http://rdf.ncbi.nlm.nih.gov/pubchem/patent/HU-0400159-A2
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_4dac022280ec96f54c694eb427655932 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D261-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D217-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-47 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D271-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K45-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-36 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4245 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4402 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D261-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D217-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K45-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D271-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-472 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-47 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-497 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D405-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-06 |
| filingDate | 2002-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_65218b74519323fd2b2411e9c052e0ea http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_36096d9ffae2a547e351ba638e1aec1b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7d6c265913b189a8bcd3bcb53e68f807 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_973bf1e6b1b8914ccbf61003290a52b8 |
| publicationDate | 2004-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | HU-0400159-A2 |
| titleOfInvention | Anthranilic acid derivatives with heteroarylsulfonyl side chain, method for their preparation, use and pharmaceutical compositions containing them |
| abstract | In the formula (I) of the compounds of this invention, R (I) is a group of formula (a), (b), (c) or (d), wherein A is -CnH2n-, wherein n is 0, 1, 2, 3, 4 or 5, D is a direct bond or oxygen, E is -CmH2m where m is 0, 1, 2, 3, 4 or 5, R (8) is hydrogen, alkyl or CpH2p-R (14). wherein p is 0, 1, 2, 3, 4 or 5; R (14) is phenyl, naphthyl or heteroaryl, which may be optionally substituted with 1, 2 or 3 substituents wherein F, CL, Br; I, CF3, OCF3, NO2, CN, COOMe, CONH2, COMe, NH2, OH, alkyl, alkoxy, dimethylamino, sulfamoyl, methylsulfonyl or methylsulfonylamino, R (9) is hydrogen or alkyl, R (10) is hydrogen, alkyl, phenyl. , naphthyl or heteroaryl, wherein the phenyl, naphthyl and heteroaryl may be optionally substituted with 1, 2 or 3 substituents wherein F, Cl, Br, I, CF 3, OCF 3, NO 2, CN, COOMe, CONH 2, COMe, NH 2, OH, alkyl, alkoxy, dimethylamino, sulfamoyl, methylsulfonyl, or methylsulfonylamino, R (11) is -cycloalkyl, phenyl, naphthyl, thienyl, furyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, indolyl, indolyl, indolyl, indolyl, indolyl, indolyl, indolyl, indazolyl; quinoxalinyl, quinazolinyl or cinnolinyl, wherein phenyl, naphthyl, thienyl, furyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, indolyl, indazolyl, quinolyl, isoquinolyl, phthalazinyl, quinolinyl or quinolinyl, quinolinyl, F, Cl, Br, I, CF 3, OCF 3, NO 2, CN, COMe, NH 2, OH, alkyl, alkoxy, dimethylamino, sulfamoyl, methylsulfonyl or methylmethylsulfonylamino, R (12) is alkyl, alkynyl, cycloalkyl, phenyl, naphthyl, or heteroaryl; phenyl, naphthyl and heteroaryl may be optionally substituted with 1, 2 or 3 substituents wherein F, Cl, Br, I, CF 3, OCF 3, NO 2, CN, COOMe, CONH 2, COMe, NH 2, OH, alkyl, alkoxy, dimethylamino, sulfamoyl, methylsulfonyl or methylsulfanylamino, R (13) is a group of the general formula CpH2p-R (14) wherein p is 0, I, 2, 3, 4 or 5, R (15) is -cycloalkyl, R (2) is hydrogen or alkyl, R (3) ) represents a heteroaryl group which is optionally 1, |
| priorityDate | 2001-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 319.