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Current Enzyme Inhibition

Editor-in-Chief

ISSN (Print): 1573-4080
ISSN (Online): 1875-6662

Research Article

Antidiabetic Potential of Ruthenium(III) Hydroxamate Complexes: Spectrophotometric Investigations

Author(s): Raj Kaushal* and Mandeep Kaur

Volume 18, Issue 3, 2022

Published on: 03 October, 2022

Page: [200 - 210] Pages: 11

DOI: 10.2174/1573408018666220825152849

Price: $65

Abstract

Background: The potential antidiabetic and antioxidant properties of four ruthenium(III) hydroxamate complexes [RuCl(H2O)(LI-III)2] (1-3) and [RuCl3(H2O)(HLIV)2] (4) were investigated on α- cell enzymes (α-amylase and α-glucosidase).

Methods: In the instance of α-amylase inhibition investigations, the antidiabetic studies of the complexes revealed that they are more active than even the Acarbose as standard, with complex 4 having an IC50 value of 52.31 g/ml. For α-glucosidase inhibition, complex 4 was observed to be the best inhibitor with a remarkable 0.35μg/ml IC50 value, which may be attributed to the size and superior lipophilicity of this complex, enabling it to interact with the biological system more effectively than complexes 1-3. The complexes with the best IC50 values were studied further for enzyme kinetics. Molecular docking studies were performed as well to investigate the interactions between the synthesized complexes and target enzymes viz., α-glucosidase and α-amylase.

Results: The obtained in-vitro results have also been supported by the results of the in-silico docking studies. Furthermore, the antiradical activity of Ru(III) complexes was assessed for its effectiveness in reducing oxidative stress.

Conclusion: All the complexes (except complex 3) exhibited remarkable antiradical activity.

Keywords: α-amylase inhibition, analytical methods, antioxidants, docking studies, α-glucosidase inhibition, kinetics, ruthenium( III)hydroxamate complexes.

Graphical Abstract
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