Diterpenoids from the Aerial Parts of Isodon serra with Selective Cytotoxic Activity

被引:1
|
作者
Li, Siqin [1 ]
Liang, Fang [1 ]
Huang, Dongdong [1 ]
Wu, Huanling [1 ]
Tan, Xiaohua [1 ]
Ma, Jiang [1 ]
Wei, Caihong [1 ]
Wang, Shixiong [1 ]
Huang, Ziying [1 ]
Yang, Guang [2 ]
He, Xin [1 ]
Yang, Ji [1 ]
机构
[1] Guangdong Pharmaceut Univ, Sch Tradit Chinese Mat Med, Guangzhou 510006, Peoples R China
[2] China Acad Chinese Med Sci, Beijing 100700, Peoples R China
来源
MOLECULES | 2024年 / 29卷 / 12期
基金
中国国家自然科学基金;
关键词
Isodon serra; diterpenoids; cytotoxic activity; structure elucidation; ENT-KAURANE DITERPENOIDS; KAURENE DITERPENOIDS; RABDOSIA-SERRA; AGENTS; TAXOL;
D O I
10.3390/molecules29122733
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
Four new diterpenoids, isodosins A-D (1-4), together with nine known compounds (5-13) were isolated and identified from the aerial parts of Isodon serra (Maxim.) Hara. The structures of the new diterpenoids were elucidated based on the analysis of HR-ESI-MS data, 1D/2D-NMR-spectroscopic data, and electronic circular dichroism (ECD) calculations. Cytotoxicities of compounds 2, 3, 5, 6, and 9 against the HepG2 and H1975 cell lines were evaluated with the MTT assay. As a result, compounds 2, 3, and 6 revealed higher levels of cytotoxicity against HepG2 cells than against H1975 cells. Moreover, compund 6 demonstrated the most efficacy in inhibiting the proliferation of HepG2 cells, with an IC50 value of 41.13 +/- 3.49 mu M. This effect was achieved by inducing apoptosis in a dose-dependent manner. Furthermore, the relationships between the structures and activities of these compounds are briefly discussed.
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收藏
页数:13
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