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Chemoenzymatic routes to enantiomerically pure 2-azatyrosine and 2-, 3- and 4-pyridylalanine derivatives

Authors :
Patrick Meffre
Valérie Rolland
Amer Moussa
Jean Martinez
Institut des Biomolécules Max Mousseron [Pôle Chimie Balard] (IBMM)
Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Montpellier (UM)-Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)
Université de Nîmes (UNIMES)
Source :
Amino Acids, Amino Acids, Springer Verlag, 2012, 42, pp.1339-1348. ⟨10.1007/s00726-010-0829-3⟩
Publication Year :
2011
Publisher :
Springer Science and Business Media LLC, 2011.

Abstract

International audience; Enantiomerically pure 2-, 3- or 4-pyridylalanine (pya) and 2-azatyrosine (azatyr) are known to present various biological activities. After incorporation into appropriate peptide sequences, these heterocyclic non natural a-amino acids could behave as new substrates or inhibitors of elastase from Pseudomonas aeruginosa.This enzyme is known to be involved in nosocomial infections and infections related to the cystic fibrosis disease. New efficient chemoenzymatic preparations of those compounds using a-chymotrypsin (a-CT) are presented.

Details

ISSN :
14382199 and 09394451
Volume :
42
Database :
OpenAIRE
Journal :
Amino Acids
Accession number :
edsair.doi.dedup.....8aeb2608bc35a3aca3d3182027d6e316
Full Text :
https://doi.org/10.1007/s00726-010-0829-3