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*For research and further manufacturing use only, not for direct human use.
Structure of 644981-35-1
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Val-Cit-PAB-MMAE is a cleavable peptide linker conjugated to the potent cytotoxic agent MMAE, designed for antibody-drug conjugate (ADC) applications. This construct features a valine-citrulline dipeptide that enables selective intracellular cleavage by cathepsin B, releasing active MMAE within target cells. The PAB spacer enhances stability in circulation while ensuring efficient payload release. The structure combines high potency with controlled delivery, enabling targeted cancer therapy with reduced off-target effects.
Val-Cit-PAB-MMAE serves as a cleavable linker-payload construct in antibody-drug conjugates, enabling site-specific delivery of the potent cytotoxic agent MMAE. The Val-Cit dipeptide facilitates protease-mediated cleavage in lysosomal environments, while the PAB spacer ensures efficient release of active MMAE. This structure combines stability in circulation with controlled intracellular activation, supporting effective tumor targeting and therapeutic efficacy in preclinical models.
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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 : H315-H319-H302
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Precautionary Statements : P264-P270-P280-P301+P310-P302+P352-P305+P351+P338-P330-P332+P313-P337+P313-P362+P364-P501
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Lot numbers can be found on the outside label of a product: