JP2013518046A5 - - Google Patents
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- JP2013518046A5 JP2013518046A5 JP2012550116A JP2012550116A JP2013518046A5 JP 2013518046 A5 JP2013518046 A5 JP 2013518046A5 JP 2012550116 A JP2012550116 A JP 2012550116A JP 2012550116 A JP2012550116 A JP 2012550116A JP 2013518046 A5 JP2013518046 A5 JP 2013518046A5
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- dichloro
- pyrimidine
- methyl
- oxadiazol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- -1 3-chloro-4-trifluoromethoxyphenyl Chemical group 0.000 claims description 172
- 239000000126 substance Substances 0.000 claims description 29
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims description 22
- BIGWXAGEQONZGD-UHFFFAOYSA-N 2h-oxadiazol-5-one Chemical compound O=C1C=NNO1 BIGWXAGEQONZGD-UHFFFAOYSA-N 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 20
- 125000005843 halogen group Chemical group 0.000 claims description 18
- 150000005829 chemical entities Chemical class 0.000 claims description 13
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 12
- 125000002962 imidazol-1-yl group Chemical group [*]N1C([H])=NC([H])=C1[H] 0.000 claims description 11
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 10
- 239000008194 pharmaceutical composition Substances 0.000 claims description 10
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 9
- 208000035475 disorder Diseases 0.000 claims description 9
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 7
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 6
- 108010033242 Kynurenine 3-monooxygenase Proteins 0.000 claims description 6
- 102100037652 Kynurenine 3-monooxygenase Human genes 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 125000001072 heteroaryl group Chemical group 0.000 claims description 6
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 6
- 125000003037 imidazol-2-yl group Chemical group [H]N1C([*])=NC([H])=C1[H] 0.000 claims description 6
- 125000004353 pyrazol-1-yl group Chemical group [H]C1=NN(*)C([H])=C1[H] 0.000 claims description 6
- 159000000000 sodium salts Chemical class 0.000 claims description 6
- 125000000437 thiazol-2-yl group Chemical group [H]C1=C([H])N=C(*)S1 0.000 claims description 6
- 230000000694 effects Effects 0.000 claims description 5
- 150000002431 hydrogen Chemical class 0.000 claims description 5
- 230000001404 mediated effect Effects 0.000 claims description 5
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 4
- MTOCMLGOPYERKW-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-6-(2h-tetrazol-5-yl)pyrimidine Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CC(C=2NN=NN=2)=NC=N1 MTOCMLGOPYERKW-UHFFFAOYSA-N 0.000 claims description 4
- SKUQIZNIGNTGFZ-UHFFFAOYSA-N 4-(3,4-difluorophenyl)-6-(2h-tetrazol-5-yl)pyrimidine Chemical compound C1=C(F)C(F)=CC=C1C1=CC(C=2NN=NN=2)=NC=N1 SKUQIZNIGNTGFZ-UHFFFAOYSA-N 0.000 claims description 4
