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Cat. No. Product Name Information
PC-45862

Palbociclib

CDK4/6 inhibitor

Palbociclib (PD0332991) is a potent and selective, orally bioavailable inhibitor of CDK4/6 with IC50 of 11 nM/16 nM.
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.
PC-45792

Roscovitine

CDK inhibitor

Roscovitine ((R)-Roscovitine, Seliciclib, CYC202) is a potent and selective CDK inhibitor with IC50 of 0.2 uM, 0.65 uM, and 0.7 uM for CDK5, Cdc2, and CDK2, respectively.
PC-42036

LY3177833

CDC7 inhibitor

LY3177833 is a potent and selective CDC7 inhibitor with IC50 of 3.3 nM.
PC-42060

AZD-5438

CDK1/2/9 inhibitor

AZD-5438 (AZD5438) potent and oral inhibitor of CDK1/2/9 with IC50 of 16/6/20 nM, respectively.
PC-42425

Senexin B

CDK8/CDK19 inhibitor

Senexin B (SNX2-1-165) is a highly potent, selective and orally available CDK8/CDK19 inhibitor with IC50 of 24-50 nM.
PC-42527

JNJ-7706621

CDK/Aurora inhibitor

JNJ-7706621 is a potent, dual CDK/Aurora kinase inhibitor with IC50 of 9/4/11/15 nM for CDK1/CDK2/Aurora A/Aurora B respectively.
PC-23612

KY-065

CDK8 inhibitor

KY-065 is a potent, selective and ATP-competitive CDK8/19 inhibitor with IC50 of 4.4/3.6 nM respectively, without affecting the activities of other CDK family members.
PC-23502

BSJ-01-175

CDK12/13 inhibitor

BSJ-01-175 is a potent, selective dual CDK12/13 covalent inhibitor with IC50 of 156 nM (CDK12/CycK) and 282.6 nM(CDK3/CycK), targets cysteine Cys1039 on CDK12 (or Cys1017 on CDK13).
PC-23151

CDK-TCIP2

CDK-TCIP2 is a bivalent molecule linking CDK9 inhibitor SNS-032 to BCL6 ligand BI3812, activates BCL6-regulated transcription, potently and specifically kills BCL6-overexpressing cells with EC50 of 0.9 nM for SUDHL5 cells.
PC-23150

CDK-TCIP1

3008612-35-6

CDK-TCIP1 is a bivalent molecule linking CDK9 inhibitor SNS-032 to BCL6 ligand BI3812, potently and specifically kills BCL6-overexpressing cells with EC50 of 7.7 nM for SUDHL5 cells.

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