Pachypodostyflavone, a New 3-methoxy Flavone and Other Constituents with Antifilarial Activities from the Stem Bark of Duguetia staudtii

A. Mbobda, A. Ngouonpe, G. Happi, B. Mountessou, Elvis Monya, Jean-Bosco Jouda, B. Toussie, B. Lenta, N. Sewald, S. Kouam, J. Tchouankeu
{"title":"Pachypodostyflavone, a New 3-methoxy Flavone and Other Constituents with Antifilarial Activities from the Stem Bark of Duguetia staudtii","authors":"A. Mbobda, A. Ngouonpe, G. Happi, B. Mountessou, Elvis Monya, Jean-Bosco Jouda, B. Toussie, B. Lenta, N. Sewald, S. Kouam, J. Tchouankeu","doi":"10.1055/a-1492-3585","DOIUrl":null,"url":null,"abstract":"Abstract A new flavone derivative named pachypodostyflavone (1), along with 8 known compounds (2–9) and a mixture of β-sitosterol and stigmasterol were isolated from the stem bark of Duguetia staudtii (Annonaceae), based on a bioassay-guided fractionation. Their structures were determined using high-resolution mass spectrometry and NMR spectroscopic data, as well as by comparison with the literature values of their analogs. Selected isolated compounds were evaluated for their in vitro antifilaricidal activities on Onchocerca ochengi microfilariae and adult worms. Inhibition of motility was evaluated spectroscopically on microfilaria and adult male worms. Viability was determined on adult female worms by the MTT/ Formazan assay. Auranofin at 10 µM and 2% DMSO were used as positive and negative controls, respectively. Compounds 1 and 7 showed potent anti-onchocerca activities with 100% activity at 250 µg/mL on both O. ochengi adult male and female worms, while compound 5 displayed 100% activity at 30 µg/mL.","PeriodicalId":199864,"journal":{"name":"Planta Medica International Open","volume":"6 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Planta Medica International Open","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/a-1492-3585","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4

Abstract

Abstract A new flavone derivative named pachypodostyflavone (1), along with 8 known compounds (2–9) and a mixture of β-sitosterol and stigmasterol were isolated from the stem bark of Duguetia staudtii (Annonaceae), based on a bioassay-guided fractionation. Their structures were determined using high-resolution mass spectrometry and NMR spectroscopic data, as well as by comparison with the literature values of their analogs. Selected isolated compounds were evaluated for their in vitro antifilaricidal activities on Onchocerca ochengi microfilariae and adult worms. Inhibition of motility was evaluated spectroscopically on microfilaria and adult male worms. Viability was determined on adult female worms by the MTT/ Formazan assay. Auranofin at 10 µM and 2% DMSO were used as positive and negative controls, respectively. Compounds 1 and 7 showed potent anti-onchocerca activities with 100% activity at 250 µg/mL on both O. ochengi adult male and female worms, while compound 5 displayed 100% activity at 30 µg/mL.
杜鹃茎皮中新型3-甲氧基黄酮及其抗丝活性成分的研究
摘要采用生物测定法分离得到了一种新的黄酮衍生物pachypodostyflavone(1)、8个已知化合物(2-9)以及β-谷甾醇和柱头甾醇的混合物。它们的结构通过高分辨率质谱和核磁共振光谱数据确定,并与它们的类似物的文献值进行比较。对分离得到的化合物进行了体外抑丝活性评价。对微丝虫和成虫雄虫的运动抑制进行了光谱学评价。采用MTT/ Formazan法测定成虫雌虫的活力。10µM的金螺脂和2% DMSO分别作为阳性和阴性对照。化合物1和7在250µg/mL浓度下对ochengi成虫雌雄均表现出100%的抗盘尾丝虫活性,而化合物5在30µg/mL浓度下表现出100%的抗盘尾丝虫活性。
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:604180095
Book学术官方微信