http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S63201155-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_03d0f52bb4069f8a19d70dcfb697c67a |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C237-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-48 |
| filingDate | 1987-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_573971b8b793312f594c224c9b31105f |
| publicationDate | 1988-08-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-S63201155-A |
| titleOfInvention | Substrate for gammaglutamyl transferase and measurement thereof |
| abstract | NEW MATERIAL:A γ-glutamyl-p-aminoanilide derivative shown by formula I (A 1 and A 2 are each lower alkylene; R 1 and R 2 are each H or lower alkyl) or a salt thereof. n EXAMPLE: γ-L-Glutamyl-p-(N,N-di-β-hydroxyethylamino)anilide. n USE: Useful as a substrate for measuring γ-glutamyl transferase active value. Having extremely excellent reactivity, solubility, etc., capable of conducting colorimetry which can measure accurately and rapidly and of readily being applied to automatic analysis, especially to dry analysis using multi-layer analysis slide of integral type by simplicity of colorimetry. n PREPARATION: For example, a p-phenylenediamine derivative shown by formula II is reacted with a 9N-position protected-γ-L-glutamic anhydride such as N- phthalyl-γ-L-glutamic anhydride, etc. Then the reaction product is deprotected to give a compound shown by formula I. n COPYRIGHT: (C)1988,JPO&Japio |
| priorityDate | 1987-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 24.