Effects of harman and norharman on the mutagenicity and binding to DNA of benzo[a]pyrene metabolites in vitro and on aryl hydrocarbon hydroxylase induction in cell culture
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference30 articles.
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2. Metabolic activation of benzo(a)pyrene proceeds by a diol-epoxide
3. Biological Reactive Intermediates;Nebert,1977
4. The reaction of 7,8-dihydro-7,8-dihydroxybenzo[a]pyrene-9,10-oxide with DNA in relation to the benzo[a]pyrene-DNA products isolated from cells
5. Mutagenicity of non-K-region diols and diol-epoxides of benz(a)anthracene and benzo(a)pyrene in S. typhimurium TA 100
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1. Harman induces CYP1A1 enzyme through an aryl hydrocarbon receptor mechanism;Toxicology and Applied Pharmacology;2010-11-15
2. Oxidative Metabolism of the Bioactive and Naturally Occurring β-Carboline Alkaloids, Norharman and Harman, by Human Cytochrome P450 Enzymes;Chemical Research in Toxicology;2008-10-16
3. Cytochrome P450 and Chemical Toxicology;Chemical Research in Toxicology;2007-12-06
4. Harman and Norharman Suppressed but NaNO2 Enhanced the Development of Preneoplastic Liver Cell Foci in 2-Amino-3,8-Dimethylimidazo[4,5-f]Quinoxaline (MeIQx)-Treated Rats;Journal of Toxicologic Pathology;2005
5. Genotoxic Effects of the Alkaloids Harman and Harmine Assessed by Comet Assay and Chromosome Aberration Test in Mammalian Cells in vitro;Pharmacology & Toxicology;2001-12
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