http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-3026900-A1

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filingDate 2017-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_88d542c2d282c42bd4674c9e85ca0636
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_800432b04aecbc9dc7b3172db5676f2b
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d02d95393a5e917b1276af6d2765f001
publicationDate 2017-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-3026900-A1
titleOfInvention Radio-pharmaceutical complexes
abstract The invention provides a method for the formation of a tissue-targeting thorium complex, said method comprising; a) forming an octadentate chelator comprising four hydroxypyridinone (HOPO) moieties, substituted in the N-position with a methyl group, and a coupling moiety terminating in a carboxylic acid group; b) coupling said octadentate chelator to at least one tissue-targeting moiety targeting prolyl endopeptidase FAP; and c) contacting said tissue-targeting chelator with an aqueous solution comprising an ion of at least one alpha-emitting thorium isotope. A method of treatment of a neoplastic or hyperplastic disease comprising admistration of such a tissue-targeting thorium complex, as well as the complex and corresponding pharmaceutical formulations are also provided.
priorityDate 2016-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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