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SU11274

Chemical Structure : SU11274

CAS No.: 658084-23-2

SU11274 (SU 11274, PKI-SU11274, SU-11274)

Catalog No.: PC-42829Not For Human Use, Lab Use Only.

SU11274 (PKI-SU11274) is a potent, selective, ATP-competitive c-Met kinase inhibitor with IC50 of 20 nM, >50-fold selectivity over Bcr-Abl, JAK2, PDGFβR.

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

Biological Activity

SU11274 (PKI-SU11274) is a potent, selective, ATP-competitive c-Met kinase inhibitor with IC50 of 20 nM, >50-fold selectivity over Bcr-Abl, JAK2, PDGFβR.
SU11274 (PKI-SU11274) induces G(1) cell cycle arrest and apoptosis with increased Annexin V staining and caspase 3 activity, specifically regulates cell growth in TPR-MET-transformed BaF3 cells with IC50 of <3 uM.
SU11274 (PKI-SU11274) differentially affects the kinase activity and subsequent signaling of various mutant forms of Met (M1268T and H1112Y).

Physicochemical Properties

M.Wt 568.0869
Formula C28H30ClN5O4S
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-Indole-5-sulfonamide, N-(3-chlorophenyl)-3-[[3,5-dimethyl-4-[(4-methyl-1-piperazinyl)carbonyl]-1H-pyrrol-2-yl]methylene]-2,3-dihydro-N-methyl-2-oxo-, (3Z)-

References

1. Sattler M, et al. Cancer Res. 2003 Sep 1;63(17):5462-9.

2. Berthou S, et al. Oncogene. 2004 Jul 8;23(31):5387-93.

3. Ma PC, et al. Cancer Res. 2005 Feb 15;65(4):1479-88.

4. Jagadeeswaran R, et al. Cancer Res. 2006 Jan 1;66(1):352-61.

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