QC6352

1851373-36-8

C24H25N3O2

DMSO : >= 25 mg/mL (64.52 mM)

Epigenetics

QC6352 is a potent KDM4C inhibitor with an IC₅₀ of 35 nM. IC50 & Target: IC50: 35 nM (KDM4C)^[1] In Vitro: QC6352 is a potent KDM4C inhibitor with an IC₅₀ of 35+/-8 nM^[1]. In a concentration-dependent manner QC6352 dramatically reduces the anchorage-independent sphere-forming capacity of BCSC1 and BCSC2. QC6352 blocks proliferation and self-renewal of BCSCs. As shown by western blot analysis the protein levels of (Epidermal growth factor receptor) EGFR are reduced in both BCSC1 and BCSC2 upon treatment with QC6352^[2]. In Vivo: QC6352 strongly affects tumor growth and final tumor weight of both BCSC1 and BCSC2 xenografts. Treatment with QC6352 is well tolerated and does not affect body weight of the mice. Results demonstrate that treatment with the KDM4 inhibitor QC6352 blocks BCSC xenograft tumor growth^[2].