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Cat. No. Product Name Information
PC-70170

GW-8510

CDK2 inhibitor

GW-8510 (GW8510) is a potent, selective inhibitor of CDK2 with IC50 of 10 nM.
PC-70116

NU-6027

CDK1/2 inhibitor

NU-6027 (NU6027) is an ATP-competitive inhibitor of CDK1 and CDK2 with Ki of 2.5 uM and 1.3 uM respectively.
PC-70115

NU6102

CDK2 inhibitor

NU6102 is a potent CDK1 and CDK2 inhibitor with IC50 of 9.5 nM and 5.4 nM against CDK1/cyclinB and CDK2/cyclinA3 respectively.
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-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-43435

TAME

APC/C inhibitor

TAME (Tosyl-L-arginine methyl ester) is a small molecule anaphase-promoting complex/cyclosome (APC/C) inhibitor that binds to the APC preferentially suppresses APC/C(Cdc20) rather than APC/C(Cdh1).
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.

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