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dc.contributor.author남상집*
dc.date.accessioned2019-08-22T16:30:05Z-
dc.date.available2019-08-22T16:30:05Z-
dc.date.issued2019*
dc.identifier.issn1660-3397*
dc.identifier.otherOAK-25242*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/251221-
dc.description.abstractMycousfurans (1 and 2), two new usnic acid congeners, along with (−)-mycousnine (3), (−)-placodiolic acid (4), and (+)-usnic acid (5), were isolated using high-performance liquid chromatography-ultraviolet (HPLC-UV)-guided fractionation of extracts of Mycosphaerella sp. isolated from a marine sediment. The planar structures of 1 and 2 were elucidated using 1D and 2D NMR spectra. The relative configurations of the stereogenic carbons of 1 and 2 were established via analysis of their nuclear Overhauser spectroscopy (NOESY) spectra, and their absolute configurations were determined using a comparison of experimental and calculated electronic circular dichroism (ECD) spectra. Compounds 1 and 2 were found to have antibacterial activity, showing moderate activity against Kocuria rhizophila and Staphylococcus aureus. © 2019 by the authors.*
dc.languageEnglish*
dc.publisherMDPI AG*
dc.subjectAntibacterial activity*
dc.subjectMycosphaerella sp*
dc.subjectMycousfurans*
dc.subjectMycousnine*
dc.subjectPlacodiolic acid*
dc.subjectUsnic acid*
dc.titleMycousfurans A and B, antibacterial usnic acid congeners from the fungus Mycosphaerella sp., isolated from a marine sediment*
dc.typeArticle*
dc.relation.issue7*
dc.relation.volume17*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.journaltitleMarine Drugs*
dc.identifier.doi10.3390/md17070422*
dc.identifier.wosidWOS:000478650600044*
dc.identifier.scopusid2-s2.0-85069859735*
dc.author.googleLee J.*
dc.author.googleKim G.J.*
dc.author.googleYang I.*
dc.author.googleWang W.*
dc.author.googleNam J.-W.*
dc.author.googleChoi H.*
dc.author.googleNam S.-J.*
dc.author.googleKang H.*
dc.contributor.scopusid남상집(57208839798)*
dc.date.modifydate20240220120010*


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