Disclosed are novel substituted 2H-isoquinolin-1-one and 3H-quinazolin-4-one derivatives useful as inhibitors of Rho kinase and for treating a variety of diseases and disorders that are mediated or sustained through the activity of Rho kinase, including cardiovascular diseases, pharmaceutical compositions comprising such compounds, methods for using such compounds and processes for making such compounds.
揭示了一种新颖的取代的2H-
异喹啉-1-酮和3H-
喹唑啉-4-酮衍
生物,可用作Rho激酶的
抑制剂,用于治疗通过Rho激酶活性介导或维持的各种疾病和疾病,包括心血管疾病,包含这些化合物的药物组合物,使用这些化合物的方法以及制备这些化合物的方法。