化学
锚定
瞬时受体电位通道
生物物理学
离子通道
作用机理
体内
TRPV1型
受体
卡普萨平
药理学
生物化学
体外
基因
生物技术
生物
医学
作者
Jack A. Terrett,Huifen Chen,Daniel G. Shore,Elisia Villemure,Robin Larouche‐Gauthier,Martin Déry,Francis Beaumier,Léa Constantineau-Forget,Chantal Grand‐Maître,Luce Lépissier,Stéphane Ciblat,Claudio F. Sturino,Yong Chen,Baihua Hu,Aijun Lu,Yunli Wang,Andrew P. Cridland,Stuart I. Ward,David H. Hackos,Rebecca M. Reese
标识
DOI:10.1021/acs.jmedchem.0c02023
摘要
Transient receptor potential ankyrin 1 (TRPA1) is a nonselective calcium-permeable ion channel highly expressed in the primary sensory neurons functioning as a polymodal sensor for exogenous and endogenous stimuli and has generated widespread interest as a target for inhibition due to its implication in neuropathic pain and respiratory disease. Herein, we describe the optimization of a series of potent, selective, and orally bioavailable TRPA1 small molecule antagonists, leading to the discovery of a novel tetrahydrofuran-based linker. Given the balance of physicochemical properties and strong
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