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LBGPEccp:14000SC01:18000SC01:YS2ANe005 - Revision history
2026-04-29T21:16:35Z
Revision history for this page on the wiki
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Editor: LBGPEccp:14000SC01:18000SC01:YS2ANe005:01 moved to LBGPEccp:14000SC01:18000SC01:YS2ANe005
2010-04-14T21:00:00Z
<p><a href="/wiki/LBGPEccp:14000SC01:18000SC01:YS2ANe005:01" class="mw-redirect" title="LBGPEccp:14000SC01:18000SC01:YS2ANe005:01">LBGPEccp:14000SC01:18000SC01:YS2ANe005:01</a> moved to <a href="/wiki/LBGPEccp:14000SC01:18000SC01:YS2ANe005" title="LBGPEccp:14000SC01:18000SC01:YS2ANe005">LBGPEccp:14000SC01:18000SC01:YS2ANe005</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>|LipidBank=PGP2412</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=PGP2412</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-myristoyl-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-myristoyl-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=&&dimyristoyl-phosphatidylethanolamine&& ethanolaminephosphoglyceride&&1,2-dimyristoyl- (3-sn-phosphatidyl) ethanolamine&&dimyristoyl-L-a-phosphatidylethanolamine<del style="font-weight: bold; text-decoration: none;">&&1,2-di-myristoyl-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=&&dimyristoyl-phosphatidylethanolamine&&ethanolaminephosphoglyceride&&1,2-dimyristoyl- (3-sn-phosphatidyl) ethanolamine&&dimyristoyl-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=175-177°C <<2481/2482>></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=175-177°C <<2481/2482>></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=[ alpha ]^{26}_D +6.7° in CHCl_3 <<2481/2482>></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=[ alpha ]^{26}_D +6.7° in CHCl_3 <<2481/2482>></div></td></tr>
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Editor: LBGPEccp:14000SC01:18000SC01:YS2ANe005:01 moved to LBGPEccp:14000SC01:18000SC01:YS2ANe005
2010-02-25T10:00:10Z
<p><a href="/wiki/LBGPEccp:14000SC01:18000SC01:YS2ANe005:01" class="mw-redirect" title="LBGPEccp:14000SC01:18000SC01:YS2ANe005:01">LBGPEccp:14000SC01:18000SC01:YS2ANe005:01</a> moved to <a href="/wiki/LBGPEccp:14000SC01:18000SC01:YS2ANe005" title="LBGPEccp:14000SC01:18000SC01:YS2ANe005">LBGPEccp:14000SC01:18000SC01:YS2ANe005</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=&&dimyristoyl-phosphatidylethanolamine&& ethanolaminephosphoglyceride&&1,2-dimyristoyl- (3-sn-phosphatidyl) ethanolamine&&dimyristoyl-L-a-phosphatidylethanolamine&&1,2-di-myristoyl-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=&&dimyristoyl-phosphatidylethanolamine&& ethanolaminephosphoglyceride&&1,2-dimyristoyl- (3-sn-phosphatidyl) ethanolamine&&dimyristoyl-L-a-phosphatidylethanolamine&&1,2-di-myristoyl-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=175-177°C <<2481/2482>></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=175-177°C <<2481/2482>></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=[ alpha ]^<del style="font-weight: bold; text-decoration: none;">26_D </del>+6.7° in CHCl_3 <<2481/2482>></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=[ alpha ]^<ins style="font-weight: bold; text-decoration: none;">{26}_D </ins>+6.7° in CHCl_3 <<2481/2482>></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 (80 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and CCl_4 ; readily soluble (> 1g/100 ml of solvent) in CHCl_3 . <<2482>></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 (80 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and CCl_4 ; readily soluble (> 1g/100 ml of solvent) in CHCl_3 . <<2482>></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>|IR Spectra=Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of alpha -tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 cm^- <del style="font-weight: bold; text-decoration: none;">^</del>1 ; <del style="font-weight: bold; text-decoration: none;">CH_2</del>^- <del style="font-weight: bold; text-decoration: none;">^</del>1 ; headgroup <del style="font-weight: bold; text-decoration: none;">PO_2</del>^- phosphate band region, 1350-1150 cm^- <del style="font-weight: bold; text-decoration: none;">^</del>1 <del style="font-weight: bold; text-decoration: none;"> </del>{{Image200|LBGPEccp:14000SC01:18000SC01:YS2ANe005SP0001.gif}} <<2483>>.</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>|IR Spectra=Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of alpha -tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 cm^<ins style="font-weight: bold; text-decoration: none;">{</ins>-1<ins style="font-weight: bold; text-decoration: none;">}</ins>; <ins style="font-weight: bold; text-decoration: none;">CH</ins>^<ins style="font-weight: bold; text-decoration: none;">{</ins>-1<ins style="font-weight: bold; text-decoration: none;">}_2 </ins>; headgroup <ins style="font-weight: bold; text-decoration: none;">PO</ins>^-<ins style="font-weight: bold; text-decoration: none;">_2 </ins> phosphate band region, 1350-1150 cm^<ins style="font-weight: bold; text-decoration: none;">{</ins>-1<ins style="font-weight: bold; text-decoration: none;">} </ins>{{Image200|LBGPEccp:14000SC01:18000SC01:YS2ANe005SP0001.gif}} <<2483>>.</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:14000SC01:18000SC01:YS2ANe005:01 moved to LBGPEccp:14000SC01:18000SC01:YS2ANe005
