New Squalene Triterpenes From the Fungus <i>Irpex laceratus</i>

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.

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Publication Details

Journal
Chemistry & Biodiversity
Published
2025-06-13
DOI
https://doi.org/10.1002/cbdv.202501271
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
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article

New Squalene Triterpenes From the Fungus Irpex laceratus

Yuchan Chen, Zhenxing Zou, Yunfei Yuan, Xiaoyi Wei et al.
Chemistry & Biodiversity
Microbial Natural Products and Biosynthesis
article

New Squalene Triterpenes From the Fungus Irpex laceratus

Yuchan Chen, Zhenxing Zou, Yunfei Yuan, Xiaoyi Wei, Haibo Tan, Chen Chen, Bin Jiang, Siyu Qin, Siran Li, Fangfang Duan, Liangnian Wei, Jiaying Lai
article en

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 IC<sub>50</sub> values of 32.5, 48.0, 76.8, and 58.8 µM, respectively.

Chemistry & BiodiversityVol. 22(10)
Central South University (CN), Guangdong Academy of Sciences (CN), South China Botanical Garden (CN), Institute of Microbiology (CN), Third Xiangya Hospital (CN)
Openalex Percentile: Top 85%
Microbial Natural Products and Biosynthesis
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