LBF18109HP01: Difference between revisions

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|LipidBank=DFA8010
|LipidBank=DFA8010
|LipidMaps=LMFA01040011
|LipidMaps=LMFA01040011
|SysName=12,13-Epoxy-11-Hydroperoxy-9-Octadecenoic Acid
|SysName=12,13-Epoxy-11-hydroperoxy-9-octadecenoic acid
|Common Name=&&12,13-Epoxy-11-Hydroperoxy-9-Octadecenoic Acid&&
|Common Name=&&12,13-Epoxy-11-hydroperoxy-9-octadecenoic acid&&
|Mass Spectra=GC-EI-MS(after methylation, reduction and trimethylsilylation)[[Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246|{{RelationTable/GetFirstAuthor|Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246}}]][[Reference:Hamberg_M:Gotthammar_B:,Lipids,1973,8,737|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Gotthammar_B:,Lipids,1973,8,737}}]]: m/e= 285[SMTO=CH-CH=CH-(CH2)7COOCH3]
|Mass Spectra=GC-EI-MS(after methylation, reduction and trimethylsilylation)[[Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246|{{RelationTable/GetFirstAuthor|Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246}}]][[Reference:Hamberg_M:Gotthammar_B:,Lipids,1973,8,737|{{RelationTable/GetFirstAuthor|Reference:Hamberg_M:Gotthammar_B:,Lipids,1973,8,737}}]]: m/e= 285[SMTO=CH-CH=CH-(CH2)7COOCH3]
|IR Spectra=After methylation and reduction[[Reference:Galliard_T:Phillips_DR:Matthew_JA:,Biochim. Biophys. Acta,1975,409,157|{{RelationTable/GetFirstAuthor|Reference:Galliard_T:Phillips_DR:Matthew_JA:,Biochim. Biophys. Acta,1975,409,157}}]][[Reference:Gardner_HW:Kleiman_R:Weisleder_D:,Lipids,1974,9,696|{{RelationTable/GetFirstAuthor|Reference:Gardner_HW:Kleiman_R:Weisleder_D:,Lipids,1974,9,696}}]][[Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246|{{RelationTable/GetFirstAuthor|Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246}}]]
|IR Spectra=After methylation and reduction[[Reference:Galliard_T:Phillips_DR:Matthew_JA:,Biochim. Biophys. Acta,1975,409,157|{{RelationTable/GetFirstAuthor|Reference:Galliard_T:Phillips_DR:Matthew_JA:,Biochim. Biophys. Acta,1975,409,157}}]][[Reference:Gardner_HW:Kleiman_R:Weisleder_D:,Lipids,1974,9,696|{{RelationTable/GetFirstAuthor|Reference:Gardner_HW:Kleiman_R:Weisleder_D:,Lipids,1974,9,696}}]][[Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246|{{RelationTable/GetFirstAuthor|Reference:Gardner_HW:Weisleder_D:Kleiman_R:,Lipids,1978,13,246}}]]

Revision as of 04:07, 14 April 2010

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Upper classes: LB LBF



12,13-Epoxy-11-hydroperoxy-9-octadecenoic acid
LBF18109HP01.png
Structural Information
12,13-Epoxy-11-hydroperoxy-9-octadecenoic acid
  • 12,13-Epoxy-11-hydroperoxy-9-octadecenoic acid
Formula C18H32O5
Exact Mass 328.224974134
Average Mass 328.44368000000003
SMILES O(C1CCCCC)C(C(OO)C=CCCCCCCCC(O)=O)1
Physicochemical Information
Major reactive products between 13-hydroperoxylinoleate (or linoleate) and soy bean extracts(pH=6.9) Gardner_HW et al.. Production mechanism Frankel_EN Gardner_HW .
Spectral Information
Mass Spectra GC-EI-MS(after methylation, reduction and trimethylsilylation) Gardner_HW et al. HambergMet al.: m/e= 285[SMTO=CH-CH=CH-(CH2)7COOCH3]
UV Spectra
IR Spectra After methylation and reduction GalliardTet al. Gardner_HW et al. Gardner_HW et al.
NMR Spectra 1H-NMR(after methylation and reduction) GalliardTet al. Gardner_HW et al. Gardner_HW et al.
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18109HP01 See above. Frankel_EN 1984
n.a. LBF18109HP01 See above. Galliard_T et al. 1975
n.a. LBF18109HP01 See above. Gardner_HW 1975
n.a. LBF18109HP01 See above. Gardner_HW et al. 1974
n.a. LBF18109HP01 See above. Gardner_HW et al. 1978
n.a. LBF18109HP01 See above. Hamberg_M et al. 1973