Three New Selaginellin Derivatives from Selaginella pulvinata and Their α-Glucosidase Inhibitory Activity

被引:2
作者
Zhu, Qin-Feng [1 ,2 ,3 ]
Luo, Tian-Tian [1 ,2 ]
Chen, Qian [1 ,2 ]
Gao, Bei-Bei [3 ]
Zeng, Ai-Fen [1 ,2 ]
Ao, Jun-Li [1 ,2 ]
Xu, Guo-Bo [1 ,2 ]
Liao, Shang-Gao [1 ,2 ]
He, Xun [1 ,2 ]
机构
[1] Guizhou Med Univ, Sch Pharm, Guiyang 550025, Peoples R China
[2] Guizhou Med Univ, State Key Lab Funct & Applicat Med Plants, Guiyang 550025, Peoples R China
[3] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Chi, Kunming 650201, Peoples R China
关键词
Selaginella pulvinata; selaginellin; selaginpulvilins V-X; alpha-glucosidase inhibitory activity; TAMARISCINA; MECHANISM;
D O I
10.1002/cbdv.202300109
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 selaginellin derivatives, selaginpulvilins V-X (1-3), together with seven known analogs (4-10) were isolated from whole plants of Selaginella pulvinata. Their structures were determined by extensive spectroscopic methods including 1D and 2D NMR, HR-ESI-MS and chemical derivatization method. Compound 1 represents a rare example of naturally occurring selaginellin with an alkynylphenol-trimmed skeleton. Biological evaluation showed that compounds 2, 6 and 8 displayed moderate inhibition against alpha-glucosidase with IC50 values of 3.71, 2.04 and 4.00 mu M, respectively.
引用
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页数:7
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