Structures and Biological Evaluations of Agelasines Isolated from the Okinawan Marine Sponge Agelas nakamurai

被引:42
作者
Abdjul, Delfly B. [1 ]
Yamazaki, Hiroyuki [1 ]
Kanno, Syu-ichi [1 ]
Takahashi, Ohgi [1 ]
Kirikoshi, Ryota [1 ]
Ukai, Kazuyo [1 ]
Namikoshi, Michio [1 ]
机构
[1] Tohoku Pharmaceut Univ, Fac Pharmaceut Sci, Sendai, Miyagi 9818558, Japan
来源
JOURNAL OF NATURAL PRODUCTS | 2015年 / 78卷 / 06期
关键词
TYROSINE-PHOSPHATASE; 1B; NATURAL-PRODUCTS; SEA SPONGE; EURYSPONGIA SP; PROTEIN; DITERPENOIDS; INHIBITOR; ALKALOIDS; TARGET; UNIT;
D O I
10.1021/acs.jnatprod.5b00375
中图分类号
Q94 [植物学];
学科分类号
071001 ;
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.
引用
收藏
页码:1428 / 1433
页数:6
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