The present invention relates to novel compounds of formula (I)
that are capable of inhibiting one or more kinases, especially SYK (Spleen Tyrosine Kinase), LRRK2 (Leucine-rich repeat kinase 2) and/or MYLK (Myosin light chain kinase) or mutants thereof. The compounds find applications in the treatment of a variety of diseases.
本发明涉及式(I)的新型化合物,这些化合物能够抑制一个或多个激酶,特别是SYK(脾
酪氨酸激酶)、LRRK2(富含亮
氨酸
重复的激酶2)和/或MYLK(肌球蛋白轻
链激酶)或其突变体。这些化合物可用于治疗各种疾病。