Prucalopride

CAS No. 179474-81-8

Prucalopride( Prucalopride | Prucalopride free base )

Catalog No. M12708 CAS No. 179474-81-8

Prucalopride is a selective, high affinity 5-HT receptor agonist for 5-HT4A and 5-HT4B receptor with Ki of 2.5 nM and 8 nM, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 29 Get Quote
10MG 47 Get Quote
25MG 61 Get Quote
50MG 73 Get Quote
100MG 126 Get Quote
200MG 178 Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Prucalopride
  • Note
    Research use only, not for human use.
  • Brief Description
    Prucalopride is a selective, high affinity 5-HT receptor agonist for 5-HT4A and 5-HT4B receptor with Ki of 2.5 nM and 8 nM, respectively.
  • Description
    Prucalopride is a selective, high affinity 5-HT receptor agonist for 5-HT4A and 5-HT4B receptor with Ki of 2.5 nM and 8 nM, respectively, exhibits >290-fold selectivity against other 5-HT receptor subtypes.(In Vitro):Prucalopride (10 μM; 24, 48, 72 h) shows anti proliferative activity in A549 cells.Prucalopride induces autophagy and apoptosis, decreases the expression of the phosphorylated protein kinase B (AKT) and mammalian target of rapamycin (mTor) in A549/A427 cells.(In Vivo):Prucalopride (5, 10 μg/kg; p.o.; single daily for 2 weeks) shortens the colonic transit time in DM model, promotes the regeneration of colonic neural stem cells and neurons.Prucalopride (5, 10 μg/kg; p.o.; single daily for 2 weeks) promotes the differentiation of colonic neural stem cells, activates the expression of glial proteins and promotes the recovery of neuronal injury to a certain extent.
  • In Vitro
    Prucalopride (10 μM; 24, 48, 72 h) shows anti proliferative activity in A549 cells.Prucalopride induces autophagy and apoptosis, decreases the expression of the phosphorylated protein kinase B (AKT) and mammalian target of rapamycin (mTor) in A549/A427 cells. Cell Proliferation Assay Cell Line:A549 cells Concentration:10 μM Incubation Time:24, 48, 72 h Result:Repressed lung cancer cells proliferation.
  • In Vivo
    Prucalopride (5, 10 μg/kg; p.o.; single daily for 2 weeks) shortens the colonic transit time in DM model, promotes the regeneration of colonic neural stem cells and neurons.Prucalopride (5, 10 μg/kg; p.o.; single daily for 2 weeks) promotes the differentiation of colonic neural stem cells, activates the expression of glial proteins and promotes the recovery of neuronal injury to a certain extent. Animal Model:Sprague dawley rats (diabetes mellitus (DM) model).Dosage:5 or 10 μg/kg Administration:Oral gavage; single daily for 2 weeks.Result:Accelerated colonic movement and shortened the colonic transit time, and markedly increased the expression levels of Ki67.Increased expression of SOX10 in the columnar epithelial nuclei and enteraden (when at 5 μg/kg), and in the columnar epithelial cells, the nuclei of lamina propria cells and enteraden (when at 10 μg/kg). Significantly increased Nestin expression, which concentrated in columnar epithelial cells and the mesenchyme. (Nestin:a marker of enteric neural stem cells in the ENS).
  • Synonyms
    Prucalopride | Prucalopride free base
  • Pathway
    Endocrinology/Hormones
  • Target
    5-HT Receptor
  • Recptor
    5-HT1A| 5-HT1B| 5-HT3| 5-HT4A| 5-HT4B
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    179474-81-8
  • Formula Weight
    367.87
  • Molecular Formula
    C18H26ClN3O3
  • Purity
    >98% (HPLC)
  • Solubility
    Ethanol: 38 mg/mL (103.29 mM); DMSO: 60 mg/mL (163.1 mM)
  • SMILES
    ClC1=CC(C(NC2CCN(CCCOC)CC2)=O)=C3C(CCO3)=C1N
  • Chemical Name
    4-amino-5-chloro-N-(1-(3-methoxypropyl)piperidin-4-yl)-2,3-dihydrobenzofuran-7-carboxamide

Shipping & Storage Information

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

Reference

1.Briejer MR, et al. Eur J Pharmacol, 2001, 423(1), 71-83.
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