AGI-5198

CAS No. 1355326-35-0

AGI-5198 ( (IDH-C35) )

Catalog No. M11453 CAS No. 1355326-35-0

AGI-5198 is the first highly potent and selective inhibitor of IDH1 R132H/R132C mutants with IC50 of 0.07 μM/0.16 μM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 29 In Stock
10MG 47 In Stock
50MG 69 In Stock
100MG 113 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    AGI-5198
  • Note
    Research use only, not for human use.
  • Brief Description
    AGI-5198 is the first highly potent and selective inhibitor of IDH1 R132H/R132C mutants with IC50 of 0.07 μM/0.16 μM.
  • Description
    AGI-5198 is the first highly potent and selective inhibitor of IDH1 R132H/R132C mutants with IC50 of 0.07 μM/0.16 μM.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    (IDH-C35)
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    Dehydrogenase
  • Recptor
    R132C-IDH1| R132H-IDH1
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    1355326-35-0
  • Formula Weight
    462.57
  • Molecular Formula
    C27H31FN4O2
  • Purity
    >98% (HPLC)
  • Solubility
    Ethanol: 14 mg/mL (30.26 mM); DMSO: 24 mg/mL (51.88 mM)
  • SMILES
    O=C(NC1CCCCC1)C(N(C2=CC=CC(F)=C2)C(CN3C=CN=C3C)=O)C4=CC=CC=C4C
  • Chemical Name
    N-cyclohexyl-2-(N-(3-fluorophenyl)-2-(2-methyl-1H-imidazol-1-yl)acetamido)-2-(o-tolyl)acetamide

Shipping & Storage Information

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

Reference

1.Rohle D, et al. Science, 2013, 340(6132), 626-630.
molnova catalog
related products
  • Qc1

    Qc1 is an inhibitor of threonine dehydrogenase (TDH) inhibitor and can be used in studies about metabolic diseases.

  • ALDH1A3-IN-2

    ALDH1A3-IN-2 is a potent ALDH1A3 inhibitor with an IC50 of 0.30 μM.ALDH1A3-IN-2 has potential for cancer disease research.

  • Enoxolone

    Enoximone is a selective phosphodiesterase inhibitor with vasodilating and positive inotropic activity that does not cause changes in myocardial oxygen consumption.