Asperpolyols A and B, two novel hydroxy polyunsaturated fatty acids, isolated from the marine-derived fungus Aspergillus versicolor M7

Asperpolyols A ((4E,8E,12E,16E)-3,7,11,15-tetrahydroxy-4,6,8,10,12,14,16-heptamethyloctadeca-4,8,12,16-tetraenoic acid) and B ((4E,8E,12E,16E)-3,7,11,15-tetrahydroxy-4,6,8,10,12,14,16-heptamethyloctadeca-4,8,12,16-tetraen-oic acid), two new hydroxy polyunsaturated fatty acids, were acquired from the extract of Aspergillus versicolor M7 isolated from seawater. Their chemical structures were determined by interpretation of 1D/2D nuclear magnetic resonance (NMR) and high-resolution electrospray ionization mass spectrometry (HRESIMS) data. Compounds 1 and 2 were evaluated for inhibiting the growth of three marine phytoplankton species, including Prorocentrum donghaiense, Heterosigma akashiwo, and Prorocentrum micans, and compound 1 exhibited weak inhibitory activity with the half-maximal inhibitory concentration (IC50) values ranging from 62.8 to 86.9 g/mL.

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Publication Details

Journal
Records of Natural Products
Published
2026-10-26
DOI
https://doi.org/10.25135/rnp.2609.4019
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
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article

Asperpolyols A and B, two novel hydroxy polyunsaturated fatty acids, isolated from the marine-derived fungus Aspergillus versicolor M7

时振振, 梁小蕊, Xiao Li, Pei Xie
Records of Natural Products
Microbial Natural Products and Biosynthesis
article

Asperpolyols A and B, two novel hydroxy polyunsaturated fatty acids, isolated from the marine-derived fungus Aspergillus versicolor M7

时振振, 梁小蕊, Xiao Li, Pei Xie
article en

Abstract

Asperpolyols A ((4E,8E,12E,16E)-3,7,11,15-tetrahydroxy-4,6,8,10,12,14,16-heptamethyloctadeca-4,8,12,16-tetraenoic acid) and B ((4E,8E,12E,16E)-3,7,11,15-tetrahydroxy-4,6,8,10,12,14,16-heptamethyloctadeca-4,8,12,16-tetraen-oic acid), two new hydroxy polyunsaturated fatty acids, were acquired from the extract of Aspergillus versicolor M7 isolated from seawater. Their chemical structures were determined by interpretation of 1D/2D nuclear magnetic resonance (NMR) and high-resolution electrospray ionization mass spectrometry (HRESIMS) data. Compounds 1 and 2 were evaluated for inhibiting the growth of three marine phytoplankton species, including Prorocentrum donghaiense, Heterosigma akashiwo, and Prorocentrum micans, and compound 1 exhibited weak inhibitory activity with the half-maximal inhibitory concentration (IC50) values ranging from 62.8 to 86.9 g/mL.

Records of Natural ProductsVol. 21(2)
Shandong Marine Resource and Environment Research Institute (CN), Weifang University of Science and Technology (CN)
Openalex Percentile: Top 14%
Microbial Natural Products and Biosynthesis
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