Propargyl-O-C1-amido-PEG3-C2-NHS ester is a non-cleavable PEG-based linker that targets the synthesis of antibody-drug conjugates (ADCs). Featuring an alkyne group, it serves as a click chemistry reagent and is capable of undergoing copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide-containing molecules. This compound is essential for creating stable ADC structures, enhancing drug delivery and efficacy in therapeutic applications.
Propargyl-O-C1-amido-PEG3-C2-NHS ester is a non-cleavable PEG-based linker that targets the synthesis of antibody-drug conjugates (ADCs). Featuring an alkyne group, it serves as a click chemistry reagent and is capable of undergoing copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide-containing molecules. This compound is essential for creating stable ADC structures, enhancing drug delivery and efficacy in therapeutic applications.
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