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Medicinal Research Reviews|March 31, 2015
History and perspectives of A2A adenosine receptor antagonists as potential therapeutic agentsDelia Preti, Pier Giovanni Baraldi, Allan R Moorman, et al.Future Medicinal Chemistry|July 7, 2015
Current status of A1 adenosine receptor allosteric enhancersRomeo Romagnoli, Pier Giovanni Baraldi, Allan R Moorman, et al.Journal of Pain Research|November 21, 2012
Skin permeability and pharmacokinetics of diclofenac epolamine administered by dermal patch in Yorkshire-Landrace pigsSusanna Tse, Kendall D Powell, Stephen J Maclennan, et al.European Journal of Medicinal Chemistry|October 7, 2004
Synthesis of 2-amino-3-heteroaroylthiophenes and evaluation of their activity as potential allosteric enhancers at the human A1 receptorPier Giovanni Baraldi, Maria Giovanna Pavani, John C Shryock, et al.Farmaco (Societa Chimica Italiana : 1989)|March 24, 2005
New heterocyclic ligands for the adenosine receptors P1 and for the ATP receptors P2Pier Giovanni Baraldi, Romeo Romagnoli, Mojgan Aghazadeh Tabrizi, et al.Bioorganic & Medicinal Chemistry Letters|December 3, 2005
Synthesis and biological characterization of [3H] (2-amino-4,5,6,7-tetrahydrobenzo[b]thiophen-3-yl)-(4-chlorophenyl)-methanone, the first radiolabelled adenosine A1 allosteric enhancerPier Giovanni Baraldi, Maria Giovanna Pavani, Edward Leung, et al.Bioorganic & Medicinal Chemistry|December 30, 2011
Pyrrolo- and pyrazolo-[3,4-e][1,2,4]triazolo[1,5-c]pyrimidines as adenosine receptor antagonistsPier Giovanni Baraldi, Giulia Saponaro, Mojgan Aghazadeh Tabrizi, et al.Bioorganic & Medicinal Chemistry|September 3, 2003
New strategies for the synthesis of A3 adenosine receptor antagonistsPier Giovanni Baraldi, Andrea Bovero, Francesca Fruttarolo, et al.Biochemical and Biophysical Research Communications|January 4, 2006
Triglyceride modulation by acifran analogs: activity towards the niacin high and low affinity G protein-coupled receptors HM74A and HM74Keyvan Mahboubi, Terri Witman-Jones, Jean E Adamus, et al.Journal of Medicinal Chemistry|July 8, 2005
New pyrrolo[2,1-f]purine-2,4-dione and imidazo[2,1-f]purine-2,4-dione derivatives as potent and selective human A3 adenosine receptor antagonistsPier Giovanni Baraldi, Delia Preti, Mojgan Aghazadeh Tabrizi, et al.Pageof 4