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Terfenadine

CAT: 0013-GTR19175883-01Size: 50 mgDry Ice: NoHazardous: No
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CAT#:0013-GTR19175883-01Size:50 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Terfenadine is a prodrug metabolized by CYP3A4 to its active form, fexofenadine, a selective H1-receptor antagonist. This compound is used in pharmacological research to study antihistamine mechanisms, CYP3A4-mediated metabolism, and non-sedative properties in both in vitro and in vivo experimental models.
CAS Number
50679-08-8
Product Name Alternative
Potassium Channel, PotassiumChannel, Terfenadine, Caspase, Ca2+Exchanger, Ca2+ Exchanger, Apoptosis, 5HT Receptor, (±) -Terfenadine, 5HTReceptor, hERG, Inhibitor, HT, HistamineReceptor, Histamine Receptor, MDL 991, MDL991, MDL-991, inhibit, KcsA, Na+Exchanger, Na+ Exchanger, Na+/Ca2+ Exchanger, mAChR
Field of Research
Cell Biology, Immunology & Inflammation, Neuroscience, Pharmacology & Drug Discovery, Protein Biochemistry
Purity
98.76% (May vary between batches)
Solubility
DMSO:47.2 mg/mL (100.07 mM) ;10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (4.24 mM)
Smiles
CC (C) (C) c1ccc (cc1) C (O) CCCN1CCC (CC1) C (O) (c1ccccc1) c1ccccc1
Molecular Formula
C32H41NO2
Molecular Weight
471.67
Storage Conditions
-20°C
Notes
For research use only.

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