## Abstract The oxygen free radical scavenging activities of 15 chromonyl‐thiazolidine‐2,4‐dione compounds (CTDs) were examined in chemical systems producing superoxide anion radicals, O (potasium superoxide–18‐crown‐6 ether–DMSO), and hydroxyl radicals, HO^•^ (a Fenton reaction: Fe(II)–H~2~O~2~–so
Free radical scavenging abilities of flavonyl-thiazolidine-2,4-dione compounds
✍ Scribed by Oya Bozdağ-Dündar; Rahmiye Ertan; Hassan Y. Aboul-Enein; Aleksandra Kładna; Irena Kruk
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 414 KB
- Volume
- 26
- Category
- Article
- ISSN
- 1522-7235
- DOI
- 10.1002/bio.1176
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✦ Synopsis
Abstract
Free radical scavenging activity of flavonyl‐thiazolidine‐2,4‐dione compounds has been evaluated using chemiluminescence, electron spin resonance spectroscopy with 5,5‐dimethyl‐1‐pyrroline‐1‐oxide as spin trap and DPPH (2,2′‐diphenyl‐1‐picrylhydrazyl) method. The examined compounds exhibited 28–50% scavenging superoxide anion radical (${\rm{O}}_2^{\bar\bullet}$), 16.7–76.7% hydroxyl radical (HO^•^) and 9–40% DPPH radical. Compounds containing carbonyl group in their structure can be considered as antioxidants with high relevance and great biological importance. Copyright © 2009 John Wiley & Sons, Ltd.
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## Abstract The antioxidant behavior of a series of new synthesized substituted thiazolyl‐thiazolidine‐2,4‐dione compounds (TZDs) was examined using chemiluminescence and electron paramagnetic resonance spin trapping techniques. 5,5‐Dimethyl‐1‐pyrroline‐__N__‐oxide (DMPO) was used as the spin trap.
## Abstract The scavenging effects of eighteen thiazolyl thiazolidine‐2,4‐dione compounds (TTCs) on superoxide radical , hydroxyl radical HO^•^, and 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH^•^) radical were evaluated by the chemiluminescence technique, electron spin resonance spectrometry (ESR) and vis
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## Abstract magnified image Novel microwave induced method for the synthesis of thiazolidine‐2,4‐dione motif under solvent phase conditions is developed. Further we report an efficient, microwave assisted method for the parallel syntheses of biologically important 5‐benzylidene‐thiazolidine‐2,4‐di