The present invention relates to compounds of formula (I) or pharmaceutical acceptable salts,
wherein R
1a
, R
1b
, R
1c
, X, and Y are defined in the description. The present invention relates also to compositions containing said compounds which are useful for inhibiting kinases such as Cdc7 and methods of treating diseases such as cancer.
The present invention provides novel compounds of formula (I) and their use in the inhibition of c-Jun N-terminal kinases. The present invention further provides the use of these compounds in medicine, in particular in the prevention and/or treatment of neurodegenerative disorders related to apoptosis and/or inflammation.
The present invention provides novel compounds of formula (I) and their use in the inhibition of c-Jun N-terminal kinases. The present invention further provides the use of these compounds in medicine, in particular in the prevention and/or treatment of neurodegenerative disorders related to apoptosis and/or inflammation.
The present invention provides pyridinonyl PDK1 inhibitors and methods of treating cancer using the same.
本发明提供了吡啶基PDK1抑制剂及其使用方法,用于治疗癌症。
JNK INHIBITORS
申请人:GRACZYK Piotr
公开号:US20090215771A1
公开(公告)日:2009-08-27
The present invention provides novel compounds of formula I and their use in the inhibition of c-Jun N-terminal kinases. The present invention further provides the use of these compounds in medicine, in particular in the prevention and/or treatment of neurodegenerative disorders related to apoptosis and/or inflammation.