about
Analysis of epoxyeicosatrienoic acids by chiral liquid chromatography/electron capture atmospheric pressure chemical ionization mass spectrometry using [13C]-analog internal standards.The rabbit pulmonary cytochrome P450 arachidonic acid metabolic pathway: characterization and significance.Epoxyeicosatrienoic acid analogs and vascular function.Glomerular stereospecific synthesis and hemodynamic actions of 8,9-epoxyeicosatrienoic acid in rat kidney.Metabolism of epoxyeicosatrienoic acids by cytosolic epoxide hydrolase: substrate structural determinants of asymmetric catalysis.Cyclooxygenase-derived metabolites of 8,9-epoxyeicosatrienoic acid are potent mitogens for cultured rat glomerular mesangial cells
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
(8S,9R)-EET
@en
type
label
(8S,9R)-EET
@en
altLabel
(8S,9R)-EpETrE
@en
(8S,9R)-epoxy-(5Z,11Z,14Z)-eicosatrienoic acid
@en
(8S,9R)-epoxy-(5Z,11Z,14Z)-icosatrienoic acid
@en
8(S),9(R)-EET
@en
8S,9R-EET
@en
8S,9R-EpETrE
@en
8S,9R-epoxy-5Z,11Z,14Z-eicosatrienoic acid
@en
prefLabel
(8S,9R)-EET
@en
P661
P662
P683
P1579
P2017
CCCCC/C=C\C/C=C\C[C@@H]1[C@@H](O1)C/C=C\CCCC(=O)O
P2063
LMFA03080019
P2067
P233
CCCCCC=CCC=CCC1C(O1)CC=CCCCC(=O)O
P234
1S/C20H32O3/c1-2-3-4-5-6-7-8-9 ...... 6-,12-9-,13-10-/t18-,19+/m1/s1
P235
DBWQSCSXHFNTMO-ZZMPYBMWSA-N