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LBG00kkk:R:R:16402BC01 - Revision history
2026-06-16T13:56:16Z
Revision history for this page on the wiki
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Editor: LBG00kkk:R:R:16402BC01:01 moved to LBG00kkk:R:R:16402BC01
2010-04-14T21:00:00Z
<p><a href="/wiki/LBG00kkk:R:R:16402BC01:01" class="mw-redirect" title="LBG00kkk:R:R:16402BC01:01">LBG00kkk:R:R:16402BC01:01</a> moved to <a href="/wiki/LBG00kkk:R:R:16402BC01" title="LBG00kkk:R:R:16402BC01">LBG00kkk:R:R:16402BC01</a></p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 06:00, 15 April 2010</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol</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= (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol</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=&& (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol&&</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=&&(S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol&&</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 ]^{25}_D =+7.5° (C0.83, CHCl_3 )<<0174>></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 ]^{25}_D =+7.5° (C0.83, CHCl_3 )<<0174>></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>|Mass Spectra=(EI 70eV)69(100), 93(22), 121(10.6), 135(15.9), 161(5.7), 175(2.9), 189(1.9), 203(2.9), 225(2.4), 272(3.9), 389(M-CH_3 , 2.1), 404(M^+ , 0.7)<<0174>>, </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>|Mass Spectra=(EI 70eV)69(100), 93(22), 121(10.6), 135(15.9), 161(5.7), 175(2.9), 189(1.9), 203(2.9), 225(2.4), 272(3.9), 389(M-CH_3 , 2.1), 404(M^+ , 0.7)<<0174>>, </div></td></tr>
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2010-02-25T10:00:10Z
<p><a href="/wiki/LBG00kkk:R:R:16402BC01:01" class="mw-redirect" title="LBG00kkk:R:R:16402BC01:01">LBG00kkk:R:R:16402BC01:01</a> moved to <a href="/wiki/LBG00kkk:R:R:16402BC01" title="LBG00kkk:R:R:16402BC01">LBG00kkk:R:R:16402BC01</a></p>
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<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>|SysName= (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol</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= (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&& (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol&&</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=&& (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol&&</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;">25_D </del>=+7.5° (C0.83, CHCl_3 )<<0174>></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;">{25}_D </ins>=+7.5° (C0.83, CHCl_3 )<<0174>></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>|Mass Spectra=(EI 70eV)69(100), 93(22), 121(10.6), 135(15.9), 161(5.7), 175(2.9), 189(1.9), 203(2.9), 225(2.4), 272(3.9), 389(M-CH_3 , 2.1), 404(M^+ , 0.7)<<0174>>, </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>|Mass Spectra=(EI 70eV)69(100), 93(22), 121(10.6), 135(15.9), 161(5.7), 175(2.9), 189(1.9), 203(2.9), 225(2.4), 272(3.9), 389(M-CH_3 , 2.1), 404(M^+ , 0.7)<<0174>>, </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>|NMR Spectra=^1 H NMR (300MHz,CDCl_3 )1.33(3H, s, CH_3 ), 1.42(3H, s, CH_3 ), 1.55-1.65(15H, m, 5CH_3 on geranylgeranyl), 1.9-2.1(12H, br m, 6CH_2 on geranylgeranyl), 3.38-3.68(3H, br m), 4.0-4.1(3H, m), 4.23-4.3(1H, m), 5.08[3H, br m, H at C(6), C(10) and C(14) on geranylgeranyl], 5.3[1H, t, J=6.8Hz H at C(2) on geranylgeranyl]<BR>^<del style="font-weight: bold; text-decoration: none;">1 ^3 </del>C NMR(75MHz,CDCl_3 )16.1(q), 16.6(q), 17.8(q), 25.5(q), 25.8(q), 26.4(t), 26.7(t), 26.87(t), 26.93(q), 39.7(t), 39.81(t), 39.87(t), 67.1(t), 68.1(t), 71.1(t), 74.9(d), 109.5(s), 120.7(d), 123.9(d), 124.3(d), 124.5(d), 131.4(s), 135.1(s), 135.4(s), 140.6(s)<<0174>>, </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>|NMR Spectra=^1 H NMR (300MHz,CDCl_3 )1.33(3H, s, CH_3 ), 1.42(3H, s, CH_3 ), 1.55-1.65(15H, m, 5CH_3 on geranylgeranyl), 1.9-2.1(12H, br m, 6CH_2 