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LBF20307PG05 - Revision history
2026-04-29T22:31:34Z
Revision history for this page on the wiki
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Editor at 08:19, 4 November 2010
2010-11-04T08:19:08Z
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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 17:19, 4 November 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>|Solubility=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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; m/e 348(M^+ ), 330, 249, 245, 217, 215, 190, 133, 119, 109 [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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; m/e 348(M^+ ), 330, 249, 245, 217, 215, 190, 133, 119, 109 [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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= lambda ^{MeOH}_{max} = 234 nm ( epsilon <del style="font-weight: bold; text-decoration: none;"> </del>17000) [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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= lambda ^{MeOH}_{max} = 234 nm (epsilon <ins style="font-weight: bold; text-decoration: none;">&#8764; </ins>17000) [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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>|IR Spectra=CHLOROFORM solution, nu 1750,1715 cm^{-1} [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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>|IR Spectra=CHLOROFORM solution, nu 1750,1715 cm^{-1} [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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=METHYL ESTER ; delta 6.3(d, J=16Hz, 1H, 13-CH), 6.1-5.95(m, 2H, 11-CH), 5,7(dd, J=6,16Hz, 1H, 14-CH), 5.7-5.1(m, 2H, 5,6-CH), 4.4-4.0(m, 1H, 15-CH), 3.69(S, 3H, OCH_3 ), 3.3-3.0(m, 1H,8-CH), 3.0-2.8(m, 2H, 10-CH) [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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=METHYL ESTER ; delta 6.3(d, J=16Hz, 1H, 13-CH), 6.1-5.95(m, 2H, 11-CH), 5,7(dd, J=6,16Hz, 1H, 14-CH), 5.7-5.1(m, 2H, 5,6-CH), 4.4-4.0(m, 1H, 15-CH), 3.69(S, 3H, OCH_3 ), 3.3-3.0(m, 1H,8-CH), 3.0-2.8(m, 2H, 10-CH) [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</div></td></tr>
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Editor at 09:01, 21 October 2010
2010-10-21T09:01:55Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 18:01, 21 October 2010</td>
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<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=7- [2R- (3S-<del style="font-weight: bold; text-decoration: none;">Hydroxy</del>-1<del style="font-weight: bold; text-decoration: none;">-trans</del>-octenyl) -5-oxo-2-cyclopenten-1R-yl] -5<del style="font-weight: bold; text-decoration: none;">-cis</del>-heptenoic 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=7- [2R- (3S-<ins style="font-weight: bold; text-decoration: none;">hydroxy-trans</ins>-1-octenyl) -5-oxo-2-cyclopenten-1R-yl] <ins style="font-weight: bold; text-decoration: none;">-cis</ins>-5-heptenoic 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=&&Prostaglandin C_2&&7- [2R- (3S-Hydroxy-1-(E)-octenyl) -5-oxo-2-cyclopenten-1R-yl] -5-(Z)-heptenoic 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=&&Prostaglandin C_2&&7- [2R- (3S-Hydroxy-1-(E)-octenyl) -5-oxo-2-cyclopenten-1R-yl] -5-(Z)-heptenoic 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>|Solubility=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</div></td></tr>
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Editor at 06:12, 28 May 2010
2010-05-28T06:12:37Z
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<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=7- [<del style="font-weight: bold; text-decoration: none;">2</del>- (3S-Hydroxy-1-trans-octenyl) -5-oxo-2-cyclopenten-1R-yl] -5-cis-heptenoic 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=7- [<ins style="font-weight: bold; text-decoration: none;">2R</ins>- (3S-Hydroxy-1-trans-octenyl) -5-oxo-2-cyclopenten-1R-yl] -5-cis-heptenoic 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=&&Prostaglandin C_2&&7- [<del style="font-weight: bold; text-decoration: none;">2</del>- (3S-Hydroxy-1-(E)-octenyl) -5-oxo-2-cyclopenten-1R-yl] -5-(Z)-heptenoic 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=&&Prostaglandin C_2&&7- [<ins style="font-weight: bold; text-decoration: none;">2R</ins>- (3S-Hydroxy-1-(E)-octenyl) -5-oxo-2-cyclopenten-1R-yl] -5-(Z)-heptenoic 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>|Solubility=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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; m/e 348(M^+ ), 330, 249, 245, 217, 215, 190, 133, 119, 109 [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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; m/e 348(M^+ ), 330, 249, 245, 217, 215, 190, 133, 119, 109 [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</div></td></tr>
