作者
Jinlong Jiang,Fa‐Xiang Ding,Xiaoyan Zhou,Thomas Bateman,Shuzhi Dong,Xin Gu,Reynalda deJesus,Barbara Pio,Haifeng Tang,Harry R. Chobanian,Dorothy Levorse,Mengwei Hu,Brande Thomas-Fowlkes,Michael Margulis,Martin Koehler,Adam B. Weinglass,Jonathan Gibson,Kevin Houle,Joel B. Yudkovitz,Caryn Hampton,Lee-Yuh Pai,Koppara Samuel,Timothy Cutarelli,Kathleen Sullivan,Emma R. Parmee,Ian W. Davies,Alexander Pasternak
摘要
A renal outer medullary potassium channel (ROMK, Kir1.1) is a putative drug target for a novel class of diuretics with potential for treating hypertension and heart failure. Our first disclosed clinical ROMK compound, 2 (MK-7145), demonstrated robust diuresis, natriuresis, and blood pressure lowering in preclinical models, with reduced urinary potassium excretion compared to the standard of care diuretics. However, 2 projected to a short human half-life (∼5 h) that could necessitate more frequent than once a day dosing. In addition, a short half-life would confer a high peak-to-trough ratio which could evoke an excessive peak diuretic effect, a common liability associated with loop diuretics such as furosemide. This report describes the discovery of a new ROMK inhibitor 22e (MK-8153), with a longer projected human half-life (∼14 h), which should lead to a reduced peak-to-trough ratio, potentially extrapolating to more extended and better tolerated diuretic effects.