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从 种子中分离鉴定两种新化合物及其抗病毒和抗炎活性。

Isolation and identification of two new compounds from the seeds of and their antiviral and anti-inflammatory activities.

机构信息

College of Physics and Optoelectronic Engineering, Shenzhen University, Shenzhen, China.

Department of Pharmacy, Shenzhen Key Laboratory of Novel Natural Health Care Products, Innovation Platform for Natural Small Molecule Drugs, Engineering Laboratory of Shenzhen Natural Small Molecule Innovative Drugs, School of Medicine, Health Science Center, Shenzhen University, Shenzhen, China.

出版信息

Nat Prod Res. 2022 Feb;36(4):974-983. doi: 10.1080/14786419.2020.1851218. Epub 2020 Nov 29.

Abstract

Eleven compounds were isolated from methanol extract taken from seeds, including two previously unknown and nine known compounds. These compounds were authenticated as a carbamate, three phenylglycosides, four phenol glycosides, two nucleosides, and one flavonoid. Their chemical structures were elucidated using 1 D/2D nuclear magnetic resonance and high resolution-MS. Antivirus activity analyses revealed that A, glucomoringin, and Vitexin possessed strong inhibitory effects against the H1N1 virus, having IC values in the range of IC = 0.26 ± 0.03, 0.98 ± 0.17, and 3.42 ± 0.37 μg/mL, respectively. Furthermore, these three compounds could decrease the levels of TNF-α, IL-6, and IL-1β, which occur in hosts because of H1N1 infections.

摘要

从种子的甲醇提取物中分离得到 11 种化合物,包括两种以前未知的和 9 种已知的化合物。这些化合物被鉴定为氨基甲酸酯、三种苯丙糖苷、四种酚糖苷、两种核苷和一种类黄酮。它们的化学结构通过 1D/2D 核磁共振和高分辨率 MS 得到阐明。抗病毒活性分析表明,A、葡萄糖苷和牡荆素对 H1N1 病毒具有很强的抑制作用,其 IC 值分别在 IC = 0.26±0.03、0.98±0.17 和 3.42±0.37μg/mL 的范围内。此外,这三种化合物可以降低 TNF-α、IL-6 和 IL-1β 的水平,这些物质是由于 H1N1 感染宿主而产生的。

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