Samantha Zanoli

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 Validation

Giovanni Maga, Federico Falchi, Marco Radi et al. · ChemMedChem · 2011 · 105 citations

Pharmacy, Medicinal Chemistry, Pharmacology +17

Indolylarylsulfones Bearing Natural and Unnatural Amino Acids. Discovery of Potent Inhibitors of HIV-1 Non-Nucleoside Wild Type and Resistant Mutant Strains Reverse Transcriptase and Coxsackie B4 Virus

Francesco Piscitelli, Antonio Coluccia, Andrea Brancale et al. · Journal of Medicinal Chemistry · 2009 · 64 citations · Full text

Life Sciences, Biochemistry, Medicinal Chemistry +17

Indolyl Aryl Sulfones as HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitors:  Role of Two Halogen Atoms at the Indole Ring in Developing New Analogues with Improved Antiviral Activity

Giuseppe La Regina, Antonio Coluccia, Francesco Piscitelli et al. · Journal of Medicinal Chemistry · 2007 · 60 citations

Life Sciences, Medicinal Chemistry, Pharmacology +17

Inhibition of Subgenomic Hepatitis C Virus RNA Replication by Acridone Derivatives: Identification of an NS3 Helicase Inhibitor

Giuseppe Manfroni, Jan Paeshuyse, Serena Massari et al. · Journal of Medicinal Chemistry · 2009 · 58 citations

Medicine, Medicinal Chemistry, Pharmacology +17

5-Alkyl-6-benzyl-2-(2-oxo-2-phenylethylsulfanyl)pyrimidin-4(3<i>H</i>)-ones, a Series of Anti-HIV-1 Agents of the Dihydro-alkoxy-benzyl-oxopyrimidine Family with Peculiar Structure−Activity Relationship Profile

Maxim B. Nawrozkij, Dante Rotili, Domenico Tarantino et al. · Journal of Medicinal Chemistry · 2008 · 52 citations

Pharmacy, Medicinal Chemistry, Pharmacology +15