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Journal of the American Chemical Society

Volumn 123, Issue 29, 2001, Pages 7054-7066

Stereochemical, structural, and thermodynamic origins of stability differences between stereoisomeric benzo[a]pyrene diol epoxide deoxyadenosine adducts in a DNA mutational hot spot sequence

(4) Yan, S a Shapiro, R a Geacintov, N E a Broyde, S a

a NEW YORK UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

METABOLICALLY ACTIVATION;

COMPUTER SIMULATION; DNA; ENZYMES; FREE ENERGY; ISOMERS; METABOLISM; MOLECULAR DYNAMICS; NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; THERMODYNAMICS;

POLYCYCLIC AROMATIC HYDROCARBONS;

DEOXYADENOSINE DERIVATIVE; DIHYDROXYBENZO[A]PYRENE OXIDE; DOUBLE STRANDED DNA; POLYCYCLIC AROMATIC HYDROCARBON;

ARTICLE; DNA ADDUCT; DNA SEQUENCE; ENANTIOMER; EXCISION REPAIR; MOLECULAR DYNAMICS; NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; STEREOISOMERISM; THERMODYNAMICS;

7,8-DIHYDRO-7,8-DIHYDROXYBENZO(A)PYRENE 9,10-OXIDE; ADENINE; BASE SEQUENCE; CARCINOGENS, ENVIRONMENTAL; DNA ADDUCTS; DRUG STABILITY; HUMANS; INTERCALATING AGENTS; MODELS, MOLECULAR; MUTAGENS; POLYCYCLIC HYDROCARBONS, AROMATIC; STEREOISOMERISM; THERMODYNAMICS;

EID: 0034822656 PISSN: 00027863 EISSN: None Source Type: Journal
DOI: 10.1021/ja0043035 Document Type: Article

Times cited : (53)

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