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Skeletocutins A-L: Antibacterial Agents from the Kenyan Wood-Inhabiting Basidiomycete, Skeletocutis sp.

机译:骨骼密汀A-L:来自肯尼亚木居住的底碱基,骨科SP的抗菌剂。

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摘要

Fermentation of the fungal strain Skeletocutis sp. originating from Mount Elgon Natural Reserve in Kenya, followed by bioassay guided fractionation led to the isolation of 12 previously undescribed metabolites named skeletocutins A-L (1-5 and 7-13) together with the known tyromycin A (6). Their structures were assigned by NMR spectroscopy complemented by HR-ESIMS. Compounds 1-6 and 11-13 exhibited selective activities against Gram-positive bacteria, while compound 10 weakly inhibited the formation of biofilm of Staphylococcus aureus. The isolated metabolites were also evaluated for inhibition of L-leucine aminopeptidase, since tyromycin A had previously been reported to possess such activities but only showed weak effects. Furthermore, all compounds were tested for antiviral activity against Hepatitis C virus (HCV), and compound 6 moderately inhibited HCV infectivity with an IC50 of 6.6 mu M.
机译:真菌菌株Skeletocutis SP的发酵。 源自肯尼亚的Elgon天然储备源自,其次是生物测定的分馏导致将12个以前未描述的代谢物分离为骨科蛋白A-L(1-5和7-13)与已知的酪霉素A(6)。 通过HR-ESIMS互补的NMR光谱分配它们的结构。 化合物1-6和11-13表现出对革兰氏阳性细菌的选择性活性,而化合物10弱抑制金黄色葡萄球菌的生物膜的形成。 还评估了分离的代谢物以抑制L-亮氨酸氨基肽酶,因为先前据报道酪霉素A具有此类活动,但仅显示出弱效应。 此外,对丙型肝炎病毒(HCV)进行抗病毒活性测试所有化合物,化合物6适度抑制HCV感染性,IC50为6.6μm。

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