(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function _classPrivateFieldInitSpec$1(obj, privateMap, value) { _checkPrivateRedeclaration$1(obj, privateMap); privateMap.set(obj, value); }
 function _checkPrivateRedeclaration$1(obj, privateCollection) { if (privateCollection.has(obj)) { throw new TypeError("Cannot initialize the same private elements twice on an object"); } }
 var Direction;
@@ -16895,7 +16931,7 @@ var SelectTool = function () {
       if (isBondingWithMacroMolecule(this.editor, event)) {
         return;
       }
-      var selected = _objectSpread$T(_objectSpread$T({}, (ci === null || ci === void 0 ? void 0 : ci.map) === 'atoms' && {
+      var selected = _objectSpread$U(_objectSpread$U({}, (ci === null || ci === void 0 ? void 0 : ci.map) === 'atoms' && {
         atoms: [ci.id]
       }), (ci === null || ci === void 0 ? void 0 : ci.map) === 'bonds' && {
         bonds: [ci.id]
@@ -17146,7 +17182,7 @@ var SelectTool = function () {
       } else if (ci.map === 'texts') {
         editor.selection(closestToSel(ci));
         var text = molecule.texts.get(ci.id);
-        var dialog = editor.event.elementEdit.dispatch(_objectSpread$T(_objectSpread$T({}, text), {}, {
+        var dialog = editor.event.elementEdit.dispatch(_objectSpread$U(_objectSpread$U({}, text), {}, {
           type: 'text'
         }));
         dialog.then(function (_ref) {
@@ -17266,28 +17302,28 @@ var SelectTool = function () {
       var render = this.editor.render;
       if (closeEdges.includes(Direction.RIGHT)) {
         render.setViewBox(function (prev) {
-          return _objectSpread$T(_objectSpread$T({}, prev), {}, {
+          return _objectSpread$U(_objectSpread$U({}, prev), {}, {
             minX: prev.minX + MOVE_STEP
           });
         });
       }
       if (closeEdges.includes(Direction.LEFT)) {
         render.setViewBox(function (prev) {
-          return _objectSpread$T(_objectSpread$T({}, prev), {}, {
+          return _objectSpread$U(_objectSpread$U({}, prev), {}, {
             minX: prev.minX - MOVE_STEP
           });
         });
       }
       if (closeEdges.includes(Direction.DOWN)) {
         render.setViewBox(function (prev) {
-          return _objectSpread$T(_objectSpread$T({}, prev), {}, {
+          return _objectSpread$U(_objectSpread$U({}, prev), {}, {
             minY: prev.minY + MOVE_STEP
           });
         });
       }
       if (closeEdges.includes(Direction.TOP)) {
         render.setViewBox(function (prev) {
-          return _objectSpread$T(_objectSpread$T({}, prev), {}, {
+          return _objectSpread$U(_objectSpread$U({}, prev), {}, {
             minY: prev.minY - MOVE_STEP
           });
         });
@@ -17388,8 +17424,8 @@ function getNewSelectedItems(editor, selectedSgroups) {
   return newSelected;
 }
 
-function ownKeys$S(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$S(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$S(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$S(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$T(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$T(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$T(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$T(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function handleHotkeyOverItem(props) {
   if (props.newAction.tool === 'eraser') {
     handleEraser(props);
@@ -17608,7 +17644,7 @@ function handleAtomTool(_ref10) {
   var hoveredItemId = _ref10.hoveredItemId,
     newAction = _ref10.newAction,
     editor = _ref10.editor;
-  var atomProps = _objectSpread$S({}, newAction.opts);
+  var atomProps = _objectSpread$T({}, newAction.opts);
   var updatedAtoms = fromAtomsAttrs(editor.render.ctab, hoveredItemId, atomProps, true);
   editor.update(updatedAtoms);
 }
@@ -17616,7 +17652,7 @@ function handleSgroupsTool(_ref11) {
   var hoveredItemId = _ref11.hoveredItemId,
     newAction = _ref11.newAction,
     editor = _ref11.editor;
-  var atomProps = _objectSpread$S({}, newAction.opts);
+  var atomProps = _objectSpread$T({}, newAction.opts);
   var action = new Action();
   var ctab = editor.render.ctab;
   var sGroup = ctab.molecule.sgroups.get(hoveredItemId);
@@ -18266,17 +18302,17 @@ var mediaSizes$1 = {
   smallHeight: 600
 };
 
-var styles$e = {"container":"LoadingCircles-module_container__MPCs0","bounce":"LoadingCircles-module_bounce__gCepS"};
+var styles$f = {"container":"LoadingCircles-module_container__MPCs0","bounce":"LoadingCircles-module_bounce__gCepS"};
 
 var LoadingCircles = function LoadingCircles() {
   return jsxs("div", {
-    className: styles$e.container,
+    className: styles$f.container,
     children: [jsx("span", {}), jsx("span", {}), jsx("span", {})]
   });
 };
 
-function ownKeys$R(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$R(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$R(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$R(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$S(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$S(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$S(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$S(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function _createForOfIteratorHelper$a(o, allowArrayLike) { var it = typeof Symbol !== "undefined" && o[Symbol.iterator] || o["@@iterator"]; if (!it) { if (Array.isArray(o) || (it = _unsupportedIterableToArray$a(o)) || allowArrayLike && o && typeof o.length === "number") { if (it) o = it; var i = 0; var F = function F() {}; return { s: F, n: function n() { if (i >= o.length) return { done: true }; return { done: false, value: o[i++] }; }, e: function e(_e) { throw _e; }, f: F }; } 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 normalCompletion = true, didErr = false, err; return { s: function s() { it = it.call(o); }, n: function n() { var step = it.next(); normalCompletion = step.done; return step; }, e: function e(_e2) { didErr = true; err = _e2; }, f: function f() { try { if (!normalCompletion && it["return"] != null) it["return"](); } finally { if (didErr) throw err; } } }; }
 function _unsupportedIterableToArray$a(o, minLen) { if (!o) return; if (typeof o === "string") return _arrayLikeToArray$a(o, minLen); var n = Object.prototype.toString.call(o).slice(8, -1); if (n === "Object" && o.constructor) n = o.constructor.name; if (n === "Map" || n === "Set") return Array.from(o); if (n === "Arguments" || /^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(n)) return _arrayLikeToArray$a(o, minLen); }
 function _arrayLikeToArray$a(arr, len) { if (len == null || len > arr.length) len = arr.length; for (var i = 0, arr2 = new Array(len); i < len; i++) arr2[i] = arr[i]; return arr2; }
@@ -18655,7 +18691,7 @@ function findClosestItem(restruct, pos, maps, skip, options) {
     var minDist = res ? res.dist : null;
     var item = findMaps[mp](restruct, pos, skip, minDist, options);
     if (item !== null) {
-      var enrichedItem = _objectSpread$R({
+      var enrichedItem = _objectSpread$S({
         map: mp
       }, item);
       if (mp === 'sgroupData') {
@@ -19939,8 +19975,8 @@ var EraserTool = function () {
   return EraserTool;
 }();
 
-function ownKeys$Q(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$Q(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$Q(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$Q(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$R(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$R(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$R(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$R(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var HandTool = function () {
   function HandTool(editor) {
     _classCallCheck$2(this, HandTool);
@@ -19985,7 +20021,7 @@ var HandTool = function () {
       var diff = Vec2.diff(this.endPos, this.begPos).scaled(1 / rnd.options.zoom);
       this.begPos = this.endPos;
       rnd.setViewBox(function (prev) {
-        return _objectSpread$Q(_objectSpread$Q({}, prev), {}, {
+        return _objectSpread$R(_objectSpread$R({}, prev), {}, {
           minX: prev.minX - diff.x,
           minY: prev.minY - diff.y
         });
@@ -20028,8 +20064,8 @@ var HandTool = function () {
   return HandTool;
 }();
 
-function ownKeys$P(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$P(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$P(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$P(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$Q(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$Q(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$Q(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$Q(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var PasteTool = function () {
   function PasteTool(editor, struct) {
     var _struct$functionalGro;
@@ -20143,7 +20179,7 @@ var PasteTool = function () {
   }, {
     key: "mouseup",
     value: function mouseup() {
-      var idsOfItemsMerged = this.mergeItems && _objectSpread$P(_objectSpread$P({}, this.mergeItems.atoms && {
+      var idsOfItemsMerged = this.mergeItems && _objectSpread$Q(_objectSpread$Q({}, this.mergeItems.atoms && {
         atoms: Array.from(this.mergeItems.atoms.values())
       }), this.mergeItems.bonds && {
         bonds: Array.from(this.mergeItems.bonds.values())
@@ -20811,8 +20847,8 @@ function normalizeAngle(angle) {
   return angleWithinFullCircle;
 }
 
-function ownKeys$O(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$O(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$O(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$O(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$P(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$P(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$P(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$P(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var SNAP_ANGLES_RELATIVE_TO_FIXED_BOND = [Math.PI / 2, -Math.PI / 2, 2 * Math.PI / 3, -(2 * Math.PI) / 3, Math.PI];
 var MAX_SNAP_DELTA = Math.PI / 18;
 var ANGLE_INDICATOR_VISIBLE_DELTA = Math.PI / 9;
@@ -20889,7 +20925,7 @@ var RotateTool = function () {
     get: function get() {
       var _this$snapInfo;
       if ((_this$snapInfo = this.snapInfo) !== null && _this$snapInfo !== void 0 && _this$snapInfo.snapAngleDrawingProps) {
-        return _objectSpread$O({
+        return _objectSpread$P({
           snapMode: this.snapInfo.snapMode
         }, this.snapInfo.snapAngleDrawingProps);
       }
@@ -21409,8 +21445,8 @@ var TemplatePreview = function () {
 function _createForOfIteratorHelper$1(o, allowArrayLike) { var it = typeof Symbol !== "undefined" && o[Symbol.iterator] || o["@@iterator"]; if (!it) { if (Array.isArray(o) || (it = _unsupportedIterableToArray$1(o)) || allowArrayLike && o && typeof o.length === "number") { if (it) o = it; var i = 0; var F = function F() {}; return { s: F, n: function n() { if (i >= o.length) return { done: true }; return { done: false, value: o[i++] }; }, e: function e(_e) { throw _e; }, f: F }; } 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 normalCompletion = true, didErr = false, err; return { s: function s() { it = it.call(o); }, n: function n() { var step = it.next(); normalCompletion = step.done; return step; }, e: function e(_e2) { didErr = true; err = _e2; }, f: function f() { try { if (!normalCompletion && it["return"] != null) it["return"](); } finally { if (didErr) throw err; } } }; }
 function _unsupportedIterableToArray$1(o, minLen) { if (!o) return; if (typeof o === "string") return _arrayLikeToArray$1(o, minLen); var n = Object.prototype.toString.call(o).slice(8, -1); if (n === "Object" && o.constructor) n = o.constructor.name; if (n === "Map" || n === "Set") return Array.from(o); if (n === "Arguments" || /^(?:Ui|I)nt(?:8|16|32)(?:Clamped)?Array$/.test(n)) return _arrayLikeToArray$1(o, minLen); }
 function _arrayLikeToArray$1(arr, len) { if (len == null || len > arr.length) len = arr.length; for (var i = 0, arr2 = new Array(len); i < len; i++) arr2[i] = arr[i]; return arr2; }
-function ownKeys$N(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$N(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$N(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$N(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$O(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$O(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$O(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$O(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function getBondFlipSign(struct, bond) {
   var _struct$atoms$get, _struct$halfBonds$get;
   var xy0 = new Vec2();
@@ -21573,7 +21609,7 @@ var TemplateTool = function () {
               this.event = event;
               (_this$templatePreview = this.templatePreview) === null || _this$templatePreview === void 0 || _this$templatePreview.hidePreview();
               if (this.functionalGroups.size) {
-                this.targetGroupsIds = getGroupIdsFromItemArrays(this.struct, _objectSpread$N(_objectSpread$N({}, ((_this$closestItem2 = this.closestItem) === null || _this$closestItem2 === void 0 ? void 0 : _this$closestItem2.map) === 'atoms' && {
+                this.targetGroupsIds = getGroupIdsFromItemArrays(this.struct, _objectSpread$O(_objectSpread$O({}, ((_this$closestItem2 = this.closestItem) === null || _this$closestItem2 === void 0 ? void 0 : _this$closestItem2.map) === 'atoms' && {
                   atoms: [this.closestItem.id]
                 }), ((_this$closestItem3 = this.closestItem) === null || _this$closestItem3 === void 0 ? void 0 : _this$closestItem3.map) === 'bonds' && {
                   bonds: [this.closestItem.id]
@@ -22907,8 +22943,8 @@ var RotateController = function () {
   return RotateController;
 }();
 
-function ownKeys$M(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$M(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$M(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$M(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$N(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$N(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$N(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$N(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function _classPrivateFieldInitSpec(obj, privateMap, value) { _checkPrivateRedeclaration(obj, privateMap); privateMap.set(obj, value); }
 function _checkPrivateRedeclaration(obj, privateCollection) { if (privateCollection.has(obj)) { throw new TypeError("Cannot initialize the same private elements twice on an object"); } }
 var SCALE = 40;
@@ -23063,7 +23099,7 @@ var Editor$3 = function () {
     key: "setOptions",
     value: function setOptions(opts) {
       var options = JSON.parse(opts);
-      this.event.apiSettings.dispatch(_objectSpread$M({}, options));
+      this.event.apiSettings.dispatch(_objectSpread$N({}, options));
       return this.render.updateOptions(opts);
     }
   }, {
@@ -23583,7 +23619,7 @@ var Cursor = function Cursor(_ref) {
   });
 };
 
-var styles$d = {"button-common-styles":"ContextMenu-module_button-common-styles__pshYr","scrollbar":"ContextMenu-module_scrollbar__fCla5","contextMenu":"ContextMenu-module_contextMenu__oqyL-","icon":"ContextMenu-module_icon__KhXEk","sameGroup":"ContextMenu-module_sameGroup__0DPIX","devider":"ContextMenu-module_devider__-K9Bc","subMenu":"ContextMenu-module_subMenu__87kBE"};
+var styles$e = {"button-common-styles":"ContextMenu-module_button-common-styles__pshYr","scrollbar":"ContextMenu-module_scrollbar__fCla5","contextMenu":"ContextMenu-module_contextMenu__oqyL-","icon":"ContextMenu-module_icon__KhXEk","sameGroup":"ContextMenu-module_sameGroup__0DPIX","devider":"ContextMenu-module_devider__-K9Bc","subMenu":"ContextMenu-module_subMenu__87kBE"};
 
 var CONTEXT_MENU_ID;
 (function (CONTEXT_MENU_ID) {
@@ -23781,8 +23817,8 @@ function ButtonGroup(_ref) {
   });
 }
 
-function ownKeys$L(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$L(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$L(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$L(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$M(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$M(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$M(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$M(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var _atom$properties = atom.properties,
   ringBondCount = _atom$properties.ringBondCount,
   hCount = _atom$properties.hCount,
@@ -23883,20 +23919,20 @@ var AtomMenuItems = function AtomMenuItems(props) {
         atoms: atomIds,
         editor: editor,
         changeAtomPromise: Promise.resolve(properties.includes(key) ? {
-          queryProperties: _objectSpread$L(_objectSpread$L({}, getPropertyValue('queryProperties')), {}, _defineProperty$1({}, key, value))
+          queryProperties: _objectSpread$M(_objectSpread$M({}, getPropertyValue('queryProperties')), {}, _defineProperty$1({}, key, value))
         } : _defineProperty$1({}, key, value))
       });
     }
   };
   return jsxs(Fragment, {
-    children: [jsx(Item, _objectSpread$L(_objectSpread$L({}, props), {}, {
+    children: [jsx(Item, _objectSpread$M(_objectSpread$M({}, props), {}, {
       onClick: handleEdit,
       children: (_props$propsFromTrigg4 = props.propsFromTrigger) !== null && _props$propsFromTrigg4 !== void 0 && _props$propsFromTrigg4.extraItemsSelected ? 'Edit selected atoms...' : 'Edit...'
-    })), jsx(Item, _objectSpread$L(_objectSpread$L({}, props), {}, {
+    })), jsx(Item, _objectSpread$M(_objectSpread$M({}, props), {}, {
       disabled: stereoDisabled,
       onClick: handleStereo,
       children: "Enhanced stereochemistry..."
-    })), jsx(Submenu, _objectSpread$L(_objectSpread$L({}, props), {}, {
+    })), jsx(Submenu, _objectSpread$M(_objectSpread$M({}, props), {}, {
       label: "Query properties",
       style: {
         overflow: 'visible'
@@ -23905,10 +23941,10 @@ var AtomMenuItems = function AtomMenuItems(props) {
         var title = _ref2.title,
           buttons = _ref2.buttons,
           key = _ref2.key;
-        return createElement(Submenu, _objectSpread$L(_objectSpread$L({}, props), {}, {
+        return createElement(Submenu, _objectSpread$M(_objectSpread$M({}, props), {}, {
           label: title,
           key: key,
-          className: styles$d.sameGroup
+          className: styles$e.sameGroup
         }), jsx(ButtonGroup, {
           buttons: buttons,
           defaultValue: getPropertyValue(key),
@@ -23917,7 +23953,7 @@ var AtomMenuItems = function AtomMenuItems(props) {
           }
         }));
       })
-    })), jsx(Item, _objectSpread$L(_objectSpread$L({}, props), {}, {
+    })), jsx(Item, _objectSpread$M(_objectSpread$M({}, props), {}, {
       onClick: handleDelete,
       children: "Delete"
     }))]
@@ -24063,8 +24099,8 @@ var useBondTypeChange = function useBondTypeChange() {
   return [handler, disabled];
 };
 
