Learn More
Medchemexpress LLC T025 | 2407433-00-3 | 99.6% | 382.42 | 100 MG

Supplier: Medchemexpress LLC HY112296100MG
T025 is an orally active and highly potent inhibitor of Cdc2-like kinase (CLKs), demonstrating Kd values of 4.8, 0.096, 6.5, 0.61, 0.074, 1.5, and 32 nM for CLK1, CLK2, CLK3, CLK4, DYRK1A, DYRK1B, and DYRK2, respectively. This compound induces caspase-3/7-mediated cell apoptosis and reduces CLK-dependent phosphorylation. T025 exhibits anti-proliferative activities in both hematological and solid cancer cell lines with IC50 values ranging from 30-300 nM, making it primarily useful for MYC-driven disease research.
- Orally active and highly potent inhibitor of Cdc2-like kinase (CLKs)
- Induces caspase-3/7-mediated cell apoptosis
- Reduces CLK-dependent phosphorylation
- Exerts anti-proliferative activities in both hematological and solid cancer cell lines
- Anti-tumor efficiency, mainly for MYC-driven disease research
By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.