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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
Theoretical evidence of a salt bridge disruption as the initiating processfor the alpha(1d)-adrenergic receptor activation: a molecular dynamics anddocking study
Authors: Carrieri, A Centeno, NB Rodrigo, J Sanz, F Carotti, A
Citation: A. Carrieri et al., Theoretical evidence of a salt bridge disruption as the initiating processfor the alpha(1d)-adrenergic receptor activation: a molecular dynamics anddocking study, PROTEINS, 43(4), 2001, pp. 382-394
Conformationally constrained butyrophenones with mixed dopaminergic (D-2) and serotoninergic (5-HT2A, 5-HT2C) affinities: Synthesis, pharmacology, 3D-QSAR, and molecular modeling of (aminoalkyl)benzo- and -thienocycloalkanones as putative atypical antipsychotics (vol 42, pg 2775, 1999)
Authors: Ravina, E Negreira, J Cid, J Masaguer, CF Rosa, E Rivas, ME Fontenla, JA Loza, MI Tristan, H Cadavid, MI Sanz, F Lozoya, E Carotti, A Carrieri, A
Citation: E. Ravina et al., Conformationally constrained butyrophenones with mixed dopaminergic (D-2) and serotoninergic (5-HT2A, 5-HT2C) affinities: Synthesis, pharmacology, 3D-QSAR, and molecular modeling of (aminoalkyl)benzo- and -thienocycloalkanones as putative atypical antipsychotics (vol 42, pg 2775, 1999), J MED CHEM, 43(6), 2000, pp. 1250-1250
Comparative molecular field analysis (CoMFA) and docking studies of non-nucleoside HIV-1 RT inhibitors (NNIs)
Authors: Barreca, ML Carotti, A Carrieri, A Chimirri, A Monforte, AM Calace, MP Rao, A
Citation: Ml. Barreca et al., Comparative molecular field analysis (CoMFA) and docking studies of non-nucleoside HIV-1 RT inhibitors (NNIs), BIO MED CH, 7(11), 1999, pp. 2283-2292
Comparative molecular field analysis of some pyridazinone-containing alpha(1)-antagonists
Authors: Cinone, N Carrieri, A Strappaghetti, G Corsano, S Barbaro, R Carotti, A
Citation: N. Cinone et al., Comparative molecular field analysis of some pyridazinone-containing alpha(1)-antagonists, BIO MED CH, 7(11), 1999, pp. 2615-2620
2-(2-phenylcyclopropyl) imidazolines: Reversed enantioselective interaction at I-1 and I-2 imidazoline receptors
Authors: Quaglia, W Bousquet, P Pigini, M Carotti, A Carrieri, A Dontenwill, M Gentili, F Giannella, M Maranca, F Piergentili, A Brasili, L
Citation: W. Quaglia et al., 2-(2-phenylcyclopropyl) imidazolines: Reversed enantioselective interaction at I-1 and I-2 imidazoline receptors, J MED CHEM, 42(15), 1999, pp. 2737-2740
Conformationally constrained butyrophenones with mixed dopaminergic (D-2) and serotoninergic (5-HT2A, 5-HT2C) affinities: Synthesis, pharmacology, 3D-QSAR, and molecular modeling of (aminoalkyl)benzo- and -thienocycloalkanones as putative atypical antipsychotics
Authors: Ravina, E Negreira, J Cid, J Masaguer, CP Rosa, E Rivas, ME Fontenla, JA Loza, MI Tristan, H Cadavid, MI Sanz, F Lozoya, E Carotti, A Carrieri, A
Citation: E. Ravina et al., Conformationally constrained butyrophenones with mixed dopaminergic (D-2) and serotoninergic (5-HT2A, 5-HT2C) affinities: Synthesis, pharmacology, 3D-QSAR, and molecular modeling of (aminoalkyl)benzo- and -thienocycloalkanones as putative atypical antipsychotics, J MED CHEM, 42(15), 1999, pp. 2774-2797
Ligand binding to I-2 imidazoline receptor: The role of lipophilicity in quantitative structure-activity relationship models
Authors: Pigini, M Bousquet, P Brasili, L Carrieri, A Cavagna, R Dontenwill, M Gentili, F Giannella, M Leonetti, F Piergentili, A Quaglia, W Carotti, A
Citation: M. Pigini et al., Ligand binding to I-2 imidazoline receptor: The role of lipophilicity in quantitative structure-activity relationship models, BIO MED CH, 6(12), 1998, pp. 2245-2260
Risultati: 1-8 |