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Epertinib hydrochloride

CAS No. 2071195-74-7

Epertinib hydrochloride ( S-22611 hydrochloride )

产品货号. M23929 CAS No. 2071195-74-7

盐酸依帕替尼显示出有效的抗肿瘤活性。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥1729 有现货
10MG ¥2736 有现货
25MG ¥4111 有现货
50MG ¥5794 有现货
100MG ¥7542 有现货
200MG ¥10170 有现货
500MG 获取报价 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥2271 有现货

生物学信息

  • 产品名称
    Epertinib hydrochloride
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    盐酸依帕替尼显示出有效的抗肿瘤活性。
  • 产品描述
    Epertinib hydrochloride shows potent antitumor activity.?Epertinib hydrochloride is a potent, orally active, reversible, and selective tyrosine kinase inhibitor of EGFR, HER2 and HER4, with IC50s of 1.48 nM, 7.15 nM and 2.49 nM, respectively.
  • 体外实验
    Epertinib hydrochloride inhibits the phosphorylation of EGFR and HER2 in NCI-N87 cells, with IC50 values of 4.5 and 1.6 nM, respectively.Epertinib hydrochloride shows inhibitory activity against MDA-MB-361 cell, with an IC50 of 26.5 nM.Epertinib hydrochloride (0-10 μM, 72 h) can selectively inhibit the proliferation of a range of cancer cell lines expressing EGFR and/or HER2. Cell Proliferation Assay Cell Line:NCI-N87 (stomach), BT-474 (breast), SK-BR-3 (breast), MDA-MB-453 (breast), MDA-MB-175VII (breast), HT115 (colon), Calu-3 (lung), fR2 (breast), and MRC-5 (lung) Concentration:0-10 μM Incubation Time:72 h Result:Inhibited the growth of NCI-N87, BT-474, SK-BR-3, MDA-MB-453, MDA-MB-175VII, HT115, Calu-3, fR2, and MRC-5, with IC50 values of 8.3 ± 2.6, 9.9 ± 0.8, 14.0 ± 3.6, 48.6 ± 3.1, 21.6 ± 4.3, 53.3 ± 8.6, 241.5 ± 29.2, 5366.7 ± 65.2, and 4964.6 ± 340.3.
  • 体内实验
    Epertinib hydrochloride (0-100 mg/kg, Orally, once daily for 28 days) shows antitumor activity.Epertinib hydrochloride (50 mg/kg, Orally, once daily for 30 days) significantly reduces the brain tumor volume.Epertinib hydrochloride (0-50 mg/kg, Orally, once daily for 10-28 days) significantly inhibits the tumor growth in a dose-dependent manner. Animal Model:Nude mice (BALB/cAJcl-nu/nu, implanted intracranially with MDA-MB-361 or BR2 cells)Dosage:12.5, 25, 50, 100 ?mg/kg Administration:Orally, once daily for 28 daysResult:Showed antitumor activity in the mammary fat pad implantation model using both cell lines and the ED50 values were comparable (24.1?mg/kg and 26.5?mg/kg for MDA-MB-361 and BR2 (MDA-MB-361-luc-BR2), respectively).Animal Model:Nude mice (BALB/cAJcl-nu/nu, implanted intracranially with MDA-MB-361 or BR2 cells)Dosage:50 mg/kg Administration:Orally, once daily for 30 days Result:Significantly reduced the brain tumor volume, indicating that epertinib could have potent antitumor activity in brain metastasis even in the presence of an intact BTB (blood-tumor barrier).Animal Model:Nude mice (BALB/cAJcl-nu/nu, prepared by subcutaneous implantation of human gastric cancer cells, NCI-N87 into the back of nude mice)Dosage:0, 6.25, 12.5, 25, and 50 mg/kg Administration:Oral gavage, daily for 10-28 days Result:Significantly inhibited the tumor growth in a dose-dependent manner.
  • 同义词
    S-22611 hydrochloride
  • 通路
    Angiogenesis
  • 靶点
    EGFR
  • 受体
    EGFR|HER4|HER2
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    2071195-74-7
  • 分子量
    596.48
  • 分子式
    C30H28Cl2FN5O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO:125 mg/mL (209.56 mM; Need ultrasonic)
  • SMILES
    CC#C/C(=N\OC[C@H]1COCCN1)/C2=CC3=C(C=C2)N=CN=C3NC4=CC(=C(C=C4)OCC5=CC(=CC=C5)F)Cl.Cl
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Tanaka H, et al. Preclinical antitumor activity of S-222611, an oral reversible tyrosine kinase inhibitor of epidermal growth factor receptor and human epidermal growth factor receptor 2. Cancer Sci. 2014 Aug;105(8):1040-8.
产品手册
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