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Editor at 06:00, 28 May 2010
2010-05-28T06:00:58Z
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<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=7- [ 2- (<del style="font-weight: bold; text-decoration: none;">3 (S) </del>-Hydroxy-1 <del style="font-weight: bold; text-decoration: none;">(E) </del>-octenyl) -5-oxo-2-cyclopenten-<del style="font-weight: bold; text-decoration: none;">1 (R) </del>-yl ] -5 <del style="font-weight: bold; text-decoration: none;">(Z) </del>-heptenoic 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=7- [2- (<ins style="font-weight: bold; text-decoration: none;">3S</ins>-Hydroxy-1<ins style="font-weight: bold; text-decoration: none;">-trans</ins>-octenyl) -5-oxo-2-cyclopenten-<ins style="font-weight: bold; text-decoration: none;">1R</ins>-yl] -5<ins style="font-weight: bold; text-decoration: none;">-cis</ins>-heptenoic 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=&&Prostaglandin C_2&&</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=&&Prostaglandin C_2<ins style="font-weight: bold; text-decoration: none;">&&7- [2- (3S-Hydroxy-1-(E)-octenyl) -5-oxo-2-cyclopenten-1R-yl] -5-(Z)-heptenoic acid</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>|Solubility=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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; m/e 348(M^+ ), 330, 249, 245, 217, 215, 190, 133, 119, 109 [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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; m/e 348(M^+ ), 330, 249, 245, 217, 215, 190, 133, 119, 109 [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</div></td></tr>
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Editor at 05:34, 23 April 2010
2010-04-23T05:34:16Z
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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=7- [ 2- (3 (S) -Hydroxy-1 (E) -octenyl) -5-oxo-2-cyclopenten-1 (R) -yl ] -5 (Z) -heptenoic 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=7- [ 2- (3 (S) -Hydroxy-1 (E) -octenyl) -5-oxo-2-cyclopenten-1 (R) -yl ] -5 (Z) -heptenoic 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=&&<del style="font-weight: bold; text-decoration: none;">PROSTAGLANDIN </del>C_2&&</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;">Prostaglandin </ins>C_2&&</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=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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; m/e 348(M^+ ), 330, 249, 245, 217, 215, 190, 133, 119, 109 [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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; m/e 348(M^+ ), 330, 249, 245, 217, 215, 190, 133, 119, 109 [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</div></td></tr>
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Editor at 21:00, 14 April 2010
2010-04-14T21:00:00Z
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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=7- [ 2- (3 (S) -Hydroxy-1 (E) -octenyl) -5-oxo-2-cyclopenten-1 (R) -yl ] -5 (Z) -heptenoic 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=7- [ 2- (3 (S) -Hydroxy-1 (E) -octenyl) -5-oxo-2-cyclopenten-1 (R) -yl ] -5 (Z) -heptenoic 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=&&PROSTAGLANDIN C_2<del style="font-weight: bold; text-decoration: none;">&&7- [ 2- (3 (S) -Hydroxy-1 (E) -octenyl) -5-oxo-2-cyclopenten-1 (R) -yl ] -5 (Z) -heptenoic acid</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>|Common Name=&&PROSTAGLANDIN C_2&&</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=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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; m/e 348(M^+ ), 330, 249, 245, 217, 215, 190, 133, 119, 109 [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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; m/e 348(M^+ ), 330, 249, 245, 217, 215, 190, 133, 119, 109 [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</div></td></tr>
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Editor at 10:00, 25 February 2010
2010-02-25T10:00:10Z
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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>|Solubility=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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; m/e 348(M^+ ), 330, 249, 245, 217, 215, 190, 133, 119, 109 [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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; m/e 348(M^+ ), 330, 249, 245, 217, 215, 190, 133, 119, 109 [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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= lambda ^<del style="font-weight: bold; text-decoration: none;">M_m _a _x </del>= 234 nm ( epsilon 17000) [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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= lambda ^<ins style="font-weight: bold; text-decoration: none;">{MeOH}_{max} </ins>= 234 nm ( epsilon 