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Organic & Biomolecular Chemistry|September 14, 2017
Efficient and regioselective one-step synthesis of 7-aryl-5-methyl- and 5-aryl-7-methyl-2-amino-[1,2,4]triazolo[1,5-a]pyrimidine derivativesSerena Massari, Jenny Desantis, Giulio Nannetti, et al.
European Journal of Medicinal Chemistry|February 23, 2024
Design, synthesis, and biological evaluation of first-in-class indomethacin-based PROTACs degrading SARS-CoV-2 main protease and with broad-spectrum antiviral activityJenny Desantis, Alessandro Bazzacco, Michela Eleuteri, et al.
Journal of Medicinal Chemistry|September 13, 2024
Between Theory and Practice: Computational/Experimental Integrated Approaches to Understand the Solubility and Lipophilicity of PROTACsAndrea Venturi, Stefano Di Bona, Jenny Desantis, et al.
European Journal of Medicinal Chemistry|September 17, 2021
Indomethacin-based PROTACs as pan-coronavirus antiviral agentsJenny Desantis, Beatrice Mercorelli, Marta Celegato, et al.
Antiviral Research|June 10, 2022
Discovery of novel SARS-CoV-2 inhibitors targeting the main protease Mpro by virtual screenings and hit optimizationBeatrice Mercorelli, Jenny Desantis, Marta Celegato, et al.
Journal of Medicinal Chemistry|April 10, 2015
A Broad Anti-influenza Hybrid Small Molecule That Potently Disrupts the Interaction of Polymerase Acidic Protein-Basic Protein 1 (PA-PB1) SubunitsSerena Massari, Giulio Nannetti, Jenny Desantis, et al.
Future Medicinal Chemistry|March 3, 2016
Recent advances in the identification of Tat-mediated transactivation inhibitors: progressing toward a functional cure of HIVOriana Tabarrini, Jenny Desantis, Serena Massari
Expert Opinion on Drug Discovery|May 31, 2022
An overview on small molecules acting as broad-spectrum agents for yellow fever infectionJenny Desantis, Tommaso Felicetti, Rolando Cannalire
International Journal of Biological Macromolecules|June 13, 2025
Novel SARS-CoV-2 allosteric inhibitors that destabilize the Main Protease Mpro dimerBeatrice Mercorelli, Alessandro Bazzacco, Michela Eleuteri, et al.
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