MX2012004289A - Derivados de azina condensada para el tratamiento de enfermedades relacionadas con el receptor de acetilcolina. - Google Patents
Derivados de azina condensada para el tratamiento de enfermedades relacionadas con el receptor de acetilcolina.Info
- Publication number
- MX2012004289A MX2012004289A MX2012004289A MX2012004289A MX2012004289A MX 2012004289 A MX2012004289 A MX 2012004289A MX 2012004289 A MX2012004289 A MX 2012004289A MX 2012004289 A MX2012004289 A MX 2012004289A MX 2012004289 A MX2012004289 A MX 2012004289A
- Authority
- MX
- Mexico
- Prior art keywords
- methyl
- esi
- alkyl
- mmol
- optionally substituted
- Prior art date
Links
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract description 22
- 201000010099 disease Diseases 0.000 title description 7
- 108010009685 Cholinergic Receptors Proteins 0.000 title description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 title description 2
- 102000034337 acetylcholine receptors Human genes 0.000 title 1
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 55
- 239000012453 solvate Substances 0.000 claims abstract description 20
- 150000003839 salts Chemical class 0.000 claims abstract description 17
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 7
- 208000024827 Alzheimer disease Diseases 0.000 claims abstract description 6
- 201000000980 schizophrenia Diseases 0.000 claims abstract description 6
- 238000002560 therapeutic procedure Methods 0.000 claims abstract description 5
- 230000002265 prevention Effects 0.000 claims abstract description 4
- -1 chloro, fluoro, methyl Chemical group 0.000 claims description 93
- 125000000217 alkyl group Chemical group 0.000 claims description 49
- FTTATHOUSOIFOQ-UHFFFAOYSA-N 1,2,3,4,6,7,8,8a-octahydropyrrolo[1,2-a]pyrazine Chemical group C1NCCN2CCCC21 FTTATHOUSOIFOQ-UHFFFAOYSA-N 0.000 claims description 45
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 41
- 229910052736 halogen Inorganic materials 0.000 claims description 40
- 150000002367 halogens Chemical class 0.000 claims description 37
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 27
- 229910052760 oxygen Inorganic materials 0.000 claims description 22
- 229910052717 sulfur Inorganic materials 0.000 claims description 21
- 229910052739 hydrogen Inorganic materials 0.000 claims description 18
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 17
- 125000003545 alkoxy group Chemical group 0.000 claims description 17
- 125000004076 pyridyl group Chemical group 0.000 claims description 17
- 125000001424 substituent group Chemical group 0.000 claims description 17
- 125000002541 furyl group Chemical group 0.000 claims description 16
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 16
- 125000000335 thiazolyl group Chemical group 0.000 claims description 16
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 15
- 229910052757 nitrogen Inorganic materials 0.000 claims description 15
- 125000004122 cyclic group Chemical group 0.000 claims description 13
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 13
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 10
- 125000005842 heteroatom Chemical group 0.000 claims description 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 9
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 8
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 8
- 229920006395 saturated elastomer Polymers 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 7
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 6
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 6
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 5
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 5
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 4
- 125000006526 (C1-C2) alkyl group Chemical group 0.000 claims description 2
- YCIPQJTZJGUXND-UHFFFAOYSA-N Aglaia odorata Alkaloid Natural products C1=CC(OC)=CC=C1C1(C(C=2C(=O)N3CCCC3=NC=22)C=3C=CC=CC=3)C2(O)C2=C(OC)C=C(OC)C=C2O1 YCIPQJTZJGUXND-UHFFFAOYSA-N 0.000 claims description 2
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 125000000732 arylene group Chemical group 0.000 claims description 2
- 125000005549 heteroarylene group Chemical group 0.000 claims description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims description 2
- VTGOHKSTWXHQJK-UHFFFAOYSA-N pyrimidin-2-ol Chemical compound OC1=NC=CC=N1 VTGOHKSTWXHQJK-UHFFFAOYSA-N 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims 3
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 1
- 108050006807 Nicotinic acetylcholine receptors Proteins 0.000 abstract description 14
- 102000019315 Nicotinic acetylcholine receptors Human genes 0.000 abstract description 13
- 230000001404 mediated effect Effects 0.000 abstract description 4
- 239000000543 intermediate Substances 0.000 description 404
- 238000004949 mass spectrometry Methods 0.000 description 236
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 135
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 111
- 239000000243 solution Substances 0.000 description 61
- QMNUDYFKZYBWQX-UHFFFAOYSA-N 1H-quinazolin-4-one Chemical compound C1=CC=C2C(=O)N=CNC2=C1 QMNUDYFKZYBWQX-UHFFFAOYSA-N 0.000 description 60
- 238000000034 method Methods 0.000 description 52
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 41
- 238000006243 chemical reaction Methods 0.000 description 38
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 36
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 32
- 238000012799 strong cation exchange Methods 0.000 description 31
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 30
- 239000000203 mixture Substances 0.000 description 29
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 28
- 239000011541 reaction mixture Substances 0.000 description 28
- 150000001875 compounds Chemical class 0.000 description 24
- 150000003254 radicals Chemical class 0.000 description 23
- 230000002829 reductive effect Effects 0.000 description 22
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 20
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 18
