CA2557115C - Azabicyclo (3.1.0) hexane derivatives useful as modulators of dopamine d3 receptors - Google Patents
Azabicyclo (3.1.0) hexane derivatives useful as modulators of dopamine d3 receptors Download PDFInfo
- Publication number
- CA2557115C CA2557115C CA2557115A CA2557115A CA2557115C CA 2557115 C CA2557115 C CA 2557115C CA 2557115 A CA2557115 A CA 2557115A CA 2557115 A CA2557115 A CA 2557115A CA 2557115 C CA2557115 C CA 2557115C
- Authority
- CA
- Canada
- Prior art keywords
- methyl
- azabicyclo
- triazol
- propyl
- thio
- 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.)
- Expired - Fee Related
Links
- 102000004073 Dopamine D3 Receptors Human genes 0.000 title claims abstract description 15
- 108090000525 Dopamine D3 Receptors Proteins 0.000 title claims abstract description 15
- QRDSDKAGXMWBID-UHFFFAOYSA-N 5-azabicyclo[3.1.0]hexane Chemical class C1CCN2CC21 QRDSDKAGXMWBID-UHFFFAOYSA-N 0.000 title description 18
- 150000001875 compounds Chemical class 0.000 claims abstract description 348
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 205
- 238000000034 method Methods 0.000 claims abstract description 166
- -1 haloC1-4alkoxy Chemical group 0.000 claims abstract description 141
- 150000003839 salts Chemical class 0.000 claims abstract description 74
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 34
- 150000002367 halogens Chemical class 0.000 claims abstract description 29
- 125000002619 bicyclic group Chemical group 0.000 claims abstract description 26
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 24
- 125000001424 substituent group Chemical group 0.000 claims abstract description 23
- 230000008569 process Effects 0.000 claims abstract description 22
- 239000000460 chlorine Substances 0.000 claims abstract description 21
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 20
- 125000002861 (C1-C4) alkanoyl group Chemical group 0.000 claims abstract description 18
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 18
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 18
- 239000003814 drug Substances 0.000 claims abstract description 18
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 18
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 18
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 18
- 239000001257 hydrogen Substances 0.000 claims abstract description 16
- 125000004076 pyridyl group Chemical group 0.000 claims abstract description 15
- 125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 13
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims abstract description 12
- 125000000842 isoxazolyl group Chemical group 0.000 claims abstract description 12
- 125000000335 thiazolyl group Chemical group 0.000 claims abstract description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 9
- 125000001544 thienyl group Chemical group 0.000 claims abstract description 9
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 7
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims abstract description 5
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims abstract description 5
- 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 103
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 95
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 92
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 70
- 208000028017 Psychotic disease Diseases 0.000 claims description 26
- 238000011282 treatment Methods 0.000 claims description 22
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 22
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims description 21
- 208000011117 substance-related disease Diseases 0.000 claims description 17
- 201000009032 substance abuse Diseases 0.000 claims description 14
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims description 12
- 231100000736 substance abuse Toxicity 0.000 claims description 11
- 241000124008 Mammalia Species 0.000 claims description 10
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 9
- 201000000980 schizophrenia Diseases 0.000 claims description 9
- WGSXKYXKAARAKD-UHFFFAOYSA-N 1-fluoro-3-isocyanato-5-(trifluoromethyl)benzene Chemical group FC1=CC(N=C=O)=CC(C(F)(F)F)=C1 WGSXKYXKAARAKD-UHFFFAOYSA-N 0.000 claims description 8
- 230000009286 beneficial effect Effects 0.000 claims description 8
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 6
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims description 6
- HIRZFMOIKMLUHF-LAUBAEHRSA-N 4-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=CC(=CC=3)C(F)(F)F)=NN=2)C)=C1C HIRZFMOIKMLUHF-LAUBAEHRSA-N 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 125000002971 oxazolyl group Chemical group 0.000 claims description 5
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 5
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 5
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 5
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 5
- 125000001425 triazolyl group Chemical group 0.000 claims description 5
- VUFRFPUOFHXBBM-HRFSGMKKSA-N 5-[5-[3-[(1r,5s)-1-(4-bromophenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-2-methylquinoline Chemical compound C1([C@@]23C[C@@H]2CN(C3)CCCSC2=NN=C(N2C)C=2C3=CC=C(N=C3C=CC=2)C)=CC=C(Br)C=C1 VUFRFPUOFHXBBM-HRFSGMKKSA-N 0.000 claims description 4
- VUFRFPUOFHXBBM-CCLHPLFOSA-N 5-[5-[3-[(1s,5r)-1-(4-bromophenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-2-methylquinoline Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC2=NN=C(N2C)C=2C3=CC=C(N=C3C=CC=2)C)=CC=C(Br)C=C1 VUFRFPUOFHXBBM-CCLHPLFOSA-N 0.000 claims description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000002541 furyl group Chemical group 0.000 claims description 4
- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 claims description 4
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims description 4
- HMMLWDCQIVJIHP-KDYSTLNUSA-N 2-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-phenyl-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]quinoline Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC2=NN=C(N2C)C=2C3=CC=C(N=C3C=CC=2)C)=CC=CC=C1 HMMLWDCQIVJIHP-KDYSTLNUSA-N 0.000 claims description 3
- BIUDHHGROGJSHN-UHFFFAOYSA-N 4-fluoro-3-(trifluoromethyl)benzaldehyde Chemical group FC1=CC=C(C=O)C=C1C(F)(F)F BIUDHHGROGJSHN-UHFFFAOYSA-N 0.000 claims description 3
- URICTYNITRPTLS-UZTOHYMASA-N 5-[5-[3-[(1s,5r)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-2-methylquinoline Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC2=NN=C(N2C)C=2C3=CC=C(N=C3C=CC=2)C)=CC=C(Cl)C(Cl)=C1 URICTYNITRPTLS-UZTOHYMASA-N 0.000 claims description 3
- NKIUMOVWDJZMRB-RBTNQOKQSA-N 5-[5-[3-[(1s,5r)-1-(4-methoxyphenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-2-methylquinoline Chemical compound C1=CC(OC)=CC=C1[C@@]1(CN(CCCSC=2N(C(C=3C4=CC=C(C)N=C4C=CC=3)=NN=2)C)C2)[C@H]2C1 NKIUMOVWDJZMRB-RBTNQOKQSA-N 0.000 claims description 3
- DRKUAUJUSZGTGW-QXNWPYRLSA-N 5-[5-[3-[(1s,5r)-1-(4-tert-butylphenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-2-methylquinoline Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC2=NN=C(N2C)C=2C3=CC=C(N=C3C=CC=2)C)=CC=C(C(C)(C)C)C=C1 DRKUAUJUSZGTGW-QXNWPYRLSA-N 0.000 claims description 3
- ZKRWPAYTJMRKLJ-BTYIYWSLSA-N 5-[5-[3-[(1s,5r)-1-[2-fluoro-4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C(=CC(=CC=3)C(F)(F)F)F)=NN=2)C)=C1C ZKRWPAYTJMRKLJ-BTYIYWSLSA-N 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 3
- ACTJTIJRIQDHEB-PGRDOPGGSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[[4-methyl-5-(oxan-4-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C2CCOCC2)C)=CC=C(Br)C=C1 ACTJTIJRIQDHEB-PGRDOPGGSA-N 0.000 claims description 2
- JJASSNLYKBIBDB-KKSFZXQISA-N (1s,5r)-1-[2-fluoro-4-(trifluoromethyl)phenyl]-3-[3-[(4-methyl-5-pyridazin-4-yl-1,2,4-triazol-3-yl)sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C=2C=NN=CC=2)C)=CC=C(C(F)(F)F)C=C1F JJASSNLYKBIBDB-KKSFZXQISA-N 0.000 claims description 2
- JCQGGPNAPQZIIU-KKSFZXQISA-N (1s,5r)-1-[2-fluoro-4-(trifluoromethyl)phenyl]-3-[3-[(4-methyl-5-pyrimidin-5-yl-1,2,4-triazol-3-yl)sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C=2C=NC=NC=2)C)=CC=C(C(F)(F)F)C=C1F JCQGGPNAPQZIIU-KKSFZXQISA-N 0.000 claims description 2
- IIBPCCLUIAWPNP-SBUREZEXSA-N (1s,5r)-1-[2-fluoro-4-(trifluoromethyl)phenyl]-3-[3-[[4-methyl-5-(2-methylpyridin-3-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound CC1=NC=CC=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C(=CC(=CC=3)C(F)(F)F)F)C[C@H]2C1 IIBPCCLUIAWPNP-SBUREZEXSA-N 0.000 claims description 2
- XMDQXTSZWZHIQV-AOMKIAJQSA-N (1s,5r)-1-[2-fluoro-4-(trifluoromethyl)phenyl]-3-[3-[[4-methyl-5-(5-methylpyrazin-2-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1=NC(C)=CN=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C(=CC(=CC=3)C(F)(F)F)F)C[C@H]2C1 XMDQXTSZWZHIQV-AOMKIAJQSA-N 0.000 claims description 2
- SWSAZAYWDBMULB-MBSDFSHPSA-N (1s,5r)-1-[2-fluoro-4-(trifluoromethyl)phenyl]-3-[3-[[4-methyl-5-[4-(trifluoromethyl)phenyl]-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C=2C=CC(=CC=2)C(F)(F)F)C)=CC=C(C(F)(F)F)C=C1F SWSAZAYWDBMULB-MBSDFSHPSA-N 0.000 claims description 2
- WXNXGSDVKPBNGU-PGRDOPGGSA-N (1s,5r)-3-[3-[(4-methyl-5-phenyl-1,2,4-triazol-3-yl)sulfanyl]propyl]-1-[6-(trifluoromethyl)pyridin-3-yl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C=2C=CC=CC=2)C)=CC=C(C(F)(F)F)N=C1 WXNXGSDVKPBNGU-PGRDOPGGSA-N 0.000 claims description 2
- OTKZOEOQKWTXMD-GHTZIAJQSA-N (1s,5r)-3-[3-[(4-methyl-5-pyridazin-4-yl-1,2,4-triazol-3-yl)sulfanyl]propyl]-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C=2C=NN=CC=2)C)=CC=C(C(F)(F)F)C=C1 OTKZOEOQKWTXMD-GHTZIAJQSA-N 0.000 claims description 2
- ZUBZEOWJXKKPSY-GHTZIAJQSA-N (1s,5r)-3-[3-[(4-methyl-5-pyrimidin-5-yl-1,2,4-triazol-3-yl)sulfanyl]propyl]-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C=2C=NC=NC=2)C)=CC=C(C(F)(F)F)C=C1 ZUBZEOWJXKKPSY-GHTZIAJQSA-N 0.000 claims description 2
- WHGLFZPJAYDODK-WMZHIEFXSA-N (1s,5r)-3-[3-[[4-methyl-5-(2-methylpyridin-3-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound CC1=NC=CC=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=CC(=CC=3)C(F)(F)F)C[C@H]2C1 WHGLFZPJAYDODK-WMZHIEFXSA-N 0.000 claims description 2
- VCUZSEOWZWQCDM-HTAPYJJXSA-N (1s,5r)-3-[3-[[4-methyl-5-(2-methylpyridin-3-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-1-[6-(trifluoromethyl)pyridin-3-yl]-3-azabicyclo[3.1.0]hexane Chemical compound CC1=NC=CC=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=NC(=CC=3)C(F)(F)F)C[C@H]2C1 VCUZSEOWZWQCDM-HTAPYJJXSA-N 0.000 claims description 2
- OWNUCKLLDLFPLN-PGRDOPGGSA-N (1s,5r)-3-[3-[[4-methyl-5-(3-methylfuran-2-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=CC(=CC=3)C(F)(F)F)=NN=2)C)=C1C OWNUCKLLDLFPLN-PGRDOPGGSA-N 0.000 claims description 2
- AEXFOTSQBUVBKJ-PGRDOPGGSA-N (1s,5r)-3-[3-[[4-methyl-5-(5-methylpyrazin-2-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1=NC(C)=CN=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=CC(=CC=3)C(F)(F)F)C[C@H]2C1 AEXFOTSQBUVBKJ-PGRDOPGGSA-N 0.000 claims description 2
- GXTDRNOVSQHWKB-HRAATJIYSA-N (1s,5r)-3-[3-[[4-methyl-5-(5-methylpyrazin-2-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-1-[6-(trifluoromethyl)pyridin-3-yl]-3-azabicyclo[3.1.0]hexane Chemical compound C1=NC(C)=CN=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=NC(=CC=3)C(F)(F)F)C[C@H]2C1 GXTDRNOVSQHWKB-HRAATJIYSA-N 0.000 claims description 2
- CCJLDYTVWAENSM-NZQKXSOJSA-N (1s,5r)-3-[3-[[4-methyl-5-(6-methylpyridin-3-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1=NC(C)=CC=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=CC(=CC=3)C(F)(F)F)C[C@H]2C1 CCJLDYTVWAENSM-NZQKXSOJSA-N 0.000 claims description 2
- RUIZWYILWQFWPT-PGRDOPGGSA-N (1s,5r)-3-[3-[[4-methyl-5-(6-methylpyridin-3-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-1-[6-(trifluoromethyl)pyridin-3-yl]-3-azabicyclo[3.1.0]hexane Chemical compound C1=NC(C)=CC=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=NC(=CC=3)C(F)(F)F)C[C@H]2C1 RUIZWYILWQFWPT-PGRDOPGGSA-N 0.000 claims description 2
- KZBPRKVXUYDFQJ-PGRDOPGGSA-N (1s,5r)-3-[3-[[4-methyl-5-(oxan-4-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-1-[4-(trifluoromethoxy)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C2CCOCC2)C)=CC=C(OC(F)(F)F)C=C1 KZBPRKVXUYDFQJ-PGRDOPGGSA-N 0.000 claims description 2
- HJAJGYFKFFRJEC-SIKLNZKXSA-N (1s,5r)-3-[3-[[4-methyl-5-(oxan-4-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C2CCOCC2)C)=CC=C(C(F)(F)F)C=C1 HJAJGYFKFFRJEC-SIKLNZKXSA-N 0.000 claims description 2
- PTRHJEYSWXFORZ-PGRDOPGGSA-N (1s,5r)-3-[3-[[4-methyl-5-[4-(trifluoromethyl)phenyl]-1,2,4-triazol-3-yl]sulfanyl]propyl]-1-[6-(trifluoromethyl)pyridin-3-yl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C=2C=CC(=CC=2)C(F)(F)F)C)=CC=C(C(F)(F)F)N=C1 PTRHJEYSWXFORZ-PGRDOPGGSA-N 0.000 claims description 2
- SYCYUYFGTJYLJB-PGRDOPGGSA-N (1s,5r)-3-[3-[[5-(1,5-dimethylpyrazol-4-yl)-4-methyl-1,2,4-triazol-3-yl]sulfanyl]propyl]-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1=NN(C)C(C)=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=CC(=CC=3)C(F)(F)F)C[C@H]2C1 SYCYUYFGTJYLJB-PGRDOPGGSA-N 0.000 claims description 2
- WUXMBXJSTUXONL-NBGIEHNGSA-N 1-[2-methoxy-5-[(1s,5r)-3-[3-[(4-methyl-5-pyridin-3-yl-1,2,4-triazol-3-yl)sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]ethanone Chemical compound C1=C(C(C)=O)C(OC)=CC=C1[C@@]1(CN(CCCSC=2N(C(C=3C=NC=CC=3)=NN=2)C)C2)[C@H]2C1 WUXMBXJSTUXONL-NBGIEHNGSA-N 0.000 claims description 2
- YQNWPSNHRUBNBO-MHECFPHRSA-N 1-[2-methoxy-5-[(1s,5r)-3-[3-[[4-methyl-5-(4-methyl-1,3-oxazol-5-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]ethanone Chemical compound C1=C(C(C)=O)C(OC)=CC=C1[C@@]1(CN(CCCSC=2N(C(C3=C(N=CO3)C)=NN=2)C)C2)[C@H]2C1 YQNWPSNHRUBNBO-MHECFPHRSA-N 0.000 claims description 2
- SIWHEXWKLXJQML-NBGIEHNGSA-N 1-[2-methoxy-5-[(1s,5r)-3-[3-[[4-methyl-5-(oxan-4-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]ethanone Chemical compound C1=C(C(C)=O)C(OC)=CC=C1[C@@]1(CN(CCCSC=2N(C(C3CCOCC3)=NN=2)C)C2)[C@H]2C1 SIWHEXWKLXJQML-NBGIEHNGSA-N 0.000 claims description 2
- XHXOKGKTIICKOZ-HFZDXXHNSA-N 1-[2-methoxy-5-[(1s,5r)-3-[3-[[4-methyl-5-[4-(trifluoromethyl)phenyl]-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]ethanone Chemical compound C1=C(C(C)=O)C(OC)=CC=C1[C@@]1(CN(CCCSC=2N(C(C=3C=CC(=CC=3)C(F)(F)F)=NN=2)C)C2)[C@H]2C1 XHXOKGKTIICKOZ-HFZDXXHNSA-N 0.000 claims description 2
- QGHRENZJUREQGK-HRAATJIYSA-N 2,4-dimethyl-5-[4-methyl-5-[3-[(1s,5r)-1-[6-(trifluoromethyl)pyridin-3-yl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-thiazole Chemical compound S1C(C)=NC(C)=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=NC(=CC=3)C(F)(F)F)C[C@H]2C1 QGHRENZJUREQGK-HRAATJIYSA-N 0.000 claims description 2
- PNKRTTBCLUZVBM-NBGIEHNGSA-N 2-methyl-5-[(1s,5r)-3-[3-[(4-methyl-5-phenyl-1,2,4-triazol-3-yl)sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]-1,3-benzothiazole Chemical compound C([C@@H]1C[C@@]1(C1)C=2C=C3N=C(SC3=CC=2)C)N1CCCSC(N1C)=NN=C1C1=CC=CC=C1 PNKRTTBCLUZVBM-NBGIEHNGSA-N 0.000 claims description 2
- CKQJENKLIZUINM-MHECFPHRSA-N 2-methyl-5-[(1s,5r)-3-[3-[[4-methyl-5-(5-methylpyrazin-2-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]-1,3-benzothiazole Chemical compound C([C@@H]1C[C@@]1(C1)C=2C=C3N=C(SC3=CC=2)C)N1CCCSC(N1C)=NN=C1C1=CN=C(C)C=N1 CKQJENKLIZUINM-MHECFPHRSA-N 0.000 claims description 2
- DRBBHLNQSPVHLL-NBGIEHNGSA-N 2-methyl-5-[(1s,5r)-3-[3-[[4-methyl-5-(6-methylpyridin-3-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]-1,3-benzothiazole Chemical compound C([C@@H]1C[C@@]1(C1)C=2C=C3N=C(SC3=CC=2)C)N1CCCSC(N1C)=NN=C1C1=CC=C(C)N=C1 DRBBHLNQSPVHLL-NBGIEHNGSA-N 0.000 claims description 2
- AWJOAMPQOUEKCN-KDYSTLNUSA-N 2-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]quinoline Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC2=NN=C(N2C)C=2C3=CC=C(N=C3C=CC=2)C)=CC=C(C(F)(F)F)C=C1 AWJOAMPQOUEKCN-KDYSTLNUSA-N 0.000 claims description 2
- FIPYQMORLUNLLH-WNCULLNHSA-N 2-methyl-6-[4-methyl-5-[3-[(1s,5r)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]quinoline Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC2=NN=C(N2C)C2=CC3=CC=C(N=C3C=C2)C)=CC=C(C(F)(F)F)C=C1 FIPYQMORLUNLLH-WNCULLNHSA-N 0.000 claims description 2
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims description 2
- JUGUEPMVIYWOOX-HFZDXXHNSA-N 3,5-dimethyl-4-[4-[(1s,5r)-3-[3-[[4-methyl-5-(4-methyl-1,3-oxazol-5-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]-1,2-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=CC(=CC=3)C3=C(ON=C3C)C)=NN=2)C)=C1C JUGUEPMVIYWOOX-HFZDXXHNSA-N 0.000 claims description 2
- CLLQEXUCEWAACY-RBISFHTESA-N 4-[(1s,5r)-3-[3-[[4-methyl-5-(2-methylquinolin-5-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]benzonitrile Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC2=NN=C(N2C)C=2C3=CC=C(N=C3C=CC=2)C)=CC=C(C#N)C=C1 CLLQEXUCEWAACY-RBISFHTESA-N 0.000 claims description 2
- LBUZXCGCCAXMJH-CCLHPLFOSA-N 4-[(1s,5r)-3-[3-[[4-methyl-5-(2-methylquinolin-5-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]phenol Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC2=NN=C(N2C)C=2C3=CC=C(N=C3C=CC=2)C)=CC=C(O)C=C1 LBUZXCGCCAXMJH-CCLHPLFOSA-N 0.000 claims description 2
- LEUDJRMEBMLZBI-FDDCHVKYSA-N 4-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-(1-methylindazol-5-yl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=C4C=NN(C)C4=CC=3)=NN=2)C)=C1C LEUDJRMEBMLZBI-FDDCHVKYSA-N 0.000 claims description 2
- FKRBBYMVCAJBHR-HFZDXXHNSA-N 4-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-[3-(5-methylthiophen-2-yl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound S1C(C)=CC=C1C1=CC=CC([C@@]23[C@@H](C2)CN(CCCSC=2N(C(C4=C(N=CO4)C)=NN=2)C)C3)=C1 FKRBBYMVCAJBHR-HFZDXXHNSA-N 0.000 claims description 2
- RDWUNZTXFIXRPP-NBGIEHNGSA-N 4-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-[4-(5-methyl-1,2-oxazol-3-yl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound O1C(C)=CC(C=2C=CC(=CC=2)[C@@]23[C@@H](C2)CN(CCCSC=2N(C(C4=C(N=CO4)C)=NN=2)C)C3)=N1 RDWUNZTXFIXRPP-NBGIEHNGSA-N 0.000 claims description 2
- MLHRKLZCJRKSHO-UHFFFAOYSA-N 4-methyl-5-[4-methyl-5-[3-[1-[3-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3CC4(CC4C3)C=3C=C(C=CC=3)C(F)(F)F)=NN=2)C)=C1C MLHRKLZCJRKSHO-UHFFFAOYSA-N 0.000 claims description 2
- NRBWMTGEADXYFF-VQBJLOOESA-N 5-[5-[1-[(1s,5r)-1-(3-chloro-4-methoxyphenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propan-2-ylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound C1=C(Cl)C(OC)=CC=C1[C@@]1(CN(CC(C)SC=2N(C(C3=C(N=CO3)C)=NN=2)C)C2)[C@H]2C1 NRBWMTGEADXYFF-VQBJLOOESA-N 0.000 claims description 2
- OTIQETSFLFLTJQ-YCRPNKLZSA-N 5-[5-[3-[(1s,5r)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=C(Cl)C(Cl)=CC=3)=NN=2)C)=C1C OTIQETSFLFLTJQ-YCRPNKLZSA-N 0.000 claims description 2
- YFAACACUMCZFCU-HRAATJIYSA-N 5-[5-[3-[(1s,5r)-1-(3-bromophenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=C(Br)C=CC=3)=NN=2)C)=C1C YFAACACUMCZFCU-HRAATJIYSA-N 0.000 claims description 2
- RDNMLFUSVMBDDY-VXKWHMMOSA-N 5-[5-[3-[(1s,5r)-1-(3-chlorophenyl)-5-methyl-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@@]4(C[C@@]4(C)C3)C=3C=C(Cl)C=CC=3)=NN=2)C)=C1C RDNMLFUSVMBDDY-VXKWHMMOSA-N 0.000 claims description 2
- QRXTUDGXPZADAH-NPMXOYFQSA-N 5-[5-[3-[(1s,5r)-1-(4-bromophenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-1-methyl-3-(trifluoromethyl)thieno[2,3-c]pyrazole Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C=2SC=3N(C)N=C(C=3C=2)C(F)(F)F)C)=CC=C(Br)C=C1 QRXTUDGXPZADAH-NPMXOYFQSA-N 0.000 claims description 2
- AVTONHYDPSFOLQ-HTAPYJJXSA-N 5-[5-[3-[(1s,5r)-1-(4-methoxyphenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound C1=CC(OC)=CC=C1[C@@]1(CN(CCCSC=2N(C(C3=C(N=CO3)C)=NN=2)C)C2)[C@H]2C1 AVTONHYDPSFOLQ-HTAPYJJXSA-N 0.000 claims description 2
- KBYDKOYJEQUBOE-NBGIEHNGSA-N 5-[5-[3-[(1s,5r)-1-(4-tert-butylphenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=CC(=CC=3)C(C)(C)C)=NN=2)C)=C1C KBYDKOYJEQUBOE-NBGIEHNGSA-N 0.000 claims description 2
- VLGWIPCXNBQWLT-BTYIYWSLSA-N 5-[5-[3-[(1s,5r)-1-[2-fluoro-5-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C(=CC=C(C=3)C(F)(F)F)F)=NN=2)C)=C1C VLGWIPCXNBQWLT-BTYIYWSLSA-N 0.000 claims description 2
- WKHUFILLPNZZHI-HFZDXXHNSA-N 5-[5-[3-[(1s,5r)-1-[3-(2,4-dimethyl-1,3-thiazol-5-yl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound S1C(C)=NC(C)=C1C1=CC=CC([C@@]23[C@@H](C2)CN(CCCSC=2N(C(C4=C(N=CO4)C)=NN=2)C)C3)=C1 WKHUFILLPNZZHI-HFZDXXHNSA-N 0.000 claims description 2
- DUOGVBWBIVGZCL-HFZDXXHNSA-N 5-[5-[3-[(1s,5r)-1-[4-(2,4-dimethyl-1,3-thiazol-5-yl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound S1C(C)=NC(C)=C1C1=CC=C([C@@]23[C@@H](C2)CN(CCCSC=2N(C(C4=C(N=CO4)C)=NN=2)C)C3)C=C1 DUOGVBWBIVGZCL-HFZDXXHNSA-N 0.000 claims description 2
- BYFBIHGWAJPFIB-YCRPNKLZSA-N 5-[5-[3-[(1s,5r)-1-[4-fluoro-3-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=C(C(F)=CC=3)C(F)(F)F)=NN=2)C)=C1C BYFBIHGWAJPFIB-YCRPNKLZSA-N 0.000 claims description 2
- JASDXILVHIDXCQ-UHFFFAOYSA-N 5-[5-[3-[1-(4-chlorophenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3CC4(CC4C3)C=3C=CC(Cl)=CC=3)=NN=2)C)=C1C JASDXILVHIDXCQ-UHFFFAOYSA-N 0.000 claims description 2
- PSAASTBVOYWQMI-CJAUYULYSA-N 1-[2-methoxy-5-[(1r,5s)-3-[3-[[4-methyl-5-(4-methyl-1,3-oxazol-5-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]propan-1-one Chemical compound C1=C(OC)C(C(=O)CC)=CC([C@]23[C@H](C2)CN(CCCSC=2N(C(C4=C(N=CO4)C)=NN=2)C)C3)=C1 PSAASTBVOYWQMI-CJAUYULYSA-N 0.000 claims 2
- UAOBDKREOZMZJQ-HXOBKFHXSA-N 4-methyl-5-[4-methyl-5-[3-[(1r,5s)-1-(2-methyl-1,3-benzothiazol-5-yl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound C([C@H]1C[C@]1(C1)C=2C=C3N=C(SC3=CC=2)C)N1CCCSC(N1C)=NN=C1C=1OC=NC=1C UAOBDKREOZMZJQ-HXOBKFHXSA-N 0.000 claims 2
- MLHRKLZCJRKSHO-UTKZUKDTSA-N 4-methyl-5-[4-methyl-5-[3-[(1r,5s)-1-[3-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@@]4(C[C@@H]4C3)C=3C=C(C=CC=3)C(F)(F)F)=NN=2)C)=C1C MLHRKLZCJRKSHO-UTKZUKDTSA-N 0.000 claims 2
- GLSJOAMLOIMSGI-KMDAROACSA-N 4-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]butylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound C([C@]1(C[C@H]1C1)C=2C=CC(=CC=2)C(F)(F)F)N1C(C)CCSC(N1C)=NN=C1C=1OC=NC=1C GLSJOAMLOIMSGI-KMDAROACSA-N 0.000 claims 2
- RDNMLFUSVMBDDY-FGZHOGPDSA-N 5-[5-[3-[(1r,5s)-1-(3-chlorophenyl)-5-methyl-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@]4(C)C3)C=3C=C(Cl)C=CC=3)=NN=2)C)=C1C RDNMLFUSVMBDDY-FGZHOGPDSA-N 0.000 claims 2
- NKIUMOVWDJZMRB-PIKZIKFNSA-N 5-[5-[3-[(1r,5s)-1-(4-methoxyphenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-2-methylquinoline Chemical compound C1=CC(OC)=CC=C1[C@]1(CN(CCCSC=2N(C(C=3C4=CC=C(C)N=C4C=CC=3)=NN=2)C)C2)[C@@H]2C1 NKIUMOVWDJZMRB-PIKZIKFNSA-N 0.000 claims 2
- DRKUAUJUSZGTGW-XJFCNFDWSA-N 5-[5-[3-[(1r,5s)-1-(4-tert-butylphenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-2-methylquinoline Chemical compound C1([C@@]23C[C@@H]2CN(C3)CCCSC2=NN=C(N2C)C=2C3=CC=C(N=C3C=CC=2)C)=CC=C(C(C)(C)C)C=C1 DRKUAUJUSZGTGW-XJFCNFDWSA-N 0.000 claims 2
- GKACMWQTMKXQPT-WMZHIEFXSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[(4-ethyl-5-pyridin-3-yl-1,2,4-triazol-3-yl)sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C=2C=NC=CC=2)CC)=CC=C(Br)C=C1 GKACMWQTMKXQPT-WMZHIEFXSA-N 0.000 claims 1
- POPJUDCEQMELRU-LAUBAEHRSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[(4-methyl-5-pyridazin-4-yl-1,2,4-triazol-3-yl)sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C=2C=NN=CC=2)C)=CC=C(Br)C=C1 POPJUDCEQMELRU-LAUBAEHRSA-N 0.000 claims 1
- HTPVMIVXLCGVPI-PGRDOPGGSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[(4-methyl-5-pyridin-3-yl-1,2,4-triazol-3-yl)sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C=2C=NC=CC=2)C)=CC=C(Br)C=C1 HTPVMIVXLCGVPI-PGRDOPGGSA-N 0.000 claims 1
- ZUWBWKOPWGGXEZ-LAUBAEHRSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[(4-methyl-5-pyrimidin-5-yl-1,2,4-triazol-3-yl)sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C=2C=NC=NC=2)C)=CC=C(Br)C=C1 ZUWBWKOPWGGXEZ-LAUBAEHRSA-N 0.000 claims 1
- SZFGGKSIQQDFKO-MGPUTAFESA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[[4-methyl-5-(1-methyltriazol-4-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound N1=NN(C)C=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=CC(Br)=CC=3)C[C@H]2C1 SZFGGKSIQQDFKO-MGPUTAFESA-N 0.000 claims 1
- ZOVUVPBEDQGAEY-HRAATJIYSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[[4-methyl-5-(2-methylpyrazol-3-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound CN1N=CC=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=CC(Br)=CC=3)C[C@H]2C1 ZOVUVPBEDQGAEY-HRAATJIYSA-N 0.000 claims 1
- WCOFNBHSYDWYKP-HTAPYJJXSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[[4-methyl-5-(3-methylfuran-2-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=CC(Br)=CC=3)=NN=2)C)=C1C WCOFNBHSYDWYKP-HTAPYJJXSA-N 0.000 claims 1
- XPYNDTGYDNWMBS-FDDCHVKYSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[[4-methyl-5-(3-methylpyridin-2-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound CC1=CC=CN=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=CC(Br)=CC=3)C[C@H]2C1 XPYNDTGYDNWMBS-FDDCHVKYSA-N 0.000 claims 1
- TVOWXONSXDBYAG-WMZHIEFXSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[[4-methyl-5-(5-methylpyridin-3-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound CC1=CN=CC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=CC(Br)=CC=3)=NN=2)C)=C1 TVOWXONSXDBYAG-WMZHIEFXSA-N 0.000 claims 1
- XWYQMRGVVCAGPL-WMZHIEFXSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[[4-methyl-5-(6-methylpyridin-3-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1=NC(C)=CC=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=CC(Br)=CC=3)C[C@H]2C1 XWYQMRGVVCAGPL-WMZHIEFXSA-N 0.000 claims 1
- GIWTTYIZASKYKT-YCRPNKLZSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[[4-methyl-5-[1-methyl-3-(trifluoromethyl)pyrazol-4-yl]-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound FC(F)(F)C1=NN(C)C=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=CC(Br)=CC=3)C[C@H]2C1 GIWTTYIZASKYKT-YCRPNKLZSA-N 0.000 claims 1
- NVNFYUKRFGJWDM-GAJHUEQPSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[[4-methyl-5-[2-methyl-6-(trifluoromethyl)pyridin-3-yl]-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound CC1=NC(C(F)(F)F)=CC=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=CC(Br)=CC=3)C[C@H]2C1 NVNFYUKRFGJWDM-GAJHUEQPSA-N 0.000 claims 1
- AIEYZNFNEQHWKO-WMZHIEFXSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[[4-methyl-5-[4-(trifluoromethyl)phenyl]-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C=2C=CC(=CC=2)C(F)(F)F)C)=CC=C(Br)C=C1 AIEYZNFNEQHWKO-WMZHIEFXSA-N 0.000 claims 1
- BUNMQAXAYZRBJI-HTAPYJJXSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[[5-(1,5-dimethylpyrazol-4-yl)-4-methyl-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1=NN(C)C(C)=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=CC(Br)=CC=3)C[C@H]2C1 BUNMQAXAYZRBJI-HTAPYJJXSA-N 0.000 claims 1
- DHPMGQUNTCQWHG-FDDCHVKYSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[[5-(2,5-dimethylfuran-3-yl)-4-methyl-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound O1C(C)=CC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=CC(Br)=CC=3)=NN=2)C)=C1C DHPMGQUNTCQWHG-FDDCHVKYSA-N 0.000 claims 1
- BCASKIBJIZNNHQ-GAJHUEQPSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[[5-(3,4-difluorophenyl)-4-methyl-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C=2C=C(F)C(F)=CC=2)C)=CC=C(Br)C=C1 BCASKIBJIZNNHQ-GAJHUEQPSA-N 0.000 claims 1
- ICMWFZOZUUSQNF-YCRPNKLZSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[[5-(5-chloro-1-methylpyrazol-4-yl)-4-methyl-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound CN1N=CC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=CC(Br)=CC=3)=NN=2)C)=C1Cl ICMWFZOZUUSQNF-YCRPNKLZSA-N 0.000 claims 1
- HRNYFPHZFKDZFM-YCRPNKLZSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[[5-(5-chlorothiophen-2-yl)-4-methyl-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C=2SC(Cl)=CC=2)C)=CC=C(Br)C=C1 HRNYFPHZFKDZFM-YCRPNKLZSA-N 0.000 claims 1
- HSORSBPOHUZXNY-KCWXNJEJSA-N 1-[2-hydroxy-5-[(1s,5r)-3-[3-[[4-methyl-5-(2-methylquinolin-5-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]ethanone Chemical compound C1=C(O)C(C(=O)C)=CC([C@@]23[C@@H](C2)CN(CCCSC=2N(C(C=4C5=CC=C(C)N=C5C=CC=4)=NN=2)C)C3)=C1 HSORSBPOHUZXNY-KCWXNJEJSA-N 0.000 claims 1
- UHFLLBIGYQQGJT-GAJHUEQPSA-N 1-[2-hydroxy-5-[(1s,5r)-3-[3-[[4-methyl-5-(4-methyl-1,3-oxazol-5-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]ethanone Chemical compound C1=C(O)C(C(=O)C)=CC([C@@]23[C@@H](C2)CN(CCCSC=2N(C(C4=C(N=CO4)C)=NN=2)C)C3)=C1 UHFLLBIGYQQGJT-GAJHUEQPSA-N 0.000 claims 1
