HRP970531A2 - Radiopharmaceuticals for imaging infection and inflammation - Google Patents
Radiopharmaceuticals for imaging infection and inflammationInfo
- Publication number
- HRP970531A2 HRP970531A2 HR08/726,507A HRP970531A HRP970531A2 HR P970531 A2 HRP970531 A2 HR P970531A2 HR P970531 A HRP970531 A HR P970531A HR P970531 A2 HRP970531 A2 HR P970531A2
- Authority
- HR
- Croatia
- Prior art keywords
- substituted
- carbamoyl
- group
- pyridinyl
- amino
- Prior art date
Links
- 239000012217 radiopharmaceutical Substances 0.000 title claims description 114
- 229940121896 radiopharmaceutical Drugs 0.000 title claims description 114
- 230000002799 radiopharmaceutical effect Effects 0.000 title claims description 114
- 208000015181 infectious disease Diseases 0.000 title claims description 31
- 230000004054 inflammatory process Effects 0.000 title claims description 31
- 206010061218 Inflammation Diseases 0.000 title claims description 30
- 238000003384 imaging method Methods 0.000 title claims description 15
- SEQKRHFRPICQDD-UHFFFAOYSA-N N-tris(hydroxymethyl)methylglycine Chemical compound OCC(CO)(CO)[NH2+]CC([O-])=O SEQKRHFRPICQDD-UHFFFAOYSA-N 0.000 claims description 307
- -1 methylenedioxy Chemical group 0.000 claims description 268
- UZMAPBJVXOGOFT-UHFFFAOYSA-N Syringetin Natural products COC1=C(O)C(OC)=CC(C2=C(C(=O)C3=C(O)C=C(O)C=C3O2)O)=C1 UZMAPBJVXOGOFT-UHFFFAOYSA-N 0.000 claims description 153
- 239000007997 Tricine buffer Substances 0.000 claims description 153
- KCFYHBSOLOXZIF-UHFFFAOYSA-N dihydrochrysin Natural products COC1=C(O)C(OC)=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2)=C1 KCFYHBSOLOXZIF-UHFFFAOYSA-N 0.000 claims description 153
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 125
- MYAJTCUQMQREFZ-UHFFFAOYSA-K tppts Chemical compound [Na+].[Na+].[Na+].[O-]S(=O)(=O)C1=CC=CC(P(C=2C=C(C=CC=2)S([O-])(=O)=O)C=2C=C(C=CC=2)S([O-])(=O)=O)=C1 MYAJTCUQMQREFZ-UHFFFAOYSA-K 0.000 claims description 113
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 110
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 109
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 109
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 100
- 150000001875 compounds Chemical class 0.000 claims description 88
- 229940092714 benzenesulfonic acid Drugs 0.000 claims description 86
- 239000003446 ligand Substances 0.000 claims description 81
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 78
- 229910052757 nitrogen Inorganic materials 0.000 claims description 77
- 238000006243 chemical reaction Methods 0.000 claims description 70
- 125000003118 aryl group Chemical group 0.000 claims description 66
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 64
- 125000000623 heterocyclic group Chemical group 0.000 claims description 61
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 60
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 claims description 60
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 60
- 235000019260 propionic acid Nutrition 0.000 claims description 60
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 claims description 58
- 239000003153 chemical reaction reagent Substances 0.000 claims description 58
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 53
- 238000000034 method Methods 0.000 claims description 49
