Date published: 2025-10-12

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VEGFR2 Kinase Inhibitor III (CAS 204005-46-9)

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Alternate Names:
Semaxanib; SU 5416
Application:
VEGFR2 Kinase Inhibitor III is a VEGFR2, Met, RET, PDGFR, and ALK inhibitor
CAS Number:
204005-46-9
Purity:
≥97%
Molecular Weight:
238.28
Molecular Formula:
C15H14N2O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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VEGFR2 Kinase Inhibitor III is a cell-permeable ATP-competitive inhibitor of Flk-1 (VEGFR2/KDR, kinase insert domain receptor), which is the major growth factor for vascular endothelial cells. This receptor is a type III tyrosine kinase receptor that functions as the main mediator of VEGF-induced endothelial proliferation, survival, and migration. Studies suggest that VEGFR2 Kinase Inhibitor III also inhibits a variety of other receptors such as Met, Flt-3/Flk-2 (FLT-3 receptor tyrosine kinases), Ret, c-Kit, PDGFR, c-Abl and Arg (ABL), and ALK. In addition, VEGFR2 kinase inhibitor III regulates the signaling pathways used by oncogenic RET-transfected cells by regulating the extracellular signal regulated kinase (ERK) and JNK pathways.


VEGFR2 Kinase Inhibitor III (CAS 204005-46-9) References

  1. Inhibition of tumor growth, angiogenesis, and microcirculation by the novel Flk-1 inhibitor SU5416 as assessed by intravital multi-fluorescence videomicroscopy.  |  Vajkoczy, P., et al. 1999. Neoplasia. 1: 31-41. PMID: 10935468
  2. Inhibition of RET tyrosine kinase by SU5416.  |  Mologni, L., et al. 2006. J Mol Endocrinol. 37: 199-212. PMID: 17032739
  3. Mechanism of inhibition of tumor angiogenesis by beta-hydroxyisovalerylshikonin.  |  Komi, Y., et al. 2009. Cancer Sci. 100: 269-77. PMID: 19200258

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

VEGFR2 Kinase Inhibitor III, 5 mg

sc-202851
5 mg
$162.00