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 18
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 18
- 239000000377 silicon dioxide Substances 0.000 description 17
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 15
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 15
- 208000035475 disorder Diseases 0.000 description 14
- 235000019439 ethyl acetate Nutrition 0.000 description 14
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- 239000002253 acid Substances 0.000 description 12
- 239000002904 solvent Substances 0.000 description 12
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 11
- 239000013058 crude material Substances 0.000 description 11
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 9
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 8
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
- 238000002953 preparative HPLC Methods 0.000 description 8
- 239000000725 suspension Substances 0.000 description 8
- 125000004429 atom Chemical group 0.000 description 7
- 238000010992 reflux Methods 0.000 description 7
- CYPYTURSJDMMMP-WVCUSYJESA-N (1e,4e)-1,5-diphenylpenta-1,4-dien-3-one;palladium Chemical compound [Pd].[Pd].C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1 CYPYTURSJDMMMP-WVCUSYJESA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 125000001072 heteroaryl group Chemical group 0.000 description 6
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000012267 brine Substances 0.000 description 5
- 239000003153 chemical reaction reagent Substances 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 239000012044 organic layer Substances 0.000 description 5
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- DLFVBJFMPXGRIB-UHFFFAOYSA-N thioacetamide Natural products CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 5
- XJKNACDCUAFDHD-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonane Chemical compound C1CC2CCN1CCN2 XJKNACDCUAFDHD-UHFFFAOYSA-N 0.000 description 4
- GGNZFQSLGOOMBV-UHFFFAOYSA-N 2-(3-chlorophenyl)-6-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-3-methylquinazolin-4-one Chemical compound N=1C2=CC=C(N3C4CCN(CC4)CC3)C=C2C(=O)N(C)C=1C1=CC=CC(Cl)=C1 GGNZFQSLGOOMBV-UHFFFAOYSA-N 0.000 description 4
- SRDHLFLAXAMBNM-UHFFFAOYSA-N 5-fluoro-2-nitro-n-[2-oxo-2-(propan-2-ylamino)ethyl]benzamide Chemical compound CC(C)NC(=O)CNC(=O)C1=CC(F)=CC=C1[N+]([O-])=O SRDHLFLAXAMBNM-UHFFFAOYSA-N 0.000 description 4
- USKFVSLMDSVSJR-QWRGUYRKSA-N 6-[(1s,4s)-5-methyl-2,5-diazabicyclo[2.2.1]heptan-2-yl]-1h-quinazolin-4-one Chemical compound N1=CNC(=O)C2=CC(N3C[C@]4(N(C[C@]3([H])C4)C)[H])=CC=C21 USKFVSLMDSVSJR-QWRGUYRKSA-N 0.000 description 4
- 102000009660 Cholinergic Receptors Human genes 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 4
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 4
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- PBCJIPOGFJYBJE-UHFFFAOYSA-N acetonitrile;hydrate Chemical compound O.CC#N PBCJIPOGFJYBJE-UHFFFAOYSA-N 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 238000003556 assay Methods 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 238000004128 high performance liquid chromatography Methods 0.000 description 4
- 239000005457 ice water Substances 0.000 description 4
- 229910000027 potassium carbonate Inorganic materials 0.000 description 4
- 229940002612 prodrug Drugs 0.000 description 4
- 239000000651 prodrug Substances 0.000 description 4
- 102000005962 receptors Human genes 0.000 description 4
- 108020003175 receptors Proteins 0.000 description 4
- 230000001225 therapeutic effect Effects 0.000 description 4
- 125000001544 thienyl group Chemical group 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- LKOQKRDNICCKCZ-UHFFFAOYSA-N 2-amino-5-hydroxy-n-methylbenzamide Chemical compound CNC(=O)C1=CC(O)=CC=C1N LKOQKRDNICCKCZ-UHFFFAOYSA-N 0.000 description 3
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 3
- HQMSFKCYMRDNAE-UHFFFAOYSA-N 5-bromo-n,2-dimethylbenzamide Chemical compound CNC(=O)C1=CC(Br)=CC=C1C HQMSFKCYMRDNAE-UHFFFAOYSA-N 0.000 description 3
- XLFJZKCYKPSSNZ-UHFFFAOYSA-N 5-fluoro-n-methyl-2-nitrobenzamide Chemical compound CNC(=O)C1=CC(F)=CC=C1[N+]([O-])=O XLFJZKCYKPSSNZ-UHFFFAOYSA-N 0.000 description 3
- SODIKESQEPOMDQ-UHFFFAOYSA-N 5-fluoro-n-methyl-2-nitrobenzenesulfonamide Chemical compound CNS(=O)(=O)C1=CC(F)=CC=C1[N+]([O-])=O SODIKESQEPOMDQ-UHFFFAOYSA-N 0.000 description 3
- MCSVSXROESVYLR-UHFFFAOYSA-N 6-bromo-3-methylquinazolin-4-one Chemical compound C1=C(Br)C=C2C(=O)N(C)C=NC2=C1 MCSVSXROESVYLR-UHFFFAOYSA-N 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- OIPILFWXSMYKGL-UHFFFAOYSA-N acetylcholine Chemical compound CC(=O)OCC[N+](C)(C)C OIPILFWXSMYKGL-UHFFFAOYSA-N 0.000 description 3
- 229960004373 acetylcholine Drugs 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 238000004587 chromatography analysis Methods 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000012458 free base Substances 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 3
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 3
- 125000002883 imidazolyl group Chemical group 0.000 description 3
- 238000011068 loading method Methods 0.000 description 3
- 150000002894 organic compounds Chemical class 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 239000012521 purified sample Substances 0.000 description 3
- 125000000168 pyrrolyl group Chemical group 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000012312 sodium hydride Substances 0.000 description 3
- 229910000104 sodium hydride Inorganic materials 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 3
- 238000000825 ultraviolet detection Methods 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- WXODYSRBIUZTDU-UHFFFAOYSA-N 2-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-n-methyl-5-nitropyridine-4-carboxamide Chemical compound C1=C([N+]([O-])=O)C(C(=O)NC)=CC(N2C3CCN(CC3)CC2)=N1 WXODYSRBIUZTDU-UHFFFAOYSA-N 0.000 description 2
