RU2008129622A - Производные никотиновой кислоты в качестве модуляторов метаботропных глутаматных рецепторов - Google Patents
Производные никотиновой кислоты в качестве модуляторов метаботропных глутаматных рецепторов Download PDFInfo
- Publication number
- RU2008129622A RU2008129622A RU2008129622/04A RU2008129622A RU2008129622A RU 2008129622 A RU2008129622 A RU 2008129622A RU 2008129622/04 A RU2008129622/04 A RU 2008129622/04A RU 2008129622 A RU2008129622 A RU 2008129622A RU 2008129622 A RU2008129622 A RU 2008129622A
- Authority
- RU
- Russia
- Prior art keywords
- pyridin
- methanone
- ylamino
- chloro
- methylpyridin
- Prior art date
Links
- 239000002253 acid Substances 0.000 title claims abstract 13
- 102000016193 Metabotropic glutamate receptors Human genes 0.000 title 1
- 108010010914 Metabotropic glutamate receptors Proteins 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract 20
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 17
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 14
- 229910052736 halogen Inorganic materials 0.000 claims abstract 14
- 150000002367 halogens Chemical group 0.000 claims abstract 14
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 14
- 239000001257 hydrogen Substances 0.000 claims abstract 14
- 150000003839 salts Chemical class 0.000 claims abstract 13
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract 12
- 239000012458 free base Substances 0.000 claims abstract 12
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract 12
- 125000000547 substituted alkyl group Chemical group 0.000 claims abstract 12
- 125000000217 alkyl group Chemical group 0.000 claims abstract 10
- 125000003282 alkyl amino group Chemical group 0.000 claims abstract 9
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract 9
- 125000004663 dialkyl amino group Chemical group 0.000 claims abstract 5
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract 5
- 150000002431 hydrogen Chemical class 0.000 claims abstract 5
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract 5
- 125000006413 ring segment Chemical group 0.000 claims abstract 5
- 125000003277 amino group Chemical group 0.000 claims abstract 4
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims abstract 4
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract 4
- -1 4-chlorophenylamino Chemical group 0.000 claims 67
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 18
- 201000010099 disease Diseases 0.000 claims 12
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 6
- WSFSSNUMVMOOMR-BJUDXGSMSA-N methanone Chemical compound O=[11CH2] WSFSSNUMVMOOMR-BJUDXGSMSA-N 0.000 claims 5
- 102000012777 Metabotropic Glutamate 5 Receptor Human genes 0.000 claims 4
- 108010065028 Metabotropic Glutamate 5 Receptor Proteins 0.000 claims 4
- 210000001035 gastrointestinal tract Anatomy 0.000 claims 4
- 230000000848 glutamatergic effect Effects 0.000 claims 4
- 230000001404 mediated effect Effects 0.000 claims 4
- 210000000653 nervous system Anatomy 0.000 claims 4
- 230000007170 pathology Effects 0.000 claims 4
- 210000001635 urinary tract Anatomy 0.000 claims 4
- 230000005540 biological transmission Effects 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 230000002265 prevention Effects 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- OTWXYJNVTOQVAZ-UHFFFAOYSA-N (2-butyl-1,3-oxazinan-3-yl)-[5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]methanone Chemical compound CCCCC1OCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 OTWXYJNVTOQVAZ-UHFFFAOYSA-N 0.000 claims 1
