Heffron Timothy P, Ndubaku Chudi O, Salphati Laurent, Alicke Bruno, Cheong Jonathan, Drobnick Joy, Edgar Kyle, Gould Stephen E, Lee Leslie B, Lesnick John D, Lewis Cristina, Nonomiya Jim, Pang Jodie, Plise Emile G, Sideris Steve, Wallin Jeffrey, Wang Lan, Zhang Xiaolin, Olivero Alan G
Genentech, Inc. , 1 DNA Way, South San Francisco, California 94080, United States.
ACS Med Chem Lett. 2016 Feb 16;7(4):351-6. doi: 10.1021/acsmedchemlett.6b00005. eCollection 2016 Apr 14.
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.
抑制磷酸肌醇3-激酶(PI3K)信号传导是治疗脑肿瘤,尤其是多形性胶质母细胞瘤(GBM)的一种有吸引力的方法。我们之前披露了我们前瞻性设计强效且能穿透血脑屏障(BBB)的PI3K抑制剂的成功方法。由于预计在人体内代谢稳定性较差,之前披露的分子最终被认为不适合临床开发。因此,我们扩展了研究,以鉴定一种能穿透血脑屏障的PI3K抑制剂,预计该抑制剂在人体内也具有代谢稳定性。这些努力需要相对于我们之前的工作鉴定出一种不同的PI3K抑制剂骨架,最终鉴定出了GDC-0084(16)。本文描述了该分子的发现及临床前特征。