The present invention relates to macrocyclic compounds of formula (I) that are useful as inhibitors of the hepatitis C virus (HCV) NS3 protease, their synthesis, and their use for treating or preventing HCV infections.
Compounds of Formula I are disclosed
As well as pharmaceutically acceptable salts thereof. Methods of using said compounds and pharmaceutical compositions containing said compounds are also disclosed.
公开了式 I 的化合物
及其药学上可接受的盐类。还公开了使用所述化合物的方法和含有所述化合物的药物组合物。