Formation of the 1,N2-glyoxal adduct of deoxyguanosine by phosphoglycolaldehyde, a product of 3′-deoxyribose oxidation in DNA

Chemical Research in Toxicology

Volumn 14, Issue 9, 2001, Pages 1247-1253

  Awada, M ^a   Dedon, P C ^a  

^a MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE DERIVATIVE; DEOXYGUANOSINE; DEOXYRIBOSE; DNA; EDETIC ACID; GLYOXAL DERIVATIVE; HYDROXYL RADICAL; IRON COMPLEX; OXYGEN; PHOSPHOGLYCOALDEHYDE; SORBITOL; UNCLASSIFIED DRUG;

ARTICLE; COMPLEX FORMATION; CONCENTRATION RESPONSE; CONTROLLED STUDY; DIASTEREOISOMER; DNA STRAND BREAKAGE; FLUORESCENCE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; OXIDATION; REACTION ANALYSIS; SIGNAL TRANSDUCTION; SYNTHESIS; ULTRAVIOLET RADIATION;

ALDEHYDES; ANIMALS; CATTLE; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; DEOXYRIBOSE; DNA ADDUCTS; DNA DAMAGE; ENDODEOXYRIBONUCLEASES; ESCHERICHIA COLI; GLYOXAL; OXIDATION-REDUCTION; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION; THYMUS GLAND;

EID: 0034813511     PISSN: 0893228X     EISSN: None     Source Type: Journal    
DOI: 10.1021/tx0155092     Document Type: Article

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