化学
连接器
基诺美
效力
组合化学
结构-活动关系
立体化学
取代基
药物发现
计算生物学
小分子
化学合成
选择性
生物化学
药理学
细胞色素P450
芳基
体内
体外
分子模型
化学空间
血浆蛋白结合
药物开发
配体效率
结合位点
甲酰胺
药效团
铅化合物
作者
Hyunyoung Moon,Xuelei Yan,Jiang Zhu,Guillaume Mata,Zhang Wang,Karl T. Haelsig,Patrick G. Schweickert,Kelsey E. Sivick,Hsin-Ting Huang,Anne M. van Abbema,Siquan Chen,Xiaoning Zhao,David W. Green,Lixia Jin,Stephen W. Young,Matthew J. Walters,Nigel P. Walker (8682108),Manmohan R. Leleti (8962166),Jay P. Powers,Jenna L. Jeffrey
标识
DOI:10.1021/acs.jmedchem.6c01334
摘要
Abstract Selective KIT inhibition is an effective strategy for treating mast cell-driven diseases, but highly conserved ATP-binding sites in class III RTKs hinder selective inhibitor design. We employed structure-guided medicinal chemistry to optimize a series of potent, selective KIT inhibitors. An initial triazolopyridine hinge-binding motif enabled potent KIT inhibition with high selectivity and, after central linker optimization, led to a “reverse” arylacetamide series with further improved potency and pharmacokinetic properties. Incorporation of a pyrazole-based linker and modification of the hinge-binding motif led to improved potency in the presence of human serum. Further tuning of the terminal aryl substituent mitigated cytochrome P450 time-dependent inhibition and improved kinome selectivity. Crystallography revealed key elements of KIT inhibition and showed that subtle modulation of linker stereoelectronic effects in the gatekeeper region can drive selectivity. These efforts yielded an optimized lead inhibitor with low-nanomolar cellular potency, high KIT selectivity, and properties favorable for chronic therapy.
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