Rational Design and Synthesis of Novel Benzimidazole Derivatives as Potential β-Glucosidase Inhibitors

Title:Rational Design and Synthesis of Novel Benzimidazole Derivatives as Potential β-Glucosidase Inhibitors

Volume: 21 Issue: 13

Author(s): Xu Liu, Ge Sun, Fengxing Li, Xia Feng, Tongguan Jia, Cheng Luo, Shijie Chen and Hua Chen*

Affiliation:

• Key Laboratory of Chemical Biology of Hebei Province, College of Chemistry and Environmental Science, Hebei University, Baoding 071002, China

Keywords: β-glucosidase inhibitors, benzimidazole, linker, solvent-exposed region, o-trihydroxyphenol, iminosugar.

Abstract: Background: β-Glucosidase has a variety of biological functions. A structural model for a potential β-glucosidase inhibitor has been proposed in the studies.

Objective: A series f new diaryl derivatives linked through benzimidazole have been randomly and rationally designed, synthesized, and evaluated for their inhibitory activities against β-glucosidase (almond). The proposed structural model provides a new strategy for the design of potent β-glucosidase inhibitors.

Methods: According to the model, a series of benzimidazole derivatives were designed and synthesized, and their inhibitory activity, Ki value, inhibitory type, and binding mode analysis (PDB ID: 2J7C) on β- glucosidase (almond) were evaluated.

Results: Two compounds 7b and 7d were the best inhibitors with IC50 values of 7.86 μM and 3.52 μM, respectively. Their Ki values were calculated to be 9.91 μM and 5.81 μM, respectively.

Conclusion: The SAR analysis suggested that such benzimidazole derivatives might bind to the active site of β-glucosidase mainly through hydrogen bonds on o-trihydroxyphenol; the additional phenyl ring on the other side towards the solvent-exposed region played a very important role in improving their inhibitory activity against β-glucosidase.

Cite this article as:

Liu Xu, Sun Ge, Li Fengxing, Feng Xia, Jia Tongguan, Luo Cheng, Chen Shijie and Chen Hua*, Rational Design and Synthesis of Novel Benzimidazole Derivatives as Potential β-Glucosidase Inhibitors, Letters in Drug Design & Discovery 2024; 21 (13) . https://dx.doi.org/10.2174/1570180820666230822141514