on geranylgeranyl), 3.38-3.68(3H, br m), 4.0-4.1(3H, m), 4.23-4.3(1H, m), 5.08[3H, br m, H at C(6), C(10) and C(14) on geranylgeranyl], 5.3[1H, t, J=6.8Hz H at C(2) on geranylgeranyl]<BR>^<ins style="font-weight: bold; text-decoration: none;">{13}</ins>C NMR(75MHz,CDCl_3 )16.1(q), 16.6(q), 17.8(q), 25.5(q), 25.8(q), 26.4(t), 26.7(t), 26.87(t), 26.93(q), 39.7(t), 39.81(t), 39.87(t), 67.1(t), 68.1(t), 71.1(t), 74.9(d), 109.5(s), 120.7(d), 123.9(d), 124.3(d), 124.5(d), 131.4(s), 135.1(s), 135.4(s), 140.6(s)<<0174>>, </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>|Chromatograms=silica gel flash chromatography (Rf=0.35, ethyl acetate-hexane(2:23) )<<0174>>, </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>|Chromatograms=silica gel flash chromatography (Rf=0.35, ethyl acetate-hexane(2:23) )<<0174>>, </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: LBG00kkk:R:R:16402BC01:01 moved to LBG00kkk:R:R:16402BC01
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<p><a href="/wiki/LBG00kkk:R:R:16402BC01:01" class="mw-redirect" title="LBG00kkk:R:R:16402BC01:01">LBG00kkk:R:R:16402BC01:01</a> moved to <a href="/wiki/LBG00kkk:R:R:16402BC01" title="LBG00kkk:R:R:16402BC01">LBG00kkk:R:R:16402BC01</a></p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 23:00, 19 February 2010</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol</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= (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&& (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol&&</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=&& (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol&&</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]^25_D =+7.5° (C0.83, CHCl_3 )<<0174>></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 ]^25_D =+7.5° (C0.83, CHCl_3 )<<0174>></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>|Mass Spectra=(EI 70eV)69(100), 93(22), 121(10.6), 135(15.9), 161(5.7), 175(2.9), 189(1.9), 203(2.9), 225(2.4), 272(3.9), 389(M-CH_3 , 2.1), 404(M^+ , 0.7)<<0174>>, </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>|Mass Spectra=(EI 70eV)69(100), 93(22), 121(10.6), 135(15.9), 161(5.7), 175(2.9), 189(1.9), 203(2.9), 225(2.4), 272(3.9), 389(M-CH_3 , 2.1), 404(M^+ , 0.7)<<0174>>, </div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H NMR (300MHz,CDCl_3 )1.33(3H, s, CH_3 ), 1.42(3H, s, CH_3 ), 1.55-1.65(15H, m, 5CH_3 on geranylgeranyl), 1.9-2.1(12H, br m, 6CH_2 on geranylgeranyl), 3.38-3.68(3H, br m), 4.0-4.1(3H, m), 4.23-4.3(1H, m), 5.08[3H, br m, H at C(6), C(10) and C(14) on geranylgeranyl], 5.3[1H, t, J=6.8Hz H at C(2) on geranylgeranyl]<BR>^1 ^3 C NMR(75MHz,CDCl_3 )16.1(q), 16.6(q), 17.8(q), 25.5(q), 25.8(q), 26.4(t), 26.7(t), 26.87(t), 26.93(q), 39.7(t), 39.81(t), 39.87(t), 67.1(t), 68.1(t), 71.1(t), 74.9(d), 109.5(s), 120.7(d), 123.9(d), 124.3(d), 124.5(d), 131.4(s), 135.1(s), 135.4(s), 140.6(s)<<0174>>, </div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H NMR (300MHz,CDCl_3 )1.33(3H, s, CH_3 ), 1.42(3H, s, CH_3 ), 1.55-1.65(15H, m, 5CH_3 on geranylgeranyl), 1.9-2.1(12H, br m, 6CH_2 on geranylgeranyl), 3.38-3.68(3H, br m), 4.0-4.1(3H, m), 4.23-4.3(1H, m), 5.08[3H, br m, H at C(6), C(10) and C(14) on geranylgeranyl], 5.3[1H, t, J=6.8Hz H at C(2) on geranylgeranyl]<BR>^1 ^3 C NMR(75MHz,CDCl_3 )16.1(q), 16.6(q), 17.8(q), 25.5(q), 25.8(q), 26.4(t), 26.7(t), 26.87(t), 26.93(q), 39.7(t), 39.81(t), 39.87(t), 67.1(t), 68.1(t), 71.1(t), 74.9(d), 109.5(s), 120.7(d), 123.9(d), 124.3(d), 124.5(d), 131.4(s), 135.1(s), 135.4(s), 140.6(s)<<0174>>, </div></td></tr>
