https://lipidbank.jp/mediawiki/index.php?action=history&feed=atom&title=LBF20406HO22
LBF20406HO22 - Revision history
2026-04-30T20:02:09Z
Revision history for this page on the wiki
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https://lipidbank.jp/mediawiki/index.php?title=LBF20406HO22&diff=55547&oldid=prev
Editor at 07:28, 21 October 2010
2010-10-21T07:28:49Z
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<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=&&8R-Hydroxy- (5Z,9E,11Z,14Z) -eicosatetraenoic acid&&(R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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>|Common Name=&&8R-Hydroxy- (5Z,9E,11Z,14Z) -eicosatetraenoic acid&&(R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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>|Optical=8(S)-ISOMER METHYL ESTER ; [ alpha ]^{22}_D =-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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>|Optical=8(S)-ISOMER METHYL ESTER ; [ alpha ]^{22}_D =-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</div></td></tr>
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Editor at 07:41, 2 June 2010
2010-06-02T07:41:19Z
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<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=&&8R-Hydroxy- (5Z,9E,11Z,14Z) -eicosatetraenoic acid&&(R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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>|Common Name=&&8R-Hydroxy- (5Z,9E,11Z,14Z) -eicosatetraenoic acid&&(R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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>|Optical=8(S)-ISOMER METHYL ESTER ; [ alpha ]^{22}_D =-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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>|Optical=8(S)-ISOMER METHYL ESTER ; [ alpha ]^{22}_D =-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</div></td></tr>
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Editor at 08:44, 1 June 2010
2010-06-01T08:44:14Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 17:44, 1 June 2010</td>
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<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= <del style="font-weight: bold; text-decoration: none;">(R) , (Z,E,Z,Z) -8</del>-Hydroxy-5,9,11,14-<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=<ins style="font-weight: bold; text-decoration: none;">8R</ins>-Hydroxy- <ins style="font-weight: bold; text-decoration: none;">(</ins>5<ins style="font-weight: bold; text-decoration: none;">-cis</ins>,9<ins style="font-weight: bold; text-decoration: none;">-trans</ins>,11<ins style="font-weight: bold; text-decoration: none;">-cis</ins>,14-<ins style="font-weight: bold; text-decoration: none;">cis) -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=&&(R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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>|Common Name=<ins style="font-weight: bold; text-decoration: none;">&&8R-Hydroxy- (5Z,9E,11Z,14Z) -eicosatetraenoic acid</ins>&&(R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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>|Optical=8(S)-ISOMER METHYL ESTER ; [ alpha ]^{22}_D =-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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>|Optical=8(S)-ISOMER METHYL ESTER ; [ alpha ]^{22}_D =-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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=ETHYL ACETATE [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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=ETHYL ACETATE [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</div></td></tr>
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Dbmanager at 21:00, 14 April 2010
2010-04-14T21:00:00Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 06:00, 15 April 2010</td>
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Dbmanager
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Dbmanager at 08:08, 10 March 2010
2010-03-10T08:08:50Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 17:08, 10 March 2010</td>
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<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= (R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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= (R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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=&&(R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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>|Common Name=&&(R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-eicosatetraenoic 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>|Optical=8(S)-ISOMER METHYL ESTER ; [ alpha ]<del style="font-weight: bold; text-decoration: none;">X</del>^{22}_D =-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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>|Optical=8(S)-ISOMER METHYL ESTER ; [ alpha ]^{22}_D =-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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=ETHYL ACETATE [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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=ETHYL ACETATE [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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, TMS ETHER ; m/e 265 [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]. 8(S)-ISOMER METHYL ESTER TMS ETHER ; m/e 406, 391, 316, 265, 243 [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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, TMS ETHER ; m/e 265 [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]. 8(S)-ISOMER METHYL ESTER TMS ETHER ; m/e 406, 391, 316, 265, 243 [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</div></td></tr>
