FI113471B - Kinoxalindion-NMDA-reseptorantagonister - Google Patents
Kinoxalindion-NMDA-reseptorantagonister Download PDFInfo
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- FI113471B FI113471B FI971026A FI971026A FI113471B FI 113471 B FI113471 B FI 113471B FI 971026 A FI971026 A FI 971026A FI 971026 A FI971026 A FI 971026A FI 113471 B FI113471 B FI 113471B
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- mmol
- dichloro
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- HOKKHZGPKSLGJE-GSVOUGTGSA-N N-Methyl-D-aspartic acid Chemical compound CN[C@@H](C(O)=O)CC(O)=O HOKKHZGPKSLGJE-GSVOUGTGSA-N 0.000 title abstract description 14
- SEPKUNXLGWMPHL-UHFFFAOYSA-N quinoxaline-2,3-dione Chemical compound C1=CC=CC2=NC(=O)C(=O)N=C21 SEPKUNXLGWMPHL-UHFFFAOYSA-N 0.000 title description 3
- 150000003839 salts Chemical class 0.000 claims abstract description 13
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims abstract description 12
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims abstract description 10
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 10
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 9
- 238000011282 treatment Methods 0.000 claims abstract description 9
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 7
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 5
- 208000012902 Nervous system disease Diseases 0.000 claims abstract description 4
- 208000025966 Neurological disease Diseases 0.000 claims abstract description 4
- 230000001154 acute effect Effects 0.000 claims abstract description 4
- 230000001684 chronic effect Effects 0.000 claims abstract description 4
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims abstract description 3
- 125000002785 azepinyl group Chemical group 0.000 claims abstract description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 3
- 125000004076 pyridyl group Chemical group 0.000 claims abstract description 3
- 125000001425 triazolyl group Chemical group 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims description 64
- 238000002360 preparation method Methods 0.000 claims description 43
- 238000000034 method Methods 0.000 claims description 20
- 238000006243 chemical reaction Methods 0.000 claims description 18
- 239000000460 chlorine Substances 0.000 claims description 17
- -1 benzotriazol-1-yl Chemical group 0.000 claims description 15
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 12
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 4
- 125000001401 1,2,4-triazol-4-yl group Chemical group N=1N=C([H])N([*])C=1[H] 0.000 claims description 3
- 241000251730 Chondrichthyes Species 0.000 claims description 3
- 125000001607 1,2,3-triazol-1-yl group Chemical group [*]N1N=NC([H])=C1[H] 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims description 2
- 230000000626 neurodegenerative effect Effects 0.000 claims 2
- 230000003301 hydrolyzing effect Effects 0.000 claims 1
- 239000005557 antagonist Substances 0.000 abstract description 11
- 208000024827 Alzheimer disease Diseases 0.000 abstract description 4
- 206010039966 Senile dementia Diseases 0.000 abstract description 2
- 208000015122 neurodegenerative disease Diseases 0.000 abstract description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 206010019196 Head injury Diseases 0.000 abstract 1
- 230000000472 traumatic effect Effects 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 105
- YMWUJEATGCHHMB-UHFFFAOYSA-N dichloromethane Substances ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 91
- 239000000203 mixture Substances 0.000 description 64
