Discovery of ATP competitive PDHK1/2 dual inhibitors

IF 2.5 4区 医学 Q3 CHEMISTRY, MEDICINAL
Hongtao Xu , Dong Ding , Xingchun Han , Kun Miao , Chungen Liang , Hongying Yun , Wei Zhu , Fabian Dey , Dan Zhao , Yao Wu , Michael Reutlinger , June Yang , Guanglei Zhai , Zhaohu Lin , Chiho Li , Waikong Wu , Bruce Xu , Li Han , Shuai Chen , Xinyi Huang , Ge Zou
{"title":"Discovery of ATP competitive PDHK1/2 dual inhibitors","authors":"Hongtao Xu ,&nbsp;Dong Ding ,&nbsp;Xingchun Han ,&nbsp;Kun Miao ,&nbsp;Chungen Liang ,&nbsp;Hongying Yun ,&nbsp;Wei Zhu ,&nbsp;Fabian Dey ,&nbsp;Dan Zhao ,&nbsp;Yao Wu ,&nbsp;Michael Reutlinger ,&nbsp;June Yang ,&nbsp;Guanglei Zhai ,&nbsp;Zhaohu Lin ,&nbsp;Chiho Li ,&nbsp;Waikong Wu ,&nbsp;Bruce Xu ,&nbsp;Li Han ,&nbsp;Shuai Chen ,&nbsp;Xinyi Huang ,&nbsp;Ge Zou","doi":"10.1016/j.bmcl.2025.130190","DOIUrl":null,"url":null,"abstract":"<div><div>Multiple screening approaches were carried out to identify novel chemistry starting for Pyruvate Dehydrogenase Kinases (PDHKs) inhibitors. Through hit triaging efforts and structure-based optimization, two series of ATP competitive inhibitors with single digit nanomolar enzymatic potency for PDHK1/2 and around 10–100-fold selectivity over PDHK4/3 were discovered. Approach of covalent inhibitor was explored to successfully improve the cellular target engagement to single digit micromolar range.</div></div>","PeriodicalId":256,"journal":{"name":"Bioorganic & Medicinal Chemistry Letters","volume":"122 ","pages":"Article 130190"},"PeriodicalIF":2.5000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioorganic & Medicinal Chemistry Letters","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0960894X2500099X","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

Multiple screening approaches were carried out to identify novel chemistry starting for Pyruvate Dehydrogenase Kinases (PDHKs) inhibitors. Through hit triaging efforts and structure-based optimization, two series of ATP competitive inhibitors with single digit nanomolar enzymatic potency for PDHK1/2 and around 10–100-fold selectivity over PDHK4/3 were discovered. Approach of covalent inhibitor was explored to successfully improve the cellular target engagement to single digit micromolar range.

Abstract Image

求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
5.70
自引率
3.70%
发文量
463
审稿时长
27 days
期刊介绍: Bioorganic & Medicinal Chemistry Letters presents preliminary experimental or theoretical research results of outstanding significance and timeliness on all aspects of science at the interface of chemistry and biology and on major advances in drug design and development. The journal publishes articles in the form of communications reporting experimental or theoretical results of special interest, and strives to provide maximum dissemination to a large, international audience.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信