bis mal peg3

Bis-Mal-PEG3 is a PEG-based linker for PROTACs, joining two essential ligands to facilitate selective protein degradation through the ubiquitin-proteasome system within cells.

N-(Mal-PEG6)-N-bis(PEG3-amine) is a Polyethylene Glycol (PEG)-based proteolysis targeting chimera (PROTAC) linker used in the synthesis of PROTACs[1].

Mal-PEG4-bis-PEG3-methyltetrazine, a cleavable 7-unit PEG ADC linker, is employed in the synthesis of antibody-drug conjugates (ADCs)[1].

Bis-(Mal-PEG3)-PH-N-succinimidyl acetate is a PEG-based PROTAC linker used in the synthesis of PROTAC molecules.

Mal-PEG4-bis-PEG3-DBCO serves as a cleavable 7-unit PEG ADC linker in the creation of antibody-drug conjugates (ADCs) [1]. It functions as a click chemistry reagent, featuring a DBCO group that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with Azide-containing molecules.

Mal-PEG2-bis-PEG3-BCN, a cleavable five-unit PEG linker, is utilized in the synthesis of antibody-drug conjugates (ADCs) [1]. It functions as a click chemistry reagent featuring a BCN group capable of engaging in strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules.

Mal-bis-PEG3-DBCO, a cleavable three-unit PEG ADC linker, is employed in the synthesis of antibody-drug conjugates (ADCs) [1]. This click chemistry reagent features a DBCO group that engages in strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules.