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Journal of Medicinal Chemistry|August 24, 2000
Synthesis and structure-activity relationships of a new set of 2-arylpyrazolo[3,4-c]quinoline derivatives as adenosine receptor antagonistsV Colotta, D Catarzi, F Varano, et al.Journal of Medicinal Chemistry|March 29, 2000
1,2,4-Triazolo[4,3-a]quinoxalin-1-one: a versatile tool for the synthesis of potent and selective adenosine receptor antagonistsV Colotta, D Catarzi, F Varano, et al.Farmaco (Societa Chimica Italiana : 1989)|April 1, 1993
Reaction of 1-aminophthalazines with alpha-halocarbonyl compounds: imidazo[2,1-a]phthalazines and their benzodiazepine receptor activitiesD Catarzi, L Cecchi, V Colotta, et al.Drug Design and Discovery|July 1, 1992
Tricyclic heteroaromatic systems. Synthesis and benzodiazepine binding activity of 1-substituted-3-methyl- and 3-phenylpyrazolo[4,5-c]quinolin-4-onesV Colotta, L Cecchi, F Melani, et al.Farmaco (Societa Chimica Italiana : 1989)|June 26, 1998
Synthesis and A1 and A2A adenosine binding activity of some pyrano[2,3-c]pyrazol-4-onesV Colotta, D Catarzi, F Varano, et al.Journal of Chemical Information and Modeling|August 29, 2007
Tandem 3D-QSARs approach as a valuable tool to predict binding affinity data: design of new Gly/NMDA receptor antagonists as a key studyM Bacilieri, F Varano, F Deflorian, et al.Pageof 5