NU7026

CAS No. 154447-35-5

NU7026( DNA-PK Inhibitor II | LY293646 )

Catalog No. M12190 CAS No. 154447-35-5

NU7026 is a potent DNA-PK inhibitor with IC50 of 0.23 μM in cell-free assays.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 30 In Stock
5MG 47 In Stock
10MG 77 In Stock
25MG 159 In Stock
50MG 314 In Stock
100MG 426 In Stock
200MG 599 In Stock
500MG Get Quote In Stock
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Biological Information

  • Product Name
    NU7026
  • Note
    Research use only, not for human use.
  • Brief Description
    NU7026 is a potent DNA-PK inhibitor with IC50 of 0.23 μM in cell-free assays.
  • Description
    NU7026 is a potent DNA-PK inhibitor with IC50 of 0.23 μM in cell-free assays, 60-fold selective for DNA-PK than PI3K and inactive against both ATM and ATR.
  • In Vitro
    NU7026 (10 μM) potentiates ionizing radiation (IR) cytotoxicity [potentiation factor at 90% cell kill (PF90)=1.51±0.04] in exponentially growing DNA-PK proficient but not deficient cells. NU7026 synergistically sensitizes I83 cells to Chlorambucil (CLB) 3.5-fold.NU7026, a novel inhibitor of the DNA repair enzyme DNA-dependent protein kinase (DNA-PK). At a dose of 10 μM, which is nontoxic to cells per se, a minimum NU7026 exposure of 4 h in combination with 3 Gy radiation is required for a significant radiosensitisation effect in CH1 human ovarian cancer cells.Solution in vitro: NU7026 is dissolved in anhydrous DMSO. NU7026 is added to cells to a final concentration of 0.25% DMSO (v/v).
  • In Vivo
    NU7026, a novel inhibitor of the DNA repair enzyme DNA-dependent protein kinase (DNA-PK). Following intravenous administration to mice at 5 mg/kg, NU7026 underwent rapid plasma clearance (0.108 L/h) and this is largely attributed to extensive metabolism. Bioavailability following interperitoneal (i.p.) and p.o. administration at 20 mg/kg is 20 and 15%, respectively.Solution in vivo:NU7026 is formulated in 10% DMSO and 5% Tween 20 in saline (i.p. and p.o.) (Mice).NU7026 is formulated in 10% ethanol, 25% PEG 200 and 5% Tween 20 in saline (i.v.).
  • Synonyms
    DNA-PK Inhibitor II | LY293646
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    ATM/ATR
  • Recptor
    ATM| ATR| DNA-PK| PI3K
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    154447-35-5
  • Formula Weight
    281.31
  • Molecular Formula
    C17H15NO3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 1 mg/mL (3.55 mM)
  • SMILES
    O=C1C=C(N2CCOCC2)OC3=C1C=CC4=CC=CC=C43
  • Chemical Name
    2-morpholino-4H-benzo[h]chromen-4-one

Shipping & Storage Information

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

Reference

1.Veuger SJ, et al. Y Res, 2003, 63(18), 6008-6015.
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