Fupentixol Dihydrochloride

CAS No. 2413-38-9

Fupentixol Dihydrochloride( Flupenthixol dihydrochloride | Flupentixol dihydrochloride | (E/Z)-Flupentixol Dihydrochloride )

Catalog No. M19923 CAS No. 2413-38-9

Flupentixol is used in therapy of schizophrenia as well as in anxiolytic and depressive disorders.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 42 In Stock
5MG 37 In Stock
10MG 52 In Stock
25MG 86 In Stock
50MG 123 In Stock
100MG 181 In Stock
200MG Get Quote In Stock
500MG 468 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Fupentixol Dihydrochloride
  • Note
    Research use only, not for human use.
  • Brief Description
    Flupentixol is used in therapy of schizophrenia as well as in anxiolytic and depressive disorders.
  • Description
    Flupentixol is used in therapy of schizophrenia as well as in anxiolytic and depressive disorders.(In Vitro):Flupentixol (2.5-40 μM; 72 h) treatment inhibits the viability of lung cancer cells in a dose-dependent manner.Flupentixol (2.5-40 μM; 24 h) induces apoptosis in lung cancer cells.Flupentixol (2.5-15 μM; 24 h) inhibits p-AKT and Bcl-2 expression levels.(In Vivo):Flupentixol (intragastric injection; 40 mg/kg; once daily; 21 d) suppresses A549 xenografted tumor growth in nude mice.
  • In Vitro
    Flupentixol (2.5-40 μM; 72 h) treatment inhibits the viability of lung cancer cells in a dose-dependent manner.Flupentixol (2.5-40 μM; 24 h) induces apoptosis in lung cancer cells.Flupentixol (2.5-15 μM; 24 h) inhibits p-AKT and Bcl-2 expression levels. Cell Viability AssayCell Line:A549, H661, SK-SEM-1, and NCAL-H520 cells Concentration:2.5, 5, 10, 20, or 40 μM Incubation Time:72 hours Result:Showed the IC50s of 5.708 μM and 6.374 μM for A549 and H661 cells, respectively.Apoptosis Analysis Cell Line:A549 and H661 cells Concentration:5, 10, 20 and 40 μM Incubation Time:24 hours Result:Increased the percentage of cells in early apoptosis compared with the negative control in both A549 and H661 (p<0.05).Induced the cleavage of PARP and caspase-3 in a dose-dependent manner.Western Blot Analysis Cell Line:A549 and H661 cells Concentration:2.5, 5, 10, and 15 μM Incubation Time:24 hours Result:Decreased AKT phosphorylation levels in a dose-dependent manner, decreased the expression levels of Bcl-2.
  • In Vivo
    Flupentixol (intragastric injection; 40 mg/kg; once daily; 21 d) suppresses A549 xenografted tumor growth in nude mice. Animal Model:BALB/C nude mice injected with A549 cellsDosage:40 mg/kg Administration: Intragastric injection; 40 mg/kg; once daily; 21 days Result:Reduced tumor volumes compared to the vehicle control (p<0.05), reduced tumor weights by 64.1% (p<0.05).
  • Synonyms
    Flupenthixol dihydrochloride | Flupentixol dihydrochloride | (E/Z)-Flupentixol Dihydrochloride
  • Pathway
    GPCR/G Protein
  • Target
    Dopamine Receptor
  • Recptor
    D1 D2
  • Research Area
    Neurological Disease
  • Indication
    schizophrenia

Chemical Information

  • CAS Number
    2413-38-9
  • Formula Weight
    507.43
  • Molecular Formula
    C23H27Cl2F3N2OS
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 95 mg/mL;Water: 95 mg/mL;Ethanol: 25 mg/mL
  • SMILES
    Cl.Cl.OCCN1CCN(CC\C=C2\c3ccccc3Sc3ccc(cc23)C(F)(F)F)CC1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Yonar D et al. Effect of cis-(Z)-flupentixol on DPPC membranes in the presence and absence of cholesterol. Chem Phys Lipids. 2016 Jun;198:61-71.
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