Cytotoxic and Anti‐inflammatory Sesquiterpenes from Ainsliaea henryi

化学 细胞毒性T细胞 消炎药 萜烯 倍半萜 传统医学 立体化学 生物化学 免疫学 生物 体外 医学
作者
Ren‐Tao Zeng,Xue‐Yun Dong,Xinggen Fang,Niao Yang,Zhi‐Ran Shi,Zhi‐Guo Zhuo,Yun‐Heng Shen,Wensheng Zhang
出处
期刊:Chemistry & Biodiversity [Wiley]
卷期号:14 (2) 被引量:11
标识
DOI:10.1002/cbdv.201600210
摘要

Three new sesquiterpenoids, 4α-hydroxyeudesm-11(13)-en-12-yl 3-methylbutanoate (1), diaspanolide E (2), and (13α)-germacra-1(10),4-dien-12,8α-olid-15-oic acid (3), along with eight known sesquiterpenoids (4 - 11), were isolated from the aerial parts of Ainsliaea henryi. The chemical structures of compounds 1 - 3 were elucidated by spectroscopic analysis (1D-, 2D-NMR, MS and HR/MS). All isolates were evaluated for their inhibitory activities against nitric oxide (NO) production in lipopolysaccharide-induced RAW264.7 macrophage cells. Compound 10 exhibited significantly inhibition against NO release with an IC50 value of 6.54 ± 0.16 μm. Also, all isolated compounds were tested for cytotoxicity against three human tumor cell lines A549, MGC803, and HCT116, among which compound 5 significantly inhibited the proliferation of MGC803 cell lines with an IC50 value of 2.2 ± 0.2 μm.
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