LBF18107OX02: Difference between revisions
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|LipidBank=DFA8042 | |LipidBank=DFA8042 | ||
|LipidMaps=LMFA01060069 | |LipidMaps=LMFA01060069 | ||
|SysName=13-Hydroxy-10- | |SysName=13-Hydroxy-10-oxo-11-octadecenoic acid | ||
|Common Name=&&13-Hydroxy-10- | |Common Name=&&13-Hydroxy-10-oxo-11-octadecenoic acid&& | ||
|Mass Spectra=GC-EI-MS(after methanolysis and hydrogenation)[[Reference:Gardner_WH:,J. Lipid. Res.,1970,11,311|{{RelationTable/GetFirstAuthor|Reference:Gardner_WH:,J. Lipid. Res.,1970,11,311}}]]: m/e=328[M], 257[M-(CH2)4CH3], 225[257-CH3OH], 199[CO(CH2)8COOCH3], 167[199-CH3OH](standard peak), 157[(CH2)7COOCH3 or CH3(CH2)4CH(OH)-(CH2)2CO] | |Mass Spectra=GC-EI-MS(after methanolysis and hydrogenation)[[Reference:Gardner_WH:,J. Lipid. Res.,1970,11,311|{{RelationTable/GetFirstAuthor|Reference:Gardner_WH:,J. Lipid. Res.,1970,11,311}}]]: m/e=328[M], 257[M-(CH2)4CH3], 225[257-CH3OH], 199[CO(CH2)8COOCH3], 167[199-CH3OH](standard peak), 157[(CH2)7COOCH3 or CH3(CH2)4CH(OH)-(CH2)2CO] | ||
|UV Spectra= lambda EtOH /max=226nm( epsilon =9900Å }1100), lambda EtOH /max=275nm( epsilon 260Å }30)[[Reference:Gardner_WH:,J. Lipid. Res.,1970,11,311|{{RelationTable/GetFirstAuthor|Reference:Gardner_WH:,J. Lipid. Res.,1970,11,311}}]] | |UV Spectra= lambda EtOH /max=226nm( epsilon =9900Å }1100), lambda EtOH /max=275nm( epsilon 260Å }30)[[Reference:Gardner_WH:,J. Lipid. Res.,1970,11,311|{{RelationTable/GetFirstAuthor|Reference:Gardner_WH:,J. Lipid. Res.,1970,11,311}}]] |
Revision as of 09:30, 13 April 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) |
IDs and Links | |
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LipidBank | DFA8042 |
LipidMaps | LMFA01060069 |
CAS | |
KEGG | {{{KEGG}}} |
KNApSAcK | {{{KNApSAcK}}} |
mol | LBF18107OX02 |
13-Hydroxy-10-oxo-11-octadecenoic acid | |
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Structural Information | |
13-Hydroxy-10-oxo-11-octadecenoic acid | |
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Formula | C18H32O4 |
Exact Mass | 312.23005951199997 |
Average Mass | 312.44428 |
SMILES | CCCCCC(O)C=CC(=O)CCCCCCCCC(O)=O |
Physicochemical Information | |
Oxidative products of linoleate by corn germ extracts Gardner_WH . Reaction products between 9-hydroperoxylinoleate and corn hydroperoxide isomerase Gardner_WH . Production mechanism Gardner_WH Gardner_HW . | |
Spectral Information | |
Mass Spectra | GC-EI-MS(after methanolysis and hydrogenation) Gardner_WH : m/e=328[M], 257[M-(CH2)4CH3], 225[257-CH3OH], 199[CO(CH2)8COOCH3], 167[199-CH3OH](standard peak), 157[(CH2)7COOCH3 or CH3(CH2)4CH(OH)-(CH2)2CO] |
UV Spectra | λ EtOH /max=226nm( ε =9900Å }1100), λ EtOH /max=275nm( ε 260Å }30) Gardner_WH |
IR Spectra | Trans unsaturation(973cm-1), conjugated C=O(1617cm-1), OH(3460,1070cm-1) Gardner_WH |
NMR Spectra | 1H-NMR Gardner_WH : C9(2.56ppm), C11(6.28ppm), C12(6.80ppm), C13(4.29ppm) |
Other Spectra | |
Chromatograms |
Reported Metabolites, References | |||||||||||||||
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