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LBF18108HP04 - Revision history
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Revision history for this page on the wiki
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Editor at 21:00, 14 April 2010
2010-04-14T21:00:00Z
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<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=Methyl-11- (3,5-epidioxy-2-ethylcyclopentyl) -9-hydroperoxy-10-undecenoic acid</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=Methyl-11- (3,5-epidioxy-2-ethylcyclopentyl) -9-hydroperoxy-10-undecenoic acid</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=&&Methyl-11- (3,5-epidioxy-2-ethylcyclopentyl) -9-hydroperoxy-10-undecenoate<del style="font-weight: bold; text-decoration: none;">&&Methyl-11- (3,5-epidioxy-2-ethylcyclopentyl) -9-hydroperoxy-10-undecenoic acid</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=&&Methyl-11- (3,5-epidioxy-2-ethylcyclopentyl) -9-hydroperoxy-10-undecenoate&&</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-MS(after reduction and TMS)[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: m/e=543[M-CH3]; 468[M-HOTMS]; 401[M-(CH2)7COOCH3]; 378[M-2xHOTMS]; 352[468-SMTO=CHCH2]; 323[352-CH2CH3]; 285[CH=CHCH(OTMS)(CH2)7COOCH3]; 259[SMTO=CH(CH2)7COOCH3]; 217[SMTO-CH=CH-CH=OTMS]</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-MS(after reduction and TMS)[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: m/e=543[M-CH3]; 468[M-HOTMS]; 401[M-(CH2)7COOCH3]; 378[M-2xHOTMS]; 352[468-SMTO=CHCH2]; 323[352-CH2CH3]; 285[CH=CHCH(OTMS)(CH2)7COOCH3]; 259[SMTO=CH(CH2)7COOCH3]; 217[SMTO-CH=CH-CH=OTMS]</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=OOH group: 3620-3010cm^{-1}[bonded], 3520cm^{-1}[free]; isolated trans unsaturation: 960cm^{-1}[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]</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=OOH group: 3620-3010cm^{-1}[bonded], 3520cm^{-1}[free]; isolated trans unsaturation: 960cm^{-1}[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]</div></td></tr>
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<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|SysName=Methyl-11- (3,5-epidioxy-2-ethylcyclopentyl) -9-hydroperoxy-10-<del style="font-weight: bold; text-decoration: none;">undecenoate</del></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|SysName=Methyl-11- (3,5-epidioxy-2-ethylcyclopentyl) -9-hydroperoxy-10-<ins style="font-weight: bold; text-decoration: none;">undecenoic acid</ins></div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&Methyl-11- (3,5-epidioxy-2-ethylcyclopentyl) -9-hydroperoxy-10-undecenoate&&</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=&&Methyl-11- (3,5-epidioxy-2-ethylcyclopentyl) -9-hydroperoxy-10-undecenoate<ins style="font-weight: bold; text-decoration: none;">&&Methyl-11- (3,5-epidioxy-2-ethylcyclopentyl) -9-hydroperoxy-10-undecenoic acid</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>|Mass Spectra=EI-MS(after reduction and TMS)[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: m/e=543[M-CH3]; 468[M-HOTMS]; 401[M-(CH2)7COOCH3]; 378[M-2xHOTMS]; 352[468-SMTO=CHCH2]; 323[352-CH2CH3]; 285[CH=CHCH(OTMS)(CH2)7COOCH3]; 259[SMTO=CH(CH2)7COOCH3]; 217[SMTO-CH=CH-CH=OTMS]</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-MS(after reduction and TMS)[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: m/e=543[M-CH3]; 468[M-HOTMS]; 401[M-(CH2)7COOCH3]; 378[M-2xHOTMS]; 352[468-SMTO=CHCH2]; 323[352-CH2CH3]; 285[CH=CHCH(OTMS)(CH2)7COOCH3]; 259[SMTO=CH(CH2)7COOCH3]; 217[SMTO-CH=CH-CH=OTMS]</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=OOH group: 3620-3010cm^{-1}[bonded], 3520cm^{-1}[free]; isolated trans unsaturation: 960cm^{-1}[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]</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=OOH group: 3620-3010cm^{-1}[bonded], 3520cm^{-1}[free]; isolated trans unsaturation: 960cm^{-1}[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]</div></td></tr>
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Editor at 02:53, 14 April 2010
