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5HP2O((PEG)2-OH)-(CH2)4-NHS

Nom chimique: 2,5-dioxopyrrolidin-1-yl 5-(2-hydroxy-2-(3-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)-3-oxopropyl)-5-oxo-2,5-dihydro-1H-pyrrol-1-yl)pentanoate

  • n° Art.:RL-8695
  • Formule:C22H32N2O11
  • Storage temperature:2-8°C
  • Masse moléculaire:500,50 g/mol

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description

5-hydroxy-1,5-dihydro-2H-pyrrol-2-ones (5HP2Os) are next-generation thiol-reactive conjugating groups superior in reactivity and stability to conventional maleimides. Maleimides are prone to hydrolysis, retro-Michael reactions and/or thiol exchange reactions, resulting in antibody and protein conjugates with poor stability. 5HP2O linkers are highly selective for cysteines, yielding conjugates with superior stability.

references

5-Hydroxy-pyrrolone based building blocks as maleimide alternatives for protein bioconjugation and single-site multi-functionalization; E. De Geyter, E. Antonatou, D. Kalaitzakis, S. Smolen, A. Iyer, L. Tack, E. Ongenae, G. Vassilikogiannakis, A. Madder; Chem. Sci. 2021; 12: 5246-5252. https://doi.org/10.1039/d0sc05881e


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