化学
克拉斯
药代动力学
突变体
效力
药理学
癌症研究
生物利用度
细胞培养
体外
代谢稳定性
细胞毒性
临床试验
表型筛选
药物发现
体内
结构-活动关系
IC50型
运输机
肿瘤细胞
作者
Alexander Sokolsky,Haolin Yin,Qinda Ye,Peter Carlsen,Chunyin Law,Matthew S. McCammant,Rocco L. Policarpo,Padmaja K Polam,Le Zhao,Fenglei Zhang,Gencheng Li,Bin Hu,Wenyu Zhu,Gia Hoang,Robert Susick,Zhenwu Li,Pei Gan,Artem Shvartsbart,Jeremy J. Roach,Chao Qi
标识
DOI:10.1021/acs.jmedchem.6c02625
摘要
Abstract The discovery of the clinical KRAS G12D inhibitor INCB161734 is described. Starting from a previously disclosed orally bioavailable tool compound 1, a concerted effort to improve the predicted human dose via modulation of potency and pharmacokinetics was undertaken. Careful consideration of the metabolic profile was key to designing low clearance compounds. In addition, the molecular size and fraction sp3 character were carefully controlled to improve permeability and crystalline solubility. From this effort, INCB161734 was identified as a balanced compound with excellent oral exposure, potent antiproliferative activity in xenograft tumor models, and excellent selectivity against wild-type K/H/NRAS. INCB161734 is currently undergoing clinical trials in patients with KRAS G12D mutations.
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