2. Protein Tyrosine Kinase/RTK
  3. FGFR
  4. FGFR2/3-IN-2

FGFR2/3-IN-2 (compound 10) 是一种具有口服活性的 FGFR2 和 FGFR3 抑制剂。FGFR2/3-IN-2 抑制 FGFR2 和 FGFR3 的 IC50 值分别为 3.7 nM 和 31.2 nM (预孵育时间 1 h)。FGFR2/3-IN-2 对 FGFR1/4 及其他激酶具有选择性，且在体内不会引起腹泻或血清磷酸盐升高。FGFR2/3-IN-2 在 SNU-16 胃癌模型中能够诱导肿瘤停滞或消退。

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FGFR2/3-IN-2 Chemical Structure

FGFR2/3-IN-2 Chemical Structure

CAS No. : 3025799-28-1

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FGFR2/3-IN-2 相关抗体

Top Publications Citing Use of Products

  • 生物活性

  • 纯度 & 产品资料

生物活性

FGFR2/3-IN-2 (compound 10) is an orally active FGFR2 and FGFR3 inhibitor. FGFR2/3-IN-2 inhibits FGFR2 and FGFR3 with IC50s of 3.7 nM and 31.2 nM (preincubation time 1 h), respectively. FGFR2/3-IN-2 spares FGFR1/4 and other kinases without causing diarrhea and serum phosphate elevation in vivo. FGFR2/3-IN-2 induces tumor stasis or regression in the SNU-16 gastric cancer model[1].

IC50 & Target[1]

FGFR1

140 nM (IC50)

FGFR2

3.7 nM (IC50)

FGFR3

31.2 nM (IC50)

分子量

522.53

Formula

C29H23FN6O3
CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.
纯度 & 产品资料

FGFR2/3-IN-2 相关分类

  • 摩尔计算器

  • 稀释计算器

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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

FGFR2/3-IN-23025799-28-1FGFRFibroblast growth factor receptormetabolic stabilitytumorgastric cancerInhibitorinhibitorinhibit

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