- RQHGIBAPHTXODB-UHFFFAOYSA-N 2-[[2-amino-5-(1,4-diazabicyclo[3.2.2]nonan-4-yl)benzoyl]amino]acetic acid Chemical compound C1=C(C(=O)NCC(O)=O)C(N)=CC=C1N1C(CC2)CCN2CC1 RQHGIBAPHTXODB-UHFFFAOYSA-N 0.000 description 2
- YIKBSICAFIIUER-UHFFFAOYSA-N 2-chloro-5-nitropyridine-4-carboxylic acid Chemical compound OC(=O)C1=CC(Cl)=NC=C1[N+]([O-])=O YIKBSICAFIIUER-UHFFFAOYSA-N 0.000 description 2
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 description 2
- SRWILAKSARHZPR-UHFFFAOYSA-N 3-chlorobenzaldehyde Chemical compound ClC1=CC=CC(C=O)=C1 SRWILAKSARHZPR-UHFFFAOYSA-N 0.000 description 2
- YLTRKOOKMIYJDB-UHFFFAOYSA-N 4-fluoro-n-methyl-2-nitrobenzamide Chemical compound CNC(=O)C1=CC=C(F)C=C1[N+]([O-])=O YLTRKOOKMIYJDB-UHFFFAOYSA-N 0.000 description 2
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 2
- RXIVJJGLXXOPFC-UHFFFAOYSA-N 5-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-n-methyl-2-nitrobenzenesulfonamide Chemical compound C1=C([N+]([O-])=O)C(S(=O)(=O)NC)=CC(N2C3CCN(CC3)CC2)=C1 RXIVJJGLXXOPFC-UHFFFAOYSA-N 0.000 description 2
- DHNJQRSDZABGBP-UHFFFAOYSA-N 5-fluoro-2-nitrobenzoyl chloride Chemical compound [O-][N+](=O)C1=CC=C(F)C=C1C(Cl)=O DHNJQRSDZABGBP-UHFFFAOYSA-N 0.000 description 2
- KXGWQWMQOSZLQY-UHFFFAOYSA-N 7-bromo-3-(3-chlorophenyl)-2-methylisoquinolin-1-one Chemical compound C=1C2=CC=C(Br)C=C2C(=O)N(C)C=1C1=CC=CC(Cl)=C1 KXGWQWMQOSZLQY-UHFFFAOYSA-N 0.000 description 2
- 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 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 208000019901 Anxiety disease Diseases 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- 101000755620 Homo sapiens Protein RIC-3 Proteins 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 2
- 102000004310 Ion Channels Human genes 0.000 description 2
- 108090000862 Ion Channels Proteins 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- 102000014415 Muscarinic acetylcholine receptor Human genes 0.000 description 2
- 108050003473 Muscarinic acetylcholine receptor Proteins 0.000 description 2
- 208000018737 Parkinson disease Diseases 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 208000028017 Psychotic disease Diseases 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 208000000323 Tourette Syndrome Diseases 0.000 description 2
- 208000016620 Tourette disease Diseases 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000000304 alkynyl group Chemical group 0.000 description 2
- 230000036506 anxiety Effects 0.000 description 2
- 239000012131 assay buffer Substances 0.000 description 2
- HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 230000006949 cholinergic function Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 125000004850 cyclobutylmethyl group Chemical group C1(CCC1)C* 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 239000001963 growth medium Substances 0.000 description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 208000026278 immune system disease Diseases 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 2
- VDBNYAPERZTOOF-UHFFFAOYSA-N isoquinolin-1(2H)-one Chemical compound C1=CC=C2C(=O)NC=CC2=C1 VDBNYAPERZTOOF-UHFFFAOYSA-N 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- LWAWSBYAHXHWDN-UHFFFAOYSA-N methyl 2-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-5-nitropyridine-4-carboxylate Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC)=CC(N2C3CCN(CC3)CC2)=N1 LWAWSBYAHXHWDN-UHFFFAOYSA-N 0.000 description 2
- SBGNWCJYDUUYTN-UHFFFAOYSA-N methyl 2-chloro-5-nitropyridine-4-carboxylate Chemical compound COC(=O)C1=CC(Cl)=NC=C1[N+]([O-])=O SBGNWCJYDUUYTN-UHFFFAOYSA-N 0.000 description 2
- RMNJNEUWTBBZPT-UHFFFAOYSA-N methyl 4-nitrobenzenesulfonate Chemical compound COS(=O)(=O)C1=CC=C([N+]([O-])=O)C=C1 RMNJNEUWTBBZPT-UHFFFAOYSA-N 0.000 description 2
- OJXLRKMXTURZJR-UHFFFAOYSA-N n-methyl-5-(2-methyl-1,3,3a,4,6,6a-hexahydropyrrolo[3,4-c]pyrrol-5-yl)-2-nitrobenzamide Chemical compound C1=C([N+]([O-])=O)C(C(=O)NC)=CC(N2CC3CN(C)CC3C2)=C1 OJXLRKMXTURZJR-UHFFFAOYSA-N 0.000 description 2
- 230000004112 neuroprotection Effects 0.000 description 2
- 239000005022 packaging material Substances 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 125000006239 protecting group Chemical group 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 125000000714 pyrimidinyl group Chemical group 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000003826 tablet Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- PYOKUURKVVELLB-UHFFFAOYSA-N trimethyl orthoformate Chemical compound COC(OC)OC PYOKUURKVVELLB-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
- 239000003643 water by type Substances 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 1
- FGWYWKIOMUZSQF-UHFFFAOYSA-N 1,1,1-triethoxypropane Chemical compound CCOC(CC)(OCC)OCC FGWYWKIOMUZSQF-UHFFFAOYSA-N 0.000 description 1
- RPEUKYFRIGEOOE-UHFFFAOYSA-N 1,3-dimethyl-1,3,2-diazaphosphinane Chemical compound CN1CCCN(C)P1 RPEUKYFRIGEOOE-UHFFFAOYSA-N 0.000 description 1
- LNNZWCVUOITPSS-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonane;2,2,2-trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.C1CC2CCN1CCN2 LNNZWCVUOITPSS-UHFFFAOYSA-N 0.000 description 1
- QNJSIGUFGXHSMG-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonane;dihydrochloride Chemical compound Cl.Cl.C1CC2CCN1CCN2 QNJSIGUFGXHSMG-UHFFFAOYSA-N 0.000 description 1
- ZWBMOMDXOYIGQW-UHFFFAOYSA-N 1,4-diazabicyclo[3.2.2]nonane;hydrochloride Chemical compound Cl.C1CC2CCN1CCN2 ZWBMOMDXOYIGQW-UHFFFAOYSA-N 0.000 description 1
- CEIIEALEIHQDBX-UHFFFAOYSA-N 1-(5-chloro-2,4-dimethoxyphenyl)-3-(5-methyl-3-isoxazolyl)urea Chemical compound C1=C(Cl)C(OC)=CC(OC)=C1NC(=O)NC1=NOC(C)=C1 CEIIEALEIHQDBX-UHFFFAOYSA-N 0.000 description 1
- FSKYZRCACCHDGR-UHFFFAOYSA-N 1h-pyrido[3,2-d]pyrimidin-4-one Chemical class C1=CN=C2C(=O)N=CNC2=C1 FSKYZRCACCHDGR-UHFFFAOYSA-N 0.000 description 1
- AVRPFRMDMNDIDH-UHFFFAOYSA-N 1h-quinazolin-2-one Chemical compound C1=CC=CC2=NC(O)=NC=C21 AVRPFRMDMNDIDH-UHFFFAOYSA-N 0.000 description 1
- KVTRUBZAMRIDHX-UHFFFAOYSA-N 2,5-diazabicyclo[2.2.1]heptane-2-carboxylic acid Chemical compound C1C2N(C(=O)O)CC1NC2 KVTRUBZAMRIDHX-UHFFFAOYSA-N 0.000 description 1
