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. Author manuscript; available in PMC: 2011 Nov 15.
Published in final edited form as: Bioorg Med Chem Lett. 2010 Sep 19;20(22):6394–6399. doi: 10.1016/j.bmcl.2010.09.088

Table 1.

Inhibition of hAMPK (α2, β1, γ1) by pyrazolopyrimidines

graphic file with name nihms238174t1.jpg
No. R1 R2 IC50(µM)a
1 graphic file with name nihms238174t2.jpg graphic file with name nihms238174t3.jpg 7.7
2 graphic file with name nihms238174t4.jpg graphic file with name nihms238174t5.jpg 3.5
3 graphic file with name nihms238174t6.jpg graphic file with name nihms238174t7.jpg 1.8
4 graphic file with name nihms238174t8.jpg graphic file with name nihms238174t9.jpg 0.28
5 graphic file with name nihms238174t10.jpg graphic file with name nihms238174t11.jpg 0.06
6 graphic file with name nihms238174t12.jpg graphic file with name nihms238174t13.jpg 0.27
7 graphic file with name nihms238174t14.jpg graphic file with name nihms238174t15.jpg 0.14
8 graphic file with name nihms238174t16.jpg graphic file with name nihms238174t17.jpg 0.22
9 graphic file with name nihms238174t18.jpg graphic file with name nihms238174t19.jpg 2.1
10 graphic file with name nihms238174t20.jpg graphic file with name nihms238174t21.jpg 2.2
11 graphic file with name nihms238174t22.jpg graphic file with name nihms238174t23.jpg 1.1
a

values were measured using the Hot Spot™ filtration binding 33P Kinase assay, Reaction Biology, Malvern, PA. Compounds were tested in ten-dose IC50 mode with three-fold dilutions starting at 10 µM. All reactions were carried out in the presence of 10 µM ATP.