Val-Cit is a cleavable linker specifically designed for the synthesis of antibody-drug conjugates (ADCs). It facilitates the selective release of cytotoxic drugs upon internalization, enhancing the therapeutic efficacy of ADCs. This compound is pivotal in cancer research, enabling the targeted delivery of therapeutics to malignant cells while minimizing systemic toxicity.
Val-Cit is a cleavable linker specifically designed for the synthesis of antibody-drug conjugates (ADCs). It facilitates the selective release of cytotoxic drugs upon internalization, enhancing the therapeutic efficacy of ADCs. This compound is pivotal in cancer research, enabling the targeted delivery of therapeutics to malignant cells while minimizing systemic toxicity.
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