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Article: Four new antibacterial xanthones from the marine-derived actinomycetes Streptomyces caelestis

TitleFour new antibacterial xanthones from the marine-derived actinomycetes Streptomyces caelestis
Authors
Liu, Ling LiXu, YingHan, ZhuangLi, Yong XinLu, LiangLai, Pok YuiZhong, Jia LiangGuo, Xian RongZhang, Xi XiangQian, Pei Yuan
KeywordsCitreamicin
Antibacterial
Streptomyces caelestis
MRSA
Issue Date2012
Citation
Marine Drugs, 2012, v. 10, n. 11, p. 2571-2583 How to Cite?
DOI: http://dx.doi.org/10.3390/md10112571
AbstractFour new polycyclic antibiotics, citreamicin θ A (1), citreamicin θ B (2), citreaglycon A (3), and dehydrocitreaglycon A (4), were isolated from marine-derived Streptomyces caelestis. The structures of these compounds were elucidated by 1D and 2D NMR spectra. All four compounds displayed antibacterial activity against Staphylococcus haemolyticus, Staphylococcus aureus, and Bacillus subtillis. Citreamicin θ A (1), citreamicin θ B (2) and citreaglycon A (3) also exhibited low MIC values of 0.25, 0.25, and 8.0 μg/mL, respectively, against methicillin-resistant Staphylococcus aureus (MRSA) ATCC 43300. © 2012 by the authors; licensee MDPI.
Persistent Identifierhttp://hdl.handle.net/10722/273520
ISSN
1660-3397
2022 Impact Factor: 5.4
2020 SCImago Journal Rankings: 0.848
ISI Accession Number ID
WOS:000311425800014

 

DC FieldValueLanguage
dc.contributor.authorLiu, Ling Li-
dc.contributor.authorXu, Ying-
dc.contributor.authorHan, Zhuang-
dc.contributor.authorLi, Yong Xin-
dc.contributor.authorLu, Liang-
dc.contributor.authorLai, Pok Yui-
dc.contributor.authorZhong, Jia Liang-
dc.contributor.authorGuo, Xian Rong-
dc.contributor.authorZhang, Xi Xiang-
dc.contributor.authorQian, Pei Yuan-
dc.date.accessioned2019-08-12T09:55:49Z-
dc.date.available2019-08-12T09:55:49Z-
dc.date.issued2012-
dc.identifier.citationMarine Drugs, 2012, v. 10, n. 11, p. 2571-2583-
dc.identifier.issn1660-3397-
dc.identifier.urihttp://hdl.handle.net/10722/273520-
dc.description.abstractFour new polycyclic antibiotics, citreamicin θ A (1), citreamicin θ B (2), citreaglycon A (3), and dehydrocitreaglycon A (4), were isolated from marine-derived Streptomyces caelestis. The structures of these compounds were elucidated by 1D and 2D NMR spectra. All four compounds displayed antibacterial activity against Staphylococcus haemolyticus, Staphylococcus aureus, and Bacillus subtillis. Citreamicin θ A (1), citreamicin θ B (2) and citreaglycon A (3) also exhibited low MIC values of 0.25, 0.25, and 8.0 μg/mL, respectively, against methicillin-resistant Staphylococcus aureus (MRSA) ATCC 43300. © 2012 by the authors; licensee MDPI.-
dc.languageeng-
dc.relation.ispartofMarine Drugs-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectCitreamicin-
dc.subjectAntibacterial-
dc.subjectStreptomyces caelestis-
dc.subjectMRSA-
dc.titleFour new antibacterial xanthones from the marine-derived actinomycetes Streptomyces caelestis-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.3390/md10112571-
dc.identifier.pmid23203278-
dc.identifier.scopuseid_2-s2.0-84870040743-
dc.identifier.volume10-
dc.identifier.issue11-
dc.identifier.spage2571-
dc.identifier.epage2583-
dc.identifier.isiWOS:000311425800014-
dc.identifier.issnl1660-3397-

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