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SU14813

Chemical Structure : SU14813

CAS No.: 627908-92-3

SU14813 (SU-14813;SU 14813)

Catalog No.: PC-42622Not For Human Use, Lab Use Only.

SU14813 is a potent, broad-spectrum RTKs inhibitor with IC50 ranging from 2 to 50 nM for VEGFR-1, VEGFR-2, PDGFRs, KIT, FLT3, and CSF1R/FMS.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

SU14813 is a potent, broad-spectrum RTKs inhibitor with IC50 ranging from 2 to 50 nM for VEGFR-1, VEGFR-2, PDGFRs, KIT, FLT3, and CSF1R/FMS.
SU14813 shows poor activity for EGFR and c-Met in biochemical assays.
SU14813 inhibits VEGFR-2, PDGFR-β, and KIT phosphorylation in porcine aorta endothelial cells with IC50 of 5.2, 9.9, and 11.2 nM respectively.
SU14813 is active in xenograft tumor models.

Physicochemical Properties

M.Wt 442.4833
Formula C23H27FN4O4
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

1H-Pyrrole-3-carboxamide, 5-[(5-fluoro-1,2-dihydro-2-oxo-3H-indol-3-ylidene)methyl]-N-[(2S)-2-hydroxy-3-(4-morpholinyl)propyl]-2,4-dimethyl-

References

1. Patyna S, et al. Mol Cancer Ther. 2006 Jul;5(7):1774-82.

2. Hu-Lowe D, et al. Mol Cancer Ther. 2011 Nov;10(11):2015.

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