Three new cassane diterpenoids from the seed kernels of Caesalpinia sinensis

被引:2
|
作者
Li, Ping [1 ]
Zhang, Bao-Hui [2 ,3 ]
Zhu, Zhi-Wei [2 ]
Jing, Wen-Hua [2 ,3 ]
Wang, Miao [2 ,3 ]
Gao, Hui-Yuan [2 ,3 ]
机构
[1] Shanxi Pharmaceut Vocat Coll, Dept Pharmaceut Engn, Taiyuan 030031, Peoples R China
[2] Shenyang Pharmaceut Univ, Sch Tradit Chinese Mat Med, Shenyang 110016, Peoples R China
[3] Shenyang Pharmaceut Univ, Key Lab Struct Based Drug Design & Discovery, Minist Educ, Shenyang 110016, Peoples R China
关键词
Caesalpinia sinensis; Cassane diterpenoids; Anti-inflammatory activity; FURANODITERPENES;
D O I
10.1016/j.phytol.2021.12.004
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Three new cassane derivatives, caesall FE (1) and caesalminaxin HC-HD (2-3), together with four known compounds (4-7) were separated from the seed kernels of Caesalpinia sinensis, and their structures were elucidated by means of analysis of comprehensive spectroscopic data, especially 1D and 2D NMR and HRESIMS. Compounds 13 represented the new examples of cassane diterpenoids containing an isomerized furan ring fused with an aromatized C ring or conjugated with one additional double bond. Biological evaluation revealed that compounds 1-7 could inhibit the overproduction of NO induced by LPS, and compounds 2 and 4-6 exhibited the inhibitory ration more than 60 % at the concentration of 50 mu M.
引用
收藏
页码:115 / 119
页数:5
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