https://lipidbank.jp/mediawiki/index.php?action=history&feed=atom&title=LBGPEccp%3A18109SC01%3A18109SC01%3AYS2ANe005
LBGPEccp:18109SC01:18109SC01:YS2ANe005 - Revision history
2026-04-29T15:47:34Z
Revision history for this page on the wiki
MediaWiki 1.43.0
https://lipidbank.jp/mediawiki/index.php?title=LBGPEccp:18109SC01:18109SC01:YS2ANe005&diff=65817&oldid=prev
Editor: LBGPEccp:18109SC01:18109SC01:YS2ANe005:01 moved to LBGPEccp:18109SC01:18109SC01:YS2ANe005
2010-04-14T21:00:00Z
<p><a href="/wiki/LBGPEccp:18109SC01:18109SC01:YS2ANe005:01" class="mw-redirect" title="LBGPEccp:18109SC01:18109SC01:YS2ANe005:01">LBGPEccp:18109SC01:18109SC01:YS2ANe005:01</a> moved to <a href="/wiki/LBGPEccp:18109SC01:18109SC01:YS2ANe005" title="LBGPEccp:18109SC01:18109SC01:YS2ANe005">LBGPEccp:18109SC01:18109SC01:YS2ANe005</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-l4">Line 4:</td>
<td colspan="2" class="diff-lineno">Line 4:</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=PGP2415</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=PGP2415</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=1,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine</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=1,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine</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=&&dioleoyl-phosphatidylethanolamine&& dioleoyl-cephalin&& 1,2-dioleoyl- (3-sn-phosphatidyl) ethanolamine&&dioleoyl-L-a-phosphatidylethanolamine<del style="font-weight: bold; text-decoration: none;">&&1,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine</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=&&dioleoyl-phosphatidylethanolamine&&dioleoyl-cephalin&&1,2-dioleoyl- (3-sn-phosphatidyl) ethanolamine&&dioleoyl-L-a-phosphatidylethanolamine&&</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=dioleoyl-PE, 195-200°C <<2507>></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=dioleoyl-PE, 195-200°C <<2507>></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= L- alpha -dioleoyl-PE, [ alpha ]^{22}_D +6.0° in CHCl_3 <<2507>></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= L- alpha -dioleoyl-PE, [ alpha ]^{22}_D +6.0° in CHCl_3 <<2507>></div></td></tr>
<!-- diff cache key wikidb:diff:1.41:old-65816:rev-65817:php=table -->
</table>
Editor
https://lipidbank.jp/mediawiki/index.php?title=LBGPEccp:18109SC01:18109SC01:YS2ANe005&diff=65816&oldid=prev
Editor: LBGPEccp:18109SC01:18109SC01:YS2ANe005:01 moved to LBGPEccp:18109SC01:18109SC01:YS2ANe005
2010-02-25T10:00:10Z
<p><a href="/wiki/LBGPEccp:18109SC01:18109SC01:YS2ANe005:01" class="mw-redirect" title="LBGPEccp:18109SC01:18109SC01:YS2ANe005:01">LBGPEccp:18109SC01:18109SC01:YS2ANe005:01</a> moved to <a href="/wiki/LBGPEccp:18109SC01:18109SC01:YS2ANe005" title="LBGPEccp:18109SC01:18109SC01:YS2ANe005">LBGPEccp:18109SC01:18109SC01:YS2ANe005</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-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>|Common Name=&&dioleoyl-phosphatidylethanolamine&& dioleoyl-cephalin&& 1,2-dioleoyl- (3-sn-phosphatidyl) ethanolamine&&dioleoyl-L-a-phosphatidylethanolamine&&1,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine&&</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=&&dioleoyl-phosphatidylethanolamine&& dioleoyl-cephalin&& 1,2-dioleoyl- (3-sn-phosphatidyl) ethanolamine&&dioleoyl-L-a-phosphatidylethanolamine&&1,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine&&</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=dioleoyl-PE, 195-200°C <<2507>></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=dioleoyl-PE, 195-200°C <<2507>></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= L- alpha -dioleoyl-PE, [ alpha ]^<del style="font-weight: bold; text-decoration: none;">22_D </del>+6.0° in CHCl_3 <<2507>></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= L- alpha -dioleoyl-PE, [ alpha ]^<ins style="font-weight: bold; text-decoration: none;">{22}_D </ins>+6.0° in CHCl_3 <<2507>></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=Insoluble in water. At 20°C, synthetic PEs are insoluble (<=1mg/100 ml of dry solvent) in acetone, ether, petroleum ether, and ethyl acetate; moderately soluble (20-100 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and CCl_4 ; readily soluble (> 1g/100 ml of solvent) in CHCl_3 <<2508/2509/2510>>.</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=Insoluble in water. At 20°C, synthetic PEs are insoluble (<=1mg/100 ml of dry solvent) in acetone, ether, petroleum ether, and ethyl acetate; moderately soluble (20-100 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and CCl_4 ; readily soluble (> 1g/100 ml of solvent) in CHCl_3 <<2508/2509/2510>>.</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>
