{"title":"Bioactive Cyclodepsipeptides from Cocultured Mangrove-Derived Aspergillus sp. and Penicillium sp.","authors":"Yu Wang, , , Guang-Ping Cao, , , Xin-Jian Qu, , , Yong-Hong Liu, , , Xiang-Xi Yi, , , Cheng-Hai Gao*, , and , Meng Bai*, ","doi":"10.1021/acs.jnatprod.5c00752","DOIUrl":null,"url":null,"abstract":"<p >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).</p>","PeriodicalId":47,"journal":{"name":"Journal of Natural Products ","volume":"88 9","pages":"2239–2246"},"PeriodicalIF":3.6000,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Natural Products ","FirstCategoryId":"99","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jnatprod.5c00752","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0
Abstract
Three new arthrichitin derivatives I–K (1–3) and three known congeners (4–6) were isolated from a coculture of mangrove-derived fungi Aspergillus sp. and Penicillium sp. using 1H 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 1 and 5 showed weak cytotoxicity against MHCC-97H cells (IC50 = 20.1 ± 0.9 and 25.8 ± 0.4 μM, respectively). Compound 4 exhibited potent anti-BPH activity (IC50 = 0.36 ± 0.02 μM).
期刊介绍:
The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained.
Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
When new compounds are reported, manuscripts describing their biological activity are much preferred.
Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.