| Literature DB >> 29126957 |
Hui Cui1, Yena Liu2, Tingmei Li3, Zhengrui Zhang1, Meng Ding1, Yuhua Long4, Zhigang She5.
Abstract
A pair of 3-arylisoindolinone enantiomers: (+)-asperglactam A (1), (-)-asperglactam A (1) and a pair of nor-bisabolane 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 α-glucosidase inhibitory activity. The enantiomers of 1-3 showed moderate inhibitory activity against α-glucosidase with IC50 values ranging from 50 to 190μM. Compound 7 exhibited significant inhibitory activity against α-glucosidase with IC50 value of 7.5μM. In addition, compound 7 was found to inhibit nitric oxide production in RAW 264.7 macrophages with IC50 value of 12.5μM.Entities:
Keywords: 3-arylisoindolinone; Aspergillus; Sesquiterpene; α-glucosidase
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Year: 2017 PMID: 29126957 DOI: 10.1016/j.fitote.2017.11.006
Source DB: PubMed Journal: Fitoterapia ISSN: 0367-326X Impact factor: 2.882