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M Witkin

Showing results (301-310 of 321) with videos related to

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Drug Development Research|February 7, 2023
Comparative anticonvulsant activity of the GABAkine KRM-II-81 and a deuterated analogXingjie Ping, Michelle J Meyer, Nicolas M Zahn, et al.
Alcoholism, Clinical and Experimental Research|April 17, 2016
A Novel, Orally Bioavailable Nociceptin Receptor Antagonist, LY2940094, Reduces Ethanol Self-Administration and Ethanol Seeking in Animal ModelsLinda M Rorick-Kehn, Roberto Ciccocioppo, Conrad J Wong, et al.
Journal of Medicinal Chemistry|April 1, 2014
Discovery of a novel series of orally active nociceptin/orphanin FQ (NOP) receptor antagonists based on a dihydrospiro(piperidine-4,7'-thieno[2,3-c]pyran) scaffoldMiguel A Toledo, Concepción Pedregal, Celia Lafuente, et al.
Journal of Medicinal Chemistry|December 10, 2016
Synthesis and Characterization of a Novel γ-Aminobutyric Acid Type A (GABA<sub>A</sub>) Receptor Ligand That Combines Outstanding Metabolic Stability, Pharmacokinetics, and Anxiolytic EfficacyMichael M Poe, Kashi Reddy Methuku, Guanguan Li, et al.
ACS Omega|August 15, 2022
Hydrochloride Salt of the GABAkine KRM-II-81Md Yeunus Mian, Branka Divović, Dishary Sharmin, et al.
Biopharmaceutics & Drug Disposition|February 23, 2022
Metabolism, pharmacokinetics, and anticonvulsant activity of a deuterated analog of the α2/3-selective GABAkine KRM-II-81Lalit K Golani, Branka Divović, Dishary Sharmin, et al.
The Journal of Pharmacology and Experimental Therapeutics|February 6, 2023
Structural Analogs of the GABAkine KRM-II-81 Are Orally Bioavailable Anticonvulsants without SedationKamal P Pandey, Branka Divović, Farjana Rashid, et al.
Neuropharmacology|January 10, 2016
In vitro pharmacological and rat pharmacokinetic characterization of LY3020371, a potent and selective mGlu<sub>2/3</sub> receptor antagonistJeffrey M Witkin, Paul L Ornstein, Charles H Mitch, et al.
ACS Chemical Neuroscience|January 4, 2024
New Imidazodiazepine Analogue, 5-(8-Bromo-6-(pyridin-2-yl)-4<i>H</i>-benzo[<i>f</i>]imidazo[1,5-<i>a</i>][1,4]diazepin-3-yl)oxazole, Provides a Simplified Synthetic Scheme, High Oral Plasma and Brain Exposures, and Produces Antiseizure Efficacy in Mice, and Antiepileptogenic Activity in Neural Networks in Brain Slices from a Patient with Mesial Temporal Lobe EpilepsyDishary Sharmin, Branka Divović, Xingjie Ping, et al.
The Journal of Pharmacology and Experimental Therapeutics|February 1, 2017
Comparative Effects of LY3020371, a Potent and Selective Metabotropic Glutamate (mGlu) 2/3 Receptor Antagonist, and Ketamine, a Noncompetitive <i>N</i>-Methyl-d-Aspartate Receptor Antagonist in Rodents: Evidence Supporting the Use of mGlu2/3 Antagonists, for the Treatment of DepressionJ M Witkin, S N Mitchell, K A Wafford, et al.
Pageof 33

Showing results (301-310 of 321) with videos related to

Sort By:
Pageof 33
Drug Development Research|February 7, 2023
Comparative anticonvulsant activity of the GABAkine KRM-II-81 and a deuterated analogXingjie Ping, Michelle J Meyer, Nicolas M Zahn, et al.
Alcoholism, Clinical and Experimental Research|April 17, 2016
A Novel, Orally Bioavailable Nociceptin Receptor Antagonist, LY2940094, Reduces Ethanol Self-Administration and Ethanol Seeking in Animal ModelsLinda M Rorick-Kehn, Roberto Ciccocioppo, Conrad J Wong, et al.
Journal of Medicinal Chemistry|April 1, 2014
Discovery of a novel series of orally active nociceptin/orphanin FQ (NOP) receptor antagonists based on a dihydrospiro(piperidine-4,7'-thieno[2,3-c]pyran) scaffoldMiguel A Toledo, Concepción Pedregal, Celia Lafuente, et al.
Journal of Medicinal Chemistry|December 10, 2016
Synthesis and Characterization of a Novel γ-Aminobutyric Acid Type A (GABA<sub>A</sub>) Receptor Ligand That Combines Outstanding Metabolic Stability, Pharmacokinetics, and Anxiolytic EfficacyMichael M Poe, Kashi Reddy Methuku, Guanguan Li, et al.
ACS Omega|August 15, 2022
Hydrochloride Salt of the GABAkine KRM-II-81Md Yeunus Mian, Branka Divović, Dishary Sharmin, et al.
Biopharmaceutics & Drug Disposition|February 23, 2022
Metabolism, pharmacokinetics, and anticonvulsant activity of a deuterated analog of the α2/3-selective GABAkine KRM-II-81Lalit K Golani, Branka Divović, Dishary Sharmin, et al.
The Journal of Pharmacology and Experimental Therapeutics|February 6, 2023
Structural Analogs of the GABAkine KRM-II-81 Are Orally Bioavailable Anticonvulsants without SedationKamal P Pandey, Branka Divović, Farjana Rashid, et al.
Neuropharmacology|January 10, 2016
In vitro pharmacological and rat pharmacokinetic characterization of LY3020371, a potent and selective mGlu<sub>2/3</sub> receptor antagonistJeffrey M Witkin, Paul L Ornstein, Charles H Mitch, et al.
ACS Chemical Neuroscience|January 4, 2024
New Imidazodiazepine Analogue, 5-(8-Bromo-6-(pyridin-2-yl)-4<i>H</i>-benzo[<i>f</i>]imidazo[1,5-<i>a</i>][1,4]diazepin-3-yl)oxazole, Provides a Simplified Synthetic Scheme, High Oral Plasma and Brain Exposures, and Produces Antiseizure Efficacy in Mice, and Antiepileptogenic Activity in Neural Networks in Brain Slices from a Patient with Mesial Temporal Lobe EpilepsyDishary Sharmin, Branka Divović, Xingjie Ping, et al.
The Journal of Pharmacology and Experimental Therapeutics|February 1, 2017
Comparative Effects of LY3020371, a Potent and Selective Metabotropic Glutamate (mGlu) 2/3 Receptor Antagonist, and Ketamine, a Noncompetitive <i>N</i>-Methyl-d-Aspartate Receptor Antagonist in Rodents: Evidence Supporting the Use of mGlu2/3 Antagonists, for the Treatment of DepressionJ M Witkin, S N Mitchell, K A Wafford, et al.
Pageof 33