Design, synthesis, structure-activity relationships and X-ray structural studies of novel 1-oxopyrimido[4,5-c]quinoline-2-acetic acid derivatives as selective and potent inhibitors of human aldose reductase.

Faculty Pharmacy Year: 2018
Type of Publication: ZU Hosted Pages:
Authors:
Journal: European Journal of Medicinal Chemistry Elsevier Volume:
Keywords : Design, synthesis, structure-activity relationships , X-ray structural    
Abstract:
Human aldose reductase (AKR1B1, AR) is a key enzyme of the polyol pathway, catalyzing the reduction of glucose to sorbitol at high glucose concentrations, as those found in diabetic condition. Indeed, AKR1B1 overexpression is related to dia
   
     
 
       

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