- UJXARZKVVMYUID-UHFFFAOYSA-N (2-butylpiperidin-1-yl)-[5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]methanone Chemical compound CCCCC1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 UJXARZKVVMYUID-UHFFFAOYSA-N 0.000 claims 1
- GWKMILBGLNCMDT-UHFFFAOYSA-N 3,4,4a,5,6,7,8,8a-octahydro-2h-quinolin-1-yl-[6-(4-chloroanilino)pyridin-3-yl]methanone Chemical compound C1=CC(Cl)=CC=C1NC1=CC=C(C(=O)N2C3CCCCC3CCC2)C=N1 GWKMILBGLNCMDT-UHFFFAOYSA-N 0.000 claims 1
- PUQAHZPHRXPSAW-UHFFFAOYSA-N 3-azabicyclo[2.2.1]heptan-3-yl-[5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]methanone Chemical compound C1=NC(C)=CC=C1NC1=NC=C(C(=O)N2C3CCC(C3)C2)C=C1Cl PUQAHZPHRXPSAW-UHFFFAOYSA-N 0.000 claims 1
- ZGZXNOYLBQRQEQ-UHFFFAOYSA-N 3-azabicyclo[3.2.2]nonan-3-yl-[6-(4-chloroanilino)pyridin-3-yl]methanone Chemical compound C1=CC(Cl)=CC=C1NC1=CC=C(C(=O)N2CC3CCC(CC3)C2)C=N1 ZGZXNOYLBQRQEQ-UHFFFAOYSA-N 0.000 claims 1
- UEKPAIMMZMCKSL-UHFFFAOYSA-N 6-(4-chloroanilino)-n,n-diethylpyridine-3-carboxamide Chemical compound N1=CC(C(=O)N(CC)CC)=CC=C1NC1=CC=C(Cl)C=C1 UEKPAIMMZMCKSL-UHFFFAOYSA-N 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 1
- DSXSVCBJSYRQQI-WWPJHQMMSA-N [(3ar,4s,7ar)-4-hydroxy-4-[2-(3-methylphenyl)ethynyl]-3,3a,5,6,7,7a-hexahydro-2h-indol-1-yl]-[6-(4-chloroanilino)pyridin-3-yl]methanone Chemical compound CC1=CC=CC(C#C[C@@]2(O)[C@H]3[C@H](N(CC3)C(=O)C=3C=NC(NC=4C=CC(Cl)=CC=4)=CC=3)CCC2)=C1 DSXSVCBJSYRQQI-WWPJHQMMSA-N 0.000 claims 1
- RCJJQWIMWHHYKR-OAHLLOKOSA-N [5-chloro-6-[(6-methoxypyridin-3-yl)amino]pyridin-3-yl]-[(2r)-2-ethylpiperidin-1-yl]methanone Chemical compound CC[C@@H]1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(OC)N=C1 RCJJQWIMWHHYKR-OAHLLOKOSA-N 0.000 claims 1
- UKUMGXODPZJWJX-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(2,3-diethylpiperidin-1-yl)methanone Chemical compound CCC1C(CC)CCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 UKUMGXODPZJWJX-UHFFFAOYSA-N 0.000 claims 1
- FCZFMKAXRZXYQE-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(2,3-dimethylpiperidin-1-yl)methanone Chemical compound CC1C(C)CCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 FCZFMKAXRZXYQE-UHFFFAOYSA-N 0.000 claims 1
- MKKRTZXTLADIPV-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(2-ethenylpiperidin-1-yl)methanone Chemical compound C1=NC(C)=CC=C1NC1=NC=C(C(=O)N2C(CCCC2)C=C)C=C1Cl MKKRTZXTLADIPV-UHFFFAOYSA-N 0.000 claims 1
- UBYMDIBFPWDBDV-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(2-ethyl-3-methylpiperidin-1-yl)methanone Chemical compound CCC1C(C)CCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 UBYMDIBFPWDBDV-UHFFFAOYSA-N 0.000 claims 1
- GGGJDPXNTLTHQM-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(2-methyl-6-propylpiperidin-1-yl)methanone Chemical compound CCCC1CCCC(C)N1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 GGGJDPXNTLTHQM-UHFFFAOYSA-N 0.000 claims 1
- LCVNVMOYCVBALJ-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(2-pentan-3-yl-1,3-oxazinan-3-yl)methanone Chemical compound CCC(CC)C1OCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 LCVNVMOYCVBALJ-UHFFFAOYSA-N 0.000 claims 1
