Human liver microsomal cytochrome P450 3A isozymes mediated vindesine biotransformation: Metabolic drug interactions
- 24 February 1993
- journal article
- Published by Elsevier in Biochemical Pharmacology
- Vol. 45 (4) , 853-861
- https://doi.org/10.1016/0006-2952(93)90169-w
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Pharmacokinetics of navelbine after oral administration in cancer patientsCancer Chemotherapy and Pharmacology, 1991
- The P450 Superfamily: Update on New Sequences, Gene Mapping, and Recommended NomenclatureDNA and Cell Biology, 1991
- In vivo and in vitro pharmacokinetics and metabolism of vincaalkaloids in rat II. Vinblastine and VincristineEuropean Journal of Drug Metabolism and Pharmacokinetics, 1990
- Expression of five forms of microsomal cytochrome P-450 in primary cultures of rabbit hepatocytes treated with various classes of inducersBiochemical Pharmacology, 1987
- Triacetyloleandomycin as inducer of cytochrome P-450 LM3c from rabbit liver microsomesBiochemical Pharmacology, 1985
- Variability in nifedipine pharmacokinetics and dynamics: A new oxidation polymorphism in manBiochemical Pharmacology, 1984
- Clinical pharmacokinetics of vindesine: Repeated treatments by intravenous bolus injectionsEuropean Journal of Cancer and Clinical Oncology, 1984
- Comparative pharmacokinetics of vindesine, vincristine and vinblastine in patients with cancerCancer Treatment Reviews, 1980
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970