LBF18107MO01: Difference between revisions

No edit summary
No edit summary
Line 15: Line 15:
|Chemical Synthesis=
|Chemical Synthesis=
|Metabolism=
|Metabolism=
|Other Spectra=ODR analysis[[Reference:Gardner:HW:Weisleder_D:Nelson_EC:,J. Org. Chem.,1984,49,508|{{RelationTable/GetFirstAuthor|Reference:Gardner:HW:Weisleder_D:Nelson_EC:,J. Org. Chem.,1984,49,508}}]]
}}
}}


{{Lipid/Footer}}
{{Lipid/Footer}}

Revision as of 21:00, 6 January 2010

LipidBank Top
(トップ)
Fatty acid
(脂肪酸)
Glycerolipid
(グリセロ脂質)
Sphingolipid
(スフィンゴ脂質)
Journals
(雑誌一覧)
How to edit
(ページの書き方)


Upper classes: LB LBF



13-Hydroxy-9,10-Dimethoxy-11-Octadecenoic Acid
LBF18107MO01.png
Structural Information
13-Hydroxy-9,10-Dimethoxy-11-Octadecenoic Acid
  • 13-Hydroxy-9,10-Dimethoxy-11-Octadecenoic Acid
Formula C20H38O5
Exact Mass 358.271924326
Average Mass 358.51272
SMILES C(CCC(O)C=CC(C(OC)CCCCCCCC(O)=O)OC)CC
Physicochemical Information
Oxidative products of 13-hydroperoxylinoleate in MeH Gardner et al..
Spectral Information
Mass Spectra GC-EI-MS(after methanolysis and trimethylsilylation) Gardner et al.: m/e=201[CHOCH3(CH2)7COOCH3](standard peak), 243[M-201] 173[SMTO=CH(CH2)4CH3]
UV Spectra
IR Spectra Methyl ester(CS2) Gardner et al.: trans olefin(973-970cm-1), OH(3600 and 3440cm-1)
NMR Spectra 1H-NMR(methyl ester; CDCl3, 300MHz) Gardner et al.: C9(3.15-3.19ppm), C10(3.58-3.62ppm), C11(5.55-5.58ppm), C12(5.71ppm), C13(4.15ppm), C9OCH3(3.27-3.29ppm), C10OCH3(3.40-3.41ppm), J11-12=15.7Hz(trans unsaturation)
Other Spectra ODR analysis Gardner et al.
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18107MO01 See above. Gardner_HW et al. 1984