| Histone deacetylation in epigenetics: an attractive target for anticancer therapy A Mai, S Massa, D Rotili, I Cerbara, S Valente, R Pezzi, S Simeoni, ... Medicinal research reviews 25 (3), 261-309, 2005 | 418 | 2005 |
| Lycium barbarum polysaccharides: Extraction, purification, structural characterisation and evidence about hypoglycaemic and hypolipidaemic effects. A review A Masci, S Carradori, MA Casadei, P Paolicelli, S Petralito, R Ragno, ... Food chemistry 254, 377-389, 2018 | 236 | 2018 |
| Design, synthesis, and biological evaluation of sirtinol analogues as class III histone/protein deacetylase (Sirtuin) inhibitors A Mai, S Massa, S Lavu, R Pezzi, S Simeoni, R Ragno, FR Mariotti, ... Journal of medicinal chemistry 48 (24), 7789-7795, 2005 | 210 | 2005 |
| Design, molecular modeling, synthesis, and anti-HIV-1 activity of new indolyl aryl sulfones. Novel derivatives of the indole-2-carboxamide R Ragno, A Coluccia, G La Regina, G De Martino, F Piscitelli, ... Journal of medicinal chemistry 49 (11), 3172-3184, 2006 | 204 | 2006 |
| Antimycobacterial pyrroles: synthesis, anti-Mycobacterium tuberculosis activity and QSAR studies R Ragno, GR Marshall, R Di Santo, R Costi, S Massa, R Rompei, M Artico Bioorganic & medicinal chemistry 8 (6), 1423-1432, 2000 | 182 | 2000 |
| 3-(4-Aroyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-alkylamides as a New Class of Synthetic Histone Deacetylase Inhibitors. 1. Design, Synthesis, Biological … A Mai, S Massa, R Ragno, I Cerbara, F Jesacher, P Loidl, G Brosch Journal of Medicinal Chemistry 46 (4), 512-524, 2003 | 144 | 2003 |
| Structure-based design, synthesis, and biological evaluation of conformationally restricted novel 2-alkylthio-6-[1-(2, 6-difluorophenyl) alkyl]-3, 4-dihydro-5-alkylpyrimidin-4 … A Mai, G Sbardella, M Artico, R Ragno, S Massa, E Novellino, G Greco, ... Journal of medicinal chemistry 44 (16), 2544-2554, 2001 | 136 | 2001 |
| Small molecule inhibitors of histone arginine methyltransferases: homology modeling, molecular docking, binding mode analysis, and biological evaluations R Ragno, S Simeoni, S Castellano, C Vicidomini, A Mai, A Caroli, ... Journal of medicinal chemistry 50 (6), 1241-1253, 2007 | 126 | 2007 |
| Mentha suaveolens Ehrh. (Lamiaceae) Essential Oil and Its Main Constituent Piperitenone Oxide: Biological Activities and Chemistry M Božović, A Pirolli, R Ragno Molecules 20 (5), 8605-8633, 2015 | 122 | 2015 |
| Calamintha nepeta (L.) Savi and its Main Essential Oil Constituent Pulegone: Biological Activities and Chemistry M Božović, R Ragno Molecules 22 (2), 290, 2017 | 117 | 2017 |
| Computer-aided design, synthesis, and anti-HIV-1 activity in vitro of 2-alkylamino-6-[1-(2, 6-difluorophenyl) alkyl]-3, 4-dihydro-5-alkylpyrimidin-4 (3 H)-ones as novel potent … R Ragno, A Mai, G Sbardella, M Artico, S Massa, C Musiu, M Mura, ... Journal of medicinal chemistry 47 (4), 928-934, 2004 | 117 | 2004 |
| 2, 6-Bis (3, 4, 5-trihydroxybenzylydene) derivatives of cyclohexanone: novel potent HIV-1 integrase inhibitors that prevent HIV-1 multiplication in cell-based assays R Costi, R Di Santo, M Artico, S Massa, R Ragno, R Loddo, M La Colla, ... Bioorganic & medicinal chemistry 12 (1), 199-215, 2004 | 110 | 2004 |
| 3-(4-Aroyl-1 H-pyrrol-2-yl)-N-hydroxy-2-propenamides, a new class of synthetic histone deacetylase inhibitors S Massa, A Mai, G Sbardella, M Esposito, R Ragno, P Loidl, G Brosch Journal of medicinal chemistry 44 (13), 2069-2072, 2001 | 102 | 2001 |
| Synthesis, biological evaluation, and binding mode of novel 1-[2-(diarylmethoxy) ethyl]-2-methyl-5-nitroimidazoles targeted at the HIV-1 reverse transcriptase R Silvestri, M Artico, G De Martino, R Ragno, S Massa, R Loddo, ... Journal of medicinal chemistry 45 (8), 1567-1576, 2002 | 95 | 2002 |
| Esential oils extraction: A 24-hour steam distillation systematic methodology M Božović, A Navarra, S Garzoli, F Pepi, R Ragno Natural product research 31 (20), 2387-2396, 2017 | 94 | 2017 |
| Docking and 3-D QSAR studies on indolyl aryl sulfones. Binding mode exploration at the HIV-1 reverse transcriptase non-nucleoside binding site and design of highly active N-(2 … R Ragno, M Artico, G De Martino, G La Regina, A Coluccia, A Di Pasquali, ... Journal of medicinal chemistry 48 (1), 213-223, 2005 | 94 | 2005 |
| High Potency of Melaleuca alternifolia Essential Oil against Multi-Drug Resistant Gram-Negative Bacteria and Methicillin-Resistant Staphylococcus aureus A Oliva, S Costantini, M De Angelis, S Garzoli, M Božović, MT Mascellino, ... Molecules 23 (10), 2584, 2018 | 93 | 2018 |
| 3-(4-Aroyl-1-methyl-1 H-2-pyrrolyl)-N-hydroxy-2-propenamides as a new class of synthetic histone deacetylase inhibitors. 2. Effect of pyrrole-C2 and/or-C4 substitutions on … A Mai, S Massa, I Cerbara, S Valente, R Ragno, P Bottoni, R Scatena, ... Journal of medicinal chemistry 47 (5), 1098-1109, 2004 | 93 | 2004 |
| In vitro inhibition of herpes simplex virus type 1 replication by Mentha suaveolens essential oil and its main component piperitenone oxide L Civitelli, S Panella, ME Marcocci, A De Petris, S Garzoli, F Pepi, ... Phytomedicine 21 (6), 857-865, 2014 | 89 | 2014 |
| 3-(4-Aroyl-1-methyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides as a New Class of Synthetic Histone Deacetylase Inhibitors. 3. Discovery of Novel Lead Compounds through … R Ragno, A Mai, S Massa, I Cerbara, S Valente, P Bottoni, R Scatena, ... Journal of medicinal chemistry 47 (6), 1351-1359, 2004 | 88 | 2004 |
Antonello MaiProfessore di Chimica Farmaceutica, Sapienza Università di RomaEmail verificata su uniroma1.it
