Ketomethylene analogues of phosphoryl dipeptides related to phosphoramidon: synthesis and inhibition of proteases

Gómez-Monterrey, I; González Muñiz, R; Pérez-Martín, C; López de Ceballos, M; Del Río, J; García-López, MT

HERO ID

4923732

Reference Type

Journal Article

Year

1992

Language

English

PMID

1524467

HERO ID 4923732
In Press No
Year 1992
Title Ketomethylene analogues of phosphoryl dipeptides related to phosphoramidon: synthesis and inhibition of proteases
Authors Gómez-Monterrey, I; González Muñiz, R; Pérez-Martín, C; López de Ceballos, M; Del Río, J; García-López, MT
Journal Archiv der Pharmazie
Volume 325
Issue 5
Page Numbers 261-265
Abstract Non-rhamnose-containing phosphoramidon analogues, in which the amide bond was replaced by the isosteric ketomethylene group, have been synthesized in order to stabilize these compounds to peptidase degradation. The key step in this synthesis was suitable alkylation of a 4-ketodiester, prepared from Z-Leu chloromethyl ketone and dimethyl malonate. The ketomethylene dipeptide derivatives P-Leu psi (COCH2)(RS)Xaa-OMe (Xaa = Trp, Phe) are good inhibitors of thermolysin, ACE and specially enkephalinase.
Doi 10.1002/ardp.19923250503
Pmid 1524467
Wosid WOS:A1992HZ23000002
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English
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