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Piperlongumine荜茇酰胺,20069-09-4

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  • ¥275 - 1775
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  • 美国
  • HY-N2329
  • 2025年12月05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

      Piplartine

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • CAS号

      20069-09-4

    • 规格

      10 mM * 1 mL/5 mg/10 mg/25 mg/50 mg/100 mg

    规格:10 mM * 1 mL产品价格:¥302.0
    规格:5 mg产品价格:¥275.0
    规格:10 mg产品价格:¥500.0
    规格:25 mg产品价格:¥750.0
    规格:50 mg产品价格:¥1184.0
    规格:100 mg产品价格:¥1775.0

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    Piperlongumine

    CAS No. : 20069-09-4

    MCE 国际站:Piperlongumine

    产品活性:Piperlongumine 是一种生物碱,具有抗炎、抗菌、抗血管生成、抗氧化、抗肿瘤和抗糖尿病等活性。在肿瘤细胞中,Piperlongumine 能够诱导 ROS 和凋亡。Piperlongumine 具有抗心肌纤维化的作用,通过抑制 ERK1/2 信号通路抑制肌成纤维细胞的转化。Piperlongumin 可用于迁移体的研究。

    研究领域:MAPK/ERK Pathway  |  Stem Cell/Wnt  |  Immunology/Inflammation  |  NF-κB  |  Metabolic Enzyme/Protease  |  Autophagy  |  Apoptosis  |  Anti-infection

    作用靶点:ERK  |  Reactive Oxygen Species  |  Autophagy  |  Apoptosis  |  Bacterial  |  Ferroptosis

    In Vitro: Piplartine (5, 10, and 15 μM) significantly decreases cell proliferation of 786-O, SKBR3, Panc1, A549, and L3.6pL cancer cells after treatment for 24 and 48 hours, induces apoptosis and ROS in these cell lines at 5 and 10 μM after 3 or 9 h of treatment.
    ?Piplartine (5 or 10 μM) induces cleaved PARP and downregulates Sp1, Sp3, Sp4, and Sp-regulated genes.
    ?Piplartine (20 μM) decreases the viability of cardiac fibroblasts (CFs). Piplartine (0-10 μM) suppresses myofibroblast transformation via suppression of the ERK1/2 signaling pathway.

    In Vivo: Piperlongumine (30 mg/kg/day, i.p. for 3 weeks) exhibits potent anti-tumor effect in athymic nude mice bearing L3.6pL cells without body weight loss.

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    Piperlongumine荜茇酰胺,20069-09-4
    ¥275 - 1775