| Literature DB >> 23057864 |
Meltem Ceylan Unlusoy1, Canan Kazak, Ornela Bayro, Eugen J Verspohl, Rahmiye Ertan, Oya Bozdag Dundar.
Abstract
Numerous compounds have been prepared in order to improve the pharmacological profile of insulinotropic activities. In the present paper, we report the synthesis and the in vitro insulin releasing activity of the 6-methyl-chromonyl-2,4-thiazolidinediones (IIIa-c, IVa-c, Va-c). Compounds IIIb, IIIc, IVa-c, Va and Vc (at lower concentration; 0.001 mg/mL) were able to increase insulin release in the presence of 5.6 mmol/L glucose. In this series, the most potent compound is IVa having methyl group at N3 position of TZD ring.Entities:
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Year: 2012 PMID: 23057864 DOI: 10.3109/14756366.2012.723207
Source DB: PubMed Journal: J Enzyme Inhib Med Chem ISSN: 1475-6366 Impact factor: 5.051