生物活性 靶点 体外研究 体内研究
ChemicalBook  CAS数据库列表  6-methyl-1,3,8-trichlorodibenzofuran

6-methyl-1,3,8-trichlorodibenzofuran

6-methyl-1,3,8-trichlorodibenzofuran,115039-00-4,结构式
6-methyl-1,3,8-trichlorodibenzofuran
  • CAS号:115039-00-4
  • 英文名:6-methyl-1,3,8-trichlorodibenzofuran
  • 中文名:6-methyl-1,3,8-trichlorodibenzofuran
  • CBNumber:CB81333417
  • 分子式:
  • 分子量:0
  • MOL File:115039-00-4.mol

6-methyl-1,3,8-trichlorodibenzofuran性质、用途与生产工艺

  • 生物活性 AhR modulator-1 (compound 6-MCDF) 是一种选择性的口服活性芳烃受体 (AhR) 调节剂。AhR modulator-1 部分地通过在肿瘤形成之前抑制前列腺 VEGF 的产生而抑制肿瘤转移。AhR modulator-1 在大鼠子宫中也具有抗雌激素特性。
  • 靶点

    Aryl hydrocarbon receptor (AhR)
    Prostatic VEGF
    Estrogenic

  • 体外研究

    AhR modulator-1 (6-MCDF; 0.1-10 μM; 48-96 hours; ASPC-1 cells) treatment exhibits dose-dependent growth inhibitory effects with growth inhibitory effects of 26, 43 and 99% at concentrations of 0.1, 1 and 10 μM, respectively.

    Cell Proliferation Assay

    Cell Line: ASPC-1 cells
    Concentration: 0.1 μM, 1 μM and 10 μM
    Incubation Time: 48 hours, 72 hours, 96 hours
    Result: Exhibited dose-dependent growth inhibitory effects.
  • 体内研究

    AhR modulator-1 (6-MCDF; 0-40 mg/kg; oral administration; daily; for 12 weeks; C57BL/6-Tg(TRAMP)8247Ng/J mice) treatment reduces the frequency of pelvic lymph node metastasis in mice fed the 40 mg/kg diet. And serum VEGF concentrations are also reduced. Prostate tumor incidence and size are not significantly reduced.

    Animal Model: C57BL/6-Tg(TRAMP)8247Ng/J (TRAMP) mice (8-week-old)
    Dosage: 0 mg/kg, 10 mg/kg, 40 mg/kg
    Administration: Oral administration; daily; for 12 weeks
    Result: The frequency of pelvic lymph node metastasis was reduced 5-fold in mice fed the 40 mg /kg diet.S erum VEGF concentrations were also reduced.
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6-methyl-1,3,8-trichlorodibenzofuran生产厂家
  • 公司名称:TargetMol Chemicals Inc.
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  • 公司名称:MedChemExpress
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  • 国家:美国
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