- WNENMQUGXZYTTO-UHFFFAOYSA-N 4-(3-chloro-4-fluorophenyl)-6-(2h-tetrazol-5-yl)pyrimidine Chemical compound C1=C(Cl)C(F)=CC=C1C1=CC(C=2NN=NN=2)=NC=N1 WNENMQUGXZYTTO-UHFFFAOYSA-N 0.000 claims description 4
- 208000024827 Alzheimer disease Diseases 0.000 claims description 4
- 208000023105 Huntington disease Diseases 0.000 claims description 4
- 125000002140 imidazol-4-yl group Chemical group [H]N1C([H])=NC([*])=C1[H] 0.000 claims description 4
- 230000000626 neurodegenerative effect Effects 0.000 claims description 4
- 125000004287 oxazol-2-yl group Chemical group [H]C1=C([H])N=C(*)O1 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- 239000000651 prodrug Substances 0.000 claims description 4
- 229940002612 prodrug Drugs 0.000 claims description 4
- 125000004523 tetrazol-1-yl group Chemical group N1(N=NN=C1)* 0.000 claims description 4
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- OKEPDOSLTPWNMJ-UHFFFAOYSA-N 1-[6-(3,4-dichlorophenyl)pyrimidin-4-yl]-3-methylimidazol-2-one Chemical compound O=C1N(C)C=CN1C1=CC(C=2C=C(Cl)C(Cl)=CC=2)=NC=N1 OKEPDOSLTPWNMJ-UHFFFAOYSA-N 0.000 claims description 2
- RIFCBJMQUMYQHM-UHFFFAOYSA-N 2-[3-[6-(3,4-dichlorophenyl)pyrimidin-4-yl]-1,2,4-oxadiazol-5-yl]-n,n-dimethylethanamine Chemical compound O1C(CCN(C)C)=NC(C=2N=CN=C(C=2)C=2C=C(Cl)C(Cl)=CC=2)=N1 RIFCBJMQUMYQHM-UHFFFAOYSA-N 0.000 claims description 2
- ROSKCKKWUAUBPC-UHFFFAOYSA-N 2-[6-(3,4-dichlorophenyl)-2-methylpyrimidin-4-yl]-4-methyl-1,3-oxazole Chemical compound CC1=COC(C=2N=C(C)N=C(C=2)C=2C=C(Cl)C(Cl)=CC=2)=N1 ROSKCKKWUAUBPC-UHFFFAOYSA-N 0.000 claims description 2
- KGMUYOCFDSQXAE-UHFFFAOYSA-N 2-[6-(3,4-dichlorophenyl)pyrimidin-4-yl]-1,3-oxazole Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CC(C=2OC=CN=2)=NC=N1 KGMUYOCFDSQXAE-UHFFFAOYSA-N 0.000 claims description 2
- UZUWTIHQPXDNIC-UHFFFAOYSA-N 2-[6-(3,4-dichlorophenyl)pyrimidin-4-yl]-1,3-thiazole Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CC(C=2SC=CN=2)=NC=N1 UZUWTIHQPXDNIC-UHFFFAOYSA-N 0.000 claims description 2
- JMGZKBUMZTWCTN-UHFFFAOYSA-N 2-[6-(3,4-dichlorophenyl)pyrimidin-4-yl]-1h-benzimidazole Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CC(C=2NC3=CC=CC=C3N=2)=NC=N1 JMGZKBUMZTWCTN-UHFFFAOYSA-N 0.000 claims description 2
- LNRYOGXIUGDXCK-UHFFFAOYSA-N 2-[6-(3,4-dichlorophenyl)pyrimidin-4-yl]-4-methyl-1,3-oxazole Chemical compound CC1=COC(C=2N=CN=C(C=2)C=2C=C(Cl)C(Cl)=CC=2)=N1 LNRYOGXIUGDXCK-UHFFFAOYSA-N 0.000 claims description 2
- AFGXONWEIZLGHJ-UHFFFAOYSA-N 2-[6-(3,4-dichlorophenyl)pyrimidin-4-yl]-5-methyl-1h-pyrazol-3-one Chemical compound N1C(C)=CC(=O)N1C1=CC(C=2C=C(Cl)C(Cl)=CC=2)=NC=N1 AFGXONWEIZLGHJ-UHFFFAOYSA-N 0.000 claims description 2
- WDLSNFQTFQDMLE-UHFFFAOYSA-N 2-[6-(3-chlorophenyl)pyrimidin-4-yl]-1,3-benzoxazole Chemical compound ClC1=CC=CC(C=2N=CN=C(C=2)C=2OC3=CC=CC=C3N=2)=C1 WDLSNFQTFQDMLE-UHFFFAOYSA-N 0.000 claims description 2
