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Structure of 1639351-92-0
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Mc-Val-Cit-PAB-Cl features a cleavable linker system designed for antibody-drug conjugates, combining a valine-citrulline dipeptide with a para-aminobenzyl carbamate (PAB) spacer. This structure enables efficient intracellular release of payload upon enzymatic cleavage in lysosomal environments, enhancing therapeutic efficacy and selectivity in targeted cancer therapies.
Mc-Val-Cit-PAB-Cl serves as a well-established linker for antibody-drug conjugates, enabling site-specific payload attachment via amine-reactive acylation. The chloroacetamide moiety provides reliable conjugation to lysine residues or N-termini under mild conditions, while the Val-Cit dipeptide spacer offers proteolytic cleavage in target cells. This structure combines bench stability, predictable bioconjugation efficiency, and proven utility in generating homogenous ADCs with controlled drug-to-antibody ratios.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: