EGFR-HER2 inhibitor TAK-285, Purity ≥98%

Cat. No.: X23-10-ZQ1055

EGFR-HER2 inhibitor TAK-285, Purity ≥98%

Synonym: TAK-285; 871026-44-7; TAK285; TAK 285; N-(2-(4-((3-Chloro-4-(3-(trifluoromethyl)phenoxy)phenyl)amino)-5H-pyrrolo[3,2-d]pyrimidin-5-yl)ethyl)-3-hydroxy-3-methylbutanamide; EGFR-HER2 inhibitor

  • MDL: MFCD22124520
  • CAS Number: 871026-44-7
  • Compound CID: 11620908
Product Size
5 mg; 10 mg; 25 mg; 50 mg; 100 mg
Price
Datasheet
MSDS
Properties
Description
TAK-285, soluble in DMSO and ethanol and insoluble in water, is a potent and specific inhibitor of the tyrosine kinase activity of EGFR. It targets EGFR/HER1, HER4, ASK1, and AuroraB.
Molecular Weight
548
Molecular Formula
C26H25ClF3N5O3
Targets
EGFR/HER1: 23 nM; HER4: 260 nM; ASK1: >10 μM; AuroraB: 1.7 μM
Form
Lyophilized powder
Purity
≥98%
Solubility
DMSO: 97 mg/mL (177.02 mM); Water: Insoluble; Ethanol: 48 mg/mL (87.59 mM)
Identity
Confirmed by NMR/HPLC/MS.
Stability
The product is stable for three years when stored at the recommended temperature in lyophilized powder.
Applications
TAK-285 can be used to study the inhibition of HER2 and EGFR in cancer research.
Storage
Store at -20ºC.
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