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Bioorganic & Medicinal Chemistry Letters|June 16, 2015
New 4-[(3-cyclohexyl-4-aryl-2,3-dihydro-1,3-thiazol-2-ylidene)amino]benzene-1-sulfonamides, synthesis and inhibitory activity toward carbonic anhydrase I, II, IX, XIIRita Meleddu, Elias Maccioni, Simona Distinto, et al.The FEBS Journal|February 26, 2011
Alizarine derivatives as new dual inhibitors of the HIV-1 reverse transcriptase-associated DNA polymerase and RNase H activities effective also on the RNase H activity of non-nucleoside resistant reverse transcriptasesFrancesca Esposito, Tatyana Kharlamova, Simona Distinto, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|October 25, 2016
Isatin: a privileged scaffold for the design of carbonic anhydrase inhibitorsClaudia Melis, Rita Meleddu, Andrea Angeli, et al.Pathogens and Disease|September 2, 2017
Design, synthesis and antiviral evaluation of novel heteroarylcarbothioamide derivatives as dual inhibitors of HIV-1 reverse transcriptase-associated RNase H and RDDP functionsAngela Corona, Valentina Onnis, Alessandro Deplano, et al.European Journal of Medicinal Chemistry|February 25, 2012
Identification of HIV-1 reverse transcriptase dual inhibitors by a combined shape-, 2D-fingerprint- and pharmacophore-based virtual screening approachSimona Distinto, Francesca Esposito, Johannes Kirchmair, et al.Phytomedicine : International Journal of Phytotherapy and Phytopharmacology|October 22, 2016
Sennoside A, derived from the traditional chinese medicine plant Rheum L., is a new dual HIV-1 inhibitor effective on HIV-1 replicationFrancesca Esposito, Ilaria Carli, Claudia Del Vecchio, et al.Journal of Enzyme Inhibition and Medicinal Chemistry|January 9, 2016
Exploring the thiazole scaffold for the identification of new agents for the treatment of fluconazole resistant CandidaRita Meleddu, Simona Distinto, Angela Corona, et al.European Journal of Medicinal Chemistry|March 4, 2017
Natural product-inspired esters and amides of ferulic and caffeic acid as dual inhibitors of HIV-1 reverse transcriptaseVijay P Sonar, Angela Corona, Simona Distinto, et al.Journal of Medicinal Chemistry|September 30, 2008
Discovery of novel PPAR ligands by a virtual screening approach based on pharmacophore modeling, 3D shape, and electrostatic similarity screeningPatrick Markt, Rasmus K Petersen, Esben N Flindt, et al.Journal of Medicinal Chemistry|January 9, 2013
Identification and characterization of new DNA G-quadruplex binders selected by a combination of ligand and structure-based virtual screening approachesStefano Alcaro, Caterina Musetti, Simona Distinto, et al.Pageof 7