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LBGPEccp:16000SC01:16000SC01:YB2ANe001 - Revision history
2026-04-29T17:36:32Z
Revision history for this page on the wiki
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Editor: LBGPEccp:16000SC01:16000SC01:YB2ANe001:01 moved to LBGPEccp:16000SC01:16000SC01:YB2ANe001
2010-04-14T21:00:00Z
<p><a href="/mediawiki/index.php?title=LBGPEccp:16000SC01:16000SC01:YB2ANe001:01&action=edit&redlink=1" class="new" title="LBGPEccp:16000SC01:16000SC01:YB2ANe001:01 (page does not exist)">LBGPEccp:16000SC01:16000SC01:YB2ANe001:01</a> moved to <a href="/wiki/LBGPEccp:16000SC01:16000SC01:YB2ANe001" title="LBGPEccp:16000SC01:16000SC01:YB2ANe001">LBGPEccp:16000SC01:16000SC01:YB2ANe001</a></p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 06:00, 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=dipalmitoylphosphatidyl-N-methylethanolamine</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=dipalmitoylphosphatidyl-N-methylethanolamine</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=&&phosphatidyl-N-methylethanolamine&&dipalmitoyl&& phosphatidyl-N-monomethylethanolamine&&dipalmitoyl&& dipalmitoylphosphatidyl-N-monomethylethanolamine&& N-methylphosphatidylethanolamine&&dipalmitoyl<del style="font-weight: bold; text-decoration: none;">&&dipalmitoylphosphatidyl-N-methylethanolamine</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=&&phosphatidyl-N-methylethanolamine&&dipalmitoyl&&phosphatidyl-N-monomethylethanolamine&&dipalmitoyl&&dipalmitoylphosphatidyl-N-monomethylethanolamine&&N-methylphosphatidylethanolamine&&dipalmitoyl&&</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=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2424>>, 184-186°C (from CHCl_3 -MeOH at 4°C <<2425>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2424>>, 182°C <<2425>></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=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2424>>, 184-186°C (from CHCl_3 -MeOH at 4°C <<2425>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2424>>, 182°C <<2425>></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>|Reflactive=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^{25}_D +8.0° <<2424>>, [ alpha ]^{23}_D +8.0° (in CHCl_3 ) <<2425>></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>|Reflactive=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^{25}_D +8.0° <<2424>>, [ alpha ]^{23}_D +8.0° (in CHCl_3 ) <<2425>></div></td></tr>
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Editor: LBGPEccp:16000SC01:16000SC01:YB2ANe001:01 moved to LBGPEccp:16000SC01:16000SC01:YB2ANe001
2010-02-25T10:00:10Z
<p><a href="/mediawiki/index.php?title=LBGPEccp:16000SC01:16000SC01:YB2ANe001:01&action=edit&redlink=1" class="new" title="LBGPEccp:16000SC01:16000SC01:YB2ANe001:01 (page does not exist)">LBGPEccp:16000SC01:16000SC01:YB2ANe001:01</a> moved to <a href="/wiki/LBGPEccp:16000SC01:16000SC01:YB2ANe001" title="LBGPEccp:16000SC01:16000SC01:YB2ANe001">LBGPEccp:16000SC01:16000SC01:YB2ANe001</a></p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 19:00, 25 February 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>|Common Name=&&phosphatidyl-N-methylethanolamine&&dipalmitoyl&& phosphatidyl-N-monomethylethanolamine&&dipalmitoyl&& dipalmitoylphosphatidyl-N-monomethylethanolamine&& N-methylphosphatidylethanolamine&&dipalmitoyl&&dipalmitoylphosphatidyl-N-methylethanolamine&&</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=&&phosphatidyl-N-methylethanolamine&&dipalmitoyl&& phosphatidyl-N-monomethylethanolamine&&dipalmitoyl&& dipalmitoylphosphatidyl-N-monomethylethanolamine&& N-methylphosphatidylethanolamine&&dipalmitoyl&&dipalmitoylphosphatidyl-N-methylethanolamine&&</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=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2424>>, 184-186°C (from CHCl_3 -MeOH at 4°C <<2425>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2424>>, 182°C <<2425>></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=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2424>>, 184-186°C (from CHCl_3 -MeOH at 4°C <<2425>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2424>>, 182°C <<2425>></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>|Reflactive=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^<del style="font-weight: bold; text-decoration: none;">25_D </del> +8.0° <<2424>>, [ alpha ]^<del style="font-weight: bold; text-decoration: none;">23_D </del> +8.0° (in CHCl_3 ) <<2425>></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>|Reflactive=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^<ins style="font-weight: bold; text-decoration: none;">{25}_D </ins> +8.0° <<2424>>, [ alpha ]^<ins style="font-weight: bold; text-decoration: none;">{23}_D </ins> +8.0° (in CHCl_3 ) <<2425>></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>}}</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>}}</div></td></tr>
