Search Results - "Sawant Basak, Aarti"
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Prescription of Oral Contraceptives by Licensed Pharmacists in the USA
Published in Journal of clinical pharmacology (01-03-2024)Get full text
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Investigation of CYP3A induction by PF‐05251749 in early clinical development: comparison of linear slope physiologically based pharmacokinetic prediction and biomarker response
Published in Clinical and translational science (01-09-2022)“…PF‐05251749 is a dual inhibitor of casein kinase 1 δ/ε under clinical development to treat disruption of circadian rhythm in Alzheimer's and Parkinson's…”
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Investigating CNS distribution of PF‐05212377, a P‐glycoprotein substrate, by translation of 5‐HT6 receptor occupancy from non‐human primates to humans
Published in Biopharmaceutics & drug disposition (01-02-2023)“…PF‐05212377 (SAM760) is a potent and selective 5‐HT6 antagonist, previously under development for the treatment of Alzheimer’s disease. In vitro, PF‐05212377…”
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Investigation of pharmacokinetic drug interaction between clesacostat and DGAT2 inhibitor ervogastat in healthy adult participants
Published in Clinical and translational science (01-02-2024)“…Co‐administration of clesacostat (acetyl‐CoA carboxylase inhibitor, PF‐05221304) and ervogastat (diacylglycerol O‐acyltransferase inhibitor, PF‐06865571) in…”
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Role of Clinical Pharmacology in Diversity and Inclusion in Global Drug Development: Current Practices and Industry Perspectives: White Paper
Published in Clinical pharmacology and therapeutics (01-10-2024)“…The 2022 United States Food and Drug Administration (US FDA) draft guidance on diversity plan (DP), which will be implemented through the Diversity Action…”
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Investigating CNS distribution of PF-05212377, a P-glycoprotein substrate, by translation of 5-HT 6 receptor occupancy from non-human primates to humans
Published in Biopharmaceutics & drug disposition (01-02-2023)“…PF-05212377 (SAM760) is a potent and selective 5-HT antagonist, previously under development for the treatment of Alzheimer's disease. In vitro, PF-05212377…”
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Design and Discovery of a Selective Small Molecule κ Opioid Antagonist (2-Methyl-N-((2′-(pyrrolidin-1-ylsulfonyl)biphenyl-4-yl)methyl)propan-1-amine, PF-4455242)
Published in Journal of medicinal chemistry (25-08-2011)“…By use of parallel chemistry coupled with physicochemical property design, a series of selective κ opioid antagonists have been discovered. The parallel…”
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Identification of Multiple 5‑HT4 Partial Agonist Clinical Candidates for the Treatment of Alzheimer’s Disease
Published in Journal of medicinal chemistry (08-11-2012)“…The cognitive impairments observed in Alzheimer’s disease (AD) are in part a consequence of reduced acetylcholine (ACh) levels resulting from a loss of…”
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Metabolism of a serotonin-4 receptor partial agonist 4-{4-[4-tetrahydrofuran-3-yloxy)-benzo[d]isoxazol-3-yloxymethyl]-piperidin-1-ylmethyl}-tetrahydropyran-4-ol (TBPT): identification of an unusual pharmacologically active cyclized oxazolidine metabolite in human
Published in Journal of pharmaceutical sciences (01-09-2013)“…4-{4-[4-Tetrahydrofuran-3-yloxy)-benzo[d]isoxazol-3-yloxymethyl]-piperidin-1-ylmethyl}-tetrahydropyran-4-ol (PF-4995274, TBPT) is a new agent that is a partial…”
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Pharmacodynamic Model of Sodium–Glucose Transporter 2 (SGLT2) Inhibition: Implications for Quantitative Translational Pharmacology
Published in The AAPS journal (01-12-2011)“…ABSTRACT Sodium–glucose co-transporter-2 (SGLT2) inhibitors are an emerging class of agents for use in the treatment of type 2 diabetes mellitus (T2DM)…”
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Metabolism and clinical pharmacokinetics of 2-methyl-n-(2′-(pyrrolidinyl-1-ylsulfonyl)-n-[1,1′-biphenyl]-4-yl)propran-1-amine: insights into monoamine oxidase- and CYP-mediated disposition by integration of in vitro ADME tools
Published in Xenobiotica (01-05-2014)“…Abstract 1. In early discovery stages, 2-methyl-N-(2′-(pyrrolidinyl-1-ylsulfonyl)-[1,1′-biphenyl]-4-yl)propan-1-amine (PBPA) demonstrated monoamine oxidase A…”
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Emerging Models of Drug Metabolism, Transporters, and Toxicity
Published in Drug metabolism and disposition (01-11-2018)“…This commentary summarizes expert mini-reviews and original research articles that have been assembled in a special issue on novel models of drug metabolism…”
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Assessing Trends in Cytokine–CYP Drug Interactions and Relevance to Drug Dosing
Published in Drug metabolism and disposition (01-11-2024)“…The regulation of drug-metabolizing enzymes and transporters by cytokines has been extensively studied in vitro and in clinic. Cytokine-mediated suppression of…”
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Physiologically Relevant, Humanized Intestinal Systems to Study Metabolism and Transport of Small Molecule Therapeutics
Published in Drug metabolism and disposition (01-11-2018)“…Intestinal disposition of small molecules involves interplay of drug metabolizing enzymes (DMEs), transporters, and host-microbiome interactions, which has…”
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Assessing trends in cytokine-CYP drug interaction and relevance to drug dosing
Published in Drug metabolism and disposition (21-02-2024)“…The regulation of drug-metabolizing enzymes and transporters by cytokines has been extensively studied, in vitro and in clinic. Cytokine-mediated suppression…”
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F30. QUINTUPLE HYPOTHESES TARGETED IN SCHIZOPHRENIA: FIGHT FIRE WITH FIRE
Published in Schizophrenia bulletin (09-04-2019)“…Abstract Background There are no effective treatments available or on the horizon for cognitive impairments associated with schizophrenia (CIAS) and primary…”
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Kynurenine pathway in schizophrenia: Galantamine-memantine combination for cognitive impairments
Published in Schizophrenia research (01-03-2018)Get full text
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Determination of receptor occupancy in the presence of mass dose: [ 11 C]GSK189254 PET imaging of histamine H 3 receptor occupancy by PF-03654746
Published in Journal of cerebral blood flow and metabolism (01-03-2017)“…Measurements of drug occupancies using positron emission tomography (PET) can be biased if the radioligand concentration exceeds "tracer" levels. Negative bias…”
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Estimation of Circulating Drug Metabolite Exposure in Human Using In Vitro Data and Physiologically Based Pharmacokinetic Modeling: Example of a High Metabolite/Parent Drug Ratio
Published in Drug metabolism and disposition (01-02-2018)“…( )-4-((4-(((4-((tetrahydrofuran-3-yl)oxy)benzo[d]isoxazol-3-yl)oxy)methyl)piperidin-1-yl)methyl)tetrahydro-2H-pyran-4-ol (TBPT), a serotonin-4 receptor…”
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