{"title":"真菌角鲨烯三萜的新发现。","authors":"Chen Chen, Linjie Wei, Yunfei Yuan, Yuchan Chen, Siran Li, Jiaying Lai, Fangfang Duan, Siyu Qin, Bin Jiang, Xiaoyi Wei, Zhenxing Zou, Haibo Tan","doi":"10.1002/cbdv.202501271","DOIUrl":null,"url":null,"abstract":"<p><p>Six undescribed squalene triterpenes, named irpelacerins A-F (1-6), together with three known lanostane triterpenoids (7-9) were isolated from the solid fermentation of the endophytic fungus Irpex laceratus, which was collected from the medicinal plant Casuarina equisetifolia L. Compounds 1-6 were a group of uncommon chain triterpenoids, which existed in the form of acyclic or monocyclic structures. Their chemical structures were determined by extensive analyses of NMR spectroscopic data, high-resolution electrospray ionization mass spectrometry, and comparison with literature analogs. Moreover, all these compounds were evaluated for their biological activities, and the results clarified that compounds 3, 6, 8, and 9 showed notable inhibitory activity against LPS-induced NO production with IC<sub>50</sub> values of 32.5, 48.0, 76.8, and 58.8 µM, respectively.</p>","PeriodicalId":9878,"journal":{"name":"Chemistry & Biodiversity","volume":" ","pages":"e01271"},"PeriodicalIF":2.3000,"publicationDate":"2025-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"New Squalene Triterpenes From the Fungus Irpex laceratus.\",\"authors\":\"Chen Chen, Linjie Wei, Yunfei Yuan, Yuchan Chen, Siran Li, Jiaying Lai, Fangfang Duan, Siyu Qin, Bin Jiang, Xiaoyi Wei, Zhenxing Zou, Haibo Tan\",\"doi\":\"10.1002/cbdv.202501271\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Six undescribed squalene triterpenes, named irpelacerins A-F (1-6), together with three known lanostane triterpenoids (7-9) were isolated from the solid fermentation of the endophytic fungus Irpex laceratus, which was collected from the medicinal plant Casuarina equisetifolia L. Compounds 1-6 were a group of uncommon chain triterpenoids, which existed in the form of acyclic or monocyclic structures. Their chemical structures were determined by extensive analyses of NMR spectroscopic data, high-resolution electrospray ionization mass spectrometry, and comparison with literature analogs. Moreover, all these compounds were evaluated for their biological activities, and the results clarified that compounds 3, 6, 8, and 9 showed notable inhibitory activity against LPS-induced NO production with IC<sub>50</sub> values of 32.5, 48.0, 76.8, and 58.8 µM, respectively.</p>\",\"PeriodicalId\":9878,\"journal\":{\"name\":\"Chemistry & Biodiversity\",\"volume\":\" \",\"pages\":\"e01271\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-06-13\",\"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.202501271\",\"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.202501271","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
摘要
从药用植物木麻黄(Casuarina equisetifolia L.)内生真菌Irpex laceratus的固体发酵中分离得到6个未描述的角烯三萜,命名为irpelacerins a - f(1-6)和3个已知的毛甾烷三萜(7-9)。其中1-6为一组不常见的链式三萜,以无环或单环结构存在。它们的化学结构是通过大量的核磁共振光谱数据分析、高分辨率电喷雾电离质谱分析以及与文献类似物的比较来确定的。结果表明,化合物3、6、8和9对lps诱导的NO产生具有显著的抑制作用,IC50值分别为32.5、48.0、76.8和58.8µM。
New Squalene Triterpenes From the Fungus Irpex laceratus.
Six undescribed squalene triterpenes, named irpelacerins A-F (1-6), together with three known lanostane triterpenoids (7-9) were isolated from the solid fermentation of the endophytic fungus Irpex laceratus, which was collected from the medicinal plant Casuarina equisetifolia L. Compounds 1-6 were a group of uncommon chain triterpenoids, which existed in the form of acyclic or monocyclic structures. Their chemical structures were determined by extensive analyses of NMR spectroscopic data, high-resolution electrospray ionization mass spectrometry, and comparison with literature analogs. Moreover, all these compounds were evaluated for their biological activities, and the results clarified that compounds 3, 6, 8, and 9 showed notable inhibitory activity against LPS-induced NO production with IC50 values of 32.5, 48.0, 76.8, and 58.8 µM, respectively.
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.