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Francesco Saverio Di Leva

Showing results (1-10 of 66) with videos related to

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Handbook of Experimental Pharmacology|June 5, 2019
Structural Insight into the Binding Mode of FXR and GPBAR1 ModulatorsFrancesco Saverio Di Leva, Daniele Di Marino, Vittorio Limongelli
Nucleic Acids Research|April 23, 2014
Mechanistic insight into ligand binding to G-quadruplex DNAFrancesco Saverio Di Leva, Ettore Novellino, Andrea Cavalli, et al.
Journal of Medicinal Chemistry|November 13, 2020
Targeting SARS-CoV-2 Proteases and Polymerase for COVID-19 Treatment: State of the Art and Future OpportunitiesRolando Cannalire, Carmen Cerchia, Andrea R Beccari, et al.
Frontiers in Molecular Biosciences|May 21, 2020
Bioinformatics and Biosimulations as Toolbox for Peptides and Peptidomimetics Design: Where Are We?Ilda D'Annessa, Francesco Saverio Di Leva, Anna La Teana, et al.
Scientific Reports|November 17, 2015
Structure-based drug design targeting the cell membrane receptor GPBAR1: exploiting the bile acid scaffold towards selective agonismFrancesco Saverio Di Leva, Carmen Festa, Barbara Renga, et al.
Journal of Natural Products|February 4, 2026
Stereocontrolled Synthesis of α-Branched Tetrahydropyrans by a One-Pot-Two-Step Photobiocatalytic Cascade of CitronellolClaudio Zippilli, Elisa De Marchi, Beatrice Di Maio, et al.
Molecular Biosystems|February 12, 2016
The ring residue proline 8 is crucial for the thermal stability of the lasso peptide caulosegnin IIJulian D Hegemann, Christopher D Fage, Shaozhou Zhu, et al.
Journal of Medicinal Chemistry|June 3, 2016
Monothiocarbamates Strongly Inhibit Carbonic Anhydrases in Vitro and Possess Intraocular Pressure Lowering Activity in an Animal Model of GlaucomaDaniela Vullo, Mariaconcetta Durante, Francesco Saverio Di Leva, et al.
Journal of Medicinal Chemistry|January 7, 2014
Design, synthesis, and biological evaluation of potent dual agonists of nuclear and membrane bile acid receptorsClaudio D'Amore, Francesco Saverio Di Leva, Valentina Sepe, et al.
Molecules (Basel, Switzerland)|March 20, 2019
Introduction of Nonacidic Side Chains on 6-Ethylcholane Scaffolds in the Identification of Potent Bile Acid Receptor Agonists with Improved Pharmacokinetic PropertiesClaudia Finamore, Giuliana Baronissi, Silvia Marchianò, et al.
Pageof 7

Showing results (1-10 of 66) with videos related to

Sort By:
Pageof 7
Handbook of Experimental Pharmacology|June 5, 2019
Structural Insight into the Binding Mode of FXR and GPBAR1 ModulatorsFrancesco Saverio Di Leva, Daniele Di Marino, Vittorio Limongelli
Nucleic Acids Research|April 23, 2014
Mechanistic insight into ligand binding to G-quadruplex DNAFrancesco Saverio Di Leva, Ettore Novellino, Andrea Cavalli, et al.
Journal of Medicinal Chemistry|November 13, 2020
Targeting SARS-CoV-2 Proteases and Polymerase for COVID-19 Treatment: State of the Art and Future OpportunitiesRolando Cannalire, Carmen Cerchia, Andrea R Beccari, et al.
Frontiers in Molecular Biosciences|May 21, 2020
Bioinformatics and Biosimulations as Toolbox for Peptides and Peptidomimetics Design: Where Are We?Ilda D'Annessa, Francesco Saverio Di Leva, Anna La Teana, et al.
Scientific Reports|November 17, 2015
Structure-based drug design targeting the cell membrane receptor GPBAR1: exploiting the bile acid scaffold towards selective agonismFrancesco Saverio Di Leva, Carmen Festa, Barbara Renga, et al.
Journal of Natural Products|February 4, 2026
Stereocontrolled Synthesis of α-Branched Tetrahydropyrans by a One-Pot-Two-Step Photobiocatalytic Cascade of CitronellolClaudio Zippilli, Elisa De Marchi, Beatrice Di Maio, et al.
Molecular Biosystems|February 12, 2016
The ring residue proline 8 is crucial for the thermal stability of the lasso peptide caulosegnin IIJulian D Hegemann, Christopher D Fage, Shaozhou Zhu, et al.
Journal of Medicinal Chemistry|June 3, 2016
Monothiocarbamates Strongly Inhibit Carbonic Anhydrases in Vitro and Possess Intraocular Pressure Lowering Activity in an Animal Model of GlaucomaDaniela Vullo, Mariaconcetta Durante, Francesco Saverio Di Leva, et al.
Journal of Medicinal Chemistry|January 7, 2014
Design, synthesis, and biological evaluation of potent dual agonists of nuclear and membrane bile acid receptorsClaudio D'Amore, Francesco Saverio Di Leva, Valentina Sepe, et al.
Molecules (Basel, Switzerland)|March 20, 2019
Introduction of Nonacidic Side Chains on 6-Ethylcholane Scaffolds in the Identification of Potent Bile Acid Receptor Agonists with Improved Pharmacokinetic PropertiesClaudia Finamore, Giuliana Baronissi, Silvia Marchianò, et al.
Pageof 7