激酶
化学
癌症研究
细胞
药物发现
医学
生物化学
作者
Timothy M. Caldwell,Yu Mi Ahn,Stacie L. Bulfer,Cynthia B. Leary,Molly M. Hood,Wei-Ping Lu,Lakshminarayana Vogeti,Subha Vogeti,Michael D. Kaufman,Scott Wise,Bertrand Le Bourdonnec,Bryan D. Smith,Daniel L. Flynn
标识
DOI:10.1016/j.bmcl.2022.128928
摘要
Based on knowledge of kinase switch-control inhibition and using a combination of structure-based drug design and standard medicinal chemistry principles, we identified a novel series of dihydropyrimidone-based CSF1R kinase inhibitors displaying exquisite selectivity for CSF1R versus a large panel of kinases and non-kinase protein targets. Starting with lead compound 3, an SAR optimization campaign led to the discovery of vimseltinib (DCC-3014; compound 20) currently undergoing clinical evaluation for the treatment of Tenosynovial Giant Cell Tumor (TGCT), a locally aggressive benign tumor associated with substantial morbidity. 2021 Elsevier ltd. All rights reserved.
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