Chelate oxorhenium to assemble new integrin antagonists

J Inorg Biochem. 2011 Jun;105(6):880-6. doi: 10.1016/j.jinorgbio.2011.03.008. Epub 2011 Mar 23.

Abstract

Assembly of independent chemical modules through oxorhenium coordination by a NS(2)+S chelation motif was applied to the synthesis of RGD (Arg-Gly-Asp) analogs. Modules were assembled through oxorhenium chelation to give a series of 18 metal complexes in good yields and satisfactory purities. Screening of these oxorhenium coordinates as antagonists of integrins αVβ3, αIIbβ3 and αVβ5 led to the identification of 3 bioactive compounds that exhibit submicromolar affinities for the 3 integrins. Preliminary studies showed that the corresponding oxotechnetium complexes are stable in mice plasma and therefore could be proposed for the molecular imaging of pathologies that overexpress integrins αVβ3 and αVβ5.

MeSH terms

  • Animals
  • Chelating Agents / chemistry*
  • Chelating Agents / metabolism
  • Integrins / antagonists & inhibitors*
  • Integrins / chemistry
  • Mice
  • Molecular Imaging
  • Peptides, Cyclic / chemical synthesis
  • Peptides, Cyclic / chemistry
  • Rhenium / chemistry*
  • Rhenium / metabolism

Substances

  • Chelating Agents
  • Integrins
  • Peptides, Cyclic
  • perrhenate
  • Rhenium