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从内生真菌链格孢属 MG1 中分离得到的具有多种抗炎和抗癌作用的聚酮化合物。

Diverse anti-inflammation and anti-cancer polyketides isolated from the endophytic fungi Alternaria sp. MG1.

机构信息

State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, People's Republic of China.

Department of Chemistry and Biochemistry, University of California, Santa Cruz, CA 95064, United States of America.

出版信息

Fitoterapia. 2021 Sep;153:105000. doi: 10.1016/j.fitote.2021.105000. Epub 2021 Jul 22.

Abstract

Six new polyketides, alternaritins A-D [(±)-1-4] and isoxanalteric acid I (8), and 25 known Alternaria toxins were isolated from the culture of an endophytic fungi Alternaria sp. MG1. 3 is a rare fungal metabolite. 6 is a new natural product, and 5, 7, and 9 are known previously but their absolute configurations have not been determined. Three enantiomers [(±)-1, (±)-7, and (±)-15] were separated via chiral HPLC resolution. The structures of those polyketides (1-9) were elucidated by spectrometric analysis using MS and NMR. The absolute configurations were established using X-ray diffraction analysis and statistical comparative analysis of the experimental ECD and OR data, in conjunction with quantum mechanical calculations. All of the compounds were evaluated for their bioactivities. Known compound 27 exerted the most potent cytotoxic activities against HT-1080 and NCI-H1299 cell lines. The new compounds, 2 and 3, showed moderate inhibition on COX-2, while a pair of isomers, 8 and 9, exhibited medium activity on COX-2 and uropathogenic Escherichia coli.

摘要

从一株内生真菌链格孢属 MG1 中分离得到 6 个新的多酮化合物交替曲菌素 A-D[(±)-1-4]和异香草醛酸 I(8)以及 25 个已知的链格孢毒素。3 是一种罕见的真菌代谢物。6 是一种新的天然产物,5、7 和 9 之前已知,但它们的绝对构型尚未确定。通过手性 HPLC 拆分分离出三种对映异构体[(±)-1、(±)-7 和(±)-15]。通过使用 MS 和 NMR 的光谱分析确定了这些多酮化合物(1-9)的结构。使用 X 射线衍射分析和实验 ECD 和 OR 数据的统计比较分析以及量子力学计算确定了绝对构型。所有化合物都进行了生物活性评估。已知化合物 27 对 HT-1080 和 NCI-H1299 细胞系表现出最强的细胞毒性活性。新化合物 2 和 3 对 COX-2 表现出中等抑制作用,而一对对映异构体 8 和 9 对 COX-2 和尿路致病性大肠杆菌表现出中等活性。

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