- OOUUSTJOZYKIFZ-MHECFPHRSA-N 1-[2-methoxy-4-[(1s,5r)-3-[3-[[4-methyl-5-(4-methyl-1,3-oxazol-5-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]ethanone Chemical compound C1=C(C(C)=O)C(OC)=CC([C@@]23[C@@H](C2)CN(CCCSC=2N(C(C4=C(N=CO4)C)=NN=2)C)C3)=C1 OOUUSTJOZYKIFZ-MHECFPHRSA-N 0.000 claims 1
- GHYALLPUTLGENT-AVRWGWEMSA-N 1-[2-methoxy-4-[(1s,5r)-3-[3-[[4-methyl-5-(4-methyl-1,3-oxazol-5-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]propan-1-one Chemical compound C1=C(OC)C(C(=O)CC)=CC=C1[C@@]1(CN(CCCSC=2N(C(C3=C(N=CO3)C)=NN=2)C)C2)[C@H]2C1 GHYALLPUTLGENT-AVRWGWEMSA-N 0.000 claims 1
- WWMANSPKRWDTJQ-SMSORMJASA-N 1-[2-methoxy-5-[(1s,5r)-3-[3-[[4-methyl-5-(2-methylquinolin-5-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]ethanone Chemical compound C1=C(C(C)=O)C(OC)=CC=C1[C@@]1(CN(CCCSC=2N(C(C=3C4=CC=C(C)N=C4C=CC=3)=NN=2)C)C2)[C@H]2C1 WWMANSPKRWDTJQ-SMSORMJASA-N 0.000 claims 1
- PSAASTBVOYWQMI-AVRWGWEMSA-N 1-[2-methoxy-5-[(1s,5r)-3-[3-[[4-methyl-5-(4-methyl-1,3-oxazol-5-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]propan-1-one Chemical class C1=C(OC)C(C(=O)CC)=CC([C@@]23[C@@H](C2)CN(CCCSC=2N(C(C4=C(N=CO4)C)=NN=2)C)C3)=C1 PSAASTBVOYWQMI-AVRWGWEMSA-N 0.000 claims 1
- CDTMYUYGZNHOPV-GTYOFVGBSA-N 1-[4-[(1s,5r)-3-[3-[[4-methyl-5-(2-methylquinolin-5-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]pyrrolidin-2-one Chemical compound C1=CC([C@]23C[C@H]2CN(C3)CCCSC2=NN=C(N2C)C=2C3=CC=C(N=C3C=CC=2)C)=CC=C1N1CCCC1=O CDTMYUYGZNHOPV-GTYOFVGBSA-N 0.000 claims 1
- ZKGLMIMJGUYTID-AVRWGWEMSA-N 1-[5-[(1s,5r)-3-[3-[[5-(3,4-difluorophenyl)-4-methyl-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]-2-hydroxyphenyl]ethanone Chemical compound C1=C(O)C(C(=O)C)=CC([C@@]23[C@@H](C2)CN(CCCSC=2N(C(C=4C=C(F)C(F)=CC=4)=NN=2)C)C3)=C1 ZKGLMIMJGUYTID-AVRWGWEMSA-N 0.000 claims 1
- DBHVXGHVYLHGTG-AFMDSPMNSA-N 1-[5-[(1s,5r)-3-[3-[[5-(3,4-difluorophenyl)-4-methyl-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]-2-methoxyphenyl]ethanone Chemical compound C1=C(C(C)=O)C(OC)=CC=C1[C@@]1(CN(CCCSC=2N(C(C=3C=C(F)C(F)=CC=3)=NN=2)C)C2)[C@H]2C1 DBHVXGHVYLHGTG-AFMDSPMNSA-N 0.000 claims 1
- ODIJMXCJWMOZFJ-PGRDOPGGSA-N 2,4-dimethyl-5-[4-methyl-5-[3-[(1s,5r)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-thiazole Chemical compound S1C(C)=NC(C)=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=CC(=CC=3)C(F)(F)F)C[C@H]2C1 ODIJMXCJWMOZFJ-PGRDOPGGSA-N 0.000 claims 1
- SQHSACZAZLANKD-YCRPNKLZSA-N 4-[5-[3-[(1s,5r)-1-(4-bromophenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-2-methyl-5-(trifluoromethyl)-1,3-oxazole Chemical compound O1C(C)=NC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=CC(Br)=CC=3)=NN=2)C)=C1C(F)(F)F SQHSACZAZLANKD-YCRPNKLZSA-N 0.000 claims 1
- FPFPTUKYJWTWPY-YWZLYKJASA-N 4-methyl-5-[4-methyl-5-[3-[(1r,5r)-1-[5-(trifluoromethyl)pyridin-2-yl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3N=CC(=CC=3)C(F)(F)F)=NN=2)C)=C1C FPFPTUKYJWTWPY-YWZLYKJASA-N 0.000 claims 1
- JWUUYXCKKOYVDZ-XOBRGWDASA-N 4-methyl-5-[4-methyl-5-[3-[(1r,5r)-1-[6-(trifluoromethyl)pyridin-2-yl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3N=C(C=CC=3)C(F)(F)F)=NN=2)C)=C1C JWUUYXCKKOYVDZ-XOBRGWDASA-N 0.000 claims 1
- UAOBDKREOZMZJQ-GAJHUEQPSA-N 4-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-(2-methyl-1,3-benzothiazol-5-yl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound C([C@@H]1C[C@@]1(C1)C=2C=C3N=C(SC3=CC=2)C)N1CCCSC(N1C)=NN=C1C=1OC=NC=1C UAOBDKREOZMZJQ-GAJHUEQPSA-N 0.000 claims 1
- OIERNJOFVGMUEF-GAJHUEQPSA-N 4-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-(2-methyl-1,3-benzothiazol-6-yl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound C([C@@H]1C[C@@]1(C1)C2=CC=C3N=C(SC3=C2)C)N1CCCSC(N1C)=NN=C1C=1OC=NC=1C OIERNJOFVGMUEF-GAJHUEQPSA-N 0.000 claims 1
- KYPWROFHQUYOCS-BTYIYWSLSA-N 4-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-[2-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C(=CC=CC=3)C(F)(F)F)=NN=2)C)=C1C KYPWROFHQUYOCS-BTYIYWSLSA-N 0.000 claims 1
- KFCVKULFYARZLT-JTSKRJEESA-N 4-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-[2-methyl-4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C(=CC(=CC=3)C(F)(F)F)C)=NN=2)C)=C1C KFCVKULFYARZLT-JTSKRJEESA-N 0.000 claims 1
- MLHRKLZCJRKSHO-LAUBAEHRSA-N 4-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-[3-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=C(C=CC=3)C(F)(F)F)=NN=2)C)=C1C MLHRKLZCJRKSHO-LAUBAEHRSA-N 0.000 claims 1
- SRVOWVHRVJSZKO-HRAATJIYSA-N 4-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-[4-(trifluoromethoxy)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=CC(OC(F)(F)F)=CC=3)=NN=2)C)=C1C SRVOWVHRVJSZKO-HRAATJIYSA-N 0.000 claims 1
- STMFIEJAIJCUPM-RXFWQSSRSA-N 4-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-[4-[6-(trifluoromethyl)pyridin-2-yl]phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=CC(=CC=3)C=3N=C(C=CC=3)C(F)(F)F)=NN=2)C)=C1C STMFIEJAIJCUPM-RXFWQSSRSA-N 0.000 claims 1
- QWTAGVPLIGQGIW-MGPUTAFESA-N 4-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-[6-(trifluoromethyl)pyridin-3-yl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=NC(=CC=3)C(F)(F)F)=NN=2)C)=C1C QWTAGVPLIGQGIW-MGPUTAFESA-N 0.000 claims 1
- YYLVZNFHPHPLKB-LAUBAEHRSA-N 4-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-phenyl-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=CC=CC=3)=NN=2)C)=C1C YYLVZNFHPHPLKB-LAUBAEHRSA-N 0.000 claims 1
- UXBIDSXSMDZFKR-MHECFPHRSA-N 5-[(1s,5r)-3-[3-[[5-(2,4-dimethyl-1,3-thiazol-5-yl)-4-methyl-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]-2-methyl-1,3-benzothiazole Chemical compound S1C(C)=NC(C)=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=C4N=C(C)SC4=CC=3)C[C@H]2C1 UXBIDSXSMDZFKR-MHECFPHRSA-N 0.000 claims 1
- MHDWNZWHPYKUAY-UJPJHGMFSA-N 5-[5-[1-[(1s,5r)-1-(2-chloro-4-methylphenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propan-2-ylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound C1([C@]23C[C@H]2CN(C3)CC(C)SC=2N(C(C3=C(N=CO3)C)=NN=2)C)=CC=C(C)C=C1Cl MHDWNZWHPYKUAY-UJPJHGMFSA-N 0.000 claims 1
- JEBLLBOUXXZBPR-HRAATJIYSA-N 5-[5-[3-[(1s,5r)-1-(3-fluorophenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=C(F)C=CC=3)=NN=2)C)=C1C JEBLLBOUXXZBPR-HRAATJIYSA-N 0.000 claims 1
- VSHFJDFDEHUHMG-HTAPYJJXSA-N 5-[5-[3-[(1s,5r)-1-(3-methoxyphenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound COC1=CC=CC([C@@]23[C@@H](C2)CN(CCCSC=2N(C(C4=C(N=CO4)C)=NN=2)C)C3)=C1 VSHFJDFDEHUHMG-HTAPYJJXSA-N 0.000 claims 1
- QYIGIFAPYBZLOA-HTAPYJJXSA-N 5-[5-[3-[(1s,5r)-1-(4-bromophenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-2,4-dimethyl-1,3-thiazole Chemical compound S1C(C)=NC(C)=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=CC(Br)=CC=3)C[C@H]2C1 QYIGIFAPYBZLOA-HTAPYJJXSA-N 0.000 claims 1
- RWAAUSOBGQKJNX-HRAATJIYSA-N 5-[5-[3-[(1s,5r)-1-(4-bromophenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-3-methyl-1,2-oxazole Chemical compound O1N=C(C)C=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=CC(Br)=CC=3)C[C@H]2C1 RWAAUSOBGQKJNX-HRAATJIYSA-N 0.000 claims 1
- JASDXILVHIDXCQ-HRAATJIYSA-N 5-[5-[3-[(1s,5r)-1-(4-chlorophenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=CC(Cl)=CC=3)=NN=2)C)=C1C JASDXILVHIDXCQ-HRAATJIYSA-N 0.000 claims 1
- QLOCSQXNJJSRQH-HRAATJIYSA-N 5-[5-[3-[(1s,5r)-1-(4-fluorophenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=CC(F)=CC=3)=NN=2)C)=C1C QLOCSQXNJJSRQH-HRAATJIYSA-N 0.000 claims 1
- LLTRSGMRUYHGQM-AOMKIAJQSA-N 5-[5-[3-[(1s,5r)-1-[2-fluoro-4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-2,4-dimethyl-1,3-oxazole Chemical compound O1C(C)=NC(C)=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C(=CC(=CC=3)C(F)(F)F)F)C[C@H]2C1 LLTRSGMRUYHGQM-AOMKIAJQSA-N 0.000 claims 1
- CRZBMVVRCINCBG-AOMKIAJQSA-N 5-[5-[3-[(1s,5r)-1-[2-fluoro-4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-2,4-dimethyl-1,3-thiazole Chemical compound S1C(C)=NC(C)=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C(=CC(=CC=3)C(F)(F)F)F)C[C@H]2C1 CRZBMVVRCINCBG-AOMKIAJQSA-N 0.000 claims 1
- ZGGNCUMBXZMKPD-HFZDXXHNSA-N 5-[5-[3-[(1s,5r)-1-[3-fluoro-4-(pyrrol-1-ylmethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C=C(F)C(CN4C=CC=C4)=CC=3)=NN=2)C)=C1C ZGGNCUMBXZMKPD-HFZDXXHNSA-N 0.000 claims 1
- ZKRWPAYTJMRKLJ-UHFFFAOYSA-N 5-[5-[3-[1-[2-fluoro-4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCN3CC4(CC4C3)C=3C(=CC(=CC=3)C(F)(F)F)F)=NN=2)C)=C1C ZKRWPAYTJMRKLJ-UHFFFAOYSA-N 0.000 claims 1
- ZZOVGFQEPXCORG-CCLHPLFOSA-N 8-fluoro-2-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]quinoline Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC2=NN=C(N2C)C=2C3=CC=C(N=C3C(F)=CC=2)C)=CC=C(C(F)(F)F)C=C1 ZZOVGFQEPXCORG-CCLHPLFOSA-N 0.000 claims 1
- 238000002360 preparation method Methods 0.000 abstract description 188
- 229940079593 drug Drugs 0.000 abstract description 14
- 239000000543 intermediate Substances 0.000 abstract description 8
- 239000000164 antipsychotic agent Substances 0.000 abstract description 4
- 238000002560 therapeutic procedure Methods 0.000 abstract description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 287
- 239000007787 solid Substances 0.000 description 166
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 164
- 238000005481 NMR spectroscopy Methods 0.000 description 147
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 128
- 239000000243 solution Substances 0.000 description 99
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 93
- 239000000203 mixture Substances 0.000 description 92
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 72
- 238000001514 detection method Methods 0.000 description 60
- 239000003480 eluent Substances 0.000 description 58
- 239000002904 solvent Substances 0.000 description 57
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 57
- 229910001868 water Inorganic materials 0.000 description 57
- 235000019441 ethanol Nutrition 0.000 description 54
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 49
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 48
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 47
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 47
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 46
- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 description 45
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 45
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 43
- 238000004808 supercritical fluid chromatography Methods 0.000 description 43
- OKKJLVBELUTLKV-MZCSYVLQSA-N Deuterated methanol Chemical compound [2H]OC([2H])([2H])[2H] OKKJLVBELUTLKV-MZCSYVLQSA-N 0.000 description 40
- 229910052938 sodium sulfate Inorganic materials 0.000 description 38
- 235000011152 sodium sulphate Nutrition 0.000 description 38
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 37
- 239000012458 free base Substances 0.000 description 37
- 238000001851 vibrational circular dichroism spectroscopy Methods 0.000 description 37
- 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 35
- 230000014759 maintenance of location Effects 0.000 description 33
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 31
- 239000007832 Na2SO4 Substances 0.000 description 30
- 239000000463 material Substances 0.000 description 28
- 230000003287 optical effect Effects 0.000 description 28
- 239000011541 reaction mixture Substances 0.000 description 27
- 229910052796 boron Inorganic materials 0.000 description 26
- 235000019439 ethyl acetate Nutrition 0.000 description 26
- 235000019253 formic acid Nutrition 0.000 description 24
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 24
- 238000001228 spectrum Methods 0.000 description 24
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 23
- 230000002829 reductive effect Effects 0.000 description 23
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 23
- 239000012044 organic layer Substances 0.000 description 22
- 239000012043 crude product Substances 0.000 description 21
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 20
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 19
- 239000003921 oil Substances 0.000 description 19
- 235000019198 oils Nutrition 0.000 description 19
- 239000012071 phase Substances 0.000 description 19
- 238000003756 stirring Methods 0.000 description 19
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 18
- 229910052757 nitrogen Inorganic materials 0.000 description 18
- 229920006395 saturated elastomer Polymers 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 17
- 208000035475 disorder Diseases 0.000 description 17
- 238000004128 high performance liquid chromatography Methods 0.000 description 17
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 16
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 16
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 16
- 238000004458 analytical method Methods 0.000 description 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 16
- 239000000706 filtrate Substances 0.000 description 15
- 230000035987 intoxication Effects 0.000 description 15
- 231100000566 intoxication Toxicity 0.000 description 15
- 239000012074 organic phase Substances 0.000 description 15
- 239000000725 suspension Substances 0.000 description 15
- 229910052799 carbon Inorganic materials 0.000 description 14
- 238000001914 filtration Methods 0.000 description 14
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 14
- 238000007792 addition Methods 0.000 description 13
- 239000000047 product Substances 0.000 description 13
- DTQVDTLACAAQTR-UHFFFAOYSA-N trifluoroacetic acid Substances OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 13
- IWDGZABFNGRZPF-WDEREUQCSA-N (1s,5r)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1=CC(C(F)(F)F)=CC=C1[C@@]1(CNC2)[C@H]2C1 IWDGZABFNGRZPF-WDEREUQCSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 12
- 230000000694 effects Effects 0.000 description 12
- 229940002612 prodrug Drugs 0.000 description 12
- 239000000651 prodrug Substances 0.000 description 12
- 239000012047 saturated solution Substances 0.000 description 12
- 208000019901 Anxiety disease Diseases 0.000 description 11
- 206010012218 Delirium Diseases 0.000 description 11
- 239000002585 base Substances 0.000 description 11
