| The mechanisms of pharmacokinetic food-drug interactions–A perspective from the UNGAP group M Koziolek, S Alcaro, P Augustijns, AW Basit, M Grimm, B Hens, CL Hoad, ... European Journal of Pharmaceutical Sciences 134, 31-59, 2019 | 358 | 2019 |
| Chalcones: a valid scaffold for monoamine oxidases inhibitors F Chimenti, R Fioravanti, A Bolasco, P Chimenti, D Secci, F Rossi, ... Journal of medicinal chemistry 52 (9), 2818-2824, 2009 | 249 | 2009 |
| Non-coding RNAs in cancer: Platforms and strategies for investigating the genomic “dark matter” K Grillone, C Riillo, F Scionti, R Rocca, G Tradigo, PH Guzzi, S Alcaro, ... Journal of Experimental & Clinical Cancer Research 39, 1-19, 2020 | 210 | 2020 |
| Synthesis, molecular modeling, and selective inhibitory activity against human monoamine oxidases of 3-carboxamido-7-substituted coumarins F Chimenti, D Secci, A Bolasco, P Chimenti, B Bizzarri, A Granese, ... Journal of medicinal chemistry 52 (7), 1935-1942, 2009 | 193 | 2009 |
| Synthesis and biological evaluation of N-substituted-3, 5-diphenyl-2-pyrazoline derivatives as cyclooxygenase (COX-2) inhibitors R Fioravanti, A Bolasco, F Manna, F Rossi, F Orallo, F Ortuso, S Alcaro, ... European journal of medicinal chemistry 45 (12), 6135-6138, 2010 | 185 | 2010 |
| Chromone, a privileged scaffold for the development of monoamine oxidase inhibitors A Gaspar, T Silva, M Yánez, D Vina, F Orallo, F Ortuso, E Uriarte, S Alcaro, ... Journal of medicinal chemistry 54 (14), 5165-5173, 2011 | 168 | 2011 |
| Synthesis, molecular modeling studies, and selective inhibitory activity against monoamine oxidase of 1-thiocarbamoyl-3, 5-diaryl-4, 5-dihydro-(1 H)-pyrazole derivatives F Chimenti, E Maccioni, D Secci, A Bolasco, P Chimenti, A Granese, ... Journal of medicinal chemistry 48 (23), 7113-7122, 2005 | 164 | 2005 |
| Inhibition of amine oxidases activity by 1-acetyl-3, 5-diphenyl-4, 5-dihydro-(1H)-pyrazole derivatives F Manna, F Chimenti, A Bolasco, D Secci, B Bizzarri, O Befani, P Turini, ... Bioorganic & Medicinal Chemistry Letters 12 (24), 3629-3633, 2002 | 163 | 2002 |
| Quercetin as the Active Principle of Hypericum hircinum Exerts a Selective Inhibitory Activity against MAO-A: Extraction, Biological Analysis, and Computational … F Chimenti, F Cottiglia, L Bonsignore, L Casu, M Casu, C Floris, D Secci, ... Journal of natural products 69 (6), 945-949, 2006 | 148 | 2006 |
| GBPM: GRID-based pharmacophore model: concept and application studies to protein–protein recognition F Ortuso, T Langer, S Alcaro Bioinformatics 22 (12), 1449-1455, 2006 | 131 | 2006 |
| A new series of flavones, thioflavones, and flavanones as selective monoamine oxidase-B inhibitors F Chimenti, R Fioravanti, A Bolasco, P Chimenti, D Secci, F Rossi, ... Bioorganic & medicinal chemistry 18 (3), 1273-1279, 2010 | 128 | 2010 |
| Inhibition of monoamine oxidases by coumarin-3-acyl derivatives: biological activity and computational study F Chimenti, D Secci, A Bolasco, P Chimenti, A Granese, O Befani, P Turini, ... Bioorganic & medicinal chemistry letters 14 (14), 3697-3703, 2004 | 127 | 2004 |
| Design and development of biomimetic nanovesicles using a microfluidic approach R Molinaro, M Evangelopoulos, JR Hoffman, C Corbo, F Taraballi, ... Advanced Materials 30 (15), 1702749, 2018 | 125 | 2018 |
| Synthesis, biological evaluation, and molecular modeling of oleuropein and its semisynthetic derivatives as cyclooxygenase inhibitors A Procopio, S Alcaro, M Nardi, M Oliverio, F Ortuso, P Sacchetta, ... Journal of agricultural and food chemistry 57 (23), 11161-11167, 2009 | 125 | 2009 |
| Ligand binding to telomeric G-quadruplex DNA investigated by funnel-metadynamics simulations F Moraca, J Amato, F Ortuso, A Artese, B Pagano, E Novellino, S Alcaro, ... Proceedings of the National Academy of Sciences 114 (11), E2136-E2145, 2017 | 124 | 2017 |
| Synthesis and selective human monoamine oxidase inhibition of 3-carbonyl, 3-acyl, and 3-carboxyhydrazido coumarin derivatives D Secci, S Carradori, A Bolasco, P Chimenti, M Yáñez, F Ortuso, S Alcaro European journal of medicinal chemistry 46 (10), 4846-4852, 2011 | 121 | 2011 |
| Selective inhibitory activity against MAO and molecular modeling studies of 2-thiazolylhydrazone derivatives F Chimenti, E Maccioni, D Secci, A Bolasco, P Chimenti, A Granese, ... Journal of medicinal chemistry 50 (4), 707-712, 2007 | 120 | 2007 |
| HCV genotypes are differently prone to the development of resistance to linear and macrocyclic protease inhibitors V Cento, C Mirabelli, R Salpini, S Dimonte, A Artese, G Costa, F Mercurio, ... PloS one 7 (7), e39652, 2012 | 113 | 2012 |
| Synthesis, stereochemical identification, and selective inhibitory activity against human monoamine oxidase-B of 2-methylcyclohexylidene-(4-arylthiazol-2-yl) hydrazones F Chimenti, E Maccioni, D Secci, A Bolasco, P Chimenti, A Granese, ... Journal of medicinal chemistry 51 (16), 4874-4880, 2008 | 113 | 2008 |
| Modeling and biological evaluation of 3, 3′-(1, 2-ethanediyl) bis [2-(4-methoxyphenyl)-thiazolidin-4-one], a new synthetic cyclooxygenase-2 inhibitor R Ottaná, E Mazzon, L Dugo, F Monforte, R Maccari, L Sautebin, ... European journal of pharmacology 448 (1), 71-80, 2002 | 110 | 2002 |
Francesco OrtusoUniversità "Magna Graecia" di CatanzaroVerified email at unicz.it
