http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-1619671-C

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-13
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-63
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-12
filingDate 1989-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1993-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1bda73af3f295593322f4f27a50df818
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ccd825236db514921505414dceaf55f4
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publicationDate 1993-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-1619671-C
titleOfInvention N,n,n-trialkyl- (dialkylphenacyl) -n- (4-dipropylamino-2-alkenyl) ammonium bromide hydrobromides showing antiviral activity with respect to coxsackie a13 virus
abstract The invention relates to nitrogen-containing compounds, in particular to N. N. hydrobromides. M-trialkyl- (dial1oshfenaci1) -M- {4-dipropylamino-2-alkenyl) ammonium bromides of grade +, 0 / & where R R is -C2H5 -CH3; R is -6H COC6Hg; X-H, which have antiviral activity. The goal is to identify more active compounds. The preparation is carried out by the reaction of N. N, p-triethyl-N- (4-bromo-3-methyl-2-butenyl) -and N. M-dimetip-M-phenacyl-N- (4-bromo-2-butenyl ) ammonium bromides with dipropylzmin in ethanol at 18 to 20 °; C. Yield%; t, ° C; Brugto-f-la: for compound 1 - 93; 105-106; C „H„ Br N; for I, 872; 135 D7; 38 2 2 BUT. 2tab
priorityDate 1989-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 34.