Pipequaline

CAS No. 77472-98-1

Pipequaline( PK-8165 | PK8165 | PK 8165 )

Catalog No. M15927 CAS No. 77472-98-1

A clinically-effective anxiolytic that acts as a non-selective partial agonist of benzodiazepine receptor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 38 In Stock
25MG 113 In Stock
50MG 211 In Stock
100MG 365 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Pipequaline
  • Note
    Research use only, not for human use.
  • Brief Description
    A clinically-effective anxiolytic that acts as a non-selective partial agonist of benzodiazepine receptor.
  • Description
    A clinically-effective anxiolytic that acts as a non-selective partial agonist of benzodiazepine receptor; exerts a partial suppression of activations by kainate, glutamate and acetylcholine in rats, also reduces the neuronal activation by kainate.
  • In Vitro
    ——
  • In Vivo
    Intravenously administered pipequaline exerts a partial suppression of activations by kainate, glutamate and acetylcholine. Microiontophoretic applications of pipequaline reduces the neuronal activation by kainate. Pipequaline produces dose-related decreases in motor activity. Pipequaline produces significant dose-related decreases in the number of head-dips made.
  • Synonyms
    PK-8165 | PK8165 | PK 8165
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    GAT
  • Recptor
    GABAA
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    77472-98-1
  • Formula Weight
    316.4394
  • Molecular Formula
    C22H24N2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: ≥ 32 mg/mL
  • SMILES
    C1CNCCC1CCC2=CC(=NC3=CC=CC=C32)C4=CC=CC=C4
  • Chemical Name
    Quinoline, 2-phenyl-4-[2-(4-piperidinyl)ethyl]-

Shipping & Storage Information

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

Reference

1. File SE. Br J Pharmacol. 1983 May;79(1):219-23. 2. Gee KW, et al. Brain Res. 1983 Mar 28;264(1):168-72. 3. Debonnel G, et al. Neuropharmacology. 1987 Sep;26(9):1337-42.
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