Half-sandwich complexes of the type [(RCOCp)M(CO)(3)] with M = Re and Tc-99(m) were synthesized from [M(OH2)(3)-(CO)(3)](+) in water. The R group can be an organic residue or a receptor binding biomolecule with a spacer to cyclopentadienyl (Cp). This provides a general route to Cp complexes of technetium without the need for starting from [TcBr(CO)(5)]. The X-ray structure Of [{C6H5CH2COC5H4}Tc(CO)(3)] has been elucidated. The compound crystallizes in the monoclinic space group P2(1)/c with a = 16.1454(9), b = 7.6300(6), and c = 12.3922(7) Angstrom and beta = 107.792(6)degrees. We have chosen a serotonergic receptor ligand (WAY) as an example for the derivatization of Cp with a bioactive molecule. WAY is linked to Cp by an aliphatic chain of variable length. The half-sandwich complexes were prepared from water and organic solvents. The structure of [(WAY4-Cp)Re(CO)(3)] could be elucidated. The compound crystallizes in the monoclinic space group P2(1)/c with a =15.7112(6), b = 6.8775(3), and c = 25.5217(12) Angstrom and beta = 103.778(5)degrees. Quantification of inhibition constants gave a clear structure-activity relationship. A single methylene group between the receptor binding site and the half-sandwich complex gave an IC50 of 217 nM for HT1A, whereas a butylene linker resulted in retention of the inhibition constant with an IC50 of 6 nM with respect to underivatized WAY. For use as radiopharmaceuticals, the compounds have also been prepared with Tc-99m in quantitative yield.
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