Propargyl-PEG2-acid is a non-cleavable linker targeting the synthesis of antibody-drug conjugates (ADCs) and PROTACs. This PEG-based compound facilitates the conjugation process through click chemistry, featuring an alkyne group that enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide-containing molecules. It serves as a vital tool for researchers in the development of innovative therapeutic strategies involving ADCs and targeted protein degradation applications.
Propargyl-PEG2-acid is a non-cleavable linker targeting the synthesis of antibody-drug conjugates (ADCs) and PROTACs. This PEG-based compound facilitates the conjugation process through click chemistry, featuring an alkyne group that enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide-containing molecules. It serves as a vital tool for researchers in the development of innovative therapeutic strategies involving ADCs and targeted protein degradation applications.
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