4.7 Article

Pseudonocardians A-C, New Diazaanthraquinone Derivatives from a Deap-Sea Actinomycete Pseudonocardia sp SCSIO 01299

Journal

MARINE DRUGS
Volume 9, Issue 8, Pages 1428-1439

Publisher

MDPI AG
DOI: 10.3390/md9081428

Keywords

marine actinomycetes; Pseudonocardia; natural products; cytotoxicity; antibacterial; South China Sea

Funding

  1. Chinese Academy of Sciences for Key Topics in Innovation Engineering [KSCX2-YW-G-065, KZCX2-YW-JC202, KSCX2-EW-G-12, LYQY200805]
  2. National Science Foundation for Young Scientists of China [41006089, 40906075]
  3. 973 program [2010CB833805]
  4. Science and Technology planning project of Guangdong Province [2010B030600010]
  5. South China Sea Institute of Oceanology for Young Scholar [SQ200903]
  6. Key Laboratory of Marine Bio-resources Sustainable Utilization [LMB091013]
  7. Chinese Academy of Sciences [08SL111002]

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Pseudonocardians A-C (2-4), three new diazaanthraquinone derivatives, along with a previously synthesized compound deoxynyboquinone (1), were produced by the strain SCSIO 01299, a marine actinomycete member of the genus Pseudonocardia, isolated from deep-sea sediment of the South China Sea. The structures of compounds 1-4 were determined by mass spectrometry and NMR experiments ((1)H, (13)C, HSQC, and HMBC). The structure of compound 1, which was obtained for the first time from a natural source, was confirmed by X-ray analysis. Compounds 1-3 exhibited potent cytotoxic activities against three tumor cell lines of SF-268, MCF-7 and NCI-H460 with IC(50) values between 0.01 and 0.21 mu M, and also showed antibacterial activities on Staphylococcus aureus ATCC 29213, Enterococcus faecalis ATCC 29212 and Bacillus thuringensis SCSIO BT01, with MIC values of 1-4 mu g mL(-1).

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