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FIIN-3,1637735-84-2

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  • ¥700 - 5350
  • MedChemExpress(MCE)已认证
  • 美国
  • HY-18603
  • 2025年12月05日
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    • 详细信息
    • 技术资料
    • 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

    • CAS号

      1637735-84-2

    • 规格

      10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg

    规格:10 mM * 1 mL产品价格:¥2282.0
    规格:1 mg产品价格:¥700.0
    规格:5 mg产品价格:¥1500.0
    规格:10 mg产品价格:¥2550.0
    规格:25 mg产品价格:¥5350.0

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    FIIN-3

    CAS No. : 1637735-84-2

    MCE 国际站:FIIN-3

    产品活性:FIIN-3 是 FGFR 的不可逆抑制剂,对FGFR1,FGFR2,FGFR3和FGFR4的IC50 值分别为13.1,21,31.4和35.3 nM。

    研究领域:JAK/STAT Signaling  |  Protein Tyrosine Kinase/RTK

    作用靶点:EGFR  |  FGFR

    In Vitro: FIIN-3 potently inhibits both WT FGFRs (EC50 in the 1- to 41-nM range) and the gatekeeper mutant of FGFR2 (EC50 of 64 nM). FIIN-3 also strongly inhibits EGFR, with an EC50 of 43 nM. FIIN-3 shows good potency against gatekeeper mutant V564F; FIIN-3 also is potent against the gatekeeper-plus-1 mutant E565K; FIIN-3 also displays antiproliferative activity (with an EC50 of 135 nM) against Ba/F3 cells transformed by the EGFR vIII fusion protein, which has a WT EGFR kinase domain. FIIN-3 shows even better activity against EGFR mutant L858R (EC50 of 17 nM) and moderate activity, displaying an EC50 of 231 nM, against the EGFR mutant L858R/T790M mutant. In WT FGFR2 Ba/F3 cells, FIIN-3 completely inhibits the FGFR2 autophosphorylation on Tyr656/657 at concentrations as low as 3 nM. In FGFR2 V564M Ba/F3 cells, FIIN-3 is capable of inhibiting the FGFR2 mutant V564M autophosphorylation with partial inhibition at 100 nM and complete inhibition observed at 300 nM.

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