Jie Bai, Si-Yao Wang, Kang Pan, Hua-Jun Luo, Kun Zou, Hui Wang
{"title":"Ligulariatinside A, a new sesquiterpene glycoside from roots of <i>Ligularia veitchiana</i>.","authors":"Jie Bai, Si-Yao Wang, Kang Pan, Hua-Jun Luo, Kun Zou, Hui Wang","doi":"10.1080/14786419.2023.2261143","DOIUrl":null,"url":null,"abstract":"<p><p>A new sesquiterpene glycoside, ligulariatinside A (<b>1</b>), along with nine known compounds, dibutyl phthalate (<b>2</b>), 1-<i>O</i>-(9<i>Z</i>,12<i>Z</i>-octadecadienoyl) glycerol (<b>3</b>), bis (2-ethylhexyl) phthalate (<b>4</b>), 4-hydroxy-3-methoxyphenylpropanol (<b>5</b>), dihydrosyringenin (<b>6</b>), caffeic acid (<b>7</b>), 6<i>β</i>-hydroxy-7(11)-eremophilen-12,8<i>α</i>-olide (<b>8</b>), together with the mixture of 6<i>β</i>,8<i>β</i>-dihydroxyeremophil-7(11)-en-12,8<i>α</i>-olide (<b>9</b>) and 6<i>β</i>,8<i>α</i>-dihydroxy-eremophil-7(11)-en-12,8<i>β</i>-olide (<b>10</b>) were isolated from roots of <i>L. veitchiana</i>. Structures of these compounds were elucidated by comprehensive analyses of HRESIMS, 1D NMR, and 2D NMR spectroscopic data. Compounds <b>2</b> and <b>4</b> are not likely natural compounds but contaminants. All isolated compounds were tested for antibacterial activity. Compounds <b>1</b>, <b>5</b>, <b>6</b>, together with the mixture of <b>9</b> and <b>10</b>, showed mild activity against <i>Vibrio anguillarum</i>, with MIC values of 50, 50, 100, and 200 μg/mL, while compound <b>7</b> showed moderate activity against <i>Vibrio anguillarum</i>, with a MIC value of 25 μg/mL.</p>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":" ","pages":"262-268"},"PeriodicalIF":1.9000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Product Research","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1080/14786419.2023.2261143","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/9/25 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
Abstract
A new sesquiterpene glycoside, ligulariatinside A (1), along with nine known compounds, dibutyl phthalate (2), 1-O-(9Z,12Z-octadecadienoyl) glycerol (3), bis (2-ethylhexyl) phthalate (4), 4-hydroxy-3-methoxyphenylpropanol (5), dihydrosyringenin (6), caffeic acid (7), 6β-hydroxy-7(11)-eremophilen-12,8α-olide (8), together with the mixture of 6β,8β-dihydroxyeremophil-7(11)-en-12,8α-olide (9) and 6β,8α-dihydroxy-eremophil-7(11)-en-12,8β-olide (10) were isolated from roots of L. veitchiana. Structures of these compounds were elucidated by comprehensive analyses of HRESIMS, 1D NMR, and 2D NMR spectroscopic data. Compounds 2 and 4 are not likely natural compounds but contaminants. All isolated compounds were tested for antibacterial activity. Compounds 1, 5, 6, together with the mixture of 9 and 10, showed mild activity against Vibrio anguillarum, with MIC values of 50, 50, 100, and 200 μg/mL, while compound 7 showed moderate activity against Vibrio anguillarum, with a MIC value of 25 μg/mL.
期刊介绍:
The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds.
The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal.
Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section.
All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.