Potassium Channel Activator 1

CAS No. 908608-06-0

Potassium Channel Activator 1( ZINC34634569 )

Catalog No. M26085 CAS No. 908608-06-0

Potassium Channel Activator 1 can be used in studies about the treatment of disorders or conditions wherein the dopaminergic system is disrupted such as mood disorders ADHD, schizophrenia, and other psychotic states.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 264 Get Quote
5MG 402 Get Quote
10MG 593 Get Quote
25MG 888 Get Quote
50MG 1242 Get Quote
100MG 1701 Get Quote
500MG 3411 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Potassium Channel Activator 1
  • Note
    Research use only, not for human use.
  • Brief Description
    Potassium Channel Activator 1 can be used in studies about the treatment of disorders or conditions wherein the dopaminergic system is disrupted such as mood disorders ADHD, schizophrenia, and other psychotic states.
  • Description
    Potassium Channel Activator 1 can be used in studies about the treatment of disorders or conditions wherein the dopaminergic system is disrupted such as mood disorders ADHD, schizophrenia, and other psychotic states.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ZINC34634569
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    Potassium Channel
  • Recptor
    NO Synthase| NOS
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    908608-06-0
  • Formula Weight
    341.4
  • Molecular Formula
    C19H23N3O3
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C(OCC=1C=CC=CC1)NC=2C(=NC(=CC2C)N3CCOCC3)C
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.3,4-oxo-isopropylidene-shikimic acid inhibits adhesion of polymorphonuclear leukocyte to TNF-alpha-induced endothelial cells in vitro.Acta Pharmacol Sin. 2004 Feb;25(2):246-50.
molnova catalog
related products
  • BMS-204352

    A potent and effective calcium-sensitive opener of maxi-K potassium channels (maxi-K) with EC50 of 392 nM at -48.4 mV in HEK293 isolated outside-out membrane patches.

  • VU0810464

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

  • Gut restricted-7

    Gut restricted-7 (GR-7) is a covalent and orally active pan-bile salt hydrolase (BSH) inhibitor. It decreases gut bacterial BSHs and decreases deconjugated bile acid levels in the feces of mice.