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EAWAG-BBD: reaction, reacID# r0667
<html><head> <title> EAWAG-BBD: reaction, reacID# r0667 </title> <!-- Piwik --> <script type="text/javascript"> var _paq = _paq || []; /* tracker methods like "setCustomDimension" should be called before "trackPageView" */ _paq.push(["setDocumentTitle", document.domain + "/" + document.title]); _paq.push(["setCookieDomain", "*.eawag-bbd.ethz.ch"]); _paq.push(['trackPageView']); _paq.push(['enableLinkTracking']); (function() { var u="//piwik.envipath.com/"; _paq.push(['setTrackerUrl', u+'piwik.php']); _paq.push(['setSiteId', '2']); var d=document, g=d.createElement('script'), s=d.getElementsByTagName('script')[0]; g.type='text/javascript'; g.async=true; g.defer=true; g.src=u+'piwik.js'; s.parentNode.insertBefore(g,s); })(); </script> <!-- End Piwik Code --> </head><body bgcolor="ffffff"> <h1>From 2-Hydroxy-1,4-benzoquinone to 1,2,4-Benzenetriol</h1> <dl> <dt><a href="http://eawag-bbd.ethz.ch/core/graphics/r0667.gif">Graphic</a> of the reaction.<p> <dt><a href="http://www.ncbi.nlm.nih.gov:80/pubmed/9721310">Medline reference</a> <dd> Zaborina O, Daubaras DL, Zago A, Xun L, Saido K, Klem T, Nikolic D, Chakrabarty AM. <i>J Bacteriol</i> (1998) <B>180</B>(17): 4667-75. <p> <dt><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=search&db=PubMed&term=hydroxybenzoquinone+AND+reductase">Search</a> Medline for <b> hydroxybenzoquinone reductase</b>. <dd>4 citations on March 09, 2012. <p><dt> </dl> <pre> <a href="/servlets/pageservlet?ptype=c&compID=c0598">2-Hydroxy-1,4-benzoquinone</a> | | NADH + H<sup>+</sup> hydroxybenzoquinone | / reductase |/ <a href="/servlets/pageservlet?ptype=ep&enzymeID=e0424">1.6.5.7</a> | <a href="http://www.genome.ad.jp/dbget-bin/www_bget?ec:1.6.5.7">Kyoto</a> |\ <a href="http://enzyme.expasy.org/EC/1.6.5.7">ExPASy</a> | \ | NAD<sup>+</sup> v <a href="/servlets/pageservlet?ptype=c&compID=c0264">1,2,4-Benzenetriol</a> </pre> <a href="http://eawag-bbd.ethz.ch/servlets/dpage?ptype=p&reacID=r0667&max_rows=0&smpth=false">Display a pathway</a> starting from this reaction. </ul> <p> </ul> <dl> <dt>EAWAG-BBD Biotransformation rules in accord with this reaction:</dt> <dd> <a href="http://eawag-bbd.ethz.ch/servlets/rule.jsp?rule=bt0107">1,4-Benzoquinone derivative -----> 1,4-Dihydroxybenzenoid (bt0107)</a><br> </dl> <hr><center> <b> [<a href="http://eawag-bbd.ethz.ch/2,4,5-t/2,4,5-t_map.html">2,4,5-Trichlorophenoxyacetic Acid</a>] [<a href="http://eawag-bbd.ethz.ch">BBD Main Menu</a>] </b> </center> <p> Page Author(s): Jiangbi Liu and Prasad Kotharu <br> August 14, 2005 <a href="/contact.html">Contact Us</a> <p><em>This is the EAWAG-BBD reaction, <b>reacID# r0667</b>.<br> It was generated on February 17, 2025 at 1:23:56 PM CST.</em> <pre>© 2025, EAWAG.</pre> </body> </html>