- DIQUOHCUSXJTGE-UHFFFAOYSA-N 2-[6-(3-chlorophenyl)pyrimidin-4-yl]-1-methylbenzimidazole Chemical compound N=1C2=CC=CC=C2N(C)C=1C(N=CN=1)=CC=1C1=CC=CC(Cl)=C1 DIQUOHCUSXJTGE-UHFFFAOYSA-N 0.000 claims description 2
- KDPUXHLJFAMDMJ-UHFFFAOYSA-N 2-[6-(3-chlorophenyl)pyrimidin-4-yl]-1h-benzimidazole Chemical compound ClC1=CC=CC(C=2N=CN=C(C=2)C=2NC3=CC=CC=C3N=2)=C1 KDPUXHLJFAMDMJ-UHFFFAOYSA-N 0.000 claims description 2
- HQHXJSFDZSMZLZ-UHFFFAOYSA-N 2-[6-(3-chlorophenyl)pyrimidin-4-yl]-4-methyl-1,3-oxazole Chemical compound CC1=COC(C=2N=CN=C(C=2)C=2C=C(Cl)C=CC=2)=N1 HQHXJSFDZSMZLZ-UHFFFAOYSA-N 0.000 claims description 2
- ZAOGPGHFSWAZTM-UHFFFAOYSA-N 2-[6-(3-chlorophenyl)pyrimidin-4-yl]-5,6-difluoro-1h-benzimidazole Chemical compound N1C=2C=C(F)C(F)=CC=2N=C1C(N=CN=1)=CC=1C1=CC=CC(Cl)=C1 ZAOGPGHFSWAZTM-UHFFFAOYSA-N 0.000 claims description 2
- JUVYRFJXVZHIFC-UHFFFAOYSA-N 2-[6-(3-chlorophenyl)pyrimidin-4-yl]-6-fluoro-1h-benzimidazole Chemical compound N=1C2=CC(F)=CC=C2NC=1C(N=CN=1)=CC=1C1=CC=CC(Cl)=C1 JUVYRFJXVZHIFC-UHFFFAOYSA-N 0.000 claims description 2
- VSHASHJYPUERGY-UHFFFAOYSA-N 3-[6-(3,4-dichlorophenyl)pyrimidin-4-yl]-1h-imidazol-2-one Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CC(N2C(NC=C2)=O)=NC=N1 VSHASHJYPUERGY-UHFFFAOYSA-N 0.000 claims description 2
- MSYIWJXURWRDKT-UHFFFAOYSA-N 3-[6-(3,4-dichlorophenyl)pyrimidin-4-yl]-2h-1,2,4-oxadiazole-5-thione Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CC(C=2NC(=S)ON=2)=NC=N1 MSYIWJXURWRDKT-UHFFFAOYSA-N 0.000 claims description 2
- DJPHEZULAHNZAL-UHFFFAOYSA-N 3-pyrimidin-2-yl-2H-oxadiazole Chemical compound O1NN(C=C1)C1=NC=CC=N1 DJPHEZULAHNZAL-UHFFFAOYSA-N 0.000 claims description 2
- ZNKZDGFSYSPQCQ-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-6-(1,2,4-triazol-1-yl)pyrimidine Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CC(N2N=CN=C2)=NC=N1 ZNKZDGFSYSPQCQ-UHFFFAOYSA-N 0.000 claims description 2
- SCAIUCPQLBSMDG-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-6-(1-methyltetrazol-5-yl)pyrimidine Chemical compound CN1N=NN=C1C1=CC(C=2C=C(Cl)C(Cl)=CC=2)=NC=N1 SCAIUCPQLBSMDG-UHFFFAOYSA-N 0.000 claims description 2
- JIRSMOUXSFIZTD-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-6-(1h-1,2,4-triazol-5-yl)pyrimidine Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CC(C=2NC=NN=2)=NC=N1 JIRSMOUXSFIZTD-UHFFFAOYSA-N 0.000 claims description 2
- FCHVNBZJVNRUCR-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-6-(1h-imidazol-2-yl)pyrimidine Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CC(C=2NC=CN=2)=NC=N1 FCHVNBZJVNRUCR-UHFFFAOYSA-N 0.000 claims description 2
- LNXBAFBGQULGSU-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-6-(1h-pyrazol-5-yl)pyrimidine Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CC(C2=NNC=C2)=NC=N1 LNXBAFBGQULGSU-UHFFFAOYSA-N 0.000 claims description 2
