Design of Next-Generation DGAT2 Inhibitor PF-07202954 with Longer Predicted Half-Life.

Kevin J Filipski, David J Edmonds,Michelle R Garnsey,Daniel J Smaltz,Karen Coffman,Kentaro Futatsugi, Jack Lee, Steven V O'Neil, Ann Wright, Deane Nason,James R Gosset, Christine C Orozco, Dan Blackler, Guila Fakhoury,Jemy A Gutierrez,Sylvie Perez,Trenton Ross,Ingrid Stock,Gregory Tesz,Robert Dullea

ACS medicinal chemistry letters(2023)

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摘要
Diacylglycerol O-acyltransferase 2 (DGAT2) inhibitors have been shown to lower liver triglyceride content and are being explored clinically as a treatment for non-alcoholic steatohepatitis (NASH). This work details efforts to find an extended-half-life DGAT2 inhibitor. A basic moiety was added to a known inhibitor template, and the basicity and lipophilicity were fine-tuned by the addition of electrophilic fluorines. A weakly basic profile was required to find an appropriate balance of potency, clearance, and permeability. This work culminated in the discovery of PF-07202954 (), a weakly basic DGAT2 inhibitor that has advanced to clinical studies. This molecule displays a higher volume of distribution and longer half-life in preclinical species, in keeping with its physicochemical profile, and lowers liver triglyceride content in a Western-diet-fed rat model.
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关键词
inhibitor,next-generation,half-life
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