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Amino-PEG6-amido-C16-Boc is a PEG-based PROTAC linker employed for the synthesis of PROTACs[1].

Amino-PEG6-amido-C16-COOH, a PEG-based PROTAC linker, facilitates the synthesis of PROTACs[1].

Amino-PEG9-amido-C16-Boc is a polyethylene glycol (PEG)-based linker utilized for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

Azide-PEG6-amido-C16-Boc is an alkyl/ether-based PROTAC linker utilized in PROTAC synthesis[1].

Azide-PEG9-amido-C12-Boc is a polyethylene glycol (PEG)-based proteolysis targeting chimera (PROTAC) linker used for the synthesis of PROTACs[1].

Azide-PEG9-amido-C16-Boc is an alkyl/ether-based PROTAC linker with utility in PROTAC synthesis [1].

Pomalidomide-amido-C1-Br is a synthesized conjugate consisting of the Pomalidomide-based cereblon ligand and a linker, functioning as an E3 ligase ligand-linker. This compound serves as a tool for designing a B-Raf PROTAC degrader, specifically PROTAC B-Raf degrader 1, which exhibits anti-cancer activity[1].

Phenol-amido-C1-PEG3-N3, also known as PROTAC Linker 21, is a PEG-based linker utilized for synthesizing PROTACs.

Azido-C1-PEG4-C3-NH2 是一种属于PEG类的PROTAC linker，可用于PROTAC分子的合成。作为点击化学试剂，Azido-C1-PEG4-C3-NH2 含有Azide基团，能够与带有Alkyne基团的分子通过铜催化的叠氮-炔环加成反应（CuAAc) 进行反应。此外，它也可以与含有DBCO或BCN基团的分子发生由环张力驱动的炔-叠氮环加成反应 (SPAAC)。

Thalidomide-O-amido-C11-COOH (化合物 IMiD acid 1) 是一种 E3 连接酶配体与连接子 CRBN (Cereblon) 的偶联物，适用于合成用于靶向降解DOT1L的PROTAC。

Azido-C1-PEG3-C3-NH2 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.