Disclosed are a class of compounds as inhibitors of kinases such as TRK, c-MET, AXL, MER and/or VEGFR2, compositions and use thereof. In particular, disclosed are a class of compounds (as shown in formula (1)) or isomers, solvates, hydrates, pharmaceutically acceptable salts, and prodrugs thereof having strong inhibition activities for kinases such as TRK, c-MET, AXL, MER and/or VEGFR2, and pharmaceutical compositions comprising said compounds. Also disclosed is use of the compounds or pharmaceutical compositions in the preparation of a medicament for treating autoimmune diseases or cancers.
公开了一类作为激酶(如 TRK、c-MET、AXL、MER 和/或 V
EGFR2)
抑制剂的化合物及其组合物和用途。特别是,公开了一类对激酶如 TRK、c-MET、AXL、MER 和/或 V
EGFR2 具有强抑制活性的化合物(如式(1)所示)或其异构体、溶解物、
水合物、药学上可接受的盐和原药,以及包含所述化合物的药物组合物。还公开了这些化合物或药物组合物在制备治疗自身免疫性疾病或癌症的药物中的用途。