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Journal of Medicinal Chemistry|September 2, 1994
8-Azaxanthine derivatives as antagonists of adenosine receptorsP Franchetti, L Messini, L Cappellacci, 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.Farmaco (Societa Chimica Italiana : 1989)|October 1, 1991
Tricyclic heteroaromatic systems. Synthesis of 1,3 and 1,2 disubstituted [1]benzopyrano[4,3-b]pyrrol-4-ones and structure-activity relationships as benzodiazepine receptor ligandsV Colotta, L Cecchi, F Melani, et al.Journal of Medicinal Chemistry|September 1, 1990
Tricyclic heteroaromatic systems. [1]benzopyranopyrrol-4-ones and [1]benzopyrano-1,2,3-triazol-4-ones as benzodiazepine receptor ligands. Synthesis and structure-activity relationshipsV Colotta, L Cecchi, F Melani, et al.Life Sciences|March 29, 2000
Effect of noise exposure on rat cardiac peripheral benzodiazepine receptorsF Salvetti, B Chelli, M Gesi, et al.Journal of Pharmaceutical Sciences|March 1, 1991
Tricyclic heteroaromatic systems: [1]benzopyrano-pyrazol-4-ones as benzodiazepine receptor ligandsV Colotta, L Cecchi, F Melani, et al.Journal of Pharmaceutical Sciences|December 1, 1986
Pyrazolo[4,5-c]quinolines. 3. Synthesis, receptor binding, and 13C NMR studyF Melani, L Cecchi, G Palazzino, 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)|June 1, 1989
Dipyrazolo[5,4-b:3',4'-d]pyridines. Synthesis, inhibition of benzodiazepine receptor binding and structure-activity relationshipsF Melani, L Cecchi, V Colotta, et al.Pageof 51