- STTZEZHKQIJKJR-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(2-pentan-3-ylpiperidin-1-yl)methanone Chemical compound CCC(CC)C1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 STTZEZHKQIJKJR-UHFFFAOYSA-N 0.000 claims 1
- GCFLCUNUJNVWKN-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(2-phenylpiperidin-1-yl)methanone Chemical compound C1=NC(C)=CC=C1NC1=NC=C(C(=O)N2C(CCCC2)C=2C=CC=CC=2)C=C1Cl GCFLCUNUJNVWKN-UHFFFAOYSA-N 0.000 claims 1
- TWZOJPNADIKKCZ-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(2-propan-2-ylpiperidin-1-yl)methanone Chemical compound CC(C)C1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 TWZOJPNADIKKCZ-UHFFFAOYSA-N 0.000 claims 1
- HLMCKZYCPCMLSH-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(2-propylazepan-1-yl)methanone Chemical compound CCCC1CCCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 HLMCKZYCPCMLSH-UHFFFAOYSA-N 0.000 claims 1
- JFVQMYLXIIQSQB-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(2-propylpiperidin-1-yl)methanone Chemical compound CCCC1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 JFVQMYLXIIQSQB-UHFFFAOYSA-N 0.000 claims 1
- ODXXMVGQRWUDQD-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(2-pyridin-2-ylpyrrolidin-1-yl)methanone Chemical compound C1=NC(C)=CC=C1NC1=NC=C(C(=O)N2C(CCC2)C=2N=CC=CC=2)C=C1Cl ODXXMVGQRWUDQD-UHFFFAOYSA-N 0.000 claims 1
- FZMFLXACJCTCMA-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(3-cyclopropylpiperidin-1-yl)methanone Chemical compound C1=NC(C)=CC=C1NC1=NC=C(C(=O)N2CC(CCC2)C2CC2)C=C1Cl FZMFLXACJCTCMA-UHFFFAOYSA-N 0.000 claims 1
- GJEHJMUTEDYLAO-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(3-propylidenepiperidin-1-yl)methanone Chemical compound C1C(=CCC)CCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 GJEHJMUTEDYLAO-UHFFFAOYSA-N 0.000 claims 1
- SZTSAJHGMRUJJW-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(3-propylpiperidin-1-yl)methanone Chemical compound C1C(CCC)CCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 SZTSAJHGMRUJJW-UHFFFAOYSA-N 0.000 claims 1
- NRMDHIOZOOKAIT-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(5-fluoro-2-propylpiperidin-1-yl)methanone Chemical compound CCCC1CCC(F)CN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 NRMDHIOZOOKAIT-UHFFFAOYSA-N 0.000 claims 1
- PLVDBWDTRCIEAJ-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-(5-methyl-2-propylpiperidin-1-yl)methanone Chemical compound CCCC1CCC(C)CN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 PLVDBWDTRCIEAJ-UHFFFAOYSA-N 0.000 claims 1
- MSMVXJRHKZIFHO-MRXNPFEDSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[(2r)-2-ethoxypyrrolidin-1-yl]methanone Chemical compound CCO[C@@H]1CCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 MSMVXJRHKZIFHO-MRXNPFEDSA-N 0.000 claims 1
- QABUURICQJOWID-MRXNPFEDSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[(2r)-2-ethylpiperidin-1-yl]methanone Chemical compound CC[C@@H]1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 QABUURICQJOWID-MRXNPFEDSA-N 0.000 claims 1
- QNYQRZYDZSRQND-CYBMUJFWSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[(2r)-2-methylpiperidin-1-yl]methanone Chemical compound C[C@@H]1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 QNYQRZYDZSRQND-CYBMUJFWSA-N 0.000 claims 1
- TWZOJPNADIKKCZ-GOSISDBHSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[(2r)-2-propan-2-ylpiperidin-1-yl]methanone Chemical compound CC(C)[C@H]1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 TWZOJPNADIKKCZ-GOSISDBHSA-N 0.000 claims 1
