Autor:	Jana Klose, Michael Bienert, Angelika Ehrlich
Rok vydání:	1998
Předmět:	Peptidomimetic Stereochemistry Chemistry Pharmacology toxicology Proline HEXA Biochemistry
Zdroj:	Letters in Peptide Science. 5:129-131
ISSN:	0929-5666
DOI:	10.1023/a:1008878921068
Popis:	Proline and Pro-derived peptidomimetics, such as meoxPro-Oic (4-methoxy-proline-octahydro indolic acid), and DBF (2-aminoethyl-6-dibenzofuran propionic acid) were introduced into thymopentin-derived penta- [SP5-] and hexa- [SP6-] peptides and penta-, hexa- and hepta-alanine. Surprisingly, we found that cyclomonomer formation in the investigated penta- and hexapeptides was drastically hindered by the presence of proline regardless of position.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::77f12ad6ad775536261b3bb18b7e232a https://doi.org/10.1023/a:1008878921068 Zobrazit plný text záznamu Full text from SpringerLink