AZD3229

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Selleck Chemicals

SKU:S8780-2MG

Regular price €144,00 EUR
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AZD3229 is an inhibitor of c-Kit and PDGFR used in studies of MAPK / ERK Signaling. In practice, this places the compound in experiments that measure mitogenic kinase cascades, proliferation control, and differentiation-linked signaling in angiogenesis, cancer, and cell signaling models.

By inhibiting c-Kit and PDGFR, AZD3229 can be used to examine mitogenic kinase cascades, proliferation control, and differentiation-linked signaling. The kinase annotation adds relevance to biochemical kinase assays, phospho-signaling studies, and selectivity profiling, together with downstream-response mapping in the same experimental setting. In angiogenesis, cancer, and cell signaling models, these readouts can be combined with viability, reporter, localization, biochemical conversion, or morphology endpoints to refine experimental interpretation.

Research Applications

  • Target-focused assays involving c-Kit and PDGFR
  • Pathway perturbation studies connected to MAPK / ERK Signaling
  • Concentration-response inhibition and target-dependence studies
  • Biochemical kinase assays, phospho-signaling studies, and selectivity profiling

Overall, AZD3229 is appropriate when a defined chemical perturbant is needed to connect c-Kit and PDGFR with measurable biochemical, transcriptional, electrophysiological, imaging, or phenotypic readouts in angiogenesis, cancer, and cell signaling models. This profile is suited to mechanistic follow-up, comparative profiling, and assay optimization under defined exposure conditions.

Targets:
c-Kit • PDGFR
Target Class:
Kinase
Pathways:
MAPK / ERK Signaling
Research Area:
Angiogenesis • Cancer • Cell Signaling
CAS No.:
2248003-60-1
Molecular Weight:
479.51
Formula:
C₂₄H₂₆FN₇O₃
SMILES:
CC(C)C1=CN(N=N1)CC(=O)NC2=CC=C(C=C2)NC3=NC=NC4=C3C(=CC(=C4)OCCOC)F
Storage Temperature:
-20°C

For Research Use Only. Not intended for diagnostic or therapeutic use.
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