<!-- diff cache key wikidb:diff:1.41:old-65815:rev-65816:php=table -->
</table>
Editor
https://lipidbank.jp/mediawiki/index.php?title=LBGPEccp:18109SC01:18109SC01:YS2ANe005&diff=65815&oldid=prev
Editor: LBGPEccp:18109SC01:18109SC01:YS2ANe005:01 moved to LBGPEccp:18109SC01:18109SC01:YS2ANe005
2010-02-19T14:00:10Z
<p><a href="/wiki/LBGPEccp:18109SC01:18109SC01:YS2ANe005:01" class="mw-redirect" title="LBGPEccp:18109SC01:18109SC01:YS2ANe005:01">LBGPEccp:18109SC01:18109SC01:YS2ANe005:01</a> moved to <a href="/wiki/LBGPEccp:18109SC01:18109SC01:YS2ANe005" title="LBGPEccp:18109SC01:18109SC01:YS2ANe005">LBGPEccp:18109SC01:18109SC01:YS2ANe005</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-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>|Common Name=&&dioleoyl-phosphatidylethanolamine&& dioleoyl-cephalin&& 1,2-dioleoyl- (3-sn-phosphatidyl) ethanolamine&&dioleoyl-L-a-phosphatidylethanolamine&&1,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine&&</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=&&dioleoyl-phosphatidylethanolamine&& dioleoyl-cephalin&& 1,2-dioleoyl- (3-sn-phosphatidyl) ethanolamine&&dioleoyl-L-a-phosphatidylethanolamine&&1,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine&&</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=dioleoyl-PE, 195-200°C <<2507>></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=dioleoyl-PE, 195-200°C <<2507>></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= L-alpha-dioleoyl-PE, [alpha]^22_D +6.0° in CHCl_3 <<2507>></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= L- alpha -dioleoyl-PE, [ alpha ]^22_D +6.0° in CHCl_3 <<2507>></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=Insoluble in water. At 20°C, synthetic PEs are insoluble (<=1mg/100 ml of dry solvent) in acetone, ether, petroleum ether, and ethyl acetate; moderately soluble (20-100 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and CCl_4 ; readily soluble (> 1g/100 ml of solvent) in CHCl_3 <<2508/2509/2510>>.</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=Insoluble in water. At 20°C, synthetic PEs are insoluble (<=1mg/100 ml of dry solvent) in acetone, ether, petroleum ether, and ethyl acetate; moderately soluble (20-100 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and CCl_4 ; readily soluble (> 1g/100 ml of solvent) in CHCl_3 <<2508/2509/2510>>.</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>
<!-- diff cache key wikidb:diff:1.41:old-65814:rev-65815:php=table -->
</table>
Editor
https://lipidbank.jp/mediawiki/index.php?title=LBGPEccp:18109SC01:18109SC01:YS2ANe005&diff=65814&oldid=prev
Editor: LBGPEccp:18109SC01:18109SC01:YS2ANe005:01 moved to LBGPEccp:18109SC01:18109SC01:YS2ANe005
2010-02-19T14:00:00Z
<p><a href="/wiki/LBGPEccp:18109SC01:18109SC01:YS2ANe005:01" class="mw-redirect" title="LBGPEccp:18109SC01:18109SC01:YS2ANe005:01">LBGPEccp:18109SC01:18109SC01:YS2ANe005:01</a> moved to <a href="/wiki/LBGPEccp:18109SC01:18109SC01:YS2ANe005" title="LBGPEccp:18109SC01:18109SC01:YS2ANe005">LBGPEccp:18109SC01:18109SC01:YS2ANe005</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-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>|Common Name=&&dioleoyl-phosphatidylethanolamine&& dioleoyl-cephalin&& 1,2-dioleoyl- (3-sn-phosphatidyl) ethanolamine&&dioleoyl-L-a-phosphatidylethanolamine&&1,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine&&</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=&&dioleoyl-phosphatidylethanolamine&& dioleoyl-cephalin&& 1,2-dioleoyl- (3-sn-phosphatidyl) ethanolamine&&dioleoyl-L-a-phosphatidylethanolamine&&1,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine&&</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=dioleoyl-PE, 195-200°C <<2507>></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=dioleoyl-PE, 195-200°C <<2507>></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= L-<del style="font-weight: bold; text-decoration: none;"><FONT FACE="Symbol">a</FONT></del>-dioleoyl-PE, [<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>22</sup></del>+6.0° in <del style="font-weight: bold; text-decoration: none;">CHCl<SUB><FONT SIZE=-1>3</FONT></SUB> </del><<2507>></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= L-<ins style="font-weight: bold; text-decoration: none;">alpha</ins>-dioleoyl-PE, [<ins style="font-weight: bold; text-decoration: none;">alpha</ins>]<ins style="font-weight: bold; text-decoration: none;">^22_D </ins>+6.0° in <ins style="font-weight: bold; text-decoration: none;">CHCl_3 </ins><<2507>></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=Insoluble in water. At 20°C, synthetic PEs are insoluble (<=1mg/100 ml of dry solvent) in acetone, ether, petroleum ether, and ethyl acetate; moderately soluble (20-100 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and <del style="font-weight: bold; text-decoration: none;">CCl<SUB><FONT SIZE=-1>4</FONT></SUB></del>; readily soluble (> 1g/100 ml of solvent) in <del style="font-weight: bold; text-decoration: none;">CHCl<SUB><FONT SIZE=-1>3</FONT></SUB> </del><<2508/2509/2510>>.