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首页> 外文期刊>Marine Drugs >20-Nor-Isopimarane Epimers Produced by Aspergillus wentii SD-310, a Fungal Strain Obtained from Deep Sea Sediment
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20-Nor-Isopimarane Epimers Produced by Aspergillus wentii SD-310, a Fungal Strain Obtained from Deep Sea Sediment

机译:由深海沉积物获得的真菌菌株aspergillus goii SD-310生产的20-Nor-Isopimaraneane差向异构体

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Four new uncommon 20-nor-isopimarane diterpenoid epimers, aspewentins I?L ( 1 – 4 ), together with a new methylated derivative of 3 , aspewentin M ( 5 ), were isolated from the deep sea sediment-derived fungus Aspergillus wentii SD-310. The very similar structures of these epimers made the separation and purification procedures difficult. The structures of compounds 1 – 5 were illustrated based on spectroscopic analysis, and the absolute configurations of compounds 1 – 5 were unambiguously determined by the combination of NOESY, time-dependent density functional (TDDFT)-ECD calculations, and X-ray crystallographic analysis. These metabolites represented the rare examples of 20-nor-isopimarane analogues possessing a cyclohexa-2,5-dien-1-one moiety. These compounds were tested for antimicrobial activities against human and aquatic pathogenic bacteria, as well as plant-pathogenic fungi. While compounds 1 and 2 exhibited inhibitory activities against zoonotic pathogenic bacteria such as Escherichia coli , Edwardsiella tarda , Vibrio harveyi , and V. parahaemolyticus , compound 5 showed potent activity against the plant pathogen Fusarium graminearum .
机译:从深海沉积物衍生的真菌Aspergillus goii SD-中分离出四种新的罕见的20-异异氮杂环烷二萜类差向异构体,Aspewentins I?L(1-4)以及一种新的甲基化衍生物3,Aspewentin M(5)。 310。这些差向异构体的非常相似的结构使分离和纯化过程变得困难。通过光谱分析说明了化合物1-5的结构,并结合NOESY,随时间变化的密度泛函(TDDFT)-ECD计算和X射线晶体学分析明确确定了化合物1-5的绝对构型。这些代谢物代表了具有环己2,5-dien-1-one部分的20-nor-isopimarane类似物的罕见实例。测试了这些化合物对人和水生病原菌以及植物致病真菌的抗菌活性。虽然化合物1和2表现出对人畜共患病原菌的抑制作用,如大肠埃希氏菌,爱德华氏菌,哈维弧菌和副溶血弧菌,化合物5对植物病原禾谷镰刀菌表现出强大的活性。

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