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V Scartoni

Showing results (1-10 of 42) with videos related to

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Mini Reviews in Medicinal Chemistry|November 27, 2009
8-azapurine nucleus: a versatile scaffold for different targetsI Giorgi, V Scartoni
Il Farmaco; Edizione Scientifica|April 1, 1987
Studies on 1,2,3-triazole derivatives as potential inhibitors of the cyclo-oxygenaseG Biagi, O Livi, V Scartoni
Farmaco (Societa Chimica Italiana : 1989)|June 1, 1996
N(9)-Substituted 2-phenyl-N(6)-benzyl-8-azaadenines: A1 adenosine receptor affinity. A comparison with the corresponding N(6)-substituted 2-phenyl-N(9)-benzyl-8-azaadeninesG Biagi, I Giorgi, O Livi, et al.
Il Farmaco; Edizione Scientifica|July 1, 1988
1,2,3-Triazoles: structural changes on two effective inhibitors of the prostaglandin synthesis in vitroG Biagi, O Livi, V Scartoni, et al.
Farmaco (Societa Chimica Italiana : 1989)|May 1, 1992
Synthesis and ADA inhibitory activity of new 2-aryl-8-azaadenosines. VIIIG Biagi, I Giorgi, O Livi, et al.
Farmaco (Societa Chimica Italiana : 1989)|September 1, 1989
Modification of the 1,2,3-triazole ring present in an effective in vitro inhibitor of the prostaglandin synthesisF Andreini, G Biagi, I Giorgi, et al.
Farmaco (Societa Chimica Italiana : 1989)|January 5, 2002
2-Alkyloxyalkylthiohypoxanthines as new potent inhibitors of xanthine oxidaseG Biagi, I Giorgi, F Pacchini, et al.
Journal of Pharmaceutical Sciences|June 1, 1992
Specific inhibition of binding to benzodiazepine receptors by 1,2,3-triazole derivativesG Biagi, O Livi, A Lucacchini, et al.
Farmaco (Societa Chimica Italiana : 1989)|February 7, 2002
New 2-(2'-phenyl-9'-benzyl-8'-azapurin-6'-ylamino)-carboxylic acid methylesters as ligands for A1 adenosine receptorsG Biagi, I Giorgi, F Pacchini, et al.
Farmaco (Societa Chimica Italiana : 1989)|January 1, 1997
Synthesis of 4,6-disubstituted- and 4,5,6-trisubstituted-2-phenyl-pyrimidines and their affinity towards A1 adenosine receptorsG Biagi, I Giorgi, O Livi, et al.
Pageof 5

Showing results (1-10 of 42) with videos related to

Sort By:
Pageof 5
Mini Reviews in Medicinal Chemistry|November 27, 2009
8-azapurine nucleus: a versatile scaffold for different targetsI Giorgi, V Scartoni
Il Farmaco; Edizione Scientifica|April 1, 1987
Studies on 1,2,3-triazole derivatives as potential inhibitors of the cyclo-oxygenaseG Biagi, O Livi, V Scartoni
Farmaco (Societa Chimica Italiana : 1989)|June 1, 1996
N(9)-Substituted 2-phenyl-N(6)-benzyl-8-azaadenines: A1 adenosine receptor affinity. A comparison with the corresponding N(6)-substituted 2-phenyl-N(9)-benzyl-8-azaadeninesG Biagi, I Giorgi, O Livi, et al.
Il Farmaco; Edizione Scientifica|July 1, 1988
1,2,3-Triazoles: structural changes on two effective inhibitors of the prostaglandin synthesis in vitroG Biagi, O Livi, V Scartoni, et al.
Farmaco (Societa Chimica Italiana : 1989)|May 1, 1992
Synthesis and ADA inhibitory activity of new 2-aryl-8-azaadenosines. VIIIG Biagi, I Giorgi, O Livi, et al.
Farmaco (Societa Chimica Italiana : 1989)|September 1, 1989
Modification of the 1,2,3-triazole ring present in an effective in vitro inhibitor of the prostaglandin synthesisF Andreini, G Biagi, I Giorgi, et al.
Farmaco (Societa Chimica Italiana : 1989)|January 5, 2002
2-Alkyloxyalkylthiohypoxanthines as new potent inhibitors of xanthine oxidaseG Biagi, I Giorgi, F Pacchini, et al.
Journal of Pharmaceutical Sciences|June 1, 1992
Specific inhibition of binding to benzodiazepine receptors by 1,2,3-triazole derivativesG Biagi, O Livi, A Lucacchini, et al.
Farmaco (Societa Chimica Italiana : 1989)|February 7, 2002
New 2-(2'-phenyl-9'-benzyl-8'-azapurin-6'-ylamino)-carboxylic acid methylesters as ligands for A1 adenosine receptorsG Biagi, I Giorgi, F Pacchini, et al.
Farmaco (Societa Chimica Italiana : 1989)|January 1, 1997
Synthesis of 4,6-disubstituted- and 4,5,6-trisubstituted-2-phenyl-pyrimidines and their affinity towards A1 adenosine receptorsG Biagi, I Giorgi, O Livi, et al.
Pageof 5