Clinical Importance of Hepatic Cytochrome P450 in Drug Metabolism

This publication has 88 references indexed in Scilit:

• In vitro oxidation of oxicam NSAIDs by a human liver cytochrome P450
  Published by Elsevier ,2002
• Loss of CYP2E1 and CYP1A2 Activity as a Function of Acetaminophen Dose: Relation to Toxicity
  Biochemical and Biophysical Research Communications, 1994
• Both cytochromes P450 2E1 and 1A1 are involved in the metabolism of chlorzoxazone
  Chemical Research in Toxicology, 1993
• Identification of Cytochrome P450 2E1 as the Predominant Enzyme Catalyzing Human Liver Microsomal Defluorination of Sevoflurane, Isoflurane, and Methoxyflurane
  Anesthesiology, 1993
• Particular ability of cytochrome P-450 CYP3A to reduce glyceryl trinitrate in rat liver microsomes: Subsequent formation of nitric oxide
  Chemico-Biological Interactions, 1993
• The P450 Superfamily: Update on New Sequences, Gene Mapping, Accession Numbers, Early Trivial Names of Enzymes, and Nomenclature
  DNA and Cell Biology, 1993
• Metabolism of minaprine in human and animal hepatocytes and liver microsomes—prediction of metabolismin vivo
  Xenobiotica, 1991
• Role of Cytochromes P45O in Drug Metabolism and Hepatotoxicity
  Seminars in Liver Disease, 1990
• Characterization of cDNAs, mRNAs, and proteins related to human liver microsomal cytochrome P-450 S-mephenytoin 4-hydroxylase
  Biochemistry, 1988
• Cytochrome P-450 isozyme selectivity in the oxidation of acetaminophen
  Chemical Research in Toxicology, 1988