AZ6197

CAS No. 2023003-94-1

AZ6197( AZ 6197 | AZ-6197 )

Catalog No. M13150 CAS No. 2023003-94-1

AZ6197 (AZ-6197) is a potent, selective, reversible inhibitor of ERK1/2 with IC50 of <0.3 nM (ERK2).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
100MG Get Quote Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    AZ6197
  • Note
    Research use only, not for human use.
  • Brief Description
    AZ6197 (AZ-6197) is a potent, selective, reversible inhibitor of ERK1/2 with IC50 of <0.3 nM (ERK2).
  • Description
    AZ6197 (AZ-6197) is a potent, selective, reversible inhibitor of ERK1/2 with IC50 of <0.3 nM (ERK2), inhibits pERK/pRSK with IC50 of 12/62 nM in A375 cells, respectively; demonstrates in vivo antitumor efficacy.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    AZ 6197 | AZ-6197
  • Pathway
    MAPK/ERK Signaling
  • Target
    ERK
  • Recptor
    ERK
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2023003-94-1
  • Formula Weight
    442.527
  • Molecular Formula
    C24H26N8O
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CC1CN2C=C(C=C2C(=O)N1CC3=CC=CC(=N3)C)C4=NC(=NC=C4C)NC5=CC=NN5C
  • Chemical Name
    (R)-3-Methyl-7-(5-methyl-2-((1-methyl-1H-pyrazol-5-yl)amino)pyrimidin-4-yl)-2-((6-methylpyridin-2-yl)methyl)-3,4-dihydropyrrolo[1,2-a]pyrazin-1(2H)-one

Shipping & Storage Information

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

Reference

1. Ward RA, et al. J Med Chem. 2017 Apr 27;60(8):3438-3450. 2. Decaudin D, et al. Oncotarget. 2018 Apr 24;9(31):21674-21686.
molnova catalog
related products
  • Tauroursodeoxycholic...

    Tauroursodeoxycholic acid (TUDCA) is a neuroprotective bile conjugate; inhibits nuclear factor-kappa B (NF-κB) activation in glial cells.

  • 1-Butanol

    1-Butanol has an antioxidant effect, can decrease hyperglycemia. 1-Butanol has anti-allergic inflammatory effects by inhibiting the degranulation of mast cells and the expression of inflammatory cytokines.

  • CC-90003

    CC-90003 (CC90003) is a potent and selective, covalent ERK1/2 inhibitor with IC50 of 10-20 nM.