NO327005B1 - Acetylenderivaer som har mGluR5 antagonistisk aktivitet - Google Patents
Acetylenderivaer som har mGluR5 antagonistisk aktivitet Download PDFInfo
- Publication number
- NO327005B1 NO327005B1 NO20042673A NO20042673A NO327005B1 NO 327005 B1 NO327005 B1 NO 327005B1 NO 20042673 A NO20042673 A NO 20042673A NO 20042673 A NO20042673 A NO 20042673A NO 327005 B1 NO327005 B1 NO 327005B1
- Authority
- NO
- Norway
- Prior art keywords
- hydroxy
- carboxylic acid
- phenylethynyl
- ethyl ester
- cyclohexyl
- Prior art date
Links
- 102000012777 Metabotropic Glutamate 5 Receptor Human genes 0.000 title claims description 6
- 108010065028 Metabotropic Glutamate 5 Receptor Proteins 0.000 title claims description 6
- 150000000475 acetylene derivatives Chemical class 0.000 title description 2
- 230000003042 antagnostic effect Effects 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 52
- 238000000034 method Methods 0.000 claims description 24
- -1 tetrahydrofuran- 3yl Chemical group 0.000 claims description 23
- 150000003839 salts Chemical group 0.000 claims description 22
- 239000002253 acid Substances 0.000 claims description 21
- 229910052739 hydrogen Inorganic materials 0.000 claims description 18
- 239000001257 hydrogen Substances 0.000 claims description 18
- 239000012458 free base Substances 0.000 claims description 15
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- 239000008194 pharmaceutical composition Substances 0.000 claims description 12
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 11
- 208000035475 disorder Diseases 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 9
- 208000002193 Pain Diseases 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 7
- 208000024827 Alzheimer disease Diseases 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 239000003814 drug Substances 0.000 claims description 6
- 150000002431 hydrogen Chemical group 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 6
- MIROVSIAGIUZPP-UHFFFAOYSA-N ethyl 5-[2-(3-chlorophenyl)ethynyl]-5-hydroxy-2,3,4,4a,6,7,8,8a-octahydroquinoline-1-carboxylate Chemical compound CCOC(=O)N1CCCC2C1CCCC2(O)C#CC1=CC=CC(Cl)=C1 MIROVSIAGIUZPP-UHFFFAOYSA-N 0.000 claims description 5
- GRNSGJOKGICXGO-UHFFFAOYSA-N tert-butyl 4-oxo-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound C1CCC(=O)C2C1N(C(=O)OC(C)(C)C)CC2 GRNSGJOKGICXGO-UHFFFAOYSA-N 0.000 claims description 5
- 208000019901 Anxiety disease Diseases 0.000 claims description 4
- 208000007101 Muscle Cramp Diseases 0.000 claims description 4
- 208000012902 Nervous system disease Diseases 0.000 claims description 4
- CFBZCLJIZQGFNC-UHFFFAOYSA-N [5-[2-(3-chlorophenyl)ethynyl]-5-hydroxy-2,3,4,4a,6,7,8,8a-octahydroquinolin-1-yl]-(furan-2-yl)methanone Chemical compound C=1C=CC(Cl)=CC=1C#CC1(O)CCCC2C1CCCN2C(=O)C1=CC=CO1 CFBZCLJIZQGFNC-UHFFFAOYSA-N 0.000 claims description 4
- 239000008186 active pharmaceutical agent Substances 0.000 claims description 4
- 230000001154 acute effect Effects 0.000 claims description 4
- 230000036506 anxiety Effects 0.000 claims description 4
- SNPPWIUOZRMYNY-UHFFFAOYSA-N bupropion Chemical compound CC(C)(C)NC(C)C(=O)C1=CC=CC(Cl)=C1 SNPPWIUOZRMYNY-UHFFFAOYSA-N 0.000 claims description 4
- 229940088679 drug related substance Drugs 0.000 claims description 4
- JATWRGYZPSSPIF-UHFFFAOYSA-N ethyl n-[3-[2-(3-fluorophenyl)ethynyl]-3-hydroxycyclohexyl]carbamate Chemical compound C1C(NC(=O)OCC)CCCC1(O)C#CC1=CC=CC(F)=C1 JATWRGYZPSSPIF-UHFFFAOYSA-N 0.000 claims description 4
- 230000000848 glutamatergic effect Effects 0.000 claims description 4
- ZFPZEYHRWGMJCV-ZHALLVOQSA-N mavoglurant Chemical compound C([C@]1(O)CCC[C@@H]2[C@H]1CCN2C(=O)OC)#CC1=CC=CC(C)=C1 ZFPZEYHRWGMJCV-ZHALLVOQSA-N 0.000 claims description 4
- 230000001404 mediated effect Effects 0.000 claims description 4
- GWKUSCMPEHTLOL-UHFFFAOYSA-N n-[3-hydroxy-3-[2-(3-methylphenyl)ethynyl]cyclohexyl]acetamide Chemical compound C1C(NC(=O)C)CCCC1(O)C#CC1=CC=CC(C)=C1 GWKUSCMPEHTLOL-UHFFFAOYSA-N 0.000 claims description 4
- 230000008054 signal transmission Effects 0.000 claims description 4
- MAUUZUNIDQAWQB-UHFFFAOYSA-N tert-butyl n-[3-hydroxy-3-[2-(3-methoxyphenyl)ethynyl]cyclohexyl]carbamate Chemical compound COC1=CC=CC(C#CC2(O)CC(CCC2)NC(=O)OC(C)(C)C)=C1 MAUUZUNIDQAWQB-UHFFFAOYSA-N 0.000 claims description 4
- 206010008120 Cerebral ischaemia Diseases 0.000 claims description 3
- 206010013654 Drug abuse Diseases 0.000 claims description 3
- 208000023105 Huntington disease Diseases 0.000 claims description 3
- 208000008238 Muscle Spasticity Diseases 0.000 claims description 3
- 208000018737 Parkinson disease Diseases 0.000 claims description 3
- 208000003251 Pruritus Diseases 0.000 claims description 3
- 206010039966 Senile dementia Diseases 0.000 claims description 3
- 208000005392 Spasm Diseases 0.000 claims description 3
- OOHWRZMAIUHACJ-PMRGXDQWSA-N [(3r)-oxolan-3-yl] 4-hydroxy-4-(2-phenylethynyl)-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound C=1C=CC=CC=1C#CC1(O)CCCC2C1CCN2C(=O)O[C@@H]1CCOC1 OOHWRZMAIUHACJ-PMRGXDQWSA-N 0.000 claims description 3
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims description 3
- 229960001058 bupropion Drugs 0.000 claims description 3
- YQWKJPIHRNCFRR-UHFFFAOYSA-N cyclopropyl-[7-hydroxy-7-[2-(3-methylphenyl)ethynyl]-3,3a,4,5,6,7a-hexahydro-1h-isoindol-2-yl]methanone Chemical compound CC1=CC=CC(C#CC2(O)C3CN(CC3CCC2)C(=O)C2CC2)=C1 YQWKJPIHRNCFRR-UHFFFAOYSA-N 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 3
- 206010015037 epilepsy Diseases 0.000 claims description 3
- CWSTVFBFMPWZTK-UHFFFAOYSA-N ethyl 4-[2-(3-fluorophenyl)ethynyl]-4-hydroxy-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound CCOC(=O)N1CCC2C1CCCC2(O)C#CC1=CC=CC(F)=C1 CWSTVFBFMPWZTK-UHFFFAOYSA-N 0.000 claims description 3
