Studies on metabolism and toxicity of styrene—VI. Regioselectivity in glutathione S-conjugation and hydrolysis of racemic, R- and S-phenyloxiranes in rat liver
- 1 March 1983
- journal article
- research article
- Published by Elsevier in Biochemical Pharmacology
- Vol. 32 (5), 777-785
- https://doi.org/10.1016/0006-2952(83)90576-2
Abstract
No abstract availableThis publication has 51 references indexed in Scilit:
- Regiospecificity and stereospecificity in the enzymatic conjugation of glutathione with (±)-benzo(a)pyrene 4,5-oxideBiochemical and Biophysical Research Communications, 1980
- Cholesterol α- and β-epoxides as obligatory intermediates in the hepatic microsomal metabolism of cholesterol to cholestanetriolBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1980
- Hepatic microsomal conversion of pregnenolone to 3β,5,6β-trihydroxy-5α-pregnan-20-one via pregnenolone α- and β-epoxidesBiochemical and Biophysical Research Communications, 1980
- Stereochemistry of leukotriene C-1Biochemical and Biophysical Research Communications, 1980
- Isolation and structure determination of enzymatically formed styrene oxide glutathione conjugatesChemico-Biological Interactions, 1979
- Evidence for the formation of a steroid S-glutathione conjugate from an epoxysteroid precursorBiochemical and Biophysical Research Communications, 1979
- Stereoselective hydrolysis of cis- and trans-stilbene oxides by hepatic microsomal epoxide hydrolaseBiochemical and Biophysical Research Communications, 1971
- Stereoselective hydrolysis of 2,3-epoxysteroids by hepatic microsomal epoxide hydrolaseBiochemical and Biophysical Research Communications, 1971
- Role of the arene oxide-oxepin system in the metabolism of aromatic substrates. IV. Stereochemical considerations of dihydrodiol formation and dehyrogenationJournal of the American Chemical Society, 1970
- Microsomal hydroxylation of ethylbenzene. Stereospecificity and the effect of phenobarbital inductionLife Sciences, 1966