Isolation of two new isomers of fusarin D from <i>Fusarium</i> sp. G10, an endophytic fungus of <i>Iris japonica</i>

<i>Fusarium</i> species are globally distributed filamentous fungi with a variety of bioactive compounds. Six fusarins (<b>1 - 6</b>), including two new isomers of fusarin D (<b>5</b> and <b>6</b>), along with six known terpenoids (<b>7 </b>-<b> 12</b>), were isolated from the endophytic fungus <i>Fusarium</i> sp. G10, which was derived from <i>Iris japonica</i> Thunb. The structures of all compounds were elucidated using various spectroscopic techniques, and their cytotoxic and antimicrobial activities were assessed. Compounds <b>2</b> and <b>3</b> demonstrated selective inhibitory effects on the DU145 and MDA-MB-231 cell lines, with IC<sub>50</sub> values ranging from 17.74 to 36.66 µM. Additionally, compound <b>11</b> demonstrated weak inhibitory activity against bacterial strains, with MIC values of 32 and 64 μg/mL.

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Publication Details

Journal
Natural Product Research
Published
2025-09-16
DOI
https://doi.org/10.1080/14786419.2025.2559760
Primary Topic
Mycotoxins in Agriculture and Food
Type
article
Field-Weighted Citation Impact
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article

Isolation of two new isomers of fusarin D from Fusarium sp. G10, an endophytic fungus of Iris japonica

Yue Zhou, Ayşe Nur Tan, Xiaoying Long, Xiaolong Tang et al.
Natural Product Research
Mycotoxins in Agriculture and Food
article

Isolation of two new isomers of fusarin D from Fusarium sp. G10, an endophytic fungus of Iris japonica

Yue Zhou, Ayşe Nur Tan, Xiaoying Long, Xiaolong Tang, Man He, Yanan An
article en

Abstract

<i>Fusarium</i> species are globally distributed filamentous fungi with a variety of bioactive compounds. Six fusarins (<b>1 - 6</b>), including two new isomers of fusarin D (<b>5</b> and <b>6</b>), along with six known terpenoids (<b>7 </b>-<b> 12</b>), were isolated from the endophytic fungus <i>Fusarium</i> sp. G10, which was derived from <i>Iris japonica</i> Thunb. The structures of all compounds were elucidated using various spectroscopic techniques, and their cytotoxic and antimicrobial activities were assessed. Compounds <b>2</b> and <b>3</b> demonstrated selective inhibitory effects on the DU145 and MDA-MB-231 cell lines, with IC<sub>50</sub> values ranging from 17.74 to 36.66 µM. Additionally, compound <b>11</b> demonstrated weak inhibitory activity against bacterial strains, with MIC values of 32 and 64 μg/mL.

Natural Product Research
Chongqing University of Arts and Sciences (CN)
Openalex Percentile: Top 82%
Mycotoxins in Agriculture and Food
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