Camostat mesilate

CAS No. 59721-29-8

Camostat mesilate( Foipan | FOY 305 )

Catalog No. M15218 CAS No. 59721-29-8

Camostat is a trypsin-like protease inhibitor, inhibits airway epithelial sodium channel (ENaC) function with IC50 of 50 nM, less potent to trpsin, prostasin and matriptase.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 46 In Stock
10MG 41 In Stock
25MG 63 In Stock
50MG 83 In Stock
100MG 116 In Stock
200MG 172 In Stock
500MG 291 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Camostat mesilate
  • Note
    Research use only, not for human use.
  • Brief Description
    Camostat is a trypsin-like protease inhibitor, inhibits airway epithelial sodium channel (ENaC) function with IC50 of 50 nM, less potent to trpsin, prostasin and matriptase.
  • Description
    Camostat is a trypsin-like protease inhibitor, inhibits airway epithelial sodium channel (ENaC) function with IC50 of 50 nM, less potent to trpsin, prostasin and matriptase.
  • In Vitro
    ——
  • In Vivo
    Animal Model:6-8 week old female BALB/c mice (lethal SARS-CoV infection model)Dosage:30 mg/kg Administration:P.o.; twice a day for 9 days Result:Effective in protecting mice against death due to a lethal infection by SARS-CoV, with a survival rate of ~60%.
  • Synonyms
    Foipan | FOY 305
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    Sodium Channel
  • Recptor
    epithelial sodium channel (ENaC)
  • Research Area
    Metabolic Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    59721-29-8
  • Formula Weight
    494.52
  • Molecular Formula
    C21H26N4O8S
  • Purity
    >98% (HPLC)
  • Solubility
    Water: 10 mg/mL (20.22 mM); DMSO: 99 mg/mL (200.19 mM)
  • SMILES
    CS(O)(=O)=O.CN(C)C(=O)COC(=O)CC1=CC=C(OC(=O)C2=CC=C(C=C2)N=C(N)N)C=C1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Coote K, et al. J Pharmacol Exp Ther, 2009, 329(2), 764-774.
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