Table 1.
Inhibition of hAMPK (α2, β1, γ1) by pyrazolopyrimidines
![]() | |||
|---|---|---|---|
| No. | R1 | R2 | IC50(µM)a |
| 1 | 7.7 | ||
| 2 | ![]() |
3.5 | |
| 3 | ![]() |
![]() |
1.8 |
| 4 | ![]() |
![]() |
0.28 |
| 5 | ![]() |
![]() |
0.06 |
| 6 | ![]() |
![]() |
0.27 |
| 7 | ![]() |
![]() |
0.14 |
| 8 | ![]() |
![]() |
0.22 |
| 9 | ![]() |
![]() |
2.1 |
| 10 | ![]() |
![]() |
2.2 |
| 11 | ![]() |
![]() |
1.1 |
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.



















