Anti-S. aureus alpha-toxin (Tosatoxumab)-MC-MMAF ADC (ADC-W-2356)

 ADC Target

  • Name
  • S. aureus alpha-toxin
  • Alternative Names
  • S. aureus alpha-toxin
  • Overview
  • Alpha-toxin, also known as alpha-hemolysin (Hla), is the major cytotoxic agent released by bacterium Staphylococcus aureus and the first identified member of the pore forming beta-barrel toxin family. This toxin consists mostly of beta-sheets (68%) with o

 ADC Antibody

  • Overview
  • Human Anti-S. aureus alpha-toxin IgG1-lambda antibody, Tosatoxumab
  • Generic name
  • Tosatoxumab
  • Host animal
  • Human

 ADC Linker

  • Name
  • MC (maleimidocaproyl)
  • Description
  • Noncleavable linkers, is considered noncleavable-meaning linker cleavage, and payload release does not depend on the differential properties between the plasma and some cytoplasmic compartments. Instead, the release of the cytotoxic drug is postulated to occur after internalization of the ADC via antigen-mediated endocytosis and delivery to lysosomal compartment, where the antibody is degraded to the level of amino acids through intracellular proteolytic degradation.

 ADC payload drug

  • Name
  • MMAF
  • Description
  • Derived from Auristatin,are water-soluble dolastatin analogs of dolastatin 10. Dolastatin 10 belongs to dolastatin family and it can powerfully bind to tubulin, thus inhibiting polymerization mediated through the binding to the vinca alkaloid binding domain, and causes cell to accumulate in metaphase arrest.

For lab research use only, not for any in vivo human use.


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