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b3dbantivirals.html
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<html>
<meta charset="utf-8">
<head>
<style>
#mols2grid.gridcontainer {
display: block;
padding-left: 1em;
max-width: 1096px;
width: 1096px;
}
#mols2grid .cell {
border: 1px solid #cccccc;
text-align: center;
vertical-align: top;
max-width: 270px;
width: 270px;
font-family: 'DejaVu', sans-serif;
font-size: 16pt;
padding: 0;
margin: 0px;
float: left;
}
#mols2grid .cell:hover {
background-color: #e3c7cb !important;
}
#mols2grid .cell .data-img {
padding: 0;
margin: 0;
}
#mols2grid .cell img, #mols2grid .cell svg {
max-width: 100%;
height: auto;
padding: 0;
}
#mols2grid .data {
overflow: hidden;
white-space: nowrap;
text-overflow: ellipsis;
display: block;
}
#mols2grid .arrow-asc:after {
content: '↑';
text-align: right;
float:right;
}
#mols2grid .arrow-desc:after {
content: '↓';
text-align: right;
float:right;
}
/* custom CSS */
</style>
<script src="https://cdnjs.cloudflare.com/ajax/libs/list.js/2.3.1/list.min.js"></script>
<link rel="stylesheet" href="https://cdn.jsdelivr.net/npm/[email protected]/dist/css/bootstrap.min.css" integrity="sha384-B0vP5xmATw1+K9KRQjQERJvTumQW0nPEzvF6L/Z6nronJ3oUOFUFpCjEUQouq2+l" crossorigin="anonymous">
<script src="https://code.jquery.com/jquery-3.6.0.min.js" integrity="sha256-/xUj+3OJU5yExlq6GSYGSHk7tPXikynS7ogEvDej/m4=" crossorigin="anonymous"></script>
<script src="https://cdn.jsdelivr.net/npm/[email protected]/dist/js/bootstrap.bundle.min.js" integrity="sha384-Piv4xVNRyMGpqkS2by6br4gNJ7DXjqk09RmUpJ8jgGtD7zP9yug3goQfGII0yAns" crossorigin="anonymous"></script>
<script src="https://unpkg.com/@rdkit/[email protected]/Code/MinimalLib/dist/RDKit_minimal.js"></script>
<!-- custom header -->
</head>
<body>
<div id="mols2grid" class="gridcontainer grid-default">
<div class="row mb-3">
<div class="list"><div class="cell" data-mols2grid-id="0"><input type="checkbox" class="position-relative float-left cached_checkbox"><div class="data data-Name"></div><a tabindex="0" class="data data-img mols2grid-tooltip" data-toggle="popover" data-content="."></a><div class="data data-IUPAC" style="display: none;"></div><div class="data data-SMILES" style="display: none;"></div></div></div>
</div>
<div class="d-inline">
<ul class="pagination float-left"></ul>
<div id="controls" class="d-flex flex-row float-right">
<div id="chkbox-dropdown" class="dropdown">
<button class="btn btn-light dropdown-toggle" type="button" id="chkboxDropdown" data-toggle="dropdown" aria-haspopup="true" aria-expanded="false">☑</button>
<div class="dropdown-menu" aria-labelledby="checkboxDropdownMenu">
<button id="btn-chkbox-all" class="dropdown-item" type="button">Check all</button>
<button id="btn-chkbox-match" class="dropdown-item" type="button">Check matching</button>
<button id="btn-chkbox-none" class="dropdown-item" type="button">Uncheck all</button>
<button id="btn-chkbox-invert" class="dropdown-item" type="button">Invert</button>
<div class="dropdown-divider"></div>
<button id="btn-chkbox-copy" class="dropdown-item" type="button">Copy to clipboard</button>
<button id="btn-chkbox-dlsmi" class="dropdown-item" type="button">Save SMILES</button>
<button id="btn-chkbox-dlcsv" class="dropdown-item" type="button">Save CSV</button>
</div>
</div>
<div id="sort-dropdown" class="dropdown pl-2">
<button class="btn btn-light dropdown-toggle" type="button" id="sortDropdown" data-toggle="dropdown" aria-haspopup="true" aria-expanded="false">
Sort by
</button>
<div class="dropdown-menu" aria-labelledby="sortDropdownMenu">
<button class="dropdown-item sort-btn " type="button" data-name="mols2grid-id">Index</button>
<button class="dropdown-item sort-btn arrow-asc active" type="button" data-name="data-Name">Name</button>
<button class="dropdown-item sort-btn " type="button" data-name="data-IUPAC">IUPAC</button>
<button class="dropdown-item sort-btn " type="button" data-name="data-SMILES">SMILES</button>
<button class="dropdown-item sort-btn" type="button" data-name="checkbox">Selected</button>
</div>
</div>
<div class="input-group row pl-4">
<input type="text" id="searchbar" class="form-control" placeholder="Search" aria-label="Search" aria-describedby="basic-addon1">
