1-Aminoindan-1, 5-dicarboxylic acid: a novel antagonist at phospholipase C-linked metabotropic glutamate receptors R Pellicciari, R Luneia, G Costantino, M Marinozzi, B Natalini, P Jakobsen, ... Journal of medicinal chemistry 38 (19), 3717-3719, 1995 | 202 | 1995 |
(S)-(+)-2-(3‘-Carboxybicyclo[1.1.1]pentyl)- glycine, a Structurally New Group I Metabotropic Glutamate Receptor Antagonist R Pellicciari, M Raimondo, M Marinozzi, B Natalini, G Costantino, ... Journal of medicinal chemistry 39 (15), 2874-2876, 1996 | 183 | 1996 |
Recent advances in the synthetic chemistry of bicyclo [1.1. 1] pentane J Kanazawa, M Uchiyama Synlett 30 (01), 1-11, 2019 | 159 | 2019 |
Synthesis and Pharmacological Characterization of All Sixteen Stereoisomers of 2-(2‘-Carboxy-3‘-phenylcyclopropyl)glycine. Focus on (2S,1‘S,2‘S,3‘R)-2-(2 … R Pellicciari, M Marinozzi, B Natalini, G Costantino, R Luneia, G Giorgi, ... Journal of medicinal chemistry 39 (11), 2259-2269, 1996 | 127 | 1996 |
Specific inhibition of kynurenate synthesis enhances extracellular dopamine levels in the rodent striatum L Amori, HQ Wu, M Marinozzi, R Pellicciari, P Guidetti, R Schwarcz Neuroscience 159 (1), 196-203, 2009 | 121 | 2009 |
The reaction of α-diazo-β-hydroxy esters with boron trifluoride etherate: Generation and rearrangement of destabilized vinyl cations. A detailed experimental and theoretical study R Pellicciari, B Natalini, BM Sadeghpour, M Marinozzi, JP Snyder, ... Journal of the American Chemical Society 118 (1), 1-12, 1996 | 115 | 1996 |
λ5-Phosphorus-Containing α-Diazo Compounds: A Valuable Tool for Accessing Phosphorus-Functionalized Molecules M Marinozzi, F Pertusati, M Serpi Chemical Reviews 116 (22), 13991-14055, 2016 | 114 | 2016 |
Synthesis and biological evaluation of 2-(3′-(1H-tetrazol-5-yl) bicyclo [1.1. 1] pent-1-yl) glycine (S-TBPG), a novel mGlu1 receptor antagonist G Costantino, K Maltoni, M Marinozzi, E Camaioni, L Prezeau, JP Pin, ... Bioorganic & medicinal chemistry 9 (2), 221-227, 2001 | 98 | 2001 |
Modulators of the kynurenine pathway of triptophan metabolism. Synthesis and preliminary biological evaluation of (S)-4-(ethylsulfonyl) benzoylalanine, the first potent and … R Pellicciari, R Rizzo, G Costantino, M Marinozzi, L Amori, P Guidetti, ... ChemMedChem 1 (5), 528-531, 2006 | 92 | 2006 |
Determination of bile salt critical micellization concentration on the road to drug discovery B Natalini, R Sardella, A Gioiello, F Ianni, A Di Michele, M Marinozzi Journal of pharmaceutical and biomedical analysis 87, 62-81, 2014 | 90 | 2014 |
Novel isoquinolinone-derived inhibitors of poly (ADP-ribose) polymerase-1: pharmacological characterization and neuroprotective effects in an in vitro model of cerebral ischemia A Chiarugi, E Meli, M Calvani, R Picca, R Baronti, E Camaioni, ... Journal of Pharmacology and Experimental Therapeutics 305 (3), 943-949, 2003 | 88 | 2003 |
Type 2 Metabotropic Glutamate (mGlu) Receptors Tonically Inhibit Transmitter Release in Rat Caudate Nucleus: In Vivo Studies with (2S,1′S,2′S,3′R)‐2‐(2 … A Cozzi, S Attucci, F Peruginelli, M Marinozzi, R Luneia, R Pellicciari, ... European Journal of Neuroscience 9 (7), 1350-1355, 1997 | 83 | 1997 |
Antioxidant activity of phenolic extracts from different cultivars of Italian onion (Allium cepa) and relative human immune cell proliferative induction A Lisanti, V Formica, F Ianni, B Albertini, M Marinozzi, R Sardella, ... Pharmaceutical biology 54 (5), 799-806, 2016 | 63 | 2016 |
The effect of mobile phase composition in the enantioseparation of pharmaceutically relevant compounds with polysaccharide‐based stationary phases R Sardella, F Ianni, A Lisanti, M Marinozzi, S Scorzoni, B Natalini Biomedical Chromatography 28 (1), 159-167, 2014 | 62 | 2014 |
Pyrazole [3, 4-e][1, 4] thiazepin-7-one derivatives as a novel class of Farnesoid X Receptor (FXR) agonists M Marinozzi, A Carotti, E Sansone, A Macchiarulo, E Rosatelli, R Sardella, ... Bioorganic & medicinal chemistry 20 (11), 3429-3445, 2012 | 58 | 2012 |
(2S, 1'S, 2'S, 3'R)-2-(2'-carboxy-3'-phenylcyclopropyl) glycine, a potent and selective antagonist of type 2 metabotropic glutamate receptors. C Thomsen, V Bruno, F Nicoletti, M Marinozzi, R Pellicciari Molecular Pharmacology 50 (1), 6-9, 1996 | 56 | 1996 |
D-3, 4-‘cyclopropylglutamate’isomers as nmda receptor ligands: Synthesis and enantioselective activity. R Pellicciari, B Natalini, M Marinozzi, JB Monahan, JP Snyder Tetrahedron letters 31 (1), 139-142, 1990 | 54 | 1990 |
Beyond bile acids: targeting Farnesoid X Receptor (FXR) with natural and synthetic ligands A Carotti, M Marinozzi, C Custodi, B Cerra, R Pellicciari, A Gioiello, ... Current topics in medicinal chemistry 14 (19), 2129-2142, 2014 | 53 | 2014 |
Spiro [2.2] pentane as a dissymmetric scaffold for conformationally constrained analogues of glutamic acid: focus on racemic 1-aminospiro [2.2] pentyl-1, 4-dicarboxylic Acids R Pellicciari, M Marinozzi, E Camaioni, M del Carmen Nùnez, ... The Journal of Organic Chemistry 67 (16), 5497-5507, 2002 | 49 | 2002 |
Computational studies in enantioselective liquid chromatography: forty years of evolution in docking-and molecular dynamics-based simulations R Sardella, E Camaioni, A Macchiarulo, A Gioiello, M Marinozzi, A Carotti TrAC Trends in Analytical Chemistry 122, 115703, 2020 | 42 | 2020 |