Esonarimod

CAS No. 101973-77-7

Esonarimod( Esonarimod | KE-298 | KE298 )

Catalog No. M17753 CAS No. 101973-77-7

Esonarimod is an antirheumatic drug.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 46 In Stock
5MG 58 In Stock
10MG 87 In Stock
25MG 177 In Stock
50MG 259 In Stock
100MG 405 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Esonarimod
  • Note
    Research use only, not for human use.
  • Brief Description
    Esonarimod is an antirheumatic drug.
  • Description
    Esonarimod is an antirheumatic drug, suppressing lymphocyte activating factor activity or biosynthesis.(In Vitro):Esonarimod (KE-298) (10 to 300 μg/mL) suppresses the production of NO by RAW264.7 cells in a dose dependent manner. The IC50 of Esonarimod is 117.5 μg/mL. Esonarimod does not affect cellular viability at these tested doses. Esonarimod has no direct effect on NOS activity in cell-free extracts of RAW264.7 cells.(In Vivo):After repeated oral administration of Esonarimod (14C-KE-298), the radioactivity decreases rapidly and no tendency towards accumulation is found.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Esonarimod | KE-298 | KE298
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    IL-1
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    101973-77-7
  • Formula Weight
    280.34
  • Molecular Formula
    C14H16O4S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CC1=CC=C(C=C1)C(=O)CC(CSC(=O)C)C(=O)O
  • Chemical Name
    Benzenebutanoic acid, alpha-((acetylthio)methyl)-4-methyl-gamma-oxo-

Shipping & Storage Information

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

Reference

1.Inoue T, et al. KE-298 and its active metabolite KE-758 suppress nitric oxide production by murine macrophage cells and peritoneal cells from rats with adjuvant induced arthritis. J Rheumatol. 2001 Jun;28(6):1229-37.
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