https://lipidbank.jp/mediawiki/index.php?action=history&feed=atom&title=LBF20306HX03 LBF20306HX03 - Revision history 2026-04-30T18:11:19Z Revision history for this page on the wiki MediaWiki 1.43.0 https://lipidbank.jp/mediawiki/index.php?title=LBF20306HX03&diff=53719&oldid=prev Editor at 05:22, 9 November 2010 2010-11-09T05:22:09Z <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 14:22, 9 November 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=XPR5001</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=XPR5001</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=LMFA03090005</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=LMFA03090005</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=8-Hydroxy- (11S,12S)-epoxy- (cis-5,trans-9,<del style="font-weight: bold; text-decoration: none;">14cis</del>) -eicosatrienoic 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=8-Hydroxy- (11S,12S)-epoxy- (cis-5,trans-9,<ins style="font-weight: bold; text-decoration: none;">cis-14</ins>) -eicosatrienoic 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;Hepoxilin A_3&amp;&amp;8-Hydroxy- (11S,12S)-epoxy- (5Z,9E,14Z) -eicosatrienoic acid&amp;&amp;8-Hydroxy-11,12 (S,S) -epoxyeicosa-5,14 (Z,Z) ,9 (E) -trienoic 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;Hepoxilin A_3&amp;&amp;8-Hydroxy- (11S,12S)-epoxy- (5Z,9E,14Z) -eicosatrienoic acid&amp;&amp;8-Hydroxy-11,12 (S,S) -epoxyeicosa-5,14 (Z,Z) ,9 (E) -trienoic 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>|Solubility=DIETHYL ETHER [[Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79}}]]</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>|Solubility=DIETHYL ETHER [[Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79}}]]</div></td></tr> </table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20306HX03&diff=53718&oldid=prev Editor at 07:41, 21 October 2010 2010-10-21T07:41:33Z <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 16:41, 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=XPR5001</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=XPR5001</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=LMFA03090005</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=LMFA03090005</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=8-Hydroxy- (11S,12S)-epoxy- (5-<del style="font-weight: bold; text-decoration: none;">cis,</del>9<del style="font-weight: bold; text-decoration: none;">-trans</del>,14cis) -eicosatrienoic 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=8-Hydroxy- (11S,12S)-epoxy- (<ins style="font-weight: bold; text-decoration: none;">cis-</ins>5<ins style="font-weight: bold; text-decoration: none;">,trans</ins>-9,14cis) -eicosatrienoic 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;Hepoxilin A_3&amp;&amp;8-Hydroxy- (11S,12S)-epoxy- (5Z,9E,14Z) -eicosatrienoic acid&amp;&amp;8-Hydroxy-11,12 (S,S) -epoxyeicosa-5,14 (Z,Z) ,9 (E) -trienoic 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;Hepoxilin A_3&amp;&amp;8-Hydroxy- (11S,12S)-epoxy- (5Z,9E,14Z) -eicosatrienoic acid&amp;&amp;8-Hydroxy-11,12 (S,S) -epoxyeicosa-5,14 (Z,Z) ,9 (E) -trienoic 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>|Solubility=DIETHYL ETHER [[Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79}}]]</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>|Solubility=DIETHYL ETHER [[Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79}}]]</div></td></tr> </table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20306HX03&diff=53717&oldid=prev Editor at 02:48, 10 June 2010 2010-06-10T02:48:11Z <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 11:48, 10 June 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l11">Line 11:</td> <td colspan="2" class="diff-lineno">Line 11:</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=METHYL ESTER TRIS-TMS ETHER ; m/e 422(M^+ ), 407, 391, 332, 311, 282, 269(base peak) [[Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173|{{RelationTable/GetFirstAuthor|Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173}}]]</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=METHYL ESTER TRIS-TMS ETHER ; m/e 422(M^+ ), 407, 391, 332, 311, 282, 269(base peak) [[Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173|{{RelationTable/GetFirstAuthor|Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173}}]]</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=Hepoxilin A3 together with hepoxilin B3 is produced from arachidonic acid or more directly from 12(S)-hydroperoxy-5,8,10,14-eicosatetraenoic acid in various animal tissues including brain, pineal gland, pancreas and skin [[Reference:Pace-Asciak_CR:,Biochim. Biophys. Acta,1994,1215,1|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:,Biochim. Biophys. Acta,1994,1215,1}}]].