LBF18108HO03: Difference between revisions

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|LipidMaps=LMFA01050127
|LipidMaps=LMFA01050127
|SysName=9,13-Dihydroxy-10-octadecenoic acid
|SysName=9,13-Dihydroxy-10-octadecenoic acid
|Common Name=&&9,13-Dihydroxy-10-octadecenoate&&
|Common Name=&&9,13-Dihydroxy-10-octadecenoic acid&&
|Mass Spectra=GC-EI-MS(after methanolysis and trimethylsilylation)[[Reference:Streckert_G:Stan_HJ:,Lipids,1975,10,847|{{RelationTable/GetFirstAuthor|Reference:Streckert_G:Stan_HJ:,Lipids,1975,10,847}}]][[Reference:Neff_WE:Frankel_EN:Scholfield_CR:Wesleder_D:,Lipids,1978,13,415|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Scholfield_CR:Wesleder_D:,Lipids,1978,13,415}}]][[Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1975,39,2027|{{RelationTable/GetFirstAuthor|Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1975,39,2027}}]][[Reference:Frankel_EN:Neff_WE:Rohwedder_WK:Khambay_BP:Garwood_RF:Weedon_BC:,Lipids,1977,12,908|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:Neff_WE:Rohwedder_WK:Khambay_BP:Garwood_RF:Weedon_BC:,Lipids,1977,12,908}}]]: m/e=429[M-43], 355, 285[CH=CH-CH(OTMS) -(CH2)7COOCH3], 259[SMTO=CH-(CH2)7COOCH3], 173[SMTO=CH-(CH2)4CH3], GC-EI-MS(after methanolysis, hydrogenation and trimethylsilylation)[[Reference:Streckert_G:Stan_HJ:,Lipids,1975,10,847|{{RelationTable/GetFirstAuthor|Reference:Streckert_G:Stan_HJ:,Lipids,1975,10,847}}]][[Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1975,39,2027|{{RelationTable/GetFirstAuthor|Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1975,39,2027}}]]
|Mass Spectra=GC-EI-MS(after methanolysis and trimethylsilylation)[[Reference:Streckert_G:Stan_HJ:,Lipids,1975,10,847|{{RelationTable/GetFirstAuthor|Reference:Streckert_G:Stan_HJ:,Lipids,1975,10,847}}]][[Reference:Neff_WE:Frankel_EN:Scholfield_CR:Wesleder_D:,Lipids,1978,13,415|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Scholfield_CR:Wesleder_D:,Lipids,1978,13,415}}]][[Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1975,39,2027|{{RelationTable/GetFirstAuthor|Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1975,39,2027}}]][[Reference:Frankel_EN:Neff_WE:Rohwedder_WK:Khambay_BP:Garwood_RF:Weedon_BC:,Lipids,1977,12,908|{{RelationTable/GetFirstAuthor|Reference:Frankel_EN:Neff_WE:Rohwedder_WK:Khambay_BP:Garwood_RF:Weedon_BC:,Lipids,1977,12,908}}]]: m/e=429[M-43], 355, 285[CH=CH-CH(OTMS) -(CH2)7COOCH3], 259[SMTO=CH-(CH2)7COOCH3], 173[SMTO=CH-(CH2)4CH3], GC-EI-MS(after methanolysis, hydrogenation and trimethylsilylation)[[Reference:Streckert_G:Stan_HJ:,Lipids,1975,10,847|{{RelationTable/GetFirstAuthor|Reference:Streckert_G:Stan_HJ:,Lipids,1975,10,847}}]][[Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1975,39,2027|{{RelationTable/GetFirstAuthor|Reference:Terao_J:Matsushita_S:,Agric. Biol. Chem.,1975,39,2027}}]]
|IR Spectra=Trans unsaturation(980cm^{-1}), olefinic(3010cm^{-1}), OH(3620-3500cm^{-1})[[Reference:Neff_WE:Frankel_EN:Scholfield_CR:Wesleder_D:,Lipids,1978,13,415|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Scholfield_CR:Wesleder_D:,Lipids,1978,13,415}}]]
|IR Spectra=Trans unsaturation(980cm^{-1}), olefinic(3010cm^{-1}), OH(3620-3500cm^{-1})[[Reference:Neff_WE:Frankel_EN:Scholfield_CR:Wesleder_D:,Lipids,1978,13,415|{{RelationTable/GetFirstAuthor|Reference:Neff_WE:Frankel_EN:Scholfield_CR:Wesleder_D:,Lipids,1978,13,415}}]]

Latest revision as of 06:34, 26 May 2010

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Upper classes: LB LBF



9,13-Dihydroxy-10-octadecenoic acid
LBF18108HO03.png
Structural Information
9,13-Dihydroxy-10-octadecenoic acid
  • 9,13-Dihydroxy-10-octadecenoic acid
Formula C18H34O4
Exact Mass 314.24570957599997
Average Mass 314.46016
SMILES CCCCCC(O)CC=CC(O)CCCCCCCC(O)=O
Physicochemical Information
Reaction products between hydroperoxylinoleate and soy bean lipoxygenase Streckert_G et al.. Autooxydation products of methyllinoleate Neff_WE et al. Terao_J et al. Frankel_EN et al..
Spectral Information
Mass Spectra GC-EI-MS(after methanolysis and trimethylsilylation) StreckertGet al. Neff_WE et al. TeraoJet al. Frankel_EN et al.: m/e=429[M-43], 355, 285[CH=CH-CH(OTMS) -(CH2)7COOCH3], 259[SMTO=CH-(CH2)7COOCH3], 173[SMTO=CH-(CH2)4CH3], GC-EI-MS(after methanolysis, hydrogenation and trimethylsilylation) StreckertGet al. TeraoJet al.
UV Spectra
IR Spectra Trans unsaturation(980cm-1), olefinic(3010cm-1), OH(3620-3500cm-1) Neff_WE et al.
NMR Spectra 1H-NMR(90MHz,CDCl3): trans olefinic protons(5.6-6.22ppm), carbinol methine protons(4.12ppm), J10-11=12.1Hz(trans unsaturation) Neff_WE et al.
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18108HO03 See above. Frankel_EN et al. 1977
n.a. LBF18108HO03 See above. Neff_WE et al. 1978
n.a. LBF18108HO03 See above. Streckert_G et al. 1975
n.a. LBF18108HO03 See above. Terao_J et al. 1975