http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0066680-A2

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2b62570f67c2899a71a144c76c503973
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S436-80
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K11-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K11-06
filingDate 2000-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fa130b78f85e6617ae3f0cd177320c2c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d175aa6412ed09863302efb0beaea57c
publicationDate 2000-11-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-0066680-A2
titleOfInvention Luminescent 4-trifluoromethyl-2-quinolones with long-wave uv-absorption and the use thereof
abstract The invention relates to a substituted 4-trifluoromethyl carbostyril according to formula (I) and is characterised in that the 4-trifluoromethyl carbostyril is provided with an absorption maximum between 350 and 420 nm and a luminescence maximum between 430 and 900 nm. The molecule can be substituted with groups that are useful for complexing metal ions and/or for binding the molecule to relevant groups of a target molecule or a solid supporting material. The carbostyril as described above can inter alia serve as an antenna molecule of a lanthanide complex. Said complexes can be templates and can be brought into contact with a directly bound or free colour molecule which absorbs in the range of 580-710 nm. Luminescence effects and decay periods can be measured after the contact with a relevant analyte.
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priorityDate 1999-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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