Design and in vitro pharmacology of a selective γ-aminobutyric acid(C) receptor antagonist

Molecular Pharmacology

Volumn 50, Issue 4, 1996, Pages 1024-1030

  Ragozzino, D ^a   Woodward, R M ^b   Murata, Y ^c   Eusebi, F ^a   Overman, L E ^c   Miledi, R ^c  

^a Centroricerca Sperim Inst R   (Italy)

^b Acea Pharmaceuticals Inc   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

(1,2,5,6 TETRAHYDRO 4 PYRIDINE)METHYLPHOSPHONIC ACID; 3 AMINOPROPYL(METHYL)PHOSPHINIC ACID; 4 AMINOBUTYRIC ACID A RECEPTOR; 4 AMINOBUTYRIC ACID B RECEPTOR; 4 AMINOBUTYRIC ACID RECEPTOR; 4 AMINOBUTYRIC ACID RECEPTOR BLOCKING AGENT; ARECAIDINE; BACLOFEN; BICUCULLINE; CHLORIDE CHANNEL; RECEPTOR SUBTYPE; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BRAIN SLICE; DRUG DESIGN; HIPPOCAMPUS; NONHUMAN; OOCYTE; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN STRUCTURE; RAT; RECEPTOR AFFINITY; RETINA; XENOPUS LAEVIS;

ANIMALS; BRAIN; DRUG DESIGN; GABA ANTAGONISTS; PHOSPHINIC ACIDS; PYRIDINES; RATS; RATS, INBRED ACI; RECEPTORS, GABA; RETINA; XENOPUS LAEVIS;

EID: 0029859986     PISSN: 0026895X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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