化学
乙酰化
嵌合体(遗传学)
赖氨酸
小分子
抑制器
计算生物学
癌症研究
生物化学
氨基酸
基因
生物
作者
Xiao Hu,Md Kabir,Yindan Lin,Yan Xiong,Ramon Parsons,Wei Gu,Jian Jin
标识
DOI:10.1021/acs.jmedchem.4c01497
摘要
The well-known tumor suppressor p53 is mutated in approximately half of all cancers. The Y220C mutation is one of the major p53 hotspot mutations. Several small-molecule stabilizers of p53Y220C have been developed. We recently developed a new technology for inducing targeted protein acetylation, termed acetylation targeting chimera (AceTAC), and the first p53Y220C AceTAC that effectively acetylated p53Y220C at lysine 382. Here, we report structure-activity relationship (SAR) studies of p53Y220C AceTACs, which led to the discovery of a novel p53Y220C AceTAC, compound
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