Preparation of some long-chain N-acyl derivatives of essential amino acids for nutritional studies
- 1 July 1980
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Biochemistry
- Vol. 58 (7) , 573-576
- https://doi.org/10.1139/o80-078
Abstract
Long-chain N-acyl derivatives of methionine, tryptophan, threonine and lysine (N6) were obtained by the reaction of succinimidyl esters of fatty acids with the unprotected amino acids; their physical properties were characterized. Substitution on the amino group of essential amino acids which are considered for food supplementation in human nutrition protects the amino acids from degradative processes in food mixtures. N-Substitution enhances the effectiveness of the fortification process and prevents the formation of off-flavors which are unpalatable to humans.This publication has 3 references indexed in Scilit:
- SIDE REACTIONS IN PEPTIDE-SYNTHESIS .10. PREVENTION OF O-ACYLATION DURING COUPLING WITH ACTIVE ESTERS1979
- Succinimidyl esters of fatty acids for amino acid acylationsCanadian Journal of Chemistry, 1976
- On the selectivity of acylation of unprotected diamino acidsCanadian Journal of Chemistry, 1968