| Literature DB >> 24607578 |
Aparna Kadam1, Bhaskar Dawane1, Manisha Pawar1, Harshala Shegokar2, Kapil Patil2, Rohan Meshram2, Rajesh Gacche3.
Abstract
Aldose reductase is the key enzyme of polypol pathway leading to accumulation of sorbitol. Sorbitol does not diffuse across the cell membranes easily and therefore accumulates within the cell, causing osmotic damage which leads to retinopathy (cataractogenesis), neuropathy and other diabetic complications. Currently, aldose reductase inhibitors like epalrestat, ranirestat and fidarestat are used for the amelioration of diabetic complications. However, such drugs are effective in patients having good glycemic control and less severe diabetic complications. In present study we have designed novel pyrazolone derivative and performed eco-friendly synthesis approach and tested the synthesized compounds as potential inhibitors of aldose reductase activity. Additional in silico analysis in current study indicates presence of highly conserved chemical environment in active site of goat lens aldose reductase. The reported data is expected to be useful for developing novel pyrazolone derivatives as lead compounds in the management of diabetic complications.Entities:
Keywords: Carbothioamide derivatives; Goat lens aldose reductase; Paired potential analysis; Polyethylene glycol (PEG-400); Pyrazolone derivatives; Virtual screening
Mesh:
Substances:
Year: 2014 PMID: 24607578 DOI: 10.1016/j.bioorg.2014.02.002
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275