adenosine (CHEBI:16335)

<!DOCTYPE html PUBLIC "-//W3C//DTD XHTML 1.0 Transitional//EN" "//www.w3.org/TR/xhtml1/DTD/xhtml1-transitional.dtd"> <html xmlns="//www.w3.org/1999/xhtml" class="fontface" lang="en"> <head> <meta http-equiv="Content-Type" content="text/html; charset=UTF-8"/> <meta name="description" content="Chemical Entities of Biological Interest (ChEBI) is a freely available dictionary of molecular entities focused on 'small' chemical compounds."/> <meta name="author" content="EBI Web Team"/> <meta name="keywords" content="chemical compounds, chemical compound, compound, ontology, biology, UniProt, ascii name, names, nomenclature, chemical, formula, IUPAC, IUPAC name, synonyms, chemical ontology, periodic table"/> <meta name="robots" content="index, nofollow" /> <meta http-equiv="Content-Language" content="en"/> <meta http-equiv="Window-target" content="_top"/> <meta name="no-email-collection" content="//www.unspam.com/noemailcollection/"/> <meta name="language" content="en"/> <meta name="revisit-after" content="14 days"/> <title> adenosine (CHEBI:16335) </title> <link rel="search" type="application/opensearchdescription+xml" title="ChEBI" href="/chebi/plugins/openSearch/openSearch.xml;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E"> <link rel="stylesheet" href="//www.ebi.ac.uk/web_guidelines/css/compliance/mini/ebi-fluid-embl.css" type="text/css"> <link rel="stylesheet" href="//ebi.emblstatic.net/web_guidelines/EBI-Icon-fonts/v1.3/fonts.css" type="text/css"> <link rel="stylesheet" href="/chebi/layouts/styles/chebiColorScheme.css;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E" type="text/css"/> <link rel="SHORTCUT ICON" href="/chebi/images/ChEBI_logo_16.ico;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E"/> <script type="text/javascript" src="/chebi/javascripts/chebi.js;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E"></script> <script type="text/javascript" src="/chebi/javascripts/jquery-1.9.1.min.js;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E"></script> <script src="//www.ebi.ac.uk/web_guidelines/js/ebi-global-search-run.js"></script> <script src="//www.ebi.ac.uk/web_guidelines/js/ebi-global-search.js"></script> <script type="text/javascript"> function showSubMenu(menu) { // First reset - hide all menus.. document.getElementById("browse").style.display = "none"; 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border-collapse: separate;margin-left: 13px;"> <tr> <td id="mainTab" class="tabStyle" onclick="window.location='searchId.do?chebiId=CHEBI:16335';" title="Click on the tab to display the main entry page for this entity.">Main</td> <td class="tabStyleBlank"></td> <td id="ontologyTab" class="tabStyle" onclick="window.location='chebiOntology.do?chebiId=CHEBI:16335';" title="Click on the tab to display the Ontological graph for this entity.">ChEBI Ontology</td> <td class="tabStyleBlank"></td> <td id="crossRefTab" class="tabStyle" onclick="window.location='displayAutoXrefs.do?chebiId=CHEBI:16335';" title="Click on the tab to display the Automatically Generated Cross-References for this entity.">Automatic Xrefs</td> <td class="tabStyleBlank"></td> <td id="reactionTab" class="tabStyle" onclick="window.location='reaction.do?chebiId=CHEBI:16335';" title="Click on the tab to display the reactions for this entity.">Reactions</td> <td class="tabStyleBlank"></td> <td id="pathwayTab" class="tabStyle" onclick="window.location='pathway.do?chebiId=CHEBI:16335';" title="Click on the tab to display the Pathways for this entity.">Pathways</td> <td class="tabStyleBlank"></td> <td id="biomodelTab" class="tabStyle" onclick="window.location='biomodel.do?chebiId=CHEBI:16335';" title="Click on the tab to display the Models for this entity.">Models</td> <td class="tabStyleBlank" style="width: 50%;"></td> </tr> </table> <script> $('#mainTab').addClass('tabStyleView'); $('#ontologyTab').removeClass('tabStyleView'); var crossRefTab = 1; if (crossRefTab > 0) { $('#crossRefTab').removeClass('tabStyleView'); } else { disableTab('crossRefTab', 'cross reference'); } var rxnCounter = 18; if (rxnCounter > 0) { $('#reactionTab').removeClass('tabStyleView'); } else { disableTab('reactionTab', 'reactions'); } var pathwayCounter = 38; if (pathwayCounter > 0) { $('#pathwayTab').removeClass('tabStyleView'); } else { disableTab('pathwayTab', 'pathways'); } var biomodelCounter = 11; if (biomodelCounter > 0) { $('#biomodelTab').removeClass('tabStyleView'); } else { disableTab('biomodelTab', 'biomodels'); } </script> <table width="100%" style="margin-top:0px;"> <tr><td style="padding-top: 0px;"> <script type='text/javascript' src="dwr/interface/VendorDWR.js"></script> <script type='text/javascript' src="dwr/engine.js"></script> <script type='text/javascript' src="dwr/util.js"></script> <script type='text/javascript' src="javascripts/vendor.js"></script> <script type="text/javascript"> var clicked = 1; function zoomIn() { //max allowed... if (clicked === 8) return; clicked++; zoom(clicked) } function zoomOut() { if (clicked === 1) return; clicked--; zoom(clicked); } function resetZoom() { clicked = 2; zoomOut(); } function zoom(count) { var image = document.getElementById('strucImg'); var src = image.src; image.src = src.substring(0, src.indexOf('dimensions=')) + 'dimensions=' + (200 * count); if (count > 1) image.style.display = "block"; else image.style.display = "none"; } </script> <table class="small-boxed-section"> <tr><td> <a href="https://docs.google.com/document/d/1_w-DwBdCCOh1gMeeP6yqGzcnkpbHYOa3AGSODe5epcg/edit#heading=h.r6hsmvl4cdti" target="_blank" titleKey="compoundResult.link.title.help" class="no-underline"> <span class="icon icon-common icon-info helpinfo" style="float: right;"></span> </a> <div style="padding-left: 4px;"> <span class="zoomImg icon icon-common icon-search-plus" title="Zoom in" onclick="zoomIn()"></span> <span class="zoomImg icon icon-common icon-search-minus" title="Zoom out" style="margin-left: 30px;" onclick="zoomOut()"></span> <span class="zoomImg icon icon-common icon-redo" title="Reset zoom" style="margin-left: 60px" onclick="resetZoom()"></span> </div> <table style="width:100%; margin: 0"> <tr> <td class="gridLayoutCellStructure"> <img src="displayImage.