可通过皮肤和气道递送的 TRPA1 抑制剂。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Tomohiro Shirai , Kazuki Kinoshita , Kentaro Kumihashi , Nanae Mugita , Masahito Yoshida , Hideo Kigoshi
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引用次数: 0

摘要

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。

Skin- and airway-deliverable TRPA1 inhibitor

Skin- and airway-deliverable TRPA1 inhibitor

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.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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