- WIPRRMYYUMAMPJ-UHFFFAOYSA-N ethyl 5-hydroxy-5-(2-phenylethynyl)-2,3,4,4a,6,7,8,8a-octahydroquinoline-1-carboxylate Chemical compound CCOC(=O)N1CCCC2C1CCCC2(O)C#CC1=CC=CC=C1 WIPRRMYYUMAMPJ-UHFFFAOYSA-N 0.000 claims description 3
- ZUHRWLSVTMLWEN-UHFFFAOYSA-N ethyl n-[3-(2-phenylethynyl)cyclohex-2-en-1-yl]carbamate Chemical compound CCOC(=O)NC1CCCC(C#CC=2C=CC=CC=2)=C1 ZUHRWLSVTMLWEN-UHFFFAOYSA-N 0.000 claims description 3
- OLWRARXBPQTFTR-UHFFFAOYSA-N ethyl n-[3-hydroxy-3-[2-(3-methylphenyl)ethynyl]cyclohexyl]carbamate Chemical compound C1C(NC(=O)OCC)CCCC1(O)C#CC1=CC=CC(C)=C1 OLWRARXBPQTFTR-UHFFFAOYSA-N 0.000 claims description 3
- 208000028867 ischemia Diseases 0.000 claims description 3
- 208000023589 ischemic disease Diseases 0.000 claims description 3
- 230000007803 itching Effects 0.000 claims description 3
- 201000006417 multiple sclerosis Diseases 0.000 claims description 3
- PLRSDRSEJPEAED-UHFFFAOYSA-N n-[3-[2-(3-fluorophenyl)ethynyl]-3-hydroxycyclohexyl]acetamide Chemical compound C1C(NC(=O)C)CCCC1(O)C#CC1=CC=CC(F)=C1 PLRSDRSEJPEAED-UHFFFAOYSA-N 0.000 claims description 3
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 claims description 3
- 208000020016 psychiatric disease Diseases 0.000 claims description 3
- 201000000980 schizophrenia Diseases 0.000 claims description 3
- 208000018198 spasticity Diseases 0.000 claims description 3
- 208000011117 substance-related disease Diseases 0.000 claims description 3
- PQTUGQRVYKKHJX-UHFFFAOYSA-N tert-butyl 7-hydroxy-7-(2-phenylethynyl)-3,3a,4,5,6,7a-hexahydro-1h-isoindole-2-carboxylate Chemical compound C12CN(C(=O)OC(C)(C)C)CC2CCCC1(O)C#CC1=CC=CC=C1 PQTUGQRVYKKHJX-UHFFFAOYSA-N 0.000 claims description 3
- SOOMTUHFRGROGM-UHFFFAOYSA-N tert-butyl n-[3-hydroxy-3-[2-(3-methylphenyl)ethynyl]cyclohexyl]carbamate Chemical compound CC1=CC=CC(C#CC2(O)CC(CCC2)NC(=O)OC(C)(C)C)=C1 SOOMTUHFRGROGM-UHFFFAOYSA-N 0.000 claims description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- 201000006474 Brain Ischemia Diseases 0.000 claims description 2
- 206010010904 Convulsion Diseases 0.000 claims description 2
- NMIXTTBVZMBIHL-WOIUINJBSA-N [(3ar,4s,7ar)-4-hydroxy-4-[2-(3-methylphenyl)ethynyl]-3,3a,5,6,7,7a-hexahydro-2h-indol-1-yl]-(furan-2-yl)methanone Chemical compound CC1=CC=CC(C#C[C@@]2(O)[C@H]3[C@H](N(CC3)C(=O)C=3OC=CC=3)CCC2)=C1 NMIXTTBVZMBIHL-WOIUINJBSA-N 0.000 claims description 2
- OOHWRZMAIUHACJ-GGQJKKPXSA-N [(3s)-oxolan-3-yl] 4-hydroxy-4-(2-phenylethynyl)-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound C=1C=CC=CC=1C#CC1(O)CCCC2C1CCN2C(=O)O[C@H]1CCOC1 OOHWRZMAIUHACJ-GGQJKKPXSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 206010008118 cerebral infarction Diseases 0.000 claims description 2
- 230000036461 convulsion Effects 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 2
- CRRWFEQGFGDINN-QWFCFKBJSA-N ethyl (3ar,4s,7ar)-4-hydroxy-4-[2-(3-methylphenyl)ethynyl]-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound C([C@]1(O)CCC[C@@H]2[C@H]1CCN2C(=O)OCC)#CC1=CC=CC(C)=C1 CRRWFEQGFGDINN-QWFCFKBJSA-N 0.000 claims description 2
- ILFYTTLEALYKPG-UHFFFAOYSA-N ethyl 4-(2-phenylethynyl)-2,3,5,6,7,7a-hexahydroindole-1-carboxylate Chemical compound C1CCC2N(C(=O)OCC)CCC2=C1C#CC1=CC=CC=C1 ILFYTTLEALYKPG-UHFFFAOYSA-N 0.000 claims description 2
- UXDUZBZETAVXED-UHFFFAOYSA-N ethyl 4-[2-(3-methoxyphenyl)ethynyl]-2,3,5,6,7,7a-hexahydroindole-1-carboxylate Chemical compound C1CCC2N(C(=O)OCC)CCC2=C1C#CC1=CC=CC(OC)=C1 UXDUZBZETAVXED-UHFFFAOYSA-N 0.000 claims description 2
- NPYOBWOVEFAZLC-UHFFFAOYSA-N ethyl 4-[2-(3-methylphenyl)ethynyl]-2,3,5,6,7,7a-hexahydroindole-1-carboxylate Chemical compound C1CCC2N(C(=O)OCC)CCC2=C1C#CC1=CC=CC(C)=C1 NPYOBWOVEFAZLC-UHFFFAOYSA-N 0.000 claims description 2
- CRRWFEQGFGDINN-UHFFFAOYSA-N ethyl 4-hydroxy-4-[2-(3-methylphenyl)ethynyl]-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound CCOC(=O)N1CCC2C1CCCC2(O)C#CC1=CC=CC(C)=C1 CRRWFEQGFGDINN-UHFFFAOYSA-N 0.000 claims description 2
- PRQIMGZKFRUZFL-UHFFFAOYSA-N ethyl 7-[2-(3-cyanophenyl)ethynyl]-7-hydroxy-3,3a,4,5,6,7a-hexahydro-1h-isoindole-2-carboxylate Chemical compound C12CN(C(=O)OCC)CC2CCCC1(O)C#CC1=CC=CC(C#N)=C1 PRQIMGZKFRUZFL-UHFFFAOYSA-N 0.000 claims description 2
- FSKINSVZNATXMA-UHFFFAOYSA-N ethyl 7-hydroxy-7-[2-(3-methylphenyl)ethynyl]-3,3a,4,5,6,7a-hexahydro-1h-isoindole-2-carboxylate Chemical compound C12CN(C(=O)OCC)CC2CCCC1(O)C#CC1=CC=CC(C)=C1 FSKINSVZNATXMA-UHFFFAOYSA-N 0.000 claims description 2
- CBYGJJTXZOIYCV-UHFFFAOYSA-N ethyl 7-hydroxy-7-[2-(4-methylphenyl)ethynyl]-3,3a,4,5,6,7a-hexahydro-1h-isoindole-2-carboxylate Chemical compound C12CN(C(=O)OCC)CC2CCCC1(O)C#CC1=CC=C(C)C=C1 CBYGJJTXZOIYCV-UHFFFAOYSA-N 0.000 claims description 2
- BVAIXRYWZUMDMR-UHFFFAOYSA-N furan-2-yl-[7-hydroxy-7-[2-(3-methylphenyl)ethynyl]-3,3a,4,5,6,7a-hexahydro-1h-isoindol-2-yl]methanone Chemical compound CC1=CC=CC(C#CC2(O)C3CN(CC3CCC2)C(=O)C=2OC=CC=2)=C1 BVAIXRYWZUMDMR-UHFFFAOYSA-N 0.000 claims description 2
- 125000002541 furyl group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000002757 morpholinyl group Chemical group 0.000 claims description 2
- YVNZPJZOIIBHQN-UHFFFAOYSA-N n-[3-hydroxy-3-[2-(3-methoxyphenyl)ethynyl]cyclohexyl]acetamide Chemical compound COC1=CC=CC(C#CC2(O)CC(CCC2)NC(C)=O)=C1 YVNZPJZOIIBHQN-UHFFFAOYSA-N 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 239000008024 pharmaceutical diluent Substances 0.000 claims description 2
- 125000004193 piperazinyl group Chemical group 0.000 claims description 2
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 2
- 125000004494 ethyl ester group Chemical group 0.000 claims 3
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims 2
- FEYFOLRTFYMDRW-UHFFFAOYSA-N ethyl 4-[2-(3-chlorophenyl)ethynyl]-4-hydroxy-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound CCOC(=O)N1CCC2C1CCCC2(O)C#CC1=CC=CC(Cl)=C1 FEYFOLRTFYMDRW-UHFFFAOYSA-N 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- USPQFPYFSLLRES-UHFFFAOYSA-N 4-[2-(3-chlorophenyl)ethynyl]-1-methylsulfonyl-3,3a,5,6,7,7a-hexahydro-2h-indol-4-ol Chemical compound CS(=O)(=O)N1CCC2C1CCCC2(O)C#CC1=CC=CC(Cl)=C1 USPQFPYFSLLRES-UHFFFAOYSA-N 0.000 claims 1
