LBF20309EO01: Difference between revisions
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|LipidBank=DFA8113 | |LipidBank=DFA8113 | ||
|LipidMaps=- | |LipidMaps=- | ||
|SysName=dl-14 (15) -Epoxy- | |SysName=dl-14 (15) -Epoxy- (cis-5,cis-8,cis-11) -eicosatrienoic acid | ||
|Common Name=&&(+-) -14 (15) -Epoxy-5Z,8Z,11Z-eicosatrienoic acid&& | |Common Name=&&(+-) -14 (15) -Epoxy- (5Z,8Z,11Z) -eicosatrienoic acid&& | ||
|Source=(±)14(15)-EpETrE is biosynthesized in rat and rabbit liver microsomes by cytochrome P450 [[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}}]][[Reference:Chacos_N:Falck_JR:Wixtrom_C:Capdevila_J:,Biochem. Biophys. Res. Commun.,1982,104,916|{{RelationTable/GetFirstAuthor|Reference:Chacos_N:Falck_JR:Wixtrom_C:Capdevila_J:,Biochem. Biophys. Res. Commun.,1982,104,916}}]]. | |Source=(±)14(15)-EpETrE is biosynthesized in rat and rabbit liver microsomes by cytochrome P450 [[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}}]][[Reference:Chacos_N:Falck_JR:Wixtrom_C:Capdevila_J:,Biochem. Biophys. Res. Commun.,1982,104,916|{{RelationTable/GetFirstAuthor|Reference:Chacos_N:Falck_JR:Wixtrom_C:Capdevila_J:,Biochem. Biophys. Res. Commun.,1982,104,916}}]]. | ||
|Chemical Synthesis= | |Chemical Synthesis= | ||
Latest revision as of 15:17, 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 | |
|---|---|
| LipidBank | DFA8113 |
| LipidMaps | - |
| CAS | |
| KEGG | {{{KEGG}}} |
| KNApSAcK | {{{KNApSAcK}}} |
| mol | LBF20309EO01 |
| (+-) -14 (15) -Epoxy- (5Z,8Z,11Z) -eicosatrienoic acid | |
|---|---|
| |
| Structural Information | |
| dl-14 (15) -Epoxy- (cis-5,cis-8,cis-11) -eicosatrienoic acid | |
| |
| (+-)14(15)-EpETrE | |
| Formula | C20H32O3 |
| Exact Mass | 320.23514489 |
| Average Mass | 320.46628 |
| SMILES | C(CCC(O1)C1CC=CCC=CCC=CCCCC(O)=O)CC |
| Physicochemical Information | |
| (±)14(15)-EpETrE is biosynthesized in rat and rabbit liver microsomes by cytochrome P450 Oliw_EH et al. Chacos_N et al.. | |
| Dramatic increases in urinary (±)14,15-DiHETrE, a (±)14(15)-EpETrE metabolite, have been documented by GC/MS in pregnancy induced hypertension Catella_F et al.. | |
| Spectral Information | |
| Mass Spectra | |
| UV Spectra | |
| IR Spectra | |
| NMR Spectra | |
| Other Spectra | |
| Chromatograms | |
| Reported Metabolites, References | ||||||||||||||||||||
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