Identification of (R)-N-((4-methoxy-6-methyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methyl-1-(1-(1-(2,2,2-trifluoroethyl)piperidin-4-yl)ethyl)-1H-indole-3-carboxamide (CPI-1205), a potent and selective inhibitor of histone methyltransferase EZH2, suitable for phase I clinical trials for B-cell lymphomasMore about Open Access at the Crick
Authors listRishi G Vaswani Victor S Gehling Les A Dakin Andrew S Cook Christopher G Nasveschuk Martin Duplessis Priyadarshini Iyer Srividya Balasubramanian Feng Zhao Andrew C Good Robert Campbell Christina Lee Nico Cantone Richard T Cummings Emmanuel Normant Steven F Bellon Brian K Albrecht Jean-Christophe Harmange Patrick Trojer James E Audia Ying Zhang Neil Justin Shuyang Chen Jon Wilson Steve Gamblin
Polycomb repressive complex 2 (PRC2) has been shown to play a major role in transcriptional silencing in part by installing methylation marks on lysine 27 of histone 3. Dysregulation of PRC2 function correlates with certain malignancies and poor prognosis. EZH2 is the catalytic engine of the PRC2 complex and thus represents a key candidate oncology target for pharmacological intervention. Here we report the optimization of our indole-based EZH2 inhibitor series that led to the identification of CPI-1205, a highly potent (biochemical IC50 = 0.002 mu M, cellular EC50 = 0.032 mu M) and selective inhibitor of EZH2. This compound demonstrates robust antitumor effects in a Karpas-422 xenograft model when dosed at 160 mg/kg BID and is currently in Phase I clinical trials. Additionally, we disclose the co-crystal structure of our inhibitor series bound to the human PRC2 complex.
Journal Journal of Medicinal Chemistry
Issue number 21