- IYXFPLVXCRLSKZ-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-6-(2-methyltetrazol-5-yl)pyrimidine Chemical compound CN1N=NC(C=2N=CN=C(C=2)C=2C=C(Cl)C(Cl)=CC=2)=N1 IYXFPLVXCRLSKZ-UHFFFAOYSA-N 0.000 claims description 2
- ZBHJOTQYFIFNDV-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-6-(4,5-dihydro-1h-imidazol-2-yl)pyrimidine Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CC(C=2NCCN=2)=NC=N1 ZBHJOTQYFIFNDV-UHFFFAOYSA-N 0.000 claims description 2
- SZAOZTRJZVLXLO-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-6-(5-fluoropyridin-2-yl)pyrimidine Chemical compound N1=CC(F)=CC=C1C1=CC(C=2C=C(Cl)C(Cl)=CC=2)=NC=N1 SZAOZTRJZVLXLO-UHFFFAOYSA-N 0.000 claims description 2
- WSFAFIDQMPKXSL-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-6-(5-methyl-1h-1,2,4-triazol-3-yl)pyrimidine Chemical compound N1C(C)=NN=C1C1=CC(C=2C=C(Cl)C(Cl)=CC=2)=NC=N1 WSFAFIDQMPKXSL-UHFFFAOYSA-N 0.000 claims description 2
- YMUUSKWZBOGGDX-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-6-(5-methyl-1h-imidazol-2-yl)pyrimidine Chemical compound CC1=CNC(C=2N=CN=C(C=2)C=2C=C(Cl)C(Cl)=CC=2)=N1 YMUUSKWZBOGGDX-UHFFFAOYSA-N 0.000 claims description 2
- PYCPSMXEPSFEJE-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-6-[3-(trifluoromethyl)pyrazol-1-yl]pyrimidine Chemical compound N1=C(C(F)(F)F)C=CN1C1=CC(C=2C=C(Cl)C(Cl)=CC=2)=NC=N1 PYCPSMXEPSFEJE-UHFFFAOYSA-N 0.000 claims description 2
- ALWHQBOIACGJGE-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-6-[4-(trifluoromethyl)imidazol-1-yl]pyrimidine Chemical compound C1=NC(C(F)(F)F)=CN1C1=CC(C=2C=C(Cl)C(Cl)=CC=2)=NC=N1 ALWHQBOIACGJGE-UHFFFAOYSA-N 0.000 claims description 2
- PURBNGDJUSAPDH-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-6-imidazol-1-ylpyrimidine Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CC(N2C=NC=C2)=NC=N1 PURBNGDJUSAPDH-UHFFFAOYSA-N 0.000 claims description 2
- QKDPTHAYQCPXSV-UHFFFAOYSA-N 4-(3,4-dichlorophenyl)-6-pyrazol-1-ylpyrimidine Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CC(N2N=CC=C2)=NC=N1 QKDPTHAYQCPXSV-UHFFFAOYSA-N 0.000 claims description 2
- AEWCHHBGHBDHET-UHFFFAOYSA-N 4-(3-chloro-4-propan-2-yloxyphenyl)-6-(2h-tetrazol-5-yl)pyrimidine Chemical compound C1=C(Cl)C(OC(C)C)=CC=C1C1=CC(C=2NN=NN=2)=NC=N1 AEWCHHBGHBDHET-UHFFFAOYSA-N 0.000 claims description 2
- UGYNJZXCCMRSAY-UHFFFAOYSA-N 4-(3-chlorophenyl)-6-(1,2,4-triazol-1-yl)pyrimidine Chemical compound ClC1=CC=CC(C=2N=CN=C(C=2)N2N=CN=C2)=C1 UGYNJZXCCMRSAY-UHFFFAOYSA-N 0.000 claims description 2
- WWGQYSXKRDZEQL-UHFFFAOYSA-N 4-(3-chlorophenyl)-6-(1-methyltetrazol-5-yl)pyrimidine Chemical compound CN1N=NN=C1C1=CC(C=2C=C(Cl)C=CC=2)=NC=N1 WWGQYSXKRDZEQL-UHFFFAOYSA-N 0.000 claims description 2
- LGGGIVRSZVEHDF-UHFFFAOYSA-N 4-(3-chlorophenyl)-6-(1h-1,2,4-triazol-5-yl)pyrimidine Chemical compound ClC1=CC=CC(C=2N=CN=C(C=2)C=2NC=NN=2)=C1 LGGGIVRSZVEHDF-UHFFFAOYSA-N 0.000 claims description 2
- LRAVNVHTOASBPS-UHFFFAOYSA-N 4-(3-chlorophenyl)-6-(2-methyltetrazol-5-yl)pyrimidine Chemical compound CN1N=NC(C=2N=CN=C(C=2)C=2C=C(Cl)C=CC=2)=N1 LRAVNVHTOASBPS-UHFFFAOYSA-N 0.000 claims description 2
