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Chemical & Pharmaceutical Bulletin|February 2, 2008
Solution-phase parallel synthesis of novel 1,2,3,4-tetrahydroisoquinoline-1-ones as anticonvulsant agentsRosaria Gitto, Eleonora Francica, Giovambattista De Sarro, et al.
International Journal of Molecular Sciences|March 6, 2021
Exploring Molecular Contacts of MUC1 at CIN85 Binding Interface to Address Future Drug Design EffortsMaria Rita Gulotta, Serena Vittorio, Rosaria Gitto, et al.
Microorganisms|August 28, 2025
Synthesis and Antifungal Evaluation Against Candida spp. of 5-Arylfuran-2-Carboxamide DerivativesSalvatore Mirabile, Giovanna Ginestra, Rosamaria Pennisi, et al.
Archiv Der Pharmazie|October 17, 2022
Structure-guided identification of a selective sulfonamide-based inhibitor targeting the human carbonic anhydrase VA isoformLaura De Luca, Andrea Angeli, Federico Ricci, et al.
Bioorganic & Medicinal Chemistry|March 22, 2020
Inhibition of HIV-1 RT activity by a new series of 3-(1,3,4-thiadiazol-2-yl)thiazolidin-4-one derivativesMaria Rosa Buemi, Rosaria Gitto, Laura Ielo, et al.
European Journal of Medicinal Chemistry|April 15, 2008
Solution-phase parallel synthesis and evaluation of anticonvulsant activity of N-substituted-3,4-dihydroisoquinoline-2(1H)-carboxamidesRosaria Gitto, Benedetta Pagano, Rita Citraro, et al.
International Journal of Molecular Sciences|October 26, 2024
Computational Approach to Identifying New Chemical Entities as Elastase Inhibitors with Potential Antiaging EffectsGiovanna Pitasi, Andrea Brancale, Sonia Floris, et al.
European Journal of Medicinal Chemistry|September 3, 2013
New scaffolds of natural origin as Integrase-LEDGF/p75 interaction inhibitors: virtual screening and activity assaysLaura De Luca, Francesca Morreale, Frauke Christ, et al.
International Journal of Molecular Sciences|January 12, 2021
In Silico Identification of Potential Druggable Binding Sites on CIN85 SH3 DomainSerena Vittorio, Thomas Seidel, Arthur Garon, et al.
Bioorganic & Medicinal Chemistry|May 23, 2015
Optimization of rhodanine scaffold for the development of protein-protein interaction inhibitorsStefania Ferro, Laura De Luca, Fatima Ezzahra Agharbaoui, et al.
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