2010-04-14T02:53:52Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 11:53, 14 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>|LipidMaps=LMFA01040053</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>|LipidMaps=LMFA01040053</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>|SysName=Methyl-11- (3,5-<del style="font-weight: bold; text-decoration: none;">Epidioxy</del>-2-<del style="font-weight: bold; text-decoration: none;">Ethylcyclopentyl</del>) -9-<del style="font-weight: bold; text-decoration: none;">Hydroperoxy</del>-10-<del style="font-weight: bold; text-decoration: none;">Undecenoate</del></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|SysName=Methyl-11- (3,5-<ins style="font-weight: bold; text-decoration: none;">epidioxy</ins>-2-<ins style="font-weight: bold; text-decoration: none;">ethylcyclopentyl</ins>) -9-<ins style="font-weight: bold; text-decoration: none;">hydroperoxy</ins>-10-<ins style="font-weight: bold; text-decoration: none;">undecenoate</ins></div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&Methyl-11- (3,5-<del style="font-weight: bold; text-decoration: none;">Epidioxy</del>-2-<del style="font-weight: bold; text-decoration: none;">Ethylcyclopentyl</del>) -9-<del style="font-weight: bold; text-decoration: none;">Hydroperoxy</del>-10-<del style="font-weight: bold; text-decoration: none;">Undecenoate</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=&&Methyl-11- (3,5-<ins style="font-weight: bold; text-decoration: none;">epidioxy</ins>-2-<ins style="font-weight: bold; text-decoration: none;">ethylcyclopentyl</ins>) -9-<ins style="font-weight: bold; text-decoration: none;">hydroperoxy</ins>-10-<ins style="font-weight: bold; text-decoration: none;">undecenoate</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>|Mass Spectra=EI-MS(after reduction and TMS)[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: m/e=543[M-CH3]; 468[M-HOTMS]; 401[M-(CH2)7COOCH3]; 378[M-2xHOTMS]; 352[468-SMTO=CHCH2]; 323[352-CH2CH3]; 285[CH=CHCH(OTMS)(CH2)7COOCH3]; 259[SMTO=CH(CH2)7COOCH3]; 217[SMTO-CH=CH-CH=OTMS]</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-MS(after reduction and TMS)[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: m/e=543[M-CH3]; 468[M-HOTMS]; 401[M-(CH2)7COOCH3]; 378[M-2xHOTMS]; 352[468-SMTO=CHCH2]; 323[352-CH2CH3]; 285[CH=CHCH(OTMS)(CH2)7COOCH3]; 259[SMTO=CH(CH2)7COOCH3]; 217[SMTO-CH=CH-CH=OTMS]</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=OOH group: 3620-3010cm^{-1}[bonded], 3520cm^{-1}[free]; isolated trans unsaturation: 960cm^{-1}[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]</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=OOH group: 3620-3010cm^{-1}[bonded], 3520cm^{-1}[free]; isolated trans unsaturation: 960cm^{-1}[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]</div></td></tr>
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Editor at 10:00, 25 February 2010
2010-02-25T10:00:10Z
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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>|Common Name=&&Methyl-11- (3,5-Epidioxy-2-Ethylcyclopentyl) -9-Hydroperoxy-10-Undecenoate&&</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=&&Methyl-11- (3,5-Epidioxy-2-Ethylcyclopentyl) -9-Hydroperoxy-10-Undecenoate&&</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-MS(after reduction and TMS)[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: m/e=543[M-CH3]; 468[M-HOTMS]; 401[M-(CH2)7COOCH3]; 378[M-2xHOTMS]; 352[468-SMTO=CHCH2]; 323[352-CH2CH3]; 285[CH=CHCH(OTMS)(CH2)7COOCH3]; 259[SMTO=CH(CH2)7COOCH3]; 217[SMTO-CH=CH-CH=OTMS]</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-MS(after reduction and TMS)[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: m/e=543[M-CH3]; 468[M-HOTMS]; 401[M-(CH2)7COOCH3]; 378[M-2xHOTMS]; 352[468-SMTO=CHCH2]; 323[352-CH2CH3]; 285[CH=CHCH(OTMS)(CH2)7COOCH3]; 259[SMTO=CH(CH2)7COOCH3]; 217[SMTO-CH=CH-CH=OTMS]</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=OOH group: 3620-3010cm^- <del style="font-weight: bold; text-decoration: none;">^</del>1 [bonded], 3520cm^- <del style="font-weight: bold; text-decoration: none;">^</del>1 [free]; isolated trans unsaturation: 960cm^- <del style="font-weight: bold; text-decoration: none;">^</del>1 [[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]</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=OOH group: 3620-3010cm^<ins style="font-weight: bold; text-decoration: none;">{</ins>-1<ins style="font-weight: bold; text-decoration: none;">}</ins>[bonded], 3520cm^<ins style="font-weight: bold; text-decoration: none;">{</ins>-1<ins style="font-weight: bold; text-decoration: none;">}</ins>[free]; isolated trans unsaturation: 960cm^<ins style="font-weight: bold; text-decoration: none;">{</ins>-1<ins style="font-weight: bold; text-decoration: none;">}</ins>[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]</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[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: