化学
兴奋剂
共价键
半胱氨酸
离子通道
药理学
化学合成
细胞内
立体化学
生物化学
受体
体外
有机化学
酶
医学
作者
Thomas Ryckmans,Aisah A. Aubdool,Jennifer V. Bodkin,Peter J. Cox,Susan D. Brain,Thomas Dupont,Emma Fairman,Yoshinobu Hashizume,Naoko Ishii,Takamasa Kato,Linda Kitching,Julie Newman,Kiyoyuki Omoto,David J. Rawson,Jade Strover
标识
DOI:10.1016/j.bmcl.2011.06.035
摘要
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.
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