- VNYSSYRCGWBHLG-AMOLWHMGSA-N leukotriene B4 Chemical compound CCCCC\C=C/C[C@@H](O)\C=C\C=C\C=C/[C@@H](O)CCCC(O)=O VNYSSYRCGWBHLG-AMOLWHMGSA-N 0.000 claims description 44
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims description 44
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 42
- 125000004429 atom Chemical group 0.000 claims description 38
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 36
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 36
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 36
- 229910052739 hydrogen Inorganic materials 0.000 claims description 34
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 34
- 229910052760 oxygen Inorganic materials 0.000 claims description 33
- 229920002554 vinyl polymer Polymers 0.000 claims description 33
- 125000005638 hydrazono group Chemical group 0.000 claims description 32
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 31
- XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 claims description 30
- 229910052799 carbon Inorganic materials 0.000 claims description 30
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 28
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 27
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 24
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 23
- 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 23
- 229910052717 sulfur Inorganic materials 0.000 claims description 23
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 21
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 21
- 125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 claims description 21
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 20
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 19
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 19
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 18
- 239000003638 chemical reducing agent Substances 0.000 claims description 18
- 239000001257 hydrogen Substances 0.000 claims description 18
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 18
- 241000124008 Mammalia Species 0.000 claims description 17
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 17
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 16
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 claims description 15
- 229910052751 metal Inorganic materials 0.000 claims description 15
- 239000002184 metal Substances 0.000 claims description 15
- 229910006069 SO3H Inorganic materials 0.000 claims description 14
- 201000010099 disease Diseases 0.000 claims description 14
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 14
- 150000003839 salts Chemical class 0.000 claims description 14
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 13
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 claims description 12
- 229920000858 Cyclodextrin Chemical group 0.000 claims description 11
- 229910052731 fluorine Inorganic materials 0.000 claims description 11
- 102000003680 Leukotriene B4 receptors Human genes 0.000 claims description 10
- 108090000093 Leukotriene B4 receptors Proteins 0.000 claims description 10
- 239000011230 binding agent Substances 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 10
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 10
- 101150024084 nhr-28 gene Proteins 0.000 claims description 10
