PEG

DNP-PEG3-azide, a PEG-based linker for PROTACs, joins two essential ligands, crucial for forming PROTAC molecules, and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

DNP-PEG4-acid is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules. This linker enables selective protein degradation leveraging the ubiquitin-proteasome system within cells.

DNP-PEG4-alcohol is a PEG-based linker for PROTACs, facilitating the formation of PROTAC molecules by joining two essential ligands, thereby enabling selective protein degradation through the ubiquitin-proteasome system within cells.

DNP-PEG4-NHS ester, a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules, enabling selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Fmoc-NMe-PEG4-C2-acid, a PEG-based linker for PROTACs, connects two essential ligands crucial for PROTAC molecule formation and facilitates selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Fmoc-PEG2-CH2CH2-NHS ester is a polyethylene glycol (PEG)-based linker constructed for the synthesis of proteolysis targeting chimeras (PROTACs).

Fmoc-PEG4-Ala-Ala-Asn-PAB is a cleavable four-unit polyethylene glycol (PEG) linker used in the synthesis of antibody-drug conjugates (ADCs)[1].

HO-PEG14-OH is a PEG-based linker for PROTACs, joining two essential ligands crucial for forming PROTAC molecules and enabling selective protein degradation through the ubiquitin-proteasome system within cells.

HO-PEG20-OH, a PEG-based linker for PROTACs, connects two essential ligands crucial for forming PROTAC molecules, facilitating selective protein degradation by leveraging the ubiquitin-proteasome system within cells.