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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 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.
Journal of Medicinal Chemistry|April 5, 2002
Structure-activity relationships in 1,4-benzodioxan-related compounds. 7. Selectivity of 4-phenylchroman analogues for alpha(1)-adrenoreceptor subtypesWilma Quaglia, Maria Pigini, Alessandro Piergentili, 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.
European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences|March 30, 2018
Ex-vivo absorption study of lysine R-lipoate salt, a new pharmaceutical form of R-ALAFrancesco Amenta, Michela Buccioni, Diego Dal Ben, et al.
Cells|March 12, 2025
A2A Adenosine Receptor Antagonists and Their Efficacy in Rat Models of Parkinson's DiseaseAndrea Spinaci, Michela Buccioni, Diego Dal Ben, et al.
European Journal of Medicinal Chemistry|July 8, 2010
1,3-Dioxolane-based ligands incorporating a lactam or imide moiety: structure-affinity/activity relationship at alpha1-adrenoceptor subtypes and at 5-HT1A receptorsSilvia Franchini, Adolfo Prandi, Annamaria Baraldi, et al.
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