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?defaultImage=true&imageIndex=0&chebiId=16335&dimensions=200" height="400" width="400" id="strucImg"> <img src="displayImage.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?defaultImage=true&imageIndex=0&chebiId=16335" class="margin-top:20px;"> </td> <td style="padding: 0"> <table width="100%" style="vertical-align:top; margin-top:5px; "> <tr> <td class="chebiDataHeader" style="width: 180px;"> ChEBI Name </td> <td><b>adenosine</b></td> </tr> <tr><td class="gap"></td></tr> <tr> <td class="chebiDataHeader" style="width: 180px;"> ChEBI ID </td> <td><b>CHEBI:16335</b></td> </tr> <tr><td class="gap"></td></tr> <tr> <td class="chebiDataHeader" style="width: 180px;"> Definition </td> <td>A ribonucleoside composed of a molecule of adenine attached to a ribofuranose moiety via a β‒N<small><sup>9</sup></small>-glycosidic bond.</td> </tr> <tr><td class="gap"></td></tr> <tr> <td class="chebiDataHeader" style="width: 180px;"> Stars </td> <td> <img src="images/goldenstar.gif"/><img src="images/goldenstar.gif"/><img src="images/goldenstar.gif"/> <span class="starsLabel">This entity has been manually annotated by the ChEBI Team.</span> </td> </tr> <tr><td class="gap"></td></tr> <tr> <td class="chebiDataHeader" style="width: 180px;"> Secondary ChEBI IDs </td> <td> CHEBI:2472, CHEBI:40558, CHEBI:40825, CHEBI:40906, CHEBI:40911, CHEBI:13734, CHEBI:22237 </td> </tr> <tr><td class="gap"></td></tr> <tr> <td class="chebiDataHeader" style="width: 180px;"> Supplier Information <span class="icon icon-common icon-basket helpinfo" style="float: right; opacity:0.5"/> </td> <td id="vendorId"> <script type ="text/javascript" > loadVendorInfo('OIRDTQYFTABQOQ-KQYNXXCUSA-N'); </script> </td> </tr> <tr><td class="gap"></td></tr> <tr> <td class="chebiDataHeader" style="width: 180px;"> Download <span class="icon icon-common icon-download helpinfo" style="float: right; opacity: 0.5"/> </td> <td> <a href="saveStructure.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?defaultImage=true&chebiId=16335&imageId=0" style="vertical-align: top" title="Save Molfile to disk">Molfile</a> <a href="saveStructure.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?xml=true&chebiId=16335&imageId=0" style="vertical-align: top" title="Save as XML">XML</a> <a href="saveStructure.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?sdf=true&chebiId=16335&imageId=0" style="vertical-align: top" title="Save as SDF">SDF</a> </td> </tr> </table> </td> </tr> <tr> <td colspan=2 valign="left" > <ul style="padding-left: 20px; margin: 0px; margin-bottom: 5px; align:left"> <form name="goToAdvancedSearch" action="advancedSearchForward.do" method="post"> <input type="hidden" name="structure" value="\ Marvin 04240612262D \ \ 19 21 0 0 1 0 999 V2000\ 0.9372 -0.2267 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0\ 0.9372 -1.0517 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\ 0.2227 -1.4642 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0\ 0.2226 -2.2892 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\ 0.9371 -2.7017 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0\ 1.6516 -2.2892 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\ 1.6516 -1.4642 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\ 2.4362 -1.2093 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0\ 2.9212 -1.8768 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\ 2.4362 -2.5442 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0\ 2.6912 -3.3290 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0\ 2.2062 -3.9963 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\ 2.6911 -4.6639 0.0000 C 0 0 2 0 0 0 0 0 0 0 0 0\ 2.4361 -5.4485 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0\ 2.9882 -6.0616 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\ 3.4757 -4.4089 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0\ 4.1432 -4.8939 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\ 3.4758 -3.5839 0.0000 C 0 0 1 0 0 0 0 0 0 0 0 0\ 4.1432 -3.0990 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0\ 1 2 1 0 0 0 0\ 2 3 1 0 0 0 0\ 2 7 2 0 0 0 0\ 3 4 2 0 0 0 0\ 4 5 1 0 0 0 0\ 5 6 2 0 0 0 0\ 6 7 1 0 0 0 0\ 6 10 1 0 0 0 0\ 7 8 1 0 0 0 0\ 8 9 2 0 0 0 0\ 9 10 1 0 0 0 0\ 11 10 1 1 0 0 0\ 11 12 1 0 0 0 0\ 11 18 1 0 0 0 0\ 12 13 1 0 0 0 0\ 13 14 1 1 0 0 0\ 13 16 1 0 0 0 0\ 14 15 1 0 0 0 0\ 16 17 1 6 0 0 0\ 16 18 1 0 0 0 0\ 18 19 1 6 0 0 0\ M END\ "/> <li><a href="advancedSearchFT.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=16335&structureSearchMethod=substructure" >Find compounds which contain this structure</a></li> <li><a href="advancedSearchFT.