CAFFEINE, AMINOIMIDAZOLECARBOXAMIDE AND DICOUMAROL, INHIBITORS OF NAD(P)H DEHYDROGENASE (QUINONE) (DT DIAPHORASE), PREVENT BOTH THE CYTO-TOXICITY AND DNA INTERSTRAND CROSSLINKING PRODUCED BY 5-(AZIRIDIN-1-YL)-2,4-DINITROBENZAMIDE (CB-1954) IN WALKER CELLS

被引:17
作者
ROBERTS, JJ
MARCHBANK, T
KOTSAKIKOVATSI, VP
BOLAND, MP
FRIEDLOS, F
KNOX, RJ
机构
关键词
D O I
10.1016/0006-2952(89)90695-3
中图分类号
R9 [药学];
学科分类号
1007 ;
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页码:4137 / 4143
页数:7
相关论文
共 27 条
[1]   DT-DIAPHORASE ACTIVITY AND THE CYTO-TOXICITY OF QUINONES IN C3H-10T1/2 MOUSE EMBRYO CELLS [J].
ATALLAH, AS ;
LANDOLPH, JR ;
ERNSTER, L ;
HOCHSTEIN, P .
BIOCHEMICAL PHARMACOLOGY, 1988, 37 (12) :2451-2459
[2]   2,4-DINITRO-5-ETHYLENEIMINOBENZAMIDE (CB 1954) - A POTENT AND SELECTIVE INHIBITOR OF GROWTH OF WALKER CARCINOMA 256 [J].
COBB, LM ;
CONNORS, TA ;
ELSON, LA ;
KHAN, AH ;
MITCHLEY, BC ;
ROSS, WCJ ;
WHISSON, ME .
BIOCHEMICAL PHARMACOLOGY, 1969, 18 (06) :1519-&
[3]   STUDIES ON REVERSAL OF SELECTIVE ANTITUMOR EFFECT OF AZIRIDINYL DERIVATIVE CB 1954 BY 4-AMINO-5-IMIDAZOLECARBOXAMIDE [J].
CONNORS, TA ;
MANDEL, HG ;
MELZACK, DH .
INTERNATIONAL JOURNAL OF CANCER, 1972, 9 (01) :126-&
[4]  
Cornish-Bowden A, 1976, PRINCIPLES ENZYME KI
[5]  
ERNSTER L, 1987, CHEM SCRIPTA, V27A, P1
[6]   PROTECTION AGAINST EFFECTS OF ANTITUMOUR AGENT CB 1954 BY CERTAIN IMIDAZOLES AND RELATED COMPOUNDS [J].
HICKMAN, JA ;
MELZACK, DH .
BIOCHEMICAL PHARMACOLOGY, 1975, 24 (21) :1947-1952
[7]   STUDIES ON PROTECTION BY IMIDAZOLES AGAINST CYTOTOXICITY OF ANTITUMOUR ALKYLATING-AGENTS MELPHALAN AND CB 1954 [J].
HICKMAN, JA ;
MELZACK, DH .
BIOCHEMICAL PHARMACOLOGY, 1976, 25 (22) :2489-2491
[8]  
JAISWAL AK, 1988, J BIOL CHEM, V263, P13572
[9]   CAFFEINE INHIBITS CELL TRANSFORMATION BY 4-NITROQUINOLINE-1-OXIDE [J].
KAKUNAGA, T .
NATURE, 1975, 258 (5532) :248-250
[10]   A NEW CYTO-TOXIC, DNA INTERSTRAND CROSSLINKING AGENT, 5-(AZIRIDIN-1-YL)-4-HYDROXYLAMINO-2-NITROBENZAMIDE, IS FORMED FROM 5-(AZIRIDIN-1-YL)-2,4-DINITROBENZAMIDE (CB-1954) BY A NITROREDUCTASE ENZYME IN WALKER CARCINOMA-CELLS [J].
KNOX, RJ ;
FRIEDLOS, F ;
JARMAN, M ;
ROBERTS, JJ .
BIOCHEMICAL PHARMACOLOGY, 1988, 37 (24) :4661-4669