Secondary Metabolites from the Marine-Derived Fungus Dichotomomyces sp. L-8 and Their Cytotoxic Activity
Li-Hong Huang,
Yan-Xiu Chen,
Jian-Chen Yu,
Jie Yuan,
Hou-Jin Li,
Wen-Zhe Ma,
Ramida Watanapokasin,
Kun-Chao Hu,
Shah Iram Niaz,
De-Po Yang,
Wen-Jian Lan
Affiliations
Li-Hong Huang
School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China
Yan-Xiu Chen
School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China
Jian-Chen Yu
Zhongshan School of Medicine, Sun Yat-sen University, 74 Zhongshan Road II, Guangzhou 510080, China
Jie Yuan
Zhongshan School of Medicine, Sun Yat-sen University, 74 Zhongshan Road II, Guangzhou 510080, China
Hou-Jin Li
School of Chemistry, Sun Yat-sen University, Guangzhou 510275, China
Wen-Zhe Ma
State Key Laboratory of Quality Research in Chinese Medicine, Macau Institute for Applied Research in Medicine and Health, Macau University of Science and Technology, Avenida Wai Long, Taipa 519020, Macau (SAR), China
Ramida Watanapokasin
Department of Biochemistry, Faculty of Medicine, Srinakharinwirot University, Bangkok 10110, Thailand
Kun-Chao Hu
School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China
Shah Iram Niaz
Institute of Chemical Sciences, Gomal University, D.I.Khan 29050, Pakistan
De-Po Yang
School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China
Wen-Jian Lan
School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China
Bioassay-guided isolation of the secondary metabolites from the fungus Dichotomomyces sp. L-8 associated with the soft coral Lobophytum crassum led to the discovery of two new compounds, dichotones A and B (1 and 2), together with four known compounds including dichotocejpin C (3), bis-N-norgliovictin (4), bassiatin (5) and (3R,6R)-bassiatin (6). The structures of these compounds were determined by 1D, 2D NMR and mass spectrometry. (3R,6R)-bassiatin (6) displayed significant cytotoxic activities against the human breast cancer cell line MDA-MB-435 and the human lung cancer cell line Calu3 with IC50 values of 7.34 ± 0.20 and 14.54 ± 0.01 μM, respectively, while bassiatin (5), the diastereomer of compound 6, was not cytotoxic.