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Volumn 131, Issue 3, 2009, Pages 1015-1024

Initiation of DNA strand cleavage by 1,2,4-benzotriazine 1,4-dioxide antitumor agents: Mechanistic insight from studies of 3-methyl-1,2,4- benzotriazine 1,4-dioxide

Author keywords

[No Author keywords available]

Indexed keywords

ANTI-TUMOR AGENTS; ANTITUMOR DRUGS; BENZOTRIAZINYL RADICAL; CHEMICAL MECHANISM; DNA DAMAGES; DNA DAMAGING AGENTS; DNA STRANDS; ENZYMATIC REDUCTION; HOMOLYSIS; HYDROXYL RADICALS; HYPOXIC CELLS; HYPOXIC CONDITION; ISOTOPIC LABELING; NEW CLASS; O-H BOND; ONE-ELECTRON REDUCTIONS; ORGANIC SUBSTRATE; SELECTIVE OXIDATION; SOLID TUMORS; TIRAPAZAMINE;

EID: 61749095311     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja8049645     Document Type: Article
Times cited : (52)

References (23)
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    • (1992) The Search For New Anticancer Drugs , pp. 87-131
    • Wilson, W.R.1
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    • Brown, J. M. Cancer Res. 1999, 59, 5863-5870.
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    • Brown, J.M.1
  • 13
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    • 2̇-) produced by this type of redox cycling can be cytotoxic, see refs 14-19. However, cellular enzymes including superoxide dismutase, catalase, glutathione peroxidase, and peroxire- doxins mitigate the deleterious effects of superoxide radical and its decomposition products (see refs 18, 20, and 21.) and, in the context of TPZ, back-oxidation of 2 clearly represents a detoxification process.
    • 2̇-) produced by this type of redox cycling can be cytotoxic, see refs 14-19. However, cellular enzymes including superoxide dismutase, catalase, glutathione peroxidase, and peroxire- doxins mitigate the deleterious effects of superoxide radical and its decomposition products (see refs 18, 20, and 21.) and, in the context of TPZ, back-oxidation of 2 clearly represents a detoxification process.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.