https://lipidbank.jp/mediawiki/index.php?action=history&feed=atom&title=LBF20303TX02 LBF20303TX02 - Revision history 2026-04-30T00:11:05Z Revision history for this page on the wiki MediaWiki 1.43.0 https://lipidbank.jp/mediawiki/index.php?title=LBF20303TX02&diff=53443&oldid=prev Editor at 07:07, 21 October 2010 2010-10-21T07:07:53Z <p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 16:07, 21 October 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l6">Line 6:</td> <td colspan="2" class="diff-lineno">Line 6:</td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=XPR2102</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=XPR2102</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidMaps=LMFA03030006</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=LMFA03030006</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=7- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-<del style="font-weight: bold; text-decoration: none;">Hydroxy</del>- (trans-1,cis-5) -octadienyl) -2H-pyran-3S-yl] -cis-5-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- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-<ins style="font-weight: bold; text-decoration: none;">hydroxy</ins>- (trans-1,cis-5) -octadienyl) -2H-pyran-3S-yl] -cis-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=&amp;&amp;Thromboxane B_3&amp;&amp;7- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-hydroxy- (1E,5Z) -octadienyl) -2H-pyran-3S-yl] -5(Z) -heptenoic acid&amp;&amp;</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&amp;&amp;Thromboxane B_3&amp;&amp;7- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-hydroxy- (1E,5Z) -octadienyl) -2H-pyran-3S-yl] -5(Z) -heptenoic acid&amp;&amp;</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-53442:rev-53443:php=table --> </table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20303TX02&diff=53442&oldid=prev Editor at 07:07, 21 October 2010 2010-10-21T07:07:27Z <p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 16:07, 21 October 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l7">Line 7:</td> <td colspan="2" class="diff-lineno">Line 7:</td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidMaps=LMFA03030006</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=LMFA03030006</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName=7- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-Hydroxy- (trans-1,cis-5) -octadienyl) -2H-pyran-3S-yl] -cis-5-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- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-Hydroxy- (trans-1,cis-5) -octadienyl) -2H-pyran-3S-yl] -cis-5-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=&amp;&amp;Thromboxane B_3&amp;&amp;7- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-hydroxy- <del style="font-weight: bold; text-decoration: none;"> </del>(1E,5Z) <del style="font-weight: bold; text-decoration: none;"> </del>-octadienyl) -2H-pyran-3S-yl ] -5(Z) -heptenoic acid&amp;&amp;</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&amp;&amp;Thromboxane B_3&amp;&amp;7- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-hydroxy- (1E,5Z) -octadienyl) -2H-pyran-3S-yl] -5(Z) -heptenoic acid&amp;&amp;</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FAB : m/e 351(M^{+1}-H_2 O), 333, 315, 307 [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FAB : m/e 351(M^{+1}-H_2 O), 333, 315, 307 [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-53441:rev-53442:php=table --> </table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20303TX02&diff=53441&oldid=prev Editor at 07:07, 21 October 2010 2010-10-21T07:07:04Z <p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 16:07, 21 