Fluroxene (2,2,2-trifluoroethyl vinyl ether) mediated destruction of cytochrome P-450 in vitro
Author:
Publisher
Elsevier BV
Subject
Pharmacology,Biochemistry
Reference17 articles.
1. Cytochrome P-450 and its Role in Drug Metabolism
2. Incorporation of radioactive-δ-aminolevulinic acid into microsomal cytochrome P450: Selective breakdown of the hemoprotein by allylisopropylacetamide and carbon tetrachloride
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1. Substrate-Dependent Irreversible Inactivation of CytochromeP-450: Conversion of Its Haem Moiety into Modified Porphyrins;Novartis Foundation Symposia;2008-05-30
2. Fluorinated Substrate Analogs: Routes of Metabolism and Selective Toxicity;Advances in Enzymology - and Related Areas of Molecular Biology;2006-11-22
3. 19F nuclear magnetic resonance analysis of trifluoroethanol metabolites in the urine of the Sprague-Dawley rat;Biochemical Pharmacology;1991-11
4. 2,2,2-Trifluoroethanol intestinal and bone marrow toxicity: The role of its metabolism to 2,2,2-trifluoroacetaldehyde and trifluoroacetic acid;Toxicology and Applied Pharmacology;1988-06
5. Multiple Aspects of the Toxicity of Fluroxene and its Metabolite 2,2,2-Trifluoroethanol;CRC Critical Reviews in Toxicology;1988-01
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