Comparative Cholinesterase, α-Glucosidase Inhibitory, Antioxidant, Molecular Docking, and Kinetic Studies on Potent Succinimide Derivatives.

INTRODUCTION

The current study was designed to synthesize derivatives of succinimide and compare their biological potency in anticholinesterase, alpha-glucosidase inhibition, and antioxidant assays.

METHODS

In this research, two succinimide derivatives including ()-1-(2,5-dioxo-1-phenylpyrrolidin-3-yl) cyclohexanecarbaldehyde (Compound ) and ()-2-(()-2,5-dioxo-1-phenylpyrrolidin-3-yl)-2-phenylpropanal (Compound ) were synthesized using Michael addition. Both the compounds, ie, and were evaluated for in-vitro acetylcholinesterase (AChE), butyrylctcholinesterase (BChE), antioxidant, and α-glucosidase inhibitory potentials. Furthermore, molecular docking was performed using Molecular Operating Environment (MOE) to explore the binding mode of both the compounds against different enzymes. Lineweaver-Burk plots of enzyme inhibitions representing the reciprocal of initial enzyme velocity versus the reciprocal of substrate concentration in the presence of synthesized compounds and standard drugs were constructed using Michaelis-Menten kinetics.

RESULTS

In AChE inhibitory assay, compounds and exhibited IC of 343.45 and 422.98 µM, respectively, against AChE enzyme. Similarly, both the compounds showed IC of 276.86 and 357.91 µM, respectively, against BChE enzyme. Compounds and displayed IC of 157.71 and 471.79 µM against α-glucosidase enzyme, respectively. In a similar pattern, compound exhibited to be more potent as compared to compound in all the three antioxidant assays. Compound exhibited IC values of 297.98, 332.94, and 825.92 µM against DPPH, ABTS, and HO free radicals, respectively. Molecular docking showed a triple fold in the AChE and BChE activity for compound compared with compound . The compound 1 revealed good interaction against both the AChE and BChE enzymes which revealed the high potency of this compound compared to compound .

CONCLUSION

Both succinimide derivatives exhibited considerable inhibitory activities against cholinesterases and α-glucosidase enzymes. Of these two, compound revealed to be more potent against all the in-vitro targets which was supported by molecular docking with the lowest binding energies. Moreover, compound also proved to have antiradical properties.