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(Cp-R)M(CO)(3) ] (M=Re or (99m) Tc) Arylsulfonamide, Arylsulfamide, and Arylsulfamate Conjugates for Selective Targeting of Human Carbonic Anhydrase IX
Authors:Can Daniel  Spingler Bernhard  Schmutz Paul  Mendes Filipa  Raposinho Paula  Fernandes Célia  Carta Fabrizio  Innocenti Alessio  Santos Isabel  Supuran Claudiu T  Alberto Roger
Institution:Institute of Inorganic Chemistry, University of Zurich, Winterthurerstrasse 190, 8057 Zurich (Switzerland).
Abstract:Enhanced receptor selectivity: Carbonic anhydrase inhibitors are relevant for both cancer diagnosis and therapy. Combining non-radioactive Re compounds with their radioactive (99m) Tc homologs enables the use of identical molecules for therapy and imaging (theragnostic). The syntheses and in?vitro evaluation of (Cp-R)M(CO)(3) ] (Cp=cyclopentadienyl, M=Re, (99m) Tc) with R being a highly potent carbonic-anhydrase-targeting vector is reported.
Keywords:bio‐organometallic chemistry  carbonic anhydrase inhibitors  radiopharmaceuticals  sulfonamides  technetium
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