October 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l6">Line 6:</td> <td colspan="2" class="diff-lineno">Line 6:</td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=XPR2102</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=XPR2102</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidMaps=LMFA03030006</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=LMFA03030006</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=7- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-<del style="font-weight: bold; text-decoration: none;">hydroxy</del>- (1-<del style="font-weight: bold; text-decoration: none;">trans,</del>5<del style="font-weight: bold; text-decoration: none;">-cis</del>) -octadienyl) -2H-pyran-3S-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- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-<ins style="font-weight: bold; text-decoration: none;">Hydroxy</ins>- (<ins style="font-weight: bold; text-decoration: none;">trans-</ins>1<ins style="font-weight: bold; text-decoration: none;">,cis</ins>-5) -octadienyl) -2H-pyran-3S-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=&amp;&amp;Thromboxane B_3&amp;&amp;7- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-hydroxy-  (1E,5Z)  -octadienyl) -2H-pyran-3S-yl ] -5(Z) -heptenoic acid&amp;&amp;</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&amp;&amp;Thromboxane B_3&amp;&amp;7- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-hydroxy-  (1E,5Z)  -octadienyl) -2H-pyran-3S-yl ] -5(Z) -heptenoic acid&amp;&amp;</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td></tr> </table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20303TX02&diff=53440&oldid=prev Editor at 03:01, 28 May 2010 2010-05-28T03:01:34Z <p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 12:01, 28 May 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l7">Line 7:</td> <td colspan="2" class="diff-lineno">Line 7:</td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidMaps=LMFA03030006</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=LMFA03030006</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName=7- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-hydroxy- (1-trans,5-cis) -octadienyl) -2H-pyran-3S-yl ] -5-cis -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- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-hydroxy- (1-trans,5-cis) -octadienyl) -2H-pyran-3S-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=&amp;&amp;Thromboxane B_3&amp;&amp;7- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-hydroxy- (<del style="font-weight: bold; text-decoration: none;">1(E)</del>,<del style="font-weight: bold; text-decoration: none;">5(Z)</del>) -octadienyl) -2H-pyran-3S-yl ] -5(Z) -heptenoic acid&amp;&amp;</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&amp;&amp;Thromboxane B_3&amp;&amp;7- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-hydroxy- <ins style="font-weight: bold; text-decoration: none;"> </ins>(<ins style="font-weight: bold; text-decoration: none;">1E</ins>,<ins style="font-weight: bold; text-decoration: none;">5Z</ins>) <ins style="font-weight: bold; text-decoration: none;"> </ins>-octadienyl) -2H-pyran-3S-yl ] -5(Z) -heptenoic acid&amp;&amp;</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FAB : m/e 351(M^{+1}-H_2 O), 333, 315, 307 [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FAB : m/e 351(M^{+1}-H_2 O), 333, 315, 307 [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td></tr> </table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20303TX02&diff=53439&oldid=prev Editor at 02:59, 28 May 2010 2010-05-28T02:59:50Z <p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 