| Cat. No. |
Product Name |
Information |
| PC-61659 |
SEL120-34A hydrochloride
CDK8/19 inhibitor
|
Romaciclib (SEL120-34A, SEL120) hydrochloride is an ATP-competitive, selective, orally active CDK8/19 inhibitor that inhibits kinase activities of CDK8/CycC and CDK19/CycC complexes with IC50 of 4.4 nM and 10.4 nM, respectively. |
| PC-61658 |
SEL120-34A
CDK8/19 inhibitor
|
Romaciclib (SEL120-34A) is an ATP-competitive, selective, orally active CDK8/19 inhibitor that inhibits kinase activities of CDK8/CycC and CDK19/CycC complexes with IC50 of 4.4 nM and 10.4 nM, respectively. |
| PC-61405 |
AZ5576
CDK9 inhibitor
|
AZ5576 (AZ-5576) is a potent, highly selective, and orally bioavailable inhibitor of CDK9 with IC50 of < 5 nM, decreases phosphorylation of Ser2-RNAPII in cells with an IC50 of 96 nM. |
| PC-61279 |
Riviciclib
CDK inhibitor
|
Riviciclib (P276-00 hydrochloride) is a potent CDK inhibitor with IC50 of 79 nM, 63 nM and 20 nM for Cdk4/cyclin D1, Cdk1/cyclin B and Cdk9/cyclin T1, respectively. |
| PC-61248 |
CYC065
CDK2/9 inhibitor
|
CYC065 (Fadraciclib) is a derivative of seliciclib and second generation CDK inhibitor with IC50 of 5/26 nM for CDK2/9. |
| PC-61246 |
Roniciclib
CDK inhibitor
|
Roniciclib (BAY 1000394) is a potent, orally active, pan-CDK inhibitor with IC50 of 7/9/11 nM for CDK1/2/4 respectively, inhibits transcriptional CDK9/7 with IC50 of 5-25 nM. |
| PC-61180 |
CDK7 and 9 inhibitor 14
CDK7/9 inhibitor
|
CDK7/9-IN-14 is a potent, selective transcriptional CDK inhibitor with Ki of 2.3 and 0.38 nM for CDK7 and CDK9, respectively. |
| PC-61146 |
CCT-251921
CDK8/CDK19 inhibitor
|
CCT-251921 (CCT251921) is a potent, selective, and orally bioavailable inhibitor of CDK8 and CDK19 with IC50of 2.3 nM and 2.6 nM respectively. |
| PC-61143 |
AZD 5597
CDK1/2 inhibitor
|
AZD 5597 is a highly potent cyclin-dependent kinase (CDK) inhibitor with IC50 of 2 nM for both CDK1 and CDK2. |
| PC-61136 |
CDK2 inhibitor 73
CDK2 inhibitor
|
CDK2 inhibitor 73 (CDK2-IN-4) is a potent, selective CDK2 inhibitor with IC50 of 44 nM for CDK2/cyclin A, displays 2,000-fold selectivity over CDK1/cyclin B (IC50=86 uM). |
| PC-61031 |
Voruciclib
CDK9 inhibitor
|
Voruciclib (P1446A-05) is a potent, selective and orally bioavailable CDK9 inhibitor with Ki of 0.63 nM and 1.68 nM for CDK9/cyclinT2 and CDK9/cyclinT1, respectively. |
| PC-61020 |
Cdc7 inhibitor 7c
Cdc7 inhibitor
|
Cdc7 inhibitor 7c (Cdc7-IN-7c) is a highly potent, selective and time-dependent Cdc7 kinase inhibitor with IC50 of 0.7 nM with slow dissociation property, with 200-fold and >14,000-fold selectivity over CDK2 and ROCK1, respectively. |