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 63
- 239000007787 solid Substances 0.000 description 52
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 45
- 239000000243 solution Substances 0.000 description 45
- 238000005481 NMR spectroscopy Methods 0.000 description 43
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 24
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 21
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 21
- 239000000047 product Substances 0.000 description 20
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 19
- 238000003818 flash chromatography Methods 0.000 description 19
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 18
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 16
- 238000010992 reflux Methods 0.000 description 16
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 15
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 14
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 12
- 239000000725 suspension Substances 0.000 description 11
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 11
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 10
- 238000001914 filtration Methods 0.000 description 10
- 239000012299 nitrogen atmosphere Substances 0.000 description 10
- 229920006395 saturated elastomer Polymers 0.000 description 10
- 239000000741 silica gel Substances 0.000 description 10
- 229910002027 silica gel Inorganic materials 0.000 description 10
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 9
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 9
- 238000000746 purification Methods 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- LVQQNALMEIGSNM-UHFFFAOYSA-N 5-(bromomethyl)-6,7-dichloro-2,3-dimethoxyquinoxaline Chemical compound ClC1=C(Cl)C(CBr)=C2N=C(OC)C(OC)=NC2=C1 LVQQNALMEIGSNM-UHFFFAOYSA-N 0.000 description 8
- 239000004471 Glycine Substances 0.000 description 8
- 238000010828 elution Methods 0.000 description 8
- 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 8
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 7
- 239000000284 extract Substances 0.000 description 7
- 239000000706 filtrate Substances 0.000 description 7
- 239000000543 intermediate Substances 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 102000004868 N-Methyl-D-Aspartate Receptors Human genes 0.000 description 6
- 108090001041 N-Methyl-D-Aspartate Receptors Proteins 0.000 description 6
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 6
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical compound [O]C GRVDJDISBSALJP-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
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 5
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 5
- 239000012267 brine Substances 0.000 description 5
- 125000000623 heterocyclic group Chemical group 0.000 description 5
- 239000002287 radioligand Substances 0.000 description 5
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 5
- 235000017557 sodium bicarbonate Nutrition 0.000 description 5
- 239000012312 sodium hydride Substances 0.000 description 5
- 229910000104 sodium hydride Inorganic materials 0.000 description 5
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- CRAYFGFTLBTRRS-UHFFFAOYSA-N 2,3-dimethoxyquinoxaline Chemical compound C1=CC=C2N=C(OC)C(OC)=NC2=C1 CRAYFGFTLBTRRS-UHFFFAOYSA-N 0.000 description 4
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 4
- 101100167062 Caenorhabditis elegans chch-3 gene Proteins 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- 238000007792 addition Methods 0.000 description 4