- FOXZZWXAFYKBSC-UHFFFAOYSA-N 5-(6-amino-5,5-dimethylhexoxy)-4-ethyl-2-(4-fluorophenyl)phenol Chemical compound C1=C(OCCCCC(C)(C)CN)C(CC)=CC(C=2C=CC(F)=CC=2)=C1O FOXZZWXAFYKBSC-UHFFFAOYSA-N 0.000 claims description 9
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 9
- 108090000765 processed proteins & peptides Chemical group 0.000 claims description 9
- 125000006850 spacer group Chemical group 0.000 claims description 9
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 8
- 101100240526 Caenorhabditis elegans nhr-20 gene Proteins 0.000 claims description 8
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 8
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical group C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims description 8
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 8
- 229910052740 iodine Inorganic materials 0.000 claims description 8
- DVECLMOWYVDJRM-UHFFFAOYSA-N pyridine-3-sulfonic acid Chemical compound OS(=O)(=O)C1=CC=CN=C1 DVECLMOWYVDJRM-UHFFFAOYSA-N 0.000 claims description 8
- 229910052794 bromium Inorganic materials 0.000 claims description 7
- 229910052801 chlorine Inorganic materials 0.000 claims description 7
- 150000007857 hydrazones Chemical class 0.000 claims description 7
- 150000003536 tetrazoles Chemical class 0.000 claims description 7
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims description 6
- SHHKMWMIKILKQW-UHFFFAOYSA-N 2-formylbenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1C=O SHHKMWMIKILKQW-UHFFFAOYSA-N 0.000 claims description 6
- 229910014033 C-OH Inorganic materials 0.000 claims description 6
- 229910014570 C—OH Inorganic materials 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 150000003573 thiols Chemical group 0.000 claims description 6
- XVFROSSJVDEYTC-UHFFFAOYSA-N 3-[[7-[3-[2-ethyl-4-(4-fluorophenyl)-5-hydroxyphenoxy]propoxy]-8-propyl-3,4-dihydro-2H-chromene-2-carbonyl]amino]propyl 2-methylpropanoate Chemical compound C1=CC=2CCC(C(=O)NCCCOC(=O)C(C)C)OC=2C(CCC)=C1OCCCOC(C(=C1)CC)=CC(O)=C1C1=CC=C(F)C=C1 XVFROSSJVDEYTC-UHFFFAOYSA-N 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 150000001413 amino acids Chemical class 0.000 claims description 5
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 5
- 125000005842 heteroatom Chemical group 0.000 claims description 5
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims description 4
- 101100294105 Caenorhabditis elegans nhr-35 gene Proteins 0.000 claims description 4
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 claims description 4
- 229910018830 PO3H Inorganic materials 0.000 claims description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims description 4
- 150000008107 benzenesulfonic acids Chemical class 0.000 claims description 4
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical group C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 4
- 239000012965 benzophenone Chemical group 0.000 claims description 4
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims description 4
- MPFLRYZEEAQMLQ-UHFFFAOYSA-N dinicotinic acid Chemical compound OC(=O)C1=CN=CC(C(O)=O)=C1 MPFLRYZEEAQMLQ-UHFFFAOYSA-N 0.000 claims description 4
- 229930195733 hydrocarbon Chemical group 0.000 claims description 4
- TWBYWOBDOCUKOW-UHFFFAOYSA-N isonicotinic acid Chemical compound OC(=O)C1=CC=NC=C1 TWBYWOBDOCUKOW-UHFFFAOYSA-N 0.000 claims description 4
