The degradation of different forms of cytochrome P-450 in vivo by fluroxene and allyl-iso-propylacetamide
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference23 articles.
1. Loss of haem in rat liver caused by the porphyrogenic agent 2-allyl-2-isopropylacetamide
2. Incorporation of radioactive-δ-aminolevulinic acid into microsomal cytochrome P450: Selective breakdown of the hemoprotein by allylisopropylacetamide and carbon tetrachloride
3. Fluroxene (2,2,2-trifluoroethyl vinyl ether) mediated destruction of cytochrome P-450 in vitro
4. The role of cytochrome P-450 in the toxicity of fluroxene (2,2,2-trifluoroethyl vinyl ether) anaesthesia in vivo
5. Further investigations of the metabolism of fluroxene and the degradation of cytochromes p-450 in vitro
Cited by 26 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. Quantum mechanical study of putative intermediates in adduct formation by the suicide substrate ethylene with cytochrome P-450;International Journal of Quantum Chemistry;2009-06-19
2. Liver Damage in Rats by Allylisopropylacetamide (AIA), an Inducer of δ-Aminolevulinic Acid Synthetase (ALAS);Acta Pharmacologica et Toxicologica;2009-03-13
3. Multiple Aspects of the Toxicity of Fluroxene and its Metabolite 2,2,2-Trifluoroethanol;CRC Critical Reviews in Toxicology;1988-01
4. Mechanisms of the Inhibition of Cytochrome P 450-Mediated Drug Oxidation by Therapeutic Agents;Drug Metabolism Reviews;1987-01
5. Cytochrome P-450-dependent H2O2production demonstrated in vivo;FEBS Letters;1986-04-07
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