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Volumn 19, Issue 5, 1993, Pages 323-332

Dna breaking activity of the carbon-centered radical generated from 2,2'azobis(2-amidinopropane) hydrochloride (AAPH)

Author keywords

2,2'azobis(2 amidinopropane)hydrochloride (AAPH); Carboncentered radical; DNA breaking; Hydroxyl radical; Spin trapping

Indexed keywords

2,2' AZOBIS(2 AMIDINOPROPANE); 2,2'-AZOBIS(2-AMIDINOPROPANE); 5,5 DIMETHYL 1 PYRROLINE 1 OXIDE; 5,5-DIMETHYL-1-PYRROLINE-1-OXIDE; AMIDINE; AMINE OXIDE; CATALASE; CYCLIC N OXIDES; DNA; FREE RADICAL; HYDROXYL RADICAL; N TERT BUTYL ALPHA PHENYLNITRONE; NITROGEN OXIDE; OXYGEN; PHENYL-N-TERT-BUTYLNITRONE; SUPEROXIDE DISMUTASE;

EID: 0027142171     PISSN: 10715762     EISSN: None     Source Type: Journal    
DOI: 10.3109/10715769309056521     Document Type: Article
Times cited : (175)

References (33)
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    • Why is the hydroxyl radical the only radical that commonly adds to DNA? Hypothesis: It has a rate combination of high electrophilicity, high thermochemical reactivity, and a mode of production that can occur near DNA
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    • Pryor, W.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.