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基于超临界流体色谱和串联质谱分子网络的环保方法从半枝莲中发现强效抗病毒化合物。

Environmentally Friendly Procedure Based on Supercritical Fluid Chromatography and Tandem Mass Spectrometry Molecular Networking for the Discovery of Potent Antiviral Compounds from Euphorbia semiperfoliata.

机构信息

Institut de Chimie des Substances Naturelles, CNRS UPR 2301, University of Paris-Saclay , 91198 Gif-sur-Yvette, France.

Laboratoire de Chimie des Produits Naturels, CNRS, UMR SPE 6134, University of Corsica , 20250 Corte, France.

出版信息

J Nat Prod. 2017 Oct 27;80(10):2620-2629. doi: 10.1021/acs.jnatprod.7b00113. Epub 2017 Sep 19.

DOI:10.1021/acs.jnatprod.7b00113
PMID:28925702
Abstract

A supercritical fluid chromatography-based targeted purification procedure using tandem mass spectrometry and molecular networking was developed to analyze, annotate, and isolate secondary metabolites from complex plant extract mixture. This approach was applied for the targeted isolation of new antiviral diterpene esters from Euphorbia semiperfoliata whole plant extract. The analysis of bioactive fractions revealed that unknown diterpene esters, including jatrophane esters and phorbol esters, were present in the samples. The purification procedure using semipreparative supercritical fluid chromatography led to the isolation and identification of two new jatrophane esters (13 and 14) and one known (15) and three new 4-deoxyphorbol esters (16-18). The structure and absolute configuration of compound 16 were confirmed by X-ray crystallography. This compound was found to display antiviral activity against Chikungunya virus (EC = 0.45 μM), while compound 15 proved to be a potent and selective inhibitor of HIV-1 replication in a recombinant virus assay (EC = 13 nM). This study showed that a supercritical fluid chromatography-based protocol and molecular networking can facilitate and accelerate the discovery of bioactive small molecules by targeting molecules of interest, while minimizing the use of toxic solvents.

摘要

建立了一种基于超临界流体色谱的靶向净化程序,结合串联质谱和分子网络,用于分析、注释和从复杂植物提取物混合物中分离次生代谢产物。该方法应用于从Euphorbia semiperfoliata 全植物提取物中靶向分离新的抗病毒二萜酯。对生物活性馏分的分析表明,样品中存在未知的二萜酯,包括巴豆烷酯和佛波酯。半制备超临界流体色谱的纯化程序导致两种新的巴豆烷酯(13 和 14)和一种已知的(15)以及三种新的 4-去氧佛波酯(16-18)的分离和鉴定。通过 X 射线晶体学确定了化合物 16 的结构和绝对构型。该化合物显示出对基孔肯雅病毒(EC = 0.45 μM)的抗病毒活性,而化合物 15 被证明是重组病毒测定中 HIV-1 复制的有效和选择性抑制剂(EC = 13 nM)。本研究表明,基于超临界流体色谱的方案和分子网络可以通过靶向感兴趣的分子,促进和加速生物活性小分子的发现,同时最大限度地减少有毒溶剂的使用。

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