- ANRMILBHZXLLOI-UHFFFAOYSA-N 4-[2-(3-chlorophenyl)ethynyl]-4-hydroxy-3,3a,5,6,7,7a-hexahydro-2H-indole-1-carboxylic acid Chemical compound OC1(C2CCN(C2CCC1)C(=O)O)C#CC1=CC(=CC=C1)Cl ANRMILBHZXLLOI-UHFFFAOYSA-N 0.000 claims 1
- OUTMOSXAPQLFAI-UHFFFAOYSA-N 4-hydroxy-4-(2-phenylethynyl)-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylic acid Chemical compound OC(=O)N1CCC2C1CCCC2(O)C#CC1=CC=CC=C1 OUTMOSXAPQLFAI-UHFFFAOYSA-N 0.000 claims 1
- 125000004217 4-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C([H])([H])* 0.000 claims 1
- PXZKSWLKUIOJGZ-UHFFFAOYSA-N [5-[2-(3-chlorophenyl)ethynyl]-5-hydroxy-2,3,4,4a,6,7,8,8a-octahydroquinolin-1-yl]-morpholin-4-ylmethanone Chemical compound C=1C=CC(Cl)=CC=1C#CC1(O)CCCC2C1CCCN2C(=O)N1CCOCC1 PXZKSWLKUIOJGZ-UHFFFAOYSA-N 0.000 claims 1
- RQTXMIDDKRXCCI-UHFFFAOYSA-N [7-hydroxy-7-[2-(3-methylphenyl)ethynyl]-3,3a,4,5,6,7a-hexahydro-1h-isoindol-2-yl]-pyridin-3-ylmethanone Chemical compound CC1=CC=CC(C#CC2(O)C3CN(CC3CCC2)C(=O)C=2C=NC=CC=2)=C1 RQTXMIDDKRXCCI-UHFFFAOYSA-N 0.000 claims 1
- PLKJVWTVHCOBFF-UHFFFAOYSA-N ethyl 4-(2-phenylethynyl)-2,3,3a,6,7,7a-hexahydroindole-1-carboxylate Chemical compound CCOC(=O)N1CCC2C1CCC=C2C#CC1=CC=CC=C1 PLKJVWTVHCOBFF-UHFFFAOYSA-N 0.000 claims 1
- RUDJFNPIFRHEMI-UHFFFAOYSA-N ethyl 5-hydroxy-5-[2-(3-methylphenyl)ethynyl]-2,3,4,4a,6,7,8,8a-octahydroquinoline-1-carboxylate Chemical compound CCOC(=O)N1CCCC2C1CCCC2(O)C#CC1=CC=CC(C)=C1 RUDJFNPIFRHEMI-UHFFFAOYSA-N 0.000 claims 1
- UGBZUTABUHFIBE-UHFFFAOYSA-N ethyl 7-[2-(3-fluorophenyl)ethynyl]-7-hydroxy-3,3a,4,5,6,7a-hexahydro-1h-isoindole-2-carboxylate Chemical compound C12CN(C(=O)OCC)CC2CCCC1(O)C#CC1=CC=CC(F)=C1 UGBZUTABUHFIBE-UHFFFAOYSA-N 0.000 claims 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 claims 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims 1
- 150000004702 methyl esters Chemical class 0.000 claims 1
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 claims 1
- UOUFRTFWWBCVPV-UHFFFAOYSA-N tert-butyl 4-(2,4-dioxo-1H-thieno[3,2-d]pyrimidin-3-yl)piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC(CC1)n1c(=O)[nH]c2ccsc2c1=O UOUFRTFWWBCVPV-UHFFFAOYSA-N 0.000 claims 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 93
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 69
- 239000011734 sodium Substances 0.000 description 42
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 41
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 40
- 238000000589 high-performance liquid chromatography-mass spectrometry Methods 0.000 description 37
- 239000000203 mixture Substances 0.000 description 28
- 239000000243 solution Substances 0.000 description 28
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 26
- 239000011541 reaction mixture Substances 0.000 description 23
- 239000000741 silica gel Substances 0.000 description 23
- 229910002027 silica gel Inorganic materials 0.000 description 23
- 238000002330 electrospray ionisation mass spectrometry Methods 0.000 description 22
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 20
- 239000003795 chemical substances by application Substances 0.000 description 20
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 15
- 238000005160 1H NMR spectroscopy Methods 0.000 description 14
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 239000003921 oil Substances 0.000 description 12
- 235000019198 oils Nutrition 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 239000012074 organic phase Substances 0.000 description 10
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 7
- 238000005481 NMR spectroscopy Methods 0.000 description 7
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 7
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 7
- 239000003480 eluent Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 241001465754 Metazoa Species 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
- 238000000746 purification Methods 0.000 description 6
- 229910052938 sodium sulfate Inorganic materials 0.000 description 6
- 235000011152 sodium sulphate Nutrition 0.000 description 6
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 5
- 238000004007 reversed phase HPLC Methods 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- 102000016193 Metabotropic glutamate receptors Human genes 0.000 description 4
- 108010010914 Metabotropic glutamate receptors Proteins 0.000 description 4
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 4
- 239000008346 aqueous phase Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000004587 chromatography analysis Methods 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 239000012043 crude product Substances 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- XMJHPCRAQCTCFT-UHFFFAOYSA-N methyl chloroformate Chemical compound COC(Cl)=O XMJHPCRAQCTCFT-UHFFFAOYSA-N 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- DYHSDKLCOJIUFX-UHFFFAOYSA-N tert-butoxycarbonyl anhydride Chemical compound CC(C)(C)OC(=O)OC(=O)OC(C)(C)C DYHSDKLCOJIUFX-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 206010020843 Hyperthermia Diseases 0.000 description 3
- INAPMGSXUVUWAF-GCVPSNMTSA-N [(2r,3s,5r,6r)-2,3,4,5,6-pentahydroxycyclohexyl] dihydrogen phosphate Chemical compound OC1[C@H](O)[C@@H](O)C(OP(O)(O)=O)[C@H](O)[C@@H]1O INAPMGSXUVUWAF-GCVPSNMTSA-N 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000004440 column chromatography Methods 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- GCFHZZWXZLABBL-UHFFFAOYSA-N ethanol;hexane Chemical compound CCO.CCCCCC GCFHZZWXZLABBL-UHFFFAOYSA-N 0.000 description 3
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- 230000036031 hyperthermia Effects 0.000 description 3
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 3
