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CP466722

Base Information
CP466722

Synonyms:CP466722;1-(6,7-Dimethoxy-4-quinazolinyl)-3-(2-pyridinyl)-1H-1,2,4-triazol-5-amine

Suppliers and Price of CP466722
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Sigma-Aldrich
  • CP466722 ≥98% (HPLC)
  • 5mg
  • $ 200.00
  • Sigma-Aldrich
  • CP466722 ≥98% (HPLC)
  • 25mg
  • $ 683.00
  • Labseeker
  • CP466722 95
  • 5g
  • $ 5250.00
  • DC Chemicals
  • CP466722 99%
  • 1 g
  • $ 1500.00
  • DC Chemicals
  • CP466722 99%
  • 250 mg
  • $ 750.00
  • Crysdot
  • CP-466722 98+%
  • 50mg
  • $ 457.00
  • Crysdot
  • CP-466722 98+%
  • 5mg
  • $ 88.00
  • Crysdot
  • CP-466722 98+%
  • 10mg
  • $ 146.00
  • ChemScene
  • CP-466722 99.40%
  • 10mg
  • $ 140.00
  • ChemScene
  • CP-466722 99.40%
  • 5mg
  • $ 80.00
Total 36 raw suppliers
Chemical Property of CP466722
Chemical Property:
  • Boiling Point:642.3±65.0 °C(Predicted) 
  • PKA:0.00±0.19(Predicted) 
  • PSA:114.59000 
  • Density:1.48 
  • LogP:1.80200 
  • Storage Temp.:2-8°C 
  • Solubility.:DMSO: soluble0.5mg/mL, clear (warmed) 
Purity/Quality:

99%, *data from raw suppliers

CP466722 ≥98% (HPLC) *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xn 
  • Hazard Codes:Xn 
  • Statements: 22 
MSDS Files:

SDS file from LookChem

Useful:
  • Description CP 466,722 is an inhibitor of ataxia-telangiectasia mutated (ATM) kinase that inhibits ionizing radiation-induced ATM autophosphorylation and phosphorylation of the ATM targets SMC1, Chk2, and p53 in HeLa cells when used at a concentration of 10 μM. It is selective for ATM over PI3K and PIKK in HFF(hTERT) and A-T(hTERT) fibroblasts, respectively. CP 466,722 decreases cell survival in response to ionizing radiation in HeLa cells. It is also cytotoxic to MCF-7 and SKBr-3 breast cancer cells (IC50s = 16.92 and 12.78 μM, respectively).
  • Uses CP466722 is a competetive, reversible inhbitor of Ataxia telangiectasia (A-T) mutated (ATM) kinase
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