amine-peg-amine

Amine-PEG-amine (MW 2000) is a polyethylene glycol (PEG) derivative that functions as a linker for PROTAC synthesis. PROTACs are small molecules used for targeted protein degradation [1].

Amine-PEG-amine (MW 20000) is a polyethylene glycol (PEG)-based linker compound utilized in the synthesis of PROTACs.

Amine-PEG-amine (MW 3400) is a polyethylene glycol (PEG) -based linker used for synthesizing proteolysis-targeting chimeras (PROTACs)[1].

Amine-PEG-amine (MW 35000), a PEG-based PROTAC linker, is utilized for the synthesis of PROTACs[1].

Amine-PEG-amine (MW 5000) is a polyethylene glycol (PEG) based linker utilized in the synthesis of proteolysis-targeting chimeras (PROTACs) [1].

Azido-PEG1-amine 是一种属于 PEG 类的 PROTAC linker，可用于合成 PROTAC 分子。

m-PEG-NH2 (MW 1000),甲氧基聚乙二醇胺, 是一种PEG为主链的PROTAC linker；m-PEG-amine可用于合成PROTAC。

Propargyl-PEG3-amine (Propargyl-PEG3-NH2) 是一种属于 PEG 类的 PROTAC linker，可用于合成 PROTAC 分子。

m-PEG12-amine是一种基于PEG的PROTAC连接器，同时也是一种在PROTACs[1]和抗体药物偶联物(ADCs)[2]的合成中使用的不可切割的12单位PEG ADC连接器。

Amino-PEG12-amine (H2N-PEG12-CH2CH2NH2) 是一种属于 PEG 类的 PROTAC linker，可用于 PROTAC 分子的合成。

Boc-NH-PEG12-NH2 (NHBoc-PEG12-amine) 是一种属于 PEG 类的 PROTAC linker，可用于 PROTAC 分子的合成。

111-Trifluoroethyl-PEG4-amine is a polyethylene glycol (PEG)-based linker suitable for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

3,4-Dibromo-Mal-PEG2-amine is a polyethylene glycol (PEG) derivative and serves as a PEG-based PROTAC linker, facilitating the synthesis of PROTACs[1].

Ald-Ph-amido-C2-PEG2-amine is a polyethylene glycol (PEG)-based linker utilized for the synthesis of PROteolysis TArgeting Chimeras (PROTACs)[1].

Amino-PEG10-amine is a PEG-based PROTAC linker employed for the conjugation of two mono diethylstilbestrol (DES)-based ligands. This compound offers an alternative approach to the synthesis of highly selective and active ER antagonists, which are crucial for the advancement of endocrine therapy in breast cancer treatment[1].

Amino-PEG11-amine 是一种基于 PEG（12 个单位）的 PROTAC 接头，能够结合两种基于单乙基雌酚的配体，是制备用于乳腺癌内分泌治疗的更具选择性和活性的 ER 拮抗剂的替代策略。

Amino-PEG3-C2-Amine, a PEG-based linker with three units, is utilized in PROTAC synthesis.

Amino-PEG4-C2-amine, a PEG-based linker (4 units) for PROTAC development, facilitates the synthesis of PROTACs.

Amino-PEG5-amine, a PEG-based linker containing 5 units, is utilized in PROTAC synthesis.

Amino-PEG7-amine 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.

Amino-PEG6-amine, a polyethylene glycol-based (PEG-based) linker with six units, is utilized for the synthesis of PROTACs.

Amino-PEG8-amine 是一种以聚乙二醇为基础的 PROTAC 连接剂，可用于PROTACs 的合成，是一种含有两个氨基(NH2)基团的共轭PEG 衍生物。

Amino-PEG9-amine 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.

Azido-PEG10-amine是一种不可降解(non-cleavable)的ADC linker和PEG类的PROTAC linker，可用于合成抗体偶联分子(ADC)和PROTAC，可以和含有Alkyne、DBCO或BCN基团的分子发生点击化学反应。