https://lipidbank.jp/mediawiki/index.php?action=history&feed=atom&title=LBF20107PG24 2026-04-30T16:16:26Z Revision history for this page on the wiki MediaWiki 1.43.0 https://lipidbank.jp/mediawiki/index.php?title=LBF20107PG24&diff=51947&oldid=prev 2010-10-21T08:16:58Z

<p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 17:16, 21 October 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l6">Line 6:</td> <td colspan="2" class="diff-lineno">Line 6:</td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=XPR1739</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=XPR1739</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidMaps=LMFA03010057</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidMaps=LMFA03010057</div></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|SysName= 9-Oxo- (11alpha,15R) -dihydroxy-16,16-dimethyl-prost-13<del style="font-weight: bold; text-decoration: none;">-trans</del>-en-1-oic acid</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|SysName=9-Oxo- (11alpha,15R) -dihydroxy-16,16-dimethyl-prost<ins style="font-weight: bold; text-decoration: none;">-trans</ins>-13-en-1-oic acid</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&amp;&amp;16,16-dimethyl Prostaglandin E_1&amp;&amp;9-Oxo- (11alpha,15R) -dihydroxy-16,16-dimethyl-prost-13(E)-en-1-oic acid&amp;&amp;</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&amp;&amp;16,16-dimethyl Prostaglandin E_1&amp;&amp;9-Oxo- (11alpha,15R) -dihydroxy-16,16-dimethyl-prost-13(E)-en-1-oic acid&amp;&amp;</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td></tr> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20107PG24&diff=51946&oldid=prev 2010-09-15T08:32:46Z

<p>New page: {{Lipid/Header}} {{Hierarchy|{{PAGENAME}}}} {{Metabolite |LipidBank=XPR1739 |LipidMaps=LMFA03010057 |SysName= 9-Oxo- (11alpha,15R) -dihydroxy-16,16-dimethyl-prost-13-trans-en-1-oic acid ...</p> <p><b>New page</b></p><div>{{Lipid/Header}}<br /> <br /> {{Hierarchy|{{PAGENAME}}}}<br /> <br /> {{Metabolite<br /> |LipidBank=XPR1739<br /> |LipidMaps=LMFA03010057<br /> |SysName= 9-Oxo- (11alpha,15R) -dihydroxy-16,16-dimethyl-prost-13-trans-en-1-oic acid<br /> |Common Name=&amp;&amp;16,16-dimethyl Prostaglandin E_1&amp;&amp;9-Oxo- (11alpha,15R) -dihydroxy-16,16-dimethyl-prost-13(E)-en-1-oic acid&amp;&amp;<br /> |Source=<br /> |Chemical Synthesis=<br /> |Metabolism=<br /> |Biological Activity= 16,16-dimethyl Prostaglandin E1 shows vascular constriction in human.[[Reference:Karim_SM:Adaikan_PG:Kottegoda_SR:,Adv. Prostaglandin Thromboxane Leukot. Res.,1980,7,969|{{RelationTable/GetFirstAuthor|Reference:Karim_SM:Adaikan_PG:Kottegoda_SR:,Adv. Prostaglandin Thromboxane Leukot. Res.,1980,7,969}}]] 16,16-dimethyl Prostaglandin E1 inhibited electrically evoked [3H]norepinephrine (NE) overflow from the isolated, superfused rabbit iris-ciliary body without affecting basal tritium efflux.[[Reference:Ohia_SE:Jumblatt_JE:,J. Pharmacol. Exp. Ther.,1990,255,11|{{RelationTable/GetFirstAuthor|Reference:Ohia_SE:Jumblatt_JE:,J. Pharmacol. Exp. Ther.,1990,255,11}}]]<br /> }}<br /> <br /> {{Lipid/Footer}}</div>

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