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Antibacterial and cytotoxic prenylated dihydrochalcones from Eriosema montanum. | LitMetric

AI Article Synopsis

  • Two new compounds, prenylated dihydrochalcones (1, 2), along with 18 known metabolites, were isolated from different parts of the plant Eriosema montanum and characterized using various spectroscopic methods and X-ray diffraction.
  • The isolated compounds demonstrated significant antibacterial activity against Gram-positive bacteria, particularly Bacillus subtilis, while showing no effectiveness against Escherichia coli.
  • Additionally, some compounds exhibited cytotoxic effects on the human breast cancer cell line MCF-7, indicating potential pharmaceutical applications, particularly for prenylated dihydrochalcones.

Article Abstract

Two new prenylated dihydrochalcones (1,2) and eighteen known secondary metabolites (3-20) were isolated from the CHCl-MeOH (1:1) extracts of the roots, the stem bark and the leaves of Eriosema montanum Baker f. (Leguminosae). The structures of the isolated compounds were characterized by NMR, IR, and UV spectroscopic and mass spectrometric analyses. The structures of compounds 5, 10, 11 and 13 were confirmed by single crystal X-ray diffraction. The antibacterial activity of the crude extracts and the isolated constituents were established against Gram-positive and Gram-negative bacteria. Among the tested compounds, 1-4 and 10 showed strong activity against the Gram-positive bacterium Bacillus subtilis with minimum inhibitory concentration (MIC) ranging from 3.1 to 8.9 μM, as did the leaf crude extract with an MIC of 3.0 μg/mL. None of the crude extracts nor the isolated compounds were active against Escherichia coli. Compounds 1, 3 and 4 showed higher cytotoxicity, evaluated against the human breast cancer cell line MCF-7, with EC of 7.0, 18.0 and 18.0 μM, respectively. These findings contribute to the phytochemical understanding of the genus Eriosema, and highlight the pharmaceutical potential of prenylated dihydrochalcones.

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Source
http://dx.doi.org/10.1016/j.fitote.2020.104809DOI Listing

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