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Volumn 118, Issue 39, 1996, Pages 9209-9217

2,7-Diaminomitosene, a monofunctional mitomycin C derivative, alkylates DNA in the major groove. Structure and base-sequence specificity of the DNA adduct and mechanism of the alkylation

Author keywords

[No Author keywords available]

Indexed keywords

2,7 DIAMINOMITOSENE; MITOMYCIN C DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0001229584     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9607401     Document Type: Article
Times cited : (50)

References (61)
  • 1
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    • note
    • 312, molar extinction coefficient at 312 nm.
  • 2
    • 0001471924 scopus 로고
    • Gottlieb, D., Shaw, P. D., Eds.; Springer-Verlag: New York
    • Szybalski, W.; Iyer, V. N. In Antibiotics 1: Mechanism of action; Gottlieb, D., Shaw, P. D., Eds.; Springer-Verlag: New York, 1967; pp 230-245.
    • (1967) Antibiotics 1: Mechanism of Action , pp. 230-245
    • Szybalski, W.1    Iyer, V.N.2
  • 4
    • 0026032132 scopus 로고
    • Hoban, P. R.; Walton, M. I.; Robson, C. N.; Godden, J.; Stratford, I. J.; Workman, P.; Harris, A. L.; Hickson, I. D. Cancer Res. 1990, 50, 4692-4697. Marshall, R. S.; Paterson, M. C.; Rauth, A. M. Biochem. Pharmacol. 1991, 41, 1351-1360.
    • (1991) Biochem. Pharmacol. , vol.41 , pp. 1351-1360
    • Marshall, R.S.1    Paterson, M.C.2    Rauth, A.M.3
  • 5
    • 0029360580 scopus 로고
    • For recent review, see: Tomasz, M. Chem. Biol. 1995, 2, 575-579.
    • (1995) Chem. Biol. , vol.2 , pp. 575-579
    • Tomasz, M.1
  • 23
    • 10244228240 scopus 로고    scopus 로고
    • note
    • (i) The term "mitosene" defines mitomycin derivatives with indoloquinone chromophore (cf. 3), while "mitosanes" are derivatives of 9,9a-dihydroindoloquinones, exemplified by MC (1).
  • 36
    • 0026703049 scopus 로고
    • (c) Ibid. 1992, 114, 7958-7959.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 7958-7959
  • 38
    • 0025360932 scopus 로고
    • The observed extent of alkylation under standard, first-order kinetic conditions (large excess of activated MC over guanine sites) may be regarded as proportional to the rate of the alkylation (Borowy-Borowski, H.; Lipman, R.; Tomasz, M. Biochemistry 1980, 29, 2999-3004).
    • (1980) Biochemistry , vol.29 , pp. 2999-3004
    • Borowy-Borowski, H.1    Lipman, R.2    Tomasz, M.3
  • 43
    • 0000785768 scopus 로고
    • Searle, C. E., Ed.; American Chemical Society: Washington, DC
    • (a) Lawley, P. D. In Chemical Carcinogenesis, ACS Monograph 182; Searle, C. E., Ed.; American Chemical Society: Washington, DC, 1984; pp 325-484.
    • (1984) Chemical Carcinogenesis, ACS Monograph 182 , pp. 325-484
    • Lawley, P.D.1
  • 50
    • 10244240840 scopus 로고    scopus 로고
    • note
    • 15


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.