11:59, 28 May 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l7">Line 7:</td> <td colspan="2" class="diff-lineno">Line 7:</td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidMaps=LMFA03030006</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=LMFA03030006</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName=7- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-hydroxy- (1-trans,5-cis) -octadienyl) -2H-pyran-3S-yl ] -5-cis -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- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-hydroxy- (1-trans,5-cis) -octadienyl) -2H-pyran-3S-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=&amp;&amp;Thromboxane B_3&amp;&amp;7- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-hydroxy- (1(E),5(Z)) -octadienyl) -2H-pyran-3S-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=&amp;&amp;Thromboxane B_3&amp;&amp;7- [Tetrahydro- (4S,6) -dihydroxy-2R- (3S-hydroxy- (1(E),5(Z)) -octadienyl) -2H-pyran-3S-yl ] -5(Z) -heptenoic acid<ins style="font-weight: bold; text-decoration: none;">&amp;&amp;</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=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FAB : m/e 351(M^{+1}-H_2 O), 333, 315, 307 [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FAB : m/e 351(M^{+1}-H_2 O), 333, 315, 307 [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-53438:rev-53439:php=table --> </table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20303TX02&diff=53438&oldid=prev Editor at 02:59, 28 May 2010 2010-05-28T02:59:08Z <p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 11:59, 28 May 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l6">Line 6:</td> <td colspan="2" class="diff-lineno">Line 6:</td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=XPR2102</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=XPR2102</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidMaps=LMFA03030006</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=LMFA03030006</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=7- [ Tetrahydro-<del style="font-weight: bold; text-decoration: none;">4 </del>(<del style="font-weight: bold; text-decoration: none;">S) </del>,6-dihydroxy-<del style="font-weight: bold; text-decoration: none;">2 </del>(<del style="font-weight: bold; text-decoration: none;">R</del>) - (<del style="font-weight: bold; text-decoration: none;">3 </del>(<del style="font-weight: bold; text-decoration: none;">S) </del>-hydroxy-1 (E) ,5 (Z) -octadienyl) -2H-pyran-<del style="font-weight: bold; text-decoration: none;">3 (S) </del>-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>|SysName=7- [Tetrahydro- (<ins style="font-weight: bold; text-decoration: none;">4S</ins>,6<ins style="font-weight: bold; text-decoration: none;">) </ins>-dihydroxy-<ins style="font-weight: bold; text-decoration: none;">2R- (3S-hydroxy- </ins>(<ins style="font-weight: bold; text-decoration: none;">1-trans,5-cis) -octadienyl</ins>) <ins style="font-weight: bold; text-decoration: none;">-2H-pyran-3S-yl ] -5-cis -heptenoic acid</ins></div></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;">|Common Name=&amp;&amp;THROMBOXANE B3&amp;&amp;</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><ins style="font-weight: bold; text-decoration: none;">|Common Name=&amp;&amp;Thromboxane B_3&amp;&amp;7- [Tetrahydro</ins>- (<ins style="font-weight: bold; text-decoration: none;">4S,6) -dihydroxy-2R- </ins>(<ins style="font-weight: bold; text-decoration: none;">3S</ins>-hydroxy- <ins style="font-weight: bold; text-decoration: none;">(</ins>1(E),5(Z<ins style="font-weight: bold; text-decoration: none;">)</ins>) -octadienyl) -2H-pyran-<ins style="font-weight: bold; text-decoration: none;">3S</ins>-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=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FAB : m/e 351(M^{+1}-H_2 O), 333, 315, 307 [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FAB : m/e 351(M^{+1}-H_2 O), 333, 315, 307 [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td></tr> <!