- OPFWKTOZVCAOFI-UHFFFAOYSA-N 2-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-5-nitropyridine-4-carboxylic acid Chemical compound C1=C([N+]([O-])=O)C(C(=O)O)=CC(N2C3CCN(CC3)CC2)=N1 OPFWKTOZVCAOFI-UHFFFAOYSA-N 0.000 description 1
- QWAXAIFIDRZQNB-UHFFFAOYSA-N 2-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-n-(3-hydroxy-2,2-dimethylpropyl)-5-nitropyridine-4-carboxamide Chemical compound C1=C([N+]([O-])=O)C(C(=O)NCC(C)(CO)C)=CC(N2C3CCN(CC3)CC2)=N1 QWAXAIFIDRZQNB-UHFFFAOYSA-N 0.000 description 1
- KGYMOXVODQDCNC-UHFFFAOYSA-N 2-(2-fluorophenyl)-1h-quinazolin-4-one Chemical compound FC1=CC=CC=C1C1=NC(=O)C2=CC=CC=C2N1 KGYMOXVODQDCNC-UHFFFAOYSA-N 0.000 description 1
- QVFOCIFHEXXYQQ-UHFFFAOYSA-N 2-(3-chlorophenyl)-3-methyl-6-(1-oxido-4-aza-1-azoniabicyclo[3.2.2]nonan-4-yl)quinazolin-4-one Chemical compound N=1C2=CC=C(N3C4CC[N+](CC4)([O-])CC3)C=C2C(=O)N(C)C=1C1=CC=CC(Cl)=C1 QVFOCIFHEXXYQQ-UHFFFAOYSA-N 0.000 description 1
- OLYJZMMCWGKVKS-UHFFFAOYSA-N 2-(3-chlorophenyl)-6-hydroxy-3-methylquinazolin-4-one Chemical compound N=1C2=CC=C(O)C=C2C(=O)N(C)C=1C1=CC=CC(Cl)=C1 OLYJZMMCWGKVKS-UHFFFAOYSA-N 0.000 description 1
- PJXZYLATNPZZCO-UHFFFAOYSA-N 2-(cyclopropylmethyl)-3H-quinazolin-4-one Chemical compound N=1C2=CC=CC=C2C(=O)NC=1CC1CC1 PJXZYLATNPZZCO-UHFFFAOYSA-N 0.000 description 1
- GLQWDUDHSNYAGG-UHFFFAOYSA-N 2-[2-(3-chlorophenyl)-6-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-4-oxoquinazolin-3-yl]-n,n-dimethylacetamide Chemical compound N=1C2=CC=C(N3C4CCN(CC4)CC3)C=C2C(=O)N(CC(=O)N(C)C)C=1C1=CC=CC(Cl)=C1 GLQWDUDHSNYAGG-UHFFFAOYSA-N 0.000 description 1
- AKOOWGZCKZVOQR-UHFFFAOYSA-N 2-[2-(3-chlorophenyl)-6-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-4-oxoquinazolin-3-yl]acetic acid Chemical compound N=1C2=CC=C(N3C4CCN(CC4)CC3)C=C2C(=O)N(CC(=O)O)C=1C1=CC=CC(Cl)=C1 AKOOWGZCKZVOQR-UHFFFAOYSA-N 0.000 description 1
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 1
- CIUSAKIVYAVQKY-UHFFFAOYSA-N 2-[6-(2,3,3a,4,6,6a-hexahydro-1h-pyrrolo[3,4-c]pyrrol-5-yl)-4-oxo-2-phenylquinazolin-3-yl]-n-propan-2-ylacetamide Chemical compound N=1C2=CC=C(N3CC4CNCC4C3)C=C2C(=O)N(CC(=O)NC(C)C)C=1C1=CC=CC=C1 CIUSAKIVYAVQKY-UHFFFAOYSA-N 0.000 description 1
- IZJWXSVSDZONEA-UHFFFAOYSA-N 2-amino-5-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-n-[2-oxo-2-(propan-2-ylamino)ethyl]benzamide Chemical compound C1=C(N)C(C(=O)NCC(=O)NC(C)C)=CC(N2C3CCN(CC3)CC2)=C1 IZJWXSVSDZONEA-UHFFFAOYSA-N 0.000 description 1
- DMDBGGXHHAAJRW-UHFFFAOYSA-N 2-amino-5-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-n-methylbenzenesulfonamide Chemical compound C1=C(N)C(S(=O)(=O)NC)=CC(N2C3CCN(CC3)CC2)=C1 DMDBGGXHHAAJRW-UHFFFAOYSA-N 0.000 description 1
- UMVPHALOKJMKDQ-UWVGGRQHSA-N 2-amino-5-[(1s,4s)-5-methyl-2,5-diazabicyclo[2.2.1]heptan-2-yl]benzamide Chemical compound C([C@]1(N(C[C@]2([H])C1)C)[H])N2C1=CC=C(N)C(C(N)=O)=C1 UMVPHALOKJMKDQ-UWVGGRQHSA-N 0.000 description 1
- MFNCPHVGSPOTKT-UHFFFAOYSA-N 2-amino-n-ethyl-5-hydroxybenzamide Chemical compound CCNC(=O)C1=CC(O)=CC=C1N MFNCPHVGSPOTKT-UHFFFAOYSA-N 0.000 description 1
- LKCKUYRPMPUHTD-UHFFFAOYSA-N 2-amino-n-propan-2-ylacetamide Chemical compound CC(C)NC(=O)CN LKCKUYRPMPUHTD-UHFFFAOYSA-N 0.000 description 1
- YJRMHIKEMDTYDR-UHFFFAOYSA-N 2-methylisoquinolin-1-one Chemical compound C1=CC=C2C(=O)N(C)C=CC2=C1 YJRMHIKEMDTYDR-UHFFFAOYSA-N 0.000 description 1
- ASGJFGPILHALRC-UHFFFAOYSA-N 3-(bromomethyl)-5-methyl-1,2-oxazole Chemical compound CC1=CC(CBr)=NO1 ASGJFGPILHALRC-UHFFFAOYSA-N 0.000 description 1
- FNVOFDGAASRDQY-UHFFFAOYSA-N 3-amino-2,2-dimethylpropan-1-ol Chemical compound NCC(C)(C)CO FNVOFDGAASRDQY-UHFFFAOYSA-N 0.000 description 1
- QWBYWPJNPKGEBO-UHFFFAOYSA-N 3-chloro-5-fluorobenzaldehyde Chemical compound FC1=CC(Cl)=CC(C=O)=C1 QWBYWPJNPKGEBO-UHFFFAOYSA-N 0.000 description 1
- WBUOVKBZJOIOAE-UHFFFAOYSA-N 3-chlorobenzonitrile Chemical compound ClC1=CC=CC(C#N)=C1 WBUOVKBZJOIOAE-UHFFFAOYSA-N 0.000 description 1
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 1
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 description 1
- IVLICPVPXWEGCA-UHFFFAOYSA-N 3-quinuclidinol Chemical compound C1C[C@@H]2C(O)C[N@]1CC2 IVLICPVPXWEGCA-UHFFFAOYSA-N 0.000 description 1
- KHJGZFUJLFVDKM-UHFFFAOYSA-N 4-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-n-methyl-2-nitrobenzamide Chemical compound C1=C([N+]([O-])=O)C(C(=O)NC)=CC=C1N1C(CC2)CCN2CC1 KHJGZFUJLFVDKM-UHFFFAOYSA-N 0.000 description 1
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 1
- OXNDMRBMCYCDGN-UHFFFAOYSA-N 5-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-2-nitro-n-[2-oxo-2-(propan-2-ylamino)ethyl]benzamide Chemical compound C1=C([N+]([O-])=O)C(C(=O)NCC(=O)NC(C)C)=CC(N2C3CCN(CC3)CC2)=C1 OXNDMRBMCYCDGN-UHFFFAOYSA-N 0.000 description 1
- WFIKWZLBRWQFFN-UHFFFAOYSA-N 5-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-n-(2-methylpropyl)-2-nitrobenzamide Chemical compound C1=C([N+]([O-])=O)C(C(=O)NCC(C)C)=CC(N2C3CCN(CC3)CC2)=C1 WFIKWZLBRWQFFN-UHFFFAOYSA-N 0.000 description 1
- GJWJBEHFFCCTOT-UHFFFAOYSA-N 5-(1-azabicyclo[2.2.2]octan-3-ylamino)-n-methyl-2-nitrobenzamide Chemical compound C1=C([N+]([O-])=O)C(C(=O)NC)=CC(NC2C3CCN(CC3)C2)=C1 GJWJBEHFFCCTOT-UHFFFAOYSA-N 0.000 description 1
- SDYSYAOAMGRABT-UHFFFAOYSA-N 5-(2,3,3a,4,6,6a-hexahydro-1h-pyrrolo[3,4-c]pyrrol-5-yl)-n-methyl-2-nitrobenzamide Chemical compound C1=C([N+]([O-])=O)C(C(=O)NC)=CC(N2CC3CNCC3C2)=C1 SDYSYAOAMGRABT-UHFFFAOYSA-N 0.000 description 1
- ZEYQWJUCBCBJGJ-AAEUAGOBSA-N 5-[(1s,4s)-2,5-diazabicyclo[2.2.1]heptan-2-yl]-2-nitro-n-[2-oxo-2-(propan-2-ylamino)ethyl]benzamide Chemical compound C([C@]1(NC[C@]2([H])C1)[H])N2C1=CC=C([N+]([O-])=O)C(C(=O)NCC(=O)NC(C)C)=C1 ZEYQWJUCBCBJGJ-AAEUAGOBSA-N 0.000 description 1
- GMEQDJAUICMKDA-UHFFFAOYSA-N 5-amino-2-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-n-methylpyridine-4-carboxamide Chemical compound C1=C(N)C(C(=O)NC)=CC(N2C3CCN(CC3)CC2)=N1 GMEQDJAUICMKDA-UHFFFAOYSA-N 0.000 description 1
- SEENCYZQHCUTSB-UHFFFAOYSA-N 5-bromo-2-methylbenzoic acid Chemical compound CC1=CC=C(Br)C=C1C(O)=O SEENCYZQHCUTSB-UHFFFAOYSA-N 0.000 description 1
