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首页> 外文期刊>Journal of natural products >Structures and Biological Evaluations of Agelasines Isolated from the Okinawan Marine Sponge Agelas nakamurai
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Structures and Biological Evaluations of Agelasines Isolated from the Okinawan Marine Sponge Agelas nakamurai

机译:冲绳海洋海绵Aeglas nakamurai分离出的Aeglasines的结构和生物学评价

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摘要

Three new N-methyladenine-containing diterpenes, 2-oxoagelasines A (1) and F (2) and 10-hydro-9-hydroxyagelasine F (3), were isolated from the Okinawan marine sponge Agelas nakamurai Hoshino together with eight known agelasine derivatives, 2-oxoagelasine B (4), agelasines A (5), B (6), D (7), E (8), F (9), and G (10), and ageline B (11). The structures of 1-3 were assigned on the basis of their spectroscopic data and their comparison with those of the literature. Compounds 3 and 5-11 inhibited the growth of Mycobacterium smegmatis with inhibition zones of 10, 14, 15, 18, 14, 20, 12, and 12 mm at 20 mu g/disc, respectively. All compounds were inactive (IC50 > 10 mu M) against Huh-7 (hepatoma) and EJ-1 (bladder carcinoma) human cancer cell lines. Three 2-oxo derivatives (1, 2, and 4) exhibited markedly reduced biological activity against M. smegmatis. Moreover, compound 10 inhibited protein tyrosine phosphatase 1B (PTP1B) activity with an IC50 value of 15 mu M.
机译:从冲绳海洋海绵Agelas nakamurai Hoshino中分离了三种新的含N-甲基腺嘌呤的二萜,2-氧代鸟氨酸A(1)和F(2)和10-氢-9-羟基鸟苷F(3)以及八种已知的Agelasine衍生物,2-氧代草氨酸B(4),Agelasine A(5),B(6),D(7),E(8),F(9)和G(10),以及年龄线B(11)。 1-3的结构是根据其光谱数据和与文献的比较来指定的。化合物3和5-11以20μg/盘分别以10、14、15、18、14、20、12和12mm的抑制区抑制耻垢分枝杆菌的生长。所有化合物均对Huh-7(肝癌)和EJ-1(膀胱癌)人类癌细胞系无活性(IC50> 10μM)。三种2-氧代衍生物(1、2和4)对耻垢分枝杆菌的生物活性明显降低。此外,化合物10抑制了蛋白酪氨酸磷酸酶1B(PTP1B)的活性,IC50值为15μM。

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