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 |
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| 5MG | 37 | In Stock |
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| 10MG | 52 | In Stock |
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| 25MG | 86 | In Stock |
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| 50MG | 123 | In Stock |
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| 100MG | 181 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | 468 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameFupentixol Dihydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionFlupentixol is used in therapy of schizophrenia as well as in anxiolytic and depressive disorders.
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DescriptionFlupentixol 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.
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In VitroFlupentixol (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.
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In VivoFlupentixol (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).
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SynonymsFlupenthixol dihydrochloride | Flupentixol dihydrochloride | (E/Z)-Flupentixol Dihydrochloride
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PathwayGPCR/G Protein
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TargetDopamine Receptor
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RecptorD1 D2
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Research AreaNeurological Disease
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Indicationschizophrenia
Chemical Information
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CAS Number2413-38-9
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Formula Weight507.43
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Molecular FormulaC23H27Cl2F3N2OS
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Purity>98% (HPLC)
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SolubilityDMSO: 95 mg/mL;Water: 95 mg/mL;Ethanol: 25 mg/mL
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SMILESCl.Cl.OCCN1CCN(CC\C=C2\c3ccccc3Sc3ccc(cc23)C(F)(F)F)CC1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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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