-- diff cache key wikidb:diff:1.41:old-53437:rev-53438:php=table --> </table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20303TX02&diff=53437&oldid=prev Editor: LBF20403TX02 moved to LBF20303TX02 2010-04-14T21:00:00Z <p><a href="/mediawiki/index.php?title=LBF20403TX02&amp;action=edit&amp;redlink=1" class="new" title="LBF20403TX02 (page does not exist)">LBF20403TX02</a> moved to <a href="/wiki/LBF20303TX02" title="LBF20303TX02">LBF20303TX02</a></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 06:00, 15 April 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l7">Line 7:</td> <td colspan="2" class="diff-lineno">Line 7:</td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidMaps=LMFA03030006</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=LMFA03030006</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName=7- [ Tetrahydro-4 (S) ,6-dihydroxy-2 (R) - (3 (S) -hydroxy-1 (E) ,5 (Z) -octadienyl) -2H-pyran-3 (S) -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- [ Tetrahydro-4 (S) ,6-dihydroxy-2 (R) - (3 (S) -hydroxy-1 (E) ,5 (Z) -octadienyl) -2H-pyran-3 (S) -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=&amp;&amp;THROMBOXANE B3<del style="font-weight: bold; text-decoration: none;">&amp;&amp;7- [ Tetrahydro-4 (S) ,6-dihydroxy-2 (R) - (3 (S) -hydroxy-1 (E) ,5 (Z) -octadienyl) -2H-pyran-3 (S) -yl ] -5 (Z) -heptenoic acid</del>&amp;&amp;</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&amp;&amp;THROMBOXANE B3&amp;&amp;</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FAB : m/e 351(M^{+1}-H_2 O), 333, 315, 307 [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FAB : m/e 351(M^{+1}-H_2 O), 333, 315, 307 [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td></tr> </table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20303TX02&diff=53436&oldid=prev Editor: LBF20403TX02 moved to LBF20303TX02 2010-02-25T10:00:10Z <p><a href="/mediawiki/index.php?title=LBF20403TX02&amp;action=edit&amp;redlink=1" class="new" title="LBF20403TX02 (page does not exist)">LBF20403TX02</a> moved to <a href="/wiki/LBF20303TX02" title="LBF20303TX02">LBF20303TX02</a></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 19:00, 25 February 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l9">Line 9:</td> <td colspan="2" class="diff-lineno">Line 9:</td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&amp;&amp;THROMBOXANE B3&amp;&amp;7- [ Tetrahydro-4 (S) ,6-dihydroxy-2 (R) - (3 (S) -hydroxy-1 (E) ,5 (Z) -octadienyl) -2H-pyran-3 (S) -yl ] -5 (Z) -heptenoic acid&amp;&amp;</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&amp;&amp;THROMBOXANE B3&amp;&amp;7- [ Tetrahydro-4 (S) ,6-dihydroxy-2 (R) - (3 (S) -hydroxy-1 (E) ,5 (Z) -octadienyl) -2H-pyran-3 (S) -yl ] -5 (Z) -heptenoic acid&amp;&amp;</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FAB : m/e 351(M^+ <del style="font-weight: bold; text-decoration: none;">^</del>1 -H_2 O), 333, 315, 307 [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FAB : m/e 351(M^<ins style="font-weight: bold; text-decoration: none;">{</ins>+1<ins style="font-weight: bold; text-decoration: none;">}</ins>-H_2 O), 333, 315, 307 [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FILM :  nu  3392, 3010, 2932, 1713, 1407, 1363, 1231, 1154, 1104, 1024, 973, 895 cm^- <del