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槐耳化学成分及其抑制神经氨酸酶活性的研究

Neuraminidase Inhibitory Activity and Constituent Characterization of Fagopyrum dibotrys.

机构信息

Institute of Medicinal Plant Development, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing 100193, China.

Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China.

出版信息

Molecules. 2017 Nov 18;22(11):1998. doi: 10.3390/molecules22111998.

DOI:10.3390/molecules22111998
PMID:29156573
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6150301/
Abstract

This study aimed to identify a new biological activity of the widely distributed species . Four extracts (ethyl acetate (EA), petroleum ether (P), ethanol (E), and water (W)) were explored for their anti-neuraminidase (NA) activity. A total of 32 compounds were identified using UHPLC-Q-Exactive Orbitrap HRMS in the EA extract, which had the best NA inhibitory effects. We used the docking data for supporting compounds' anti-neuraminidase activity. Among them, five compounds including one flavonoid, three organic acids, and one glucoside were discovered for the first time in . Docking studies and NA activity assay revealed the remarkable NA inhibitory activity of eight components in EA extract, especially rutin, hesperidin, procyanidin B₂, and quercitrin. Therefore, could be used to develop anti-influenza drugs.

摘要

本研究旨在确定广泛分布的物种的新生物活性。探索了四种提取物(乙酸乙酯(EA)、石油醚(P)、乙醇(E)和水(W))的抗神经氨酸酶(NA)活性。在 EA 提取物中使用 UHPLC-Q-Exactive Orbitrap HRMS 鉴定了 32 种化合物,EA 提取物具有最佳的 NA 抑制作用。我们使用对接数据来支持化合物的抗神经氨酸酶活性。其中,五种化合物包括一种类黄酮、三种有机酸和一种糖苷,首次在中发现。对接研究和 NA 活性测定显示,EA 提取物中八种成分具有显著的 NA 抑制活性,特别是芦丁、橙皮苷、原花青素 B₂和槲皮素。因此,可用于开发抗流感药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde2/6150301/22f0de395df9/molecules-22-01998-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde2/6150301/2f5d4061a513/molecules-22-01998-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde2/6150301/9631bee8b1d7/molecules-22-01998-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde2/6150301/e40de1de20c1/molecules-22-01998-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde2/6150301/c509023a6f65/molecules-22-01998-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde2/6150301/2dba0c684b25/molecules-22-01998-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde2/6150301/22f0de395df9/molecules-22-01998-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde2/6150301/2f5d4061a513/molecules-22-01998-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde2/6150301/9631bee8b1d7/molecules-22-01998-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde2/6150301/e40de1de20c1/molecules-22-01998-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde2/6150301/c509023a6f65/molecules-22-01998-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde2/6150301/2dba0c684b25/molecules-22-01998-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde2/6150301/22f0de395df9/molecules-22-01998-g006.jpg

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