Six Undescribed Lanostane‐Type Triterpenoids From <i>Ganoderma lucidum</i>

Six previously undescribed lanostane triterpenoids (1-6), together with 21 known analogues (7-27) were isolated from the fruiting bodies of the medicinal fungus Ganoderma lucidum. Compounds 1-3 are lucidenate-type triterpenoids, whereas compounds 4-6 are ganoderate-type derivatives. The planar structures and relative configurations of the six new compounds were established by comprehensive analysis of HRESIMS and 1D & 2D NMR spectroscopic data. The absolute configurations of compounds 1-3 were determined by ECD calculations or the modified Mosher's method. On the basis of the single-crystal X-ray diffraction data for compound 7, together with biogenetic considerations, the absolute configurations at C-25 of compounds 4-6 were assigned as 25R. Evaluation of the isolated compounds for anti-inflammatory activity revealed no significant inhibition of LPS-induced nitric oxide (NO) production in RAW264.7 macrophages.

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Journal
Chemistry & Biodiversity
Published
2026-05-01
DOI
https://doi.org/10.1002/cbdv.71265
Primary Topic
Fungal Biology and Applications
Type
article
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article

Six Undescribed Lanostane‐Type Triterpenoids From Ganoderma lucidum

Ze Liu, Zi-Wei Jia, Wei‐Ming Huang, Wen‐Jun Xu et al.
Chemistry & Biodiversity
Fungal Biology and Applications
article

Six Undescribed Lanostane‐Type Triterpenoids From Ganoderma lucidum

Ze Liu, Zi-Wei Jia, Wei‐Ming Huang, Wen‐Jun Xu, Ping Ying, Ling‐Yi Kong
article en

Abstract

Six previously undescribed lanostane triterpenoids (1-6), together with 21 known analogues (7-27) were isolated from the fruiting bodies of the medicinal fungus Ganoderma lucidum. Compounds 1-3 are lucidenate-type triterpenoids, whereas compounds 4-6 are ganoderate-type derivatives. The planar structures and relative configurations of the six new compounds were established by comprehensive analysis of HRESIMS and 1D & 2D NMR spectroscopic data. The absolute configurations of compounds 1-3 were determined by ECD calculations or the modified Mosher's method. On the basis of the single-crystal X-ray diffraction data for compound 7, together with biogenetic considerations, the absolute configurations at C-25 of compounds 4-6 were assigned as 25R. Evaluation of the isolated compounds for anti-inflammatory activity revealed no significant inhibition of LPS-induced nitric oxide (NO) production in RAW264.7 macrophages.

Chemistry & BiodiversityVol. 23(5)
China Pharmaceutical University (CN), Lishui University (CN)
Openalex Percentile: Top 5%
Fungal Biology and Applications
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