- 238000003818 flash chromatography Methods 0.000 description 11
- 238000010992 reflux Methods 0.000 description 11
- 235000017557 sodium bicarbonate Nutrition 0.000 description 11
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 11
- 238000003556 assay Methods 0.000 description 10
- FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 10
- 229960004132 diethyl ether Drugs 0.000 description 10
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 10
- 125000004043 oxo group Chemical group O=* 0.000 description 10
- 229910000027 potassium carbonate Inorganic materials 0.000 description 10
- 125000006239 protecting group Chemical group 0.000 description 10
- 239000000741 silica gel Substances 0.000 description 10
- 229910002027 silica gel Inorganic materials 0.000 description 10
- 238000000746 purification Methods 0.000 description 9
- BSMNRYCSBFHEMQ-GZMMTYOYSA-N (1s,5r)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane Chemical compound C1=C(Cl)C(Cl)=CC=C1[C@@]1(CNC2)[C@H]2C1 BSMNRYCSBFHEMQ-GZMMTYOYSA-N 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 208000019022 Mood disease Diseases 0.000 description 8
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 8
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 8
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 8
- 239000012267 brine Substances 0.000 description 8
- 239000013078 crystal Substances 0.000 description 8
- 238000001704 evaporation Methods 0.000 description 8
- 230000008020 evaporation Effects 0.000 description 8
- 125000005842 heteroatom Chemical group 0.000 description 8
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 8
- 102000005962 receptors Human genes 0.000 description 8
- 108020003175 receptors Proteins 0.000 description 8
- 238000011894 semi-preparative HPLC Methods 0.000 description 8
- 208000019116 sleep disease Diseases 0.000 description 8
- 229910000029 sodium carbonate Inorganic materials 0.000 description 8
- 235000017550 sodium carbonate Nutrition 0.000 description 8
- 229910000104 sodium hydride Inorganic materials 0.000 description 8
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 8
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 7
- 101150041968 CDC13 gene Proteins 0.000 description 7
- 102000015554 Dopamine receptor Human genes 0.000 description 7
- 108050004812 Dopamine receptor Proteins 0.000 description 7
- MFESCIUQSIBMSM-UHFFFAOYSA-N I-BCP Chemical compound ClCCCBr MFESCIUQSIBMSM-UHFFFAOYSA-N 0.000 description 7
- 201000001880 Sexual dysfunction Diseases 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 7
- 210000004027 cell Anatomy 0.000 description 7
- 238000001816 cooling Methods 0.000 description 7
- 206010013663 drug dependence Diseases 0.000 description 7
- 125000005843 halogen group Chemical group 0.000 description 7
- 239000010410 layer Substances 0.000 description 7
- 239000002244 precipitate Substances 0.000 description 7
- 231100000872 sexual dysfunction Toxicity 0.000 description 7
- 208000020685 sleep-wake disease Diseases 0.000 description 7
- 239000003039 volatile agent Substances 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
- QCZWAZSRPCRGMC-UHFFFAOYSA-N 5-[5-(3-chloropropylsulfanyl)-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCCl)=NN=2)C)=C1C QCZWAZSRPCRGMC-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 6
- 206010013654 Drug abuse Diseases 0.000 description 6
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- ZVDDJPSHRNMSKV-UHFFFAOYSA-N acetaldehyde;hydrochloride Chemical compound Cl.CC=O ZVDDJPSHRNMSKV-UHFFFAOYSA-N 0.000 description 6
- 239000002249 anxiolytic agent Substances 0.000 description 6
- 230000000949 anxiolytic effect Effects 0.000 description 6
- 229910000024 caesium carbonate Inorganic materials 0.000 description 6
- XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Chemical compound [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 description 6
- ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 description 6
- 239000012230 colorless oil Substances 0.000 description 6
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 230000000147 hypnotic effect Effects 0.000 description 6
- 238000001727 in vivo Methods 0.000 description 6
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 6
- 239000008188 pellet Substances 0.000 description 6
- 239000000932 sedative agent Substances 0.000 description 6
- 230000001624 sedative effect Effects 0.000 description 6
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 6
- 230000003595 spectral effect Effects 0.000 description 6
- BPLKQGGAXWRFOE-UHFFFAOYSA-M trimethylsulfoxonium iodide Chemical compound [I-].C[S+](C)(C)=O BPLKQGGAXWRFOE-UHFFFAOYSA-M 0.000 description 6
- CXNIUSPIQKWYAI-UHFFFAOYSA-N xantphos Chemical compound C=12OC3=C(P(C=4C=CC=CC=4)C=4C=CC=CC=4)C=CC=C3C(C)(C)C2=CC=CC=1P(C=1C=CC=CC=1)C1=CC=CC=C1 CXNIUSPIQKWYAI-UHFFFAOYSA-N 0.000 description 6
- ZCHPFSLSIJTHFX-KWQFWETISA-N (1s,5r)-1-[2-fluoro-4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound FC1=CC(C(F)(F)F)=CC=C1[C@@]1(CNC2)[C@H]2C1 ZCHPFSLSIJTHFX-KWQFWETISA-N 0.000 description 5
- KWTSXDURSIMDCE-QMMMGPOBSA-N (S)-amphetamine Chemical compound C[C@H](N)CC1=CC=CC=C1 KWTSXDURSIMDCE-QMMMGPOBSA-N 0.000 description 5
- IWYDHOAUDWTVEP-ZETCQYMHSA-N (S)-mandelic acid Chemical class OC(=O)[C@@H](O)C1=CC=CC=C1 IWYDHOAUDWTVEP-ZETCQYMHSA-N 0.000 description 5
- 125000001305 1,2,4-triazol-3-yl group Chemical group [H]N1N=C([*])N=C1[H] 0.000 description 5
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 5
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
- 208000022497 Cocaine-Related disease Diseases 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 239000004793 Polystyrene Substances 0.000 description 5
- 239000000556 agonist Substances 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- 229940025084 amphetamine Drugs 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 238000004587 chromatography analysis Methods 0.000 description 5
- 238000007796 conventional method Methods 0.000 description 5
- 235000019788 craving Nutrition 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 5
- 230000008030 elimination Effects 0.000 description 5
- 238000003379 elimination reaction Methods 0.000 description 5
- 230000005764 inhibitory process Effects 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 229920002223 polystyrene Polymers 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 239000002002 slurry Substances 0.000 description 5
- 239000012453 solvate Substances 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- VSCBATMPTLKTOV-UHFFFAOYSA-N 2-tert-butylimino-n,n-diethyl-1,3-dimethyl-1,3,2$l^{5}-diazaphosphinan-2-amine Chemical compound CCN(CC)P1(=NC(C)(C)C)N(C)CCCN1C VSCBATMPTLKTOV-UHFFFAOYSA-N 0.000 description 4
- 208000031091 Amnestic disease Diseases 0.000 description 4
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
- 206010012289 Dementia Diseases 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 208000003863 Marijuana Abuse Diseases 0.000 description 4
- 208000026251 Opioid-Related disease Diseases 0.000 description 4
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 230000008485 antagonism Effects 0.000 description 4
- 229910000085 borane Inorganic materials 0.000 description 4
- 239000000872 buffer Substances 0.000 description 4
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 description 4
- 239000006196 drop Substances 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 229910052740 iodine Inorganic materials 0.000 description 4
- 125000002950 monocyclic group Chemical group 0.000 description 4
- 230000002085 persistent effect Effects 0.000 description 4
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical compound C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 4
- 229950010883 phencyclidine Drugs 0.000 description 4
- 235000011181 potassium carbonates Nutrition 0.000 description 4
- SMUQFGGVLNAIOZ-UHFFFAOYSA-N quinaldine Chemical compound C1=CC=CC2=NC(C)=CC=C21 SMUQFGGVLNAIOZ-UHFFFAOYSA-N 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000000523 sample Substances 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- 239000012312 sodium hydride Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000003826 tablet Substances 0.000 description 4
- 230000001225 therapeutic effect Effects 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- 229910052723 transition metal Inorganic materials 0.000 description 4
- 150000003624 transition metals Chemical class 0.000 description 4
- 229940087668 (+)- acetylmandelic acid Drugs 0.000 description 3
- KHJRUTSPEDPIBP-GXSJLCMTSA-N (1s,5r)-1-(4-bromophenyl)-3-azabicyclo[3.1.0]hexane Chemical compound C1=CC(Br)=CC=C1[C@@]1(CNC2)[C@H]2C1 KHJRUTSPEDPIBP-GXSJLCMTSA-N 0.000 description 3
- HGWUUOXXAIISDB-UHFFFAOYSA-N 3-azabicyclo[3.1.0]hexane Chemical compound C1NCC2CC21 HGWUUOXXAIISDB-UHFFFAOYSA-N 0.000 description 3
- LIYKWEUNIHOULB-UHFFFAOYSA-N 3-benzyl-1-[5-(trifluoromethyl)pyridin-2-yl]-3-azabicyclo[3.1.0]hexane Chemical compound N1=CC(C(F)(F)F)=CC=C1C1(CN(CC=2C=CC=CC=2)C2)C2C1 LIYKWEUNIHOULB-UHFFFAOYSA-N 0.000 description 3
- 125000004199 4-trifluoromethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C(F)(F)F 0.000 description 3
- XARCVMREUVYIHA-UHFFFAOYSA-N 5-[5-(3-chloropropylsulfanyl)-4-methyl-1,2,4-triazol-3-yl]-2,4-dimethyl-1,3-oxazole Chemical compound O1C(C)=NC(C)=C1C1=NN=C(SCCCCl)N1C XARCVMREUVYIHA-UHFFFAOYSA-N 0.000 description 3
- KZPOSKZBSHRFCE-UHFFFAOYSA-N 5-[5-(3-chloropropylsulfanyl)-4-methyl-1,2,4-triazol-3-yl]-2-methylquinoline Chemical compound C=1C=CC2=NC(C)=CC=C2C=1C1=NN=C(SCCCCl)N1C KZPOSKZBSHRFCE-UHFFFAOYSA-N 0.000 description 3
- HQULYFAKUZDRPB-UHFFFAOYSA-N 6-bromo-2-[4-(trifluoromethoxy)phenoxy]-1,3-benzothiazole Chemical compound BrC1=CC2=C(N=C(S2)OC2=CC=C(C=C2)OC(F)(F)F)C=C1 HQULYFAKUZDRPB-UHFFFAOYSA-N 0.000 description 3
- HJHYMLQMBHHNRJ-UHFFFAOYSA-N 8-fluoro-2-methylquinoline Chemical compound C1=CC=C(F)C2=NC(C)=CC=C21 HJHYMLQMBHHNRJ-UHFFFAOYSA-N 0.000 description 3
- 208000007848 Alcoholism Diseases 0.000 description 3
- 208000029197 Amphetamine-Related disease Diseases 0.000 description 3
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 3
- 208000007271 Substance Withdrawal Syndrome Diseases 0.000 description 3
- KPCZJLGGXRGYIE-UHFFFAOYSA-N [C]1=CC=CN=C1 Chemical group [C]1=CC=CN=C1 KPCZJLGGXRGYIE-UHFFFAOYSA-N 0.000 description 3
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 3
- 239000012346 acetyl chloride Substances 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 239000000443 aerosol Substances 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 3
- 238000012435 analytical chromatography Methods 0.000 description 3
- 230000002547 anomalous effect Effects 0.000 description 3
- 239000005557 antagonist Substances 0.000 description 3
- 239000003125 aqueous solvent Substances 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 229960003920 cocaine Drugs 0.000 description 3
- 238000004440 column chromatography Methods 0.000 description 3
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 230000018109 developmental process Effects 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 230000006870 function Effects 0.000 description 3
- 150000003840 hydrochlorides Chemical class 0.000 description 3
- 239000012442 inert solvent Substances 0.000 description 3
- 238000002329 infrared spectrum Methods 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
- YICYREKXXVXWCS-UHFFFAOYSA-N methyl 2-bromo-2-(4-methoxyphenyl)acetate Chemical compound COC(=O)C(Br)C1=CC=C(OC)C=C1 YICYREKXXVXWCS-UHFFFAOYSA-N 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 235000015320 potassium carbonate Nutrition 0.000 description 3
- 238000002953 preparative HPLC Methods 0.000 description 3
- 125000004940 pyridazin-4-yl group Chemical group N1=NC=C(C=C1)* 0.000 description 3
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 description 3
- 238000010898 silica gel chromatography Methods 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000008279 sol Substances 0.000 description 3
- 239000008259 solid foam Substances 0.000 description 3
- 125000003396 thiol group Chemical group [H]S* 0.000 description 3
- WTVXIBRMWGUIMI-UHFFFAOYSA-N trifluoro($l^{1}-oxidanylsulfonyl)methane Chemical group [O]S(=O)(=O)C(F)(F)F WTVXIBRMWGUIMI-UHFFFAOYSA-N 0.000 description 3
- 238000010626 work up procedure Methods 0.000 description 3
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 description 2
- KMPAEWQDBFWCEZ-FZMZJTMJSA-N (1s,5r)-3-(3-chloropropyl)-1-[2-fluoro-4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound FC1=CC(C(F)(F)F)=CC=C1[C@@]1(CN(CCCCl)C2)[C@H]2C1 KMPAEWQDBFWCEZ-FZMZJTMJSA-N 0.000 description 2
- GCJUIWFGXMGLBW-UONOGXRCSA-N (1s,5r)-3-(3-chloropropyl)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1=CC(C(F)(F)F)=CC=C1[C@@]1(CN(CCCCl)C2)[C@H]2C1 GCJUIWFGXMGLBW-UONOGXRCSA-N 0.000 description 2
- OBCUSTCTKLTMBX-VIFPVBQESA-N (2s)-2-acetyloxy-2-phenylacetic acid Chemical compound CC(=O)O[C@H](C(O)=O)C1=CC=CC=C1 OBCUSTCTKLTMBX-VIFPVBQESA-N 0.000 description 2
- TUFADSGTJUOBEH-ZWNOBZJWSA-N (5aR,9aR)-6-propyl-5a,7,8,9,9a,10-hexahydro-5H-pyrido[2,3-g]quinazolin-2-amine Chemical compound NC1=NC=C2C[C@H]3N(CCC)CCC[C@@H]3CC2=N1 TUFADSGTJUOBEH-ZWNOBZJWSA-N 0.000 description 2
- QVVAWONRFLJUBP-UHFFFAOYSA-N 1,3-benzothiazol-3-ium;chloride Chemical compound Cl.C1=CC=C2SC=NC2=C1 QVVAWONRFLJUBP-UHFFFAOYSA-N 0.000 description 2
- GFCSAENYPAUFBQ-UHFFFAOYSA-N 1-[3-fluoro-4-(pyrrol-1-ylmethyl)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound FC1=CC(C23C(C2)CNC3)=CC=C1CN1C=CC=C1 GFCSAENYPAUFBQ-UHFFFAOYSA-N 0.000 description 2
- WJKHDCRPNISRMI-UHFFFAOYSA-N 1-[5-(trifluoromethyl)pyridin-2-yl]-3-azabicyclo[3.1.0]hexane Chemical compound N1=CC(C(F)(F)F)=CC=C1C1(CNC2)C2C1 WJKHDCRPNISRMI-UHFFFAOYSA-N 0.000 description 2
- WMDXIWLQHQYKNZ-UHFFFAOYSA-N 1-benzyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,5-dihydropyrrole Chemical compound O1C(C)(C)C(C)(C)OB1C(C1)=CCN1CC1=CC=CC=C1 WMDXIWLQHQYKNZ-UHFFFAOYSA-N 0.000 description 2
- GBTPNDDGLRQGRY-UHFFFAOYSA-N 2,2,2-trifluoro-1-[1-(3-methoxyphenyl)-3-azabicyclo[3.1.0]hexan-3-yl]ethanone Chemical compound COC1=CC=CC(C23C(C2)CN(C3)C(=O)C(F)(F)F)=C1 GBTPNDDGLRQGRY-UHFFFAOYSA-N 0.000 description 2
