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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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