In vitro inhibition of CYP2B1 monooxygenase by β-myrcene and other monoterpenoid compounds
- 1 June 1997
- journal article
- Published by Elsevier BV in Toxicology Letters
- Vol. 92 (1), 39-46
- https://doi.org/10.1016/s0378-4274(97)00034-9
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Cytochrome P450 specificities of alkoxyresorufin O-dealkylation in human and rat liverBiochemical Pharmacology, 1994
- Influence of β-myrcene on sister-chromatid exchanges induced by mutagens in V79 and HTC cellsMutation Research Letters, 1991
- Evaluation of the mutagenicity of β‐myrcene in mammalian cells in vitroEnvironmental and Molecular Mutagenesis, 1991
- The Cytochrome P450 I Gene Family of Microsomal Hemoproteins and Their Role in the Metabolic Activation of ChemicalsDrug Metabolism Reviews, 1990
- Regulation of the mammalian cytochrome P1-450 (CYP1A1) geneInternational Journal of Biochemistry, 1989
- Stable expression of rat cytochrome P-450IIB1 cDNA in Chinese hamster cells (V79) and metabolic activation of aflatoxin B1.Proceedings of the National Academy of Sciences, 1988
- Mutagenic activation of aflatoxin B1 by several forms of purified cytochrome P-450Mutation Research Letters, 1986
- Ethoxy-, pentoxy- and benzyloxyphenoxazones and homologues: a series of substrates to distinguish between different induced cytochromes P-450Biochemical Pharmacology, 1985
- Monographs on fragrance raw materialsFood and Cosmetics Toxicology, 1979
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976