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藤黄檀中呋喃二萜类化合物及其他成分的抗炎活性。

Anti-inflammatory activities of furanoditerpenoids and other constituents from Fibraurea tinctoria.

作者信息

Su Chung-Ren, Chen Yuh-Fung, Liou Meei-Jen, Tsai Huei-Yann, Chang Wen-Shin, Wu Tian-Shung

机构信息

Department of Chemistry, National Cheng Kung University, No.1, University Road, Tainan 701, Taiwan.

出版信息

Bioorg Med Chem. 2008 Nov 1;16(21):9603-9. doi: 10.1016/j.bmc.2008.09.023. Epub 2008 Sep 12.

Abstract

Five new furanoditerpenoids, epi-8-hydroxycolumbin (1), fibaruretin B (2), C (3), E (5), and F (6), were isolated from the stems of Fibraurea tinctoria, as well as fibaruretin D (4) from the natural source for the first time, and 39 known compounds. The structures (1-6) were elucidated on the basis of spectroscopic analysis. All the isolated furanoditerpenoids (1-16) were examined for their in vitro activity and some were in vivo anti-inflammatory activity. Compounds 8 and 9 showed significant anti-inflammatory action administered at a dose of 100mg/kg of reducing carrageenan mice paw edema, whereas compound 7, 9, 10, 14, and 16 were more potent to inhibit NO production. The inhibitory effects of these compounds are dose-dependent (1-4 microg/ml).

摘要

从黄藤茎中分离得到5个新的呋喃二萜类化合物,表-8-羟基哥伦比亚苷(1)、黄藤素B(2)、C(3)、E(5)和F(6),同时首次从天然来源中分离得到黄藤素D(4),以及39个已知化合物。通过光谱分析确定了化合物(1-6)的结构。对所有分离得到的呋喃二萜类化合物(1-16)进行了体外活性检测,部分化合物进行了体内抗炎活性检测。化合物8和9在100mg/kg剂量下对角叉菜胶致小鼠足肿胀具有显著抗炎作用,而化合物7、9、10、14和16对一氧化氮生成的抑制作用更强。这些化合物的抑制作用呈剂量依赖性(1-4μg/ml)。

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