{"title":"NMR Screening Approach for Discovery of 5-Hydroxymethylfurfural Derivatives from Marine Fungus Fusarium oxysporum SP7.","authors":"Yu-Hua Zhang, Kai-Lei Chen, Yu-Peng Xuan, Ya-Jie Zhou, Wen-Jian Lan, Hou-Jin Li","doi":"10.1002/cbdv.202500248","DOIUrl":null,"url":null,"abstract":"<p><p>By tracing the characteristic proton and carbon nuclear magnetic resonance signals of the furan ring and aldehyde group, four novel 5-hydroxymethylfurfural derivatives, fusaroxysporins A-D (1-4), together with ten known compounds were obtained from the marine fungus Fusarium oxysporum SP7. Their structures were elucidated by comprehensive spectroscopic analysis. The possible biogenic synthesis pathways of these compounds were speculated. Compound 1 showed moderate cytotoxic activity against the human type II alveolar epithelial cell A-549 and the human hepatocarcinoma cell line HepG2 with the IC50 values of 48.0 and 92.0 μM, respectively, while the other compounds had no activity (IC50 > 200 μM).</p>","PeriodicalId":9878,"journal":{"name":"Chemistry & Biodiversity","volume":" ","pages":"e202500248"},"PeriodicalIF":2.3000,"publicationDate":"2025-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry & Biodiversity","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/cbdv.202500248","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
By tracing the characteristic proton and carbon nuclear magnetic resonance signals of the furan ring and aldehyde group, four novel 5-hydroxymethylfurfural derivatives, fusaroxysporins A-D (1-4), together with ten known compounds were obtained from the marine fungus Fusarium oxysporum SP7. Their structures were elucidated by comprehensive spectroscopic analysis. The possible biogenic synthesis pathways of these compounds were speculated. Compound 1 showed moderate cytotoxic activity against the human type II alveolar epithelial cell A-549 and the human hepatocarcinoma cell line HepG2 with the IC50 values of 48.0 and 92.0 μM, respectively, while the other compounds had no activity (IC50 > 200 μM).
期刊介绍:
Chemistry & Biodiversity serves as a high-quality publishing forum covering a wide range of biorelevant topics for a truly international audience. This journal publishes both field-specific and interdisciplinary contributions on all aspects of biologically relevant chemistry research in the form of full-length original papers, short communications, invited reviews, and commentaries. It covers all research fields straddling the border between the chemical and biological sciences, with the ultimate goal of broadening our understanding of how nature works at a molecular level.
Since 2017, Chemistry & Biodiversity is published in an online-only format.