2010-02-19T14:00:10Z
<p><a href="/wiki/LBGPEccp:14000SC01:18000SC01:YS2ANe005:01" class="mw-redirect" title="LBGPEccp:14000SC01:18000SC01:YS2ANe005:01">LBGPEccp:14000SC01:18000SC01:YS2ANe005:01</a> moved to <a href="/wiki/LBGPEccp:14000SC01:18000SC01:YS2ANe005" title="LBGPEccp:14000SC01:18000SC01:YS2ANe005">LBGPEccp:14000SC01:18000SC01:YS2ANe005</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 23:00, 19 February 2010</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l6">Line 6:</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=&&dimyristoyl-phosphatidylethanolamine&& ethanolaminephosphoglyceride&&1,2-dimyristoyl- (3-sn-phosphatidyl) ethanolamine&&dimyristoyl-L-a-phosphatidylethanolamine&&1,2-di-myristoyl-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=&&dimyristoyl-phosphatidylethanolamine&& ethanolaminephosphoglyceride&&1,2-dimyristoyl- (3-sn-phosphatidyl) ethanolamine&&dimyristoyl-L-a-phosphatidylethanolamine&&1,2-di-myristoyl-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=175-177°C <<2481/2482>></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=175-177°C <<2481/2482>></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=[alpha]^26_D +6.7° in CHCl_3 <<2481/2482>></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=[ alpha ]^26_D +6.7° in CHCl_3 <<2481/2482>></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 (80 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and CCl_4 ; readily soluble (> 1g/100 ml of solvent) in CHCl_3 . <<2482>></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 (80 mg/100 ml of dry solvent) in EtOH, pyridine, benzene, and CCl_4 ; readily soluble (> 1g/100 ml of solvent) in CHCl_3 . <<2482>></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>|IR Spectra=Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of alpha-tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 cm^- ^1 ; CH_2^- ^1 ; headgroup PO_2^- phosphate band region, 1350-1150 cm^- ^1 {{Image200|LBGPEccp:14000SC01:18000SC01:YS2ANe005SP0001.gif}} <<2483>>.</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>|IR Spectra=Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of <ins style="font-weight: bold; text-decoration: none;"> </ins>alpha -tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 cm^- ^1 ; CH_2^- ^1 ; headgroup PO_2^- phosphate band region, 1350-1150 cm^- ^1 {{Image200|LBGPEccp:14000SC01:18000SC01:YS2ANe005SP0001.gif}} <<2483>>.</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:14000SC01:18000SC01:YS2ANe005:01 moved to LBGPEccp:14000SC01:18000SC01:YS2ANe005
2010-02-19T14:00:00Z
<p><a href="/wiki/LBGPEccp:14000SC01:18000SC01:YS2ANe005:01" class="mw-redirect" title="LBGPEccp:14000SC01:18000SC01:YS2ANe005:01">LBGPEccp:14000SC01:18000SC01:YS2ANe005:01</a> moved to <a href="/wiki/LBGPEccp:14000SC01:18000SC01:YS2ANe005" title="LBGPEccp:14000SC01:18000SC01:YS2ANe005">LBGPEccp:14000SC01:18000SC01:YS2ANe005</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 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=&&dimyristoyl-phosphatidylethanolamine&& ethanolaminephosphoglyceride&&1,2-dimyristoyl- (3-sn-phosphatidyl) ethanolamine&&dimyristoyl-L-a-phosphatidylethanolamine&&1,2-di-myristoyl-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=&&dimyristoyl-phosphatidylethanolamine&& ethanolaminephosphoglyceride&&1,2-dimyristoyl- (3-sn-phosphatidyl) ethanolamine&&dimyristoyl-L-a-phosphatidylethanolamine&&1,2-di-myristoyl-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=175-177°C <<2481/2482>></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=175-177°C <<2481/2482>></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=[<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>26</sup></del>+6.7° in <del style="font-weight: bold; text-decoration: none;">CHCl<SUB><FONT SIZE=-1>3</FONT></SUB> </del><<2481/2482>></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=[<ins style="font-weight: bold; text-decoration: none;">alpha</ins>]<ins style="font-weight: