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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D271-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K11-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D271-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-78
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-52
filingDate 1985-05-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1988-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c7c10fc565aaebab78050612b060d932
publicationDate 1988-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4769467-A
titleOfInvention Fluorogenic 2,1,3-benzoxadiazoles and fluorometric amine/thiol assays therewith
abstract Fluorogenic compounds are disclosed which are reactive with biologically important analytes including primary amines, secondary amines, and/or thiols and are of the general formula: <IMAGE> wherein X is a group such as <IMAGE> -CN, -CO2CH3, or SO2R, and wherein R is <IMAGE> OR3, or Cl; R1 and R2 are hydrogen atoms or alkyl groups having 1 to 3 carbon atoms and R3 is a phenyl or benzyl group. The inventive compounds form a fluorescent adduct with the above analytes at the number 7 position of the benzoxadiazole ring. The fluorescent adduct thereby formed enables detection of very minute amounts of analyte (picomoles) using conventional fluorescent analytical methods.
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priorityDate 1983-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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