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Saccharobisindole, Neoasterric Methyl Ester, and 7-Chloro-4(1H)-quinolone: Three New Compounds Isolated from the Marine Bacterium Saccharomonospora sp.

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dc.contributor.authorKim, Sohee-
dc.contributor.authorLe, Tu Cam-
dc.contributor.authorHan, Sang-Ah-
dc.contributor.authorHillman, Prima F.-
dc.contributor.authorHong, Ahreum-
dc.contributor.authorHwang, Sunghoon-
dc.contributor.authorDu, Young Eun-
dc.contributor.authorKim, Hiyoung-
dc.contributor.authorOh, Dong-Chan-
dc.contributor.authorCha, Sun-Shin-
dc.contributor.authorLee, Jihye-
dc.contributor.authorNam, Sang-Jip-
dc.contributor.authorFenical, William-
dc.date.accessioned2024-08-08T01:22:54Z-
dc.date.available2024-08-08T01:22:54Z-
dc.date.created2022-02-10-
dc.date.created2022-02-10-
dc.date.issued2022-01-
dc.identifier.citationMarine Drugs, Vol.20 No.1, p. 35-
dc.identifier.issn1660-3397-
dc.identifier.urihttps://hdl.handle.net/10371/205546-
dc.description.abstractAnalysis of the chemical components from the culture broth of the marine bacterium Saccharomonospora sp. CNQ-490 has yielded three novel compounds: saccharobisindole (1), neoasterric methyl ester (2), and 7-chloro-4(1H)-quinolone (3), in addition to acremonidine E (4), pinselin (5), penicitrinon A (6), and penicitrinon E (7). The chemical structures of the three novel compounds were elucidated by the interpretation of 1D, 2D nuclear magnetic resonance (NMR), and high-resolution mass spectrometry (HRMS) data. Compound 2 generated weak inhibition activity against Bacillus subtilis KCTC2441 and Staphylococcus aureus KCTC1927 at concentrations of 32 mu g/mL and 64 mu g/mL, respectively, whereas compounds 1 and 3 did not have any observable effects. In addition, compound 2 displayed weak anti-quorum sensing (QS) effects against S. aureus KCTC1927 and Micrococcus luteus SCO560.-
dc.language영어-
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)-
dc.titleSaccharobisindole, Neoasterric Methyl Ester, and 7-Chloro-4(1H)-quinolone: Three New Compounds Isolated from the Marine Bacterium Saccharomonospora sp.-
dc.typeArticle-
dc.identifier.doi10.3390/md20010035-
dc.citation.journaltitleMarine Drugs-
dc.identifier.wosid000747804000001-
dc.identifier.scopusid2-s2.0-85121995406-
dc.citation.number1-
dc.citation.startpage35-
dc.citation.volume20-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorOh, Dong-Chan-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusXANTHONE DERIVATIVES-
dc.subject.keywordPlusCITRININ DERIVATIVES-
dc.subject.keywordPlusMETABOLITES-
dc.subject.keywordPlusALKALOIDS-
dc.subject.keywordAuthorSaccharomonospora sp-
dc.subject.keywordAuthormarine natural products-
dc.subject.keywordAuthorantibacterial activity-
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  • College of Pharmacy
  • Department of Manufacturing Pharmacy
Research Area Chemical biology of natural products, Drug discovery from microbial natural products, Study of insect-microbial symbiosis, 미생물 유래 생리활성 천연물 발굴, 천연물 구조 분석

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