tetrazine-biotin

Tetrazine-biotin is a cleavable linker vital in ADC synthesis. Tetrazine-biotin joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled drug release, optimizing ADC effectiveness.

Tetrazine-SS-PEG4-Biotin, a cleavable 4-unit PEG ADC linker, is employed for the synthesis of antibody-drug conjugates (ADCs)[1].

Tetrazine-SS-Biotin, a cleavable ADC linker, finds utility in ADC (antibody-drug conjugate) synthesis [1].

Tetrazine-diazo-PEG4-biotin functions as a cleavable 4-unit PEG ADC linker in the preparation of antibody-drug conjugates (ADCs) [1]. This compound acts as a click chemistry reagent, incorporating a Tetrazine group capable of conducting an inverse electron demand Diels-Alder reaction (iEDDA) with molecules possessing TCO groups.

Tetrazine-PEG4-biotin is a cleavable linker consisting of a four-unit PEG (polyethylene glycol) chain, designed for the synthesis of antibody-drug conjugates (ADCs)[1].

Biotin-MeTz shiyi is a click chemistry reagent characterized by a terminal methyl tetrazine group. As a biotin derivative, it is used for the preparation of biotinylated conjugates.

Biotin-PEG3-Me-Tet, an ADC linker consisting of three PEG units, utilizes its Tetrazine group to participate in a specific inverse electron demand Diels-Alder reaction (iEDDA) with compounds containing TCO groups.