C9: 4.26-4.35; C10: 5.47-5.52; C11: 5.44-6.03; C12: 2.66-2.92; C13: 4.42-4.53; C15: 4.53-4.66; C16: 1.90-2.16; OOH: 7.89-7.94; 13C-NMR[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: C9: 86.3-86.6; C10: 129.8-132.4; C11: 132.4-135.0; C12: 45.9-50.8; C13: 79.8-80.5C14: 39.3-44.1; C15: 81.7-83.0;</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[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: C9: 4.26-4.35; C10: 5.47-5.52; C11: 5.44-6.03; C12: 2.66-2.92; C13: 4.42-4.53; C15: 4.53-4.66; C16: 1.90-2.16; OOH: 7.89-7.94; 13C-NMR[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: C9: 86.3-86.6; C10: 129.8-132.4; C11: 132.4-135.0; C12: 45.9-50.8; C13: 79.8-80.5C14: 39.3-44.1; C15: 81.7-83.0;</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=Photoenhancement of linoleate peroxidation(TypeII)[[Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197}}]][[Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73}}]][[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]. It is produced from a 13-peroxyradical of linoleate via 1,3-cyclization[[Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197}}]][[Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73}}]][[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]].</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=Photoenhancement of linoleate peroxidation(TypeII)[[Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197}}]][[Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73}}]][[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]. It is produced from a 13-peroxyradical of linoleate via 1,3-cyclization[[Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197}}]][[Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73}}]][[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]].</div></td></tr>
</table>
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<td colspan="1" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 23:00, 19 February 2010</td>
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Editor
https://lipidbank.jp/mediawiki/index.php?title=LBF18108HP04&diff=48876&oldid=prev
Editor at 14:00, 19 February 2010
2010-02-19T14:00:00Z
<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, 19 February 2010</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l9">Line 9:</td>
<td colspan="2" class="diff-lineno">Line 9:</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=&&Methyl-11- (3,5-Epidioxy-2-Ethylcyclopentyl) -9-Hydroperoxy-10-Undecenoate&&</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=&&Methyl-11- (3,5-Epidioxy-2-Ethylcyclopentyl) -9-Hydroperoxy-10-Undecenoate&&</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-MS(after reduction and TMS)[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: m/e=543[M-CH3]; 468[M-HOTMS]; 401[M-(CH2)7COOCH3]; 378[M-2xHOTMS]; 352[468-SMTO=CHCH2]; 323[352-CH2CH3]; 285[CH=CHCH(OTMS)(CH2)7COOCH3]; 259[SMTO=CH(CH2)7COOCH3]; 217[SMTO-CH=CH-CH=OTMS]</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-MS(after reduction and TMS)[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: m/e=543[M-CH3]; 468[M-HOTMS]; 401[M-(CH2)7COOCH3]; 378[M-2xHOTMS]; 352[468-SMTO=CHCH2]; 323[352-CH2CH3]; 285[CH=CHCH(OTMS)(CH2)7COOCH3]; 259[SMTO=CH(CH2)7COOCH3]; 217[SMTO-CH=CH-CH=OTMS]</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=OOH group: 3620-3010cm<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>[bonded], 3520cm<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>[free]; isolated trans unsaturation: 960cm<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>[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]</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=OOH group: 3620-3010cm<ins style="font-weight: bold; text-decoration: none;">^</ins>- <ins style="font-weight: bold; text-decoration: none;">^</ins>1 [bonded], 3520cm<ins style="font-weight: bold; text-decoration: none;">^</ins>- <ins style="font-weight: bold; text-decoration: none;">^</ins>1 [free]; isolated trans unsaturation: 960cm<ins style="font-weight: bold; text-decoration: none;">^</ins>- <ins style="font-weight: bold; text-decoration: none;">^</ins>1 [[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]</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=-1></del>1<del style="font-weight: bold; text-decoration: none;"></FONT></SUP></del>H-NMR[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: C9: 4.26-4.35; C10: 5.47-5.52; C11: 5.44-6.03; C12: 2.66-2.92; C13: 4.42-4.53; C15: 4.53-4.66; C16: 