Description
Mubritinib is an EGFR2 (HER2) inhibitor that underwent clinical trials, showing some promise as an anticancer chemotherapeutic in the treatment of bladder, kidney, and prostate cancer, but was not pursued further.
| Product Unit Size | Cost | Quantity | Stock |
|---|
Mubritinib is an EGFR2 (HER2) inhibitor that underwent clinical trials, showing some promise as an anticancer chemotherapeutic in the treatment of bladder, kidney, and prostate cancer, but was not pursued further.
| Cas No. | 366017-09-6 |
|---|---|
| Purity | ≥99% |
| Formula | C25H23F3N4O2 |
| Formula Wt. | 468.47 |
| Chemical Name | 1-(4-{4-[(2-{(E)-2-[4-(trifluoromethyl)phenyl]ethenyl}-1,3-oxazol-4-yl)methoxy]phenyl}butyl)-1H-1,2,3-triazole |
| IUPAC Name | 4-[[4-[4-(triazol-1-yl)butyl]phenoxy]methyl]-2-[(E)-2-[4- (trifluoromethyl)phenyl]ethenyl]-1,3-oxazole |
| Synonym | TAK-165 |
| Appearance | White to off white powder |
| Store Temp | Ambient |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
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| Info Sheet |
Nagasawa J, Mizokami A, Koshida K, et al. Novel HER2 selective tyrosine kinase inhibitor, TAK-165, inhibits bladder, kidney and androgen-independent prostate cancer in vitro and in vivo. Int J Urol. 2006 May;13(5):587-92. PMID: 16771730.
FAK inhibitor.
Pyrimidine nucleoside analog; DNA synthesis inh...
Fatty acid synthase inhibitor.
β-lactamase inhibitor.
Endogenous peptide, produced by activation of P...
Triazole; demethylation inhibitor, NMDA agonist...
Nucleoside (thymidine) analog; DNA chain termin...
Fast skeletal muscle troponin complex activator...
DNA alkylator.
Peptide fragment of HER2/neu/erbB2 receptor.
Benzisoxazole; 5-HT7 and NMDA agonist, D-amino ...
Synthesis impurity
STING inhibitor
Nucleoside (deoxyadenosine) analog; DNA chain t...
Nucleoside (guanosine) analog; DNA chain termin...
Macrolide; ET antagonist, proteasome inhibitor....
Pyrimidine derivative; kinesin Eg5 inhibitor.
Protease inhibitor
HDAC inhibitor, RNA splicing inhibitor.
OVA antigen.