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TYRPHOSTIN AG 879

Base Information Edit
  • Chemical Name:TYRPHOSTIN AG 879
  • CAS No.:148741-30-4
  • Molecular Formula:C18H24 N2 O S
  • Molecular Weight:316.46
  • Hs Code.:2930909090
  • Mol file:148741-30-4.mol
TYRPHOSTIN AG 879

Synonyms:2-Propenethioamide,3-[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]-2-cyano-, (E)-; AG 879;Tyrphostin AG 879

Suppliers and Price of TYRPHOSTIN AG 879
Supply Marketing:Edit
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
  • Usbiological
  • AG 879
  • 10mg
  • $ 446.00
  • TRC
  • Tyrphostin AG 879
  • 100mg
  • $ 835.00
  • Tocris
  • AG 879 ≥99%(HPLC)
  • 10
  • $ 183.00
  • Sigma-Aldrich
  • Tyrphostin AG 879 99% (HPLC)
  • 5mg
  • $ 134.00
  • Sigma-Aldrich
  • AG 879
  • 5mg
  • $ 129.00
  • DC Chemicals
  • AG 879 >98%
  • 250 mg
  • $ 900.00
  • DC Chemicals
  • AG 879 >98%
  • 1 g
  • $ 1900.00
  • CSNpharm
  • Tyrphostin AG 879
  • 1mg
  • $ 27.00
  • CSNpharm
  • Tyrphostin AG 879
  • 50mg
  • $ 297.00
  • Crysdot
  • Tyrphostin AG 879 95+%
  • 50mg
  • $ 451.00
Total 22 raw suppliers
Chemical Property of TYRPHOSTIN AG 879 Edit
Chemical Property:
  • Vapor Pressure:4.5E-08mmHg at 25°C 
  • Boiling Point:443.8°Cat760mmHg 
  • Flash Point:222.2°C 
  • PSA:102.13000 
  • Density:1.161g/cm3 
  • LogP:4.88058 
  • Storage Temp.:Store at -20°C 
  • Solubility.:DMSO: at 26 mg/mlsoluble 
Purity/Quality:

98%,99%, *data from raw suppliers

AG 879 *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Description AG-879 (148741-30-4) inhibits NGF-induced neurite growth in PC12 cells via selective inhibition of NGF receptor(pp140c-trk) autophosphorylation (IC50 = 10 μM). No inhibition of EGF, or PDGF receptor phosphorylation is observed at typical working concentrations.
  • Uses Tyrphostin AG 879 is a dual EGFR/HER2 inhibitor that was administered together with androgen withdrawal therapy and was shown to sensitize prostate cancer cells to apoptosis.
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