Date published: 2025-11-1

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SU 4312 (CAS 5812-07-7)

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Application:
SU 4312 is a potent and selective VEGFR (Flk/Flt) inhibitor
CAS Number:
5812-07-7
Purity:
98%
Molecular Weight:
264.3
Molecular Formula:
C17H16N2O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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SU 4312 is a selective and potent vascular endothelial cell growth factor receptor (VEGFR) inhibitor. Inhibition of VEGFR-2 in neonatal rodent models of stroke, has been shown to limit endothelial cell proliferation and promote cell death. It has been suggested that SU 4312 may interfere with endothelial cell activation in azheimer′s disease because it could block vessel formation.


SU 4312 (CAS 5812-07-7) References

  1. In vivo characterization of endothelial cell activation in a transgenic mouse model of Alzheimer's disease.  |  Schultheiss, C., et al. 2006. Angiogenesis. 9: 59-65. PMID: 16821113
  2. Vascular endothelial growth factor receptor-2 inhibition promotes cell death and limits endothelial cell proliferation in a neonatal rodent model of stroke.  |  Shimotake, J., et al. 2010. Stroke. 41: 343-9. PMID: 20101028
  3. Prolonged blockade of VEGF receptors does not damage retinal photoreceptors or ganglion cells.  |  Miki, A., et al. 2010. J Cell Physiol. 224: 262-72. PMID: 20232317
  4. The anti-cancer agent SU4312 unexpectedly protects against MPP(+) -induced neurotoxicity via selective and direct inhibition of neuronal NOS.  |  Cui, W., et al. 2013. Br J Pharmacol. 168: 1201-14. PMID: 23062100
  5. Vascular Endothelial Growth Factor-A (VEGF-A) Mediates Activin A-Induced Human Trophoblast Endothelial-Like Tube Formation.  |  Li, Y., et al. 2015. Endocrinology. 156: 4257-68. PMID: 26327470
  6. Substantial protection against MPTP-associated Parkinson's neurotoxicity in vitro and in vivo by anti-cancer agent SU4312 via activation of MEF2D and inhibition of MAO-B.  |  Guo, B., et al. 2017. Neuropharmacology. 126: 12-24. PMID: 28807675
  7. Inhibitors of the VEGF Receptor Suppress HeLa S3 Cell Proliferation via Misalignment of Chromosomes and Rotation of the Mitotic Spindle, Causing a Delay in M-Phase Progression.  |  Okumura, D., et al. 2018. Int J Mol Sci. 19: PMID: 30545129

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

SU 4312, 5 mg

sc-200637
5 mg
$97.00

SU 4312, 25 mg

sc-200637A
25 mg
$360.00

Hi I have a question regarding SU 4312 (CAS 5812-07-7). I am wondering about the mechanism of inhibition? How does this inhibitor work? Does it bind to the extracellular domain of VEGFR-1 and 2 or it just inhibit the kinase domaine?

Asked by: Parinaz
Thank you for your question. We do not have any information on the mechanism of inhibition of this compound; you would have to rely on third party resources for such information.
Answered by: Tech Support Europe
Date published: 2024-05-15
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Rated 5 out of 5 by from Schultheiss et alSchultheiss et al. (PubMed ID 16821113) used SU 4312 to block angiogenesis via VEGF antagonism in transgenic mice with Alzheimer s disease. -SCBT Publication Review
Date published: 2015-06-01
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SU 4312 is rated 5.0 out of 5 by 1.
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