The present disclosure relates to novel compounds and pharmaceutical compositions thereof which are useful as inhibitors of proteasomes. The compounds provided herein are capable of inhibiting all three of CT-L, T-L, and PGPH activities of proteasomes, and are useful in treating various conditions or diseases associated with proteasomes.
本公开涉及新型化合物及其药物组合物,这些化合物可用作
蛋白酶体的
抑制剂。本文提供的化合物能够抑制
蛋白酶体的CT-L、T-L和
PGPH三种活性,并可用于治疗与
蛋白酶体相关的各种疾病或症状。