Bridged bicyclic heteroaryl substituted triazoles and pharmaceutical compositions containing the compounds are disclosed as being useful in inhibiting the activity of the receptor protein tyrosine kinase AxI. Methods of using the compounds in treating diseases or conditions associated with AxI activity are also disclosed.
本发明公开了桥接的双环杂芳基取代的三唑类化合物以及含有该化合物的制药组合物,用于抑制受体
蛋白酪氨酸激酶AxI的活性。本发明还公开了使用该化合物治疗与AxI活性相关的疾病或病况的方法。