http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-054702-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0a910d33c239980f3a705e312c5bad6a |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C311-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C311-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C311-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C311-17 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D405-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D409-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D217-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-26 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D317-64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-233 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D215-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C317-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-62 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-47 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-65 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-88 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D251-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C311-29 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-34 |
| filingDate | 2005-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2b27b67708fd86e09f488636bf53c711 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_935c70f6ca50e82f5d89cfa8d37e5aca http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7180264136e2837b75c6c7254ce276a9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a21096e1f6c8eae764d6cb82501b55b |
| publicationDate | 2007-07-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-054702-A1 |
| titleOfInvention | COMPOUNDS DERIVED FROM SULFONAMIDE, A METHOD OF PREPARATION, PHARMACEUTICAL COMPOSITION AND USE OF THE COMPOUND FOR THE PREPARATION OF A MEDICINAL PRODUCT |
| abstract | Compositions that comprise them, processes for their preparation and their use to manufacture medicines. Its use in therapy consists of treatment for inflammatory disease states. Claim 1: A compound characterized in that it responds to formula (1), wherein: A is phenyl, naphthyl, pyridinyl, furyl, thienyl, isoxazolyl, pyrazolyl, benzthienyl, quinolinyl or isoquinolinyl, and A is optionally substituted by halo, C1- alkyl 6, C1-6 alkoxy, C1-4 alkylthio, C1-4 fluoroalkyl, C1-4 fluoroalkoxy, pyridinyloxy, benzyloxy, nitro, cyano, C (O) 2H, C (O) 2C1-4alkyl, S (O) 2C1alkyl 4, S (O) 2NH2, S (O) 2NH1-4alkyl, S (O) 2N (C1-4alkyl) 2, C (O) C1-4alkyl, C (O) NH2, C (O) NH1-4alkyl, C (O) N (C1-4 alkyl) 2, NHC (O) C1-4 alkyl, NR10R11, phenoxy (optionally substituted by halo, C1-6 alkyl, C1-6 alkoxy, C1-4 alkylthio, C1-4 fluoroalkyl, fluoroalkoxy C1-4, nitro, cyano, C (O) 2H, C (O) 2 alkylC1-4, S (O) 2alkylC1-4, S (O) 2NH2, S (O) 2NHalkylC1-4, S (O) 2N ( C1-4 alkyl) 2, C (O) C1-4 alkyl, benzyloxy, C (O) NH2, C (O) NH1-4 alkyl, C (O) N (C1-4 alkyl) 2, NHC (O) C1-4 alkyl or NR14R15), phenyl (optionally substituted by halo, C1-6 alkyl, C1-6 alkoxy, C1-4 alkylthio, fluoroal C1-4 chyl, C1-4 fluoroalkoxy, nitro, cyano, C (O) 2H, C (O) 2C1-4 alkyl, S (O) 2C1-4 alkyl, S (O) 2NH, S (O) 2NHC1-4 alkyl S (O) 2N (C 1-4 alkyl) 2, C (O) C 1-4 alkyl, benzyloxy, C (O) NH 2, C (O) NH C 1-4 alkyl, C (O) N (C 1-4 alkyl) 2, NHC ( O) C1-4 alkyl or NR16R17), pyridinyloxy (optionally substituted by halo, C1-6 alkyl, C1-4 alkoxy, C1-4 alkylthio, C1-4 fluoroalkyl, C1-4 fluoroalkoxy, nitro, cyano, C (O) 2H , C (O) 2 C1-4alkyl, S (O) 2C1-4alkyl, S (O) NH2, S (O) 2NC1-4alkyl, S (O) 2N (C1-4alkyl) 2, C (O) C1-4alkyl , benzyloxy, C (O) NH2, C (O) NH1-4alkyl, C (O) N (C1-4alkyl) 2 NHC (O) C1-4alkyl, or NR18R19) or pyrazolyl (optionally substituted by halo, C1- alkyl 6, C1-6 alkoxy, C1-4 alkylthio, C1-4 fluoroalkyl, C1-4 fluoroalkoxy, nitro, cyano, C (O) 2H, C (O) 2C1-4 alkyl, S (O) 2C1-4 alkyl, S ( O) 2NH2, S (O) 2NH1-4alkyl, S (O) 2N (C1-4alkyl) 2, C (O) C1-4alkyl, C (O) NH2, C (O) NH1-4alkyl, C (O) N (C1-4alkyl) 2, NHC (O) C1-4alkyl, or NR20R21; R10, R11, R14, R15, R16, R17, R18, R19, R20 and R21 are, independently, hydrogen, C1-4 alkyl or C3-7 cycloalkyl; R 1 is hydrogen, C 1-6 alkyl, phenyl, C (6-) pyridinyl, C 3-6 cycloalkyl, (C 3-6 cycloalkyl) CH 2 or C 3-4 alkenyl; L is a bond, C1-4 alkylene (optionally substituted by C1-4 alkyl or C1-4 haloalkyl), C1-4 alkylene (optionally substituted by C1-4 alkyl or C1-4 haloalkyl), CH2C (O) NH, CH (CH3) C (O) NH, C1-4 alkylene (optionally substituted by C1-4 alkyl or C1-4 haloalkyl), C1-4 alkylene (optionally substituted by C1-4 alkyl or C1-4 haloalkyl), C1-4-S (O) alkylene (optionally substituted by C1-4 alkyl or C1-4 haloalkyl) or C1-4 alkylene) -S (O) 2 (optionally substituted by C1-4 alkyl or C1-4 haloalkyl); W is cyclohexyl, phenyl, methylenedioxyphenyl, thienyl, pyrazolyl, thiazolyl, isoxazolyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, 1,3,5-triazinyl, 1,2,3-triazinyl, 1,2,4-triazinyl, benzofuranyl, benzthienyl, indolyl, indolinyl, dihydroindolinyl, indazolyl, benzimidazolyl, benzoxazolyl, benzthiazolyl, quinolinyl, tetrahydroquinolinyl, isoquinolinyl, quinoxalinyl, quinazolinyl, cinnolinyl, phthalazinyl, [1,8] -naphthyridinyl, quintalidinyl 1H) -onyl, isoquinolin-1 (2H) -onyl, phthalazin-1 (2H) -onyl, 1H-indazolyl, 1,3-dihydro-2H- indole-2-onyl, isoindolin-1-onyl, 3,4 -dihydro-1H-isochromen-1-onyl or 1H-isochromen-1-onyl; W is optionally substituted by halo, C1-6 alkyl, C1-4 alkoxy, C1-4 alkylthio, C1-4 fluoroalkyl, C1-4 fluoroalkoxy, nitro, cyano, OH, C (O) 2H, C (O) 2C1 alkyl 4, S (O) 2 C1-4alkyl, S (O) 2NH2, S (O) 2NC1-4alkyl, S (O) 2N (C1-4alkyl) 2, benzyloxy, imidazolyl, C (O) C1-4alkyl, C ( O) NH2, C (O) NH1-4alkyl, C (O) N (C1-4alkyl) 2, NHC (O) C1-4alkyl or NR12R13; R12 and R13 are, independently, hydrogen, C1-4 alkyl or C3-7 cycloalkyl; or a salt acceptable for pharmaceutical use thereof. |
| priorityDate | 2004-10-29-04:00^^<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: 76.