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KEGG COMPOUND: C00423

<!doctype html> <html><head> <title>KEGG COMPOUND: C00423</title> <link type="text/css" rel="stylesheet" href="/css/gn2.css?1744370736"> <link type="text/css" rel="stylesheet" href="/css/bget.css?1744370736"> <meta name="viewport" content="width=device-width, initial-scale=1.0"> <link type="text/css" rel="stylesheet" href="/css/bgetm.css?1744370736" media="only screen and (max-width: 768px)"> <style>.kcfd{display:none;}</style> <script> <!-- var getElementsByClassName = document.getElementsByClassName ? function (cl){ return document.getElementsByClassName(cl); } : function (cl){ var elms = []; var objs = document.getElementsByTagName('*'); for(var i=0;i<objs.length;i++){ var obj = objs[i]; if(obj.className == cl){ elms.push(obj); } } return elms; }; function toggleField(clk,cl,show,hide){ var objs = getElementsByClassName(cl); for(var i=0;i<objs.length;i++){ var obj = objs[i]; if(!obj.style.display||obj.style.display == 'none'){ obj.style.display = 'block'; clk.innerHTML = 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for(var i=1;i<=1;i++){ if(document.getElementById('kcfb'+i)){ document.getElementById('kcfb'+i).onclick = function(e){toggleData(this,e);}; } } } function Link_XtrctSeq2(form) { var dna_from; var dna_to; var dna_len; var plus_up = Number(form.XtrctSeq_UP.value) ; var plus_down = Number(form.XtrctSeq_DOWN.value); var vector = Number(form.VECTOR.value); var org = form.ORG.value; var chr = form.CHR.value; var kid = form.KEGGID.value; var url; if (plus_up == 0 && plus_down == 0) { url = "/entry/-f+-n+n+" + kid; } else { if (vector == 1) { dna_from = Number(form.FROM.value) - plus_up; dna_to = Number(form.TO.value) + plus_down; } else { dna_from = Number(form.FROM.value) - plus_down; dna_to = Number(form.TO.value) + plus_up; } url = "/dbget-bin/cut_sequence_genes.pl?FROM=" + dna_from + "&TO=" + dna_to +"&VECTOR=" + vector + "&ORG=" + org; if (chr) url += "&CHR=" + chr; } //window.open( url, "_self" ); location.href = url; } function go_taxonomy(form,params){ for(var key in params){ if(form[key]){ form.setAttribute(key,params[key]); } else{ var obj = document.createElement('input'); obj.setAttribute('type','hidden'); obj.setAttribute('name',key); obj.setAttribute('value',params[key]); form.appendChild(obj); } } form.submit(); } window.onload=function(){window.focus();init();}; //---> </script> </head> <body> <div> <table border=0 cellpadding=0 cellspacing=0><tr><td> <table border=0 cellpadding=0 cellspacing=0 width="650"><tr><td width=70><a href="/kegg/kegg2.html"><img align="middle" alt="KEGG" border=0 src="/Fig/bget/kegg2.gif"></a></td><td>&nbsp;&nbsp;&nbsp;</td><td><a name="compound:C00423"></a><font class="title2">COMPOUND: C00423</font></td><td class="tar vbot"><button class="btn" onclick="javascript:void(window.open(&#39;/kegg/document/help_bget_compound.html&#39;,&#39;KEGG_Help&#39;,&#39;toolbar=no,location=no,directories=no,width=720,height=640,resizable=yes,scrollbars=yes&#39;));return false;">Help</button></td></tr></table><form method="post" action="/entry/" enctype="application/x-www-form-urlencoded" id="form1" name="form1"></form><table class="w1" width="650"> <tr> <td class="fr2 w1"> <table width="650" class="w2"> <tr><th class="th20 deft tal vmid"><span class="nowrap">Entry</span></th> <td class="td20 defd"><table class="w1" width="100%"><tr><td class="tal pd0"><code><span class="nowrap">C00423&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Compound&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<br> </span></code></td></tr></table></td></tr> <tr><th class="th21 deft tal vtop"><span class="nowrap">Name</span></th> <td class="td21 defd"><div class="cel"><div class="cel">trans-Cinnamate;<br> trans-Cinnamic acid;<br> (E)-Cinnamate;<br> (2E)-3-Phenylprop-2-enoate<br> </div></div></td></tr> <tr><th