Two new diarylheptanoids and a new phenylhexanol derivative from the bulbils of Dioscorea opposita Thunb. and their α-glucosidase inhibitory activity
Autor: | Xi-Ling Fan, Yan-Ling Liu, Xu Chen, Meng-Huan Guo, Xiaoke Zheng, Weisheng Feng, Chen He, Zhiyou Hao, Yan-Gang Cao, Hong-Wei Li, Meng-Na Wang, Ying-Jie Ren |
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Rok vydání: | 2021 |
Předmět: |
biology
010405 organic chemistry Stereochemistry Plant Science biology.organism_classification 01 natural sciences Biochemistry In vitro 0104 chemical sciences 010404 medicinal & biomolecular chemistry chemistry.chemical_compound chemistry Docking (molecular) Dioscorea Binding site Agronomy and Crop Science Two-dimensional nuclear magnetic resonance spectroscopy α glucosidase inhibitory Derivative (chemistry) Diarylheptanoids Biotechnology |
Zdroj: | Phytochemistry Letters. 44:142-148 |
ISSN: | 1874-3900 |
DOI: | 10.1016/j.phytol.2021.06.016 |
Popis: | Two previously undescribed diarylheptanoids, diosniponol E (1) and F (2), and a new phenylhexanol derivative, (rel-2R,4R)-6-(4-hydroxy-3-methoxyphenyl)-hexane-1,2,4-triol (3), together with seven known compounds, were isolated from the bulbils of Dioscorea opposita Thunb.. Their structures were elucidated by HRESIMS and 1D/2D NMR as well as by comparison with the literature, and absolute configurations of compounds 1 and 2 were deduced by comparison of their experimental and calculated electronic circular dichroic (ECD) spectra. All the isolated compounds were evaluated in vitro for their α-glucosidase inhibitory activity. The results indicated that compounds 3 and 7 exhibited inhibitory effect against α-glucosidase with the IC50 values of 16.2 ± 2.2 and 8.7 ± 1.6 μM, respectively. Molecular docking experiments were performed to identify the probable binding mode of compound 7 in the binding sites of α-glucosidase and molecular dynamics simulations were performed to evaluate the stability over time of the main interactions observed in docking experiments. |
Databáze: | OpenAIRE |
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