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Current Medicinal Chemistry|January 11, 2005
Oligonucleotides and oligonucleotide conjugates: a new approach for cancer treatmentTatiana Da Ros, Giampiero Spalluto, Maurizio Prato, et al.
Chemmedchem|December 21, 2006
Highlights on the development of A(2A) adenosine receptor agonists and antagonistsGloria Cristalli, Barbara Cacciari, Diego Dal Ben, et al.
Purinergic Signalling|April 12, 2008
Pyrazolo-triazolo-pyrimidines as adenosine receptor antagonists: A complete structure-activity profileBarbara Cacciari, Chiara Bolcato, Giampiero Spalluto, et al.
Chemical Communications (Cambridge, England)|January 6, 2004
Demystifying the three dimensional structure of G protein-coupled receptors (GPCRs) with the aid of molecular modelingStefano Moro, Francesca Deflorian, Giampiero Spalluto, et al.
Purinergic Signalling|March 28, 2008
Pyrazolo-triazolo-pyrimidines as adenosine receptor antagonists: Effect of the N-5 bond type on the affinity and selectivity at the four adenosine receptor subtypesChiara Bolcato, Claudia Cusan, Giorgia Pastorin, et al.
Farmaco (Societa Chimica Italiana : 1989)|April 26, 2005
Synthesis, biological studies and molecular modeling investigation of 1,3-dimethyl-2,4-dioxo-6-methyl-8-(substituted) 1,2,3,4-tetrahydro [1,2,4]-triazolo [3,4-f]-purines as potential adenosine receptor antagonistsGiorgia Pastorin, Chiara Bolcato, Barbara Cacciari, et al.
Bioorganic & Medicinal Chemistry|March 28, 2006
The application of a 3D-QSAR (autoMEP/PLS) approach as an efficient pharmacodynamic-driven filtering method for small-sized virtual library: application to a lead optimization of a human A3 adenosine receptor antagonistStefano Moro, Magdalena Bacilieri, Barbara Cacciari, et al.
Medicinal Chemistry (Shariqah (United Arab Emirates))|February 9, 2019
Structure Activity Relationship of 4-Amino-2-thiopyrimidine Derivatives as Platelet Aggregation InhibitorsBarbara Cacciari, Pamela Crepaldi, Chun Yan Cheng, et al.
Nano Letters|June 10, 2005
Carbon nanotube substrates boost neuronal electrical signalingViviana Lovat, Davide Pantarotto, Laura Lagostena, et al.
Journal of Medicinal Chemistry|January 5, 2002
7-Substituted 5-amino-2-(2-furyl)pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines as A2A adenosine receptor antagonists: a study on the importance of modifications at the side chain on the activity and solubilityPier Giovanni Baraldi, Barbara Cacciari, Romeo Romagnoli, et al.
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