- 235000019270 ammonium chloride Nutrition 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 239000012298 atmosphere Substances 0.000 description 4
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 229960002989 glutamic acid Drugs 0.000 description 4
- 125000005843 halogen group Chemical group 0.000 description 4
- 150000002391 heterocyclic compounds Chemical class 0.000 description 4
- 235000006408 oxalic acid Nutrition 0.000 description 4
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 4
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 4
- HJUGFYREWKUQJT-UHFFFAOYSA-N tetrabromomethane Chemical compound BrC(Br)(Br)Br HJUGFYREWKUQJT-UHFFFAOYSA-N 0.000 description 4
- ABJFBJGGLJVMAQ-UHFFFAOYSA-N 1,4-dihydroquinoxaline-2,3-dione Chemical class C1=CC=C2NC(=O)C(=O)NC2=C1 ABJFBJGGLJVMAQ-UHFFFAOYSA-N 0.000 description 3
- 125000006083 1-bromoethyl group Chemical group 0.000 description 3
- FWBADBLIFHGDFP-UHFFFAOYSA-N 5-(1-bromopropyl)-6,7-dichloro-2,3-dimethoxyquinoxaline Chemical compound COC1=C(OC)N=C2C(C(Br)CC)=C(Cl)C(Cl)=CC2=N1 FWBADBLIFHGDFP-UHFFFAOYSA-N 0.000 description 3
- KGZCECNIGBHRHP-UHFFFAOYSA-N 5-(chloromethyl)-2,3-dimethoxy-6,7-dimethylquinoxaline Chemical compound CC1=C(C)C(CCl)=C2N=C(OC)C(OC)=NC2=C1 KGZCECNIGBHRHP-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- YNHIGQDRGKUECZ-UHFFFAOYSA-L bis(triphenylphosphine)palladium(ii) dichloride Chemical compound [Cl-].[Cl-].[Pd+2].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 YNHIGQDRGKUECZ-UHFFFAOYSA-L 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000012065 filter cake Substances 0.000 description 3
- 235000013922 glutamic acid Nutrition 0.000 description 3
- 239000004220 glutamic acid Substances 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 239000011630 iodine Substances 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 239000000546 pharmaceutical excipient Substances 0.000 description 3
- 229910000027 potassium carbonate Inorganic materials 0.000 description 3
- 235000011181 potassium carbonates Nutrition 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 229940086542 triethylamine Drugs 0.000 description 3
- XWMGFDLVGGMTOO-UHFFFAOYSA-N (2,3-dimethoxy-6,7-dimethylquinoxalin-5-yl)methanol Chemical compound CC1=C(C)C(CO)=C2N=C(OC)C(OC)=NC2=C1 XWMGFDLVGGMTOO-UHFFFAOYSA-N 0.000 description 2
- IBRBMZRLVYKVRF-UHFFFAOYSA-N 1,2,4-trichloro-5-nitrobenzene Chemical compound [O-][N+](=O)C1=CC(Cl)=C(Cl)C=C1Cl IBRBMZRLVYKVRF-UHFFFAOYSA-N 0.000 description 2
- XWBMMWWAXFDZMI-UHFFFAOYSA-N 1-(2h-benzotriazol-5-yl)-n,n-dimethylmethanamine Chemical compound CN(C)CC1=CC=C2NN=NC2=C1 XWBMMWWAXFDZMI-UHFFFAOYSA-N 0.000 description 2
- KXONSAKSCCVAGI-UHFFFAOYSA-N 1-(6,7-dichloro-2,3-dimethoxyquinoxalin-5-yl)ethanol Chemical compound ClC1=C(Cl)C(C(C)O)=C2N=C(OC)C(OC)=NC2=C1 KXONSAKSCCVAGI-UHFFFAOYSA-N 0.000 description 2
- NCOIBUPOQWVYGO-UHFFFAOYSA-N 1-(6,7-dichloro-2,3-dimethoxyquinoxalin-5-yl)propan-1-ol Chemical compound COC1=C(OC)N=C2C(C(O)CC)=C(Cl)C(Cl)=CC2=N1 NCOIBUPOQWVYGO-UHFFFAOYSA-N 0.000 description 2
- DHAXJRMFAGWCHT-UHFFFAOYSA-N 1-[(6,7-dichloro-2,3-dimethoxyquinoxalin-5-yl)methyl]triazole-4-carbaldehyde Chemical compound C=12N=C(OC)C(OC)=NC2=CC(Cl)=C(Cl)C=1CN1C=C(C=O)N=N1 DHAXJRMFAGWCHT-UHFFFAOYSA-N 0.000 description 2
- UUFQTNFCRMXOAE-UHFFFAOYSA-N 1-methylmethylene Chemical compound C[CH] UUFQTNFCRMXOAE-UHFFFAOYSA-N 0.000 description 2
- GYQDMMSNDKWZLY-UHFFFAOYSA-N 2,3,6,7-tetrachloro-5-nitroquinoxaline Chemical compound ClC1=C(Cl)N=C2C([N+](=O)[O-])=C(Cl)C(Cl)=CC2=N1 GYQDMMSNDKWZLY-UHFFFAOYSA-N 0.000 description 2
