PKI-166 (hydrochloride)


CAS No. : 2230253-82-2

2230253-82-2
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Cat. No. : HY-110328
M.Wt: 366.84
Formula: C20H19ClN4O
Purity: >98 %
Solubility: 10 mM in DMSO
Introduction of 2230253-82-2 :

PKI-166 hydrochloride is a potent, selective and orally active EGFR tyrosine kinase inhibitor, with an IC50 of 0.7 nM[1]. IC50 & Target: IC50: 0.7 nM (EGFR tyrosine kinase)[1] In Vitro: PKI-166 hydrochloride (0-0.5 μM; 1 hour; pretreatment) inhibits EGFR autophosphorylation in human pancreatic cancer cells[1].
PKI-166 hydrochloride (0.03 μM; 6 days) enhances the cytotoxicity mediated by gemcitabine[1].
In Vivo: PKI-166 hydrochloride (100 mg/kg; p.o.; daily; for 29 days) inhibits of pancreatic cancer growth[1].

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