class="th20 deft tal vtop"><span class="nowrap">Formula</span></th> <td class="td20 defd"><div class="cel">C9H8O2<br> </div></td></tr> <tr><th class="th21 deft tal vtop"><span class="nowrap">Exact mass</span></th> <td class="td21 defd"><div class="cel">148.0524<br> </div></td></tr> <tr><th class="th20 deft tal vtop"><span class="nowrap">Mol weight</span></th> <td class="td20 defd"><div class="cel">148.16<br> </div></td></tr> <tr><th class="th21 deft tal vtop"><span class="nowrap">Structure</span></th> <td class="td21 defd"><a href="/Fig/compound/C00423.gif"><img name="img0" src="/Fig/compound/C00423.gif" style="max-width:600px" border=0></a><br> <button class="btn" onclick="location.href='/entry/-f+m+C00423';return false;">Mol file</button><button class="btn" onclick="location.href='/entry/-f+k+C00423';return false;">KCF file</button><button class="btn" onclick="location.href='/tools-bin/strsearch_view?ENTRY=C00423&amp;PROGRAM=simcomp&amp;DATABASE=compound';return false;">DB search</button></td></tr> <tr><th class="th20 deft tal vtop"><span class="nowrap">Reaction</span></th> <td class="td20 defd"><div class="cel"><a href="/entry/R00697">R00697</a> <a href="/entry/R01426">R01426</a> <a href="/entry/R02252">R02252</a> <a href="/entry/R02253">R02253</a> <a href="/entry/R02254">R02254</a> <a href="/entry/R02255">R02255</a> <a href="/entry/R02256">R02256</a> <a href="/entry/R06745">R06745</a> <br> <a href="/entry/R06781">R06781</a> <a href="/entry/R06783">R06783</a> <a href="/entry/R07796">R07796</a> <a href="/entry/R08422">R08422</a> <a href="/entry/R08423">R08423</a> <a href="/entry/R11070">R11070</a> <a href="/entry/R12535">R12535</a><br> </div></td></tr> <tr><th class="th21 deft tal vtop"><span class="nowrap">Pathway</span></th> <td class="td21 defd"><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/pathway/map00130+C00423">map00130</a>&nbsp;&nbsp;</span></td><td>Ubiquinone and other terpenoid-quinone biosynthesis</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/pathway/map00360+C00423">map00360</a>&nbsp;&nbsp;</span></td><td>Phenylalanine metabolism</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/pathway/map00940+C00423">map00940</a>&nbsp;&nbsp;</span></td><td>Phenylpropanoid biosynthesis</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/pathway/map00996+C00423">map00996</a>&nbsp;&nbsp;</span></td><td>Biosynthesis of various alkaloids</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/pathway/map00999+C00423">map00999</a>&nbsp;&nbsp;</span></td><td>Biosynthesis of various plant secondary metabolites</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/pathway/map01060+C00423">map01060</a>&nbsp;&nbsp;</span></td><td>Biosynthesis of plant secondary metabolites</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/pathway/map01070+C00423">map01070</a>&nbsp;&nbsp;</span></td><td>Biosynthesis of plant hormones</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/pathway/map01100+C00423">map01100</a>&nbsp;&nbsp;</span></td><td>Metabolic pathways</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/pathway/map01110+C00423">map01110</a>&nbsp;&nbsp;</span></td><td>Biosynthesis of secondary metabolites</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/pathway/map01120+C00423">map01120</a>&nbsp;&nbsp;</span></td><td>Microbial metabolism in diverse environments</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/pathway/map01220+C00423">map01220</a>&nbsp;&nbsp;</span></td><td>Degradation of aromatic compounds</td></tr></table></td></tr> <tr><th class="th20 deft tal vtop"><span class="nowrap">Module</span></th> <td class="td20 defd"><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/module/M00039+C00423">M00039</a>&nbsp;&nbsp;</span></td><td>Monolignol biosynthesis, phenylalanine/tyrosine =&gt; monolignol</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/module/M00137+C00423">M00137</a>&nbsp;&nbsp;</span></td><td>Flavanone biosynthesis, phenylalanine =&gt; naringenin</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap"><a href="/module/M00545+C00423">M00545</a>&nbsp;&nbsp;</span></td><td>Trans-cinnamate degradation, trans-cinnamate =&gt; acetyl-CoA</td></tr></table></td></tr> <tr><th class="th21 deft tal vtop"><span class="nowrap">Enzyme</span></th> <td class="td21 defd"><div class="cel"><a href="/entry/1.3.1.31">1.3.1.31</a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="/entry/1.3.8.15">1.3.8.15</a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="/entry/1.14.12.19">1.14.12.19</a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="/entry/1.14.13.14">1.14.13.14</a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<br> <a href="/entry/1.14.14.91">1.14.14.91</a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="/entry/2.4.1.177">2.4.1.177</a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="/entry/2.8.3.17">2.8.3.17</a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="/entry/4.1.1.102">4.1.1.102</a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<br> <a href="/entry/4.3.1.24">4.3.1.24</a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="/entry/4.3.1.25">4.3.1.25</a>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<a href="/entry/6.2.1.12">6.2.1.12</a><br> </div></td></tr> <tr><th class="th20 deft tal vtop"><span class="nowrap">Brite</span></th> <td class="td20 defd"><div class="cel"><span class="nowrap">Phytochemical compounds [BR:<a href="/brite/br08003+C00423">br08003</a>]<br> &nbsp;Phenylpropanoids<br> &nbsp;&nbsp;Monolignols<br> &nbsp;&nbsp;&nbsp;Others<br> &nbsp;&nbsp;&nbsp;&nbsp;C00423&nbsp;&nbsp;trans-Cinnamate<br> </span></div><button class="btn" onclick="location.href='/kegg-bin/search_brite?option=-a&amp;search_string=C00423';return false;">BRITE hierarchy</button></td></tr> <tr><th class="th21 deft tal vtop"><span class="nowrap">Other DBs</span></th> <td class="td21 defd"><table class="w1"><tr><td class="vtop pd0"><span class="nowrap">CAS:&nbsp;</span></td><td>140-10-3</td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap">PubChem:&nbsp;</span></td><td><a href="https://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?sid=3713">3713</a></td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap">ChEBI:&nbsp;</span></td><td><a href="https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:15669">15669</a> <a href="https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:35697">35697</a></td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap">KNApSAcK:&nbsp;</span></td><td><a href="http://kanaya.naist.jp/knapsack_jsp/information.jsp?sname=C_ID&word=C00000170">C00000170</a> <a href="http://kanaya.naist.jp/knapsack_jsp/information.jsp?sname=C_ID&word=C00029961">C00029961</a></td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap">PDB-CCD:&nbsp;</span></td><td><a href="https://www.ebi.ac.uk/pdbe-srv/pdbechem/chemicalCompound/show/TCA">TCA</a>[<a href="https://pdbj.org/mine/summary/TCA">PDBj</a>] </td></tr></table><table class="w1"><tr><td class="vtop pd0"><span class="nowrap">NIKKAJI:&nbsp;</span></td><td><a href="https://jglobal.jst.go.jp/en/redirect?Nikkaji_No=J2.024I">J2.024I</a></td></tr></table></td></tr> <tr><th class="th20 deft tal vtop"><span class="nowrap">KCF data</span></th> <td class="td20 defd"><button class="btn" id="kcfb1">Show</button><div class="kcfd" id="kcfd1"><br>ATOM&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;11<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;1&nbsp;&nbsp;&nbsp;O6a O&nbsp;&nbsp;&nbsp;&nbsp;13.3700&nbsp;&nbsp;-16.9400<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;2&nbsp;&nbsp;&nbsp;C6a C&nbsp;&nbsp;&nbsp;&nbsp;14.5824&nbsp;&nbsp;-16.2400<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;3&nbsp;&nbsp;&nbsp;C2b