Journal of medicinal chemistry · 2026
Discovery of Jatrophane Diterpenoids as JAG1-Notch Signaling Inhibitors for the Treatment of Liver Fibrosis.
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Zhu Xin-Ying, Wu Shu-Qi, Gan Lu, Yang Xianyuan, Liao Yi-Ling, An Nan, Fan Run-Zhu, Huang Jia-Luo, Tang Gui-Hua, Zhang Chuan-Rui, Yin Sheng
Аннотация
Liver fibrosis is an urgent clinical condition that lacks effective therapies. In this study, molecular networking-guided fractionation of the medicinal plant Euphorbia hylonoma yielded a focused jatrophane diterpenoid library (1-32), featuring 26 previously undescribed structures. Subsequent antifibrotic screening of this library in TGF-β1-stimulated hepatic stellate cells (HSCs) identified euphylonoid D (1) as a novel hit, enabling a preliminary structure-activity relationship (SAR) analysis of this class. In a CCl4-induced mouse model, 1 significantly alleviated liver fibrosis while exhibiting a favorable safety profile. Mechanistic studies revealed that 1 acts as the first small-molecule inhibitor of Jagged-1 (JAG1), a classic Notch ligand, thereby suppressing Notch signaling, leading to the attenuation of liver fibrosis. These findings not only validate JAG1 as a therapeutic target for liver fibrosis but also highlight 1 as a promising lead for developing novel antifibrotic agents.