ELLIPTICINES AS POTENT INHIBITORS OF MICROSOMES-DEPENDENT CHEMICAL MUTAGENESIS

被引:38
作者
LESCA, P [1 ]
LECOINTE, P [1 ]
PAOLETTI, C [1 ]
MANSUY, D [1 ]
机构
[1] ECOLE NORM SUPER, CHIM LAB, F-75231 PARIS 5, FRANCE
关键词
D O I
10.1016/0009-2797(79)90052-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
9-Hydroxyellipticine (9-OHE), an inhibitor of microsomal monooxygenase activities has been shown to exert a large or even complete decrease of the mutagenicity, on the Salmonella strains of a great number of compounds (aromatic amines, polycyclic aromatic hydrocarbons, fungal toxins, azo compounds, tobacco smoke condensate). 9-OHE and 9-fluoroellipticine are more potent inhibitors than ellipticine itself. The inhibitions exerted by 9-OHE are not even equalled by 10-fold higher doses of 7,8-benzoflavone (7,8-BF). There is a good correlation between these data and the interaction properties of ellipticines with microsomal cytochromes P-450. © 1979.
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页码:279 / 287
页数:9
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