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dc.contributor.author남상집*
dc.date.accessioned2017-02-15T08:02:03Z-
dc.date.available2017-02-15T08:02:03Z-
dc.date.issued2017*
dc.identifier.issn0960-894X*
dc.identifier.issn1464-3405*
dc.identifier.otherOAK-20079*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/234509-
dc.description.abstractActivity-guided fractionations of the tunicate Pseudodistoma antinboja yielded four new compounds of the cadiolide class (cadiolides J-M, 1, 3-5) along with a known one (cadiolide H, 2). The structures were defined by spectroscopic methods including X-ray crystallographic analysis. These compounds were evaluated for their antibacterial activity and exhibited potent antibacterial activity against all of the drug resistant strains tested with MICs comparable to those of marketed drugs such as vancomycin and linezolid. (C) 2016 Elsevier Ltd. All rights reserved.*
dc.languageEnglish*
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD*
dc.subjectTunicate*
dc.subjectPseudodistoma antinboja*
dc.subjectAntibacterial activity*
dc.titleCadiolides J-M, antibacterial polyphenyl butenolides from the Korean tunicate Pseudodistoma antinboja*
dc.typeArticle*
dc.relation.issue3*
dc.relation.volume27*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage574*
dc.relation.lastpage577*
dc.relation.journaltitleBIOORGANIC & MEDICINAL CHEMISTRY LETTERS*
dc.identifier.doi10.1016/j.bmcl.2016.12.016*
dc.identifier.wosidWOS:000392900600038*
dc.identifier.scopusid2-s2.0-85009160511*
dc.author.googleWang, Weihong*
dc.author.googleKim, Hiyoung*
dc.author.googlePatil, Rahul S.*
dc.author.googleGirl, Awadut G.*
dc.author.googleWon, Dong Hwan*
dc.author.googleHahn, Dongyup*
dc.author.googleSung, Youjung*
dc.author.googleLee, Jusung*
dc.author.googleChoi, Hyukjae*
dc.author.googleNam, Sang-Jip*
dc.author.googleKang, Heonjoong*
dc.contributor.scopusid남상집(57208839798)*
dc.date.modifydate20240220120010*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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