Fexofenadine Hydrochloride

CAS: 153439-40-8

Ref. TR-F322490

Produktinformation

• Name: Fexofenadine Hydrochloride
• Synonyme: 2-[4-[(1RS)-1-hydroxy-4-[4-(hydroxydiphenylmethyl)piperidin-1-yl]butyl]phenyl]-2-methylpropanoic acid hydrochloride, Allegra, MDL 16455A, Telfast, Telfast BD, 2-(4-[1-Hydroxy-4-[4-(hydroxydiphenylmethyl)piperidin-1-yl]butyl]phenyl)-2-methylpropanoic acid hydrochloride, 2-[4-(1-Hydroxy-4-{4-[Hydroxy(Diphenyl)Methyl]Piperidin-1-Yl}Butyl)Phenyl]-2-Methylpropanoic Acid Hydrochloride (1:1), 2-[4-[1-Hydroxy-4-[4-(Hydroxy-Diphenyl-Methyl)-1-Piperidyl]-Butyl]Phenyl]-2-Methyl-Propanoic Acid Hydrochloride, Alernex, Alpha,Alpha-Dimethyl-4-[1-Hydroxy-4-[4-(Hydroxydiphenylmethyl)-1-Piperidinyl]Butyl]-Benzeneacetic Acid Hydrochloride, Benzeneacetic acid, 4-[1-hydroxy-4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]butyl]-α,α-dimethyl-, hydrochloride, Benzeneacetic acid, 4-[1-hydroxy-4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]butyl]-α,α-dimethyl-, hydrochloride (1:1), Carboxyterfenadine,Terfenadinecarboxylate, Fastofen, Feksine, Fexadyne, Fexodine, Fexofen, Fexofenadine HCl, Fexofenadine-D10 Hcl, Fexofendine Hcl, Mdl 16455A, Rapido, Terfenidine Carboxylate Hydrochloride, Vivafeks, Α,Α-Dimethyl-4-[1-Hydroxy-4-[4-(Hydroxydiphenylmethyl)-1-Piperidinyl]Butyl]Benzeneacetic Acid
• CAS: 153439-40-8

Beschreibung

Applications The active metabolite of Terfenadine (T114500), a H1-histamine receptor antagonist.
References Pratt, E., et al.: Diabet Med., 18, 515 (2001), Mizutani, N., et al.: J. Pharmacol. Sci., 93, 437 (2003), Scadding, G., et al.: Clin. Drug Invest., 25, 153 (2005), Asai, M., et al.: N. Engl. J. Med., 354, 307 (2006),

• Marke: TRC

Chemische Eigenschaften

• Molekulargewicht: 538.12
• Formel: C₃₂H₄₀ClNO₄
• Farbe/Form: Off-White
• InChl: /h3-8,10-13,15-18,28-29,34,37H,9,14,19-23H2,1-2H3,(H,35,36), InChI=1S/C32H39NO4.ClH/c1-31(2,30(35)36)25-17-15-24(16-18-25)29(34)14-9-21-33-22-19-28(20-23-33)32(37,26-10-5-3-6-11-26)27-12-7-4-8-13-27, 1H
• InChI Key: InChIKey=RRJFVPUCXDGFJB-UHFFFAOYSA-N
• SMILES: CC(C)(C(=O)O)c1ccc(C(O)CCCN2CCC(C(O)(c3ccccc3)c3ccccc3)CC2)cc1.Cl