1.90-2.16; OOH: 7.89-7.94; 13C-NMR[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: C9: 86.3-86.6; C10: 129.8-132.4; C11: 132.4-135.0; C12: 45.9-50.8; C13: 79.8-80.5C14: 39.3-44.1; C15: 81.7-83.0;</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[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: C9: 4.26-4.35; C10: 5.47-5.52; C11: 5.44-6.03; C12: 2.66-2.92; C13: 4.42-4.53; C15: 4.53-4.66; C16: 1.90-2.16; OOH: 7.89-7.94; 13C-NMR[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: C9: 86.3-86.6; C10: 129.8-132.4; C11: 132.4-135.0; C12: 45.9-50.8; C13: 79.8-80.5C14: 39.3-44.1; C15: 81.7-83.0;</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=Photoenhancement of linoleate peroxidation(TypeII)[[Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197}}]][[Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73}}]][[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]. It is produced from a 13-peroxyradical of linoleate via 1,3-cyclization[[Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197}}]][[Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73}}]][[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]].</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Source=Photoenhancement of linoleate peroxidation(TypeII)[[Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197}}]][[Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73}}]][[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]. It is produced from a 13-peroxyradical of linoleate via 1,3-cyclization[[Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197}}]][[Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73}}]][[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]].</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>|Chemical Synthesis=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chemical Synthesis=</div></td></tr>
</table>
Editor
https://lipidbank.jp/mediawiki/index.php?title=LBF18108HP04&diff=48875&oldid=prev
Editor at 21:00, 6 January 2010
2010-01-06T21:00:00Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 06:00, 7 January 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>|Metabolism=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Metabolism=</div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">|Biological Activity=It reacts with DNA in the presence of Fe ions and ascorbic acid[[Reference:Fujimoto_K:Neff_WE:Frankel_EN:,Biochim. Biophys. Acta,1984,795,100|{{RelationTable/GetFirstAuthor|Reference:Fujimoto_K:Neff_WE:Frankel_EN:,Biochim. Biophys. Acta,1984,795,100}}]].</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>
</table>
Editor
https://lipidbank.jp/mediawiki/index.php?title=LBF18108HP04&diff=48874&oldid=prev
Editor at 11:55, 25 November 2009
2009-11-25T11:55:00Z
<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;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:55, 25 November 2009</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>|IR Spectra=OOH group: 3620-3010cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>[bonded], 3520cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>[free]; isolated trans unsaturation: 960cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]</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=OOH group: 3620-3010cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>[bonded], 3520cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>[free]; isolated trans unsaturation: 960cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]</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=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: C9: 4.26-4.35; C10: 5.47-5.52; C11: 5.44-6.03; C12: 2.66-2.92; C13: 4.42-4.53; C15: 4.53-4.66; C16: 1.90-2.16; OOH: 7.89-7.94; 13C-NMR[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: C9: 86.3-86.6; C10: 129.8-132.4; C11: 132.4-135.0; C12: 45.9-50.8; C13: 79.8-80.5C14: 39.3-44.1; C15: 81.7-83.0;</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=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: C9: 4.26-4.35; C10: 5.47-5.52; C11: 5.44-6.03; C12: 2.66-2.92; C13: 4.42-4.53; C15: 4.53-4.66; C16: 1.90-2.16; OOH: 7.89-7.94; 13C-NMR[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: C9: 86.3-86.6; C10: 129.8-132.4; C11: 132.4-135.0; C12: 45.9-50.8; C13: 79.8-80.5C14: 39.3-44.1; C15: 81.7-83.0;</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>|Source=Photoenhancement of linoleate peroxidation(TypeII)[[Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197}}]][[Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73}}]][[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]<del