Alkaloidal Metabolites from a Marine-Derived Aspergillus sp Fungus

被引:40
|
作者
Liao, Lijuan [1 ]
You, Minjung [1 ]
Chung, Beom Koo [2 ]
Oh, Dong-Chan [1 ]
Oh, Ki-Bong [2 ]
Shin, Jongheon [1 ]
机构
[1] Seoul Natl Univ, Coll Pharm, Inst Nat Prod Res, Seoul 151742, South Korea
[2] Seoul Natl Univ, Coll Agr & Life Sci, Dept Agr Biotechnol, Seoul 151921, South Korea
来源
JOURNAL OF NATURAL PRODUCTS | 2015年 / 78卷 / 03期
基金
新加坡国家研究基金会;
关键词
CONSTITUENT AMINO-ACIDS; ABSOLUTE-CONFIGURATION; NATURAL-PRODUCTS; MARFEYS METHOD; A-C; FUMIQUINAZOLINES; GROWTH; LC/MS;
D O I
10.1021/np500683u
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Fumiquinazoline S (1), a new quinazoline-containing alkaloid, and the known fumiquinazolines F (6) and L (7) of the same structural class were isolated from the solid-substrate culture of an Aspergillus sp. fungus collected from marine-submerged wood. In addition, isochaetominines A-C (2-4) and 14-epi-isochaetominine C (5), new alkaloids possessing an unusual amino acid-based tetracyclic core framework related to the fumiquinazolines, were isolated from the same fungal strain. The structures of these compounds were determined by combined spectroscopic methods, and the absolute configurations were assigned by NOESY, ROESY, and advanced Marfeys analyses along with biogenetic considerations. The new compounds exhibited weak inhibition against Na+/K+-ATPase.
引用
收藏
页码:349 / 354
页数:6
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