ISSN : 2663-2187

Synthesis, Biological Evaluation and Molecular Docking Studies of 3,5- Disubstituted-2,4-Thiazolidinedione Derivatives as Potential Antihyperlipidemic Agents

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P. Laxmi Madhuri , G. Rajitha
» doi: 10.33472/AFJBS.6.13.2024.1267-1276

Abstract

Hyperlipidemia, characterized by elevated cholesterol levels, triglycerides, and low-density lipoproteins (LDL), is a major contributor to atherosclerosis and subsequent cardiovascular events. The coexistence of diabetes and hyperlipidemia poses a significant challenge due to their synergistic effects on cardiovascular risk. Novel 3,5- disubstituted thiazolidinediones were synthesized by the reaction of thiazolidinediones with biphenylcarbox aldehyde by Knoevenagel condensation reactions and the obtained products upon treatment with alkyl /aryl halides gave the synthesized products. The synthesized compounds were characterized by IR, NMR, and Mass spectra. The synthesized compounds were evaluated for anti-hyper lipidemic in alloxan-induced hyperglycemic rats and the compounds IId &IIf exhibited good control over hyperlipidemia when compared with pioglitazone. These studies were further asserted by molecular docking studies at the PPARα.

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