Enantioselective Hydrolysis ofN-Acyl Amino Acid Esters by Tripeptide-type L-Histidine Derivative in a Bilayer Vesicular System

Autor:	Katsutoshi Ohkubo, Hitoshi Ishida, Masahiko Kawata, Kazuhiro Yamaki
Rok vydání:	1991
Předmět:	chemistry.chemical_classification Hydrolysis chemistry Stereochemistry Vesicle Bilayer Enantioselective synthesis lipids (amino acids peptides and proteins) Phenylalanine General Chemistry Tripeptide Histidine Amino acid
Zdroj:	Chemistry Letters. 20:1723-1726
ISSN:	1348-0715 0366-7022
DOI:	10.1246/cl.1991.1723
Popis:	Peculiar enantioselective hydrolysis of N-acyl amino acid esters was found in the bilayer vesicular systems containing the tripeptide-type histidine derivative, Z-L-Leu-L-His-L-Leu. The enantioselectivity for the hydrolysis of long chain N-acyl phenylalanine p-nitrophenyl ester, C16-Phe-PNP, appeared in the binding process and was governed by an entropy factor.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::4ee43ecd789bbbf2147a2e5b3b917f48 https://doi.org/10.1246/cl.1991.1723 Zobrazit plný text záznamu