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Search results for: 'p53 and mdm2 proteins interaction inhibitor chiral'

Search results for: 'p53 and mdm2 proteins interaction inhibitor chiral'

A8736 THZ531

Target: Cyclin-Dependent Kinases

Summary: CDK12 and CDK13 covalent inhibitor

≥55.8 mg/mL
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
A3417 Flavopiridol

Target: Cyclin-Dependent Kinases

Summary: Pan-cdk inhibitor

insoluble in H2O; ≥40.2 mg/mL
A8412 Dinaciclib (SCH727965)

2 Citation

Target: Cyclin-Dependent Kinases

Summary: Potent CDK inhibitor
A8642 R547

2 Citation

Target: Cyclin-Dependent Kinases

Summary: CDK1/2/4 inhibitor,ATP-competitive

Soluble in DMSO
A1794 LY2835219

Target: Cyclin-Dependent Kinases

Summary: CDK4/6 inhibitor,potent and selective

≥30.15 mg/mL
A5700 BS-181 HCl

Target: Cyclin-Dependent Kinases

Summary: CDK7 inhibitor,highly selective

insoluble in H2O; ≥20.85 mg/mL
A8335 Palbociclib (PD0332991) Isethionate

1 Citation

Target: Cyclin-Dependent Kinases

Summary: CDK4/6 inhibitor,highly selective

≥28.7 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
A4115 JNJ-7706621

1 Citation

Target: Cyclin-Dependent Kinases|Aurora Kinases

Summary: Potent CDK/Aurora kinase inhibitor

insoluble in EtOH; insoluble in H2O; ≥19.7 mg/mL