{"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}
引用次数: 0
Abstract
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.