T9652

Terfenadin

≥97.5% (HPLC), powder, H1 histamine receptor antagonist

• Synonym(e): α-[4-(1,1-Dimethylethyl)-phenyl]-4-(hydroxydiphenylmethyl)-1-piperidinbutanol
• Empirische Formel (Hill-System): C₃₂H₄₁NO₂
• CAS-Nummer: 50679-08-8
• Molekulargewicht: 471.67
• NACRES: NA.77
• PubChem Substance ID: 24277779
• UNSPSC Code: 12161501
• EC Number: 256-710-8
• MDL number: MFCD00079622

Eigenschaften

• Produktname: Terfenadin,
• Quality Segment: 200
• solubility: chloroform: soluble 250 mg plus 5 ml of solvent, clear to very slightly hazy, colorless to faintly yellow, H₂O: soluble 0.01 mg/mL at 30 °C, 1 M HCl: soluble 0.12 mg/mL at 30 °C, hexane: soluble 0.34 mg/mL at 30 °C, 0.1 M tartaric acid: soluble 0.45 mg/mL, 0.1 M citric acid: soluble 1.1 mg/mL, methanol: soluble 37.5 mg/mL at 30 °C, ethanol: soluble in salt form 37.8 mg/mL at 30 °C
• originator: Sanofi Aventis
• storage temp.: 2-8°C
• SMILES string: CC(C)(C)c1ccc(cc1)C(O)CCCN2CCC(CC2)C(O)(c3ccccc3)c4ccccc4
• 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
• Gene Information: human ... ABCB1(5243), CYP2C8(1558), CYP3A4(1576), HRH1(3269), IL4(3565), IL5(3567), KCNH1(3756), KCNH2(3757) ; mouse ... Abcb1a(18671), Abcb1b(18669) ; rat ... Hrh1(24448)

Beschreibung

Application

Terfenadine has been used to study the role of histamine in itch related to proteinase-activated receptors (PARs) in mice[1]. Terfenadine has also been used to block histamine receptor type 1 to study the pathogenesis of 2,4-dinitrobenzene sulfonic acid (DNBS)-induced ulcerative colitis in rats[2].

Terfenadine has been used as a positive control in electrophysiology recordings. It has also been used as a constituent of internal standard solution in liquid chromatography-mass spectrometry (LC-MS).[3]

Biochem/physiol Actions

Nicht sedierender H1 Histamin-Rezeptor-Antagonist der zweiten Generation.

Non-sedating second generation H1 histamine receptor antagonist. Mainly metabolized by Cyp3A4, 5, 7. Inhibits CYP2C8.

Terfenadine acts a potential anti-histamine and is used in the treatment of allergic rhinitis and chronic urticaria.

Features and Benefits

This compound is a featured product for ADME Tox research. Click here to discover more featured ADME Tox products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

This compound is featured on the Potassium Channels page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

This compound was developed by Sanofi Aventis. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Preparation Note

250 mg of Terfenadine dissolves in 5ml of chloroform to yield a clear, colorless solution. Terfenadine is also soluble at 30^° C in 0.1 M citric acid (1.1 mg/ml), water (0.01 mg/ml), methanol (37.5 mg/ml), hexane (0.34 mg/ml), ethanol (37.8 mg/ml), 1 M hydrochloric acid (0.12 mg/ml), and 0.1 M tartaric acid (0.45 mg/ml).

Sicherheitshinweise

• hcodes: H413
• pcodes: P273 - P501
• Hazard Classifications: Aquatic Chronic 4
• Lagerklasse: 11 - Combustible Solids
• flash_point_f: Not applicable
• flash_point_c: Not applicable