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Bioorganic & Medicinal Chemistry|October 15, 2010
Molecular modeling study on potent and selective adenosine A(3) receptor agonistsDiego Dal Ben, Michela Buccioni, Catia Lambertucci, et al.Bioorganic Chemistry|January 31, 2026
Adenine nucleotides as potent and selective GPR17 modulatorsDiego Dal Ben, Catia Lambertucci, Michela Buccioni, et al.Expert Opinion on Therapeutic Patents|April 7, 2022
A patent review of adenosine A2B receptor antagonists (2016-present)Beatrice Francucci, Diego Dal Ben, Catia Lambertucci, et al.Journal of Medicinal Chemistry|January 7, 2005
Design, synthesis, and biological evaluation of prazosin-related derivatives as multipotent compoundsAlessandra Antonello, Patrizia Hrelia, Amedeo Leonardi, et al.European Journal of Pharmacology|October 11, 2005
(+)-Cyclazosin, a selective alpha1B-adrenoceptor antagonist: functional evaluation in rat and rabbit tissuesGabriella Marucci, Piero Angeli, Michela Buccioni, et al.Journal of Medicinal Chemistry|April 4, 2003
1,3-dioxolane-based ligands as a novel class of alpha1-adrenoceptor antagonistsLivio Brasili, Claudia Sorbi, Silvia Franchini, et al.Molecules (Basel, Switzerland)|March 6, 2021
Combined Therapy of A1AR Agonists and A2AAR Antagonists in NeuroinflammationGabriella Marucci, Diego Dal Ben, Catia Lambertucci, et al.Current Medicinal Chemistry|February 21, 2022
A2A Adenosine Receptor Antagonists and their Potential in Neurological DisordersCatia Lambertucci, Gabriella Marucci, Daniela Catarzi, et al.Expert Opinion on Therapeutic Patents|November 16, 2019
Update on novel purinergic P2X3 and P2X2/3 receptor antagonists and their potential therapeutic applicationsGabriella Marucci, Diego Dal Ben, Michela Buccioni, et al.Medicinal Chemistry (Shariqah (United Arab Emirates))|March 14, 2008
Synthesis and pharmacological profile of a series of 1-substituted-2-carbonyl derivatives of Diphenidol: novel M4 muscarinic receptor antagonistsLucilla Varoli, Piero Angeli, Michela Buccioni, et al.Pageof 11