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Neurochemical Research|October 1, 1994
Solubilization and characterization of [3H]imipramine and [3H]paroxetine binding sites from calf striatumA Rotondo, G Giannaccini, C Quattrone, et al.Life Sciences|January 1, 1990
Stress-related changes of benzodiazepine binding inhibitory activity (B.B.I.A.) in humansD Marazziti, S Michelini, G Giannaccini, et al.Receptors & Channels|January 1, 1993
Novel adenosine receptor ligands: 1,3-disubstituted[1]benzopyrano[2,3-c]pyrazol-4-ones. Synthesis and structure-activity relationshipsV Colotta, L Cecchi, D Catarzi, et al.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)|March 1, 1990
Specific inhibition of benzodiazepine receptor binding by some N-(2-methyl or 1,2-dimethylindol-3-ylglyoxylyl)amino acid derivativesG Primofiore, A M Marini, F Da Settimo, et al.Farmaco (Societa Chimica Italiana : 1989)|August 1, 1993
Tricyclic heteroaromatic systems pyrazolo[1,5-a]quinoxalines: synthesis and benzodiazepine receptor activityV Colotta, L Cecchi, D Catarzi, et al.Journal of Medicinal Chemistry|January 1, 1987
3-[(2-ethoxyphenoxy)methyl]piperidine derivatives. Synthesis and antidepressant activityA Balsamo, I Giorgi, A Lapucci, et al.Il Farmaco; Edizione Scientifica|August 1, 1986
Synthesis of new 6H-indolo[2,3-b] [1,8]naphthyridines and their specific inhibition of benzodiazepine receptorA Da Settimo, G Primofiore, P L Ferrarini, et al.Journal of Medicinal Chemistry|September 2, 1994
Structure-activity relationships of 1,2,4-triazolo[1,5-a] quinoxalines and their 1-deaza analogues imidazo[1,2-a]quinoxalines at the benzodiazepine receptorD Catarzi, L Cecchi, V Colotta, et al.Pageof 51