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Wei Lemaire

Showing results (1-10 of 35) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 22, 2003
The glycine transporter type 1 inhibitor N-[3-(4'-fluorophenyl)-3-(4'-phenylphenoxy)propyl]sarcosine potentiates NMDA receptor-mediated responses in vivo and produces an antipsychotic profile in rodent behaviorGene G Kinney, Cyrille Sur, Maryann Burno, et al.
European Journal of Pharmacology|August 15, 2002
A nonpeptide oxytocin receptor antagonist radioligand highly selective for human receptorsWei Lemaire, Julie A O'Brien, Maryann Burno, et al.
Nuclear Medicine and Biology|March 22, 2008
A novel radioligand for glycine transporter 1: characterization and use in autoradiographic and in vivo brain occupancy studiesZhizhen Zeng, Julie A O'Brien, Wei Lemaire, et al.
Analytical Biochemistry|September 10, 2003
Development of a scintillation proximity assay for analysis of Na+/Cl- -dependent neurotransmitter transporter activityJacinta B Williams, Pierre J Mallorga, Wei Lemaire, et al.
Bioorganic & Medicinal Chemistry Letters|November 4, 2024
Virtual screening for early identification of potent and selective histone deacetylase 6 inhibitor seriesShawn J Stachel, Deping Wang, Anthony T Ginnetti, et al.
Bioorganic & Medicinal Chemistry Letters|September 22, 2006
Synthesis and SAR of GlyT1 inhibitors derived from a series of N-((4-(morpholine-4-carbonyl)-1-(propylsulfonyl)piperidin-4-yl)methyl)benzamidesZhijian Zhao, Julie A O'Brien, Wei Lemaire, et al.
Bioorganic & Medicinal Chemistry Letters|January 28, 2014
Benzimidazole CB2 agonists: design, synthesis and SARKausik K Nanda, Darrell A Henze, Kimberly Della Penna, et al.
Journal of Biomolecular Screening|February 11, 2016
Kinetic Analysis of Membrane Potential Dye Response to NaV1.7 Channel Activation Identifies Antagonists with Pharmacological Selectivity against NaV1.5Michael Finley, Jason Cassaday, Tony Kreamer, et al.
Molecular Pharmacology|August 16, 2003
A family of highly selective allosteric modulators of the metabotropic glutamate receptor subtype 5Julie A O'Brien, Wei Lemaire, Tsing-Bau Chen, et al.
Bioorganic & Medicinal Chemistry Letters|April 8, 2014
Discovery of dual orexin receptor antagonists with rat sleep efficacy enabled by expansion of the acetonitrile-assisted/diphosgene-mediated 2,4-dichloropyrimidine synthesisAnthony J Roecker, Swati P Mercer, C Meacham Harrell, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 22, 2003
The glycine transporter type 1 inhibitor N-[3-(4'-fluorophenyl)-3-(4'-phenylphenoxy)propyl]sarcosine potentiates NMDA receptor-mediated responses in vivo and produces an antipsychotic profile in rodent behaviorGene G Kinney, Cyrille Sur, Maryann Burno, et al.
European Journal of Pharmacology|August 15, 2002
A nonpeptide oxytocin receptor antagonist radioligand highly selective for human receptorsWei Lemaire, Julie A O'Brien, Maryann Burno, et al.
Nuclear Medicine and Biology|March 22, 2008
A novel radioligand for glycine transporter 1: characterization and use in autoradiographic and in vivo brain occupancy studiesZhizhen Zeng, Julie A O'Brien, Wei Lemaire, et al.
Analytical Biochemistry|September 10, 2003
Development of a scintillation proximity assay for analysis of Na+/Cl- -dependent neurotransmitter transporter activityJacinta B Williams, Pierre J Mallorga, Wei Lemaire, et al.
Bioorganic & Medicinal Chemistry Letters|November 4, 2024
Virtual screening for early identification of potent and selective histone deacetylase 6 inhibitor seriesShawn J Stachel, Deping Wang, Anthony T Ginnetti, et al.
Bioorganic & Medicinal Chemistry Letters|September 22, 2006
Synthesis and SAR of GlyT1 inhibitors derived from a series of N-((4-(morpholine-4-carbonyl)-1-(propylsulfonyl)piperidin-4-yl)methyl)benzamidesZhijian Zhao, Julie A O'Brien, Wei Lemaire, et al.
Bioorganic & Medicinal Chemistry Letters|January 28, 2014
Benzimidazole CB2 agonists: design, synthesis and SARKausik K Nanda, Darrell A Henze, Kimberly Della Penna, et al.
Journal of Biomolecular Screening|February 11, 2016
Kinetic Analysis of Membrane Potential Dye Response to NaV1.7 Channel Activation Identifies Antagonists with Pharmacological Selectivity against NaV1.5Michael Finley, Jason Cassaday, Tony Kreamer, et al.
Molecular Pharmacology|August 16, 2003
A family of highly selective allosteric modulators of the metabotropic glutamate receptor subtype 5Julie A O'Brien, Wei Lemaire, Tsing-Bau Chen, et al.
Bioorganic & Medicinal Chemistry Letters|April 8, 2014
Discovery of dual orexin receptor antagonists with rat sleep efficacy enabled by expansion of the acetonitrile-assisted/diphosgene-mediated 2,4-dichloropyrimidine synthesisAnthony J Roecker, Swati P Mercer, C Meacham Harrell, et al.
Pageof 4