Cytotoxic guaianolides and seco-guaianolides from Artemisia atrovirens

被引:10
|
作者
Zheng, Yongzhe [1 ,2 ,3 ]
Ke, Chang-Qiang [1 ,2 ]
Zhou, Shuaizhen [1 ,2 ]
Feng, Lu [1 ,2 ]
Tang, Chunping [1 ,2 ]
Ye, Yang [1 ,2 ,3 ,4 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Mat Medial, State Key Lab Drug Res, Shanghai 201203, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Mat Medial, Nat Prod Chem Dept, Shanghai 201203, Peoples R China
[3] Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
[4] Shanghai Tech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
基金
中国国家自然科学基金;
关键词
Artemisia atrovirens; Guaianolide; TDDFT ECD calculation; Cytotoxicity; SESQUITERPENE LACTONES; ABSOLUTE-CONFIGURATIONS; CONSTITUENTS; ARGYI;
D O I
10.1016/j.fitote.2021.104900
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A phytochemical investigation of a medicinal plant Artemisia atrovirens was carried out, resulting in the characterization of a novel bis-nor seco-guaianolide, seco-atrovirenolide A (1), a new 1,10-seco-guaianolide derivative, seco-atrovirenoic acid A (2), and a new artifact 10-methanoyloxy-seco-atrovirenoic acid A (3), together with eight known guaianolide and seco-guaianolide derivatives (4-11). The structures of new compounds were fully established by extensive analysis of MS, 1D and 2D NMR spectroscopic data. The absolute configurations of the isolated compounds were confirmed by TDDFT ECD calculation, Mosher's method, and X-ray crystal diffraction experiment. All the compounds were tested in vitro for their cytotoxicity against HL-60 and A549 cell lines. Some of them showed moderate inhibitory activity against HL-60 cell lines with IC50 values ranging from 5.99 to 11.74 mu M.
引用
收藏
页数:8
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