Nordqvist Anneli, Granberg Kenneth L
Medicinal Chemistry, Cardiovascular, Renal and Metabolism, IMED Biotech Unit, AstraZeneca, Gothenburg, Sweden.
Medicinal Chemistry, Cardiovascular, Renal and Metabolism, IMED Biotech Unit, AstraZeneca, Gothenburg, Sweden.
Vitam Horm. 2019;109:151-188. doi: 10.1016/bs.vh.2018.10.008. Epub 2018 Dec 11.
Two mineralocorticoid receptor antagonists, spironolactone and eplerenone, are currently approved by the FDA. Several non-steroid based ligands are in clinical trials for indications including heart failure, hypertension and diabetic kidney disease, and even more structurally distinct chemical series are reported in the literature with preclinical data from animal models. Design of new ligands that are both selective over the other oxosteroid receptors (GR, PR and AR) and possess properties compatible with oral dosing, despite the overall lipophilic binding pocket of MR, remains a challenge. High-throughput screening has been successfully used to identify novel starting points in several drug discovery programs, and these were optimized using property based drug design, often aided by protein-ligand X-ray complex structures.
目前,两种盐皮质激素受体拮抗剂——螺内酯和依普利酮已获美国食品药品监督管理局(FDA)批准。几种非甾体类配体正处于临床试验阶段,用于治疗心力衰竭、高血压和糖尿病肾病等疾病,甚至有更多结构不同的化学系列在文献中被报道,并伴有来自动物模型的临床前数据。尽管盐皮质激素受体具有整体亲脂性结合口袋,但设计出对其他氧类固醇受体(糖皮质激素受体、孕激素受体和雄激素受体)具有选择性且具有与口服给药相兼容特性的新型配体仍然是一项挑战。高通量筛选已成功用于在多个药物研发项目中确定新的起点,并通过基于性质的药物设计对这些起点进行优化,蛋白质-配体X射线复合物结构常常为此提供帮助。