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Acetylcysteine

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  • ¥546
  • LABLEAD
  • A6436
  • 2026年01月10日
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    • 详细信息
    • 询价记录
    • 文献和实验
    • 技术资料
    • 库存

      9999

    • 规格

      5g

    货号:A6436

    储存条件:粉末-20°C可保存3年;液体-80°C可保存12月。

    产品描述

    Acetylcysteine is a thiol-containing antioxidant that has been shown to inhibit the binding activity of NF-κB in response to multiple agonists in various cell types. Preincubation of human umbilical vein endothelial cells with acetylcysteine (0 – 40mM) for 1h dose-dependently inhibited IL-1b-induced monocytic cell adhesion. The IC50 value of acetylcysteine was 20mM, and the 95% inhibition was observed at 40mM. Acetylcysteine treatment also resulted in a reduction in surface expression of E-selectin and VCAM-1 of 56% and 70%, respectively, in endothelial cells. In addition, acetylcysteine promoted long-term survival of serum-deprived PC12 cells with an ED50 value of around 30nM. It dose-dependently prevented internucleosomal DNA cleavage at the doses of 10 – 80mM. The presence of acetylcysteine also promoted the survival of neonatal rat sympathetic neurons. In PC12 cells, the thymidine incorporation and proliferation were almost completely blocked by 60mM acetylcysteine with an ED50 value of approximately 30mM. Administration of SAMP8 mice with acetylcysteine (100mg/kg, once daily, s.c.) for four weeks improved their cognition in both the T‐maze footshock avoidance paradigm and the lever press appetitive task when compared to mice treated with saline.

    作用机制

    Acetylcysteine is a thiol and mucolytic agent that acts as an antioxidant by maintaining the balance of intracellular glutathione. The free sulfhydryl group allows acetylcysteine to reduce disulphide bonds, thereby decreasing mucus viscosity and facilitating mucociliary clearance.

    产品信息

    CAS号

    616-91-1

    分子式

    C5H9NO3S

    分子

    163.19

    溶解度

     

    DMSO

    30.0 mg/mL (183.8 mM)

    Water

    30.0 mg/mL (183.8 mM)

    Ethanol

    30.0 mg/mL (183.8 mM)

     

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    相关实验
    • In Vitro Drug Metabolism: Thiol Conjugation

      , the structures of these intermediates often can be deduced by analysis of the corresponding glutathione or N -acetylcysteine conjugates. A practical approach in this regard, therefore, is to screen drug candidates in vitro for the formation of reactive

    • In Vitro Screening for Antioxidant Activity

      in triggering pathophysiological change (6 ). Increased levels of these compounds may respond to α-tocopherol, glutathione (GSH), phytonutrients like carotenoids and flavonoids, ascorbate, coenzyme Q10 (ubiquinone), N-acetylcysteine, transresveratol in red wine

    • 类器官培养与应用——肝类器官

      - 0.2% 0.2% - - - - - -   HEPES - - - - - - 10mM 10mM 10mM   N2 - - - - - - 1× 1× 1×   N-Acetylcysteine - - - - - - 1mM 1mM 1mM   Leu15-Gastrin I human

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