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=16335&structureSearchMethod=similarity">Find compounds which resemble this structure</a></li> <li><a href='javascript:$(goToAdvancedSearch).submit()'>Take structure to the Advanced Search</a></li> </form> </ul> <a id="structureImageGallery_more" href="javascript:fold('structureImageGallery', 'structureImageGallery_more', 'more structures >>','<< hide structures');" title="Expand to see more structures.">more structures >></a> </td> </tr> </table> </td></tr> <script type="text/javascript" src="javascripts/JSmol.min.js"></script> <script type="text/javascript"> var use = "HTML5"; jmol_isReady = function(applet) { document.title = (applet._id + " is ready") Jmol._getElement(applet, "appletdiv").style.border = "none"; } var Info = { width : 200, height : 200, color : "#000", serverURL : "http://chemapps.stolaf.edu/jmol/jsmol/php/jsmol.php", use : "HTML5", readyFunction : null, disableInitialConsole: true, disableJ2SLoadMonitor: true, bondWidth: 4, zoomScaling: 1.5, pinchScaling: 2.0, mouseDragFactor: 0.5, touchDragFactor: 0.15, multipleBondSpacing: 4, spinRateX: 0.2, spinRateY: 0.5, spinFPS: 20, spin:true, debug: false } var lastPrompt=0; function enlargeJsmol(id){ var style= document.getElementById('jmolApplet'+id+'_appletinfotablediv').style; if(style.width == '200px'){ style.height = '400px'; style.width = '400px'; document.getElementById('expand'+id).innerHTML ="reduce"; } else { style.height = '200px'; style.width = '200px'; document.getElementById('expand'+id).innerHTML ="expand"; } } </script> <tr><td> <div id="structureImageGallery" style="display: none;"> <div style="padding: 5px; 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var jmolApplet0; jmol = Jmol.getApplet("jmolApplet0", Info); var s = 'load inline "' + mol + '"; '; javascript: Jmol.script(jmolApplet0, s); </script> <div> <img src="/chebi/images/save_file.gif;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E" height="18" width="18" border="0" title="Save Molfile to disk" alt="Save molfile"> <a href="saveStructure.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?defaultImage=false&chebiId=16335&imageIndex=1&imageId=17090" title="Save Molfile to disk">Molfile</a> <a href="#" onclick="enlargeJsmol(0)" style="float:right;" id="expand0" >expand</a> </div> </div> </div> </td></tr> </table> <script type='text/javascript' src='/chebi/dwr/interface/WikipediaDWR.js;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E'></script> <script type='text/javascript' src='/chebi/javascripts/wikipedia.js;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E'></script> <div style="padding:5px"></div> <table class="chebiTableContent" > <tr> <td class="chebiDataHeader" style="width: 90%"> Wikipedia <a href="https://docs.google.com/document/d/1_w-DwBdCCOh1gMeeP6yqGzcnkpbHYOa3AGSODe5epcg/edit#heading=h.14609qwvoroj" target="_blank" class="no-underline" title="Please click here to get further information on Wikipedia"><span class="icon icon-common icon-info helpinfo"></span></a> </td> <td class="chebiDataHeader"> License <a href="http://en.wikipedia.org/wiki/Wikipedia:Text_of_the_GNU_Free_Documentation_License" target="_blank" class="no-underline"> <span class="icon icon-common icon-info helpinfo"></span> </a> </td> </tr> <tr> <td colspan="2" id="wikipediaId"> <img src="/chebi/images/wait_red_indicator.gif;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E" height="16px" width="16px" id="wikiWaitIndicator" alt="Waiting for wikipedia content"> <script type ="text/javascript" > loadWikiContent('Adenosine'); </script> </td> </tr> <tr><td> <a href="http://en.wikipedia.org/wiki/Adenosine" target="_blank">Read full article at Wikipedia</a> </td></tr> </table> <table class="small-boxed-section"><tr><td> <a href="https://docs.google.com/document/d/1_w-DwBdCCOh1gMeeP6yqGzcnkpbHYOa3AGSODe5epcg/edit#heading=h.c6nol7kqsqf9" target="_blank" class="no-underline" title="Please click here to get further information on Formulae"><span class="icon icon-common icon-info helpinfo" style="position: absolute; right: 20px;"></span></a> <table class="chebiTableContent" style="margin: 3px;"> <td class="chebiDataHeader" style="width: 150px; height: 15px;"> Formula </td> <td> C10H13N5O4<br/> </td> </table> <table class="chebiTableContent" style="margin: 3px;"> <tr> <td class="chebiDataHeader" style="width: 150px; height: 15px;"> Net Charge </td> <td> 0 </td> </tr> </table> <table class="chebiTableContent" style="margin: 3px;"> <tr> <td class="chebiDataHeader" style="width: 150px; height: 15px;"> Average Mass </td> <td> 267.24152 </td> </tr> </table> <table class="chebiTableContent" style="margin: 3px;"> <tr> <td class="chebiDataHeader" style="width: 150px; height: 15px;"> Monoisotopic Mass </td> <td> 267.09675 </td> </tr> </table> <table class="chebiTableContent" style="margin: 3px;"> <tr> <td class="chebiDataHeader" style="width: 150px; height: 