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Bioactive Metabolites from Mangrove Endophytic Fungus Aspergillus sp. 16-5B

机译:红树林内生真菌曲霉菌的生物活性代谢产物。 16-5B

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Chemical investigation of the endophytic fungus Aspergillus sp. 16-5B cultured on Czapek’s medium led to the isolation of four new metabolites, aspergifuranone (1), isocoumarin derivatives (±) 2 and (±) 3, and (R)-3-demethylpurpurester A (4), together with the known purpurester B (5) and pestaphthalides A (6). Their structures were determined by analysis of 1D and 2D NMR spectroscopic data. The absolute configuration of Compound 1 was determined by comparison of the experimental and calculated electronic circular dichroism (ECD) spectra, and that of Compound 4 was revealed by comparing its optical rotation data and CD with those of the literature. The structure of Compound 6 was further confirmed by single-crystal X-ray diffraction experiment using CuKα radiation. All isolated compounds were evaluated for their α-glucosidase inhibitory activities, and Compound 1 showed significant inhibitory activity with IC50 value of 9.05 ± 0.60 μM. Kinetic analysis showed that Compound 1 was a noncompetitive inhibitor of α-glucosidase. Compounds 2 and 6 exhibited moderate inhibitory activities.
机译:内生真菌曲霉菌的化学研究。在Czapek培养基上培养的16-5B导致分离出四种新的代谢物,即曲霉古拉酮(1),异香豆素衍生物(±)2和(±)3和(R)-3-脱甲基紫酸酯A(4),以及已知的紫酯B(5)和香豆酚A(6)。通过分析1D和2D NMR光谱数据确定其结构。化合物1的绝对构型是通过比较实验和计算的电子圆二色性(ECD)光谱确定的,化合物4的绝对构型是通过将其旋光度数据和CD与文献资料相比较来揭示的。通过使用CuKα辐射的单晶X射线衍射实验进一步证实了化合物6的结构。评价所有分离的化合物的α-葡萄糖苷酶抑制活性,化合物1显示出显着的抑制活性,IC 50 值为9.05±0.60μM。动力学分析表明化合物1是α-葡糖苷酶的非竞争性抑制剂。化合物2和6表现出中等的抑制活性。

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