bold; text-decoration: none;">^26_D </ins>+6.7° in <ins style="font-weight: bold; text-decoration: none;">CHCl_3 </ins><<2481/2482>></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 (80 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>. <<2482>></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 (80 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>. <<2482>></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>|IR Spectra=Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of <del style="font-weight: bold; text-decoration: none;"><FONT FACE="Symbol">a</FONT></del>-tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 cm<del style="font-weight: bold; text-decoration: none;"><SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=</del>-1<del style="font-weight: bold; text-decoration: none;">>1</FONT></SUP></del>; <del style="font-weight: bold; text-decoration: none;">CH<SUB><FONT SIZE=</del>-1<del style="font-weight: bold; text-decoration: none;">>2</FONT></SUB> deformation, scissoring band region, 1500-1400 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP></del>; headgroup <del style="font-weight: bold; text-decoration: none;">PO<SUB><FONT SIZE=-1>2</FONT></SUB><SUP><FONT SIZE=</del>-<del style="font-weight: bold; text-decoration: none;">1>-</FONT></SUP> </del>phosphate band region, 1350-1150 cm<del style="font-weight: bold; text-decoration: none;"><SUP><FONT SIZE=</del>-1<del style="font-weight: bold; text-decoration: none;">>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP> </del>{{Image200|LBGPEccp:14000SC01:18000SC01:YS2ANe005SP0001.gif}} <<2483>>.</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>|IR Spectra=Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of <ins style="font-weight: bold; text-decoration: none;">alpha</ins>-tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 cm<ins style="font-weight: bold; text-decoration: none;">^</ins>- <ins style="font-weight: bold; text-decoration: none;">^</ins>1 ; <ins style="font-weight: bold; text-decoration: none;">CH_2^</ins>- <ins style="font-weight: bold; text-decoration: none;">^</ins>1 ; headgroup <ins style="font-weight: bold; text-decoration: none;">PO_2^</ins>- <ins style="font-weight: bold; text-decoration: none;"> </ins>phosphate band region, 1350-1150 cm<ins style="font-weight: bold; text-decoration: none;">^</ins>- <ins style="font-weight: bold; text-decoration: none;">^</ins>1 <ins style="font-weight: bold; text-decoration: none;"> </ins>{{Image200|LBGPEccp:14000SC01:18000SC01:YS2ANe005SP0001.gif}} <<2483>>.</div></td></tr>
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2010-02-18T15:00:00Z
<p><a href="/wiki/LBGPEccp:14000SC01:18000SC01:YS2ANe005:01" class="mw-redirect" title="LBGPEccp:14000SC01:18000SC01:YS2ANe005:01">LBGPEccp:14000SC01:18000SC01:YS2ANe005:01</a> moved to <a href="/wiki/LBGPEccp:14000SC01:18000SC01:YS2ANe005" title="LBGPEccp:14000SC01:18000SC01:YS2ANe005">LBGPEccp:14000SC01:18000SC01:YS2ANe005</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 00:00, 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>|LipidBank=PGP2412</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=PGP2412</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-myristoyl-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-myristoyl-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=dimyristoyl-phosphatidylethanolamine <del style="font-weight: bold; text-decoration: none;">ethanolaminephosphoglyceride1</del>,2-dimyristoyl- (3-sn-phosphatidyl) <del style="font-weight: bold; text-decoration: none;">ethanolaminedimyristoyl</del>-L-a-<del style="font-weight: bold; text-decoration: none;">phosphatidylethanolamine1</del>,2-di-myristoyl-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>dimyristoyl-phosphatidylethanolamine<ins style="font-weight: bold; text-decoration: none;">&& ethanolaminephosphoglyceride&&1</ins>,2-dimyristoyl- (3-sn-phosphatidyl) <ins style="font-weight: bold; text-decoration: none;">ethanolamine&&dimyristoyl</ins>-L-a-<ins style="font-weight: bold; text-decoration: none;">phosphatidylethanolamine&&1</ins>,2-di-myristoyl-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=175-177°C 2481/2482</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=175-177°C <ins style="font-weight: bold; text-decoration: none;"><<</ins>2481/2482<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=[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;">subsup26</del>/sup+6.7° in <del style="font-weight: bold; text-decoration: none;">CHClSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB 2481/2482</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=[<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>26<</ins>/sup<ins style="font-weight: bold; text-decoration: none;">></ins>+6.7° 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>2481/2482<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 (80 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. 