The present invention relates to compounds and methods useful as inhibitors of protein kinases, including B-Raf and several receptor tyrosine and cytoplasmic tyrosine kinases. The present invention is directed to new substituted pyrimidinyloxy urea compounds of Formulas II, III and IV and compositions and their application as pharmaceuticals for the treatment of disease. Methods of modulating of protein kinase activity in a human or animal subject are also provided for the treatment diseases such as cancers.
本发明涉及化合物和方法,用作蛋白激酶的
抑制剂,包括B-Raf以及几种受体
酪氨酸激酶和细胞质
酪氨酸激酶。本发明涉及新的取代
嘧啶氧基
脲化合物II、III和IV的配方及其作为药物治疗疾病的应用。还提供了在人类或动物主体中调节蛋白激酶活性的方法,用于治疗癌症等疾病。