Polycyclic aryl and polycyclic 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 catalytic activity are also disclosed.
多环芳基和多环杂芳基取代的三唑类化合物以及含有这些化合物的药物组合物被披露为在抑制受体
蛋白酪氨酸激酶Axl的活性方面是有用的。还披露了使用这些化合物治疗与Axl催化活性相关的疾病或症状的方法。