Erlotinib Hydrochloride

Erlotinib Hydrochloride
  • CAS No.:183319-69-9
  • Grade:99.94%
  • Formula:C22H24ClN3O4
  • M.W.:429.90
  • Solvent:≥ 0.5 mg/mL (1.16 mM); Clear solution

Overview

Erlotinib (CP-358774) Hydrochloride is a selective, orally active EGFR tyrosine kinase inhibitor. Erlotinib Hydrochloride also acts as a substrate and inhibitor of OATP2B1 , with an IC 50 of approximately 0.079 μM for inhibiting OATP2B1-mediated uptake of estrone 3-sulfate. Erlotinib Hydrochloride blocks EGFR phosphorylation, downstream signal transduction, as well as the growth and proliferation of cancer cells. Erlotinib Hydrochloride inhibits MMP-10-mediated renal injury, fibrotic lesions, the ERK1/2 , GSK-3β and β-catenin signaling pathways, as well as the deposition of fibronectin, α-SMA, collagen and renal injury markers. Erlotinib Hydrochloride is metabolized via CYP3A to produce the active metabolite OSI-420. Erlotinib Hydrochloride can be used in research related to non-small cell lung cancer , gastric cancer , papillary renal cell carcinoma, EGFR inhibitor resistance and renal fibrosis.

Application

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Product Information

  • Catalog No.: HY-12008
  • CAS No.: 183319-69-9
  • Molecular Formula: C22H24ClN3O4
  • Molecular Weight: 429.90
  • Purity: 99.94%
  • Storage: 4°C, sealed storage, away from moisture * In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
  • Solubility: ≥ 0.5 mg/mL (1.16 mM); Clear solution
  • Availability: In-stock

Source

Original product source


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