United States (Change Country)SU11274 Chemical Structure
SU11274 is a highly specific inhibitor of c-Met , with in vitro IC50 for the Met enzyme at 0.012 μmol/L. The inhibitor did not affect other tyrosine kinase oncoproteins, including BCR-ABL, TEL-JAK2, TEL-PDGF_R, or TEL-ABL. Inhibition of the Met kinase activity by SU11274 led to time- and dose-dependent reduced cell growth. [1]
Further study shows SU11274 belongs to a class of small molecule RTK inhibitors that exert their activity by competing for the Mg-ATP complex binding pocket, which results in inhibition of kinase activity and subsequent downstream signaling. [2]
[1] Oncogene 2004;23:5387–5393
[2] Cancer Res 2005;65:1479-1488
| Molecular Weight (WM): | 568.09 |
|---|---|
| Formula: | C28H30CIN5O4S |
| Solubility(R.T.:25°C): | DMSO 92mg/mL |
| Water <1mg/mL | |
| Ethanol 2mg/mL |
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;Cancer Sci, 2011, 102(12), 2164-71. SU11274 purchased from Selleck
Data independently produced by ;Dr. Zhang of Tianjin Medical University SU11274 purchased from Selleck
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