化学
药理学
泼尼松龙
体内
糖皮质激素受体
兴奋剂
部分激动剂
不利影响
炎症
糖皮质激素
受体
药物发现
副作用(计算机科学)
内分泌学
内科学
生物化学
生物
生物技术
程序设计语言
医学
计算机科学
作者
Lena Ripa,K. A. P. Edman,Matthew Dearman,Goran Edenro,Ramon Hendrickx,Victoria Ullah,Hui‐Fang Chang,Matti Lepistö,Dave Chapman,Stefan Geschwindner,Lisa Wissler,Petter Svanberg,Karolina Lawitz,Jesper Malmberg,Antonios Nikitidis,Roine I. Olsson,James Bird,Antoni Llinas,Tove Hegelund-Myrbäck,Markus Berger
标识
DOI:10.1021/acs.jmedchem.7b01690
摘要
Synthetic glucocorticoids (GC) are essential for the treatment of a broad range of inflammatory diseases. However, their use is limited by target related adverse effects on, e.g., glucose homeostasis and bone metabolism. Starting from a nonsteroidal GR ligand (4) that is a full agonist in reporter gene assays, we exploited key functional triggers within the receptor, generating a range of structurally diverse partial agonists. Of these, only a narrow subset exhibited full anti-inflammatory efficacy and a significantly reduced impact on adverse effect markers in human cell assays compared to prednisolone. This led to the discovery of AZD9567 (15) with excellent in vivo efficacy when dosed orally in a rat model of joint inflammation. Compound 15 is currently being evaluated in clinical trials comparing the efficacy and side effect markers with those of prednisolone.
科研通智能强力驱动
Strongly Powered by AbleSci AI