- UYIHWNXDBBIQIE-UHFFFAOYSA-N n-[6-(2-benzylidenehydrazinyl)pyridin-3-yl]sulfonyl-3-[1-[2-oxo-2-(2-phenylethylamino)ethyl]-5-phenylmethoxyindol-3-yl]prop-2-enamide Chemical compound C=1C=CC=CC=1CCNC(=O)CN(C1=CC=C(OCC=2C=CC=CC=2)C=C11)C=C1C=CC(=O)NS(=O)(=O)C(C=N1)=CC=C1NN=CC1=CC=CC=C1 UYIHWNXDBBIQIE-UHFFFAOYSA-N 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 125000001639 phenylmethylene group Chemical group [H]C(=*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 4
- 229920001515 polyalkylene glycol Chemical group 0.000 claims description 4
- 230000005855 radiation Effects 0.000 claims description 4
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 4
- ZKQNARWAMJYUPK-UHFFFAOYSA-N 3-[2-[2-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]ethoxy]-6-[5-[(5-oxo-1-prop-2-enyl-7,8-dihydro-6h-naphthalen-2-yl)oxy]pentoxy]phenyl]propanoic acid Chemical compound NCCOCCOCCOCCOC1=CC=CC(OCCCCCOC=2C(=C3CCCC(=O)C3=CC=2)CC=C)=C1CCC(O)=O ZKQNARWAMJYUPK-UHFFFAOYSA-N 0.000 claims description 3
- BKAWJIRCKVUVED-UHFFFAOYSA-N 5-(2-hydroxyethyl)-4-methylthiazole Chemical compound CC=1N=CSC=1CCO BKAWJIRCKVUVED-UHFFFAOYSA-N 0.000 claims description 3
- XUONGGHFXKBBNC-UHFFFAOYSA-N 7-[3-[2-ethyl-4-(4-fluorophenyl)-5-hydroxyphenoxy]propoxy]-n-[3-(2-methylpropanoylamino)propyl]-8-propyl-3,4-dihydro-2h-chromene-2-carboxamide Chemical compound C1=CC=2CCC(C(=O)NCCCNC(=O)C(C)C)OC=2C(CCC)=C1OCCCOC(C(=C1)CC)=CC(O)=C1C1=CC=C(F)C=C1 XUONGGHFXKBBNC-UHFFFAOYSA-N 0.000 claims description 3
- 239000004215 Carbon black (E152) Chemical group 0.000 claims description 3
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- ZXHVAUBONBIMSG-UHFFFAOYSA-N n-[6-(4,6-diphenylpyridin-2-yl)oxy-2,2-dimethylhexyl]-4-[[[2-oxo-2-(2-sulfanylethylamino)ethyl]-(2-sulfanylethyl)amino]methyl]benzamide Chemical compound C=1C=C(CN(CCS)CC(=O)NCCS)C=CC=1C(=O)NCC(C)(C)CCCCOC(N=1)=CC(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 ZXHVAUBONBIMSG-UHFFFAOYSA-N 0.000 claims description 3
- 239000000523 sample Substances 0.000 claims description 3
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical group O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 claims description 3
- NTUROZDXWLPVHB-UHFFFAOYSA-M sodium;3-diphenylphosphanylbenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=CC(P(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 NTUROZDXWLPVHB-UHFFFAOYSA-M 0.000 claims description 3
- AXJZCJSXNZZMDU-UHFFFAOYSA-N (5-methyl-1h-imidazol-4-yl)methanol Chemical compound CC=1N=CNC=1CO AXJZCJSXNZZMDU-UHFFFAOYSA-N 0.000 claims description 2
- 125000006743 (C1-C60) alkyl group Chemical group 0.000 claims description 2
- CDMRYARHYKNFLS-UHFFFAOYSA-N 2,2-dimethylpentanamide Chemical compound CCCC(C)(C)C(N)=O CDMRYARHYKNFLS-UHFFFAOYSA-N 0.000 claims description 2
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims description 2
- JSBIFLBZSZFTCT-UHFFFAOYSA-N 2-formylbenzenesulfonic acid 6-hydrazinyl-N-[2-[(5-hydrazinylidene-1-prop-2-enyl-7,8-dihydro-6H-naphthalen-2-yl)oxy]ethyl]pyridine-3-carboxamide Chemical compound OS(=O)(=O)C1=CC=CC=C1C=O.C1=NC(NN)=CC=C1C(=O)NCCOC1=CC=C(C(CCC2)=NN)C2=C1CC=C JSBIFLBZSZFTCT-UHFFFAOYSA-N 0.000 claims description 2
- UGHBBNXOHJPVAQ-UHFFFAOYSA-N 2-formylbenzenesulfonic acid 6-hydrazinyl-N-[6-[(5-hydrazinylidene-1-prop-2-enyl-7,8-dihydro-6H-naphthalen-2-yl)oxy]hexyl]pyridine-3-carboxamide Chemical compound OS(=O)(=O)C1=CC=CC=C1C=O.C1=NC(NN)=CC=C1C(=O)NCCCCCCOC1=CC=C(C(CCC2)=NN)C2=C1CC=C UGHBBNXOHJPVAQ-UHFFFAOYSA-N 0.000 claims description 2
