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设计和药理学评价 TrpA1 通道非亲电型参考激动剂 PF-4840154。

Design and pharmacological evaluation of PF-4840154, a non-electrophilic reference agonist of the TrpA1 channel.

机构信息

Pfizer Worldwide Medicinal Chemistry, Ramsgate Road, Sandwich, Kent CT139NJ, United Kingdom.

出版信息

Bioorg Med Chem Lett. 2011 Aug 15;21(16):4857-9. doi: 10.1016/j.bmcl.2011.06.035. Epub 2011 Jun 21.

Abstract

TrpA1 is an ion channel involved in nociceptive and inflammatory pain. It is implicated in the detection of chemical irritants through covalent binding to a cysteine-rich intracellular region of the protein. While performing an HTS of the Pfizer chemical collection, a class of pyrimidines emerged as a non-reactive, non-covalently binding family of agonists of the rat and human TrpA1 channel. Given the issues identified with the reference agonist Mustard Oil (MO) in screening, a new, non-covalently binding agonist was optimized and proved to be a superior agent to MO for screening purposes. Compound 16a (PF-4840154) is a potent, selective agonist of the rat and human TrpA1 channel and elicited TrpA1-mediated nocifensive behaviour in mouse.

摘要

TRPA1 是一种参与伤害性和炎性疼痛的离子通道。它通过与蛋白质富含半胱氨酸的细胞内区域共价结合,参与化学刺激物的检测。在对辉瑞化学药物库进行高通量筛选时,一类嘧啶类化合物作为大鼠和人 TRPA1 通道的非反应性、非共价结合激动剂出现。鉴于在筛选中发现芥子油(MO)作为参考激动剂存在问题,优化了一种新的非共价结合激动剂,并证明它是一种优于 MO 的筛选用药物。化合物 16a(PF-4840154)是一种有效的大鼠和人 TRPA1 通道选择性激动剂,可诱发小鼠的 TRPA1 介导的伤害性行为。

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