<div class="input-group-append">
<button id="searchBtn" class="btn btn-light dropdown-toggle" type="button" data-toggle="dropdown" aria-haspopup="true" aria-expanded="false">🔎</button>
<div class="dropdown-menu dropdown-menu-right">
<button id="txtSearch" class="search-btn dropdown-item active">Text</button>
<button id="smartsSearch" class="search-btn dropdown-item">SMARTS</button>
</div>
</div>
</div>
</div>
</div>
</div>
<script>
// list.js
var listObj = new List('mols2grid', {
valueNames: [{data: ['mols2grid-id']}, 'data-img', 'data-SMILES', 'data-Name', 'data-IUPAC', {attr: 'data-content', name: 'mols2grid-tooltip'}],
item: '<div class="cell" data-mols2grid-id="0"><input type="checkbox" class="position-relative float-left cached_checkbox"><div class="data data-Name"></div><a tabindex="0" class="data data-img mols2grid-tooltip" data-toggle="popover" data-content="."></a><div class="data data-IUPAC" style="display: none;"></div><div class="data data-SMILES" style="display: none;"></div></div>',
page: 12,
pagination: {
name: "pagination",
item: '<li class="page-item"><a class="page page-link" href="#" onclick="event.preventDefault()"></a></li>',
innerWindow: 1,
outerWindow: 1,
},
});
listObj.remove("mols2grid-id", "0");
listObj.add([{"data-img": null, "mols2grid-id": 2, "data-Name": "127779-20-8", "data-IUPAC": "n-[4-[3-(tert-butylcarbamoyl)-3,4,4a,5,6,7,8,8a-octahydro-1h-isoquinolin-2-yl]-3-hydroxy-1-phenylbutan-2-yl]-2-(quinoline-2-carbonylamino)butanediamide", "data-SMILES": "CC(C)(C)NC(=O)C1CC2CCCCC2CN1CC(O)C(Cc1ccccc1)NC(=O)C(CC(N)=O)NC(=O)c1ccc2ccccc2n1", "mols2grid-tooltip": "<strong>IUPAC</strong>: n-[4-[3-(tert-butylcarbamoyl)-3,4,4a,5,6,7,8,8a-octahydro-1h-isoquinolin-2-yl]-3-hydroxy-1-phenylbutan-2-yl]-2-(quinoline-2-carbonylamino)butanediamide<br><strong>SMILES</strong>: CC(C)(C)NC(=O)C1CC2CCCCC2CN1CC(O)C(Cc1ccccc1)NC(=O)C(CC(N)=O)NC(=O)c1ccc2ccccc2n1"}, {"data-img": null, "mols2grid-id": 11, "data-Name": "129618-40-2", "data-IUPAC": "2-cyclopropyl-7-methyl-2,4,9,15-tetrazatricyclo[9.4.0.03,8]pentadeca-1(11),3,5,7,12,14-hexaen-10-one", "data-SMILES": "Cc1ccnc2c1NC(=O)c1cccnc1N2C1CC1", "mols2grid-tooltip": "<strong>IUPAC</strong>: 2-cyclopropyl-7-methyl-2,4,9,15-tetrazatricyclo[9.4.0.03,8]pentadeca-1(11),3,5,7,12,14-hexaen-10-one<br><strong>SMILES</strong>: Cc1ccnc2c1NC(=O)c1cccnc1N2C1CC1"}, {"data-img": null, "mols2grid-id": 18, "data-Name": "174484-81-2", "data-IUPAC": "n-[3-[1-[4-hydroxy-6-oxo-2-(2-phenylethyl)-2-propyl-3h-pyran-5-yl]propyl]phenyl]-5-(trifluoromethyl)pyridine-2-sulfonamide", "data-SMILES": "CCCC1(CCc2ccccc2)CC(O)=C(C(CC)c2cccc(NS(=O)(=O)c3ccc(C(F)(F)F)cn3)c2)C(=O)O1", "mols2grid-tooltip": "<strong>IUPAC</strong>: n-[3-[1-[4-hydroxy-6-oxo-2-(2-phenylethyl)-2-propyl-3h-pyran-5-yl]propyl]phenyl]-5-(trifluoromethyl)pyridine-2-sulfonamide<br><strong>SMILES</strong>: CCCC1(CCc2ccccc2)CC(O)=C(C(CC)c2cccc(NS(=O)(=O)c3ccc(C(F)(F)F)cn3)c2)C(=O)O1"}, {"data-img": null, "mols2grid-id": 26, "data-Name": "394730-60-0", "data-IUPAC": "n-(4-amino-1-cyclobutyl-3,4-dioxobutan-2-yl)-3-[2-(tert-butylcarbamoylamino)-3,3-dimethylbutanoyl]-6,6-dimethyl-3-azabicyclo[3.1.0]hexane-2-carboxamide", "data-SMILES": "CC(C)(C)NC(=O)NC(C(=O)N1CC2C(C1C(=O)NC(CC1CCC1)C(=O)C(N)=O)C2(C)C)C(C)(C)C", "mols2grid-tooltip": "<strong>IUPAC</strong>: n-(4-amino-1-cyclobutyl-3,4-dioxobutan-2-yl)-3-[2-(tert-butylcarbamoylamino)-3,3-dimethylbutanoyl]-6,6-dimethyl-3-azabicyclo[3.1.0]hexane-2-carboxamide<br><strong>SMILES</strong>: CC(C)(C)NC(=O)NC(C(=O)N1CC2C(C1C(=O)NC(CC1CCC1)C(=O)C(N)=O)C2(C)C)C(C)(C)C"}, {"data-img": null, "mols2grid-id": 4, "data-Name": "aciclovir", "data-IUPAC": "2-amino-9-(2-hydroxyethoxymethyl)-3h-purin-6-one", "data-SMILES": "Nc1nc(=O)c2ncn(COCCO)c2[nH]1", "mols2grid-tooltip": "<strong>IUPAC</strong>: 2-amino-9-(2-hydroxyethoxymethyl)-3h-purin-6-one<br><strong>SMILES</strong>: Nc1nc(=O)c2ncn(COCCO)c2[nH]1"}, {"data-img": null, "mols2grid-id": 16, "data-Name": "adefovir dipivoxil", "data-IUPAC": "[2-(6-aminopurin-9-yl)ethoxymethyl-(2,2-dimethylpropanoyloxymethoxy)phosphoryl]oxymethyl 2,2-dimethylpropanoate", "data-SMILES": "CC(C)(C)C(=O)OCOP(=O)(COCCn1cnc2c(N)ncnc21)OCOC(=O)C(C)(C)C", "mols2grid-tooltip": "<strong>IUPAC</strong>: [2-(6-aminopurin-9-yl)ethoxymethyl-(2,2-dimethylpropanoyloxymethoxy)phosphoryl]oxymethyl 2,2-dimethylpropanoate<br><strong>SMILES</strong>: CC(C)(C)C(=O)OCOP(=O)(COCCn1cnc2c(N)ncnc21)OCOC(=O)C(C)(C)C"}, {"data-img": null, "mols2grid-id": 20, "data-Name": "arbidol", "data-IUPAC": "ethyl 6-bromo-4-[(dimethylamino)methyl]-5-hydroxy-1-methyl-2-(phenylsulfanylmethyl)indole-3-carboxylate", "data-SMILES": "CCOC(=O)c1c(CSc2ccccc2)n(C)c2cc(Br)c(O)c(CN(C)C)c12", "mols2grid-tooltip": "<strong>IUPAC</strong>: ethyl 6-bromo-4-[(dimethylamino)methyl]-5-hydroxy-1-methyl-2-(phenylsulfanylmethyl)indole-3-carboxylate<br><strong>SMILES</strong>: CCOC(=O)c1c(CSc2ccccc2)n(C)c2cc(Br)c(O)c(CN(C)C)c12"}, {"data-img": null, "mols2grid-id": 30, "data-Name": "atazanavir", "data-IUPAC": "methyl n-[1-[2-[2-hydroxy-3-[[2-(methoxycarbonylamino)-3,3-dimethylbutanoyl]amino]-4-phenylbutyl]-2-[(4-pyridin-2-ylphenyl)methyl]hydrazinyl]-3,3-dimethyl-1-oxobutan-2-yl]carbamate", "data-SMILES": "COC(=O)NC(C(=O)NC(Cc1ccccc1)C(O)CN(Cc1ccc(-c2ccccn2)cc1)NC(=O)C(NC(=O)OC)C(C)(C)C)C(C)(C)C", "mols2grid-tooltip": "<strong>IUPAC</strong>: methyl n-[1-[2-[2-hydroxy-3-[[2-(methoxycarbonylamino)-3,3-dimethylbutanoyl]amino]-4-phenylbutyl]-2-[(4-pyridin-2-ylphenyl)methyl]hydrazinyl]-3,3-dimethyl-1-oxobutan-2-yl]carbamate<br><strong>SMILES</strong>: COC(=O)NC(C(=O)NC(Cc1ccccc1)C(O)CN(Cc1ccc(-c2ccccn2)cc1)NC(=O)C(NC(=O)OC)C(C)(C)C)C(C)(C)C"}, {"data-img": null, "mols2grid-id": 23, "data-Name": "brivudine", "data-IUPAC": "5-(2-bromoethenyl)-1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione", "data-SMILES": "O=c1[nH]c(=O)n(C2CC(O)C(CO)O2)cc1C=CBr", "mols2grid-tooltip": "<strong>IUPAC</strong>: 5-(2-bromoethenyl)-1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione<br><strong>SMILES</strong>: O=c1[nH]c(=O)n(C2CC(O)C(CO)O2)cc1C=CBr"}, {"data-img": null, "mols2grid-id": 9, "data-Name": "chembl195725", "data-IUPAC": "oxolan-3-yl n-[4-[(4-aminophenyl)sulfonyl-(2-methylpropyl)amino]-3-hydroxy-1-phenylbutan-2-yl]carbamate", "data-SMILES": "CC(C)CN(CC(O)C(Cc1ccccc1)NC(=O)OC1CCOC1)S(=O)(=O)c1ccc(N)cc1", "mols2grid-tooltip": "<strong>IUPAC</strong>: oxolan-3-yl n-[4-[(4-aminophenyl)sulfonyl-(2-methylpropyl)amino]-3-hydroxy-1-phenylbutan-2-yl]carbamate<br><strong>SMILES</strong>: CC(C)CN(CC(O)C(Cc1ccccc1)NC(=O)OC1CCOC1)S(=O)(=O)c1ccc(N)cc1"}, {"data-img": null, "mols2grid-id": 27, "data-Name": "darunavir", "data-IUPAC": "2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-4-yl n-[4-[(4-aminophenyl)sulfonyl-(2-methylpropyl)amino]-3-hydroxy-1-phenylbutan-2-yl]carbamate", "data-SMILES": "CC(C)CN(CC(O)C(Cc1ccccc1)NC(=O)OC1COC2OCCC12)S(=O)(=O)c1ccc(N)cc1", "mols2grid-tooltip": "<strong>IUPAC</strong>: 2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-4-yl n-[4-[(4-aminophenyl)sulfonyl-(2-methylpropyl)amino]-3-hydroxy-1-phenylbutan-2-yl]carbamate<br><strong>SMILES</strong>: CC(C)CN(CC(O)C(Cc1ccccc1)NC(=O)OC1COC2OCCC12)S(=O)(=O)c1ccc(N)cc1"}, {"data-img": null, "mols2grid-id": 0, "data-Name": "didanosine", "data-IUPAC": "9-[5-(hydroxymethyl)oxolan-2-yl]-1h-purin-6-one", "data-SMILES": "O=c1[nH]cnc2c1ncn2C1CCC(CO)O1", "mols2grid-tooltip": "<strong>IUPAC</strong>: 9-[5-(hydroxymethyl)oxolan-2-yl]-1h-purin-6-one<br><strong>SMILES</strong>: O=c1[nH]cnc2c1ncn2C1CCC(CO)O1"}, {"data-img": null, "mols2grid-id": 12, "data-Name": "doxorubicin", "data-IUPAC": "n-[2-[4-[3-(propan-2-ylamino)pyridin-2-yl]piperazine-1-carbonyl]-1h-indol-5-yl]methanesulfonamide", "data-SMILES": "CC(C)Nc1cccnc1N1CCN(C(=O)c2cc3cc(NS(C)(=O)=O)ccc3[nH]2)CC1", "mols2grid-tooltip": "<strong>IUPAC</strong>: n-[2-[4-[3-(propan-2-ylamino)pyridin-2-yl]piperazine-1-carbonyl]-1h-indol-5-yl]methanesulfonamide<br><strong>SMILES</strong>: CC(C)Nc1cccnc1N1CCN(C(=O)c2cc3cc(NS(C)(=O)=O)ccc3[nH]2)CC1"}, {"data-img": null, "mols2grid-id": 15, "data-Name": "efavirenz", "data-IUPAC": "6-chloro-4-(2-cyclopropylethynyl)-4-(trifluoromethyl)-1h-3,1-benzoxazin-2-one", "data-SMILES": "O=C1Nc2ccc(Cl)cc2C(C#CC2CC2)(C(F)(F)F)O1", "mols2grid-tooltip": "<strong>IUPAC</strong>: 6-chloro-4-(2-cyclopropylethynyl)-4-(trifluoromethyl)-1h-3,1-benzoxazin-2-one<br><strong>SMILES</strong>: