GSK2606414

CAS No. 1337531-36-8

GSK2606414( GSK2606414 | GSK-2606414 | GSK PERK Inhibitor )

Catalog No. M11350 CAS No. 1337531-36-8

GSK2606414 is an orally available, potent, and selective PERK inhibitor with IC50 of 0.4 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 93 In Stock
2MG 58 In Stock
5MG 90 In Stock
10MG 123 In Stock
50MG 325 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    GSK2606414
  • Note
    Research use only, not for human use.
  • Brief Description
    GSK2606414 is an orally available, potent, and selective PERK inhibitor with IC50 of 0.4 nM.
  • Description
    GSK2606414 is an orally available, potent, and selective PERK inhibitor with IC50 of 0.4 nM, displaying at least 100-fold selectivity over the other EIF2AKs assayed.(In Vitro):GSK2606414 inhibits PERK activation in cells.(In Vivo):GSK2606414 (50 and 150 mg/kg, p.o.) inhibits the growth of a human tumor xenograft in mice.
  • In Vitro
    GSK2606414 inhibits PERK activation in cells.
  • In Vivo
    GSK2606414 (50 and 150 mg/kg, p.o.) inhibits the growth of a human tumor xenograft in mice.
  • Synonyms
    GSK2606414 | GSK-2606414 | GSK PERK Inhibitor
  • Pathway
    Apoptosis
  • Target
    PERK
  • Recptor
    eIF-2AK1 (HRI)| eIF-2AK2 (PKR)| eIF-2AK3 (PERK)
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    1337531-36-8
  • Formula Weight
    451.44
  • Molecular Formula
    C24H20F3N5O
  • Purity
    >98% (HPLC)
  • Solubility
    Ethanol: 19 mg/mL (42.08 mM); DMSO: 90 mg/mL (199.36 mM)
  • SMILES
    FC(C1=CC(CC(N2CCC3=C2C=CC(C4=CN(C)C5=NC=NC(N)=C54)=C3)=O)=CC=C1)(F)F
  • Chemical Name
    1-(5-(4-amino-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)indolin-1-yl)-2-(3-(trifluoromethyl)phenyl)ethanone

Shipping & Storage Information

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

Reference

1.Axten JM, et al. J Med Chem. 2012, 55(16), 7193-7207.
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