Val-Cit-PAB-Exatecan is a drug-linker conjugate designed for antibody-drug conjugate (ADC) applications. This compound features a DNA topoisomerase I inhibitor, DX-8951, linked via a cathepsin-cleavable linker, Val-Cit-PAB. Its primary mechanism involves targeted delivery of the cytotoxic agent to cancer cells, thereby enhancing therapeutic efficacy while minimizing systemic toxicity. Val-Cit-PAB-Exatecan is utilized in research focused on developing effective ADC therapies for various malignancies.
Val-Cit-PAB-Exatecan is a drug-linker conjugate designed for antibody-drug conjugate (ADC) applications. This compound features a DNA topoisomerase I inhibitor, DX-8951, linked via a cathepsin-cleavable linker, Val-Cit-PAB. Its primary mechanism involves targeted delivery of the cytotoxic agent to cancer cells, thereby enhancing therapeutic efficacy while minimizing systemic toxicity. Val-Cit-PAB-Exatecan is utilized in research focused on developing effective ADC therapies for various malignancies.
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