Isolation and evaluation of virucidal activities of flavanone glycosides and rosmarinic acid derivatives from Dracocephalum spp. against feline calicivirus

苯丙素 糖苷 黄烷酮 化学 猫杯状病毒 立体化学 生物 生物化学 类黄酮 病毒 生物合成 病毒学 抗氧化剂
作者
Mirza Synthia Sabrin,Selenge Erdenechimeg,Yohei Takeda,Javzan Batkhuu,Haruko Ogawa,Dulamjav Jamsransuren,Keisuke Suganuma,Toshihiro Murata
出处
期刊:Phytochemistry [Elsevier BV]
卷期号:191: 112896-112896 被引量:10
标识
DOI:10.1016/j.phytochem.2021.112896
摘要

Feline calicivirus is one of the surrogate viruses of human norovirus. This study aimed to identify virucidal compounds, chemical constituents of plants from the genus Dracocephalum, which are rich in flavonoids and phenylpropanoid oligomers. Four undescribed compounds, including a flavanone glucoside, two stilbenoid glycosides, and a phenylpropanoid amide glycoside, as well as 17 known compounds, were isolated from the Mongolian plants Dracocephalum fruticulosum Stephan ex Willd., and D. nutans L. belonging to the family Lamiaceae. The structures of the compounds were determined based on NMR, MS, and electronic CD spectroscopic data. In addition to these 21 compounds, 15 previously reported compounds from D. foetidum Bunge in C.F. von Ledebour were included, and a total of 36 compounds were evaluated for their virucidal activities against feline calicivirus. Some of the flavanone glycosides and phenylpropanoid oligomers showed virucidal activities, and their structural features are discussed. The findings suggest that isosakuranetin glycosides and phenylpropanoid oligomers may have the potential for norovirus inactivation.

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