Chemical constituents of Anacolosa pervilleana and their antiviral activities

被引:49
|
作者
Bourjot, Melanie [1 ]
Leyssen, Pieter [2 ]
Eydoux, Cecilia [3 ]
Guillemot, Jean-Claude [3 ]
Canard, Bruno [3 ]
Rasoanaivo, Philippe [4 ]
Gueritte, Francoise [1 ]
Litaudon, Marc [1 ]
机构
[1] CNRS, ICSN, LabEx LERMIT, Ctr Rech Gif, F-91198 Gif Sur Yvette, France
[2] Rega Inst Med Res KU Leuven, Lab Virol & Expt Chemotherapy, B-3000 Louvain, Belgium
[3] ESIL Case 925, AFMB, AMU, Lab Architecture & Fonct Macromol Biol,UMR7257, F-13288 Marseille, France
[4] IMRA, Antananarivo 102, Madagascar
关键词
Anacolosa pervilleana; Acetylenic acid; Sambunigrin; Antiviral; Chikungunya virus; Dengue virus; IDENTIFICATION; GLUCOSIDES; INHIBITORS; ACIDS;
D O I
10.1016/j.fitote.2012.05.004
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In an effort to identify novel inhibitors of Chikungunya (CHIN) and Dengue (DENV) virus replication, a systematic study with 820 ethyl acetate extracts of Madagascan plants was performed in a virus-cell-based assay for CHIKV and a DENV NS5 RNA-dependant RNA polymerase (RdRp) assay. The extract obtained from the leaves of Anacolosa pervilleana was selected for its significant activity in both assays. One new (E)-tridec-2-en-4-ynedioic acid named anacolosine (1), together with three known acetylenic acids, the octadeca-9,11,13-triynoic acid (2), (13E)-octadec-13-en-9,11-diynoic acid (3), (13E)-octadec-13-en-11-ynoic acid (4), two terpenoids, lupenone (5) and beta-amyrone (6), and one cyanogenic glycoside, (S)-sambunigrin (7) were isolated. Their structures were elucidated by comprehensive analyses of NMR spectroscopy and mass spectrometry data. The inhibitory potency of these compounds was evaluated on CHIKV, DENV RdRp and West-Nile polymerase virus (WNV RdRp). Both terpenoids showed a moderate activity against CHIKV (EC50 77 and 86 mu M, respectively) and the acetylenic acids produced IC50 values around 3 mu M in the DENV RdRp assay. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1076 / 1080
页数:5
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