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Showing results (21-30 of 42) with videos related to

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Farmaco (Societa Chimica Italiana : 1989)|December 1, 1996
New chiral inhibitors of induced platelet aggregation: the enantiomeric specificity of (R)- and (S)-methyl and ethyl esters of 1-(4-[(1-hydroxycarbonyl)-ethoxy]-benzyl)-1H-1,2,3-triazole as a tool for determining their biological targetG Biagi, I Giorgi, O Livi, et al.
Farmaco (Societa Chimica Italiana : 1989)|January 1, 1992
An 1,2,3-triazole derivative bioisoster of a potent in vitro prostaglandin synthesis inhibitor: preparation and biological activityG Biagi, G Dell'Omodarme, I Giorgi, et al.
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.
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.
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.
Farmaco (Societa Chimica Italiana : 1989)|January 1, 1995
Synthesis of new N(6)-substituted 2-phenyl-8-azaadenosines. Their affinity for adenosine A1 and A2 receptors. A comparison with the corresponding 2-phenyl-9-benzyl-8-azaadenines. VIG Biagi, I Giorgi, O Livi, et al.
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Showing results (21-30 of 42) with videos related to

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Pageof 5
Farmaco (Societa Chimica Italiana : 1989)|December 1, 1996
New chiral inhibitors of induced platelet aggregation: the enantiomeric specificity of (R)- and (S)-methyl and ethyl esters of 1-(4-[(1-hydroxycarbonyl)-ethoxy]-benzyl)-1H-1,2,3-triazole as a tool for determining their biological targetG Biagi, I Giorgi, O Livi, et al.
Farmaco (Societa Chimica Italiana : 1989)|January 1, 1992
An 1,2,3-triazole derivative bioisoster of a potent in vitro prostaglandin synthesis inhibitor: preparation and biological activityG Biagi, G Dell'Omodarme, I Giorgi, et al.
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.
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.
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.
Farmaco (Societa Chimica Italiana : 1989)|January 1, 1995
Synthesis of new N(6)-substituted 2-phenyl-8-azaadenosines. Their affinity for adenosine A1 and A2 receptors. A comparison with the corresponding 2-phenyl-9-benzyl-8-azaadenines. VIG Biagi, I Giorgi, O Livi, et al.
Pageof 5