Medicinal plants are known as sources of potential antimicrobial compounds belonging to different classes. The aim of the present work was to evaluate the antimicrobial potential of the crude extract, fractions, and some isolated secondary metabolites from the leaves of , a Cameroonian medicinal plant traditionally used for the treatment of microbial infections. Repeated column chromatography of the ethyl acetate and n-butanol fractions led to the isolation of seventeen previously known compounds (), among which three steroids (), one triterpene (), four flavonoids (), two stilbenoids ( and ) four ellagic acid derivatives (), one geraniinic acid derivative (), one coumarine (), and one glyceride (). Their structures were elucidated mainly by means of extensive spectroscopic and spectrometric (1D and 2D NMR and, MS) analysis and comparison with the published data. The crude extract, fractions, and isolated compounds were all screened for their antimicrobial activity. None of the natural compounds was active against strains. However, the crude extract, fractions, and compounds showed varying levels of antibacterial properties against at least one of the tested bacterial strains, with minimal inhibitory concentrations (MICs) ranging from 250 to 1000 μg/mL. The -butanol (-BuOH) fraction was the most active against ATCC 25922, with an MIC value of 250 μg/mL. Among the isolated compounds, schweinfurthin B () exhibited the best activity against NR 46003 with a MIC value of 62.5 μg/mL. In addition, schweinfurthin O () and isomacarangin () also exhibited moderate activity against the same strain with a MIC value of 125 μg/mL. Therefore, pharmacomodulation was performed on compound and three new semisynthetic derivatives () were prepared by allylation and acetylation reactions and screened for their in vitro antimicrobial activity. None of the semisynthetic derivatives showed antimicrobial activity against the same tested strains. The chemophenetic significance of the isolated compounds is also discussed in this paper.
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http://dx.doi.org/10.3390/molecules27248820 | DOI Listing |
Sci Rep
January 2025
Institute of Chemistry, University of Miskolc, Miskolc-Egyetemváros, Miskolc, 3515, Hungary.
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Department of Biochemistry, College of Sciences, King Saud University, Riyadh, Saudi Arabia.
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December 2024
Nanotechnology Research Center, Research Institute of Petroleum Industry (RIPI), West Blvd. Azadi Sports Complex, P.O. Box 14665, 1998 Tehran, Iran.
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Department of Analytical Chemistry, University of Belgrade-Faculty of Chemistry, Studentski trg 12-16, 11158 Belgrade, Serbia. Electronic address:
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Institute of Food Science Technology, National Taiwan University, No. 1, Sec. 4, Roosevelt Rd., Taipei, Taiwan, R.O.C.
This study reveals the anti-tyrosinase activity of Ganoderma formosanum extracts, pinpointing compounds including gluconic acid, mesalamine, L-pyroglutamic acid, esculetin, 5-hydroxyindole, and salicylic acid, as effective melanin production inhibitors in melanoma cells and zebrafish embryos. Furthermore, multiple molecular docking simulations provided insights into interactions between the identified compounds and tyrosinase, increasing binding affinity up to -16.36 kcal/mol.
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