PI3K/AKT/mTOR通路
胶质母细胞瘤
血脑屏障
mTOR抑制剂的发现与发展
计算生物学
癌症研究
医学
药理学
代谢稳定性
神经科学
信号转导
化学
生物
中枢神经系统
体外
细胞生物学
生物化学
作者
Timothy P. Heffron,Chudi Ndubaku,Laurent Salphati,Bruno Alicke,Jonathan Cheong,Joy Drobnick,Kyle A. Edgar,Stephen E. Gould,Leslie B. Lee,John Lesnick,Cristina Lewis,Jim Nonomiya,Jodie Pang,Emile G. Plise,Steve Sideris,Jeffrey J. Wallin,Lan Wang,Xiaolin Zhang,Alan G. Olivero
标识
DOI:10.1021/acsmedchemlett.6b00005
摘要
Inhibition of phosphoinositide 3-kinase (PI3K) signaling is an appealing approach to treat brain tumors, especially glioblastoma multiforme (GBM). We previously disclosed our successful approach to prospectively design potent and blood-brain barrier (BBB) penetrating PI3K inhibitors. The previously disclosed molecules were ultimately deemed not suitable for clinical development due to projected poor metabolic stability in humans. We, therefore, extended our studies to identify a BBB penetrating inhibitor of PI3K that was also projected to be metabolically stable in human. These efforts required identification of a distinct scaffold for PI3K inhibitors relative to our previous efforts and ultimately resulted in the identification of GDC-0084 (16). The discovery and preclinical characterization of this molecule are described within.
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