| Literature DB >> 18565754 |
Oya Bozdağ-Dündar1, Eugen J Verspohl, Net Daş-Evcimen, Rebecca M Kaup, Katrin Bauer, Mutlu Sarikaya, Begüm Evranos, Rahmiye Ertan.
Abstract
A new series of flavonyl-2,4-thiazolidinediones (Va-c, VIa-c) was prepared by Knoevenagel reaction. The synthesized compounds were tested for their ability to inhibit rat kidney aldose reductase (AR) and for their insulinotropic activities in INS-1 cells. Compound Vb was able to increase insulin release in the presence of 5.6mmol/l glucose. Compounds VIa-c displayed moderate to high AR inhibitory activity levels. Particularly, compound VIa showed the highest AR inhibitory activity (86.57%).Entities:
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Year: 2008 PMID: 18565754 DOI: 10.1016/j.bmc.2008.05.059
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641