scholarly journals Synthesis and Biological Evaluation of 2-Heteroarylthioalkanoic Acid Analogues of Clofibric Acid as Peroxisome Proliferator-Activated Receptor α Agonists

2009 ◽  
Vol 52 (20) ◽  
pp. 6224-6232 ◽  
Author(s):  
Letizia Giampietro ◽  
Alessandra Ammazzalorso ◽  
Antonella Giancristofaro ◽  
Fabio Lannutti ◽  
Giancarlo Bettoni ◽  
...  
Author(s):  
Shivkant Patel ◽  
Ashim Kumar Sen ◽  
Dillip Kumar Dash ◽  
Piyushkumar Sadhu ◽  
Mamta Kumari ◽  
...  

Thiazolidinedione derivative have Antihyperglycemic activity, they are agonists for the peroxisome proliferator-activated receptor (PPAR), which controls glucose synthesis, transport, and utilization via regulating the transcription of insulin-responsive genes. A number of novel insulin sensitizers are currently being researched. Several of these are derivatives of Thiazolidinedione, but others have different chemical structures. In this work, we created some new Thiazolidinedione derivative based on structure–activity relationship as closely as feasible. The Thiazolidine-2,4-Dione derivatives were manually developed and synthesized using the proper synthetic techniques, then tested in vitro for antihyperglycemic action using the Sucrose loading model (SLM) and the Alloxan induced diabetes model (AIDM). The newly synthesized Thiazolidine-2,4-Dione derivative was characterized using infrared (IR) and proton (H) nuclear magnetic resonance. In this study we found that Compound M-4 has a lot of antihyperglycemic action, thus it's a good idea to think about using it as a lead material for the creation of anti-diabetic drugs.


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