15px;">InChI</td> <td>InChI=1S/C10H13N5O4/c11-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>8-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>5-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>9(13-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>2-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>12-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>8)<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>15(3-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>14-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>5)<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>10-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>7(18)<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>6(17)<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>4(1-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>16)<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>19-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>10/h2-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>4,6-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>7,10,16-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>18H,1H2,(H2,11,12,13)<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>/t4-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>,6-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>,7-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>,10-<img alt="" src="images/invisible_space.gif" width="0" height="0" border="0"/>/m1/s1</td> </tr> </table> <table class="chebiTableContent" style="margin: 3px;"> <tr> <td class="chebiDataHeader" style="width: 150px; height: 15px;">InChIKey</td> <td>OIRDTQYFTABQOQ-KQYNXXCUSA-N</td> </tr> </table> <table class="chebiTableContent" style="margin: 3px;"> <tr> <td class="chebiDataHeader" style="width: 150px; height: 15px;">SMILES</td> <td>Nc1ncnc2n(cnc12)[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O</td> </tr> </table> </td></tr></table> <div style="padding:5px"></div> <table class="chebiTableContent"> <tr> <td class="chebiDataHeader" width="30%" align="left"> Metabolite of Species <a href="https://docs.google.com/document/d/1_w-DwBdCCOh1gMeeP6yqGzcnkpbHYOa3AGSODe5epcg/edit#heading=h.q9ft3vb1a2cz" target="_blank" class="no-underline" title="Please click here to get further information on Metabolite of species"><span class="icon icon-common icon-info helpinfo"></span></a> </td> <td class="chebiDataHeader" width="70%" align="left">Details</td> </tr> <tr> <td class="chebiDataContent"> <i>Mus musculus</i> <a href="http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&id=txid10090" target="_blank">(NCBI:txid10090)</a> </td> <td class="chebiDataContent"> Source: BioModels - MODEL1507180067 See: <a href="//europepmc.org/abstract/MED/19425150" target="_blank">PubMed</a> </td> </tr> <tr> <td class="chebiDataContent"> <i>Chlamydomonas reinhardtii</i> <a href="http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&id=txid3055" target="_blank">(NCBI:txid3055)</a> </td> <td class="chebiDataContent"> See: <a href="//europepmc.org/abstract/MED/25515814" target="_blank">PubMed</a> </td> </tr> <tr> <td class="chebiDataContent"> <i>Daphnia magna</i> <a href="http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&id=txid35525" target="_blank">(NCBI:txid35525)</a> </td> <td class="chebiDataContent"> See: Mixtures of similarly acting compounds in Daphnia magna: From gene to metabolite and beyondTine Vandenbrouck, Oliver A.H. Jones, Nathalie Dom, Julian L. Griffin, Wim De CoenEnvironment International 36 (2010) 254-268 </td> </tr> <tr> <td class="chebiDataContent"> <i>Saccharomyces cerevisiae</i> <a href="http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&id=txid4932" target="_blank">(NCBI:txid4932)</a> </td> <td class="chebiDataContent"> Source: yeast.sf.net See: <a href="//europepmc.org/abstract/MED/24678285" target="_blank">PubMed</a> </td> </tr> <tr> <td class="chebiDataContent"> <i>Escherichia coli</i> <a href="http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&id=txid562" target="_blank">(NCBI:txid562)</a> </td> <td class="chebiDataContent"> See: <a href="//europepmc.org/abstract/MED/21988831" target="_blank">PubMed</a> </td> </tr> <tr> <td class="chebiDataContent"> <i>Cordyceps sinensis</i> <a href="http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&id=txid72228" target="_blank">(NCBI:txid72228)</a> </td> <td class="chebiDataContent"> Found in mycelium <a href="http://purl.obolibrary.org/obo/BTO_0001436" target="_blank">(BTO:0001436)</a>. Ethanolic extract of dried mycelia See: <a href="//europepmc.org/abstract/MED/21848266" target="_blank">PubMed</a> </td> </tr> <tr> <td class="chebiDataContent"> <i>Homo sapiens</i> <a href="http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&id=txid9606" target="_blank">(NCBI:txid9606)</a> </td> <td class="chebiDataContent"> See: <a href="//dx.doi.org/10.1038/nbt.2488" target="_blank">DOI</a> </td> </tr> </table> <div style="padding:5px"></div>   <table class="chebiTableContent"> <tr width="100%" height="15px"> <td class="chebiDataHeader" colspan="2"> Roles Classification <a href="https://docs.google.com/document/d/1_w-DwBdCCOh1gMeeP6yqGzcnkpbHYOa3AGSODe5epcg/edit#heading=h.r0vkewxosv0s" target="_blank" class="no-underline" title="Please click here to get further information on Roles Classification"><span class="icon icon-common icon-info helpinfo"></span></a> </td> </tr> <tr> <td class= "roleHeader"> <a href="chebiOntology.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI:24432" target="_blank">Biological Role</a>(s):</td> <td > <a href="/chebi/chebiOntology.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=35480">analgesic</a> <div class="roleDefinition">An agent capable of relieving pain without the loss of consciousness or without producing anaesthesia. In addition, analgesic is a role played by a compound which is exhibited by a capability to cause a reduction of pain symptoms.</div> <a href="/chebi/chebiOntology.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=77746">human metabolite</a> <div class="roleDefinition">Any mammalian metabolite produced during a metabolic reaction in humans (<ital>Homo sapiens</ital>).