化学
神经母细胞瘤RAS病毒癌基因同源物
体内
赫拉
克拉斯
癌症研究
药理学
生物化学
生物
突变
基因
生物技术
作者
Joachim Bröeker,Alex G. Waterson,Timothy R. Hodges,Jason R. Abbott,Allison L. Arnold,Jark Böttcher,Nina Braun,Jianwen Cui,Julian E. Fuchs,Thomas Gerstberger,Sebastian Gogg,Sabine Hanner,Lorenz Herdeis,Lucas W. Howell,Andreas Mantoulidis,Moriz Mayer,Jason Phan,Francesca Rocchetti,K. Nathan Sankar,Dhruba Sarkar
标识
DOI:10.1021/acs.jmedchem.5c00576
摘要
KRAS is one of the most highly validated cancer targets. Here we describe the design and synthesis of two reversible pan-KRAS inhibitors, BI-2865 and BI-2493. From our KRASG12C inhibitor program, we identified BI-2865, a potent noncovalent KRAS inhibitor that showed cellular activity against a broad spectrum of KRAS alleles and selectivity against HRAS and NRAS. Spirocyclization led to the discovery of BI-2493, a highly rigid analogue exhibiting better potency, metabolic stability, and permeability. BI-2493 shows in vivo efficacy in various KRAS mutant and KRAS wild-type amplified xenograft models and represents a promising starting point for further optimization.
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