含碳硼烷衍生物作为TEAD自棕榈酰化抑制剂的发现和生物学评价。

IF 2.3 4区 医学 Q3 CHEMISTRY, MEDICINAL Bioorganic & Medicinal Chemistry Letters Pub Date : 2025-06-01 Epub Date: 2025-02-24 DOI:10.1016/j.bmcl.2025.130155
Chaofan Li , Yingshuang Zhang , Ziyin Zhang , Yirong Zhang , Yuxuan Song , Linyuan Wang , Changxian Yuan , Guanxiang Hao , Nan Sun , Hongjing Li , Zhiguang Zhang , Yundong He , Sinan Wang
{"title":"含碳硼烷衍生物作为TEAD自棕榈酰化抑制剂的发现和生物学评价。","authors":"Chaofan Li ,&nbsp;Yingshuang Zhang ,&nbsp;Ziyin Zhang ,&nbsp;Yirong Zhang ,&nbsp;Yuxuan Song ,&nbsp;Linyuan Wang ,&nbsp;Changxian Yuan ,&nbsp;Guanxiang Hao ,&nbsp;Nan Sun ,&nbsp;Hongjing Li ,&nbsp;Zhiguang Zhang ,&nbsp;Yundong He ,&nbsp;Sinan Wang","doi":"10.1016/j.bmcl.2025.130155","DOIUrl":null,"url":null,"abstract":"<div><div>Transcriptional enhanced associate domain (TEAD) proteins are key downstream effectors of the Hippo signaling pathway that play a crucial role in various cell processes including tissue development, regeneration, cell proliferation and cancer. TEADs contain a hydrophobic auto-palmitoylation pocket that can bind palmitic acid and stabilize TEADs from being degraded. Inhibitors targeting this palmitoylation pocket typically consist of hydrophobic pharmacophores. Carboranes is a cage-shaped molecule exhibiting superior hydrophobicity compared to adamantane or phenyl groups. Herein, we incorporated carborane into known TEAD inhibitors for better interaction with the hydrophobic palmitate pocket. Compounds <strong>1f</strong> and <strong>1l</strong> are identified as TEAD transcription inhibitors with strong anti-proliferation and anti-migration activities toward prostate cancer cell lines. They also significantly reduced TEAD-regulated downstream gene expressions.</div></div>","PeriodicalId":256,"journal":{"name":"Bioorganic & Medicinal Chemistry Letters","volume":"121 ","pages":"Article 130155"},"PeriodicalIF":2.3000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Discovery and biological evaluation of carborane-containing derivatives as TEAD auto palmitoylation inhibitors\",\"authors\":\"Chaofan Li ,&nbsp;Yingshuang Zhang ,&nbsp;Ziyin Zhang ,&nbsp;Yirong Zhang ,&nbsp;Yuxuan Song ,&nbsp;Linyuan Wang ,&nbsp;Changxian Yuan ,&nbsp;Guanxiang Hao ,&nbsp;Nan Sun ,&nbsp;Hongjing Li ,&nbsp;Zhiguang Zhang ,&nbsp;Yundong He ,&nbsp;Sinan Wang\",\"doi\":\"10.1016/j.bmcl.2025.130155\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Transcriptional enhanced associate domain (TEAD) proteins are key downstream effectors of the Hippo signaling pathway that play a crucial role in various cell processes including tissue development, regeneration, cell proliferation and cancer. TEADs contain a hydrophobic auto-palmitoylation pocket that can bind palmitic acid and stabilize TEADs from being degraded. Inhibitors targeting this palmitoylation pocket typically consist of hydrophobic pharmacophores. Carboranes is a cage-shaped molecule exhibiting superior hydrophobicity compared to adamantane or phenyl groups. Herein, we incorporated carborane into known TEAD inhibitors for better interaction with the hydrophobic palmitate pocket. Compounds <strong>1f</strong> and <strong>1l</strong> are identified as TEAD transcription inhibitors with strong anti-proliferation and anti-migration activities toward prostate cancer cell lines. They also significantly reduced TEAD-regulated downstream gene expressions.</div></div>\",\"PeriodicalId\":256,\"journal\":{\"name\":\"Bioorganic & Medicinal Chemistry Letters\",\"volume\":\"121 \",\"pages\":\"Article 130155\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-06-01\",\"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/S0960894X25000642\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/2/24 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioorganic & Medicinal Chemistry Letters","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0960894X25000642","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/24 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

摘要

转录增强相关结构域(TEAD)蛋白是Hippo信号通路的关键下游效应蛋白,在包括组织发育、再生、细胞增殖和癌症在内的各种细胞过程中起着至关重要的作用。TEADs含有一个疏水的自棕榈酰化口袋,可以结合棕榈酸并稳定TEADs不被降解。靶向这种棕榈酰化口袋的抑制剂通常由疏水药效团组成。碳硼烷是一种笼形分子,与金刚烷或苯基相比,具有优越的疏水性。在这里,我们将碳硼烷加入到已知的TEAD抑制剂中,以更好地与疏水棕榈酸袋相互作用。化合物1f和1l被鉴定为TEAD转录抑制剂,对前列腺癌细胞具有较强的抗增殖和抗迁移活性。它们还显著降低了tead调控的下游基因表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Discovery and biological evaluation of carborane-containing derivatives as TEAD auto palmitoylation inhibitors
Transcriptional enhanced associate domain (TEAD) proteins are key downstream effectors of the Hippo signaling pathway that play a crucial role in various cell processes including tissue development, regeneration, cell proliferation and cancer. TEADs contain a hydrophobic auto-palmitoylation pocket that can bind palmitic acid and stabilize TEADs from being degraded. Inhibitors targeting this palmitoylation pocket typically consist of hydrophobic pharmacophores. Carboranes is a cage-shaped molecule exhibiting superior hydrophobicity compared to adamantane or phenyl groups. Herein, we incorporated carborane into known TEAD inhibitors for better interaction with the hydrophobic palmitate pocket. Compounds 1f and 1l are identified as TEAD transcription inhibitors with strong anti-proliferation and anti-migration activities toward prostate cancer cell lines. They also significantly reduced TEAD-regulated downstream gene expressions.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
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.
期刊最新文献
Rational design, synthesis, and biological evaluation of chalcone hybrids including benzoylpiperazin (phenylacetylpiperazin)-thiophene as anti- Alzheimer's agents Rational design and N-terminal acylation of a lactam-cyclized 11-residue antimicrobial peptide for improved antibacterial potency OracleScreen-LILRB4 (HTS-Oracle v3): machine learning-guided discovery of myeloid immune checkpoint binders validated in patient-derived cells Discovery of a potent sGC stimulator with once-daily dosing potential for the treatment of hypertension Solid-phase synthesis and antimicrobial activities of lipid-neomycin conjugates
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1