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| Content Provider | Springer Nature Link |
|---|---|
| Author | Dewi, Rizna Triana Tachibana, Sanro Darmawan, Ahmad |
| Copyright Year | 2013 |
| Abstract | Butyrolactone I and II from Aspergillus terreus MC751 as well as three synthetic butyrolactone I derivatives were assessed for α-glucosidase inhibitory and antioxidant activities. Butyrolactone I (1), which has a prenyl side chain and an alpha hydroxy-lactone group, was the most potent α-glucosidase inhibitor and also had antioxidant activities with IC50 values of 52.17 ± 5.68 and 51.39 ± 3.68 μM, respectively. In contrast, butyrolactone II (2) lacking a prenyl side chain was the most potent antioxidant with an IC50 of 17.64 ± 6.41 μM, but was less active against α-glucosidase. Acetylation of all hydroxyl groups of butyrolactone I significantly decreased both the α-glucosidase inhibitory and antioxidant activity. The prenyl and alpha hydroxy-lactone groups seem to have a synergic effect on the inhibitory activity but not antioxidant activity. This is the first structure–activity relationship report on the α-glucosidase inhibition and antioxidant activity by butyrolactone derivatives. |
| Starting Page | 454 |
| Ending Page | 460 |
| Page Count | 7 |
| File Format | |
| ISSN | 10542523 |
| Journal | Medicinal Chemistry Research |
| Volume Number | 23 |
| Issue Number | 1 |
| e-ISSN | 15548120 |
| Language | English |
| Publisher | Springer US |
| Publisher Date | 2013-06-05 |
| Publisher Place | New York |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Aspergillus terreus MC75 Butyrolactones derivatives α-Glucosidase inhibitory activity Antioxidant Pharmacology/Toxicology Biochemistry Cell Biology |
| Content Type | Text |
| Resource Type | Article |
| Subject | Organic Chemistry Pharmacology, Toxicology and Pharmaceutics |
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