- DXXBFAXBSVZRKA-UHFFFAOYSA-N 2,3,6,7-tetrachloroquinoxalin-5-amine Chemical compound ClC1=C(Cl)N=C2C(N)=C(Cl)C(Cl)=CC2=N1 DXXBFAXBSVZRKA-UHFFFAOYSA-N 0.000 description 2
- UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 2
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 description 2
- AFXPDOCNMCKWCH-UHFFFAOYSA-N 2-iodo-3,4-dimethyl-6-nitroaniline Chemical compound CC1=CC([N+]([O-])=O)=C(N)C(I)=C1C AFXPDOCNMCKWCH-UHFFFAOYSA-N 0.000 description 2
- ALHUXMDEZNLFTA-UHFFFAOYSA-N 2-methylquinoxaline Chemical compound C1=CC=CC2=NC(C)=CN=C21 ALHUXMDEZNLFTA-UHFFFAOYSA-N 0.000 description 2
- COFYIPIXKADKRY-UHFFFAOYSA-N 4,5-dichloro-3-methyl-2-nitroaniline Chemical compound CC1=C(Cl)C(Cl)=CC(N)=C1[N+]([O-])=O COFYIPIXKADKRY-UHFFFAOYSA-N 0.000 description 2
- LLSKXUJDISAQFP-UHFFFAOYSA-N 4,5-dichloro-3-methylbenzene-1,2-diamine Chemical compound CC1=C(N)C(N)=CC(Cl)=C1Cl LLSKXUJDISAQFP-UHFFFAOYSA-N 0.000 description 2
- PINGKGKKUSYUAW-UHFFFAOYSA-N 4,5-dimethyl-2-nitroaniline Chemical compound CC1=CC(N)=C([N+]([O-])=O)C=C1C PINGKGKKUSYUAW-UHFFFAOYSA-N 0.000 description 2
- NIALCPJNHZUBSE-UHFFFAOYSA-N 6,7-dichloro-2,3-dimethoxy-5-(1,2,4-triazol-1-ylmethyl)quinoxaline Chemical compound C=12N=C(OC)C(OC)=NC2=CC(Cl)=C(Cl)C=1CN1C=NC=N1 NIALCPJNHZUBSE-UHFFFAOYSA-N 0.000 description 2
- BGEWWFCMXJVJLH-UHFFFAOYSA-N 6,7-dichloro-2,3-dimethoxy-5-methylquinoxaline Chemical compound ClC1=C(Cl)C(C)=C2N=C(OC)C(OC)=NC2=C1 BGEWWFCMXJVJLH-UHFFFAOYSA-N 0.000 description 2
- KLRNHQAMURJZGV-UHFFFAOYSA-N 6,7-dichloro-2,3-dimethoxyquinoxaline-5-carbaldehyde Chemical compound ClC1=C(Cl)C(C=O)=C2N=C(OC)C(OC)=NC2=C1 KLRNHQAMURJZGV-UHFFFAOYSA-N 0.000 description 2
- YRVWYBQQAWRTKI-UHFFFAOYSA-N 6,7-dichloro-5-(1,2,4-triazol-1-ylmethyl)-1,4-dihydroquinoxaline-2,3-dione Chemical compound ClC=1C(Cl)=CC=2NC(=O)C(=O)NC=2C=1CN1C=NC=N1 YRVWYBQQAWRTKI-UHFFFAOYSA-N 0.000 description 2
- RYKHPSSYBOXZSD-UHFFFAOYSA-N 6,7-dichloro-5-(1-chloroethyl)-2,3-dimethoxyquinoxaline Chemical compound ClC1=C(Cl)C(C(C)Cl)=C2N=C(OC)C(OC)=NC2=C1 RYKHPSSYBOXZSD-UHFFFAOYSA-N 0.000 description 2
- JLFLGSYJXFGJPO-UHFFFAOYSA-N 6,7-dichloro-5-iodo-2,3-dimethoxyquinoxaline Chemical compound ClC1=C(Cl)C(I)=C2N=C(OC)C(OC)=NC2=C1 JLFLGSYJXFGJPO-UHFFFAOYSA-N 0.000 description 2
- JJNMOOWTCJCOFU-UHFFFAOYSA-N 6,7-dichloro-5-methyl-1,4-dihydroquinoxaline-2,3-dione Chemical compound N1C(=O)C(=O)NC2=C1C=C(Cl)C(Cl)=C2C JJNMOOWTCJCOFU-UHFFFAOYSA-N 0.000 description 2
- APKFPKLTEJAOJI-UHFFFAOYSA-N 6-butyldec-5-en-5-ylstannane Chemical compound CCCCC([SnH3])=C(CCCC)CCCC APKFPKLTEJAOJI-UHFFFAOYSA-N 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- 102000003678 AMPA Receptors Human genes 0.000 description 2
- 108090000078 AMPA Receptors Proteins 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-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
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
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- MMYRDQRTZWTYGH-UHFFFAOYSA-N methyl 6,7-dimethoxy-1,4-dihydroquinoxaline-5-carboxylate Chemical compound N1C=CNC2=CC(OC)=C(OC)C(C(=O)OC)=C21 MMYRDQRTZWTYGH-UHFFFAOYSA-N 0.000 description 1
- ZRHIENWSKPCKRU-UHFFFAOYSA-N methyl 6,7-dimethoxy-2,3-dioxo-1,4-dihydroquinoxaline-5-carboxylate Chemical compound N1C(=O)C(=O)NC2=C1C=C(OC)C(OC)=C2C(=O)OC ZRHIENWSKPCKRU-UHFFFAOYSA-N 0.000 description 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- OYSZWLKHERKDHI-UHFFFAOYSA-N n-[[1-[(6,7-dichloro-2,3-dimethoxyquinoxalin-5-yl)methyl]triazol-4-yl]methyl]butan-1-amine Chemical compound N1=NC(CNCCCC)=CN1CC1=C(Cl)C(Cl)=CC2=NC(OC)=C(OC)N=C12 OYSZWLKHERKDHI-UHFFFAOYSA-N 0.000 description 1
