Suppr超能文献

从山竹子叶中分离得到的具有prenylated 结构的酚类化合物及其抗猪流行性腹泻病毒活性

Prenylated Phenolic Compounds from the Leaves of Sabia limoniacea and Their Antiviral Activities against Porcine Epidemic Diarrhea Virus.

机构信息

Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy , Seoul National University , Seoul 08826 , Republic of Korea.

Department of Botany , Hanoi University of Pharmacy , Hanoi , Vietnam.

出版信息

J Nat Prod. 2019 Apr 26;82(4):702-713. doi: 10.1021/acs.jnatprod.8b00435. Epub 2019 Mar 19.

Abstract

Porcine epidemic diarrhea virus (PEDV), a serious swine epidemic, has been rampant in Asia since the 1990s. Despite the widespread use of PEDV vaccines, the occurrence of PEDV variants requires the discovery of new substances that inhibit these viruses. During a search for PEDV inhibitory materials from natural sources, seven new sabphenosides (1-7) and a new flavonoid (8), as well as eight known phenolic compounds (9-16), were obtained from the leaves of Sabia limoniacea. The structural determination of the new phenolic derivatives (1-8) was accomplished using comprehensive spectroscopic methods. Their absolute configurations were assigned by a combination of the ECD exciton chirality method following selective reduction and calculation of their ECD spectra. The bioactivities of the isolated compounds were measured based on their abilities to inhibit viral replication of PEDV. Among the test compounds, 15 and 16 exhibited the most promising antiviral activities, with IC values of 7.5 ± 0.7 μM and 8.0 ± 2.5 μM against PEDV replication. This study suggests that compounds 15 and 16 could serve as new scaffolds for the treatment of PEDV infection through the inhibition of PEDV replication.

摘要

猪流行性腹泻病毒(PEDV)是一种严重的猪传染病,自 20 世纪 90 年代以来一直在亚洲肆虐。尽管广泛使用了 PEDV 疫苗,但 PEDV 变异株的出现需要发现新的抑制这些病毒的物质。在从天然来源中寻找抑制 PEDV 的物质时,从 Sabia limoniacea 的叶子中获得了七种新的 Sabphenosides(1-7)和一种新的类黄酮(8),以及八种已知的酚类化合物(9-16)。通过综合光谱方法确定了新酚类衍生物(1-8)的结构。通过选择性还原和计算其 ECD 光谱相结合的方法,确定了它们的绝对构型。根据抑制 PEDV 复制的能力,测定了分离化合物的生物活性。在测试的化合物中,化合物 15 和 16 表现出最有希望的抗病毒活性,对 PEDV 复制的 IC 值分别为 7.5±0.7 μM 和 8.0±2.5 μM。本研究表明,化合物 15 和 16 可通过抑制 PEDV 复制,作为治疗 PEDV 感染的新骨架。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验