Stilbenoids and Flavonoids from Cajanus cajan (L.) Millsp. and Their a-Glucosidase Inhibitory Activities

被引:2
|
作者
Zhao, Yaxian [1 ,2 ,3 ]
Zhao, Xinman [1 ,2 ,3 ]
Guo, Mengjia [1 ,2 ,3 ]
Varier, Krishnapriya M. [1 ,2 ,3 ]
Gajendran, Babu [1 ,2 ,3 ]
Liu, Shaohuan [1 ,2 ,3 ]
Tao, Ling [1 ,2 ,3 ]
Shen, Xiangchun [1 ,2 ,3 ]
Zhang, Nenling [1 ,2 ,3 ]
机构
[1] Guizhou Med Univ, Sch Pharmaceut Sci, State Key Lab Funct & Applicat Med Plants, Guiyang 550025, Peoples R China
[2] Guizhou Med Univ, Sch Pharmaceut Sci, High Efficacy Applicat Nat Med Resources Engn Ctr, Guiyang 550025, Peoples R China
[3] Guizhou Med Univ, Sch Pharmaceut Sci, Key Lab Optimal Utilizat Nat Med Resources, Guiyang 550025, Peoples R China
来源
MOLECULES | 2023年 / 28卷 / 09期
基金
中国国家自然科学基金;
关键词
Cajanus cajan; stilbenoid; flavonoid; alpha-glucosidase inhibitory activity; DERIVATIVES; CELLS;
D O I
10.3390/molecules28093779
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
Two new stilbenoids, cajanstilbenoid C (1) and cajanstilbenoid D (2), together with eight other known stilbenoids (3-10) and seventeen known flavonoids (11-27), were isolated from the petroleum ether and ethyl acetate portions of the 95% ethanol extract of leaves of Cajanus cajan (L.) Millsp. The planar structures of the new compounds were elucidated by NMR and high-resolution mass spectrometry, and their absolute configurations were determined by comparison of their experimental and calculated electronic circular dichroism (ECD) values. All the compounds were assayed for their inhibitory activities against yeast a-glucosidase. The results demonstrated that compounds 3, 8-9, 11, 13, 19-21, and 24-26 had strong inhibitory activities against a-glucosidase, with compound 11 (IC50 = 0.87 +/- 0.05 mu M) exhibiting the strongest activity. The structure-activity relationships were preliminarily summarized. Moreover, enzyme kinetics showed that compound 8 was a noncompetitive inhibitor, compounds 11, 24-26 were anticompetitive, and compounds 9 and 13 were mixed-competitive.
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页数:11
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