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Journal of Medicinal Chemistry|December 24, 2004
Design, synthesis, and pharmacological characterization of novel, potent NMDA receptor antagonistsPaola Conti, Marco De Amici, Giovanni Grazioso, et al.
Chemmedchem|August 7, 2012
Synthesis and biological evaluation of CTP synthetase inhibitors as potential agents for the treatment of African trypanosomiasisLucia Tamborini, Andrea Pinto, Terry K Smith, et al.
British Journal of Cancer|February 12, 2019
Inhibition of SIRT1 deacetylase and p53 activation uncouples the anti-inflammatory and chemopreventive actions of NSAIDsGiulia Dell'Omo, Daniela Crescenti, Cristina Vantaggiato, et al.
Journal of Medicinal Chemistry|September 1, 2015
Characterization of 2,4-Diamino-6-oxo-1,6-dihydropyrimidin-5-yl Ureido Based Inhibitors of Trypanosoma brucei FolD and Testing for Antiparasitic ActivityThomas C Eadsforth, Andrea Pinto, Rosaria Luciani, et al.
The Journal of Biological Chemistry|February 22, 2011
The glial glutamate transporter 1 (GLT1) is expressed by pancreatic beta-cells and prevents glutamate-induced beta-cell deathEliana S Di Cairano, Alberto M Davalli, Lucia Perego, et al.
European Journal of Medicinal Chemistry|September 5, 2025
From pan-active to parasite-selective antiparasitic agents: A scaffold hopping approachChiara Borsari, Nuno Santarem, Dina Coertzen, et al.
ACS Infectious Diseases|May 8, 2024
Discovery of 1,3,4-Oxadiazole Derivatives as Broad-Spectrum Antiparasitic AgentsAlexandra Ioana Corfu, Nuno Santarem, Sara Luelmo, et al.
Journal of Medicinal Chemistry|September 30, 2005
Synthesis, binding affinity at glutamic acid receptors, neuroprotective effects, and molecular modeling investigation of novel dihydroisoxazole amino acidsPaola Conti, Marco De Amici, Giovanni Grazioso, et al.
Journal of Medicinal Chemistry|May 26, 2026
First-in-Class Covalent Inhibitors of PFKFB3: Discovery and Characterization in PDAC ModelsAlessandra Fiore, Antonio Scarano, Giulia Antonini, et al.
European Journal of Medicinal Chemistry|January 27, 2020
Identification of a 2,4-diaminopyrimidine scaffold targeting Trypanosoma brucei pteridine reductase 1 from the LIBRA compound library screening campaignPasquale Linciano, Gregorio Cullia, Chiara Borsari, et al.
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