Binding of 1-Benzopyran-4-one Derivatives to Aldose Reductase: A Free Energy Perturbation Study-Reference-Cited by-同舟云学术

Binding of 1-Benzopyran-4-one Derivatives to Aldose Reductase: A Free Energy Perturbation Study

Published:2002-05 Issue:5 Volume:10 Page:1427-1436
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Rastelli Giulio,Costantino Luca,Gamberini M.Cristina,Del Corso Antonella,Mura Umberto,Petrash J.Mark,Ferrari Anna Maria,Pacchioni Sara

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference45 articles.

1. New aldose reductase inhibitors as potential agents for the prevention of long-term diabetic complications

2. Diabetes complications and their potential prevention: Aldose reductase inhibition and other approaches

3. Eggler, J. F., Larson, E. R., Lipinski, C. A., Mylari, B. L., Urban, F. J. In A Perspective of Aldose Reductase Inhibitors. Advances In Medical Chemistry. Jai: Greenwich, CT, 1993; Vol. 2, p. 197.

4. 1-Benzopyran-4-one Antioxidants as Aldose Reductase Inhibitors

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