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Search results for: 'research area dna damage atm kinase'

Search results for: 'research area dna damage atm kinase'

A8385 BMS265246

Target: Cyclin-Dependent Kinases

Summary: CDK1/2 inhibitor,potent and selective

insoluble in H2O; insoluble in EtOH; ≥17.25 mg/mL
A8641 LEE011

Target: Cyclin-Dependent Kinases

Summary: CDK4/6 inhibitor

insoluble in H2O; insoluble in EtOH; ≥10.88 mg/mL
B3277 AMG 925

Target: Cyclin-Dependent Kinases|FLT3

Summary: FLT3/CDK4 inhibitor,potent and selective

insoluble in DMSO; insoluble in H2O; insoluble in EtOH
B3672 Indirubin

Target: Cyclin-Dependent Kinases|GSK-3

Summary: cyclin-dependent kinases and GSK-3β inhibitor

insoluble in H2O; insoluble in H2O; insoluble in EtOH; ≥13.1 mg/mL
A3721 PHA-767491

Target: Cyclin-Dependent Kinases|MK2|Cdc7

Summary: Cdc7/cdk9 inhibitor, potent, ATP-competitive

insoluble in H2O; insoluble in EtOH; ≥10.65 mg/mL
B1299 1-NM-PP1

Target: Cyclin-Dependent Kinases|Bcr-Abl|Src|Ca2 /calmodulin-dependent protein kinases (CaMKs)|c-Fyn

Summary: Pp60c-src inhibitor

insoluble in H2O; ≥16.55 mg/mL
A3294 CDK9 inhibitor

1 Citation

Target: Cyclin-Dependent Kinases

Summary: CDK9 inhibitor

Soluble in DMSO
A3336 CVT-313

1 Citation

Target: Cyclin-Dependent Kinases

Summary: Cdk2 inhibitor

≥20 mg/mL
A8885 Ro 3306

4 Citation

Target: Cyclin-Dependent Kinases

Summary: An ATP-competitive, potent CDK1 inhibitor

insoluble in EtOH; insoluble in H2O; ≥4.39 mg/mL
A8882 THZ1

12 Citation

Target: Cyclin-Dependent Kinases

Summary: Covalent CDK7 inhibitor,potent and selective

≥28.3 mg/mL