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Chemmedchem|May 8, 2009
Combined strategies for the discovery of ionotropic glutamate receptor antagonistsAlba Chimirri, Laura De Luca, Stefania Ferro, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|September 14, 2020
Rational design of small molecules able to inhibit α-synuclein amyloid aggregation for the treatment of Parkinson's diseaseSerena Vittorio, Ilenia Adornato, Rosaria Gitto, et al.
Bioorganic & Medicinal Chemistry Letters|July 27, 2024
Exploitation of the nitro- and/or 4-Trifluoromethyl-decorated phenyl fragment to develop small inhibitors of Alpha-Syn fibril aggregationGiovanna Pitasi, Marc Fornt-Suñé, Federica Bucolo, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|April 1, 2015
Searching for indole derivatives as potential mushroom tyrosinase inhibitorsStefania Ferro, Giovanna Certo, Laura De Luca, et al.
Farmaco (Societa Chimica Italiana : 1989)|October 19, 2002
Synthesis and pharmacological properties of new 3-ethoxycarbonyl-11H-[1,2,4]triazolo[4,5-c][2,3]benzodiazepinesA Chimirri, Rosaria Gitto, S Quartarone, et al.
Chemmedchem|December 21, 2025
Investigating the Ligand-Binding Properties of N-arylbenzimidazoles as Novel Elastase InhibitorsGiovanna Pitasi, Sonia Floris, Francesca Mancuso, et al.
Bioorganic & Medicinal Chemistry|February 26, 2016
Structure-guided design of new indoles as negative allosteric modulators (NAMs) of N-methyl-D-aspartate receptor (NMDAR) containing GluN2B subunitMaria Rosa Buemi, Laura De Luca, Stefania Ferro, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|July 19, 2012
Fragment hopping approach directed at design of HIV IN-LEDGF/p75 interaction inhibitorsLaura De Luca, Stefania Ferro, Francesca Morreale, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|July 18, 2013
Synthesis and biological evaluation of novel antiviral agents as protein-protein interaction inhibitorsStefania Ferro, Laura De Luca, Francesca Morreale, et al.
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