克拉斯
化学
效力
共价键
癌症研究
烷基化
药理学
生物化学
细胞培养
IC50型
体外
突变
细胞
突变体
共价结合
动力学
细胞生长
结构-活动关系
血浆蛋白结合
调节器
重组DNA
作者
Nicholas Endres,Steven Do,Rana Mroue,Jack A. Terrett,Matt Saabye,Angela Oh,Thomas Hunsaker,Emily Chan,John C. Tran (1471192),Lan K. Nguyen,Qihui Lian,Taylur P. Ma (14723765),Thomas P. Garner,Luca Gerosa,Maureen H. Beresini,Aaron Boudreau,Sarah M. Bronner,Patrick Cyr (1566223),Noriko Ishisoko,Yevgeniy Izrayelit
标识
DOI:10.1021/acs.jmedchem.5c02272
摘要
High Resolution Image Download MS PowerPoint Slide KRAS G12C is one of the most prevalent oncogenic mutations in nonsmall cell lung cancer. Herein we describe the discovery and optimization of divarasib (GDC-6036), an orally available, highly potent, and selective covalent KRAS G12C inhibitor. We demonstrate a significant noncovalent binding component of divarasib that contributes to its potency and rapid kinetics. Divarasib has greater potency and kinetics of alkylation compared with other KRAS G12C inhibitors in vitro and shows robust tumor growth inhibition in multiple KRAS G12C-positive cell lines.
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