O=C1Nc2ccc(Cl)cc2C(C#CC2CC2)(C(F)(F)F)O1"}, {"data-img": null, "mols2grid-id": 24, "data-Name": "entecavir", "data-IUPAC": "2-amino-9-[4-hydroxy-3-(hydroxymethyl)-2-methylidenecyclopentyl]-1h-purin-6-one", "data-SMILES": "C=C1C(CO)C(O)CC1n1cnc2c(=O)[nH]c(N)nc21", "mols2grid-tooltip": "<strong>IUPAC</strong>: 2-amino-9-[4-hydroxy-3-(hydroxymethyl)-2-methylidenecyclopentyl]-1h-purin-6-one<br><strong>SMILES</strong>: C=C1C(CO)C(O)CC1n1cnc2c(=O)[nH]c(N)nc21"}, {"data-img": null, "mols2grid-id": 31, "data-Name": "etravirine", "data-IUPAC": "4-[6-amino-5-bromo-2-(4-cyanoanilino)pyrimidin-4-yl]oxy-3,5-dimethylbenzonitrile", "data-SMILES": "Cc1cc(C#N)cc(C)c1Oc1nc(Nc2ccc(C#N)cc2)nc(N)c1Br", "mols2grid-tooltip": "<strong>IUPAC</strong>: 4-[6-amino-5-bromo-2-(4-cyanoanilino)pyrimidin-4-yl]oxy-3,5-dimethylbenzonitrile<br><strong>SMILES</strong>: Cc1cc(C#N)cc(C)c1Oc1nc(Nc2ccc(C#N)cc2)nc(N)c1Br"}, {"data-img": null, "mols2grid-id": 5, "data-Name": "indinavir", "data-IUPAC": "1-[4-benzyl-2-hydroxy-5-[(2-hydroxy-2,3-dihydro-1h-inden-1-yl)amino]-5-oxopentyl]-n-tert-butyl-4-(pyridin-3-ylmethyl)piperazine-2-carboxamide", "data-SMILES": "CC(C)(C)NC(=O)C1CN(Cc2cccnc2)CCN1CC(O)CC(Cc1ccccc1)C(=O)NC1c2ccccc2CC1O", "mols2grid-tooltip": "<strong>IUPAC</strong>: 1-[4-benzyl-2-hydroxy-5-[(2-hydroxy-2,3-dihydro-1h-inden-1-yl)amino]-5-oxopentyl]-n-tert-butyl-4-(pyridin-3-ylmethyl)piperazine-2-carboxamide<br><strong>SMILES</strong>: CC(C)(C)NC(=O)C1CN(Cc2cccnc2)CCN1CC(O)CC(Cc1ccccc1)C(=O)NC1c2ccccc2CC1O"}, {"data-img": null, "mols2grid-id": 33, "data-Name": "maraviroc", "data-IUPAC": "4,4-difluoro-n-[3-[3-(3-methyl-5-propan-2-yl-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]octan-8-yl]-1-phenylpropyl]cyclohexane-1-carboxamide", "data-SMILES": "Cc1nnc(C(C)C)n1C1CC2CCC(C1)N2CCC(NC(=O)C1CCC(F)(F)CC1)c1ccccc1", "mols2grid-tooltip": "<strong>IUPAC</strong>: 4,4-difluoro-n-[3-[3-(3-methyl-5-propan-2-yl-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]octan-8-yl]-1-phenylpropyl]cyclohexane-1-carboxamide<br><strong>SMILES</strong>: Cc1nnc(C(C)C)n1C1CC2CCC(C1)N2CCC(NC(=O)C1CCC(F)(F)CC1)c1ccccc1"}, {"data-img": null, "mols2grid-id": 14, "data-Name": "mesna", "data-IUPAC": "trisodium;phosphonatoformate", "data-SMILES": "O=C(O)P(=O)(O)O", "mols2grid-tooltip": "<strong>IUPAC</strong>: trisodium;phosphonatoformate<br><strong>SMILES</strong>: O=C(O)P(=O)(O)O"}, {"data-img": null, "mols2grid-id": 21, "data-Name": "mls003373964", "data-IUPAC": "4-amino-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]pyrimidin-2-one", "data-SMILES": "Nc1ccn(C2CSC(CO)O2)c(=O)n1", "mols2grid-tooltip": "<strong>IUPAC</strong>: 4-amino-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]pyrimidin-2-one<br><strong>SMILES</strong>: Nc1ccn(C2CSC(CO)O2)c(=O)n1"}, {"data-img": null, "mols2grid-id": 7, "data-Name": "n-[3-hydroxy-5-[[3-methyl-2-[[[methyl-[(2-propan-2-yl-4-thiazolyl)methyl]amino]-oxomethyl]amino]-1-oxobutyl]amino]-1,6-diphenylhexan-2-yl]carbamic acid 5-thiazolylmethyl ester", "data-IUPAC": "1,3-thiazol-5-ylmethyl n-[3-hydroxy-5-[[3-methyl-2-[[methyl-[(2-propan-2-yl-1,3-thiazol-4-yl)methyl]carbamoyl]amino]butanoyl]amino]-1,6-diphenylhexan-2-yl]carbamate", "data-SMILES": "CC(C)c1nc(CN(C)C(=O)NC(C(=O)NC(Cc2ccccc2)CC(O)C(Cc2ccccc2)NC(=O)OCc2cncs2)C(C)C)cs1", "mols2grid-tooltip": "<strong>IUPAC</strong>: 1,3-thiazol-5-ylmethyl n-[3-hydroxy-5-[[3-methyl-2-[[methyl-[(2-propan-2-yl-1,3-thiazol-4-yl)methyl]carbamoyl]amino]butanoyl]amino]-1,6-diphenylhexan-2-yl]carbamate<br><strong>SMILES</strong>: CC(C)c1nc(CN(C)C(=O)NC(C(=O)NC(Cc2ccccc2)CC(O)C(Cc2ccccc2)NC(=O)OCc2cncs2)C(C)C)cs1"}, {"data-img": null, "mols2grid-id": 3, "data-Name": "nelfinavir mesylate", "data-IUPAC": "n-tert-butyl-2-[2-hydroxy-3-[(3-hydroxy-2-methylbenzoyl)amino]-4-phenylsulfanylbutyl]-3,4,4a,5,6,7,8,8a-octahydro-1h-isoquinoline-3-carboxamide", "data-SMILES": "Cc1c(O)cccc1C(=O)NC(CSc1ccccc1)C(O)CN1CC2CCCCC2CC1C(=O)NC(C)(C)C", "mols2grid-tooltip": "<strong>IUPAC</strong>: n-tert-butyl-2-[2-hydroxy-3-[(3-hydroxy-2-methylbenzoyl)amino]-4-phenylsulfanylbutyl]-3,4,4a,5,6,7,8,8a-octahydro-1h-isoquinoline-3-carboxamide<br><strong>SMILES</strong>: Cc1c(O)cccc1C(=O)NC(CSc1ccccc1)C(O)CN1CC2CCCCC2CC1C(=O)NC(C)(C)C"}, {"data-img": null, "mols2grid-id": 