Discovery of novel non-steroidal reverse indole mineralocorticoid receptor antagonists

被引:10
|
作者
Ogawa, Anthony K. [1 ]
Bunte, Ellen Vande [1 ]
Mal, Rudrajit [1 ]
Lan, Ping [1 ]
Sun, Zhongxiang [1 ]
Crespo, Alejandro [2 ]
Wiltsie, Judyann [1 ]
Clemas, Joseph [1 ]
Gibson, Jack [1 ]
Contino, Lisa [1 ]
Lisnock, JeanMarie [1 ]
Zhou, Gaochao [1 ]
Garcia-Calvo, Margarita [1 ]
Jochnowitz, Nina [1 ]
Ma, Xiuying [1 ]
Pan, Yi [1 ]
Brown, Patricia [1 ]
Zamlynny, Beata [1 ]
Bateman, Thomas [1 ]
Leung, Dennis [2 ]
Xu, Ling [2 ]
Tong, Xinchun [2 ]
Liu, Kun [1 ]
Crook, Martin [1 ]
Sinclair, Peter [1 ]
机构
[1] Merck & Co Inc, Early Dev & Discovery Sci, 2000 Galloping Hill Rd, Kenilworth, NJ 07033 USA
[2] Merck & Co Inc, Early Dev & Discovery Sci, 126 E Lincoln Ave, Rahway, NJ 07065 USA
关键词
Mineralocorticoid receptor antagonist; Hypertension; Spironolactone; Eplerenone; MILD PATIENTS HOSPITALIZATION; ALDOSTERONE; EPLERENONE; POTENT; IDENTIFICATION; HYPERKALEMIA; SURVIVAL;
D O I
10.1016/j.bmcl.2016.04.052
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Reported herein are a series of reverse indoles that represent novel non-steroidal mineralocorticoid receptor (MR) antagonists. The key structure-activity relationships (SAR) are presented below. This reverse indole series is exemplified by a compound that demonstrated efficacy in an acute natriuresis rodent model comparable to marketed MR antagonists, spironolactone and eplerenone. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2866 / 2869
页数:4
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