Pyridine, quinoline, and isoquinoline N-oxides as kinase inhibitors
    5.
    发明授权
    Pyridine, quinoline, and isoquinoline N-oxides as kinase inhibitors 有权
    吡啶,喹啉和异喹啉N-氧化物作为激酶抑制剂

    公开(公告)号:US07678811B2

    公开(公告)日:2010-03-16

    申请号:US11775457

    申请日:2007-07-10

    摘要: This invention relates to urea compounds containing a pyridine, quinoline, or isoquinoline functionality which is oxidized at the nitrogen heteroatom and which are useful in the treatment of (i) raf mediated diseases, for example, cancer, (ii) p38 mediated diseases such as inflammation and osteoporosis, and (iii) VEGF mediated diseases such as angogenesis disorders.

    摘要翻译: 本发明涉及含有吡啶,喹啉或异喹啉官能团的脲化合物,其在氮杂原子处被氧化并且可用于治疗(i)raf介导的疾病,例如癌症,(ii)p38介导的疾病,例如 炎症和骨质疏松症,和(iii)VEGF介导的疾病,如血管发生障碍。