The present work reports the isolation and biological evaluation of three dimeric xanthones from sp. EJC01.1 isolated as endophytic from , a typical plant of the Amazon. The compounds phomoxanthone A (), phomoxanthone B () and dicerandrol B () were isolated by chromatographic procedures and identified by spectroscopic methods of 1D and 2D NMR and MS. The extracts and compound showed antimicrobial activities against , , , and . The compound phomoxanthone A () showed greater inhibitory activity against (MIC of 7.81 µg mL); in addition, it also pronounced inhibitory effect against promastigote forms of (IC of 16.38 ± 1.079 µg mL) and epimastigote forms (IC of 28.61 ± 1.071 µg mL). To provide more information about the antibacterial activity of compound 1, an unprecedented molecular docking study was performed using S-ribosyl-homocysteine lyase (LuxS) (PDB ID 2FQO), which showed a possible interaction of phomoxanthone A with two of the residues (His58 and Cys126) that are fundamental for the catalysis mechanism in , which may be associated with the higher activity, when compared to other bacteria, observed in experimental studies. Additionally, quantum studies (DFT) were performed, for which a low gap value (5.982 eV) was observed, which corroborates the reactivity of phomoxanthone A. Thus, phomoxanthone A can be a good agent against pathogenic bacteria.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9598121PMC
http://dx.doi.org/10.3390/antibiotics11101332DOI Listing

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