申请人:MUJICA-FERNAUD Teresa
公开号:US20080146589A1
公开(公告)日:2008-06-19
Novel compounds of the formula I
in which
R
1
, R
2
, R
3
and Het are as defined herein, which
are inhibitors of tyrosine kinases and/or Raf kinases and can be employed for the treatment of tumours, for neuroprotection and for protection of the stress proteins of the skin.
本发明提供一种化合物(I)的新型,其中R1,R2,R3和Het的定义如本文所述,这些化合物是酪氨酸激酶和/或Raf激酶的抑制剂,并可用于治疗肿瘤,神经保护和皮肤应激蛋白的保护。