For research use only. Not for therapeutic Use.
(±)8(9)-<wbr></wbr>EET is biosynthesized in rat and rabbit liver microsomes by cytochrome P450. (±)8(9)-<wbr></wbr>EET is a major P450 metabolite in the renal cortex. (±)8(9)-<wbr></wbr>EET reduces the glomerular filtration rate through cyclooxygenase-<wbr></wbr>dependent preglomerular vasoconstriction.
Catalog Number | R016238 |
Synonyms | (±)8,9-EpETrE |
Molecular Formula | C20H32O3 |
Purity | ≥95% |
Storage | -20°C |
InChI | InChI=1S/C20H32O3/c1-2-3-4-5-6-7-8-9-12-15-18-19(23-18)16-13-10-11-14-17-20(21)22/h6-7,9-10,12-13,18-19H,2-5,8,11,14-17H2,1H3,(H,21,22)/b7-6-,12-9-,13-10-/t18-,19+/m1/s1 |
InChIKey | DBWQSCSXHFNTMO-ZZMPYBMWSA-N |
SMILES | CCCCC/C=CC/C=CC[C@@H](O1)[C@@H]1C/C=CCCCC(O)=O |
Reference | 1.Chacos, N.,Falck, J.R.,Wixtrom, C., et al. Novel epoxides formed during the liver cytochrome P-450 oxidation of arachidonic acid. Biochemical and Biophysical Research Communications 104, 916-922 (1982). |