http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2622977-T3

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filingDate 2010-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2017-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2622977-T3
titleOfInvention Homogeneous tests with dissolution phase
abstract A test method for an analyte in a sample, the test method comprising: forming a reaction mixture in an aqueous solution, in any order or simultaneously adding sample, a specific chemiluminescent labeled binding partner, a binding partner specific labeled with activator, wherein the activator brand activates the chemiluminescent label, and a selective signal inhibitor, where all components are soluble in aqueous solution, where the specific binding partner labeled with chemiluminescent and the partner Specific binding labeled with activator bind to analyte present in the sample to form a binding complex; adding to the reaction mixture an activating solution, wherein the activating solution releases a detectable chemiluminescent signal correlated with the amount of specific binding partner labeled with chemiluminescent bound to analyte and specific binding partner labeled with activator bound to analyte in the mixture reaction, wherein the selective signal inhibitor is selected from the group consisting of ** Formula ** wherein: the chemiluminescent-labeled specific binding partner comprises a chemiluminescent label compound directly or indirectly connected to a binding torque member specific, wherein the chemiluminescent brand is selected from compounds of acidane cetenedithioacetal, acridan esters, thioesters of acridane, acridane sulfonamides, and derivatives of acridane enol of formula VIII: ** Formula ** wherein R1 is selected from alkyl, alkenyl groups , alkynyl, aryl and aralkyl of 1-20 carbon atoms, any of which may be substituted with 1-3 groups selected from carbonyl groups, carboxyl groups, tri (C1-C8 alkyl) silyl groups, an SO3- group, an OSO3-2 group, glycosyl groups, a PO3- group, a OPO3-2 group, halogen atoms, a hydroxyl group, a thiol group, amino groups, quaternary ammonium groups or quaternary phosphonium groups, wherein X is selected from alkyl, aryl, C1-C8 aralkyl groups, the alkyl groups having or aryl carboxyl of 1-20 carbon atoms, tri (C1-C8 alkyl) silyl groups, a SO3- group, glycosyl groups and phosphoryl groups of the formula PO (OR ') (OR ") wherein R' and R" are independently selected from the alkyl, cyanoalkyl, aryl and aralkyl C1-C8 groups, trialkylsilyl groups, alkali metal cations, alkaline earth cations, ammonium and trialkylphosphonium cations, wherein Z is selected from O and S atoms, wherein R6 is selected from alkyl, phenyl, benzyl, alkoxyalkyl and substituted C1-C4 carboxyalkyl groups os or unsubstituted, where R7-14 is each hydrogen or 1 or 2 alkyl, alkoxy, hydroxy and halogen substituents are selected and the rest of R7-14 is hydrogen or where each of R7-14 is hydrogen and R1 it is a labeling substituent or wherein one of R7-14 is a labeling substituent and the others of R7-14 are hydrogen. wherein the specific binding partner labeled with activator comprises a compound with activator label directly or indirectly connected to a member of a specific binding pair wherein the activator brand is selected from transition metal salts, transition metal complexes and enzymes , wherein the activator brand has peroxidase activity, and wherein the activator solution comprises a peroxide compound.
priorityDate 2009-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419520830
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCG1NJB6
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23667635
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397365
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP02190
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP02178
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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP29287
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP14393
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Total number of triples: 447.