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Synthesis and binding properties of 2-amino-5-phosphono-3-pentenoic acid photoaffinity ligands as probes for the glutamate recognition site of the NMDA receptor

Author
HECKENDORN, R; ALLGEIER, H; BAUD, J; GUNZENHAUSER, W; ANGST, C
Ciba-Geigy Ltd, res. dep., pharmaceuticals div., 4002 Basel, Switzerland
Source

Journal of medicinal chemistry (Print). 1993, Vol 36, Num 23, pp 3721-3726 ; ref : 27 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)
Activité biologique Affinité Azide Composé aliphatique Composé benzénique Déshydroaminoacide In vitro Phénols Récepteur NMDA α-Aminoacide Acide phosphonique Déc-3-énoïque acide(2-amino-6-[4-azido-2-hydroxy-3-iodobenzamido]-4-sodiophosphonométhyl)
Keyword (en)
Biological activity Affinity Organic azide Aliphatic compound Benzenic compound Dehydroaminoacid In vitro Phenols NMDA receptor α-Aminoacid
Keyword (es)
Actividad biológica Afinidad Azida orgánica Compuesto alifático Compuesto bencénico Deshidroaminoácido In vitro Fenoles Receptor NMDA α-Aminoácido
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C03 Noncondensed benzenic compounds

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
3830714

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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