1, "data-Name": "nsc606170", "data-IUPAC": "4-amino-1-[5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one", "data-SMILES": "Nc1ccn(C2CCC(CO)O2)c(=O)n1", "mols2grid-tooltip": "<strong>IUPAC</strong>: 4-amino-1-[5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one<br><strong>SMILES</strong>: Nc1ccn(C2CCC(CO)O2)c(=O)n1"}, {"data-img": null, "mols2grid-id": 35, "data-Name": "ophthalmadine", "data-IUPAC": "1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-iodopyrimidine-2,4-dione", "data-SMILES": "O=c1[nH]c(=O)n(C2CC(O)C(CO)O2)cc1I", "mols2grid-tooltip": "<strong>IUPAC</strong>: 1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-iodopyrimidine-2,4-dione<br><strong>SMILES</strong>: O=c1[nH]c(=O)n(C2CC(O)C(CO)O2)cc1I"}, {"data-img": null, "mols2grid-id": 13, "data-Name": "ornidazole", "data-IUPAC": "adamantan-1-amine;hydron;chloride", "data-SMILES": "NC12CC3CC(CC(C3)C1)C2", "mols2grid-tooltip": "<strong>IUPAC</strong>: adamantan-1-amine;hydron;chloride<br><strong>SMILES</strong>: NC12CC3CC(CC(C3)C1)C2"}, {"data-img": null, "mols2grid-id": 19, "data-Name": "oseltamivir", "data-IUPAC": "ethyl 4-acetamido-5-amino-3-pentan-3-yloxycyclohexene-1-carboxylate", "data-SMILES": "CCOC(=O)C1=CC(OC(CC)CC)C(NC(C)=O)C(N)C1", "mols2grid-tooltip": "<strong>IUPAC</strong>: ethyl 4-acetamido-5-amino-3-pentan-3-yloxycyclohexene-1-carboxylate<br><strong>SMILES</strong>: CCOC(=O)C1=CC(OC(CC)CC)C(NC(C)=O)C(N)C1"}, {"data-img": null, "mols2grid-id": 22, "data-Name": "racivir", "data-IUPAC": "4-amino-5-fluoro-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]pyrimidin-2-one", "data-SMILES": "Nc1nc(=O)n(C2CSC(CO)O2)cc1F", "mols2grid-tooltip": "<strong>IUPAC</strong>: 4-amino-5-fluoro-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]pyrimidin-2-one<br><strong>SMILES</strong>: Nc1nc(=O)n(C2CSC(CO)O2)cc1F"}, {"data-img": null, "mols2grid-id": 8, "data-Name": "ribavirin", "data-IUPAC": "1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,4-triazole-3-carboxamide", "data-SMILES": "NC(=O)c1ncn(C2OC(CO)C(O)C2O)n1", "mols2grid-tooltip": "<strong>IUPAC</strong>: 1-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,4-triazole-3-carboxamide<br><strong>SMILES</strong>: NC(=O)c1ncn(C2OC(CO)C(O)C2O)n1"}, {"data-img": null, "mols2grid-id": 17, "data-Name": "schembl10264224", "data-IUPAC": "oxolan-3-yl n-[4-[(4-aminophenyl)sulfonyl-(2-methylpropyl)amino]-1-phenyl-3-phosphonooxybutan-2-yl]carbamate", "data-SMILES": "CC(C)CN(CC(OP(=O)(O)O)C(Cc1ccccc1)NC(=O)OC1CCOC1)S(=O)(=O)c1ccc(N)cc1", "mols2grid-tooltip": "<strong>IUPAC</strong>: oxolan-3-yl n-[4-[(4-aminophenyl)sulfonyl-(2-methylpropyl)amino]-1-phenyl-3-phosphonooxybutan-2-yl]carbamate<br><strong>SMILES</strong>: CC(C)CN(CC(OP(=O)(O)O)C(Cc1ccccc1)NC(=O)OC1CCOC1)S(=O)(=O)c1ccc(N)cc1"}, {"data-img": null, "mols2grid-id": 10, "data-Name": "stavudine", "data-IUPAC": "1-[5-(hydroxymethyl)-2,5-dihydrofuran-2-yl]-5-methylpyrimidine-2,4-dione", "data-SMILES": "Cc1cn(C2C=CC(CO)O2)c(=O)[nH]c1=O", "mols2grid-tooltip": "<strong>IUPAC</strong>: 1-[5-(hydroxymethyl)-2,5-dihydrofuran-2-yl]-5-methylpyrimidine-2,4-dione<br><strong>SMILES</strong>: Cc1cn(C2C=CC(CO)O2)c(=O)[nH]c1=O"}, {"data-img": null, "mols2grid-id": 29, "data-Name": "telaprevir", "data-IUPAC": "2-[2-[[2-cyclohexyl-2-(pyrazine-2-carbonylamino)acetyl]amino]-3,3-dimethylbutanoyl]-n-[1-(cyclopropylamino)-1,2-dioxohexan-3-yl]-3,3a,4,5,6,6a-hexahydro-1h-cyclopenta[c]pyrrole-3-carboxamide", "data-SMILES": "CCCC(NC(=O)C1C2CCCC2CN1C(=O)C(NC(=O)C(NC(=O)c1cnccn1)C1CCCCC1)C(C)(C)C)C(=O)C(=O)NC1CC1", "mols2grid-tooltip": "<strong>IUPAC</strong>: 2-[2-[[2-cyclohexyl-2-(pyrazine-2-carbonylamino)acetyl]amino]-3,3-dimethylbutanoyl]-n-[1-(cyclopropylamino)-1,2-dioxohexan-3-yl]-3,3a,4,5,6,6a-hexahydro-1h-cyclopenta[c]pyrrole-3-carboxamide<br><strong>SMILES</strong>: CCCC(NC(=O)C1C2CCCC2CN1C(=O)C(NC(=O)C(NC(=O)c1cnccn1)C1CCCCC1)C(C)(C)C)C(=O)C(=O)NC1CC1"}, {"data-img": null, "mols2grid-id": 32, "data-Name": "telbivudine", "data-IUPAC": "1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione", "data-SMILES": "Cc1cn(C2CC(O)C(CO)O2)c(=O)[nH]c1=O", "mols2grid-tooltip": "<strong>IUPAC</strong>: 1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione<br><strong>SMILES</strong>: