Synthetic macromolecular inhibitors of human leukocyte elastase. I: Synthesis of peptidyl carbamates bound to water-soluble polymers. Poly-α,β-[N-(2-hydroxyethyl)-D,L-aspartamide] and poly-α-[N5-(2-hydroxyethyl)-L-glutamine]
- Author
- RYPACEK, F; BANKS, W. R; NOSKOVA, D; DIGENIS, G. A
Czechoslovak acad. sci., inst. macromolecular chemistry, 16206 Prague, Czechoslovakia - Source
Journal of medicinal chemistry (Print). 1994, Vol 37, Num 12, pp 1850-1856 ; ref : 29 ref
- CODEN
- JMCMAR
- ISSN
- 0022-2623
- Scientific domain
- Pharmacology drugs
- Publisher
- American Chemical Society, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aspartique dérivé polymère Carbamate organique Glutamique acide dérivé polymère Inhibiteur Leukocyte elastase Peptide polymère Préparation Enzyme Hydrolases Proteinases Serine endopeptidases
- Keyword (en)
- Aspartic derivative polymer Organic carbamate Glutamic acid derivative polymer Inhibitor Leukocyte elastase Aminoacid polymer Preparation Enzyme Hydrolases Proteinases Serine endopeptidases
- Keyword (es)
- Aspartico derivado polímero Carbamato orgánico Glutámico ácido derivado polímero Inhibidor Leukocyte elastase Péptido polímero Preparación Enzima Hydrolases Proteinases Serine endopeptidases
- Classification
- Pascal
- 001 Exact sciences and technology / 001D Applied sciences / 001D09 Physicochemistry of polymers / 001D09D Organic polymers / 001D09D02 Preparation, kinetics, thermodynamics, mechanism and catalysts / 001D09D02B Polymerization
- Discipline
- Physical chemistry of polymers
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4147586
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1021/jm00038a014 
https://dx.doi.org/10.1021/jm00038a014
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