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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>|SysName= (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol</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= (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&& (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol&&</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=&& (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol&&</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>25</sup></del>=+7.5° (C0.83, <del style="font-weight: bold; text-decoration: none;">CHCl<SUB><FONT SIZE=-1>3</FONT></SUB></del>)<<0174>></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;">^25_D </ins>=+7.5° (C0.83, <ins style="font-weight: bold; text-decoration: none;">CHCl_3 </ins>)<<0174>></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>|Mass Spectra=(EI 70eV)69(100), 93(22), 121(10.6), 135(15.9), 161(5.7), 175(2.9), 189(1.9), 203(2.9), 225(2.4), 272(3.9), 389(M-<del style="font-weight: bold; text-decoration: none;">CH<SUB><FONT SIZE=-1>3</FONT></SUB></del>, 2.1), 404(M<del style="font-weight: bold; text-decoration: none;"><SUP><FONT SIZE=-1></del>+<del style="font-weight: bold; text-decoration: none;"></FONT></SUP></del>, 0.7)<<0174>>, </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>|Mass Spectra=(EI 70eV)69(100), 93(22), 121(10.6), 135(15.9), 161(5.7), 175(2.9), 189(1.9), 203(2.9), 225(2.4), 272(3.9), 389(M-<ins style="font-weight: bold; text-decoration: none;">CH_3 </ins>, 2.1), 404(M<ins style="font-weight: bold; text-decoration: none;">^</ins>+ , 0.7)<<0174>>, </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>|NMR Spectra=<del style="font-weight: bold; text-decoration: none;"><SUP><FONT SIZE=-</del>1<del style="font-weight: bold; text-decoration: none;">>1</FONT></SUP></del>H NMR (300MHz,<del style="font-weight: bold; text-decoration: none;">CDCl<SUB><FONT SIZE=-1>3</FONT></SUB></del>)1.33(3H, s, <del style="font-weight: bold; text-decoration: none;">CH<SUB><FONT SIZE=-1>3</FONT></SUB></del>), 1.42(3H, s, <del style="font-weight: bold; text-decoration: none;">CH<SUB><FONT SIZE=-1>3</FONT></SUB></del>), 1.55-1.65(15H, m, <del style="font-weight: bold; text-decoration: none;">5CH<SUB><FONT SIZE=-1>3</FONT></SUB> </del>on geranylgeranyl), 1.9-2.1(12H, br m, <del style="font-weight: bold; text-decoration: none;">6CH<SUB><FONT SIZE=-1>2</FONT></SUB> </del>on geranylgeranyl), 3.38-3.68(3H, br m), 4.0-4.1(3H, m), 4.23-4.3(1H, m), 5.08[3H, br m, H at C(6), C(10) and C(14) on geranylgeranyl], 5.3[1H, t, J=6.8Hz H at C(2) on geranylgeranyl]<BR><del style="font-weight: bold; text-decoration: none;"><SUP><FONT SIZE=-1>1</FONT></SUP><SUP><FONT SIZE=-</del>1<del style="font-weight: bold; text-decoration: none;">></del>3<del style="font-weight: bold; text-decoration: none;"></FONT></SUP></del>C NMR(75MHz,<del style="font-weight: bold; text-decoration: none;">CDCl<SUB><FONT SIZE=-1>3</FONT></SUB></del>)16.1(q), 16.6(q), 17.8(q), 25.5(q), 25.8(q), 26.4(t), 26.7(t), 26.87(t), 26.93(q), 39.7(t), 39.81(t), 39.87(t), 67.1(t), 68.1(t), 71.1(t), 74.9(d), 109.5(s), 120.7(d), 123.9(d), 124.3(d), 124.5(d), 131.4(s), 135.1(s), 135.4(s), 140.6(s)<<0174>>, </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>|NMR Spectra=<ins style="font-weight: bold; text-decoration: none;">^</ins>1 H NMR (300MHz,<ins style="font-weight: bold; text-decoration: none;">CDCl_3 </ins>)1.33(3H, s, <ins style="font-weight: bold; text-decoration: none;">CH_3 </ins>), 1.42(3H, s, <ins style="font-weight: bold; text-decoration: none;">CH_3 </ins>), 1.55-1.65(15H, m, <ins style="font-weight: bold; text-decoration: none;">5CH_3 </ins>on geranylgeranyl), 1.9-2.1(12H, br m, <ins style="font-weight: bold; text-decoration: none;">6CH_2 </ins>on geranylgeranyl), 3.38-3.68(3H, br m), 4.0-4.1(3H, m), 4.23-4.3(1H, m), 5.08[3H, br m, H at C(6), C(10) and C(14) on geranylgeranyl], 5.3[1H, t, J=6.8Hz H at C(2) on geranylgeranyl]<BR><ins style="font-weight: bold; text-decoration: none;">^</ins>1 <ins style="font-weight: bold; text-decoration: none;">^</ins>3 C NMR(75MHz,<ins style="font-weight: bold; text-decoration: none;">CDCl_3 </ins>)16.1(q), 16.6(q), 17.8(q), 25.5(q), 25.8(q), 26.4(t), 26.7(t), 26.87(t), 26.93(q), 39.7(t), 39.81(t), 39.87(t), 67.1(t), 68.1(t), 71.1(t), 74.9(d), 109.5(s), 120.7(d), 123.9(d), 124.3(d), 124.5(d), 131.4(s), 135.1(s), 135.4(s), 140.6(s)<<0174>>, </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>|Chromatograms=silica gel flash chromatography (Rf=0.35, ethyl acetate-hexane(2:23) )<<0174>>, </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>|Chromatograms=silica gel flash chromatography (Rf=0.35, ethyl acetate-hexane(2:23) )<<0174>>, </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: LBG00kkk:R:R:16402BC01:01 moved to LBG00kkk:R:R:16402BC01
