Cariporide

CAS No. 159138-80-4

Cariporide ( HOE642;HOE-642 )

Catalog No. M12272 CAS No. 159138-80-4

Cariporide (HOE642)is a potent, selective sodium-hydrogen exchange subtype 1 (NHE1) inhibitor with IC50 of 50 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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10MG 50 In Stock
25MG 102 In Stock
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Biological Information

  • Product Name
    Cariporide
  • Note
    Research use only, not for human use.
  • Brief Description
    Cariporide (HOE642)is a potent, selective sodium-hydrogen exchange subtype 1 (NHE1) inhibitor with IC50 of 50 nM.
  • Description
    Cariporide (HOE642)is a potent, selective sodium-hydrogen exchange subtype 1 (NHE1) inhibitor with IC50 of 50 nM, little to no activity against NHE3 and NHE2 (IC50=3 and 10 uM); inhibits the amiloride sensitive sodium influx in rabbit erythrocytes, reduces the swelling of human platelets induced by intracellular acidification, and delays pH recovery in rat cardiomyocytes; reduces and prevents ventricular premature beats, ventricular tachycardia, and ventricular fibrillation after oral treatment in vivo, shows cardioprotective and antiarrhythmic effects in ischaemic and reperfused hearts.Heart Arrhythmia Phase 2 Discontinued
  • Synonyms
    HOE642;HOE-642
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    Sodium Channel
  • Recptor
    NHE2
  • Research Area
    Cardiovascular Disease
  • Indication
    Heart Arrhythmia

Chemical Information

  • CAS Number
    159138-80-4
  • Formula Weight
    283.35
  • Molecular Formula
    C12H17N3O3S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 79 mg/mL (278.8 mM) ( < 1 mg/ml refers to the product slightly soluble or insoluble )
  • SMILES
    O=C(/N=C(N)\N)C1=CC=C(C(C)C)C(S(=O)(C)=O)=C1
  • Chemical Name
    N-(Aminoiminomethyl)-4-(1-methylethyl)-3-(methylsulfonyl)benzamide

Shipping & Storage Information

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

Reference

1. Scholz W, et al. Cardiovasc Res. 1995 Feb;29(2):260-8.
2. Russ U, et al. Pflugers Arch. 1996 Nov-Dec;433(1-2):26-34.
3. Xue YX, et al. Eur J Pharmacol. 1996 Dec 19;317(2-3):309-16.
4. Aye NN, et al. Eur J Pharmacol. 1997 Nov 27;339(2-3):121-7.
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