http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007155976-A1

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filingDate 2004-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dd4c560c3e6a89d081daf61fd670f089
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a0953456fd863d0bdb3fc9bc8e5599b4
publicationDate 2007-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2007155976-A1
titleOfInvention Prosthetic groups useful in the synthesis of radiopharmaceutical compounds
abstract The present invention relates to compositions and methods for preparing radiopharmaceutical compounds in high chemical-purity and isotopic-purity. The present invention provides polymer-bound precursors to radiopharmaceutical compounds that can be converted to radiopharmaceutical compounds in one step. In a preferred embodiment, a radiopharmaceutical precursor is bound to a polymeric support via a prosthetic group comprising an alkenyl-tin bond. The radiopharmaceutical precursor is converted to a radiopharmaceutical compound in one step involving cleavage of the alkenyl-tin bond and incorporation of a radioisotope to form the radiopharmaceutical compound. Importantly, the polymeric support containing the toxic tin by-product can be easily removed from the radiopharmaceutical compound by filtration. The present invention can be used to install a large number of different radioisotopes. In a preferred embodiment, the radioisotope is 211 At, 123 I or 131 I.
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Total number of triples: 530.