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- W1567686906 abstract "Oxidation of tienilic acid by human cytochromes P-450 (CYP) 2C9, 2C18, 2C8 and 2C19 was studied using recombinant enzymes expressed in yeast. CYP 2C9 was the best catalyst for 5-hydroxylation of tienilic acid (Km= 5 ±1 μM, kcat= 1.7 ± 0.2 min−1), 30-fold more potent in terms of kcat/Km than CYP 2C18 (Km= 150 ± 15 μM, kcat= 1.8 ± 0.2 min−1 and 300-fold more potent than CYP 2C8 (Km= 145 ± 15 μM, kcat= 0.2 ± 0.1 min−1). CYP 2C19 was unable to catalyze this hydroxylation under our experimental conditions. During this study, a marked effect of the ionic strength on the activities (hydroxylations of tienilic acid and tolbutamide) of these cytochromes P-450 expressed in the yeast strain 334 was observed. The effect was particularly great in the case of CYP 2C18, with a tenfold decrease of activity upon increasing ionic strength from 0.02 to 0.1. Specific-covalent binding of tienilic acid metabolites to cytochrome P-450 (incubations in the presence of 5 mM glutathione) was markedly higher upon tienilic acid oxidation by CYP 2C9 than by CYP 2C18 and CYP 2C8. Mechanism-based inactivation of cytochrome P-450 during tienilic acid oxidation was observed in the case of CYP 2C9 but was not detectable with CYP 2C18 and CYP 2C8. Tienilic acid thus appears to be a mechanism-based inhibitor specific for CYP 2C9 in human liver. Experiments performed with human liver microsomes confirmed that tienilic acid 5-hydroxylase underwent a time-dependent inactivation (apparent t½= 10 ± 5 min) during 5-hydroxylation of tienilic acid." @default.
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- W1567686906 date "1996-11-01" @default.
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- W1567686906 title "Oxidation of Tienilic Acid by Human Yeast-Expressed Cytochromes P-450 2C8, 2C9, 2C18 and 2C19. Evidence that this Drug is A Mechanism-Based Inhibitor Specific for Cytochrome P-450 2C9" @default.
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- W1567686906 doi "https://doi.org/10.1111/j.1432-1033.1996.00797.x" @default.
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