http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2573412-T3
Outgoing Links
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bb75b0b19820e3833ebdcb31603b242b |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P3-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P9-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-437 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-4188 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D491-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D491-048 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D495-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D473-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D473-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D519-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D473-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D473-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D513-04 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D473-28 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-048 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-5377 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4188 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-437 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P3-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P3-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P3-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D513-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D519-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D495-04 |
filingDate | 2011-09-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2016-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a222e59b0e2d74c1227f1b85d9886841 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aa664d49af2c945bdbc872a23907bef9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_02dc83a1c6204c016dd6784b09685b0f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a96a02a1f7d93a6aaf5ec4d9ad6e44d9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ceb04cf56bd267a49e37d285762d49a1 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a597af462ab57f5d59adc232967d48cb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5653b3aa7cea21fc6d0353e66fe124bc |
publicationDate | 2016-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | ES-2573412-T3 |
titleOfInvention | Fused hetero-ring imidazole derivative that has the effect of AMPK (activation of adenosine monophosphate activated protein kinase) |
abstract | A compound characterized in that it is represented by formula (I): ** Formula ** its pharmaceutically acceptable salt or a solvate thereof, wherein a group represented by the formula: ** Formula ** is a group represented by the formula: ** Formula ** halogen, hydroxy, cyano, nitro, carboxy, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted cycloalkyl , substituted or unsubstituted cycloalkenyl, substituted or unsubstituted heterocyclyl, substituted or unsubstituted alkyloxy, substituted or unsubstituted aryloxy, substituted or unsubstituted heteroaryloxy, substituted or unsubstituted cycloalkyloxy, substituted or unsubstituted cycloalkenyloxy, substituted or unsubstituted heterocyclyloxy, alkylthio substituted or unsubstituted, substituted or unsubstituted arylthio, substituted or unsubstituted heteroarylthio, substituted cycloalkylthio oo unsubstituted, substituted or unsubstituted cycloalkenylthio, substituted or unsubstituted heterocyclylthio, substituted or unsubstituted alkylsulfonyl, substituted or unsubstituted arylsulfonyl, substituted or unsubstituted heteroarylsulfonyl, substituted or unsubstituted cycloalkylsulfonyl, substituted or unsubstituted cycloalkenynyl sulfonyl, substituted, substituted or unsubstituted acyl, substituted or unsubstituted carbamoyl, substituted or unsubstituted sulfamoyl, or substituted or unsubstituted amino; m is an integer from 1 to 3; R2 is hydrogen, or substituted or unsubstituted alkyl; X is -O-; and Y is substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; with the proviso that the compounds shown below are excluded: ** Formula ** where, unless otherwise defined, the following definitions apply: "alkyl" refers to a linear or branched C1-alkyl group to C10; "alkenyl" refers to a linear or branched C2 to C8 alkenyl group having one or more double bonds; "alkynyl" refers to a linear or branched C2 to C8 alkynyl group having one or more triple bonds; "cycloalkyl" has from C3 to C15 carbon atoms; "cycloalkenyl" has C3 to C10 carbon atoms; "heterocyclic" refers to a non-aromatic heterocyclic group; the alkyl part of "alkylcarbonyl", the alkenyl part of "alkenylcarbonyl", the cycloalkyl part of "cycloalkylcarbonyl", the cycloalkenyl part of "cycloalkenylcarbonyl" and the heterocyclyl part of "heterocyclylcarbonyl", refer respectively to the "alkyl" above , the anterior "alkenyl", the anterior "cycloalkyl", the anterior "cycloalkenyl" and the anterior "heterocyclyl"; the alkyl part of "alkyloxy", "alkylthio", "alkylsulfonyl" and "alkyloxycarbonyl" refers to the above "alkyl"; the cycloalkyl part of "cycloalkyloxy", "cycloalkylthio" and "cycloalkylsulfonyl" refers to the above "cycloalkyl"; the cycloalkenyl part of "cycloalkenyloxy", "cycloalkenylthio" and "cycloalkenylsulfonyl" refers to the above "cycloalkenyl"; the heterocyclyl part of "heterocyclyloxy", "heterocyclylthio" and "heterocyclyl sulfonyl" refers to the above "heterocyclic"; "substituted alkyl", "substituted alkenyl", "substituted alkynyl", "substituted aryl", "substituted heteroaryl", "substituted cycloalkyl", "substituted cycloalkenyl", "substituted heterocyclyl", "substituted alkyloxy", "substituted aryloxy", "substituted heteroaryloxy", "substituted cycloalkyloxy", "substituted cycloalkenyloxy", "substituted heterocyclyloxy", "substituted alkylthio", "substituted arylthio", "substituted heteroarylthio", "substituted cycloalkylthio", "substituted cycloalkenylthio", "substituted hetericyclithium" "substituted alkylsulfonyl", "substituted arylsulfonyl", "substituted heteroarylsulfonyl", "substituted cycloalkylsulfonyl", "substituted cycloalkenylsulfonyl", "substituted heterocyclylsulfonyl", "substituted acyl", "substituted carbamoyl", "substituted sulfamoyl" or "substituted amino" be substituted with 1 to 4 substituents selected from the group consisting of a) halogen; b) hydroxy; c) carboxy; d) nitro; e) cyano. |
priorityDate | 2010-09-10-04:00^^<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: 382.