Six new tigliane diterpenoids with anti-inflammatory activity from Euphorbia kansuensis

被引:3
|
作者
Yan, Xue-Long [1 ,2 ,3 ]
Chen, Bei-Ling [1 ,2 ]
Yuan, Fang-Yu [4 ]
Zhu, Qin-Feng [1 ,2 ]
Zhang, Xu [1 ,2 ]
Lin, Yan [1 ,2 ]
Long, Qing-De [1 ,2 ]
Liao, Shang-Gao [1 ,2 ]
机构
[1] Guizhou Med Univ, State Key Lab Funct & Applicat Med Plants, Guian New Dist 550025, Guizhou, Peoples R China
[2] Guizhou Med Univ, Sch Pharm, Guian New Dist 550025, Guizhou, Peoples R China
[3] Guizhou Med Univ, Sch Basic Med Sci, Guian New Dist 550025, Guizhou, Peoples R China
[4] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Guangdong, Peoples R China
关键词
Euphorbia kansuensis; Anti-inflammatory; NO inhibitory activity; Tigliane diterpenoid; ESTERS; CONSTITUENTS; PLANTS;
D O I
10.1016/j.arabjc.2022.103807
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Six new tigliane diterpenoids, euphkanoids A -F (1-6), along with 12 known diterpenoids (7-18) were isolated from the roots of Euphorbia kansuensis, a traditional Chinese medicinal plant. Their structures were elucidated by spectroscopic analysis, ECD calculation and chemical methods. Compounds 1-3 represent the unusual examples of tigliane diterpenoids with a conjugated olefinic aldehyde moiety. 1-18 and two hydrolyzed analogues (1c and 4a) were screened for the inhibitory effects on nitric oxide (NO) production induced by lipopolysaccharide (LPS) in RAW264.7 cells. The results showed that 1-3 and 6 markedly inhibited NO production with IC(50 )values in the range of 4.8-11.3 lM, which were more active than the positive control quercetin (IC50 = 12.3 lM). (C) 2022 The Author(s). Published by Elsevier B.V. on behalf of King Saud University.
引用
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页数:9
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