溴尿嘧啶
计算机科学
计算生物学
万维网
医学
化学
生物
生物化学
表观遗传学
基因
作者
Jeffrey A. Boerth,Marianne Schimpl,Simon C. C. Lucas,Jingwen Zhang,Erin Code,Kevin J. Embrey,Philip B. Rawlins,Haixia Wang,Richard Storer,Paolo Di Fruscia,Jennifer E. Nelson,Alexander G. Milbradt,Ulf Börjesson,Andrea Gohlke,Victoria Korboukh,Ariamala Gopalsamy
标识
DOI:10.1021/acsmedchemlett.5c00120
摘要
Suppression of oncogenic gene expression is an effective strategy for the treatment of cancer. The SWI/SNF (SWItch/Sucrose Non-Fermentable) complex plays an important role in regulating gene activation or repression, and its dysregulation has been linked to aberrant transcription activity in many types of cancer. Targeting the subunits of this complex, such as SMARCA2, SMARCA4, and PBRM1, which are part of the bromodomain family VIII, has significant therapeutic potential. Herein we report the discovery of pyrimidoindolones as a novel series of bromodomain family VIII binders identified through an NMR-based fragment screen. These binders have been optimized to achieve sub-μM affinity for the family VIII proteins SMARCA2, SMARCA4, and PRBM1, with promising physicochemical properties.
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