Discovery of MK-8153, a Potent and Selective ROMK Inhibitor and Novel Diuretic/Natriuretic.

Journal: Journal Of Medicinal Chemistry
Published:
Abstract

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.

Authors
Jinlong Jiang, Fa-xiang Ding, Xiaoyan Zhou, Thomas Bateman, Shuzhi Dong, Xin Gu, Reynalda Keh Dejesus, Barbara Pio, Haifeng Tang, Harry Chobanian, Dorothy Levorse, Mengwei Hu, Brande Thomas Fowlkes, Michael Margulis, Martin Koehler, Adam Weinglass, Jack Gibson, Kevin Houle, Joel Yudkovitz, Caryn Hampton, Lee-yuh Pai, Koppara Samuel, Timothy Cutarelli, Kathleen Sullivan, Emma Parmee, Ian Davies, Alexander Pasternak