Two new fusarochromanone derivatives, deacetylfusarochromene () and deacetamidofusarochrom-2',3-diene (), along with the previously reported metabolites fusarochromanone TDP-2 (), fusarochromene (), 2,2-dimethyl-5-amino-6-(2'-ene-4'-hydroxylbutyryl)-4-chromone (), fusarochromanone (), (-)-chrysogine (), and equisetin (), were isolated from the marine fungus UBOCC-A-117302. The structures of the compounds were determined by extensive spectrometric (HRMS) and spectroscopic (1D and 2D NMR) analyses, as well as specific rotation. Among them, and showed inhibition of three protein kinases with IC values ranging from 1.42 to 25.48 μM. Cytotoxicity and antimicrobial activity of all isolated compounds were also evaluated. Six fusarochromanone derivatives (-) exhibited diverse activities against three cell lines, RPE-1, HCT-116, and U2OS (IC values ranging from 0.058 to 84.380 μM). Equisetin () showed bactericidal activities against and (MBC values of 7.8 and 31.25 µM, respectively), and bacteriostatic activity against (MIC value of 31.25 µM). Compounds and showed bacteriostatic activities against (MIC of 125 µM).
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11509758 | PMC |
http://dx.doi.org/10.3390/md22100444 | DOI Listing |
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