Design, Synthesis, and Biological Evaluation of Chromone Derivatives as STAT1 Inhibitors for Treatment of Nonalcoholic Steatohepatitis

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Authors: Zhipeng Zhang, Hongyan Lai, Shaofang Tian, Yingjie Song, Cunwuliji Na, Xiang Shi, Changhong He, Liuye Shi, Shengyun Wang, Fawad Ali, Fu Shu, Baoshun Zhang
Cited by: 1
References: 46

Abstract

Nonalcoholic steatohepatitis (NASH) is a chronic liver disease with a high global incidence rate, intricately linked to metabolic disorders. It is characterized by steatosis, inflammation, and hepatocyte ballooning. STAT1 is a transcription factor involved in metabolic regulation and progression of inflammatory responses. In this study, we have identified STAT1 as a novel therapeutic target for NASH. Using our established STAT1 inhibitor screening platform, we identified the compound ZDZ-553, which is characterized by a chromone skeleton, demonstrates potent inhibitory activity against STAT1, and exhibits a favorable safety profile. In the NASH mouse model experiment, ZDZ-553 significantly ameliorated liver steatosis and inflammatory responses. These findings collectively suggest that ZDZ-553 could be a promising candidate for treatment of NASH, highlighting the therapeutic potential of targeting STAT1.

Fields of Study & Subjects

Cytokine Signaling Pathways and Interactions Liver Disease Diagnosis and Treatment Hepatitis C virus research

Publication details

Journal / source
Journal of Medicinal Chemistry
Publisher
American Chemical Society (ACS)
Volume
69
Issue
3
Pages
2509–2538
Publication date
27 January 2026
Language
EN