Atrasentan

Atrasentan

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  • $47
  • Alomone
  • ZK-0039505
  • 以色列
  • 2025年11月20日
  • 见官方网站
  • Synthetic
  • 见官方网站
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  • 企业认证

    • 详细信息
    • 技术资料
    • 供应商

      上海再康生物科技有限公司

    • 库存

      大量

    • 靶点

      见官方网站

    • 级别

    • 目录编号

      A-455

    • 克隆性

      多克隆

    • 抗原来源

      Synthetic

    • 保质期

      6个月

    • 抗体英文名

      Atrasentan

    • 抗体名

      Atrasentan

    • 标记物

      见官方网站

    • 宿主

      Synthetic

    • 适应物种

      见官方网站

    • 免疫原

      见官方网站

    • 亚型

      见官方网站

    • 形态

      液体或冻干粉

    • 应用范围

      见官方网站

    • 浓度

      见官方网站

    • 保存条件

      -20°C

    • 规格

      1 mg, 5 mg, 10 mg, 25 mg, 50 mg

    Atrasentan

    (+)-A-127722, A-147627, ABT-627
    A Potent and Selective Antagonist of Endothelin A Receptors
    Cat #: A-455
    Sizes: 1 mg, 5 mg, 10 mg, 25 mg, 50 mg
    Source: Synthetic
    MW: 510.62 Da.
    Target: ET-A receptors
    CLICK HERE TO RECEIVE A 1 mg FREE TRIAL SAMPLE!

    Atrasentan (A-127722), is a synthetic compound that acts as a potent and selective antagonist of endothelin A (ET-A) receptor. Atrasentan is highly selective towards ET-A receptor, exhibiting 1000-fold selectivity over ET-B receptors1. It inhibits endothelin-1 radioligand binding with an IC50 value of 0.36 nM and Endothelin-1-stimulated phosphoinositol hydrolysis with an IC50 of 0.16 nM1.

    ET-A receptors are predominantly detected in peripheral tissues, especially in vascular smooth muscle tissues where they mediate vasoconstriction. They are also expressed in several regions of the brain. ET-A receptor has high affinity for endothelin-1 and endothelin-2 and relatively low affinity for endothelin-3, while the ET-B receptor has equally high affinity for all endothelin isopeptides2.

    Alomone Labs is pleased to offer Atrasentan (#A-455).


    AtrasentanReferences
    1. Winn, M. et al. (1996) J. Med. Chem. 39, 1039.
    2. Saeki, T. et al. (1991) Biochem. Biophys. Res. Commun. 179, 286.
    • Our Bioassay
    • Specifications
    • Related Products
    Our bioassay

    Alomone Labs Atrasentan inhibits ET-A receptor-mediated Ca2+ mobilization in CHO cells.
    Dose response curve of Atrasentan (#A-455) inhibition of ET-A receptor-mediated, Endothelin-1-evoked Ca2+ mobilization. IC50 was determined at 0.124 nM. Cells were loaded with Calcium 6 dye, incubated with Atrasentan, and stimulated with 15 nM Endothelin-1 (EC80). Changes in intracellular Ca2+ levels were detected as changes in maximum relative fluorescence (RLU) using FLIPRTETRA™.
    Purity>98%.
    Effective concentration0.01-10 nM.
    Chemical name(2R,3R,4S)-4-(1,3-benzodioxol-5-yl)-1-[2-(dibutylamino)-2-oxoethyl]-2-(4-methozkphenyl)pyrrolidine-3-carbozklic acid.
    Molecular formulaC29H38N2O6.
    CAS number173937-91-2.
    ActivityAtrasentan is a potent and highly selective antagonist of ET-A endothelin receptors, exhibiting a 1000-fold selectivity for ET-A over ET-B receptors, inhibiting Endothelin-1 radioligand binding with an IC50 of 0.36 nM and Endothelin-1-stimulated phosphoinositol hydrolysis with IC50 of 0.16 nM1.
    Storage before reconstitutionProduct before reconstitution should be stored at -20oC.
    ReconstitutionSoluble in DMSO. Centrifuge all products before use (10000 x g 5 min).
    Storage after reconstitutionUp to three months at -20°C.
     

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