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从 的根部中分离得到一个新的环烯醚萜苷。

A new iridoid glucoside from the roots of .

机构信息

VNU University of Science, Vietnam National University, Thanh Xuan, Hanoi 11400, Vietnam.

Institute of Marine Biochemistry, Vietnam Academy of Science and Technology, Hanoi 10072, Vietnam.

出版信息

J Asian Nat Prod Res. 2023 Dec;25(12):1223-1228. doi: 10.1080/10286020.2023.2211510. Epub 2023 May 26.

Abstract

A new iridoid glucoside, moridoside (), and nine known compounds, asperulosidic acid (), 6---acetylscandoside (), geniposidic acid (), 2-hydroxymethylanthraquinone (), 2-hydroxymethyl-3-hydroxyanthraquinone (), damnacanthol (), lucidine-ω-methyl ether (), 2-hydroxy-1-methoxyanthraquinone (), and 3,8-dihydroxy-1,2-dimethoxyanthraquinone () were isolated from the methanol extract of How. roots. Their structural identification was carried out based on the spectroscopic evidence. All compounds were evaluated for their nitric oxide (NO) production inhibitory activities in LPS-stimulated RAW264.7 macrophages. Compounds significantly inhibited the production of NO with IC values of 28.4, 33.6, and 30.5 μM, respectively.

摘要

从玄参根的甲醇提取物中分离得到了一个新的环烯醚萜苷(moridoside ())和 9 个已知化合物,分别为asperulosidic acid ()、6---acetylscandoside ()、geniposidic acid ()、2-hydroxymethylanthraquinone ()、2-hydroxymethyl-3-hydroxyanthraquinone ()、damnacanthol ()、lucidine-ω-methyl ether ()、2-hydroxy-1-methoxyanthraquinone ()和 3,8-dihydroxy-1,2-dimethoxyanthraquinone ()。基于光谱证据对它们的结构进行了鉴定。所有化合物均在 LPS 刺激的 RAW264.7 巨噬细胞中评估了其一氧化氮 (NO) 产生抑制活性。化合物 显著抑制了 NO 的产生,其 IC 值分别为 28.4、33.6 和 30.5 μM。

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