PEG

Amino-PEG9-amine (Legacy Tebubio ref. 282T14254). Amino-PEG9-amine is a PEG-based linker used in PROTACs, joining two essential ligands to facilitate the formation of PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system within cells.

Amino-PEG9-Boc (Legacy Tebubio ref. 282T14255). Amino-PEG9-Boc is a PEG-based linker for PROTACs, essential for joining two ligands in PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system within cells.

Aminooxy-PEG2-azide (Legacy Tebubio ref. 282T14262). Aminooxy-PEG2-azide, a PEG-based PROTAC linker, is utilized for the synthesis of PROTACs[1] and serves as a non-cleavable 2-unit PEG ADC linker in the synthesis of antibody-drug conjugates (ADCs)[2].

Aminooxy-PEG3-azide (Legacy Tebubio ref. 282T14264). Aminooxy-PEG3-azide is an ADC linker belonging to the class of PEGs, as well as three-unit PEGs, which can be used for the synthesis of antibody-coupled reactive molecules (ADCs).

Aminooxy-PEG4-alcohol (Legacy Tebubio ref. 282T14271). Aminooxy-PEG4-alcohol is both a non-cleavable 4-unit PEG ADC linker and a PEG-based PROTAC linker.

Aminooxy-PEG4-C2-Boc (Legacy Tebubio ref. 282T14273). Aminooxy-PEG4-C2-Boc is a PEG-based linker for PROTACs that connects two essential ligands, facilitating selective protein degradation via the ubiquitin-proteasome system within cells.

Aminooxy-PEG5-azide (Legacy Tebubio ref. 282T14276). Aminooxy-PEG5-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs [1].

APN-C3-PEG4-azide (Legacy Tebubio ref. 282T14310). APN-C3-PEG4-azide is a PEG-based linker for PROTACs, facilitating the conjugation of two essential ligands vital for PROTAC molecule formation. This linker supports selective protein degradation via the cell's ubiquitin-proteasome system.

Azide-PEG4-Tos (Legacy Tebubio ref. 282T14395). Azide-PEG4-Tos is a PEG-based linker for PROTACs that connects two essential ligands, facilitating the formation of PROTAC molecules and enabling selective protein degradation via the ubiquitin-proteasome system within cells.