化学
耐受性
生物利用度
渗透剂(生化)
激酶
药理学
磷酸肌醇3激酶
PI3K/AKT/mTOR通路
生物化学
医学
信号转导
不利影响
有机化学
作者
Robin A. Fairhurst,Pascal Furet,Patricia Imbach‐Weese,Frédéric Stauffer,Heinrich Rueeger,Clive McCarthy,Sebastien Ripoche,Susanne Oswald,Bertrand Arnaud,Aline Jary,Michel Maira,Christian Schnell,Daniel Guthy,Markus Wartmann,Michael Kiffe,Sandrine Desrayaud,Francesca Blasco,Toni Widmer,Frank H. Seiler,Sascha Gutmann
标识
DOI:10.1021/acs.jmedchem.2c00267
摘要
Balanced pan-class I phosphoinositide 3-kinase inhibition as an approach to cancer treatment offers the prospect of treating a broad range of tumor types and/or a way to achieve greater efficacy with a single inhibitor. Taking buparlisib as the starting point, the balanced pan-class I PI3K inhibitor 40 (NVP-CLR457) was identified with what was considered to be a best-in-class profile. Key to the optimization to achieve this profile was eliminating a microtubule stabilizing off-target activity, balancing the pan-class I PI3K inhibition profile, minimizing CNS penetration, and developing an amorphous solid dispersion formulation. A rationale for the poor tolerability profile of 40 in a clinical study is discussed.
科研通智能强力驱动
Strongly Powered by AbleSci AI