• 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

m-PEG3-SH

CAS No. 31521-83-2

m-PEG3-SH ( M-PEG3-Thiol; 2-(2-(2-Methoxyethoxy)Ethoxy)Ethanethiol )

产品货号. M26973 CAS No. 31521-83-2

m-PEG3-SH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
50MG ¥340 有现货
100MG 获取报价 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
    m-PEG3-SH
  • 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
    m-PEG3-SH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
  • 产品描述
    m-PEG3-SH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.(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
    M-PEG3-Thiol; 2-(2-(2-Methoxyethoxy)Ethoxy)Ethanethiol
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    Apoptosis; Bcr-Abl; HDAC
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    31521-83-2
  • 分子量
    180.3
  • 分子式
    C7H16O3S
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    COCCOCCOCCS
  • 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.Rabizadeh E, et al. Pivanex, a histone deacetylase inhibitor, induces changes in BCR-ABL expression and when combined with STI571, acts synergistically in a chronic myelocytic leukemia cell line. Leuk Res. 2007 Aug;31(8):1115-23. Epub 2007 Jan 30.
产品手册
关联产品
  • Acetyl-PHF6 amide(TF...

    Acetyl-PHF6 amide TFA is a tau derived hexapeptide.

  • P7C3

    The P7C3 class of neuroprotective aminopropyl carbazoles has been shown to block neuronal cell death in models of neurodegeneration.

  • Neoechinulin A

    Neoechinulin A has anti-inflammatory effect against LPS-stimulated RAW264.7 macrophages through inhibition of the NF-κB and p38 MAPK pathways.