This work describes the isolation and structural elucidation of compounds from the leaves of (Aubl.) DC. (goiaba-brava) and evaluates the antimicrobial activity of the crude extract, fractions and isolated compounds against bacteria and fungi. Column chromatography was used to fractionate and purify the extract of the leaves and the chemical structures of the compounds were determined using spectroscopic techniques. The antibacterial and antifungal activities were assessed using the broth microdilution method. The phytochemical investigation isolated 11 compounds: α-bisabolol, α-bisabolol oxide B, α-cadinol, β-sitosterol, -pentacosane, -tetracosane, quercetin, kaempferol, avicularin, juglanin and guaijaverin. The crude ethanolic extract and its fractions were tested against 15 bacteria and 9 yeasts. The crude extract inhibited the in vitro growth of yeasts at concentration of 4 to 32 μg/mL. The hexane, dichloromethane, ethyl acetate and aqueous fractions inhibited sp. at concentrations of 4 to 256 μg/mL, whereas the sp. isolates were inhibited only by the hexane and dichloromethane fractions in minimal inhibitory concentrations (MICs) at 16 to 64 μg/mL. The flavonoid quercetin-3--α-arabinofuranose (avicularin) was the most active compound, inhibiting species in concentrations of 2 to 32 μg/mL. The MIC values suggest potential activity of this plant species against yeast.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152266PMC
http://dx.doi.org/10.3390/molecules22071100DOI Listing

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