Cytotoxic and Anti-inflammatory Sesquiterpenes from Ainsliaea henryi

被引:15
|
作者
Zeng, Ren-Tao [1 ]
Dong, Xue-Yun [1 ]
Fang, Xing [1 ]
Yang, Niao [1 ]
Shi, Zhi-Ran [3 ]
Zhuo, Zhi-Guo [1 ]
Shen, Yun-Heng [1 ]
Zhang, Wei-Dong [1 ,2 ,3 ]
机构
[1] Second Mil Med Univ, Sch Pharm, Dept Phytochem, Shanghai 200433, Peoples R China
[2] Shanghai Inst Pharmaceut Ind, Shanghai 200400, Peoples R China
[3] China Pharmaceut Univ, Sch Tradit Chinese Med, Nanjing 210009, Jiangsu, Peoples R China
关键词
Ainsliaea species; Ainsliaea henryi; Sesquiterpenoids; NO production; Cytotoxic activities; ACERIFOLIA SCH BIP; NITRIC-OXIDE; LACTONES; MACROCEPHALA; DERIVATIVES; NAKAI;
D O I
10.1002/cbdv.201600210
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
Three new sesquiterpenoids, 4-hydroxyeudesm-11(13)-en-12-yl 3-methylbutanoate (1), diaspanolide E (2), and (13)-germacra-1(10),4-dien-12,8-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 m. 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 m.
引用
收藏
页数:7
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