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H3B-120

CAS No. 2194903-42-7

H3B-120 ( —— )

产品货号. M26243 CAS No. 2194903-42-7

H3B-120 是一种高选择性、竞争性、变构氨基甲酰磷酸合成酶 1 (CPS1) 抑制剂 (IC50: 1.5 μM; Ki: 1.4 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 ¥3345 有现货
25MG ¥5605 有现货
50MG ¥7979 有现货
100MG ¥10773 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
    H3B-120
  • 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
    H3B-120 是一种高选择性、竞争性、变构氨基甲酰磷酸合成酶 1 (CPS1) 抑制剂 (IC50: 1.5 μM; Ki: 1.4 μM),具有抗癌活性。
  • 产品描述
    H3B-120 is a highly selective, competitive, and allosteric carbamoyl phosphate synthetase 1 (CPS1) inhibitor (IC50: 1.5 μM; Ki: 1.4 μM) with anti-cancer activity.(In Vitro):H3B-120 (25, 50, 75, 100 μM) inhibits urea production in a dose-dependent manner, although the cellular potency decreases significantly compared with enzymatic assays.?The half-life of H3B-120 is only 40 min.?H3B-120 has no inhibition of CPS2 activity of CAD (CPS2, aspartyl transcarbamylase, dihydroorotase).
  • 体外实验
    H3B-120 has no inhibition of CPS2 activity of CAD (CPS2, aspartyl transcarbamylase, dihydroorotase).H3B-120 achieves inhibition by binding to an allosteric pocket situated between the integrating and ATP A domains. H3B-120 (25, 50, 75, 100 μM) inhibits urea production in a dose-dependent manner, although the cellular potency decreases significantly compared with enzymatic assays. The half-life of H3B-120 is only 40 min.
  • 体内实验
    ——
  • 同义词
    ——
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    Akt| p38 MAPK
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    2194903-42-7
  • 分子量
    372.49
  • 分子式
    C19H24N4O2S
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 62.5 mg/mL (167.79 mM)
  • SMILES
    CN(Cc1ccccc1)C(=O)N1CCC(CC1)C(=O)Nc1nc(C)cs1
  • 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.?Bai ZT,?et al. Inhibition of invasion by N-trans-feruloyloctopamine via AKT, p38MAPK and EMT related signals in hepatocellular carcinoma cells. Bioorg Med Chem Lett.?2017 Feb 15;27(4):989-993.
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