m-PEG12-OH
CAS No. 2050595-03-2
m-PEG12-OH ( Dodecaethylene Glycol Monomethyl Ether )
产品货号. M26969 CAS No. 2050595-03-2
m-PEG12-OH 是一种基于 PEG 的 PROTAC 连接体,可用于 PROTAC 的合成。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 25MG | ¥92 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称m-PEG12-OH
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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
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产品简述m-PEG12-OH 是一种基于 PEG 的 PROTAC 连接体,可用于 PROTAC 的合成。
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产品描述m-PEG12-OH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. m-PEG12-OH is also a non-cleavable 12 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs).(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. ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker.
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体外实验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.
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体内实验——
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同义词Dodecaethylene Glycol Monomethyl Ether
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通路Others
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靶点Other Targets
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受体DENV NS2B-NS3 protease
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研究领域——
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适应症——
化学信息
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CAS Number2050595-03-2
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分子量560.67
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分子式C25H52O13
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纯度>98% (HPLC)
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溶解度——
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SMILESCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
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Jujuboside D
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Vilanterol
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PKC ζ pseudosubstrat...
Inhibitor of protein kinase C (PKC) ζ; attached to cell permeabilisation Antennapedia domain vector peptide. Consists of amino acids 113 - 129 of PKC ζ pseudosubstrate domain linked by a disulphide bridge to the Antennapedia domain vector peptide. The Antennapedia peptide is actively taken up by intact cells, at 4 or 37°C, ensuring rapid and effective uptake of the inhibitor peptide. Once inside the cell, the disulphide bonds are subjected to reduction in the cytoplasm leading to release of the inhibitor peptide. Induces mast cell degranulation by a PKC ζ-independent pathway.
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