</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=Hepoxilin A3 together with hepoxilin B3 is produced from arachidonic acid or more directly from 12(S)-hydroperoxy-5,8,10,14-eicosatetraenoic acid in various animal tissues including brain, pineal gland, pancreas and skin [[Reference:Pace-Asciak_CR:,Biochim. Biophys. Acta,1994,1215,1|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:,Biochim. Biophys. Acta,1994,1215,1}}]].</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>|Chemical Synthesis=<del style="font-weight: bold; text-decoration: none;">&lt;!--1072--&gt; </del>{{Image200|LBF20306HX03FT0001.gif}}</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>|Chemical Synthesis=<ins style="font-weight: bold; text-decoration: none;">[[Reference:Corey_EJ:Su_W:,Tetrahedron_Lett.,1984,25,5119|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Su_W:,Tetrahedron_Lett.,1984,25,5119}}]] </ins>{{Image200|LBF20306HX03FT0001.gif}}</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>|Metabolism=The presence of hepoxilin synthase was suggested by a finding that intact cells (skin) and tissue slices (brain hippocampus and pineal gland) transformed 12(S)-hydroperoxy-5,8,10,14-eicosatetraenoic acid to hepoxilins A3 and B3, but tissue boiling inhibited the hepoxilin production [[Reference:Pace-Asciak_CR:Reynaud_D:Demin_PM:,Lipids,1995,30,107|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Reynaud_D:Demin_PM:,Lipids,1995,30,107}}]].</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>|Metabolism=The presence of hepoxilin synthase was suggested by a finding that intact cells (skin) and tissue slices (brain hippocampus and pineal gland) transformed 12(S)-hydroperoxy-5,8,10,14-eicosatetraenoic acid to hepoxilins A3 and B3, but tissue boiling inhibited the hepoxilin production [[Reference:Pace-Asciak_CR:Reynaud_D:Demin_PM:,Lipids,1995,30,107|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Reynaud_D:Demin_PM:,Lipids,1995,30,107}}]].</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>|Symbol=HxA3</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>|Symbol=HxA3</div></td></tr> </table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20306HX03&diff=53716&oldid=prev Editor at 07:18, 2 June 2010 2010-06-02T07:18:17Z <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 16:18, 2 June 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=XPR5001</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=XPR5001</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=LMFA03090005</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=LMFA03090005</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=8-Hydroxy- (11S,12S)-epoxy- (5-cis,9-trans,14cis) -<del style="font-weight: bold; text-decoration: none;">icosatrienoic </del>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=8-Hydroxy- (11S,12S)-epoxy- (5-cis,9-trans,14cis) -<ins style="font-weight: bold; text-decoration: none;">eicosatrienoic </ins>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;Hepoxilin A_3&amp;&amp;8-Hydroxy- (11S,12S)-epoxy- (5Z,9E,14Z) -eicosatrienoic acid&amp;&amp;8-Hydroxy-11,12 (S,S) -epoxyeicosa-5,14 (Z,Z) ,9 (E) -trienoic 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;Hepoxilin A_3&amp;&amp;8-Hydroxy- (11S,12S)-epoxy- (5Z,9E,14Z) -eicosatrienoic acid&amp;&amp;8-Hydroxy-11,12 (S,S) -epoxyeicosa-5,14 (Z,Z) ,9 (E) -trienoic 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>|Solubility=DIETHYL ETHER [[Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79}}]]</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>|Solubility=DIETHYL ETHER [[Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79}}]]</div></td></tr> </table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20306HX03&diff=53715&oldid=prev Editor at 11:41, 1 June 2010 2010-06-01T11:41:28Z <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 20:41, 1 June 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=XPR5001</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=XPR5001</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=LMFA03090005</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=LMFA03090005</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=8-Hydroxy-11,12 (S,S) -epoxyeicosa-5,14 (Z,Z) ,9 (E) -trienoic 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;">8-Hydroxy- (11S,12S)-epoxy- (5-cis,9-trans,14cis) -icosatrienoic acid</ins></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><del style="font-weight: bold; text-decoration: none;">|Common Name=&amp;&amp;HEPOXILIN A3</del>&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><ins style="font-weight: bold; text-decoration: none;">|Common Name=&amp;&amp;Hepoxilin A_3&amp;&amp;8-Hydroxy- (11S,12S)-epoxy- (5Z,9E,14Z) -eicosatrienoic acid&amp;&amp;</ins>8-Hydroxy-11,12 (S,S) -epoxyeicosa-5,14 (Z,Z) ,9 (E) -trienoic 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>|Solubility=DIETHYL ETHER [[Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79}}]]</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>|Solubility=DIETHYL ETHER [[Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79}}]]</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=METHYL ESTER TRIS-TMS ETHER ; m/e 422(M^+ ), 407, 391, 332, 311, 282, 269(base peak) [[Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173|{{RelationTable/GetFirstAuthor|Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173}}]]</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=METHYL ESTER TRIS-TMS ETHER ; m/e 422(M^+ ), 407, 391, 332, 311, 282, 269(base peak) [[Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173|{{RelationTable/GetFirstAuthor|Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173}}]]</div></td></tr> </table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20306HX03&diff=53714&oldid=prev Editor: LBF20406HX01 moved to LBF20306HX03 2010-04-14T21:00:00Z <p><a href="/mediawiki/index.php?title=LBF20406HX01&amp;action=edit&amp;redlink=1" class="new" title="LBF20406HX01 (page does not exist)">LBF20406HX01</a> moved to <a href="/wiki/LBF20306HX03" title="LBF20306HX03">LBF20306HX03</a></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 06:00, 15 April 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l7">Line 7:</td> <td colspan="2" class="diff-lineno">Line 7:</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=LMFA03090005</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=LMFA03090005</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>|SysName=8-Hydroxy-11,12 (S,S) -epoxyeicosa-5,14 (Z,Z) ,9 (E) -trienoic acid</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>|SysName=8-Hydroxy-11,12 (S,S) -epoxyeicosa-5,14 (Z,Z) ,9 (E) -trienoic acid</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>|Common Name=&amp;&amp;HEPOXILIN A3<del style="font-weight: bold; text-decoration: none;">&amp;&amp;8-Hydroxy-11,12 (S,S) -epoxyeicosa-5,14 (Z,Z) ,9 (E) -trienoic acid</del>&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>|Common Name=&amp;&amp;HEPOXILIN A3&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>|Solubility=DIETHYL ETHER [[Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79}}]]</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>|Solubility=DIETHYL ETHER [[Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79}}]]</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=METHYL ESTER TRIS-TMS ETHER ; m/e 422(M^+ ), 407, 391, 332, 311, 282, 269(base peak) [[Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173|{{RelationTable/GetFirstAuthor|Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173}}]]</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=METHYL ESTER TRIS-TMS ETHER ; m/e 422(M^+ ), 407, 391, 332, 311, 282, 269(base