-function ownKeys$K(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$K(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$K(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$K(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$L(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$L(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$L(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$L(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var nonQueryBondNames = getNonQueryBondNames(tools);
 var BondMenuItems = function BondMenuItems(props) {
   var _props$propsFromTrigg;
@@ -24086,13 +24122,13 @@ var BondMenuItems = function BondMenuItems(props) {
   var handleDelete = useDelete$1();
   var bondNamesWithoutEmptyValue = nonQueryBondNames.slice(1);
   return jsxs(Fragment, {
-    children: [jsx(Item, _objectSpread$K(_objectSpread$K({}, props), {}, {
+    children: [jsx(Item, _objectSpread$L(_objectSpread$L({}, props), {}, {
       onClick: handleEdit,
       children: (_props$propsFromTrigg = props.propsFromTrigger) !== null && _props$propsFromTrigg !== void 0 && _props$propsFromTrigg.extraItemsSelected ? 'Edit selected bonds...' : 'Edit...'
     })), bondNamesWithoutEmptyValue.map(function (name, i) {
       var iconName = getIconName(name);
-      var classNames = styles$d.sameGroup + (i === bondNamesWithoutEmptyValue.length - 1 ? styles$d.devider : '');
-      return createElement(Item, _objectSpread$K(_objectSpread$K({
+      var classNames = styles$e.sameGroup + (i === bondNamesWithoutEmptyValue.length - 1 ? styles$e.devider : '');
+      return createElement(Item, _objectSpread$L(_objectSpread$L({
         className: classNames
       }, props), {}, {
         id: name,
@@ -24100,37 +24136,37 @@ var BondMenuItems = function BondMenuItems(props) {
         key: name
       }), iconName && jsx(Icon, {
         name: iconName,
-        className: styles$d.icon
+        className: styles$e.icon
       }), jsx("span", {
         children: formatTitle(tools[name].title)
       }));
-    }), jsx(Submenu, _objectSpread$K(_objectSpread$K({}, props), {}, {
+    }), jsx(Submenu, _objectSpread$L(_objectSpread$L({}, props), {}, {
       label: "Query bonds",
-      className: styles$d.subMenu,
+      className: styles$e.subMenu,
       children: queryBondNames.map(function (name) {
         var iconName = getIconName(name);
         return jsxs(Item, {
-          className: styles$d.sameGroup,
+          className: styles$e.sameGroup,
           id: name,
           onClick: handleTypeChange,
           children: [iconName && jsx(Icon, {
             name: iconName,
-            className: styles$d.icon
+            className: styles$e.icon
           }), jsx("span", {
             children: formatTitle(tools[name].title)
           })]
         }, name);
       })
-    })), jsx(Item, _objectSpread$K(_objectSpread$K({}, props), {}, {
+    })), jsx(Item, _objectSpread$L(_objectSpread$L({}, props), {}, {
       hidden: sGroupAttachHidden,
       onClick: handleSGroupAttach,
       children: "Attach S-Group..."
-    })), jsx(Item, _objectSpread$K(_objectSpread$K({}, props), {}, {
+    })), jsx(Item, _objectSpread$L(_objectSpread$L({}, props), {}, {
       hidden: sGroupEditHidden,
       disabled: sGroupEditDisabled,
       onClick: handleSGroupEdit,
       children: "Edit S-Group..."
-    })), jsx(Item, _objectSpread$K(_objectSpread$K({}, props), {}, {
+    })), jsx(Item, _objectSpread$L(_objectSpread$L({}, props), {}, {
       onClick: handleDelete,
       children: "Delete"
     }))]
@@ -24199,8 +24235,8 @@ var useFunctionalGroupRemove = function useFunctionalGroupRemove() {
   return handler;
 };
 
-function ownKeys$J(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$J(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$J(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$J(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$K(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$K(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$K(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$K(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var FunctionalGroupMenuItems = function FunctionalGroupMenuItems(props) {
   var _useFunctionalGroupEo = useFunctionalGroupEoc(),
     _useFunctionalGroupEo2 = _slicedToArray$1(_useFunctionalGroupEo, 3),
@@ -24209,7 +24245,7 @@ var FunctionalGroupMenuItems = function FunctionalGroupMenuItems(props) {
     ExpandOrContractDisabled = _useFunctionalGroupEo2[2];
   var handleRemove = useFunctionalGroupRemove();
   return jsxs(Fragment, {
-    children: [jsx(Item, _objectSpread$J(_objectSpread$J({}, props), {}, {
+    children: [jsx(Item, _objectSpread$K(_objectSpread$K({}, props), {}, {
       disabled: function disabled(params) {
         return ExpandOrContractDisabled(params);
       },
@@ -24220,7 +24256,7 @@ var FunctionalGroupMenuItems = function FunctionalGroupMenuItems(props) {
         return handleExpandOrContract(params, true);
       },
       children: "Expand Abbreviation"
-    })), jsx(Item, _objectSpread$J(_objectSpread$J({}, props), {}, {
+    })), jsx(Item, _objectSpread$K(_objectSpread$K({}, props), {}, {
       disabled: function disabled(params) {
         return ExpandOrContractDisabled(params);
       },
@@ -24231,15 +24267,15 @@ var FunctionalGroupMenuItems = function FunctionalGroupMenuItems(props) {
         return handleExpandOrContract(params, false);
       },
       children: "Contract Abbreviation"
-    })), jsx(Item, _objectSpread$J(_objectSpread$J({}, props), {}, {
+    })), jsx(Item, _objectSpread$K(_objectSpread$K({}, props), {}, {
       onClick: handleRemove,
       children: "Remove Abbreviation"
     }))]
   });
 };
 
-function ownKeys$I(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$I(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$I(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$I(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$J(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$J(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$J(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$J(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var bondNames = getBondNames(tools);
 var SelectionMenuItems = function SelectionMenuItems(props) {
   var _useBondEdit = useBondEdit(),
@@ -24260,18 +24296,18 @@ var SelectionMenuItems = function SelectionMenuItems(props) {
     atomStereoDisabled = _useAtomStereo2[1];
   var handleDelete = useDelete$1();
   return jsxs(Fragment, {
-    children: [jsx(Item, _objectSpread$I(_objectSpread$I({}, props), {}, {
+    children: [jsx(Item, _objectSpread$J(_objectSpread$J({}, props), {}, {
       disabled: bondEditDisabled,
       onClick: handleBondEdit,
       children: "Edit selected bonds..."
-    })), jsx(Item, _objectSpread$I(_objectSpread$I({}, props), {}, {
+    })), jsx(Item, _objectSpread$J(_objectSpread$J({}, props), {}, {
       disabled: atomEditDisabled,
       onClick: handleAtomEdit,
       children: "Edit selected atoms..."
-    })), jsx(Submenu, _objectSpread$I(_objectSpread$I({}, props), {}, {
+    })), jsx(Submenu, _objectSpread$J(_objectSpread$J({}, props), {}, {
       label: "Bond type",
       disabled: bondTypeChangeDisabled,
-      className: styles$d.subMenu,
+      className: styles$e.subMenu,
       children: bondNames.map(function (name) {
         var iconName = getIconName(name);
         return jsxs(Item, {
@@ -24279,17 +24315,17 @@ var SelectionMenuItems = function SelectionMenuItems(props) {
           onClick: handleTypeChange,
           children: [iconName && jsx(Icon, {
             name: iconName,
-            className: styles$d.icon
+            className: styles$e.icon
           }), jsx("span", {
             children: formatTitle(tools[name].title)
           })]
         }, name);
       })
-    })), jsx(Item, _objectSpread$I(_objectSpread$I({}, props), {}, {
+    })), jsx(Item, _objectSpread$J(_objectSpread$J({}, props), {}, {
       disabled: atomStereoDisabled,
       onClick: handleAtomStereo,
       children: "Enhanced stereochemistry..."
-    })), jsx(Item, _objectSpread$I(_objectSpread$I({}, props), {}, {
+    })), jsx(Item, _objectSpread$J(_objectSpread$J({}, props), {}, {
       onClick: handleDelete,
       children: "Delete"
     }))]
@@ -24372,8 +24408,8 @@ var useRGroupAttachmentPointEdit = function useRGroupAttachmentPointEdit() {
   return [handler, disabled, hidden];
 };
 
-function ownKeys$H(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$H(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$H(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$H(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$I(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$I(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$I(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$I(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var RGroupAttachmentPointMenuItems = function RGroupAttachmentPointMenuItems(props) {
   var handleRemove = useDelete();
   var _useRGroupAttachmentP = useRGroupAttachmentPointEdit(),
@@ -24382,23 +24418,23 @@ var RGroupAttachmentPointMenuItems = function RGroupAttachmentPointMenuItems(pro
     rgroupAttachmentPointDisabled = _useRGroupAttachmentP2[1],
     rgroupAttachmentPointHidden = _useRGroupAttachmentP2[2];
   return jsxs(Fragment, {
-    children: [jsx(Item, _objectSpread$H(_objectSpread$H({}, props), {}, {
+    children: [jsx(Item, _objectSpread$I(_objectSpread$I({}, props), {}, {
       disabled: rgroupAttachmentPointDisabled,
       hidden: rgroupAttachmentPointHidden,
       onClick: handleEditRGroupAttachmentPoint,
       children: "Edit..."
-    })), jsx(Item, _objectSpread$H(_objectSpread$H({}, props), {}, {
+    })), jsx(Item, _objectSpread$I(_objectSpread$I({}, props), {}, {
       onClick: handleRemove,
       children: "Remove"
     }))]
   });
 };
 