</div> <a href="/chebi/chebiOntology.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=78675">fundamental metabolite</a> <div class="roleDefinition">Any metabolite produced by all living cells.</div> </td> </tr> <tr><td style ="border-bottom :1px solid #999999;" colspan="2"></td></tr> <tr> <td class= "roleHeader"> <a href="chebiOntology.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI:33232" target="_blank">Application</a>(s):</td> <td > <a href="/chebi/chebiOntology.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=38070">anti-arrhythmia drug</a> <div class="roleDefinition">A drug used for the treatment or prevention of cardiac arrhythmias. Anti-arrhythmia drugs may affect the polarisation-repolarisation phase of the action potential, its excitability or refractoriness, or impulse conduction or membrane responsiveness within cardiac fibres.</div> <a href="/chebi/chebiOntology.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=35620">vasodilator agent</a> <div class="roleDefinition">A drug used to cause dilation of the blood vessels.</div> <a href="/chebi/chebiOntology.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=35480">analgesic</a> <div class="roleDefinition">An agent capable of relieving pain without the loss of consciousness or without producing anaesthesia. In addition, analgesic is a role played by a compound which is exhibited by a capability to cause a reduction of pain symptoms.</div> </td> </tr> <tr><td style ="border-bottom :1px solid #999999;" colspan="2"></td></tr> </table> <a href="chebiOntology.do?chebiId=CHEBI:16335" style="margin-left: 13px;">View more via ChEBI Ontology</a>  <table width="100%"> <tr> <a name="termLineage" class="anchoredHighInfo"> <td class="chebiDataHeader" align="left" colspan="2" width="200"> ChEBI Ontology <a href="https://docs.google.com/document/d/1_w-DwBdCCOh1gMeeP6yqGzcnkpbHYOa3AGSODe5epcg/edit#heading=h.udsjepca86vc" target="_blank" class="no-underline" title="Please click here to get further information on the ChEBI Ontology"><span class="icon icon-common icon-info helpinfo"></span></a> </td> </a> </tr> <tr> <td width="110px"> Outgoing </td> <td > adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>) <font style="font-weight:bold;"> has functional parent </font> adenine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16708">CHEBI:16708</a>) <br/> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>) <font style="font-weight:bold;"> has role </font> analgesic (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A35480">CHEBI:35480</a>) <br/> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>) <font style="font-weight:bold;"> has role </font> anti-arrhythmia drug (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A38070">CHEBI:38070</a>) <br/> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>) <font style="font-weight:bold;"> has role </font> fundamental metabolite (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A78675">CHEBI:78675</a>) <br/> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>) <font style="font-weight:bold;"> has role </font> human metabolite (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A77746">CHEBI:77746</a>) <br/> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>) <font style="font-weight:bold;"> has role </font> vasodilator agent (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A35620">CHEBI:35620</a>) <br/> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>) <font style="font-weight:bold;"> is a </font> adenosines (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A22260">CHEBI:22260</a>) <br/> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>) <font style="font-weight:bold;"> is a </font> purines <small>D</small>-ribonucleoside (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A142355">CHEBI:142355</a>) <br/> </td> </tr> <tr><td style ="border-bottom :1px solid #999999;" colspan="2"></td></tr> <tr> <td width="110px"> Incoming </td> <td > α-<i>N</i>-(9-β-<small>D</small>-ribofuranosylpurin-6-yl)glycinamide (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A77005">CHEBI:77005</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> (−)-<i>N</i><small><sup>6</sup></small>-(2-phenylisopropyl)adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A192091">CHEBI:192091</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> 1-methyladenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16020">CHEBI:16020</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> 1-tuberculosinyladenosine(1+) (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A85603">CHEBI:85603</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> 2-methylthio-<i>N</i><small><sup>6</sup></small>-(Δ<small><sup>2</sup></small>-isopentenyl)adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A62875">CHEBI:62875</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> 2-methylthio-<i>N</i><small><sup>6</sup></small>-(<i>cis</i>-4-hydroxy-Δ<small><sup>2</sup></small>-isopentenyl)adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A62879">CHEBI:62879</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> 2-thio-<i>N</i><small><sup>6</sup></small>-(Δ<small><sup>2</sup></small>-isopentenyl)adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A73551">CHEBI:73551</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> 3'-<i>O</i>-salicyl-AMP (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A60351">CHEBI:60351</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> 