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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>{{Lipid/Footer}}</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>{{Lipid/Footer}}</div></td></tr>
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Editor: LBGPEccp:16000SC01:16000SC01:YB2ANe001:01 moved to LBGPEccp:16000SC01:16000SC01:YB2ANe001
2010-02-19T14:00:10Z
<p><a href="/mediawiki/index.php?title=LBGPEccp:16000SC01:16000SC01:YB2ANe001:01&action=edit&redlink=1" class="new" title="LBGPEccp:16000SC01:16000SC01:YB2ANe001:01 (page does not exist)">LBGPEccp:16000SC01:16000SC01:YB2ANe001:01</a> moved to <a href="/wiki/LBGPEccp:16000SC01:16000SC01:YB2ANe001" title="LBGPEccp:16000SC01:16000SC01:YB2ANe001">LBGPEccp:16000SC01:16000SC01:YB2ANe001</a></p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 23:00, 19 February 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>|Common Name=&&phosphatidyl-N-methylethanolamine&&dipalmitoyl&& phosphatidyl-N-monomethylethanolamine&&dipalmitoyl&& dipalmitoylphosphatidyl-N-monomethylethanolamine&& N-methylphosphatidylethanolamine&&dipalmitoyl&&dipalmitoylphosphatidyl-N-methylethanolamine&&</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=&&phosphatidyl-N-methylethanolamine&&dipalmitoyl&& phosphatidyl-N-monomethylethanolamine&&dipalmitoyl&& dipalmitoylphosphatidyl-N-monomethylethanolamine&& N-methylphosphatidylethanolamine&&dipalmitoyl&&dipalmitoylphosphatidyl-N-methylethanolamine&&</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=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2424>>, 184-186°C (from CHCl_3 -MeOH at 4°C <<2425>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2424>>, 182°C <<2425>></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=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2424>>, 184-186°C (from CHCl_3 -MeOH at 4°C <<2425>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2424>>, 182°C <<2425>></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>|Reflactive=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [alpha]^25_D +8.0° <<2424>>, [alpha]^23_D +8.0° (in CHCl_3 ) <<2425>></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>|Reflactive=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [ alpha ]^25_D +8.0° <<2424>>, [ alpha ]^23_D +8.0° (in CHCl_3 ) <<2425>></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>}}</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>}}</div></td></tr>
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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>{{Lipid/Footer}}</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>{{Lipid/Footer}}</div></td></tr>
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Editor: LBGPEccp:16000SC01:16000SC01:YB2ANe001:01 moved to LBGPEccp:16000SC01:16000SC01:YB2ANe001
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<p><a href="/mediawiki/index.php?title=LBGPEccp:16000SC01:16000SC01:YB2ANe001:01&action=edit&redlink=1" class="new" title="LBGPEccp:16000SC01:16000SC01:YB2ANe001:01 (page does not exist)">LBGPEccp:16000SC01:16000SC01:YB2ANe001:01</a> moved to <a href="/wiki/LBGPEccp:16000SC01:16000SC01:YB2ANe001" title="LBGPEccp:16000SC01:16000SC01:YB2ANe001">LBGPEccp:16000SC01:16000SC01:YB2ANe001</a></p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 23:00, 19 February 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=dipalmitoylphosphatidyl-N-methylethanolamine</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=dipalmitoylphosphatidyl-N-methylethanolamine</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=&&phosphatidyl-N-methylethanolamine&&dipalmitoyl&& phosphatidyl-N-monomethylethanolamine&&dipalmitoyl&& dipalmitoylphosphatidyl-N-monomethylethanolamine&& N-methylphosphatidylethanolamine&&dipalmitoyl&&dipalmitoylphosphatidyl-N-methylethanolamine&&</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=&&phosphatidyl-N-methylethanolamine&&dipalmitoyl&& phosphatidyl-N-monomethylethanolamine&&dipalmitoyl&& dipalmitoylphosphatidyl-N-monomethylethanolamine&& N-methylphosphatidylethanolamine&&dipalmitoyl&&dipalmitoylphosphatidyl-N-methylethanolamine&&</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>|Melting