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Journal of Medicinal Chemistry|January 27, 2007
Selective inhibitory activity against MAO and molecular modeling studies of 2-thiazolylhydrazone derivativesFranco Chimenti, Elias Maccioni, Daniela Secci, et al.Chemmedchem|March 24, 2016
Hit Identification of a Novel Dual Binder for h-telo/c-myc G-Quadruplex by a Combination of Pharmacophore Structure-Based Virtual Screening and Docking RefinementRoberta Rocca, Giosuè Costa, Anna Artese, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|January 19, 2017
Through scaffold modification to 3,5-diaryl-4,5-dihydroisoxazoles: new potent and selective inhibitors of monoamine oxidase BRita Meleddu, Simona Distinto, Roberto Cirilli, et al.ACS Medicinal Chemistry Letters|May 22, 2020
New Dihydrothiazole Benzensulfonamides: Looking for Selectivity toward Carbonic Anhydrase Isoforms I, II, IX, and XIIRita Meleddu, Simona Distinto, Filippo Cottiglia, et al.Journal of Chemical Information and Modeling|July 22, 2008
Discovery of novel cathepsin S inhibitors by pharmacophore-based virtual high-throughput screeningPatrick Markt, Caroline McGoohan, Brian Walker, et al.Biochimica Et Biophysica Acta. General Subjects|December 28, 2016
Identification of G-quadruplex DNA/RNA binders: Structure-based virtual screening and biophysical characterizationRoberta Rocca, Federica Moraca, Giosuè Costa, et al.Molecules (Basel, Switzerland)|September 28, 2024
Privileged Scaffold Hybridization in the Design of Carbonic Anhydrase InhibitorsDaniela Secci, Erica Sanna, Simona Distinto, et al.ACS Medicinal Chemistry Letters|November 20, 2024
New Structural Features of Isatin Dihydrothiazole Hybrids for Selective Carbonic Anhydrase InhibitorsDaniela Secci, Simona Distinto, Alessia Onali, et al.Journal of Natural Products|October 18, 2017
Phenylpropenoids from Bupleurum fruticosum as Anti-Human Rhinovirus Species A Selective Capsid BindersBenedetta Fois, Giulia Bianco, Vijay P Sonar, et al.European Journal of Medicinal Chemistry|March 3, 2015
(3Z)-3-(2-[4-(aryl)-1,3-thiazol-2-yl]hydrazin-1-ylidene)-2,3-dihydro-1H-indol-2-one derivatives as dual inhibitors of HIV-1 reverse transcriptaseRita Meleddu, Simona Distinto, Angela Corona, et al.Pageof 7