- 235000019341 magnesium sulphate Nutrition 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 229910000027 potassium carbonate Inorganic materials 0.000 description 3
- 239000012266 salt solution Substances 0.000 description 3
- 238000010898 silica gel chromatography Methods 0.000 description 3
- 230000007306 turnover Effects 0.000 description 3
- IOIJLLZBQXYQSU-UHFFFAOYSA-N 1-ethynyl-3-methylbenzene Chemical compound Cc1cccc(c1)C#[C-] IOIJLLZBQXYQSU-UHFFFAOYSA-N 0.000 description 2
- FSWGHKSIVFQREG-UHFFFAOYSA-N 2-benzyl-1,3,3a,4,7,7a-hexahydroisoindol-4-ol Chemical compound C1C2C(O)C=CCC2CN1CC1=CC=CC=C1 FSWGHKSIVFQREG-UHFFFAOYSA-N 0.000 description 2
- YUFXDPVFXIMAFZ-UHFFFAOYSA-N 3-(ethylamino)cyclopent-2-en-1-one Chemical compound CCNC1=CC(=O)CC1 YUFXDPVFXIMAFZ-UHFFFAOYSA-N 0.000 description 2
- JBCRNGVTLQWOOW-UHFFFAOYSA-N 3-(methylamino)cyclohex-2-en-1-one Chemical compound CNC1=CC(=O)CCC1 JBCRNGVTLQWOOW-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- 241000282412 Homo Species 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
- 239000007832 Na2SO4 Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 239000000556 agonist Substances 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- 230000037396 body weight Effects 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- RZEKVGVHFLEQIL-UHFFFAOYSA-N celecoxib Chemical compound C1=CC(C)=CC=C1C1=CC(C(F)(F)F)=NN1C1=CC=C(S(N)(=O)=O)C=C1 RZEKVGVHFLEQIL-UHFFFAOYSA-N 0.000 description 2
- ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 description 2
- 239000010779 crude oil Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- DGMRZLVGDMPVFF-UHFFFAOYSA-N ethyl 4-hydroxy-1,3,3a,4,5,6,7,7a-octahydroisoindole-2-carboxylate Chemical compound C1CCC(O)C2CN(C(=O)OCC)CC21 DGMRZLVGDMPVFF-UHFFFAOYSA-N 0.000 description 2
- XZKVJGZUIXNXQM-UHFFFAOYSA-N ethyl 5-hydroxy-5-(2-trimethylsilylethynyl)-2,3,4,4a,6,7,8,8a-octahydroquinoline-1-carboxylate Chemical compound C1CCC(C#C[Si](C)(C)C)(O)C2C1N(C(=O)OCC)CCC2 XZKVJGZUIXNXQM-UHFFFAOYSA-N 0.000 description 2
- TZJGCBFQRXKUCY-UHFFFAOYSA-N ethyl 7-hydroxy-7-(2-phenylethynyl)-3,3a,4,5,6,7a-hexahydro-1h-isoindole-2-carboxylate Chemical compound C12CN(C(=O)OCC)CC2CCCC1(O)C#CC1=CC=CC=C1 TZJGCBFQRXKUCY-UHFFFAOYSA-N 0.000 description 2
- NDCRUBFLEOYBDR-UHFFFAOYSA-N ethyl 7-oxo-3,3a,4,5,6,7a-hexahydro-1h-isoindole-2-carboxylate Chemical compound C1CCC(=O)C2CN(C(=O)OCC)CC21 NDCRUBFLEOYBDR-UHFFFAOYSA-N 0.000 description 2
- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 description 2
- RLGDZRATANMWQX-UHFFFAOYSA-N ethyl n-[3-(2-phenylethynyl)cyclohex-3-en-1-yl]carbamate Chemical compound C1C(NC(=O)OCC)CCC=C1C#CC1=CC=CC=C1 RLGDZRATANMWQX-UHFFFAOYSA-N 0.000 description 2
- GRZACXOEKBCYKP-UHFFFAOYSA-N ethyl n-[3-hydroxy-3-[2-(3-methoxyphenyl)ethynyl]cyclohexyl]carbamate Chemical compound C1C(NC(=O)OCC)CCCC1(O)C#CC1=CC=CC(OC)=C1 GRZACXOEKBCYKP-UHFFFAOYSA-N 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- GNSLYOGEBCFYDE-UHFFFAOYSA-N lithium;ethynylbenzene Chemical compound [Li+].[C-]#CC1=CC=CC=C1 GNSLYOGEBCFYDE-UHFFFAOYSA-N 0.000 description 2
- DIMRKPVRDZGMGG-UHFFFAOYSA-N methyl n-[3-[2-(3-fluorophenyl)ethynyl]-3-hydroxycyclohexyl]-n-methylcarbamate Chemical compound C1C(N(C)C(=O)OC)CCCC1(O)C#CC1=CC=CC(F)=C1 DIMRKPVRDZGMGG-UHFFFAOYSA-N 0.000 description 2
- RDQKZAOIHHZXHM-UHFFFAOYSA-N methyl n-[3-[2-(3-fluorophenyl)ethynyl]-3-hydroxycyclohexyl]carbamate Chemical compound C1C(NC(=O)OC)CCCC1(O)C#CC1=CC=CC(F)=C1 RDQKZAOIHHZXHM-UHFFFAOYSA-N 0.000 description 2
- HXOVKZPUZJYARX-UHFFFAOYSA-N methyl n-ethyl-n-(3-oxocyclopenten-1-yl)carbamate Chemical compound COC(=O)N(CC)C1=CC(=O)CC1 HXOVKZPUZJYARX-UHFFFAOYSA-N 0.000 description 2
- QFDARFXTWHWDOZ-UHFFFAOYSA-N methyl n-ethyl-n-[3-hydroxy-3-[2-(3-methylphenyl)ethynyl]cyclopentyl]carbamate Chemical compound C1C(N(CC)C(=O)OC)CCC1(O)C#CC1=CC=CC(C)=C1 QFDARFXTWHWDOZ-UHFFFAOYSA-N 0.000 description 2
- JLFQJQDCRITDFB-UHFFFAOYSA-N methyl n-methyl-n-(3-oxocyclohexen-1-yl)carbamate Chemical compound COC(=O)N(C)C1=CC(=O)CCC1 JLFQJQDCRITDFB-UHFFFAOYSA-N 0.000 description 2
- JICQALMMGYCIDX-UHFFFAOYSA-N methyl n-methyl-n-(3-oxocyclohexyl)carbamate Chemical compound COC(=O)N(C)C1CCCC(=O)C1 JICQALMMGYCIDX-UHFFFAOYSA-N 0.000 description 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- 235000011181 potassium carbonates Nutrition 0.000 description 2
- 238000002953 preparative HPLC Methods 0.000 description 2
- RZJQGNCSTQAWON-UHFFFAOYSA-N rofecoxib Chemical compound C1=CC(S(=O)(=O)C)=CC=C1C1=C(C=2C=CC=CC=2)C(=O)OC1 RZJQGNCSTQAWON-UHFFFAOYSA-N 0.000 description 2
- 229910000104 sodium hydride Inorganic materials 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- GRNSGJOKGICXGO-NXEZZACHSA-N tert-butyl (3ar,7ar)-4-oxo-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound C1CCC(=O)[C@H]2[C@@H]1N(C(=O)OC(C)(C)C)CC2 GRNSGJOKGICXGO-NXEZZACHSA-N 0.000 description 2
- MRMYRYLVMIZVQM-UHFFFAOYSA-N tert-butyl 4-hydroxy-2,3,3a,4,5,6,7,7a-octahydroindole-1-carboxylate Chemical compound C1CCC(O)C2C1N(C(=O)OC(C)(C)C)CC2 MRMYRYLVMIZVQM-UHFFFAOYSA-N 0.000 description 2
- XRYXQDYFSBOZFJ-UHFFFAOYSA-N tert-butyl 4-oxo-6,7-dihydro-5h-indole-1-carboxylate Chemical compound C1CCC(=O)C2=C1N(C(=O)OC(C)(C)C)C=C2 XRYXQDYFSBOZFJ-UHFFFAOYSA-N 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- FBJRTQKSLCSQGD-UATJXVQHSA-N (3ar,4s,7ar)-4-[2-(3-methylphenyl)ethynyl]-1,2,3,3a,5,6,7,7a-octahydroindol-4-ol;hydrochloride Chemical compound Cl.CC1=CC=CC(C#C[C@@]2(O)[C@@H]3CCN[C@@H]3CCC2)=C1 FBJRTQKSLCSQGD-UATJXVQHSA-N 0.000 description 1
- XESFFARYEHPMLK-RNFRBKRXSA-N (3ar,7ar)-4-oxo-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylic acid Chemical compound C1CCC(=O)[C@H]2[C@@H]1N(C(=O)O)CC2 XESFFARYEHPMLK-RNFRBKRXSA-N 0.000 description 1
- KASJZXHXXNEULX-UHFFFAOYSA-N 1,5,6,7-tetrahydroindol-4-one Chemical compound O=C1CCCC2=C1C=CN2 KASJZXHXXNEULX-UHFFFAOYSA-N 0.000 description 1
- ACEVACUFIJRHNX-UHFFFAOYSA-N 2,3,4,4a,6,7,8,8a-octahydro-1h-quinolin-5-one;oxalic acid Chemical compound OC(=O)C(O)=O.N1CCCC2C(=O)CCCC21 ACEVACUFIJRHNX-UHFFFAOYSA-N 0.000 description 1
- DTWCFCILAJVNPE-UHFFFAOYSA-N 3-methoxycyclopent-2-en-1-one Chemical compound COC1=CC(=O)CC1 DTWCFCILAJVNPE-UHFFFAOYSA-N 0.000 description 1
- WDYVUKGVKRZQNM-UHFFFAOYSA-N 6-phosphonohexylphosphonic acid Chemical compound OP(O)(=O)CCCCCCP(O)(O)=O WDYVUKGVKRZQNM-UHFFFAOYSA-N 0.000 description 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- 208000007848 Alcoholism Diseases 0.000 description 1
- GAOKTGXOJBFNHY-UHFFFAOYSA-N CC(C)(C)OC(=O)N1CCCC2C1CCCC2(O)C#CC1=CC=CC(Cl)=C1 Chemical compound CC(C)(C)OC(=O)N1CCCC2C1CCCC2(O)C#CC1=CC=CC(Cl)=C1 GAOKTGXOJBFNHY-UHFFFAOYSA-N 0.000 description 1
- 101150041968 CDC13 gene Proteins 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229910021595 Copper(I) iodide Inorganic materials 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- 208000004454 Hyperalgesia Diseases 0.000 description 1
- 208000035154 Hyperesthesia Diseases 0.000 description 1
- 108090001060 Lipase Proteins 0.000 description 1
- 239000004367 Lipase Substances 0.000 description 1
- 102000004882 Lipase Human genes 0.000 description 1
- 238000003820 Medium-pressure liquid chromatography Methods 0.000 description 1
- 241001661345 Moesziomyces antarcticus Species 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- 108010084311 Novozyme 435 Proteins 0.000 description 1
- 235000019502 Orange oil Nutrition 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 208000025569 Tobacco Use disease Diseases 0.000 description 1
- 206010043903 Tobacco abuse Diseases 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- IKESQGSAZLNOMK-GRMSKOJTSA-N acetic acid;tert-butyl (3as,4r,7as)-4-acetyloxy-2,3,3a,4,5,6,7,7a-octahydroindole-1-carboxylate Chemical compound CC(O)=O.CC(=O)O[C@@H]1CCC[C@@H]2N(C(=O)OC(C)(C)C)CC[C@H]12 IKESQGSAZLNOMK-GRMSKOJTSA-N 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 206010001584 alcohol abuse Diseases 0.000 description 1
- 208000025746 alcohol use disease Diseases 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229940047495 celebrex Drugs 0.000 description 1
- 229960000590 celecoxib Drugs 0.000 description 1
- 230000001684 chronic effect Effects 0.000 description 1
- 229960003920 cocaine Drugs 0.000 description 1
- 239000012230 colorless oil Substances 0.000 description 1
- LSXDOTMGLUJQCM-UHFFFAOYSA-M copper(i) iodide Chemical compound I[Cu] LSXDOTMGLUJQCM-UHFFFAOYSA-M 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000003412 degenerative effect Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000008298 dragée Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000009982 effect on human Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- UIQMAEKKEOSTQR-UHFFFAOYSA-N ethyl 4-hydroxy-4-(2-phenylethynyl)-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound CCOC(=O)N1CCC2C1CCCC2(O)C#CC1=CC=CC=C1 UIQMAEKKEOSTQR-UHFFFAOYSA-N 0.000 description 1
- CQSKFJMMPQUHFD-UHFFFAOYSA-N ethyl 5-oxo-2,3,4,4a,6,7,8,8a-octahydroquinoline-1-carboxylate Chemical compound C1CCC(=O)C2C1N(C(=O)OCC)CCC2 CQSKFJMMPQUHFD-UHFFFAOYSA-N 0.000 description 1
- TUSJQDVXPJUEDX-UHFFFAOYSA-N ethyl n-[3-hydroxy-3-(2-phenylethynyl)cyclohexyl]carbamate Chemical compound C1C(NC(=O)OCC)CCCC1(O)C#CC1=CC=CC=C1 TUSJQDVXPJUEDX-UHFFFAOYSA-N 0.000 description 1
- QRZWUUZVBTZPSX-UHFFFAOYSA-N ethyl n-methyl-n-[3-(2-phenylethynyl)cyclohex-3-en-1-yl]carbamate Chemical compound C1C(N(C)C(=O)OCC)CCC=C1C#CC1=CC=CC=C1 QRZWUUZVBTZPSX-UHFFFAOYSA-N 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000003818 flash chromatography Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 230000003834 intracellular effect Effects 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 235000019421 lipase Nutrition 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- 229960000994 lumiracoxib Drugs 0.000 description 1
- KHPKQFYUPIUARC-UHFFFAOYSA-N lumiracoxib Chemical compound OC(=O)CC1=CC(C)=CC=C1NC1=C(F)C=CC=C1Cl KHPKQFYUPIUARC-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- ONCGDBBUYYQAAN-UHFFFAOYSA-N methyl n-[3-[2-(3-chlorophenyl)ethynyl]-3-hydroxycyclohexyl]-n-methylcarbamate Chemical compound C1C(N(C)C(=O)OC)CCCC1(O)C#CC1=CC=CC(Cl)=C1 ONCGDBBUYYQAAN-UHFFFAOYSA-N 0.000 description 1
- UQTWICKBCPTKJI-UHFFFAOYSA-N methyl n-[3-hydroxy-3-[2-(3-methoxyphenyl)ethynyl]-5,5-dimethylcyclohexyl]-n-methylcarbamate Chemical compound C1C(N(C)C(=O)OC)CC(C)(C)CC1(O)C#CC1=CC=CC(OC)=C1 UQTWICKBCPTKJI-UHFFFAOYSA-N 0.000 description 1
- CLJAAHZISOTDIY-UHFFFAOYSA-N methyl n-[3-hydroxy-3-[2-(3-methoxyphenyl)ethynyl]cyclohexyl]-n-methylcarbamate Chemical compound C1C(N(C)C(=O)OC)CCCC1(O)C#CC1=CC=CC(OC)=C1 CLJAAHZISOTDIY-UHFFFAOYSA-N 0.000 description 1
- ZFDQIQJVKUEROE-UHFFFAOYSA-N methyl n-[3-hydroxy-3-[2-(3-methylphenyl)ethynyl]cyclohexyl]-n-methylcarbamate Chemical compound C1C(N(C)C(=O)OC)CCCC1(O)C#CC1=CC=CC(C)=C1 ZFDQIQJVKUEROE-UHFFFAOYSA-N 0.000 description 1
- POQHKMYYVSOTOH-UHFFFAOYSA-N methyl n-[3-hydroxy-5,5-dimethyl-3-[2-(3-methylphenyl)ethynyl]cyclohexyl]-n-methylcarbamate Chemical compound C1C(N(C)C(=O)OC)CC(C)(C)CC1(O)C#CC1=CC=CC(C)=C1 POQHKMYYVSOTOH-UHFFFAOYSA-N 0.000 description 1
- 239000004530 micro-emulsion Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- XBXCNNQPRYLIDE-UHFFFAOYSA-M n-tert-butylcarbamate Chemical compound CC(C)(C)NC([O-])=O XBXCNNQPRYLIDE-UHFFFAOYSA-M 0.000 description 1
- 210000000653 nervous system Anatomy 0.000 description 1
- 229940127240 opiate Drugs 0.000 description 1
- 239000010502 orange oil Substances 0.000 description 1
- GEVPUGOOGXGPIO-UHFFFAOYSA-N oxalic acid;dihydrate Chemical compound O.O.OC(=O)C(O)=O GEVPUGOOGXGPIO-UHFFFAOYSA-N 0.000 description 1
