Hydroxy-PEG10-acid (Legacy Tebubio ref. 282T18031). Hydroxy-PEG10-acid (HO-PEG10-CH2CH2COOH) is a PEG-based PROTAC linker that can be used to synthesize PROTACs[1].
Hydroxy-PEG12-Boc (Legacy Tebubio ref. 282T18035). Hydroxy-PEG12-Boc (Hydroxy-PEG12-T-Butyl Ester) is a PEG-based PROTAC linker. Hydroxy-PEG12-Boc can be used in the synthesis of PROTACs.
Iodoacetamide-PEG3-azide (Legacy Tebubio ref. 282T18052). Iodoacetamide-PEG3-azide, a PEG-derived PROTAC linker, is utilized in the synthesis of PROTACs. [1]
Lenalidomide-PEG1-azide (Legacy Tebubio ref. 282T18067). Lenalidomide-PEG1-azide is an E3 ligase ligand-linker conjugate that incorporates the cereblon ligand based on Lenalidomide and a linker. It is designed for use in the development of PROTAC BRD4 Degrader-2[1].
m-C-tri(CH2-PEG1-NHS ester) (Legacy Tebubio ref. 282T18076). m-C-tri(CH2-PEG1-NHS ester) is a non-cleavable one-unit polyethylene glycol (PEG) linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
m-PEG-mal (MW 2000) (Legacy Tebubio ref. 282T18093). m-PEG-mal (MW 2000) is a PEG-based linker used in PROTACs to join two essential ligands, facilitating selective protein degradation via the ubiquitin-proteasome system within cells.
m-PEG11-acid (Legacy Tebubio ref. 282T18123). m-PEG11-acid is a non-cleavable 11-unit polyethylene glycol (PEG) linker used in the synthesis of antibody-drug conjugates (ADCs) [1] and as a PEG-based linker for PROTAC synthesis [2].