- JFVQMYLXIIQSQB-QGZVFWFLSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[(2r)-2-propylpiperidin-1-yl]methanone Chemical compound CCC[C@@H]1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 JFVQMYLXIIQSQB-QGZVFWFLSA-N 0.000 claims 1
- FCZFMKAXRZXYQE-TZMCWYRMSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[(2r,3r)-2,3-dimethylpiperidin-1-yl]methanone Chemical compound C[C@@H]1[C@H](C)CCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 FCZFMKAXRZXYQE-TZMCWYRMSA-N 0.000 claims 1
- VNSFTQGCSOLRBI-RTBURBONSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[(2r,6r)-2-ethyl-6-propylpiperidin-1-yl]methanone Chemical compound CCC[C@@H]1CCC[C@@H](CC)N1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 VNSFTQGCSOLRBI-RTBURBONSA-N 0.000 claims 1
- QABUURICQJOWID-INIZCTEOSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[(2s)-2-ethylpiperidin-1-yl]methanone Chemical compound CC[C@H]1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 QABUURICQJOWID-INIZCTEOSA-N 0.000 claims 1
- QNYQRZYDZSRQND-ZDUSSCGKSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[(2s)-2-methylpiperidin-1-yl]methanone Chemical compound C[C@H]1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 QNYQRZYDZSRQND-ZDUSSCGKSA-N 0.000 claims 1
- TWZOJPNADIKKCZ-SFHVURJKSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[(2s)-2-propan-2-ylpiperidin-1-yl]methanone Chemical compound CC(C)[C@@H]1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 TWZOJPNADIKKCZ-SFHVURJKSA-N 0.000 claims 1
- JFVQMYLXIIQSQB-KRWDZBQOSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[(2s)-2-propylpiperidin-1-yl]methanone Chemical compound CCC[C@H]1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 JFVQMYLXIIQSQB-KRWDZBQOSA-N 0.000 claims 1
- FCZFMKAXRZXYQE-JSGCOSHPSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[(2s,3s)-2,3-dimethylpiperidin-1-yl]methanone Chemical compound C[C@H]1[C@@H](C)CCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 FCZFMKAXRZXYQE-JSGCOSHPSA-N 0.000 claims 1
- LGCIZDYPKPLDMP-CQSZACIVSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[(3r)-3-ethylpiperidin-1-yl]methanone Chemical compound C1[C@H](CC)CCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 LGCIZDYPKPLDMP-CQSZACIVSA-N 0.000 claims 1
- LGCIZDYPKPLDMP-AWEZNQCLSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[(3s)-3-ethylpiperidin-1-yl]methanone Chemical compound C1[C@@H](CC)CCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 LGCIZDYPKPLDMP-AWEZNQCLSA-N 0.000 claims 1
- JIWDGCYERQLPRJ-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[2-(1,2-difluoropropyl)piperidin-1-yl]methanone Chemical compound CC(F)C(F)C1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 JIWDGCYERQLPRJ-UHFFFAOYSA-N 0.000 claims 1
- HCGQCDQUALDBFH-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[2-(2-fluoropropyl)piperidin-1-yl]methanone Chemical compound CC(F)CC1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 HCGQCDQUALDBFH-UHFFFAOYSA-N 0.000 claims 1
- YOUIQGSPMLFUQR-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[2-(5-methylfuran-2-yl)piperidin-1-yl]methanone Chemical compound O1C(C)=CC=C1C1N(C(=O)C=2C=C(Cl)C(NC=3C=NC(C)=CC=3)=NC=2)CCCC1 YOUIQGSPMLFUQR-UHFFFAOYSA-N 0.000 claims 1
