LIVI, ORESTE Statistiche

LIVI, ORESTE  

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Titolo Data di pubblicazione Autore(i) File
An 1,2,3-Triazole Derivative Bioisoster of a Potent in Vitro Prostaglandin Synthesis Inhibitor: Preparation and Biological Activity 1-gen-1992 Biagi, Giuliana; Dell'Omodarme, Giuliana; Giorgi, Irene; Livi, Oreste; Scartoni, Valerio
1,2,3-Triazole[4,5-d]pyridazines II. New Derivatives Tested on the Adenosine Receptors 1-gen-1994 Biagi, Giuliana; Giorgi, Irene; Livi, Oreste; Scartoni, Valerio; Martini, Claudia; Tacchi, P; Merlino, Stefano; Pasero, Marco
2,9-Disubstituted-N6-(arylcarbamoyl)-8-azaadenines as new selective A3 adenosine receptor antagonists: Synthesis, biochemical and molecular modelling studies 1-gen-2005 G., Biagi; Bianucci, ANNA MARIA PAOLA; Coi, Alessio; Costa, Barbara; L., Fabbrini; Giorgi, Irene; Livi, Oreste; I., Micco; F., Pacchini; E., Santini; M., Leonardi; F., AHMAD NOFAL; O., LEROY SALERNI; V., Scartoni
A 3D model of human A1 adenosine receptor. An evaluation of the binding free energy with ligands 1-gen-1997 Bianucci, ANNA MARIA PAOLA; BIGI U., M; Biagi, G; Giorgi, Irene; Livi, Oreste; Scartoni, V.
A 3D Model of the Human A1 Adenosine Receptor. An Evaluation of the Binding Free-Energy with Ligands 1-gen-1998 Bianucci, ANNA MARIA PAOLA; M. U., Bigi; G., Biagi; Giorgi, Irene; Livi, Oreste; V., Scartoni
A QSAR study of A1adenosine receptor antagonists by a new neural network model 1-gen-2001 Bianucci, ANNA MARIA PAOLA; G., Biagi; Giorgi, Irene; Livi, Oreste; Micheli, Alessio; V., Scartoni; Sperduti, Alessandro; Starita, Antonina
Bioisosterism, Enantioselectivity and Molecular Modelling of New Effective Substituted 2-Phenyl Adenines and 8-AZA Analogues. Different Binding Modes to A1 Adenosine Receptors 1-gen-2001 Bianucci, ANNA MARIA PAOLA; G., Biagi; Coi, Alessio; Giorgi, Irene; Livi, Oreste; F., Pacchini; V., Scartoni; Lucacchini, Antonio; Costa, Barbara
Interaction of an improved model of human A1 adenosine receptor with ligands 1-gen-1998 G., Biagi; Bianucci, ANNA MARIA PAOLA; U. M., Bigi; Giorgi, Irene; Livi, Oreste; V., Scartoni
Interactions of an improved model of the the Human A1 Adenosine Receptor with Ligands 1-gen-1998 Bianucci, ANNA MARIA PAOLA; BIGI M., U; Giorgi, Irene; Livi, Oreste; Scartoni, V.
Introduction of a hydroxy function on N6 8-azaadenine substituents to improve the solubility and the effectiveness of antagonists towards A1 adenosine receptors 1-gen-1999 Bianucci, ANNA MARIA PAOLA; G., Biagi; Giorgi, Irene; Livi, Oreste; Scartoni, V.
NEW 1,2,3-TRIAZOLO[1,5-a]QUINOXALINES: SYNTHESIS AND BINDING TO BENZODIAZEPINE AND ADENOSINE RECEPTORS. II 1-gen-2002 Biagi, G; Giorgi, Irene; Livi, Oreste; V., Scartoni; Betti, Laura; Giannaccini, Gino; Trincavelli, MARIA LETIZIA
NEW 1,2,3-TRIAZOLO[4,5-D]1,2,4-TRIAZOLO[3,4-D]PYRIDAZINE DERIVATIVES. II 1-gen-2002 Biagi, Giuliana; F., Ciambrone; I., Giorgi; Livi, Oreste; V., Scartoni; P. L., Barili
New N6-cycloalkyl-1H-1,2,3-triazolo[4,5-c]Pyridines as potent of A1 Adenosine Receptor Antagonists 1-gen-1999 Bianucci, ANNA MARIA PAOLA; Biagi, G; Giorgi, Irene; Livi, Oreste; Scartoni, V.
Steroeselectivity as an evidence for a double insertion of Antagonists within A1 Adenosine Receptors 1-gen-1999 Bianucci, ANNA MARIA PAOLA; G., Biagi; Giorgi, Irene; Livi, Oreste; Scartoni, V.
Structural modifications of benzanilide derivatives, effective potassium channel openers. X In corso di stampa Calderone, Vincenzo; A., Coi; F. L., Fiamingo; Giorgi, I; M., Leonardi; Livi, Oreste; A., Martelli; E., Martinotti
Synthesis of analogs of (±)-EHNA as potent inhibitors of ADA 1-gen-1999 Bianucci, ANNA MARIA PAOLA; Biagi, G; Giorgi, Irene; Livi, Oreste; Scartoni, V.
Synthesis, biological activity and molecular modelling of new trisubstituted 8-azaadenines with high affinity for A1 adenosine receptors In corso di stampa I., Giorgi; A. M., Bianucci; Biagi, Giuliana; Livi, Oreste; V., Scartoni; M., Leonardi; B., Pietra; A., Coi; I., Massarelli; F., AHMAD NOFAL; F. L., Fiamingo; P., Anastasi; G., Giannini