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*For research and further manufacturing use only, not for direct human use.
Structure of 159857-80-4
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MC-Val-Cit-PAB is a cleavable linker designed for antibody-drug conjugate (ADC) applications. This moiety integrates a valine-citrulline dipeptide spacer with a para-aminobenzoyl (PAB) group, enabling site-specific drug attachment and efficient intracellular release via protease-sensitive bond cleavage. The structure ensures stability in circulation while facilitating targeted payload delivery.
MC-Val-Cit-PAB serves as a well-established linker module in antibody-drug conjugates, enabling site-specific payload attachment via cleavable ester bonds. Its Val-Cit dipeptide sequence ensures efficient intracellular release of the cytotoxic agent under lysosomal protease activity. The PAB (para-aminobenzoyl) moiety enhances conjugate stability and facilitates purification. This construct offers robust bench stability, predictable conjugation efficiency, and compatibility with standard NHS-ester coupling protocols in therapeutic development workflows.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: