Sfoglia per Autore
An 1,2,3-Triazole Derivative Bioisoster of a Potent in Vitro Prostaglandin Synthesis Inhibitor: Preparation and Biological Activity
1992-01-01 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
1994-01-01 Biagi, Giuliana; Giorgi, Irene; Livi, Oreste; Scartoni, Valerio; Martini, Claudia; Tacchi, P; Merlino, Stefano; Pasero, Marco
A 3D model of human A1 adenosine receptor. An evaluation of the binding free energy with ligands
1997-01-01 Bianucci, ANNA MARIA PAOLA; BIGI U., M; Biagi, G; Giorgi, Irene; Livi, Oreste; Scartoni, V.
Interaction of an improved model of human A1 adenosine receptor with ligands
1998-01-01 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
1998-01-01 Bianucci, ANNA MARIA PAOLA; BIGI M., U; Giorgi, Irene; Livi, Oreste; Scartoni, V.
A 3D Model of the Human A1 Adenosine Receptor. An Evaluation of the Binding Free-Energy with Ligands
1998-01-01 Bianucci, ANNA MARIA PAOLA; M. U., Bigi; G., Biagi; Giorgi, Irene; Livi, Oreste; V., Scartoni
Introduction of a hydroxy function on N6 8-azaadenine substituents to improve the solubility and the effectiveness of antagonists towards A1 adenosine receptors
1999-01-01 Bianucci, ANNA MARIA PAOLA; G., Biagi; Giorgi, Irene; Livi, Oreste; Scartoni, V.
Synthesis of analogs of (±)-EHNA as potent inhibitors of ADA
1999-01-01 Bianucci, ANNA MARIA PAOLA; Biagi, G; Giorgi, Irene; Livi, Oreste; Scartoni, V.
New N6-cycloalkyl-1H-1,2,3-triazolo[4,5-c]Pyridines as potent of A1 Adenosine Receptor Antagonists
1999-01-01 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
1999-01-01 Bianucci, ANNA MARIA PAOLA; G., Biagi; Giorgi, Irene; Livi, Oreste; Scartoni, V.
Bioisosterism, Enantioselectivity and Molecular Modelling of New Effective Substituted 2-Phenyl Adenines and 8-AZA Analogues. Different Binding Modes to A1 Adenosine Receptors
2001-01-01 Bianucci, ANNA MARIA PAOLA; G., Biagi; Coi, Alessio; Giorgi, Irene; Livi, Oreste; F., Pacchini; V., Scartoni; Lucacchini, Antonio; Costa, Barbara
A QSAR study of A1adenosine receptor antagonists by a new neural network model
2001-01-01 Bianucci, ANNA MARIA PAOLA; G., Biagi; Giorgi, Irene; Livi, Oreste; Micheli, Alessio; V., Scartoni; Sperduti, Alessandro; Starita, Antonina
NEW 1,2,3-TRIAZOLO[4,5-D]1,2,4-TRIAZOLO[3,4-D]PYRIDAZINE DERIVATIVES. II
2002-01-01 Biagi, Giuliana; F., Ciambrone; I., Giorgi; Livi, Oreste; V., Scartoni; P. L., Barili
NEW 1,2,3-TRIAZOLO[1,5-a]QUINOXALINES: SYNTHESIS AND BINDING TO BENZODIAZEPINE AND ADENOSINE RECEPTORS. II
2002-01-01 Biagi, G; Giorgi, Irene; Livi, Oreste; V., Scartoni; Betti, Laura; Giannaccini, Gino; Trincavelli, MARIA LETIZIA
2,9-Disubstituted-N6-(arylcarbamoyl)-8-azaadenines as new selective A3 adenosine receptor antagonists: Synthesis, biochemical and molecular modelling studies
2005-01-01 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
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
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
| 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 | |
| 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. | |
| 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. | |
| 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 | |
| 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. | |
| 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. | |
| 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. | |
| 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 | |
| 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 | |
| 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 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 | |
| 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 | |
| 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 | |
| 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 |
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