生物活性 靶点 体外研究 3-[1-[3-(1H-咪唑-1-基)丙基]-1H-吲哚-3-基]-4-(苯氨基)-1H-吡咯-2,5-二酮 试剂级价格
ChemicalBook  CAS数据库列表  3-[1-[3-(1H-咪唑-1-基)丙基]-1H-吲哚-3-基]-4-(苯氨基)-1H-吡咯-2,5-二酮

3-[1-[3-(1H-咪唑-1-基)丙基]-1H-吲哚-3-基]-4-(苯氨基)-1H-吡咯-2,5-二酮

3-[1-[3-(1H-咪唑-1-基)丙基]-1H-吲哚-3-基]-4-(苯氨基)-1H-吡咯-2,5-二酮,257879-35-9,结构式
3-[1-[3-(1H-咪唑-1-基)丙基]-1H-吲哚-3-基]-4-(苯氨基)-1H-吡咯-2,5-二酮
  • CAS号:257879-35-9
  • 英文名:PKCβ Inhibitor
  • 中文名:3-[1-[3-(1H-咪唑-1-基)丙基]-1H-吲哚-3-基]-4-(苯氨基)-1H-吡咯-2,5-二酮
  • CBNumber:CB12628270
  • 分子式:C24H21N5O2
  • 分子量:411.46
  • MOL File:257879-35-9.mol
3-[1-[3-(1H-咪唑-1-基)丙基]-1H-吲哚-3-基]-4-(苯氨基)-1H-吡咯-2,5-二酮化学性质
  • 溶解度 :DMF: 10 mg/ml; DMSO: 10 mg/ml; Ethanol: 1 mg/ml; PBS (pH 7.2): 0.25 mg/ml
  • 形态 :A solid
  • 颜色 :Yellow to orange

3-[1-[3-(1H-咪唑-1-基)丙基]-1H-吲哚-3-基]-4-(苯氨基)-1H-吡咯-2,5-二酮性质、用途与生产工艺

  • 生物活性 PKCβ inhibitor 1 是有效的,ATP 竞争性和选择性 PKCβ 抑制剂,对人 PKCβ1 和 PKCβ2 的 IC50 分别为 21 和 5 nM。与 PKCβ2 相比,PKCβ inhibitor 1 对其他 PKC 同工酶 (PKCα、PKCγ 和 PKCε) 具有 60 倍以上的选择性。
  • 靶点

    human PKCβ1

    21 nM (IC 50 )

    human PKCβ2

    5 nM (IC 50 )

    PKCα

    331 nM (IC 50 )

  • 体外研究

    PKCβ inhibitor 1 (0-30 μM; 48 hours) suppresses tumor cell proliferation in a time- and dose-dependent manner.
    PKCβ inhibitor 1 (14 μM; 2-48 hours) induces apoptosis in 2F7 cells.
    PKCβ inhibitor 1 (15 μM; 2-48 hours) inhibits cell cycle progression in 2F7 and BCBL-1 cells.
    PKCβ (15 or 14 μM, respectively; 2-48 hours) inhibitor 1 reduces the expression of phospho-PKCβ in BCBL-1 and 2F7 cells.
    PKCβ inhibitor 1(0-48 hours) suppresses GSK3β, mTOR, and S6 phosphorylation.

    Cell Proliferation Assay

    Cell Line: 2F7, BCBL-1 cells
    Concentration: 0, 5, 10, 20, and 30 μM
    Incubation Time: 48 hours
    Result: A dose-dependent reduction in viability of the 2F7 and BCBL-1 cells starting at 5 μM and increasing with elevated inhibitor concentration.

    Apoptosis Analysis

    Cell Line: 2F7 cells
    Concentration: 14 μM
    Incubation Time: 2-48 hours
    Result: Apoptotic induction in 2.1% of the 2F7 cells above background after 2 hours of treatment, increasing through 48 hours of treatment.

    Cell Cycle Analysis

    Cell Line: BCBL-1 Cells
    Concentration: 15 μM (the IC 50 )
    Incubation Time: 2-48 hours
    Result: Inhibits cell cycle progression in 2F7 and BCBL-1 cells.

    Western Blot Analysis

    Cell Line: BCBL-1 and 2F7 cell lines
    Concentration: 15 or 14 μM (at the IC 50 respectively)
    Incubation Time: 2-48 hours
    Result: The expression of phospho-PKCβ in BCBL-1 and 2F7 cells reduced.
3-[1-[3-(1H-咪唑-1-基)丙基]-1H-吲哚-3-基]-4-(苯氨基)-1H-吡咯-2,5-二酮上下游产品信息
上游原料
下游产品
3-[1-[3-(1H-咪唑-1-基)丙基]-1H-吲哚-3-基]-4-(苯氨基)-1H-吡咯-2,5-二酮 试剂级价格
  • 更新日期:2024/11/08
  • 产品编号:HY-13335
  • 产品名称:3-[1-[3-(1H-咪唑-1-基)丙基]-1H-吲哚-3-基]-4-(苯氨基)-1H-吡咯-2,5-二酮 PKCβ inhibitor 1
  • CAS编号:257879-35-9
  • 包装:500μg
  • 价格:1100元
  • 更新日期:2024/11/08
  • 产品编号:HY-13335
  • 产品名称:3-[1-[3-(1H-咪唑-1-基)丙基]-1H-吲哚-3-基]-4-(苯氨基)-1H-吡咯-2,5-二酮 PKCβ inhibitor 1
  • CAS编号:257879-35-9
  • 包装:1mg
  • 价格:1800元
3-[1-[3-(1H-咪唑-1-基)丙基]-1H-吲哚-3-基]-4-(苯氨基)-1H-吡咯-2,5-二酮生产厂家
  • 公司名称:ChemeGen 中国
  • 联系电话: 18818260767
  • 电子邮件:sales@chemegen.com
  • 国家:中国
  • 产品数:11217
  • 优势度:58