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- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- 规格:
10 mM * 1 mL///1 mg
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E7090
CAS No. : 1622204-21-0
MCE 国际站:E7090
产品活性:E7090 是一种有效的,具有口服活性的选择性 FGFR 抑制剂,对 FGFR1/FGFR2/FGFR3/FGFR4 的 IC50 值分别为 0.71 nM、0.50 nM、1.2 nM 和120 nM。
研究领域:Protein Tyrosine Kinase/RTK
作用靶点:FGFR
In Vitro: E7090 inhibits the growth of SNU-16, human gastric cancer cell line harboring FGFR2 amplification with an IC50 value of 3 nM.
E7090 inhibits SNU-16 cell proliferation with an IC50 value of 5.7 nM.
E7090 inhibits proliferation of human cancer cell lines harboring various types of FGFRs gene abnormalities such as amplification, mutation, or translocation in vitro, which are confirmed by the inhibition of FGFR signaling.
E7090 has interaction kinetics with FGFR1 kinases intermediate between those of the two representative inhibitors, and the residence time of E7090 succinate is 19 minutes.
In Vivo: Pharmacodynamics analysis reveals that E7090 inhibits phosphorylation of FGFRs in SNU-16 xenograft tumors in a dose-dependent manner.
E7090 (6.25-50 mg/kg, orally, once daily) treatment prolongs survival in a 4T1 mouse lung metastasis model.
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