• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

Regorafenib hydrochloride

CAS No. 835621-07-3

Regorafenib hydrochloride ( BAY73-4506 hydrochloride )

产品货号. M16096 CAS No. 835621-07-3

Regorafenib hydrochloride (BAY73-4506) is a potent, orally active multikinase inhibitor.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥243 有现货
10MG ¥381 有现货
50MG ¥786 有现货
100MG ¥1191 有现货
200MG 获取报价 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Regorafenib 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
    Regorafenib hydrochloride (BAY73-4506) is a potent, orally active multikinase inhibitor.
  • 产品描述
    Regorafenib hydrochloride (BAY73-4506) is a potent, orally active multikinase inhibitor that potently inhibits endothelial cell kinases in biochemical and cellular kinase phosphorylation assays with nanomolar range (IC50=3-200 nM); inhibits VEGFR1/2/3, PDGFRβ, FGFR1, KIT, RET and B-RAF etc.; exhibits potent dose-dependent TGI in various preclinical human xenograft models in mice.Colon Cancer Approved
  • 同义词
    BAY73-4506 hydrochloride
  • 通路
    Angiogenesis
  • 靶点
    VEGFR
  • 受体
    VEGFR
  • 研究领域
    Cancer
  • 适应症
    Colon Cancer

化学信息

  • CAS Number
    835621-07-3
  • 分子量
    519.28
  • 分子式
    C21H16Cl2F4N4O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO: ≥ 5.6 mg/mL
  • SMILES
    CNC(=O)C1=NC=CC(=C1)OC2=CC(=C(C=C2)NC(=O)NC3=CC(=C(C=C3)Cl)C(F)(F)F)F.Cl
  • 化学全称
    2-Pyridinecarboxamide, 4-[4-[[[[4-chloro-3-(trifluoromethyl)phenyl]amino]carbonyl]amino]-3-fluorophenoxy]-N-methyl-, hydrochloride (1:1)

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. Wilhelm SM, et al. Int J Cancer. 2011 Jul 1;129(1):245-55.
2. Mross K, et al. Clin Cancer Res. 2012 May 1;18(9):2658-67.
3. Abou-Elkacem L, et al. Mol Cancer Ther. 2013 Jul;12(7):1322-31.
产品手册
关联产品
  • Jaceidin

    Jaceidin is a membrane-permeable inhibitor of VEGFR with anti-tumor activities.

  • Sulfatinib (b)

    Sulfatinib (HMPL-012) is a potent, multi-targeted tyrosine kinase inhibitor of VEGFR-1/2/3, FGFR1, CSF1R with IC50 of 2/24/1 nM, 15 nM, 4 nM, respectively.

  • Pazopanib hydrochlor...

    A potent, orally available, pan-VEGFR inhibitor with IC50 of 10, 30, and 47 nM for VEGFR-1, -2, and -3, respectively.