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 | |
---|---|
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.
Polyketide; protein translation inhibitor, mamm...
Cysteine-ITC conjugate, antioxidant; aldehyde d...
Endogenous tachykinin peptide, involved in infl...
Prodrug
FGFR inhibitor.
Peptide, derivative of AT I, cleavage product o...
Cyclic hexapeptide isolated from Phomopsis lept...
β-lactamase inhibitor.
Opioid peptide; μOR agonist.
ERK1/2 inhibitor.
Nav1.7 and Nav1.8 N1+ channel blocker.
GABA potentiator, voltage-gated Na+ and ATP-sen...
Hydrophobic β-lactam; penicillin binding prote...
5-HT3 antagonist.
Diterpenoid found in Rabdosia rubescens; potent...
Alkaloid compound originally found in Corydalis...
Chloramphenicol derivative; protein translation...
Diterpene found in coffee beans.
Phenol found in Zingiber; 5-HT3 antagonist.