4.4 Article

Antituberculosis compounds from a deep-sea-derived fungus Aspergillus sp SCSIO Ind09F01

Journal

NATURAL PRODUCT RESEARCH
Volume 31, Issue 16, Pages 1958-1962

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/14786419.2016.1266353

Keywords

Deep sea fungi; Aspergillus sp; anti-tuberculosis; alkaloids

Funding

  1. Strategic Priority Research Programme of the Chinese Academy of Sciences [XDA11030403]
  2. National Natural Science Foundation of China [31270402, 41376162, 41476135]
  3. Guangzhou Science and Technology Project [201604010081]
  4. Pearl River S&T Nova Programme of Guangzhou [201610010017]

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Eleven diketopiperazine and fumiquinazoline alkaloids (1-11) together with a tetracyclic triterpenoid helvolic acid (12) were obtained from the cultures of a deep-sea derived fungus Aspergillus sp. SCSIO Ind09F01. The structures of these compounds (1-12) were determined mainly by the extensive NMR, ESIMS spectra data and by comparison with previously described compounds. Besides, anti-tuberculosis, cytotoxic, antibacterial, COX-2 inhibitory and antiviral activities of these compounds were evaluated. Gliotoxin (3), 12,13-dihydroxy-fumitremorgin C (11) and helvolic acid (12) exhibited very strong anti-tuberculosis activity towards Mycobacterium tuberculosis with the prominent MIC50 values of <0.03, 2.41 and 0.894M, respectively, which was here reported for the first time. Meanwhile gliotoxin also displayed significant selective cytotoxicities against K562, A549 and Huh-7 cell lines with the IC50 values of 0.191, 0.015 and 95.4M, respectively. [GRAPHICS] .

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