http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-3485068-D1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_153afaf9d74a0fe68cb8addfea16743a
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2326-12
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-28
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-28
filingDate 1984-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1991-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b329377414e1424d97f3d585fcb4efb8
publicationDate 1991-10-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-3485068-D1
titleOfInvention METHOD FOR DETERMINING THE ACTIVITY OF PEROXIDASE, BY MEANS OF END DILUTION, AND BY MEANS OF CARRYING OUT THE SAME.
abstract Determn. of peroxidase activity by end dilution titration under peroxidase and pt. dilution titration determng. conditions comprises reaction of a peroxidase and a benzidine deriv. of formula (I) or its salt. R1 = H, halogen, NH2, 1-4C alkyl, 1-4C alkoxy, COOH, SO3H or carboxypropoxy; R2 = H, halogen or 1-4C alkyl. Reaction is in presence of a colour-retarding amt. of non- or low chromogenic benzene deriv. of formula (II) to retard colour development for sufficiently long to permit a sharp dilution end pt., and then peroxidase activity is determined. R3, R4 = OH, NH2, 1-4C alkylamino or benzylamino.
priorityDate 1983-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 19.