Efficient 125I-radiolabeling of biomolecules using a strain-promoted oxidation-controlled cyclooctyne-1,2-quinone cycloaddition reaction

Chem Commun (Camb). 2020 Jan 2;56(3):415-418. doi: 10.1039/c9cc08982a.

Abstract

We report a novel 1,2-catechol based radioiodinated precursor for radioiodination of bicyclo[6.1.0]nonyne (BCN) installed biologically active molecules using a strain-promoted oxidation-controlled cyclooctyne-1,2-quinone cycloaddition reaction (SPOCQ) under ambient conditions. Compared to the reported methodologies, the new strategy demonstrates some clear advantages, including high in vitro and in vivo stability, high radiochemical yield, and exceptionally fast reaction kinetics at micro-molar concentration.

MeSH terms

  • Animals
  • Bridged Bicyclo Compounds / chemical synthesis
  • Bridged Bicyclo Compounds / chemistry
  • Catechols / chemistry
  • Cycloaddition Reaction*
  • Heart / diagnostic imaging
  • Iodine Radioisotopes / chemistry
  • Isotope Labeling
  • Kinetics
  • Mice
  • Mice, Inbred ICR
  • Oxidation-Reduction
  • Quinones / chemistry*
  • Radiopharmaceuticals / chemical synthesis
  • Radiopharmaceuticals / chemistry*
  • Single Photon Emission Computed Tomography Computed Tomography

Substances

  • Bridged Bicyclo Compounds
  • Catechols
  • Iodine Radioisotopes
  • Quinones
  • Radiopharmaceuticals
  • bicyclo(6.1.0)nonyne
  • Iodine-125
  • catechol