Revaprazan hydrochloride

CAS No. 178307-42-1

Revaprazan hydrochloride( SB-641257 | YH-1885 )

Catalog No. M12683 CAS No. 178307-42-1

Revaprazan (SB-641257;YH-1885) potent potassium-competitive acid blocker (P-CAB) that inhibits H+,K+-ATPase in a reversible and K+-competitive manner.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
10MG 33 In Stock
25MG 67 In Stock
50MG 104 In Stock
100MG 163 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Revaprazan hydrochloride
  • Note
    Research use only, not for human use.
  • Brief Description
    Revaprazan (SB-641257;YH-1885) potent potassium-competitive acid blocker (P-CAB) that inhibits H+,K+-ATPase in a reversible and K+-competitive manner.
  • Description
    Revaprazan (SB-641257;YH-1885) potent potassium-competitive acid blocker (P-CAB) that inhibits H+,K+-ATPase in a reversible and K+-competitive manner; reduces gastric acid secretion, also exerts anti-inflammatory action against Helicobacter pylori-induced COX-2 expression by inactivating Akt signaling.Ulcer Approved.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    SB-641257 | YH-1885
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    Proton Pump
  • Recptor
    H+/K+-ATPase
  • Research Area
    Other Indications
  • Indication
    Ulcer

Chemical Information

  • CAS Number
    178307-42-1
  • Formula Weight
    398.91
  • Molecular Formula
    C22H24ClFN4
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 10 mM ( < 1 mg/ml refers to the product slightly soluble or insoluble )
  • SMILES
    Cl.CC1N(CCc2ccccc12)c3nc(Nc4ccc(F)cc4)nc(C)c3C
  • Chemical Name
    N-(4-fluorophenyl)-4,5-dimethyl-6-(1-methyl-3,4-dihydro-1H-isoquinolin-2-yl)pyrimidin-2-amine hydrochloride

Shipping & Storage Information

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

Reference

1. Li H, et al. Drug Metab Dispos. 2001 Jan;29(1):54-9. 2. Lee JS, et al. J Clin Biochem Nutr. 2012 Sep;51(2):77-83. 3. Inatomi N, et al. Pharmacol Ther. 2016 Dec;168:12-22.
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