http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7018851-B2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-582
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filingDate 2003-02-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2006-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dcc0f6df3062b40f6b9d6bc2bbc029a7
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publicationDate 2006-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-7018851-B2
titleOfInvention Biospecific binding reactants labeled with new luminescent lanthanide chelates and their use
abstract This invention relates to a luminescent lanthanide chelate comprising a lanthanide ion and a chelating ligand of formula (I) n nwhereinn n R 1 is selected from the group consisting H, —COOH, —COO − , —CH 2 COOH and —CH 2 COO − ; G 1 is a group consisting of one or two moieties each moiety being selected from the group consisting of ethynediyl, ethenylene, phenylene, biphenylene, naphthylene, pyridylene, pyrazinylene, pyrimidinylene, pyridazinylene, furylene, thienylene, pyrrolylene, imidazolylene, pyrazolylene, thiazolylene, isothiazolylene, oxazolylene, isoxazolylene, fyrazanylene, 1,2,4-triazol-3,5-ylene and oxadiazolylene; G 2 for coupling to a biospecific binding reactant is selected from the group consisting of amino, aminooxy, carbonyl, aldehyde or mercapto groups and activated forms made of them; Z is selected from the group consisting of carboxyalkyl amine, ether, thioether, carbonyl and unsubstituted or substitute methyl (—CR 2 —) wherein group R 2 is selected from the group consisting of H, methyl, ethyl and carboxylalkyl; and the lanthanide ion is europium(III), terbium(III), dysprosiym(III) or samarium(III). This invention further relates to a detectable molecule comprising the lanthanide chelate and the use of the molecule in a method of carrying out a biospecific binding assay.
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