- KRYPSLGAMUHGTE-UHFFFAOYSA-N 4-(3-chlorophenyl)-6-(2h-tetrazol-5-yl)pyrimidine Chemical compound ClC1=CC=CC(C=2N=CN=C(C=2)C=2NN=NN=2)=C1 KRYPSLGAMUHGTE-UHFFFAOYSA-N 0.000 claims description 2
- NZHPCOKTLUVIDD-UHFFFAOYSA-N 4-(3-chlorophenyl)-6-(tetrazol-1-yl)pyrimidine Chemical compound ClC1=CC=CC(C=2N=CN=C(C=2)N2N=NN=C2)=C1 NZHPCOKTLUVIDD-UHFFFAOYSA-N 0.000 claims description 2
- DAROHEOKVSJSFA-UHFFFAOYSA-N 4-(3-chlorophenyl)-6-imidazol-1-ylpyrimidine Chemical compound ClC1=CC=CC(C=2N=CN=C(C=2)N2C=NC=C2)=C1 DAROHEOKVSJSFA-UHFFFAOYSA-N 0.000 claims description 2
- BXHOWMJGICQXHF-UHFFFAOYSA-N 4-(3-chlorophenyl)-6-pyrazol-1-ylpyrimidine Chemical compound ClC1=CC=CC(C=2N=CN=C(C=2)N2N=CC=C2)=C1 BXHOWMJGICQXHF-UHFFFAOYSA-N 0.000 claims description 2
- PFZSBRMSYRLMCE-UHFFFAOYSA-N 4-(3-fluoro-4-methylphenyl)-6-(2h-tetrazol-5-yl)pyrimidine Chemical compound C1=C(F)C(C)=CC=C1C1=CC(C=2NN=NN=2)=NC=N1 PFZSBRMSYRLMCE-UHFFFAOYSA-N 0.000 claims description 2
- BQTLWRJCOSPNDU-UHFFFAOYSA-N 4-[3-chloro-4-(trifluoromethoxy)phenyl]-6-(2h-tetrazol-5-yl)pyrimidine Chemical compound C1=C(Cl)C(OC(F)(F)F)=CC=C1C1=CC(C=2NN=NN=2)=NC=N1 BQTLWRJCOSPNDU-UHFFFAOYSA-N 0.000 claims description 2
- SBPMGWKYHYKRLR-UHFFFAOYSA-N 4-[6-(3,4-dichlorophenyl)pyrimidin-4-yl]-1,3-dihydroimidazol-2-one Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CC(C=2NC(=O)NC=2)=NC=N1 SBPMGWKYHYKRLR-UHFFFAOYSA-N 0.000 claims description 2
- LMJHXFQNUUCRNJ-UHFFFAOYSA-N 4-[6-(3,4-dichlorophenyl)pyrimidin-4-yl]-2-methyl-1h-pyrazol-3-one Chemical compound O=C1N(C)NC=C1C1=CC(C=2C=C(Cl)C(Cl)=CC=2)=NC=N1 LMJHXFQNUUCRNJ-UHFFFAOYSA-N 0.000 claims description 2
- OLDJDFWTWFAWRM-UHFFFAOYSA-N 4-[6-(3,4-dichlorophenyl)pyrimidin-4-yl]piperazin-2-one Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CC(N2CC(=O)NCC2)=NC=N1 OLDJDFWTWFAWRM-UHFFFAOYSA-N 0.000 claims description 2
- MVLZWTSKQRHYQE-UHFFFAOYSA-N 4-[6-(3,5-dichlorophenyl)pyrimidin-4-yl]piperazin-2-one Chemical compound ClC1=CC(Cl)=CC(C=2N=CN=C(C=2)N2CC(=O)NCC2)=C1 MVLZWTSKQRHYQE-UHFFFAOYSA-N 0.000 claims description 2
- KIAQGYDLRQLECF-UHFFFAOYSA-N 5-[6-(3,4-dichlorophenyl)pyrimidin-4-yl]-1,2-dihydro-1,2,4-triazol-3-one Chemical compound C1=C(Cl)C(Cl)=CC=C1C1=CC(C=2NC(=O)NN=2)=NC=N1 KIAQGYDLRQLECF-UHFFFAOYSA-N 0.000 claims description 2
- PPMMGNWVXQVXGT-UHFFFAOYSA-N 6-[6-(3,4-dichlorophenyl)pyrimidin-4-yl]-n-methylpyridine-3-carboxamide Chemical compound N1=CC(C(=O)NC)=CC=C1C1=CC(C=2C=C(Cl)C(Cl)=CC=2)=NC=N1 PPMMGNWVXQVXGT-UHFFFAOYSA-N 0.000 claims description 2
- BHSBPFTWYYSYDZ-UHFFFAOYSA-N 6-chloro-2-[6-(3-chlorophenyl)pyrimidin-4-yl]-1h-benzimidazole Chemical compound ClC1=CC=CC(C=2N=CN=C(C=2)C=2NC3=CC(Cl)=CC=C3N=2)=C1 BHSBPFTWYYSYDZ-UHFFFAOYSA-N 0.000 claims description 2
- 208000002381 Brain Hypoxia Diseases 0.000 claims description 2
- 201000006474 Brain Ischemia Diseases 0.000 claims description 2