-function ownKeys$G(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$G(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$G(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$G(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$H(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$H(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$H(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$H(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var props = {
   animation: false,
-  className: styles$d.contextMenu
+  className: styles$e.contextMenu
 };
 var ContextMenu = function ContextMenu() {
   var _useAppContext = useAppContext(),
@@ -24411,31 +24447,31 @@ var ContextMenu = function ContextMenu() {
     editor.contextMenu[id] = visible;
   }, [getKetcherInstance]);
   return jsxs(Fragment, {
-    children: [jsx(Menu, _objectSpread$G(_objectSpread$G({}, props), {}, {
+    children: [jsx(Menu, _objectSpread$H(_objectSpread$H({}, props), {}, {
       id: CONTEXT_MENU_ID.FOR_BONDS,
       onVisibilityChange: function onVisibilityChange(visible) {
         return trackVisibility(CONTEXT_MENU_ID.FOR_BONDS, visible);
       },
       children: jsx(BondMenuItems, {})
-    })), jsx(Menu, _objectSpread$G(_objectSpread$G({}, props), {}, {
+    })), jsx(Menu, _objectSpread$H(_objectSpread$H({}, props), {}, {
       id: CONTEXT_MENU_ID.FOR_ATOMS,
       onVisibilityChange: function onVisibilityChange(visible) {
         return trackVisibility(CONTEXT_MENU_ID.FOR_ATOMS, visible);
       },
       children: jsx(AtomMenuItems, {})
-    })), jsx(Menu, _objectSpread$G(_objectSpread$G({}, props), {}, {
+    })), jsx(Menu, _objectSpread$H(_objectSpread$H({}, props), {}, {
       id: CONTEXT_MENU_ID.FOR_SELECTION,
       onVisibilityChange: function onVisibilityChange(visible) {
         return trackVisibility(CONTEXT_MENU_ID.FOR_SELECTION, visible);
       },
       children: jsx(SelectionMenuItems, {})
-    })), jsx(Menu, _objectSpread$G(_objectSpread$G({}, props), {}, {
+    })), jsx(Menu, _objectSpread$H(_objectSpread$H({}, props), {}, {
       id: CONTEXT_MENU_ID.FOR_FUNCTIONAL_GROUPS,
       onVisibilityChange: function onVisibilityChange(visible) {
         return trackVisibility(CONTEXT_MENU_ID.FOR_FUNCTIONAL_GROUPS, visible);
       },
       children: jsx(FunctionalGroupMenuItems, {})
-    })), jsx(Menu, _objectSpread$G(_objectSpread$G({}, props), {}, {
+    })), jsx(Menu, _objectSpread$H(_objectSpread$H({}, props), {}, {
       id: CONTEXT_MENU_ID.FOR_R_GROUP_ATTACHMENT_POINT,
       onVisibilityChange: function onVisibilityChange(visible) {
         return trackVisibility(CONTEXT_MENU_ID.FOR_R_GROUP_ATTACHMENT_POINT, visible);
@@ -24760,8 +24796,8 @@ var functionGroupInfoSelector = function functionGroupInfoSelector(state) {
   return state.functionalGroups.functionalGroupInfo;
 };
 
-function ownKeys$F(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$F(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$F(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$F(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$G(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$G(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$G(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$G(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var HOVER_PANEL_PADDING$1 = 20;
 var MAX_INFO_PANEL_SIZE = 200;
 function getPanelPosition$1(clientX, clientY, render, sGroup) {
@@ -24846,7 +24882,7 @@ var InfoPanel = function InfoPanel(props) {
     className: clsx(classes$E.infoPanel, className),
     children: jsx(StructRender, {
       struct: molecule,
-      options: _objectSpread$F(_objectSpread$F({}, render.options), {}, {
+      options: _objectSpread$G(_objectSpread$G({}, render.options), {}, {
         downScale: true,
         cachePrefix: 'infoPanel',
         needCache: false,
@@ -24965,8 +25001,8 @@ var InfoTooltip$1 = connect(function (store) {
 })(InfoTooltip);
 
 var _excluded$o = ["Tag", "className", "indigoVerification", "struct", "tool", "toolOpts", "options", "onInit", "onSelectionChange", "onElementEdit", "onEnhancedStereoEdit", "onQuickEdit", "onBondEdit", "onZoomIn", "onZoomOut", "onRgroupEdit", "onSgroupEdit", "onRemoveFG", "onMessage", "onAromatizeStruct", "onDearomatizeStruct", "onAttachEdit", "onCipChange", "onConfirm", "onShowInfo", "onApiSettings", "showAttachmentPoints", "onUpdateFloatingTools", "onShowMacromoleculesErrorMessage"];
-function ownKeys$E(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$E(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$E(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$E(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$F(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$F(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$F(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$F(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function _callSuper$9(t, o, e) { return o = _getPrototypeOf$2(o), _possibleConstructorReturn$2(t, _isNativeReflectConstruct$9() ? Reflect.construct(o, e || [], _getPrototypeOf$2(t).constructor) : o.apply(t, e)); }
 function _isNativeReflectConstruct$9() { try { var t = !Boolean.prototype.valueOf.call(Reflect.construct(Boolean, [], function () {})); } catch (t) {} return (_isNativeReflectConstruct$9 = function _isNativeReflectConstruct() { return !!t; })(); }
 function setupEditor(editor, props) {
@@ -25050,7 +25086,7 @@ var StructEditor = function (_Component) {
     value: function handleHorizontalScroll(event) {
       var _this2 = this;
       this.editor.render.setViewBox(function (prev) {
-        return _objectSpread$E(_objectSpread$E({}, prev), {}, {
+        return _objectSpread$F(_objectSpread$F({}, prev), {}, {
           minX: prev.minX - getSmoothScrollDelta(event.wheelDelta, _this2.editor.zoom())
         });
       });
@@ -25060,7 +25096,7 @@ var StructEditor = function (_Component) {
     value: function handleScroll(event) {
       var _this3 = this;
       this.editor.render.setViewBox(function (prev) {
-        return _objectSpread$E(_objectSpread$E({}, prev), {}, {
+        return _objectSpread$F(_objectSpread$F({}, prev), {}, {
           minX: prev.minX + getSmoothScrollDelta(event.deltaX, _this3.editor.zoom()),
           minY: prev.minY + getSmoothScrollDelta(event.deltaY, _this3.editor.zoom())
         });
@@ -25080,7 +25116,7 @@ var StructEditor = function (_Component) {
     key: "componentDidMount",
     value: function componentDidMount() {
       var _this4 = this;
-      this.editor = new Editor$3(this.editorRef.current, _objectSpread$E({}, this.props.options));
+      this.editor = new Editor$3(this.editorRef.current, _objectSpread$F({}, this.props.options));
       var ketcher = ketcherProvider.getKetcher();
       if (ketcher !== null && ketcher !== void 0 && ketcher.editor.macromoleculeConvertionError) {
         this.props.onShowMacromoleculesErrorMessage(ketcher.editor.macromoleculeConvertionError);
@@ -25213,7 +25249,7 @@ var StructEditor = function (_Component) {
         clientX = _this$state$clientX === void 0 ? 0 : _this$state$clientX,
         _this$state$clientY = _this$state.clientY,
         clientY = _this$state$clientY === void 0 ? 0 : _this$state$clientY;
-      return jsxs(Tag, _objectSpread$E(_objectSpread$E({
+      return jsxs(Tag, _objectSpread$F(_objectSpread$F({
         className: clsx(classes$G.canvas, className)
       }, props), {}, {
         "data-testid": "ketcher-canvas",
@@ -25445,8 +25481,8 @@ var _excluded$n = ["schema", "value", "onChange", "innerRef", "type", "isFocused
   _excluded7$1 = ["children", "onChange", "innerRef"];
 function _callSuper$8(t, o, e) { return o = _getPrototypeOf$2(o), _possibleConstructorReturn$2(t, _isNativeReflectConstruct$8() ? Reflect.construct(o, e || [], _getPrototypeOf$2(t).constructor) : o.apply(t, e)); }
 function _isNativeReflectConstruct$8() { try { var t = !Boolean.prototype.valueOf.call(Reflect.construct(Boolean, [], function () {})); } catch (t) {} return (_isNativeReflectConstruct$8 = function _isNativeReflectConstruct() { return !!t; })(); }
-function ownKeys$D(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$D(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$D(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$D(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$E(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$E(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$E(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$E(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function GenericInput(_ref) {
   _ref.schema;
     var value = _ref.value,
@@ -25469,7 +25505,7 @@ function GenericInput(_ref) {
     }
   }, [inputRef, isFocused]);
   return jsxs(Fragment, {
-    children: [jsx("input", _objectSpread$D({
+    children: [jsx("input", _objectSpread$E({
       type: type,
       value: value !== null && value !== void 0 ? value : '',
       onInput: onChange,
@@ -25495,7 +25531,7 @@ function TextArea(_ref2) {
     onChange = _ref2.onChange,
     innerRef = _ref2.innerRef,
     rest = _objectWithoutProperties(_ref2, _excluded2$4);
-  return jsx("textarea", _objectSpread$D({
+  return jsx("textarea", _objectSpread$E({
     value: value !== null && value !== void 0 ? value : '',
     ref: innerRef,
     onInput: onChange
@@ -25513,7 +25549,7 @@ function CheckBox(_ref3) {
     rest = _objectWithoutProperties(_ref3, _excluded3$1);
   return jsxs("div", {
     className: classes$C.fieldSetItem,
-    children: [jsx("input", _objectSpread$D({
+    children: [jsx("input", _objectSpread$E({
       type: "checkbox",
       checked: Boolean(value),
       onClick: onChange,
@@ -25576,7 +25612,7 @@ function FieldSet(_ref5) {
         className: classes$C.fieldSetItem,
         children: jsxs("label", {
           className: classes$C.fieldSetLabel,
-          children: [jsx("input", _objectSpread$D({
+          children: [jsx("input", _objectSpread$E({
             ref: innerRef,
             type: type,
             defaultChecked: type === 'radio' ? selected(val, checked) : selected(val, value),
@@ -25617,7 +25653,7 @@ function Slider(_ref6) {
     rest = _objectWithoutProperties(_ref6, _excluded5$1);
   return jsxs("div", {
     className: classes$C.slider,
-    children: [jsx("input", _objectSpread$D({
+    children: [jsx("input", _objectSpread$E({
       ref: innerRef,
       type: "checkbox",
       checked: value,
@@ -25651,7 +25687,7 @@ function inputCtrl(component, schema, _onChange) {
       type: 'text'
     };
   }
-  return _objectSpread$D({
+  return _objectSpread$E({
     onChange: function onChange(ev) {
       var val = !component.val ? ev : component.val(ev, schema);
       _onChange(val);
@@ -25713,7 +25749,7 @@ function componentMap(props) {
 var AnyComponentWithRef = React__default.forwardRef(function (_ref7, ref) {
   var Component = _ref7.Component,
     props = _objectWithoutProperties(_ref7, _excluded6$1);
-  return jsx(Component, _objectSpread$D(_objectSpread$D({}, props), {}, {
+  return jsx(Component, _objectSpread$E(_objectSpread$E({}, props), {}, {
     innerRef: ref
   }));
 });
@@ -25735,7 +25771,7 @@ var Input = function (_PureComponent) {
         _this$props.onChange;
         var innerRef = _this$props.innerRef,
         restProps = _objectWithoutProperties(_this$props, _excluded7$1);
-      return jsx(AnyComponentWithRef, _objectSpread$D(_objectSpread$D({
+      return jsx(AnyComponentWithRef, _objectSpread$E(_objectSpread$E({
         Component: this.component,
         ref: innerRef
       }, this.ctrl), restProps));
@@ -25744,7 +25780,7 @@ var Input = function (_PureComponent) {
   return Input;
 }(PureComponent);
 var Input$1 = React__default.forwardRef(function (props, ref) {
-  return jsx(Input, _objectSpread$D({
+  return jsx(Input, _objectSpread$E({
     innerRef: ref
   }, props));
 });
@@ -25822,8 +25858,8 @@ var _excluded$m = ["schema", "result"],
   _excluded8 = ["dataError"],
   _excluded9 = ["title", "name", "schema"],
   _excluded10 = ["pattern", "maxLength", "enum", "enumNames"];
-function ownKeys$C(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$C(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$C(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$C(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$D(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$D(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$D(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$D(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function _callSuper$7(t, o, e) { return o = _getPrototypeOf$2(o), _possibleConstructorReturn$2(t, _isNativeReflectConstruct$7() ? Reflect.construct(o, e || [], _getPrototypeOf$2(t).constructor) : o.apply(t, e)); }
 function _isNativeReflectConstruct$7() { try { var t = !Boolean.prototype.valueOf.call(Reflect.construct(Boolean, [], function () {})); } catch (t) {} return (_isNativeReflectConstruct$7 = function _isNativeReflectConstruct() { return !!t; })(); }
 var Form = function (_Component) {
@@ -25842,7 +25878,7 @@ var Form = function (_Component) {
         valid = _this$schema$serializ.valid,
         errors = _this$schema$serializ.errors;
       var errs = getErrorsObj(errors);
-      var initialState = _objectSpread$C(_objectSpread$C({}, init), {}, {
+      var initialState = _objectSpread$D(_objectSpread$D({}, init), {}, {
         init: true
       });
       onUpdate(initialState, valid, errs);
@@ -25928,7 +25964,7 @@ function Label(_ref) {
     children = _ref.children,
     props = _objectWithoutProperties(_ref, _excluded2$3);
   var tooltip = props.tooltip ? props.tooltip : null;
-  return jsxs("label", _objectSpread$C(_objectSpread$C({}, props), {}, {
+  return jsxs("label", _objectSpread$D(_objectSpread$D({}, props), {}, {
     children: [title && labelPos !== 'after' ? jsx("span", {
       title: tooltip,
       children: title
@@ -25963,11 +25999,11 @@ function Field(props) {
     dataError = _stateStore$field.dataError,
     fieldOpts = _objectWithoutProperties(_stateStore$field, _excluded4);
   var Component = component;
-  var formField = component ? jsx(Component, _objectSpread$C(_objectSpread$C({
+  var formField = component ? jsx(Component, _objectSpread$D(_objectSpread$D({
     name: name,
     schema: desc,
     className: className
-  }, fieldOpts), rest)) : jsx(Input$1, _objectSpread$C(_objectSpread$C(_objectSpread$C({
+  }, fieldOpts), rest)) : jsx(Input$1, _objectSpread$D(_objectSpread$D(_objectSpread$D({
     name: name,
     schema: desc
   }, fieldOpts), rest), {}, {
@@ -26029,7 +26065,7 @@ function FieldWithModal(props) {
       className: clsx(_defineProperty$1(_defineProperty$1(_defineProperty$1({}, classes$B.dataError, dataError), classes$B.inputWithEditButtonWrapper, true), classes$B.inputWrapper, true)),
       onMouseEnter: handlePopoverOpen,
       onMouseLeave: handlePopoverClose,
-      children: [jsx(Input$1, _objectSpread$C(_objectSpread$C({
+      children: [jsx(Input$1, _objectSpread$D(_objectSpread$D({
         name: name,
         schema: desc
       }, fieldOpts), rest)), jsx(IconButton, {
@@ -26094,7 +26130,7 @@ function CustomQueryField(props) {
       onMouseEnter: handlePopoverOpen,
       onMouseLeave: handlePopoverClose,
       className: clsx(_defineProperty$1(_defineProperty$1({}, classes$B.dataError, dataError), classes$B.inputWrapper, true)),
-      children: jsx(Input$1, _objectSpread$C(_objectSpread$C({
+      children: jsx(Input$1, _objectSpread$D(_objectSpread$D({
         type: "textarea",
         "data-testid": "atomCustomQuery",
         name: name,
@@ -26123,7 +26159,7 @@ var SelectOneOf = function SelectOneOf(props) {
     selectDesc["enum"].push(item);
     selectDesc.enumNames.push(schema[item].title || item);
   });
-  return jsx(Field, _objectSpread$C(_objectSpread$C({
+  return jsx(Field, _objectSpread$D(_objectSpread$D({
     name: name,
     options: getSelectOptionsFromSchema(selectDesc),
     title: title
@@ -26156,7 +26192,7 @@ function propSchema(schema, _ref2) {
         _schemaCopy$propertie["enum"];
         _schemaCopy$propertie.enumNames;
         var rest = _objectWithoutProperties(_schemaCopy$propertie, _excluded10);
-      schemaCopy.properties[formatName] = _objectSpread$C(_objectSpread$C({}, rest), {}, {
+      schemaCopy.properties[formatName] = _objectSpread$D(_objectSpread$D({}, rest), {}, {
         format: formatName
       });
     });
@@ -26315,11 +26351,11 @@ var ColorPicker = function ColorPicker(props) {
   });
 };
 
