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filingDate 2014-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b2cc68f452c0856becaf63a254065149
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publicationDate 2014-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2014196304-A
titleOfInvention Compound
abstract Provided is a compound that is activated in vivo from a compound having relatively little biological activity, that is, a so-called “prodrug” to a compound having relatively biological activity, and a method for targeted treatment of cancer using the compound. . A peptide comprising the amino acid sequence -Arg-Ser-Cit-Gly-Hof-Tyr-Leu- and having a cap-forming group c, fluorescein, fluorescein derivative, monosaccharide, D-amino acid at the N-terminus or C-terminus of the peptide, Alternatively, a prodrug comprising a peptide having a selection from proline imino acid, and a biologically active compound, anticancer agent or vascular disrupting agent bound to the peptide. [Selection figure] None
priorityDate 2007-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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