Mono-acylated o-phenylendiamines derivatives of formula I
1
wherein X and R are as described herein, have been found useful for the treatment of diseases mediated by the inhibition of histone deacetylase, such as cancer.
其中X和R如本文所述,具有以下结构的I1式单酰化的
邻苯二胺衍
生物,已被发现对通过抑制组蛋白
去乙酰化酶介导的疾病,如癌症的治疗有用。