Amiloride hydrochloride dihydrate

CAS No. 17440-83-4

Amiloride hydrochloride dihydrate ( MK870; MK-870; MK 870; Amiloride Hydrochloride )

Catalog No. M12644 CAS No. 17440-83-4

A pyrazine compound inhibiting SODIUM reabsorption through SODIUM CHANNELS in renal EPITHELIAL CELLS.

Purity : >98%(HPLC)

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

Biological Information

  • Product Name
    Amiloride hydrochloride dihydrate
  • Note
    Research use only, not for human use.
  • Brief Description
    A pyrazine compound inhibiting SODIUM reabsorption through SODIUM CHANNELS in renal EPITHELIAL CELLS.
  • Description
    A pyrazine compound inhibiting sodium reabsorption through sodium channels in renal epithelial cells. This inhibition creates a negative potential in the luminal membranes of principal cells, located in the distal convoluted tubule and collecting duct. Negative potential reduces secretion of potassium and hydrogen ions. Amiloride is used in conjunction with diuretics to spare potassium loss.
  • Synonyms
    MK870; MK-870; MK 870; Amiloride Hydrochloride
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    Sodium Channel
  • Recptor
    Amiloride-sensitive sodium channel
  • Research Area
    Cardiovascular Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    17440-83-4
  • Formula Weight
    302.12
  • Molecular Formula
    C6H8ClN7O·HCl·2H2O
  • Purity
    >98%(HPLC)
  • Solubility
    DMSO: 60 mg/mL (198.59 mM)
  • SMILES
    C1(=C(N=C(C(=N1)Cl)N)N)C(=O)N=C(N)N.O.O.Cl
  • Chemical Name
    3,5-Diamino-N-(aminoiminomethyl)-6-chloropyrazinecarboxamide hydrochloride

Shipping & Storage Information

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

Reference

1.Kelly O, et al. Am J Physiol Renal Physiol. 2003 Dec;285(6):F1279-90.
molnova catalog
related products
  • CNV1014802 hydrochlo...

    CNV1014802 (GSK-1014802, Raxatrigine, Vixotrigine) is a potent, selective Nav1.7 sodium channel blocker.

  • Ouabain

    Ouabain is a selective Na+/K+ -ATPase inhibitor binds to α2 /α3 subunit with Ki of 41 nM/15 nM.

  • Lacosamide

    An anticonvulsant compound that enhances the slow inactivation of voltage-gated sodium channels without affecting the fast inactivation of voltage-gated sodium channels.