- 230000016273 neuron death Effects 0.000 description 1
- 230000003961 neuronal insult Effects 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 239000010502 orange oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- 210000000578 peripheral nerve Anatomy 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004353 pyrazol-1-yl group Chemical group [H]C1=NN(*)C([H])=C1[H] 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003252 quinoxalines Chemical class 0.000 description 1
- 239000002464 receptor antagonist Substances 0.000 description 1
- 229940044551 receptor antagonist Drugs 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000004258 retinal degeneration Effects 0.000 description 1
- 238000001896 rotating frame Overhauser effect spectroscopy Methods 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 229940001584 sodium metabisulfite Drugs 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- 239000012321 sodium triacetoxyborohydride Substances 0.000 description 1
- 229940063675 spermine Drugs 0.000 description 1
- 210000000278 spinal cord Anatomy 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- KUYMVWXKHQSIAS-UHFFFAOYSA-N tert-butyl 2-chloroacetate Chemical compound CC(C)(C)OC(=O)CCl KUYMVWXKHQSIAS-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
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- NHGXDBSUJJNIRV-UHFFFAOYSA-M tetrabutylammonium chloride Chemical compound [Cl-].CCCC[N+](CCCC)(CCCC)CCCC NHGXDBSUJJNIRV-UHFFFAOYSA-M 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- DZXKSFDSPBRJPS-UHFFFAOYSA-N tin(2+);sulfide Chemical compound [S-2].[Sn+2] DZXKSFDSPBRJPS-UHFFFAOYSA-N 0.000 description 1
- GZNAASVAJNXPPW-UHFFFAOYSA-M tin(4+) chloride dihydrate Chemical compound O.O.[Cl-].[Sn+4] GZNAASVAJNXPPW-UHFFFAOYSA-M 0.000 description 1
- FWPIDFUJEMBDLS-UHFFFAOYSA-L tin(II) chloride dihydrate Substances O.O.Cl[Sn]Cl FWPIDFUJEMBDLS-UHFFFAOYSA-L 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- PIEPQKCYPFFYMG-UHFFFAOYSA-N tris acetate Chemical compound CC(O)=O.OCC(N)(CO)CO PIEPQKCYPFFYMG-UHFFFAOYSA-N 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
Classifications
-
- 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
-
- 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
- A61P25/20—Hypnotics; Sedatives
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Biomedical Technology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurosurgery (AREA)
- Medicinal Chemistry (AREA)
- Neurology (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Anesthesiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Steroid Compounds (AREA)
Claims (8)
1. Förening kännetecknad av att den har farmein R\/X i H yVv° I (i) r2 N H eller ett farmaceutiskt godtagbart sait därav, 5 väri Rl och R^ vardera oberoende är Cl, Br, CH3, CH2CH3 eller CF3; R3 är H, CH3 eller CH2CH3; och X är 5-ledad heterocyklisk grupp som innehäller upp tili 4 kväveatomer, bunden via en kväveatom, där nämnda grupp eventuellt är substituerad med C^-C^-alkyl eller (CH2)nNR4R5, väri n är ett heltal frän 1 till 5 och R4 och R^ är vardera 10 oberoende H, C^-Cö-alkyl, C3-Cg-cykloalkyl eller Cj-C4-alkyl substituerad med fenyl eller pyridyl, eller R4 och R^ är sammanbundna för att tillsammans med den kväveatom, tili vilken de är bundna, bilda en pyrrolidin-, piperidin-, piperazin-, N-• (C]-C4-alkyl)piperazin-, morfolin- eller azepingrupp, eller när X är triazolyl, kan , . nämnda grupp eventuellt vara bensokondenserad. 15