2482</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 (80 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>. <ins style="font-weight: bold; text-decoration: none;"><<</ins>2482<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>|IR Spectra=Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of FONT FACE=<del style="font-weight: bold; text-decoration: none;">Symbola</del>/FONT-tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 <del style="font-weight: bold; text-decoration: none;">cmSUPFONT </del>SIZE=-1-/FONT/<del style="font-weight: bold; text-decoration: none;">SUPSUPFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">11</del>/FONT/SUP; <del style="font-weight: bold; text-decoration: none;">CHSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">12</del>/FONT/SUB deformation, scissoring band region, 1500-1400 <del style="font-weight: bold; text-decoration: none;">cmSUPFONT </del>SIZE=-1-/FONT/<del style="font-weight: bold; text-decoration: none;">SUPSUPFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">11</del>/FONT/SUP; headgroup <del style="font-weight: bold; text-decoration: none;">POSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">12</del>/FONT/<del style="font-weight: bold; text-decoration: none;">SUBSUPFONT </del>SIZE=-1-/FONT/SUP phosphate band region, 1350-1150 <del style="font-weight: bold; text-decoration: none;">cmSUPFONT </del>SIZE=-1-/FONT/<del style="font-weight: bold; text-decoration: none;">SUPSUPFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">11</del>/FONT/SUP {{Image200|LBGPEccp:14000SC01:18000SC01:YS2ANe005SP0001.gif}} 2483.</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>|IR Spectra=Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of <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>-tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 <ins style="font-weight: bold; text-decoration: none;">cm<SUP><FONT </ins>SIZE=-1<ins style="font-weight: bold; text-decoration: none;">></ins>-<ins style="font-weight: bold; text-decoration: none;"><</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/<ins style="font-weight: bold; text-decoration: none;">SUP><SUP><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>1<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/SUP<ins style="font-weight: bold; text-decoration: none;">></ins>; <ins style="font-weight: bold; text-decoration: none;">CH<SUB><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>2<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/SUB<ins style="font-weight: bold; text-decoration: none;">> </ins>deformation, scissoring band region, 1500-1400 <ins style="font-weight: bold; text-decoration: none;">cm<SUP><FONT </ins>SIZE=-1<ins style="font-weight: bold; text-decoration: none;">></ins>-<ins style="font-weight: bold; text-decoration: none;"><</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/<ins style="font-weight: bold; text-decoration: none;">SUP><SUP><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>1<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/SUP<ins style="font-weight: bold; text-decoration: none;">></ins>; headgroup <ins style="font-weight: bold; text-decoration: none;">PO<SUB><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>2<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/<ins style="font-weight: bold; text-decoration: none;">SUB><SUP><FONT </ins>SIZE=-1<ins style="font-weight: bold; text-decoration: none;">></ins>-<ins style="font-weight: bold; text-decoration: none;"><</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/SUP<ins style="font-weight: bold; text-decoration: none;">> </ins>phosphate band region, 1350-1150 <ins style="font-weight: bold; text-decoration: none;">cm<SUP><FONT </ins>SIZE=-1<ins style="font-weight: bold; text-decoration: none;">></ins>-<ins style="font-weight: bold; text-decoration: none;"><</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/<ins style="font-weight: bold; text-decoration: none;">SUP><SUP><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>1<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/SUP<ins style="font-weight: bold; text-decoration: none;">> </ins>{{Image200|LBGPEccp:14000SC01:18000SC01:YS2ANe005SP0001.gif}} <ins style="font-weight: bold; text-decoration: none;"><<</ins>2483<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>
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Editor: LBGPEccp:14000SC01:18000SC01:YS2ANe005:01 moved to LBGPEccp:14000SC01:18000SC01:YS2ANe005
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<p><a href="/wiki/LBGPEccp:14000SC01:18000SC01:YS2ANe005:01" class="mw-redirect" title="LBGPEccp:14000SC01:18000SC01:YS2ANe005:01">LBGPEccp:14000SC01:18000SC01:YS2ANe005:01</a> moved to <a href="/wiki/LBGPEccp:14000SC01:18000SC01:YS2ANe005" title="LBGPEccp:14000SC01:18000SC01:YS2ANe005">LBGPEccp:14000SC01:18000SC01:YS2ANe005</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 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=PGP2412</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=PGP2412</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-myristoyl-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-myristoyl-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>dimyristoyl-phosphatidylethanolamine<del style="font-weight: bold; text-decoration: none;">&& ethanolaminephosphoglyceride&&1</del>,2-dimyristoyl- (3-sn-phosphatidyl) <del style="font-weight: bold; text-decoration: none;">ethanolamine&&dimyristoyl</del>-L-a-<del style="font-weight: bold; text-decoration: none;">phosphatidylethanolamine&&1</del>,2-di-myristoyl-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=dimyristoyl-phosphatidylethanolamine <ins style="font-weight: bold; text-decoration: none;">ethanolaminephosphoglyceride1</ins>,2-dimyristoyl- (3-sn-phosphatidyl) <ins style="font-weight: bold; text-decoration: none;">ethanolaminedimyristoyl</ins>-L-a-<ins style="font-weight: bold; text-decoration: none;">phosphatidylethanolamine1</ins>,2-di-myristoyl-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=175-177°C <del style="font-weight: bold; text-decoration: none;"><<</del>2481/2482<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=175-177°C 2481/2482</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=[<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>26<</del>/sup<del style="font-weight: bold; text-decoration: none;">></del>+6.7° 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>2481/2482<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=[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;">subsup26</ins>/sup+6.7° in <ins style="font-weight: bold; text-decoration: none;">CHClSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB 2481/2482</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 (80 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>. <del style="font-weight: bold; text-decoration: none;"><<</del>2482<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 (80 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. 2482</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>|IR Spectra=Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of <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>-tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 <del style="font-weight: bold; text-decoration: none;">cm<SUP><FONT </del>SIZE=-1<del style="font-weight: bold; text-decoration: none;">></del>-<del style="font-weight: bold; text-decoration: none;"><</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/<del style="font-weight: bold; text-decoration: none;">SUP><SUP><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>1<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/SUP<del style="font-weight: bold; text-decoration: none;">></del>; <del style="font-weight: bold; text-decoration: none;">CH<SUB><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>2<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/SUB<del style="font-weight: bold; text-decoration: none;">> </del>deformation, scissoring band region, 1500-1400 <del style="font-weight: bold; text-decoration: none;">cm<SUP><FONT </del>SIZE=-1<del style="font-weight: bold; text-decoration: none;">></del>-<del style="font-weight: bold; text-decoration: none;"><</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/<del style="font-weight: bold; text-decoration: none;">SUP><SUP><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>1<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/SUP<del style="font-weight: bold; text-decoration: none;">></del>; headgroup <del style="font-weight: bold; text-decoration: none;">PO<SUB><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>2<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/<del style="font-weight: bold; text-decoration: none;">SUB><SUP><FONT </del>SIZE=-1<del style="font-weight: bold; text-decoration: none;">></del>-<del style="font-weight: bold; text-decoration: none;"><</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/SUP<del style="font-weight: bold; text-decoration: none;">> </del>phosphate band region, 1350-1150 <del style="font-weight: bold; text-decoration: none;">cm<SUP><FONT </del>SIZE=-1<del style="font-weight: bold; text-decoration: none;">></del>-<del style="font-weight: bold; text-decoration: none;"><</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/<del style="font-weight: bold; text-decoration: none;">SUP><SUP><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>1<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/SUP<del style="font-weight: bold; text-decoration: none;">> </del>{{Image200|LBGPEccp:14000SC01:18000SC01:<del style="font-weight: bold; text-decoration: none;">YS2ANe005:01SP0001</del>.gif}} <del style="font-weight: bold; text-decoration: none;"><<</del>2483<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>|IR Spectra=Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of FONT FACE=<ins style="font-weight: bold; text-decoration: none;">Symbola</ins>/FONT-tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 <ins style="font-weight: bold; text-decoration: none;">cmSUPFONT </ins>SIZE=-1-/FONT/<ins style="font-weight: bold; text-decoration: none;">SUPSUPFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">11</ins>/FONT/SUP; <ins style="font-weight: bold; text-decoration: none;">CHSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">12</ins>/FONT/SUB deformation, scissoring band region, 1500-1400 <ins style="font-weight: bold; text-decoration: none;">cmSUPFONT </ins>SIZE=-1-/FONT/<ins style="font-weight: bold; text-decoration: none;">SUPSUPFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">11</ins>/FONT/SUP; headgroup <ins style="font-weight: bold; text-decoration: none;">POSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">12</ins>/FONT/<ins style="font-weight: bold; text-decoration: none;">SUBSUPFONT </ins>SIZE=-1-/FONT/SUP phosphate band region, 1350-1150 <ins style="font-weight: bold; text-decoration: none;">cmSUPFONT </ins>SIZE=-1-/FONT/<ins style="font-weight: bold; text-decoration: none;">SUPSUPFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">11</ins>/FONT/SUP {{Image200|LBGPEccp:14000SC01:18000SC01:<ins style="font-weight: bold; text-decoration: none;">YS2ANe005SP0001</ins>.gif}} 2483.</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:14000SC01:18000SC01:YS2ANe005:01 moved to LBGPEccp:14000SC01:18000SC01:YS2ANe005
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https://lipidbank.jp/mediawiki/index.php?title=LBGPEccp:14000SC01:18000SC01:YS2ANe005&diff=65668&oldid=prev
Editor at 04:57, 27 July 2009
2009-07-27T04:57:13Z
<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 13:57, 27 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=PGP2412</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=PGP2412</div></td></tr>
<tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l8">Line 8:</td>
<td colspan="2" class="diff-lineno">Line 10:</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>|IR Spectra=Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of <FONT FACE="Symbol">a</FONT>-tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>; CH<SUB><FONT SIZE=-1>2</FONT></SUB> deformation, scissoring band region, 1500-1400 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>; headgroup PO<SUB><FONT SIZE=-1>2</FONT></SUB><SUP><FONT SIZE=-1>-</FONT></SUP> phosphate band region, 1350-1150 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP> {{Image200|LBGPEccp:14000SC01:18000SC01:YS2ANe005:01SP0001.gif}} <<2483>>.</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>|IR Spectra=Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of <FONT FACE="Symbol">a</FONT>-tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>; CH<SUB><FONT SIZE=-1>2</FONT></SUB> deformation, scissoring band region, 1500-1400 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>; headgroup PO<SUB><FONT SIZE=-1>2</FONT></SUB><SUP><FONT SIZE=-1>-</FONT></SUP> phosphate band region, 1350-1150 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP> {{Image200|LBGPEccp:14000SC01:18000SC01:YS2ANe005:01SP0001.gif}} <<2483>>.</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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Editor
https://lipidbank.jp/mediawiki/index.php?title=LBGPEccp:14000SC01:18000SC01:YS2ANe005&diff=65667&oldid=prev
Editor at 04:48, 27 July 2009
2009-07-27T04:48:50Z
