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European Journal of Medicinal Chemistry|July 10, 2017
First dual AK/GSK-3β inhibitors endowed with antioxidant properties as multifunctional, potential neuroprotective agentsSimone Brogi, Anna Ramunno, Lida Savi, et al.
Journal of Medicinal Chemistry|May 3, 2012
Design, synthesis, and pharmacological characterization of indol-3-ylacetamides, indol-3-yloxoacetamides, and indol-3-ylcarboxamides: potent and selective CB2 cannabinoid receptor inverse agonistsSerena Pasquini, Claudia Mugnaini, Alessia Ligresti, et al.
The Journal of Pharmacology and Experimental Therapeutics|December 2, 2011
Characterization of COR627 and COR628, two novel positive allosteric modulators of the GABA(B) receptorM Paola Castelli, Angelo Casu, Paola Casti, et al.
Mini Reviews in Medicinal Chemistry|February 20, 2015
Development of HuperTacrines as non-toxic, cholinesterase inhibitors for the potential treatment of Alzheimer's diseaseMourad Chioua, Marta Pérez, Oscar M Bautista-Aguilera, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Multifunctional cholinesterase and amyloid Beta fibrillization modulators. Synthesis and biological investigationStefania Butini, Margherita Brindisi, Simone Brogi, et al.
Molecular Diversity|June 25, 2026
Thiazolidinedione-triazole hybrids: design, synthesis, and biological evaluation as dual inhibitors of α-amylase and aldose reductase with antioxidant activity for antidiabetic therapyEman E Nasr, Mohamed R Elnagar, Nahed Nasser Eid El-Sayed, et al.
European Journal of Medicinal Chemistry|March 8, 2013
Synthesis and structure-activity relationship studies in serotonin 5-HT(1A) receptor agonists based on fused pyrrolidone scaffoldsAndrea Cappelli, Monica Manini, Salvatore Valenti, et al.
Bioorganic Chemistry|June 12, 2019
Bridged bicyclic 2,3-dioxabicyclo[3.3.1]nonanes as antiplasmodial agents: Synthesis, structure-activity relationships and studies on their biomimetic reaction with Fe(II)Sarah D'Alessandro, Gloria Alfano, Luisa Di Cerbo, et al.
ACS Infectious Diseases|October 31, 2019
Screening and Phenotypical Characterization of <i>Schistosoma mansoni</i> Histone Deacetylase 8 (<i>Sm</i>HDAC8) Inhibitors as Multistage Antischistosomal AgentsFulvio Saccoccia, Margherita Brindisi, Roberto Gimmelli, et al.
European Journal of Medicinal Chemistry|January 17, 2016
Synthesis and biological evaluation of fluorinated 1,5-diarylpyrrole-3-alkoxyethyl ether derivatives as selective COX-2 inhibitors endowed with anti-inflammatory activityAngela Di Capua, Claudia Sticozzi, Simone Brogi, et al.
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