Betahistine dihydrochloride

Betahistine Dihydrochloride is a histamine H3 receptors inhibitor used as an antivertigo drug. (In Vitro) :Betahistine dihydrochloride (0-10 μM) inhibits [125I]iodoproxyfan binding to membranes of CHO (rH3 (445) R) and CHO (hH3 (445) R) cells with IC50 values of 1.9 μM and 3.3 μM, respectively. Lead to Ki values of 1.4 μM and 2.5 μM, respectively.Betahistine dihydrochloride (0-10 μM) has a regulating function on cAMP formation in CHO (rH3 (445) R), CHO (rH3 (413) R), and CHO (hH3 (445) R) cells. At low concentrations, betahistine behaves an apparent inverse agonist, and progressively enhances cAMP formation with EC50 values of 0.1 nM, 0.05 nM and 0.3 nM, respectively. In contrast, at concentrations higher than 10 nM, betahistine inhibits cAMP formation with an EC50 value of 0.1 μM in CHO (rH3 (445) R) and full agonist activity. (In Vivo) :Betahistine dihydrochloride (intraperitoneal or oral administration; 0.1-30 mg/kg; single dose) with acute administration has increased tele-methylhistamine (t-MeHA) levels with an ED50 of 0.4 mg/kg, indicating the inverse agonism. Besides, after acute oral administration, it increases t-MeHA levels with an ED50 of 2 mg/kg in male Swissmice.Betahistine dihydrochloride (oral adminstration; 1 and 5 mg/kg; daily for 3 weeks) attenuates the severity of arthritis and reduces the levels of pro-inflammatory cytokines in the paw tissues of CIA mice.

5579-84-0

Pharmacology & Drug Discovery

>98% (HPLC)

Ethanol: 1 mg/mL (4.78 mM) ; Water: 38 mg/mL (181.71 mM) ; DMSO: 38 mg/mL (181.71 mM)

Cl.Cl.CNCCC1=CC=CC=N1

C8H14Cl2N2

209.12

Storage temperature: -20°C. Stability: ≥ 2 years