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Brett R Beno

Showing results (21-30 of 37) with videos related to

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Bioorganic & Medicinal Chemistry Letters|March 30, 2007
Conformationally restricted homotryptamines 3. Indole tetrahydropyridines and cyclohexenylamines as selective serotonin reuptake inhibitorsJeffrey A Deskus, James R Epperson, Charles P Sloan, et al.
Journal of Medicinal Chemistry|September 16, 2005
Conformationally restricted homotryptamines. 2. Indole cyclopropylmethylamines as selective serotonin reuptake inhibitorsRonald J Mattson, John D Catt, Derek J Denhart, et al.
Bioorganic & Medicinal Chemistry Letters|March 29, 2011
Investigation of the mode of binding of a novel series of N-benzyl-4-heteroaryl-1-(phenylsulfonyl)piperazine-2-carboxamides to the hepatitis C virus polymeraseRobert G Gentles, Steven Sheriff, Brett R Beno, et al.
Plos One|August 11, 2012
High-throughput screening and rapid inhibitor triage using an infectious chimeric Hepatitis C virusMichael J Wichroski, Jie Fang, Betsy J Eggers, et al.
Journal of Medicinal Chemistry|August 5, 2024
Atropisomerism Observed in Galactose-Based Monosaccharide Inhibitors of Galectin-3 Comprising 2-Methyl-4-phenyl-2,4-dihydro-3<i>H</i>-1,2,4-triazole-3-thioneDavid S Yoon, Chunjian Liu, Prasada Rao Jalagam, et al.
Bioorganic & Medicinal Chemistry Letters|March 20, 2012
Synthesis and SAR studies of novel heteroaryl fused tetracyclic indole-diamide compounds: potent allosteric inhibitors of the hepatitis C virus NS5B polymeraseMin Ding, Feng He, Thomas W Hudyma, et al.
Bioorganic & Medicinal Chemistry Letters|February 3, 2005
De novo design, synthesis, and in vitro activity of LFA-1 antagonists based on a bicyclic[5.5]hydantoin scaffoldDominique Potin, Michele Launay, Eric Nicolai, et al.
Journal of Medicinal Chemistry|September 3, 2011
Small molecule receptor protein tyrosine phosphatase γ (RPTPγ) ligands that inhibit phosphatase activity via perturbation of the tryptophan-proline-aspartate (WPD) loopSteven Sheriff, Brett R Beno, Weixu Zhai, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 26, 2015
Discovery of D1 Dopamine Receptor Positive Allosteric Modulators: Characterization of Pharmacology and Identification of Residues that Regulate Species SelectivityMartin A Lewis, Lisa Hunihan, John Watson, et al.
ACS Medicinal Chemistry Letters|January 8, 2019
Structure-Property Basis for Solving Transporter-Mediated Efflux and Pan-Genotypic Inhibition in HCV NS5B InhibitorsKap-Sun Yeung, Brett R Beno, Kathy Mosure, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

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Pageof 4
Bioorganic & Medicinal Chemistry Letters|March 30, 2007
Conformationally restricted homotryptamines 3. Indole tetrahydropyridines and cyclohexenylamines as selective serotonin reuptake inhibitorsJeffrey A Deskus, James R Epperson, Charles P Sloan, et al.
Journal of Medicinal Chemistry|September 16, 2005
Conformationally restricted homotryptamines. 2. Indole cyclopropylmethylamines as selective serotonin reuptake inhibitorsRonald J Mattson, John D Catt, Derek J Denhart, et al.
Bioorganic & Medicinal Chemistry Letters|March 29, 2011
Investigation of the mode of binding of a novel series of N-benzyl-4-heteroaryl-1-(phenylsulfonyl)piperazine-2-carboxamides to the hepatitis C virus polymeraseRobert G Gentles, Steven Sheriff, Brett R Beno, et al.
Plos One|August 11, 2012
High-throughput screening and rapid inhibitor triage using an infectious chimeric Hepatitis C virusMichael J Wichroski, Jie Fang, Betsy J Eggers, et al.
Journal of Medicinal Chemistry|August 5, 2024
Atropisomerism Observed in Galactose-Based Monosaccharide Inhibitors of Galectin-3 Comprising 2-Methyl-4-phenyl-2,4-dihydro-3<i>H</i>-1,2,4-triazole-3-thioneDavid S Yoon, Chunjian Liu, Prasada Rao Jalagam, et al.
Bioorganic & Medicinal Chemistry Letters|March 20, 2012
Synthesis and SAR studies of novel heteroaryl fused tetracyclic indole-diamide compounds: potent allosteric inhibitors of the hepatitis C virus NS5B polymeraseMin Ding, Feng He, Thomas W Hudyma, et al.
Bioorganic & Medicinal Chemistry Letters|February 3, 2005
De novo design, synthesis, and in vitro activity of LFA-1 antagonists based on a bicyclic[5.5]hydantoin scaffoldDominique Potin, Michele Launay, Eric Nicolai, et al.
Journal of Medicinal Chemistry|September 3, 2011
Small molecule receptor protein tyrosine phosphatase γ (RPTPγ) ligands that inhibit phosphatase activity via perturbation of the tryptophan-proline-aspartate (WPD) loopSteven Sheriff, Brett R Beno, Weixu Zhai, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 26, 2015
Discovery of D1 Dopamine Receptor Positive Allosteric Modulators: Characterization of Pharmacology and Identification of Residues that Regulate Species SelectivityMartin A Lewis, Lisa Hunihan, John Watson, et al.
ACS Medicinal Chemistry Letters|January 8, 2019
Structure-Property Basis for Solving Transporter-Mediated Efflux and Pan-Genotypic Inhibition in HCV NS5B InhibitorsKap-Sun Yeung, Brett R Beno, Kathy Mosure, et al.
Pageof 4