化学
表观遗传学
小分子
乙酰化
效力
体内
赖氨酸
分子
体外
选择性
结构-活动关系
立体化学
计算生物学
费斯特共振能量转移
生物物理学
组合化学
纳米技术
生物化学
荧光
基因
遗传学
氨基酸
有机化学
生物
物理
催化作用
量子力学
材料科学
作者
Allyn T. Londregan,Karlygash Aitmakhanova,James M. Bennett,Laura J. Byrnes,Daniel P. Canterbury,Xiayun Cheng,Thomas Christott,Jennifer Clemens,Steven B. Coffey,João M. Dias,Matthew Dowling,Gillian Farnie,Oleg Fedorov,Kimberly F. Fennell,Vicki Gamble,C. Gileadi,Charline Giroud,Michael Harris,Brett D. Hollingshead,K. Huber
标识
DOI:10.1021/acs.jmedchem.2c01421
摘要
A series of small-molecule YEATS4 binders have been discovered as part of an ongoing research effort to generate high-quality probe molecules for emerging and/or challenging epigenetic targets. Analogues such as 4d and 4e demonstrate excellent potency and selectivity for YEATS4 binding versus YEATS1,2,3 and exhibit good physical properties and in vitro safety profiles. A new X-ray crystal structure confirms direct binding of this chemical series to YEATS4 at the lysine acetylation recognition site of the YEATS domain. Multiple analogues engage YEATS4 with nanomolar potency in a whole-cell nanoluciferase bioluminescent resonance energy transfer assay. Rodent pharmacokinetic studies demonstrate the competency of several analogues as in vivo-capable binders.
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