Bicyclic aryl substituted triazoles or heteroaryl substituted triazoles and pharmaceutical compositions containing the compounds are disclosed as being useful in inhibiting the activity of the receptor protein tyrosine kinase Axl. Methods of using the compounds in treating diseases or conditions associated with Axl activity are also disclosed.
本文介绍了具有双环芳基取代的三唑或杂环芳基取代的三唑及含有这些化合物的制药组合物,这些化合物有助于抑制受体
蛋白酪氨酸激酶Axl的活性。本文还介绍了使用这些化合物治疗与Axl活性相关的疾病或症状的方法。