2010-02-18T15:00:00Z
<p><a href="/wiki/LBG00kkk:R:R:16402BC01:01" class="mw-redirect" title="LBG00kkk:R:R:16402BC01:01">LBG00kkk:R:R:16402BC01:01</a> moved to <a href="/wiki/LBG00kkk:R:R:16402BC01" title="LBG00kkk:R:R:16402BC01">LBG00kkk:R:R:16402BC01</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=EEL0208</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=EEL0208</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= (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol</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= (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol</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= (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol</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>(S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol<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;">subsup25</del>/sup=+7.5° (C0.83, <del style="font-weight: bold; text-decoration: none;">CHClSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB)0174</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>25<</ins>/sup<ins style="font-weight: bold; text-decoration: none;">></ins>=+7.5° (C0.83, <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>0174<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>|Mass Spectra=(EI 70eV)69(100), 93(22), 121(10.6), 135(15.9), 161(5.7), 175(2.9), 189(1.9), 203(2.9), 225(2.4), 272(3.9), 389(M-<del style="font-weight: bold; text-decoration: none;">CHSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB, 2.1), 404(<del style="font-weight: bold; text-decoration: none;">MSUPFONT </del>SIZE=-1+/FONT/SUP, 0.7)0174, </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>|Mass Spectra=(EI 70eV)69(100), 93(22), 121(10.6), 135(15.9), 161(5.7), 175(2.9), 189(1.9), 203(2.9), 225(2.4), 272(3.9), 389(M-<ins style="font-weight: bold; text-decoration: none;">CH<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>, 2.1), 404(<ins style="font-weight: bold; text-decoration: none;">M<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>, 0.7)<ins style="font-weight: bold; text-decoration: none;"><<</ins>0174<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>|NMR Spectra=<del style="font-weight: bold; text-decoration: none;">SUPFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">11</del>/FONT/<del style="font-weight: bold; text-decoration: none;">SUPH </del>NMR (300MHz,<del style="font-weight: bold; text-decoration: none;">CDClSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB)1.33(3H, s, <del style="font-weight: bold; text-decoration: none;">CHSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB), 1.42(3H, s, <del style="font-weight: bold; text-decoration: none;">CHSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB), 1.55-1.65(15H, m, <del style="font-weight: bold; text-decoration: none;">5CHSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB on geranylgeranyl), 1.9-2.1(12H, br m, <del style="font-weight: bold; text-decoration: none;">6CHSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">12</del>/FONT/SUB on geranylgeranyl), 3.38-3.68(3H, br m), 4.0-4.1(3H, m), 4.23-4.3(1H, m), 5.08[3H, br m, H at C(6), C(10) and C(14) on geranylgeranyl], 5.3[1H, t, J=6.8Hz H at C(2) on geranylgeranyl]<del style="font-weight: bold; text-decoration: none;">BRSUPFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">11</del>/FONT/<del style="font-weight: bold; text-decoration: none;">SUPSUPFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/<del style="font-weight: bold; text-decoration: none;">SUPC </del>NMR(75MHz,<del style="font-weight: bold; text-decoration: none;">CDClSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB)16.1(q), 16.6(q), 17.8(q), 25.5(q), 25.8(q), 26.4(t), 26.7(t), 26.87(t), 26.93(q), 39.7(t), 39.81(t), 39.87(t), 67.1(t), 68.1(t), 71.1(t), 74.9(d), 109.5(s), 120.7(d), 123.9(d), 124.3(d), 124.5(d), 131.4(s), 135.1(s), 135.4(s), 140.6(s)0174, </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>|NMR Spectra=<ins style="font-weight: bold; text-decoration: none;"><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>/<ins style="font-weight: bold; text-decoration: none;">SUP>H </ins>NMR (300MHz,<ins style="font-weight: bold; text-decoration: none;">CDCl<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>)1.33(3H, s, <ins style="font-weight: bold; text-decoration: none;">CH<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>), 1.42(3H, s, <ins style="font-weight: bold; text-decoration: none;">CH<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>), 1.55-1.65(15H, m, <ins style="font-weight: bold; text-decoration: none;">5CH<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>on geranylgeranyl), 1.9-2.1(12H, br m, <ins style="font-weight: bold; text-decoration: none;">6CH<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>on geranylgeranyl), 3.38-3.68(3H, br m), 4.0-4.1(3H, m), 4.23-4.3(1H, m), 5.08[3H, br m, H at C(6), C(10) and C(14) on geranylgeranyl], 5.3[1H, t, J=6.8Hz H at C(2) on geranylgeranyl]<ins style="font-weight: bold; text-decoration: none;"><BR><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>/<ins style="font-weight: bold; text-decoration: none;">SUP><SUP><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>3<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/<ins style="font-weight: bold; text-decoration: none;">SUP>C </ins>NMR(75MHz,<ins style="font-weight: bold; text-decoration: none;">CDCl<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>)16.1(q), 16.6(q), 17.8(q), 25.5(q), 25.8(q), 26.4(t), 26.7(t), 26.87(t), 26.93(q), 39.7(t), 39.81(t), 39.87(t), 67.1(t), 68.1(t), 71.1(t), 74.9(d), 109.5(s), 120.7(d), 123.9(d), 124.3(d), 124.5(d), 131.4(s), 135.1(s), 135.4(s), 140.6(s)<ins style="font-weight: bold; text-decoration: none;"><<</ins>0174<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>|Chromatograms=silica gel flash chromatography (Rf=0.35, ethyl acetate-hexane(2:23) )0174, </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>|Chromatograms=silica gel flash chromatography (Rf=0.35, ethyl acetate-hexane(2:23) )<ins style="font-weight: bold; text-decoration: none;"><<</ins>0174<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>
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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: LBG00kkk:R:R:16402BC01:01 moved to LBG00kkk:R:R:16402BC01
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<p><a href="/wiki/LBG00kkk:R:R:16402BC01:01" class="mw-redirect" title="LBG00kkk:R:R:16402BC01:01">LBG00kkk:R:R:16402BC01:01</a> moved to <a href="/wiki/LBG00kkk:R:R:16402BC01" title="LBG00kkk:R:R:16402BC01">LBG00kkk:R:R:16402BC01</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=EEL0208</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=EEL0208</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= (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol</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= (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol</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>(S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol<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= (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol</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>25<</del>/sup<del style="font-weight: bold; text-decoration: none;">></del>=+7.5° (C0.83, <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>0174<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;">subsup25</ins>/sup=+7.5° (C0.83, <ins style="font-weight: