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Terfenadine is a selective histamine H1-receptor antagonist with anti-allergic effects that lacks central nervous system depressant activity. It is a prodrug that undergoes extensive first-pass hepatic metabolism by the cytochrome P450 enzyme CYP3A4 to its pharmacologically active metabolite fexofenadine (Cay-18191). Terfenadine is reported to be cardiotoxic, inducing QT interval prolongation by blocking cardiac potassium channels.Formal Name: alpha-[4-(1,1-dimethylethyl)phenyl]-4-(hydroxydiphenylmethyl)-1-piperidinebutanol. CAS Number: 50679-08-8. Synonyms: MDL 9918, NSC 665802, (±)-Terfenadine, DL-Terfenadine. Molecular Formula: C32H41NO2. Formula Weight: 471.7. Purity: >98%. Formulation: (Request formulation change), A crystalline solid. Solubility: DMF: 10 mg/ml, DMF:PBS(pH 7.2)(1:1): 0.33 mg/ml, DMSO: 10 mg/ml, Ethanol: 0.25 mg/ml. SMILES: CC(C)(C)C1=CC=C(C(O)CCCN2CCC(C(C3=CC=CC=C3)(O)C4=CC=CC=C4)CC2)C=C1. InChi Code: InChI=1S/C32H41NO2/c1-31(2,3)26-18-16-25(17-19-26)30(34)15-10-22-33-23-20-29(21-24-33)32(35,27-11-6-4-7-12-27)28-13-8-5-9-14-28/h4-9,11-14,16-19,29-30,34-35H,10,15,20-24H2,1-3H3. InChi Key: GUGOEEXESWIERI-UHFFFAOYSA-N.
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