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Journal Abstract Search
174 related items for PubMed ID: 6111423
1. The 1980 Bernard B. Brodie award lecture. Drug metabolism by cytochrome P-450: progress and perspectives. Coon MJ. Drug Metab Dispos; 1981; 9(1):1-4. PubMed ID: 6111423 [No Abstract] [Full Text] [Related]
4. Studies on the molecular function of cytochrome P-450 during drug metabolism. Estabrook RW, Matsubara T, Mason JI, Werringloer J, Baron J. Drug Metab Dispos; 1973; 1(1):98-110. PubMed ID: 4149428 [No Abstract] [Full Text] [Related]
6. Interaction of constitutive and phenobarbital-induced cytochrome P-450 isozymes during the sequential oxidation of benzphetamine. Explanation for the difference in benzphetamine-induced hydrogen peroxide production and 455-nm complex formation in microsomes from untreated and phenobarbital-treated rats. Jeffery EH, Mannering GJ. Mol Pharmacol; 1983 May; 23(3):748-57. PubMed ID: 6865917 [Abstract] [Full Text] [Related]
8. Drug metabolism in a reconstituted system by diabetes-dependent hepatic cytochrome P-450. Past MR, Cook DE. Res Commun Chem Pathol Pharmacol; 1982 Jul; 37(1):81-90. PubMed ID: 6812187 [Abstract] [Full Text] [Related]
10. [Features of the metabolism of various drugs involving cytochrome P-450 isoenzymes]. Filimonova AA, Ziganshin AU, Ziganshina LE. Eksp Klin Farmakol; 2007 Jul; 70(3):69-77. PubMed ID: 17650639 [Abstract] [Full Text] [Related]
11. Interactions of drug metabolites with hepatic cytochrome P-450. Some implications for drug metabolism. Bast A. Pharm Weekbl Sci; 1982 Aug 20; 4(4):113-4. PubMed ID: 7133961 [No Abstract] [Full Text] [Related]
14. Reductive cleavage of hydroperoxides by cytochrome P-450. Vaz AD, Coon MJ. Methods Enzymol; 1990 Aug 20; 186():278-82. PubMed ID: 2233300 [No Abstract] [Full Text] [Related]
15. The characterization of an inhibitory complex formed with cytochrome P-450 and a metabolite of 1,1-disubstituted hydrazines. Hines RN, Prough RA. J Pharmacol Exp Ther; 1980 Jul 20; 214(1):80-6. PubMed ID: 7391974 [No Abstract] [Full Text] [Related]
19. The antibiotic tiamulin is a potent inducer and inhibitor of cytochrome P4503A via the formation of a stable metabolic intermediate complex. Studies in primary hepatocyte cultures and liver microsomes of the pig. Witkamp RF, Nijmeijer SM, Monshouwer M, Van Miert AS. Drug Metab Dispos; 1995 May 20; 23(5):542-7. PubMed ID: 7587928 [Abstract] [Full Text] [Related]