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)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 43 In Stock
5MG 72 In Stock
10MG 110 In Stock
25MG 178 In Stock
50MG 332 In Stock
100MG 494 In Stock
200MG Get Quote In Stock
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Biological Information

  • Product Name
    Vesnarinone
  • Note
    Research use only, not for human use.
  • Brief Description
    Vesnarinone (INN) is a mixed phosphodiesterase 3 inhibitor and ion-channel modifier that has modest, dose-dependent, positive inotropic activity.
  • Description
    Vesnarinone 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.
  • 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. 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.
  • In Vivo
    Vesnarinone (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.
  • Synonyms
    RG-0210 | RG 0210 | Piteranometozine | Vesnarinone
  • Pathway
    PI3K/Akt/mTOR signaling
  • Target
    GSK-3
  • Recptor
    Others
  • Research Area
    Infection
  • Indication
    ——

Chemical Information

  • CAS Number
    81840-15-5
  • Formula Weight
    395.46
  • Molecular Formula
    C22H25N3O4
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 16.67 mg/mL. 42.15 mM;
  • SMILES
    N1C(=O)CCc2cc(ccc12)N1CCN(CC1)C(=O)c1cc(c(cc1)OC)OC
  • Chemical Name
    6-[4-(3,4-dimethoxybenzoyl)piperazin-1-yl]-3,4-dihydro-1H-quinolin-2-one

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • 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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