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dc.contributor.author임경민*
dc.contributor.author남상집*
dc.date.accessioned2017-10-27T11:45:00Z-
dc.date.available2017-10-27T11:45:00Z-
dc.date.issued2017*
dc.identifier.issn1660-3397*
dc.identifier.otherOAK-21252*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/237079-
dc.description.abstractIntensive study of the organic extract of the marine-derived bacterium Saccharomonospora sp. CNQ-490 has yielded three new α-pyrones, saccharomonopyrones A–C (1–3). The chemical structures of these compounds were assigned from the interpretation of 1D, 2D NMR and mass spectrometry data. Saccharomonopyrone A (1) is the first α-pyrone microbial natural product bearing the ethyl-butyl ether chain in the molecule, while saccharomonopyrones B and C possess unusual 3-methyl and a 6-alkyl side-chain within a 3,4,5,6-tetrasubstituted α-pyrone moiety. Saccharomonopyrone A exhibited weak antioxidant activity using a cation radical scavenging activity assay with an IC50 value of 140 µM. © 2017 by the authors. Licensee MDPI.*
dc.languageEnglish*
dc.publisherMDPI AG*
dc.subjectMarine natural products*
dc.subjectSaccharomonospora sp.*
dc.subjectα-pyrones*
dc.titleSaccharomonopyrones A–C, new α-pyrones from a marine sediment-derived bacterium Saccharomonospora sp. CNQ-490*
dc.typeArticle*
dc.relation.issue8*
dc.relation.volume15*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.journaltitleMarine Drugs*
dc.identifier.doi10.3390/md15080239*
dc.identifier.wosidWOS:000408763400005*
dc.identifier.scopusid2-s2.0-85029697768*
dc.author.googleYim C.-Y.*
dc.author.googleLe T.C.*
dc.author.googleLee T.G.*
dc.author.googleYang I.*
dc.author.googleChoi H.*
dc.author.googleLee J.*
dc.author.googleKang K.-Y.*
dc.author.googleLee J.S.*
dc.author.googleLim K.-M.*
dc.author.googleYee S.-T.*
dc.author.googleKang H.*
dc.author.googleNam S.-J.*
dc.author.googleFenical W.*
dc.contributor.scopusid임경민(8916551700)*
dc.contributor.scopusid남상집(57208839798)*
dc.date.modifydate20240220115649*


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