https://lipidbank.jp/mediawiki/index.php?action=history&feed=atom&title=LBF20207PG76 2026-04-30T19:09:38Z Revision history for this page on the wiki MediaWiki 1.43.0 https://lipidbank.jp/mediawiki/index.php?title=LBF20207PG76&diff=53149&oldid=prev 2010-10-21T08:49:02Z

<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 17:49, 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=XPR8051</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=XPR8051</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=LMFA03010097</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=LMFA03010097</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=(8R,9S,11R,12R,15S) -11<del style="font-weight: bold; text-decoration: none;">,18</del>-<del style="font-weight: bold; text-decoration: none;">Diacetoxy</del>-9,15-dihydroxyprost- (cis-5,trans-13) -dienoic 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=<ins style="font-weight: bold; text-decoration: none;">Methyl- </ins>(8R,9S,11R,12R,15S) -11-<ins style="font-weight: bold; text-decoration: none;">Acetoxy</ins>-9,15-dihydroxyprost- (cis-5,trans-13) -dienoic 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;Prostaglandin F_2 alpha-11-acetate methyl ester&amp;&amp;Methyl- (8R,9S,11R,12R,15S) -11-Acetoxy-9,15-dihydroxyprost- (5Z,13E) -dienoic 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;Prostaglandin F_2 alpha-11-acetate methyl ester&amp;&amp;Methyl- (8R,9S,11R,12R,15S) -11-Acetoxy-9,15-dihydroxyprost- (5Z,13E) -dienoic 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>|Melting Point=55°(hexane)[[Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875|{{RelationTable/GetFirstAuthor|Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875}}]]</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>|Melting Point=55°(hexane)[[Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875|{{RelationTable/GetFirstAuthor|Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875}}]]</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-53148:rev-53149:php=table --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20207PG76&diff=53148&oldid=prev 2010-10-21T08:48:26Z

<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 17:48, 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=XPR8051</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=XPR8051</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=LMFA03010097</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=LMFA03010097</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=<del style="font-weight: bold; text-decoration: none;">Methyl- </del>(8R,9S,11R,12R,15S) -11-<del style="font-weight: bold; text-decoration: none;">Acetoxy</del>-9,15-dihydroxyprost- (5-<del style="font-weight: bold; text-decoration: none;">cis,</del>13<del style="font-weight: bold; text-decoration: none;">-trans</del>) -dienoic acid|Common Name=&amp;&amp;Prostaglandin F_2 alpha-11-acetate methyl ester&amp;&amp;Methyl- (8R,9S,11R,12R,15S) -11-Acetoxy-9,15-dihydroxyprost- (5Z,13E) -dienoic acid&amp;&amp;</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=(8R,9S,11R,12R,15S) -11<ins style="font-weight: bold; text-decoration: none;">,18</ins>-<ins style="font-weight: bold; text-decoration: none;">Diacetoxy</ins>-9,15-dihydroxyprost- (<ins style="font-weight: bold; text-decoration: none;">cis-</ins>5<ins style="font-weight: bold; text-decoration: none;">,trans</ins>-13) -dienoic acid</div></td></tr> <tr><td colspan="2" class="diff-side-deleted"></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>|Common Name=&amp;&amp;Prostaglandin F_2 alpha-11-acetate methyl ester&amp;&amp;Methyl- (8R,9S,11R,12R,15S) -11-Acetoxy-9,15-dihydroxyprost- (5Z,13E) -dienoic 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>|Melting Point=55°(hexane)[[Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875|{{RelationTable/GetFirstAuthor|Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875}}]]</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>|Melting Point=55°(hexane)[[Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875|{{RelationTable/GetFirstAuthor|Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875}}]]</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>|Mass Spectra=CIMS m/z 411 ([M^+ +1], 1), 392(7), 350(6), 332(98),314(100),288(2),282(15). [[Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875|{{RelationTable/GetFirstAuthor|Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875}}]]</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>|Mass Spectra=CIMS m/z 411 ([M^+ +1], 1), 392(7), 350(6), 332(98),314(100),288(2),282(15). [[Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875|{{RelationTable/GetFirstAuthor|Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875}}]]</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-53147:rev-53148:php=table --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20207PG76&diff=53147&oldid=prev 2010-09-16T02:26:01Z

<p>New page: {{Lipid/Header}} {{Hierarchy|{{PAGENAME}}}} {{Metabolite |LipidBank=XPR8051 |LipidMaps=LMFA03010097 |SysName=Methyl- (8R,9S,11R,12R,15S) -11-Acetoxy-9,15-dihydroxyprost- (5-cis,13-trans)...</p> <p><b>New page</b></p><div>{{Lipid/Header}}<br /> <br /> {{Hierarchy|{{PAGENAME}}}}<br /> <br /> {{Metabolite<br /> |LipidBank=XPR8051<br /> |LipidMaps=LMFA03010097<br /> |SysName=Methyl- (8R,9S,11R,12R,15S) -11-Acetoxy-9,15-dihydroxyprost- (5-cis,13-trans) -dienoic acid|Common Name=&amp;&amp;Prostaglandin F_2 alpha-11-acetate methyl ester&amp;&amp;Methyl- (8R,9S,11R,12R,15S) -11-Acetoxy-9,15-dihydroxyprost- (5Z,13E) -dienoic acid&amp;&amp;<br /> |Melting Point=55°(hexane)[[Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875|{{RelationTable/GetFirstAuthor|Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875}}]]<br /> |Mass Spectra=CIMS m/z 411 ([M^+ +1], 1), 392(7), 350(6), 332(98),314(100),288(2),282(15). [[Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875|{{RelationTable/GetFirstAuthor|Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875}}]]<br /> |IR Spectra= nu ^{KBr}_{max}3700, 3610, 3510, 1740, 1730, and 970 cm^{-1}[[Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875|{{RelationTable/GetFirstAuthor|Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875}}]]<br /> |NMR Spectra=^1 H-NMR(270MHz,CDCl_3 ) delta ppm0.88(3H,t,J=6.0Hz),1.26(6H,brs),2.04(3H,s),2.32(2H,t,J=7.2Hz),2.39(1H,ddd,J=15.2,9.0,5.4Hz),2.55(1H,ddd,J=11.8,8.4,7.0Hz),3.67(3H,s),4.08(1H,q,J=6.1Hz),4.17(1H,dd,J=5.4,3.5Hz),4.90(1H,ddd,J=9.0,7.0,3.8Hz),5.41(2H,m),5.53(1H,m),5.55(1H,m).[[Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875|{{RelationTable/GetFirstAuthor|Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875}}]]<br /> |Source=Prostaglandin F_2 alpha -11-acetate methyl ester was isolated from soft coral, Lobophyton depressum.[[Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875|{{RelationTable/GetFirstAuthor|Reference:Carmely_S:Kashman_Y:Loya_Y:Benayahu_Y:,Tetrahedron Lett.,1980,21,875}}]]<br /> |Chemical Synthesis=<br /> |Metabolism=<br /> }}<br /> <br /> {{Lipid/Footer}}</div>

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