Point=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2424>>, 184-186°C (from <del style="font-weight: bold; text-decoration: none;">CHCl<SUB><FONT SIZE=-1>3</FONT></SUB></del>-MeOH at 4°C <<2425>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2424>>, 182°C <<2425>></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>|Melting Point=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2424>>, 184-186°C (from <ins style="font-weight: bold; text-decoration: none;">CHCl_3 </ins>-MeOH at 4°C <<2425>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2424>>, 182°C <<2425>></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>|Reflactive=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [<del style="font-weight: bold; text-decoration: none;"><FONT FACE="Symbol">a</FONT></del>]<del style="font-weight: bold; text-decoration: none;"><sub>D</sub><sup>25</sup> </del>+8.0° <<2424>>, [<del style="font-weight: bold; text-decoration: none;"><FONT FACE="Symbol">a</FONT></del>]<del style="font-weight: bold; text-decoration: none;"><sub>D</sub><sup>23</sup> </del>+8.0° (in <del style="font-weight: bold; text-decoration: none;">CHCl<SUB><FONT SIZE=-1>3</FONT></SUB></del>) <<2425>></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>|Reflactive=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [<ins style="font-weight: bold; text-decoration: none;">alpha</ins>]<ins style="font-weight: bold; text-decoration: none;">^25_D </ins>+8.0° <<2424>>, [<ins style="font-weight: bold; text-decoration: none;">alpha</ins>]<ins style="font-weight: bold; text-decoration: none;">^23_D </ins>+8.0° (in <ins style="font-weight: bold; text-decoration: none;">CHCl_3 </ins>) <<2425>></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>}}</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>}}</div></td></tr>
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Editor: LBGPEccp:16000SC01:16000SC01:YB2ANe001:01 moved to LBGPEccp:16000SC01:16000SC01:YB2ANe001
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<p><a href="/mediawiki/index.php?title=LBGPEccp:16000SC01:16000SC01:YB2ANe001:01&action=edit&redlink=1" class="new" title="LBGPEccp:16000SC01:16000SC01:YB2ANe001:01 (page does not exist)">LBGPEccp:16000SC01:16000SC01:YB2ANe001:01</a> moved to <a href="/wiki/LBGPEccp:16000SC01:16000SC01:YB2ANe001" title="LBGPEccp:16000SC01:16000SC01:YB2ANe001">LBGPEccp:16000SC01:16000SC01:YB2ANe001</a></p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 00:00, 19 February 2010</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l4">Line 4:</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>|LipidBank=PGP2403</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=PGP2403</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=dipalmitoylphosphatidyl-N-methylethanolamine</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=dipalmitoylphosphatidyl-N-methylethanolamine</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=phosphatidyl-N-<del style="font-weight: bold; text-decoration: none;">methylethanolaminedipalmitoyl </del>phosphatidyl-N-<del style="font-weight: bold; text-decoration: none;">monomethylethanolaminedipalmitoyl </del>dipalmitoylphosphatidyl-N-monomethylethanolamine N-<del style="font-weight: bold; text-decoration: none;">methylphosphatidylethanolaminedipalmitoyldipalmitoylphosphatidyl</del>-N-methylethanolamine</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;">&&</ins>phosphatidyl-N-<ins style="font-weight: bold; text-decoration: none;">methylethanolamine&&dipalmitoyl&& </ins>phosphatidyl-N-<ins style="font-weight: bold; text-decoration: none;">monomethylethanolamine&&dipalmitoyl&& </ins>dipalmitoylphosphatidyl-N-monomethylethanolamine<ins style="font-weight: bold; text-decoration: none;">&& </ins>N-<ins style="font-weight: bold; text-decoration: none;">methylphosphatidylethanolamine&&dipalmitoyl&&dipalmitoylphosphatidyl</ins>-N-methylethanolamine<ins style="font-weight: bold; text-decoration: none;">&&</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>|Melting Point=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C 2424, 184-186°C (from <del style="font-weight: bold; text-decoration: none;">CHClSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB-MeOH at 4°C 2425; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C 2424, 182°C 2425</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>|Melting Point=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <ins style="font-weight: bold; text-decoration: none;"><<</ins>2424<ins style="font-weight: bold; text-decoration: none;">>></ins>, 184-186°C (from <ins style="font-weight: bold; text-decoration: none;">CHCl<SUB><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>3<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/SUB<ins style="font-weight: bold; text-decoration: none;">></ins>-MeOH at 4°C <ins style="font-weight: bold; text-decoration: none;"><<</ins>2425<ins style="font-weight: bold; text-decoration: none;">>></ins>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <ins style="font-weight: bold; text-decoration: none;"><<</ins>2424<ins style="font-weight: bold; text-decoration: none;">>></ins>, 182°C <ins style="font-weight: bold; text-decoration: none;"><<</ins>2425<ins style="font-weight: bold; text-decoration: none;">>></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>|Reflactive=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [FONT FACE=<del style="font-weight: bold; text-decoration: none;">Symbola</del>/FONT]<del style="font-weight: bold; text-decoration: none;">subD</del>/<del style="font-weight: bold; text-decoration: none;">subsup25</del>/sup +8.0° 2424, [FONT FACE=<del style="font-weight: bold; text-decoration: none;">Symbola</del>/FONT]<del style="font-weight: bold; text-decoration: none;">subD</del>/<del style="font-weight: bold; text-decoration: none;">subsup23</del>/sup +8.0° (in <del style="font-weight: bold; text-decoration: none;">CHClSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB) 2425</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>|Reflactive=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [<ins style="font-weight: bold; text-decoration: none;"><</ins>FONT FACE=<ins style="font-weight: bold; text-decoration: none;">"Symbol">a<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">></ins>]<ins style="font-weight: bold; text-decoration: none;"><sub>D<</ins>/<ins style="font-weight: bold; text-decoration: none;">sub><sup>25<</ins>/sup<ins style="font-weight: bold; text-decoration: none;">> </ins>+8.0° <ins style="font-weight: bold; text-decoration: none;"><<</ins>2424<ins style="font-weight: bold; text-decoration: none;">>></ins>, [<ins style="font-weight: bold; text-decoration: none;"><</ins>FONT FACE=<ins style="font-weight: bold; text-decoration: none;">"Symbol">a<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">></ins>]<ins style="font-weight: bold; text-decoration: none;"><sub>D<</ins>/<ins style="font-weight: bold; text-decoration: none;">sub><sup>23<</ins>/sup<ins style="font-weight: bold; text-decoration: none;">> </ins>+8.0° (in <ins style="font-weight: bold; text-decoration: none;">CHCl<SUB><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>3<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/SUB<ins style="font-weight: bold; text-decoration: none;">></ins>) <ins style="font-weight: bold; text-decoration: none;"><<</ins>2425<ins style="font-weight: bold; text-decoration: none;">>></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>}}</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>}}</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;"><br></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;"><br></td></tr>
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Editor: LBGPEccp:16000SC01:16000SC01:YB2ANe001:01 moved to LBGPEccp:16000SC01:16000SC01:YB2ANe001
2010-01-27T20:00:00Z
