CAS 83799-24-0
:Fexofénadine
- 2-(4-[1-Hydroxy-4-[4-(hydroxy-diphenyl-methyl)-piperidin-1-yl]-butyl]-phenyl)-2-methyl-propionic acid
- 2-(4-[1-Hydroxy-4-[4-(hydroxydiphenylmethyl)piperidin-1-yl]butyl]phenyl)-2-methylpropanoic acid
- 2-[4-(1-Hydroxy-4-{4-[Hydroxy(Diphenyl)Methyl]Piperidin-1-Yl}Butyl)Phenyl]-2-Methylpropanoic Acid
- 4-[1-Hydroxy-4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]butyl]-α,α-dimethylbenzeneacetic acid
- 4-[4-[4-(Hydroxydiphenylmethyl)-1-piperidinyl]-1-hydroxybutyl]-α,α-dimethylphenylacetic acid
- Benzeneacetic acid, 4-[1-hydroxy-4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]butyl]-α,α-dimethyl-
- Carboxyterfenadine
- Fexet
- Mdl 16455
- Telfast 120
- Terfenadine acid metabolite
- Terfenadine carboxylate
- Voir plus de synonymes
2-(4-{1-hydroxy-4-[4-(hydroxydiphenylmethyl)piperidin-1-yl]butyl}phenyl)-2-methylpropanoic acid
CAS :Formule :C32H39NO4Degré de pureté :95%Couleur et forme :SolidMasse moléculaire :501.6564Fexofenadine
CAS :Formule :C32H39NO4Degré de pureté :≥ 98.0%Couleur et forme :White to beige powderMasse moléculaire :501.66Fexofenadine Hydrochloride
CAS :Formule :C32H39NO4·HClDegré de pureté :>98.0%(T)(HPLC)Couleur et forme :White to Almost white powder to crystalMasse moléculaire :538.13Fexofenadine
CAS :Fexofenadine, a non-sedating antihistamine, treats allergies like hay fever and urticaria.Formule :C32H39NO4Degré de pureté :99.35%Couleur et forme :White To Off-White SolidMasse moléculaire :501.66Fexofenadine
CAS :Produit contrôléApplications The active metabolite of Terfenadine (T114500), a H1-histamine receptor antagonist.
References Garteiz, D.A., et al.: Arzneim.-Forsch., 32, 1185 (1982), Rampe, D., et al.: Mol. Pharmacol., 44, 1240 (1993), Obradovic, T., et al.: Pharm. Res., 24, 318 (2007),Formule :C32H39NO4Couleur et forme :Off-WhiteMasse moléculaire :501.66Fexofenadine
CAS :Fexofenadine is a selective histamine H1 receptor antagonist that has been shown to be effective in the treatment of allergic rhinitis. It is well tolerated and does not have any significant drug interactions. Fexofenadine is metabolized by cytochrome P450 (CYP) enzymes and undergoes extensive first-pass metabolism. This means that it should not interact with CYP inhibitors such as ketoconazole or cimetidine, but may increase the effects of CYP inducers such as phenobarbital or rifampin. Fexofenadine has been shown to inhibit the activity of human multidrug resistance protein 1 (MDR1) and P-glycoprotein (P-gp).
Degré de pureté :Min. 95 Area-%Couleur et forme :White Off-White PowderMasse moléculaire :501.66 g/mol






