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New furostanol saponins with anti-inflammatory and cytotoxic activities from the rhizomes of Smilax davidiana

机译:来自Smilax Davidiana的根茎的抗炎和细胞毒性活动的新的Furoostanol saponins

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Graphical abstract Display Omitted Highlights ? Seven new furostanol glycosides were isolated from the ethanol extract of Smilax davidiana . ? The structures of new compounds were determined on the basis of NMR spectroscopy and HR-ESI-MS. ? Compounds 3 , 5 and 7 were found to have modest anti-inflammatory effects. ? Davidianoside F ( 6 ) showed activity against MCF-7 and HELA cell lines. Abstract Seven new furostanol saponins have been isolated from the rhizomes of Smilax davidiana . Their structures were established by 2D NMR spectroscopic techniques ( 1 H, 1 H-COSY, NOESY, HSQC and HMBC), mass spectrometry and comparison with the literature. The isolated compounds were subjected to evaluate anti-inflammatory and cytotoxic activities in vitro. Compounds 3 , 5 and 7 were found to have modest anti-inflammatory effects through suppression of IL-1β production and promote the expression of IL-10 in LPS-stimulated RAW 264.7 cells. Davidianoside F ( 6 ) showed activity against MCF-7 and HELA cell lines at the concentration of 10.2μM and 4.3μM, respectively. ]]>
机译:图形抽象显示省略了亮点?从Smileax Davidiana的乙醇提取物中分离出七种新的Furoostanol糖苷。还基于NMR光谱和HR-ESI-MS测定新化合物的结构。还发现化合物3,5和7具有适度的抗炎作用。还DavidianoSide F(6)显示针对MCF-7和HeLa细胞系的活性。摘要七种新的Furostanol saponins已从Smilax Davidiana的根茎中分离出来。它们的结构由2D NMR光谱技术(1小时,1 H-Cozy,Noesy,HSQC和HMBC),质谱和与文献进行比较。对分离的化合物进行体外评估抗炎和细胞毒性活性。发现化合物3,5和7通过抑制IL-1β产生并促进IL-10在LPS刺激的原料264.7细胞中的表达具有适度的抗炎作用。 DavidianoSide F(6)分别显示针对MCF-7和HeLa细胞系的活性分别以10.2μm和4.3μm的浓度。 ]]>

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