Lanostane-type triterpenoids from the fungus <i>Inonotus obliquus</i>

Triterpenoids of the lanostane type are the primary characteristic compounds isolated from <i>Inonotus obliquus</i>. Phytochemical investigations on the EtOAc extract of the fungus led to the isolation of three new lanostane-type triterpenoids (compounds <b>1-3</b>) and 18 known derivatives. Their structures were determined from spectroscopic data, including NMR and HR-ESI-MS data, and quantum chemical calculations. The isolated lanostane-type triterpenoids exhibit a range of structures, characterised by the different C-17 side chains such as a 21, 24-cyclopentanol moiety, a γ-lactone ring, and a tetrahydrofuran ring. The <sup>13</sup>C chemical shifts variation for both C-21 and C-24 in 21, 24-cyclolanostanes were examined and summarised, offering a useful diagnostic tool to determine the relative configuration of the 21, 24-cyclopentanol moiety in the four types of 21, 24-cyclolanostanes.

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Publication Details

Journal
Natural Product Research
Published
2025-12-27
DOI
https://doi.org/10.1080/14786419.2025.2605555
Primary Topic
Fungal Biology and Applications
Type
article
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article

Lanostane-type triterpenoids from the fungus Inonotus obliquus

Hui Xiong, T. Zhang, Guang-zhong Yang, Di-Jun Chen et al.
Natural Product Research
Fungal Biology and Applications
article

Lanostane-type triterpenoids from the fungus Inonotus obliquus

Hui Xiong, T. Zhang, Guang-zhong Yang, Di-Jun Chen, Yu Chen, Chuang Zhu, Wen-Li Zeng
article en

Abstract

Triterpenoids of the lanostane type are the primary characteristic compounds isolated from <i>Inonotus obliquus</i>. Phytochemical investigations on the EtOAc extract of the fungus led to the isolation of three new lanostane-type triterpenoids (compounds <b>1-3</b>) and 18 known derivatives. Their structures were determined from spectroscopic data, including NMR and HR-ESI-MS data, and quantum chemical calculations. The isolated lanostane-type triterpenoids exhibit a range of structures, characterised by the different C-17 side chains such as a 21, 24-cyclopentanol moiety, a γ-lactone ring, and a tetrahydrofuran ring. The <sup>13</sup>C chemical shifts variation for both C-21 and C-24 in 21, 24-cyclolanostanes were examined and summarised, offering a useful diagnostic tool to determine the relative configuration of the 21, 24-cyclopentanol moiety in the four types of 21, 24-cyclolanostanes.

Natural Product Research
Minzu University of China (CN)
Openalex Percentile: Top 30%
Fungal Biology and Applications
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Lanostane-type triterpenoids from the fungus <i>Inonotus obliquus</i> — Hui Xiong, T. Zhang, et al. · Natural Product Research (2025) | TGRS Research Map | TGRS