The present invention relates to novel fluoro-substituted 3,5-dicyano-4-(1H-indazol-5-yl)-2,6-dimethyl-1,4-dihy-dropyridine derivatives having protein tyrosine kinase inhibitory activity, to a process for the manufacture thereof and to the use thereof for the treatment of c-Met-mediated diseases or c-Met-mediated conditions, particularly cancer and other proliferative disorders.
本发明涉及一种具有
蛋白酪氨酸激酶抑制活性的新型
氟取代的3,5-二
氰基-4-(1H-
吲唑-5-基)-2,6-二甲基-1,4-二氢-
吡啶衍生物,以及其制造方法和用于治疗c-Met介导的疾病或c-Met介导的病状,特别是癌症和其他增殖性疾病的用途。