https://lipidbank.jp/mediawiki/index.php?action=history&feed=atom&title=LBF20406HO12 2026-04-30T20:02:40Z Revision history for this page on the wiki MediaWiki 1.43.0 https://lipidbank.jp/mediawiki/index.php?title=LBF20406HO12&diff=55351&oldid=prev 2010-10-21T07:26:10Z

<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 16:26, 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=DFA8130</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=DFA8130</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=LMFA03060021</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=LMFA03060021</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-Hydroxy- (5-cis<del style="font-weight: bold; text-decoration: none;">,9</del>-<del style="font-weight: bold; text-decoration: none;">trans</del>,<del style="font-weight: bold; text-decoration: none;">11</del>-<del style="font-weight: bold; text-decoration: none;">cis,</del>14<del style="font-weight: bold; text-decoration: none;">-cis</del>) -eicosatetraenoic 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=8R-Hydroxy- (<ins style="font-weight: bold; text-decoration: none;">cis-</ins>5<ins style="font-weight: bold; text-decoration: none;">,trans</ins>-<ins style="font-weight: bold; text-decoration: none;">9,</ins>cis-<ins style="font-weight: bold; text-decoration: none;">11</ins>,<ins style="font-weight: bold; text-decoration: none;">cis</ins>-14) -eicosatetraenoic 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;8R-Hydroxy- (5Z,9E,11Z,14Z) -eicosatetraenoic 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;8R-Hydroxy- (5Z,9E,11Z,14Z) -eicosatetraenoic 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>|UV Spectra= lambda max: 237nm  epsilon : 27,000</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>|UV Spectra= lambda max: 237nm  epsilon : 27,000</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-55350:rev-55351:php=table --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20406HO12&diff=55350&oldid=prev 2010-06-02T07:33:49Z

<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 16:33, 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=DFA8130</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=DFA8130</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=LMFA03060021</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=LMFA03060021</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-Hydroxy- (5-cis,9-trans,11-cis,14-cis) -<del style="font-weight: bold; text-decoration: none;">icosatetraenoic </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=8R-Hydroxy- (5-cis,9-trans,11-cis,14-cis) -<ins style="font-weight: bold; text-decoration: none;">eicosatetraenoic </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;8R-Hydroxy- (5Z,9E,11Z,14Z) -eicosatetraenoic 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;8R-Hydroxy- (5Z,9E,11Z,14Z) -eicosatetraenoic 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>|UV Spectra= lambda max: 237nm  epsilon : 27,000</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>|UV Spectra= lambda max: 237nm  epsilon : 27,000</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-55349:rev-55350:php=table --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20406HO12&diff=55349&oldid=prev 2010-06-01T08:28:08Z

<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 17:28, 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=DFA8130</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=DFA8130</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=LMFA03060021</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=LMFA03060021</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-<del style="font-weight: bold; text-decoration: none;">hydroxy</del>-<del style="font-weight: bold; text-decoration: none;">5Z</del>,<del style="font-weight: bold; text-decoration: none;">9E</del>,<del style="font-weight: bold; text-decoration: none;">11Z</del>,<del style="font-weight: bold; text-decoration: none;">14Z</del>-<del style="font-weight: bold; text-decoration: none;">eicosatetraenoic </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=8R-<ins style="font-weight: bold; text-decoration: none;">Hydroxy</ins>- <ins style="font-weight: bold; text-decoration: none;">(5-cis</ins>,<ins style="font-weight: bold; text-decoration: none;">9-trans</ins>,<ins style="font-weight: bold; text-decoration: none;">11-cis</ins>,<ins style="font-weight: bold; text-decoration: none;">14-cis) </ins>-<ins style="font-weight: bold; text-decoration: none;">icosatetraenoic </ins>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;8R-<del style="font-weight: bold; text-decoration: none;">hydroxy</del>-5Z,9E,11Z,14Z-eicosatetraenoic 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>|Common Name=&amp;&amp;8R-<ins style="font-weight: bold; text-decoration: none;">Hydroxy</ins>- <ins style="font-weight: bold; text-decoration: none;">(</ins>5Z,9E,11Z,14Z<ins style="font-weight: bold; text-decoration: none;">) </ins>-eicosatetraenoic 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>|UV Spectra= lambda max: 237nm  epsilon : 27,000</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>|UV Spectra= lambda max: 237nm  epsilon : 27,000</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=8(R)-HETE is a metabolite of arachidonic acid by the 8-lipoxygenase pathway in marine organisms [[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]][[Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829|{{RelationTable/GetFirstAuthor|Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829}}]].</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=8(R)-HETE is a metabolite of arachidonic acid by the 8-lipoxygenase pathway in marine organisms [[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]][[Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829|{{RelationTable/GetFirstAuthor|Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829}}]].</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-55348:rev-55349:php=table --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20406HO12&diff=55348&oldid=prev 2010-05-10T09:16:33Z

