http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20010025055-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P1-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-437
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-444
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K-
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-16
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-444
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 1998-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2001-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20010025055-A
titleOfInvention Anti-Viral Compounds
abstract The present invention relates to compounds of formula (I) which inhibit the growth of picornavirus, hepatitis virus, enterovirus, cardiovirus, polio virus, coxsackievirus of the A and B groups, echo virus and mengo virus. In the above formula or pharmaceutically acceptable salts thereof, A is hydrogen, halo, CN, C 1 -C 4 alkyl, -C≡CH, CO (C 1 -C 4 alkyl), CO 2 (C 1 -C 4 alkyl) ), Or CONR 2 R 3 , R 2 and R 3 are independently hydrogen or C 1 -C 4 alkyl, A ′ is hydrogen, halo, C 1 -C 6 alkyl, benzyl, naphthyl, thienyl, furyl , Pyridyl, pyrrolyl, COR 4 , S (O) n R 4 , or a group of formula (II), R 4 is C 1 -C 6 alkyl, phenyl or substituted phenyl, n is 0, 1 Or 2, R 5 is independently hydrogen or halo at each position, m is 1, 2, 3 or 4, R 6 is hydrogen, halo, CF 3 , OH, CO 2 H, NH 2 , NO 2 , CONHOCH 3 , C 1 -C 4 alkyl or CO 2 (C 1 -C 4 alkyl), C 1 -C 4 alkoxy.n n n <Formula I>n n n n n n n n <Formula II>
priorityDate 1998-05-20-04:00^^<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: 415.