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Isolation of chemical constituents from Spilanthes calva DC: Toxicity, anthelmintic efficacy and in silico studies

机译:从尖齿锦葵DC中分离化学成分:毒性,驱虫功效和计算机模拟研究

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摘要

Aqueous and ethanol extracts of this Spilanthes calva DC is widely used in folk medicine in South India for treating various parasitic diseases. In vitro anthelmintic activities of crude aqueous and alcoholic extract of aerial parts of the plant was investigated to provide experimental evidence for its use in folk medicine. Investigations of in vitro anthelmintic efficacy were evaluated separately on adult Pheretima posthuma and Ascaridia galli compared with Albendazole. Ethanol extract showed more anthelmintic activity than aqueous extract. Six compounds were isolated from ethanol extract compounds 3, 4 and 6 showed significant anthelmintic activity with LC50 values of 12, 11, 9.9 and 11.47, 10.56, 8.35 respectively against both the worms. The oral LD50 of the aqueous and ethanol extracts estimated in mice is greater than 5000. mg/kg. Molecular docking studies were carried out for compound 6 by using ArgusLab 4.0.1. and Molegrow 2012.2.5.0 generated the enzyme binding interaction which suggested the lactone ring attained a non-coplanar conformation with benzisoxazole can contribute two significant hydrogen bonding interaction with Tyr 50 and Gln 134. This could be attributed to the slight structural resemblance with Albendazole and hydrogen bonding, π-π and non-polar interactions towards the inhibitor-binding cavity of the β-tubulin enzyme. Our study shows ingredients in S.calva DC ethanol extract contains an effective anthelmintic composition that could potentially developed as a promising plant origin anthelmintic.
机译:这种尖齿cal DC的水和乙醇提取物被广泛用于印度南部的民间医学中,用于治疗各种寄生虫病。研究了植物地上部分的粗制水和酒精提取物的体外驱虫活性,为其在民间医学中的使用提供了实验证据。与阿苯达唑相比,分别评估了成人成年Phutima posthuma和Ascaridia galli的体外驱虫效果。乙醇提取物显示出比水性提取物更高的驱虫活性。从乙醇提取物中分离出六种化合物,化合物3、4和6表现出明显的驱虫活性,对两种蠕虫的LC50值分别为12、11、9.9和11.47、10.56、8.35。在小鼠中估计的水提取物和乙醇提取物的口服LD50大于5000. mg / kg。使用ArgusLab 4.0.1对化合物6进行了分子对接研究。 Molegrow and Molegrow 2012.2.5.0产生了酶结合相互作用,这表明内酯环与苯并异恶唑形成非共面构象可以与Tyr 50和Gln 134产生两个重要的氢键相互作用。这可能是由于与阿苯达唑和氢的结构相似结合,β-微管蛋白酶抑制剂结合腔的π-π和非极性相互作用。我们的研究表明,S.calva DC乙醇提取物中的成分包含有效的驱虫药成分,有可能被开发为有前途的植物性驱虫药。

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