AG 126

CAS No. 118409-62-4

AG 126 ( AG 126; Tyrphostin AG 126; UNII-7YA4AMD1JC )

Catalog No. M17173 CAS No. 118409-62-4

The tyrphostin AG-126 selectively inhibits the phosphorylation of ERK1 (p44) and ERK2 (p42) at 25-50 μM.

Purity : 98%

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 39 In Stock
5MG 60 In Stock
10MG 105 In Stock
25MG 210 In Stock
50MG 311 In Stock
100MG 462 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    AG 126
  • Note
    Research use only, not for human use.
  • Brief Description
    The tyrphostin AG-126 selectively inhibits the phosphorylation of ERK1 (p44) and ERK2 (p42) at 25-50 μM.
  • Description
    AG 126 selectively inhibits the phosphorylation. It also acts as a cell-permeable inhibitor of lipopolysaccharide (LPS)-induced synthesis of tumor necrosis factor-α and nitric oxide in murine peritoneal macrophages.
  • Synonyms
    AG 126; Tyrphostin AG 126; UNII-7YA4AMD1JC
  • Pathway
    Cytoskeleton/Cell Adhesion Molecules
  • Target
    Akt
  • Recptor
    COX-2; ERK1,2
  • Research Area
    Inflammation/Immunology
  • Indication
    ——

Chemical Information

  • CAS Number
    118409-62-4
  • Formula Weight
    215.17
  • Molecular Formula
    C10H5N3O3
  • Purity
    98%
  • Solubility
    DMSO : 100 mg/mL. 464.75 mM;
  • SMILES
    C1=CC(=C(C=C1C=C(C#N)C#N)O)[N+](=O)[O-]
  • Chemical Name
    Propanedinitrile, ((3-hydroxy-4-nitrophenyl)methylene)-

Shipping & Storage Information

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

Reference

1. Novogrodsky, A.,Vanichkin, A.,Patya, M., et al. Prevention of lipopolysaccharide-induced lethal toxicity by tyrosine kinase inhibitors. Science 264(5163), 1319-1322 (1994).
molnova catalog
related products
  • Iso-H7 dihydrochlori...

    Iso-H7 dihydrochloride is a less potent inhibitor of phosphokinase C than H-7.

  • Lenaldekar

    Lenaldekar inhibits T-cell expansion and autoimmune encephalomyelitis.

  • GSK-690693

    A potent, ATP competitive, pan-AKT inhibitor with IC50 of 2, 13, and 9 nM against AKT1, 2, and 3, respectively.