NFAT Inhibitor

CAS No. 249537-73-3

NFAT Inhibitor( —— )

Catalog No. M29714 CAS No. 249537-73-3

NFAT inhibitor is a cell-permeable compound that selectively inhibits calcineurin-mediated dephosphorylation of NFAT.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 237 In Stock
10MG 429 In Stock
25MG 704 In Stock
50MG 981 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock

Biological Information

  • Product Name
    NFAT Inhibitor
  • Note
    Research use only, not for human use.
  • Brief Description
    NFAT inhibitor is a cell-permeable compound that selectively inhibits calcineurin-mediated dephosphorylation of NFAT.
  • Description
    NFAT inhibitor is a cell-permeable compound that selectively inhibits calcineurin-mediated dephosphorylation of NFAT.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Nuclear factor of activated Tcells (NFAT)
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    249537-73-3
  • Formula Weight
    1685.94
  • Molecular Formula
    C75H120N20O22S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?H2O : 100 mg/mL (59.38 mM)
  • SMILES
    ——
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • β-Casomorphin (1-5),...

    β-Casomorphin (1-5), amide, bovine is a peptide of bovine β-Casomorphin.

  • 2-Carboxybenzaldehyd...

    The major peak of 2-Carboxybenzaldehyde reductase activity in human liver co-purifies with hAFAR protein. Sulphydryl substances and some proteins play important roles in preserving the molecular and catalytic properties of 2-Carboxybenzaldehyde reductase.

  • (Z)-Butylidenephthal...

    (Z)-Butylidenephthalide ((Z)-3-Butylidenephthalide) has antitumor and hypoglycemic effects, and can effectively inhibit the tumor growth of glioma and inhibit R-glucosidase activity.