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Results: 1-8 |
Results: 8
High affinity central benzodiazepine receptor ligands. Part 2: Quantitative structure-activity relationships and comparative molecular field analysisof pyrazolo[4,3-c]quinolin-3-ones
Authors: Savini, L Chiasserini, L Pellerano, C Biggio, G Maciocco, E Serra, M Cinone, N Carrieri, A Altomare, C Carotti, A
Citation: L. Savini et al., High affinity central benzodiazepine receptor ligands. Part 2: Quantitative structure-activity relationships and comparative molecular field analysisof pyrazolo[4,3-c]quinolin-3-ones, BIO MED CH, 9(2), 2001, pp. 431-444
Clozapine, but not haloperidol, increases brain concentrations of neuroactive steroids in the rat
Authors: Barbaccia, ML Affricano, D Purdy, RH Maciocco, E Spiga, F Biggio, G
Citation: Ml. Barbaccia et al., Clozapine, but not haloperidol, increases brain concentrations of neuroactive steroids in the rat, NEUROPSYCH, 25(4), 2001, pp. 489-497
Increase in expression of the GABA(A) receptor alpha(4) subunit gene induced by withdrawal of, but not by long-term treatment with, benzodiazepine full or partial agonists
Authors: Follesa, P Cagetti, E Mancuso, L Biggio, F Manca, A Maciocco, E Massa, F Desole, MS Carta, M Busonero, F Sanna, E Biggio, G
Citation: P. Follesa et al., Increase in expression of the GABA(A) receptor alpha(4) subunit gene induced by withdrawal of, but not by long-term treatment with, benzodiazepine full or partial agonists, MOL BRAIN R, 92(1-2), 2001, pp. 138-148
Physicochemical characterization and in vivo properties of Zolpidem in solid dispersions with polyethylene glycol 4000 and 6000
Authors: Trapani, G Franco, M Latrofa, A Pantaleo, MR Provenzano, MR Sanna, E Maciocco, E Liso, G
Citation: G. Trapani et al., Physicochemical characterization and in vivo properties of Zolpidem in solid dispersions with polyethylene glycol 4000 and 6000, INT J PHARM, 184(1), 1999, pp. 121-130
Synthesis and dopamine D-2-Iike receptor binding affinity of substituted 5-phenyl-pyrrole-3-carboxamides
Authors: Pinna, GRA Curzu, MM Sechi, M Chelucci, G Maciocco, E
Citation: Gra. Pinna et al., Synthesis and dopamine D-2-Iike receptor binding affinity of substituted 5-phenyl-pyrrole-3-carboxamides, FARMACO, 54(8), 1999, pp. 542-550
Characterization of the electrophysiological and pharmacological effects of 4-iodo-2,6-diisopropylphenol, a propofol analogue devoid of sedative-anaesthetic properties
Authors: Sanna, E Motzo, C Usala, M Serra, M Dazzi, L Maciocco, E Trapani, G Latrofa, A Liso, G Biggio, G
Citation: E. Sanna et al., Characterization of the electrophysiological and pharmacological effects of 4-iodo-2,6-diisopropylphenol, a propofol analogue devoid of sedative-anaesthetic properties, BR J PHARM, 126(6), 1999, pp. 1444-1454
Molecular and neurochemical evaluation of the effects of etizolam on GABA(A) receptors under normal and stress conditions
Authors: Sanna, E Pau, D Tuveri, F Massa, F Maciocco, E Acquas, C Floris, C Fontana, SN Maira, G Biggio, G
Citation: E. Sanna et al., Molecular and neurochemical evaluation of the effects of etizolam on GABA(A) receptors under normal and stress conditions, ARZNEI-FOR, 49(2), 1999, pp. 88-95
Synthesis and D-2-like binding affinity of 4,5-dihydro-1H-benzo[g]indole-3-carboxamide derivatives as conformationally restricted 5-phenyl-pyrrole-3-carboxamide analogs
Authors: Pinna, GA Curzu, MM Sechi, M Chelucci, G Vianello, P Maciocco, E
Citation: Ga. Pinna et al., Synthesis and D-2-like binding affinity of 4,5-dihydro-1H-benzo[g]indole-3-carboxamide derivatives as conformationally restricted 5-phenyl-pyrrole-3-carboxamide analogs, FARMACO, 53(10-11), 1998, pp. 684-689
Risultati: 1-8 |