2. Förening enligt patentkrav 1, kännetecknad av att Rl och R^ bäda är Cl.
. 3. Förening enligt patentkrav 1 eller 2, kännetecknad av att R^ är CH2CH3.
4. Förening enligt nägot av patentkraven 1 tili 3, kännetecknad av att X är 1,2,3- : '.· triazol-l-yl, bensotriazol-l-yl eller 1,2,4-triazol-4-yl. ' »
5. Förfarande för att framställä en förening med farmein (I) enligt patentkrav 1, ’: 20 kännetecknat av att det innefattar att man omsätter en förening med farmein (II) med en förening med farmein XH ätföljt av hydrolys av den resulterande produkten med farmein (III) enligt följande reaktionsschema, väri Rl, R^, r3 och X har den i » .: patentkrav 1 angivna betydelsen och hai är klor eller brom 43 113471 Rl^^hal R3\^X if χΗ II j| -► r2^\^\n<^^och3 r2 n^\0Ch3 (n) (m) h3o+ r3^x i H H
6. Farmaceutisk komposition, kännetecknad av att den innefattar en förening med formeln (I), eller ett farmaceutiskt godtagbart sait därav, tillsammans med ett farmaceutiskt godtagbart utspädningsmedel eller bärare. 5
7. Förening med formeln (I), eller ett farmaceutiskt godtagbart sait därav, att ; användas som ett läkemedel vid behandling av akuta neurodegenerativa och kronis- : ka neurologiska sjukdomar.
8. Användning av en förening med formeln (I), eller av ett farmaceutiskt godtagbart sait därav, för framställning av ett läkemedel att användas vid behandling av 10 akuta neurodegenerativa och kroniska neurologiska sjukdomar. > * »
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9418443A GB9418443D0 (en) | 1994-09-13 | 1994-09-13 | Therapeutic agents |
| GB9418443 | 1994-09-13 | ||
| PCT/EP1995/003483 WO1996008485A1 (en) | 1994-09-13 | 1995-09-01 | Quinoxalinedione nmda receptor antagonists |
| EP9503483 | 1995-09-01 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI971026A0 FI971026A0 (sv) | 1997-03-12 |
| FI971026A FI971026A (sv) | 1997-03-12 |
| FI113471B true FI113471B (sv) | 2004-04-30 |
Family
ID=10761258
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI971026A FI113471B (sv) | 1994-09-13 | 1997-03-12 | Kinoxalindion-NMDA-reseptorantagonister |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US5783572A (sv) |
| EP (1) | EP0781279B1 (sv) |
| JP (1) | JP2898097B2 (sv) |
| AT (1) | ATE202099T1 (sv) |
| CA (1) | CA2199845C (sv) |
| DE (1) | DE69521323T2 (sv) |
| DK (1) | DK0781279T3 (sv) |
| ES (1) | ES2158126T3 (sv) |
| FI (1) | FI113471B (sv) |
| GB (1) | GB9418443D0 (sv) |
| GR (1) | GR3036270T3 (sv) |
| MX (1) | MX9701894A (sv) |
| PT (1) | PT781279E (sv) |
| WO (1) | WO1996008485A1 (sv) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6110911A (en) * | 1995-06-07 | 2000-08-29 | Warner-Lambert Company | Cyclic amine derivatives of substituted quinoxaline 2,3-diones as glutamate receptor antagonists |
