A Stable Solid Model for Protein Sulfenyl Iodides
- 1 February 1973
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 70 (2) , 328-330
- https://doi.org/10.1073/pnas.70.2.328
Abstract
The first simple sulfenyl iodide that is a pure stable crystalline solid is reported. This product, ISCMe(2)CH(NHCbz)CONH-Ph-p-Cl(10), contains linkages that simulate the two peptide linkages vicinal to the -SI moiety in a protein sulfenyl iodide. Unlike typical simple sulfenyl iodides, solid 10 remains unchanged at ambient conditions for more than ten weeks; however, it is quite reactive in solution. Under proper circumstances, therefore, a sulfenyl iodide is proved to be a stable but highly reactive species. The model 10 and related compounds should afford prospects for better understanding of the unusual stabilities of certain protein sulfenyl iodides and of ways in which other such compounds may function in mediating iodination reactions in the thyroid gland.Keywords
This publication has 5 references indexed in Scilit:
- On the chemical iodination of tyrosine with protein sulfenyl iodide and sulfenyl periodide derivatives the behaviour of thiol protein-iodine systemsBiochimica et Biophysica Acta (BBA) - Protein Structure, 1971
- Biologically oriented organic sulfur chemistry. V. Alkanesulfenyl iodidesThe Journal of Organic Chemistry, 1970
- Studies on dihydrofolic reductase, II. The activation of dihydrofolic reductase from chicken liver by iodine.Proceedings of the National Academy of Sciences, 1966
- The Reaction of β-Lactoglobulin Sulfenyl Iodide with Several Antithyroid Agents*Biochemistry, 1964
- THE REACTION OF TOBACCO MOSAIC VIRUS WITH IODINEJournal of Biological Chemistry, 1955