style="font-weight: bold; text-decoration: none;">;></del>. It is produced from a 13-peroxyradical of linoleate via 1,3-cyclization[[Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197}}]][[Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73}}]][[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]<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>|Source=Photoenhancement of linoleate peroxidation(TypeII)[[Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197}}]][[Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73}}]][[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]. It is produced from a 13-peroxyradical of linoleate via 1,3-cyclization[[Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197}}]][[Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73}}]][[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]].</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>|Chemical Synthesis=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chemical Synthesis=</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Metabolism=</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Metabolism=</div></td></tr>
</table>
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<td colspan="1" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="1" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 19:00, 25 November 2009</td>
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2009-11-24T22:00:01Z
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<table style="background-color: #fff; color: #202122;" data-mw="interface">
<col class="diff-marker" />
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<tr class="diff-title" lang="en">
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 07:00, 25 November 2009</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l11">Line 11:</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|IR Spectra=OOH group: 3620-3010cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>[bonded], 3520cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>[free]; isolated trans unsaturation: 960cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]</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=OOH group: 3620-3010cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>[bonded], 3520cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>[free]; isolated trans unsaturation: 960cm<SUP><FONT SIZE=-1>-</FONT></SUP><SUP><FONT SIZE=-1>1</FONT></SUP>[[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]]</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=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: C9: 4.26-4.35; C10: 5.47-5.52; C11: 5.44-6.03; C12: 2.66-2.92; C13: 4.42-4.53; C15: 4.53-4.66; C16: 1.90-2.16; OOH: 7.89-7.94; 13C-NMR[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: C9: 86.3-86.6; C10: 129.8-132.4; C11: 132.4-135.0; C12: 45.9-50.8; C13: 79.8-80.5C14: 39.3-44.1; C15: 81.7-83.0;</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=<SUP><FONT SIZE=-1>1</FONT></SUP>H-NMR[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: C9: 4.26-4.35; C10: 5.47-5.52; C11: 5.44-6.03; C12: 2.66-2.92; C13: 4.42-4.53; C15: 4.53-4.66; C16: 1.90-2.16; OOH: 7.89-7.94; 13C-NMR[[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]]: C9: 86.3-86.6; C10: 129.8-132.4; C11: 132.4-135.0; C12: 45.9-50.8; C13: 79.8-80.5C14: 39.3-44.1; C15: 81.7-83.0;</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;">|Source=Photoenhancement of linoleate peroxidation(TypeII)[[Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197}}]][[Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73}}]][[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]];>. It is produced from a 13-peroxyradical of linoleate via 1,3-cyclization[[Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Prog. Lipid Res.,1984,23,197}}]][[Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:,Chem. Phys. Lipids,1987,44,73}}]][[Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Weisleder_D:,Lipids,1982,17,780}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1984,106,3577}}]][[Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223|{{RelationTable/GetFirstAuthor|Reference:Oconnor_DE:Mihelich_ED:Coleman_MC:,J. Am. Chem. Soc.,1981,103,223}}]];>.</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;">|Chemical Synthesis=</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;">|Metabolism=</ins></div></td></tr>
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