https://lipidbank.jp/mediawiki/index.php?action=history&feed=atom&title=LBF181nnXX01
LBF181nnXX01 - Revision history
2026-04-30T05:47:30Z
Revision history for this page on the wiki
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https://lipidbank.jp/mediawiki/index.php?title=LBF181nnXX01&diff=49448&oldid=prev
Editor at 21:00, 14 April 2010
2010-04-14T21:00:00Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 06:00, 15 April 2010</td>
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<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=2-Cyclopentene-1-tridecanoic 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=2-Cyclopentene-1-tridecanoic 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=&&Chaulmoogric acid&&13- (2-Cyclopenten-1-yl) tridecanoic acid&&13- (Cyclopent-2-enyl) -n<del style="font-weight: bold; text-decoration: none;">-tridecanoic acid&&2-Cyclopentene-1</del>-tridecanoic 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=&&Chaulmoogric acid&&13- (2-Cyclopenten-1-yl) tridecanoic acid&&13- (Cyclopent-2-enyl) -n-tridecanoic 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>|Melting Point=68.5 °C</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>|Melting Point=68.5 °C</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>|Boiling Point=247.5 °C at 20 mmHg</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>|Boiling Point=247.5 °C at 20 mmHg</div></td></tr>
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Editor
https://lipidbank.jp/mediawiki/index.php?title=LBF181nnXX01&diff=49447&oldid=prev
Editor at 05:26, 14 April 2010
2010-04-14T05:26:12Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 14:26, 14 April 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>|Melting Point=68.5 °C</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>|Melting Point=68.5 °C</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>|Boiling Point=247.5 °C at 20 mmHg</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>|Boiling Point=247.5 °C at 20 mmHg</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>|Solubility=soluble in acetone, chloroform and ether.[[Reference:Cole_HI:Cardoso_HT:,J. Am. Chem. Soc.,1939,61,2349| {{RelationTable/GetFirstAuthor|Reference:Cole_HI:Cardoso_HT:,J. Am. Chem. Soc.,1939,61,2349}}]][[Reference:Barrowcliff_M:Power_FB.,J. Chem. Soc.,1907,91,557| {{RelationTable/GetFirstAuthor|Reference:Barrowcliff_M:Power_FB.,J. Chem. Soc.,1907,91,557}}]][[Reference:Power_FB:Barrowcliff_M.,J. Chem. Soc.,1905,87,884| {{RelationTable/GetFirstAuthor|Reference:Power_FB:Barrowcliff_M.,J. Chem. Soc.,1905,87,884}}]][[<del style="font-weight: bold; text-decoration: none;">Reference:</del>Reference:Power_FB:Gornall_FH.,J. Chem. Soc.,1904,85,838851|{{RelationTable/GetFirstAuthor|Reference:Power_FB:Gornall_FH.,J. Chem. Soc.,1904,85,838851}}]]</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>|Solubility=soluble in acetone, chloroform and ether.[[Reference:Cole_HI:Cardoso_HT:,J. Am. Chem. Soc.,1939,61,2349| {{RelationTable/GetFirstAuthor|Reference:Cole_HI:Cardoso_HT:,J. Am. Chem. Soc.,1939,61,2349}}]][[Reference:Barrowcliff_M:Power_FB.,J. Chem. Soc.,1907,91,557| {{RelationTable/GetFirstAuthor|Reference:Barrowcliff_M:Power_FB.,J. Chem. Soc.,1907,91,557}}]][[Reference:Power_FB:Barrowcliff_M.,J. Chem. Soc.,1905,87,884| {{RelationTable/GetFirstAuthor|Reference:Power_FB:Barrowcliff_M.,J. Chem. Soc.,1905,87,884}}]][[Reference:Power_FB:Gornall_FH.,J. Chem. Soc.,1904,85,838851|{{RelationTable/GetFirstAuthor|Reference:Power_FB:Gornall_FH.,J. Chem. Soc.,1904,85,838851}}]]</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=Seed of Taraktogenos kurzii (Synonym: Hydnocarpus kurzii.); oil of Gynocardia odorata (chaulmoogra); 2 Oncoba spp..</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=Seed of Taraktogenos kurzii (Synonym: Hydnocarpus kurzii.); oil of Gynocardia odorata (chaulmoogra); 2 Oncoba spp..</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chemical Synthesis=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chemical Synthesis=</div></td></tr>
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Editor
https://lipidbank.jp/mediawiki/index.php?title=LBF181nnXX01&diff=49446&oldid=prev
Editor at 05:15, 14 April 2010
2010-04-14T05:15:28Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 14:15, 14 April 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>|Melting Point=68.5 °C</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>|Melting Point=68.5 °C</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>|Boiling Point=247.5 °C at 20 mmHg</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>|Boiling Point=247.5 °C at 20 mmHg</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>|Solubility=soluble in acetone, chloroform and ether.[[Reference:Cole_HI:Cardoso_HT:,J. Am. Chem. Soc.,1939,61,2349|{{RelationTable/GetFirstAuthor|Reference:Cole_HI:Cardoso_HT:,J. Am. Chem. Soc.,1939,61,2349}}]]</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>|Solubility=soluble in acetone, chloroform and ether.