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European Journal of Medicinal Chemistry|July 4, 2014
High affinity ligands and potent antagonists for the α1D-adrenergic receptor. Novel 3,8-disubstituted [1]benzothieno[3,2-d]pyrimidine derivativesGiuseppe Romeo, Loredana Salerno, Valeria Pittalà, et al.Chemmedchem|April 3, 2016
The Length and Flexibility of the 2-Substituent of 9-Ethyladenine Derivatives Modulate Affinity and Selectivity for the Human A2A Adenosine ReceptorAjiroghene Thomas, Michela Buccioni, Diego Dal Ben, et al.Biochemical Pharmacology|October 29, 2013
Different efficacy of adenosine and NECA derivatives at the human A3 adenosine receptor: insight into the receptor activation switchDiego Dal Ben, Michela Buccioni, Catia Lambertucci, et al.Bioorganic & Medicinal Chemistry Letters|February 27, 2010
Discovery of a new series of 5-HT1A receptor agonistsSilvia Franchini, Adolfo Prandi, Claudia Sorbi, et al.Bioorganic & Medicinal Chemistry Letters|April 4, 2020
New 8-amino-1,2,4-triazolo[4,3-a]pyrazin-3-one derivatives. Evaluation of different moieties on the 6-aryl ring to obtain potent and selective human A2A adenosine receptor antagonistsMatteo Falsini, Costanza Ceni, Daniela Catarzi, et al.ACS Medicinal Chemistry Letters|April 19, 2019
Investigation on 2',3'-O-Substituted ATP Derivatives and Analogs as Novel P2X3 Receptor AntagonistsDiego Dal Ben, Michela Buccioni, Catia Lambertucci, et al.Bioorganic & Medicinal Chemistry Letters|October 10, 2006
New pyrimido[5,4-b]indoles and [1]benzothieno[3,2-d]pyrimidines: high affinity ligands for the alpha(1)-adrenoceptor subtypesGiuseppe Romeo, Luisa Materia, Gabriella Marucci, et al.Bioorganic Chemistry|August 26, 2019
New A2A adenosine receptor antagonists: a structure-based upside-down interaction in the receptor cavityCatia Lambertucci, Andrea Spinaci, Michela Buccioni, et al.Drug Metabolism Letters|April 10, 2009
In vitro metabolism studies of new adenosine A 2A receptor antagonistsGabriella Marucci, Sara Finaurini, Michela Buccioni, et al.Journal of Medicinal Chemistry|November 19, 2019
Structure-Based Optimization of Coumarin hA3 Adenosine Receptor AntagonistsMaria João Matos, Santiago Vilar, Saleta Vazquez-Rodriguez, et al.Pageof 10