LBF20306HO01: Difference between revisions
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{{Lipid/Header}} | |||
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|LipidBank=DFA8106 | |LipidBank=DFA8106 | ||
|LipidMaps=LMFA03050004 | |LipidMaps=LMFA03050004 | ||
|SysName= (+-) 5, 6- | |SysName=dl-5, 6-Dihydroxy- (cis-8,cis-11,cis-14) -eicosatrienoic acid | ||
|Common Name=&&(+-) -5, 6-Dihydroxy- (8Z,11Z,14Z) -eicosatrienoic acid&& | |||
|Source= | |||
|Chemical Synthesis= | |||
|Metabolism=Epoxide hydrolases convert the EpETrEs into vicinal diols[[Reference:Oliw_EH:Guengerich_FP:Oates_JA:,J. Biol. Chem.,1982,257,3771|{{RelationTable/GetFirstAuthor|Reference:Oliw_EH:Guengerich_FP:Oates_JA:,J. Biol. Chem.,1982,257,3771}}]], with the concurrent loss of much of their biological activity. (±)5,6-DiHETrE is a substrate for sheep seminal vesicle cyclooxygenase, producing 5,6-dihydroxy PGE1 and F1 metabolites in vitro[[Reference:Oliw_EH:,Biochim. Biophys. Acta,1984,795,384|{{RelationTable/GetFirstAuthor|Reference:Oliw_EH:,Biochim. Biophys. Acta,1984,795,384}}]]. | |||
|Symbol=(+-)5,6-DiHETrE | |||
}} | }} | ||
{{Lipid/Footer}} |
Latest revision as of 07:19, 21 October 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 | DFA8106 |
LipidMaps | LMFA03050004 |
CAS | |
KEGG | {{{KEGG}}} |
KNApSAcK | {{{KNApSAcK}}} |
mol | LBF20306HO01 |
(+-) -5, 6-Dihydroxy- (8Z,11Z,14Z) -eicosatrienoic acid | |
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Structural Information | |
dl-5, 6-Dihydroxy- (cis-8,cis-11,cis-14) -eicosatrienoic acid | |
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(+-)5,6-DiHETrE | |
Formula | C20H34O4 |
Exact Mass | 338.24570957599997 |
Average Mass | 338.48156 |
SMILES | C(CC=CCC=CCC=CCC(O)C(O)CCCC(O)=O)CCC |
Physicochemical Information | |
Epoxide hydrolases convert the EpETrEs into vicinal diols Oliw_EH et al., with the concurrent loss of much of their biological activity. (±)5,6-DiHETrE is a substrate for sheep seminal vesicle cyclooxygenase, producing 5,6-dihydroxy PGE1 and F1 metabolites in vitro Oliw_EH . | |
Spectral Information | |
Mass Spectra | |
UV Spectra | |
IR Spectra | |
NMR Spectra | |
Other Spectra | |
Chromatograms |
Reported Metabolites, References | |||||||||||||||
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