-var styles$c = {"measureInput":"measure-input-module_measureInput__uZQ-j","select":"measure-input-module_select__1ZFmv"};
+var styles$d = {"measureInput":"measure-input-module_measureInput__uZQ-j","select":"measure-input-module_select__1ZFmv"};
 
 var _excluded$l = ["schema", "value", "onChange", "name", "className"];
-function ownKeys$B(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$B(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$B(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$B(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$C(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$C(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$C(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$C(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var selectOptions$1 = getSelectOptionsFromSchema({
   "enum": ['cm', 'px', 'pt', 'inch']
 });
@@ -26363,8 +26399,8 @@ var MeasureInput = function MeasureInput(_ref) {
     calcValue();
   }, [value, measure, calcValue]);
   var desc = schema || schema.properties[name];
-  return jsxs("div", _objectSpread$B(_objectSpread$B({
-    className: clsx(styles$c.measureInput, className)
+  return jsxs("div", _objectSpread$C(_objectSpread$C({
+    className: clsx(styles$d.measureInput, className)
   }, rest), {}, {
     children: [jsx("span", {
       children: rest.title || desc.title
@@ -26381,7 +26417,7 @@ var MeasureInput = function MeasureInput(_ref) {
         onChange: handleMeasChange,
         options: selectOptions$1,
         value: measure,
-        className: styles$c.select
+        className: styles$d.select
       })]
     })]
   }));
@@ -26400,8 +26436,8 @@ function convertValue(value, measureFrom, measureTo) {
 var classes$z = {"button-common-styles":"buttons-module_button-common-styles__qWDOz","scrollbar":"buttons-module_scrollbar__SpaVV","openButton":"buttons-module_openButton__wErm9"};
 
 var _excluded$k = ["children", "type", "server", "className"];
-function ownKeys$A(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$A(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$A(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$A(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$B(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$B(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$B(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$B(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function _callSuper$6(t, o, e) { return o = _getPrototypeOf$2(o), _possibleConstructorReturn$2(t, _isNativeReflectConstruct$6() ? Reflect.construct(o, e || [], _getPrototypeOf$2(t).constructor) : o.apply(t, e)); }
 function _isNativeReflectConstruct$6() { try { var t = !Boolean.prototype.valueOf.call(Reflect.construct(Boolean, [], function () {})); } catch (t) {} return (_isNativeReflectConstruct$6 = function _isNativeReflectConstruct() { return !!t; })(); }
 var OpenButton = function (_Component) {
@@ -26446,7 +26482,7 @@ var OpenButton = function (_Component) {
         _this$props2.server;
         var className = _this$props2.className,
         props = _objectWithoutProperties(_this$props2, _excluded$k);
-      return jsxs("button", _objectSpread$A(_objectSpread$A({
+      return jsxs("button", _objectSpread$B(_objectSpread$B({
         onClick: function onClick() {
           return _this2.btn.click();
         },
@@ -26711,8 +26747,8 @@ var fieldGroups = {
 };
 
