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Chem Biodivers ; 20(12): e202301512, 2023 Dec.
Article in English | MEDLINE | ID: mdl-37921566

ABSTRACT

Four new phomalones A-D (1-4), together with five known analogues (5-9) were isolated from the deep-sea-derived fungus Trichobotrys effuse FS522. Their structures of the new compounds established by analysis of their NMR and HR-ESI-MS spectroscopic data, and the absolute configurations of 2 was determined by electronic circular dichroism (ECD) calculations. compounds 4, 6 and 8 substantially inhibited the production of nitric oxide (NO) with IC50 values of 4.64, 13.90, and 34.07 µM.


Subject(s)
Ascomycota , Anti-Inflammatory Agents/pharmacology , Magnetic Resonance Spectroscopy/methods , Molecular Structure , Pyrans/chemistry , Pyrans/pharmacology , Heterocyclic Compounds, 3-Ring/chemistry , Heterocyclic Compounds, 3-Ring/pharmacology
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