Cc1cn(C2CC(O)C(CO)O2)c(=O)[nH]c1=O"}, {"data-img": null, "mols2grid-id": 28, "data-Name": "thiazol-5-ylmethyl (2r,5r)-5-((s)-2-(3-((2-isopropylthiazol-4-yl)methyl)-3-methylureido)-4-morpholinobutanamido)-1,6-diphenylhexan-2-ylcarbamate", "data-IUPAC": "1,3-thiazol-5-ylmethyl n-[5-[[2-[[methyl-[(2-propan-2-yl-1,3-thiazol-4-yl)methyl]carbamoyl]amino]-4-morpholin-4-ylbutanoyl]amino]-1,6-diphenylhexan-2-yl]carbamate", "data-SMILES": "CC(C)c1nc(CN(C)C(=O)NC(CCN2CCOCC2)C(=O)NC(CCC(Cc2ccccc2)NC(=O)OCc2cncs2)Cc2ccccc2)cs1", "mols2grid-tooltip": "<strong>IUPAC</strong>: 1,3-thiazol-5-ylmethyl n-[5-[[2-[[methyl-[(2-propan-2-yl-1,3-thiazol-4-yl)methyl]carbamoyl]amino]-4-morpholin-4-ylbutanoyl]amino]-1,6-diphenylhexan-2-yl]carbamate<br><strong>SMILES</strong>: CC(C)c1nc(CN(C)C(=O)NC(CCN2CCOCC2)C(=O)NC(CCC(Cc2ccccc2)NC(=O)OCc2cncs2)Cc2ccccc2)cs1"}, {"data-img": null, "mols2grid-id": 34, "data-Name": "thymidine,.alpha.,.alpha.-trifluoro-", "data-IUPAC": "1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-(trifluoromethyl)pyrimidine-2,4-dione", "data-SMILES": "O=c1[nH]c(=O)n(C2CC(O)C(CO)O2)cc1C(F)(F)F", "mols2grid-tooltip": "<strong>IUPAC</strong>: 1-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-(trifluoromethyl)pyrimidine-2,4-dione<br><strong>SMILES</strong>: O=c1[nH]c(=O)n(C2CC(O)C(CO)O2)cc1C(F)(F)F"}, {"data-img": null, "mols2grid-id": 25, "data-Name": "zanamivir", "data-IUPAC": "3-acetamido-4-(diaminomethylideneamino)-2-(1,2,3-trihydroxypropyl)-3,4-dihydro-2h-pyran-6-carboxylic acid", "data-SMILES": "CC(=O)NC1C(N=C(N)N)C=C(C(=O)O)OC1C(O)C(O)CO", "mols2grid-tooltip": "<strong>IUPAC</strong>: 3-acetamido-4-(diaminomethylideneamino)-2-(1,2,3-trihydroxypropyl)-3,4-dihydro-2h-pyran-6-carboxylic acid<br><strong>SMILES</strong>: CC(=O)NC1C(N=C(N)N)C=C(C(=O)O)OC1C(O)C(O)CO"}, {"data-img": null, "mols2grid-id": 6, "data-Name": "zidovudine", "data-IUPAC": "1-[4-azido-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione", "data-SMILES": "Cc1cn(C2CC(N=[N+]=[N-])C(CO)O2)c(=O)[nH]c1=O", "mols2grid-tooltip": "<strong>IUPAC</strong>: 1-[4-azido-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione<br><strong>SMILES</strong>: Cc1cn(C2CC(N=[N+]=[N-])C(CO)O2)c(=O)[nH]c1=O"}]);
// filter
if (window.parent.mols2grid_lists === undefined) {
window.parent.mols2grid_lists = {};
}
window.parent.mols2grid_lists["default"] = listObj;
// selection
class MolStorage extends Map {
multi_set(_id, _smiles) {
for (let i=0; i < _id.length; i++) {
this.set(_id[i], _smiles[i]);
}
}
multi_del(_id) {
for (let i=0; i < _id.length; i++) {
this.delete(_id[i]);
};
}
to_dict() {
var content = "{";
for (let [key, value] of this) {
content += key + ":" + JSON.stringify(value) + ",";
}
content = content.length > 1 ? content.slice(0, -1) : content;
content += "}";
return content
}
download_smi(fileName) {
var content = "SMILES index\n";
for (let [key, value] of this) {
content += value + " " + key + "\n";
}
var a = document.createElement("a");
var file = new Blob([content], {type: "text/plain"});
a.href = URL.createObjectURL(file);
a.download = fileName;
a.click();
a.remove();
}
}
var SELECTION = new MolStorage();
// kernel
var kernel_env = null;
if (window.parent.IPython !== undefined) {
// Jupyter notebook
kernel_env = "jupyter";
var kernel = window.parent.IPython.notebook.kernel;
kernel.execute('from mols2grid.select import register as _m2g_reg')
function add_selection(grid_id, _id, smiles) {
SELECTION.multi_set(_id, smiles);
kernel.execute("_m2g_reg.add_selection('"+grid_id+"', "+JSON.stringify(_id)+","+JSON.stringify(smiles)+")");
}
function del_selection(grid_id, _id) {
SELECTION.multi_del(_id);
kernel.execute("_m2g_reg.del_selection('"+grid_id+"', "+JSON.stringify(_id)+")");
}
} else if (window.parent.google !== undefined) {
// Google colab
kernel_env = "colab";
var kernel = window.parent.google.colab.kernel;
function add_selection(grid_id, _id, smiles) {
SELECTION.multi_set(_id, smiles);
(async function() {
const result = await kernel.invokeFunction('_m2g_reg.add_selection',
[grid_id, _id, smiles], {});
})();
}
function del_selection(grid_id, _id) {
SELECTION.multi_del(_id);
(async function() {
const result = await kernel.invokeFunction('_m2g_reg.del_selection',
