Reaction schemes for the degradation of cytochromes P-450 by allyl-iso-propylacetamide and fluroxene
Author:
Publisher
Elsevier BV
Subject
Pharmacology,Biochemistry
Reference27 articles.
1. Loss of haem in rat liver caused by the porphyrogenic agent 2-allyl-2-isopropylacetamide
2. Destruction of Cytochrome P 450 by Secobarbital and Other Barbiturates Containing Allyl Groups
3. Incorporation of radioactive-δ-aminolevulinic acid into microsomal cytochrome P450: Selective breakdown of the hemoprotein by allylisopropylacetamide and carbon tetrachloride
4. Loss of haem from cytochrome P-450 caused by lipid peroxidation and 2-allyl-2-isoprophylacetamide. An abnormal pathway not involving production of carbon monoxide
5. Fluroxene (2,2,2-trifluoroethyl vinyl ether) mediated destruction of cytochrome P-450 in vitro
Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. The effect of oxygen upon the kinetics of glucose oxidase inactivation;The Canadian Journal of Chemical Engineering;1993-12
2. Resistance of the 2,2,2-trifluoroethoxy aryl moiety to the cytochrome P-450 metabolism in rat liver microsomes;Bioorganic & Medicinal Chemistry Letters;1993-02
3. The effect of oxygen upon the kinetics of enzyme inactivation: In vitro investigations using glutamine synthetase;The Canadian Journal of Chemical Engineering;1992-12
4. Substrate inactivation of enzymes in vitro and in vivo;Biotechnology Advances;1989-01
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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