Isolation of Premyrsinane, Myrsinane, and Tigliane Diterpenoids from Euphorbia pithyusa Using a Chikungunya Virus Cell-Based Assay and Analogue Annotation by Molecular Networking

被引:41
作者
Esposito, Melissa [1 ,2 ]
Nothias, Louis-Felix [2 ]
Retailleau, Pascal [2 ]
Costa, Jean [1 ]
Roussi, Fanny [2 ]
Neyts, Johan [3 ]
Leyssen, Pieter [3 ]
Touboul, David [2 ]
Litaudon, Marc [2 ]
Paolini, Julien [1 ]
机构
[1] Univ Corsica, CNRS, UMR 6134, SPE,Lab Nat Prod Chem, F-20250 Corte, France
[2] Univ Paris Saclay, CNRS, UPR 2301, Inst Nat Subst Chem, Gif Sur Yvette, France
[3] Katholieke Univ Leuven, Lab Virol & Expt Chemotherapy, Rega Inst Med Res, B-3000 Leuven, Belgium
来源
JOURNAL OF NATURAL PRODUCTS | 2017年 / 80卷 / 07期
关键词
ANTIVIRAL ACTIVITY; REPLICATION; INHIBITORS; ESTERS; POTENT; CYCLOMYRSINANE; DEREPLICATION; DISCOVERY; STRATEGY; FALCATA;
D O I
10.1021/acs.jnatprod.7b00233
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Six new premyrsinol esters (1-6) and one new myrsinol ester (8) were isolated from an aerial parts extract of Euphorbia pithyusa, together with a known premyrsinol (7) and two known dideoxyphorbol esters (9 and 10), following a bioactivity-guided purification procedure using a chikungunya virus (CHIKV) tell-based assay. The structures of the new diterpene,esters (1-6 and 8) were elucidated by MS and NMR. spectroscopic data interpretation. Compounds. 1-10 were evaluated against CHIKV replication, and results showed that the 4 beta-dideoxyphorbol ester 10 was the most active compound, with an EC50 value of 4:0 +/- 0.3 mu M and a selectivity index of 10.6. To gain more insight into the structural diversity of diterpenoids produced by E. pithyusa, the initial extract and chromatographic fractions were analyzed by LC-MS/MS. The generated data were procedure and revealed that dozens of unknown premyrsinane, myrsinane, and tigliane analogues were present. annotated using a molecular networking
引用
收藏
页码:2051 / 2059
页数:9
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