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ACY-775,1375466-18-4

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  • MedChemExpress(MCE)已认证
  • 美国
  • HY-19328
  • 2025年12月05日
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    • 详细信息
    • 文献和实验
    • 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.

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • CAS号

      1375466-18-4

    • 规格

      10 mM * 1 mL/5 mg/10 mg/25 mg

    规格:10 mM * 1 mL产品价格:¥1287.0
    规格:5 mg产品价格:¥1170.0
    规格:10 mg产品价格:¥1950.0
    规格:25 mg产品价格:¥4030.0

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    ACY-775

    CAS No. : 1375466-18-4

    MCE 国际站:ACY-775

    产品活性:ACY-775 是一个有效的,选择性强的组蛋白脱乙酰酶 6 (HDAC6) 抑制剂 IC50 值为 7.5  nM。ACY775 还抑制 MBLAC2

    研究领域:Cell Cycle/DNA Damage  |  Epigenetics

    作用靶点:HDAC

    In Vitro: In vehicle-treated cells, α-tubulin is mainly presented in the deacetylated form, while histone 3 is clearly acetylated. Upon treatment with ACY-775, a clear enhancement of the acetylation of α-tubulin is visible, while histone acetylation remains unaltered. Acetylation of α-tubulin is visualized by immunofluorescence and the intensity in the neurites of the neurons is quantified and normalized to the length of the fluorescent signal. In vehicle-treated DRG neurons, acetylated α-tubulin is already present. Upon treatment with ACY-775 the signal intensity of acetylated α-tubulin increases significantly. Significant increase in motility of mitochondria and also the total number of mitochondria within the neurites are observed compare with vehicle-treated DRG neurons. A significantly higher number of retrogradely transport mitochondria is observed in DRG neurons treated with ACY-775 compare with vehicle-treated cells.

    In Vivo: Biodistribution profiles of ACY-738, ACY-775, and tubastatin A are examined after acute dosing at 5 or 50 mg/kg over 2 h. At t=30 min after acute 50 mg/kg injection, respective plasma levels of ACY-738 and ACY-775 are 515 ng/mL (1.9 μM) and 1359 ng/mL (4.1 μM). Elimination from plasma is rapid, with plasmatic half-life of 12 min and concentration below 10 ng/mL after 2 h. Nevertheless, areas under concentration time curves for brain and plasm calculated over 2 h for both ACY-738 and ACY-775 lead to ratios >1. When ACY-738 (5 mg/kg) or ACY-775 (50 mg/kg) are administered repeatedly in wild-type mice at 24 h, 4 h, and 30 min before killing, significant increases in α-tubulin acetylation are observed in all tested brain regions.

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