bold; text-decoration: none;">CHClSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB)0174</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>|Mass Spectra=(EI 70eV)69(100), 93(22), 121(10.6), 135(15.9), 161(5.7), 175(2.9), 189(1.9), 203(2.9), 225(2.4), 272(3.9), 389(M-<del style="font-weight: bold; text-decoration: none;">CH<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>, 2.1), 404(<del style="font-weight: bold; text-decoration: none;">M<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>, 0.7)<del style="font-weight: bold; text-decoration: none;"><<</del>0174<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>|Mass Spectra=(EI 70eV)69(100), 93(22), 121(10.6), 135(15.9), 161(5.7), 175(2.9), 189(1.9), 203(2.9), 225(2.4), 272(3.9), 389(M-<ins style="font-weight: bold; text-decoration: none;">CHSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB, 2.1), 404(<ins style="font-weight: bold; text-decoration: none;">MSUPFONT </ins>SIZE=-1+/FONT/SUP, 0.7)0174, </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>|NMR Spectra=<del style="font-weight: bold; text-decoration: none;"><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>/<del style="font-weight: bold; text-decoration: none;">SUP>H </del>NMR (300MHz,<del style="font-weight: bold; text-decoration: none;">CDCl<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>)1.33(3H, s, <del style="font-weight: bold; text-decoration: none;">CH<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>), 1.42(3H, s, <del style="font-weight: bold; text-decoration: none;">CH<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>), 1.55-1.65(15H, m, <del style="font-weight: bold; text-decoration: none;">5CH<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>on geranylgeranyl), 1.9-2.1(12H, br m, <del style="font-weight: bold; text-decoration: none;">6CH<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>on geranylgeranyl), 3.38-3.68(3H, br m), 4.0-4.1(3H, m), 4.23-4.3(1H, m), 5.08[3H, br m, H at C(6), C(10) and C(14) on geranylgeranyl], 5.3[1H, t, J=6.8Hz H at C(2) on geranylgeranyl]<del style="font-weight: bold; text-decoration: none;"><BR><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>/<del style="font-weight: bold; text-decoration: none;">SUP><SUP><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>3<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/<del style="font-weight: bold; text-decoration: none;">SUP>C </del>NMR(75MHz,<del style="font-weight: bold; text-decoration: none;">CDCl<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>)16.1(q), 16.6(q), 17.8(q), 25.5(q), 25.8(q), 26.4(t), 26.7(t), 26.87(t), 26.93(q), 39.7(t), 39.81(t), 39.87(t), 67.1(t), 68.1(t), 71.1(t), 74.9(d), 109.5(s), 120.7(d), 123.9(d), 124.3(d), 124.5(d), 131.4(s), 135.1(s), 135.4(s), 140.6(s)<del style="font-weight: bold; text-decoration: none;"><<</del>0174<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>|NMR Spectra=<ins style="font-weight: bold; text-decoration: none;">SUPFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">11</ins>/FONT/<ins style="font-weight: bold; text-decoration: none;">SUPH </ins>NMR (300MHz,<ins style="font-weight: bold; text-decoration: none;">CDClSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB)1.33(3H, s, <ins style="font-weight: bold; text-decoration: none;">CHSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB), 1.42(3H, s, <ins style="font-weight: bold; text-decoration: none;">CHSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB), 1.55-1.65(15H, m, <ins style="font-weight: bold; text-decoration: none;">5CHSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB on geranylgeranyl), 1.9-2.1(12H, br m, <ins style="font-weight: bold; text-decoration: none;">6CHSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">12</ins>/FONT/SUB on geranylgeranyl), 3.38-3.68(3H, br m), 4.0-4.1(3H, m), 4.23-4.3(1H, m), 5.08[3H, br m, H at C(6), C(10) and C(14) on geranylgeranyl], 5.3[1H, t, J=6.8Hz H at C(2) on geranylgeranyl]<ins style="font-weight: bold; text-decoration: none;">BRSUPFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">11</ins>/FONT/<ins style="font-weight: bold; text-decoration: none;">SUPSUPFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/<ins style="font-weight: bold; text-decoration: none;">SUPC </ins>NMR(75MHz,<ins style="font-weight: bold; text-decoration: none;">CDClSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB)16.1(q), 16.6(q), 17.8(q), 25.5(q), 25.8(q), 26.4(t), 26.7(t), 26.87(t), 26.93(q), 39.7(t), 39.81(t), 39.87(t), 67.1(t), 68.1(t), 71.1(t), 74.9(d), 109.5(s), 120.7(d), 123.9(d), 124.3(d), 124.5(d), 131.4(s), 135.1(s), 135.4(s), 140.6(s)0174, </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>|Chromatograms=silica gel flash chromatography (Rf=0.35, ethyl acetate-hexane(2:23) )<del style="font-weight: bold; text-decoration: none;"><<</del>0174<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>|Chromatograms=silica gel flash chromatography (Rf=0.35, ethyl acetate-hexane(2:23) )0174, </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;"><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: LBG00kkk:R:R:16402BC01:01 moved to LBG00kkk:R:R:16402BC01
2010-01-20T01:38:51Z
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Editor at 13:00, 26 July 2009
2009-07-26T13:00:00Z
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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 22:00, 26 July 2009</td>
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<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=EEL0208</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=EEL0208</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>|Chromatograms=silica gel flash chromatography (Rf=0.35, ethyl acetate-hexane(2:23) )<<0174>>, </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>|Chromatograms=silica gel flash chromatography (Rf=0.35, ethyl acetate-hexane(2:23) )<<0174>>, </div></td></tr>
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https://lipidbank.jp/mediawiki/index.php?title=LBG00kkk:R:R:16402BC01&diff=60789&oldid=prev
Editor at 12:00, 8 July 2009
2009-07-08T12:00:00Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 21:00, 8 July 2009</td>
</tr><tr><td colspan="4" class="diff-notice" lang="en"><div class="mw-diff-empty">(No difference)</div>
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Editor at 11:00, 8 July 2009
2009-07-08T11:00:00Z
<p></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;">Revision as of 20:00, 8 July 2009</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l2">Line 2:</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=EEL0208</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=EEL0208</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= (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol</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= (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol</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;">|Common Name=&& (S) -1,2-O-Isopropylidene-3-O-geranylgeranylglycerol&&</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>|Reflactive=[<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>25</sup>=+7.5° (C0.83, CHCl<SUB><FONT SIZE=-1>3</FONT></SUB>)<<0174>></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>25</sup>=+7.5° (C0.83, CHCl<SUB><FONT SIZE=-1>3</FONT></SUB>)<<0174>></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>|Mass Spectra=(EI 70eV)69(100), 93(22), 121(10.6), 135(15.9), 161(5.7), 175(2.9), 189(1.9), 203(2.9), 225(2.4), 272(3.9), 389(M-CH<SUB><FONT SIZE=-1>3</FONT></SUB>, 2.1), 404(M<SUP><FONT SIZE=-1>+</FONT></SUP>, 0.7)<<0174>>, </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>|Mass Spectra=(EI 70eV)69(100), 93(22), 121(10.6), 135(15.9), 161(5.7), 175(2.9), 189(1.9), 203(2.9), 225(2.4), 272(3.9), 389(M-CH<SUB><FONT SIZE=-1>3</FONT></SUB>, 2.1), 404(M<SUP><FONT SIZE=-1>+</FONT></SUP>, 0.7)<<0174>>, </div></td></tr>
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