- HEFDZAFSWJOKNO-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[2-(5-methylthiophen-2-yl)pyrrolidin-1-yl]methanone Chemical compound S1C(C)=CC=C1C1N(C(=O)C=2C=C(Cl)C(NC=3C=NC(C)=CC=3)=NC=2)CCC1 HEFDZAFSWJOKNO-UHFFFAOYSA-N 0.000 claims 1
- OKKROUZDCTVERP-UHFFFAOYSA-N [5-chloro-6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]-[2-(ethoxymethyl)piperidin-1-yl]methanone Chemical compound CCOCC1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C)N=C1 OKKROUZDCTVERP-UHFFFAOYSA-N 0.000 claims 1
- UTLOKJWQYPPGFN-CQSZACIVSA-N [5-chloro-6-[[6-(trifluoromethyl)pyridin-3-yl]amino]pyridin-3-yl]-[(2r)-2-ethylpiperidin-1-yl]methanone Chemical compound CC[C@@H]1CCCCN1C(=O)C(C=C1Cl)=CN=C1NC1=CC=C(C(F)(F)F)N=C1 UTLOKJWQYPPGFN-CQSZACIVSA-N 0.000 claims 1
- DYAMDVYBLGVRFS-UHFFFAOYSA-N [6-(4-chloroanilino)pyridin-3-yl]-(3-methylpiperidin-1-yl)methanone Chemical compound C1C(C)CCCN1C(=O)C(C=N1)=CC=C1NC1=CC=C(Cl)C=C1 DYAMDVYBLGVRFS-UHFFFAOYSA-N 0.000 claims 1
- FLPISVAYDJFBMX-UHFFFAOYSA-N [6-(4-methoxyanilino)pyridin-3-yl]-morpholin-4-ylmethanone;hydrochloride Chemical compound Cl.C1=CC(OC)=CC=C1NC1=CC=C(C(=O)N2CCOCC2)C=N1 FLPISVAYDJFBMX-UHFFFAOYSA-N 0.000 claims 1
- KQHFREGDHFYKIR-UHFFFAOYSA-N azepan-1-yl-[6-[(6-methylpyridin-3-yl)amino]pyridin-3-yl]methanone Chemical compound C1=NC(C)=CC=C1NC1=CC=C(C(=O)N2CCCCCC2)C=N1 KQHFREGDHFYKIR-UHFFFAOYSA-N 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical compound C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 claims 1
- 230000002496 gastric effect Effects 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 239000000825 pharmaceutical preparation Substances 0.000 claims 1
- 230000008054 signal transmission Effects 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/10—Laxatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/06—Antimigraine agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Child & Adolescent Psychology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Addiction (AREA)
- Ophthalmology & Optometry (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Gastroenterology & Hepatology (AREA)
- Nutrition Science (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05027934.8 | 2005-12-20 | ||
| EP05027934 | 2005-12-20 | ||
| EP06120424.4 | 2006-09-11 | ||
| EP06120424 | 2006-09-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2008129622A true RU2008129622A (ru) | 2010-01-27 |
Family
ID=37744569
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2008129622/04A RU2008129622A (ru) | 2005-12-20 | 2006-12-18 | Производные никотиновой кислоты в качестве модуляторов метаботропных глутаматных рецепторов |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20090005363A1 (https=) |
| EP (1) | EP1966144A1 (https=) |
| JP (1) | JP2009519986A (https=) |
| KR (1) | KR20080076962A (https=) |
| AR (1) | AR058554A1 (https=) |
| AU (1) | AU2006329007A1 (https=) |
| BR (1) | BRPI0620066A2 (https=) |
| CA (1) | CA2627630A1 (https=) |
| PE (1) | PE20071171A1 (https=) |
| RU (1) | RU2008129622A (https=) |
| TW (1) | TW200732323A (https=) |
| WO (1) | WO2007071358A1 (https=) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010502664A (ja) | 2006-09-11 | 2010-01-28 | ノバルティス アクチエンゲゼルシャフト | 代謝型グルタミン酸受容体の調節剤としてのニコチン酸誘導体 |
| JP5341084B2 (ja) * | 2007-08-03 | 2013-11-13 | エフ.ホフマン−ラ ロシュ アーゲー | Taar1リガンドとしてのピリジンカルボキシアミド及びベンズアミド誘導体 |
| AU2008309621A1 (en) * | 2007-10-12 | 2009-04-16 | Novartis Ag | Metabotropic glutamate receptor modulators for the treatment of Parkinson's Disease |
