EGFR-HER2 inhibitor Erlotinib, Purity ≥98%

Cat. No.: X23-10-ZQ1059

EGFR-HER2 inhibitor Erlotinib, Purity ≥98%

Synonym: Erlotinib; 183321-74-6; N-(3-Ethynylphenyl)-6,7-bis(2-methoxyethoxy)quinazolin-4-amine; Tarceva; Erlotinib free base; 4-[(3-Ethynylphenyl)amino]-6,7-bis(2-methoxyethoxy)quinazoline; EGFR-HER2 inhibitor

  • MDL: MFCD02089651
  • CAS Number: 183321-74-6
  • Compound CID: 176870
Product Size
5 g; 10 g; 20 g
Price
Datasheet
MSDS
Properties
Description
Erlotinib, soluble in DMSO and warmed ethanol and insoluble in water, is a potent and specific inhibitor of the tyrosine kinase activity of EGFR. It targets EGFR.
Molecular Weight
393.443
Molecular Formula
C22H23N3O4
Targets
EGFR: 2 nM (IC50, cell free assay)
Form
Lyophilized powder
Purity
≥98%
Solubility
DMSO: 68 mg/mL (172.83 mM); Water: Insoluble; Warmed ethanol: 13 mg/mL
Identity
Confirmed by NMR/HPLC/MS.
Stability
The product is stable for three years when stored at the recommended temperature in lyophilized powder.
Applications
Erlotinib can be used to study the inhibition of EGFR tyrosine kinase in cancer research.
Storage
Store at -20ºC.
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