{"title":"薯蓣内生镰刀菌L46新α-吡啶酮的分离纯化","authors":"Ruo-Dan Tian, Ying-Fei Zhao, Fei-Fan Wang, Song-Jie Zhan, Chun-Nan Wen, Miao Liu, Bing-Ji Ma","doi":"10.1002/cbdv.202500223","DOIUrl":null,"url":null,"abstract":"<p><p>Fusarilactones D and E (1 and 2), two new α-pyrone derivatives, and four known compounds, namely, phomapyrone C (3), fusarester C (4), neovasifuranone B (5), and neovasifuranone A (6), were isolated from Fusarium sp. L46, an endophytic fungus isolated from Dioscorea opposita leaves. Their structures were determined using 1D and 2D NMR spectra, HRESIMS, and optical rotation measurements. Compounds 3-5 were assessed for their inhibitory activity on pancreatic lipase.</p>","PeriodicalId":9878,"journal":{"name":"Chemistry & Biodiversity","volume":" ","pages":"e00223"},"PeriodicalIF":2.3000,"publicationDate":"2025-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"New α-Pyrones From Endophytic Fusarium Sp. L46 Isolated From Dioscorea opposita.\",\"authors\":\"Ruo-Dan Tian, Ying-Fei Zhao, Fei-Fan Wang, Song-Jie Zhan, Chun-Nan Wen, Miao Liu, Bing-Ji Ma\",\"doi\":\"10.1002/cbdv.202500223\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Fusarilactones D and E (1 and 2), two new α-pyrone derivatives, and four known compounds, namely, phomapyrone C (3), fusarester C (4), neovasifuranone B (5), and neovasifuranone A (6), were isolated from Fusarium sp. L46, an endophytic fungus isolated from Dioscorea opposita leaves. Their structures were determined using 1D and 2D NMR spectra, HRESIMS, and optical rotation measurements. Compounds 3-5 were assessed for their inhibitory activity on pancreatic lipase.</p>\",\"PeriodicalId\":9878,\"journal\":{\"name\":\"Chemistry & Biodiversity\",\"volume\":\" \",\"pages\":\"e00223\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-06-18\",\"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.202500223\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry & Biodiversity","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/cbdv.202500223","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
New α-Pyrones From Endophytic Fusarium Sp. L46 Isolated From Dioscorea opposita.
Fusarilactones D and E (1 and 2), two new α-pyrone derivatives, and four known compounds, namely, phomapyrone C (3), fusarester C (4), neovasifuranone B (5), and neovasifuranone A (6), were isolated from Fusarium sp. L46, an endophytic fungus isolated from Dioscorea opposita leaves. Their structures were determined using 1D and 2D NMR spectra, HRESIMS, and optical rotation measurements. Compounds 3-5 were assessed for their inhibitory activity on pancreatic lipase.
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.