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BMS-986308 的发现:一种用于心力衰竭治疗的肾脏外髓质钾通道抑制剂。

Discovery of BMS-986308: A Renal Outer Medullary Potassium Channel Inhibitor for the Treatment of Heart Failure.

机构信息

Bristol Myers Squibb Research & Early Development, Princeton, New Jersey 08540, United States.

Biocon Bristol Myers Squibb Research Center, Syngene International Limited, Bangalore 560099, India.

出版信息

J Med Chem. 2024 Jun 13;67(11):9731-9744. doi: 10.1021/acs.jmedchem.4c00893. Epub 2024 May 29.

Abstract

Recent literature reports highlight the importance of the renal outer medullary potassium (ROMK) channel in renal sodium and potassium homeostasis and emphasize the potential impact that ROMK inhibitors could have as a novel mechanism diuretic in heart failure patients. A series of piperazine-based ROMK inhibitors were designed and optimized to achieve excellent ROMK potency, hERG selectivity, and ADME properties, which led to the identification of compound (BMS-986308). BMS-986308 demonstrated efficacy in the volume-loaded rat diuresis model as well as promising in vitro and in vivo profiles and was therefore advanced to clinical development.

摘要

最近的文献报道强调了肾外髓质钾(ROMK)通道在肾脏钠钾平衡中的重要性,并强调了 ROMK 抑制剂作为心力衰竭患者新型利尿机制的潜在影响。设计并优化了一系列基于哌嗪的 ROMK 抑制剂,以实现优异的 ROMK 效力、hERG 选择性和 ADME 特性,从而鉴定出化合物(BMS-986308)。BMS-986308在容量负荷大鼠利尿模型中表现出疗效,并且具有有前景的体外和体内特征,因此被推进到临床开发。

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