Propargyl-PEG4-CH2CH2-Boc is a non-cleavable ADC linker designed for the synthesis of antibody-drug conjugates (ADCs) targeting Galectin-3. This versatile linker incorporates PEG and an alkyl/ether moiety, making it suitable for the development of PROTACs (PROteolysis TArgeting Chimeras). As a click chemistry reagent, it features an alkyne group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide-containing compounds, enhancing the efficacy of bioconjugation processes in chemical biology research.
Propargyl-PEG4-CH2CH2-Boc is a non-cleavable ADC linker designed for the synthesis of antibody-drug conjugates (ADCs) targeting Galectin-3. This versatile linker incorporates PEG and an alkyl/ether moiety, making it suitable for the development of PROTACs (PROteolysis TArgeting Chimeras). As a click chemistry reagent, it features an alkyne group that facilitates copper-catalyzed azide-alkyne cycloaddition (CuAAc) with azide-containing compounds, enhancing the efficacy of bioconjugation processes in chemical biology research.
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