Anti-Inflammatory Constituents from Bidens frondosa

Molecules

Jiamei Le²  Wenquan Lu²  Xiaojuan Xiong¹  Zhijun Wu²  Wansheng Chen² 

[1] College of Chemical and Biological Engineering, Yichun University, Jiangxi 336000, China; E-Mail:;Department of Pharmacy, Changzheng Hospital, Second Military Medical University, Shanghai 200003, China; E-Mails:

关键词: Bidens frondosa;    polyacetylene glucoside;    phenylpropanoid glucoside;    flavonoid glycoside;    anti-inflammatory activity;   

DOI  :  10.3390/molecules201018496

来源: mdpi

【 摘 要 】

A new polyacetylene glucoside (3E,5E,11E)-tridecatriene-7,9-diyne-1,2,13-triol-2-O-β-d-glucopyranoside (1), a new phenylpropanoid glucoside 2′-butoxyethylconiferin (2), and a new flavonoid glycoside 8,3′,4′-trihydroxyflavone-7-O-(6′′-O-p-coumaroyl)-β-d-glucopyranoside (3), have been isolated from Bidens frondosa together with fifty-three known compounds 4–56. The structures of these compounds were established by spectroscopic methods. mainly ESIMS, 1D- and 2D-NMR spectroscopic data. and comparison with literature data. Compounds 1–34, 36, 39, 43, 47, 51, and 52 were tested for inhibition of nuclear factor kappa B (NF-κB) in 293-NF-κB-luciferase report cell line induced by lipopolysaccharide (LPS), and compounds 1, 2, 3, 9, 15, 21, 24 and 51 were tested for the production of TNF-α, IL-1β, IL-6, IL-10 in RAW 264.7 macrophages induced by LPS. In conclusion, the isolated compounds 1, 2, 3, 9, 15, 21, 24 and 51 exhibited significant activity in anti-inflammatory activity assays.

【 授权许可】

CC BY   
© 2015 by the authors; licensee MDPI, Basel, Switzerland.