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Beilstein J. Org. Chem. 2025, 21, 327–339, doi:10.3762/bjoc.21.23
Graphical Abstract
Figure 1: Chemical structures of compounds 1–6, prototenellin D and pretenellin B [7].
Figure 2: Key 1H-1H COSY, HMBC and ROESY correlations of 1.
Figure 3: Comparison of experimental (black) and simulated Boltzmann-averaged (red: (2’S,3’S,12S)-1; green: (...
Figure 4: A plausible biosynthetic pathway of 1–3.
Figure 5: Biofilm inhibition and eradication assessment via CV staining assay. A) S. aureus biofilm inhibitio...
Figure 6: A) Metabolic activity in biomass of S. aureus biofilm treated with farinosones D (1) or A (2). Erro...
Beilstein J. Org. Chem. 2021, 17, 1385–1391, doi:10.3762/bjoc.17.97
Figure 1: Structures of fulvoferruginin (1) and the newly isolated derivatives fulvoferruginins B–F (2–6).
Figure 2: KEY HMBC (arrows) and COSY (thick bonds) correlations of compounds 2 and 3.
Figure 3: Key ROESY correlations of metabolite 3.