http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100638709-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-135
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-5375
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-12
filingDate 2004-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2006-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2006-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100638709-B1
titleOfInvention N-substituted sulfamoylbenzoic acid derivatives, preparation method thereof and pharmaceutical composition for antiviral comprising the same
abstract The present invention relates to an N -substituted-sulfamoylbenzoic acid derivative useful as an antiviral agent, and more particularly, a novel N represented by the following Chemical Formula 1 having an excellent antiproliferative effect of Hepatitis C virus (HCV). The present invention relates to a -substituted-sulfamoylbenzoic acid derivative, a pharmaceutically acceptable salt thereof, a preparation method thereof, and an antiviral pharmaceutical composition comprising the compound as an active ingredient. The novel N -substituted-sulfamoylbenzoic acid derivatives represented by the general formula (1) according to the present invention are excellent in inhibiting the proliferation of hepatitis C virus (HCV) and have low toxicity, thus preventing and treating hepatitis C. It can be usefully used as.n n n [Formula 1]n n n n n n n n In Formula 1, R 1 represents a hydroxyl group or a -NR 2 R 3 group.n n n In the substituent for R 1 , R 2 represents a hydrogen atom, a C 1 -C 4 straight or crushed alkyl group, or a-(CH 2 ) m -R 4 group, and in the substituent for R 2 , R 4 represents a phenyl group or a heterocyclic ring, and m represents an integer of 0 to 4.n n n And, in the substituents representing R 1, R 3 is C 1 - C 4 straight or branched chain of the alkyl group, or - (CH 2) n -R 5 represents a group, in the substituent indicates the R 3, R 5 is a C A dialkylamino group of 2 -C 6 , a heterocyclic ring, or a heterocyclic ring in which a straight or pulverized alkyl group of C 1 -C 4 is substituted, n represents an integer of 0 to 4.n n n Antiviral agents, N-substituted-sulfamoylbenzoic acid derivatives, hepatitis C virus, HCV, pharmaceutically acceptable salts, antivirals, pharmaceutical compositions, hepatitis C, prophylaxis, treatment
priorityDate 2004-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID321320
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419486080
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP33493
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCO57273
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ0A443
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419558257
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID11103
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID86625863
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419589977
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP22956
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCO57275
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID135398633
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP30738
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ3ZK55
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10473
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCV5IVB1
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ0A2Q9
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9J7Z2
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCO57266
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ88920
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP11640
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP0C137
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP52680
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ0A3Q4
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA4GCL3
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP05080
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCO57269
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP0C139
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ33339
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ04853
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419524198
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA4GCM4
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9IMM4
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP25328
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP19740
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP18517
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA4GCK2
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419548968
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP0C135
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID87075864
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419567032
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP11619
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCE0J6W8
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457584123
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ04266
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ8AZL8
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ8JJE2
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP22174
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415734038
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA4GCJ1
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA3DSK5
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419508115
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA4ZCW2
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ08IG7
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419573201
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP08269
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ04265
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA4ZCW8
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA4GBY2
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP08271
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ91E95
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ80872
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP22173
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCA3DRP5
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415788016
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP12918
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ66096
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ91A27
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419523391

Total number of triples: 374.