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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-56
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-505
filingDate 1994-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1998-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_74f869dacc6f45075f13c6088540df8a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_da734d54cb5c2950f01142b56a33909a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_de52358dfc58599ce8224a5af482b7a3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bab9c7ad62244f6f824897dbce6c969c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_da1ecec70028f1c1c8d6177bbefc31e0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_48d56df0d938cd08c34b5cb27fc7c5a7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10bf274f83d83d927aeba617b5d384cc
publicationDate 1998-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-0140021-B1
titleOfInvention Pyrimidine Acyclonucleoside Derivatives
abstract The present invention relates to a novel pyrimidine acyclonucleoside derivative represented by the following structural formula (I) and an antiviral agent comprising the same as an active ingredient.n n n n n n n n In the above formula, R 1 is an ethyl group or isopropyl group, R 2 is a substituted or unsubstituted phenyl selenenyl group, the substituent is one or more selected from alkyl groups and halogen atoms of C 1 ~ C 2 , R 3 is hydrogen An atom, a C 1 to C 3 alkyl group, a C 1 to C 3 hydroxyalkyl group, an acyloxyalkyl group or a substituted or unsubstituted phenyl group may be selected from the group consisting of C 1 to C 3 alkyl group and C 1 to C 3 alkoxy group Or a halogen atom, X is an oxygen atom or a sulfur atom.
priorityDate 1994-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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