style="font-weight: bold; text-decoration: none;">^</del>1 <del style="font-weight: bold; text-decoration: none;"> </del>[[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FILM :  nu  3392, 3010, 2932, 1713, 1407, 1363, 1231, 1154, 1104, 1024, 973, 895 cm^<ins style="font-weight: bold; text-decoration: none;">{</ins>-1<ins style="font-weight: bold; text-decoration: none;">} </ins>[[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=^1 H-NMR(CDCl_3 , TMS) :  delta  5.85(dd, J=17.5, 6.3Hz,1H, 14-CH), 5.71(dd, J=17.5, 7.5Hz, 1H, 13-CH), 5.55(td, J=20.0, 12.5Hz, 1H, 18-CH), 5.48-5.31(m, 4H, 5,6,11,17-CH), 4.41(dd, J=12.5, 7.5Hz, 1H, 12-CH), 4.23(dt, J=12.5, 6.3Hz, 1H, 15-CH), 4.08(m, 1H, 9-CH), 2.40-2.24(m, 4H, 4,16-CH), 2.18-1.96(m, 7H, 2,7,10,19-CH), 1.81(m, 2H, 3-CH), 1.74-1.63(m, 2H, 3-CH), 1.45(tdd, J=8.8, 5.0, 5.0Hz, 1H, 8-CH), 0.96(t, J=7.5Hz, 3H, 20-CH) [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]] ^<del style="font-weight: bold; text-decoration: none;">1 ^3 </del>C-NMR(CDCl_3 ) : 177.25, 136.52, 135.22, 130.75, 129.22, 127.49, 123.66, 123.59, 92.56, 71.58, 69.20, 64.95, 44.99, 36.01, 34.72, 32.89, 26.31, 24.80, 24.58, 24.58, 20.76, 14.21[[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=^1 H-NMR(CDCl_3 , TMS) :  delta  5.85(dd, J=17.5, 6.3Hz,1H, 14-CH), 5.71(dd, J=17.5, 7.5Hz, 1H, 13-CH), 5.55(td, J=20.0, 12.5Hz, 1H, 18-CH), 5.48-5.31(m, 4H, 5,6,11,17-CH), 4.41(dd, J=12.5, 7.5Hz, 1H, 12-CH), 4.23(dt, J=12.5, 6.3Hz, 1H, 15-CH), 4.08(m, 1H, 9-CH), 2.40-2.24(m, 4H, 4,16-CH), 2.18-1.96(m, 7H, 2,7,10,19-CH), 1.81(m, 2H, 3-CH), 1.74-1.63(m, 2H, 3-CH), 1.45(tdd, J=8.8, 5.0, 5.0Hz, 1H, 8-CH), 0.96(t, J=7.5Hz, 3H, 20-CH) [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]] ^<ins style="font-weight: bold; text-decoration: none;">{13}</ins>C-NMR(CDCl_3 ) : 177.25, 136.52, 135.22, 130.75, 129.22, 127.49, 123.66, 123.59, 92.56, 71.58, 69.20, 64.95, 44.99, 36.01, 34.72, 32.89, 26.31, 24.80, 24.58, 24.58, 20.76, 14.21[[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]] {{Image200|LBF20303TX02FT0001.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:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]] {{Image200|LBF20303TX02FT0001.gif}}</div></td></tr> </table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20303TX02&diff=53435&oldid=prev Editor: LBF20403TX02 moved to LBF20303TX02 2010-02-19T14:00:10Z <p><a href="/mediawiki/index.php?title=LBF20403TX02&amp;action=edit&amp;redlink=1" class="new" title="LBF20403TX02 (page does not exist)">LBF20403TX02</a> moved to <a href="/wiki/LBF20303TX02" title="LBF20303TX02">LBF20303TX02</a></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 23:00, 19 February 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l10">Line 10:</td> <td colspan="2" class="diff-lineno">Line 10:</td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FAB : m/e 351(M^+ ^1 -H_2 O), 333, 315, 307 [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FAB : m/e 351(M^+ ^1 -H_2 O), 333, 315, 307 [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FILM : nu 3392, 3010, 2932, 1713, 1407, 1363, 1231, 1154, 1104, 1024, 973, 895 cm^- ^1  [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FILM : <ins style="font-weight: bold; text-decoration: none;"> </ins>nu <ins style="font-weight: bold; text-decoration: none;"> </ins>3392, 3010, 2932, 1713, 1407, 1363, 1231, 1154, 1104, 1024, 973, 895 cm^- ^1  [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=^1 H-NMR(CDCl_3 , TMS) : delta 5.85(dd, J=17.5, 6.3Hz,1H, 14-CH), 5.71(dd, J=17.5, 7.5Hz, 1H, 13-CH), 5.55(td, J=20.0, 12.5Hz, 1H, 18-CH), 5.48-5.31(m, 4H, 5,6,11,17-CH), 4.41(dd, J=12.5, 7.5Hz, 1H, 12-CH), 4.23(dt, J=12.5, 6.3Hz, 