Institut de Chimie des Substances Naturelles, CNRS ICSN, UPR 2301, Université Paris-Saclay, 91198, Gif-sur-Yvette, France.
97351, Matoury, Guyane Française, France.
Phytochemistry. 2019 Nov;167:112101. doi: 10.1016/j.phytochem.2019.112101. Epub 2019 Aug 29.
In an effort to identify inhibitors of Chikungunya virus (CHIKV) replication, a systematic study of 594 extracts of plant species originating from the French Guiana plateau region was performed in a virus-cell-based assay for CHIKV assay. The extract obtained from the stem bark of Sagotia racemosa was selected for its potent antiviral activity. Using a classical bioassay-guided procedure, three undescribed degraded diterpenoids, i.e. trigohowilols C and D and trigoflavidol D, as well as trigoxyphin K, stictic acid, hyperhomosekikaic acid and five known flavonoids were isolated. The structures of these compounds were elucidated by extensive NMR spectroscopic data analysis. Although trigohowilols C and D were isolated from the most active fraction they didn't show any antiviral activity. By using the Feature-Based Molecular Networking (FBMN) and Network Annotation Propagation (NAP) workflows, it has been shown that the strong anti-CHIKV activity found for this fraction might be due to the presence of analogues of 12-O-tetradecanoylphorbol-13-acetate (TPA), one of the most potent inhibitors of CHIKV replication identified to date.
为了寻找抑制基孔肯雅病毒(CHIKV)复制的抑制剂,我们在基于细胞的 CHIKV 测定法中对源自法属圭亚那高原地区的 594 种植物提取物进行了系统研究。从 Sagotia racemosa 的茎皮中获得的提取物因其强大的抗病毒活性而被选中。使用经典的生物测定指导程序,从该提取物中分离出了三种未描述的降解二萜类化合物,即 trigohowilols C 和 D 以及 trigoflavidol D,以及 trigoxyphin K、stictic acid、hyperhomosekikaic acid 和五种已知的黄酮类化合物。通过广泛的 NMR 光谱数据分析确定了这些化合物的结构。尽管 trigohowilols C 和 D 是从最活跃的部分中分离出来的,但它们没有显示出任何抗病毒活性。通过使用基于特征的分子网络(FBMN)和网络注释传播(NAP)工作流程,表明该部分具有很强的抗 CHIKV 活性,可能是由于存在 12-O-十四烷酰佛波醇-13-乙酸酯(TPA)的类似物,这是迄今为止发现的最有效的 CHIKV 复制抑制剂之一。