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Saccharobisindole, neoasterric methyl ester, and 7‐chloro‐4(1h)‐quinolone: Three new compounds isolated from the marine bacterium saccharomonospora sp.

Title
Saccharobisindole, neoasterric methyl ester, and 7‐chloro‐4(1h)‐quinolone: Three new compounds isolated from the marine bacterium saccharomonospora sp.
Authors
Kim S.Le T.C.Han S.-A.Hillman P.F.Hong A.Hwang S.Du Y.E.Kim H.Oh D.-C.Cha S.-S.Lee J.Nam S.-J.Fenical W.
Ewha Authors
남상집차선신
SCOPUS Author ID
남상집scopus; 차선신scopus
Issue Date
2022
Journal Title
Marine Drugs
ISSN
1660-3397JCR Link
Citation
Marine Drugs vol. 20, no. 1
Keywords
Antibacterial activityMarine natural productsSaccharomonospora sp
Publisher
MDPI
Indexed
SCIE; SCOPUS WOS scopus
Document Type
Article
Abstract
Analysis 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 μg/mL and 64 μg/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. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
DOI
10.3390/md20010035
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자연과학대학 > 화학·나노과학전공 > Journal papers
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