Non-arene oxide aromatic ring hydroxylation of 2,2',5,5'-tetrachlorobiphenyl as the major metabolic pathway catalyzed by phenobarbital-induced rat liver microsomes.-Reference-Cited by-同舟云学术

Non-arene oxide aromatic ring hydroxylation of 2,2',5,5'-tetrachlorobiphenyl as the major metabolic pathway catalyzed by phenobarbital-induced rat liver microsomes.

Published:1983-07 Issue:13 Volume:258 Page:8304-8311
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Preston B D,Miller J A,Miller E C

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference45 articles.

1. Arene Oxides: A New Aspect of Drug Metabolism

2. Deuterium isotope effects during formation of phenols by hepatic monoxygenases. Evidence for an alternative to the arene oxide pathway

3. Aromatic hydroxylation of ellipticine in rats: Lack of an NIH shift

4. Metabolism of symmetrical hexachlorobiphenyl isomers in the rat

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