Stefano Alcaro
Stefano Alcaro
Net4Science spinoff & Dipartimento di Scienze della Salute - UMG di Catanzaro (Italy)
Verified email at unicz.it
TitleCited byYear
Mass spectrometry
AL Burlingame, TA Baillie, DH Russell
Analytical chemistry 64 (12), 467-502, 1992
166*1992
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
1592009
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
1342005
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
1272009
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
1122002
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
1112006
Chromone, a privileged scaffold for the development of monoamine oxidase inhibitors
A Gaspar, T Silva, M Yįnez, D Vina, F Orallo, F Ortuso, E Uriarte, S Alcaro, ...
Journal of medicinal chemistry 54 (14), 5165-5173, 2011
1052011
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
982004
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
942010
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
902007
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
882012
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
882008
N-myristoylation determines dual targeting of mammalian NADH-cytochrome b (5) reductase to ER and mitochondrial outer membranes by a mechanism of kinetic partitioning
S Colombo, R Longhi, S Alcaro, F Ortuso, T Sprocati, A Flora, N Borgese
The Journal of cell biology 168 (5), 735-745, 2005
842005
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
832006
Homoisoflavonoids: natural scaffolds with potent and selective monoamine oxidase-B inhibition properties
N Desideri, A Bolasco, R Fioravanti, L Proietti Monaco, F Orallo, M Yáñez, ...
Journal of medicinal chemistry 54 (7), 2155-2164, 2011
812011
Hybrid ligand–alkylating agents targeting telomeric G-quadruplex structures
F Doria, M Nadai, M Folini, M Di Antonio, L Germani, C Percivalle, C Sissi, ...
Organic & biomolecular chemistry 10 (14), 2798-2806, 2012
802012
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
802010
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
792009
Modeling and biological evaluation of 3, 3′-(1, 2-ethanediyl) bis [2-(4-methoxyphenyl)-thiazolidin-4-one], a new synthetic cyclooxygenase-2 inhibitor
R Ottanį, E Mazzon, L Dugo, F Monforte, R Maccari, L Sautebin, ...
European journal of pharmacology 448 (1), 71-80, 2002
762002
Chiral 3, 3′-(1, 2-Ethanediyl)-bis [2-(3, 4-dimethoxyphenyl)-4-thiazolidinones] with anti-inflammatory activity. Part 11: Evaluation of COX-2 selectivity and modelling
MG Vigorita, R Ottaną, F Monforte, R Maccari, MT Monforte, A Trovato, ...
Bioorganic & medicinal chemistry 11 (6), 999-1006, 2003
752003
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