Synthesis, Biological Evaluation, and Docking Study of Rhinacanthin-Related Derivatives as α-Glucosidase Inhibitors

Chúng tôi vui mừng thông báo rằng TS. Lê Thị Kim Dung và các đồng nghiệp  đã xuất bản công trình có tựa đề “Synthesis, Biological Evaluation, and Docking Study of Rhinacanthin-Related Derivatives as α-Glucosidase Inhibitors” trên tạp chí ACS Omega.

Tóm tắt:

This study describes the design, synthesis, and in vitro evaluation of 25 rhinacanthin-related derivatives as potential α-glucosidase inhibitors. The synthesized compounds were characterized using 1H and 13C NMR spectroscopy as well as mass spectrometry. Most of the synthesized compounds demonstrated significant inhibitory activity, with IC50 ranging from 1.45 ± 0.04 to 31.91 ± 3.31 μM, compared to the positive control, acarbose (IC50 = 836.00 ± 47.19 μM). In particular, compounds 6 and 12 exhibited the highest anti-α-glucosidase activity and acted as competitive inhibitors, with Ki values of 14.11 and 4.14 μM, respectively. Molecular docking analysis was performed and revealed that key π–π stacking interactions with residue F300, together with hydrogen bonds involving N241, H279, E304, and R312, contributed significantly to the enhanced α-glucosidase inhibitory activity of the active compounds. These findings suggest that compounds 6 and 12 are promising candidates for developing α-glucosidase inhibitors with potential antidiabetic effects.