AZD 2932

AZD 2932

CAT N°: 17741
Price:

From 48.00 40.80

AZD 2932 is an inhibitor of VEGFR2, PDGFR?, CSF1R, c-KIT, and FLT3 receptor tyrosine kinases (IC50s = 4, 8, 100, 9, and 7 nM, respectively).{41214} It also inhibits Pdgfr? phosphorylation (IC50 = 2 nM) in lysates from C6 rat glial tumors grown in athymic mice. AZD 2932 (12.5-50 mg/kg) reduces tumor growth and inhibits Pdgfr? and Vegfr2 phosphorylation in a 1:1 ratio in a C6 mouse xenograft model. Xenograft models using non-PDGFR expressing tumor cells were insensitive to AZD 2932 treatment.

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • 4-[(6,7-dimethoxy-4-quinazolinyl)oxy]-N-[1-(1-methylethyl)-1H-pyrazol-4-yl]-benzeneacetamide
  • Correlated keywords
    • VEFGR-2 PDGFR-? CFS-1R c-FMS cKIT FLT-3 AZD2932 AXD2932 AXD-2932 quinazoline endothelial
  • Product Overview:
    AZD 2932 is an inhibitor of VEGFR2, PDGFR?, CSF1R, c-KIT, and FLT3 receptor tyrosine kinases (IC50s = 4, 8, 100, 9, and 7 nM, respectively).{41214} It also inhibits Pdgfr? phosphorylation (IC50 = 2 nM) in lysates from C6 rat glial tumors grown in athymic mice. AZD 2932 (12.5-50 mg/kg) reduces tumor growth and inhibits Pdgfr? and Vegfr2 phosphorylation in a 1:1 ratio in a C6 mouse xenograft model. Xenograft models using non-PDGFR expressing tumor cells were insensitive to AZD 2932 treatment.

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