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. Author manuscript; available in PMC: 2010 Aug 25.
Published in final edited form as: J Med Chem. 2010 Feb 25;53(4):1799–1809. doi: 10.1021/jm901647p

Figure 5.

Figure 5

Inhibition of agonist-induced cAMP production by the A2AAR hit compounds. Activity is measured at 10 µM concentration of the compounds, as compared to no compound in the control. Data is normalized where 0 % represents the unstimulated condition (black bars) and 100 % represents the accumulation of intracellular cAMP observed for stimulation with compound 3a at 10 nM or 10 µM concentrations (shaded and open bars respectively).