Toward the Discovery of Novel Anti‐HIV Drugs. Second‐Generation Inhibitors of the Cellular ATPase DDX3 with Improved Anti‐HIV Activity: Synthesis, Structure–Activity Relationship Analysis, Cytotoxicity Studies, and Target ValidationGiovanni Maga, Maurizio Botta, Federico Falchi et al.|ChemMedChem|2011Cited by 105
New Nitrogen Containing Substituents at the Indole-2-carboxamide Yield High Potent and Broad Spectrum Indolylarylsulfone HIV-1 Non-Nucleoside Reverse Transcriptase InhibitorsGiuseppe La Regina, Romano Silvestri, Alberta Samuele et al.|Journal of Medicinal Chemistry|2012Cited by 61
Discovery of Chiral Cyclopropyl Dihydro-Alkylthio-Benzyl-Oxopyrimidine (<i>S</i>-DABO) Derivatives as Potent HIV-1 Reverse Transcriptase Inhibitors with High Activity Against Clinically Relevant MutantsMarco Radi, Maurizio Botta, Mercedes Armand‐Ugón et al.|Journal of Medicinal Chemistry|2009Cited by 38
2-(Alkyl/Aryl)Amino-6-Benzylpyrimidin-4(3<i>H</i>)-ones as Inhibitors of Wild-Type and Mutant HIV-1: Enantioselectivity StudiesDante Rotili, Antonello Mai, Rino Ragno et al.|Journal of Medicinal Chemistry|2012Cited by 31