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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C311-17
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-36
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filingDate 1986-01-31-04:00^^<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_af5fd18861195783c2ad59cbddcdcd7a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c2340fec5d8e2aa52b7b382f6ad2fc2d
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publicationDate 1993-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-1363764-C
titleOfInvention N-2-fluorenesulfonyl-o-propionyl-threo-d,l-phenylserine ethyl ester showing antiviral activity with respect to echo 11 virus
abstract The invention relates to esters of substituted amino acids, in particular to ethyl ester M-2-fluorensulfonyl-0-propioNyl-threo-0, L-phenylserine (EPS), which may find application in medicine. The chain is the creation of new derivatives of this series it exhibits antiviral activity against ECHO virus G. The production of EPS is carried out from ethyl phosphate L-2-fluorensulfonyl-threo-0.1.-phen1llserine and propionic acid chloride with absolute chloroform upon boiling. Yield 93, 1%, mp 138-140 °; C. EFS is only active against ECHO P at a dose of 500 μg / mp and a therapeutic index of 2.);, -. | Mi 4 .. to @ s "-.1
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/LT-4663-B
priorityDate 1986-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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