m-peg-azide

m-PEG-azide (MW 10000) 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-azide (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-azide (MW 20000) 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-azide (MW 5000) 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.

4-Arm-PEG-Azide (MW 400) (4-Arm-PEG-N3 (MW 400)) 是一种 PEG 衍生物，由聚乙二醇单元及叠氮基团 (azide) 构成。其 Azide 基团可与含 Alkyne 基团的分子在铜催化条件下进行叠氮-炔环加成反应 (CuAAc)，也能与含 DBCO 或 BCN 基团的分子进行环张力驱动的炔-叠氮环加成 (SPAAC)。

4-Arm-PEG-Azide (MW 1000) (4-Arm-PEG-N3 (MW 1000)) 是一种 PEG 衍生物，由 PEG 单元和叠氮基团（azide）构成。它含有 Azide 基团，可与含 Alkyne 基团的分子进行铜催化叠氮-炔环加成反应 (CuAAc)，也能与含 DBCO 或 BCN 基团的分子进行环张力驱动的炔-叠氮环加成反应 (SPAAC)。

4-Arm-PEG-Azide (MW .400) (4-Arm-PEG-N3 (MW .400)) 是 PEG 衍生物，由 PEG 单元与叠氮基团 (azide) 组成。其 Azide 基团可以通过铜催化的叠氮-炔环加成反应 (CuAAc) 与含有 Alkyne 基团的分子反应，也能够通过环张力驱动的炔-叠氮环加成反应 (SPAAC) 作用于含有 DBCO 或 BCN 基团的分子。

4-Arm-PEG-Azide (MW 600) (4-Arm-PEG-N3 (MW 600)) 是一种由 PEG 分子与叠氮基团组成的聚乙二醇衍生物。其 Azide 基团能够与含 Alkyne 基团的分子通过铜催化的叠氮-炔环加成反应 (CuAAc) 发生交联，也可与含 DBCO 或 BCN 基团的分子进行环张力驱动的叠氮-炔环加成反应 (SPAAC)。

4-Arm-PEG-Azide (MW 2000) (4-Arm-PEG-N3 (MW 2000)) 是一种 PEG 衍生物，包含 PEG 单元和叠氮基团 (azide)。该化合物拥有 Azide 基团，可参与与含有 Alkyne 基团的分子进行铜催化的叠氮-炔环加成反应 (CuAAc)。此外，它还能与含有 DBCO 或 BCN 基团的分子发生环张力驱动的炔-叠氮环加成反应 (SPAAC)。

4-Arm PEG-Azide (MW 5000) (4-Arm PEG-N3 (MW 5000)) 是一种四臂的多乙二醇衍生物，其每个臂的末端含有一个叠氮基团，并连接至一个季戊四醇核心。

4-Arm PEG-Azide (MW 20000) (4-Arm PEG-N3 (MW 20000)) 是一个多臂的聚乙二醇衍生物，四个末端各自含有叠氮基，并连接于季戊四醇核心。

4-Arm PEG-Azide (MW 40000) (4-Arm PEG-N3 (MW 40000)) 是一种以季戊四醇为核心的多臂 PEG 衍生物，每个臂的末端均含有一个叠氮基。

4-Arm PEG-Azide (MW 10000) (4-Arm PEG-N3 (MW 10000)) 是一种多臂的聚乙二醇衍生物，每个臂在末端具有一个叠氮基，并且与季戊四醇核心相连。

m-PEG10-azide 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-PEG2-azide, a PEG-based PROTAC linker, is utilized in the synthesis of PROTACs.

m-PEG3-azide 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-PEG4-azide, also referred to as 13-Azido-2,5,8,11-tetraoxatridecane, functions as a PEG-based PROTAC linker suitable for PROTACs synthesis[1].

m-PEG5-azide 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-PEG6-azide is a six-unit polyethylene glycol linker functionalized with an azide moiety, serving as a non-cleavable linker for the synthesis of antibody-drug conjugates (ADCs).

m-PEG7-azide 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-PEG8-azide 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-azide 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-PEG12-azide, a PEG-based PROTAC linker, is utilized in the synthesis of PROTACs [1].

m-PEG16-azide 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.