Identification of c8-modified deoxyinosine and N2-and C8-modified deoxyguanosine as major products of the in vitro reaction of N-hydroxy-6-aminochrysene with DNA and the formation of these adducts in isolated rat hepatocytes treated with 6-nitrochrysene and 6-aminochrysene

Carcinogenesis

Volumn 8, Issue 11, 1987, Pages 1703-1709

  Delclos, K Barry ^a   Miller, Dwight W ^a   Lay, Jackson O ^a   Casciano, Daniel A ^a   Walker, Ralph P ^a   Fu, Peter P ^a   Kadlubar, Fred F ^a  

^a NATIONAL CENTER FOR TOXICOLOGICAL RESEARCH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

6 CHRYSENAMINE; 6 NITROCHRYSENE; 6-CHRYSENAMINE; 6-NITROCHRYSENE; CARCINOGEN; CHRYSENE DERIVATIVE; DEOXYGUANOSINE; DEOXYINOSINE; DIAGNOSTIC AGENT; DNA; DRUG DERIVATIVE; INOSINE; N HYDROXY 6 AMINOCHRYSENE; N-HYDROXY-6-AMINOCHRYSENE; PHENANTHRENE DERIVATIVE; TRITIUM;

ANIMAL; ARTICLE; BIOTRANSFORMATION; LIVER; MASS SPECTROMETRY; METABOLISM; RAT;

ANIMAL; BIOTRANSFORMATION; CARCINOGENS; CHRYSENES; DEOXYGUANOSINE; DNA; INOSINE; LIVER; PHENANTHRENES; RATS; SPECTRUM ANALYSIS, MASS; SUPPORT, U.S. GOV'T, NON-P.H.S.; SUPPORT, U.S. GOV'T, P.H.S.; TRITIUM;

EID: 0023449786     PISSN: 01433334     EISSN: None     Source Type: Journal    
DOI: 10.1093/carcin/8.11.1703     Document Type: Article

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