Ecdysterols and triterpene glycoside from Achyranthes aspera L. and their NO production inhibitory activity

Hoàng Thi Ngoc Lan, Nguyen Thi Ngoc Mai, Bui Thi Thao Anh, Duong Thi Dung, Bui Huu Tai, Phan Van Kiem
{"title":"Ecdysterols and triterpene glycoside from Achyranthes aspera L. and their NO production inhibitory activity","authors":"Hoàng Thi Ngoc Lan, Nguyen Thi Ngoc Mai, Bui Thi Thao Anh, Duong Thi Dung, Bui Huu Tai, Phan Van Kiem","doi":"10.15625/2525-2518/18462","DOIUrl":null,"url":null,"abstract":"Phytochemical study on the methanolic extract of the aerial parts of Achyranthes aspera led to the isolation of six compounds including five ecdysterols, makisterone A (1), achyranthesterone A (2), 24(28)-dehydromakisterone A (3), podecdysone C (4), 20-hydroxyecdysone (5), and 3-O-α-L-rhamnopyranosyl-(1→3)-β-D-glucuronopyranosyl-oleanolic acid 28-O-β-D-glucopyranosyl ester (6). Compounds 1-5 were first isolated from A. aspera. Their chemical structures were identified by 1D and 1D NMR spectra in comparison with the published data in literature. Al five ecdysterol significantly showed NO production inhibition effects in LPS-activated RAW264.7 cells with the IC50 values ranging from 27.21 to 40.47 µM compared to that of positive control compound, L-NMMA, 32.24 µM.","PeriodicalId":506542,"journal":{"name":"Vietnam Journal of Science and Technology","volume":"42 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Vietnam Journal of Science and Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15625/2525-2518/18462","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Phytochemical study on the methanolic extract of the aerial parts of Achyranthes aspera led to the isolation of six compounds including five ecdysterols, makisterone A (1), achyranthesterone A (2), 24(28)-dehydromakisterone A (3), podecdysone C (4), 20-hydroxyecdysone (5), and 3-O-α-L-rhamnopyranosyl-(1→3)-β-D-glucuronopyranosyl-oleanolic acid 28-O-β-D-glucopyranosyl ester (6). Compounds 1-5 were first isolated from A. aspera. Their chemical structures were identified by 1D and 1D NMR spectra in comparison with the published data in literature. Al five ecdysterol significantly showed NO production inhibition effects in LPS-activated RAW264.7 cells with the IC50 values ranging from 27.21 to 40.47 µM compared to that of positive control compound, L-NMMA, 32.24 µM.
牛膝中的蜕皮甾醇和三萜糖苷及其抑制 NO 生成的活性
通过对牛膝气生部分甲醇提取物进行植物化学研究,分离出了六种化合物,包括五种蜕皮甾醇,即makisterone A (1)、achyranthesterone A (2)、24(28)-dehydromakisterone A (3)、podecdysone C (4)、20-hydroxyecdysone (5)和3-O-α-L-rhamopyranosyl、24(28)-dehydromakisterone A (3)、podecdysone C (4)、20-hydroxyecdysone (5) 和 3-O-α-L-rhamnopyranosyl-(1→3)-β-D-glucuronopyranosyl-oleanolic acid 28-O-β-D-glucopyranosyl ester (6)。化合物 1-5 最早是从 A. aspera 中分离出来的。通过一维和一维核磁共振光谱与文献发表的数据进行对比,确定了它们的化学结构。与阳性对照化合物 L-NMMA 的 32.24 µM 相比,这五种蜕皮甾醇在 LPS 激活的 RAW264.7 细胞中明显表现出抑制 NO 生成的作用,IC50 值介于 27.21 至 40.47 µM 之间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信