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https://lipidbank.jp/mediawiki/index.php?title=LBF20406HO22&diff=55542&oldid=prev
Editor at 10:00, 25 February 2010
2010-02-25T10:00:10Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 19:00, 25 February 2010</td>
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<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= (R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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= (R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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=&&(R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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>|Common Name=&&(R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-eicosatetraenoic 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>|Optical=8(S)-ISOMER METHYL ESTER ; [ alpha ]X^<del style="font-weight: bold; text-decoration: none;">22_D </del>=-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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>|Optical=8(S)-ISOMER METHYL ESTER ; [ alpha ]X^<ins style="font-weight: bold; text-decoration: none;">{22}_D </ins>=-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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=ETHYL ACETATE [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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=ETHYL ACETATE [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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, TMS ETHER ; m/e 265 [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]. 8(S)-ISOMER METHYL ESTER TMS ETHER ; m/e 406, 391, 316, 265, 243 [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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, TMS ETHER ; m/e 265 [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]. 8(S)-ISOMER METHYL ESTER TMS ETHER ; m/e 406, 391, 316, 265, 243 [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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=METHYL ESTER ; lambda <del style="font-weight: bold; text-decoration: none;">_m _a _x </del>= 235.8nm ( epsilon 28,000)[[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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=METHYL ESTER ; lambda <ins style="font-weight: bold; text-decoration: none;">_{max} </ins>= 235.8nm ( epsilon 28,000)[[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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>|NMR Spectra=8(S)-ISOMER METHYL ESTER ; ^1 H-NMR(CDCl_3 ) : delta 6.56(dd, J=14.5, 11.1Hz, 1H, 10-CH), 6.00(brt, J=11.1, 9.7Hz, 1H, 11-CH), 5.72(dd, J=7.3, 14.5Hz, 1H, 9-CH), 5.59-5.16(m, 5H), 4.23(q, 1H,8-CH), 3.71(s, 3H,OCH_3 ), 2.95(t, 2H,13-CH), 2.35(t, 4H, 4,7-CH), 2.11(sextet, 4H), 1.73(pentet, 2H, 3-CH), 1.56(brs, S, 1H, OH), 1.32(m, 6H), 0.91(t, 3H, 20-CH) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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>|NMR Spectra=8(S)-ISOMER METHYL ESTER ; ^1 H-NMR(CDCl_3 ) : delta 6.56(dd, J=14.5, 11.1Hz, 1H, 10-CH), 6.00(brt, J=11.1, 9.7Hz, 1H, 11-CH), 5.72(dd, J=7.3, 14.5Hz, 1H, 9-CH), 5.59-5.16(m, 5H), 4.23(q, 1H,8-CH), 3.71(s, 3H,OCH_3 ), 2.95(t, 2H,13-CH), 2.35(t, 4H, 4,7-CH), 2.11(sextet, 4H), 1.73(pentet, 2H, 3-CH), 1.56(brs, S, 1H, OH), 1.32(m, 6H), 0.91(t, 3H, 20-CH) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td></tr>
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Editor
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Editor at 14:00, 19 February 2010
2010-02-19T14:00:10Z
<p></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 23:00, 19 February 2010</td>
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<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= (R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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= (R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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=&&(R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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>|Common Name=&&(R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-eicosatetraenoic 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>|Optical=8(S)-ISOMER METHYL ESTER ; [alpha]X^22_D =-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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>|Optical=8(S)-ISOMER METHYL ESTER ; [ alpha ]X^22_D =-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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=ETHYL ACETATE [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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=ETHYL ACETATE [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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, TMS ETHER ; m/e 265 [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]. 8(S)-ISOMER METHYL ESTER TMS ETHER ; m/e 406, 391, 316, 265, 243 [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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, TMS ETHER ; m/e 265 [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]. 