m-peg-oh

m-PEG-OH (MW 2000) is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG-OH (MW5000) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].

m-PEG-OH (MW 1000) 是一种大分子引发剂，可用于合成两亲性嵌段共聚物。这种共聚物能够形成纳米级胶束，用于递送活性药物。被胶束包裹的疏水性抗癌剂Paclitaxel (HY-B0015) 相较于游离形式的Paclitaxel，具有更强的抗癌活性，并能优先在肿瘤组织中积聚，在健康器官中的分布有限。

m-PEG-OH (MW 10000) 是一种大分子引发剂，用于合成两亲性嵌段共聚物。两亲性嵌段共聚物可用于制备纳米胶束，以传递活性药物。胶束包裹的疏水性抗癌剂，Paclitaxel (HY-B0015)，比游离的Paclitaxel具有更强的抗癌活性。该药物优先在肿瘤组织中累积，而在健康器官中的分布非常有限。

m-PEG-OH (MW 550) (mPEG-Hydroxy (MW 550)) 是聚乙二醇 (PEG) 的一种衍生物，常用于药物传递领域。

m-PEG-OH (MW 750) (mPEG-Hydroxy (MW 750)) 是一种用于药物递送的聚乙二醇 (PEG) 衍生物。

m-PEG-OH (MW 350) (mPEG-Hydroxy (MW 350)) 是聚乙二醇 (PEG) 的一种衍生物，常用于药物递送系统。

m-PEG-OH (MW 20000) 能作为大分子引发剂，用于合成两亲性嵌段共聚物。这种共聚物可用于制备纳米级胶束，以递送活性药物。被胶束封装后的疏水性抗癌剂Paclitaxel(HY-B0015)的细胞杀伤活性比游离形式更强，同时更倾向于在肿瘤组织中积累，而在健康器官中的分布有限。

m-PEG12-OH (Dodecaethylene Glycol Monomethyl Ether) 是一种基于 PEG 的 PROTAC 接头，可用于 PROTAC 的合成。它也是一种不可切割的 12 单元 PEG ADC 接头，用于合成抗体-药物偶联物。

m-PEG3-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG7-CH2-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Bis(m-PEG4)-N-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG11-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG3-S-PEG2-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG36-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG48-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Mal-PEG4-Glu(OH)-NH-m-PEG24 is a polyethylene glycol-based (PEG-based) linker, specifically designed for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

NH2-PEG4-Glu(OH)-NH-m-PEG24 is a PEG-based PROTAC linker suitable for PROTAC synthesis[1].