- PTSAXAZDPIJLSG-UHFFFAOYSA-N 5-fluoro-2-nitro-n-propan-2-ylbenzamide Chemical compound CC(C)NC(=O)C1=CC(F)=CC=C1[N+]([O-])=O PTSAXAZDPIJLSG-UHFFFAOYSA-N 0.000 description 1
- GIWMPSXRNSNUIE-UHFFFAOYSA-N 5-fluoro-2-nitro-n-propylbenzamide Chemical compound CCCNC(=O)C1=CC(F)=CC=C1[N+]([O-])=O GIWMPSXRNSNUIE-UHFFFAOYSA-N 0.000 description 1
- FIAHHCYZKNNOQH-UHFFFAOYSA-N 5-fluoro-2-nitrobenzamide Chemical compound NC(=O)C1=CC(F)=CC=C1[N+]([O-])=O FIAHHCYZKNNOQH-UHFFFAOYSA-N 0.000 description 1
- KPWHHDVNRKIFRI-UHFFFAOYSA-N 5-fluoro-2-nitrobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC(F)=CC=C1[N+]([O-])=O KPWHHDVNRKIFRI-UHFFFAOYSA-N 0.000 description 1
- ALKFOTRKZGCLFU-UHFFFAOYSA-N 5-fluoro-2-nitrobenzenesulfonyl chloride Chemical compound [O-][N+](=O)C1=CC=C(F)C=C1S(Cl)(=O)=O ALKFOTRKZGCLFU-UHFFFAOYSA-N 0.000 description 1
- GHYZIXDKAPMFCS-UHFFFAOYSA-N 5-fluoro-2-nitrobenzoic acid Chemical compound OC(=O)C1=CC(F)=CC=C1[N+]([O-])=O GHYZIXDKAPMFCS-UHFFFAOYSA-N 0.000 description 1
- MPMIQYFCHBLYRH-UHFFFAOYSA-N 5-fluoro-n-(2-methylpropyl)-2-nitrobenzamide Chemical compound CC(C)CNC(=O)C1=CC(F)=CC=C1[N+]([O-])=O MPMIQYFCHBLYRH-UHFFFAOYSA-N 0.000 description 1
- MTEZWNKWMRQSHO-UHFFFAOYSA-N 5-fluoro-n-[[1-(hydroxymethyl)cyclobutyl]methyl]-2-nitrobenzamide Chemical compound C=1C(F)=CC=C([N+]([O-])=O)C=1C(=O)NCC1(CO)CCC1 MTEZWNKWMRQSHO-UHFFFAOYSA-N 0.000 description 1
- ZSSNZFQUIHKYGJ-UHFFFAOYSA-N 6-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-3-methylthieno[2,3-d]pyrimidin-4-one Chemical compound C=1C=2C(=O)N(C)C=NC=2SC=1N1CCN2CCC1CC2 ZSSNZFQUIHKYGJ-UHFFFAOYSA-N 0.000 description 1
- BHXKPERUDPFBCV-UHFFFAOYSA-N 6-(1-azabicyclo[2.2.2]octan-3-yloxy)-2-(3-chlorophenyl)-3-methylquinazolin-4-one Chemical compound N=1C2=CC=C(OC3C4CCN(CC4)C3)C=C2C(=O)N(C)C=1C1=CC=CC(Cl)=C1 BHXKPERUDPFBCV-UHFFFAOYSA-N 0.000 description 1
- FDEGQLVPLYMGDB-HOTGVXAUSA-N 6-[(1s,4s)-5-methyl-2,5-diazabicyclo[2.2.1]heptan-2-yl]-3-[(5-methyl-1,2-oxazol-3-yl)methyl]quinazolin-4-one Chemical compound C([C@]1(N(C[C@]2([H])C1)C)[H])N2C(C=C1C2=O)=CC=C1N=CN2CC=1C=C(C)ON=1 FDEGQLVPLYMGDB-HOTGVXAUSA-N 0.000 description 1
- BHXKPERUDPFBCV-FQEVSTJZSA-N 6-[[(3r)-1-azabicyclo[2.2.2]octan-3-yl]oxy]-2-(3-chlorophenyl)-3-methylquinazolin-4-one Chemical compound N=1C2=CC=C(O[C@@H]3C4CCN(CC4)C3)C=C2C(=O)N(C)C=1C1=CC=CC(Cl)=C1 BHXKPERUDPFBCV-FQEVSTJZSA-N 0.000 description 1
- NSLQTXVXWPLWBL-NRFANRHFSA-N 6-[[(3r)-1-azabicyclo[2.2.2]octan-3-yl]oxy]-3-ethyl-2-phenylquinazolin-4-one Chemical compound N=1C2=CC=C(O[C@@H]3C4CCN(CC4)C3)C=C2C(=O)N(CC)C=1C1=CC=CC=C1 NSLQTXVXWPLWBL-NRFANRHFSA-N 0.000 description 1
- NSLQTXVXWPLWBL-OAQYLSRUSA-N 6-[[(3s)-1-azabicyclo[2.2.2]octan-3-yl]oxy]-3-ethyl-2-phenylquinazolin-4-one Chemical compound N=1C2=CC=C(O[C@H]3C4CCN(CC4)C3)C=C2C(=O)N(CC)C=1C1=CC=CC=C1 NSLQTXVXWPLWBL-OAQYLSRUSA-N 0.000 description 1
- XZJMEPGBWRNNND-UHFFFAOYSA-N 6-bromo-3-methylthieno[2,3-d]pyrimidin-4-one Chemical compound O=C1N(C)C=NC2=C1C=C(Br)S2 XZJMEPGBWRNNND-UHFFFAOYSA-N 0.000 description 1
- ZLRZHWUEWCVYHG-UHFFFAOYSA-N 6-bromo-3h-quinolin-4-one Chemical compound N1=CCC(=O)C2=CC(Br)=CC=C21 ZLRZHWUEWCVYHG-UHFFFAOYSA-N 0.000 description 1
- JYDXUDOZEQAXBH-UHFFFAOYSA-N 6-hydroxy-1h-3,1-benzoxazine-2,4-dione Chemical compound N1C(=O)OC(=O)C2=CC(O)=CC=C21 JYDXUDOZEQAXBH-UHFFFAOYSA-N 0.000 description 1
- IAARRMOBNGVINM-UHFFFAOYSA-N 6-hydroxy-3-methylquinazolin-4-one Chemical compound C1=C(O)C=C2C(=O)N(C)C=NC2=C1 IAARRMOBNGVINM-UHFFFAOYSA-N 0.000 description 1
- ZZSFZIKRCCTBSV-UHFFFAOYSA-N 7-bromo-2-methylisoquinolin-1-one Chemical compound C1=C(Br)C=C2C(=O)N(C)C=CC2=C1 ZZSFZIKRCCTBSV-UHFFFAOYSA-N 0.000 description 1
- NMNLXVSNJLUKQW-UHFFFAOYSA-N 7-bromo-3-(3-chlorophenyl)-2h-isoquinolin-1-one Chemical compound ClC1=CC=CC(C=2NC(=O)C3=CC(Br)=CC=C3C=2)=C1 NMNLXVSNJLUKQW-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- HJCMDXDYPOUFDY-WHFBIAKZSA-N Ala-Gln Chemical compound C[C@H](N)C(=O)N[C@H](C(O)=O)CCC(N)=O HJCMDXDYPOUFDY-WHFBIAKZSA-N 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 description 1
- OKTJSMMVPCPJKN-NJFSPNSNSA-N Carbon-14 Chemical compound [14C] OKTJSMMVPCPJKN-NJFSPNSNSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 108091006146 Channels Proteins 0.000 description 1
- 101000983970 Conus catus Alpha-conotoxin CIB Proteins 0.000 description 1
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 108091006027 G proteins Proteins 0.000 description 1
- 102000030782 GTP binding Human genes 0.000 description 1
- 108091000058 GTP-Binding Proteins 0.000 description 1
- 201000004311 Gilles de la Tourette syndrome Diseases 0.000 description 1
- 239000007821 HATU Substances 0.000 description 1
- 239000007995 HEPES buffer Substances 0.000 description 1
- 239000012981 Hank's balanced salt solution Substances 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 208000002193 Pain Diseases 0.000 description 1
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 1
- 102100022368 Protein RIC-3 Human genes 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- OKJPEAGHQZHRQV-UHFFFAOYSA-N Triiodomethane Natural products IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 1
- GXBMIBRIOWHPDT-UHFFFAOYSA-N Vasopressin Natural products N1C(=O)C(CC=2C=C(O)C=CC=2)NC(=O)C(N)CSSCC(C(=O)N2C(CCC2)C(=O)NC(CCCN=C(N)N)C(=O)NCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(CCC(N)=O)NC(=O)C1CC1=CC=CC=C1 GXBMIBRIOWHPDT-UHFFFAOYSA-N 0.000 description 1
- 102000002852 Vasopressins Human genes 0.000 description 1
- 108010004977 Vasopressins Proteins 0.000 description 1
- 108010084455 Zeocin Proteins 0.000 description 1
- WDORHSVOZYQOQO-UHFFFAOYSA-N acetamide;2h-isoquinolin-1-one Chemical class CC(N)=O.C1=CC=C2C(=O)NC=CC2=C1 WDORHSVOZYQOQO-UHFFFAOYSA-N 0.000 description 1
- PAAZCQANMCYGAW-UHFFFAOYSA-N acetic acid;2,2,2-trifluoroacetic acid Chemical compound CC(O)=O.OC(=O)C(F)(F)F PAAZCQANMCYGAW-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000000556 agonist Substances 0.000 description 1
