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Current Medicinal Chemistry|January 11, 2005
Non peptidic alphavbeta3 antagonists: recent developmentsBarbara Cacciari, Giampiero SpallutoMini Reviews in Medicinal Chemistry|April 26, 2018
A2A Adenosine Receptor Antagonists as Therapeutic Candidates: Are They Still an Interesting Challenge?Barbara Cacciari, Giampiero Spalluto, Stephanie FedericoCurrent Topics in Medicinal Chemistry|February 7, 2003
Medicinal chemistry of A2A adenosine receptor antagonistsBarbara Cacciari, Giorgia Pastorin, Giampiero SpallutoJournal of Medicinal Chemistry|September 2, 2005
Autocorrelation of molecular electrostatic potential surface properties combined with partial least squares analysis as new strategy for the prediction of the activity of human A(3) adenosine receptor antagonistsStefano Moro, Magdalena Bacilieri, Barbara Cacciari, et al.Future Medicinal Chemistry|November 7, 2023
Chemical and biological versatility of pyrazolo[3,4-d]pyrimidines: one scaffold, multiple modes of actionAlessandro Trentini, Stefania Hanau, Maria Cristina Manfrinato, et al.Journal of Pharmaceutical Sciences|September 17, 2010
Solid lipid microparticles for the stability enhancement of a dopamine prodrugAlessandro Dalpiaz, Barbara Cacciari, Matteo Mezzena, et al.Future Medicinal Chemistry|July 12, 2021
Thio-substituted derivatives of 4-amino-pyrazolo[3,4-d]pyrimidine-6-thiol as antiproliferative agentsBarbara Cacciari, Romeo Romagnoli, Arianna Romani, et al.Mini Reviews in Medicinal Chemistry|December 27, 2005
A2B adenosine receptor antagonists: recent developmentsBarbara Cacciari, Giorgia Pastorin, Chiara Bolcato, et al.The Journal of Organic Chemistry|March 8, 1996
Synthesis and Properties of Substituted CBI Analogs of CC-1065 and the Duocarmycins Incorporating the 7-Methoxy-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (MCBI) Alkylation Subunit: Magnitude of Electronic Effects on the Functional ReactivityDale L. Boger, Jeffrey A. McKie, Hui Cai, et al.Current Topics in Medicinal Chemistry|May 7, 2016
Pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidines and Structurally Simplified Analogs. Chemistry and SAR Profile as Adenosine Receptor AntagonistsSara Redenti, Antonella Ciancetta, Giorgia Pastorin, et al.Pageof 5