 var _excluded$j = ["initState", "formState", "server", "onOpenFile", "onReset", "appOpts"];
-function ownKeys$z(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$z(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$z(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$z(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$A(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$A(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$A(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$A(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var defaultSettings = getDefaultOptions();
 var HeaderContent$1 = function HeaderContent(_ref) {
   var server = _ref.server,
@@ -26965,7 +27001,7 @@ var SettingsDialog = function SettingsDialog(props) {
       formState: formState,
       initState: initState
     }),
-    children: jsx(Form$1, _objectSpread$z(_objectSpread$z({
+    children: jsx(Form$1, _objectSpread$A(_objectSpread$A({
       schema: optionsSchema,
       init: initState
     }, formState), {}, {
@@ -27038,8 +27074,8 @@ function ErrorsCheck(props) {
 var style = {"button-common-styles":"Check-module_button-common-styles__WPocW","scrollbar":"Check-module_scrollbar__3jzOc","dialog_body":"Check-module_dialog_body__wHZMM","buttons":"Check-module_buttons__cjuqO","buttonSecondary":"Check-module_buttonSecondary__2482r","buttonPrimary":"Check-module_buttonPrimary__1h5p1","buttonsRight":"Check-module_buttonsRight__L1v9A","wrapper":"Check-module_wrapper__27SOp","checkInfo":"Check-module_checkInfo__Iqq6t","settings":"Check-module_settings__knuQF","warnings":"Check-module_warnings__b4ozd","centeredContainer":"Check-module_centeredContainer__t61r8","warningsContainer":"Check-module_warningsContainer__vSbyK","checkBoxesDisabled":"Check-module_checkBoxesDisabled__EAdRo"};
 
 var _excluded$i = ["formState", "checkState", "onCheck", "onApply", "onCancel"];
-function ownKeys$y(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$y(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$y(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$y(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$z(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$z(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$z(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$z(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var checkSchema = {
   title: 'Check',
   type: 'object',
@@ -27133,7 +27169,7 @@ function CheckDialog(props) {
   return jsx(Dialog, {
     title: "Structure Check",
     className: style.dialog_body,
-    params: _objectSpread$y(_objectSpread$y({}, restProps), {}, {
+    params: _objectSpread$z(_objectSpread$z({}, restProps), {}, {
       onCancel: onCancel
     }),
     buttons: [],
@@ -27145,7 +27181,7 @@ function CheckDialog(props) {
       isCheckedWithNewSettings: isCheckedWithNewSettings
     }),
     withDivider: true,
-    children: jsx(Form$1, _objectSpread$y(_objectSpread$y({
+    children: jsx(Form$1, _objectSpread$z(_objectSpread$z({
       schema: checkSchema,
       init: checkState
     }, formState), {}, {
@@ -27205,7 +27241,7 @@ var mapDispatchToProps$c = function mapDispatchToProps(dispatch, ownProps) {
 };
 var Check = connect(mapStateToProps$e, mapDispatchToProps$c)(CheckDialog);
 
-var styles$b = {"button-common-styles":"FormulaInput-module_button-common-styles__xQ8ZA","scrollbar":"FormulaInput-module_scrollbar__8TUkb","chem_input":"FormulaInput-module_chem_input__oprB3"};
+var styles$c = {"button-common-styles":"FormulaInput-module_button-common-styles__xQ8ZA","scrollbar":"FormulaInput-module_scrollbar__8TUkb","chem_input":"FormulaInput-module_chem_input__oprB3"};
 
 var formulaRegexp = /\b(\d*)([A-Z][a-z]{0,3}#?)(\d*)\s*\b/g;
 var errorRegexp = /error:.*/g;
@@ -27219,7 +27255,7 @@ function formulaInputMarkdown(contentData) {
     }
   };
   return jsx("div", {
-    className: styles$b.chem_input,
+    className: styles$c.chem_input,
     onKeyPress: function onKeyPress(e) {
       return e.preventDefault();
     },
@@ -27420,8 +27456,8 @@ var DialogActionButton = function DialogActionButton(_ref) {
 
 var _excluded$g = ["file", "structStr", "fragment", "version", "imagoVersions", "onOk"],
   _excluded2$2 = ["onRecognize", "isFragment", "onImage", "onChangeImago"];
-function ownKeys$x(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$x(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$x(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$x(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$y(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$y(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$y(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$y(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 function isImage(file) {
   var _file$type;
   return file === null || file === void 0 || (_file$type = file.type) === null || _file$type === void 0 ? void 0 : _file$type.includes('image');
@@ -27503,7 +27539,7 @@ function RecognizeDialog(prop) {
   return jsxs(Dialog, {
     title: "Import Structure from Image",
     className: classes$v.recognize,
-    params: _objectSpread$x(_objectSpread$x({}, props), {}, {
+    params: _objectSpread$y(_objectSpread$y({}, props), {}, {
       onOk: onOk
     }),
     result: function result() {
@@ -27830,8 +27866,8 @@ var ElementNumber = function ElementNumber(props) {
   });
 };
 
-function ownKeys$w(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$w(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$w(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$w(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$x(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$x(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$x(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$x(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var atomProps$1 = atom.properties;
 var AtomElement = function AtomElement(_ref) {
   var formState = _ref.formState;
@@ -27843,7 +27879,7 @@ var AtomElement = function AtomElement(_ref) {
     label = _formState$result.label;
   var dispatch = useDispatch();
   var openNestedDialog = function openNestedDialog(modalName, props, onChange) {
-    openDialog(dispatch, modalName, _objectSpread$w(_objectSpread$w({}, props), {}, {
+    openDialog(dispatch, modalName, _objectSpread$x(_objectSpread$x({}, props), {}, {
       isNestedModal: true
     })).then(function (el) {
       var _el$values;
@@ -27904,8 +27940,8 @@ var AtomElement = function AtomElement(_ref) {
 };
 
 var _excluded$e = ["formState", "stereoParity", "isMultipleAtoms", "isRestoredModal"];
-function ownKeys$v(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$v(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$v(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$v(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$w(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$w(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$w(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$w(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var atomProps = atom.properties;
 var querySpecificFields = [{
   name: 'ringBondCount',
@@ -28031,7 +28067,7 @@ var Atom = function Atom(props) {
             "data-testid": field.name
           }, field.name);
         } else {
-          return jsx(Field, _objectSpread$v({}, field), field.name);
+          return jsx(Field, _objectSpread$w({}, field), field.name);
         }
       })
     })
@@ -28065,7 +28101,7 @@ var Atom = function Atom(props) {
     },
     buttons: ['Cancel', 'OK'],
     withDivider: true,
-    children: jsx(Form$1, _objectSpread$v(_objectSpread$v({
+    children: jsx(Form$1, _objectSpread$w(_objectSpread$w({
       schema: atom,
       customValid: customValid,
       init: isRestoredModal ? null : rest
@@ -28126,8 +28162,8 @@ var AtomContainer = connect(mapStateToProps$a)(Atom);
 var classes$s = {"attachPoints":"Attach-module_attachPoints__5QEAv"};
 
 var _excluded$d = ["formState"];
-function ownKeys$u(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$u(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$u(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$u(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$v(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$v(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$v(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$v(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var AttachPoints = function AttachPoints(props) {
   var formState = props.formState,
     rest = _objectWithoutProperties(props, _excluded$d);
@@ -28146,7 +28182,7 @@ var AttachPoints = function AttachPoints(props) {
     },
     buttons: ['Cancel', 'OK'],
     withDivider: true,
-    children: jsxs(Form$1, _objectSpread$u(_objectSpread$u({
+    children: jsxs(Form$1, _objectSpread$v(_objectSpread$v({
       schema: attachmentPoints,
       init: rest
     }, formState), {}, {
@@ -28169,8 +28205,8 @@ var AttachPointsContainer = connect(mapStateToProps$9)(AttachPoints);
 var classes$r = {"automap":"Automap-module_automap__531ko"};
 
 var _excluded$c = ["formState"];
-function ownKeys$t(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$t(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$t(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$t(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$u(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$u(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$u(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$u(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var automapSchema = {
   title: 'Reaction Auto-Mapping',
   type: 'object',
@@ -28202,10 +28238,10 @@ var Automap = function Automap(props) {
     buttonsNameMap: {
       OK: 'Apply'
     },
-    children: jsx(Form$1, _objectSpread$t(_objectSpread$t({
+    children: jsx(Form$1, _objectSpread$u(_objectSpread$u({
       schema: automapSchema
     }, formState), {}, {
-      children: jsx(Field, _objectSpread$t(_objectSpread$t({
+      children: jsx(Field, _objectSpread$u(_objectSpread$u({
         name: "mode",
         options: getSelectOptionsFromSchema(automapSchema.properties.mode)
       }, props), {}, {
@@ -28234,8 +28270,8 @@ var AutomapContainer = connect(mapStateToProps$8, mapDispatchToProps$8)(Automap)
 var classes$q = {"bond":"Bond-module_bond__EDfLY","customQueryWrapper":"Bond-module_customQueryWrapper__mKGLY"};
 
 var _excluded$b = ["formState"];
-function ownKeys$s(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$s(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$s(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$s(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$t(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$t(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$t(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$t(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var Bond = function Bond(props) {
   var formState = props.formState,
     rest = _objectWithoutProperties(props, _excluded$b);
@@ -28293,7 +28329,7 @@ var Bond = function Bond(props) {
     },
     buttons: ['Cancel', 'OK'],
     withDivider: true,
-    children: jsxs(Form$1, _objectSpread$s(_objectSpread$s({
+    children: jsxs(Form$1, _objectSpread$t(_objectSpread$t({
       schema: bond,
       init: rest
     }, formState), {}, {
@@ -28379,8 +28415,8 @@ var BondContainer = connect(mapStateToProps$7)(Bond);
 
 var classes$p = {"field":"IfThenSelect-module_field__9YaPA"};
 
