Identification of 4-(3-Pyridyl)-4-oxobutyl-2′-deoxycytidine Adducts Formed in the Reaction of DNA with 4-(Acetoxymethylnitrosamino)-1-(3-pyridyl)-1-butanone: A Chemically Activated Form of Tobacco-Specific Carcinogens
Author:
Affiliation:
1. Masonic Cancer Center, University of Minnesota, 2231 6th Street SE, Room 2-148 CCRB, Minneapolis, Minnesota 55455, United States
Funder
National Cancer Institute
Publisher
American Chemical Society (ACS)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acsomega.7b00072
Reference35 articles.
1. Biochemistry, Biology, and Carcinogenicity of Tobacco-Specific N-Nitrosamines
2. Cytochrome P450 2A-Catalyzed Metabolic Activation of Structurally Similar Carcinogenic Nitrosamines: N‘-Nitrosonornicotine Enantiomers, N-Nitrosopiperidine, and N-Nitrosopyrrolidine
3. Cytochrome P450 Enzymes as Catalysts of Metabolism of 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone, a Tobacco Specific Carcinogen
4. Progress and Challenges in Selected Areas of Tobacco Carcinogenesis
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