http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-1806133-C

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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

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