</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=Insoluble in water. At 20°C, synthetic PEs are insoluble (<=1mg/100 ml of dry solvent) in acetone, ether, petroleum ether, and ethyl acetate; moderately soluble (20-100 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and <ins style="font-weight: bold; text-decoration: none;">CCl_4 </ins>; readily soluble (> 1g/100 ml of solvent) in <ins style="font-weight: bold; text-decoration: none;">CHCl_3 </ins><<2508/2509/2510>>.</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>
<!-- diff cache key wikidb:diff:1.41:old-65813:rev-65814:php=table -->
</table>
Editor
https://lipidbank.jp/mediawiki/index.php?title=LBGPEccp:18109SC01:18109SC01:YS2ANe005&diff=65813&oldid=prev
Editor: LBGPEccp:18109SC01:18109SC01:YS2ANe005:01 moved to LBGPEccp:18109SC01:18109SC01:YS2ANe005
2010-02-18T15:00:00Z
<p><a href="/wiki/LBGPEccp:18109SC01:18109SC01:YS2ANe005:01" class="mw-redirect" title="LBGPEccp:18109SC01:18109SC01:YS2ANe005:01">LBGPEccp:18109SC01:18109SC01:YS2ANe005:01</a> moved to <a href="/wiki/LBGPEccp:18109SC01:18109SC01:YS2ANe005" title="LBGPEccp:18109SC01:18109SC01:YS2ANe005">LBGPEccp:18109SC01:18109SC01:YS2ANe005</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 00:00, 19 February 2010</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l4">Line 4:</td>
<td colspan="2" class="diff-lineno">Line 4:</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=PGP2415</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=PGP2415</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=1,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine</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=1,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine</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=dioleoyl-phosphatidylethanolamine dioleoyl-cephalin 1,2-dioleoyl- (3-sn-phosphatidyl) <del style="font-weight: bold; text-decoration: none;">ethanolaminedioleoyl</del>-L-a-<del style="font-weight: bold; text-decoration: none;">phosphatidylethanolamine1</del>,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine</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>dioleoyl-phosphatidylethanolamine<ins style="font-weight: bold; text-decoration: none;">&& </ins>dioleoyl-cephalin<ins style="font-weight: bold; text-decoration: none;">&& </ins>1,2-dioleoyl- (3-sn-phosphatidyl) <ins style="font-weight: bold; text-decoration: none;">ethanolamine&&dioleoyl</ins>-L-a-<ins style="font-weight: bold; text-decoration: none;">phosphatidylethanolamine&&1</ins>,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine<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=dioleoyl-PE, 195-200°C 2507</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=dioleoyl-PE, 195-200°C <ins style="font-weight: bold; text-decoration: none;"><<</ins>2507<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= L-FONT FACE=<del style="font-weight: bold; text-decoration: none;">Symbola</del>/FONT-dioleoyl-PE, [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;">subsup22</del>/sup+6.0° in <del style="font-weight: bold; text-decoration: none;">CHClSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB 2507</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= L-<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>-dioleoyl-PE, [<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>22<</ins>/sup<ins style="font-weight: bold; text-decoration: none;">></ins>+6.0° 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>2507<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>|Solubility=Insoluble in water. At 20°C, synthetic PEs are insoluble (=1mg/100 ml of dry solvent) in acetone, ether, petroleum ether, and ethyl acetate; moderately soluble (20-100 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and <del style="font-weight: bold; text-decoration: none;">CClSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">14</del>/FONT/SUB; readily soluble ( 1g/100 ml of solvent) in <del style="font-weight: bold; text-decoration: none;">CHClSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB 2508/2509/2510.