GF109203X

CAS No. 133052-90-1

GF109203X( BIM I | GF 109203X | G? 6850 )

Catalog No. M11312 CAS No. 133052-90-1

GF109203X is a potent PKC inhibitor with IC50 of 20 nM, 17 nM, 16 nM, and 20 nM for PKCα, PKCβI, PKCβII, and PKCγ, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 63 In Stock
5MG 58 In Stock
10MG 96 In Stock
25MG 188 In Stock
50MG 343 In Stock
100MG 458 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    GF109203X
  • Note
    Research use only, not for human use.
  • Brief Description
    GF109203X is a potent PKC inhibitor with IC50 of 20 nM, 17 nM, 16 nM, and 20 nM for PKCα, PKCβI, PKCβII, and PKCγ, respectively.
  • Description
    GF109203X is a potent PKC inhibitor with IC50 of 20 nM, 17 nM, 16 nM, and 20 nM for PKCα, PKCβI, PKCβII, and PKCγ, respectively, showing more than 3000-fold selectivity for PKC as compared to EGFR, PDGFR and insulin receptor.
  • In Vitro
    ——
  • In Vivo
    Animal Model: Quinpirole-treated shrews Dosage:0-20 mg/kg Administration:i.p.Result:Reduced the mean frequency of Quinpirole-induced vomiting.Blocked Quinpirole-mediated ERK1/2 phosphorylation in shrew brainstems.
  • Synonyms
    BIM I | GF 109203X | G? 6850
  • Pathway
    Angiogenesis
  • Target
    PDGFR
  • Recptor
    PDGFR| PKCα| PKCβ1| PKCβ2| PKCγ
  • Research Area
    Metabolic Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    133052-90-1
  • Formula Weight
    412.48
  • Molecular Formula
    C25H24N4O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:82 mg/mL (198.79 mM); Ethanol:<1 mg/mL (<1 mM); Water:<1 mg/mL (<1 mM)
  • SMILES
    O=C(C(C1=CN(CCCN(C)C)C2=C1C=CC=C2)=C3C4=CNC5=C4C=CC=C5)NC3=O.
  • Chemical Name
    3-(1-(3-(dimethylamino)propyl)-1H-indol-3-yl)-4-(1H-indol-3-yl)-1H-pyrrole-2,5-dione

Shipping & Storage Information

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

Reference

1. Toullec D, et al. J Biol Chem. 1991, 266(24), 15771-15781.
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