The present invention relates to thiopyrimidine-based compounds that are inhibitors of protein kinases including JAK kinases. In particular, the compounds are selective for JAK1, JAK2 or JAK3 kinases and combinations thereof such as JAK1 and JAK2. The kinase inhibitors can be used in the treatment of kinase associated diseases such as immunological and inflammatory diseases including organ transplants; hyperproliferative diseases including cancer and myeloproliferative diseases; viral diseases; metabolic diseases and vascular diseases.
本发明涉及一种基于噻
嘧啶的化合物,这些化合物是蛋白激酶(包括JAK激酶)的
抑制剂。特别地,这些化合物选择性地作用于JAK1、JAK2或JAK3激酶及其组合,例如JAK1和JAK2。这些激酶
抑制剂可用于治疗与激酶相关的疾病,如免疫和炎症性疾病,包括器官移植;增殖过度性疾病,包括癌症和骨髓增生性疾病;病毒性疾病;代谢性疾病和血管性疾病。