{"title":"A new biopotentially active isoflavone glycoside from the stem of Ficus arnottiana Miq.","authors":"Shweta Singh, R. Yadava, R. Yadav, V. Surywanshi","doi":"10.13171/mjc02303201671singh","DOIUrl":null,"url":null,"abstract":"A new bioactive isoflavone glycoside with a molecular formula C34H42O20, melting point 261°C-263°C and [M]+ 770 was isolated from the methanol soluble fraction of 90% methanolic extract of the stem of Ficus arnottiana Miq. The compound was illustrated as a new bioactive isoflavone glycoside 5,6,5ˈ-trihydroxy-8,3ˈ-dimethoxy-isoflavone 5ˈ-O-α-L-rhamnopyranosyl (1→3) O-α-L xylopyranosyl 5-O-β-D-glucopyranoside were characterized with the help of various chemical reactions, Fourier transforms infrared spectroscopy (FT-IR), Nuclear magnetic resonance spectroscopy (1HNMR), Mass spectrometry (LC-MS) and chemical degradations. Isolated compounds were also used for the antimicrobial activity of micro-organisms worked successfully tested against all strains: Escherichia coli, Bacillus cereus, and Staphylococcus aureus, while the least activity by Pseudomonas aeruginosa.","PeriodicalId":18513,"journal":{"name":"Mediterranean Journal of Chemistry","volume":"59 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mediterranean Journal of Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.13171/mjc02303201671singh","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
A new bioactive isoflavone glycoside with a molecular formula C34H42O20, melting point 261°C-263°C and [M]+ 770 was isolated from the methanol soluble fraction of 90% methanolic extract of the stem of Ficus arnottiana Miq. The compound was illustrated as a new bioactive isoflavone glycoside 5,6,5ˈ-trihydroxy-8,3ˈ-dimethoxy-isoflavone 5ˈ-O-α-L-rhamnopyranosyl (1→3) O-α-L xylopyranosyl 5-O-β-D-glucopyranoside were characterized with the help of various chemical reactions, Fourier transforms infrared spectroscopy (FT-IR), Nuclear magnetic resonance spectroscopy (1HNMR), Mass spectrometry (LC-MS) and chemical degradations. Isolated compounds were also used for the antimicrobial activity of micro-organisms worked successfully tested against all strains: Escherichia coli, Bacillus cereus, and Staphylococcus aureus, while the least activity by Pseudomonas aeruginosa.