糖皮质激素受体
化学
糖皮质激素
兴奋剂
药物发现
受体
转换抑制
体外
药理学
生物化学
内分泌学
基因
生物
交易激励
转录因子
作者
Markus Berger,Hartmut Rehwinkel,Norbert Schmees,Heike Schäcke,K. A. P. Edman,Lisa Wissler,Andreas Reichel,Stefan Jaroch
标识
DOI:10.1016/j.bmcl.2016.12.047
摘要
We report on the discovery of two new lead series for the development of glucocorticoid receptor agonists. Firstly, the discovery of tetrahydronaphthalenes led to metabolically stable and dissociated compounds. Their binding mode to the glucocorticoid receptor could be elucidated through an X-ray structure. Closer inspection into the reaction path and analyses of side products revealed a new amino alcohol series also addressing the glucocorticoid receptor and demonstrating strong anti-inflammatory activity in vitro.
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