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Bioorganic & Medicinal Chemistry|June 15, 2007
Synthesis, resolution, stereochemistry, and molecular modeling of (R)- and (S)-2-acetyl-1-(4'-chlorophenyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline AMPAR antagonistsRosaria Gitto, Rita Ficarra, Rosanna Stancanelli, et al.European Journal of Medicinal Chemistry|June 16, 2019
Exploiting the 1-(4-fluorobenzyl)piperazine fragment for the development of novel tyrosinase inhibitors as anti-melanogenic agents: Design, synthesis, structural insights and biological profileLaura Ielo, Batel Deri, Maria Paola Germanò, et al.Journal of Medicinal Chemistry|November 5, 2011
Synthesis and biological characterization of 3-substituted-1H-indoles as ligands of GluN2B-containing N-methyl-D-aspartate receptorsRosaria Gitto, Laura De Luca, Stefania Ferro, et al.Bioorganic Chemistry|December 4, 2025
Depigmenting action and bioimaging of luminescent BODIPY-based piperazinyl phenol derivativesSalvatore Mirabile, Anna Barattucci, Paola Maria Bonaccorsi, et al.Journal of Medicinal Chemistry|April 29, 2017
Probing Molecular Interactions between Human Carbonic Anhydrases (hCAs) and a Novel Class of BenzenesulfonamidesElvira Bruno, Maria Rosa Buemi, Anna Di Fiore, et al.European Journal of Medicinal Chemistry|December 12, 2018
Exploring structural properties of potent human carbonic anhydrase inhibitors bearing a 4-(cycloalkylamino-1-carbonyl)benzenesulfonamide moietyMaria Rosa Buemi, Anna Di Fiore, Laura De Luca, et al.European Journal of Medicinal Chemistry|April 3, 2025
O-derivatization of natural tropolone and β-thujaplicin leading to effective inhibitors of human carbonic anhydrases IX and XIIFrancesco Melfi, Ilaria D'Agostino, Simone Carradori, et al.Pageof 11