๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Enzymatic synthesis of peptidyl amino alcohols and peptidyl amino aldehydes-serine proteinase inhibitors

โœ Scribed by Joanna V. Potetinova; Tatiana L. Voyushina; Valentin M. Stepanov


Book ID
104364903
Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
256 KB
Volume
7
Category
Article
ISSN
0960-894X

No coin nor oath required. For personal study only.

โœฆ Synopsis


An enzymatic synthesis of peptidyl amino alcohols is described. The reactions were performed in organic solvents using as a catalyst subtilisin distributed on the surface of macroporous silica. Subsequent mild oxidation of peptidyl amino alcohols results in peptide aldehydes -the potent specific inhibitors of serine proteinases.


๐Ÿ“œ SIMILAR VOLUMES


The synthesis and evaluation of peptidyl
โœ Michael D. Mullican; David J. Lauffer; Roger J. Gillespie; Saroop S. Matharu; Da ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 306 KB

The tetrapeptide aldehyde AC-Tyr-Val-Ala-AspH (1, L-709,049) has been reported to be a potent reversible inhibitor of Interleukln-1 B Converting E e (ICE). We have prepared a series of analogs of 1, in order to explore the active site of ICE. The e ects of truncation, methylation of the amide nitrog