17000) [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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>|IR Spectra=CHLOROFORM solution, nu 1750,1715 cm^- <del style="font-weight: bold; text-decoration: none;">^</del>1 <del style="font-weight: bold; text-decoration: none;"> </del>[[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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>|IR Spectra=CHLOROFORM solution, nu 1750,1715 cm^<ins style="font-weight: bold; text-decoration: none;">{</ins>-1<ins style="font-weight: bold; text-decoration: none;">} </ins>[[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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=METHYL ESTER ; delta 6.3(d, J=16Hz, 1H, 13-CH), 6.1-5.95(m, 2H, 11-CH), 5,7(dd, J=6,16Hz, 1H, 14-CH), 5.7-5.1(m, 2H, 5,6-CH), 4.4-4.0(m, 1H, 15-CH), 3.69(S, 3H, OCH_3 ), 3.3-3.0(m, 1H,8-CH), 3.0-2.8(m, 2H, 10-CH) [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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=METHYL ESTER ; delta 6.3(d, J=16Hz, 1H, 13-CH), 6.1-5.95(m, 2H, 11-CH), 5,7(dd, J=6,16Hz, 1H, 14-CH), 5.7-5.1(m, 2H, 5,6-CH), 4.4-4.0(m, 1H, 15-CH), 3.69(S, 3H, OCH_3 ), 3.3-3.0(m, 1H,8-CH), 3.0-2.8(m, 2H, 10-CH) [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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
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<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 23:00, 19 February 2010</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l10">Line 10:</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>|Solubility=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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; m/e 348(M^+ ), 330, 249, 245, 217, 215, 190, 133, 119, 109 [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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; m/e 348(M^+ ), 330, 249, 245, 217, 215, 190, 133, 119, 109 [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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=lambda ^M_m _a _x = 234 nm (epsilon 17000) [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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= lambda <ins style="font-weight: bold; text-decoration: none;"> </ins>^M_m _a _x = 234 nm ( epsilon <ins style="font-weight: bold; text-decoration: none;"> </ins>17000) [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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>|IR Spectra=CHLOROFORM solution, nu 1750,1715 cm^- ^1 [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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>|IR Spectra=CHLOROFORM solution, <ins style="font-weight: bold; text-decoration: none;"> </ins>nu <ins style="font-weight: bold; text-decoration: none;"> </ins>1750,1715 cm^- ^1 [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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=METHYL ESTER ; delta 6.3(d, J=16Hz, 1H, 13-CH), 6.1-5.95(m, 2H, 11-CH), 5,7(dd, J=6,16Hz, 1H, 14-CH), 5.7-5.1(m, 2H, 5,6-CH), 4.4-4.0(m, 1H, 15-CH), 3.69(S, 3H, OCH_3 ), 3.3-3.0(m, 1H,8-CH), 3.0-2.8(m, 2H, 10-CH) [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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=METHYL ESTER ; <ins style="font-weight: bold; text-decoration: none;"> </ins>delta <ins style="font-weight: bold; text-decoration: none;"> </ins>6.3(d, J=16Hz, 1H, 13-CH), 6.1-5.95(m, 2H, 11-CH), 5,7(dd, J=6,16Hz, 1H, 14-CH), 5.7-5.1(m, 2H, 5,6-CH), 4.4-4.0(m, 1H, 15-CH), 3.69(S, 3H, OCH_3 ), 3.3-3.0(m, 1H,8-CH), 3.0-2.8(m, 2H, 10-CH) [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]] {{Image200|LBF20307PG05FT0001.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:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]] {{Image200|LBF20307PG05FT0001.gif}}</div></td></tr>
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Editor
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Editor at 14:00, 19 February 2010
2010-02-19T14:00:00Z
<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 23:00, 19 February 2010</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l9">Line 9:</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>|Common Name=&&PROSTAGLANDIN C_2&&7- [ 2- (3 (S) -Hydroxy-1 (E) -octenyl) -5-oxo-2-cyclopenten-1 (R) -yl ] -5 (Z) -heptenoic 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=&&PROSTAGLANDIN C_2&&7- [ 2- (3 (S) -Hydroxy-1 (E) -octenyl) -5-oxo-2-cyclopenten-1 (R) -yl ] -5 (Z) -heptenoic 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>|Solubility=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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=METHANOL, CHLOROFORM [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Mass Spectra=METHYL ESTER; m/e 348(M<del style="font-weight: bold; text-decoration: none;"><SUP><FONT SIZE=-1></del>+<del style="font-weight: bold; text-decoration: none;"></FONT></SUP></del>), 330, 249, 245, 217, 215, 190, 133, 119, 109 [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Mass Spectra=METHYL