Bioactive Cyclodepsipeptides from Cocultured Mangrove-Derived <i>Aspergillus</i> sp. and <i>Penicillium</i> sp.

Three new arthrichitin derivatives I-K (<b>1</b>-<b>3</b>) and three known congeners (<b>4</b>-<b>6</b>) were isolated from a coculture of mangrove-derived fungi <i>Aspergillus</i> sp. and <i>Penicillium</i> sp. using <sup>1</sup>H NMR-guided fractionation. Their structures were determined by comprehensive spectroscopic analysis (1D/2D NMR, HRESIMS, ESI-MS/MS), Marfey's analysis, DP4+ probability, and experimental/computed ECD comparison. All compounds were evaluated for antibacterial effects and cytotoxicity. Notably, compounds <b>1</b> and <b>5</b> showed weak cytotoxicity against MHCC-97H cells (IC<sub>50</sub> = 20.1 ± 0.9 and 25.8 ± 0.4 μM, respectively). Compound <b>4</b> exhibited potent anti-BPH activity (IC<sub>50</sub> = 0.36 ± 0.02 μM).

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Publication Details

Journal
Journal of Natural Products
Published
2025-09-02
DOI
https://doi.org/10.1021/acs.jnatprod.5c00752
Citations
1
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
1.39

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article

Bioactive Cyclodepsipeptides from Cocultured Mangrove-Derived Aspergillus sp. and Penicillium sp.

Guang-Ping Cao, Xin-Jian Qu, Meng Bai, Xiangxi Yi et al.
1 citations
Journal of Natural Products
Microbial Natural Products and Biosynthesis
1.39
article

Bioactive Cyclodepsipeptides from Cocultured Mangrove-Derived Aspergillus sp. and Penicillium sp.

Guang-Ping Cao, Xin-Jian Qu, Meng Bai, Xiangxi Yi, Chenghai Gao, Yonghong Liu, Yu Wang
article en
1 citations

Abstract

Three new arthrichitin derivatives I-K (<b>1</b>-<b>3</b>) and three known congeners (<b>4</b>-<b>6</b>) were isolated from a coculture of mangrove-derived fungi <i>Aspergillus</i> sp. and <i>Penicillium</i> sp. using <sup>1</sup>H NMR-guided fractionation. Their structures were determined by comprehensive spectroscopic analysis (1D/2D NMR, HRESIMS, ESI-MS/MS), Marfey's analysis, DP4+ probability, and experimental/computed ECD comparison. All compounds were evaluated for antibacterial effects and cytotoxicity. Notably, compounds <b>1</b> and <b>5</b> showed weak cytotoxicity against MHCC-97H cells (IC<sub>50</sub> = 20.1 ± 0.9 and 25.8 ± 0.4 μM, respectively). Compound <b>4</b> exhibited potent anti-BPH activity (IC<sub>50</sub> = 0.36 ± 0.02 μM).

Journal of Natural ProductsVol. 88(9)
Guangxi University (CN), Guangxi University of Chinese Medicine (CN)
Natural Science Foundation of Guangxi Zhuang Autonomous Region, Guangxi Traditional Chinese Medical University, Guangxi Key Research and Development Program
Openalex Percentile: Top 16%
Microbial Natural Products and Biosynthesis
1.39
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