## 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.
Scavenging capacities of some thiazolyl thiazolidine-2,4-dione compounds on superoxide radical, hydroxyl radical, and DPPH radical
✍ Scribed by Irena Kruk; Oya Bozdağ-Dündar; Meltem Ceylan-Ünlüsoy; Rahmiye Ertan; Hassan Y. Aboul-Enein; Teresa Michalska
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 288 KB
- Volume
- 24
- Category
- Article
- ISSN
- 1522-7235
- DOI
- 10.1002/bio.1105
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✦ Synopsis
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 visible spectrophotometry, respectively. The examined compounds were shown to have 27–59%
scavenging ability, 19–69% HO^•^ scavenging activity and 2–32% DPPH^•^ scavenging ability. This property of the tested compound seems to be important in the prevention of various diseases of free radicals etiology. Copyright © 2009 John Wiley & Sons, Ltd.
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