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 KRAS(G12C) 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.
Discovery of BI-2493, a Pan-KRAS Inhibitor Showing In Vivo Efficacy.
发现 BI-2493,一种泛 KRAS 抑制剂,显示出体内疗效
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| 期刊: | Journal of Medicinal Chemistry | 影响因子: | 6.800 |
| 时间: | 2025 | 起止号: | 2025 Aug 14; 68(15):15649-15668 |
| doi: | 10.1021/acs.jmedchem.5c00576 | 研究方向: | 其它 |
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