Search Results - "Ogilvie, Brian"

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  1. 1

    An Assessment of the In Vitro Inhibition of Cytochrome P450 Enzymes, UDP-Glucuronosyltransferases, and Transporters by Phosphodiester- or Phosphorothioate-Linked Oligonucleotides by Kazmi, Faraz, Yerino, Phyllis, McCoy, Chase, Parkinson, Andrew, Buckley, David B., Ogilvie, Brian W.

    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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    Journal Article
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    GLUCURONIDATION CONVERTS GEMFIBROZIL TO A POTENT, METABOLISM-DEPENDENT INHIBITOR OF CYP2C8: IMPLICATIONS FOR DRUG-DRUG INTERACTIONS by OGILVIE, Brian W, DONGLU ZHANG, WENYING LI, RODRIGUES, A. David, GIPSON, Amy E, HOLSAPPLE, Jeff, TOREN, Paul, PARKINSON, Andrew

    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 by Martin, Parthena, Czerwiński, Maciej, Limaye, Pallavi B., Ogilvie, Brian W., Smith, Steven, Boyd, Brooks

    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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    In vitro evaluation of fenfluramine and norfenfluramine as victims of drug interactions by Martin, Parthena, Czerwiński, Maciej, Limaye, Pallavi B., Muranjan, Seema, Ogilvie, Brian W., Smith, Steven, Boyd, Brooks

    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 by PARKINSON, Andrew, KAZMI, Faraz, BUCKLEY, David B, YERINO, Phyllis, PARIS, Brandy L, HOLSAPPLE, Jeff, TOREN, Paul, OTRADOVEC, Steve M, OGILVIE, Brian W

    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 by Ogilvie, Brian W., Torres, Rosarelis, Dressman, Marlene A., Kramer, William G., Baroldi, Paolo

    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 by Czerwiński, Maciej, Gilligan, Krystal, Westland, Kevin, Ogilvie, Brian W.

    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 by PARIS, Brandy L, OGILVIE, Brian W, SCHEINKOENIG, Julie A, NDIKUM-MOFFOR, Florence, GIBSON, Remi, PARKINSON, Andrew

    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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    Scientific Archives in the Age of Digitization by Ogilvie, Brian

    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 by Ye, Christine, Sweeny, David, Sukbuntherng, Juthamas, Zhang, Qingling, Tan, Weiwei, Wong, Simon, Madan, Ajay, Ogilvie, Brian, Parkinson, Andrew, Antonian, Lida

    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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