- UWBHMRBRLOJJAA-UHFFFAOYSA-N oxaluric acid Chemical compound NC(=O)NC(=O)C(O)=O UWBHMRBRLOJJAA-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000008177 pharmaceutical agent Substances 0.000 description 1
- 239000002831 pharmacologic agent Substances 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 229960000371 rofecoxib Drugs 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000007962 solid dispersion Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000005477 standard model Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- MRMYRYLVMIZVQM-MXWKQRLJSA-N tert-butyl (3ar,4s,7ar)-4-hydroxy-2,3,3a,4,5,6,7,7a-octahydroindole-1-carboxylate Chemical compound [C@H]1([C@H](CCC2)O)[C@@H]2N(C(=O)OC(C)(C)C)CC1 MRMYRYLVMIZVQM-MXWKQRLJSA-N 0.000 description 1
- ZAPZZFRGOMWRCG-WOIUINJBSA-N tert-butyl (3ar,4s,7ar)-4-hydroxy-4-[2-(3-methylphenyl)ethynyl]-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound CC1=CC=CC(C#C[C@@]2(O)[C@H]3[C@H](N(CC3)C(=O)OC(C)(C)C)CCC2)=C1 ZAPZZFRGOMWRCG-WOIUINJBSA-N 0.000 description 1
- GRNSGJOKGICXGO-UWVGGRQHSA-N tert-butyl (3as,7as)-4-oxo-3,3a,5,6,7,7a-hexahydro-2h-indole-1-carboxylate Chemical compound C1CCC(=O)[C@@H]2[C@H]1N(C(=O)OC(C)(C)C)CC2 GRNSGJOKGICXGO-UWVGGRQHSA-N 0.000 description 1
- NIISILKXKMNSLC-UHFFFAOYSA-N tert-butyl 7-hydroxy-7-[2-(3-methylphenyl)ethynyl]-3,3a,4,5,6,7a-hexahydro-1h-isoindole-2-carboxylate Chemical compound CC1=CC=CC(C#CC2(O)C3CN(CC3CCC2)C(=O)OC(C)(C)C)=C1 NIISILKXKMNSLC-UHFFFAOYSA-N 0.000 description 1
- SGPWUVURFSJYQO-UHFFFAOYSA-N tert-butyl 7-oxo-3,3a,4,5,6,7a-hexahydro-1h-isoindole-2-carboxylate Chemical compound C1CCC(=O)C2CN(C(=O)OC(C)(C)C)CC21 SGPWUVURFSJYQO-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000000472 traumatic effect Effects 0.000 description 1
- CWMFRHBXRUITQE-UHFFFAOYSA-N trimethylsilylacetylene Chemical group C[Si](C)(C)C#C CWMFRHBXRUITQE-UHFFFAOYSA-N 0.000 description 1
- 238000000825 ultraviolet detection Methods 0.000 description 1
- 229940087652 vioxx Drugs 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 229940018503 zyban Drugs 0.000 description 1
Classifications
-
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/16—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by singly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/24—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a ring other than a six-membered aromatic ring
-
- 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
- A61P25/08—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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/32—Alcohol-abuse
-
- 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
- A61P25/34—Tobacco-abuse
-
- 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
- A61P25/36—Opioid-abuse
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/16—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
- C07C233/23—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/04—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms
- C07D215/08—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms with acylated ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
- C07D215/20—Oxygen 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
- C07D401/02—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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- 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
- C07D405/02—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 two hetero rings
- C07D405/06—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 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
- C07D405/02—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 two hetero rings
- C07D405/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Addiction (AREA)
- Pain & Pain Management (AREA)
- Psychology (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Indole Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Quinoline Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0128996.6A GB0128996D0 (en) | 2001-12-04 | 2001-12-04 | Organic compounds |
PCT/EP2002/013670 WO2003047581A1 (fr) | 2001-12-04 | 2002-12-03 | Derives d'acetylene possedant une activite antagoniste mglur 5 |
Publications (2)
Publication Number | Publication Date |
---|---|
NO20042673L NO20042673L (no) | 2004-06-25 |
NO327005B1 true NO327005B1 (no) | 2009-04-06 |
Family
ID=9926969
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20042673A NO327005B1 (no) | 2001-12-04 | 2004-06-25 | Acetylenderivaer som har mGluR5 antagonistisk aktivitet |
Country Status (32)
Country | Link |
---|---|
US (4) | US7348353B2 (fr) |
EP (1) | EP1453512B8 (fr) |
JP (2) | JP4176020B2 (fr) |
KR (2) | KR100980901B1 (fr) |
CN (2) | CN101366714B (fr) |
AR (2) | AR037682A1 (fr) |
AT (1) | ATE327755T1 (fr) |
AU (1) | AU2002358585B2 (fr) |
BR (1) | BR0214666A (fr) |
CA (1) | CA2466560C (fr) |
CO (1) | CO5590929A2 (fr) |
CY (1) | CY1105460T1 (fr) |
DE (1) | DE60211944T2 (fr) |
DK (1) | DK1453512T3 (fr) |
EC (1) | ECSP045139A (fr) |
EG (1) | EG24936A (fr) |
ES (1) | ES2263842T3 (fr) |
GB (1) | GB0128996D0 (fr) |
HK (1) | HK1071510A1 (fr) |
HU (1) | HU229429B1 (fr) |
IL (1) | IL161990A0 (fr) |
MX (1) | MXPA04005456A (fr) |
MY (1) | MY137774A (fr) |
NO (1) | NO327005B1 (fr) |
NZ (1) | NZ533266A (fr) |
PE (1) | PE20030640A1 (fr) |
PL (1) | PL212996B1 (fr) |
PT (1) | PT1453512E (fr) |
RU (1) | RU2341515C2 (fr) |
TW (1) | TWI328578B (fr) |
WO (1) | WO2003047581A1 (fr) |
ZA (1) | ZA200403713B (fr) |
Families Citing this family (44)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0128996D0 (en) | 2001-12-04 | 2002-01-23 | Novartis Ag | Organic compounds |
US7772188B2 (en) | 2003-01-28 | 2010-08-10 | Ironwood Pharmaceuticals, Inc. | Methods and compositions for the treatment of gastrointestinal disorders |
GB0325956D0 (en) * | 2003-11-06 | 2003-12-10 | Addex Pharmaceuticals Sa | Novel compounds |
EP1734963A4 (fr) | 2004-04-02 | 2008-06-18 | Merck & Co Inc | Methode destinee a traiter des hommes presentant des troubles metaboliques et anthropometriques |
