Search Results - "Prueksaritanont, T"
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Validation of a microdose probe drug cocktail for clinical drug interaction assessments for drug transporters and CYP3A
Published in Clinical pharmacology and therapeutics (01-04-2017)“…A microdose cocktail containing midazolam, dabigatran etexilate, pitavastatin, rosuvastatin, and atorvastatin has been established to allow simultaneous…”
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UGT2B17 Genetic Polymorphisms Dramatically Affect the Pharmacokinetics of MK-7246 in Healthy Subjects in a First-in-Human Study
Published in Clinical pharmacology and therapeutics (01-07-2012)“…MK‐7246, an antagonist of the chemoattractant receptor on T helper type 2 (Th2) cells, is being developed for the treatment of respiratory diseases. In a…”
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Hepatic Metabolism of MK-0457, a Potent Aurora Kinase Inhibitor: Interspecies Comparison and Role of Human Cytochrome P450 and Flavin-Containing Monooxygenase
Published in Drug metabolism and disposition (01-09-2007)“…MK-0457 ( N -[4({4-(4-methylpiperazin-1-yl)-6-[(3-methyl-1 H -pyrazol-5 -yl)amino]pyrimidin-2-yl}thio)phenyl]cyclopropanecarboxamide), an Aurora kinase…”
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Effects of fibrates on human organic anion-transporting polypeptide 1B1-, multidrug resistance protein 2- and P-glycoprotein-mediated transport
Published in Xenobiotica (01-07-2005)“…The effects of different fibric acid derivatives (bezafibrate, clofibrate, clofibric acid, fenofibrate, fenofibric acid and gemfibrozil) on human organic anion…”
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Preclinical pharmacokinetics of MK-0974, an orally active calcitonin-gene related peptide (CGRP)-receptor antagonist, mechanism of dose dependency and species differences
Published in Xenobiotica (01-01-2009)“…The underlying mechanism for low oral bioavailability of MK-0974, a potent calcitonin-gene related peptide (CGRP)-receptor antagonist, in monkeys and for…”
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Comparative studies of drug-metabolizing enzymes in dog, monkey, and human small intestines, and in Caco-2 cells
Published in Drug metabolism and disposition (01-06-1996)“…Drug-metabolizing enzymes were studied in subcellular fractions of dog, monkey, and human small intestines, and in the human adenocarcinoma cell line Caco-2, a…”
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Bioavailability of cyclosporine with concomitant rifampin administration is markedly less than predicted by hepatic enzyme induction
Published in Clinical pharmacology and therapeutics (01-11-1992)“…The pharmacokinetics of cyclosporine was studied in six healthy volunteers after administration of the drug orally (10 mg/kg) and intravenously (3 mg/kg) with…”
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Concurrent Administration of the Erythromycin Breath Test (EBT) and Oral Midazolam as In Vivo Probes for CYP3A Activity
Published in Journal of clinical pharmacology (01-12-1999)“…Given the prominent role of CYP3A in the metabolism of drugs, it is important to identify whether new chemical entities will affect this enzyme system and…”
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Interactions between Simvastatin and Troglitazone or Pioglitazone in Healthy Subjects
Published in Journal of clinical pharmacology (01-05-2001)“…Two randomized, two‐period crossover studies were conducted to evaluate the effects of repeat oral dosing of troglitazone (Study I) and pioglitazone (Study II)…”
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Stereoselective hepatic disposition of a diastereomeric pair of αvβ3 antagonists in rat
Published in Xenobiotica (01-11-2003)“…1. The study investigated mechanisms underlying the stereoselective hepatic disposition observed in rats of a zwitterionic diastereomeric pair ((3S)-3-{(3R or…”
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Drug–Drug Interaction Studies: Regulatory Guidance and An Industry Perspective
Published in The AAPS journal (01-07-2013)“…Recently, the US Food and Drug Administration and European Medicines Agency have issued new guidance for industry on drug interaction studies, which outline…”
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Interspecies comparison and role of human cytochrome P450 and flavin-containing monooxygenase in hepatic metabolism of L-775,606, a potent 5-HT(1D) receptor agonist
Published in Xenobiotica (01-01-2000)“…1. Quantitative species differences and human liver enzymes involved in the metabolism of L-775,606, a potent and selective 5-HT1D receptor agonist developed…”
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An extended point-area deconvolution approach for assessing drug input rates
Published in Pharmaceutical research (01-10-2001)“…To describe an extended point-area deconvolution approach for evaluating drug input rates based on the application of piecewise cubic polynomial functions…”
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Simvastatin Does Not Affect CYP3A Activity, Quantified by the Erythromycin Breath Test and Oral Midazolam Pharmacokinetics, in Healthy Male Subjects
Published in Journal of clinical pharmacology (01-11-2000)“…Potential for inhibition of CYP3A activity by simvastatin, an HMG‐CoA reductase inhibitor, was evaluated in 12 healthy male subjects who received placebo or 80…”
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Cyclosporine metabolism by rat liver microsomes. Evidence for involvement of enzyme(s) other than cytochromes P-450 3A
Published in Drug metabolism and disposition (01-07-1993)“…Cyclosporine (CyA) metabolism was investigated in liver microsomes obtained from untreated male and female Sprague-Dawley rats, and rats pretreated with…”
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The human hepatic metabolism of simvastatin hydroxy acid is mediated primarily by CYP3A, and not CYP2D6
Published in British journal of clinical pharmacology (01-07-2003)“…Aims To identify the cytochrome P450 (CYP) isoforms responsible for the metabolism of simvastatin hydroxy acid (SVA), the most potent metabolite of…”
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Interspecies comparison and role of human cytochrome P450 and flavin-containing monooxygenase in hepatic metabolism of L-775,606, a potent 5-HT1D receptor agonist
Published in Xenobiotica (2000)“…1. Quantitative species differences and human liver enzymes involved in the metabolism of L-775,606, a potent and selective 5-HT1D receptor agonist developed…”
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FK 506 metabolism in male and female rat liver microsomes
Published in Drug metabolism and disposition (01-01-1994)“…The main metabolite of the immunosuppressant FK 506 in hepatic microsomes from male and female Sprague-Dawley rats was identified by mass spectrometry as an…”
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Effects of Fibrates on Metabolism of Statins in Human Hepatocytes
Published in Drug metabolism and disposition (01-11-2002)“…This study investigated the metabolic interaction between fibrates and statin hydroxy acids in human hepatocytes. Gemfibrozil (GFZ) modestly affected the…”
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