首页> 外文期刊>Journal of Medicinal Chemistry >Discovery of 2-Aminopyrimidines as Potent Agonists for the Bitter Taste Receptor TAS2R14
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Discovery of 2-Aminopyrimidines as Potent Agonists for the Bitter Taste Receptor TAS2R14

机译:发现2-氨基嘧啶作为苦味受体的有效激动剂TAS2R14

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摘要

The bitter taste receptor TAS2R14 is a G protein-coupled receptor that is found on the tongue as well as in the human airway smooth muscle and other extraoral tissues. Because its activation causes bronchodilatation, TAS2R14 is a potential target for the treatment of asthma or chronic obstructive pulmonary disease. Structural variations of flufenamic acid, a nonsteroidal anti-inflammatory drug, led us to 2-aminopyridines showing considerable efficacy and potency in an IP(1)accumulation assay. In combination with an exchange of the carboxylic moiety by a tetrazole unit, a set of promising new TAS2R14 agonists was developed. The most potent ligand 28.1 (EC50 = 72 nM) revealed a six-fold higher potency than flufenamic acid and a maximum efficacy of 129. Besides its unprecedented TAS2R14 activation, 28.1 revealed marked selectivity over a panel of 24 non-bitter taste human G protein-coupled receptors.
机译:苦味受体 TAS2R14是一种 G 蛋白偶联受体,存在于舌头以及人体气道平滑肌和其他口外组织中。由于其激活会导致支气管扩张,TAS2R14是治疗哮喘或慢性阻塞性肺疾病的潜在靶标。氟芬那酸(一种非甾体类抗炎药)的结构变化使我们发现 2-氨基吡啶在 IP(1) 积累测定中显示出相当大的疗效和效力。结合四唑单元对羧基部分的交换,开发了一组有前途的新型TAS2R14激动剂。最有效的配体 28.1 (EC50 = 72 nM) 显示出比氟芬那酸高 6 倍的效力和 129% 的最大功效。除了前所未有的TAS2R14激活外,28.1 还显示出对 24 种非苦味人类 G 蛋白偶联受体的显着选择性。

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