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Interactions of alkyltin salts with biological dithiols: Dealkylation and induction of a regular beta-turn structure in peptides
- Source :
- Journal of the American Chemical Society. Nov 10, 2004, Vol. 126 Issue 44, 14400-14410
- Publication Year :
- 2004
-
Abstract
- The high-resolution NMR study and DFT calculation of the interaction between alkyltin compounds and a biological molecule are reported. It was seen that 9-residue peptide containing a CXC motif extracted from the neuronal peptide stannin (SNN) has no preferred structure, but upon the addition of trimethyltin (TMT), dealkylates TMT to dimethyltin (DMT), and adopts a unique stable type-I beta-turn conformation.
Details
- Language :
- English
- ISSN :
- 00027863
- Volume :
- 126
- Issue :
- 44
- Database :
- Gale General OneFile
- Journal :
- Journal of the American Chemical Society
- Publication Type :
- Academic Journal
- Accession number :
- edsgcl.126137616