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Tacrolimus

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  • ¥312 - 3169
  • MedChemExpress(MCE)已认证
  • 美国
  • HY-13756
  • 2025年07月16日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      4°C, protect from light

    • 英文名

      FK506; Fujimycin; FR900506

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • CAS号

      104987-11-3

    • 规格

      5 mg/10 mg/50 mg/100 mg/200 mg/500 mg

    规格:5 mg产品价格:¥312.0
    规格:10 mg产品价格:¥500.0
    规格:50 mg产品价格:¥700.0
    规格:100 mg产品价格:¥1250.0
    规格:200 mg产品价格:¥2000.0
    规格:500 mg产品价格:¥3169.0

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    Tacrolimus

    CAS No. : 104987-11-3

    MCE 国际站:Tacrolimus

    产品活性:Tacrolimus (FK506),大环内酯类,与 FK506 结合蛋白 (FKBP) 结合形成复合物并抑制钙调神经磷酸酶 (calcineurin phosphatase),从而抑制 T 淋巴细胞信号转导和 IL-2 转录。具有强免疫抑制特性。

    研究领域:Metabolic Enzyme/Protease  |  Autophagy  |  Apoptosis  |  Immunology/Inflammation  |  Anti-infection

    作用靶点:Phosphatase  |  FKBP  |  Bacterial  |  Autophagy  |  Antibiotic

    In Vitro: Tacrolimus (FK506) inhibits calcium-dependent events, such as IL-2 gene transcription, NO synthase activation, cell degranulation, and apoptosis. Tacrolimus also potentiates the actions of glucocorticoids and progesterone by binding to FKBPs contained within the hormone receptor complex, preventing degradation. The agent may enhance expression of the TGFβ-1 gene in a fashion analogous to that demonstrated for CsA. T cell proliferation in response to ligation of the T cell receptor is inhibited by Tacrolimus. Treatment with a low concentration of Tacrolimus (FK506,10 μg/L) does not significantly affect the proliferation of MH3924A cells (P=0.135). Upon treatment with higher concentrations of Tacrolimus (100-1,000 μg/L), the proliferation of MH3924A cells is significantly enhanced (P<0.01). Treatment with AMD3100 at any concentration (10, 50 or 100 μg/L), has no obvious effect on MH3924A cell proliferation (P>0.05). However, when different concentrations of AMD3100 are combined with 100 μg/L Tacrolimus, the in vitro proliferation of MH3924A cells is increased (P<0.01).

    In Vivo: The therapeutic effect of Tacrolimus is investigated on progression and perpetuation of colitis by administering Tacrolimus to Dextran sulfate sodium (DSS)-treated mice from Days 10 to 16 or to 23. At Days 17 and 24, colon length is significantly shortened, and colon weight is significantly higher in DSS-treated control animals than in normal animals. In addition, colon weight per unit length in the control group is more than twice that in the normal group. While both 7 and 14 d treatment with Tacrolimus significantly suppresses increases in colon weight per unit length in DSS-treated animals compared with the control group, this treatment does not actually restore the colon shortening. In addition, this inhibitory effect of Tacrolimus on increases in colon weight per unit length is more pronounced with 14-d than 7-d treatment, as shown by the inhibitory percentages (59% vs. 28%).

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