Please use this identifier to cite or link to this item: https://doi.org/10.3390/molecules171112469
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dc.titleA novel antibacterial compound from siegesbeckia glabrescens
dc.contributor.authorKim, Y.-S
dc.contributor.authorKim, H
dc.contributor.authorJung, E
dc.contributor.authorKim, J.-H
dc.contributor.authorHwang, W
dc.contributor.authorKang, E.-J
dc.contributor.authorLee, S
dc.contributor.authorHa, B.-J
dc.contributor.authorLee, J
dc.contributor.authorPark, D
dc.date.accessioned2020-10-27T04:51:07Z
dc.date.available2020-10-27T04:51:07Z
dc.date.issued2012
dc.identifier.citationKim, 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
dc.identifier.issn1420-3049
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/180817
dc.description.abstractThe 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.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectantifungal agent
dc.subjectantiinfective agent
dc.subjectplant extract
dc.subjectvaleric acid derivative
dc.subjectarticle
dc.subjectAsteraceae
dc.subjectchemical structure
dc.subjectchemistry
dc.subjectdrug effect
dc.subjectGram negative bacterium
dc.subjectgrowth, development and aging
dc.subjectisolation and purification
dc.subjectmicrobial sensitivity test
dc.subjectplant
dc.subjectStaphylococcus aureus
dc.subjectyeast
dc.subjectAnti-Bacterial Agents
dc.subjectAntifungal Agents
dc.subjectAsteraceae
dc.subjectGram-Negative Bacteria
dc.subjectMicrobial Sensitivity Tests
dc.subjectMolecular Structure
dc.subjectPentanoic Acids
dc.subjectPlant Components, Aerial
dc.subjectPlant Extracts
dc.subjectStaphylococcus aureus
dc.subjectYeasts
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.3390/molecules171112469
dc.description.sourcetitleMolecules
dc.description.volume17
dc.description.issue11
dc.description.page12469-12477
dc.published.statePublished
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