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Pharmaceuticals (Basel, Switzerland)|October 11, 2019
Non-Nucleoside Agonists of the Adenosine Receptors: An OverviewDiego Dal Ben, Catia Lambertucci, Michela Buccioni, et al.
European Journal of Medicinal Chemistry|October 12, 2010
Synthesis and α1-adrenoceptor antagonist activity of tamsulosin analoguesGianni Sagratini, Piero Angeli, Michela Buccioni, et al.
Bioorganic & Medicinal Chemistry|March 12, 2002
Structure--activity relationships among novel phenoxybenzamine-related beta-chloroethylaminesDario Giardinà, Mauro Crucianelli, Piero Angeli, et al.
Expert Opinion on Therapeutic Patents|January 15, 2019
GPR17 receptor modulators and their therapeutic implications: review of recent patentsGabriella Marucci, Diego Dal Ben, Catia Lambertucci, et al.
FEBS Letters|March 8, 2006
Endocannabinoid system in Xenopus laevis development: CB1 receptor dynamicsBeatrice Migliarini, Migliarini Beatrice, Gabriella Marucci, et al.
Cells|July 11, 2025
Radioligands Targeting the Purinergic P2X ReceptorsDiego Dal Ben, Michela Buccioni, Catia Lambertucci, et al.
Mini Reviews in Medicinal Chemistry|August 13, 2016
Overview on Radiolabel-Free in vitro Assays for GPCRsMichela Buccioni, Claudia Santinelli, Piero Angeli, et al.
Purinergic Signalling|October 21, 2016
2',3'-O-Substituted ATP derivatives as potent antagonists of purinergic P2X3 receptors and potential analgesic agentsDiego Dal Ben, Anna Marchenkova, Ajiroghene Thomas, et al.
Chemmedchem|January 21, 2010
Molecular modeling studies on the human neuropeptide S receptor and its antagonistsDiego Dal Ben, Ippolito Antonini, Michela Buccioni, et al.
Bioorganic & Medicinal Chemistry Letters|January 15, 2019
Novel human adenosine receptor antagonists based on the 7-amino-thiazolo[5,4-d]pyrimidine scaffold. Structural investigations at the 2-, 5- and 7-positions to enhance affinity and tune selectivityFlavia Varano, Daniela Catarzi, Matteo Falsini, et al.
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