Citrifuran E–I, Five Dimeric Polyketides With Potential Anti‐inflammatory Activity From <i>Aspergillus</i> sp. AWG 1–15

Five novel dimeric polyketides, citrifuran E-I (1-5), were isolated from the fungus Aspergillus sp. AWG 1-15. These polyketides were rare heterodimers of azaphilone and furanone derivatives. Their relative and absolute configurations were determined based on high-resolution electrospray ionization mass spectrometry and spectroscopic analyses (one- and two-dimensional nuclear magnetic resonance), electronic circular dichroism calculations, and chemical derivatization. All compounds were assessed for anti-inflammatory activity by measuring their effects on nitric oxide production induced by lipopolysaccharide in RAW 264.7 cells. Compounds 1-4 exhibited moderate inhibitory activity, with the minimum inhibitory concentration (IC<sub>50</sub>) values ranging from 12.6 to 37.3 µM, compared to the positive control N<sup>G</sup>-monomethyl-L-arginine (IC<sub>50</sub> = 40.6 µM).

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Publication Details

Journal
Chemistry & Biodiversity
Published
2025-04-07
DOI
https://doi.org/10.1002/cbdv.202500695
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Citrifuran E–I, Five Dimeric Polyketides With Potential Anti‐inflammatory Activity From Aspergillus sp. AWG 1–15

Qun Jiang, Guo-Ping Yin, Ran He, Yiyang Chen et al.
Chemistry & Biodiversity
Microbial Natural Products and Biosynthesis
article

Citrifuran E–I, Five Dimeric Polyketides With Potential Anti‐inflammatory Activity From Aspergillus sp. AWG 1–15

Qun Jiang, Guo-Ping Yin, Ran He, Yiyang Chen, Minghua Yang, Ling-Yi Kong
article en

Abstract

Five novel dimeric polyketides, citrifuran E-I (1-5), were isolated from the fungus Aspergillus sp. AWG 1-15. These polyketides were rare heterodimers of azaphilone and furanone derivatives. Their relative and absolute configurations were determined based on high-resolution electrospray ionization mass spectrometry and spectroscopic analyses (one- and two-dimensional nuclear magnetic resonance), electronic circular dichroism calculations, and chemical derivatization. All compounds were assessed for anti-inflammatory activity by measuring their effects on nitric oxide production induced by lipopolysaccharide in RAW 264.7 cells. Compounds 1-4 exhibited moderate inhibitory activity, with the minimum inhibitory concentration (IC<sub>50</sub>) values ranging from 12.6 to 37.3 µM, compared to the positive control N<sup>G</sup>-monomethyl-L-arginine (IC<sub>50</sub> = 40.6 µM).

Chemistry & BiodiversityVol. 22(8)
China Pharmaceutical University (CN), State Key Laboratory of Natural Medicine
National Natural Science Foundation of China, Overseas Expertise Introduction Center for Discipline Innovation of Food Nutrition and Human Health (111 Center)
Clean water and sanitation
Openalex Percentile: Top 92%
Microbial Natural Products and Biosynthesis
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