- 125000004450 alkenylene group Chemical group 0.000 description 1
- 230000003281 allosteric effect Effects 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 230000036592 analgesia Effects 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- 230000000843 anti-fungal effect Effects 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- KBZOIRJILGZLEJ-LGYYRGKSSA-N argipressin Chemical compound C([C@H]1C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CSSC[C@@H](C(N[C@@H](CC=2C=CC(O)=CC=2)C(=O)N1)=O)N)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCC(N)=O)C1=CC=CC=C1 KBZOIRJILGZLEJ-LGYYRGKSSA-N 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 238000011914 asymmetric synthesis Methods 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 229960004365 benzoic acid Drugs 0.000 description 1
- MUALRAIOVNYAIW-UHFFFAOYSA-N binap Chemical compound C1=CC=CC=C1P(C=1C(=C2C=CC=CC2=CC=1)C=1C2=CC=CC=C2C=CC=1P(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 MUALRAIOVNYAIW-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 210000003169 central nervous system Anatomy 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 229960004106 citric acid Drugs 0.000 description 1
- 208000010877 cognitive disease Diseases 0.000 description 1
- 230000001149 cognitive effect Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- GBRBMTNGQBKBQE-UHFFFAOYSA-L copper;diiodide Chemical compound I[Cu]I GBRBMTNGQBKBQE-UHFFFAOYSA-L 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 125000006165 cyclic alkyl group Chemical group 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 239000003405 delayed action preparation Substances 0.000 description 1
- 229910052805 deuterium Inorganic materials 0.000 description 1
- MXFYYFVVIIWKFE-UHFFFAOYSA-N dicyclohexyl-[2-[2,6-di(propan-2-yloxy)phenyl]phenyl]phosphane Chemical group CC(C)OC1=CC=CC(OC(C)C)=C1C1=CC=CC=C1P(C1CCCCC1)C1CCCCC1 MXFYYFVVIIWKFE-UHFFFAOYSA-N 0.000 description 1
- 229960004132 diethyl ether Drugs 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- XHFGWHUWQXTGAT-UHFFFAOYSA-N dimethylamine hydrochloride Natural products CNC(C)C XHFGWHUWQXTGAT-UHFFFAOYSA-N 0.000 description 1
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 1
- 230000006806 disease prevention Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000009510 drug design Methods 0.000 description 1
- OCFIUNGSKQZESJ-UHFFFAOYSA-N echinozolinone Natural products C1=CC=C2C(=O)N(CCO)C=NC2=C1 OCFIUNGSKQZESJ-UHFFFAOYSA-N 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 239000003797 essential amino acid Substances 0.000 description 1
- 235000020776 essential amino acid Nutrition 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- HFTNNOZFRQLFQB-UHFFFAOYSA-N ethenoxy(trimethyl)silane Chemical compound C[Si](C)(C)OC=C HFTNNOZFRQLFQB-UHFFFAOYSA-N 0.000 description 1
- 229940052303 ethers for general anesthesia Drugs 0.000 description 1
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- RFHAOTPXVQNOHP-UHFFFAOYSA-N fluconazole Chemical compound C1=NC=NN1CC(C=1C(=CC(F)=CC=1)F)(O)CN1C=NC=N1 RFHAOTPXVQNOHP-UHFFFAOYSA-N 0.000 description 1
- 229960004884 fluconazole Drugs 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 235000011087 fumaric acid Nutrition 0.000 description 1
- 229960002598 fumaric acid Drugs 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 102000050217 human RIC3 Human genes 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 1
- 229910000043 hydrogen iodide Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 230000004179 hypothalamic–pituitary–adrenal axis Effects 0.000 description 1
- 239000012729 immediate-release (IR) formulation Substances 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000000099 in vitro assay Methods 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 238000004255 ion exchange chromatography Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 108010082117 matrigel Proteins 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- DUMHGDILCXSHNL-UHFFFAOYSA-N methyl 2-[[2-amino-5-(1,4-diazabicyclo[3.2.2]nonan-4-yl)benzoyl]amino]acetate Chemical compound C1=C(N)C(C(=O)NCC(=O)OC)=CC(N2C3CCN(CC3)CC2)=C1 DUMHGDILCXSHNL-UHFFFAOYSA-N 0.000 description 1
- IXVNSGSUEVSJIF-UHFFFAOYSA-N methyl 5-bromo-2-nitrobenzoate Chemical compound COC(=O)C1=CC(Br)=CC=C1[N+]([O-])=O IXVNSGSUEVSJIF-UHFFFAOYSA-N 0.000 description 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000003068 molecular probe Substances 0.000 description 1
- 230000003551 muscarinic effect Effects 0.000 description 1
- DHTZMTGBKXYJHP-UHFFFAOYSA-N n-(cyclopropylmethyl)-5-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-2-nitrobenzamide Chemical compound [O-][N+](=O)C1=CC=C(N2C3CCN(CC3)CC2)C=C1C(=O)NCC1CC1 DHTZMTGBKXYJHP-UHFFFAOYSA-N 0.000 description 1
- QKYGBQXQXGFTLO-UHFFFAOYSA-N n-(cyclopropylmethyl)-5-fluoro-2-nitrobenzamide Chemical compound [O-][N+](=O)C1=CC=C(F)C=C1C(=O)NCC1CC1 QKYGBQXQXGFTLO-UHFFFAOYSA-N 0.000 description 1
- PYOOQBCXRZMONQ-UHFFFAOYSA-N n-cyclobutyl-5-fluoro-2-nitrobenzamide Chemical compound [O-][N+](=O)C1=CC=C(F)C=C1C(=O)NC1CCC1 PYOOQBCXRZMONQ-UHFFFAOYSA-N 0.000 description 1
- IWOLOJWHROVYDV-UHFFFAOYSA-N n-cyclopropyl-5-fluoro-2-nitrobenzamide Chemical compound [O-][N+](=O)C1=CC=C(F)C=C1C(=O)NC1CC1 IWOLOJWHROVYDV-UHFFFAOYSA-N 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 210000000653 nervous system Anatomy 0.000 description 1
- 208000015122 neurodegenerative disease Diseases 0.000 description 1
- 239000002858 neurotransmitter agent Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000036407 pain Effects 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 210000001428 peripheral nervous system Anatomy 0.000 description 1
- 229940124531 pharmaceutical excipient Drugs 0.000 description 1
- CWCMIVBLVUHDHK-ZSNHEYEWSA-N phleomycin D1 Chemical compound N([C@H](C(=O)N[C@H](C)[C@@H](O)[C@H](C)C(=O)N[C@@H]([C@H](O)C)C(=O)NCCC=1SC[C@@H](N=1)C=1SC=C(N=1)C(=O)NCCCCNC(N)=N)[C@@H](O[C@H]1[C@H]([C@@H](O)[C@H](O)[C@H](CO)O1)O[C@@H]1[C@H]([C@@H](OC(N)=O)[C@H](O)[C@@H](CO)O1)O)C=1N=CNC=1)C(=O)C1=NC([C@H](CC(N)=O)NC[C@H](N)C(N)=O)=NC(N)=C1C CWCMIVBLVUHDHK-ZSNHEYEWSA-N 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates 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