- IGHBFUFAFNZSME-KLSJZZFUSA-N 2-formylbenzenesulfonic acid;6-hydrazinyl-n-[3-[[(e)-1-hydrazinyl-3-[3-(2-phenylethoxy)-6-(phenylsulfanylmethyl)pyridin-2-yl]prop-2-enylidene]amino]propyl]pyridine-3-carboxamide Chemical compound OS(=O)(=O)C1=CC=CC=C1C=O.C1=NC(NN)=CC=C1C(=O)NCCCNC(=NN)\C=C\C1=NC(CSC=2C=CC=CC=2)=CC=C1OCCC1=CC=CC=C1 IGHBFUFAFNZSME-KLSJZZFUSA-N 0.000 claims description 2
- XXOXQSDXISQREA-NBYYMMLRSA-N 2-formylbenzenesulfonic acid;6-hydrazinyl-n-[3-[[(e)-1-hydrazinyl-3-[3-(2-phenylethoxy)-6-[(2,3,5,6-tetrafluorophenyl)sulfanylmethyl]pyridin-2-yl]prop-2-enylidene]amino]propyl]pyridine-3-carboxamide Chemical compound OS(=O)(=O)C1=CC=CC=C1C=O.C1=NC(NN)=CC=C1C(=O)NCCCNC(=NN)\C=C\C1=NC(CSC=2C(=C(F)C=C(F)C=2F)F)=CC=C1OCCC1=CC=CC=C1 XXOXQSDXISQREA-NBYYMMLRSA-N 0.000 claims description 2
- OVZQCPHCHSEOHI-ZUQRMPMESA-N 2-formylbenzenesulfonic acid;6-hydrazinyl-n-[3-[[(e)-1-hydrazinyl-3-[6-[(4-hydroxyphenyl)sulfanylmethyl]-3-(2-phenylethoxy)pyridin-2-yl]prop-2-enylidene]amino]propyl]pyridine-3-carboxamide Chemical compound OS(=O)(=O)C1=CC=CC=C1C=O.C1=NC(NN)=CC=C1C(=O)NCCCNC(=NN)\C=C\C1=NC(CSC=2C=CC(O)=CC=2)=CC=C1OCCC1=CC=CC=C1 OVZQCPHCHSEOHI-ZUQRMPMESA-N 0.000 claims description 2
- LZEZPHLWAVGZCF-UHFFFAOYSA-N 2-formylbenzenesulfonic acid;6-hydrazinyl-n-[3-[[hydrazinyl-[1-[3-[(4-phenylphenyl)methyl]-2h-chromen-7-yl]cyclopentyl]methylidene]amino]propyl]pyridine-3-carboxamide Chemical compound OS(=O)(=O)C1=CC=CC=C1C=O.C1=NC(NN)=CC=C1C(=O)NCCCNC(=NN)C1(C=2C=C3OCC(CC=4C=CC(=CC=4)C=4C=CC=CC=4)=CC3=CC=2)CCCC1 LZEZPHLWAVGZCF-UHFFFAOYSA-N 0.000 claims description 2
- RGIIAYDCZSXHGL-UHFFFAOYSA-N 2-pyridin-4-ylethanesulfonic acid Chemical compound OS(=O)(=O)CCC1=CC=NC=C1 RGIIAYDCZSXHGL-UHFFFAOYSA-N 0.000 claims description 2
- YWGYBQCOVFJZGN-UHFFFAOYSA-N 3-[4-[5-(4,6-diphenylpyridin-2-yl)oxypentoxy]-3-ethoxyphenyl]-n-(6-hydrazinylpyridin-3-yl)sulfonylprop-2-enamide Chemical compound C=1C=C(OCCCCCOC=2N=C(C=C(C=2)C=2C=CC=CC=2)C=2C=CC=CC=2)C(OCC)=CC=1C=CC(=O)NS(=O)(=O)C1=CC=C(NN)N=C1 YWGYBQCOVFJZGN-UHFFFAOYSA-N 0.000 claims description 2
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 2
- AVEQSMYLPHITNI-UHFFFAOYSA-N 6-[6-[4-(1,3-benzodioxol-5-yl)phenyl]pyridin-2-yl]oxy-n-[1-[(6-hydrazinylpyridin-3-yl)sulfonylamino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]-2,2-dimethylhexanamide Chemical compound C=1C=CC(C=2C=CC(=CC=2)C=2C=C3OCOC3=CC=2)=NC=1OCCCCC(C)(C)C(=O)NC(C(=O)NS(=O)(=O)C=1C=NC(NN)=CC=1)CC1=CC=C(O)C=C1 AVEQSMYLPHITNI-UHFFFAOYSA-N 0.000 claims description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 2
- 101100495921 Arabidopsis thaliana CHR27 gene Proteins 0.000 claims description 2
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims description 2
- 125000005865 C2-C10alkynyl group Chemical group 0.000 claims description 2
- 101100240528 Caenorhabditis elegans nhr-23 gene Proteins 0.000 claims description 2
- 101100294121 Caenorhabditis elegans nhr-57 gene Proteins 0.000 claims description 2
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- IXLHRLDPOPMXDU-UHFFFAOYSA-N tert-butyl n-[3-[2-[2-[3-[5-[5-[6-(4,6-diphenylpyridin-2-yl)oxy-2-methylhexan-2-yl]tetrazol-2-yl]pentanoylamino]propoxy]ethoxy]ethoxy]propyl]carbamate Chemical compound CC(C)(C)OC(=O)NCCCOCCOCCOCCCNC(=O)CCCCN1N=NC(C(C)(C)CCCCOC=2N=C(C=C(C=2)C=2C=CC=CC=2)C=2C=CC=CC=2)=N1 IXLHRLDPOPMXDU-UHFFFAOYSA-N 0.000 description 1
