The present invention relates to substituted isoxazolo-quinazolines which modulate the activity of protein kinases and are therefore useful in treating diseases caused by dysregulated protein kinase activity, in particular human MPS1 and PERK. The present invention also provides methods for preparing these compounds, pharmaceutical compositions comprising these compounds, and methods of treating diseases utilizing such these compounds or the pharmaceutical compositions containing them.
本发明涉及替代
异噁唑喹唑啉,可调节蛋白激酶活性,因此在治疗由蛋白激酶活性失调引起的疾病方面具有用处,特别是人类
MPS1和PERK。本发明还提供了制备这些化合物的方法,包括这些化合物的药物组合物,以及利用这些化合物或含有它们的药物组合物治疗疾病的方法。