4-Aminopyridine

CAS No. 504-24-5

4-Aminopyridine ( 4-AP; BRL 34915; Dalfampridine; Fampridine; NSC 15041 )

Catalog No. M14717 CAS No. 504-24-5

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

Purity : >98%(HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
50MG 45 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    4-Aminopyridine
  • Note
    Research use only, not for human use.
  • Brief Description
    4-Aminopyridine is a nonselective K+ channel blocker that binds from the cytoplasmic side of the cell membrane.
  • Description
    4-Aminopyridine is a nonselective K+ channel blocker that binds from the cytoplasmic side of the cell membrane. Target: Potassium Channel 4-Aminopyridine(4AP) is a nonselective K+ channel blocker that binds from the cytoplasmic side of the cell membrane.
  • Synonyms
    4-AP; BRL 34915; Dalfampridine; Fampridine; NSC 15041
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    Potassium Channel
  • Recptor
    Potassium Channel
  • Research Area
    Other Indications
  • Indication
    ——

Chemical Information

  • CAS Number
    504-24-5
  • Formula Weight
    94.11
  • Molecular Formula
    C5H6N2
  • Purity
    >98%(HPLC)
  • Solubility
    Soluble in Water
  • SMILES
    C1=CN=CC=C1N
  • Chemical Name
    pyridin-4-amine

Shipping & Storage Information

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

Reference

1. Sherratt, R.M., H. Bostock, and T.A. Sears, Effects of 4-aminopyridine on normal and demyelinated mammalian nerve fibres. nature, 1980. 283(5747): p. 570-2.
2. Bouchard, R. and D. Fedida, Closed- and open-state binding of 4-aminopyridine to the cloned human potassium channel Kv1.
5. J Pharmacol Exp Ther, 1995. 275(2): p. 864-76.
molnova catalog
related products
  • BMS-813160

    BMS-813160 is the first dualCCR2/CCR5antagonist to enter Clinical development for cardiovascular.

  • 2,2,2-Trichloroethan...

    2,2,2-Trichloroethanol is an agonist of the nonclassical K2P channels TREK-1 and TRAAK.

  • P-1075

    P-1075 is a potent sulfonylurea receptor 2-associated ATP-sensitive potassium channels (SUR2-KIR6) activator (EC50 = 45 nM).