蛋白激酶B
AKT1型
激酶
化学
蛋白激酶A
PI3K/AKT/mTOR通路
磷酸化
药理学
癌症研究
原癌基因蛋白质c-akt
生物化学
信号转导
生物
作者
James F. Blake,Rui Xu,Josef R. Bencsik,Dengming Xiao,Nicholas C. Kallan,Stephen T. Schlachter,Ian S. Mitchell,Keith L. Spencer,Anna L. Banka,Eli M. Wallace,Susan L. Gloor,Matthew Martinson,Richard Woessner,Guy Vigers,Barbara J. Brandhuber,Jun Liang,Brian S. Safina,Jun Li,Birong Zhang,Christine Chabot
摘要
The discovery and optimization of a series of 6,7-dihydro-5H-cyclopenta[d]pyrimidine compounds that are ATP-competitive, selective inhibitors of protein kinase B/Akt is reported. The initial design and optimization was guided by the use of X-ray structures of inhibitors in complex with Akt1 and the closely related protein kinase A. The resulting compounds demonstrate potent inhibition of all three Akt isoforms in biochemical assays and poor inhibition of other members of the cAMP-dependent protein kinase/protein kinase G/protein kinase C extended family and block the phosphorylation of multiple downstream targets of Akt in human cancer cell lines. Biological studies with one such compound, 28 (GDC-0068), demonstrate good oral exposure resulting in dose-dependent pharmacodynamic effects on downstream biomarkers and a robust antitumor response in xenograft models in which the phosphatidylinositol 3-kinase-Akt-mammalian target of rapamycin pathway is activated. 28 is currently being evaluated in human clinical trials for the treatment of cancer.
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