化学
氟苯那酸
效力
受体
支气管扩张
药理学
兴奋剂
结构-活动关系
羧酸
立体化学
生物化学
体外
哮喘
内科学
支气管扩张剂
医学
作者
Lukas Waterloo,Harald Hübner,Fabrizio Fierro,Tara Pfeiffer,Regine Brox,Stefan Löber,Dorothée Weikert,Masha Y. Niv,Peter Gmeiner
标识
DOI:10.1021/acs.jmedchem.2c01997
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 IP1accumulation 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.
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