http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2004224986-A1

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filingDate 2004-02-18^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e7dc8698dbc56fee35134095a7f7d300
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a82e0a2ecfa677234d3708f00001d437
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9ec12913b743246d0091f1c30d90326b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_26127d18515a11e0fa6cffe42c347164
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5b4c14f45911623beee4207711e4885a
publicationDate 2004-11-11^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2004224986-A1
titleOfInvention Piperidinyl targeting compounds that selectively bind integrins
abstract The present invention relates to the synthesis and biological application of piperidinoyl carboxylic acid integrin antagonists affinity moiety of IFormula (I): n n n and Formula (II): n n n These affinity moieties maybe used with imaging agents or liposomes to target cells that express the α v β 3 , α v β 5 , or α v β 6 integrin receptors.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2009124804-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2009058314-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9694089-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11426473-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8680278-B2
priorityDate 2002-08-16^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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