| US5874426A (en) * | 1995-06-07 | 1999-02-23 | Warner-Lambert Company | Cyclic amine derivatives of substituted quinoxaline 2,3-diones as glutamate receptor antagonists |
| MY132385A (en) * | 1995-08-31 | 2007-10-31 | Novartis Ag | 2,3-dioxo-1,2,3,4-tetrahydro-quinoxalinyl derivatives |
| GB9605027D0 (en) | 1996-03-09 | 1996-05-08 | Pfizer Ltd | Quinoxalinediones |
| AU5367598A (en) * | 1996-11-25 | 1998-06-22 | Warner-Lambert Company | Urea and thiourea derivatives of substituted quinoxaline 2,3-diones as glutamate receptor antagonists |
| US6172065B1 (en) | 1997-03-04 | 2001-01-09 | Warner-Lambert Company | Urea and thiourea derivatives of substituted quinoxaline 2,3-diones as glutamate receptor antagonists |
| US6340758B1 (en) * | 1997-05-16 | 2002-01-22 | Warner-Lambert Company | Conformationally semi-constrained quinoxaline 2,3-diones as neuroprotective agents |
| TW526195B (en) | 1997-06-10 | 2003-04-01 | Novartis Ag | Crystal modifications of 1-(2,6-difluorobenzyl)-1H-1,2,3-triazole-4-carboxamide and their use |
| DE19936521A1 (de) * | 1999-08-06 | 2001-02-15 | Gruenenthal Gmbh | Substituierte Pyrrolidin-2,3,4-trion-3-oxim-Derivate |
| JP2005506292A (ja) * | 2001-03-08 | 2005-03-03 | エモリー ユニバーシティ | ｐＨに依存するＮＭＤＡレセプターアンタゴニスト |
| US7732162B2 (en) | 2003-05-05 | 2010-06-08 | Probiodrug Ag | Inhibitors of glutaminyl cyclase for treating neurodegenerative diseases |
| US20060142186A1 (en) * | 2004-12-23 | 2006-06-29 | Voyager Pharmaceutical Corporation | Leuprolide acetate and acetylcholinesterase inhibitors or NMDA receptor antagonists for the treatment of alzheimer's disease |
| WO2008055945A1 (en) | 2006-11-09 | 2008-05-15 | Probiodrug Ag | 3-hydr0xy-1,5-dihydr0-pyrr0l-2-one derivatives as inhibitors of glutaminyl cyclase for the treatment of ulcer, cancer and other diseases |
| ATE554085T1 (de) | 2006-11-30 | 2012-05-15 | Probiodrug Ag | Neue inhibitoren von glutaminylcyclase |
| EP2117540A1 (en) | 2007-03-01 | 2009-11-18 | Probiodrug AG | New use of glutaminyl cyclase inhibitors |
| JP5667440B2 (ja) | 2007-04-18 | 2015-02-12 | プロビオドルグ エージー | グルタミニルシクラーゼ阻害剤としてのチオ尿素誘導体 |
| CN103058957A (zh) | 2007-06-29 | 2013-04-24 | 埃莫里大学 | 用于神经保护的nmda受体拮抗剂 |
| SG178953A1 (en) | 2009-09-11 | 2012-04-27 | Probiodrug Ag | Heterocylcic derivatives as inhibitors of glutaminyl cyclase |
| US9181233B2 (en) | 2010-03-03 | 2015-11-10 | Probiodrug Ag | Inhibitors of glutaminyl cyclase |
| AU2011226074B2 (en) | 2010-03-10 | 2015-01-22 | Vivoryon Therapeutics N.V. | Heterocyclic inhibitors of glutaminyl cyclase (QC, EC 2.3.2.5) |
| US8541596B2 (en) | 2010-04-21 | 2013-09-24 | Probiodrug Ag | Inhibitors |
| BR112013014484A2 (pt) * | 2010-12-13 | 2016-07-19 | Viamet Pharmaceuticals Inc | compostos inibidores de metaloenzimas |
| ES2570167T3 (es) | 2011-03-16 | 2016-05-17 | Probiodrug Ag | Derivados de benzimidazol como inhibidores de glutaminil ciclasa |
