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
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Biological Information

  • Product Name
    Cetirizine dihydrochloride
  • Note
    Research use only, not for human use.
  • Brief Description
    A second-generation antihistamine that acts as a selective H1 receptor antagonist.
  • Description
    A 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.
  • 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. 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%.
  • 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. 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.
  • Synonyms
    P-071
  • Pathway
    GPCR/G Protein
  • Target
    Histamine Receptor
  • Recptor
    H1receptor
  • Research Area
    Inflammation/Immunology
  • Indication
    Allergy

Chemical Information

  • CAS Number
    83881-52-1
  • Formula Weight
    461.8097
  • Molecular Formula
    C21H27Cl3N2O3
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    Cl.OC(=O)COCCN1CCN(CC1)C(C1=CC=CC=C1)C1=CC=C(Cl)C=C1
  • Chemical Name
    Acetic acid, 2-[2-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]ethoxy]-, hydrochloride (1:2)

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

molnova catalog
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