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首页> 外文期刊>Planta medica: Natural products and medicinal plant research >Anti-inflammatory Ingenane Diterpenoids from the Roots of Euphorbia kansui
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Anti-inflammatory Ingenane Diterpenoids from the Roots of Euphorbia kansui

机译:抗炎ingenane二萜来自邻戟属植物的根源

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Bioassay-guided fractionation of the ethanolic extract of the roots of Euphorbia kansui led to the isolation of two new in-genane diterpenoids, euphorkans A (1) and B (2), together with 16 known analogues (3-18). Their structures were determined by combined spectral and chemical methods. All the isolates were evaluated for their inhibitory effects on lipopoly-saccharide-induced nitric oxide production in RAW264.7 macrophage cells. Compounds 1-6 and 10-13 exhibited pronounced inhibitory activity with IC50 values in the range of 2.78-10.6 mu M, and were more potent than the positive control, quercetin (IC50 = 15.8 mu M). Compounds 1 and 5 were selected for further assays toward the key inflammation mediators TNF-alpha and IL-6, and showed a significant inhibition in a dose-dependent manner. The preliminary mechanistic study revealed that 1 and 5 inhibited NF-kappa B activity, which may exert a role in their anti-inflammatory activity.
机译:乙酸根的乙醇提取物的生物测定分馏导致了两个新的异丙内二萜,昆基(1)和B(2)的分离,与16个已知的类似物(3-18)。 它们的结构通过组合的光谱和化学方法测定。 评价所有分离株的抑制作用对Raw264.7巨噬细胞中的脂多糖诱导的一氧化氮产生的抑制作用。 化合物1-6和10-13在2.78-10.6μm的范围内具有IC 50值的明显抑制活性,并且比阳性对照,槲皮素(IC50 =15.8μm)更有效。 选择化合物1和5用于朝向关键炎症介质TNF-α和IL-6的进一步测定,并以剂量依赖性方式显示出显着的抑制作用。 初步机械研究表明,1和5抑制了NF-Kappa B活性,这可能在其抗炎活动中发挥作用。

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