Influence of benzo[a]pyrenediol epoxide chirality on solution conformations of DNA covalent adducts: the (-)-trans-anti-[BP]G.cntdot.C adduct structure and comparison with the (+)-trans-anti[BP]G.cntdot.C enantiomer-Reference-Cited by-同舟云学术

Influence of benzo[a]pyrenediol epoxide chirality on solution conformations of DNA covalent adducts: the (-)-trans-anti-[BP]G.cntdot.C adduct structure and comparison with the (+)-trans-anti[BP]G.cntdot.C enantiomer

Published:1992-07-16 Issue:23 Volume:31 Page:5245-5252
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

De Los Santos Carlos,Cosman Monique,Hingerty Brian E.,Ibanez Victor,Margulis Leonid A.,Geacintov Nicholas E.,Broyde Suse,Patel Dinshaw J.

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/bi00138a002

Reference45 articles.

1. The correlation between benzol[a]pyrene-induced mutagenicity and DNA adduct formation in Salmonella typhimurium TA100

2. Targeting DNA sites with chiral metal complexes

3. Mutation in mammalian cells by stereoisomers of anti-benzo[a]pyrene-diolepoxide in relation to the extent and nature of the DNA reaction products

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