{"title":"Benzo[c]phenanthridine alkaloids and glycosylated flavonoids from the roots of Zanthoxylum gilletii (Rutaceae)","authors":"Liliane Clotilde Dzouemo, Emmanuel Ngeufa Happi, Mouthe Gervais Happi, Willifred Dongmo Tekapi Tsopgni, J. Wansi","doi":"10.53365/nrfhh/154598","DOIUrl":null,"url":null,"abstract":"The roots of <i>Zanthoxylum gilletii</i> have been chemically investigated and led to the isolation and characterization of nine compounds including three benzo[<i>c</i>]phenanthridine alkaloids oxychelerythrine (<b>1</b>), angoline (<b>2</b>) and arnottianamide (<b>3</b>); two glycosylated flavonoids hesperidin (<b>4</b>) and its analogue neohesperidin (<b>5</b>) along with four common specialized metabolites including sesamin (<b>6</b>), lupeol (<b>7</b>), β-sitosterol (<b>8</b>) and its derivative daucosterol (<b>9</b>). Their structures were established based on their recorded 1D and 2D-NMR data. Some compounds (<b>1</b>, <b>2</b>, <b>3</b>, <b>6</b> and <b>7</b>) did not display a cytotoxic activity until the highest concentration of 200 μM against the human cell lines MCF-7 and A549. The chemotaxonomic relevance of this study has been discussed. To the best of our knowledge, except for the five compounds <b>3</b>, <b>6</b>-<b>9</b>, all the four others have been for the first time isolated from <i>Z. gilletii</i> (Rutaceae).","PeriodicalId":394827,"journal":{"name":"Natural Resources for Human Health","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Resources for Human Health","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.53365/nrfhh/154598","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
The roots of Zanthoxylum gilletii have been chemically investigated and led to the isolation and characterization of nine compounds including three benzo[c]phenanthridine alkaloids oxychelerythrine (1), angoline (2) and arnottianamide (3); two glycosylated flavonoids hesperidin (4) and its analogue neohesperidin (5) along with four common specialized metabolites including sesamin (6), lupeol (7), β-sitosterol (8) and its derivative daucosterol (9). Their structures were established based on their recorded 1D and 2D-NMR data. Some compounds (1, 2, 3, 6 and 7) did not display a cytotoxic activity until the highest concentration of 200 μM against the human cell lines MCF-7 and A549. The chemotaxonomic relevance of this study has been discussed. To the best of our knowledge, except for the five compounds 3, 6-9, all the four others have been for the first time isolated from Z. gilletii (Rutaceae).