## 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 exhi
Free radical scavenging activity of novel thiazolidine-2,4-dione derivatives
✍ Scribed by Berczyński, Paweł; Kruk, Irena; Piechowska, Teresa; Ceylan-Unlusoy, Meltem; Bozdağ-Dündar, Oya; Aboul-Enein, Hassan Y.
- Book ID
- 121797415
- Publisher
- John Wiley and Sons
- Year
- 2012
- Tongue
- English
- Weight
- 403 KB
- Volume
- 28
- Category
- Article
- ISSN
- 1522-7235
- DOI
- 10.1002/bio.2454
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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 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