PEG

m-PEG12-Thiol is a PEG-based linker for PROTACs that joins two essential ligands, crucial for forming PROTAC molecules, and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG24-acid is a PEG-based linker for PROTACs, joining two essential ligands that are crucial for forming PROTAC molecules; this linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

m-PEG24-Mal is a PEG-based linker for PROTACs, facilitating the conjugation of two essential ligands necessary for PROTAC molecule formation, thereby enabling selective protein degradation through the ubiquitin-proteasome system within cells.

m-PEG37-acid is a PEG-based linker for PROTACs that connects two essential ligands, critical for forming PROTAC molecules, thereby facilitating selective protein degradation via the ubiquitin-proteasome system within cells.

Mal-amido-PEG12-NHS ester is a polyethylene glycol (PEG)-derived linker used in the synthesis of proteolysis-targeting chimeras (PROTACs), facilitating the conjugation of target-specific ligands for protein degradation[1].

Mal-PEG1-Val-Cit-PABC-OH is a 1-unit polyethylene glycol (PEG) ADC linker with cleavable properties, used in the synthesis of antibody-drug conjugates (ADCs) to facilitate drug-antibody conjugation[1].

Methyltetrazine-PEG4-acid, a PEG-based linker, is employed in the synthesis of PROTACs[1].

N-(Acid-PEG2)-N-bis(PEG3-azide) is a polyethylene glycol (PEG)-based linker used in synthesizing proteolysis targeting chimeras (PROTACs), a unique class of molecules designed for targeted protein degradation[1].

N-(Amino-PEG3)-N-bis(PEG4-Boc) is a polyethylene glycol (PEG) derivative frequently used as a linker in the synthesis of proteolysis targeting chimeras (PROTACs) [1].