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首页- Products - GPCR/G Protein - Antibacterial - N-Acetyltyramine

N-Acetyltyramine

CAS No. 1202-66-0

N-Acetyltyramine ( —— )

产品货号. M28125 CAS No. 1202-66-0

N-Acetyltyramine is the active compound extracted from a fermentation broth of strain M3-10 which produces quorum-sensing inhibitor (QSI) compound. N-Acetyltyramine inhibits Chromobacterium violaceum ATCC 12472 violacein production and virulence factors, such as pyoverdine production, as well as swarming and twitching motilities, produced by Pseudomonas aeruginosa PAO1.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ￥413 有现货
10MG ￥648 有现货
25MG ￥1077 有现货
50MG ￥1596 有现货
100MG ￥2373 有现货
200MG ￥3548 有现货
500MG ￥5638 有现货
1G 获取报价 有现货
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生物学信息

  • 产品名称
    N-Acetyltyramine
  • 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
    N-Acetyltyramine is the active compound extracted from a fermentation broth of strain M3-10 which produces quorum-sensing inhibitor (QSI) compound. N-Acetyltyramine inhibits Chromobacterium violaceum ATCC 12472 violacein production and virulence factors, such as pyoverdine production, as well as swarming and twitching motilities, produced by Pseudomonas aeruginosa PAO1.
  • 产品描述
    N-Acetyltyramine is the active compound extracted from a fermentation broth of strain M3-10 which produces quorum-sensing inhibitor (QSI) compound. N-Acetyltyramine inhibits Chromobacterium violaceum ATCC 12472 violacein production and virulence factors, such as pyoverdine production, as well as swarming and twitching motilities, produced by Pseudomonas aeruginosa PAO1.(In Vitro):N-Acetyltyramine enhances cytotoxicity of doxorubicin in resistant P388 murine leukemia cells (IC50 = 0.13 μg/ml).
  • 同义词
    ——
  • 通路
    GPCR/G Protein
  • 靶点
    Antibacterial
  • 受体
    Wee1
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    1202-66-0
  • 分子量
    179.2
  • 分子式
    C10H13NO2
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    CC(=O)NCCc1ccc(O)cc1
  • 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.Huang PQ, et al. Discovery of ZN-c3, a Highly Potent and Selective Wee1 Inhibitor Undergoing Evaluation in Clinical Trials for the Treatment of Cancer. J Med Chem. 2021 Sep 9;64(17):13004-13024.
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