C&nbsp;&nbsp;&nbsp;&nbsp;15.7949&nbsp;&nbsp;-16.9400<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;4&nbsp;&nbsp;&nbsp;C2b C&nbsp;&nbsp;&nbsp;&nbsp;17.0073&nbsp;&nbsp;-16.2400<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;5&nbsp;&nbsp;&nbsp;C8y C&nbsp;&nbsp;&nbsp;&nbsp;18.2197&nbsp;&nbsp;-16.9400<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;6&nbsp;&nbsp;&nbsp;O6a O&nbsp;&nbsp;&nbsp;&nbsp;14.5824&nbsp;&nbsp;-14.8402<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;7&nbsp;&nbsp;&nbsp;C8x C&nbsp;&nbsp;&nbsp;&nbsp;18.2197&nbsp;&nbsp;-18.3399<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;8&nbsp;&nbsp;&nbsp;C8x C&nbsp;&nbsp;&nbsp;&nbsp;19.4322&nbsp;&nbsp;-19.0399<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;9&nbsp;&nbsp;&nbsp;C8x C&nbsp;&nbsp;&nbsp;&nbsp;20.6446&nbsp;&nbsp;-18.3399<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;10&nbsp;&nbsp;C8x C&nbsp;&nbsp;&nbsp;&nbsp;20.6446&nbsp;&nbsp;-16.9400<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;11&nbsp;&nbsp;C8x C&nbsp;&nbsp;&nbsp;&nbsp;19.4322&nbsp;&nbsp;-16.2400<br> BOND&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;11<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;1&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;1&nbsp;&nbsp;&nbsp;2 1<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;2&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;2&nbsp;&nbsp;&nbsp;3 1<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;3&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;3&nbsp;&nbsp;&nbsp;4 2<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;4&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;4&nbsp;&nbsp;&nbsp;5 1<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;5&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;2&nbsp;&nbsp;&nbsp;6 2<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;6&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;5&nbsp;&nbsp;&nbsp;7 2<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;7&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;7&nbsp;&nbsp;&nbsp;8 1<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;8&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;8&nbsp;&nbsp;&nbsp;9 2<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;9&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;9&nbsp;&nbsp;10 1<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;10&nbsp;&nbsp;&nbsp;10&nbsp;&nbsp;11 2<br> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;11&nbsp;&nbsp;&nbsp;&nbsp;5&nbsp;&nbsp;11 1<br> </div></td></tr> </table></td></tr></table> <br><span style="font-size:12px"><a href="/entry/cpd_ja:C00423">&raquo; Japanese version</a></span><br><br></td><td class="vtop"><div class="aw" style="margin-top:46px;"><div class="fm at th20">&nbsp;&nbsp;All links&nbsp;&nbsp;</div> <div class="fm"><pre class="fm" style="margin-left:1em"> <span style="color:#006"><a href="/dbget-bin/get_linkdb?-t+6+cpd:C00423">Chemical substance (18)</a></span> <a href="/dbget-bin/get_linkdb?-t+pubchem+cpd:C00423">PubChem (1)</a> <a href="/dbget-bin/get_linkdb?-t+chebi+cpd:C00423">ChEBI (2)</a> <a href="/dbget-bin/get_linkdb?-t+hmdb+cpd:C00423">HMDB (1)</a> <a href="/dbget-bin/get_linkdb?-t+knapsack+cpd:C00423">KNApSAcK (2)</a> <a href="/dbget-bin/get_linkdb?-t+massbank+cpd:C00423">MASSBANK (10)</a> <a href="/dbget-bin/get_linkdb?-t+nikkaji+cpd:C00423">NIKKAJI (1)</a> <a href="/dbget-bin/get_linkdb?-t+pdb-ccd+cpd:C00423">PDB-CCD (1)</a> <a href="/dbget-bin/get_linkdb?-t+alldb+cpd:C00423">All databases (18)</a> <br><a href="/dbget-bin/get_linkdb?-N+cpd:C00423">Download RDF</a> </pre> </div></div> </td></tr></table> <a href="/dbget/">DBGET</a> integrated database retrieval system</div> </body> </html>

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