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| Content Provider | MDPI |
|---|---|
| Author | Liu, Yayue Chen, Senhua Liu, Zhaoming Lu, Yongjun Xia, Guoping Liu, Hongju He, Lei She, Zhigang |
| Abstract | Chemical investigation of the endophytic fungus Aspergillus sp. 16-5B cultured on Czapek’s medium led to the isolation of four new metabolites, aspergifuranone (1), isocoumarin derivatives (±) 2 and (±) 3, and (R)-3-demethylpurpurester A (4), together with the known purpurester B (5) and pestaphthalides A (6). Their structures were determined by analysis of 1D and 2D NMR spectroscopic data. The absolute configuration of Compound 1 was determined by comparison of the experimental and calculated electronic circular dichroism (ECD) spectra, and that of Compound 4 was revealed by comparing its optical rotation data and CD with those of the literature. The structure of Compound 6 was further confirmed by single-crystal X-ray diffraction experiment using CuKα radiation. All isolated compounds were evaluated for their α-glucosidase inhibitory activities, and Compound 1 showed significant inhibitory activity with IC50 value of 9.05 ± 0.60 μM. Kinetic analysis showed that Compound 1 was a noncompetitive inhibitor of α-glucosidase. Compounds 2 and 6 exhibited moderate inhibitory activities. |
| File Size | 809984 |
| Ending Page | 3102 |
| Page Count | 12 |
| Starting Page | 3091 |
| File Format | |
| e-ISSN | 16603397 |
| DOI | 10.3390/md13053091 |
| Journal | Marine Drugs |
| Issue Number | 5 |
| Volume Number | 13 |
| Language | English |
| Publisher Date | 2015-05-19 |
| Access Restriction | Open |
| Subject Keyword | marine fungi; Aspergillus sp. α-glucosidase inhibitor theoretical calculations ECD optical rotation |
| Content Type | Text |
| Resource Type | Article |
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