https://lipidbank.jp/mediawiki/index.php?action=history&feed=atom&title=LBF22408AM01 2026-04-30T21:48:54Z Revision history for this page on the wiki MediaWiki 1.43.0 https://lipidbank.jp/mediawiki/index.php?title=LBF22408AM01&diff=56783&oldid=prev 2010-11-08T10:01:21Z

<p></p> <table style="background-color: #fff; color: #202122;" data-mw="interface"> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="en"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 19:01, 8 November 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=XPR7056</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=XPR7056</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=LMFA08040018</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=LMFA08040018</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=N-16,16-<del style="font-weight: bold; text-decoration: none;">Dimethy</del>- (cis-5,cis-8,cis-11,cis-14) -docosatetraenoylethanolamine</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=N-16,16-<ins style="font-weight: bold; text-decoration: none;">Dimethyl</ins>- (cis-5,cis-8,cis-11,cis-14) -docosatetraenoylethanolamine</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;N-16,16-<del style="font-weight: bold; text-decoration: none;">Dimethy</del>- (5Z,8Z,11Z,14Z) -docosatetraenoylethanolamine&amp;&amp;16,16-Dimethyldocosa- (5Z,8Z,11Z,14Z) -tetraenoylethanolamine&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;N-16,16-<ins style="font-weight: bold; text-decoration: none;">Dimethyl</ins>- (5Z,8Z,11Z,14Z) -docosatetraenoylethanolamine&amp;&amp;16,16-Dimethyldocosa- (5Z,8Z,11Z,14Z) -tetraenoylethanolamine&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>|NMR Spectra=^1 H NMR (CDCl3)  delta 5.79 (br s, lH, NH), 5.38 (m, 6H, 5,6,8,9,11,12-vinyl-H), 5.21 (m, 2H, 14,15-vinyl-H), 3.44, 3.43 (s&amp;d overlapped, 4H, OCH2-CH2-N), 3.36 (s, 3H, OCH3), 2.92 (t, 2H, J=6.0Hz, 13-CH2), 2.80 (m, 4H, 7,10-CH2), 2.18 (t, 2H, J=7.7Hz, 2-CH2), 2.12 (m, 2H, 4-CH2), 1.71(p, 2H, J=7.7Hz, 3-CH2), 1.25 (m, 10H, 17-21CH2), 1.08 (s, 6H, gem-Me2), 0.86 (m, 3H, 22-CH2) [[Reference:Seltzman_HH:Fleming_DN:Thomas_BF:Gilliam_AF:McCallion_DS:Pertwee_RG:Compton_DR:Martin_BR:,J. Med. Chem.,1997,40,3626|{{RelationTable/GetFirstAuthor|Reference:Seltzman_HH:Fleming_DN:Thomas_BF:Gilliam_AF:McCallion_DS:Pertwee_RG:Compton_DR:Martin_BR:,J. Med. Chem.,1997,40,3626}}]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H NMR (CDCl3)  delta 5.79 (br s, lH, NH), 5.38 (m, 6H, 5,6,8,9,11,12-vinyl-H), 5.21 (m, 2H, 14,15-vinyl-H), 3.44, 3.43 (s&amp;d overlapped, 4H, OCH2-CH2-N), 3.36 (s, 3H, OCH3), 2.92 (t, 2H, J=6.0Hz, 13-CH2), 2.80 (m, 4H, 7,10-CH2), 2.18 (t, 2H, J=7.7Hz, 2-CH2), 2.12 (m, 2H, 4-CH2), 1.71(p, 2H, J=7.7Hz, 3-CH2), 1.25 (m, 10H, 17-21CH2), 1.08 (s, 6H, gem-Me2), 0.86 (m, 3H, 22-CH2) [[Reference:Seltzman_HH:Fleming_DN:Thomas_BF:Gilliam_AF:McCallion_DS:Pertwee_RG:Compton_DR:Martin_BR:,J. Med. Chem.,1997,40,3626|{{RelationTable/GetFirstAuthor|Reference:Seltzman_HH:Fleming_DN:Thomas_BF:Gilliam_AF:McCallion_DS:Pertwee_RG:Compton_DR:Martin_BR:,J. Med. Chem.,1997,40,3626}}]]</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> <!-- diff cache key wikidb:diff:1.41:old-56782:rev-56783:php=table --> </table>

