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G Biagi

Showing results (61-70 of 95) with videos related to

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Farmaco (Societa Chimica Italiana : 1989)|August 1, 1996
1,2,3-Triazolo [4,5-d] pyridazines--V. Preparation and adenosine receptor binding of new 4-amino derivativesG Biagi, I Giorgi, O Livi, et al.
Farmaco (Societa Chimica Italiana : 1989)|October 1, 1995
N(6) or N(9) substituted 2-phenyl-8-azaadenines: affinity for A1 adenosine receptors. VIIG Biagi, I Giorgi, O Livi, et al.
Drug Design and Discovery|May 1, 1997
A 3D model of the human A1 adenosine receptor. An evaluation of the binding free-energy with ligandsA M Bianucci, M U Bigi, G Biagi, et al.
Farmaco (Societa Chimica Italiana : 1989)|March 1, 1994
N(6)-substituted 2-phenyl-9-benzyl-8-azaadenines. Affinity for adenosine A1 and A2 receptors. A comparison with 2-N-butyl analogous derivatives. VG Biagi, I Giorgi, O Livi, et al.
Farmaco (Societa Chimica Italiana : 1989)|February 1, 1994
2-Aryl-8-azaadenosines: structure-activity relationships in the binding with A1 and A2 receptors. A comparison with the corresponding 9-benzyl-8-azaadenines. IIIG Biagi, I Giorgi, O Livi, et al.
Thrombosis and Haemostasis|December 29, 1989
Association of reduced factor VIII with impaired platelet reactivity to adrenalin and collagen after total thyroidectomyG Palareti, G Biagi, C Legnani, et al.
European Journal of Medicinal Chemistry|August 26, 2000
5-(4'-Substituted-2'-nitroanilino)-1,2,3-triazoles as new potential potassium channel activators. IG Biagi, V Calderone, I Giorgi, et al.
Farmaco (Societa Chimica Italiana : 1989)|November 1, 1990
Studies on 1,2,3-triazole derivatives as in vitro inhibitors of prostaglandin synthesisG Biagi, G Dell'Omodarme, M Ferretti, et al.
Thorax|October 1, 1992
Air transport and the fate of pneumothorax in pleural adhesionsM M Haid, P Paladini, M Maccherini, et al.
Farmaco (Societa Chimica Italiana : 1989)|January 5, 2002
Some structural changes on triazolyl-benzotriazoles and triazolyl-benzimidazolones as potential potassium channel activators. IIIG Biagi, V Calderone, I Giorgi, et al.
Pageof 10

Showing results (61-70 of 95) with videos related to

Sort By:
Pageof 10
Farmaco (Societa Chimica Italiana : 1989)|August 1, 1996
1,2,3-Triazolo [4,5-d] pyridazines--V. Preparation and adenosine receptor binding of new 4-amino derivativesG Biagi, I Giorgi, O Livi, et al.
Farmaco (Societa Chimica Italiana : 1989)|October 1, 1995
N(6) or N(9) substituted 2-phenyl-8-azaadenines: affinity for A1 adenosine receptors. VIIG Biagi, I Giorgi, O Livi, et al.
Drug Design and Discovery|May 1, 1997
A 3D model of the human A1 adenosine receptor. An evaluation of the binding free-energy with ligandsA M Bianucci, M U Bigi, G Biagi, et al.
Farmaco (Societa Chimica Italiana : 1989)|March 1, 1994
N(6)-substituted 2-phenyl-9-benzyl-8-azaadenines. Affinity for adenosine A1 and A2 receptors. A comparison with 2-N-butyl analogous derivatives. VG Biagi, I Giorgi, O Livi, et al.
Farmaco (Societa Chimica Italiana : 1989)|February 1, 1994
2-Aryl-8-azaadenosines: structure-activity relationships in the binding with A1 and A2 receptors. A comparison with the corresponding 9-benzyl-8-azaadenines. IIIG Biagi, I Giorgi, O Livi, et al.
Thrombosis and Haemostasis|December 29, 1989
Association of reduced factor VIII with impaired platelet reactivity to adrenalin and collagen after total thyroidectomyG Palareti, G Biagi, C Legnani, et al.
European Journal of Medicinal Chemistry|August 26, 2000
5-(4'-Substituted-2'-nitroanilino)-1,2,3-triazoles as new potential potassium channel activators. IG Biagi, V Calderone, I Giorgi, et al.
Farmaco (Societa Chimica Italiana : 1989)|November 1, 1990
Studies on 1,2,3-triazole derivatives as in vitro inhibitors of prostaglandin synthesisG Biagi, G Dell'Omodarme, M Ferretti, et al.
Thorax|October 1, 1992
Air transport and the fate of pneumothorax in pleural adhesionsM M Haid, P Paladini, M Maccherini, et al.
Farmaco (Societa Chimica Italiana : 1989)|January 5, 2002
Some structural changes on triazolyl-benzotriazoles and triazolyl-benzimidazolones as potential potassium channel activators. IIIG Biagi, V Calderone, I Giorgi, et al.
Pageof 10