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FEN1 Inhibitor C2

CAS No. 1995893-58-7

FEN1 Inhibitor C2 ( FEN1-IN-4 )

产品货号. M22114 CAS No. 1995893-58-7

FEN1-IN-4 是人皮瓣核酸内切酶 1 (hFEN1) 的抑制剂。FEN1 抑制剂 C2 抑制选择性损害缺乏 Cdc4 和 Mre11a 的结肠癌细胞的增殖,这两种细胞在结直肠癌中经常发生突变。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥462 有现货
5MG ¥721 有现货
10MG ¥1158 有现货
25MG ¥2049 有现货
50MG ¥3216 有现货
100MG ¥4965 有现货
200MG 获取报价 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    FEN1 Inhibitor C2
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    FEN1-IN-4 是人皮瓣核酸内切酶 1 (hFEN1) 的抑制剂。FEN1 抑制剂 C2 抑制选择性损害缺乏 Cdc4 和 Mre11a 的结肠癌细胞的增殖,这两种细胞在结直肠癌中经常发生突变。
  • 产品描述
    FEN1-IN-4 is an inhibitor of human flap endonuclease-1 (hFEN1)FEN1 Inhibitor C2 inhibition selectively impairs proliferation of colon cancer cells deficient in Cdc4 and Mre11a, both frequently mutated in colorectal cancers.?FEN1 has also emerged as a potential chemosensitizing target due to its role in LP-BER since it is critical for repair of MMS (methyl methanesulfonate)-induced alkylation damage, and its knockdown or inhibition increases sensitivity to TMZ (temozolomide) in glioblastoma and colorectal cancer cell lines.
  • 体外实验
    FEN1 inhibition selectively impairs proliferation of colon cancer cells deficient in Cdc4 and Mre11a, both frequently mutated in colorectal cancers. FEN1 has also emerged as a potential chemosensitizing target due to its role in LP-BER since it is critical for repair of Methyl methanesulfonate-induced alkylation damage, and its knockdown or inhibition increases sensitivity to Temozolomide in glioblastoma and colorectal cancer cell lines.
  • 体内实验
    ——
  • 同义词
    FEN1-IN-4
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    hFEN1
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    1995893-58-7
  • 分子量
    232.24
  • 分子式
    C12H12N2O3
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO:100 mg/mL (430.59 mM; Need ultrasonic)
  • SMILES
    On1c(=O)n(CC2CC2)c2ccccc2c1=O
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Jack C Exell, et al. Cellularly Active N-hydroxyurea FEN1 Inhibitors Block Substrate Entry to the Active Site. Nat Chem Biol. 2016 Oct;12(10):815-21.
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