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J Med Chem ; 48(23): 7482-5, 2005 Nov 17.
Article in English | MEDLINE | ID: mdl-16279808

ABSTRACT

Two 3,5-disubstituted sulfonamide catechol ligands were synthesized. Tris(ligand) iron(III) complexes were prepared and investigated as MRI contrast agents. Longitudinal relaxivity (r1) values were determined for the complexes. The r1 values in water were substantially higher than those of typical six-coordinate iron(III) complexes. The r1 values in plasma under the same conditions increased. The iron(III) complexes were administered to rats, and the kidney and liver signal intensities were measured by T1-weighted MR imaging experiments.


Subject(s)
Catechols/chemical synthesis , Contrast Media/chemical synthesis , Ferric Compounds/chemical synthesis , Iron Chelating Agents/chemical synthesis , Sulfonamides/chemical synthesis , Animals , Catechols/chemistry , Catechols/pharmacology , Contrast Media/chemistry , Contrast Media/pharmacology , Female , Ferric Compounds/chemistry , Ferric Compounds/pharmacology , Gadolinium DTPA/pharmacology , Iron Chelating Agents/chemistry , Iron Chelating Agents/pharmacology , Kidney/anatomy & histology , Ligands , Liver/anatomy & histology , Magnetic Resonance Imaging , Rats , Rats, Inbred F344 , Structure-Activity Relationship , Sulfonamides/chemistry , Sulfonamides/pharmacology
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