GB0503646D0 (en) * | 2005-02-22 | 2005-03-30 | Novartis Ag | Organic compounds |
GB0508319D0 (en) * | 2005-04-25 | 2005-06-01 | Novartis Ag | Organic compounds |
GB0508318D0 (en) * | 2005-04-25 | 2005-06-01 | Novartis Ag | Organic compounds |
GB0508314D0 (en) * | 2005-04-25 | 2005-06-01 | Novartis Ag | Organic compounds |
GB0514296D0 (en) * | 2005-07-12 | 2005-08-17 | Novartis Ag | Organic compounds |
EP2272509A1 (fr) * | 2006-09-11 | 2011-01-12 | Novartis AG | Nouvelles utilisations des récepteurs du glutamate métabotropique |
MX354786B (es) | 2007-06-04 | 2018-03-21 | Synergy Pharmaceuticals Inc | Agonistas de guanilato ciclasa utiles para el tratamiento de trastornos gastrointestinales, inflamacion, cancer y otros trastornos. |
US8969514B2 (en) | 2007-06-04 | 2015-03-03 | Synergy Pharmaceuticals, Inc. | Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases |
TW200924745A (en) * | 2007-10-12 | 2009-06-16 | Novartis Ag | Organic compounds |
AU2012254934B2 (en) * | 2007-10-12 | 2013-10-17 | Novartis Ag | Metabotropic glutamate receptor modulators for the treatment of Parkinson's disease |
CA2726917C (fr) | 2008-06-04 | 2018-06-26 | Synergy Pharmaceuticals Inc. | Agonistes de guanylate cyclase utile dans le traitement de troubles gastro-intestinaux, d'une inflammation, d'un cancer et d'autres troubles |
CN102131503A (zh) * | 2008-06-30 | 2011-07-20 | 诺瓦提斯公司 | 用于治疗帕金森病的包含mGluR调节剂的组合产品 |
NZ590753A (en) | 2008-08-12 | 2012-06-29 | Novartis Ag | Processes for the preparation of 4-oxo-octahydro-indole-1-carbocylic acid methyl ester and derivatives thereof |
US8334287B2 (en) | 2009-07-17 | 2012-12-18 | Hoffmann-La Roche Inc. | Imidazoles |
US20120157464A1 (en) | 2009-07-23 | 2012-06-21 | Novartis Ag | Use of azabicycloalkyl derivatives or pyrrolidine-2-one derivatives for the treatment or prevention of ataxia |
TWI558398B (zh) | 2009-09-22 | 2016-11-21 | 諾華公司 | 菸鹼乙醯膽鹼受體α7活化劑之用途 |
WO2011048150A1 (fr) | 2009-10-20 | 2011-04-28 | Novartis Ag | Utilisation de 1h-quinazoline-2,4-diones |
MX2012012615A (es) * | 2010-04-30 | 2012-12-17 | Novartis Ag | Marcadores predictivos utiles en el tratamiento del sindrome fragil x (fxs). |
BR112012033290A2 (pt) | 2010-06-24 | 2016-11-22 | Novartis Ag | uso de 1h-quinazolina-2,4-dionas |
US9616097B2 (en) | 2010-09-15 | 2017-04-11 | Synergy Pharmaceuticals, Inc. | Formulations of guanylate cyclase C agonists and methods of use |
WO2012084873A1 (fr) | 2010-12-20 | 2012-06-28 | Novartis Ag | Esters d'acides 4-(hétéro)aryl-éthynyl-octahydro-indole-1-carboxyliques |
EP2668159A1 (fr) | 2011-01-24 | 2013-12-04 | Novartis AG | Dérivés de 4-tolyl-éthynyl-octahydro-indole-1-ester |
JP2014503568A (ja) | 2011-01-27 | 2014-02-13 | ノバルティス アーゲー | ニコチン酸アセチルコリン受容体α7活性化因子の使用 |
CA2830458A1 (fr) | 2011-03-18 | 2012-09-27 | Novartis Ag | Combinaisons d'activateurs des recepteurs nicotiniques a l'acetylcholine alpha 7 et d'antagonistes des mglur5 destinees a etre utilisees dans la dyskinesie induite par la dopaminedans la maladie de parkinson |
EP2753331A1 (fr) | 2011-09-07 | 2014-07-16 | Novartis AG | Utilisation de 1h-quinazoline-2,4-diones dans la prévention ou le traitement de l'épilepsie photosensible |
WO2013131981A1 (fr) | 2012-03-08 | 2013-09-12 | Novartis Ag | Marqueurs de prédiction utiles dans le diagnostic et le traitement du syndrome de l'x fragile (fxs) |
GB201215033D0 (en) | 2012-08-23 | 2012-10-10 | Novartis Ag | Diazepinone derivatives |
BR112015016992A8 (pt) | 2013-01-15 | 2018-01-23 | Novartis Ag | uso de agonistas do receptor alfa 7 nicotínico de acetilcolina |
WO2014111751A1 (fr) | 2013-01-15 | 2014-07-24 | Novartis Ag | Utilisation d'agonistes du récepteur nicotinique alpha 7 pour le traitement de la narcolepsie |
EP2970384A1 (fr) | 2013-03-15 | 2016-01-20 | Synergy Pharmaceuticals Inc. | Agonistes de la guanylate cyclase et leurs utilisations |
WO2014151200A2 (fr) | 2013-03-15 | 2014-09-25 | Synergy Pharmaceuticals Inc. | Compositions utiles pour le traitement de troubles gastro-intestinaux |
JP6606491B2 (ja) | 2013-06-05 | 2019-11-13 | シナジー ファーマシューティカルズ インコーポレイテッド | グアニル酸シクラーゼcの超高純度アゴニスト、その作成および使用方法 |
KR102290249B1 (ko) * | 2013-06-12 | 2021-08-17 | 노파르티스 아게 | 변형 방출 제제 |
CN105669686B (zh) * | 2014-11-19 | 2018-08-03 | 上海合全药业股份有限公司 | 一种6-(叔丁氧羰基)八氢呋喃[2,3-c]吡啶-4-羧酸的合成方法 |
AU2018310881C1 (en) | 2017-07-31 | 2021-12-16 | Novartis Ag | Use of mavoglurant in the reduction of cocaine use or in preventing relapse into cocaine use |
KR20200035262A (ko) | 2017-07-31 | 2020-04-02 | 노파르티스 아게 | 알코올 사용 감소 또는 알코올 사용 재발 예방에 있어서 마보글루란트의 용도 |
AU2020215849B2 (en) | 2019-01-29 | 2023-07-27 | Novartis Ag | The use of an mGluR5 antagonist for treating opioid analgesic tolerance |
EP4181918A2 (fr) | 2020-07-17 | 2023-05-24 | Novartis AG | Utilisation d'antagonistes de mglur5 |
JP2023552833A (ja) | 2020-12-11 | 2023-12-19 | ノバルティス アーゲー | アンフェタミン中毒の治療のためのmGluR5拮抗薬の使用 |
WO2022130136A1 (fr) | 2020-12-14 | 2022-06-23 | Novartis Ag | Utilisation d'antagonistes de mglur5 pour traiter un trouble lié aux jeux d'argent |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2741009A1 (de) * | 1976-09-22 | 1978-03-23 | Sandoz Ag | 4-styryl-4-indolinol-derivate, ihre verwendung und herstellung |
DE2802833A1 (de) | 1978-01-23 | 1979-07-26 | Sandoz Ag | 4-styryl-4-indolinol-derivate, ihre verwendung und herstellung |
US5264456A (en) | 1989-12-29 | 1993-11-23 | Allergan, Inc. | Acetylenes disubstituted with a furyl group and a substituted phenyl group having retinoid like activity |
US5284957A (en) | 1992-09-03 | 1994-02-08 | Eli Lilly And Company | Excitatory amino acid receptor antagonists |
US5593994A (en) | 1994-09-29 | 1997-01-14 | The Dupont Merck Pharmaceutical Company | Prostaglandin synthase inhibitors |
AU6709596A (en) | 1995-08-22 | 1997-03-19 | Japan Tobacco Inc. | Amide compounds and use of the same |
