The disclosure relates to compounds of Formula (I) as allosteric chromenone inhibitors of phosphoinositide 3‑kinase (PI3K) useful in the treatment of diseases or disorders associated with PI3K modulation, Formula (I) or pharmaceutically acceptable salts thereof wherein R, R1, R2,R3, R4, R5, R6, R7, and R8, are as defined herein. The disclosure also relates to methods of making and using compounds of Formula (I) or pharmaceutically acceptable salts thereof.
本披露涉及式(I)的化合物,作为
磷脂酰肌醇3-激酶(
PI3K)的变构异构酮
抑制剂,有助于治疗与
PI3K调节相关的疾病或疾病,式(I)或其药学上可接受的盐,其中R,R1,R2,R3,R4,R5,R6,R7和R8如本文所定义。本披露还涉及制备和使用式(I)的化合物或其药学上可接受的盐的方法。