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SU5416

Chemical Structure : SU5416

CAS No.: 204005-46-9

SU5416 (Semaxinib;SU-5416;SU 5416)

Catalog No.: PC-42557Not For Human Use, Lab Use Only.

A potent and specific VEGFR2 (KDR/Flk-1) inhibitor with IC50 of 1.04 uM.

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

Biological Activity

A potent and specific VEGFR2 (KDR/Flk-1) inhibitor with IC50 of 1.04 uM; displays no inhibitory activity against EGFR and FGFR; inhibits autophosphorylation of the Flk-1 receptor with IC50 of 1.23 uM in ELISA assays, inhibits VEGF-driven mitogenesis of HUVECs with IC50 of 0.04 uM; affects tumor vascular density and vascular leakage in vivo.

Solid Tumors

Phase 1 Discontinued

Physicochemical Properties

M.Wt 238.2845
Formula C15H14N2O
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

DMSO: 22.5 mg/mL

Chemical Name/SMILES

2H-Indol-2-one, 3-[(3,5-dimethyl-1H-pyrrol-2-yl)methylene]-1,3-dihydro-

References

1. Fong TA, et al. Cancer Res. 1999 Jan 1;59(1):99-106.

2. Shaheen RM, et al. Cancer Res. 1999 Nov 1;59(21):5412-6.

3. Mendel DB, et al. Anticancer Drug Des. 2000 Feb;15(1):29-41.

4. Mendel DB, et al. Clin Cancer Res. 2000 Dec;6(12):4848-58.

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