CPI-169

1802175-07-0

C27H36N4O5S

DMSO : >= 59 mg/mL (111.60 mM)

Epigenetics

CPI-169 is a novel and potent EZH2 inhibitor, with IC₅₀s of 0.24 nM, 0.51 nM, and 6.1 nM for EZH2 WT, EZH2 Y641N, and EZH1, respectively. IC50 & Target: IC50: 0.24 nM (EZH2 WT), 0.51 nM (EZH2 Y641N), 6.1 nM (EZH1) In Vitro: CPI-169 inhibits the catalytic activity of PRC2 with an IC₅₀ of < 1nM, decreases cellular levels of H3K27me3 with an EC₅₀ of 70 nM, and triggers cell cycle arrest and apoptosis in a variety of cell lines^[1]. In KARPAS-422 cells, CPI-169 shows a dose-dependent inhibitory effect on cell viability, and produces synergy anti-proliferative activity when used in combination with ABT-199. In 16 out of 25 NHL cell lines, CPI-169 also suppresses cell growth with GI₅₀ of <5 uM^[2]. In Vivo: CPI-169 (200 mpk, s.c. BID) is well tolerated in mice with no observed toxic effect or body weight loss. CPI-169 treatment leads to tumor growth inhibition (TGI) of an EZH2 mutant KARPAS-422 DLBCL xenograft. CPI-169 (100 mpk, BID) with a single dose of CHOP leads tumors to rapidly regress and become unpalpable^[1]. In mice bearing KARPAS-422 xenografts, CPI-169 (200 mg/kg, s.c.) effectively suppresses H3K27me3 levels and results in lymphoma tumor regression without affecting body weight or causing any overt adverse effects^[2].