The invention relates to novel aminothiazole derivatives which are inhibitors of the transforming growth factor, (“TGF”)-β signalling pathway, in particular, the phosphorylation of smad2 or smad3 by the TGF-β type I or activin-like kinase (“ALK”)-5 receptor, methods for their preparation and their use in medicine, specifically in the treatment and prevention of a disease state mediated by this pathway.
本发明涉及一种新型的
氨基
噻唑衍
生物,该衍
生物是转化生长因子(“TGF”)-β信号通路的
抑制剂,特别是抑制TGF-β类型I或类激活素样激酶(“ALK”)-5受体对smad2或smad3的
磷酸化,以及该衍
生物的制备方法和在医学上的应用,具体地用于治疗和预防由该通路介导的疾病状态。