| WO2009047303A2 (en) * | 2007-10-12 | 2009-04-16 | Novartis Ag | Metabotropic glutamate receptor modulators for the treatment of pervasive developmental disorder |
| MX2010014222A (es) * | 2008-06-30 | 2011-03-29 | Novartis Ag Star | Combinaciones que comprenden moduladores de mglur para el tratamiento de enfermedad de parkinson. |
| CN102256963B (zh) * | 2008-12-19 | 2014-06-11 | 贝林格尔.英格海姆国际有限公司 | 作为ccr2受体拮抗剂用于治疗炎症、哮喘和copd的环状嘧啶-4-甲酰胺 |
| US8748623B2 (en) | 2009-02-17 | 2014-06-10 | Syntrix Biosystems, Inc. | Pyridinecarboxamides as CXCR2 modulators |
| EP2959902A1 (en) | 2009-07-23 | 2015-12-30 | Novartis AG | Use of azabicycloalkyl derivatives for the treatment or prevention of ataxia |
| NZ598891A (en) * | 2009-08-24 | 2014-05-30 | Neuralstem Inc | Synthesis of a neurostimulative piperazine |
| RU2012116124A (ru) * | 2009-09-21 | 2013-10-27 | Вандербилт Юниверсити | О-БЕНЗИЛ НИКОТИНАМИДНЫЕ АНАЛОГИ КАК ПОЗИТИВНЫЕ АЛЛОСТЕРИЧЕСКИЕ МОДУЛЯТОРЫ mGluR5 |
| JO3250B1 (ar) | 2009-09-22 | 2018-09-16 | Novartis Ag | إستعمال منشطات مستقبل نيكوتينيك أسيتيل كولين ألفا 7 |
| EP2490691A1 (en) | 2009-10-20 | 2012-08-29 | Novartis AG | Use of 1h-quinazoline-2,4-diones |
| ES2674275T3 (es) | 2009-12-17 | 2018-06-28 | Centrexion Therapeutics Corporation | Antagonistas del receptor CCR2 y usos de los mismos |
| WO2011149963A1 (en) * | 2010-05-24 | 2011-12-01 | Vanderbilt University | Substituted-6-methylnicotinamides as mglur5 positive allosteric modulators |
| AU2011268865A1 (en) | 2010-06-24 | 2013-01-31 | Novartis Ag | Use of 1H-quinazoline-2,4-diones |
| EP2608672B1 (en) | 2010-08-23 | 2020-12-16 | Syntrix Biosystems, Inc. | Aminopyridine- and aminopyrimidinecarboxamides as cxcr2 modulators |
| AR084515A1 (es) * | 2010-12-22 | 2013-05-22 | Merz Pharma Gmbh & Co Kgaa | Derivados heterociclicos nitrogenados, composiciones farmaceuticas que los contienen y uso de los mismos en el tratamiento de enfermedades asociadas al sistema nervioso central tales como parkinson y alzheimer, entre otras |
| AR084516A1 (es) * | 2010-12-22 | 2013-05-22 | Merz Pharma Gmbh & Co Kgaa | Moduladores de receptores de glutamato metabotropicos |
| WO2012101060A1 (en) | 2011-01-27 | 2012-08-02 | Novartis Ag | Use of nicotinic acetylcholine receptor alpha 7 activators |
| MX2014002693A (es) | 2011-09-07 | 2014-06-04 | Novartis Ag | Uso de 1h-quinazolina-2,4-dionas para usarse en la prevencion o el tratamiento de epilepsia fotosensible. |
| RU2672468C1 (ru) * | 2011-12-22 | 2018-11-15 | Конекшис Лайф Сайенсиз Пвт. Лтд. | Производные аза-адамантанов и их применение |
| MX362819B (es) | 2013-01-15 | 2019-02-18 | Novartis Ag | Uso de agonistas del receptor nicotinico de acetilcolina alfa 7 para el tratamiento de la narcolepsia. |
| KR101879919B1 (ko) | 2013-01-15 | 2018-07-18 | 노파르티스 아게 | 알파 7 니코틴성 아세틸콜린 수용체 작용물질의 용도 |
| TW201444821A (zh) | 2013-03-13 | 2014-12-01 | Janssen Pharmaceutica Nv | 經取代之哌啶化合物及其作為食慾素受體調節劑之用途 |
| TWI621618B (zh) | 2013-03-13 | 2018-04-21 | 比利時商健生藥品公司 | 經取代2-氮雜雙環類及其作為食慾素受體調控劑之用途 |
| TW201444849A (zh) | 2013-03-13 | 2014-12-01 | Janssen Pharmaceutica Nv | 經取代的7-氮雜雙環類及其作為食慾激素受體調節劑之用途 |
| US10561676B2 (en) | 2013-08-02 | 2020-02-18 | Syntrix Biosystems Inc. | Method for treating cancer using dual antagonists of CXCR1 and CXCR2 |
