Abstract
One previously undescribed acetylenic polyketide, arunropsisol A (1), one new p-terphenyl derivative, aruterphenylol A (5), together with three known acetylenic polyketides, four benzene derivatives, and one macrolide, were isolated from the solid fermentation of the marine-derived fungus Microsphaeropsis arundinis P1B. Their structures were elucidated through a combination of spectroscopic, computational ECD, and X-ray diffraction methods. Arunropsisol A (1) is characterized by a novel carbon-skeleton, featuring a rare four-carbon 3-oxobut-1-yn-1-yl side chain, which suggests a biosynthetic relationship via oxidative cleavage of a common five-carbon isopentenyl-derived precursor. All isolated compounds were evaluated for their anti-inflammatory activity.
| Original language | English |
|---|---|
| Article number | 146956 |
| Journal | Journal of Molecular Structure |
| Volume | 1376 |
| DOIs | |
| State | Published - 5 Dec 2026 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 14 Life Below Water
Keywords
- Absolute configuration
- Anti-inflammatory activity
- Marine-derived fungus
- Microsphaeropsis arundinis
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