首页> 外国专利> Azaindoles substituted with either triazine or pyrimidine useful as inhibitors of janus kinases consisting of JAK1, JAK2, JAK3, and TYK2

Azaindoles substituted with either triazine or pyrimidine useful as inhibitors of janus kinases consisting of JAK1, JAK2, JAK3, and TYK2

机译:被三嗪或嘧啶取代的氮杂吲哚可用作由JAK1,JAK2,JAK3和TYK2组成的janus激酶的抑制剂

摘要

Disclosed are compounds of formula (I) and methods for their preparation. The compounds have an azaindole core and are substituted with either a pyrimidine or triazine moiety. Additionally, R1 is NR-CR2-C(O)-NR2 X is N or CR The compounds of formula (I) are useful as inhibitors of Janus kinases, a family of tyrosine kinases consisting of JAK1, JAK2, JAK3 and TYK2. The compounds are therefore useful as pharmaceuticals for treating a disease or condition such as a proliferative disorder, a cardiac disorder, a neurodegenerative disorder, an autoimmune disorder, a condition associated with organ transplantation, an inflammatory disorder, or an immunologically mediated disorder. In particular the pharmaceuticals are useful for treating asthma, transplant rejection and rheumatoid arthritis.
机译:公开了式(I)的化合物及其制备方法。该化合物具有氮杂吲哚核,并被嘧啶或三嗪部分取代。另外,R1是NR-CR2-C(O)-NR2 X是N或CR。式(I)化合物可用作Janus激酶的抑制剂,Janus激酶是由JAK1,JAK2,JAK3和TYK2组成的酪氨酸激酶家族。因此,该化合物可用作治疗疾病或病症例如增生性疾病,心脏疾病,神经退行性疾病,自身免疫疾病,与器官移植有关的疾病,炎性疾病或免疫介导的疾病的药物。特别地,所述药物可用于治疗哮喘,移植排斥和类风湿关节炎。

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