3-Arylisoindolinone and sesquiterpene derivatives from the mangrove endophytic fungi Aspergillus versicolor SYSU-SKS025

被引:37
作者
Cui, Hui [1 ]
Liu, Yena [2 ]
Li, Tingmei [3 ]
Zhang, Zhengrui [1 ]
Ding, Meng [1 ]
Long, Yuhua [3 ]
She, Zhigang [1 ]
机构
[1] Sun Yat Sen Univ, Sch Chem, Guangzhou 510275, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China, Canc Ctr, Guangzhou 510060, Guangdong, Peoples R China
[3] South China Normal Univ, Sch Chem & Environm, Guangzhou 510006, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
3-arylisoindolinone; Sesquiterpene; Aspergillus; alpha-glucosidase; DIAPORTHE-PHASEOLORUM SKS019;
D O I
10.1016/j.fitote.2017.11.006
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A pair of 3-arylisoindolinone enantiomers: (+)-asperglactam A (1), (-)-asperglactam A (1) and a pair of norbisabolane enantiomers: (+)-1-hydroxyboivinianic acid (2), (-)-1-hydroxyboivinianic acid (2), along with seven known compounds (3 - 8) were obtained from the mangrove endophytic fungus Aspergillus versicolor SYSU-SKS025. Their structures were determined on the basis of HRESIMS and NMR spectroscopic data, and X-ray diffraction. (+)-Asperglactam A (1) and (-)-asperglactam A (1) are the first optically pure examples in the 3-arylisoindolinone family, which are rarely found in natural sources. All isolated compounds were evaluated for a-glucosidase inhibitory activity. The enantiomers of 1 - 3 showed moderate inhibitory activity against alpha-glucosidase with IC50 values ranging from 50 to 190 mu M. Compound 7 exhibited significant inhibitory activity against alpha-glucosidase with IC50 value of 7.5 mu M. In addition, compound 7 was found to inhibit nitric oxide production in RAW 264.7 macrophages with IC50 value of 12.5 mu M.
引用
收藏
页码:177 / 181
页数:5
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