Journal of Medicinal Chemistry p. 2252 - 2259 (1987)
Update date:2022-08-05
Topics: Synthesis Analogues Antagonist activity
Blackburn, Thomas P.
Cox, Barry
Guildford, Allen J.
Count, David J. Le
Middlemiss, Derek N.
et al.
A series of 2-<(2-aminoethyl)thio>quinolines substituted at the 3-position with alkyl, aryl, or heteroaryl groups has been prepared in the search for novel and selective 5-HT2 antagonists.The affinity of the compounds for 5-HT1 recep
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