"目錄號: HY-15289
GPCR/G ProteinImmunology/Inflammation-
Ciproxifan(FUB-359)馬來酸鹽是高活性的H3受體拮抗劑窝革,IC50為9.2 nM,對其它亞型受體的親和力較低缀踪。
相關產(chǎn)品
Pitolisant hydrochloride-Perphenazine-Osthole-Clemastine fumarate-Clemizole hydrochloride-Promethazine hydrochloride-Azelastine hydrochloride-Bepotastine Beslilate-Diphenylpyraline hydrochloride-Famotidine-Histamine-Alcaftadine-Bilastine-Cetirizine dihydrochloride-Desloratadine-
生物活性
Description
Ciproxifan maleate(FUB-359 maleate) is a highly potent and selective histamin H3-receptor antagonist with IC50 of 9.2 nM, with low apparent affinity at other receptor subtypes.IC50 value: Target: H3 receptorIn vitro, Ciproxifan behaved as a competitive antagonist at the H3 autoreceptor controlling 3H histamine release from synaptosomes and displayed similar Ki values (0.5-1.9 nM) at the H3 receptor controlling the electrically-induced contraction of guinea pig ileum or at the brain H3 receptor labeled with 125I-iodoproxyfan. This appears to be an orally bioavailable, extremely selective and potent H3-receptor antagonist whose vigilance- and attention-promoting effects are promising for therapeutic applications in aging disorders.
References