Journal of medicinal chemistry · 2021
Discovery of MK-8153, a Potent and Selective ROMK Inhibitor and Novel Diuretic/Natriuretic.
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Jiang Jinlong, Ding Fa-Xiang, Zhou Xiaoyan, Bateman Thomas J, Dong Shuzhi, Gu Xin, Keh deJesus Reynalda, Pio Barbara, Tang Haifeng, Chobanian Harry R, Levorse Dorothy, Hu Mengwei, Thomas-Fowlkes Brande, Margulis Michael, Koehler Martin, Weinglass Adam, Gibson Jack, Houle Kevin, Yudkovitz Joel, Hampton Caryn, Pai Lee-Yuh, Samuel Koppara, Cutarelli Timothy, Sullivan Kathleen, Parmee Emma R, Davies Ian, Pasternak Alexander
Аннотация
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.