8(S)-ISOMER METHYL ESTER TMS ETHER ; m/e 406, 391, 316, 265, 243 [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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=METHYL ESTER ; lambda _m _a _x = 235.8nm (epsilon 28,000)[[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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=METHYL ESTER ; <ins style="font-weight: bold; text-decoration: none;"> </ins>lambda <ins style="font-weight: bold; text-decoration: none;"> </ins>_m _a _x = 235.8nm ( epsilon <ins style="font-weight: bold; text-decoration: none;"> </ins>28,000)[[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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>|NMR Spectra=8(S)-ISOMER METHYL ESTER ; ^1 H-NMR(CDCl_3 ) : delta 6.56(dd, J=14.5, 11.1Hz, 1H, 10-CH), 6.00(brt, J=11.1, 9.7Hz, 1H, 11-CH), 5.72(dd, J=7.3, 14.5Hz, 1H, 9-CH), 5.59-5.16(m, 5H), 4.23(q, 1H,8-CH), 3.71(s, 3H,OCH_3 ), 2.95(t, 2H,13-CH), 2.35(t, 4H, 4,7-CH), 2.11(sextet, 4H), 1.73(pentet, 2H, 3-CH), 1.56(brs, S, 1H, OH), 1.32(m, 6H), 0.91(t, 3H, 20-CH) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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>|NMR Spectra=8(S)-ISOMER METHYL ESTER ; ^1 H-NMR(CDCl_3 ) : <ins style="font-weight: bold; text-decoration: none;"> </ins>delta <ins style="font-weight: bold; text-decoration: none;"> </ins>6.56(dd, J=14.5, 11.1Hz, 1H, 10-CH), 6.00(brt, J=11.1, 9.7Hz, 1H, 11-CH), 5.72(dd, J=7.3, 14.5Hz, 1H, 9-CH), 5.59-5.16(m, 5H), 4.23(q, 1H,8-CH), 3.71(s, 3H,OCH_3 ), 2.95(t, 2H,13-CH), 2.35(t, 4H, 4,7-CH), 2.11(sextet, 4H), 1.73(pentet, 2H, 3-CH), 1.56(brs, S, 1H, OH), 1.32(m, 6H), 0.91(t, 3H, 20-CH) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td></tr>
<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=[[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]] {{Image200|LBF20406HO22FT0001.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=[[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]] {{Image200|LBF20406HO22FT0001.gif}}</div></td></tr>
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<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>
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<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= (R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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= (R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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=&&(R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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>|Common Name=&&(R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-eicosatetraenoic 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>|Optical=8(S)-ISOMER METHYL ESTER ; [<del style="font-weight: bold; text-decoration: none;"><FONT FACE=""Symbol"">a</FONT></del>]X<del style="font-weight: bold; text-decoration: none;"><sub>D</sub><sup>22</sup></del>=-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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>|Optical=8(S)-ISOMER METHYL ESTER ; [<ins style="font-weight: bold; text-decoration: none;">alpha</ins>]X<ins style="font-weight: bold; text-decoration: none;">^22_D </ins>=-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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=ETHYL ACETATE [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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=ETHYL ACETATE [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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, TMS ETHER ; m/e 265 [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]. 8(S)-ISOMER METHYL ESTER TMS ETHER ; m/e 406, 391, 316, 265, 243 [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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, TMS ETHER ; m/e 265 [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]. 8(S)-ISOMER METHYL ESTER TMS ETHER ; m/e 406, 391, 316, 265, 243 [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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=METHYL ESTER ; <del style="font-weight: bold; text-decoration: none;"><FONT FACE=""Symbol"">l</FONT> <SUB><FONT SIZE=-1>m</FONT></SUB><SUB><FONT SIZE=-1>a</FONT></SUB><SUB><FONT SIZE=-1>x</FONT></SUB> </del>= 235.8nm (<del style="font-weight: bold; text-decoration: none;"><FONT FACE=""Symbol"">e</FONT> </del>28,000)[[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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=METHYL ESTER ; <ins style="font-weight: bold; text-decoration: none;">lambda _m _a _x </ins>= 235.8nm (<ins style="font-weight: bold; text-decoration: none;">epsilon </ins>28,000)[[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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>|NMR Spectra=8(S)-ISOMER METHYL ESTER ; <del style="font-weight: bold; text-decoration: none;"><SUP><FONT SIZE=-</del>1<del style="font-weight: bold; text-decoration: none;">>1</FONT></SUP></del>H-NMR(<del style="font-weight: bold; text-decoration: none;">CDCl<SUB><FONT SIZE=-1>3</FONT></SUB></del>) : <del style="font-weight: bold; text-decoration: none;"><FONT FACE=""Symbol"">d</FONT> </del>6.56(dd, J=14.5, 11.1Hz, 1H, 10-CH), 6.00(brt, J=11.1, 9.7Hz, 1H, 11-CH), 5.72(dd, J=7.3, 14.5Hz, 1H, 9-CH), 5.59-5.16(m, 5H), 4.23(q, 1H,8-CH), 3.71(s, 3H,<del style="font-weight: bold; text-decoration: none;">OCH<SUB><FONT SIZE=-1>3</FONT></SUB></del>), 2.95(t, 2H,13-CH), 2.35(t, 4H, 4,7-CH), 2.11(sextet, 4H), 1.73(pentet, 2H, 3-CH), 1.56(brs, S, 1H, OH), 1.32(m, 6H), 0.91(t, 3H, 20-CH) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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>|NMR Spectra=8(S)-ISOMER METHYL ESTER ; <ins style="font-weight: bold; text-decoration: none;">^</ins>1 H-NMR(<ins style="font-weight: bold; text-decoration: none;">CDCl_3 </ins>) : <ins style="font-weight: bold; text-decoration: none;">delta </ins>6.56(dd, J=14.5, 11.1Hz, 1H, 10-CH), 6.00(brt, J=11.1, 9.7Hz, 1H, 11-CH), 5.72(dd, J=7.3, 14.5Hz, 1H, 9-CH), 5.59-5.16(m, 5H), 4.23(q, 1H,8-CH), 3.71(s, 3H,<ins style="font-weight: bold; text-decoration: none;">OCH_3 </ins>), 2.95(t, 2H,13-CH), 2.35(t, 4H, 4,7-CH), 2.11(sextet, 4H), 1.73(pentet, 2H, 3-CH), 1.56(brs, S, 1H, OH), 1.32(m, 6H), 0.91(t, 3H, 20-CH) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td></tr>