peak) [[Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173|{{RelationTable/GetFirstAuthor|Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173}}]]</div></td></tr> </table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20306HX03&diff=53713&oldid=prev Editor: LBF20406HX01 moved to LBF20306HX03 2010-02-25T10:00:10Z <p><a href="/mediawiki/index.php?title=LBF20406HX01&amp;action=edit&amp;redlink=1" class="new" title="LBF20406HX01 (page does not exist)">LBF20406HX01</a> moved to <a href="/wiki/LBF20306HX03" title="LBF20306HX03">LBF20306HX03</a></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <tr class="diff-title" lang="en"> <td colspan="1" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="1" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 19:00, 25 February 2010</td> </tr><tr><td colspan="2" class="diff-notice" lang="en"><div class="mw-diff-empty">(No difference)</div> </td></tr></table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20306HX03&diff=53712&oldid=prev Editor: LBF20406HX01 moved to LBF20306HX03 2010-02-19T14:00:10Z <p><a href="/mediawiki/index.php?title=LBF20406HX01&amp;action=edit&amp;redlink=1" class="new" title="LBF20406HX01 (page does not exist)">LBF20406HX01</a> moved to <a href="/wiki/LBF20306HX03" title="LBF20306HX03">LBF20306HX03</a></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <tr class="diff-title" lang="en"> <td colspan="1" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="1" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 23:00, 19 February 2010</td> </tr><tr><td colspan="2" class="diff-notice" lang="en"><div class="mw-diff-empty">(No difference)</div> </td></tr></table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20306HX03&diff=53711&oldid=prev Editor: LBF20406HX01 moved to LBF20306HX03 2010-02-19T14:00:00Z <p><a href="/mediawiki/index.php?title=LBF20406HX01&amp;action=edit&amp;redlink=1" class="new" title="LBF20406HX01 (page does not exist)">LBF20406HX01</a> moved to <a href="/wiki/LBF20306HX03" title="LBF20306HX03">LBF20306HX03</a></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 23:00, 19 February 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l9">Line 9:</td> <td colspan="2" class="diff-lineno">Line 9:</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;HEPOXILIN A3&amp;&amp;8-Hydroxy-11,12 (S,S) -epoxyeicosa-5,14 (Z,Z) ,9 (E) -trienoic 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;HEPOXILIN A3&amp;&amp;8-Hydroxy-11,12 (S,S) -epoxyeicosa-5,14 (Z,Z) ,9 (E) -trienoic 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>|Solubility=DIETHYL ETHER [[Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79}}]]</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>|Solubility=DIETHYL ETHER [[Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Mizuno_K:Yamamoto_S:,Prostaglandins,1983,25,79}}]]</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>|Mass Spectra=METHYL ESTER TRIS-TMS ETHER ; m/e 422(M<del style="font-weight: bold; text-decoration: none;">&lt;SUP&gt;&lt;FONT SIZE=-1&gt;</del>+<del style="font-weight: bold; text-decoration: none;">&lt;/FONT&gt;&lt;/SUP&gt;</del>), 407, 391, 332, 311, 282, 269(base peak) [[Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173|{{RelationTable/GetFirstAuthor|Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173}}]]</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>|Mass Spectra=METHYL ESTER TRIS-TMS ETHER ; m/e 422(M<ins style="font-weight: bold; text-decoration: none;">^</ins>+ ), 407, 391, 332, 311, 282, 269(base peak) [[Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173|{{RelationTable/GetFirstAuthor|Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173}}]]</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=Hepoxilin A3 together with hepoxilin B3 is produced from arachidonic acid or more directly from 12(S)-hydroperoxy-5,8,10,14-eicosatetraenoic acid in various animal tissues including brain, pineal gland, pancreas and skin [[Reference:Pace-Asciak_CR:,Biochim. Biophys. Acta,1994,1215,1|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:,Biochim. Biophys. Acta,1994,1215,1}}]].