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Cat. No. Product Name Information
PC-72776

Senexin C

CDK8/19 inhibitor

Senexin C is a novel potent, selective and orally bioavailable CDK8/19 inhibitor with Kd of 1.4 and 2.9 nM for CDK8/CycC and CDK19/CycC, respectively.
PC-72755

AS-0141

CDC7 inhibitor

Monzosertib (AS 0141) is a potent, selective, orally bioavailable CDC7 inhibitor with IC50 of 2.4 nM.
PC-72673

BRD6688

HDAC2 inhibitor

BRD6688 is a potent, kinetically selective HDAC2 inhibitor with IC50 of 21/100 nM for HDAC1/2, >115-fold selectivity versus HDAC3.
PC-72642

SY-1365

CDK7 inhibitor

SY-1365 (Mevociclib, SY1365) is a potent, selective, covalent CDK7 inhibitor with Ki of 17.4 nM.
PC-72637

CDDD2-94

CDK4 inhibitor

CDDD2-94 is a highly potent and selective CDK4 inhibitor with Ki of 2 nM, 140-fold more selective for CDK4 over CDK6 (Ki=279 nM).
PC-72622

PF-06842874

CDK4/6 inhibitor

PF-06842874 is a potent, selective CDK4/6 inhibitor.
PC-72467

LY3405105

CDK7 inhibitor

LY3405105 (LY-3405105) is a potent, selective, orally active CDK7 inhibitor with an IC50 of 92.8 nM, shows potential antineoplastic activity.
PC-72466

SY-5102

CDK7 inhibitor

SY-5102 (SY5102) is a highly potent, selective, noncovalent, orally available CDK7 inhibitor with SPR Kd of 0.03 nM (binding to CDK7/Cyclin H).
PC-72216

MFH290

CDK12/13 inhibitor

MFH290 (MFH-290) is a potent, highly selective, covalent inhibitor of CDK12/13 with IC50 of 25/49 nM.
PC-38299

(R)-CR8

CDK inhibitor

(R)-CR8 is a potent CDK1/2/5/7/9 inhibitor, inhibits CDK1/cyclin B (IC50, 90 nM), CDK2/cyclin A (72 nM), CDK2/cyclin E (41 nM), CDK5/p25 ( 110 nM), CDK7/cyclin H (1.1 uM), CDK9/cyclin T (0.18 uM) and CK1δ/ε (0.4 uM).
PC-38278

KB-0742

CDK9 inhibitor

KB-0742 (KB0742) is a potent, orally bioavailable, selective CDK9 inhibitor with IC50 of 6 nM (CDK9/cyclin T1 inhibition).
PC-38149

A-1592668

CDK9 inhibitor

A-1592668 (A 1592668) is a novel potent, CDK9-selective inhibitor with IC50 of 1.2 nM, >1000 fold selectivity over CDK1/2/7/8.

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