- 239000002243 precursor Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- DBABZHXKTCFAPX-UHFFFAOYSA-N probenecid Chemical compound CCCN(CCC)S(=O)(=O)C1=CC=C(C(O)=O)C=C1 DBABZHXKTCFAPX-UHFFFAOYSA-N 0.000 description 1
- 229960003081 probenecid Drugs 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- VVWRJUBEIPHGQF-UHFFFAOYSA-N propan-2-yl n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)N=NC(=O)OC(C)C VVWRJUBEIPHGQF-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- NSETWVJZUWGCKE-UHFFFAOYSA-N propylphosphonic acid Chemical compound CCCP(O)(O)=O NSETWVJZUWGCKE-UHFFFAOYSA-N 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- 230000004224 protection Effects 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000000018 receptor agonist Substances 0.000 description 1
- 229940044601 receptor agonist Drugs 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229960001367 tartaric acid Drugs 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 125000005958 tetrahydrothienyl group Chemical group 0.000 description 1
- 125000004632 tetrahydrothiopyranyl group Chemical group S1C(CCCC1)* 0.000 description 1
- 238000003354 tissue distribution assay Methods 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 229940062627 tribasic potassium phosphate Drugs 0.000 description 1
- GKASDNZWUGIAMG-UHFFFAOYSA-N triethyl orthoformate Chemical compound CCOC(OCC)OCC GKASDNZWUGIAMG-UHFFFAOYSA-N 0.000 description 1
- 238000001665 trituration Methods 0.000 description 1
- 238000004704 ultra performance liquid chromatography Methods 0.000 description 1
- 229960003726 vasopressin Drugs 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
-
- 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
- A61P25/28—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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biomedical Technology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hospice & Palliative Care (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25110109P | 2009-10-13 | 2009-10-13 | |
| EP09172872 | 2009-10-13 | ||
| PCT/EP2010/065160 WO2011045258A1 (en) | 2009-10-13 | 2010-10-11 | Condensed azine - derivatives for the treatment of diseases related to the acetylcholine receptor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2012004289A true MX2012004289A (es) | 2012-06-12 |
Family
ID=42040651
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2012004289A MX2012004289A (es) | 2009-10-13 | 2010-10-11 | Derivados de azina condensada para el tratamiento de enfermedades relacionadas con el receptor de acetilcolina. |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8841289B2 (enExample) |
| EP (1) | EP2488520B1 (enExample) |
| JP (1) | JP2013507417A (enExample) |
| KR (1) | KR20120100913A (enExample) |
| CN (1) | CN102666540A (enExample) |
| AU (1) | AU2010305825A1 (enExample) |
| BR (1) | BR112012008518A2 (enExample) |
| CA (1) | CA2776835A1 (enExample) |
| IN (1) | IN2012DN02968A (enExample) |
| MX (1) | MX2012004289A (enExample) |
| RU (1) | RU2012119488A (enExample) |
| WO (1) | WO2011045258A1 (enExample) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2012291133A1 (en) | 2011-07-29 | 2014-02-20 | Taisho Pharmaceutical Co., Ltd. | Amidine compound or salt thereof |
| WO2013132253A1 (en) | 2012-03-07 | 2013-09-12 | Institute Of Cancer Research: Royal Cancer Hospital (The) | 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use |
| AU2013264943B2 (en) * | 2012-05-22 | 2018-02-01 | King Abdullah University Of Science And Technology | Combination comprising parthenolide for use in the treatment of Alzheimer's Disease and other neurodegenerative disorders |
| EP3044221B1 (en) | 2013-09-11 | 2018-02-21 | Institute of Cancer Research: Royal Cancer Hospital (The) | 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use |
| WO2016034703A1 (en) | 2014-09-05 | 2016-03-10 | AbbVie Deutschland GmbH & Co. KG | Fused heterocyclic or carbocyclic compounds carrying a substituted cycloaliphatic radical and use thereof for treating vasopressin-related diseases |
| ES2764660T3 (es) | 2014-12-16 | 2020-06-04 | Axovant Sciences Gmbh | Compuestos de amida de quinuclidina sustituida geminal como agonistas de receptores alfa-7 nicotínicos de acetilcolina |
| AR103297A1 (es) | 2014-12-30 | 2017-05-03 | Forma Therapeutics Inc | Pirrolo y pirazolopirimidinas como inhibidores de la proteasa 7 específica de ubiquitina |
| MA41291A (fr) | 2014-12-30 | 2017-11-07 | Forma Therapeutics Inc | Dérivés de la pyrrolotriazinone et de l'imidazotriazinone en tant qu'inhibiteurs de la protéase spécifique de l'ubiquitine n° 7 (usp7) pour le traitement d'un cancer |
| JP2018504430A (ja) | 2015-02-05 | 2018-02-15 | フォーマ セラピューティクス，インコーポレイテッド | ユビキチン特異的プロテアーゼ７阻害物質としてのキナゾリノン及びアザキナゾリノン |
| WO2016126929A1 (en) | 2015-02-05 | 2016-08-11 | Forma Therapeutics, Inc. | Thienopyrimidinones as ubiquitin-specific protease 7 inhibitors |
| US9938300B2 (en) | 2015-02-05 | 2018-04-10 | Forma Therapeutics, Inc. | Isothiazolopyrimidinones, pyrazolopyrimidinones, and pyrrolopyrimidinones as ubiquitin-specific protease 7 inhibitors |
| CN106146410B (zh) * | 2015-04-03 | 2018-10-12 | 中南大学 | 6-氨基-4(3h)-喹唑啉酮衍生物及其合成方法和用途 |
| CN106279211B (zh) | 2015-06-03 | 2020-09-15 | 北京大学 | 一种噻唑并嘧啶酮化合物及其制备方法和应用 |
| WO2016201096A1 (en) | 2015-06-10 | 2016-12-15 | Forum Pharmaceuticals, Inc. | Aminobenzisoxazole compounds as agonists of a7-nicotinic acetylcholine receptors |
| HK1253295A1 (zh) | 2015-08-12 | 2019-06-14 | Axovant Sciences Gmbh | 作为7-烟碱乙酰胆碱受体的激动剂的偕取代的氨基苯并异恶唑化合物 |
| JP7071917B2 (ja) | 2015-12-09 | 2022-05-19 | カデント セラピューティクス，インコーポレーテッド | ヘテロ芳香族ｎｍｄａ受容体モジュレーターおよびその使用 |
| EP3386990B1 (en) | 2015-12-09 | 2023-04-19 | Novartis AG | Thienopyrimidinone nmda receptor modulators and uses thereof |
| EP3558318B1 (en) | 2016-12-22 | 2023-12-20 | Novartis AG | Nmda receptor modulators and uses thereof |
