The Selective 5-HT1B Receptor Inverse Agonist 1‘-Methyl-5-[[2‘-methyl-4‘- (5-methyl-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]carbonyl]-2,3,6,7-tetrahydro- spiro[furo[2,3-f]indole-3,4‘-piperidine] (SB-224289) Potently Blocks Terminal 5-HT Autoreceptor Function Both in Vitro and in Vivo
Author:
Affiliation:
1. SmithKline Beecham Pharmaceuticals, Discovery Research, New Frontiers Science Park (North), Third Avenue, Harlow, Essex CM19 5AW, England
Publisher
American Chemical Society (ACS)
Subject
Drug Discovery,Molecular Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/jm970457s
Reference59 articles.
1. Cell-specific coupling of the cloned human 5-HT1F receptor to multiple signal transduction pathways
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