http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-1806133-C
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_be91b86eb1f4554580a36df612d284a7 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C311-38 |
filingDate | 1991-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 1993-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_96b085954de21737000337cd148a087c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49ec7e4b628c11acfce32f9082cc6cc0 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_df02d4a0bf9769590808c03256c1c3bf http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_40c3a0a4e269d9f701fc083066a776f6 |
publicationDate | 1993-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | RU-1806133-C |
titleOfInvention | 6-(n-benzyloxycarbonyl)arginylaminonaphthalene-1-sulfamides bromohydrates as substrates for analysis of peptidases by fluorescent method |
abstract | Usage: as substrates for fluorescence analysis of peptidases. SUMMARY OF THE INVENTION: 6- (Na-benzyloxycarbonyl) arginylamino-naphthalene-1-sulfamide bromohydrates of the formula: 1-RiR2NS02 (naphthalene NAGD M01 -Z) HBr, where, R2 is linear or branched (Ct-C) alkyl, CsHn, cyclohexyl, ben - zil, or, C2I5, or NRiR2 hexamethylene, piperidine, morpholine, Z-benzyloxycarbonyl. Reagent 1: 6- (N a-benzyloxycarbonyl) arginyl bromide. Reagent -2: corresponding aminonaphthalene sulfamide. Reaction conditions: in dry pyridine and toluene. 3 tab. |
priorityDate | 1991-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 40.