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dc.contributor.author남상집*
dc.date.accessioned2021-08-12T16:31:50Z-
dc.date.available2021-08-12T16:31:50Z-
dc.date.issued2021*
dc.identifier.issn1523-7060*
dc.identifier.otherOAK-29483*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/258715-
dc.description.abstractDumulmycin (1) was isolated from Streptomyces sp. DM28, a bacterial strain from a riverine sediment sample. The structure of 1 was elucidated as a bicyclic macrolide possessing 19-membered and 5-membered rings by spectroscopic analysis. The stereochemistry of 1 was determined by J-based configuration analysis, ROESY NMR data, DP4 calculations, and the modified Mosher's method. Genetic analysis identified a trans-acyltransferase polyketide biosynthetic gene cluster for 1. Dumulmycin exhibited in vitro antitubercular activity (MIC50 = 27.1 μM). © 2021 American Chemical Society.*
dc.languageEnglish*
dc.publisherAmerican Chemical Society*
dc.titleDumulmycin, an antitubercular bicyclic macrolide from a riverine sediment-derived streptomyces sp.*
dc.typeArticle*
dc.relation.issue9*
dc.relation.volume23*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage3359*
dc.relation.lastpage3363*
dc.relation.journaltitleOrganic Letters*
dc.identifier.doi10.1021/acs.orglett.1c00847*
dc.identifier.wosidWOS:000649477300025*
dc.identifier.scopusid2-s2.0-85106162085*
dc.author.googleAn J.S.*
dc.author.googleShin B.*
dc.author.googleKim T.H.*
dc.author.googleHwang S.*
dc.author.googleShin Y.-H.*
dc.author.googleCui J.*
dc.author.googleDu Y.E.*
dc.author.googleYi J.*
dc.author.googleNam S.-J.*
dc.author.googleHong S.*
dc.author.googleShin J.*
dc.author.googleJang J.*
dc.author.googleYoon Y.J.*
dc.author.googleOh D.-C.*
dc.contributor.scopusid남상집(57208839798)*
dc.date.modifydate20240220120010*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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