Pharmacological discrimination of GluR5 and GluR6 kainate receptor subtypes by (3S,4aR,6R,8aR)-6-[2-(1(2)H-tetrazole-5-yl)ethyl]decahydroisoquinoline-3 carboxylic-acid

Molecular Pharmacology

Volumn 49, Issue 4, 1996, Pages 581-585

  Bleakman, David ^a   Schoepp, Darryle D ^a   Ballyk, Barbara ^b   Bufton, Hywel ^c   Sharpe, Erica F ^a   Thomas, Kathy ^a   Ornstein, Paul L ^a   Kamboj, Rajender K ^b  

^a ELI LILLY AND COMPANY   (United States)

^b NPS Pharmaceutical Inc   (United States)

^c UNIVERSITY OF BRISTOL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

6 NITRO 7 SULFAMOYLBENZO[F]QUINOXALINE 2,3 DIONE; AMPA RECEPTOR; DECAHYDRO 6 [2 (1H TETRAZOL 5 YL)ETHYL] 3 ISOQUINOLINECARBOXYLIC ACID; KAINIC ACID RECEPTOR; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; RECEPTOR SUBTYPE;

ANIMAL CELL; ARTICLE; CONCENTRATION RESPONSE; HUMAN CELL; KIDNEY CELL; NEUROTRANSMISSION; NONHUMAN; PRIORITY JOURNAL; PURKINJE CELL; RECEPTOR BINDING; SPINAL GANGLION;

ANIMALS; CELL LINE; GANGLIA, SPINAL; HUMANS; ISOQUINOLINES; PURKINJE CELLS; QUINOXALINES; RATS; RATS, SPRAGUE-DAWLEY; RECEPTORS, AMPA; RECEPTORS, KAINIC ACID; TETRAZOLES;

EID: 0029979667     PISSN: 0026895X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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