(1-Amino-2-propenyl)phosphonic acid, an inhibitor of alanine racemase and D-alanine:D-alanine ligase

DL-(1-Amino-2-propenyl)phosphonic acid was synthesized through the sequential oxidation, sulfoxide elimination, and deprotection of diphenyl [1-[(benzyloxycarbonyl)amino]-3-(phenylthio)propyl] phosphonate. This analogue of vinylglycine is a strong inhibitor of the alanine racemases from Pseudomonas...

Full description

Saved in:
Bibliographic Details
Published inJournal of medicinal chemistry Vol. 29; no. 4; pp. 579 - 581
Main Authors Vo Quang Yen, Carniato, Denis, Vo Quang, Liliane, Lacoste, Anne Marie, Neuzil, Eugene, Le Goffic, Francois
Format Journal Article
LanguageEnglish
Published Washington, DC American Chemical Society 01.04.1986
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:DL-(1-Amino-2-propenyl)phosphonic acid was synthesized through the sequential oxidation, sulfoxide elimination, and deprotection of diphenyl [1-[(benzyloxycarbonyl)amino]-3-(phenylthio)propyl] phosphonate. This analogue of vinylglycine is a strong inhibitor of the alanine racemases from Pseudomonas aeruginosa and Streptococcus faecalis and of the D-Ala:D-Ala ligase from this latter species. This molecule is ineffective against the whole bacterial cells. Unlike vinylglycine, this unsaturated phosphonate does not inhibit the following mammalian enzymes: aspartate aminotransferase, alanine aminotransferase, D-amino acid oxidase, which indicates its specificity. Thus, its incorporation in a peptide structure could induce interesting antimicrobial properties.
Bibliography:istex:1913FB7AB7799B3B74D297C98F65EB4EEB72D3A2
ark:/67375/TPS-PKHDS367-T
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0022-2623
1520-4804
DOI:10.1021/jm00154a024