- JLSFKHJNJFXGAB-UHFFFAOYSA-N 2,4-dimethyl-1,3-oxazole-5-carboxylic acid Chemical compound CC1=NC(C)=C(C(O)=O)O1 JLSFKHJNJFXGAB-UHFFFAOYSA-N 0.000 description 2
- ZJZBJTWOACCRHE-UHFFFAOYSA-N 2-(1-benzyl-2,5-dihydropyrrol-3-yl)-5-(trifluoromethyl)pyridine Chemical compound N1=CC(C(F)(F)F)=CC=C1C(C1)=CCN1CC1=CC=CC=C1 ZJZBJTWOACCRHE-UHFFFAOYSA-N 0.000 description 2
- LLBKPUXRAXHRPH-UHFFFAOYSA-N 2-(1-benzyl-2,5-dihydropyrrol-3-yl)-6-(trifluoromethyl)pyridine Chemical compound FC(F)(F)C1=CC=CC(C=2CN(CC=3C=CC=CC=3)CC=2)=N1 LLBKPUXRAXHRPH-UHFFFAOYSA-N 0.000 description 2
- 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 2
- MVGIHUANEKVSMB-UHFFFAOYSA-N 3-(3-chloropropylsulfanyl)-4-methyl-5-[4-(trifluoromethyl)phenyl]-1,2,4-triazole Chemical compound CN1C(SCCCCl)=NN=C1C1=CC=C(C(F)(F)F)C=C1 MVGIHUANEKVSMB-UHFFFAOYSA-N 0.000 description 2
- JTYIJNUNIZZGBL-UHFFFAOYSA-N 3-(3-chloropropylsulfanyl)-5-(3,4-difluorophenyl)-4-methyl-1,2,4-triazole Chemical compound CN1C(SCCCCl)=NN=C1C1=CC=C(F)C(F)=C1 JTYIJNUNIZZGBL-UHFFFAOYSA-N 0.000 description 2
- KMRLIBSAUBEIOP-YUIIUQSRSA-N 3-[(1s,5r)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]butan-1-ol Chemical compound C1([C@]23C[C@H]2CN(C3)C(CCO)C)=CC=C(C(F)(F)F)C=C1 KMRLIBSAUBEIOP-YUIIUQSRSA-N 0.000 description 2
- NCEGIWIYCGJXAY-UHFFFAOYSA-N 3-[4-(trifluoromethyl)phenyl]pyrrole-2,5-dione Chemical compound C1=CC(C(F)(F)F)=CC=C1C1=CC(=O)NC1=O NCEGIWIYCGJXAY-UHFFFAOYSA-N 0.000 description 2
- HXYSQUKTBYWEEW-UHFFFAOYSA-N 3-benzyl-1-[6-(trifluoromethyl)pyridin-2-yl]-3-azabicyclo[3.1.0]hexane Chemical compound FC(F)(F)C1=CC=CC(C23C(C2)CN(CC=2C=CC=CC=2)C3)=N1 HXYSQUKTBYWEEW-UHFFFAOYSA-N 0.000 description 2
- LVSQXDHWDCMMRJ-UHFFFAOYSA-N 4-hydroxybutan-2-one Chemical compound CC(=O)CCO LVSQXDHWDCMMRJ-UHFFFAOYSA-N 0.000 description 2
- CYJRNFFLTBEQSQ-UHFFFAOYSA-N 8-(3-methyl-1-benzothiophen-5-yl)-N-(4-methylsulfonylpyridin-3-yl)quinoxalin-6-amine Chemical compound CS(=O)(=O)C1=C(C=NC=C1)NC=1C=C2N=CC=NC2=C(C=1)C=1C=CC2=C(C(=CS2)C)C=1 CYJRNFFLTBEQSQ-UHFFFAOYSA-N 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 206010001605 Alcohol poisoning Diseases 0.000 description 2
- 241000218236 Cannabis Species 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 208000017781 Cocaine intoxication Diseases 0.000 description 2
- 229910021592 Copper(II) chloride Inorganic materials 0.000 description 2
- LVZWSLJZHVFIQJ-UHFFFAOYSA-N Cyclopropane Chemical compound C1CC1 LVZWSLJZHVFIQJ-UHFFFAOYSA-N 0.000 description 2
- 101150049660 DRD2 gene Proteins 0.000 description 2
- 206010012239 Delusion Diseases 0.000 description 2
- 208000024254 Delusional disease Diseases 0.000 description 2
- 238000003775 Density Functional Theory Methods 0.000 description 2
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 206010016754 Flashback Diseases 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- 239000007995 HEPES buffer Substances 0.000 description 2
- 208000004547 Hallucinations Diseases 0.000 description 2
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 2
- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 2
- JRNVZBWKYDBUCA-UHFFFAOYSA-N N-chlorosuccinimide Chemical compound ClN1C(=O)CCC1=O JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- 208000018737 Parkinson disease Diseases 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 208000011963 Substance-induced psychotic disease Diseases 0.000 description 2
- 231100000393 Substance-induced psychotic disorder Toxicity 0.000 description 2
- 239000004809 Teflon Substances 0.000 description 2
- 229920006362 Teflon® Polymers 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 238000000862 absorption spectrum Methods 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 125000002252 acyl group Chemical group 0.000 description 2
- 239000004479 aerosol dispenser Substances 0.000 description 2
- 206010001584 alcohol abuse Diseases 0.000 description 2
- 208000025746 alcohol use disease Diseases 0.000 description 2
- 208000028505 alcohol-related disease Diseases 0.000 description 2
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 description 2
- 230000029936 alkylation Effects 0.000 description 2
- 238000005804 alkylation reaction Methods 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- 229940039407 aniline Drugs 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 230000027455 binding Effects 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- ILAHWRKJUDSMFH-UHFFFAOYSA-N boron tribromide Chemical compound BrB(Br)Br ILAHWRKJUDSMFH-UHFFFAOYSA-N 0.000 description 2
- 125000005620 boronic acid group Chemical group 0.000 description 2
- 210000004556 brain Anatomy 0.000 description 2
- VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 description 2
- 229960001948 caffeine Drugs 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 201000001843 cannabis dependence Diseases 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 235000010980 cellulose Nutrition 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004296 chiral HPLC Methods 0.000 description 2
- 201000001272 cocaine abuse Diseases 0.000 description 2
- 150000001934 cyclohexanes Chemical class 0.000 description 2
- 231100000868 delusion Toxicity 0.000 description 2
- 238000010511 deprotection reaction Methods 0.000 description 2
- ZHXTWWCDMUWMDI-UHFFFAOYSA-N dihydroxyboron Chemical compound O[B]O ZHXTWWCDMUWMDI-UHFFFAOYSA-N 0.000 description 2
- 229960003638 dopamine Drugs 0.000 description 2
- 239000002552 dosage form Substances 0.000 description 2
- 230000001544 dysphoric effect Effects 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 150000004675 formic acid derivatives Chemical class 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 239000007903 gelatin capsule Substances 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 239000000380 hallucinogen Substances 0.000 description 2
- 208000011331 hallucinogen-persisting perception disease Diseases 0.000 description 2
- 239000011539 homogenization buffer Substances 0.000 description 2
- 150000002431 hydrogen Chemical group 0.000 description 2
- 150000003949 imides Chemical class 0.000 description 2
- 238000001990 intravenous administration Methods 0.000 description 2
- 125000001786 isothiazolyl group Chemical group 0.000 description 2
- 239000007937 lozenge Substances 0.000 description 2
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 125000005948 methanesulfonyloxy group Chemical group 0.000 description 2
- ZQYLDVNTWDEAJI-UHFFFAOYSA-N methyl 2-(4-methoxyphenyl)acetate Chemical compound COC(=O)CC1=CC=C(OC)C=C1 ZQYLDVNTWDEAJI-UHFFFAOYSA-N 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 239000003176 neuroleptic agent Substances 0.000 description 2
- 229960002715 nicotine Drugs 0.000 description 2
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 2
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 2
- 208000002851 paranoid schizophrenia Diseases 0.000 description 2
- 208000007100 phencyclidine abuse Diseases 0.000 description 2
- YBYRMVIVWMBXKQ-UHFFFAOYSA-N phenylmethanesulfonyl fluoride Chemical compound FS(=O)(=O)CC1=CC=CC=C1 YBYRMVIVWMBXKQ-UHFFFAOYSA-N 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 238000002600 positron emission tomography Methods 0.000 description 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
- 239000003380 propellant Substances 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 229950003275 quinelorane Drugs 0.000 description 2
- 239000002287 radioligand Substances 0.000 description 2
- 239000013074 reference sample Substances 0.000 description 2
- 238000012552 review Methods 0.000 description 2
- 238000002821 scintillation proximity assay Methods 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 2
- 235000009518 sodium iodide Nutrition 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid group Chemical class S(O)(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- IOGXOCVLYRDXLW-UHFFFAOYSA-N tert-butyl nitrite Chemical compound CC(C)(C)ON=O IOGXOCVLYRDXLW-UHFFFAOYSA-N 0.000 description 2
- 239000012414 tert-butyl nitrite Substances 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- 125000005951 trifluoromethanesulfonyloxy group Chemical group 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 239000003643 water by type Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- VCGRFBXVSFAGGA-UHFFFAOYSA-N (1,1-dioxo-1,4-thiazinan-4-yl)-[6-[[3-(4-fluorophenyl)-5-methyl-1,2-oxazol-4-yl]methoxy]pyridin-3-yl]methanone Chemical compound CC=1ON=C(C=2C=CC(F)=CC=2)C=1COC(N=C1)=CC=C1C(=O)N1CCS(=O)(=O)CC1 VCGRFBXVSFAGGA-UHFFFAOYSA-N 0.000 description 1
- SYCYUYFGTJYLJB-LMNIDFBRSA-N (1S)-3-[3-[[5-(1,5-dimethylpyrazol-4-yl)-4-methyl-1,2,4-triazol-3-yl]sulfanyl]propyl]-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound CN1N=CC(=C1C)C=1N(C(=NN1)SCCCN1C[C@]2(CC2C1)C1=CC=C(C=C1)C(F)(F)F)C SYCYUYFGTJYLJB-LMNIDFBRSA-N 0.000 description 1
- BSMNRYCSBFHEMQ-KCJUWKMLSA-N (1r,5s)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane Chemical compound C1=C(Cl)C(Cl)=CC=C1[C@]1(CNC2)[C@@H]2C1 BSMNRYCSBFHEMQ-KCJUWKMLSA-N 0.000 description 1
- KHJRUTSPEDPIBP-KOLCDFICSA-N (1r,5s)-1-(4-bromophenyl)-3-azabicyclo[3.1.0]hexane Chemical compound C1=CC(Br)=CC=C1[C@]1(CNC2)[C@@H]2C1 KHJRUTSPEDPIBP-KOLCDFICSA-N 0.000 description 1
- IWDGZABFNGRZPF-MNOVXSKESA-N (1r,5s)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1=CC(C(F)(F)F)=CC=C1[C@]1(CNC2)[C@@H]2C1 IWDGZABFNGRZPF-MNOVXSKESA-N 0.000 description 1
- VAHRZLJELMJYTJ-VNJAQMQMSA-N (1s,5r)-1-(4-bromophenyl)-3-[3-[(4-methyl-5-pyridin-3-yl-1,2,4-triazol-3-yl)sulfanyl]propyl]-3-azabicyclo[3.1.0]hexane;hydrochloride Chemical compound Cl.C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C=2C=NC=CC=2)C)=CC=C(Br)C=C1 VAHRZLJELMJYTJ-VNJAQMQMSA-N 0.000 description 1
- QEZIHZXJMGTKOH-YUIIUQSRSA-N (1s,5r)-3-(4-chlorobutan-2-yl)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound C1([C@]23C[C@H]2CN(C3)C(CCCl)C)=CC=C(C(F)(F)F)C=C1 QEZIHZXJMGTKOH-YUIIUQSRSA-N 0.000 description 1
- DMIQAPWKNMHJQK-XUCJAIGXSA-N (1s,5r)-3-(4-chlorobutan-2-yl)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane;hexane Chemical compound CCCCCC.C1([C@]23C[C@H]2CN(C3)C(CCCl)C)=CC=C(C(F)(F)F)C=C1 DMIQAPWKNMHJQK-XUCJAIGXSA-N 0.000 description 1
- WAFBUQPEOUFQIX-UULHHVIKSA-N (1s,5r)-3-[3-[[4-methyl-5-(6-methylpyridin-3-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane;hydrochloride Chemical compound Cl.C1=NC(C)=CC=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C=CC(=CC=3)C(F)(F)F)C[C@H]2C1 WAFBUQPEOUFQIX-UULHHVIKSA-N 0.000 description 1
- UOFQUIZUQYNTJK-MGBOEYOKSA-N (1s,5r)-3-[3-[[4-methyl-5-(oxan-4-yl)-1,2,4-triazol-3-yl]sulfanyl]propyl]-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexane;hydrochloride Chemical compound Cl.C1([C@]23C[C@H]2CN(C3)CCCSC=2N(C(=NN=2)C2CCOCC2)C)=CC=C(C(F)(F)F)C=C1 UOFQUIZUQYNTJK-MGBOEYOKSA-N 0.000 description 1
- DIIFZCPZIRQDIJ-UHFFFAOYSA-N (3,5-dimethyl-1,2-oxazol-4-yl)boronic acid Chemical compound CC1=NOC(C)=C1B(O)O DIIFZCPZIRQDIJ-UHFFFAOYSA-N 0.000 description 1
- MIOPJNTWMNEORI-XVKPBYJWSA-N (R)-camphorsulfonic acid Chemical compound C1C[C@]2(CS(O)(=O)=O)C(=O)C[C@H]1C2(C)C MIOPJNTWMNEORI-XVKPBYJWSA-N 0.000 description 1
- 125000003088 (fluoren-9-ylmethoxy)carbonyl group Chemical group 0.000 description 1
- VTWKXBJHBHYJBI-VURMDHGXSA-N (nz)-n-benzylidenehydroxylamine Chemical compound O\N=C/C1=CC=CC=C1 VTWKXBJHBHYJBI-VURMDHGXSA-N 0.000 description 1
- KZPYGQFFRCFCPP-UHFFFAOYSA-N 1,1'-bis(diphenylphosphino)ferrocene Chemical compound [Fe+2].C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1 KZPYGQFFRCFCPP-UHFFFAOYSA-N 0.000 description 1
- 125000004605 1,2,3,4-tetrahydroisoquinolinyl group Chemical group C1(NCCC2=CC=CC=C12)* 0.000 description 1
- 125000004607 1,2,3,4-tetrahydroquinolinyl group Chemical group N1(CCCC2=CC=CC=C12)* 0.000 description 1
- 125000005943 1,2,3,6-tetrahydropyridyl group Chemical group 0.000 description 1
- XGYCWCIGCYGQFU-UHFFFAOYSA-N 1,2-thiazolidine 1,1-dioxide Chemical compound O=S1(=O)CCCN1 XGYCWCIGCYGQFU-UHFFFAOYSA-N 0.000 description 1
- RCHDLEVSZBOHOS-UHFFFAOYSA-N 1,4-dichlorobut-2-yne Chemical compound ClCC#CCCl RCHDLEVSZBOHOS-UHFFFAOYSA-N 0.000 description 1
- LGRHOXLDDMBJQT-UHFFFAOYSA-N 1-(2-fluoro-4-methylphenyl)-3-azabicyclo[3.1.0]hexane Chemical compound FC1=CC(C)=CC=C1C1(CNC2)C2C1 LGRHOXLDDMBJQT-UHFFFAOYSA-N 0.000 description 1
- MOAXKJFXKNHAMF-UHFFFAOYSA-N 1-(3-chloro-4-methoxyphenyl)-3-azabicyclo[3.1.0]hexane Chemical compound C1=C(Cl)C(OC)=CC=C1C1(CNC2)C2C1 MOAXKJFXKNHAMF-UHFFFAOYSA-N 0.000 description 1
- TUUFTWPXUNSKMA-UHFFFAOYSA-N 1-(3-methoxyphenyl)-3-azabicyclo[3.1.0]hexane Chemical compound COC1=CC=CC(C23C(C2)CNC3)=C1 TUUFTWPXUNSKMA-UHFFFAOYSA-N 0.000 description 1
- PDPNDIOORXPPHH-UHFFFAOYSA-N 1-(4-methoxyphenyl)cyclopropane-1,2-dicarboxylic acid Chemical compound C1=CC(OC)=CC=C1C1(C(O)=O)C(C(O)=O)C1 PDPNDIOORXPPHH-UHFFFAOYSA-N 0.000 description 1
- GGJILJYXZOJJSB-UHFFFAOYSA-N 1-(trifluoromethyl)thieno[2,3-c]pyrazole Chemical compound FC(F)(F)n1ncc2ccsc12 GGJILJYXZOJJSB-UHFFFAOYSA-N 0.000 description 1
- ASOKPJOREAFHNY-UHFFFAOYSA-N 1-Hydroxybenzotriazole Chemical group C1=CC=C2N(O)N=NC2=C1 ASOKPJOREAFHNY-UHFFFAOYSA-N 0.000 description 1
- KHWKHOXPNILXFK-NBGIEHNGSA-N 1-[2-hydroxy-5-[(1s,5r)-3-[3-[[4-methyl-5-[4-(trifluoromethyl)phenyl]-1,2,4-triazol-3-yl]sulfanyl]propyl]-3-azabicyclo[3.1.0]hexan-1-yl]phenyl]ethanone Chemical compound C1=C(O)C(C(=O)C)=CC([C@@]23[C@@H](C2)CN(CCCSC=2N(C(C=4C=CC(=CC=4)C(F)(F)F)=NN=2)C)C3)=C1 KHWKHOXPNILXFK-NBGIEHNGSA-N 0.000 description 1
- KSISJODFSDRWQJ-UHFFFAOYSA-N 1-[3-(trifluoromethoxy)phenyl]-3-azabicyclo[3.1.0]hexane Chemical compound FC(F)(F)OC1=CC=CC(C23C(C2)CNC3)=C1 KSISJODFSDRWQJ-UHFFFAOYSA-N 0.000 description 1
- XAGZJIQIVXSURR-UHFFFAOYSA-N 1-[4-(trifluoromethyl)phenyl]piperidin-2-one Chemical group C1=CC(C(F)(F)F)=CC=C1N1C(=O)CCCC1 XAGZJIQIVXSURR-UHFFFAOYSA-N 0.000 description 1
- LHYKTQVFLKHQSR-UHFFFAOYSA-N 1-amino-3-methylurea Chemical compound CNC(=O)NN LHYKTQVFLKHQSR-UHFFFAOYSA-N 0.000 description 1
- PYOFNPHTKBSXOM-UHFFFAOYSA-N 1-methylindazol-5-amine Chemical compound NC1=CC=C2N(C)N=CC2=C1 PYOFNPHTKBSXOM-UHFFFAOYSA-N 0.000 description 1
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 1