3'-phosphoadenylyl selenate (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A28450">CHEBI:28450</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> 3-iodo-4-aminobenzyl-5'-<i>N</i>-methylcarboxamidoadenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A73285">CHEBI:73285</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> 3-iodobenzyl-5'-<i>N</i>-methylcarboxamidoadenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A73286">CHEBI:73286</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> 5'-<i>O</i>-sulfamoyladenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A43716">CHEBI:43716</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> 5'-<i>S</i>-methyl-5'-thioadenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A17509">CHEBI:17509</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> 5'-chloro-5'-deoxyadenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A47133">CHEBI:47133</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> 5'-deoxyadenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A17319">CHEBI:17319</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> 5'-ethylthioadenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A74046">CHEBI:74046</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> 9-ribosyl-<i>trans</i>-zeatin (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A71693">CHEBI:71693</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> <i>N</i>-[(9-β-<small>D</small>-ribofuranosyl-2-methylthiopurin-6-yl)carbamoyl]threonine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A21457">CHEBI:21457</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> <i>N</i>-[(9-β-<small>D</small>-ribofuranosylpurin-6-yl)carbamoyl]threonine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A21440">CHEBI:21440</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> <i>N</i>-ethyl-5'-carboxamidoadenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A73284">CHEBI:73284</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> <i>N</i><small><sup>6</sup></small>,2'-<i>O</i>-dimethyladenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A229469">CHEBI:229469</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> <i>N</i><small><sup>6</sup></small>,<i>N</i><small><sup>6</sup></small>-dimethyladenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A28284">CHEBI:28284</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> <i>N</i><small><sup>6</sup></small>-(Δ<small><sup>2</sup></small>-isopentenyl)adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A62881">CHEBI:62881</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> <small>L</small>-adenosylselenohomocysteine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A77028">CHEBI:77028</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> adenosine phosphate (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A22256">CHEBI:22256</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> adenylyl selenate (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A2485">CHEBI:2485</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> aspartyl adenylate β-ketophosphonate isostere (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A74089">CHEBI:74089</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> CGS-21680 (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A73283">CHEBI:73283</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> cordysinin B (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A69426">CHEBI:69426</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> diadenosyl diphosphate (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A64369">CHEBI:64369</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> diadenosyl hexaphosphate (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A63736">CHEBI:63736</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> diadenosyl pentaphosphate (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A63737">CHEBI:63737</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> diadenosyl tetraphosphate (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A63738">CHEBI:63738</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> diadenosyl triphosphate (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A63739">CHEBI:63739</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> nucleocidin (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A166872">CHEBI:166872</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> propionyl adenylate (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A74517">CHEBI:74517</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> sangivamycin (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A85997">CHEBI:85997</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> succinyladenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A71169">CHEBI:71169</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> thioadenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A26953">CHEBI:26953</a>) <font style="font-weight:bold;"> has functional parent </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> adenosine residue (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A62885">CHEBI:62885</a>) <font style="font-weight:bold;"> is substituent group from </font> adenosine (<a href="/chebi/searchId.do;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E?chebiId=CHEBI%3A16335">CHEBI:16335</a>)<br/> </td> </tr> </table> <div style="padding:5px"></div>  <table