Marine Drugs · 2021 · 30 citations · 13 references
Natural SciencesChemistryMicrobiologyMycologyOrganic ChemistryStructure-activity RelationshipsFungal BiochemistryFungal Natural Product BiosynthesisFungal Secondary MetabolitesMarine Bioactive CompoundsMarine Natural ProductsAnti-inflammatory ActivityBioactive Fungal MetabolitesCircular DichroismElectronic Circular DichroismFungal Bioactive CompoundsMarine Fungal MetabolitesNitric OxideStructure Elucidation Of Fungal Metabolites
Four undescribed compounds, guhypoxylonols A (1), B (2), C (3), and D (4), were isolated from the mangrove endophytic fungus Aspergillus sp. GXNU-Y45, together with seven previously reported metabolites. The structures of 1–4 were elucidated based on analysis of HRESIMS and NMR spectroscopic data. The absolute configurations of the stereogenic carbons in 1–3 were established through a combination of spectroscopic data and electronic circular dichroism (ECD). Compounds 1–11 were evaluated for their anti-inflammatory activity. Compounds 1, 3, 4, and 6 showed an inhibitory activity against the production of nitric oxide (NO), with the IC50 values of 14.42 ± 0.11, 18.03 ± 0.14, 16.66 ± 0.21, and 21.05 ± 0.13 μM, respectively.
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Anti-inflammatory meroterpenoids from the mangrove endophytic fungus Talaromyces amestolkiae YX1
Senhua Chen, Meng Ding, Weiyang Liu et al. · Phytochemistry · 2017 · 89 citations