[grid_id, _id], {});
})();
}
} else {
function add_selection(grid_id, _id, smiles) {
SELECTION.multi_set(_id, smiles);
}
function del_selection(grid_id, _id) {
SELECTION.multi_del(_id);
}
}
// sort
var sort_field = "data-Name";
var sort_order = "asc";
function mols2gridSortFunction(itemA, itemB, options) {
var x = itemA.values()[options.valueName];
var y = itemB.values()[options.valueName];
if (typeof x === "number") {
if (isFinite(x - y)) {
return x - y;
} else {
return isFinite(x) ? -1 : 1;
}
} else {
x = x.toLowerCase();
y = y.toLowerCase();
return (x < y) ? -1: (x > y) ? 1: 0;
}
}
function checkboxSort(itemA, itemB, options) {
if (itemA.elm !== undefined) {
var checkedA = itemA.elm.firstChild.checked;
if (itemB.elm !== undefined) {
var checkedB = itemB.elm.firstChild.checked;
if (checkedA && !checkedB) {
return -1;
} else if (!checkedA && checkedB) {
return 1;
} else {
return 0;
}
} else {
return -1;
}
} else if (itemB.elm !== undefined) {
return 1;
} else {
return 0;
}
}
$('#mols2grid button.sort-btn').click(function(e) {
var _field = $(this).attr("data-name");
if (_field == sort_field) {
$(this).removeClass("arrow-" + sort_order)
sort_order = (sort_order === "desc") ? "asc" : "desc";
} else {
$('#mols2grid button.sort-btn.active').removeClass("active arrow-" + sort_order);
sort_order = "asc";
sort_field = _field;
$(this).addClass("active");
}
$(this).addClass("arrow-" + sort_order)
if (sort_field == "checkbox") {
listObj.sort("mols2grid-id", {order: sort_order, sortFunction: checkboxSort});
} else {
listObj.sort(_field, {order: sort_order, sortFunction: mols2gridSortFunction});
}
});
// tooltips
$.fn.tooltip.Constructor.Default.whiteList.span = ['style']
listObj.on("updated", function (list) {
$(function () {
// hide previous popovers
$('#mols2grid a.page-link').click(function(e) {
$('.mols2grid-tooltip[data-toggle="popover"]').popover('hide')
});
// create new popover
$('.mols2grid-tooltip[data-toggle="popover"]').popover({
placement: 'bottom',
trigger: 'click hover',
html: true,
sanitize: false,
});
})
});
// selection modifyers and export options
// check all
$('#btn-chkbox-all').click(function (e) {
var _id = [];
var _smiles = [];
listObj.items.forEach(function (item) {
if (item.elm) {
item.elm.getElementsByTagName("input")[0].checked = true;
} else {
item.show()
item.elm.getElementsByTagName("input")[0].checked = true;
item.hide()
}
_id.push(item.values()["mols2grid-id"]);
_smiles.push(item.values()["data-SMILES"]);
});
add_selection("default", _id, _smiles);
});
// check matching
$('#btn-chkbox-match').click(function (e) {
var _id = [];
var _smiles = [];
listObj.matchingItems.forEach(function (item) {
if (item.elm) {
item.elm.getElementsByTagName("input")[0].checked = true;
} else {
item.show()
item.elm.getElementsByTagName("input")[0].checked = true;
item.hide()
}
_id.push(item.values()["mols2grid-id"]);
_smiles.push(item.values()["data-SMILES"]);
});
add_selection("default", _id, _smiles);
});
// uncheck all
$('#btn-chkbox-none').click(function (e) {
var _id = [];
listObj.items.forEach(function (item) {
if (item.elm) {
item.elm.getElementsByTagName("input")[0].checked = false;
} else {
item.show()
item.elm.getElementsByTagName("input")[0].checked = false;
item.hide()
}
_id.push(item.values()["mols2grid-id"]);
});
del_selection("default", _id);
});
// invert
$('#btn-chkbox-invert').click(function (e) {
var _id_add = [];
var _id_del = [];
var _smiles = [];
listObj.items.forEach(function (item) {
if (item.elm) {
var chkbox = item.elm.getElementsByTagName("input")[0]
chkbox.checked = !chkbox.checked;
} else {
item.show()
var chkbox = item.elm.getElementsByTagName("input")[0]
chkbox.checked = !chkbox.checked;
item.hide()
}
if (chkbox.checked) {
_id_add.push(item.values()["mols2grid-id"]);
_smiles.push(item.values()["data-SMILES"]);
} else {
_id_del.push(item.values()["mols2grid-id"]);
}
});
del_selection("default", _id_del);
add_selection("default", _id_add, _smiles);
});
// copy to clipboard
$("#btn-chkbox-copy").click(function(e) {
navigator.clipboard.writeText(SELECTION.to_dict());
});
// export smiles
$("#btn-chkbox-dlsmi").click(function(e) {
SELECTION.download_smi("selection.smi");
});
// export CSV
