Pyridyloxobutylation of Guanine Residues by 4-[(Acetoxymethyl)nitrosamino]-1-(3-pyridyl)-1-butanone Generates Substrates of O6-Alkylguanine−DNA Alkyltransferase
Author:
Affiliation:
1. Division of Chemical Carcinogenesis and Division of Carcinogenesis and Molecular Epidemiology, American Health Foundation, 1 Dana Road, Valhalla, New York 10595
Publisher
American Chemical Society (ACS)
Subject
Toxicology,General Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/tx960067t
Reference24 articles.
Cited by 17 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Metabolism and DNA Adduct Formation of Tobacco-Specific N-Nitrosamines;International Journal of Molecular Sciences;2022-05-04
2. DNA Polymerases η and ζ Combine to Bypass O2-[4-(3-Pyridyl)-4-oxobutyl]thymine, a DNA Adduct Formed from Tobacco Carcinogens;Chemical Research in Toxicology;2016-02-22
3. Generation and Characterization of a Novel CYP2A13-Transgenic Mouse Model;Drug Metabolism and Disposition;2014-06-06
4. Mass Spectrometric Analysis of Relative Levels of Pyridyloxobutylation Adducts Formed in the Reaction of DNA with a Chemically Activated Form of the Tobacco-Specific Carcinogen 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone;Chemical Research in Toxicology;2005-05-17
5. Stable Isotope Labeling−Mass Spectrometry Analysis of Methyl- and Pyridyloxobutyl-Guanine Adducts of 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone in p53-Derived DNA Sequences;Biochemistry;2005-01-15
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