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Bioorganic & Medicinal Chemistry|January 23, 2009
Development of 3-substituted-1H-indole derivatives as NR2B/NMDA receptor antagonistsRosaria Gitto, Laura De Luca, Stefania Ferro, et al.
Bioconjugate Chemistry|August 15, 2018
Graphene Quantum Dots Based Systems As HIV InhibitorsDaniela Iannazzo, Alessandro Pistone, Stefania Ferro, et al.
Bioorganic & Medicinal Chemistry|January 25, 2014
Design and synthesis of N₁-aryl-benzimidazoles 2-substituted as novel HIV-1 non-nucleoside reverse transcriptase inhibitorsAnna-Maria Monforte, Stefania Ferro, Laura De Luca, et al.
Archiv Der Pharmazie|June 24, 2022
Synthesis and biological evaluation of sulfonamide-based compounds as inhibitors of carbonic anhydrase from Vibrio choleraeFrancesca Mancuso, Andrea Angeli, Viviana De Luca, et al.
International Journal of Molecular Sciences|December 11, 2022
Ligand-Based Discovery of a Small Molecule as Inhibitor of α-Synuclein Amyloid FormationLaura De Luca, Serena Vittorio, Samuel Peña-Díaz, et al.
ACS Medicinal Chemistry Letters|November 20, 2020
In Silico-Guided Identification of New Potent Inhibitors of Carbonic Anhydrases Expressed in Vibrio choleraeFrancesca Mancuso, Laura De Luca, Andrea Angeli, et al.
Archiv Der Pharmazie|June 20, 2006
3D pharmacophore models for 1,2,3,4-tetrahydroisoquinoline derivatives acting as anticonvulsant agentsLaura De Luca, Rosaria Gitto, Maria Letizia Barreca, et al.
Archiv Der Pharmazie|June 15, 2007
New 4-[(1-benzyl-1H-indol-3-yl)carbonyl]-3-hydroxyfuran-2(5H)-ones, beta-diketo acid analogs as HIV-1 integrase inhibitorsStefania Ferro, Maria Letizia Barreca, Laura De Luca, et al.
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