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Antibacterial 3,6-Disubstituted 4-Hydroxy-5,6-dihydro-2H-pyran-2-ones from Serratia plymuthica MF371-2
Swedish Univ Agr Sci, Uppsala, Sweden.
Swedish Univ Agr Sci, Uppsala, Sweden.
Swedish Univ Agr Sci, Uppsala, Sweden.
Swedish Univ Agr Sci, Uppsala, Sweden; Medivir AB, Huddinge, Sweden.
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2017 (English)In: Journal of natural products (Print), ISSN 0163-3864, E-ISSN 1520-6025, Vol. 80, no 11, p. 2997-3002Article in journal (Refereed) Published
Abstract [en]

Bioassay-guided fractionation of culture extracts of Serratia plymuthica strain MF371-2 resulted in the isolation of two new antibacterial compounds with potent activity against Gram-positive bacteria, including Staphylococcus aureus LMG 15975 (MRSA). A spectroscopic investigation, in combination with synthesis, enabled the characterization of the compounds as 3-butyryl-4-hydroxy-6-heptyl-5,6-dihydro2H-pyran-2-one (plymuthipyranone A, 1) and 3-butyry1-4-hydroxy-6-nony1-5,6-dihydro-2H-pyran-2-one (plymuthipyranone B, 2). The MIC values for 1 and 2 against S. aureus LMG 15975 were determined to be 1-2 mu g mL(-1) and 0.8 mu g mL(-1), respectively. Compound 2 was found to have potent activity against many strains of S. aureus, including several mupirocin-resistant strains, other species of Staphylococcus, and vancomycin-resistant enterococci. Compound 2 was slightly cytotoxic for human cells, with CC50 values between 4.7 and 40 mu g mL(-1), but the CC50/MIC ratio was >= 10 for many tested combinations of human cells and bacteria, suggesting its possible use as an antibacterial agent. Several analogues were synthesized with different alkyl groups in the 3- and 6-positions (6-13), and their biological properties were evaluated. It was concluded that the activity of the compounds increased with the lengths of the alkyl and acyl substituents.

Place, publisher, year, edition, pages
2017. Vol. 80, no 11, p. 2997-3002
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Pharmaceutical Sciences
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URN: urn:nbn:se:uu:diva-343492DOI: 10.1021/acs.jnatprod.7b00565ISI: 000416500400016PubMedID: 29083894OAI: oai:DiVA.org:uu-343492DiVA, id: diva2:1186216
Available from: 2018-02-27 Created: 2018-02-27 Last updated: 2018-03-12Bibliographically approved

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