Lipids & Polymers

Bis-PEG4-PFP ester (Legacy Tebubio ref. 282T14640). Bis-PEG4-PFP ester is a PEG-based linker for PROTACs, joining two essential ligands and enabling selective protein degradation through the ubiquitin-proteasome system within cells.

Bis-PEG4-sulfonic acid (Legacy Tebubio ref. 282T14641). Bis-PEG4-sulfonic acid is a PEG-based linker for PROTACs, facilitating the conjugation of essential ligands critical for PROTAC molecule formation. It enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Bis-PEG6-acid (Legacy Tebubio ref. 282T14645). Bis-PEG6-acid is a PEG-based linker for PROTACs that joins two essential ligands, facilitating selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Bis-PEG7-NHS ester (Legacy Tebubio ref. 282T14648). Bis-PEG7-NHS ester is a cleavable ADC linker utilized in the synthesis of antibody-drug conjugates (ADCs) [1].

Bis-PEG9-NHS ester (Legacy Tebubio ref. 282T14652). Bis-PEG9-NHS ester, a cleavable ADC linker, is utilized in the synthesis of antibody-drug conjugates (ADCs)[1].

Bis-propargyl-PEG6 (Legacy Tebubio ref. 282T14659). Bis-propargyl-PEG6 is a polyethylene glycol (PEG) derivative commonly employed as a PEG-based PROTAC linker during the synthesis of PROTACs. Its application includes the generation of polymer-linked multimers of guanosine-3', 5'-cyclic monophosphates[1].

Bis-propargyl-PEG7 (Legacy Tebubio ref. 282T14660). Bis-propargyl-PEG7 is a polyethylene glycol (PEG)-based linker utilized in the synthesis of proteolysis targeting chimeras (PROTACs). It is particularly employed for the synthesis of polymer-linked multimers of guanosine-3',5'-cyclic monophosphates[1].

Boc-Aminooxy-PEG2-C2-amine (Legacy Tebubio ref. 282T14709). Boc-Aminooxy-PEG2-C2-amine is a polyethylene glycol (PEG)-based linker molecule designed for use in the synthesis of proteolysis-targeting chimeras (PROTACs) [1].

Boc-Aminooxy-PEG2 (Legacy Tebubio ref. 282T14711). Boc-Aminooxy-PEG2 is a PEG-based linker for PROTACs, facilitating the formation of PROTAC molecules by joining two essential ligands and enabling selective protein degradation via the ubiquitin-proteasome system within cells.