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Updated: Sep 12, 2025

Optimized Analysis of In Vivo and In Vitro Hepatic Steatosis
Published on: March 11, 2017
Discovery of Highly Potent, Selective, and Liver-Targeted THR-β Agonists for the Treatment of Metabolic
Ju Liang1,2,3, Yipei Gu2, Liuyu Hu2
1School of Pharmaceutical Science and Technology, Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences, Hangzhou 310024, China.
Abstract:
With the improvement of living standards, metabolic-disorder-associated steatohepatitis (MASH) has posed a serious threat to public health. In 2024, THR-β agonist Resmetirom was approved by the FDA as the first market drug for the treatment of MASH. In this work, we discovered a new class of THR-β agonists through structure-based rational design. Compound 12 exhibited much higher agonistic activity (EC50 = 11.0 nM) and higher selectivity for THR-β over THR-α (THR-β/α = 34.1) compared to the market drug Resmetirom. More importantly, good pharmacokinetic properties of 12 was observed with an excellent liver to heart ratio of 335:1. Notably, compound 12 exhibited superior ability to improve steatosis, ballooning, inflammation and fibrosis, while Resmetirom did not show any improvement in inflammation, suggesting that 12 is a highly promising THR-β agonist and warrants extensive preclinical investigation as a potential clinical development candidate for the treatment of MASH.
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