<p><a href="/mediawiki/index.php?title=LBGPEccp:16000SC01:16000SC01:YB2ANe001:01&action=edit&redlink=1" class="new" title="LBGPEccp:16000SC01:16000SC01:YB2ANe001:01 (page does not exist)">LBGPEccp:16000SC01:16000SC01:YB2ANe001:01</a> moved to <a href="/wiki/LBGPEccp:16000SC01:16000SC01:YB2ANe001" title="LBGPEccp:16000SC01:16000SC01:YB2ANe001">LBGPEccp:16000SC01:16000SC01:YB2ANe001</a></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 05:00, 28 January 2010</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l4">Line 4:</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>|LipidBank=PGP2403</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=PGP2403</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=dipalmitoylphosphatidyl-N-methylethanolamine</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=dipalmitoylphosphatidyl-N-methylethanolamine</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;">&&</del>phosphatidyl-N-<del style="font-weight: bold; text-decoration: none;">methylethanolamine&&dipalmitoyl&& </del>phosphatidyl-N-<del style="font-weight: bold; text-decoration: none;">monomethylethanolamine&&dipalmitoyl&& </del>dipalmitoylphosphatidyl-N-monomethylethanolamine<del style="font-weight: bold; text-decoration: none;">&& </del>N-<del style="font-weight: bold; text-decoration: none;">methylphosphatidylethanolamine&&dipalmitoyl&&dipalmitoylphosphatidyl</del>-N-methylethanolamine<del style="font-weight: bold; text-decoration: none;">&&</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=phosphatidyl-N-<ins style="font-weight: bold; text-decoration: none;">methylethanolaminedipalmitoyl </ins>phosphatidyl-N-<ins style="font-weight: bold; text-decoration: none;">monomethylethanolaminedipalmitoyl </ins>dipalmitoylphosphatidyl-N-monomethylethanolamine N-<ins style="font-weight: bold; text-decoration: none;">methylphosphatidylethanolaminedipalmitoyldipalmitoylphosphatidyl</ins>-N-methylethanolamine</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>|Melting Point=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <del style="font-weight: bold; text-decoration: none;"><<</del>2424<del style="font-weight: bold; text-decoration: none;">>></del>, 184-186°C (from <del style="font-weight: bold; text-decoration: none;">CHCl<SUB><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>3<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/SUB<del style="font-weight: bold; text-decoration: none;">></del>-MeOH at 4°C <del style="font-weight: bold; text-decoration: none;"><<</del>2425<del style="font-weight: bold; text-decoration: none;">>></del>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <del style="font-weight: bold; text-decoration: none;"><<</del>2424<del style="font-weight: bold; text-decoration: none;">>></del>, 182°C <del style="font-weight: bold; text-decoration: none;"><<</del>2425<del style="font-weight: bold; text-decoration: none;">>></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>|Melting Point=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C 2424, 184-186°C (from <ins style="font-weight: bold; text-decoration: none;">CHClSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB-MeOH at 4°C 2425; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C 2424, 182°C 2425</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>|Reflactive=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [<del style="font-weight: bold; text-decoration: none;"><</del>FONT FACE=<del style="font-weight: bold; text-decoration: none;">"Symbol">a<</del>/FONT<del style="font-weight: bold; text-decoration: none;">></del>]<del style="font-weight: bold; text-decoration: none;"><sub>D<</del>/<del style="font-weight: bold; text-decoration: none;">sub><sup>25<</del>/sup<del style="font-weight: bold; text-decoration: none;">> </del>+8.0° <del style="font-weight: bold; text-decoration: none;"><<</del>2424<del style="font-weight: bold; text-decoration: none;">>></del>, [<del style="font-weight: bold; text-decoration: none;"><</del>FONT FACE=<del style="font-weight: bold; text-decoration: none;">"Symbol">a<</del>/FONT<del style="font-weight: bold; text-decoration: none;">></del>]<del style="font-weight: bold; text-decoration: none;"><sub>D<</del>/<del style="font-weight: bold; text-decoration: none;">sub><sup>23<</del>/sup<del style="font-weight: bold; text-decoration: none;">> </del>+8.0° (in <del style="font-weight: bold; text-decoration: none;">CHCl<SUB><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>3<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/SUB<del style="font-weight: bold; text-decoration: none;">></del>) <del style="font-weight: bold; text-decoration: none;"><<</del>2425<del style="font-weight: bold; text-decoration: none;">>></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>|Reflactive=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [FONT FACE=<ins style="font-weight: bold; text-decoration: none;">Symbola</ins>/FONT]<ins style="font-weight: bold; text-decoration: none;">subD</ins>/<ins style="font-weight: bold; text-decoration: none;">subsup25</ins>/sup +8.0° 2424, [FONT FACE=<ins style="font-weight: bold; text-decoration: none;">Symbola</ins>/FONT]<ins style="font-weight: bold; text-decoration: none;">subD</ins>/<ins style="font-weight: bold; text-decoration: none;">subsup23</ins>/sup +8.0° (in <ins style="font-weight: bold; text-decoration: none;">CHClSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB) 2425</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>}}</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>}}</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;"><br></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;"><br></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>{{Lipid/Footer}}</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>{{Lipid/Footer}}</div></td></tr>
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Editor: LBGPEccp:16000SC01:16000SC01:YB2ANe001:01 moved to LBGPEccp:16000SC01:16000SC01:YB2ANe001
2010-01-20T01:39:08Z
<p><a href="/mediawiki/index.php?title=LBGPEccp:16000SC01:16000SC01:YB2ANe001:01&action=edit&redlink=1" class="new" title="LBGPEccp:16000SC01:16000SC01:YB2ANe001:01 (page does not exist)">LBGPEccp:16000SC01:16000SC01:YB2ANe001:01</a> moved to <a href="/wiki/LBGPEccp:16000SC01:16000SC01:YB2ANe001" title="LBGPEccp:16000SC01:16000SC01:YB2ANe001">LBGPEccp:16000SC01:16000SC01:YB2ANe001</a></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
<col class="diff-marker" />
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 10:39, 20 January 2010</td>
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https://lipidbank.jp/mediawiki/index.php?title=LBGPEccp:16000SC01:16000SC01:YB2ANe001&diff=65682&oldid=prev
Editor at 13:00, 26 July 2009
2009-07-26T13:00:00Z
<p></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
<col class="diff-marker" />
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<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 22:00, 26 July 2009</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l1">Line 1:</td>
<td colspan="2" class="diff-lineno">Line 1:</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;">{{Lipid/Header}}</ins></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;"></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>{{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=PGP2403</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=PGP2403</div></td></tr>
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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>|Reflactive=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>25</sup> +8.0° <<2424>>, [<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>23</sup> +8.0° (in CHCl<SUB><FONT SIZE=-1>3</FONT></SUB>) <<2425>></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>|Reflactive=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>25</sup> +8.0° <<2424>>, [<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>23</sup> +8.0° (in CHCl<SUB><FONT SIZE=-1>3</FONT></SUB>) <<2425>></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>}}</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>}}</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;"></ins></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;">{{Lipid/Footer}}</ins></div></td></tr>
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https://lipidbank.jp/mediawiki/index.php?title=LBGPEccp:16000SC01:16000SC01:YB2ANe001&diff=65681&oldid=prev
Editor at 12:00, 8 July 2009
2009-07-08T12:00:00Z
<p></p>
<p><b>New page</b></p><div>{{Metabolite<br />
|LipidBank=PGP2403<br />
|SysName=dipalmitoylphosphatidyl-N-methylethanolamine<br />
|Common Name=&&phosphatidyl-N-methylethanolamine&&dipalmitoyl&& phosphatidyl-N-monomethylethanolamine&&dipalmitoyl&& dipalmitoylphosphatidyl-N-monomethylethanolamine&& N-methylphosphatidylethanolamine&&dipalmitoyl&&dipalmitoylphosphatidyl-N-methylethanolamine&&<br />
|Melting Point=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, 177-178°C <<2424>>, 184-186°C (from CHCl<SUB><FONT SIZE=-1>3</FONT></SUB>-MeOH at 4°C <<2425>>; 1,2-dipalmitoyl-DL-N-methylphosphatidylethanolamine, 170-171°C <<2424>>, 182°C <<2425>><br />
|Reflactive=1,2-dipalmitoyl-L-N-methylphosphatidylethanolamine, [<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>25</sup> +8.0° <<2424>>, [<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>23</sup> +8.0° (in CHCl<SUB><FONT SIZE=-1>3</FONT></SUB>) <<2425>><br />
}}</div>
Editor