Two undescribed bisabolane-type sesquiterpenoids from the endophytic fungus <i>Penicillium herquei</i>

Sixteen compounds, including two undescribed bisabolane-type sesquiterpenoids (1, 2), four aromatic derivatives (3–6), two cyclopeptides (7, 8), two acyclic sesquiterpenes (9–10), four fatty acid esters (11–14) and two fatty acids (15–16), were separated from the endophytic fungus Penicillium herquei. Their structures were established by analysis of spectroscopic data, HRESIMS spectra, NMR data and comparison with data in relevant literature. It is the first time that all of these compounds were isolated from P. herquei. The in vitro cytotoxicity of all isolated was evaluated against four tumor cell lines (HCT116, A549, HeLa, and Hepg2 cells) by the MTT assay, and compounds 1, 2, 4, 7 and 8 exhibited cytotoxicity with IC50 values ranging from 9.7 ± 0.8 to 37.4 ± 2.5 μM.

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Publication Details

Journal
Journal of Asian Natural Products Research
Published
2026-07-16
DOI
https://doi.org/10.1080/10286020.2026.2701131
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Two undescribed bisabolane-type sesquiterpenoids from the endophytic fungus Penicillium herquei

L Li, Jing Huang, Yi-yang Xiong, Zhou Xian-li et al.
Journal of Asian Natural Products Research
Microbial Natural Products and Biosynthesis
article

Two undescribed bisabolane-type sesquiterpenoids from the endophytic fungus Penicillium herquei

L Li, Jing Huang, Yi-yang Xiong, Zhou Xian-li, Meng-Yi Deng
article en

Abstract

Sixteen compounds, including two undescribed bisabolane-type sesquiterpenoids (1, 2), four aromatic derivatives (3–6), two cyclopeptides (7, 8), two acyclic sesquiterpenes (9–10), four fatty acid esters (11–14) and two fatty acids (15–16), were separated from the endophytic fungus Penicillium herquei. Their structures were established by analysis of spectroscopic data, HRESIMS spectra, NMR data and comparison with data in relevant literature. It is the first time that all of these compounds were isolated from P. herquei. The in vitro cytotoxicity of all isolated was evaluated against four tumor cell lines (HCT116, A549, HeLa, and Hepg2 cells) by the MTT assay, and compounds 1, 2, 4, 7 and 8 exhibited cytotoxicity with IC50 values ranging from 9.7 ± 0.8 to 37.4 ± 2.5 μM.

Journal of Asian Natural Products Research
Southwest Jiaotong University (CN)
National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 10%
Microbial Natural Products and Biosynthesis
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