class="chebiTableContent" > <tr> <td class="chebiDataHeader" width="100%" align="left"> IUPAC Name <a href="https://docs.google.com/document/d/1_w-DwBdCCOh1gMeeP6yqGzcnkpbHYOa3AGSODe5epcg/edit#heading=h.w9s830q3ije3" target="_blank" class="no-underline" title="Please click here to get further information on IUPAC Names"><span class="icon icon-common icon-info helpinfo"></span></a> </td> </tr> <tr> <td class="chebiDataContent" > adenosine </td> </tr> </table> <div style="padding:5px"></div>  <table class="chebiTableContent" > <tr> <td class="chebiDataHeader" width="80%" align="left"> Synonyms <a href="https://docs.google.com/document/d/1_w-DwBdCCOh1gMeeP6yqGzcnkpbHYOa3AGSODe5epcg/edit#heading=h.b2rxgvwlpfxt" target="_blank" class="no-underline" title="Please click here to get further information on synonyms"><span class="icon icon-common icon-info helpinfo"></span></a> </td> <td class="chebiDataHeader" width="20%" align="left"> Sources </td> </tr> <tr> <td class="chebiDataContent" > (2<i>R</i>,3<i>R</i>,4<i>S</i>,5<i>R</i>)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol </td> <td class="chebiDataContent" > DrugBank </td> </tr> <tr> <td class="chebiDataContent" > 6-Amino-9-beta-D-ribofuranosyl-9H-purine </td> <td class="chebiDataContent" > ChemIDplus </td> </tr> <tr> <td class="chebiDataContent" > 9-beta-D-Ribofuranosidoadenine </td> <td class="chebiDataContent" > ChemIDplus </td> </tr> <tr> <td class="chebiDataContent" > 9-β-<small>D</small>-ribofuranosyl-9<i>H</i>-purin-6-amine </td> <td class="chebiDataContent" > ChEBI </td> </tr> <tr> <td class="chebiDataContent" > 9-beta-D-Ribofuranosyl-9H-purin-6-amine </td> <td class="chebiDataContent" > ChemIDplus </td> </tr> <tr> <td class="chebiDataContent" > 9-β-<small>D</small>-ribofuranosyladenine </td> <td class="chebiDataContent" > HMDB </td> </tr> <tr> <td class="chebiDataContent" > Ade-Rib </td> <td class="chebiDataContent" > CBN </td> </tr> <tr> <td class="chebiDataContent" > adenine riboside </td> <td class="chebiDataContent" > HMDB </td> </tr> <tr> <td class="chebiDataContent" > Adenosin </td> <td class="chebiDataContent" > ChEBI </td> </tr> <tr> <td class="chebiDataContent" > ADENOSINE </td> <td class="chebiDataContent" > PDBeChem </td> </tr> <tr> <td class="chebiDataContent" > Adenosine </td> <td class="chebiDataContent" > KEGG COMPOUND </td> </tr> <tr> <td class="chebiDataContent" > adenosine </td> <td class="chebiDataContent" > <a href="http://www.uniprot.org/uniprot/?query="adenosine"&sort=score" target="_blank"> UniProt </a> </td> </tr> <tr> <td class="chebiDataContent" > Ado </td> <td class="chebiDataContent" > CBN </td> </tr> <tr> <td class="chebiDataContent" > β-<small>D</small>-adenosine </td> <td class="chebiDataContent" > ChemIDplus </td> </tr> </table> <div style="padding:5px"></div> <table class="chebiTableContent" > <tr> <td class="chebiDataHeader" width="80%" align="left"> Brand Names <a href="https://docs.google.com/document/d/1_w-DwBdCCOh1gMeeP6yqGzcnkpbHYOa3AGSODe5epcg/edit#heading=h.e7as0c2lypko" target="_blank" class="no-underline" title="Please click here to get further information on Brand Names"><span class="icon icon-common icon-info helpinfo"></span></a> </td> <td class="chebiDataHeader" width="20%" align="left"> Sources </td> </tr> <tr > <td class="chebiDataContent" > Adenocard </td> <td class="chebiDataContent"> DrugBank </td> </tr> <tr > <td class="chebiDataContent" > Adenocor </td> <td class="chebiDataContent"> DrugBank </td> </tr> <tr > <td class="chebiDataContent" > Adenoscan </td> <td class="chebiDataContent"> DrugBank </td> </tr> </table> <div style="padding:5px"></div> <table class="chebiTableContent"> <tr> <td class="chebiDataHeader" width="80%" align="left"> Manual Xrefs <a href="https://docs.google.com/document/d/1_w-DwBdCCOh1gMeeP6yqGzcnkpbHYOa3AGSODe5epcg/edit#heading=h.9zlqnai7mu5k" target="_blank" class="no-underline" title="Please click here to get further information on Database Links"><span class="icon icon-common icon-info helpinfo"></span></a> </td> <td class="chebiDataHeader" width="20%" align="left"> Databases </td> </tr> <tr> <td class="chebiDataContent" > <a href="http://drugcentral.org/drugcard/90/view" target="_blank">90</a> </td> <td class="chebiDataContent" > DrugCentral  </td> </tr> <tr> <td class="chebiDataContent" > <a href="http://en.wikipedia.org/wiki/Adenosine" target="_blank">Adenosine</a> </td> <td class="chebiDataContent" > Wikipedia  </td> </tr> <tr> <td class="chebiDataContent" > <a href="http://biocyc.org/META/NEW-IMAGE?type=NIL&object=ADENOSINE&redirect=T" target="_blank">ADENOSINE</a> </td> <td class="chebiDataContent" > MetaCyc  </td> </tr> <tr> <td class="chebiDataContent" > <a href="https://www.ebi.ac.uk/pdbe-srv/pdbechem/chemicalCompound/show/ADN" target="_blank">ADN</a> </td> <td class="chebiDataContent" > PDBeChem  </td> </tr> <tr> <td class="chebiDataContent" > <a href="https://www.ebi.ac.uk/pdbe-srv/pdbechem/chemicalCompound/show/ArF00" target="_blank">ArF00</a> </td> <td class="chebiDataContent" > PDBeChem  </td> </tr> <tr> <td class="chebiDataContent" > <a href="https://www.ebi.ac.uk/pdbe-srv/pdbechem/chemicalCompound/show/ArS00" target="_blank">ArS00</a> </td> <td class="chebiDataContent" > PDBeChem  </td> </tr> <tr> <td class="chebiDataContent" > <a href="http://www.knapsackfamily.com/knapsack_core/information.php?sname=C_ID&word=C00007444" target="_blank">C00007444</a> </td> <td class="chebiDataContent" > KNApSAcK  </td> </tr> <tr> <td