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European Journal of Medicinal Chemistry|November 5, 2016
Chemical exploration of 4-(4-fluorobenzyl)piperidine fragment for the development of new tyrosinase inhibitorsStefania Ferro, Laura De Luca, Maria Paola Germanò, et al.
Bioorganic & Medicinal Chemistry|September 3, 2008
Improvement of water solubility of non-competitive AMPA receptor antagonists by complexation with beta-cyclodextrinRosanna Stancanelli, Vincenza Crupi, Laura De Luca, et al.
European Journal of Medicinal Chemistry|April 8, 2014
Diketoacid chelating ligands as dual inhibitors of HIV-1 integration processDominga Rogolino, Mauro Carcelli, Carlotta Compari, et al.
Frontiers in Medicine|April 2, 2026
Dry Eye Disease and personality: a systematic reviewAlessandro Meduri, Emanuele Maria Merlo, Giorgio Sparacino, et al.
Journal of Medicinal Chemistry|March 27, 2012
Synthesis, structure-activity relationship studies, and X-ray crystallographic analysis of arylsulfonamides as potent carbonic anhydrase inhibitorsRosaria Gitto, Francesca M Damiano, Pavel Mader, et al.
International Ophthalmology|December 22, 2025
Precision and efficacy in congenital cataract surgery: a retrospective study of the 27-gauge vitrectomy systemMaura Mancini, Alessandro Meduri, Claudio Brancato, et al.
European Journal of Medicinal Chemistry|December 28, 2010
2-hydroxyisoquinoline-1,3(2H,4H)-diones as inhibitors of HIV-1 integrase and reverse transcriptase RNase H domain: influence of the alkylation of position 4Muriel Billamboz, Fabrice Bailly, Cédric Lion, et al.
Bioorganic & Medicinal Chemistry Letters|February 6, 2007
Discovery of novel benzimidazolones as potent non-nucleoside reverse transcriptase inhibitors active against wild-type and mutant HIV-1 strainsMaria Letizia Barreca, Angela Rao, Laura De Luca, et al.
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