<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 18:16, 10 May 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l13">Line 13:</td> <td colspan="2" class="diff-lineno">Line 13:</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 precursor of 8(R)-HETE, 8(R)-HpETE, is the putative intermediate in the biosynthesis of marine prostaglandins via the allene oxide synthase pathway.[[Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829|{{RelationTable/GetFirstAuthor|Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829}}]].</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 precursor of 8(R)-HETE, 8(R)-HpETE, is the putative intermediate in the biosynthesis of marine prostaglandins via the allene oxide synthase pathway.[[Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829|{{RelationTable/GetFirstAuthor|Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829}}]].</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=8(R)-HETE</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=8(R)-HETE</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>|Biological Activity=8(R)-HETE induces maturation of starfish oocytes at a concentration of 0.071 mu M [[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]]. This activity if neglible in the 8(S)-enantiomer [[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]].</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>|Biological Activity=8(R)-HETE induces maturation of starfish oocytes at a concentration of 0.071 <ins style="font-weight: bold; text-decoration: none;">&amp;</ins>mu<ins style="font-weight: bold; text-decoration: none;">; </ins>M [[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]]. This activity if neglible in the 8(S)-enantiomer [[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]].</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>}}</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>}}</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;"><br></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;"><br></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>{{Lipid/Footer}}</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>{{Lipid/Footer}}</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-55347:rev-55348:php=table --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20406HO12&diff=55347&oldid=prev 2010-04-14T21:00:00Z

<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 06:00, 15 April 2010</td> </tr><tr><td colspan="4" class="diff-notice" lang="en"><div class="mw-diff-empty">(No difference)</div> </td></tr> <!-- diff cache key wikidb:diff:1.41:old-55346:rev-55347 --> </table>

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<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 15:32, 10 March 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l5">Line 5:</td> <td colspan="2" class="diff-lineno">Line 5:</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>{{Metabolite</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>{{Metabolite</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>|LipidBank=DFA8130</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=DFA8130</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>|LipidMaps=<del style="font-weight: bold; text-decoration: none;">-</del></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>|LipidMaps=<ins style="font-weight: bold; text-decoration: none;">LMFA03060021</ins></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=8R-hydroxy-5Z,9E,11Z,14Z-eicosatetraenoic 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=8R-hydroxy-5Z,9E,11Z,14Z-eicosatetraenoic 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;8R-hydroxy-5Z,9E,11Z,14Z-eicosatetraenoic 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;8R-hydroxy-5Z,9E,11Z,14Z-eicosatetraenoic acid&amp;&amp;</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-55345:rev-55346:php=table --> </table>

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<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 19:00, 25 February 2010</td> </tr><tr><td colspan="4" class="diff-notice" lang="en"><div class="mw-diff-empty">(No difference)</div> </td></tr> <!-- diff cache key wikidb:diff:1.41:old-55344:rev-55345 --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20406HO12&diff=55344&oldid=prev 2010-02-19T14:00:10Z

<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 23:00, 19 February 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l8">Line 8:</td> <td colspan="2" class="diff-lineno">Line 8:</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=8R-hydroxy-5Z,9E,11Z,14Z-eicosatetraenoic 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=8R-hydroxy-5Z,9E,11Z,14Z-eicosatetraenoic 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;8R-hydroxy-5Z,9E,11Z,14Z-eicosatetraenoic 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;8R-hydroxy-5Z,9E,11Z,14Z-eicosatetraenoic acid&amp;&amp;</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>|UV Spectra=<del style="font-weight: bold; text-decoration: none;">lambdamax</del>: 237nm epsilon: 27,000</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>|UV Spectra= <ins style="font-weight: bold; text-decoration: none;">lambda max</ins>: 237nm <ins style="font-weight: bold; text-decoration: none;"> </ins>epsilon : 27,000</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=8(R)-HETE is a metabolite of arachidonic acid by the 8-lipoxygenase pathway in marine organisms [[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]][[Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829|{{RelationTable/GetFirstAuthor|Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829}}]].</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=8(R)-HETE is a metabolite of arachidonic acid by the 8-lipoxygenase pathway in marine organisms [[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]][[Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829|{{RelationTable/GetFirstAuthor|Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829}}]].</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=</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=</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 precursor of 8(R)-HETE, 8(R)-HpETE, is the putative intermediate in the biosynthesis of marine prostaglandins via the allene oxide synthase pathway.[[Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829|{{RelationTable/GetFirstAuthor|Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829}}]].</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 precursor of 8(R)-HETE, 8(R)-HpETE, is the putative intermediate in the biosynthesis of marine prostaglandins via the allene oxide synthase pathway.[[Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829|{{RelationTable/GetFirstAuthor|Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829}}]].</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=8(R)-HETE</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=8(R)-HETE</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>|Biological Activity=8(R)-HETE induces maturation of starfish oocytes at a concentration of 0.<del style="font-weight: bold; text-decoration: none;">071muM </del>[[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]]. This activity if neglible in the 8(S)-enantiomer [[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]].</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>|Biological Activity=8(R)-HETE induces maturation of starfish oocytes at a concentration of 0.<ins style="font-weight: bold; text-decoration: none;">071 mu M </ins>[[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]]. This activity if neglible in the 8(S)-enantiomer [[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]].</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>}}</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>}}</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;"><br></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;"><br></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>{{Lipid/Footer}}</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>{{Lipid/Footer}}</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-55343:rev-55344:php=table --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20406HO12&diff=55343&oldid=prev 2010-02-19T14:00:00Z

