Computer-generated graphic models of the N2-substituted deoxyguanosine adducts of 2-acetylaminofluorene and benzo[a]pyrene and the O6-substituted deoxyguanosine adduct of 1-naphthylamine in the DNA double helix

Author:

Beland Frederick A.

Publisher

Elsevier BV

Subject

Toxicology,General Medicine

Reference31 articles.

1. Identification of the persistently bound form of the carcinogen N-acetyl-2-aminofluorene to rat liver DNA in vivo;Westra;Chem.-Biol. Interact.,1976

2. Persistent binding of a new product of the carcinogen N-hydroxy-N-2-acetylaminofluorene with guanine in rat liver DNA in vivo;Kreik;Cancer Res.,1972

3. Enzymatic conversion of benzo(a)pyrene leading predominantly to the diol-epoxide r-7, t-8-dihydroxy-t-9,10-oxy-7,8,9,10-tetrahydrobenzo(a)pyrene through a single enantiomer of r-7, t-8-dihydroxy-7,8-dihydrobenzo(a)pyrene;Yang,1976

4. (±)-7α, 8β-dihydroxy-9β, 10β-epoxy-7,8,9,10-tetrahydrobenzo(a)pyrene is an intermediate in the metabolism and binding to DNA of benzo(a)pyrene;King,1976

5. Benzo(a)pyrene diol epoxides as intermediates in nucleic acid binding in vitro and in vivo;Weinstein;Science,1976

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