Editor https://lipidbank.jp/mediawiki/index.php?title=LBF22408AM01&diff=56782&oldid=prev 2010-10-22T07:12:17Z

<p>New page: {{Lipid/Header}} {{Hierarchy|{{PAGENAME}}}} {{Metabolite |LipidBank=XPR7056 |LipidMaps=LMFA08040018 |SysName=N-16,16-Dimethy- (cis-5,cis-8,cis-11,cis-14) -docosatetraenoylethanolamine |C...</p> <p><b>New page</b></p><div>{{Lipid/Header}}<br /> <br /> {{Hierarchy|{{PAGENAME}}}}<br /> <br /> {{Metabolite<br /> |LipidBank=XPR7056<br /> |LipidMaps=LMFA08040018<br /> |SysName=N-16,16-Dimethy- (cis-5,cis-8,cis-11,cis-14) -docosatetraenoylethanolamine<br /> |Common Name=&amp;&amp;N-16,16-Dimethy- (5Z,8Z,11Z,14Z) -docosatetraenoylethanolamine&amp;&amp;16,16-Dimethyldocosa- (5Z,8Z,11Z,14Z) -tetraenoylethanolamine&amp;&amp;<br /> |NMR Spectra=^1 H NMR (CDCl3) delta 5.79 (br s, lH, NH), 5.38 (m, 6H, 5,6,8,9,11,12-vinyl-H), 5.21 (m, 2H, 14,15-vinyl-H), 3.44, 3.43 (s&amp;d overlapped, 4H, OCH2-CH2-N), 3.36 (s, 3H, OCH3), 2.92 (t, 2H, J=6.0Hz, 13-CH2), 2.80 (m, 4H, 7,10-CH2), 2.18 (t, 2H, J=7.7Hz, 2-CH2), 2.12 (m, 2H, 4-CH2), 1.71(p, 2H, J=7.7Hz, 3-CH2), 1.25 (m, 10H, 17-21CH2), 1.08 (s, 6H, gem-Me2), 0.86 (m, 3H, 22-CH2) [[Reference:Seltzman_HH:Fleming_DN:Thomas_BF:Gilliam_AF:McCallion_DS:Pertwee_RG:Compton_DR:Martin_BR:,J. Med. Chem.,1997,40,3626|{{RelationTable/GetFirstAuthor|Reference:Seltzman_HH:Fleming_DN:Thomas_BF:Gilliam_AF:McCallion_DS:Pertwee_RG:Compton_DR:Martin_BR:,J. Med. Chem.,1997,40,3626}}]]<br /> |Source=<br /> |Chemical Synthesis=This compound was synthesized from 16,16-dimethyldocosa-cis-5,8,11,14-tetraenoic methyl ester, NaCN and ethanolamine by heating (50°C in methanol)in a sealed tube. Yield 82 %. [[Reference:Seltzman_HH:Fleming_DN:Thomas_BF:Gilliam_AF:McCallion_DS:Pertwee_RG:Compton_DR:Martin_BR:,J. Med. Chem.,1997,40,3626|{{RelationTable/GetFirstAuthor|Reference:Seltzman_HH:Fleming_DN:Thomas_BF:Gilliam_AF:McCallion_DS:Pertwee_RG:Compton_DR:Martin_BR:,J. Med. Chem.,1997,40,3626}}]]<br /> |Metabolism=<br /> |Biological Activity={{Image200|LBF20408AM01FT7056.gif}} &lt;!--7056--&gt;<br /> }}<br /> <br /> {{Lipid/Footer}}</div>

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