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Chemoenzymatic routes to enantiomerically pure 2-azatyrosine and 2-, 3- and 4-pyridylalanine derivatives
- 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.
- Subjects :
- Pseudomonas aeruginosa elastase
Stereochemistry
Clinical Biochemistry
Peptide
Stereoisomerism
010402 general chemistry
medicine.disease_cause
01 natural sciences
Biochemistry
Structure-Activity Relationship
Azatyrosine
medicine
Chymotrypsin
Structure–activity relationship
Enzyme Inhibitors
chemistry.chemical_classification
Alanine
Molecular Structure
[CHIM.ORGA]Chemical Sciences/Organic chemistry
010405 organic chemistry
Pseudomonas aeruginosa
Organic Chemistry
Elastase
0104 chemical sciences
3. Good health
Kinetics
Enzyme
chemistry
Heterocyclic a-amino acids
Subjects
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