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.
Sesquiterpene lactone derived from Artemesia.
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ROS1, MET, Ron, Axl, TIE-2, VEGFR2 inhibitor.
Synthesis impurity
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Sulforaphane-cysteine conjugate.
NO donor.
Endogenous peptide involved in vascular contrac...
ITC found in cruciferous vegetables.
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Synthetic peptide hormone, met-enkephalin analo...
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Bipyridamine toxin.
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