法苏迪尔
Rho相关蛋白激酶
丝氨酸
炎症
激酶
化学
磷酸化
医学
生物化学
免疫学
作者
Yaodong You,Kun Zhu,Jie Wang,Qi Liang,Wen Li,Lin Wang,Baojun Guo,Jing Zhou,Xuanlin Feng,Jianyou Shi
标识
DOI:10.1016/j.cclet.2023.108336
摘要
Rho-associated coiled-coil-containing protein kinase (ROCK) belongs to the serine-threonine family, and ROCK is involved in a variety of biological processes including cell migration, adhesion, proliferation and differentiation through phosphorylation of different downstream substrates. The aberrant activation of ROCK is associated with the pathological conditions in different systems including various diseases, including cancer, neurological diseases, inflammation, cardiovascular diseases and glaucoma. Therefore, the ROCK inhibitors have potential applicability for treating the aforementioned diseases. Four small molecule ROCK inhibitors have been approved for clinical use: fasudil, ripasudil, netarsudil and belumosudil. In recent years, more small molecule ROCK inhibitors have been identified. This paper reviews the ROCK inhibitors reported in past seven years. We mainly focused on the summarization of the structure–activity relationships, inhibitory efficacy, pharmacological mechanisms and the relevant clinical studies of the reported ROCK inhibitors. Besides the small molecular inhibitors, the peptides and biological extracts which exhibit ROCK inhibitory effects are also included. We also provide suggestions for the future development of the potent ROCK inhibitors.
科研通智能强力驱动
Strongly Powered by AbleSci AI