化学
微粒体
还原酶
细胞色素
乙醇
细胞色素P450
基质(水族馆)
氧化还原
体外
IC50型
氧化物
立体化学
酶
生物化学
有机化学
生物
生态学
作者
Lenka Skálová,Milan Nobilis,Barbora Szotáková,Vladimı́r Wsól,Ε. Kvasnieková
出处
期刊:Drug metabolism and drug interactions
日期:1998-06-01
卷期号:14 (4): 221-234
被引量:6
标识
DOI:10.1515/dmdi.1998.14.4.221
摘要
Benfluron N-oxide [5-(2-N-oxo-2-N,N'-dimethylaminoethoxy)-7-oxo-7-H-benzo[c]fluorene] is a biologically active substance which displays a cytostatic effect on several experimental tumour cells. The main metabolic pathway of benfluron N-oxide in vitro and in vitro--its reduction to the parent tertiary amine benfluron--and the role of cytochrome P450 in this reduction were studied. The value of the benfluron N-oxide/benfluron redox potential as a criterion of suitability of the substrate for cytochrome P450 reductase activity was determined. Results of induction and inhibition studies on rats suggest that cytochromes P4502B and P4502E1 participate in microsomal reduction of benfluron N-oxide. Unlike most cytochrome P450 catalysed reactions, the reduction of benfluron N-oxide also occurs under aerobic conditions. Microsomes induced by phenobarbital, ethanol or beta-naphthoflavone showed no significantly greater inhibitory effect of oxygen on benfluron N-oxide reduction.
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