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Cat. No. Product Name Information
PC-60188

Olomoucine

CDK inhibitor

Olomoucine is a potent, ATP-competetive CDKs inhibitor with IC50 of 7, 7, 7, 3 uM for Cdc2/cyclin B, Cdk2/cyclin A, Cdk2/cyclin E, and Cdk/p35 kinase.
PC-42103

M2I-1

Mad2 inhibitor

M2I-1 is the first small molecule Mad2 inhibitor that targets the binding of Mad2 to Cdc20.
PC-45559

NU-6300

CDK2 inhibitor

NU-6300 is the first covalent, irreversible, ATP-Competitive CDK2 inhibitor with Ki of 6 nM.
PC-45599

NU-2058

CDK1/2 inhibitor

NU-2058 is an ATP-competitive inhibitor of CDK1 and CDK2 with Ki of 5 uM and 12 uM respectively.
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).

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