https://lipidbank.jp/mediawiki/index.php?action=history&feed=atom&title=LBF20406LT04
LBF20406LT04 - Revision history
2026-04-30T21:02:25Z
Revision history for this page on the wiki
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https://lipidbank.jp/mediawiki/index.php?title=LBF20406LT04&diff=55730&oldid=prev
Editor at 06:23, 9 November 2010
2010-11-09T06:23:27Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 15:23, 9 November 2010</td>
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<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|SysName=N,N-Dimethyl- (5S,12R) -dihydroxy- (cis-6,trans-8,trans-<del style="font-weight: bold; text-decoration: none;">11</del>,cis-14) -eicosatetraenamide</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,N-Dimethyl- (5S,12R) -dihydroxy- (cis-6,trans-8,trans-<ins style="font-weight: bold; text-decoration: none;">10</ins>,cis-14) -eicosatetraenamide</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=&&Leukotriene B_4 dimethylamide&&N,N-Dimethyl- (5S,12R) -dihydroxy- (6Z,8E,10E,14Z) -eicosatetraenamide&&</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=&&Leukotriene B_4 dimethylamide&&N,N-Dimethyl- (5S,12R) -dihydroxy- (6Z,8E,10E,14Z) -eicosatetraenamide&&</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td></tr>
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Editor at 07:50, 21 October 2010
2010-10-21T07:50:45Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 16:50, 21 October 2010</td>
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<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|SysName=N,N-Dimethyl- (5S,12R) -dihydroxy- (6-<del style="font-weight: bold; text-decoration: none;">cis</del>,<del style="font-weight: bold; text-decoration: none;">8</del>-<del style="font-weight: bold; text-decoration: none;">trans</del>,<del style="font-weight: bold; text-decoration: none;">11</del>-<del style="font-weight: bold; text-decoration: none;">trans,</del>14<del style="font-weight: bold; text-decoration: none;">-cis</del>) -eicosatetraenamide</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,N-Dimethyl- (5S,12R) -dihydroxy- (<ins style="font-weight: bold; text-decoration: none;">cis-</ins>6<ins style="font-weight: bold; text-decoration: none;">,trans</ins>-<ins style="font-weight: bold; text-decoration: none;">8</ins>,<ins style="font-weight: bold; text-decoration: none;">trans</ins>-<ins style="font-weight: bold; text-decoration: none;">11</ins>,<ins style="font-weight: bold; text-decoration: none;">cis</ins>-14) -eicosatetraenamide</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=&&Leukotriene B_4 dimethylamide&&N,N-Dimethyl- (5S,12R) -dihydroxy- (6Z,8E,10E,14Z) -eicosatetraenamide&&</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=&&Leukotriene B_4 dimethylamide&&N,N-Dimethyl- (5S,12R) -dihydroxy- (6Z,8E,10E,14Z) -eicosatetraenamide&&</div></td></tr>
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Editor at 07:44, 2 June 2010
2010-06-02T07:44:14Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 16:44, 2 June 2010</td>
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<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|SysName=N,N-Dimethyl- (5S,12R) -dihydroxy- (6-cis,8-trans,11-trans,14-cis) -<del style="font-weight: bold; text-decoration: none;">icosatetraenamide</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>|SysName=N,N-Dimethyl- (5S,12R) -dihydroxy- (6-cis,8-trans,11-trans,14-cis) -<ins style="font-weight: bold; text-decoration: none;">eicosatetraenamide</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>|Common Name=&&Leukotriene B_4 dimethylamide&&N,N-Dimethyl- (5S,12R) -dihydroxy- (6Z,8E,10E,14Z) -eicosatetraenamide&&</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=&&Leukotriene B_4 dimethylamide&&N,N-Dimethyl- (5S,12R) -dihydroxy- (6Z,8E,10E,14Z) -eicosatetraenamide&&</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td></tr>
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Editor at 09:39, 1 June 2010
2010-06-01T09:39:19Z
