Description
A histamine H1 receptor antagonist (Ki = 1.9 nM); binds competitively with the H1 receptor inverse agonist mepyramine in polymorphonuclear leukocytes (IC50 = 80 µM); metabolized to cetirizine in vivo; prevents histamine-induced recruitment of rolling leukocytes in rat mesentery post-capillary venules in situ (10 µM); decreases anxiety-like behavior in mice in the elevated plus maze and light-dark exploration test
Formal name: 2-[2-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]ethoxy]-ethanol
Synonyms: NSC 169188|U.C.B 4492
Molecular weight: 374.9
CAS: 68-88-2
Purity: ≥98%
Formulation: A solution in ethanol
Product Type|Biochemicals|Receptor Pharmacology|Antagonists||Research Area|Immunology & Inflammation|Allergy||Research Area|Immunology & Inflammation|Innate Immunity||Research Area|Neuroscience|Behavioral Neuroscience|Anxiety