Diphenylpyraline hydrochloride

CAS No. 132-18-3

Diphenylpyraline hydrochloride( Diphenylpyraline hydrochloride | Diafen hydrochloride | Diaphen )

Catalog No. M11298 CAS No. 132-18-3

Diphenylpyraline Hcl is a first-generation antihistamine with anticholinergic effects, acts as a dopamine reuptake inhibitor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1G 43 In Stock

Biological Information

  • Product Name
    Diphenylpyraline hydrochloride
  • Note
    Research use only, not for human use.
  • Brief Description
    Diphenylpyraline Hcl is a first-generation antihistamine with anticholinergic effects, acts as a dopamine reuptake inhibitor.
  • Description
    Diphenylpyraline Hcl is a first-generation antihistamine with anticholinergic effects, acts as a dopamine reuptake inhibitor, shows to be useful in the treatment of Parkinsonism.(In Vitro):Diphenylpyraline hydrochloride (10 μM) markedly inhibits dopamine uptakein mouse nucleus accumbens slices.(In Vivo):Diphenylpyraline hydrochloride (intraperitoneal injection; 5-10 mg/kg) elevates extracellular dopamine levels (~200%) in mouse nucleus accumbens and induces locomotor activation in mice.
  • In Vitro
    Diphenylpyraline hydrochloride (10 μM) markedly inhibits dopamine uptakein mouse nucleus accumbens slices.
  • In Vivo
    ——
  • Synonyms
    Diphenylpyraline hydrochloride | Diafen hydrochloride | Diaphen
  • Pathway
    GPCR/G Protein
  • Target
    Histamine Receptor
  • Recptor
    H1 receptor
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    132-18-3
  • Formula Weight
    317.85
  • Molecular Formula
    C19H23NO·HCl
  • Purity
    >98% (HPLC)
  • Solubility
    Soluble in DMSO
  • SMILES
    CN1CCC(OC(C2=CC=CC=C2)C3=CC=CC=C3)CC1.[H]Cl
  • Chemical Name
    Piperidine, 4-(diphenylmethoxy)-1-methyl-, hydrochloride

Shipping & Storage Information

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

Reference

1.Lapa GB, et al. Eur J Pharmacol. 2005, 506(3):237-40.
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