Conformations of adducts formed between the genotoxic benzo[a]pyrene-7,8-dione and nucleosides studied by density functional theory

Biophysical Chemistry

Volumn 125, Issue 1, 2007, Pages 151-158

  Lee, Hyun Mee ^a   Chae, Youn Hee ^a   Kwon, Cheol ^a   Kim, Seog K ^a  

^a Yeungnam University   (South Korea)

Author keywords

Adduct; Benzo a pyrene 7,8 dione; Density functional theory; DNA; Stereoisomer

Indexed keywords

2' DEOXYNUCLEOSIDE; BENZO[A]PYRENE; BENZO[A]PYRENE 7,8 DIONE; NUCLEOSIDE DERIVATIVE; OXIDOREDUCTASE; QUINONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CONFORMATION; DENSITY FUNCTIONAL THEORY; DNA STRAND; GENOTOXICITY; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; QUANTUM MECHANICS;

BENZOPYRENES; COMPUTER SIMULATION; DEOXYRIBONUCLEOSIDES; DNA ADDUCTS; GUANOSINE; MOLECULAR CONFORMATION; N-GLYCOSYL HYDROLASES; NUCLEIC ACID CONFORMATION; QUANTUM THEORY; STEREOISOMERISM;

MAMMALIA;

EID: 33750724711     PISSN: 03014622     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bpc.2006.07.015     Document Type: Article

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