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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 1998-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_24ea1870eb912fc6f533346326fa47fe
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cb666d727f057068d7d08e88a840f4d8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5c5f1f273cd6fdb436800262705ec66f
publicationDate 1998-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9831363-A1
titleOfInvention Anti-viral compounds
abstract The present invention relates to compounds of Formula (I), which inhibit the growth of picornaviruses, such as rhinoviruses, Hepatitus viruses, enteroviruses, cardioviruses, polioviruses, coxsackieviruses of the A and B groups, echo virus and Mengo virus, wherein: R is C1-C6 alkyl, phenyl, or substituted phenyl; Y and Y1 are independently hydrogen, halo, nitro, or trifluoromethyl; X is N-OH, O, or CHR1; R1 is hydrogen, halo, CN, C¿1?-C4 alkyl, -C CH, CONR?2R3, COR2¿, or CO¿2?R?2; R2 and R3¿ are independently hydrogen or C¿1?-C4 alkyl; or a pharmaceutically acceptable salt thereof.
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priorityDate 1997-01-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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