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dc.contributor.author남상집*
dc.date.accessioned2016-08-28T10:08:54Z-
dc.date.available2016-08-28T10:08:54Z-
dc.date.issued2013*
dc.identifier.issn0163-3864*
dc.identifier.otherOAK-10044*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/223686-
dc.description.abstractTwo new cyclic hexapeptides, nocardiamides A (1) and B (2), were isolated from the culture broth of marine-derived actinomycete CNX037 strain that was identified as a Nocardiopsis species. The planar structures of nocardiamides A (1) and B (2) were assigned on the basis of 1D and 2D NMR and HRESIMS spectroscopic analyses. Their absolute configurations were deduced by the advanced Marfey's method and chiral-phase HPLC analysis. The challenge of locating two d- and one l-valine residue in 1 and 2 was accomplished by total synthesis using solid-phase peptide synthetic methods. Both 1 and 2 showed negligible antimicrobial activities against seven indicator strains and exhibited no cytotoxicity against HCT-116. © 2013 The American Chemical Society and American Society of Pharmacognosy.*
dc.languageEnglish*
dc.titleNocardiamides A and B, two cyclohexapeptides from the marine-derived actinomycete Nocardiopsis sp. CNX037*
dc.typeArticle*
dc.relation.issue4*
dc.relation.volume76*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage694*
dc.relation.lastpage701*
dc.relation.journaltitleJournal of Natural Products*
dc.identifier.doi10.1021/np400009a*
dc.identifier.wosidWOS:000318264700029*
dc.identifier.scopusid2-s2.0-84876889883*
dc.author.googleWu Z.-C.*
dc.author.googleLi S.*
dc.author.googleNam S.-J.*
dc.author.googleLiu Z.*
dc.author.googleZhang C.*
dc.contributor.scopusid남상집(57208839798)*
dc.date.modifydate20240220120010*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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