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].
Molekulargewicht:
884.99
Formel:
C49H32N12O2S2
Target-Kategorie:
EGFR|||CDK
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