EP2223920A3 (fr) | 1996-06-19 | 2011-09-28 | Aventis Pharma Limited | Composes azabicycliques substitues |
TW544448B (en) * | 1997-07-11 | 2003-08-01 | Novartis Ag | Pyridine derivatives |
WO1999062869A1 (fr) | 1998-06-04 | 1999-12-09 | Kumiai Chemical Industry Co., Ltd. | Derives de phenylacetylene et bactericides a usage agricole ou horticole |
CN1187048C (zh) | 1998-10-02 | 2005-02-02 | 诺瓦提斯公司 | mGLuR拮抗剂用于治疗疼痛和焦虑 |
IL146697A0 (en) | 1999-07-06 | 2002-07-25 | Lilly Co Eli | SELECTIVE iGluR5 RECEPTOR FOR THE TREATMENT OF MIGRAINE |
GB0007108D0 (en) | 2000-03-23 | 2000-05-17 | Novartis Ag | Organic compounds |
IL155202A0 (en) | 2000-10-20 | 2003-11-23 | Biocryst Pharm Inc | Biaryl compounds as serine protease inhibitors |
WO2002046166A1 (fr) * | 2000-12-04 | 2002-06-13 | F. Hoffmann-La Roche Ag | Derives phenylethenyle ou phenylethinyle servant d'antagonistes de recepteur de glutamate |
GB0103045D0 (en) * | 2001-02-07 | 2001-03-21 | Novartis Ag | Organic Compounds |
US7138404B2 (en) | 2001-05-23 | 2006-11-21 | Hoffmann-La Roche Inc. | 4-aminopyrimidine derivatives |
GB0128996D0 (en) * | 2001-12-04 | 2002-01-23 | Novartis Ag | Organic compounds |
JP2005517640A (ja) | 2001-12-04 | 2005-06-16 | エフ.ホフマン−ラ ロシュ アーゲー | 置換2−アミノ−シクロアルカンカルボキサアミドならびにシステインプロテアーゼインヒビターとしてのその使用 |
TW200303309A (en) | 2001-12-04 | 2003-09-01 | Bristol Myers Squibb Co | Novel n-[4-(1h-imidazol-1-yl)-2-fluorophenyl]-3-trifluoromethyl)-1h-pyrazole-5-carboxamides as factor Xa inhibitors |
-
2001
- 2001-12-04 GB GBGB0128996.6A patent/GB0128996D0/en not_active Ceased
-
2002
- 2002-12-01 EG EG2002121297A patent/EG24936A/xx active
- 2002-12-02 PE PE2002001157A patent/PE20030640A1/es not_active Application Discontinuation
- 2002-12-02 TW TW091134933A patent/TWI328578B/zh not_active IP Right Cessation
- 2002-12-02 AR ARP020104641A patent/AR037682A1/es not_active Application Discontinuation
- 2002-12-03 MY MYPI20024525A patent/MY137774A/en unknown
- 2002-12-03 HU HU0402191A patent/HU229429B1/hu unknown
- 2002-12-03 EP EP02792867A patent/EP1453512B8/fr not_active Expired - Lifetime
- 2002-12-03 CA CA2466560A patent/CA2466560C/fr not_active Expired - Fee Related
- 2002-12-03 CN CN200810166366.0A patent/CN101366714B/zh not_active Expired - Lifetime
- 2002-12-03 DK DK02792867T patent/DK1453512T3/da active
- 2002-12-03 KR KR1020107002745A patent/KR100980901B1/ko not_active IP Right Cessation
- 2002-12-03 US US10/497,363 patent/US7348353B2/en not_active Expired - Lifetime
- 2002-12-03 IL IL16199002A patent/IL161990A0/xx not_active IP Right Cessation
- 2002-12-03 BR BR0214666-5A patent/BR0214666A/pt not_active Application Discontinuation
- 2002-12-03 NZ NZ533266A patent/NZ533266A/en not_active IP Right Cessation
- 2002-12-03 MX MXPA04005456A patent/MXPA04005456A/es active IP Right Grant
- 2002-12-03 CN CNB028232968A patent/CN100430059C/zh not_active Expired - Lifetime
- 2002-12-03 KR KR1020047008477A patent/KR100959204B1/ko not_active IP Right Cessation
- 2002-12-03 PL PL368739A patent/PL212996B1/pl unknown
- 2002-12-03 DE DE60211944T patent/DE60211944T2/de not_active Expired - Lifetime
- 2002-12-03 JP JP2003548836A patent/JP4176020B2/ja not_active Expired - Lifetime
- 2002-12-03 WO PCT/EP2002/013670 patent/WO2003047581A1/fr active Application Filing
- 2002-12-03 ES ES02792867T patent/ES2263842T3/es not_active Expired - Lifetime
- 2002-12-03 PT PT02792867T patent/PT1453512E/pt unknown
- 2002-12-03 RU RU2004120781/04A patent/RU2341515C2/ru not_active IP Right Cessation
- 2002-12-03 AT AT02792867T patent/ATE327755T1/de active
- 2002-12-03 AU AU2002358585A patent/AU2002358585B2/en not_active Ceased
-
2004
- 2004-05-14 ZA ZA2004/03713A patent/ZA200403713B/en unknown
- 2004-06-04 EC EC2004005139A patent/ECSP045139A/es unknown
- 2004-06-07 CO CO04053105A patent/CO5590929A2/es active IP Right Grant
- 2004-06-25 NO NO20042673A patent/NO327005B1/no not_active IP Right Cessation
-
2005
- 2005-02-28 HK HK05101701A patent/HK1071510A1/xx not_active IP Right Cessation
-
2006
- 2006-08-03 CY CY20061101091T patent/CY1105460T1/el unknown
-
2008
- 2008-02-29 US US12/040,081 patent/US20080146647A1/en not_active Abandoned
- 2008-07-09 JP JP2008179005A patent/JP5036648B2/ja not_active Expired - Lifetime
-
2011
- 2011-09-22 US US13/239,467 patent/US8536229B2/en not_active Expired - Lifetime
-
2012
- 2012-11-20 AR ARP120104356A patent/AR088921A2/es not_active Application Discontinuation
-
2013
- 2013-08-15 US US13/967,719 patent/US20130331568A1/en not_active Abandoned
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
NO327005B1 (no) | Acetylenderivaer som har mGluR5 antagonistisk aktivitet | |
KR100586349B1 (ko) | 아릴술폰아미드 및 그의 유사체, 및 신경 변성 질병 치료에있어서 그의 용도 | |
US5476874A (en) | New HIV protease inhibitors | |
JPH09500147A (ja) | 抗炎症剤としてのイソキサゾリン化合物 | |
FR2567885A1 (fr) | Derives 3-aminopropoxyaryliques, leur preparation, leur application comme medicaments et compositions pharmaceutiques les contenant | |
US4782058A (en) | 1,3,4,6,7,11b-Hexahydro-6-phenyl-2H-pyrazino-(2,1-a)isoquinolines, for anti-histamine or anti-depression treatment | |
DE69317651T2 (de) | Indol derivate als steroid 5 alpha-reductase inhibitoren | |
KR100546534B1 (ko) | 아릴술폰아미드 및 그의 동족체, 및 신경 변성 질병 치료에 있어서 그의 용도 | |
US5641785A (en) | Oxazoloquinolinone derivatives, their preparation and their therapeutic application as inhibitors of monoamine oxidase | |
KR20010040254A (ko) | 아미노알킬페놀 유도체 및 관련 화합물 | |
US5747540A (en) | HIV protease inhibitors useful for the treatment of AIDS | |
JP3908798B2 (ja) | ベンゾシクロアルケン類、その製造法および剤 | |
US6265402B1 (en) | Use of 2-phenylmorpholin-5-one derivatives | |
IE57907B1 (en) | Phenethylamine derivatives | |
JPH0342276B2 (fr) | ||
EP1517896A2 (fr) | Phenyl- et pyridyl-diazaheterocycles ayant une activite modulatrice du tnf | |
JPH0450301B2 (fr) | ||
JPH06345695A (ja) | リグナン類縁体の製法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MK1K | Patent expired |