Please use this identifier to cite or link to this item: https://doi.org/10.3390/molecules171112469
Title: A novel antibacterial compound from siegesbeckia glabrescens
Authors: Kim, Y.-S
Kim, H
Jung, E
Kim, J.-H
Hwang, W
Kang, E.-J
Lee, S 
Ha, B.-J
Lee, J
Park, D
Keywords: antifungal agent
antiinfective agent
plant extract
valeric acid derivative
article
Asteraceae
chemical structure
chemistry
drug effect
Gram negative bacterium
growth, development and aging
isolation and purification
microbial sensitivity test
plant
Staphylococcus aureus
yeast
Anti-Bacterial Agents
Antifungal Agents
Asteraceae
Gram-Negative Bacteria
Microbial Sensitivity Tests
Molecular Structure
Pentanoic Acids
Plant Components, Aerial
Plant Extracts
Staphylococcus aureus
Yeasts
Issue Date: 2012
Citation: Kim, Y.-S, Kim, H, Jung, E, Kim, J.-H, Hwang, W, Kang, E.-J, Lee, S, Ha, B.-J, Lee, J, Park, D (2012). A novel antibacterial compound from siegesbeckia glabrescens. Molecules 17 (11) : 12469-12477. ScholarBank@NUS Repository. https://doi.org/10.3390/molecules171112469
Rights: Attribution 4.0 International
Abstract: The crude methanol extract of the dried aerial parts of Siegesbeckia glabrescens (Compositae) showed antibacterial activity against the foodborne pathogen Staphylococcus aureus. Bioactivity-guided separation led to the isolation of 3-(dodecanoyloxy)-2-(isobutyryloxy)-4-methylpentanoic acid from nature for the first time. The structure was determined by spectroscopic data analysis (UV, MS, and NMR). The minimal inhibitory concentration (MIC) of 3-(dodecanoyloxy)-2-(isobutyryloxy)-4-methylpentanoic acid against S. aureus was found to be 3.12 ?g/mL. In addition, in a further antimicrobial activity assay against Gram-positive (B. subtilis, E faecalis, P. acnes, S. epidermidis, S. schleiferi subsp. coagulans, S. agalactiae and S. pyrogens), and Gram-negative bacteria (E coli and P. aeruginosa), and yeast strains (C. alibicans and F. neoformans), the antimicrobial activity of the compound was found to be specific for Gram-positive bacteria. The MIC values of the compound for Gram-positive bacteria ranged from 3.12 to 25 ?g/mL. Furthermore, it was found that the 2-(isobutyryloxy)-4-methylpentanoic acid substituent may operate as a key factor in the antibacterial activity of the compound, together with the laurate group. © 2012 by the authors.
Source Title: Molecules
URI: https://scholarbank.nus.edu.sg/handle/10635/180817
ISSN: 1420-3049
DOI: 10.3390/molecules171112469
Rights: Attribution 4.0 International
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