EGFR/CDK2-IN-2
Product Specifications
Target
EGFR, CDK
Related Pathways
Tyrosine Kinase/Adaptors, Cell Cycle/Checkpoint, JAK/STAT signaling, Angiogenesis
Bioactivity
EGFR/CDK2-IN-2 (compound 6a) is a dual inhibitor targeting EGFR and CDK-2, with IC50 values of 19.6 nM and 87.9 nM, respectively. It induces apoptosis in MCF-7 cells and arrests cell cycle progression in the S phase, demonstrating notable anticancer activity with an IC50 of 0.39 μM [1].
Molecular Formula
C49H32N12O2S2
Molecular Weight
884.99
Shipping Conditions
Ice Packs
Storage Temperature
-20°C
Available Sizes
Frequently Asked Questions
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