Skin- and airway-deliverable TRPA1 inhibitor

IF 3.3 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Bioorganic & Medicinal Chemistry Pub Date : 2024-06-24 DOI:10.1016/j.bmc.2024.117812
Tomohiro Shirai , Kazuki Kinoshita , Kentaro Kumihashi , Nanae Mugita , Masahito Yoshida , Hideo Kigoshi
{"title":"Skin- and airway-deliverable TRPA1 inhibitor","authors":"Tomohiro Shirai ,&nbsp;Kazuki Kinoshita ,&nbsp;Kentaro Kumihashi ,&nbsp;Nanae Mugita ,&nbsp;Masahito Yoshida ,&nbsp;Hideo Kigoshi","doi":"10.1016/j.bmc.2024.117812","DOIUrl":null,"url":null,"abstract":"<div><p>This study explored the potential of perfumery compounds as sources of transient receptor potential ankyrin 1 (TRPA1) inhibitors that could be formulated for effective delivery to the skin and airways. A highly potent, small, and selective TRPA1 inhibitor, 2-methyl-4-phenyl-1-pentanol (<strong>1</strong>), was discovered in perfumery compounds. Compound <strong>1</strong> demonstrated promising inhibitory activity against a broad range of TRPA1 agonists. A single stereoisomer of <strong>1</strong> was identified as the most effective TRPA1 inhibitor, indicating the potential for stereoselective synthesis to enhance its potency. Additionally, the structure–activity relationship of <strong>1</strong> was evaluated to elucidate the structural features of TRPA1 inhibitors within the fragrance-like compounds. Notably, the topical application of <strong>1</strong> alleviated sensory irritation in individuals with sensitive skin, while the inhalation of <strong>1</strong> resulted in a significant reduction in ammonia irritation, underscoring its efficacy in both skin and airway applications.</p></div>","PeriodicalId":255,"journal":{"name":"Bioorganic & Medicinal Chemistry","volume":null,"pages":null},"PeriodicalIF":3.3000,"publicationDate":"2024-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bioorganic & Medicinal Chemistry","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0968089624002268","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

This study explored the potential of perfumery compounds as sources of transient receptor potential ankyrin 1 (TRPA1) inhibitors that could be formulated for effective delivery to the skin and airways. A highly potent, small, and selective TRPA1 inhibitor, 2-methyl-4-phenyl-1-pentanol (1), was discovered in perfumery compounds. Compound 1 demonstrated promising inhibitory activity against a broad range of TRPA1 agonists. A single stereoisomer of 1 was identified as the most effective TRPA1 inhibitor, indicating the potential for stereoselective synthesis to enhance its potency. Additionally, the structure–activity relationship of 1 was evaluated to elucidate the structural features of TRPA1 inhibitors within the fragrance-like compounds. Notably, the topical application of 1 alleviated sensory irritation in individuals with sensitive skin, while the inhalation of 1 resulted in a significant reduction in ammonia irritation, underscoring its efficacy in both skin and airway applications.

Abstract Image

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
可通过皮肤和气道递送的 TRPA1 抑制剂。
这项研究探索了香水化合物作为瞬态受体电位艳基蛋白 1(TRPA1)抑制剂来源的潜力,这种抑制剂可以配制成有效的药物输送到皮肤和呼吸道。在香水化合物中发现了一种高效、小型、选择性 TRPA1 抑制剂--2-甲基-4-苯基-1-戊醇(1)。化合物 1 对多种 TRPA1 激动剂具有良好的抑制活性。1 的单一立体异构体被鉴定为最有效的 TRPA1 抑制剂,这表明立体选择性合成有可能提高其效力。此外,还对 1 的结构-活性关系进行了评估,以阐明香味类化合物中 TRPA1 抑制剂的结构特征。值得注意的是,局部使用 1 可减轻对皮肤敏感者的感觉刺激,而吸入 1 则可显著减少氨气刺激,这证明了它在皮肤和呼吸道应用方面的功效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Bioorganic & Medicinal Chemistry
Bioorganic & Medicinal Chemistry 医学-生化与分子生物学
CiteScore
6.80
自引率
2.90%
发文量
413
审稿时长
17 days
期刊介绍: Bioorganic & Medicinal Chemistry provides an international forum for the publication of full original research papers and critical reviews on molecular interactions in key biological targets such as receptors, channels, enzymes, nucleotides, lipids and saccharides. The aim of the journal is to promote a better understanding at the molecular level of life processes, and living organisms, as well as the interaction of these with chemical agents. A special feature will be that colour illustrations will be reproduced at no charge to the author, provided that the Editor agrees that colour is essential to the information content of the illustration in question.
期刊最新文献
A methamphetamine vaccine using short monoamine and diamine peptide linkers and poly-mannose Research progress of BRD4 in head and neck squamous cell carcinoma: Therapeutic application of novel strategies and mechanisms Design, synthesis and biological evaluation of novel diphenylamine analogues as NLRP3 inflammasome inhibitors Synthesis of phenanthridine derivatives by a water-compatible gold-catalyzed hydroamination Current pharmacophore based approaches for the development of new anti-Alzheimer’s agents
×
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学术文献互助
Book学术文献互助群
群 号:481959085
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