Terfenadine
- CAS No.
- 50679-08-8
- Chemical Name:
- Terfenadine
- Synonyms
- seldane;Terfenadin;Cyater;Terdin;terfen;Terfex;Aldaban;mdl9918;rmi9918;Teldane
- CBNumber:
- CB7695393
- Molecular Formula:
- C32H41NO2
- Molecular Weight:
- 471.67
- MOL File:
- 50679-08-8.mol
- Modify Date:
- 2024/7/2 8:55:17
Melting point | 145-152 °C |
---|---|
Boiling point | 572.76°C (rough estimate) |
Density | 1.0488 (rough estimate) |
refractive index | 1.6310 (estimate) |
storage temp. | 2-8°C |
solubility | chloroform: soluble250 mg plus 5 ml of solvent, clear to very slightly hazy, colorless to faintly yellow |
form | Solid |
pka | pKa 9.21(H2O t = 25 I = 0.025) (Uncertain) |
color | White to Off-White |
Water Solubility | 0.001 g/100 mL (30 ºC) |
CAS DataBase Reference | 50679-08-8(CAS DataBase Reference) |
NIST Chemistry Reference | Seldane(50679-08-8) |
SAFETY
Risk and Safety Statements
Symbol(GHS) | GHS07,GHS08,GHS09 |
---|---|
Signal word | Danger |
Hazard statements | H413 |
Precautionary statements | P273-P501 |
Safety Statements | 24/25 |
WGK Germany | 2 |
RTECS | TM4969000 |
HS Code | 29333999 |
Toxicity | LD50 orally in mice: >2000 mg/kg (Carr, Meyer) |
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Terfenadine Chemical Properties,Uses,Production
Chemical Properties
White Solid
Uses
Terfenadine has been used to study the role of histamine in itch related to proteinase-activated receptors (PARs) in mice. 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.
World Health Organization (WHO)
The first clinically interesting histamine H-receptor1 antagonists were introduced in the late 1940s and early 1950s. Several H-antihistaminics have a similar cardiac effect to that seen with astemizole1 and terfenadine. Serious cardiovascular adverse reactions have been reported when used concomitantly with imidazole antifungals and macrolide antibiotics. See also under astemizole.
Biological Activity
Histamine H 1 receptor antagonist. Also blocks hERG and K ATP channels (IC 50 values are 204 nM and 1.2 μ M respectively). Inhibits the delayed rectifier K + current (I Kr ) in guinea pig ventricular myocytes (IC 50 = 50 nM). Activity prolongs QT and induces Torsades de pointes (TdP); cardiotoxic in vivo .
Pharmacology
Terfenadine not only differs from the other antihistamine drugs in its chemical structure, but also in that its action begins within 1–2 h and last approximately 12 h, reaching its peak of action in 3–4 h.
Terfenadine Preparation Products And Raw materials
Raw materials
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OCEAN TRADING CORPORATION | +91(22) 24921669 | New Delhi, India | 6211 | 58 | Inquiry |
Medilink Pharmachem | +91 (79) 3007-0133 | New Delhi, India | 424 | 50 | Inquiry |
Hangzhou FandaChem Co.,Ltd. | 008657128800458; +8615858145714 | China | 9337 | 55 | Inquiry |
CONIER CHEM AND PHARMA LIMITED | +8618523575427 | China | 49391 | 58 | Inquiry |
career henan chemical co | +86-0371-86658258 +8613203830695 | China | 29826 | 58 | Inquiry |
TargetMol Chemicals Inc. | +1-781-999-5354 +1-00000000000 | United States | 19892 | 58 | Inquiry |
Hefei TNJ Chemical Industry Co.,Ltd. | 0551-65418671 | China | 34571 | 58 | Inquiry |
Shaanxi Dideu Medichem Co. Ltd | +86-029-89586680 +86-18192503167 | China | 9030 | 58 | Inquiry |
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