-function ownKeys$r(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$r(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$r(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$r(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$s(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$s(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$s(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$s(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var IfThenSelect = function IfThenSelect(props) {
   var rgroupLabels = props.rgroupLabels,
     label = props.label,
@@ -28398,7 +28434,7 @@ var IfThenSelect = function IfThenSelect(props) {
       desc.enumNames.push("IF R".concat(label, " THEN R").concat(rgroupLabel));
     }
   });
-  return jsx(Field, _objectSpread$r(_objectSpread$r({
+  return jsx(Field, _objectSpread$s(_objectSpread$s({
     schema: desc,
     className: classes$p.field
   }, props), {}, {
@@ -28410,8 +28446,8 @@ var IfThenSelect = function IfThenSelect(props) {
 var classes$o = {"button-common-styles":"RgroupLogic-module_button-common-styles__P-ABP","scrollbar":"RgroupLogic-module_scrollbar__gDniy","rgroupLogic":"RgroupLogic-module_rgroupLogic__q4RTy","resth":"RgroupLogic-module_resth__RL2qE"};
 
 var _excluded$a = ["formState", "label", "rgroupLabels"];
-function ownKeys$q(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$q(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$q(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$q(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$r(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$r(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$r(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$r(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var RgroupLogic = function RgroupLogic(props) {
   var formState = props.formState,
     label = props.label,
@@ -28432,7 +28468,7 @@ var RgroupLogic = function RgroupLogic(props) {
     },
     buttons: ['Cancel', 'OK'],
     withDivider: true,
-    children: jsxs(Form$1, _objectSpread$q(_objectSpread$q({
+    children: jsxs(Form$1, _objectSpread$r(_objectSpread$r({
       schema: rgroupLogic,
       customValid: {
         range: function range(r) {
@@ -28471,15 +28507,15 @@ var RgroupLogicContainer = connect(mapStateToProps$6)(RgroupLogic);
 
 var classes$n = {"button-common-styles":"Open-module_button-common-styles__NBSQP","scrollbar":"Open-module_scrollbar__sRvYM","open":"Open-module_open__m8V9g","textareaEditor":"Open-module_textareaEditor__ZbEVj","footerContent":"Open-module_footerContent__Q0hTw","buttonsContainer":"Open-module_buttonsContainer__L1HqU","openButton":"Open-module_openButton__cj3oU","cancelButton":"Open-module_cancelButton__0TQzA","copyButton":"Open-module_copyButton__KlXKd"};
 
-var styles$a = {"analyzingFileWrapper":"AnalyzingFile-module_analyzingFileWrapper__j0Ltf","fileBox":"AnalyzingFile-module_fileBox__ywFIh"};
+var styles$b = {"analyzingFileWrapper":"AnalyzingFile-module_analyzingFileWrapper__j0Ltf","fileBox":"AnalyzingFile-module_fileBox__ywFIh"};
 
 var ICON_NAME = 'file-thumbnail';
 var AnalyzingFile = function AnalyzingFile(_ref) {
   var fileName = _ref.fileName;
   return jsxs("div", {
-    className: styles$a.analyzingFileWrapper,
+    className: styles$b.analyzingFileWrapper,
     children: [fileName && jsxs("div", {
-      className: styles$a.fileBox,
+      className: styles$b.fileBox,
       children: [jsx(Icon, {
         name: ICON_NAME
       }), jsx("p", {
@@ -28489,13 +28525,13 @@ var AnalyzingFile = function AnalyzingFile(_ref) {
   });
 };
 
-var styles$9 = {"optionsContainer":"OpenOptions-module_optionsContainer__-WqT8","dropContainer":"OpenOptions-module_dropContainer__PL6Tg","buttonLabelWrapper":"OpenOptions-module_buttonLabelWrapper__h2YsI","buttonLabel":"OpenOptions-module_buttonLabel__LiY--","textLabelWrapper":"OpenOptions-module_textLabelWrapper__Vx8NF","textLabel":"OpenOptions-module_textLabel__TlOfz","dropIconWrapper":"OpenOptions-module_dropIconWrapper__ibBQx"};
+var styles$a = {"optionsContainer":"OpenOptions-module_optionsContainer__-WqT8","dropContainer":"OpenOptions-module_dropContainer__PL6Tg","buttonLabelWrapper":"OpenOptions-module_buttonLabelWrapper__h2YsI","buttonLabel":"OpenOptions-module_buttonLabel__LiY--","textLabelWrapper":"OpenOptions-module_textLabelWrapper__Vx8NF","textLabel":"OpenOptions-module_textLabel__TlOfz","dropIconWrapper":"OpenOptions-module_dropIconWrapper__ibBQx"};
 
-var styles$8 = {"isHovered":"FileDrop-module_isHovered__c-CDn","isDisabled":"FileDrop-module_isDisabled__Ejuyq"};
+var styles$9 = {"isHovered":"FileDrop-module_isHovered__c-CDn","isDisabled":"FileDrop-module_isDisabled__Ejuyq"};
 
 var _excluded$9 = ["buttonLabel", "textLabel", "iconName", "disabled", "disabledText"];
-function ownKeys$p(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
-function _objectSpread$p(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$p(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$p(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+function ownKeys$q(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$q(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$q(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$q(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var FileDrop = function FileDrop(_ref) {
   var buttonLabel = _ref.buttonLabel,
     textLabel = _ref.textLabel,
@@ -28503,7 +28539,7 @@ var FileDrop = function FileDrop(_ref) {
     disabled = _ref.disabled,
     disabledText = _ref.disabledText,
     rest = _objectWithoutProperties(_ref, _excluded$9);
-  var _useDropzone = useDropzone(_objectSpread$p({
+  var _useDropzone = useDropzone(_objectSpread$q({
       multiple: false,
       disabled: disabled
     }, rest)),
@@ -28512,33 +28548,33 @@ var FileDrop = function FileDrop(_ref) {
     isDragActive = _useDropzone.isDragActive,
     open = _useDropzone.open;
   var getClassesString = useMemo(function () {
-    var classes = [styles$9.dropContainer, isDragActive ? styles$8.isHovered : null, disabled ? styles$8.isDisabled : null];
+    var classes = [styles$a.dropContainer, isDragActive ? styles$9.isHovered : null, disabled ? styles$9.isDisabled : null];
     return classes.join(' ');
   }, [isDragActive]);
-  return jsxs("div", _objectSpread$p(_objectSpread$p({
+  return jsxs("div", _objectSpread$q(_objectSpread$q({
     onKeyDown: open
   }, getRootProps({
     className: getClassesString
   })), {}, {
-    children: [jsx("input", _objectSpread$p({}, getInputProps())), jsx("div", {
-      className: styles$9.dropIconWrapper,
+    children: [jsx("input", _objectSpread$q({}, getInputProps())), jsx("div", {
+      className: styles$a.dropIconWrapper,
       children: jsx(Icon, {
         name: iconName
       })
     }), disabled ? jsx("p", {
-      className: styles$9.textLabel,
+      className: styles$a.textLabel,
       children: disabledText
     }) : jsxs(Fragment, {
       children: [jsx("div", {
-        className: styles$9.textLabelWrapper,
+        className: styles$a.textLabelWrapper,
         children: jsx("p", {
-          className: styles$9.textLabel,
+          className: styles$a.textLabel,
           children: textLabel
         })
       }), jsx("div", {
-        className: styles$9.buttonLabelWrapper,
+        className: styles$a.buttonLabelWrapper,
         children: jsx("p", {
-          className: styles$9.buttonLabel,
+          className: styles$a.buttonLabel,
           children: buttonLabel
         })
       })]
@@ -28558,21 +28594,21 @@ var OpenOptions = function OpenOptions(_ref) {
     isRecognizeDisabled = _ref.isRecognizeDisabled,
     errorHandler = _ref.errorHandler;
   return jsxs("div", {
-    className: styles$9.optionsContainer,
+    className: styles$a.optionsContainer,
     children: [jsxs("div", {
       onClick: selectClipboard,
-      className: styles$9.dropContainer,
+      className: styles$a.dropContainer,
       children: [jsx("div", {
-        className: styles$9.dropIconWrapper,
+        className: styles$a.dropIconWrapper,
         children: jsx(Icon, {
           name: ICON_NAMES.PASTE
         })
       }), jsx("div", {
-        className: styles$9.textLabelWrapper
+        className: styles$a.textLabelWrapper
       }), jsx("div", {
-        className: styles$9.buttonLabelWrapper,
+        className: styles$a.buttonLabelWrapper,
         children: jsx("p", {
-          className: styles$9.buttonLabel,
+          className: styles$a.buttonLabel,
           children: "Paste from clipboard"
         })
       })]
@@ -28616,6 +28652,144 @@ var TextEditor = function TextEditor(_ref) {
   });
 };
 
