Antituberculosis compounds from a deep-sea-derived fungus Aspergillus sp. SCSIO Ind09F01
2017
Luo, Xiaowei | Zhou, Xuefeng | Lin, Xiuping | Qin, Xiaochu | Zhang, Tianyu | Wang, Junfeng | Tu, Zhengchao | Yang, Bin | Liao, Shengrong | Tian, Yongqi | Pang, Xiaoyan | Kaliyaperumal, Kumaravel | Li, Jian Lin | Tao, Huaming | Liu, Yonghong
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 0.894 μM, 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 95.4 μM, respectively.
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