Eudesmane-type sesquiterpenes from the rhizomes of Atractylodes macrocephala and their bioactivities

被引:4
|
作者
Zhang, Hai-Xin [1 ]
Si, Jin-Guang [1 ]
Li, Jing-Rong [1 ,2 ]
Yu, Meng [1 ]
Zhao, Chen-Xu [1 ]
Zhang, Tao [1 ]
Zou, Zhong-Mei [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Inst Med Plant Dev, Beijing 100193, Peoples R China
[2] Guizhou Med Univ, Med Sci, Guiyang 550000, Peoples R China
基金
中国国家自然科学基金;
关键词
Atractylodes macrocephala Koidz; Compositae; Sesquiterpene; Isolation; Bioactivities; INHIBITORY-ACTIVITY; TERPENOIDS;
D O I
10.1016/j.phytochem.2022.113545
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
Fifteen undescribed eudesmane-type sesquiterpenes, named atramacronoids D-R, along with fourteen known analogues were isolated from the rhizomes of Atractylodes macrocephala. The structures of atramacronoids D-R were elucidated based on extensive spectroscopic data analysis, Snatzke's rule, electronic circular dichroism (ECD) calculations, and X-ray crystallographic analysis. Notably, of the undescribed isolates, atramacronoids D and E are the first example of eudesmanolactam-phenol and eudesmanolactam-ethyl hybrids obtained from plants, respectively. A pair of enantiomers, (+)-and (-)-atramacronoids F, were successfully resolved by chiral -phase HPLC. Atramacronoid D exhibited weak cytotoxicity against SGC-7901 cells. Atramacronoid E significantly promoted the proliferation of LPS-induced IEC-6 cells.
引用
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页数:13
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