Search Results - "Ogilvie, Brian"
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An Assessment of the In Vitro Inhibition of Cytochrome P450 Enzymes, UDP-Glucuronosyltransferases, and Transporters by Phosphodiester- or Phosphorothioate-Linked Oligonucleotides
Published in Drug metabolism and disposition (01-08-2018)“…Oligonucleotides represent an expanding class of pharmacotherapeutics in development for various indications. Typically, oligonucleotides are developed with…”
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Evaluation of Ketoconazole and Its Alternative Clinical CYP3A4/5 Inhibitors as Inhibitors of Drug Transporters: The In Vitro Effects of Ketoconazole, Ritonavir, Clarithromycin, and Itraconazole on 13 Clinically-Relevant Drug Transporters
Published in Drug metabolism and disposition (01-03-2016)“…Ketoconazole is a potent CYP3A4/5 inhibitor and, until recently, recommended by the Food and Drug Administration (FDA) and the European Medicines Agency as a…”
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Impact of donor diversity on phase I and phase II activities in cryopreserved human hepatocytes and human liver microsomes
Published in Drug metabolism and pharmacokinetics (01-04-2024)Get full text
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The Reliability of Estimating Ki Values for Direct, Reversible Inhibition of Cytochrome P450 Enzymes from Corresponding IC50 Values: A Retrospective Analysis of 343 Experiments
Published in Drug metabolism and disposition (01-11-2015)“…In the present study, we conducted a retrospective analysis of 343 in vitro experiments to ascertain whether observed (experimentally determined) values of Ki…”
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Prediction of the Overall Renal Tubular Secretion and Hepatic Clearance of Anionic Drugs and a Renal Drug-Drug Interaction Involving Organic Anion Transporter 3 in Humans by In Vitro Uptake Experiments
Published in Drug metabolism and disposition (01-06-2011)“…The present study investigated prediction of the overall renal tubular secretion and hepatic clearances of anionic drugs based on in vitro transport studies…”
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The Proton Pump Inhibitor, Omeprazole, but Not Lansoprazole or Pantoprazole, Is a Metabolism-Dependent Inhibitor of CYP2C19: Implications for Coadministration with Clopidogrel
Published in Drug metabolism and disposition (01-11-2011)“…As a direct-acting inhibitor of CYP2C19 in vitro, lansoprazole is more potent than omeprazole and other proton pump inhibitors (PPIs), but lansoprazole does…”
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GLUCURONIDATION CONVERTS GEMFIBROZIL TO A POTENT, METABOLISM-DEPENDENT INHIBITOR OF CYP2C8: IMPLICATIONS FOR DRUG-DRUG INTERACTIONS
Published in Drug metabolism and disposition (01-01-2006)“…Gemfibrozil more potently inhibits CYP2C9 than CYP2C8 in vitro, and yet the opposite inhibitory potency is observed in the clinic. To investigate this apparent…”
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In vitro evaluation suggests fenfluramine and norfenfluramine are unlikely to act as perpetrators of drug interactions
Published in Pharmacology research & perspectives (01-06-2022)“…Studies support the safety and efficacy of fenfluramine (FFA) as an antiseizure medication (ASM) in Dravet syndrome, Lennox‐Gastaut syndrome, or CDKL5…”
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System-Dependent Outcomes during the Evaluation of Drug Candidates as Inhibitors of Cytochrome P450 (CYP) and Uridine Diphosphate Glucuronosyltransferase (UGT) Enzymes: Human Hepatocytes versus Liver Microsomes versus Recombinant Enzymes
Published in DRUG METABOLISM AND PHARMACOKINETICS (01-01-2010)“…The ability of a drug to cause clinically significant drug-drug interactions due to direct or metabolism-dependent inhibition of cytochrome P450 (CYP) can…”
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In vitro evaluation of fenfluramine and norfenfluramine as victims of drug interactions
Published in Pharmacology research & perspectives (01-06-2022)“…Fenfluramine (FFA) has potent antiseizure activity in severe, pharmacoresistant childhood‐onset developmental and epileptic encephalopathies (e.g., Dravet…”
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An Evaluation of the Dilution Method for Identifying Metabolism-Dependent Inhibitors of Cytochrome P450 Enzymes
Published in Drug metabolism and disposition (01-08-2011)“…Metabolism-dependent inhibition (MDI) of cytochrome P450 is usually assessed in vitro by examining whether the inhibitory potency of a drug candidate increases…”
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Clinical assessment of drug-drug interactions of tasimelteon, a novel dual melatonin receptor agonist
Published in Journal of clinical pharmacology (01-09-2015)“…Tasimelteon ([1R‐trans]‐N‐[(2‐[2,3‐dihydro‐4‐benzofuranyl] cyclopropyl) methyl] propanamide), a novel dual melatonin receptor agonist that demonstrates…”
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Effects of monocyte chemoattractant protein‐1, macrophage inflammatory protein‐1α, and interferon‐α2a on P450 enzymes in human hepatocytes in vitro
Published in Pharmacology research & perspectives (01-12-2019)“…Some immunomodulatory agents stimulate the release of cytokines capable of suppressing P450 enzymes and potentially affecting pharmacokinetics of…”
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In Vitro Inhibition and Induction of Human Liver Cytochrome P450 Enzymes by Milnacipran
Published in Drug metabolism and disposition (01-10-2009)“…Milnacipran (Savella) inhibits both norepinephrine and serotonin reuptake and is distinguished by a nearly 3-fold greater potency in inhibiting norepinephrine…”
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Microsomal cytochrome P450 enzyme activities in nonalcoholic steatohepatitis livers
Published in Drug metabolism and pharmacokinetics (01-01-2019)Get full text
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Construction of Triple-Transfected Cells [Organic Anion-Transporting Polypeptide (OATP) 1B1/Multidrug Resistance-Associated Protein (MRP) 2/MRP3 and OATP1B1/MRP2/MRP4] for Analysis of the Sinusoidal Function of MRP3 and MRP4
Published in Drug metabolism and disposition (01-10-2009)“…Multidrug resistance-associated protein (MRP) 3/ ABCC3 and MRP4/ ABCC4 are ATP-binding cassette (ABC) transporters expressed in the sinusoidal membrane of…”
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An in Vitro Evaluation of the Victim and Perpetrator Potential of the Anticancer Agent Laromustine (VNP40101M), Based on Reaction Phenotyping and Inhibition and Induction of Cytochrome P450 Enzymes
Published in Drug metabolism and disposition (01-09-2009)“…Laromustine (VNP40101M, also known as Cloretazine) is a novel sulfonylhydrazine alkylating (anticancer) agent. Laromustine generates two types of reactive…”
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Scientific Archives in the Age of Digitization
Published in Isis (01-03-2016)“…Historians are increasingly working with material that is not only digital but has been digitized. Early digitization projects aimed to encode data for…”
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Distribution, metabolism, and excretion of the anti-angiogenic compound SU5416
Published in Toxicology in vitro (01-03-2006)“…SU5416, 3-(3,5-dimethyl-1 H-pyrrol-2-ylmethylene)-1,3-dihydro-indol-2-one, is a potent inhibitor of vascular endothelial growth factor (VEGF) receptor tyrosine…”
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