Six new phenylpropanoids from Kaempferia galanga L . and their anti-inflammatory activity

被引:2
|
作者
Zhu, Yunfang [1 ,2 ]
Chen, Lu [1 ,2 ]
Zeng, Jia [3 ]
Xu, Jingwen [1 ,2 ]
Hu, Hui [4 ]
He, Xiangjiu [1 ,2 ]
Wang, Yihai [1 ,2 ]
机构
[1] Guangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R China
[2] Guangdong Engn Res Ctr Lead Cpds & Drug Discovery, Guangzhou 510006, Peoples R China
[3] Beijing Univ Chinese Med, Sch Life Sci, Beijing 100029, Peoples R China
[4] Humanwell Healthcare Grp Co Ltd, Wuhan 430000, Peoples R China
关键词
Kaempferia galanga L; Zingiberaceae; phenylpropanoid; 2+2] cycloaddition natural product; cyclobutane derivative; anti-inflammatory activity; CYCLOBUTANE DERIVATIVES; ACID; PHOTODIMERS; NEOLIGNANS;
D O I
10.1016/j.fitote.2024.106028
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Kaempferia galanga L. is an aromatic medicinal plant belonging to the Zingiberaceae family. Its rhizome has been widely used as traditional Chinese medicine and a flavor spice for a long time. In this study, six previously undescribed phenylpropanoids, including four [2 +2]- cycloaddition-derived cyclobutane natural products ( 1- 4 ), and two phenylpropanoids ( 5- 6 ) were isolated from the rhizomes of K. galanga L. Their structures were elucidated by spectroscopic methods, single-crystal X-ray diffraction, NMR calculation, and ECD spectra calculation. These cyclobutane derivatives were isolated from K. galanga for the first time. Furthermore, compounds 1-6 were evaluated for the potential inhibitory activities on NO production and NF- kappa B nuclear translocation in LPStriggered RAW 264.7 macrophages. The results showed that the isolated compounds have a moderate antiinflammatory activity measured on their potency to inhibit NO production and the expression of iNOS and COX-2. Additionally, compound 2 effectively suppressed NF- kappa B nuclear translocation at a concentration of 40 mu M.
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页数:10
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