{"title":"来自 Barringtonia macrocarpa 的异龙脑二萜衍生物。","authors":"","doi":"10.1080/14786419.2023.2217467","DOIUrl":null,"url":null,"abstract":"<div><div>From the MeOH residue of <em>Barringtonia macrocarpa</em> branches and leaves, one new isoryanodane diterpene, barringisol (<strong>1</strong>), and two new isoryanodane diterpene glucosides, barringisosides A and B (<strong>2</strong> and <strong>3</strong>), were obtained using various chromatographic isolations. The structural characterization was confirmed by spectroscopic methods including 1D, 2D NMR and HR-ESI-QTOF-MS. This is the first isolation of isoryanodane diterpene derivatives from <em>Barringtonia</em> species. Moreover, the <em>in vitro</em> cytotoxicity of <strong>1</strong>−<strong>3</strong> on three human cancer cell lines (HepG2, LNCaP and MCF7) was also accessed using SRB assays.</div></div>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":null,"pages":null},"PeriodicalIF":1.9000,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Isoryanodane diterpene derivatives from Barringtonia macrocarpa\",\"authors\":\"\",\"doi\":\"10.1080/14786419.2023.2217467\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>From the MeOH residue of <em>Barringtonia macrocarpa</em> branches and leaves, one new isoryanodane diterpene, barringisol (<strong>1</strong>), and two new isoryanodane diterpene glucosides, barringisosides A and B (<strong>2</strong> and <strong>3</strong>), were obtained using various chromatographic isolations. The structural characterization was confirmed by spectroscopic methods including 1D, 2D NMR and HR-ESI-QTOF-MS. This is the first isolation of isoryanodane diterpene derivatives from <em>Barringtonia</em> species. Moreover, the <em>in vitro</em> cytotoxicity of <strong>1</strong>−<strong>3</strong> on three human cancer cell lines (HepG2, LNCaP and MCF7) was also accessed using SRB assays.</div></div>\",\"PeriodicalId\":18990,\"journal\":{\"name\":\"Natural Product Research\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2024-09-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Natural Product Research\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1478641923017102\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Product Research","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1478641923017102","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Isoryanodane diterpene derivatives from Barringtonia macrocarpa
From the MeOH residue of Barringtonia macrocarpa branches and leaves, one new isoryanodane diterpene, barringisol (1), and two new isoryanodane diterpene glucosides, barringisosides A and B (2 and 3), were obtained using various chromatographic isolations. The structural characterization was confirmed by spectroscopic methods including 1D, 2D NMR and HR-ESI-QTOF-MS. This is the first isolation of isoryanodane diterpene derivatives from Barringtonia species. Moreover, the in vitro cytotoxicity of 1−3 on three human cancer cell lines (HepG2, LNCaP and MCF7) was also accessed using SRB assays.
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.