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首页> 外文期刊>Medicinal chemistry research: an international journal for rapid communications on design and mechanisms of action of biologically active agents >Bioguided chemical characterization of the antiproliferative fraction of edible pseudo bulbs of Malaxis acuminata D. Don by HPLC-ESI-QTOF-MS
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Bioguided chemical characterization of the antiproliferative fraction of edible pseudo bulbs of Malaxis acuminata D. Don by HPLC-ESI-QTOF-MS

机译:Malaxis Acuminata D的抗增殖级数的生物化化学表征D. WPLC-ESI-QTOF-MS

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Abstract The edible pseudo bulbs of Malaxis acuminata D. Don are used as a constituent of an Indian drug ‘Astavarga’ and in several marketed Ayurvedic formulations. The aim of the present work was to investigate the in vitro antiproliferative activity of the ethanolic extract and its fractions of the pseudo bulbs of Malaxis acuminata and to develop the HPLC-ESI-QTOF-MS/MS method for rapid de-replication of the phytoconstituents present in the bioactive fraction. The antiproliferative activity was evaluated against four human cancer cell lines, such as A549 (non-small cell lung cancer cells), DU145 (human prostate carcinoma), DLD1 (human colorectal adenocarcinoma), and MCF-7 (human breast adenocarcinoma) using the sulphorhodamine B assay. Eleven compounds including two flavonoids, three bisphenanthrene compounds, three stillbenoid compounds, two phenanthrene derivatives, and one prenylated benzoic acid were identified and characterized by HPLC-ESI-QTOF-MS/MS analysis along with the isolation of three steroidal compounds by column chromatography. The present investigation indicated that pseudo bulbs of Malaxis acuminata possessed a potent antiproliferative activity. LC–MS/MS analysis provided rapid dereplication of compounds, which might be responsible for its antiproliferative activity.
机译:摘要Malaxis Acuminata D. Don的可食用伪灯泡被用作印度药物“Astavarga”和几个销售的阿育吠陀制剂的组成部分。本作本作作品的目的是探讨乙醇提取物的体外抗增殖活性及其丙糊螨伪灯泡的级分,并开发HPLC-ESI-QTOF-MS / MS方法,用于快速去除植物植物酶存在于生物活性分数中。评估抗增殖活性,抗四种人癌细胞系,例如A549(非小细胞肺癌细胞),DU145(人道前列腺癌),DLD1(人结肠直肠腺癌)和MCF-7(人乳腺腺癌)使用该方法硫代胺B测定。在包括两种类黄酮,三种双苯甲酸丁二烯化合物,三个缬属苯甲酸丁衍生物和两种苯甲酸苯甲酸和一种戊烯化苯甲酸的11种化合物,并通过HPLC-ESI-QTOF-MS / MS分析,以及通过柱色谱分离的三种甾体化合物的分离。本研究表明,马克萨斯毒液的假灯泡具有有效的抗增殖活性。 LC-MS / MS分析提供了快速全体化化合物,这可能对其抗增殖活动负责。

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