<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 13:48, 27 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 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><del style="font-weight: bold; text-decoration: none;">{{Lipid/Header}}</del></div></td><td colspan="2" class="diff-side-added"></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><del style="font-weight: bold; text-decoration: none;"></del></div></td><td colspan="2" class="diff-side-added"></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=PGP2412</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=PGP2412</div></td></tr>
<tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l10">Line 10:</td>
<td colspan="2" class="diff-lineno">Line 8:</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>|IR Spectra=Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of <FONT FACE="Symbol">a</FONT>-tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>; CH<SUB><FONT SIZE=-1>2</FONT></SUB> deformation, scissoring band region, 1500-1400 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>; headgroup PO<SUB><FONT SIZE=-1>2</FONT></SUB><SUP><FONT SIZE=-1>-</FONT></SUP> phosphate band region, 1350-1150 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP> {{Image200|LBGPEccp:14000SC01:18000SC01:YS2ANe005:01SP0001.gif}} <<2483>>.</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>|IR Spectra=Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of <FONT FACE="Symbol">a</FONT>-tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>; CH<SUB><FONT SIZE=-1>2</FONT></SUB> deformation, scissoring band region, 1500-1400 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>; headgroup PO<SUB><FONT SIZE=-1>2</FONT></SUB><SUP><FONT SIZE=-1>-</FONT></SUP> phosphate band region, 1350-1150 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP> {{Image200|LBGPEccp:14000SC01:18000SC01:YS2ANe005:01SP0001.gif}} <<2483>>.</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" 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><del style="font-weight: bold; text-decoration: none;"></del></div></td><td colspan="2" class="diff-side-added"></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><del style="font-weight: bold; text-decoration: none;">{{Lipid/Footer}}</del></div></td><td colspan="2" class="diff-side-added"></td></tr>
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Editor
https://lipidbank.jp/mediawiki/index.php?title=LBGPEccp:14000SC01:18000SC01:YS2ANe005&diff=65666&oldid=prev
Editor at 14:00, 26 July 2009
2009-07-26T14:00:00Z
<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 23:00, 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=PGP2412</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=PGP2412</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=175-177°C <<2481/2482>></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=175-177°C <<2481/2482>></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=[<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>26</sup>+6.7° in CHCl<SUB><FONT SIZE=-1>3</FONT></SUB> <<2481/2482>></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=[<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>26</sup>+6.7° in CHCl<SUB><FONT SIZE=-1>3</FONT></SUB> <<2481/2482>></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 (80 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>. <<2482>></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 (80 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>. <<2482>></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>|IR Spectra=Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of <FONT FACE="Symbol">a</FONT>-tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>; CH<SUB><FONT SIZE=-1>2</FONT></SUB> deformation, scissoring band region, 1500-1400 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>; headgroup PO<SUB><FONT SIZE=-1>2</FONT></SUB><SUP><FONT SIZE=-1>-</FONT></SUP> phosphate band region, 1350-1150 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP> {{Image200|LBGPEccp:14000SC01:18000SC01:YS2ANe005:01SP0001.gif}} <<2483>>.</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>|IR Spectra=Fourier transform IR spectra for dimyristoyl-PE in the dry state (anhydrous), either in the pure state (A, C and E) or in the presence of 20 mol% of <FONT FACE="Symbol">a</FONT>-tocopherol (B, D and F). Ester C=O stretching vibration mode region,1800-1700 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>; CH<SUB><FONT SIZE=-1>2</FONT></SUB> deformation, scissoring band region, 1500-1400 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>; headgroup PO<SUB><FONT SIZE=-1>2</FONT></SUB><SUP><FONT SIZE=-1>-</FONT></SUP> phosphate band region, 1350-1150 cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP> {{Image200|LBGPEccp:14000SC01:18000SC01:YS2ANe005:01SP0001.gif}} <<2483>>.</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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Editor