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PD 173074

Cell-permeable, potent inhibitor of FGF and VEGF receptors.
 
ENZ-CHM112-0005 5 mg 184.00 USD
 
ENZ-CHM112-0010 10 mg 296.00 USD
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A cell-permeable compound that acts as a potent, ATP-competitive, and reversible inhibitor of FGF and VEGF receptors. PD 173074 inhibits PDGFR and c-Src only at much higher concentration. Shown to inhibit the autophosphorylation of endogenous FGFR1 and overexpressed VEGFR2.

Product Specification

Alternative Name:1-t-Butyl-3-(6-(3,5-dimethoxyphenyl)-2-(4-diethylaminobutylamino)-pyrido[2,3-d]pyrimidin-7-yl)urea
 
Formula:C28H41N7O3
 
MW:523.7
 
CAS:219580-11-7
 
Purity:≥99% (HPLC)
 
Appearance:White powder solid.
 
Solubility:Soluble in DMSO or methanol.
 
Shipping:Ambient
 
Short Term Storage:-20°C
 
Long Term Storage:-80°C
 
ENZ-CHM112 structure
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ENZ-CHM112 structure

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For Research Use Only. Not for use in diagnostic procedures.
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