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Cat.No. Product Name Information/Activity

BCC5665 (R)-(-)-α-Methylhistamine dihydrobromide (R)-(-)-α-Methylhistamine dihydrobromide is a potent and selective H3 histamine receptor agonist with a Kd of 50.3 nM. (R)-(-)-α-Methylhistamine dihydrobromide can cross the blood-brain barrier, and can enhance memory retention, attenuates memory impairment in rats.

(R)-(-)-α-Methylhistamine dihydrobromide chemical structure

BCC6700 (S)-(+)-α-Methylhistamine dihydrobromide 75614-93-6

(S)-(+)-α-Methylhistamine dihydrobromide chemical structure

BCC6701 Nα-Methylhistamine dihydrochloride 16503-22-3

Nα-Methylhistamine dihydrochloride chemical structure

BCC7378 Proxyfan oxalate 177708-09-7 Proxyfan oxalate chemical structure

BCC7963 A 331440 dihydrochloride Selective H<sub>3</sub> antagonist A 331440 dihydrochloride chemical structure

BCC1863 Pitolisant hydrochloride Pitolisant hydrochloride is a potent and selective nonimidazole inverse agonist at the recombinant human histamine H3 receptor (Ki=0.16 nM). Pitolisant hydrochloride chemical structure

Pitolisant hydrochloride chemical structure

BCC7291 Carcinine ditrifluoroacetate 56897-53-1 Carcinine ditrifluoroacetate chemical structure

BCC6781 Clobenpropit dihydrobromide Clobenpropit dihydrobromide is a potent histamine H3R antagonist/inverse agonist with a pEC50 of 8.07 for histamine H3LR. Clobenpropit dihydrobromide acts as partial agonist at histamine H4 receptors (Ki 13 nM). Clobenpropit dihydrobromide also binds to serotonin 5-HT3 receptors (Ki 7.4 nM) and α2A/α2C adrenoceptors (Ki 17.4/7.8 nM). Clobenpropit dihydrobromide increases apoptosis. Clobenpropit dihydrobromide chemical structure

Clobenpropit dihydrobromide chemical structure

BCC7352 Conessine 546-06-5 Conessine chemical structure

BCC7357 GT 2016 152241-24-2 GT 2016 chemical structure

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