ESTER; m/e 348(M<ins style="font-weight: bold; text-decoration: none;">^</ins>+ ), 330, 249, 245, 217, 215, 190, 133, 119, 109 [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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;"><FONT FACE="Symbol">l</FONT> <SUP><FONT SIZE=-1>M</FONT></SUP><SUP><FONT SIZE=-1>e</FONT></SUP><SUP><FONT SIZE=-1>O</FONT></SUP><SUP><FONT SIZE=-1>H</FONT></SUP><SUB><FONT SIZE=-1>m</FONT></SUB><SUB><FONT SIZE=-1>a</FONT></SUB><SUB><FONT SIZE=-1>x</FONT></SUB> </del>= 234 nm (<del style="font-weight: bold; text-decoration: none;"><FONT FACE="Symbol">e</FONT> </del>17000) [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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 ^M_m _a _x </ins>= 234 nm (<ins style="font-weight: bold; text-decoration: none;">epsilon </ins>17000) [[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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>|IR Spectra=CHLOROFORM solution, <del style="font-weight: bold; text-decoration: none;"><FONT FACE="Symbol">n</FONT> </del>1750,1715 cm<del style="font-weight: bold; text-decoration: none;"><SUP><FONT SIZE=</del>-1<del style="font-weight: bold; text-decoration: none;">>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP> </del>[[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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>|IR Spectra=CHLOROFORM solution, <ins style="font-weight: bold; text-decoration: none;">nu </ins>1750,1715 cm<ins style="font-weight: bold; text-decoration: none;">^</ins>- <ins style="font-weight: bold; text-decoration: none;">^</ins>1 <ins style="font-weight: bold; text-decoration: none;"> </ins>[[Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]]</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=METHYL ESTER ; <del style="font-weight: bold; text-decoration: none;"><FONT FACE="Symbol">d</FONT> </del>6.3(d, J=16Hz, 1H, 13-CH), 6.1-5.95(m, 2H, 11-CH), 5,7(dd, J=6,16Hz, 1H, 14-CH), 5.7-5.1(m, 2H, 5,6-CH), 4.4-4.0(m, 1H, 15-CH), 3.69(S, 3H, <del style="font-weight: bold; text-decoration: none;">OCH<SUB><FONT SIZE=-1>3</FONT></SUB></del>), 3.3-3.0(m, 1H,8-CH), 3.0-2.8(m, 2H, 10-CH) [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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=METHYL ESTER ; <ins style="font-weight: bold; text-decoration: none;">delta </ins>6.3(d, J=16Hz, 1H, 13-CH), 6.1-5.95(m, 2H, 11-CH), 5,7(dd, J=6,16Hz, 1H, 14-CH), 5.7-5.1(m, 2H, 5,6-CH), 4.4-4.0(m, 1H, 15-CH), 3.69(S, 3H, <ins style="font-weight: bold; text-decoration: none;">OCH_3 </ins>), 3.3-3.0(m, 1H,8-CH), 3.0-2.8(m, 2H, 10-CH) [[Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903|{{RelationTable/GetFirstAuthor|Reference:Floyd_MB:Schaub_RE:Siuta_GJ:Skotnicki_JS:Grudzinskas_CV:Weiss_MJ:Dessy_F:VanHumbeeck_L:,J. Med. Chem.,1980,23,903}}]]</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:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]] {{Image200|LBF20307PG05FT0001.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:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]] {{Image200|LBF20307PG05FT0001.gif}}</div></td></tr>
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https://lipidbank.jp/mediawiki/index.php?title=LBF20307PG05&diff=53923&oldid=prev
Editor at 21:00, 6 January 2010
2010-01-06T21:00:00Z
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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>
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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:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]] {{Image200|LBF20307PG05FT0001.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:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761|{{RelationTable/GetFirstAuthor|Reference:Corey_EJ:Cyr_CR:,Tetrah. Lett.,1974,,1761}}]] {{Image200|LBF20307PG05FT0001.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=Prostaglandin A isomerase converts prostaglandin A2 to C2, and the enzyme is found in human serum [[Reference:Polet_H:Levine_L:,J. Biol. Chem.,1975,250,351|{{RelationTable/GetFirstAuthor|Reference:Polet_H:Levine_L:,J. Biol. Chem.,1975,250,351}}]] and in the plasma of rabbit, cat, pig, dog and rat [[Reference:Jones_RL:Cammock_S:Horton_EW:,Biochim. Biophys. Acta,1972,280,588|{{RelationTable/GetFirstAuthor|Reference:Jones_RL:Cammock_S:Horton_EW:,Biochim. Biophys. Acta,1972,280,588}}]].</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=Prostaglandin A isomerase converts prostaglandin A2 to C2, and the enzyme is found in human serum [[Reference:Polet_H:Levine_L:,J. Biol. Chem.,1975,250,351|{{RelationTable/GetFirstAuthor|Reference:Polet_H:Levine_L:,J. Biol. Chem.,1975,250,351}}]] and in the plasma of rabbit, cat, pig, dog and rat [[Reference:Jones_RL:Cammock_S:Horton_EW:,Biochim. Biophys. Acta,1972,280,588|{{RelationTable/GetFirstAuthor|Reference:Jones_RL:Cammock_S:Horton_EW:,Biochim. Biophys. Acta,1972,280,588}}]].</div></td></tr>
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