DMH-1,1206711-16-1

DMH-1,1206711-16-1

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  • ¥246 - 4520
  • MedChemExpress(MCE)已认证
  • 美国
  • HY-12273
  • 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.

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • CAS号

      1206711-16-1

    • 规格

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

    规格:10 mM * 1 mL产品价格:¥957.0
    规格:1 mg产品价格:¥246.0
    规格:5 mg产品价格:¥543.0
    规格:10 mg产品价格:¥870.0
    规格:25 mg产品价格:¥1820.0
    规格:50 mg产品价格:¥2910.0
    规格:100 mg产品价格:¥4520.0

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    DMH-1

    CAS No. : 1206711-16-1

    MCE 国际站:DMH-1

    产品活性:DMH-1 是一种有效的,具有选择性的 BMP 抑制剂,对 ALK1/ALK2/ALK3/ALK6的IC50 值分别为 27/107.9/<5/47.6 nM。

    研究领域:Autophagy  |  TGF-beta/Smad

    作用靶点:Autophagy  |  TGF-β Receptor

    In Vitro: DMH-1 (0.5 μM) induces regulation of OCT4, Nanog, and PAX6 protein expression. DMH-1 significantly reduces the percentage of cells expressing the pluripotency marker proteins OCT4 and Nanog in both SM3 and CA6 cells. PAX6 expression is significantly up-regulated by day 5 and day 7 in CA6 and SM3 cells, respectively. DMH-1 induces regulation of pluripotency and neural precursor marker mRNAs. PAX6 can regulate the expression of SOX1 independently by manipulating the DMH-1 concentration during the neural induction of hiPSCs. DMH-1 (5 μM and 10 μM) inhibits CDDP-induced autophagy in HeLa cells and enhances the ability of CDDP to reduce HeLa cell viability, inhibits tamoxifen-induced autophagy in MCF-7 cells and enhances the ability of Tamoxifen (HY-13757A) to reduce MCF-7 cell viability, inhibits 5-FU-induced autophagy in both MCF-7 and HeLa cells but does not affect the inhibitory effects of 5-FU on MCF-7 and HeLa cell viability. DMH-1 enhances the apoptotic induction effects of CDDP on HeLa cells after 24 h treatment. DMH-1 inhibits HeLa and MCF-7 cell proliferation. DMH-1 (20 μM) reduces the canonical phosphorylation of Smads 1,5 and 9. DMH-1 in combination with Cisplatin significantly decreases Ki-67 positive staining in the OVCAR8 cells. DMH-1 (20 μM) upregulates JAG1, reduces CYP1B1 and increases HAPLN1 expression in both OVCAR8 and NCI-RES cells.

    In Vivo: DMH1 (5 mg/kg, i.p.) treatment significantly reduces the tumor growth in human lung cancer xenograft model.

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