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Bioorganic & Medicinal Chemistry|April 29, 2009
Synthesis and evaluation of pharmacological profile of 1-aryl-6,7-dimethoxy-3,4-dihydroisoquinoline-2(1H)-sulfonamidesRosaria Gitto, Stefania Ferro, Stefano Agnello, et al.Chemmedchem|July 1, 2009
Pharmacophore-based discovery of small-molecule inhibitors of protein-protein interactions between HIV-1 integrase and cellular cofactor LEDGF/p75Laura De Luca, Maria Letizia Barreca, Stefania Ferro, et al.Chemmedchem|September 12, 2022
Design, Synthesis, and in Vitro Evaluation of 4-(4-Hydroxyphenyl)piperazine-Based Compounds Targeting TyrosinaseSalvatore Mirabile, Maria Paola Germanò, Antonella Fais, et al.Chemmedchem|July 5, 2021
Evaluation of 4-(4-Fluorobenzyl)piperazin-1-yl]-Based Compounds as Competitive Tyrosinase Inhibitors Endowed with Antimelanogenic EffectsSalvatore Mirabile, Serena Vittorio, Maria Paola Germanò, et al.Chemmedchem|July 23, 2026
1-Aryl-6,7-Dimethoxy-3,4-Dihydroisoquinoline-2(1H)-Sulfonamides as hCA XII Selective Inhibitors: Experimental and Theoretical Studies to Interrogate the Isoform SelectivityFederico Ricci, Anna Di Fiore, Andrea Angeli, et al.European Journal of Medicinal Chemistry|December 4, 2017
Inhibitory effects and structural insights for a novel series of coumarin-based compounds that selectively target human CA IX and CA XII carbonic anhydrasesLaura De Luca, Francesca Mancuso, Stefania Ferro, et al.European Journal of Medicinal Chemistry|September 1, 2023
Computational methods to analyze and predict the binding mode of inhibitors targeting both human and mushroom tyrosinaseFederico Ricci, Kristina Schira, Lyna Khettabi, et al.Molecular Informatics|September 12, 2019
A Combination of Pharmacophore and Docking-based Virtual Screening to Discover new Tyrosinase InhibitorsSerena Vittorio, Thomas Seidel, Maria Paola Germanò, et al.Chemmedchem|September 4, 2008
Computational studies to discover a new NR2B/NMDA receptor antagonist and evaluation of pharmacological profileRosaria Gitto, Laura De Luca, Stefania Ferro, et al.Journal of Medicinal Chemistry|March 27, 2012
Synthesis, structure-activity relationship studies, and X-ray crystallographic analysis of arylsulfonamides as potent carbonic anhydrase inhibitorsRosaria Gitto, Francesca M Damiano, Pavel Mader, et al.Pageof 11