Identification of potent, selective KDM5 inhibitors

Abstract This communication describes the identification and optimization of a series of pan-KDM5 inhibitors derived from compound 1 , a hit initially identified against KDM4C. Compound 1 was optimized to afford compound 20 , a 10 nM inhibitor of KDM5A. Compound 20 is highly selective for the KDM5 enzymes versus other histone lysine demethylases and demonstrates activity in a cellular assay measuring the increase in global histone 3 lysine 4 tri-methylation (H3K4me3). In addition compound 20 has good ADME properties, excellent mouse PK, and is a suitable starting point for further optimization.