| Cat. No. |
Product Name |
Information |
| PC-60298 |
MSC2530818
CDK8 inhibitor
|
MSC-2530818 (MSC 2530818, MSC2530818) is a potent, selective, and orally bioavailable CDK8 inhibitor with IC50 of 2.6 nM. |
| PC-45559 |
NU-6300
CDK2 inhibitor
|
NU-6300 is the first covalent, irreversible, ATP-Competitive CDK2 inhibitor with Ki of 6 nM. |
| PC-44628 |
Senexin-A
CDK8/CDK19 inhibitor
|
Senexin-A is a selective inhibitor of CDK8 (IC50=0.28 uM) and CDK19, inhibits CDK8 and CDK19 ATP site binding with Kd50 of 0.83 uM and 0.31 uM, respectively. |
| PC-45491 |
SU-9516
CDK2 inhibitor
|
SU-9516 is a potent, selective CDK2 inhibitor with IC50 of 22 nM. |
| PC-46009 |
THZ1 hydrochloride
CDK7 inhibitor
|
THZ1 hydrochloride is a potent, selective, covalent CDK7 inhibitor with IC50 of 3.2 nM. |
| PC-46008 |
THZ1
CDK7 inhibitor
|
THZ1 is a potent, selective, covalent CDK7 inhibitor with IC50 of 3.2 nM, also weakly inhibits CDK12 with IC50 of 250 nM. |
| PC-42578 |
PHA-848125
CDK/TRK inhibitor
|
Milciclib (PHA-848125) is a potent, selective, brain penetrant and orally available dual CDK and TRK inhibitor with IC50 of 45 and 53 nM for CDK2/cyclin A and TrkA, respectively. |
| PC-45913 |
AT-7519 hydrochloride
CDK2 inhibitor
|
AT-7519 hydrochloride (AT7519) is a potent, selective CDK2 inhibitor with IC50 of 47 nM, also inhibits CDK1/4/5 with IC50 of 190/67/18 nM and shows selectivity over some kinases (Aurora A, IR kinase, MEK, PDK1, c-Abl, IC50>10 uM). |
| PC-45912 |
AT-7519 trifluoroacetate
CDK2 inhibitor
|
AT-7519 trifluoroacetate (AT7519) is a potent, selective CDK2 inhibitor with IC50 of 47 nM, also inhibits CDK1/4/5 with IC50 of 190/67/18 nM and shows selectivity over some kinases (Aurora A, IR kinase, MEK, PDK1, c-Abl, IC50>10 uM). |
| PC-45911 |
AT-7519
CDK2 inhibitor
|
AT-7519 (AT7519) is a potent, selective CDK2 inhibitor with IC50 of 47 nM, also inhibits CDK1/4/5 with IC50 of 190/67/18 nM and shows selectivity over some kinases (Aurora A, IR kinase, MEK, PDK1, c-Abl, IC50>10 uM). |
| PC-42052 |
SNS-032
CDK2/7/9 inhibitor
|
SNS-032 (BMS-387032) is a potent and selective inhibitor of CDK 2/7/9 with IC50 of 48 nM/62 nM/4 nM, respectively. |
| PC-42616 |
Dinaciclib
CDK inhibitor
|
Dinaciclib (SCH 727965) is a potent and selective CDK inhibitor with IC50 of 1, 1, 3 and 4 nM against CDK2, CDK5, CDK1 and CDK9, respectively. |
