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Results: 1-10 |
Results: 10
Interaction between aromatic residues. Molecular dynamics and ab initio exploration of the potential energy surface of the tryptophan-histidine pair
Authors: Gervasio, FL Procacci, P Cardini, G Guarna, A Giolitti, A Schettino, V
Citation: Fl. Gervasio et al., Interaction between aromatic residues. Molecular dynamics and ab initio exploration of the potential energy surface of the tryptophan-histidine pair, J PHYS CH B, 104(5), 2000, pp. 1108-1114
Ala scan analogues of HOE 140. Synthesis and biological activities
Authors: Quartara, L Ricci, R Meini, S Patacchini, R Giolitti, A Amadesi, S Rizzi, C Rizzi, A Varani, K Borea, PA Maggi, CA Regoli, D
Citation: L. Quartara et al., Ala scan analogues of HOE 140. Synthesis and biological activities, EUR J MED C, 35(11), 2000, pp. 1001-1010
The rise and fall of the early Center-Left (An interview with Antonio Giolitti)
Authors: Ricciardi, A Giolitti, A
Citation: A. Ricciardi et A. Giolitti, The rise and fall of the early Center-Left (An interview with Antonio Giolitti), PONTE, 56(4), 2000, pp. 85-115
Molecular determinants of peptide and nonpeptide NK-2 receptor antagonistsbinding sites of the human tachykinin NK-2 receptor by site-directed mutagenesis
Authors: Giolitti, A Cucchi, P Renzetti, AR Rotondaro, L Zappitelli, S Maggi, CA
Citation: A. Giolitti et al., Molecular determinants of peptide and nonpeptide NK-2 receptor antagonistsbinding sites of the human tachykinin NK-2 receptor by site-directed mutagenesis, NEUROPHARM, 39(8), 2000, pp. 1422-1429
Regio- and stereoselective cycloadditions of cyclic nitrones to maleic diamide forced in a peptide: Synthesis of potent ligands of human NK-2 receptor
Authors: Valenza, S Cordero, FM Brandi, A Guidi, A Altamura, M Giolitti, A Giuntini, F Pasqui, F Renzetti, AR Maggi, CA
Citation: S. Valenza et al., Regio- and stereoselective cycloadditions of cyclic nitrones to maleic diamide forced in a peptide: Synthesis of potent ligands of human NK-2 receptor, J ORG CHEM, 65(13), 2000, pp. 4003-4008
Discovery of potent cyclic pseudopeptide human tachykinin NK-2 receptor antagonists
Authors: Giannotti, D Perrotta, E Di Bugno, C Nannicini, R Harmat, NJS Giolitti, A Patacchini, R Renzetti, AR Rotondaro, L Giuliani, S Altamura, M Maggi, CA
Citation: D. Giannotti et al., Discovery of potent cyclic pseudopeptide human tachykinin NK-2 receptor antagonists, J MED CHEM, 43(22), 2000, pp. 4041-4044
Theoretical investigation of histidine-tryptophan preferential interactions
Authors: Alagona, G Ghio, C Giolitti, A Monti, S
Citation: G. Alagona et al., Theoretical investigation of histidine-tryptophan preferential interactions, THEOR CH AC, 101(1-3), 1999, pp. 143-150
Relevance of aromatic residues in transmembrane segments V to VII for binding of peptide and nonpeptide antagonists to the human tachykinin NK2 receptor
Authors: Renzetti, AR Catalioto, RM Criscuoli, M Cucchi, P Ferrer, C Giolitti, A Guelfi, M Rotondaro, L Warner, FJ Maggi, CA
Citation: Ar. Renzetti et al., Relevance of aromatic residues in transmembrane segments V to VII for binding of peptide and nonpeptide antagonists to the human tachykinin NK2 receptor, J PHARM EXP, 290(2), 1999, pp. 487-495
MEN 11270, a novel selective constrained peptide antagonist with high affinity at the human B-2 kinin receptor
Authors: Meini, S Quartara, L Rizzi, A Patacchini, R Cucchi, P Giolitti, A Calo, G Regoli, D Criscuoli, M Maggi, CA
Citation: S. Meini et al., MEN 11270, a novel selective constrained peptide antagonist with high affinity at the human B-2 kinin receptor, J PHARM EXP, 289(3), 1999, pp. 1250-1256
Effects of tyrosine289phenylalanine mutation on binding and functional properties of the human tachykinin NK2 receptor stably expressed in Chinese hamster ovary cells
Authors: Renzetti, AR Catalioto, RM Carloni, C Criscuoli, M Cucchi, P Giolitti, A Zappitelli, S Rotondaro, L Maggi, CA
Citation: Ar. Renzetti et al., Effects of tyrosine289phenylalanine mutation on binding and functional properties of the human tachykinin NK2 receptor stably expressed in Chinese hamster ovary cells, BIOCH PHARM, 57(8), 1999, pp. 899-906
Risultati: 1-10 |