| DE102015011861B4 (de) | 2015-09-10 | 2018-03-01 | Rudolf Schindler | Neue cyclische Carboxamide als NMDA NR2B Rezeptor Inhibitoren |
| ES2812698T3 (es) | 2017-09-29 | 2021-03-18 | Probiodrug Ag | Inhibidores de glutaminil ciclasa |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ221729A (en) * | 1986-09-15 | 1989-07-27 | Janssen Pharmaceutica Nv | Imidazolyl methyl-substituted benzimidazole derivatives and pharmaceutical compositions |
| GB8827822D0 (en) * | 1988-11-29 | 1988-12-29 | Janssen Pharmaceutica Nv | (1h-azol-1-ylmethyl)substituted quinoline derivatives |
| DK715888D0 (da) * | 1988-12-22 | 1988-12-22 | Ferrosan As | Quinoxalinforbindelser, deres fremstilling og anvendelse |
| DE4217952A1 (de) * | 1992-05-30 | 1993-12-02 | Basf Ag | Chinoxalin-2,3(1H,4H)-dione |
| AU672617B2 (en) * | 1992-06-22 | 1996-10-10 | Regents Of The University Of California, The | Glycine receptor antagonists and the use thereof |
-
1994
- 1994-09-13 GB GB9418443A patent/GB9418443D0/en active Pending
-
1995
- 1995-09-01 MX MX9701894A patent/MX9701894A/es not_active IP Right Cessation
- 1995-09-01 ES ES95931989T patent/ES2158126T3/es not_active Expired - Lifetime
- 1995-09-01 US US08/793,896 patent/US5783572A/en not_active Expired - Fee Related
- 1995-09-01 PT PT95931989T patent/PT781279E/pt unknown
- 1995-09-01 JP JP8509872A patent/JP2898097B2/ja not_active Expired - Fee Related
- 1995-09-01 DK DK95931989T patent/DK0781279T3/da active
- 1995-09-01 CA CA002199845A patent/CA2199845C/en not_active Expired - Fee Related
- 1995-09-01 AT AT95931989T patent/ATE202099T1/de not_active IP Right Cessation
- 1995-09-01 DE DE69521323T patent/DE69521323T2/de not_active Expired - Fee Related
- 1995-09-01 WO PCT/EP1995/003483 patent/WO1996008485A1/en active IP Right Grant
- 1995-09-01 EP EP95931989A patent/EP0781279B1/en not_active Expired - Lifetime
-
1997
- 1997-03-12 FI FI971026A patent/FI113471B/sv active
-
2001
- 2001-07-24 GR GR20010401119T patent/GR3036270T3/el not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| GR3036270T3 (en) | 2001-10-31 |
| EP0781279B1 (en) | 2001-06-13 |
| DE69521323D1 (de) | 2001-07-19 |
| GB9418443D0 (en) | 1994-11-02 |
| MX9701894A (es) | 1997-06-28 |
| ES2158126T3 (es) | 2001-09-01 |
| FI971026A0 (sv) | 1997-03-12 |
| DE69521323T2 (de) | 2001-09-20 |
| US5783572A (en) | 1998-07-21 |
| WO1996008485A1 (en) | 1996-03-21 |
| JPH09511523A (ja) | 1997-11-18 |
| CA2199845A1 (en) | 1996-03-21 |
| ATE202099T1 (de) | 2001-06-15 |
| EP0781279A1 (en) | 1997-07-02 |
| CA2199845C (en) | 2000-08-01 |
| JP2898097B2 (ja) | 1999-05-31 |
| DK0781279T3 (da) | 2001-09-03 |
| PT781279E (pt) | 2001-09-28 |
| FI971026A (sv) | 1997-03-12 |
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