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首页> 外文期刊>The Journal of Antibiotics: An International Journal >Anthranilamides: New antimicroalgal active substances from a marine Streptomyces sp.
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Anthranilamides: New antimicroalgal active substances from a marine Streptomyces sp.

机译:邻氨基苯甲酰胺:来自海洋链霉菌属的新型抗藻类活性物质。

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摘要

2-[Methyl-(3-phenylpropionyl)amino]-benzoic acid (1e) was isolated from a culture of marine Streptomyces sp. strain B7747. Analogous compounds have potential importance as phytotoxic substances, hence compound 1e and the analogues 1a similar to 1d and 1f similar to 3a were synthesised. Antimicroalgal activity of the anthranilamide analogues showed that esters 1b, 1f and 2b were more active than the free acids. The minimum inhibitory concentration (MIG) against Chlorella vulgaris, Chlorella sorokiniana, Chlorella salina and Scenedesmus subspicatus ranged from 20 to 107 mu g/ml. All anthranilamides were inactive against Staphylococcus aureus, Escherichia coli, and Mucor miehei. [References: 13]
机译:从海洋链霉菌属种的培养物中分离出2- [甲基-(3-苯基丙酰基)氨基]-苯甲酸(1e)。菌株B7747。类似的化合物作为植物毒性物质具有潜在的重要性,因此合成了化合物1e和类似于1d的类似物1a和类似于3a的类似物1f。邻氨基苯甲酰胺类似物的抗藻活性表明,酯1b,1f和2b比游离酸更具活性。对寻常小球藻,小球藻小球藻,盐藻和盐生小球藻的最小抑菌浓度(MIG)为20至107μg/ ml。所有邻氨基苯甲酰胺对金黄色葡萄球菌,大肠杆菌和Mucor miehei均无活性。 [参考:13]

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