info:eu-repo/semantics/article
QSAR prediction of inhibition of aldose reductase for flavonoids
Fecha
2008-06Registro en:
Mercader, Andrew Gustavo; Duchowicz, Pablo Román; Fernández, Francisco Marcelo; Castro, Eduardo Alberto; Bennardi, Daniel Oscar; et al.; QSAR prediction of inhibition of aldose reductase for flavonoids; Pergamon-Elsevier Science Ltd; Bioorganic & Medicinal Chemistry; 16; 6-2008; 7470-7476
0968-0896
CONICET Digital
CONICET
Autor
Mercader, Andrew Gustavo
Duchowicz, Pablo Román
Fernández, Francisco Marcelo
Castro, Eduardo Alberto
Bennardi, Daniel Oscar
Autino, Juan Carlos
Romanelli, Gustavo Pablo
Resumen
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 backbone50) 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