Cholestyramine

Cholestyramine

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  • ¥500 - 600
  • MedChemExpress(MCE)已认证
  • 美国
  • HY-104081
  • 2025年07月06日
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    • 详细信息
    • 技术资料
    • 保存条件

      Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.

    • 英文名

      Cholestyramine resin; Colestyramine

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • CAS号

      11041-12-6

    • 规格

      500 mg/1 g

    规格:500 mg产品价格:¥500.0
    规格:1 g产品价格:¥600.0

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    Cholestyramine

    CAS No. : 11041-12-6

    MCE 国际站:Cholestyramine

    产品活性:Cholestyramine (Colestyramine) 是胆汁酸结合树脂,它可以抑制肠胆汁酸吸收导致增加粪便胆汁酸排泄,进而又增加胆固醇胆汁酸合成。

    研究领域:Others

    作用靶点:Others

    In Vitro: Cholestyramine (0.1-50 μg/mL) produced the most dramatic results after a 24-hour exposure; an efflux rate of 65% compared with control cells. Cholestyramine is an anion-exchange resin and is insoluble in water. alcohol, chloro-form, and ether. For the assay, cholestyramine is initially wetted with a small amount of DMSO further diluting with media. A blank sample prepared with dimethylsulfoxide DMSO without cholestyramine displayed no differences from the control samples.

    In Vivo: Cholestyramine is a bile acid binding resin and can inhibit intestinal bile acid absorption which results in the? increasing bile acid synthesis from cholesterol. Results reveal that GSPE treatment alone, and co-administration with Cholestyramine, regulate BA, cholesterol and TG metabolism differently compare to Cholestyramine administration alone. Notably, GSPE decreases intestinal apical sodium-dependent bile acid transporter (Asbt) gene expression, while Cholestyramine significantly induces expression. Administration with GSPE or Cholestyramine robustly induces hepatic BA biosynthetic gene expression, especially cholesterol 7α-hydroxylase (Cyp7a1), compare to control, while co-administration further enhances expression. Treatment with Cholestyramine induces both intestinal and hepatic cholesterologenic gene expression, while co-administration with GSPE attenuates the Cholestyramine-inducing increase in the liver but not in the intestine. Cholestyramine also induces hepatic lipogenic gene expression, which is attenuated by co-administration with GSPE.

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