化学
体内
糖皮质激素
药理学
体外
结构-活动关系
生物活性
酶抑制剂
敌手
糖皮质激素受体
生物化学
作用机理
抗糖皮质激素
作者
Lorna Duffy,Mark Mills,Andrew W. Phillips,Ian R. Strutt,Thomas W. Hornsby,Morgan Jouanneau,Bohdan Waszkowycz,Sally L. Lee,Adam Peall,Utsav Bali,Iain A. S. Walters,Hazel Hunt
标识
DOI:10.1021/acs.jmedchem.5c03567
摘要
Glucocorticoid receptor antagonists (GR antagonists) are a class of compounds developed to inhibit the activation of the glucocorticoid receptor and they have been used to treat a range of conditions such as Cushing's syndrome, diabetes, glaucoma, and depression. We report herein the discovery and optimization of a series of selective piperazine-based GR antagonists and discuss how key learnings from the discovery of relacorilant (CORT125134) were utilized to identify a simplified scaffold. Several compounds were identified with the desired profile and 3 key compounds were progressed to in vivo proof of concept studies.
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