Role of aromacity, ring strain, and stereochemistry of selected disulfides and their congeners in the oxidative linkage of DNA strands at the major groove. A computational study

Journal of Chemical Information and Modeling

Volumn 46, Issue 6, 2006, Pages 2527-2536

  Izsak, Robert ^a   Jojart, Balazs ^a   Csizmadia, Imre G ^a,b   Viskolcz, Bela ^a  

^a UNIVERSITY OF SZEGED   (Hungary)

^b UNIVERSITY OF TORONTO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSTS; COMPUTATIONAL METHODS; DNA; MOLECULAR DYNAMICS; OXIDATION; STEREOCHEMISTRY; THERMODYNAMICS;

AROMATIC DISULFIDES; CONGENERS; DEOXYRIBOSE MODELS; MOLECULAR COMPUTATIONS;

SULFUR COMPOUNDS;

DISULFIDE; DNA; OXYGEN; SELENIUM; SULFUR;

ARTICLE; BIOLOGY; CATALYSIS; CHEMICAL MODEL; CHEMICAL STRUCTURE; CHEMISTRY; COMPUTER SIMULATION; CONFORMATION; HYDROGEN BOND; METHODOLOGY; OXIDATION REDUCTION REACTION; STEREOISOMERISM; THERMODYNAMICS;

CATALYSIS; COMPUTATIONAL BIOLOGY; COMPUTER SIMULATION; DISULFIDES; DNA; HYDROGEN BONDING; MODELS, CHEMICAL; MODELS, MOLECULAR; NUCLEIC ACID CONFORMATION; OXIDATION-REDUCTION; OXYGEN; SELENIUM; STEREOISOMERISM; SULFUR; THERMODYNAMICS;

EID: 33845771367     PISSN: 15499596     EISSN: 1549960X     Source Type: Journal    
DOI: 10.1021/ci060123o     Document Type: Article

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