</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=Hepoxilin A3 together with hepoxilin B3 is produced from arachidonic acid or more directly from 12(S)-hydroperoxy-5,8,10,14-eicosatetraenoic acid in various animal tissues including brain, pineal gland, pancreas and skin [[Reference:Pace-Asciak_CR:,Biochim. Biophys. Acta,1994,1215,1|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:,Biochim. Biophys. Acta,1994,1215,1}}]].</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>|Chemical Synthesis=&lt;!--1072--&gt; {{Image200|LBF20306HX03FT0001.gif}}</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>|Chemical Synthesis=&lt;!--1072--&gt; {{Image200|LBF20306HX03FT0001.gif}}</div></td></tr> </table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20306HX03&diff=53710&oldid=prev Editor: LBF20406HX01 moved to LBF20306HX03 2010-01-26T16:30:00Z <p><a href="/mediawiki/index.php?title=LBF20406HX01&amp;action=edit&amp;redlink=1" class="new" title="LBF20406HX01 (page does not exist)">LBF20406HX01</a> moved to <a href="/wiki/LBF20306HX03" title="LBF20306HX03">LBF20306HX03</a></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 01:30, 27 January 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l11">Line 11:</td> <td colspan="2" class="diff-lineno">Line 11:</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=METHYL ESTER TRIS-TMS ETHER ; m/e 422(M&lt;SUP&gt;&lt;FONT SIZE=-1&gt;+&lt;/FONT&gt;&lt;/SUP&gt;), 407, 391, 332, 311, 282, 269(base peak) [[Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173|{{RelationTable/GetFirstAuthor|Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173}}]]</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=METHYL ESTER TRIS-TMS ETHER ; m/e 422(M&lt;SUP&gt;&lt;FONT SIZE=-1&gt;+&lt;/FONT&gt;&lt;/SUP&gt;), 407, 391, 332, 311, 282, 269(base peak) [[Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173|{{RelationTable/GetFirstAuthor|Reference:Walker_IC:Jones_RL:Wilson_NH:,Prostaglandins,1979,18,173}}]]</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=Hepoxilin A3 together with hepoxilin B3 is produced from arachidonic acid or more directly from 12(S)-hydroperoxy-5,8,10,14-eicosatetraenoic acid in various animal tissues including brain, pineal gland, pancreas and skin [[Reference:Pace-Asciak_CR:,Biochim. Biophys. Acta,1994,1215,1|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:,Biochim. Biophys. Acta,1994,1215,1}}]].</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=Hepoxilin A3 together with hepoxilin B3 is produced from arachidonic acid or more directly from 12(S)-hydroperoxy-5,8,10,14-eicosatetraenoic acid in various animal tissues including brain, pineal gland, pancreas and skin [[Reference:Pace-Asciak_CR:,Biochim. Biophys. Acta,1994,1215,1|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:,Biochim. Biophys. Acta,1994,1215,1}}]].</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>|Chemical Synthesis= {{Image200|LBF20306HX03FT0001.gif}}</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>|Chemical Synthesis=<ins style="font-weight: bold; text-decoration: none;">&lt;!--1072--&gt; </ins>{{Image200|LBF20306HX03FT0001.gif}}</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>|Metabolism=The presence of hepoxilin synthase was suggested by a finding that intact cells (skin) and tissue slices (brain hippocampus and pineal gland) transformed 12(S)-hydroperoxy-5,8,10,14-eicosatetraenoic acid to hepoxilins A3 and B3, but tissue boiling inhibited the hepoxilin production [[Reference:Pace-Asciak_CR:Reynaud_D:Demin_PM:,Lipids,1995,30,107|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Reynaud_D:Demin_PM:,Lipids,1995,30,107}}]].</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>|Metabolism=The presence of hepoxilin synthase was suggested by a finding that intact cells (skin) and tissue slices (brain hippocampus and pineal gland) transformed 12(S)-hydroperoxy-5,8,10,14-eicosatetraenoic acid to hepoxilins A3 and B3, but tissue boiling inhibited the hepoxilin production [[Reference:Pace-Asciak_CR:Reynaud_D:Demin_PM:,Lipids,1995,30,107|{{RelationTable/GetFirstAuthor|Reference:Pace-Asciak_CR:Reynaud_D:Demin_PM:,Lipids,1995,30,107}}]].</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>|Symbol=HxA3</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>|Symbol=HxA3</div></td></tr> </table> Editor