[[Reference:Cole_HI:Cardoso_HT:,J. Am. Chem. Soc.,1939,61,2349| {{RelationTable/GetFirstAuthor|Reference:Cole_HI:Cardoso_HT:,J. Am. Chem. Soc.,1939,61,2349<ins style="font-weight: bold; text-decoration: none;">}}]][[Reference:Barrowcliff_M:Power_FB.,J. Chem. Soc.,1907,91,557| {{RelationTable/GetFirstAuthor|Reference:Barrowcliff_M:Power_FB.,J. Chem. Soc.,1907,91,557}}]][[Reference:Power_FB:Barrowcliff_M.,J. Chem. Soc.,1905,87,884| {{RelationTable/GetFirstAuthor|Reference:Power_FB:Barrowcliff_M.,J. Chem. Soc.,1905,87,884}}]][[Reference:Reference:Power_FB:Gornall_FH.,J. Chem. Soc.,1904,85,838851|{{RelationTable/GetFirstAuthor|Reference:Power_FB:Gornall_FH.,J. Chem. Soc.,1904,85,838851</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>|Source=Seed of Taraktogenos kurzii (Synonym: Hydnocarpus kurzii.); oil of Gynocardia odorata (chaulmoogra); 2 Oncoba spp..</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=Seed of Taraktogenos kurzii (Synonym: Hydnocarpus kurzii.); oil of Gynocardia odorata (chaulmoogra); 2 Oncoba spp..</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chemical Synthesis=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chemical Synthesis=</div></td></tr>
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Editor
https://lipidbank.jp/mediawiki/index.php?title=LBF181nnXX01&diff=49445&oldid=prev
Editor at 04:52, 14 April 2010
2010-04-14T04:52:43Z
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidMaps=LMFA01140017</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=LMFA01140017</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=2-Cyclopentene-1-tridecanoic 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=2-Cyclopentene-1-tridecanoic 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=&&Chaulmoogric acid&&13- (2-<del style="font-weight: bold; text-decoration: none;">cyclopenten</del>-1-yl) tridecanoic acid&&13- (Cyclopent-2-enyl) -n-tridecanoic acid&&2-Cyclopentene-1-tridecanoic 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=&&Chaulmoogric acid&&13- (2-<ins style="font-weight: bold; text-decoration: none;">Cyclopenten</ins>-1-yl) tridecanoic acid&&13- (Cyclopent-2-enyl) -n-tridecanoic acid&&2-Cyclopentene-1-tridecanoic 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>|Melting Point=68.5 °C</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>|Melting Point=68.5 °C</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>|Boiling Point=247.5 °C at 20 mmHg</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>|Boiling Point=247.5 °C at 20 mmHg</div></td></tr>
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Editor
https://lipidbank.jp/mediawiki/index.php?title=LBF181nnXX01&diff=49444&oldid=prev
Dbmanager at 10:00, 25 February 2010
2010-02-25T10:00:10Z
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Dbmanager at 14:00, 19 February 2010
2010-02-19T14:00:10Z
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Dbmanager
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Dbmanager at 14:00, 19 February 2010
2010-02-19T14:00:00Z
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Dbmanager
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Dbmanager at 21:00, 6 January 2010
2010-01-06T21:00:00Z
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Dbmanager at 08:00, 9 December 2009
2009-12-09T08:00:48Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 17:00, 9 December 2009</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l5">Line 5:</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>{{Metabolite</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Metabolite</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=DFA0265</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=DFA0265</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|LipidMaps=<del style="font-weight: bold; text-decoration: none;">LMFA01030196</del></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|LipidMaps=<ins style="font-weight: bold; text-decoration: none;">LMFA01140017</ins></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName=2-Cyclopentene-1-tridecanoic 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=2-Cyclopentene-1-tridecanoic 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=&&Chaulmoogric acid&&13- (2-cyclopenten-1-yl) tridecanoic acid&&13- (Cyclopent-2-enyl) -n-tridecanoic acid&&2-Cyclopentene-1-tridecanoic 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=&&Chaulmoogric acid&&13- (2-cyclopenten-1-yl) tridecanoic acid&&13- (Cyclopent-2-enyl) -n-tridecanoic acid&&2-Cyclopentene-1-tridecanoic acid&&</div></td></tr>
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Dbmanager
https://lipidbank.jp/mediawiki/index.php?title=LBF181nnXX01&diff=49439&oldid=prev
Editor at 11:55, 25 November 2009
2009-11-25T11:55:00Z
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<table style="background-color: #fff; color: #202122;" data-mw="interface">
<tr class="diff-title" lang="en">
<td colspan="1" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="1" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:55, 25 November 2009</td>
</tr><tr><td colspan="2" class="diff-notice" lang="en"><div class="mw-diff-empty">(No difference)</div>
</td></tr></table>
Editor