The Selective 5-HT1BReceptor 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
Year: 1998
Type: article
Source: Journal of Medicinal Chemistry
DOI: 10.1021/jm970457s
Authors: Laramie M. Gaster, Frank E. Blaney, Susannah Davies, D. Malcolm Duckworth, Peter Ham, Sarah Jenkins, Andrew J. Jennings, Graham F. Joiner, Frank D. King, Keith R. Mulholland, Paul A. Wyman, Jim J. Hagan, Jon Hatcher, Brian J. Jones, Derek N. Middlemiss, Gary W. Price, Graham Riley, Claire Roberts, Carol Routledge, Julie Selkirk, Paula D. Slade
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2016502217
