Artematrovirenins A-P, guaiane-type sesquiterpenoids with cytotoxicities against two hepatoma cell lines from Artemisia atrovirens

被引:21
|
作者
Su, Li-Hua [1 ,2 ]
Ma, Yun-Bao [1 ]
Geng, Chang-An [1 ]
Li, Tian-Ze [1 ]
Huang, Xiao-Yan [1 ]
Hu, Jing [1 ]
Zhang, Xin [1 ,2 ]
Tang, Shuang [1 ,2 ]
Shen, Cheng [1 ,2 ]
Gao, Zhen [1 ,2 ]
Zhang, Xue-Mei [1 ]
Chen, Ji-Jun [1 ,2 ]
机构
[1] Chinese Acad Sci, State Key Lab Phytochem & Plant Resources West Ch, Yunnan Key Lab Nat Med Chem, Kunming Inst Bot, Kunming 650201, Yunnan, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
Artemisia atrovirens; guaiane-type sesquiterpenoids; artematrovirenins A-P; HepG2 and Huh7 cell lines; antihepatic cytotoxicity; LACTONES; CONSTITUENTS; GUAIANOLIDES;
D O I
10.1016/j.bioorg.2021.105072
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
Random screening revealed that the EtOH extract of Artemisia atrovirens showed significant cytotoxicity against two human hepatoma cell lines (HepG2 and Huh7) with the inhibitory ratio of 98.9% and 99.7% at the concentration of 100 mu g/mL. Further bioactivity-guided isolation of active fraction led to 16 new guaiane-type sesquiterpenoids, artematrovirenins A-P (1-16). Their structures were elucidated by extensive spectroscopic data. The absolute stereochemistry of compounds 1 and 14 was determined by single-crystal X-ray diffraction analyses. Pharmacological evaluation suggested that five compounds (3, 5, 8, 10, and 15) exhibited cytotoxicity, compounds 3 and 5 displayed cytotoxicity against HepG2 cell line with an IC50 values of 8.0 and 16.0 mu M, as well as against Huh7 cell line with values of 18.2 and 32.2 mu M.
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页数:11
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