LBF20309EO01: Difference between revisions

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|LipidBank=DFA8113
|LipidBank=DFA8113
|LipidMaps=-
|LipidMaps=-
|SysName=dl-14 (15) -Epoxy-5Z,8Z,11Z-eicosatrienoic acid
|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 06:17, 21 October 2010

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Upper classes: LB LBF



(+-) -14 (15) -Epoxy- (5Z,8Z,11Z) -eicosatrienoic acid
LBF20309EO01.png
Structural Information
dl-14 (15) -Epoxy- (cis-5,cis-8,cis-11) -eicosatrienoic acid
  • (+-) -14 (15) -Epoxy- (5Z,8Z,11Z) -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
Biospecies ID Compound Name Reference Comment
n.a. LBF20309EO01 See above. Catella_F et al. 1990
n.a. LBF20309EO01 See above. Chacos_N et al. 1982
n.a. LBF20309EO01 See above. Oliw_EH et al. 1982