</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=Insoluble in water. At 20°C, synthetic PEs are insoluble (<ins style="font-weight: bold; text-decoration: none;"><</ins>=1mg/100 ml of dry solvent) in acetone, ether, petroleum ether, and ethyl acetate; moderately soluble (20-100 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and <ins style="font-weight: bold; text-decoration: none;">CCl<SUB><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>4<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/SUB<ins style="font-weight: bold; text-decoration: none;">></ins>; readily soluble (<ins style="font-weight: bold; text-decoration: none;">> </ins>1g/100 ml of solvent) 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>2508/2509/2510<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>
<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>
<!-- diff cache key wikidb:diff:1.41:old-65812:rev-65813:php=table -->
</table>
Editor
https://lipidbank.jp/mediawiki/index.php?title=LBGPEccp:18109SC01:18109SC01:YS2ANe005&diff=65812&oldid=prev
Editor: LBGPEccp:18109SC01:18109SC01:YS2ANe005:01 moved to LBGPEccp:18109SC01:18109SC01:YS2ANe005
2010-01-27T20:00:00Z
<p><a href="/wiki/LBGPEccp:18109SC01:18109SC01:YS2ANe005:01" class="mw-redirect" title="LBGPEccp:18109SC01:18109SC01:YS2ANe005:01">LBGPEccp:18109SC01:18109SC01:YS2ANe005:01</a> moved to <a href="/wiki/LBGPEccp:18109SC01:18109SC01:YS2ANe005" title="LBGPEccp:18109SC01:18109SC01:YS2ANe005">LBGPEccp:18109SC01:18109SC01:YS2ANe005</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 05:00, 28 January 2010</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l4">Line 4:</td>
<td colspan="2" class="diff-lineno">Line 4:</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=PGP2415</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=PGP2415</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=1,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine</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=1,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine</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>dioleoyl-phosphatidylethanolamine<del style="font-weight: bold; text-decoration: none;">&& </del>dioleoyl-cephalin<del style="font-weight: bold; text-decoration: none;">&& </del>1,2-dioleoyl- (3-sn-phosphatidyl) <del style="font-weight: bold; text-decoration: none;">ethanolamine&&dioleoyl</del>-L-a-<del style="font-weight: bold; text-decoration: none;">phosphatidylethanolamine&&1</del>,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine<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=dioleoyl-phosphatidylethanolamine dioleoyl-cephalin 1,2-dioleoyl- (3-sn-phosphatidyl) <ins style="font-weight: bold; text-decoration: none;">ethanolaminedioleoyl</ins>-L-a-<ins style="font-weight: bold; text-decoration: none;">phosphatidylethanolamine1</ins>,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine</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=dioleoyl-PE, 195-200°C <del style="font-weight: bold; text-decoration: none;"><<</del>2507<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=dioleoyl-PE, 195-200°C 2507</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= L-<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>-dioleoyl-PE, [<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>22<</del>/sup<del style="font-weight: bold; text-decoration: none;">></del>+6.0° 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>2507<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= L-FONT FACE=<ins style="font-weight: bold; text-decoration: none;">Symbola</ins>/FONT-dioleoyl-PE, [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;">subsup22</ins>/sup+6.0° in <ins style="font-weight: bold; text-decoration: none;">CHClSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB 2507</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=Insoluble in water. At 20°C, synthetic PEs are insoluble (<del style="font-weight: bold; text-decoration: none;"><</del>=1mg/100 ml of dry solvent) in acetone, ether, petroleum ether, and ethyl acetate; moderately soluble (20-100 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and <del style="font-weight: bold; text-decoration: none;">CCl<SUB><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>4<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/SUB<del style="font-weight: bold; text-decoration: none;">></del>; readily soluble (<del style="font-weight: bold; text-decoration: none;">> </del>1g/100 ml of solvent) 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>2508/2509/2510<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>|Solubility=Insoluble in water. At 20°C, synthetic PEs are insoluble (=1mg/100 ml of dry solvent) in acetone, ether, petroleum ether, and ethyl acetate; moderately soluble (20-100 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and <ins style="font-weight: bold; text-decoration: none;">CClSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">14</ins>/FONT/SUB; readily soluble ( 1g/100 ml of solvent) in <ins style="font-weight: bold; text-decoration: none;">CHClSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB 2508/2509/2510.</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>