$("#btn-chkbox-dlcsv").click(function(e) {
var sep = "\t"
// same order as subset + tooltip
var columns = Array.from(listObj.items[0].elm.querySelectorAll("div.data"))
.map(elm => elm.classList[1]);
// remove 'data-'
var header = columns.map(name => name.slice(5));
// csv content
header = ["index"].concat(header).join(sep);
var content = header + "\n";
for (let [index, smiles] of SELECTION.entries()) {
var data = listObj.items[index].values();
content += index;
columns.forEach((key) => {
content += sep + data[key];
})
content += "\n";
}
var a = document.createElement("a");
var file = new Blob([content], {type: "text/csv"});
a.href = URL.createObjectURL(file);
a.download = "selection.csv";
a.click();
a.remove();
});
// update selection on checkbox click
listObj.on("updated", function (list) {
$("input:checkbox").change(function() {
var _id = parseInt($(this).closest(".cell").attr("data-mols2grid-id"));
if (this.checked) {
var _smiles = $($(this).siblings(".data-SMILES")[0]).text();
add_selection("default", [_id], [_smiles]);
} else {
del_selection("default", [_id]);
}
});
});
// generate images for the currently displayed molecules
var draw_opts = {"fixedBondLength": 30, "width": 270, "height": 140};
var json_draw_opts = JSON.stringify(draw_opts);
var smarts_matches = {};
// Load RDKit
window
.initRDKitModule()
.then(function(RDKit) {
console.log('RDKit version: ', RDKit.version());
window.RDKit = RDKit;
window.RDKitModule = RDKit;
// search bar
function SmartsSearch(query, columns) {
var smiles_col = columns[0];
smarts_matches = {};
var query = $('#mols2grid #searchbar').val();
var qmol = RDKit.get_qmol(query);
if (qmol.is_valid()) {
listObj.items.forEach(function (item) {
var smiles = item.values()[smiles_col]
var mol = RDKit.get_mol(smiles, '{"removeHs": false }');
if (mol.is_valid()) {
var results = mol.get_substruct_matches(qmol);
if (results === "\{\}") {
item.found = false;
} else {
item.found = true;
results = JSON.parse(results);
var highlights = {"atoms": [], "bonds": []};
results.forEach(function (match) {
highlights["atoms"].push(...match.atoms)
highlights["bonds"].push(...match.bonds)
});
var index = item.values()["mols2grid-id"];
smarts_matches[index] = highlights;
}
} else {
item.found = false;
}
mol.delete();
});
}
qmol.delete();
}
var search_type = "Text";
$('#mols2grid .search-btn').click(function() {
search_type = $(this).text();
$('#mols2grid button.search-btn.active').removeClass("active");
$(this).addClass("active");
});
$('#mols2grid #searchbar').on("keyup", function(e) {
var query = e.target.value;
if (search_type === "Text") {
smarts_matches = {};
listObj.search(query, ['data-Name', 'data-IUPAC', 'data-SMILES']);
} else {
listObj.search(query, ["data-SMILES"], SmartsSearch);
}
});
// generate images for the currently displayed molecules
RDKit.prefer_coordgen(true);
function draw_mol(smiles, index, template_mol) {
var mol = RDKit.get_mol(smiles, '{"removeHs": false }');
var svg = "";
if (mol.is_valid()) {
var highlights = smarts_matches[index];
if (highlights) {
var details = Object.assign({}, draw_opts, highlights);
details = JSON.stringify(details);
mol.generate_aligned_coords(template_mol, true);
} else {
var details = json_draw_opts;
}
svg = mol.get_svg_with_highlights(details);
}
mol.delete();
if (svg == "") {
return '<svg width="270" height="140" xmlns="http://www.w3.org/2000/svg" version="1.1" viewBox="0 0 270 140"></svg>';
}
return svg;
}
listObj.on("updated", function (list) {
var query = $('#mols2grid #searchbar').val();
var template_mol;
if (query === "") {
smarts_matches = {};
template_mol = null;
} else {
template_mol = RDKit.get_qmol(query);
template_mol.set_new_coords(true);
}
$('#mols2grid .cell').each(function() {
var $t = $(this);
var smiles = $t.children(".data-SMILES").first().text();
var index = parseInt(this.getAttribute("data-mols2grid-id"));
var svg = draw_mol(smiles, index, template_mol);
$t.children(".data-img").html(svg);
});
if (template_mol) {
template_mol.delete();
}
});
// trigger update to activate tooltips, draw images, setup callbacks...
listObj.update();
// resize iframe to fit content
if (window.frameElement) {
window.parent.fit_height(window.frameElement);
}
});
</script>
</body>
</html>