• Title of article

    QSAR prediction of inhibition of aldose reductase for flavonoids Original Research Article

  • Author/Authors

    Andrew G. Mercader، نويسنده , , Pablo R. Duchowicz، نويسنده , , Francisco M. Fernandez، نويسنده , , Eduardo A. Castro، نويسنده , , Daniel O. Bennardi، نويسنده , , Juan C. Autino، نويسنده , , Gustavo P. Romanelli، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2008
  • Pages
    7
  • From page
    7470
  • To page
    7476
  • Abstract
    We performed a predictive analysis based on quantitative structure–activity relationships (QSAR) of an important property of flavonoids, which is the inhibition (IC50) of aldose reductase (AR). The importance of AR inhibition is that it prevents cataract formation in diabetic patients. The best linear model constructed from 55 molecular structures incorporated six molecular descriptors, selected from more than a thousand geometrical, topological, quantum-mechanical, and electronic types of descriptors. As a practical application, we used the obtained QSAR model to predict the AR inhibitory effect of newly synthesized flavonoids that present 2-, 7-substitutions in the benzopyrane backbone.
  • Keywords
    Flavone derivative , Cataract prevention , Enhanced replacement method , Genetic Algorithm , Aldose reductase inhibition , Replacement Method , QSAR , Dragon molecular descriptors
  • Journal title
    Bioorganic and Medicinal Chemistry
  • Serial Year
    2008
  • Journal title
    Bioorganic and Medicinal Chemistry
  • Record number

    1306798