化学
蛋白激酶B
选择性
酶
酶抑制剂
激酶
生物化学
结构-活动关系
立体化学
磷酸化
体外
催化作用
作者
Nicholas C. Kallan,Keith L. Spencer,James F. Blake,Rui Xu,Justin Heizer,Josef R. Bencsik,Ian S. Mitchell,Susan L. Gloor,Matthew Martinson,Tyler Risom,Stefan Groß,Tony Morales,Wen‐I Wu,Guy Vigers,Barbara J. Brandhuber,Nicholas J. Skelton
标识
DOI:10.1016/j.bmcl.2011.02.073
摘要
A novel series of spirochromane pan-Akt inhibitors is reported. SAR optimization furnished compounds with improved enzyme potencies and excellent selectivity over the related AGC kinase PKA. Attempted replacement of the phenol hinge binder provided compounds with excellent Akt enzyme and cell activities but greatly diminished selectivity over PKA.
科研通智能强力驱动
Strongly Powered by AbleSci AI