- RUIDQYPOYMXDLP-UHFFFAOYSA-N 2,2,2-trifluoro-1-[1-(4-methoxyphenyl)-3-azabicyclo[3.1.0]hexan-3-yl]ethanone Chemical compound C1=CC(OC)=CC=C1C1(CN(C2)C(=O)C(F)(F)F)C2C1 RUIDQYPOYMXDLP-UHFFFAOYSA-N 0.000 description 1
- QCLMKWSJCKTRGR-UHFFFAOYSA-N 2,2,2-trifluoro-1-[1-[4-(5-methyl-1,2-oxazol-3-yl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]ethanone Chemical compound O1C(C)=CC(C=2C=CC(=CC=2)C23C(C2)CN(C3)C(=O)C(F)(F)F)=N1 QCLMKWSJCKTRGR-UHFFFAOYSA-N 0.000 description 1
- VHOVLXMLZLNXEO-UHFFFAOYSA-N 2,5-dihydro-1h-pyrrol-3-ylboronic acid Chemical compound OB(O)C1=CCNC1 VHOVLXMLZLNXEO-UHFFFAOYSA-N 0.000 description 1
- GFISDBXSWQMOND-UHFFFAOYSA-N 2,5-dimethoxyoxolane Chemical compound COC1CCC(OC)O1 GFISDBXSWQMOND-UHFFFAOYSA-N 0.000 description 1
- KYNNBXCGXUOREX-UHFFFAOYSA-N 2-(3-bromophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1 KYNNBXCGXUOREX-UHFFFAOYSA-N 0.000 description 1
- KNNHPOGBBNRNDH-UHFFFAOYSA-N 2-[(2-chloro-6-fluorophenyl)methylsulfanyl]ethanamine Chemical compound NCCSCC1=C(F)C=CC=C1Cl KNNHPOGBBNRNDH-UHFFFAOYSA-N 0.000 description 1
- BLXXCCIBGGBDHI-UHFFFAOYSA-N 2-[3-(trifluoromethyl)phenyl]acetic acid Chemical compound OC(=O)CC1=CC=CC(C(F)(F)F)=C1 BLXXCCIBGGBDHI-UHFFFAOYSA-N 0.000 description 1
- ZMTIBXQPXBUWPQ-UHFFFAOYSA-N 2-[4-(trifluoromethoxy)phenyl]acetic acid Chemical compound OC(=O)CC1=CC=C(OC(F)(F)F)C=C1 ZMTIBXQPXBUWPQ-UHFFFAOYSA-N 0.000 description 1
- OBCUSTCTKLTMBX-UHFFFAOYSA-N 2-acetyloxy-2-phenylacetic acid Chemical class CC(=O)OC(C(O)=O)C1=CC=CC=C1 OBCUSTCTKLTMBX-UHFFFAOYSA-N 0.000 description 1
- 125000004174 2-benzimidazolyl group Chemical group [H]N1C(*)=NC2=C([H])C([H])=C([H])C([H])=C12 0.000 description 1
- GSKMWMFOQQBVMI-UHFFFAOYSA-N 2-bromo-5-(trifluoromethyl)pyridine Chemical compound FC(F)(F)C1=CC=C(Br)N=C1 GSKMWMFOQQBVMI-UHFFFAOYSA-N 0.000 description 1
- DOWNSQADAFSSAR-UHFFFAOYSA-N 2-bromo-6-(trifluoromethyl)pyridine Chemical compound FC(F)(F)C1=CC=CC(Br)=N1 DOWNSQADAFSSAR-UHFFFAOYSA-N 0.000 description 1
- XGYLSRFSXKAYCR-UHFFFAOYSA-N 2-chloro-4-methylaniline Chemical compound CC1=CC=C(N)C(Cl)=C1 XGYLSRFSXKAYCR-UHFFFAOYSA-N 0.000 description 1
- PNLQPWWBHXMFCA-UHFFFAOYSA-N 2-chloroprop-1-ene Chemical compound CC(Cl)=C PNLQPWWBHXMFCA-UHFFFAOYSA-N 0.000 description 1
- YKPDYPPZLUZONK-UHFFFAOYSA-N 2-fluoro-3-(trifluoromethyl)aniline Chemical compound NC1=CC=CC(C(F)(F)F)=C1F YKPDYPPZLUZONK-UHFFFAOYSA-N 0.000 description 1
- ARHDUOQIXLGANT-UHFFFAOYSA-N 2-fluoro-4-(trifluoromethyl)aniline Chemical compound NC1=CC=C(C(F)(F)F)C=C1F ARHDUOQIXLGANT-UHFFFAOYSA-N 0.000 description 1
- ZQEXBVHABAJPHJ-UHFFFAOYSA-N 2-fluoro-4-methylaniline Chemical compound CC1=CC=C(N)C(F)=C1 ZQEXBVHABAJPHJ-UHFFFAOYSA-N 0.000 description 1
- DRKWGMXFFCPZLW-UHFFFAOYSA-N 2-fluoro-5-(trifluoromethyl)aniline Chemical compound NC1=CC(C(F)(F)F)=CC=C1F DRKWGMXFFCPZLW-UHFFFAOYSA-N 0.000 description 1
- ZNIGVBCUUZGYDU-UHFFFAOYSA-N 2-methyl-1,3-benzothiazol-5-amine;dihydrochloride Chemical compound [Cl-].[Cl-].[NH3+]C1=CC=C2SC(C)=[NH+]C2=C1 ZNIGVBCUUZGYDU-UHFFFAOYSA-N 0.000 description 1
- HFUJOSYKJMNSFQ-UHFFFAOYSA-N 2-methyl-1,3-benzothiazol-6-amine Chemical compound C1=C(N)C=C2SC(C)=NC2=C1 HFUJOSYKJMNSFQ-UHFFFAOYSA-N 0.000 description 1
- PAXQXJDYVORMOO-UHFFFAOYSA-N 2-methyl-4-(trifluoromethyl)aniline Chemical compound CC1=CC(C(F)(F)F)=CC=C1N PAXQXJDYVORMOO-UHFFFAOYSA-N 0.000 description 1
- AXJACLJMUNBPKI-BFSXKHHNSA-N 2-methyl-5-[4-methyl-5-[3-[(1s,5r)-1-[4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-1,2,4-triazol-3-yl]quinoline;hydrochloride Chemical compound Cl.C1([C@]23C[C@H]2CN(C3)CCCSC2=NN=C(N2C)C=2C3=CC=C(N=C3C=CC=2)C)=CC=C(C(F)(F)F)C=C1 AXJACLJMUNBPKI-BFSXKHHNSA-N 0.000 description 1
- SURRWOVCCLTBGC-UHFFFAOYSA-N 3-(2,4-dimethyl-1,3-oxazol-5-yl)-4-methyl-1h-1,2,4-triazole-5-thione Chemical compound O1C(C)=NC(C)=C1C1=NNC(=S)N1C SURRWOVCCLTBGC-UHFFFAOYSA-N 0.000 description 1
- FPQQSJJWHUJYPU-UHFFFAOYSA-N 3-(dimethylamino)propyliminomethylidene-ethylazanium;chloride Chemical compound Cl.CCN=C=NCCCN(C)C FPQQSJJWHUJYPU-UHFFFAOYSA-N 0.000 description 1
- OZLMWITUNBVEPK-UHFFFAOYSA-N 3-[5-(3-chloropropylsulfanyl)-4-methyl-1,2,4-triazol-3-yl]pyridine Chemical compound CN1C(SCCCCl)=NN=C1C1=CC=CN=C1 OZLMWITUNBVEPK-UHFFFAOYSA-N 0.000 description 1
- CRRVZRDISHOQQL-UHFFFAOYSA-N 3-fluoro-4-(trifluoromethyl)aniline Chemical compound NC1=CC=C(C(F)(F)F)C(F)=C1 CRRVZRDISHOQQL-UHFFFAOYSA-N 0.000 description 1
- WQKQODZOQAFYPR-UHFFFAOYSA-N 3-fluoro-5-(trifluoromethyl)aniline Chemical compound NC1=CC(F)=CC(C(F)(F)F)=C1 WQKQODZOQAFYPR-UHFFFAOYSA-N 0.000 description 1
- PZVWKCGKIADPAU-UHFFFAOYSA-N 4-(1,3-benzothiazol-2-ylsulfanyl)aniline Chemical compound C1=CC(N)=CC=C1SC1=NC2=CC=CC=C2S1 PZVWKCGKIADPAU-UHFFFAOYSA-N 0.000 description 1
- FDEYRPOSQNXRGR-UHFFFAOYSA-N 4-(1-benzyl-2,5-dihydropyrrol-3-yl)-2-fluorobenzonitrile Chemical compound C1=C(C#N)C(F)=CC(C=2CN(CC=3C=CC=CC=3)CC=2)=C1 FDEYRPOSQNXRGR-UHFFFAOYSA-N 0.000 description 1
- OQAUECMPHZGGPM-UHFFFAOYSA-N 4-(3-azabicyclo[3.1.0]hexan-1-yl)benzonitrile Chemical compound C1=CC(C#N)=CC=C1C1(CNC2)C2C1 OQAUECMPHZGGPM-UHFFFAOYSA-N 0.000 description 1
- GNSKTKGGZXYRDR-UHFFFAOYSA-N 4-(3-benzyl-3-azabicyclo[3.1.0]hexan-1-yl)-2-fluorobenzonitrile Chemical compound C1=C(C#N)C(F)=CC(C23C(C2)CN(CC=2C=CC=CC=2)C3)=C1 GNSKTKGGZXYRDR-UHFFFAOYSA-N 0.000 description 1
- PLVKORSUGOABDB-UHFFFAOYSA-N 4-[3-(2,2,2-trifluoroacetyl)-2-azabicyclo[3.1.0]hexan-1-yl]benzonitrile Chemical compound N1C(C(=O)C(F)(F)F)CC2CC21C1=CC=C(C#N)C=C1 PLVKORSUGOABDB-UHFFFAOYSA-N 0.000 description 1
- IDXDBQIHKBXNHG-UHFFFAOYSA-N 4-[3-(2,2,2-trifluoroacetyl)-3-azabicyclo[3.1.0]hexan-1-yl]benzaldehyde Chemical compound C1N(C(=O)C(F)(F)F)CC2CC21C1=CC=C(C=O)C=C1 IDXDBQIHKBXNHG-UHFFFAOYSA-N 0.000 description 1
- KVCQTKNUUQOELD-UHFFFAOYSA-N 4-amino-n-[1-(3-chloro-2-fluoroanilino)-6-methylisoquinolin-5-yl]thieno[3,2-d]pyrimidine-7-carboxamide Chemical compound N=1C=CC2=C(NC(=O)C=3C4=NC=NC(N)=C4SC=3)C(C)=CC=C2C=1NC1=CC=CC(Cl)=C1F KVCQTKNUUQOELD-UHFFFAOYSA-N 0.000 description 1
- CSFDTBRRIBJILD-UHFFFAOYSA-N 4-chloro-2-fluoroaniline Chemical compound NC1=CC=C(Cl)C=C1F CSFDTBRRIBJILD-UHFFFAOYSA-N 0.000 description 1
- CQJCPOVTPNWVBW-UHFFFAOYSA-N 4-methoxy-3-(trifluoromethyl)aniline Chemical compound COC1=CC=C(N)C=C1C(F)(F)F CQJCPOVTPNWVBW-UHFFFAOYSA-N 0.000 description 1
- ZIXUNDOOBLSXPE-UHFFFAOYSA-N 4-methyl-1,3-oxazole-5-carboxylic acid Chemical compound CC=1N=COC=1C(O)=O ZIXUNDOOBLSXPE-UHFFFAOYSA-N 0.000 description 1
- YKBFUPQGQNUMIA-UHFFFAOYSA-N 4-methyl-3-(2-methylquinolin-5-yl)-1h-1,2,4-triazole-5-thione Chemical compound C=1C=CC2=NC(C)=CC=C2C=1C1=NNC(=S)N1C YKBFUPQGQNUMIA-UHFFFAOYSA-N 0.000 description 1
- NQITUZDGXBAHQQ-UHFFFAOYSA-N 4-methyl-3-(4-methyl-1,3-oxazol-5-yl)-1h-1,2,4-triazole-5-thione Chemical compound N1=COC(C=2N(C(=S)NN=2)C)=C1C NQITUZDGXBAHQQ-UHFFFAOYSA-N 0.000 description 1
- PTVZQOAHCSKAAS-UHFFFAOYSA-N 4-methyl-3-thiosemicarbazide Chemical compound CNC(=S)NN PTVZQOAHCSKAAS-UHFFFAOYSA-N 0.000 description 1
- ODGIMMLDVSWADK-UHFFFAOYSA-N 4-trifluoromethylaniline Chemical compound NC1=CC=C(C(F)(F)F)C=C1 ODGIMMLDVSWADK-UHFFFAOYSA-N 0.000 description 1
- IRDPYOIOLAFBAZ-MFKMUULPSA-N 5-[(1r,5s)-3-azabicyclo[3.1.0]hexan-1-yl]-2-methyl-1,3-benzothiazole Chemical compound C1=C2SC(C)=NC2=CC([C@]23[C@H](C2)CNC3)=C1 IRDPYOIOLAFBAZ-MFKMUULPSA-N 0.000 description 1
- ALNZIBXWDANKLC-VPRHZQQDSA-N 5-[5-[3-[(1s,5r)-1-[2-fluoro-4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-2,4-dimethyl-1,3-oxazole;hydrochloride Chemical compound Cl.O1C(C)=NC(C)=C1C(N1C)=NN=C1SCCCN1C[C@@]2(C=3C(=CC(=CC=3)C(F)(F)F)F)C[C@H]2C1 ALNZIBXWDANKLC-VPRHZQQDSA-N 0.000 description 1
- XHSASHVDEMJIMD-NVJCMEIXSA-N 5-[5-[3-[(1s,5r)-1-[2-fluoro-4-(trifluoromethyl)phenyl]-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole;hydrochloride Chemical compound Cl.N1=COC(C=2N(C(SCCCN3C[C@]4(C[C@H]4C3)C=3C(=CC(=CC=3)C(F)(F)F)F)=NN=2)C)=C1C XHSASHVDEMJIMD-NVJCMEIXSA-N 0.000 description 1
- WDDOLFDBAGPKBI-IKZMBGHXSA-N 5-[5-[3-[(1s,5r)-1-[3-fluoro-5-(trifluoromethyl)phenyl]-2-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-4-methyl-1,3-oxazole Chemical compound N1=COC(C=2N(C(SCCCC3N[C@]4(C[C@H]4C3)C=3C=C(C=C(F)C=3)C(F)(F)F)=NN=2)C)=C1C WDDOLFDBAGPKBI-IKZMBGHXSA-N 0.000 description 1
- BSFCVAYFJQLZEU-UHFFFAOYSA-N 5-bromo-2,4-dimethyl-1,3-thiazole Chemical compound CC1=NC(C)=C(Br)S1 BSFCVAYFJQLZEU-UHFFFAOYSA-N 0.000 description 1
- IBOZOWZSXZNIHI-UHFFFAOYSA-N 6-(trifluoromethyl)pyridin-3-amine Chemical compound NC1=CC=C(C(F)(F)F)N=C1 IBOZOWZSXZNIHI-UHFFFAOYSA-N 0.000 description 1
- SLHOJTDTIDHLRK-WXVAWEFUSA-N 6-[5-[3-[(1s,5r)-1-(4-chlorophenyl)-3-azabicyclo[3.1.0]hexan-3-yl]propylsulfanyl]-4-methyl-1,2,4-triazol-3-yl]-2-methylquinoline Chemical compound C1([C@]23C[C@H]2CN(C3)CCCSC2=NN=C(N2C)C2=CC3=CC=C(N=C3C=C2)C)=CC=C(Cl)C=C1 SLHOJTDTIDHLRK-WXVAWEFUSA-N 0.000 description 1
- YZXVYUZDVBWITQ-UHFFFAOYSA-N 6-azabicyclo[3.1.0]hexane Chemical compound C1CCC2NC21 YZXVYUZDVBWITQ-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 206010001596 Alcohol induced persisting dementia Diseases 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 208000024827 Alzheimer disease Diseases 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 208000000044 Amnesia Diseases 0.000 description 1
- 235000003911 Arachis Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- 206010003805 Autism Diseases 0.000 description 1
- 208000020706 Autistic disease Diseases 0.000 description 1
- 108010001478 Bacitracin Proteins 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 238000009010 Bradford assay Methods 0.000 description 1
- 208000021465 Brief psychotic disease Diseases 0.000 description 1
- COVZYZSDYWQREU-UHFFFAOYSA-N Busulfan Chemical compound CS(=O)(=O)OCCCCOS(C)(=O)=O COVZYZSDYWQREU-UHFFFAOYSA-N 0.000 description 1
- PQFSLFFWDHKKJA-UHFFFAOYSA-N C(=O)O.C12CNCC2C1 Chemical compound C(=O)O.C12CNCC2C1 PQFSLFFWDHKKJA-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-NJFSPNSNSA-N Carbon-14 Chemical compound [14C] OKTJSMMVPCPJKN-NJFSPNSNSA-N 0.000 description 1
- 208000017164 Chronobiology disease Diseases 0.000 description 1
- 208000028698 Cognitive impairment Diseases 0.000 description 1
- 241000699802 Cricetulus griseus Species 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical class [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- 206010012225 Delirium tremens Diseases 0.000 description 1
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 description 1
- 101100534540 Dictyostelium discoideum syn7A gene Proteins 0.000 description 1
- 102000004980 Dopamine D2 Receptors Human genes 0.000 description 1
- 108090001111 Dopamine D2 Receptors Proteins 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 208000030814 Eating disease Diseases 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- DULCUDSUACXJJC-UHFFFAOYSA-N Ethyl phenylacetate Chemical class CCOC(=O)CC1=CC=CC=C1 DULCUDSUACXJJC-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 208000019454 Feeding and Eating disease Diseases 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 101150026303 HEX1 gene Proteins 0.000 description 1
- GVGLGOZIDCSQPN-PVHGPHFFSA-N Heroin Chemical compound O([C@H]1[C@H](C=C[C@H]23)OC(C)=O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4OC(C)=O GVGLGOZIDCSQPN-PVHGPHFFSA-N 0.000 description 1
- 208000003698 Heroin Dependence Diseases 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- 208000001271 Inhalant Abuse Diseases 0.000 description 1
- WTDRDQBEARUVNC-LURJTMIESA-N L-DOPA Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-LURJTMIESA-N 0.000 description 1
- WTDRDQBEARUVNC-UHFFFAOYSA-N L-Dopa Natural products OC(=O)C(N)CC1=CC=C(O)C(O)=C1 WTDRDQBEARUVNC-UHFFFAOYSA-N 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
- 235000010643 Leucaena leucocephala Nutrition 0.000 description 1
- 240000007472 Leucaena leucocephala Species 0.000 description 1
- GDBQQVLCIARPGH-UHFFFAOYSA-N Leupeptin Natural products CC(C)CC(NC(C)=O)C(=O)NC(CC(C)C)C(=O)NC(C=O)CCCN=C(N)N GDBQQVLCIARPGH-UHFFFAOYSA-N 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- 206010026749 Mania Diseases 0.000 description 1
- 238000007192 Meerwein reaction reaction Methods 0.000 description 1
- 208000026139 Memory disease Diseases 0.000 description 1
- 208000016285 Movement disease Diseases 0.000 description 1
- 101100534544 Mus musculus Stx7 gene Proteins 0.000 description 1
- AYCPARAPKDAOEN-LJQANCHMSA-N N-[(1S)-2-(dimethylamino)-1-phenylethyl]-6,6-dimethyl-3-[(2-methyl-4-thieno[3,2-d]pyrimidinyl)amino]-1,4-dihydropyrrolo[3,4-c]pyrazole-5-carboxamide Chemical compound C1([C@H](NC(=O)N2C(C=3NN=C(NC=4C=5SC=CC=5N=C(C)N=4)C=3C2)(C)C)CN(C)C)=CC=CC=C1 AYCPARAPKDAOEN-LJQANCHMSA-N 0.000 description 1
- MBBZMMPHUWSWHV-BDVNFPICSA-N N-methylglucamine Chemical compound CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO MBBZMMPHUWSWHV-BDVNFPICSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- 229910003310 Ni-Al Inorganic materials 0.000 description 1
- 206010057852 Nicotine dependence Diseases 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 208000021384 Obsessive-Compulsive disease Diseases 0.000 description 1
- 208000027099 Paranoid disease Diseases 0.000 description 1
- 208000027089 Parkinsonian disease Diseases 0.000 description 1
- 206010034010 Parkinsonism Diseases 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 208000034592 Polysubstance dependence Diseases 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- 206010061921 Psychotic disorder due to a general medical condition Diseases 0.000 description 1
- 238000001069 Raman spectroscopy Methods 0.000 description 1
- 208000020186 Schizophreniform disease Diseases 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 208000019568 Shared Paranoid disease Diseases 0.000 description 1
- 208000028810 Shared psychotic disease Diseases 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 231100000643 Substance intoxication Toxicity 0.000 description 1
- 208000011962 Substance-induced mood disease Diseases 0.000 description 1
- 231100000395 Substance-induced mood disorder Toxicity 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 238000006069 Suzuki reaction reaction Methods 0.000 description 1
