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European Journal of Medicinal Chemistry|December 31, 2015
Drug design, synthesis, in vitro and in silico evaluation of selective monoaminoxidase B inhibitors based on 3-acetyl-2-dichlorophenyl-5-aryl-2,3-dihydro-1,3,4-oxadiazole chemical scaffoldSimona Distinto, Rita Meleddu, Matilde Yanez, et al.European Journal of Medicinal Chemistry|September 21, 2019
Review about the multi-target profile of resveratrol and its implication in the SGK1 inhibitionGiada Catalogna, Federica Moraca, Lucia D'Antona, et al.European Journal of Medicinal Chemistry|December 3, 2019
Mediterranean products as promising source of multi-target agents in the treatment of metabolic syndromeDonatella Bagetta, Annalisa Maruca, Antonio Lupia, et al.European Journal of Medicinal Chemistry|November 12, 2017
Design, synthesis and biochemical evaluation of novel multi-target inhibitors as potential anti-Parkinson agentsSimone Carradori, Francesco Ortuso, Anél Petzer, et al.Journal of Amino Acids|March 28, 2013
Design, Synthesis, and Evaluation of New Tripeptides as COX-2 InhibitorsErmelinda Vernieri, Isabel Gomez-Monterrey, Ciro Milite, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|February 19, 2021
Selective inhibition of carbonic anhydrase IX and XII by coumarin and psoralen derivativesRita Meleddu, Serenella Deplano, Elias Maccioni, et al.European Journal of Medicinal Chemistry|August 10, 2019
The Mediterranean Diet as source of bioactive compounds with multi-targeting anti-cancer profileAnnalisa Maruca, Raffaella Catalano, Donatella Bagetta, et al.European Journal of Medicinal Chemistry|April 29, 2019
Benzoic acid-derived nitrones: A new class of potential acetylcholinesterase inhibitors and neuroprotective agentsCatarina Oliveira, Donatella Bagetta, Fernando Cagide, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|August 20, 2019
Benzo[b]tiophen-3-ol derivatives as effective inhibitors of human monoamine oxidase: design, synthesis, and biological activityPaolo Guglielmi, Daniela Secci, Anél Petzer, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|August 22, 2019
Exploring new structural features of the 4-[(3-methyl-4-aryl-2,3-dihydro-1,3-thiazol-2-ylidene)amino]benzenesulphonamide scaffold for the inhibition of human carbonic anhydrasesSimona Distinto, Rita Meleddu, Francesco Ortuso, et al.Pageof 13