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Mubritinib (TAK 165) Chemical Structure
Mubritinib (TAK 165) is a potent EGFR and p34cdc2 inhibitor with IC50 of 6 nM and 0.2 µM, respectively. Mubritinib(TAK 165) also inhibits p33cdk2 and p33cdk5.Mubritinib(TAK 165) displays > 4000-fold selectivity over EGFR, FGFR, PDGFR, JAK1 and Src. Mubritinib(TAK 165) exhibits potent antiproliferative effects in ErbB2-overexpressing cancer cell lines (IC50 = 5 nM in BT474 breast cancer cells) and significantly inhibits bladder, breast and prostate cancer xenograft growth in vivo. [1][2]
[2] J. Med. Chem. 1997;40: 408-412
| Molecular Weight (WM): | 468.47 |
|---|---|
| Formula: | C25H23F3N4O2 |
| Solubility(R.T.:25°C): | DMSO 13mg/mL |
| Water <1mg/mL | |
| Ethanol <1mg/mL |
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