• 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 - Others - Other Targets - Thymidylate Kinase Inhibitor, YMU1

Thymidylate Kinase Inhibitor, YMU1

CAS No. 902589-96-2

Thymidylate Kinase Inhibitor, YMU1 ( —— )

产品货号. M24937 CAS No. 902589-96-2

YMU1 is a human thymidylate kinase (hTMPK) inhibitor. YMU1 stabilizes the conformation of ligand-induced degradation (LID) region of hTMPK and blocks the catalytic site or ATP-binding site.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥583 有现货
10MG ¥915 有现货
25MG ¥1847 有现货
50MG ¥2973 有现货
100MG ¥4787 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
    Thymidylate Kinase Inhibitor, YMU1
  • 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
    YMU1 is a human thymidylate kinase (hTMPK) inhibitor. YMU1 stabilizes the conformation of ligand-induced degradation (LID) region of hTMPK and blocks the catalytic site or ATP-binding site.
  • 产品描述
    YMU1 is a human thymidylate kinase (hTMPK) inhibitor. YMU1 stabilizes the conformation of ligand-induced degradation (LID) region of hTMPK and blocks the catalytic site or ATP-binding site.
  • 同义词
    ——
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    hTMPK
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    902589-96-2
  • 分子量
    378.5
  • 分子式
    C17H22N4O4S
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO:10 mM
  • SMILES
    CCOC(=O)N1CCN(CC1)C(=O)CN2C(=O)C3=C(S2)N=C(C=C3C)C
  • 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.Dong B , Jaeger A M , Hughes P F , et al. Targeting therapy-resistant prostate cancer via a direct inhibitor of the human heat shock transcription factor 1[J]. Science Translational Medicine, 2020, 12(574):eabb5647.
产品手册
关联产品
  • Thiorphan

    Thiorphan is an ?neprilysin ?inhibitor?(NEP;?IC50 : 0.007 μM).

  • Bacopaside N2

    Bacopaside N2 is a natural product.

  • Cetrorelix

    Cetrorelix Acetate is gonadotropin-releasing hormone?(GnRH)?receptor antagonist with an?IC50?of 1.21 nM.