Propafenone
CAS No. 54063-53-5
Propafenone( —— )
Catalog No. M14930 CAS No. 54063-53-5
An antiarrhythmia agent that is particularly effective in ventricular arrhythmias. It also has weak beta-blocking activity.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 34 | In Stock |
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10MG | 45 | In Stock |
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25MG | 61 | In Stock |
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50MG | 98 | In Stock |
|
100MG | 129 | In Stock |
|
200MG | 181 | In Stock |
|
500MG | Get Quote | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NamePropafenone
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NoteResearch use only, not for human use.
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Brief DescriptionAn antiarrhythmia agent that is particularly effective in ventricular arrhythmias. It also has weak beta-blocking activity.
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DescriptionAn antiarrhythmia agent that is particularly effective in ventricular arrhythmias. It also has weak beta-blocking activity.
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In VitroPropafenone (5-25 μM) inhibits esophageal squamous cell carcinoma (ESCC) cell proliferation.Propafenone causes mitochondrial dysfunction by a decreased mitochondrial membrane potential and reduced expression of Bcl-xL and Bcl-2. Propafenone (10 and 20 μm) treatment significantly down regulates the expression levels of the anti-apoptotic proteins Bcl-xL and Bcl-2 in ESCC cells. Propafenone also reduces expression of p-ERK. Cell Proliferation Assay Cell Line:The human ESCC cell lines KYSE30, KYSE150 and KYSE270 Concentration:5, 10, 15, 20, and 25 μm Incubation Time:24, 48, and 72 hours Result:Gradually decreased cell proliferation over time and potently inhibited cell proliferation with increasing concentrations in KYSE30, KYSE150 and KYSE270 cells.Western Blot Analysis Cell Line:The human ESCC cell lines KYSE30, KYSE150 and KYSE270 Concentration:0, 10, and 20 μm Incubation Time:72 hours Result:Significant downregulation of Bcl-xL and Bcl-2 expression levels was observed.
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In VivoPropafenone (20 mg/kg; intraperitoneal injection every other day) markedly suppresses the tumor burden with a decrease of 69.2%.Propafenone also significantly inhibits tumor cell proliferation (mean index decreased from 56.3±6.7% in the DMSO-treated group to 20.7±5.1% in the 10 mg/kg propafenone-treated group and 11.3±4.0% in the 20 mg/kg propafenone-treated group). Animal Model:Female BALB/c nude mice bearing KYSE270-derived xenografts (6-8 weeks)Dosage:10 mg/kg or 20 mg/kg Administration:Intraperitoneally injected Result:Exerted a significantly inhibitory effect on the growth of tumor xenografts.
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Synonyms——
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PathwayEndocrinology/Hormones
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TargetMRP
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RecptorMRP1| Potassium Channel| Sodium Channel
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Research Area——
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Indication——
Chemical Information
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CAS Number54063-53-5
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Formula Weight341.44
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Molecular FormulaC21H27NO3
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Purity>98% (HPLC)
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SolubilityWater: 93.28 mg/L
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SMILESCCCNCC(O)COC1=CC=CC=C1C(=O)CCC1=CC=CC=C1
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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.Overington JP, et al. Nat Rev Drug Discov. 2006 Dec;5(12):993-6.
molnova catalog
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