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Search results for: 'research area cell cycle c myc'

Search results for: 'research area cell cycle c myc'

A8477 MK-8776 (SCH-900776)

Target: Chk

Summary: Chk1 inhibitor,potent and selective

insoluble in H2O; insoluble in EtOH; ≥18.8 mg/mL
A1980 SNS-032 (BMS-387032)

2 Citation

Target: Cyclin-Dependent Kinases

Summary: CDK inhibitor

insoluble in H2O; ≥19.05 mg/mL
A8316 PD 0332991 (Palbociclib) HCl

5 Citation

Target: Cyclin-Dependent Kinases

Summary: CDK4/6 inhibitor,highly selective

≥14.48 mg/mL
A8335 Palbociclib (PD0332991) Isethionate

1 Citation

Target: Cyclin-Dependent Kinases

Summary: CDK4/6 inhibitor,highly selective

≥28.7 mg/mL
A4112 Barasertib (AZD1152-HQPA)

3 Citation

Target: Aurora Kinases

Summary: Aurora Kinase B inhibitor, Potent and selective

≥25.4 mg/mL
A8182 3-Deazaneplanocin A (DZNep) hydrochloride

1 Citation

Target: EZH2

Summary: SAHH and EZH2 inhibitor

insoluble in EtOH; ≥14.94 mg/mL
A1905 3-Deazaneplanocin,DZNep

6 Citation

Target: Hydrolase

Summary: S-adenosylhomocysteine and EZH2 inhibitor

insoluble in EtOH; ≥17.07 mg/mL
A3573 LY2801653

Target: MET

Summary: MET inhibitor

≥27.65 mg/mL