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Cat. No. Product Name Information
PC-60793

JNJ-39758979

Histamine H4 antagonist

JNJ-39758979 (JNJ39758979) is a potent, selective, orally bioavailable histamine H4 receptor (H4R) antagonist with Ki of 12.5 nM, >80-fold selectivity over other histamine receptors.
PC-60533

Seliforant

Histamine H4 antagonist

Seliforant (SENS-111, SENS111) is a novel potent, selective histamine H4 receptor antagonist.
PC-60377

S 38093

Histamine H3 antagonist

S 38093 is a brain-penetrant H3 receptor antagonist/inverse agonist that shows procognitive properties in vivo.
PC-45168

Loratadine

Histamine H1 agonist

A tricyclic antihistamine that acts as a selective inverse agonist of peripheral histamine H1-receptors..
PC-45167

Cetirizine dihydrochloride

Histamine H1 antagonist

Cetirizine dihydrochloride is a second-generation antihistamine that acts as a selective H1 receptor antagonist, inhibits eosinophil chemotaxis during the allergic response.
PC-45166

Cetirizine

Histamine H1 antagonist

Cetirizine is a second-generation antihistamine that acts as a selective H1 receptor antagonist, inhibits eosinophil chemotaxis during the allergic response.
PC-42380

VUF10460

Histamine H4 agonist

VUF10460 is a potent, selective histamine H4 receptor (H4R) agonist with pKi of 7.46 and 8.22 for rat and human H4, respectively.
PC-45369

Decloxizine

Histamin H1 antagonist

Decloxizine (UCB-1402, NSC-289116) is a potent histamine 1 (H1) receptor antagonist.
PC-42908

ABT-239

Histamine H3 antagonist

ABT-239 is a potent and selective Histamine H3 receptor antagonist with Ki of 0.1-5.8 nM (human, rat H3).
PC-42911

Pitolisant hydrochloride

H3 receptor antagonist

Pitolisant hydrochloride (Ciproxidine, BF2649) is a potent and selective antagonist of H3 receptor with Ki/EC50 of 0.16/1.5 nM.
PC-42910

Pitolisant oxalate

H3 receptor antagonist

Pitolisant oxalate (Tiprolisant oxalate) is a potent and selective antagonist of H3 receptor with Ki/EC50 of 0.16/1.5 nM.
PC-42909

Pitolisant

H3 receptor antagonist

Pitolisant (Tiprolisant, BF-2649, BF 2.649) is a potent and selective antagonist of H3 receptor with Ki/EC50 of 0.16/1.5 nM.

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