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Mubritinib (TAK 165)

Catalog No. S2216 Product Citations1 Product Citation(s)
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Mubritinib (TAK 165) Chemical Structure

Bio Information

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]

References:

[2] J. Med. Chem. 1997;40: 408-412

Chemical Information

Molecular Weight (WM): 468.47
Formula:

C25H23F3N4O2

Solubility(R.T.:25°C): DMSO 13mg/mL 
Water <1mg/mL 
Ethanol <1mg/mL 

Quality Control

View current batch:
H-NMR HPLC H-NMR HPLC

Research Area

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Mubritinib (TAK 165) has been referenced in 1 publications.

A guide to picking the most selective kinase inhibitor tool compounds for pharmacological validation of drug targets.

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