Abstract
Five new flavanones, davidones A-E (1–5), one new isoflavonoid, cyclolicoisoflavones A3 (8), together with seven known compounds were isolated from the petroleum ether and the ethyl acetate fractions of the roots of Sophora davidii (Franch.) Skeels. The structures of new compounds were established by 1D and 2D NMR and MS data. The absolute configuration of 1–5 was assigned by NMR calculations and comparing its experimental and calculated ECD spectra. Flavanones were the main active principles responsible for the glucose transporter 4 (GLUT-4) translocation activities of SD-PE and SD-EtOAc. Compounds 1–7 and acacetin (12) promoted GLUT-4 translocation by the range of 1.35–3.00 folds, respectively.
| Original language | English |
|---|---|
| Article number | 104500 |
| Journal | Bioorganic Chemistry |
| Volume | 106 |
| DOIs | |
| Publication status | Published - Jan 2021 |
Bibliographical note
Publisher Copyright:© 2020 Elsevier Inc.
Keywords
- Antidiabetic
- ECD
- Flavonoids
- GLUT-4
- Sophora davidii
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