The present invention relates to a class of small molecule hydroxamic acid compounds capable of inhibiting histone deacetylases (HDACs). The present invention also relates to methods of preparation of hydroxamic acid HDAC inhibitor compounds of the invention, which are N-substituted-1,2,3,4-tetrahydroisoquinoline hydroxamic acid derivatives, and their incorporation into pharmaceutical compositions and methods of administration. The present invention also relates to N-substituted-1,2,3,4-tetrahydroisoquinoline hydroxamic acid derivatives, which may be prepared as a hydroxamic acid HDAC inhibitor compound library that can be utilized in screening methods known in the art.
本发明涉及一类小分子羟基酰胺酸化合物,能够抑制组蛋白
去乙酰化酶(H
DACs)。本发明还涉及制备本发明的羟基酰胺酸H
DAC抑制剂化合物的方法,这些化合物是N-取代-1,2,3,4-
四氢异喹啉羟基酰胺衍
生物,并将它们纳入药物组合物和给药方法中。本发明还涉及N-取代-1,2,3,4-
四氢异喹啉羟基酰胺衍
生物,可以制备为羟基酰胺H
DAC抑制剂化合物库,可用于筛选方法。