http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1303031-C

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-505
filingDate 1987-08-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1992-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_66899e3449ad58840efb5b32be79acde
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_99f5c6745cfab8db435ebe9479aa71e7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_932dd8cb0daaac86b0fd1f9a85f4e180
publicationDate 1992-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1303031-C
titleOfInvention Pyrimidine derivatives
abstract Abstract Compounds of the formula wherein R1 is halogen, C1-4-alkyl, halo-(C1-4-alkyl) or C2-4-alkanoy1, R2 is hydrogen, hydroxy, C1-4-alkoxy, C1-4-alkylthio or phenyl-(C1-4-alkoxy) or, when X is O, also acyloxy, R3 is hydrogen or C1-4-alkyl, R4 is a carbocyclic group or a heterocyclic group, RS is hydrogen or fluorine, m stands for zero, 1 or 2, X is O or NH and Y is a direct bond, -CH=CH-, -C=C- or a group of the formula of (Z)n-A- (a) in which A is a C1-8-alkylene group which is optionally substituted by one or two phenyl groups, Z is O, S, SO or SO2 and n stands for zero or 1, with the proviso that R1 is different from iodine, when R2 is hydroxy or benzoyloxy, R3 is hydrogen, R4 is unsubstituted phenyl, R5 is hydrogen, m stands for zero, X is O, and Y is a direct bond, and tautomers thereof, possess antiviral activity and can be used in the form of medicaments for the control and prevention of viral infections. They can be manufactured according to methods known per se.
priorityDate 1986-08-18-04:00^^<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: 793.