Jie Wang, Wen-Bin Gao, Fan-Wei Liu, Qi Liu, Bo Song, Jin Ye, Ying Chen, Cai-Lin Zhao, Wei Dong, Li-Na Guo, Bo Song
{"title":"Two new furanone derivatives from the endophytic fungus <i>Byssochlamys</i> sp. and their cytotoxic activities.","authors":"Jie Wang, Wen-Bin Gao, Fan-Wei Liu, Qi Liu, Bo Song, Jin Ye, Ying Chen, Cai-Lin Zhao, Wei Dong, Li-Na Guo, Bo Song","doi":"10.1080/14786419.2023.2275269","DOIUrl":null,"url":null,"abstract":"<p><p>Two new furanone derivatives, byssochlanones A-B (<b>1</b>-<b>2</b>) were purified from the endophytic fungus <i>Byssochlamys</i> sp. isolated from the wetland plant, <i>Phragmites australis</i>. Their structures were elucidated on the basis of extensive spectroscopic analyses. Compounds <b>1</b>-<b>2</b> represented typical furanone analogues which are not common in natural products. The absolute configuration of compounds <b>1</b>-<b>2</b> were identified through quantum-chemical electronic circular dichroism (ECD) calculation compared with their experimental CD. In addition, compounds <b>1</b>-<b>2</b> were tested for their cytotoxic activities against HCT-8 and Hela cancer cell lines, and compound <b>2</b> showed moderate activity against HCT-8 cells with IC<sub>50</sub> value of 21.3 <i>μ</i>M.</p>","PeriodicalId":18990,"journal":{"name":"Natural Product Research","volume":" ","pages":"4292-4296"},"PeriodicalIF":1.9000,"publicationDate":"2024-12-01","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/10.1080/14786419.2023.2275269","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/10/27 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
Abstract
Two new furanone derivatives, byssochlanones A-B (1-2) were purified from the endophytic fungus Byssochlamys sp. isolated from the wetland plant, Phragmites australis. Their structures were elucidated on the basis of extensive spectroscopic analyses. Compounds 1-2 represented typical furanone analogues which are not common in natural products. The absolute configuration of compounds 1-2 were identified through quantum-chemical electronic circular dichroism (ECD) calculation compared with their experimental CD. In addition, compounds 1-2 were tested for their cytotoxic activities against HCT-8 and Hela cancer cell lines, and compound 2 showed moderate activity against HCT-8 cells with IC50 value of 21.3 μM.
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.