<!-- diff cache key wikidb:diff:1.41:old-65811:rev-65812:php=table -->
</table>
Editor
https://lipidbank.jp/mediawiki/index.php?title=LBGPEccp:18109SC01:18109SC01:YS2ANe005&diff=65811&oldid=prev
Editor: LBGPEccp:18109SC01:18109SC01:YS2ANe005:01 moved to LBGPEccp:18109SC01:18109SC01:YS2ANe005
2010-01-20T01:39:08Z
<p><a href="/wiki/LBGPEccp:18109SC01:18109SC01:YS2ANe005:01" class="mw-redirect" title="LBGPEccp:18109SC01:18109SC01:YS2ANe005:01">LBGPEccp:18109SC01:18109SC01:YS2ANe005:01</a> moved to <a href="/wiki/LBGPEccp:18109SC01:18109SC01:YS2ANe005" title="LBGPEccp:18109SC01:18109SC01:YS2ANe005">LBGPEccp:18109SC01:18109SC01:YS2ANe005</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 10:39, 20 January 2010</td>
</tr><tr><td colspan="4" class="diff-notice" lang="en"><div class="mw-diff-empty">(No difference)</div>
</td></tr>
<!-- diff cache key wikidb:diff:1.41:old-65810:rev-65811 -->
</table>
Editor
https://lipidbank.jp/mediawiki/index.php?title=LBGPEccp:18109SC01:18109SC01:YS2ANe005&diff=65810&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" />
<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 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=PGP2415</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=PGP2415</div></td></tr>
<tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l5">Line 5:</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>|Melting Point=dioleoyl-PE, 195-200°C <<2507>></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=dioleoyl-PE, 195-200°C <<2507>></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= L-<FONT FACE="Symbol">a</FONT>-dioleoyl-PE, [<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>22</sup>+6.0° in CHCl<SUB><FONT SIZE=-1>3</FONT></SUB> <<2507>></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= L-<FONT FACE="Symbol">a</FONT>-dioleoyl-PE, [<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>22</sup>+6.0° in CHCl<SUB><FONT SIZE=-1>3</FONT></SUB> <<2507>></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=Insoluble in water. At 20°C, synthetic PEs are insoluble (=1mg/100 ml of dry solvent) in acetone, ether, petroleum ether, and ethyl acetate; moderately soluble (20-100 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and CCl<SUB><FONT SIZE=-1>4</FONT></SUB>; readily soluble (> 1g/100 ml of solvent) in CHCl<SUB><FONT SIZE=-1>3</FONT></SUB> <<2508/2509/2510>>.</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=Insoluble in water. At 20°C, synthetic PEs are insoluble (<ins style="font-weight: bold; text-decoration: none;"><</ins>=1mg/100 ml of dry solvent) in acetone, ether, petroleum ether, and ethyl acetate; moderately soluble (20-100 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and CCl<SUB><FONT SIZE=-1>4</FONT></SUB>; readily soluble (> 1g/100 ml of solvent) in CHCl<SUB><FONT SIZE=-1>3</FONT></SUB> <<2508/2509/2510>>.</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>
<!-- diff cache key wikidb:diff:1.41:old-65809:rev-65810:php=table -->
</table>
Editor
https://lipidbank.jp/mediawiki/index.php?title=LBGPEccp:18109SC01:18109SC01:YS2ANe005&diff=65809&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=PGP2415<br />
|SysName=1,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine<br />
|Common Name=&&dioleoyl-phosphatidylethanolamine&& dioleoyl-cephalin&& 1,2-dioleoyl- (3-sn-phosphatidyl) ethanolamine&&dioleoyl-L-a-phosphatidylethanolamine&&1,2-di-oleoyl-sn-glycero- (3) -phosphoethanolamine&&<br />
|Melting Point=dioleoyl-PE, 195-200°C <<2507>><br />
|Reflactive= L-<FONT FACE="Symbol">a</FONT>-dioleoyl-PE, [<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>22</sup>+6.0° in CHCl<SUB><FONT SIZE=-1>3</FONT></SUB> <<2507>><br />
|Solubility=Insoluble in water. At 20°C, synthetic PEs are insoluble (=1mg/100 ml of dry solvent) in acetone, ether, petroleum ether, and ethyl acetate; moderately soluble (20-100 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and CCl<SUB><FONT SIZE=-1>4</FONT></SUB>; readily soluble (> 1g/100 ml of solvent) in CHCl<SUB><FONT SIZE=-1>3</FONT></SUB> <<2508/2509/2510>>.<br />
}}</div>
Editor