
Vesnarinone
CAS No. 81840-15-5
Vesnarinone( RG-0210 | RG 0210 | Piteranometozine | Vesnarinone )
Catalog No. M17603 CAS No. 81840-15-5
Vesnarinone (INN) is a mixed phosphodiesterase 3 inhibitor and ion-channel modifier that has modest, dose-dependent, positive inotropic activity.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 43 | In Stock |
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5MG | 72 | In Stock |
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10MG | 110 | In Stock |
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25MG | 178 | In Stock |
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50MG | 332 | In Stock |
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100MG | 494 | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameVesnarinone
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NoteResearch use only, not for human use.
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Brief DescriptionVesnarinone (INN) is a mixed phosphodiesterase 3 inhibitor and ion-channel modifier that has modest, dose-dependent, positive inotropic activity.
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DescriptionVesnarinone is a cardiotonic agent, mixed phosphodiesterase 3 inhibitor and ion-channel modifier that has modest, dose-dependent, positive inotropic activity, but minimal negative chronotropic activity. Vesnarinone improves ventricular performance most in patients with the worst degree of heart failure.(In Vitro):Vesnarinone (60 and 100 μg/mL; 48 h) inhibits the cell growth in a dose-dependent manner.Vesnarinone (60 μg/mL; 48 h) induces G1 arrest and apoptosis.Vesnarinone (60 μg/mL; 0, 12, 24, and 48 h) treatment increases p21-mRNA expression and decreases p21 protein slightly.(In Vivo):Vesnarinone (oral gavage; 300 mg/kg; once daily; 6 w) binds covalently to rat liver in vivo.
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In VitroVesnarinone (60 and 100 μg/mL; 48 h) inhibits the cell growth in a dose-dependent manner.Vesnarinone (60 μg/mL; 48 h) induces G1 arrest and apoptosis.Vesnarinone (60 μg/mL; 0, 12, 24, and 48 h) treatment increases p21-mRNA expression and decreases p21 protein slightly. Cell Viability AssayCell Line:OSC3, OSC4, and OSC5 cells Concentration:60 μg/mL and 100 μg/mL Incubation Time:48 hours Result:Observed more than 50% inhibition in cells treated with 100 μg/mL, and reduced 30±40% the production of MTT formazan in cells treated with 60 μg/mL.Apoptosis Analysis Cell Line:OSC3, OSC4, and OSC5 cells Concentration:60 μg/mL Incubation Time:48 hours Result:Decreased the tumor cell population in the S phase and increased in the G1 phase.Western Blot Analysis Cell Line:OSC3, OSC4, and OSC5 cells Concentration:60 μg/mL Incubation Time:0, 12, 24, and 48 hours Result:Increased the expression of p21-mRNA after 12±24 h vesnarinone treatment.
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In VivoVesnarinone (oral gavage; 300 mg/kg; once daily; 6 w) binds covalently to rat liver in vivo. Animal Model:Female Lewis rats (200 g)Dosage:300 mg/kg Administration:Oral gavage; 300 mg/kg; once daily; 6 weeks Result:Observed covalently modified liver proteins.
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SynonymsRG-0210 | RG 0210 | Piteranometozine | Vesnarinone
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PathwayPI3K/Akt/mTOR signaling
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TargetGSK-3
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RecptorOthers
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Research AreaInfection
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Indication——
Chemical Information
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CAS Number81840-15-5
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Formula Weight395.46
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Molecular FormulaC22H25N3O4
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Purity>98% (HPLC)
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SolubilityDMSO : 16.67 mg/mL. 42.15 mM;
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SMILESN1C(=O)CCc2cc(ccc12)N1CCN(CC1)C(=O)c1cc(c(cc1)OC)OC
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Chemical Name6-[4-(3,4-dimethoxybenzoyl)piperazin-1-yl]-3,4-dihydro-1H-quinolin-2-one
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.Katayama Y, et al. Inhibitory effects of Vesnarinone on cloned cardiac delayed rectifier K(+) channels expressed in a mammalian cell line. J Pharmacol Exp Ther. 2000 Jul;294(1):339-46.
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