The present invention provides a novel class of macrocyclic compounds, which are useful as cysteine protease inhibitors. Also provided are novel intermediates and methods of preparing the compounds. The invention also provides pharmaceutical compositions comprising the compounds. The compounds and compositions are useful in methods of treating or preventing one or more diseases associated with cysteine protease activity, particularly those associated with calpain activity.
本发明提供了一类新型的大环化合物,可用作半胱
氨酸蛋白酶抑制剂。还提供了新型中间体和制备这些化合物的方法。该发明还提供了包含这些化合物的药物组合物。这些化合物和组合物可用于治疗或预防与半胱
氨酸
蛋白酶活性有关的一种或多种疾病,特别是与
钙蛋白酶活性有关的疾病。