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SU 4312

Chemical Structure : SU 4312

CAS No.: 5812-07-7

SU 4312 (NSC 86429)

Catalog No.: PC-61860Not For Human Use, Lab Use Only.

SU 4312 (NSC 86429) is a selective, cell-permeable, brain-penetrant inhibitor of VEGFR2 and PDGFR tyrosine kinase with IC50 of 0.8 and 19.4 uM, respectively.

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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

SU 4312 (NSC 86429) is a selective, cell-permeable, brain-penetrant inhibitor of VEGFR2 and PDGFR tyrosine kinase with IC50 of 0.8 and 19.4 uM, respectively; displays no significant inhibitory activity against EGFR, HER2, and IGF-1R (>100 uM); exhibits neuroprotection against MPP(+) at least partly via selective and direct inhibition of nNOS; inhibits VEGF-dependent angiogenesis in a zebrafish assay (IC50=1.8 uM) without affecting normal cells.

Physicochemical Properties

M.Wt 264.3
Formula C17H16N2O
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

3-[[4-(dimethylamino)phenyl]methylene]-1,3-dihydro-2H-indol-2-one

References

1. Sun L, et al. J Med Chem. 1998 Jul 2;41(14):2588-603.

2. Tran TC, et al. Cancer Res. 2007 Dec 1;67(23):11386-92.

3. Cui W, et al. Br J Pharmacol. 2013 Mar;168(5):1201-14.

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