| Literature DB >> 29295795 |
Yating Sun1, Jingtang Liu2, Lei Li2, Chi Gong3, Shuping Wang2, Fan Yang4, Huiming Hua5, Houwen Lin6.
Abstract
Two new butenolide derivatives (±)-asperteretal D ((±)-1) and asperteretal E (2) containing rare 2-benzyl-3-phenyl substituted lactone core, together with nine known analogues (3-11) were obtained from a fungus Aspergillus terreus derived from the marine sponge Phakellia fusca. All the structures were elucidated on the basis of extensive NMR spectroscopic data. The chiral chromatography analyses allowed the separation of the (±)-asperteretal D, of which the absolute configurations were determined by comparing the experimental to calculated electronic circular dichroic (ECD) spectra. Compounds (±)-1, 2-5, and 7 exhibited potent inhibitory activities against α-glucosidase with IC50 values ranging from 8.65 to 20.3 µM (positive control acarbose with an IC50 value of 320 µM). In addition, derivatives 5-8 also showed moderate antioxidant activities.Entities:
Keywords: Antioxidant activity; Aspergillus terreus; Butenolide derivatives; α-Glucosidase inhibitors
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Year: 2017 PMID: 29295795 DOI: 10.1016/j.bmcl.2017.12.049
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823