The formation of dihydrodiols in the chemical or enzymic oxidation of dibenz[a,c]anthracene, dibenz[a,h]anthracene and chrysene
Author:
Publisher
Elsevier BV
Subject
Toxicology,General Medicine
Reference20 articles.
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4. The formation of dihydrodiols by chemical or enzymic oxidation of 3-methylcholanthrene;Tierney;Chem.-Biol. Interact.,1978
5. The formation of dihydrodiols by the chemical or enzymic oxidation of benz[a]anthracene and 7,12-dimethylbenz[a]anthracene;Tierney;Chem.-Biol. Interact.,1978
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1. Synthesis, Absolute Configuration, and Bacterial Mutagenicity of the 8 Stereoisomeric Vicinal Diol Epoxides at the Terminal Benzo Ring of Carcinogenic Dibenz[a,h]anthracene;Chemical Research in Toxicology;2011-11-16
2. Alternative pathways of polycyclic aromatic hydrocarbons activation: the formation of polar DNA adducts.;Acta Biochimica Polonica;1999-06-30
3. Metabolic Activation of Chrysene by Human Hepatic and Pulmonary Cytochrome P450 Enzymes;Polycyclic Aromatic Compounds;1996-11
4. Metabolic Activation of the Potent Carcinogen Dibenzo[a,h]anthracene by cDNA-Expressed Human Cytochromes P450;Archives of Biochemistry and Biophysics;1996-04
5. Bisdihydrodiols, rather than dihydrodiol oxides, are the principal microsomal metabolites of tumorigenic trans-3,4-dihydroxy-3,4-dihydrodibenz[a,h]anthracene;Chemical Research in Toxicology;1994-01
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