Abstract
The present chapter describe a series of synthetic organoselenium compounds such as ebselen analogues, diaryl selenides, spirodioxyselenurane, spirodiazaselenuranes and its Glutathione peroxidise (GPx) catalytic activity. These ebselen related compounds either by modifying the basic structure of ebselen or incorporating some structural features of the native enzyme, a number of small-molecules of selenium compounds as functional mimics of GPx are discussed. In addition to this, spirodioxyselenuranes and spirodiazaselenuranes are important class of hypervalent selenium compounds, whose stability highly depends on the nature of the substituents attached to the nitrogen atom. The glutathione peroxidase (GPx) mimetic activity of all the selenium compounds showed significantly by facilitating the oxidation of the selenium centre. In contrast to this, ebselen analogue shows significant antioxidant activity compared with spirodiazaselenuranes and its derivatives.
Reference60 articles.
1. Berzelius JJ. Undersökning af enny Mineral-kropp, funnen ide orenare sorterna af detvid Fahlun tillverkade svafle, Discovery of Selenium. Afhandlingar i Fysik, Kemi och Mineralogi. 1818;6:42
2. Löwig CJ. Poggendorff’s Ueber schwefelwasserstoff-und selenwasserstoffäther (about hydrogen sulfide and selenium hydrogen ether). Annals of Physics. 1836;37:552
3. Rathke B. Ueber das Selenmercaptan. Justus Liebigs Annalen der Chemie. 1869;152:211
4. Hutton JG. The correlation of certain lesions in animals with certain soil types. Journal of the American Chemical Society. 1931;23:1076
5. Franke KW. A toxicant occurring naturally in certain samples of plant foodstuffs. I. Results obtained in preliminary feeding trials. The Journal of Nutrition. 1934;8:597