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首页> 外文期刊>Journal of Biologically Active Products from Nature >In vitro evaluation of antioxidant, antiproliferative potentials of bioactive extract-cum-rutin compound Isolated from Memecylon edule leaves and its molecular docking study
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In vitro evaluation of antioxidant, antiproliferative potentials of bioactive extract-cum-rutin compound Isolated from Memecylon edule leaves and its molecular docking study

机译:从Memecylon edule叶中分离的生物活性提取物-芦丁化合物的抗氧化剂,抗增殖潜力的体外评估及其分子对接研究

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The current study was planned to investigate the antioxidant and anti-proliferative potential of leaf crude extracts and isolated compound (rutin) from Memecylon edule by performing the standard antioxidant and MTT assays. Results suggested that different solvents crude leaf extracts of M. edule expressed varying degree of antioxidant potential on all tested methods (DPPH, NO, OH, O2- radicals) based on dose depended manner and they also had good reducing ability. Significant high antiradical potential was found in ethyl acetate extract (DPPH IC50 value 26.77 mug/ml, NO IC50 value 27.04 mug/ml, OH IC50 value 30.94 mug/ml, O2-IC50 value 50.75 mug/ml and FRAP EC50 value 40.43 mug/ml) followed by other extracts. The anti-proliferative activity of potential extract (ethyl acetate extract) which possess high antioxidant activity, and isolated rutin compound was tested (by MTT assay) against U-937 and HT-60 cell lines and the results show dose dependent activity. In addition, docking studies of reportedrutin compound exhibits strong inhibition on the active site of VEGFR2 than the co-crystallized ligand N,2-dimethyl-6-(7-(2-morpholinoethoxy) Quinolin-4-yloxy)benzofuran-3-carboxamide.
机译:目前的研究计划通过执行标准的抗氧化剂和MTT分析来研究叶粗提物和Memecylon药中分离的化合物(芦丁)的抗氧化和抗增殖潜力。结果表明,不同剂量的丹参粗叶提取物在所有测试方法(DPPH,NO,OH,O2-自由基)上均表现出不同程度的抗氧化潜能,且剂量依赖方式也不同,它们也具有良好的还原能力。在乙酸乙酯提取物中发现了显着的高抗自由基能力(DPPH IC50值为26.77杯/毫升,NO IC50值为27.04杯/毫升,OH IC50值为30.94杯/毫升,O2-IC50值为50.75杯/毫升,FRAP EC50值为40.43杯/毫升),然后其他提取物。具有高抗氧化活性的潜在提取物(乙酸乙酯提取物)的抗增殖活性,并测试了分离的芦丁化合物(通过MTT分析)对U-937和HT-60细胞系的抗增殖活性,结果显示了剂量依赖性活性。此外,报道的芦丁化合物的对接研究比共结晶的配体N,2-二甲基-6-(7-(2-吗啉代乙氧基)喹啉-4-基氧基)苯并呋喃-3-羧酰胺对VEGFR2的活性位点具有较强的抑制作用。 。

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