1H, 15-CH), 4.08(m, 1H, 9-CH), 2.40-2.24(m, 4H, 4,16-CH), 2.18-1.96(m, 7H, 2,7,10,19-CH), 1.81(m, 2H, 3-CH), 1.74-1.63(m, 2H, 3-CH), 1.45(tdd, J=8.8, 5.0, 5.0Hz, 1H, 8-CH), 0.96(t, J=7.5Hz, 3H, 20-CH) [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]] ^1 ^3 C-NMR(CDCl_3 ) : 177.25, 136.52, 135.22, 130.75, 129.22, 127.49, 123.66, 123.59, 92.56, 71.58, 69.20, 64.95, 44.99, 36.01, 34.72, 32.89, 26.31, 24.80, 24.58, 24.58, 20.76, 14.21[[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=^1 H-NMR(CDCl_3 , TMS) : <ins style="font-weight: bold; text-decoration: none;"> </ins>delta <ins style="font-weight: bold; text-decoration: none;"> </ins>5.85(dd, J=17.5, 6.3Hz,1H, 14-CH), 5.71(dd, J=17.5, 7.5Hz, 1H, 13-CH), 5.55(td, J=20.0, 12.5Hz, 1H, 18-CH), 5.48-5.31(m, 4H, 5,6,11,17-CH), 4.41(dd, J=12.5, 7.5Hz, 1H, 12-CH), 4.23(dt, J=12.5, 6.3Hz, 1H, 15-CH), 4.08(m, 1H, 9-CH), 2.40-2.24(m, 4H, 4,16-CH), 2.18-1.96(m, 7H, 2,7,10,19-CH), 1.81(m, 2H, 3-CH), 1.74-1.63(m, 2H, 3-CH), 1.45(tdd, J=8.8, 5.0, 5.0Hz, 1H, 8-CH), 0.96(t, J=7.5Hz, 3H, 20-CH) [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]] ^1 ^3 C-NMR(CDCl_3 ) : 177.25, 136.52, 135.22, 130.75, 129.22, 127.49, 123.66, 123.59, 92.56, 71.58, 69.20, 64.95, 44.99, 36.01, 34.72, 32.89, 26.31, 24.80, 24.58, 24.58, 20.76, 14.21[[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]] {{Image200|LBF20303TX02FT0001.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:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]] {{Image200|LBF20303TX02FT0001.gif}}</div></td></tr> </table> Editor https://lipidbank.jp/mediawiki/index.php?title=LBF20303TX02&diff=53434&oldid=prev Editor: LBF20403TX02 moved to LBF20303TX02 2010-02-19T14:00:00Z <p><a href="/mediawiki/index.php?title=LBF20403TX02&amp;action=edit&amp;redlink=1" class="new" title="LBF20403TX02 (page does not exist)">LBF20403TX02</a> moved to <a href="/wiki/LBF20303TX02" title="LBF20303TX02">LBF20303TX02</a></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 23:00, 19 February 2010</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l9">Line 9:</td> <td colspan="2" class="diff-lineno">Line 9:</td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&amp;&amp;THROMBOXANE B3&amp;&amp;7- [ Tetrahydro-4 (S) ,6-dihydroxy-2 (R) - (3 (S) -hydroxy-1 (E) ,5 (Z) -octadienyl) -2H-pyran-3 (S) -yl ] -5 (Z) -heptenoic acid&amp;&amp;</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&amp;&amp;THROMBOXANE B3&amp;&amp;7- [ Tetrahydro-4 (S) ,6-dihydroxy-2 (R) - (3 (S) -hydroxy-1 (E) ,5 (Z) -octadienyl) -2H-pyran-3 (S) -yl ] -5 (Z) -heptenoic acid&amp;&amp;</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Solubility=DIETHYL ETHER [[Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:,Biochim. Biophys. Acta,1980,618,389}}]], ETHYL ACETATE, CHLOROFORM [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FAB : m/e 351(M<del style="font-weight: bold; text-decoration: none;">&lt;SUP&gt;&lt;FONT SIZE=-1&gt;</del>+<del style="font-weight: bold; text-decoration: none;">&lt;/FONT&gt;&lt;/SUP&gt;&lt;SUP&gt;&lt;FONT SIZE=-</del>1<del style="font-weight: bold; text-decoration: none;">&gt;1&lt;/FONT&gt;&lt;/SUP&gt;</del>-<del style="font-weight: bold; text-decoration: none;">H&lt;SUB&gt;&lt;FONT SIZE=-1&gt;2&lt;/FONT&gt;&lt;/SUB&gt;</del>O), 333, 315, 307 [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FAB : m/e 351(M<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;">H_2 </ins>O), 333, 315, 307 [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FILM : <del style="font-weight: bold; text-decoration: none;">&lt;FONT FACE="Symbol"&gt;n&lt;/FONT&gt; </del>3392, 3010, 2932, 1713, 1407, 1363, 1231, 1154, 1104, 1024, 973, 