class="chebiDataContent" > <a href="http://www.genome.ad.jp/dbget-bin/www_bget?cpd:C00212" target="_blank">C00212</a> </td> <td class="chebiDataContent" > KEGG COMPOUND  </td> </tr> <tr> <td class="chebiDataContent" > <a href="http://www.genome.ad.jp/dbget-bin/www_bget?drug:D00045" target="_blank">D00045</a> </td> <td class="chebiDataContent" > KEGG DRUG  </td> </tr> <tr> <td class="chebiDataContent" > <a href="http://www.drugbank.ca/cgi-bin/getCard.cgi?CARD=DB00640" target="_blank">DB00640</a> </td> <td class="chebiDataContent" > DrugBank  </td> </tr> <tr> <td class="chebiDataContent" > <a href="http://www.ecmdb.ca/compounds/ECMDB00050?" target="_blank">ECMDB00050</a> </td> <td class="chebiDataContent" > ECMDB  </td> </tr> <tr> <td class="chebiDataContent" > <a href="http://www.hmdb.ca/metabolites/HMDB0000050" target="_blank">HMDB0000050</a> </td> <td class="chebiDataContent" > HMDB  </td> </tr> <tr> <td class="chebiDataContent" > <a href="http://lincsportal.ccs.miami.edu/SmallMolecules/view/LSM-28568" target="_blank">LSM-28568</a> </td> <td class="chebiDataContent" > LINCS  </td> </tr> <tr> <td class="chebiDataContent" > <a href="http://www.ymdb.ca/compounds/YMDB00058?" target="_blank">YMDB00058</a> </td> <td class="chebiDataContent" > YMDB  </td> </tr> <tr> <td><a target="_blank" href="displayAutoXrefs.do?chebiId=CHEBI:16335">View more database links</a></td> </tr> </table> <div style="padding:5px"></div> <table class="chebiTableContent" > <tr> <td class="chebiDataHeader" width="30%" align="left"> Registry Numbers <a href="https://docs.google.com/document/d/1_w-DwBdCCOh1gMeeP6yqGzcnkpbHYOa3AGSODe5epcg/edit#heading=h.jyjwjdev8xw" target="_blank" class="no-underline" title="Please click here to get further information on Registry Numbers"><span class="icon icon-common icon-info helpinfo"></span></a> </td> <td class="chebiDataHeader" width="40%" align="left"> Types </td> <td class="chebiDataHeader" width="30%" align="left"> Sources </td> </tr> <tr> <td class="chebiDataContent" > 53385 </td> <td class="chebiDataContent"> Gmelin Registry Number </td> <td class="chebiDataContent" > Gmelin </td> </tr> <tr> <td class="chebiDataContent" > 58-61-7 </td> <td class="chebiDataContent"> CAS Registry Number </td> <td class="chebiDataContent" > KEGG COMPOUND </td> </tr> <tr> <td class="chebiDataContent" > <a href="https://chem.nlm.nih.gov/chemidplus/rn/58-61-7" target="_blank">58-61-7</a> </td> <td class="chebiDataContent"> CAS Registry Number </td> <td class="chebiDataContent" > ChemIDplus </td> </tr> <tr> <td class="chebiDataContent" > <a href="http://webbook.nist.gov/cgi/cbook.cgi?ID=58-61-7" target="_blank">58-61-7</a> </td> <td class="chebiDataContent"> CAS Registry Number </td> <td class="chebiDataContent" > NIST Chemistry WebBook </td> </tr> <tr> <td class="chebiDataContent" > 93029 </td> <td class="chebiDataContent"> Reaxys Registry Number </td> <td class="chebiDataContent" > Reaxys </td> </tr> </table> <div style="padding:5px"></div> <script type='text/javascript' src='/chebi/dwr/interface/CitationDWR.js;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E'></script>  <script type='text/javascript' src='/chebi/javascripts/citations.js;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E'></script> <table class="chebiTableContent"> <tr id="citationHeader"> <td class="chebiDataHeader" width="30%" align="left"> Citations <a href="https://docs.google.com/document/d/1_w-DwBdCCOh1gMeeP6yqGzcnkpbHYOa3AGSODe5epcg/edit#heading=h.qcvldn6t3ojb" target="_blank" class="no-underline" title="Please click here to get further information on Citations"><span class="icon icon-common icon-info helpinfo"></span></a> <img src="/chebi/images/wait_red_indicator.gif;jsessionid=DBBF37C2330F6F95796EC8A6B84EF69E" height="16px" width="16px" id="citationWait" alt="Waiting for Citations"> </td> <td class="chebiDataHeader" width="40%" align="left"> Types </td> <td class="chebiDataHeader" width="30%" align="left"> Sources </td> </tr> <tbody id="citations"> <tr> <td class="chebiDataContent"> 11213237 </td> <td class="chebiDataContent"> PubMed citation </td> <td class="chebiDataContent"> Europe PMC </td> </tr> <script>dbCitations.push(new dbCitation("11213237","PubMed citation","Europe PMC"));</script> <tr> <td class="chebiDataContent"> 11820865 </td> <td class="chebiDataContent"> PubMed citation </td> <td class="chebiDataContent"> 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Europe PMC </td> </tr> <script>dbCitations.push(new dbCitation("17190852","PubMed citation","Europe PMC"));</script> <tr> <td class="chebiDataContent"> 18000974 </td> <td class="chebiDataContent"> PubMed citation </td> <td class="chebiDataContent"> Europe PMC </td> </tr> <script>dbCitations.push(new dbCitation("18000974","PubMed citation","Europe PMC"));</script> <tr> <td class="chebiDataContent"> 323854 </td> <td class="chebiDataContent"> PubMed citation </td> <td class="chebiDataContent"> Europe PMC </td> </tr> <script>dbCitations.push(new dbCitation("323854","PubMed citation","Europe PMC"));</script> </tbody> </table> <script>testCitationConnection();</script> <div style="padding:5px"></div> <table class="chebiTableContent"> <tr> <td class="chebiDataHeader"> Last Modified <a href="https://docs.google.com/document/d/1_w-DwBdCCOh1gMeeP6yqGzcnkpbHYOa3AGSODe5epcg/edit#heading=h.fkjgfwxjxa8w" target="_blank" titleKey="structure.link.title.lastmodified" class="no-underline"> <span 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adenosine (CHEBI:16335)