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首页> 外文期刊>Molecules >Secondary Metabolites from Vietnamese Marine Invertebrates with Activity against Trypanosoma brucei and T. cruzi
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Secondary Metabolites from Vietnamese Marine Invertebrates with Activity against Trypanosoma brucei and T. cruzi

机译:来自越南海洋无脊椎动物的次生代谢产物,具有抗布鲁氏锥虫和克鲁氏锥虫的活性

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Marine-derived natural products from invertebrates comprise an extremely diverse and promising source of the compounds from a wide variety of structural classes. This study describes the discovery of five marine natural products with activity against Trypanosoma species by natural product library screening using whole cell in vitro assays. We investigated the anti-trypanosomal activity of the extracts from the soft corals and echinoderms living in Vietnamese seas. Of the samples screened, the methanolic extracts of several marine organisms exhibited potent activities against cultures of Trypanosoma brucei and T. cruzi (EC_(50) < 5.0 μg/mL). Among the compounds isolated from these extracts, laevigatol B (1) from Lobophytum crassum and L. laevigatum, (24S)-ergost-4-ene-3-one (2) from Sinularia dissecta, astropectenol A (3) from Astropecten polyacanthus, and cholest-8-ene-3β,5α,6β,7α-tetraol (4) from Diadema savignyi showed inhibitory activity against T. brucei with EC_(50) values ranging from 1.57 ± 0.14 to 14.6 ± 1.36 μM, relative to the positive control, pentamidine (EC_(50) = 0.015 ± 0.003 μM). Laevigatol B (1) and 5α-cholest-8(14)-ene-3β,7α-diol (5) exhibited also significant inhibitory effects on T. cruzi. The cytotoxic activity of the pure compounds on mammalian cells was also assessed and found to be insignificant in all cases. This is the first report on the inhibitory effects of marine organisms collected in Vietnamese seas against Trypanosoma species responsible for neglected tropical diseases.
机译:来自无脊椎动物的海洋来源的天然产物构成了来自各种结构类别的化合物的极其多样化和有希望的来源。这项研究描述了通过使用全细胞体外测定法筛选天然产物库,发现了五种对锥虫具有活性的海洋天然产物。我们调查了生活在越南海域的软珊瑚和棘皮动物提取物的抗锥虫活性。在筛选的样品中,几种海洋生物的甲醇提取物表现出对布鲁氏锥虫和克氏锥虫培养物的有效活性(EC_(50)<5.0μg/ mL)。从这些提取物中分离出的化合物中,包括来自景天树的Laevigatol B(1)和来自Sinularia dissecta的(24S)-ergost-4-ene-3-one(2),来自Astropecten polyacanthus的astropectenol A(3), Diadema savignyi的cholest-8-ene-3β,5α,6β,7α-四醇(4)表现出对T. brucei的抑制活性,EC_(50)值在1.57±0.14至14.6±1.36μM之间,相对于阳性对照喷他idine(EC_(50)= 0.015±0.003μM)。 Laevigatol B(1)和5α-胆甾8(14)-烯-3β,7α-二醇(5)对T. cruzi也有明显的抑制作用。还评估了纯化合物对哺乳动物细胞的细胞毒性活性,发现在所有情况下均无意义。这是关于越南海域海洋生物对导致被忽视的热带病的锥虫物种具有抑制作用的第一份报告。

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