Accueil>>Lipids>> P450>>(±)8(9)-EET-d11

(±)8(9)-EET-d11 (Synonyms: (±)8,9-EET-d11, (±)8,9-EpETrE-d11)

Catalog No.GC46264

A neuropeptide with diverse biological activities

Products are for research use only. Not for human use. We do not sell to patients.

(±)8(9)-EET-d11 Chemical Structure

Cas No.: N/A

Taille Prix Stock Qté
10 μg
168,00 $US
En stock
25 μg
399,00 $US
En stock
50 μg
756,00 $US
En stock

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

(±)8(9)-EET-d11 contains 11 deuterium atoms at the 16, 16', 17, 17', 18, 18', 19, 19', 20, 20, and 20 positions. It is intended for use as an internal standard for the quantification of (±)8(9)-EET by GC- or LC-mass spectrometry (MS). (±)8(9)-EET is biosynthesized from arachidonic acid in rat and rabbit liver microsomes by CYP450.1,2 (±)8(9)-EET is a major P450 metabolite in the renal cortex.3 (±)8(9)-EET reduces GFR through cyclooxygenase-dependent preglomerular vasoconstriction.4

1.Chacos, N., Falck, J.R., Wixtrom, C., et al.Novel epoxides formed during the liver cytochrome P-450 oxidation of arachidonic acidBiochem. Biophys. Res. Commun.104(3)916-922(1982) 2.Oliw, E.H., Guengerich, F.P., and Oates, J.A.Oxygenation of arachidonic acid by hepatic monooxygenases. Isolation and metabolism of four epoxide intermediatesJ. Biol. Chem.257(7)3771-3781(1982) 3.Zhang, J.Y., Prakash, C., Yamashita, K., et al.Regiospecific and enantioselective metabolism of 8,9-epoxyeicosatrienoic acid by cyclooxygenaseBiochem. Biophys. Res. Commun.183(1)138-143(1992) 4.Katoh, T., Takahashi, K., Capdevila, J., et al.Glomerular stereospecific synthesis and hemodynamic actions of 8,9-epoxyeicosatrienoic acid in rat kidneyAm. J. Physiol.261(4 Pt 2)F578-F586(1991)

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Average Rating: 5 ★★★★★ (Based on Reviews and 28 reference(s) in Google Scholar.)

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