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Actinopolymorphols E and F, pyrazine alkaloids from a marine sediment-derived bacterium Streptomyces sp

DC Field Value Language
dc.contributor.authorKim, Sohee-
dc.contributor.authorHillman, Prima F.-
dc.contributor.authorLee, Ji Young-
dc.contributor.authorLee, Juri-
dc.contributor.authorLee, Jihye-
dc.contributor.authorCha, Sun-Shin-
dc.contributor.authorOh, Dong-Chan-
dc.contributor.authorNam, Sang-Jip-
dc.contributor.authorFenical, William-
dc.date.accessioned2022-10-18T00:32:56Z-
dc.date.available2022-10-18T00:32:56Z-
dc.date.created2022-10-13-
dc.date.issued2022-11-
dc.identifier.citationJournal of Antibiotics, Vol.75 No.11, pp.619-625-
dc.identifier.issn0021-8820-
dc.identifier.urihttps://hdl.handle.net/10371/186394-
dc.description.abstractHPLC-UV-guided fractionation of crude extract from the marine sediment-derived bacterium Streptomyces sp. CNP-944 has yielded two new pyrazine alkaloids, actinopolymorphols E and F (1 and 2), in addition to the previously reported biosynthetic product, actinopolymorphol G (3), and the known actinopolymorphol D (4). The chemical structures of 1-3 were determined based on the interpretation of the 1D, 2D NMR, and MS spectroscopic data. Compound 2 displayed weak antibacterial activities against Kocuria rhizophila, Bacillus subtilis, and Staphylococcus aureus with minimum inhibitory concentration (MIC) values of 16, 64, and 64 mu g ml(-1), respectively.-
dc.language영어-
dc.publisherNature Publishing Group-
dc.titleActinopolymorphols E and F, pyrazine alkaloids from a marine sediment-derived bacterium Streptomyces sp-
dc.typeArticle-
dc.identifier.doi10.1038/s41429-022-00562-2-
dc.citation.journaltitleJournal of Antibiotics-
dc.identifier.wosid000854677300002-
dc.identifier.scopusid2-s2.0-85138018197-
dc.citation.endpage625-
dc.citation.number11-
dc.citation.startpage619-
dc.citation.volume75-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorOh, Dong-Chan-
dc.type.docTypeArticle-
dc.description.journalClass1-
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