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亲脂性
化学
配体效率
甲酰胺
选择性
铅化合物
立体化学
药理学
片段(逻辑)
组合化学
候选药物
药物发现
配体(生物化学)
药品
受体
效力
体外
药代动力学
生物化学
计算机科学
算法
催化作用
医学
作者
Katherine L. Lee,Catherine M. Ambler,David R. Anderson,Brian P. Boscoe,Andrea G. Bree,Joanne Brodfuehrer,Jeanne S. Chang,Chulho Choi,Seung-Won Chung,Kevin J. Curran,Jacqueline E. Day,Christoph M. Dehnhardt,Ken Dower,Susan E. Drozda,Richard K. Frisbie,Lori K. Gavrin,Joel Goldberg,Seungil Han,Martin Hegen,David Hepworth
标识
DOI:10.1021/acs.jmedchem.7b00231
摘要
Through fragment-based drug design focused on engaging the active site of IRAK4 and leveraging three-dimensional topology in a ligand-efficient manner, a micromolar hit identified from a screen of a Pfizer fragment library was optimized to afford IRAK4 inhibitors with nanomolar potency in cellular assays. The medicinal chemistry effort featured the judicious placement of lipophilicity, informed by co-crystal structures with IRAK4 and optimization of ADME properties to deliver clinical candidate PF-06650833 (compound 40). This compound displays a 5-unit increase in lipophilic efficiency from the fragment hit, excellent kinase selectivity, and pharmacokinetic properties suitable for oral administration.
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