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Poststatin, a new inhibitor of prolyl endopeptidase. IV. The chemical synthesis of poststain.

Authors :
Tsuda M
Muraoka Y
Nagai M
Takeuchi T
Aoyagi T
Source :
The Journal of antibiotics [J Antibiot (Tokyo)] 1996 Mar; Vol. 49 (3), pp. 287-91.
Publication Year :
1996

Abstract

Total synthesis of poststatin was achieved by both liquid phase and solid phase methods. In both methods, the (2R,3S)-3-amino-2-hydroxyvaleric acid moiety was incorporated into protected pentapeptides, and was oxidized to (S)-3-amino-2-oxovaleric acid (postine). Deprotection of the oxidized pentapeptides gave a specimen identical with natural poststatin in physico-chemical properties and prolyl endopeptidase inhibitory activity.

Details

Language :
English
ISSN :
0021-8820
Volume :
49
Issue :
3
Database :
MEDLINE
Journal :
The Journal of antibiotics
Publication Type :
Academic Journal
Accession number :
8626246
Full Text :
https://doi.org/10.7164/antibiotics.49.287