Cetirizine dihydrochloride
CAS No. 83881-52-1
Cetirizine dihydrochloride( P-071 )
Catalog No. M16110 CAS No. 83881-52-1
A second-generation antihistamine that acts as a selective H1 receptor antagonist.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 50MG | 32 | In Stock |
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| 100MG | 45 | In Stock |
|
| 200MG | 65 | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameCetirizine dihydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionA second-generation antihistamine that acts as a selective H1 receptor antagonist.
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DescriptionA second-generation antihistamine that acts as a selective H1 receptor antagonist; used in the treatment of allergies.Allergy Approved(In Vitro):Cetirizine (>5 μM) at higher concentrations can reduce the release of GM-CSF and IL-8 from A549 cells stimulated with IL-1β. Cetirizine exerts anti-inflammatory effects beyond histamine H1-receptor antagonist.(In Vivo):Cetirizine (20 mg/kg, mice, orally) exerts its anti-inflammatory effects by inhibiting MIF as well as IL-8 production in mice immunized and challenged with ragweed pollen.
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In VitroCetirizine (>5 μM) at higher concentrations can reduce the release of GM-CSF and IL-8 from A549 cells stimulated with IL-1β. Cetirizine exerts anti-inflammatory effects beyond histamine H1-receptor antagonist. Cell Viability AssayCell Line:Human airway epithelial cell line A549.Concentration:0-10 μM.Incubation Time:24 h.Result:The survival of A549 cells incubated with various concentrations of cetirizine (0.1, 1, 2.5, 5, and 10 μM) for 24 hours were all higher than 90% when comparing with the control group by MTT test.Cetirizine, 5 and 10 μM, suppressed GM-CSF release by 70.71 and 61.55%, respectively.Preincubation with cetirizine, 10 μM, suppressed the IL-8 secretion by 75.04%.
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In VivoCetirizine (20 mg/kg, mice, orally) exerts its anti-inflammatory effects by inhibiting MIF as well as IL-8 production in mice immunized and challenged with ragweed pollen. Animal Model:Male 8-week-old BALB/c mice (25-30 g) immunized and challenged with ragweed pollen.Dosage:2 or 20 mg/kg.Administration:Orally, diluted in sterile water on days 18, 19, and 20.
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SynonymsP-071
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PathwayGPCR/G Protein
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TargetHistamine Receptor
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RecptorH1receptor
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Research AreaInflammation/Immunology
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IndicationAllergy
Chemical Information
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CAS Number83881-52-1
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Formula Weight461.8097
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Molecular FormulaC21H27Cl3N2O3
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESCl.OC(=O)COCCN1CCN(CC1)C(C1=CC=CC=C1)C1=CC=C(Cl)C=C1
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Chemical NameAcetic acid, 2-[2-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]ethoxy]-, hydrochloride (1:2)
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
molnova catalog
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