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Cinnarizine is a calcium channel inhibitor and histamine H4 receptor antagonist (Ki = 142 nM). It inhibits L- and T-type calcium channels in isolated guinea pig atrial cells in a voltage-dependent manner. Cinnarizine inhibits L-type calcium currents in isolated guinea pig type II vestibular hair cells (IC50 = 1.5 µM). In vivo, cinnarizine (10 mg/kg) inhibits ethanol-induced gastric ulcer formation in rats. Formulations containing cinnarizine have been used in the treatment of nausea and vomiting due to vertigo, Meniere's disease, or chemotherapy.Formal Name: 1-(diphenylmethyl)-4-(3-phenyl-2-propen-1-yl)-piperazine. CAS Number: 298-57-7. Molecular Formula: C26H28N2. Formula Weight: 368.5. Purity: >98%. Formulation: (Request formulation change), A crystalline solid. Solubility: DMF: 14 mg/ml, DMF:PBS(pH7.2) (1:2): 0.3 mg/mol, DMSO: 2 mg/ml, Ethanol: 3 mg/ml. lambdamax: 227, 251 nm. SMILES: C1(C(C2=CC=CC=C2)N3CCN(C/C=C/C4=CC=CC=C4)CC3)=CC=CC=C1. InChi Code: InChI=1S/C26H28N2/c1-4-11-23(12-5-1)13-10-18-27-19-21-28(22-20-27)26(24-14-6-2-7-15-24)25-16-8-3-9-17-25/h1-17,26H,18-22H2/b13-10+. InChi Key: DERZBLKQOCDDDZ-JLHYYAGUSA-N.
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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