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Chelate oxorhenium to assemble new integrin antagonists.

Journal of inorganic biochemistry (2011-04-23)
Julien Le Gal, Marta Gonera, Marie-Anne Lelait, Denis Servent, Christophe Dugave
RÉSUMÉ

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.

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Sigma-Aldrich
Ammonium perrhenate, ≥99%
Sigma-Aldrich
Sodium perrhenate, 99.99% trace metals basis
Sigma-Aldrich
Potassium perrhenate, 99%
Sigma-Aldrich
Ammonium perrhenate, 99.999% trace metals basis
Sigma-Aldrich
Potassium perrhenate, 99.98% trace metals basis