+var serverSelector = function serverSelector(state) {
+  return state.options.app.server ? state.server : null;
+};
+
+var styles$8 = {"wrapper":"CDXStructuresViewer-module_wrapper__7nZbQ","structuresWrapper":"CDXStructuresViewer-module_structuresWrapper__kZN0N","menuListWrapper":"CDXStructuresViewer-module_menuListWrapper__za1za","header":"CDXStructuresViewer-module_header__107Fj","fileName":"CDXStructuresViewer-module_fileName__BkvUb","menuItem":"CDXStructuresViewer-module_menuItem__21Wb1","centerWrapper":"CDXStructuresViewer-module_centerWrapper__T26wg","imageWrapper":"CDXStructuresViewer-module_imageWrapper__m54Wi","image":"CDXStructuresViewer-module_image__7Q-Ah"};
+
+var editorOptionsSelector = function editorOptionsSelector(state) {
+  var _state$editor;
+  return (_state$editor = state.editor) === null || _state$editor === void 0 || (_state$editor = _state$editor.render) === null || _state$editor === void 0 ? void 0 : _state$editor.options;
+};
+
+function ownKeys$p(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
+function _objectSpread$p(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$p(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$p(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
+var CDXStructuresViewer = function CDXStructuresViewer(_ref) {
+  var _ref$structList = _ref.structList,
+    structList = _ref$structList === void 0 ? [] : _ref$structList,
+    inputHandler = _ref.inputHandler,
+    fileName = _ref.fileName;
+  var server = useSelector(serverSelector);
+  var editorOptions = useSelector(editorOptionsSelector);
+  var _useState = useState(0),
+    _useState2 = _slicedToArray$1(_useState, 2),
+    selectedIndex = _useState2[0],
+    setSelectedIndex = _useState2[1];
+  var _useState3 = useState({}),
+    _useState4 = _slicedToArray$1(_useState3, 2),
+    itemsMap = _useState4[0],
+    setItemsMap = _useState4[1];
+  var _useState5 = useState(false),
+    _useState6 = _slicedToArray$1(_useState5, 2),
+    loading = _useState6[0],
+    setLoading = _useState6[1];
+  useEffect(function () {
+    if (!itemsMap[selectedIndex] || itemsMap[selectedIndex].error) {
+      inputHandler('');
+    } else {
+      inputHandler(itemsMap[selectedIndex].base64struct);
+    }
+  }, [inputHandler, itemsMap, selectedIndex]);
+  var getImages = useCallback(function () {
+    var itemsList = {};
+    setLoading(true);
+    var promises = structList.map(function (str) {
+      return parseStruct(str, server).then(function (struct) {
+        return {
+          base64struct: str,
+          struct: struct
+        };
+      })["catch"](function (error) {
+        return {
+          base64struct: str,
+          error: error.message || error
+        };
+      });
+    });
+    Promise.allSettled(promises).then(function (values) {
+      values.forEach(function (el, index) {
+        if (el.status === 'fulfilled') {
+          itemsList[index] = el.value;
+        }
+      });
+      setItemsMap(itemsList);
+      setLoading(false);
+      setSelectedIndex(0);
+    });
+  }, [server, structList]);
+  useEffect(function () {
+    getImages();
+  }, [getImages]);
+  var renderStructure = function renderStructure(structure) {
+    if (structure !== null && structure !== void 0 && structure.error) {
+      var _itemsMap$selectedInd;
+      return jsxs("div", {
+        children: ["Error: ", (_itemsMap$selectedInd = itemsMap[selectedIndex]) === null || _itemsMap$selectedInd === void 0 ? void 0 : _itemsMap$selectedInd.error]
+      });
+    }
+    if (structure !== null && structure !== void 0 && structure.struct) {
+      return jsx(StructRender, {
+        className: styles$8.image,
+        struct: structure.struct,
+        options: _objectSpread$p(_objectSpread$p({}, editorOptions), {}, {
+          autoScale: true,
+          needCache: false
+        })
+      });
+    }
+    return null;
+  };
+  var renderStructures = function renderStructures() {
+    if (!(structList !== null && structList !== void 0 && structList.length)) {
+      return jsx("div", {
+        className: styles$8.centerWrapper,
+        children: jsx("div", {
+          children: "No embedded structures found in the file"
+        })
+      });
+    }
+    var menuList = Object.values(itemsMap) || [];
+    return jsxs("div", {
+      className: styles$8.structuresWrapper,
+      children: [jsxs("div", {
+        className: styles$8.menuListWrapper,
+        children: [jsx("div", {
+          className: styles$8.header,
+          children: "Select structure"
+        }), jsx(MenuList, {
+          children: menuList.map(function (value, index) {
+            return jsxs(MenuItem, {
+              selected: index === selectedIndex,
+              onClick: function onClick() {
+                return setSelectedIndex(index);
+              },
+              children: ["Structure ".concat(index + 1), value.error && jsx(Icon, {
+                name: "error"
+              })]
+            }, value.base64struct + index);
+          })
+        })]
+      }), jsx("div", {
+        className: styles$8.imageWrapper,
+        children: renderStructure(itemsMap[selectedIndex])
+      })]
+    });
+  };
+  return jsxs("div", {
+    className: styles$8.wrapper,
+    children: [jsxs("div", {
+      children: ["File: ", jsx("span", {
+        className: styles$8.fileName,
+        children: fileName
+      })]
+    }), loading ? jsx("div", {
+      className: styles$8.centerWrapper,
+      children: jsx(LoadingCircles, {})
+    }) : renderStructures()]
+  });
+};
+
 function ownKeys$o(e, r) { var t = Object.keys(e); if (Object.getOwnPropertySymbols) { var o = Object.getOwnPropertySymbols(e); r && (o = o.filter(function (r) { return Object.getOwnPropertyDescriptor(e, r).enumerable; })), t.push.apply(t, o); } return t; }
 function _objectSpread$o(e) { for (var r = 1; r < arguments.length; r++) { var t = null != arguments[r] ? arguments[r] : {}; r % 2 ? ownKeys$o(Object(t), !0).forEach(function (r) { _defineProperty$1(e, r, t[r]); }) : Object.getOwnPropertyDescriptors ? Object.defineProperties(e, Object.getOwnPropertyDescriptors(t)) : ownKeys$o(Object(t)).forEach(function (r) { Object.defineProperty(e, r, Object.getOwnPropertyDescriptor(t, r)); }); } return e; }
 var ViewSwitcher = function ViewSwitcher(props) {
@@ -28629,6 +28803,8 @@ var ViewSwitcher = function ViewSwitcher(props) {
         return jsx(OpenOptions, _objectSpread$o({}, props));
       case props.states.textEditor:
         return jsx(TextEditor, _objectSpread$o({}, props));
+      case props.states.presentationViewer:
+        return jsx(CDXStructuresViewer, _objectSpread$o({}, props));
       default:
         return null;
     }
@@ -28641,7 +28817,8 @@ function _objectSpread$n(e) { for (var r = 1; r < arguments.length; r++) { var t
 var MODAL_STATES = {
   idle: 'idle',
   textEditor: 'textEditor',
-  imageRec: 'imageRec'
+  imageRec: 'imageRec',
+  presentationViewer: 'presentationViewer'
 };
 var FooterContent$1 = function FooterContent(_ref) {
   var structStr = _ref.structStr,
@@ -28683,18 +28860,22 @@ var Open = function Open(props) {
     _useState2 = _slicedToArray$1(_useState, 2),
     structStr = _useState2[0],
     setStructStr = _useState2[1];
-  var _useState3 = useState(''),
+  var _useState3 = useState([]),
     _useState4 = _slicedToArray$1(_useState3, 2),
-    fileName = _useState4[0],
-    setFileName = _useState4[1];
-  var _useState5 = useState(),
+    structList = _useState4[0],
+    setStructList = _useState4[1];
+  var _useState5 = useState(''),
     _useState6 = _slicedToArray$1(_useState5, 2),
-    opener = _useState6[0],
-    setOpener = _useState6[1];
-  var _useState7 = useState(MODAL_STATES.idle),
+    fileName = _useState6[0],
+    setFileName = _useState6[1];
+  var _useState7 = useState(),
     _useState8 = _slicedToArray$1(_useState7, 2),
-    currentState = _useState8[0],
-    setCurrentState = _useState8[1];
+    opener = _useState8[0],
+    setOpener = _useState8[1];
+  var _useState9 = useState(MODAL_STATES.idle),
+    _useState10 = _slicedToArray$1(_useState9, 2),
+    currentState = _useState10[0],
+    setCurrentState = _useState10[1];
   useEffect(function () {
     if (server) {
       fileOpener(server).then(function (chosenOpener) {
@@ -28706,8 +28887,14 @@ var Open = function Open(props) {
   }, [server]);
   var onFileLoad = function onFileLoad(files) {
     var onLoad = function onLoad(fileContent) {
-      setStructStr(fileContent);
-      setCurrentState(MODAL_STATES.textEditor);
+      if (fileContent.isPPTX) {
+        setStructStr('');
+        setStructList(fileContent.structures);
+        setCurrentState(MODAL_STATES.presentationViewer);
+      } else {
+        setStructStr(fileContent);
+        setCurrentState(MODAL_STATES.textEditor);
+      }
     };
     var onError = function onError() {
       return errorHandler('Error processing file');
@@ -28734,7 +28921,7 @@ var Open = function Open(props) {
       fragment: false
     });
   };
-  var withFooterContent = currentState === MODAL_STATES.textEditor && !isAnalyzingFile;
+  var withFooterContent = (currentState === MODAL_STATES.textEditor || currentState === MODAL_STATES.presentationViewer) && !isAnalyzingFile;
   if (currentState === MODAL_STATES.imageRec) {
     return jsx(Recognize, _objectSpread$n({}, rest));
   }
@@ -28768,7 +28955,8 @@ var Open = function Open(props) {
       isRecognizeDisabled: isRecognizeDisabled,
       structStr: structStr,
       inputHandler: setStructStr,
-      autoFocus: true
+      autoFocus: true,
+      structList: structList
     })
   });
 };
@@ -32467,8 +32655,8 @@ var KetcherBuilder = function () {
                 initApp(element, appRoot, staticResourcesUrl, {
                   buttons: buttons || {},
                   errorHandler: errorHandler || null,
-                  version: "2.18.0-rc.2" ,
-                  buildDate: "2024-01-17T14:23:52" ,
+                  version: "2.18.0-rc.3" ,
+                  buildDate: "2024-01-31T10:46:48" ,
                   buildNumber: ''
                 }, structService, resolve, togglerComponent);
               });