A compound of formula (I) wherein A and B are optionally substituted cyclohexenyl or phenyl groups, X is carbonyl or sulfonyl, and Y is 5-7 atoms-linker, is useful as histone deacetylase inhibitors, particularly for inhibiting cell proliferation.
1
式(I)的化合物,其中A和B为可选择的取代
环己烯基或苯基,X为羰基或磺酰基,Y为5-7原子链连接体,可用作组蛋白
去乙酰化酶抑制剂,特别是用于抑制细胞增殖。