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Volumn 44, Issue 17, 2001, Pages 2834-2842

Selective activation of mitomycin A by thiols to form DNA cross-links and monoadducts: Biochemical basis for the modulation of mitomycin cytotoxicity by the quinone redox potential

Author keywords

[No Author keywords available]

Indexed keywords

AMMONIUM DERIVATIVE; AMMONIUM HYDROXIDE; DEOXYGUANOSINE; DITHIOTHREITOL; DNA; GLUTATHIONE; MERCAPTOETHANOL; MITOMYCIN A; MITOMYCIN C; QUINONE DERIVATIVE; THIOL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0035899188     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm010072g     Document Type: Article
Times cited : (39)

References (50)
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  • 20
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    • Free-radical mechanisms involved in the formation of sequence dependent bistranded DNA lesions by the antitumor antibiotics bleomycin, neocarzinostatin and calicheamycin
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    • Dedon, P.C.1    Goldberg, I.H.2
  • 23
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    • Studies on dynemycin. A non-radical cycloaromatization pathway for the azabicyclo [7.3.1]enediyne core structure initiated by thiolate addition
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    • Studies on the mode of action of mitomycin C(7) aminoethylene disulfides (BMS-181174 and KW-2149): Reactivity of 7-N-(mercaptoethyl)mitomycin C
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    • Wang, S.1    Kohn, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.