
Bioorganic and Medicinal Chemistry Letters p. 3103 - 3108 (1999)
Update date:2022-08-11
Topics:
Tozer, Matthew J.
Buck, Ildiko M.
Cooke, Tracey
Barret Kalindjian
McDonald, Iain M.
Pether, Michael J.
Steel, Katherine I. M.
4-Chlorophenylmethanesulfonamide and (4-chlorobenzyl)sulfamide derivatives of histamine homologues were prepared and found to be potent and selective histamine H3 receptor antagonists. High receptor affinity and low differences in the data from the bioassays were achieved with the imidazol-4-ylbutyl analogues.
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