<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 23:00, 19 February 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l8">Line 8:</td> <td colspan="2" class="diff-lineno">Line 8:</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=8R-hydroxy-5Z,9E,11Z,14Z-eicosatetraenoic 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=8R-hydroxy-5Z,9E,11Z,14Z-eicosatetraenoic 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;8R-hydroxy-5Z,9E,11Z,14Z-eicosatetraenoic 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;8R-hydroxy-5Z,9E,11Z,14Z-eicosatetraenoic acid&amp;&amp;</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>|UV Spectra=<del style="font-weight: bold; text-decoration: none;">&lt;FONT FACE="Symbol"&gt;l&lt;/FONT&gt;max</del>: 237nm <del style="font-weight: bold; text-decoration: none;">&lt;FONT FACE="Symbol"&gt;e&lt;/FONT&gt;</del>: 27,000</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>|UV Spectra=<ins style="font-weight: bold; text-decoration: none;">lambdamax</ins>: 237nm <ins style="font-weight: bold; text-decoration: none;">epsilon</ins>: 27,000</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=8(R)-HETE is a metabolite of arachidonic acid by the 8-lipoxygenase pathway in marine organisms [[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]][[Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829|{{RelationTable/GetFirstAuthor|Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829}}]].</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=8(R)-HETE is a metabolite of arachidonic acid by the 8-lipoxygenase pathway in marine organisms [[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]][[Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829|{{RelationTable/GetFirstAuthor|Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829}}]].</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=</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=</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 precursor of 8(R)-HETE, 8(R)-HpETE, is the putative intermediate in the biosynthesis of marine prostaglandins via the allene oxide synthase pathway.[[Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829|{{RelationTable/GetFirstAuthor|Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829}}]].</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 precursor of 8(R)-HETE, 8(R)-HpETE, is the putative intermediate in the biosynthesis of marine prostaglandins via the allene oxide synthase pathway.[[Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829|{{RelationTable/GetFirstAuthor|Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829}}]].</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=8(R)-HETE</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=8(R)-HETE</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>|Biological Activity=8(R)-HETE induces maturation of starfish oocytes at a concentration of 0.<del style="font-weight: bold; text-decoration: none;">071&lt;FONT FACE="Symbol"&gt;m&lt;/FONT&gt;M </del>[[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]]. This activity if neglible in the 8(S)-enantiomer [[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]].</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>|Biological Activity=8(R)-HETE induces maturation of starfish oocytes at a concentration of 0.<ins style="font-weight: bold; text-decoration: none;">071muM </ins>[[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]]. This activity if neglible in the 8(S)-enantiomer [[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]].</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>}}</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>}}</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;"><br></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;"><br></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>{{Lipid/Footer}}</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>{{Lipid/Footer}}</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-55342:rev-55343:php=table --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20406HO12&diff=55342&oldid=prev 2010-01-06T21:00:00Z

<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 06:00, 7 January 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l12">Line 12:</td> <td colspan="2" class="diff-lineno">Line 12:</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=</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=</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 precursor of 8(R)-HETE, 8(R)-HpETE, is the putative intermediate in the biosynthesis of marine prostaglandins via the allene oxide synthase pathway.[[Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829|{{RelationTable/GetFirstAuthor|Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829}}]].</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 precursor of 8(R)-HETE, 8(R)-HpETE, is the putative intermediate in the biosynthesis of marine prostaglandins via the allene oxide synthase pathway.[[Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829|{{RelationTable/GetFirstAuthor|Reference:Brash_AR:Baertschi_SW:Ingram_CD:Harris_TM:,J. Biol. Chem.,1987,262,15829}}]].</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><ins style="font-weight: bold; text-decoration: none;">|Symbol=8(R)-HETE</ins></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><ins style="font-weight: bold; text-decoration: none;">|Biological Activity=8(R)-HETE induces maturation of starfish oocytes at a concentration of 0.071&lt;FONT FACE="Symbol"&gt;m&lt;/FONT&gt;M [[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]]. This activity if neglible in the 8(S)-enantiomer [[Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040|{{RelationTable/GetFirstAuthor|Reference:Meijer_L:Brash_AR:Bryant_RW:Ng_K:Maclouf_J:Sprecher_H:,J. Biol. Chem.,1986,261,17040}}]].</ins></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>}}</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>}}</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;"><br></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;"><br></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>{{Lipid/Footer}}</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>{{Lipid/Footer}}</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-55341:rev-55342:php=table --> </table>

Editor