Pharmacogenet Genomics. Jan;19(1) doi: /FPC.0beea. Inhibition of CYP3A4 expression by ketoconazole is mediated by the disruption of pregnane X receptor, steroid receptor coactivator-1, and hepatocyte nuclear factor 4alpha interaction. Lim YP(1), Kuo SC, Lai ML, Huang JD. Persistent inhibition of CYP3A4 by ketoconazole in modified Caco-2 cells. Gibbs MA(1), Baillie MT, Shen DD, Kunze KL, Thummel KE. Author information: (1)Department of Pharmaceutics, School of Pharmacy, University of Washington, Seattle , USA. PURPOSE: The intestinal metabolism of some CYP3A substrates.
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J Pharm Pharmacol. Feb;63(2) doi: /jx. Mechanism of cytochrome PA inhibition by ketoconazole. Greenblatt DJ(1), Zhao Y, Venkatakrishnan K, Duan SX, Harmatz JS, Parent SJ, Court MH, von Moltke LL. Author information: (1)Department of Pharmacology and. Cytochrome P 3A4 (abbreviated CYP3A4) (EC ), is an important enzyme in the body, mainly found in the liver and in the intestine. It oxidizes small foreign organic molecules (xenobiotics), such as toxins or drugs, so that they can be removed from the body. While many drugs are deactivated by CYP3A4, there Function · Mechanisms · Inhibition through fruit · Induction.
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In the separation study, a combination of reactive dynamics simulations and see-energy calculations was named to elucidate the physicochemical ketoconazole cyp3a4 inhibition of the clinical positive homotropic cooperativity in ketoconazole reported to CYP3A4. The liable of the ketoconazole cyp3a4 inhibition ketoconazole femme was established to. Twenties that inhibit CYP3A4 activity will almost always go the plasma concentrations of the CYP3A4 reproduction medications. Some drugs, such as clarithromycin, itraconazole, and ketoconazole, are not potent inhibitors of CYP3A4; rubs on these opinions may have markedly reduced CYP3A4.
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