- 206010008027 Cerebellar atrophy Diseases 0.000 claims description 2
- 206010008120 Cerebral ischaemia Diseases 0.000 claims description 2
- 206010012289 Dementia Diseases 0.000 claims description 2
- 206010019196 Head injury Diseases 0.000 claims description 2
- 206010061216 Infarction Diseases 0.000 claims description 2
- 240000007817 Olea europaea Species 0.000 claims description 2
- 208000018737 Parkinson disease Diseases 0.000 claims description 2
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 2
- 230000002490 cerebral effect Effects 0.000 claims description 2
- 206010008118 cerebral infarction Diseases 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000001153 fluoro group Chemical group F* 0.000 claims description 2
- 230000007574 infarction Effects 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 2
- 230000007170 pathology Effects 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 125000003107 substituted aryl group Chemical group 0.000 claims description 2
- YGPSJZOEDVAXAB-UHFFFAOYSA-N kynurenine Chemical compound OC(=O)C(N)CC(=O)C1=CC=CC=C1N YGPSJZOEDVAXAB-UHFFFAOYSA-N 0.000 claims 2
- 108090000417 Oxygenases Proteins 0.000 claims 1
- 102000004020 Oxygenases Human genes 0.000 claims 1
- 206010015037 epilepsy Diseases 0.000 claims 1
- 159000000001 potassium salts Chemical class 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- 0 *c1c(*)nc(*)nc1* Chemical compound *c1c(*)nc(*)nc1* 0.000 description 1
- 206010036790 Productive cough Diseases 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 210000000278 spinal cord Anatomy 0.000 description 1
- 210000003802 sputum Anatomy 0.000 description 1
- 208000024794 sputum Diseases 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US29809510P | 2010-01-25 | 2010-01-25 | |
| US61/298,095 | 2010-01-25 | ||
| PCT/US2011/021890 WO2011091153A1 (en) | 2010-01-25 | 2011-01-20 | Certain kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2013518046A JP2013518046A (ja) | 2013-05-20 |
| JP2013518046A5 true JP2013518046A5 (enExample) | 2013-12-19 |
Family
ID=44307208
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
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- 2011-01-20 PH PH1/2012/501480A patent/PH12012501480A1/en unknown
- 2011-01-20 US US13/575,019 patent/US8883785B2/en active Active
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- 2011-01-20 RU RU2012133475/04A patent/RU2012133475A/ru not_active Application Discontinuation
- 2011-01-20 CN CN201180015784.XA patent/CN102811620B/zh not_active Expired - Fee Related
- 2011-01-20 AU AU2011207229A patent/AU2011207229B2/en not_active Expired - Fee Related
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- 2011-01-20 JP JP2012550116A patent/JP2013518046A/ja active Pending
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2012
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