| BR112020026637A2 (pt) * | 2018-06-27 | 2021-03-30 | Reborna Biosciences, Inc. | Agente profilático ou terapêutico para atrofia muscular espinhal |
| HU231414B1 (hu) | 2018-07-13 | 2023-08-28 | Richter Gedeon Nyrt. | Tiadiazin származékok |
| AU2019309448B2 (en) | 2018-07-26 | 2024-08-29 | Domain Therapeutics | Substituted quinazolinone derivatives and their use as positive allosteric modulators of mGluR4 |
| JOP20210020A1 (ar) | 2018-08-03 | 2021-01-25 | Cadent Therapeutics Inc | معدلات عطرية غير متجانسة لمستقبل nmda واستخداماتها |
| WO2021198191A1 (en) | 2020-03-30 | 2021-10-07 | Enyo Pharma | Quinazolinone derivatives and uses thereof for treating a cancer |
| WO2021198188A1 (en) | 2020-03-30 | 2021-10-07 | Enyo Pharma | Quinazolinone derivatives and uses thereof for treating a cancer |
| WO2022047145A1 (en) | 2020-08-28 | 2022-03-03 | Arvinas Operations, Inc. | Rapidly accelerating fibrosarcoma protein degrading compounds and associated methods of use |
| CN112898290B (zh) * | 2021-01-29 | 2022-08-05 | 中南大学 | 异噁唑甲酰胺基-4(3h)-喹唑啉酮衍生物及其合成方法和用途 |
| EP4584258A1 (en) | 2022-09-07 | 2025-07-16 | Arvinas Operations, Inc. | Rapidly accelerated fibrosarcoma (raf) degrading compounds and associated methods of use |
| TW202539670A (zh) * | 2024-02-23 | 2025-10-16 | 大陸商海思科醫藥集團股份有限公司 | Braf抑制劑的製備方法 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE0000540D0 (sv) | 2000-02-18 | 2000-02-18 | Astrazeneca Ab | New compounds |
| JP2005504730A (ja) * | 2001-04-20 | 2005-02-17 | バーテックス ファーマシューティカルズ インコーポレイテッド | Ｇｓｋ−３インヒビターとして有用な組成物 |
| US7148236B2 (en) * | 2002-01-17 | 2006-12-12 | Merck & Co., Inc. | Modulators of acetylcholine receptors |
| GB0220581D0 (en) | 2002-09-04 | 2002-10-09 | Novartis Ag | Organic Compound |
| TW200536830A (en) * | 2004-02-06 | 2005-11-16 | Chugai Pharmaceutical Co Ltd | 1-(2H)-isoquinolone derivative |
| ES2423006T3 (es) * | 2005-07-26 | 2013-09-17 | Sanofi | Derivados de isoquinolona sustituidos con piperidinilo como inhibidores de la cinasa Rho |
| JP5256202B2 (ja) * | 2006-09-11 | 2013-08-07 | エム・エス・ディー・オス・ベー・フェー | キナゾリノンおよびイソキノリノンアセトアミド誘導体 |
| ATE502027T1 (de) * | 2006-12-27 | 2011-04-15 | Sanofi Aventis | Substituierte isochinoline und ihre verwendung als rho-kinase-inhibitoren |
| JP2010229035A (ja) * | 2007-08-01 | 2010-10-14 | Taisho Pharmaceutical Co Ltd | ピリドピリミジン−４−オン誘導体 |
| US8343960B2 (en) * | 2007-11-14 | 2013-01-01 | Neurosearch A/S | 1,4-diaza-bicyclo[3.2.2]nonyl pyrimidine derivatives and their medical use |
| CN101960691B (zh) | 2008-02-29 | 2013-04-24 | 核心技术国际有限公司 | 电池组的充电装置和电池组的品质判断装置 |
-
2010
- 2010-10-11 IN IN2968DEN2012 patent/IN2012DN02968A/en unknown
- 2010-10-11 BR BR112012008518A patent/BR112012008518A2/pt not_active Application Discontinuation
- 2010-10-11 CA CA2776835A patent/CA2776835A1/en not_active Abandoned
- 2010-10-11 US US13/501,587 patent/US8841289B2/en active Active
- 2010-10-11 AU AU2010305825A patent/AU2010305825A1/en not_active Abandoned
- 2010-10-11 MX MX2012004289A patent/MX2012004289A/es not_active Application Discontinuation
- 2010-10-11 CN CN2010800465507A patent/CN102666540A/zh active Pending
- 2010-10-11 EP EP10771062.6A patent/EP2488520B1/en active Active
- 2010-10-11 WO PCT/EP2010/065160 patent/WO2011045258A1/en not_active Ceased
- 2010-10-11 KR KR1020127009340A patent/KR20120100913A/ko not_active Withdrawn
- 2010-10-11 RU RU2012119488/04A patent/RU2012119488A/ru unknown
- 2010-10-11 JP JP2012533593A patent/JP2013507417A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| JP2013507417A (ja) | 2013-03-04 |
| WO2011045258A1 (en) | 2011-04-21 |
| US20120208796A1 (en) | 2012-08-16 |
| EP2488520A1 (en) | 2012-08-22 |
| RU2012119488A (ru) | 2013-11-20 |
| US8841289B2 (en) | 2014-09-23 |
| KR20120100913A (ko) | 2012-09-12 |
| IN2012DN02968A (enExample) | 2015-07-31 |
| BR112012008518A2 (pt) | 2016-04-05 |
| CA2776835A1 (en) | 2011-04-21 |
| CN102666540A (zh) | 2012-09-12 |
| AU2010305825A1 (en) | 2012-04-19 |
| EP2488520B1 (en) | 2015-09-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MX2012004289A (es) | Derivados de azina condensada para el tratamiento de enfermedades relacionadas con el receptor de acetilcolina. | |
| AU2016333721B2 (en) | Spiro[3H-indole-3,2´-pyrrolidin]-2(1H)-one compounds and derivatives as MDM2-p53 inhibitors | |
| CA2956129C (en) | New spiro[3h-indole-3,2'-pyrrolidin]-2(1h)-one compounds and derivatives as mdm2-p53 inhibitors | |
| KR101560066B1 (ko) | 테트라히드로-피리도-피리미딘 유도체 | |
| KR20180133906A (ko) | Ehmt1 및 ehmt2 저해제로서의 아민-치환된 아릴 또는 헤테로아릴 화합물 | |
| AU2007258435A1 (en) | Heterocyclic aspartyl protease inhibitors | |
| CA2944475A1 (en) | Bicyclic-fused heteroaryl or aryl compounds | |
| WO2014177524A1 (en) | C-linked heterocycloalkyl substituted pyrimidines and their uses | |
| EP2209775A1 (en) | Heterobicyclic compounds as histamine h4-receptor antagonists | |
| CN104974161B (zh) | 作为PARP抑制剂的4H-吡唑并[1,5-α]苯并咪唑化合物的类似物 | |
| NZ584430A (en) | Quinazolinedione derivatives, preparation thereof and therapeutic uses thereof | |
| IL191213A (en) | Transformed derivatives in the cycles of pyrimidone | |
| NZ749946A (en) | Novel compound or pharmaceutically acceptable salt thereof | |
| EP3548468A1 (en) | Tricyclic rho kinase inhibitors | |
| JP7801084B2 (ja) | Ｅｇｆｒ阻害剤としてのインドリン化合物及び誘導体 | |
| WO2012085167A1 (en) | Metabotropic glutamate receptor modulators | |
| JP7312171B2 (ja) | ピラゾロピリジノン化合物 | |
| JP2024545518A (ja) | Ｃｄｋ９阻害剤及びその使用 | |
| AU2022371404A1 (en) | Covalent egfr inhibitors and methods of use thereof | |
| JP7689923B2 (ja) | チエノピリジノン化合物 | |
| AU2009224760A1 (en) | 2-Aminoquinolines as 5-HT5A receptor antagonists | |
| RU2827549C2 (ru) | Соединения тиенопиридинона | |
| RU2806751C2 (ru) | Соединения на основе пиразолопиридинона | |
| MX2010011136A (es) | Derivados de pirrolo [2,3-d] pirimidin-2-il-amina como inhibidores pkc-theta. | |
| AU2006314136A1 (en) | Substituted bicyclic pyrimidone derivatives |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| GB | Transfer or rights |
Owner name: MERCK SHARP & DOHME B.V. |
|
| FA | Abandonment or withdrawal |