CBL0137 hydrochloride产品图

CBL0137 hydrochloride

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  • ¥700 - 9900
  • MedChemExpress(MCE)已认证
  • 美国
  • HY-18935A
  • 2026年05月21日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      4°C, sealed storage, away from moisture

    • 英文名

      Curaxin-137 hydrochloride; CBL-C137 hydrochloride

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • CAS号

      1197397-89-9

    • 规格

      10 mM * 1 mL/2 mg/5 mg/10 mg/25 mg/50 mg

    规格:10 mM * 1 mL产品价格:¥1231.0
    规格:2 mg产品价格:¥700.0
    规格:5 mg产品价格:¥1500.0
    规格:10 mg产品价格:¥2600.0
    规格:25 mg产品价格:¥5600.0
    规格:50 mg产品价格:¥9900.0

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    CBL0137 hydrochloride

    CAS No. : 1197397-89-9

    MCE 国际站:CBL0137 hydrochloride

    产品活性:CBL0137 hydrochloride 是组蛋白分子伴侣 FACT 的抑制剂。CBL0137 hydrochlorideye 也可以激活 p53 并抑制 NF-κB,对于它们的 EC50 值分别为 0.37 和 0.47 μM。

    研究领域:Apoptosis  |  NF-κB

    作用靶点:MDM-2/p53  |  NF-κB

    In Vitro: Treatment with CBL0137 hydrochloride leads to complete absence of living cells at concentrations above 2.5 μM. CBL0137 hydrochloride causes a greater reduction in the number of colonies formed of not only MiaPaCa-2 cells when combines with gemcitabine, but also gemcitabine-resistant PANC-1 cells. Treatment of human pancreatic cancer cells with CBL0137 hydrochloride results in a dose dependent reduction of protein and mRNA levels of RRM1 and RRM2.

    In Vivo: The CBL0137 hydrochloride monotherapy group and the CBL0137 hydrochloride-gemcitabine combination group samples show large necrotic fields, numerous apoptotic bodies and loss of tumor cells. Sub-optimal doses of 50 to 60 mg/kg CBL0137 hydrochloride causes similar enhancement of gemcitabine antitumor activity as that produced by the maximum tolerated dose (MTD) of 90 mg/kg as indicated by the lack of statistically significant differences among the combination groups. CBL0137 hydrochloride inhibits FACT function through depletion of the pool of active FACT involved in transcription elongation. CBL0137 hydrochloride, given by oral gavage at a nontoxic dose of 30 mg/kg per day on a 5 days on/2 days off schedule, suppresses tumor growth in xenografts of colon (DLD-1), renal cell carcinoma (Caki-1), and melanoma (Mel-7) tumor cell lines and transplanted surgical samples from patients with pancreatic ductal adenocarcinoma.

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