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- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K51/00—Preparations containing radioactive substances for use in therapy or testing in vivo
- A61K51/02—Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
- A61K51/04—Organic compounds
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- A61K51/02—Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
- A61K51/04—Organic compounds
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- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/39—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
- C07C323/40—Y being a hydrogen or a carbon atom
- C07C323/41—Y being a hydrogen or an acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/734—Ethers
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/76—Nitrogen atoms to which a second hetero atom is attached
- C07D213/77—Hydrazine radicals
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/02—Acyclic radicals, not substituted by cyclic structures
- C07H15/12—Acyclic radicals, not substituted by cyclic structures attached to a nitrogen atom of the saccharide radical
Landscapes
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- Organic Chemistry (AREA)
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- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
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- Molecular Biology (AREA)
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- Oncology (AREA)
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- Biochemistry (AREA)
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- Genetics & Genomics (AREA)
- Communicable Diseases (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Peptides Or Proteins (AREA)
- Plural Heterocyclic Compounds (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
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US72650796A | 1996-10-07 | 1996-10-07 |
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HRP970531A2 true HRP970531A2 (en) | 1998-08-31 |
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HR08/726,507A HRP970531A2 (en) | 1996-10-07 | 1997-10-07 | Radiopharmaceuticals for imaging infection and inflammation |
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EP (2) | EP1293214A3 (ja) |
JP (1) | JP2001525796A (ja) |
KR (1) | KR20000048922A (ja) |
CN (1) | CN1239895A (ja) |
AR (1) | AR013324A1 (ja) |
AT (1) | ATE240123T1 (ja) |
AU (1) | AU736481C (ja) |
BR (1) | BR9712281A (ja) |
CA (1) | CA2267767A1 (ja) |
DE (1) | DE69722038T2 (ja) |
ES (1) | ES2198010T3 (ja) |
HR (1) | HRP970531A2 (ja) |
HU (1) | HUP0001167A3 (ja) |
IL (1) | IL129263A0 (ja) |
NZ (1) | NZ335539A (ja) |
WO (1) | WO1998015295A2 (ja) |
ZA (1) | ZA978956B (ja) |
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US20030124053A1 (en) * | 1996-10-07 | 2003-07-03 | Barrett John Andrew | Radiopharmaceuticals for imaging infection and inflammation |
AU3119199A (en) * | 1998-04-03 | 1999-10-25 | Du Pont Pharmaceuticals Company | Radiopharmaceuticals for imaging infection and inflammation and for imaging and treatment of cancer |
US6685914B1 (en) | 1999-09-13 | 2004-02-03 | Bristol-Myers Squibb Pharma Company | Macrocyclic chelants for metallopharmaceuticals |
CA2427911A1 (en) * | 2000-11-03 | 2002-05-10 | Bristol Myers Squibb Company | Simultaneous dual isotope imaging of cardiac perfusion and cardiac inflammation |
