• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号
首页- Products - Chromatin/Epigenetic - Histone Demethylase - Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate

Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate

CAS No. 303141-21-1

Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate ( DC-S239 )

产品货号. M28480 CAS No. 303141-21-1

Ethyl 2-amino-4-methyl-5-[(3-硝基苯基)carbamoyl]thiophene-3-carboxylate 是组蛋白甲基转移酶 SETD7 的选择性抑制剂 (IC50 = 4.59 μM),具有抗癌活性。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥2001 有现货
10MG ¥3216 有现货
25MG ¥5370 有现货
50MG ¥7655 有现货
100MG ¥10368 有现货
500MG ¥20817 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate
  • 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
    Ethyl 2-amino-4-methyl-5-[(3-硝基苯基)carbamoyl]thiophene-3-carboxylate 是组蛋白甲基转移酶 SETD7 的选择性抑制剂 (IC50 = 4.59 μM),具有抗癌活性。
  • 产品描述
    Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate is a selective inhibitor of histone methyltransferase SETD7 (IC50 = 4.59 μM) with anticancer activity.(In Vitro):Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate (0-100 μM) inhibits the proliferation of MCF7, HL60 and MV4-11 cells in a dose-dependent manner with the IC50 values of 10.93 μM and 16.43 μM, respectively. Ethyl 2-amino-4-methyl-5-[(3-nitrophenyl)carbamoyl]thiophene-3-carboxylate inhibits DNMT1, DOT1L, EZH2, NSD1, SETD8 and G9a by less than 45%, whereas it inhibits SET7 by 90% at concentrations of 100 μM.
  • 体外实验
    DC-S239 inhibits DNMT1, DOT1L, EZH2, NSD1, SETD8 and G9a by less than 45%, while it inhibits SET7 by 90% at concentrations of 100 μM.DC-S239 (0-100 μM, 120 h) can inhibit the proliferation of MCF7, HL60 and MV4-11 cells in a dose-dependent manner but no significant effect on the activity of HCT116 and DHL4 cells.Cell Viability Assay Cell Line:MCF7, HL60, DHL4, MV4-11 and HCT116 cell lines Concentration:0-100 μM Incubation Time:120 h Result:Inhibited MCF7 and HL60 with the IC50 values of 10.93 μM and 16.43 μM, respectively.
  • 体内实验
    ——
  • 同义词
    DC-S239
  • 通路
    Chromatin/Epigenetic
  • 靶点
    Histone Demethylase
  • 受体
    D1
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    303141-21-1
  • 分子量
    349.36
  • 分子式
    C15H15N3O5S
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 125 mg/mL (357.80 mM)
  • SMILES
    CCOC(c1c(N)sc(C(Nc2cc([N+]([O-])=O)ccc2)=O)c1C)=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

产品手册
关联产品
  • PF-06821497

    PF-06821497 是一种 EZH2 选择性抑制剂,具有显着的肿瘤生长抑制作用。

  • Zavondemstat

    Zavondemstat (QC8222; TACH 101) 是一种组蛋白赖氨酸脱甲基酶 4D (KDM4D) 抑制剂,具有抗肿瘤活性。

  • KHK-IN-2

    KHK-IN-2 是一种选择性、有效的酮己糖激酶 (KHK) 抑制剂,IC50 为 0.45 μM。