- 206010043118 Tardive Dyskinesia Diseases 0.000 description 1
- 208000025569 Tobacco Use disease Diseases 0.000 description 1
- 206010043903 Tobacco abuse Diseases 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 208000012886 Vertigo Diseases 0.000 description 1
- 206010047700 Vomiting Diseases 0.000 description 1
- 108010046516 Wheat Germ Agglutinins Proteins 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- ZUSWDTWYONAOPH-UHFFFAOYSA-N [2-(trifluoromethyl)phenyl]hydrazine;hydrochloride Chemical group [Cl-].[NH3+]NC1=CC=CC=C1C(F)(F)F ZUSWDTWYONAOPH-UHFFFAOYSA-N 0.000 description 1
- BJVVSQMKGWOWBI-UHFFFAOYSA-N [4-(3-azabicyclo[3.1.0]hexan-1-yl)-2-fluorophenyl]methanamine;dihydrochloride Chemical compound Cl.Cl.C1=C(F)C(CN)=CC=C1C1(CNC2)C2C1 BJVVSQMKGWOWBI-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000012445 acidic reagent Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 238000012382 advanced drug delivery Methods 0.000 description 1
- 230000016571 aggressive behavior Effects 0.000 description 1
- 201000007930 alcohol dependence Diseases 0.000 description 1
- 208000029650 alcohol withdrawal Diseases 0.000 description 1
- 208000006246 alcohol withdrawal delirium Diseases 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 230000006986 amnesia Effects 0.000 description 1
- 201000002472 amphetamine abuse Diseases 0.000 description 1
- 239000003708 ampul Substances 0.000 description 1
- 239000003263 anabolic agent Substances 0.000 description 1
- 229940070021 anabolic steroids Drugs 0.000 description 1
- 230000000561 anti-psychotic effect Effects 0.000 description 1
- 230000036506 anxiety Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- 239000008365 aqueous carrier Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 125000005279 aryl sulfonyloxy group Chemical group 0.000 description 1
- 239000012131 assay buffer Substances 0.000 description 1
- 125000003828 azulenyl group Chemical group 0.000 description 1
- 229960003071 bacitracin Drugs 0.000 description 1
- 229930184125 bacitracin Natural products 0.000 description 1
- CLKOFPXJLQSYAH-ABRJDSQDSA-N bacitracin A Chemical compound C1SC([C@@H](N)[C@@H](C)CC)=N[C@@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]1C(=O)N[C@H](CCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CC=2N=CNC=2)C(=O)N[C@H](CC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)NCCCC1 CLKOFPXJLQSYAH-ABRJDSQDSA-N 0.000 description 1
- OYLGJCQECKOTOL-UHFFFAOYSA-L barium fluoride Chemical compound [F-].[F-].[Ba+2] OYLGJCQECKOTOL-UHFFFAOYSA-L 0.000 description 1
- 229910001632 barium fluoride Inorganic materials 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- 125000004604 benzisothiazolyl group Chemical group S1N=C(C2=C1C=CC=C2)* 0.000 description 1
- 125000004603 benzisoxazolyl group Chemical group O1N=C(C2=C1C=CC=C2)* 0.000 description 1
- 150000008038 benzoazepines Chemical class 0.000 description 1
- 229940049706 benzodiazepine Drugs 0.000 description 1
- 125000003310 benzodiazepinyl group Chemical class N1N=C(C=CC2=C1C=CC=C2)* 0.000 description 1
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 description 1
- 125000004622 benzoxazinyl group Chemical group O1NC(=CC2=C1C=CC=C2)* 0.000 description 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 description 1
- HRCFATLJUADPJI-UHFFFAOYSA-N bicyclo[3.1.0]hexane;hydrochloride Chemical compound Cl.C1CCC2CC21 HRCFATLJUADPJI-UHFFFAOYSA-N 0.000 description 1
- 239000012620 biological material Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- MPQAQJSAYDDROO-VMAIWCPRSA-N bis[(1r,3r,4s,5r)-4,6,6-trimethyl-3-bicyclo[3.1.1]heptanyl]boron Chemical compound C([C@H]([C@@H]1C)[B][C@@H]2C[C@@H]3C[C@@H](C3(C)C)[C@H]2C)[C@H]2C(C)(C)[C@@H]1C2 MPQAQJSAYDDROO-VMAIWCPRSA-N 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 150000001638 boron Chemical class 0.000 description 1
- 125000005998 bromoethyl group Chemical group 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 201000009322 cannabis abuse Diseases 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 206010007776 catatonia Diseases 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- MMFVFNVXXDFELX-UHFFFAOYSA-N chloroform;n,n-diethylethanamine Chemical compound ClC(Cl)Cl.CCN(CC)CC MMFVFNVXXDFELX-UHFFFAOYSA-N 0.000 description 1
- VDANGULDQQJODZ-UHFFFAOYSA-N chloroprocaine Chemical compound CCN(CC)CCOC(=O)C1=CC=C(N)C=C1Cl VDANGULDQQJODZ-UHFFFAOYSA-N 0.000 description 1
- 229960002023 chloroprocaine Drugs 0.000 description 1
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 1
- 229960001231 choline Drugs 0.000 description 1
- 125000000259 cinnolinyl group Chemical group N1=NC(=CC2=CC=CC=C12)* 0.000 description 1
- 238000002983 circular dichroism Methods 0.000 description 1
- 201000006145 cocaine dependence Diseases 0.000 description 1
- 229940110456 cocoa butter Drugs 0.000 description 1
- 235000019868 cocoa butter Nutrition 0.000 description 1
- 230000019771 cognition Effects 0.000 description 1
- 208000010877 cognitive disease Diseases 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000011340 continuous therapy Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- WZHCOOQXZCIUNC-UHFFFAOYSA-N cyclandelate Chemical compound C1C(C)(C)CC(C)CC1OC(=O)C(O)C1=CC=CC=C1 WZHCOOQXZCIUNC-UHFFFAOYSA-N 0.000 description 1
- 238000005888 cyclopropanation reaction Methods 0.000 description 1
- 150000001942 cyclopropanes Chemical class 0.000 description 1
- 125000004856 decahydroquinolinyl group Chemical group N1(CCCC2CCCCC12)* 0.000 description 1
- 230000017858 demethylation Effects 0.000 description 1
- 238000010520 demethylation reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000003001 depressive effect Effects 0.000 description 1
- 229910052805 deuterium Inorganic materials 0.000 description 1
- 229960002069 diamorphine Drugs 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 229940043237 diethanolamine Drugs 0.000 description 1
- 125000000723 dihydrobenzofuranyl group Chemical group O1C(CC2=C1C=CC=C2)* 0.000 description 1
- NYOWONIQQNXXDL-UHFFFAOYSA-N dimethyl 1-(4-methoxyphenyl)cyclopropane-1,2-dicarboxylate Chemical compound COC(=O)C1CC1(C(=O)OC)C1=CC=C(OC)C=C1 NYOWONIQQNXXDL-UHFFFAOYSA-N 0.000 description 1
- 125000000532 dioxanyl group Chemical group 0.000 description 1
- 125000005879 dioxolanyl group Chemical group 0.000 description 1
- 235000014632 disordered eating Nutrition 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 125000005883 dithianyl group Chemical group 0.000 description 1
- 229940052760 dopamine agonists Drugs 0.000 description 1
- 239000003136 dopamine receptor stimulating agent Substances 0.000 description 1
- BSMNRYCSBFHEMQ-UHFFFAOYSA-N dov-216,303 Chemical compound C1=C(Cl)C(Cl)=CC=C1C1(CNC2)C2C1 BSMNRYCSBFHEMQ-UHFFFAOYSA-N 0.000 description 1
- 238000012377 drug delivery Methods 0.000 description 1
- 238000009510 drug design Methods 0.000 description 1
- 230000000857 drug effect Effects 0.000 description 1
- 230000000142 dyskinetic effect Effects 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 239000012259 ether extract Substances 0.000 description 1
- RDULEYWUGKOCMR-UHFFFAOYSA-N ethyl 2-chloro-3-oxobutanoate Chemical compound CCOC(=O)C(Cl)C(C)=O RDULEYWUGKOCMR-UHFFFAOYSA-N 0.000 description 1
- FCZCIXQGZOUIDN-UHFFFAOYSA-N ethyl 2-diethoxyphosphinothioyloxyacetate Chemical compound CCOC(=O)COP(=S)(OCC)OCC FCZCIXQGZOUIDN-UHFFFAOYSA-N 0.000 description 1
- NBEMQPLNBYYUAZ-UHFFFAOYSA-N ethyl acetate;propan-2-one Chemical compound CC(C)=O.CCOC(C)=O NBEMQPLNBYYUAZ-UHFFFAOYSA-N 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229940012017 ethylenediamine Drugs 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 230000030135 gastric motility Effects 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 201000002270 hallucinogen abuse Diseases 0.000 description 1
- 201000006138 hallucinogen dependence Diseases 0.000 description 1
- 125000005280 halo alkyl sulfonyloxy group Chemical group 0.000 description 1
- HJLHTTJLVALHOP-UHFFFAOYSA-N hexane;hydron;chloride Chemical compound Cl.CCCCCC HJLHTTJLVALHOP-UHFFFAOYSA-N 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- ZXRCAYWYTOIRQS-UHFFFAOYSA-N hydron;phenol;chloride Chemical compound Cl.OC1=CC=CC=C1 ZXRCAYWYTOIRQS-UHFFFAOYSA-N 0.000 description 1
- GXBDUKNALWQPMX-UHFFFAOYSA-N hydron;pyrrole-2,5-dione;chloride Chemical class Cl.O=C1NC(=O)C=C1 GXBDUKNALWQPMX-UHFFFAOYSA-N 0.000 description 1
- PSXRWZBTVAZNSF-UHFFFAOYSA-N hydron;quinoline;chloride Chemical compound Cl.N1=CC=CC2=CC=CC=C21 PSXRWZBTVAZNSF-UHFFFAOYSA-N 0.000 description 1
- 125000002632 imidazolidinyl group Chemical group 0.000 description 1
- 125000002636 imidazolinyl group Chemical group 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 description 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 1
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000004594 isoindolinyl group Chemical group C1(NCC2=CC=CC=C12)* 0.000 description 1
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000005928 isopropyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 description 1
- 125000005956 isoquinolyl group Chemical group 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- GDBQQVLCIARPGH-ULQDDVLXSA-N leupeptin Chemical compound CC(C)C[C@H](NC(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C=O)CCCN=C(N)N GDBQQVLCIARPGH-ULQDDVLXSA-N 0.000 description 1
- 108010052968 leupeptin Proteins 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 230000004807 localization Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 208000024714 major depressive disease Diseases 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000007721 medicinal effect Effects 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
- FWVOAIHAIWHHDM-UHFFFAOYSA-N methyl 2-(3,4-dichlorophenyl)acetate Chemical compound COC(=O)CC1=CC=C(Cl)C(Cl)=C1 FWVOAIHAIWHHDM-UHFFFAOYSA-N 0.000 description 1
- HTBBVKFFDDQVER-UHFFFAOYSA-N methyl 2-(3-chlorophenyl)acetate Chemical compound COC(=O)CC1=CC=CC(Cl)=C1 HTBBVKFFDDQVER-UHFFFAOYSA-N 0.000 description 1
- OXYLCGRXCQARQV-UHFFFAOYSA-N methyl 2-(3-fluorophenyl)acetate Chemical compound COC(=O)CC1=CC=CC(F)=C1 OXYLCGRXCQARQV-UHFFFAOYSA-N 0.000 description 1
- AJPPKGMEHMXPMC-UHFFFAOYSA-N methyl 2-(4-fluorophenyl)acetate Chemical compound COC(=O)CC1=CC=C(F)C=C1 AJPPKGMEHMXPMC-UHFFFAOYSA-N 0.000 description 1
- YWVRILIISWHRDP-UHFFFAOYSA-N methyl 2-[2-(trifluoromethyl)phenyl]acetate Chemical compound COC(=O)CC1=CC=CC=C1C(F)(F)F YWVRILIISWHRDP-UHFFFAOYSA-N 0.000 description 1
- BSJFQYCYYUQYSN-UHFFFAOYSA-N methyl 2-bromo-2-[4-(trifluoromethoxy)phenyl]acetate Chemical compound COC(=O)C(Br)C1=CC=C(OC(F)(F)F)C=C1 BSJFQYCYYUQYSN-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 125000002757 morpholinyl group Chemical group 0.000 description 1
- 230000008450 motivation Effects 0.000 description 1
- ACTNHJDHMQSOGL-UHFFFAOYSA-N n',n'-dibenzylethane-1,2-diamine Chemical compound C=1C=CC=CC=1CN(CCN)CC1=CC=CC=C1 ACTNHJDHMQSOGL-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 238000002610 neuroimaging Methods 0.000 description 1
- 230000000701 neuroleptic effect Effects 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- 239000012038 nucleophile Substances 0.000 description 1
- UZGLIIJVICEWHF-UHFFFAOYSA-N octogen Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)CN([N+]([O-])=O)C1 UZGLIIJVICEWHF-UHFFFAOYSA-N 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 229940127240 opiate Drugs 0.000 description 1
- 201000005040 opiate dependence Diseases 0.000 description 1
- 201000000988 opioid abuse Diseases 0.000 description 1
- 229940005483 opioid analgesics Drugs 0.000 description 1
- 229940126701 oral medication Drugs 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- 125000001715 oxadiazolyl group Chemical group 0.000 description 1
- 125000003145 oxazol-4-yl group Chemical group O1C=NC(=C1)* 0.000 description 1
- 125000005968 oxazolinyl group Chemical group 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 239000004031 partial agonist Substances 0.000 description 1
- 235000010603 pastilles Nutrition 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
- XOKSLPVRUOBDEW-UHFFFAOYSA-N pinane of uncertain configuration Natural products CC1CCC2C(C)(C)C1C2 XOKSLPVRUOBDEW-UHFFFAOYSA-N 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000004237 preparative chromatography Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- MFDFERRIHVXMIY-UHFFFAOYSA-N procaine Chemical compound CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 MFDFERRIHVXMIY-UHFFFAOYSA-N 0.000 description 1
- 229960004919 procaine Drugs 0.000 description 1
- RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 208000020016 psychiatric disease Diseases 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 125000003072 pyrazolidinyl group Chemical group 0.000 description 1
- 125000002755 pyrazolinyl group Chemical group 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- 125000005493 quinolyl group Chemical group 0.000 description 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 102220082749 rs143241583 Human genes 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 208000022610 schizoaffective disease Diseases 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 238000013207 serial dilution Methods 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 230000000392 somatic effect Effects 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 201000006152 substance dependence Diseases 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000002511 suppository base Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- DYHSDKLCOJIUFX-UHFFFAOYSA-N tert-butoxycarbonyl anhydride Chemical compound CC(C)(C)OC(=O)OC(=O)OC(C)(C)C DYHSDKLCOJIUFX-UHFFFAOYSA-N 0.000 description 1
- 125000001981 tert-butyldimethylsilyl group Chemical group [H]C([H])([H])[Si]([H])(C([H])([H])[H])[*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 125000003039 tetrahydroisoquinolinyl group Chemical group C1(NCCC2=CC=CC=C12)* 0.000 description 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 125000005958 tetrahydrothienyl group Chemical group 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 description 1
- 238000003354 tissue distribution assay Methods 0.000 description 1
