Skip to main content
. Author manuscript; available in PMC: 2014 Dec 1.
Published in final edited form as: Biochem Pharmacol. 2013 Sep 7;86(11):10.1016/j.bcp.2013.08.063. doi: 10.1016/j.bcp.2013.08.063

Fig. 4.

Fig. 4

Concentration-dependent inhibition of hENT4 adenosine transport by the most potent dipyridamole analogues. Graded concentrations of test compounds were incubated with cells for 15 min prior to addition of [3H]adenosine for an uptake period of 2 min. Data are presented as percent inhibition relative to vehicle control (mean ± S.D.; n = 3). Compounds shown are the ones with IC50s ≤ 200 nM for hENT4.