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Secondary Metabolites from the Marine-Derived Fungus Dichotomomyces sp . L-8 and Their Cytotoxic Activity

机译:海洋衍生真菌Dichotomomyces sp的次生代谢产物。 L-8及其细胞毒活性

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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 (3 R ,6 R )-bassiatin ( 6 ). The structures of these compounds were determined by 1D, 2D NMR and mass spectrometry. (3 R ,6 R ) - 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 IC 50 values of 7.34 ± 0.20 and 14.54 ± 0.01 μM, respectively, while bassiatin ( 5 ), the diastereomer of compound 6 , was not cytotoxic.
机译:生物测定指导从真菌Dichotomomyces sp分离次生代谢产物。 L-8与柔软的珊瑚叶蜡bo相关联,导致发现了两个新化合物,二甲酮A和B(1和2),以及四个已知化合物,包括二甲ce菌素C(3),bis-N-norgliovictin(4), bassatin(5)和(3 R,6 R)-bassatin(6)。这些化合物的结构通过1D,2D NMR和质谱测定。 (3 R,6 R)-蝶呤(6)对人乳腺癌细胞MDA-MB-435和人肺癌细胞Calu3具有显着的细胞毒活性,IC 50值为7.34±0.20和14.54±0.01μM,分别是化合物6的非对映体巴西苷(5)没有细胞毒性。

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