Linaggrenoids A-I, structurally diverse lindenane sesquiterpenoids with anti-hepatic fibrosis effects from Lindera aggregata

被引:0
作者
Li, Wen-Xian [1 ,2 ,3 ]
Gan, Lu [4 ]
Liao, Yi-Ling [4 ]
Wu, Yu-Wei [3 ]
Zhang, Bai-Hui [3 ]
Guo, De-an [1 ,2 ,3 ]
Li, Wei [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
[2] Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Zhongshan Inst Drug Discovery, Shanghai Inst Mat Med, Zhongshan 528400, Peoples R China
[4] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Peoples R China
基金
中国国家自然科学基金;
关键词
Lindera aggregata; Lauraceae; Lindenane sesquiterpenoid; Anti-hepatic fibrosis activity; CHLORANTHUS; JAPONICUS; LACTONES; ROOTS;
D O I
10.1016/j.phytochem.2025.114477
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Linaggrenoid A (1), a highly rearranged lindenane sesquiterpenoid, together with eight undescribed lindenane sesquiterpenoid linaggrenoids B-I (2-9) and eight known analogs (10-17), were isolated from the root tubers of Lindera aggregata. Their structures, including absolute configurations, were established using spectroscopic and computational methods, as well as single-crystal X-ray diffraction. Linaggrenoids A and H (1 and 8), featuring a 5/6/3 and 3/5/6 carbocyclic ring system, respectively, demonstrated potential as anti-hepatic fibrosis agents by suppressing the expression of fibronectin, collagen I, and alpha-smooth muscle actin in TGF-beta 1-induced LX-2 cells.
引用
收藏
页数:10
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