EP1356827A1 (en) * | 2002-04-24 | 2003-10-29 | Mallinckrodt Inc. | Method for obtaining a 2-18F-fluor-2-deoxy-D-glucose (18F-FDG)-solution |
US7319149B2 (en) | 2003-06-13 | 2008-01-15 | Bristol-Myers Squibb Pharma Company | Chelants and macrocyclic metal complex radiopharmaceuticals thereof |
MY155320A (en) * | 2007-10-05 | 2015-09-30 | Acucela Inc | Alkoxy compounds for disease treatment |
CN104193673B (zh) * | 2014-08-14 | 2016-03-23 | 南开大学 | 一种以三联吡啶为骨架含苯砜基的顺磁荧光双功能探针 |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2665159B1 (fr) * | 1990-07-24 | 1992-11-13 | Rhone Poulenc Sante | Nouveaux derives de la pyridine et de la quinoleine, leur preparation et les compositions pharmaceutiques qui les contiennent. |
US5879657A (en) * | 1993-03-30 | 1999-03-09 | The Dupont Merck Pharmaceutical Company | Radiolabeled platelet GPIIb/IIIa receptor antagonists as imaging agents for the diagnosis of thromboembolic disorders |
US5750088A (en) * | 1993-03-30 | 1998-05-12 | The Dupont Merck Pharmaceutical Company | Stable hydrazones linked to a peptide moiety as reagents for the preparation of radiopharmaceuticals |
-
1997
- 1997-10-06 CA CA002267767A patent/CA2267767A1/en not_active Abandoned
- 1997-10-06 IL IL12926397A patent/IL129263A0/xx unknown
- 1997-10-06 HU HU0001167A patent/HUP0001167A3/hu unknown
- 1997-10-06 WO PCT/US1997/018096 patent/WO1998015295A2/en active IP Right Grant
- 1997-10-06 NZ NZ335539A patent/NZ335539A/en unknown
- 1997-10-06 KR KR1019990702953A patent/KR20000048922A/ko not_active Application Discontinuation
- 1997-10-06 EP EP02079932A patent/EP1293214A3/en not_active Withdrawn
- 1997-10-06 EP EP97947259A patent/EP0999856B1/en not_active Expired - Lifetime
- 1997-10-06 JP JP51768098A patent/JP2001525796A/ja active Pending
- 1997-10-06 AU AU52381/98A patent/AU736481C/en not_active Ceased
- 1997-10-06 ES ES97947259T patent/ES2198010T3/es not_active Expired - Lifetime
- 1997-10-06 DE DE69722038T patent/DE69722038T2/de not_active Expired - Fee Related
- 1997-10-06 AT AT97947259T patent/ATE240123T1/de not_active IP Right Cessation
- 1997-10-06 CN CN97180342A patent/CN1239895A/zh active Pending
- 1997-10-06 BR BR9712281-5A patent/BR9712281A/pt not_active Application Discontinuation
- 1997-10-07 HR HR08/726,507A patent/HRP970531A2/hr not_active Application Discontinuation
- 1997-10-07 AR ARP970104629A patent/AR013324A1/es unknown
- 1997-10-07 ZA ZA978956A patent/ZA978956B/xx unknown
Also Published As
Publication number | Publication date |
---|---|
NZ335539A (en) | 2001-06-29 |
IL129263A0 (en) | 2000-02-17 |
KR20000048922A (ko) | 2000-07-25 |
EP0999856B1 (en) | 2003-05-14 |
DE69722038D1 (de) | 2003-06-18 |
EP1293214A2 (en) | 2003-03-19 |
JP2001525796A (ja) | 2001-12-11 |
EP1293214A3 (en) | 2003-03-26 |
WO1998015295A3 (en) | 1998-08-27 |
HUP0001167A3 (en) | 2002-03-28 |
WO1998015295A2 (en) | 1998-04-16 |
ZA978956B (en) | 1999-04-16 |
CA2267767A1 (en) | 1998-04-16 |
AR013324A1 (es) | 2000-12-27 |
AU736481C (en) | 2002-06-06 |
ES2198010T3 (es) | 2004-01-16 |
DE69722038T2 (de) | 2004-02-19 |
BR9712281A (pt) | 1999-08-31 |
AU736481B2 (en) | 2001-07-26 |
CN1239895A (zh) | 1999-12-29 |
AU5238198A (en) | 1998-05-05 |
ATE240123T1 (de) | 2003-05-15 |
EP0999856A2 (en) | 2000-05-17 |
HUP0001167A2 (hu) | 2000-06-28 |
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