| US10046002B2 (en) | 2013-08-02 | 2018-08-14 | Syntrix Biosystems Inc. | Method for treating cancer using chemokine antagonists |
| US8969365B2 (en) | 2013-08-02 | 2015-03-03 | Syntrix Biosystems, Inc. | Thiopyrimidinecarboxamides as CXCR1/2 modulators |
| JPWO2015098991A1 (ja) * | 2013-12-26 | 2017-03-23 | 東レ株式会社 | N−アルキルアミド誘導体及びその医薬用途 |
| KR102455043B1 (ko) * | 2014-09-11 | 2022-10-13 | 얀센 파마슈티카 엔.브이. | 치환된 2-아자바이사이클 및 오렉신 수용체 조절제로서의 이의 용도 |
| PT3317270T (pt) | 2015-07-02 | 2020-08-24 | Centrexion Therapeutics Corp | (4-((3r,4r)-3-metoxitetrahidro-pirano-4-ilamino)piperidina-1-il)(5-metil-6-(((2r,6s)-6-(p-tolil)tetrahidro-2h-pirano-2-il)metilamino)pirimidina-4-il)citrato de metanona |
| US20190231525A1 (en) | 2016-08-01 | 2019-08-01 | Mitraltech Ltd. | Minimally-invasive delivery systems |
| DE102018104201A1 (de) * | 2018-02-23 | 2019-08-29 | Westfälische Wilhelms-Universität Münster | Verfahren zur Herstellung fluorierten heterocyclischen aliphatischer Verbindungen |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE817911C (de) * | 1947-12-16 | 1951-10-22 | Chem Fab Tempelhof Preuss & Te | Verfahren zur Darstellung von in 6-Stellung basisch substituierten Pyridin-3-carbonsaeureamiden |
| WO1999018066A1 (en) * | 1997-10-02 | 1999-04-15 | Sankyo Company, Limited | Amidocarboxylic acid derivatives |
| AU9781098A (en) * | 1997-10-02 | 1999-04-27 | Merck & Co., Inc. | Inhibitors of prenyl-protein transferase |
| CN1158264C (zh) * | 1997-11-21 | 2004-07-21 | Nps药物有限公司 | 用于治疗中枢神经系统疾病的代谢性谷氨酸受体拮抗剂 |
| DK1196397T3 (da) * | 1999-06-02 | 2006-01-02 | Nps Pharma Inc | Metabotrope glutamatreceptorantagonister og anvendelse deraf til behandling af sygdomme i centralnervesystemet |
| WO2001007416A1 (de) * | 1999-07-28 | 2001-02-01 | Lonza Ag | Verfahren zur herstellung von pyridazincarbonsäurederivaten |
| US6479510B2 (en) * | 2000-08-18 | 2002-11-12 | Pharmacia & Upjohn Company | Quinuclidine-substituted aryl compounds for treatment of disease |
| WO2003022214A2 (en) * | 2001-09-06 | 2003-03-20 | Millennium Pharmaceuticals, Inc. | Piperazine and homopiperazine compounds |
| US7595311B2 (en) * | 2002-05-24 | 2009-09-29 | Exelixis, Inc. | Azepinoindole derivatives as pharmaceutical agents |
| KR101025633B1 (ko) * | 2002-09-19 | 2011-03-30 | 일라이 릴리 앤드 캄파니 | 오피오이드 수용체 안타고니스트로서의 디아릴 에테르 |
| US20040067985A1 (en) * | 2002-10-04 | 2004-04-08 | Fortuna Haviv | Method of inhibiting angiogenesis |
| NZ551468A (en) * | 2003-12-24 | 2010-05-28 | Biota Scient Management | Polycyclic agents for the treatment of respiratory syncytial virus infections |
| WO2005110982A2 (en) * | 2004-04-07 | 2005-11-24 | Neurogen Corporation | Substituted 1-benzyl-4-substituted piperazine analogues |
| DE102004020908A1 (de) * | 2004-04-28 | 2005-11-17 | Grünenthal GmbH | Substituierte 5,6,7,8,-Tetrahydro-pyrido[4,3-d]pyrimidin-2-yl- und 5,6,7,8,-Tetrahydro-chinazolin-2-yl-Verbindungen |
| SE0401969D0 (sv) * | 2004-08-02 | 2004-08-02 | Astrazeneca Ab | Piperidine derivatives |
| ES2377758T3 (es) * | 2004-11-12 | 2012-03-30 | Bristol-Myers Squibb Company | Compuestos tricíclicos basados en tiazolo[4,5-b]piridina imidazo-fusionada y composiciones farmacéuticas que los comprenden |
| WO2006064286A1 (en) * | 2004-12-13 | 2006-06-22 | Medivir Uk Ltd | Cathepsin s inhibitors |
| WO2006094639A1 (en) * | 2005-03-04 | 2006-09-14 | F.Hoffmann-La Roche Ag | Pyridine-2-carboxamide derivatives as mglur5 antagonists |
