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OTX008

CAS No. 1638140-55-2

OTX008 ( Calixarene 0118;PTX-008 )

产品货号. M12472 CAS No. 1638140-55-2

OTX008 (Calixarene 0118, PTX-008) is a calixarene derivative designed to bind the Galectin-1 (Gal1) amphipathic β-sheet conformation.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
100MG 获取报价 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
    OTX008
  • 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
    OTX008 (Calixarene 0118, PTX-008) is a calixarene derivative designed to bind the Galectin-1 (Gal1) amphipathic β-sheet conformation.
  • 产品描述
    OTX008 (Calixarene 0118, PTX-008) is a calixarene derivative designed to bind the Galectin-1 (Gal1) amphipathic β-sheet conformation; inhibits Gal1 expression and ERK1/2 and AKT-dependent survival pathways, and induces G2/M cell cycle arrest through CDK1; inhibits proliferation and invasion at micromolar concentrations in cancer cells; inhibits growth of A2780-1A9 xenografts in vivo.Solid Tumors Phase 1 Clinical
  • 同义词
    Calixarene 0118;PTX-008
  • 通路
    Cytoskeleton/Cell Adhesion Molecules
  • 靶点
    Galectin
  • 受体
    Galectin
  • 研究领域
    Cancer
  • 适应症
    Solid Tumors

化学信息

  • CAS Number
    1638140-55-2
  • 分子量
    937.18
  • 分子式
    C52H72N8O8
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    ——
  • 化学全称
    Acetamide, 2,2',2'',2'''-[(2-methylpentacyclo[19.3.1.13,7.19,13.115,19]octacosa-1(25),3,5,7(28),9,11,13(27),15,17,19(26),21,23-dodecaene-25,26,27,28-tetrayl)tetrakis(oxy)]tetrakis[N-[2-(dimethylamino)ethyl]-

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. Dings RP, et al. J Med Chem. 2012 Jun 14;55(11):5121-9.
2. Astorgues-Xerri L, et al. Eur J Cancer. 2014 Sep;50(14):2463-77.
3. Dings RP, et al. Cancer Lett. 2008 Jul 8;265(2):270-80.
4. Zucchetti M, et al. Cancer Chemother Pharmacol. 2013 Oct;72(4):879-87.
产品手册
关联产品
  • LLS30

    LLS30 is a potent, allosteric Galectin-1 (Gal-1) inhibitor.

  • OTX008 (b)

    OTX008 (Calixarene 0118, PTX-008) is a calixarene derivative designed to bind the Galectin-1 (Gal1) amphipathic β-sheet conformation.

  • GB1107

    GB1107 (GB-1107, GB 1107) is a potent, selective, orally active inhibitor of Galectin-3 (Gal-3) with Kd of 37 nM (human Galectin-3).