The Cytochalasins and Polyketides from a Mangrove Endophytic Fungus Xylaria arbuscula QYF

Twelve compounds, including four undescribed cytochalasins, xylariachalasins A-D (<b>1</b>-<b>4</b>), four undescribed polyketides (<b>5</b>-<b>8</b>), and four known cytochalasins (<b>9</b>-<b>12</b>), were isolated from the mangrove endophytic fungus <i>Xylaria arbuscula</i> QYF. Their structures and absolute configurations were established by extensive spectroscopic analyses (1D and 2D NMR, HRESIMS), electronic circular dichroism (ECD) calculations, <sup>13</sup>C NMR calculation and DP4+ analysis, single-crystal X-ray diffraction, and the modified Mosher ester method. Compounds <b>1</b> and <b>2</b> are rare cytochalasin hydroperoxides. In bioactivity assays, Compound <b>2</b> exhibited moderate antimicrobial activities against <i>Staphylococcus aureus</i> and <i>Candida albicans</i> with MIC values of 12.5 μM for both Compound <b>10</b> exhibited significant cytotoxic activity against MDA-MB-435 with an IC<sub>50</sub> value of 3.61 ± 1.60 μM.

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Publication Details

Journal
Marine Drugs
Published
2024-09-05
DOI
https://doi.org/10.3390/md22090407
Citations
8
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
3.58

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article

The Cytochalasins and Polyketides from a Mangrove Endophytic Fungus Xylaria arbuscula QYF

Yihao Yin, Zhigang She, Tingshun Zhu, Xinyu Ye et al.
8 citations
Marine Drugs
Microbial Natural Products and Biosynthesis
3.58
article

The Cytochalasins and Polyketides from a Mangrove Endophytic Fungus Xylaria arbuscula QYF

Yihao Yin, Zhigang She, Tingshun Zhu, Xinyu Ye, Fei Cao, Wencong Yang, Yufeng Liu, Bo Wang, Qi Tan, Jianying Wu, Siqi Fu
article en
8 citations

Abstract

Twelve compounds, including four undescribed cytochalasins, xylariachalasins A-D (<b>1</b>-<b>4</b>), four undescribed polyketides (<b>5</b>-<b>8</b>), and four known cytochalasins (<b>9</b>-<b>12</b>), were isolated from the mangrove endophytic fungus <i>Xylaria arbuscula</i> QYF. Their structures and absolute configurations were established by extensive spectroscopic analyses (1D and 2D NMR, HRESIMS), electronic circular dichroism (ECD) calculations, <sup>13</sup>C NMR calculation and DP4+ analysis, single-crystal X-ray diffraction, and the modified Mosher ester method. Compounds <b>1</b> and <b>2</b> are rare cytochalasin hydroperoxides. In bioactivity assays, Compound <b>2</b> exhibited moderate antimicrobial activities against <i>Staphylococcus aureus</i> and <i>Candida albicans</i> with MIC values of 12.5 μM for both Compound <b>10</b> exhibited significant cytotoxic activity against MDA-MB-435 with an IC<sub>50</sub> value of 3.61 ± 1.60 μM.

Marine DrugsVol. 22(9)
Sun Yat-sen University (CN), Hebei University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 7%
Microbial Natural Products and Biosynthesis
3.58
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