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<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|SysName=N,N-<del style="font-weight: bold; text-decoration: none;">dimethy</del>-5S,12R-dihydroxy-<del style="font-weight: bold; text-decoration: none;">6Z</del>,<del style="font-weight: bold; text-decoration: none;">8E</del>,<del style="font-weight: bold; text-decoration: none;">10E</del>,<del style="font-weight: bold; text-decoration: none;">14Z</del>-<del style="font-weight: bold; text-decoration: none;">eicosatetraenamide</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>|SysName=N,N-<ins style="font-weight: bold; text-decoration: none;">Dimethyl</ins>- <ins style="font-weight: bold; text-decoration: none;">(</ins>5S,12R<ins style="font-weight: bold; text-decoration: none;">) </ins>-dihydroxy- <ins style="font-weight: bold; text-decoration: none;">(6-cis</ins>,<ins style="font-weight: bold; text-decoration: none;">8-trans</ins>,<ins style="font-weight: bold; text-decoration: none;">11-trans</ins>,<ins style="font-weight: bold; text-decoration: none;">14-cis) </ins>-<ins style="font-weight: bold; text-decoration: none;">icosatetraenamide</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>|Common Name=&&<del style="font-weight: bold; text-decoration: none;">LeukotrieneB4 dimethyl amide</del>&&</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&<ins style="font-weight: bold; text-decoration: none;">Leukotriene B_4 dimethylamide&&N,N-Dimethyl- (5S,12R) -dihydroxy- (6Z,8E,10E,14Z) -eicosatetraenamide</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=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td></tr>
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Editor at 21:00, 14 April 2010
2010-04-14T21:00:00Z
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName=N,N-dimethy-5S,12R-dihydroxy-6Z,8E,10E,14Z-eicosatetraenamide</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=N,N-dimethy-5S,12R-dihydroxy-6Z,8E,10E,14Z-eicosatetraenamide</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=&&LeukotrieneB4 dimethyl amide<del style="font-weight: bold; text-decoration: none;">&&N,N-dimethy-5S,12R-dihydroxy-6Z,8E,10E,14Z-eicosatetraenamide</del>&&</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&LeukotrieneB4 dimethyl amide&&</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=</div></td></tr>
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Editor at 10:00, 25 February 2010
2010-02-25T10:00:10Z
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Editor at 14:00, 19 February 2010
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Editor at 21:00, 6 January 2010
2010-01-06T21:00:00Z
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</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l11">Line 11:</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chemical Synthesis=</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>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Metabolism=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Metabolism=</div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">|Biological Activity=Leukotriene B4 dimethylamide inhibits LTB4 induced degranulation of human neutrophils at the concentration of 130 nM (Ki) and release of lysozyme of PMNL.[[Reference:Falcone_RC:Aharony_D:,J. Pharmacol. Exp. Ther.,1990,255,565|{{RelationTable/GetFirstAuthor|Reference:Falcone_RC:Aharony_D:,J. Pharmacol. Exp. Ther.,1990,255,565}}]][[Reference:Shimazaki_T:Kobayashi_Y:Sato_F:Iwama_T:Shikada_K:,Prostaglandins,1990,39,459|{{RelationTable/GetFirstAuthor|Reference:Shimazaki_T:Kobayashi_Y:Sato_F:Iwama_T:Shikada_K:,Prostaglandins,1990,39,459}}]][[Reference:Showell_HJ:Otterness_IG:Marfat_A:Corey_EJ:,Biochem. Biophys. Res. Commun.,1982,106,741|{{RelationTable/GetFirstAuthor|Reference:Showell_HJ:Otterness_IG:Marfat_A:Corey_EJ:,Biochem. Biophys. Res. Commun.,1982,106,741}}]] The effect may be due to the antagonistic effect against LTB4 receptor.[[Reference:Falcone_RC:Aharony_D:,J. Pharmacol. Exp. Ther.,1990,255,565|{{RelationTable/GetFirstAuthor|Reference:Falcone_RC:Aharony_D:,J. Pharmacol. Exp. Ther.,1990,255,565}}]]</ins></div></td></tr>
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