• 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

PEG3-O-CH2COOH

CAS No. 51951-05-4

PEG3-O-CH2COOH ( PROTAC Linker 8 )

产品货号. M27009 CAS No. 51951-05-4

PEG3-O-CH2COOH (PROTAC Linker 8) is a PEG-based PROTAC linker can be used in the synthesis of SNIPERs.

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
25MG ¥300 有现货
50MG ¥405 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
    PEG3-O-CH2COOH
  • 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
    PEG3-O-CH2COOH (PROTAC Linker 8) is a PEG-based PROTAC linker can be used in the synthesis of SNIPERs.
  • 产品描述
    PEG3-O-CH2COOH (PROTAC Linker 8) is a PEG-based PROTAC linker can be used in the synthesis of SNIPERs.(In Vitro):PEG3-O-CH2COOH (Compound 15b) is a PROTAC linker can be used in the synthesis of a series of SNIPER(ER)s. SNIPERs that recruit inhibitor of the apoptosis protein (IAP) ubiquitin ligases to specifically degrade targeted proteins.
  • 同义词
    PROTAC Linker 8
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    Voltage-gated sodium channel
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    51951-05-4
  • 分子量
    208.2
  • 分子式
    C8H16O6
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    OCCOCCOCCOCC(O)=O
  • 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.Cheng HC, Incardona J. Models of torsades de pointes: effects of FPL64176, DPI201106, dofetilide, and chromanol 293B in isolated rabbit and guinea pig hearts. J Pharmacol Toxicol Methods. 2009 Sep-Oct;60(2):174-84.
产品手册
关联产品
  • Loreclezole

    Loreclezole is a selective GABAA receptor modulator and acts as a positive allosteric modulator of β2 or β3-subunit-containing receptors.

  • Rat CGRP-(8-37)

    CGRP-(8-37) is a truncated version of calcitonin gene-related peptide (CGRP) that binds to the CGRP receptor with similar affinity but does not activate the receptor,It is a highly selective CGRP receptor antagonist.

  • MCU-i4

    MCU-i4 is a novel negative modulator of the MCU, binding MICU1 and impairing muscle cell growth.