<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=[[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]] {{Image200|LBF20406HO22FT0001.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=[[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]] {{Image200|LBF20406HO22FT0001.gif}}</div></td></tr>
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Editor
https://lipidbank.jp/mediawiki/index.php?title=LBF20406HO22&diff=55539&oldid=prev
Editor at 21:00, 6 January 2010
2010-01-06T21:00:00Z
<p></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<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-l8">Line 8:</td>
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<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= (R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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= (R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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=&&(R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-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>|Common Name=&&(R) , (Z,E,Z,Z) -8-Hydroxy-5,9,11,14-eicosatetraenoic 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>|<del style="font-weight: bold; text-decoration: none;">Reflactive</del>=8(S)-ISOMER METHYL ESTER ; [<FONT FACE=""Symbol"">a</FONT>]X<sub>D</sub><sup>22</sup>=-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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;">Optical</ins>=8(S)-ISOMER METHYL ESTER ; [<FONT FACE=""Symbol"">a</FONT>]X<sub>D</sub><sup>22</sup>=-4.75°(C=0.4, CHLOROFORM) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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=ETHYL ACETATE [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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=ETHYL ACETATE [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]</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, TMS ETHER ; m/e 265 [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]. 8(S)-ISOMER METHYL ESTER TMS ETHER ; m/e 406, 391, 316, 265, 243 [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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, TMS ETHER ; m/e 265 [[Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747|{{RelationTable/GetFirstAuthor|Reference:Bundy_GL:Nidy_EG:Epps_DE:Mizsak_SA:Wnuk_RJ:,J. Biol. Chem.,1986,261,747}}]]. 8(S)-ISOMER METHYL ESTER TMS ETHER ; m/e 406, 391, 316, 265, 243 [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</div></td></tr>
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<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=[[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]] {{Image200|LBF20406HO22FT0001.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=[[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]] {{Image200|LBF20406HO22FT0001.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=</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=</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=The compound is involved in the maturation of starfish oocyte [[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>
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Editor
https://lipidbank.jp/mediawiki/index.php?title=LBF20406HO22&diff=55538&oldid=prev
Editor at 11:55, 25 November 2009
2009-11-25T11:55:00Z
<p></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<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 20:55, 25 November 2009</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l14">Line 14:</td>
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<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>|NMR Spectra=8(S)-ISOMER METHYL ESTER ; <SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR(CDCl<SUB><FONT SIZE=-1>3</FONT></SUB>) : <FONT FACE=""Symbol"">d</FONT> 6.56(dd, J=14.5, 11.1Hz, 1H, 10-CH), 6.00(brt, J=11.1, 9.7Hz, 1H, 11-CH), 5.72(dd, J=7.3, 14.5Hz, 1H, 9-CH), 5.59-5.16(m, 5H), 4.23(q, 1H,8-CH), 3.71(s, 3H,OCH<SUB><FONT SIZE=-1>3</FONT></SUB>), 2.95(t, 2H,13-CH), 2.35(t, 4H, 4,7-CH), 2.11(sextet, 4H), 1.73(pentet, 2H, 3-CH), 1.56(brs, S, 1H, OH), 1.32(m, 6H), 0.91(t, 3H, 20-CH) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</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>|NMR Spectra=8(S)-ISOMER METHYL ESTER ; <SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR(CDCl<SUB><FONT SIZE=-1>3</FONT></SUB>) : <FONT FACE=""Symbol"">d</FONT> 6.56(dd, J=14.5, 11.1Hz, 1H, 10-CH), 6.00(brt, J=11.1, 9.7Hz, 1H, 11-CH), 5.72(dd, J=7.3, 14.5Hz, 1H, 9-CH), 5.59-5.16(m, 5H), 4.23(q, 1H,8-CH), 3.71(s, 3H,OCH<SUB><FONT SIZE=-1>3</FONT></SUB>), 2.95(t, 2H,13-CH), 2.35(t, 4H, 4,7-CH), 2.11(sextet, 4H), 1.73(pentet, 2H, 3-CH), 1.56(brs, S, 1H, OH), 1.32(m, 6H), 0.91(t, 3H, 20-CH) [[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td></tr>
<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=[[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]]<del style="font-weight: bold; text-decoration: none;">;> </del>{{Image200|LBF20406HO22FT0001.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=[[Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039|{{RelationTable/GetFirstAuthor|Reference:Yadagiri_P:Lumin_S:Mosset_P:Capdevila_J:Falck_JR:,Tetrah. Lett.,1986,27,6039}}]] {{Image200|LBF20406HO22FT0001.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=</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=</div></td></tr>
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