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首页- Products - Others - Other Targets - Thalidomide-O-amido-PEG2-C2-NH2 TFA

Thalidomide-O-amido-PEG2-C2-NH2 TFA

CAS No. 1957235-75-4

Thalidomide-O-amido-PEG2-C2-NH2 TFA ( Cereblon Ligand-Linker Conjugates 10 TFA; E3 Ligase Ligand-Linker Conjugates 24 TFA )

产品货号. M26947 CAS No. 1957235-75-4

Thalidomide-O-amido-PEG2-C2-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 2-unit PEG linker used in PROTAC technology.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥729 有现货
10MG ¥1069 有现货
25MG ¥1798 有现货
50MG ¥2665 有现货
100MG ¥3993 有现货
200MG ¥6043 有现货
500MG ¥14013 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Thalidomide-O-amido-PEG2-C2-NH2 TFA
  • 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
    Thalidomide-O-amido-PEG2-C2-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 2-unit PEG linker used in PROTAC technology.
  • 产品描述
    Thalidomide-O-amido-PEG2-C2-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and 2-unit PEG linker used in PROTAC technology.(In Vitro):PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
  • 同义词
    Cereblon Ligand-Linker Conjugates 10 TFA; E3 Ligase Ligand-Linker Conjugates 24 TFA
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    H2 receptor
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    1957235-75-4
  • 分子量
    576.5
  • 分子式
    C23H27F3N4O10
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    OC(=O)C(F)(F)F.NCCOCCOCCNC(=O)COc1cccc2C(=O)N(C3CCC(=O)NC3=O)C(=O)c12
  • 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.Agut J, Sánchez JC, Sacristán A, Action of ebrotidine, ranitidine and cimetidine on the specific binding to histamine H1- and H2-receptors. Arzneimittelforschung. 1997 Apr;47(4A):447-9.
产品手册
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