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Benoit Deprez

Showing results (51-60 of 83) with videos related to

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Communications Biology|July 24, 2024
Identification of new correctors for traffic-defective ABCB4 variants by a high-content screening approachMounia Lakli, Julie Dumont, Virginie Vauthier, et al.
European Journal of Medicinal Chemistry|March 21, 2026
Discovery of pyrimidine-based small activators of insulin degrading enzymeJamal El Bakali, Cyril Ronco, Valérie Landry, et al.
Journal of Medicinal Chemistry|December 6, 2022
Tricyclic SpiroLactams Kill Mycobacteria In Vitro and In Vivo by Inhibiting Type II NADH DehydrogenasesSushovan Dam, Salia Tangara, Claire Hamela, et al.
European Journal of Medicinal Chemistry|April 17, 2014
Imidazole-derived 2-[N-carbamoylmethyl-alkylamino]acetic acids, substrate-dependent modulators of insulin-degrading enzyme in amyloid-β hydrolysisJulie Charton, Marion Gauriot, Qing Guo, et al.
Journal of Medicinal Chemistry|May 14, 2014
Ligand efficiency driven design of new inhibitors of Mycobacterium tuberculosis transcriptional repressor EthR using fragment growing, merging, and linking approachesBaptiste Villemagne, Marion Flipo, Nicolas Blondiaux, et al.
European Journal of Medicinal Chemistry|October 30, 2025
A new chemotype that opens the S2∗ pocket of the 3CL protease exhibits antiviral activity against SARS-CoV-2Laura Mourot, Fatima-Zahra Chaibi, Nour Bou-Karroum, et al.
Journal of Medicinal Chemistry|October 7, 2017
Controlling Plasma Stability of Hydroxamic Acids: A MedChem ToolboxPaul Hermant, Damien Bosc, Catherine Piveteau, et al.
Journal of Medicinal Chemistry|April 18, 2017
Topical Intestinal Aminoimidazole Agonists of G-Protein-Coupled Bile Acid Receptor 1 Promote Glucagon Like Peptide-1 Secretion and Improve Glucose ToleranceManuel Lasalle, Vanessa Hoguet, Nathalie Hennuyer, et al.
Nucleic Acids Research|December 14, 2011
Structural activation of the transcriptional repressor EthR from Mycobacterium tuberculosis by single amino acid change mimicking natural and synthetic ligandsXavier Carette, Nicolas Blondiaux, Eve Willery, et al.
Journal of Medicinal Chemistry|February 7, 2025
Discovery of New Nanomolar Selective IRAP InhibitorsBen He, Nour Bou Karroum, Ronan Gealageas, et al.
Pageof 9

Showing results (51-60 of 83) with videos related to

Sort By:
Pageof 9
Communications Biology|July 24, 2024
Identification of new correctors for traffic-defective ABCB4 variants by a high-content screening approachMounia Lakli, Julie Dumont, Virginie Vauthier, et al.
European Journal of Medicinal Chemistry|March 21, 2026
Discovery of pyrimidine-based small activators of insulin degrading enzymeJamal El Bakali, Cyril Ronco, Valérie Landry, et al.
Journal of Medicinal Chemistry|December 6, 2022
Tricyclic SpiroLactams Kill Mycobacteria In Vitro and In Vivo by Inhibiting Type II NADH DehydrogenasesSushovan Dam, Salia Tangara, Claire Hamela, et al.
European Journal of Medicinal Chemistry|April 17, 2014
Imidazole-derived 2-[N-carbamoylmethyl-alkylamino]acetic acids, substrate-dependent modulators of insulin-degrading enzyme in amyloid-β hydrolysisJulie Charton, Marion Gauriot, Qing Guo, et al.
Journal of Medicinal Chemistry|May 14, 2014
Ligand efficiency driven design of new inhibitors of Mycobacterium tuberculosis transcriptional repressor EthR using fragment growing, merging, and linking approachesBaptiste Villemagne, Marion Flipo, Nicolas Blondiaux, et al.
European Journal of Medicinal Chemistry|October 30, 2025
A new chemotype that opens the S2∗ pocket of the 3CL protease exhibits antiviral activity against SARS-CoV-2Laura Mourot, Fatima-Zahra Chaibi, Nour Bou-Karroum, et al.
Journal of Medicinal Chemistry|October 7, 2017
Controlling Plasma Stability of Hydroxamic Acids: A MedChem ToolboxPaul Hermant, Damien Bosc, Catherine Piveteau, et al.
Journal of Medicinal Chemistry|April 18, 2017
Topical Intestinal Aminoimidazole Agonists of G-Protein-Coupled Bile Acid Receptor 1 Promote Glucagon Like Peptide-1 Secretion and Improve Glucose ToleranceManuel Lasalle, Vanessa Hoguet, Nathalie Hennuyer, et al.
Nucleic Acids Research|December 14, 2011
Structural activation of the transcriptional repressor EthR from Mycobacterium tuberculosis by single amino acid change mimicking natural and synthetic ligandsXavier Carette, Nicolas Blondiaux, Eve Willery, et al.
Journal of Medicinal Chemistry|February 7, 2025
Discovery of New Nanomolar Selective IRAP InhibitorsBen He, Nour Bou Karroum, Ronan Gealageas, et al.
Pageof 9