VU0810464

CAS No. 2126040-21-7

VU0810464( —— )

Catalog No. M21143 CAS No. 2126040-21-7

VU0810464 is a non-ureaG protein-gated inwardly-rectifying potassium channels (GIRK Kir3) activator.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 101 In Stock
5MG 91 In Stock
10MG 145 In Stock
25MG 244 In Stock
50MG 319 In Stock
100MG 425 In Stock
200MG 578 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    VU0810464
  • Note
    Research use only, not for human use.
  • Brief Description
    VU0810464 is a non-ureaG protein-gated inwardly-rectifying potassium channels (GIRK Kir3) activator.
  • Description
    VU0810464 is a non-ureaG protein-gated inwardly-rectifying potassium channels (GIRK Kir3) activator.
  • In Vitro
    VU0810464 (0, 0.1, 0.3, 1, 3, 10, 30 μM) produces a concentration‐dependent response curves of currents in SAN and HPC cells, in addition, VU0810464 is9‐fold higher potency for Kir3 channel activation in neurons as compared to SAN cells.
  • In Vivo
    VU0810464 (intraperitoneal?injection;30 mg/kg,10 mg/kg; 30mg/kg; pre-treated 30 mins) produces a dose-dependent reduction of SIH response in Male C57BL/6J mice. To test if VU0810464 plays it role through Kir3 channel activation, VU0810464 (10 mg/kg) suppresses the SIH response in wild‐ type mice, but has no impact on Kcnj3?/? mice.VU0810464 (intraperitoneal?injection?; 30 mg/kg; 15, 30, 45, or 60 min post‐injection) displays a favourable distribution to the brain (Kp,uu = 0.83), has a improvement over ML297 (Kp,uu= 0.32).Clearance of VU0810464 is rapid,brain and plasma half-lives is 20 min in a PK study. Animal Model:Male C57BL/6J mice, Kcnj3?/? siblings female and maleC57BL/6J miceDosage:10 mg/kg; 30mg/kg Administration:Intraperitoneal?injection Result:Reduced stress‐induced hyperthermia (SIH), a physiological test of anxiolytic efficacy in wild mice, but had no impact in and Kcnj3 (Girk1) ?/?mice.
  • Synonyms
    ——
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    Potassium Channel
  • Recptor
    GIRK
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2126040-21-7
  • Formula Weight
    349.83
  • Molecular Formula
    C18H21ClFN3O
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:250 mg/mL (714.63 mM)
  • SMILES
    Cc1cc(NC(=O)Cc2ccc(F)c(Cl)c2)n(C2CCCCC2)n1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Discovery and Characterization of 1H?Pyrazol-5-yl-2-phenylacetamides as Novel Non-Urea-Containing GIRK1/2 Potassium Channel Activators[J]. Acs Chemical Neuroscience 2017 8(9):1873-1879.
molnova catalog
related products
  • 4-Aminopyridine

    4-Aminopyridine is a nonselective K+ channel blocker that binds from the cytoplasmic side of the cell membrane.

  • ML277

    ML277 was identified as a potent activator of KCNQ1 channels (EC(50)=260 nM).

  • DCEBIO

    DCEBIO stimulates the secretion of Cl- through the activation of the hIK1 K + channel and the activation of the apical Cl- conductance.