-
2006
- 2006-12-18 AU AU2006329007A patent/AU2006329007A1/en not_active Abandoned
- 2006-12-18 CA CA002627630A patent/CA2627630A1/en not_active Abandoned
- 2006-12-18 EP EP06829702A patent/EP1966144A1/en not_active Withdrawn
- 2006-12-18 KR KR1020087014836A patent/KR20080076962A/ko not_active Withdrawn
- 2006-12-18 JP JP2008546217A patent/JP2009519986A/ja active Pending
- 2006-12-18 RU RU2008129622/04A patent/RU2008129622A/ru not_active Application Discontinuation
- 2006-12-18 AR ARP060105586A patent/AR058554A1/es not_active Application Discontinuation
- 2006-12-18 WO PCT/EP2006/012181 patent/WO2007071358A1/en not_active Ceased
- 2006-12-18 BR BRPI0620066-4A patent/BRPI0620066A2/pt not_active IP Right Cessation
- 2006-12-18 US US12/158,387 patent/US20090005363A1/en not_active Abandoned
- 2006-12-19 TW TW095147659A patent/TW200732323A/zh unknown
- 2006-12-20 PE PE2006001666A patent/PE20071171A1/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| TW200732323A (en) | 2007-09-01 |
| BRPI0620066A2 (pt) | 2011-11-01 |
| AR058554A1 (es) | 2008-02-13 |
| PE20071171A1 (es) | 2008-01-22 |
| US20090005363A1 (en) | 2009-01-01 |
| WO2007071358A1 (en) | 2007-06-28 |
| CA2627630A1 (en) | 2007-06-28 |
| KR20080076962A (ko) | 2008-08-20 |
| JP2009519986A (ja) | 2009-05-21 |
| EP1966144A1 (en) | 2008-09-10 |
| AU2006329007A1 (en) | 2007-06-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU2008129622A (ru) | Производные никотиновой кислоты в качестве модуляторов метаботропных глутаматных рецепторов | |
| AU2019283921B2 (en) | Indole carboxamide compounds useful as kinase inhibitors | |
| EP3454862B1 (en) | Spirocyclic degronimers for target protein degradation | |
| JP2023071767A (ja) | Brm標的化化合物および関連使用方法 | |
| AU2024203200A1 (en) | Bifunctional molecules containing an e3 ubiquitine ligase binding moiety linked to a bcl6 targeting moiety | |
| RU2345996C1 (ru) | Аннелированные азагетероциклические амиды, включающие пиримидиновый фрагмент, способ их получения и применения | |
| JP6585158B2 (ja) | ヤヌスキナーゼの阻害に有用なピロロ[2,3−d]ピリミジン誘導体 | |
| JP2022009742A (ja) | Hivの処置のためのアミド化合物 | |
| JP5925394B2 (ja) | 抗レトロウイルス剤としての(ヘテロ)アリールアセトアミド誘導体 | |
| CN120077051A (zh) | Kras抑制剂 | |
| KR20230040386A (ko) | 시스테인 프로테아제의 억제제 및 이의 사용 방법 | |
| AU2017382406A1 (en) | EGFR proteolysis targeting chimeric molecules and associated methods of use | |
| WO2019099868A2 (en) | Degraders and degrons for targeted protein degradation | |
| CN109790143A (zh) | 用于靶蛋白降解的胺连接的c3-戊二酰亚胺降解决定子体 | |
| CN108366992A (zh) | 蛋白水解靶向嵌合体化合物及其制备和应用方法 | |
| AU2018238138A1 (en) | Substituted dihydroindene-4-carboxamides and analogs thereof, and methods using same | |
| CN101883774A (zh) | 噻吩并嘧啶和吡唑并嘧啶化合物及其用作mtor激酶和pi3激酶抑制剂的用途 | |
| KR102404865B1 (ko) | 항종양제 | |
| US20240336643A1 (en) | Bifunctional compounds that degrade alk and uses thereof | |
| WO2021173677A1 (en) | Potent and selective degraders of alk | |
| JP2025523393A (ja) | 二環式置換グルタルイミドセレブロンバインダー | |
| MXPA04005209A (es) | Antagonistas del receptor de adenosina a2a. | |
| KR20200027992A (ko) | 무스카린성 아세틸콜린 수용체 m4의 길항제 | |
| JPWO2015163339A1 (ja) | 新規二環性または三環性複素環化合物 | |
| JP2017504628A (ja) | 縮合イミダゾール化合物 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA92 | Acknowledgement of application withdrawn (lack of supplementary materials submitted) |
Effective date: 20110504 |