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Journal of Medicinal Chemistry|May 10, 2012
Water-soluble pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidines as human A₃ adenosine receptor antagonistsPier Giovanni Baraldi, Giulia Saponaro, Romeo Romagnoli, et al.Journal of Medicinal Chemistry|June 17, 2011
New 2-heterocyclyl-imidazo[2,1-i]purin-5-one derivatives as potent and selective human A3 adenosine receptor antagonistsPier Giovanni Baraldi, Delia Preti, Abdel Naser Zaid, et al.Bioorganic & Medicinal Chemistry|December 21, 2011
Structure-activity relationships of 2-amino-3-aroyl-4-[(4-arylpiperazin-1-yl)methyl]thiophenes. Part 2: Probing the influence of diverse substituents at the phenyl of the arylpiperazine moiety on allosteric enhancer activity at the A₁ adenosine receptorRomeo Romagnoli, Pier Giovanni Baraldi, Maria Dora Carrion, et al.Journal of Medicinal Chemistry|September 3, 2014
Synthesis and biological evaluation of novel allosteric enhancers of the A1 adenosine receptor based on 2-amino-3-(4'-chlorobenzoyl)-4-substituted-5-arylethynyl thiopheneRomeo Romagnoli, Pier Giovanni Baraldi, Adriaan P IJzerman, et al.Pageof 4