895 cm<del style="font-weight: bold; text-decoration: none;">&lt;SUP&gt;&lt;FONT SIZE=-1&gt;-&lt;/FONT&gt;&lt;/SUP&gt;&lt;SUP&gt;&lt;FONT SIZE=</del>-1<del style="font-weight: bold; text-decoration: none;">&gt;1&lt;/FONT&gt;&lt;/SUP&gt; </del>[[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=FILM : <ins style="font-weight: bold; text-decoration: none;">nu </ins>3392, 3010, 2932, 1713, 1407, 1363, 1231, 1154, 1104, 1024, 973, 895 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:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=<del style="font-weight: bold; text-decoration: none;">&lt;SUP&gt;&lt;FONT SIZE=-1&gt;</del>1<del style="font-weight: bold; text-decoration: none;">&lt;/FONT&gt;&lt;/SUP&gt;</del>H-NMR(<del style="font-weight: bold; text-decoration: none;">CDCl&lt;SUB&gt;&lt;FONT SIZE=-1&gt;3&lt;/FONT&gt;&lt;/SUB&gt;</del>, TMS) : <del style="font-weight: bold; text-decoration: none;">&lt;FONT FACE="Symbol"&gt;d&lt;/FONT&gt; </del>5.85(dd, J=17.5, 6.3Hz,1H, 14-CH), 5.71(dd, J=17.5, 7.5Hz, 1H, 13-CH), 5.55(td, J=20.0, 12.5Hz, 1H, 18-CH), 5.48-5.31(m, 4H, 5,6,11,17-CH), 4.41(dd, J=12.5, 7.5Hz, 1H, 12-CH), 4.23(dt, J=12.5, 6.3Hz, 1H, 15-CH), 4.08(m, 1H, 9-CH), 2.40-2.24(m, 4H, 4,16-CH), 2.18-1.96(m, 7H, 2,7,10,19-CH), 1.81(m, 2H, 3-CH), 1.74-1.63(m, 2H, 3-CH), 1.45(tdd, J=8.8, 5.0, 5.0Hz, 1H, 8-CH), 0.96(t, J=7.5Hz, 3H, 20-CH) [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]] <del style="font-weight: bold; text-decoration: none;">&lt;SUP&gt;&lt;FONT SIZE=-</del>1<del style="font-weight: bold; text-decoration: none;">&gt;1&lt;/FONT&gt;&lt;/SUP&gt;&lt;SUP&gt;&lt;FONT SIZE=-1&gt;</del>3<del style="font-weight: bold; text-decoration: none;">&lt;/FONT&gt;&lt;/SUP&gt;</del>C-NMR(<del style="font-weight: bold; text-decoration: none;">CDCl&lt;SUB&gt;&lt;FONT SIZE=-1&gt;3&lt;/FONT&gt;&lt;/SUB&gt;</del>) : 177.25, 136.52, 135.22, 130.75, 129.22, 127.49, 123.66, 123.59, 92.56, 71.58, 69.20, 64.95, 44.99, 36.01, 34.72, 32.89, 26.31, 24.80, 24.58, 24.58, 20.76, 14.21[[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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=<ins style="font-weight: bold; text-decoration: none;">^</ins>1 H-NMR(<ins style="font-weight: bold; text-decoration: none;">CDCl_3 </ins>, TMS) : <ins style="font-weight: bold; text-decoration: none;">delta </ins>5.85(dd, J=17.5, 6.3Hz,1H, 14-CH), 5.71(dd, J=17.5, 7.5Hz, 1H, 13-CH), 5.55(td, J=20.0, 12.5Hz, 1H, 18-CH), 5.48-5.31(m, 4H, 5,6,11,17-CH), 4.41(dd, J=12.5, 7.5Hz, 1H, 12-CH), 4.23(dt, J=12.5, 6.3Hz, 1H, 15-CH), 4.08(m, 1H, 9-CH), 2.40-2.24(m, 4H, 4,16-CH), 2.18-1.96(m, 7H, 2,7,10,19-CH), 1.81(m, 2H, 3-CH), 1.74-1.63(m, 2H, 3-CH), 1.45(tdd, J=8.8, 5.0, 5.0Hz, 1H, 8-CH), 0.96(t, J=7.5Hz, 3H, 20-CH) [[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]] <ins style="font-weight: bold; text-decoration: none;">^</ins>1 <ins style="font-weight: bold; text-decoration: none;">^</ins>3 C-NMR(<ins style="font-weight: bold; text-decoration: none;">CDCl_3 </ins>) : 177.25, 136.52, 135.22, 130.75, 129.22, 127.49, 123.66, 123.59, 92.56, 71.58, 69.20, 64.95, 44.99, 36.01, 34.72, 32.89, 26.31, 24.80, 24.58, 24.58, 20.76, 14.21[[Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]]</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:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]] {{Image200|LBF20303TX02FT0001.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:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769|{{RelationTable/GetFirstAuthor|Reference:Nakamura_N:Nagai_H:Yoneda:M:Suga_H:Kawamura_M:Iguchi_S:,Chem. Pharm. Bull. (Tokyo),1993,41,1769}}]] {{Image200|LBF20303TX02FT0001.gif}}</div></td></tr> </table> Editor