- 238000003325 tomography Methods 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 238000000844 transformation Methods 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- QAEDZJGFFMLHHQ-UHFFFAOYSA-N trifluoroacetic anhydride Chemical compound FC(F)(F)C(=O)OC(=O)C(F)(F)F QAEDZJGFFMLHHQ-UHFFFAOYSA-N 0.000 description 1
- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 description 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 1
- 125000000725 trifluoropropyl group Chemical group [H]C([H])(*)C([H])([H])C(F)(F)F 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 231100000889 vertigo Toxicity 0.000 description 1
- 238000001845 vibrational spectrum Methods 0.000 description 1
- 238000003260 vortexing Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/32—Alcohol-abuse
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/34—Tobacco-abuse
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/36—Opioid-abuse
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Addiction (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Endocrinology (AREA)
- Anesthesiology (AREA)
- Gynecology & Obstetrics (AREA)
- Pain & Pain Management (AREA)
- Reproductive Health (AREA)
- Otolaryngology (AREA)
- Nutrition Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0403990.5 | 2004-02-23 | ||
| GB0403990A GB0403990D0 (en) | 2004-02-23 | 2004-02-23 | Compounds |
| GB0404083A GB0404083D0 (en) | 2004-02-24 | 2004-02-24 | Compounds |
| GB0404083.8 | 2004-02-24 | ||
| GB0417120A GB0417120D0 (en) | 2004-07-30 | 2004-07-30 | Compounds |
| GB0417120.3 | 2004-07-30 | ||
| PCT/EP2005/001940 WO2005080382A1 (en) | 2004-02-23 | 2005-02-21 | Azabicyclo (3.1.0) hexane derivatives useful as modulators of dopamine d3 receptors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2557115A1 CA2557115A1 (en) | 2005-09-01 |
| CA2557115C true CA2557115C (en) | 2012-10-02 |
Family
ID=34890800
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2557115A Expired - Fee Related CA2557115C (en) | 2004-02-23 | 2005-02-21 | Azabicyclo (3.1.0) hexane derivatives useful as modulators of dopamine d3 receptors |
Country Status (25)
| Country | Link |
|---|---|
| US (3) | US7855298B2 (https=) |
| EP (3) | EP2070922B1 (https=) |
| JP (1) | JP4960217B2 (https=) |
| KR (1) | KR101143718B1 (https=) |
| CN (1) | CN1946714B (https=) |
| AR (1) | AR047890A1 (https=) |
| AT (3) | ATE451364T1 (https=) |
| AU (2) | AU2005215918C1 (https=) |
| BR (1) | BRPI0507945A (https=) |
| CA (1) | CA2557115C (https=) |
| CY (3) | CY1109854T1 (https=) |
| DE (1) | DE602005018190D1 (https=) |
| DK (3) | DK2060570T3 (https=) |
| ES (2) | ES2380990T3 (https=) |
| HR (3) | HRP20100114T1 (https=) |
| IL (1) | IL177184A0 (https=) |
| MA (1) | MA28438B1 (https=) |
| NO (1) | NO20064309L (https=) |
| PE (1) | PE20051173A1 (https=) |
| PL (3) | PL2060570T3 (https=) |
| PT (3) | PT2070922E (https=) |
| RU (1) | RU2434011C2 (https=) |
| SI (3) | SI1745040T1 (https=) |
| TW (1) | TW200538113A (https=) |
| WO (1) | WO2005080382A1 (https=) |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20051173A1 (es) * | 2004-02-23 | 2006-02-14 | Glaxo Group Ltd | Compuestos azabiciclico (3.1.0) hexanos como moduladores de receptores de dopamina d3 |
| US20070043100A1 (en) | 2005-08-16 | 2007-02-22 | Hagen Eric J | Novel polymorphs of azabicyclohexane |
| GB0507602D0 (en) * | 2005-04-14 | 2005-05-18 | Glaxo Group Ltd | Compounds |
| GB0507601D0 (en) * | 2005-04-14 | 2005-05-18 | Glaxo Group Ltd | Compounds |
| GB0507680D0 (en) * | 2005-04-15 | 2005-05-25 | Glaxo Group Ltd | Compounds |
| GB0512099D0 (en) * | 2005-06-14 | 2005-07-20 | Glaxo Group Ltd | Compounds |
| WO2006133945A1 (en) | 2005-06-14 | 2006-12-21 | Glaxo Group Limited | Novel compounds |
| WO2007006117A1 (en) * | 2005-07-13 | 2007-01-18 | Nicogen Inc. | Novel cyp2a6 inhibitors |
| NZ592836A (en) * | 2005-07-27 | 2013-01-25 | Dov Pharmaceutical Inc | Novel 1-aryl-3-azabicyclo[3.1.0]hexanes: preparation and use to treat neuropsychiatric disorders |
| GB0517191D0 (en) * | 2005-08-22 | 2005-09-28 | Glaxo Group Ltd | Compounds |
| GB0517187D0 (en) * | 2005-08-22 | 2005-09-28 | Glaxo Group Ltd | Compounds |
| WO2007022933A1 (en) * | 2005-08-22 | 2007-03-01 | Glaxo Group Limited | Triazole derivatives as modulators of dopamine d3 receptors |
| GB0517193D0 (en) * | 2005-08-22 | 2005-09-28 | Glaxo Group Ltd | Novel use |
| GB0517175D0 (en) * | 2005-08-22 | 2005-09-28 | Glaxo Group Ltd | Compounds |
| AR060237A1 (es) * | 2006-04-03 | 2008-06-04 | Glaxo Group Ltd | Compuesto de 3-azabiciclo[3.1.0]hexano como moduladores del receptor de dopamina d3, su uso para la preparacion de un medicamento para el tratamiento de afecciones psicoticas y composicion farmaceutica que lo comprende. |
| GB0703387D0 (en) * | 2007-02-21 | 2007-03-28 | Glaxo Group Ltd | Novel compounds |
| GB0607899D0 (en) * | 2006-04-03 | 2006-05-31 | Glaxo Group Ltd | Process for preparing heterocyclic derivatives |
| US8222266B2 (en) * | 2006-04-03 | 2012-07-17 | Glaxo Group Limited | Azabicyclo [3.1.0] hexyl derivatives as modulators of dopamine D3 receptors |
| US8163927B2 (en) * | 2006-04-03 | 2012-04-24 | Glaxo Group Limited | Azabicyclo [3.1.0] hexane derivatives as modulators of dopamine D3 receptors |
| GB0608452D0 (en) * | 2006-04-27 | 2006-06-07 | Glaxo Group Ltd | Novel compounds |
| US20080045725A1 (en) | 2006-04-28 | 2008-02-21 | Murry Jerry A | Process For The Synthesis of (+) And (-)-1-(3,4-Dichlorophenyl)-3-Azabicyclo[3.1.0]Hexane |
| GB0616574D0 (en) * | 2006-08-21 | 2006-09-27 | Glaxo Group Ltd | Compounds |
| US8138377B2 (en) | 2006-11-07 | 2012-03-20 | Dov Pharmaceutical, Inc. | Arylbicyclo[3.1.0]hexylamines and methods and compositions for their preparation and use |
| US20090069374A1 (en) * | 2007-06-06 | 2009-03-12 | Phil Skolnick | Novel 1-Heteroaryl-3-Azabicyclo[3.1.0]Hexanes, Methods For Their Preparation And Their Use As Medicaments |
| US9133159B2 (en) | 2007-06-06 | 2015-09-15 | Neurovance, Inc. | 1-heteroaryl-3-azabicyclo[3.1.0]hexanes, methods for their preparation and their use as medicaments |
| GB0719235D0 (en) * | 2007-10-02 | 2007-11-14 | Glaxo Group Ltd | Novel compounds |
| GB0719234D0 (en) * | 2007-10-02 | 2007-11-14 | Glaxo Group Ltd | Novel compounds |
| CN102816106A (zh) | 2008-06-24 | 2012-12-12 | 默沙东公司 | 用于制备基本上立体异构纯的稠合二环脯氨酸化合物的生物催化方法 |
| US8536185B2 (en) | 2008-09-22 | 2013-09-17 | Cayman Chemical Company, Incorporated | Multiheteroaryl compounds as inhibitors of H-PGDS and their use for treating prostaglandin D2 mediated diseases |
| BR112012000657A2 (pt) | 2009-06-26 | 2016-11-16 | Panacea Biotec Ltd | novos azabicilohexanos |
| US20140206740A1 (en) | 2011-07-30 | 2014-07-24 | Neurovance, Inc. | Use Of (1R,5S)-(+)-(Napthalen-2-yl)-3-Azabicyclo[3.1.0]Hexane In The Treatment Of Conditions Affected By Monoamine Neurotransmitters |
| US20160279098A1 (en) * | 2013-11-11 | 2016-09-29 | Euthymics Bioscience, Inc. | Novel methods |
| HK1250029A1 (zh) | 2015-08-05 | 2018-11-23 | Indivior Uk Limited | 具有双环结构的多巴胺d3受体拮抗剂 |
| JP7250405B2 (ja) | 2018-01-26 | 2023-04-03 | 塩野義製薬株式会社 | ドーパミンｄ３受容体拮抗作用を有する環式化合物 |
| CN116113627B (zh) | 2020-06-22 | 2025-06-03 | 科赛普特治疗公司 | 季吲哚糖皮质激素受体拮抗剂 |
| US12115154B2 (en) | 2020-12-16 | 2024-10-15 | Srx Cardio, Llc | Compounds for the modulation of proprotein convertase subtilisin/kexin type 9 (PCSK9) |
| IL313667A (en) | 2021-12-21 | 2024-08-01 | Corcept Therapeutics Inc | Glucocorticoid receptor antagonists INDAZOL CYCLES |
| CA3243549A1 (en) | 2021-12-21 | 2023-06-29 | Corcept Therapeutics Incorporated | INDAZOLE PIPERAZINE-BASED GLUCOCORTICOID RECEPTOR ANTAGONISTS |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI274750B (en) * | 1999-01-12 | 2007-03-01 | Abbott Gmbh & Co Kg | Triazole compounds showing high affinity to dopamine D3 receptor and pharmaceutical composition comprising the same |
| GB0015562D0 (en) * | 2000-06-23 | 2000-08-16 | Pfizer Ltd | Heterocycles |
| JP4272423B2 (ja) | 2000-11-14 | 2009-06-03 | スミスクライン ビーチャム ピー エル シー | ドーパミンｄ３受容体のモジュレーターとして有用なテトラヒドロベンズアゼピン誘導体（抗精神病剤） |
| US6569887B2 (en) * | 2001-08-24 | 2003-05-27 | Dov Pharmaceuticals Inc. | (−)-1-(3,4-Dichlorophenyl)-3-azabicyclo[3.1.0]hexane, compositions thereof, and uses as a dopamine-reuptake |
| EP1440059B1 (en) | 2001-10-22 | 2008-04-16 | Pfizer Products Inc. | 3-azabicyclo(3.1.0)hexane derivatives as opioid receptor antagonists |
| IL166510A0 (en) * | 2002-08-09 | 2006-01-15 | Nps Pharma Inc | 1,2,4"oxadiazole as modulators of metabotropic glutamate receptor-5 |
| PE20051173A1 (es) * | 2004-02-23 | 2006-02-14 | Glaxo Group Ltd | Compuestos azabiciclico (3.1.0) hexanos como moduladores de receptores de dopamina d3 |
| GB0507601D0 (en) * | 2005-04-14 | 2005-05-18 | Glaxo Group Ltd | Compounds |
| GB0507602D0 (en) * | 2005-04-14 | 2005-05-18 | Glaxo Group Ltd | Compounds |
| GB0507680D0 (en) * | 2005-04-15 | 2005-05-25 | Glaxo Group Ltd | Compounds |
| WO2006133945A1 (en) * | 2005-06-14 | 2006-12-21 | Glaxo Group Limited | Novel compounds |
| GB0517175D0 (en) * | 2005-08-22 | 2005-09-28 | Glaxo Group Ltd | Compounds |
| GB0517191D0 (en) * | 2005-08-22 | 2005-09-28 | Glaxo Group Ltd | Compounds |
| GB0517193D0 (en) * | 2005-08-22 | 2005-09-28 | Glaxo Group Ltd | Novel use |
| WO2007022933A1 (en) * | 2005-08-22 | 2007-03-01 | Glaxo Group Limited | Triazole derivatives as modulators of dopamine d3 receptors |
| GB0517187D0 (en) * | 2005-08-22 | 2005-09-28 | Glaxo Group Ltd | Compounds |
| AR060237A1 (es) * | 2006-04-03 | 2008-06-04 | Glaxo Group Ltd | Compuesto de 3-azabiciclo[3.1.0]hexano como moduladores del receptor de dopamina d3, su uso para la preparacion de un medicamento para el tratamiento de afecciones psicoticas y composicion farmaceutica que lo comprende. |
| GB0616574D0 (en) * | 2006-08-21 | 2006-09-27 | Glaxo Group Ltd | Compounds |
-
2005
- 2005-02-21 PE PE2005000205A patent/PE20051173A1/es not_active Application Discontinuation
- 2005-02-21 AT AT05707610T patent/ATE451364T1/de active
- 2005-02-21 SI SI200530923T patent/SI1745040T1/sl unknown
- 2005-02-21 TW TW094105108A patent/TW200538113A/zh unknown
- 2005-02-21 AT AT08169935T patent/ATE542816T1/de active
- 2005-02-21 SI SI200531398T patent/SI2070922T1/sl unknown
- 2005-02-21 US US10/598,200 patent/US7855298B2/en not_active Expired - Fee Related
- 2005-02-21 PT PT08169934T patent/PT2070922E/pt unknown
- 2005-02-21 ES ES08169935T patent/ES2380990T3/es not_active Expired - Lifetime
- 2005-02-21 PL PL08169935T patent/PL2060570T3/pl unknown
- 2005-02-21 WO PCT/EP2005/001940 patent/WO2005080382A1/en not_active Ceased
- 2005-02-21 EP EP08169934A patent/EP2070922B1/en not_active Expired - Lifetime
- 2005-02-21 DK DK08169935.7T patent/DK2060570T3/da active
- 2005-02-21 PT PT05707610T patent/PT1745040E/pt unknown
- 2005-02-21 JP JP2007500152A patent/JP4960217B2/ja not_active Expired - Fee Related
- 2005-02-21 SI SI200531503T patent/SI2060570T1/sl unknown
- 2005-02-21 RU RU2006133909/04A patent/RU2434011C2/ru not_active IP Right Cessation
- 2005-02-21 AR ARP050100632A patent/AR047890A1/es not_active Application Discontinuation
- 2005-02-21 ES ES05707610T patent/ES2337590T3/es not_active Expired - Lifetime
- 2005-02-21 KR KR1020067016833A patent/KR101143718B1/ko not_active Expired - Fee Related
- 2005-02-21 EP EP08169935A patent/EP2060570B1/en not_active Expired - Lifetime
- 2005-02-21 CA CA2557115A patent/CA2557115C/en not_active Expired - Fee Related
- 2005-02-21 DE DE602005018190T patent/DE602005018190D1/de not_active Expired - Lifetime
- 2005-02-21 BR BRPI0507945-4A patent/BRPI0507945A/pt active Search and Examination
- 2005-02-21 AT AT08169934T patent/ATE520686T1/de active
- 2005-02-21 PT PT08169935T patent/PT2060570E/pt unknown
- 2005-02-21 PL PL08169934T patent/PL2070922T3/pl unknown
- 2005-02-21 DK DK05707610.1T patent/DK1745040T3/da active
- 2005-02-21 EP EP05707610A patent/EP1745040B9/en not_active Expired - Lifetime
- 2005-02-21 DK DK08169934.0T patent/DK2070922T3/da active
- 2005-02-21 HR HR20100114T patent/HRP20100114T1/hr unknown
- 2005-02-21 AU AU2005215918A patent/AU2005215918C1/en not_active Ceased
- 2005-02-21 PL PL05707610T patent/PL1745040T3/pl unknown
- 2005-02-21 CN CN2005800126155A patent/CN1946714B/zh not_active Expired - Fee Related
-
2006
- 2006-07-31 IL IL177184A patent/IL177184A0/en unknown
- 2006-08-22 MA MA29286A patent/MA28438B1/fr unknown
- 2006-09-22 NO NO20064309A patent/NO20064309L/no not_active Application Discontinuation
-
2009
- 2009-09-01 AU AU2009212887A patent/AU2009212887A1/en not_active Abandoned
- 2009-12-16 US US12/639,129 patent/US8263782B2/en not_active Expired - Fee Related
- 2009-12-16 US US12/639,282 patent/US8283474B2/en not_active Expired - Fee Related
-
2010
- 2010-03-01 CY CY20101100197T patent/CY1109854T1/el unknown
-
2011
- 2011-10-26 HR HR20110781T patent/HRP20110781T1/hr unknown
- 2011-11-07 CY CY20111101073T patent/CY1112011T1/el unknown
-
2012
- 2012-03-29 HR HR20120281T patent/HRP20120281T1/hr unknown
- 2012-04-11 CY CY20121100356T patent/CY1113029T1/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2557115C (en) | Azabicyclo (3.1.0) hexane derivatives useful as modulators of dopamine d3 receptors | |
| RU2689777C1 (ru) | Конденсированные трициклические производные бензимидазолов в качестве модуляторов активности tnf | |
| US7947683B2 (en) | 3-(1,2,4-triazol-3-ylalkyl) azabicyclo (3.1.0) hexane derivatives as modulators of dopamine D3 receptors | |
| US7799815B2 (en) | Triazole derivatives as modulators of dopamine D3 receptors | |
| US7875643B2 (en) | Azabicyclo (3.1.0) hexane derivatives useful as modulators of dopamine D3 receptors | |
| US7803820B2 (en) | 3-triazolylthiaalkyl-3-azabicyclo (3-1-O) hexanes and their use as dopamine D3 receptor ligands | |
| EP1891057B1 (en) | Azabicyclo[3.1.0]hexane derivaives as dopamin d3 receptor modulators | |
| HK1132995A (en) | Azabicyclo(3.1.0) hexane derivatives useful as modulators of dopamine d3 receptors | |
| HK1133431A (en) | Azabicyclo(3.1.0) hexane derivatives useful as modulators of dopamine d3 receptors | |
| MXPA06009652A (en) | Azabicyclo (3.1.0) hexane derivatives useful as modulators of dopamine d3 receptors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKLA | Lapsed |
Effective date: 20180221 |