生物活性 靶点 体外研究 体内研究
ChemicalBook  CAS数据库列表  (-)-反式-3-(3,4-亚甲基二氧基苄基)-2-(3,4,5-三甲氧基苄基)丁内酯

(-)-反式-3-(3,4-亚甲基二氧基苄基)-2-(3,4,5-三甲氧基苄基)丁内酯

(-)-反式-3-(3,4-亚甲基二氧基苄基)-2-(3,4,5-三甲氧基苄基)丁内酯,40456-50-6,结构式
(-)-反式-3-(3,4-亚甲基二氧基苄基)-2-(3,4,5-三甲氧基苄基)丁内酯
  • CAS号:40456-50-6
  • 英文名:(3R)-3α-(3,4,5-Trimethoxybenzyl)-4β-(1,3-benzodioxole-5-ylmethyl)tetrahydrofuran-2-one
  • 中文名:(-)-反式-3-(3,4-亚甲基二氧基苄基)-2-(3,4,5-三甲氧基苄基)丁内酯
  • CBNumber:CB22190075
  • 分子式:C22H24O7
  • 分子量:400.42
  • MOL File:40456-50-6.mol
(-)-反式-3-(3,4-亚甲基二氧基苄基)-2-(3,4,5-三甲氧基苄基)丁内酯化学性质
  • 沸点 :564.9±45.0 °C(Predicted)
  • 密度 :1.266±0.06 g/cm3(Predicted)
  • 储存条件 :Store at -20°C
  • 溶解度 :Soluble in DMSO
  • 形态 :A solid

(-)-反式-3-(3,4-亚甲基二氧基苄基)-2-(3,4,5-三甲氧基苄基)丁内酯性质、用途与生产工艺

  • 生物活性 Yatein 是从 A. chilensis 中提取的木质素,具有抗增殖活性。Yatein 能通过中断立早基因的表达,抑制单纯疱疹病毒 1 型 (HSV-1) 的复制。
  • 靶点

    HSV-1

  • 体外研究

    Yatein induces cell-cycle arrest at G2/M phase (5 μM; 24 hours) and enhances G2/M phase-related protein expression (5 μM; 6-12 hours) in human lung adenocarcinoma A549 and CL1-5 cells.
    Yatein (5 μM; 6-12 hours) induces DNA damage through activation of the ATM/ATR pathway in human A549 and CL1-5 cells.
    Yatein (5 μM; 6 hours) affects microtubule dynamics by inhibiting tubulin polymerization.

    Cell Viability Assay

    Cell Line: A549 cells, CL1-5 cells
    Concentration: 1.25 μM , 2.5 μM , 5 μM
    Incubation Time: 24 hours
    Result: Induced cell-cycle arrest at G2/M phase in both cell lines.

    Cell Viability Assay

    Cell Line: A549 cells, CL1-5 cells
    Concentration: 5 μM
    Incubation Time: 6 hours, 12 hours
    Result: Upregulated the expression of cyclin B1, but not Cdc2 and Cdc25c, induced Cdc2 phosphorylation.
  • 体内研究

    Yatein (20 mg/kg; i.p.; five times per week; for 42 days) exhibits in vivo antitumor effects in a human lung adenocarcinoma xenograft mouse model.

    Animal Model: Male NOD/SCID mice (6-8 weeks), with A549 cells xenograft
    Dosage: 20 mg/kg
    Administration: Intraperitoneal injection, five times per week, for 42 days
    Result: Significantly slowed tumor growth and moderately increased both cyclin B1 expression and Cdc2 phosphorylation.
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