化学
孤儿受体
邻氨基苯甲酸
G蛋白偶联受体
药理学
消炎药
受体
立体化学
生物化学
医学
转录因子
基因
作者
Nader M. Boshta,Michael Lewash,Meryem Köse,Vigneshwaran Namasivayam,Soumya Sarkar,Jan Voss,Andy J. Liedtke,Anna Junker,Maoqun Tian,Anne Stößel,Mahmoud Rashed,Ahmed Mahal,Nicole Merten,Cécile Pégurier,Jörg Hockemeyer,Evi Kostenis,Christa E. Müller
标识
DOI:10.1021/acs.jmedchem.4c01755
摘要
83.2 nM). Receptor-ligand docking studies revealed that the compounds' binding site is characterized by positively charged arginine residues and a lipophilic pocket. These findings yield valuable insights into this poorly characterized receptor providing a basis for future drug development.
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