The present invention is directed to compounds that are inhibitors of cysteine protease, in particular, cathepsins B, K, L, F, and S and are therefore useful in treating diseases mediated by these proteases. The present invention is directed to pharmaceutical compositions comprising these compounds and processes for preparing them.
                            本发明涉及一种抑制半胱
氨酸
蛋白酶的化合物,特别是包括B、K、L、F和S型半胱
氨酸
蛋白酶,在治疗由这些
蛋白酶介导的疾病中具有用途。本发明涉及包括这些化合物的药物组合物和其制备方法。