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*For research and further manufacturing use only, not for direct human use.
Structure of 870487-08-4
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Boc-Val-Cit-OH is a protected tripeptide linker featuring a valine-citrulline sequence with a C-terminal hydroxyl group. This stable, bench-ready intermediate integrates efficiently into antibody-drug conjugate (ADC) architectures, enabling site-specific payload attachment through cleavable linkers. The Boc group ensures compatibility with standard peptide synthesis protocols and provides enhanced stability during handling.
Boc-Val-Cit-OH serves as a key building block in the synthesis of antibody-drug conjugates (ADCs), enabling site-specific drug attachment via its cleavable Val-Cit dipeptide linker. The Boc group provides stable protection of the N-terminus, while the C-terminal carboxylic acid facilitates efficient coupling reactions. This compound exhibits excellent bench stability, compatibility with standard peptide synthesis protocols, and reliable cleavage under physiological conditions, making it a practical choice for constructing bioconjugates in therapeutic development.
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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: