Inhibition of rat hepatic mixed function oxidases by antimalarial drugs: Selectivity for cytochromes P-450 and P-448
- 1 October 1984
- journal article
- research article
- Published by Elsevier in Chemico-Biological Interactions
- Vol. 51 (3) , 285-294
- https://doi.org/10.1016/0009-2797(84)90154-6
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Determination of cytochrome P-448 activity in biological tissuesBiochemical Journal, 1984
- Cytochrome P-448 and the activation of toxic chemicals and carcinogensXenobiotica, 1984
- The binding to oxidised cytochromes P-450 and inhibition of mixed-function oxidases by aryl-substituted benzimidazoles and related compoundsChemico-Biological Interactions, 1983
- Inhibition of drug metabolism by the antimalarial drugs chloroquine and primaquine in the ratBiochemical Pharmacology, 1983
- Studies on the substrate-binding sites of liver microsomal cytochrome P-448Biochemical Journal, 1982
- Purification and characterization of microsomal cytochrome P-450sXenobiotica, 1982
- A class of strong inhibitors of microsomal monooxygenases: The elupticinesChemico-Biological Interactions, 1979
- Inhibitors of hepatic mixed function oxidases—II Some benzimidazole, benzoxazole and benzothiazole derivativesBiochemical Pharmacology, 1976
- Structure-activity relationships in the effects of 1-alkylimidazoles on microsomal oxidation in vitro and in vivoBiochemical Pharmacology, 1974
- Imidazole derivatives—A new class of microsomal enzyme inhibitorsBiochemical Pharmacology, 1972