ES2548913T3 - Derivados heterocíclicos como inhibidores de glutaminil ciclasa - Google Patents
Derivados heterocíclicos como inhibidores de glutaminil ciclasa Download PDFInfo
- Publication number
- ES2548913T3 ES2548913T3 ES10751952.2T ES10751952T ES2548913T3 ES 2548913 T3 ES2548913 T3 ES 2548913T3 ES 10751952 T ES10751952 T ES 10751952T ES 2548913 T3 ES2548913 T3 ES 2548913T3
- Authority
- ES
- Spain
- Prior art keywords
- phenyl
- alkyl
- benzo
- substituted
- imidazol
- 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.)
- Active
Links
- 125000000623 heterocyclic group Chemical group 0.000 title abstract description 34
- 102000003642 glutaminyl-peptide cyclotransferase Human genes 0.000 title description 4
- 108010081484 glutaminyl-peptide cyclotransferase Proteins 0.000 title description 4
- 239000003112 inhibitor Substances 0.000 title description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 121
- -1 cyano, hydroxyl Chemical group 0.000 abstract description 109
- 150000001875 compounds Chemical class 0.000 abstract description 72
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract description 31
- 125000004452 carbocyclyl group Chemical group 0.000 abstract description 19
- 125000001072 heteroaryl group Chemical group 0.000 abstract description 15
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 15
- 125000000217 alkyl group Chemical group 0.000 abstract description 11
- 125000002950 monocyclic group Chemical group 0.000 abstract description 10
- 229910052736 halogen Inorganic materials 0.000 abstract description 9
- 150000002367 halogens Chemical class 0.000 abstract description 9
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract description 7
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract description 6
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 abstract description 6
- 150000003839 salts Chemical class 0.000 abstract description 6
- 125000003118 aryl group Chemical group 0.000 abstract description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract description 5
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract description 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract description 3
- 125000005213 alkyl heteroaryl group Chemical group 0.000 abstract description 3
- 125000004043 oxo group Chemical group O=* 0.000 abstract description 3
- 239000012453 solvate Substances 0.000 abstract description 3
- 229910052799 carbon Inorganic materials 0.000 abstract description 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000004001 thioalkyl group Chemical group 0.000 abstract 1
- 238000000034 method Methods 0.000 description 46
- 206010012289 Dementia Diseases 0.000 description 18
- 230000008569 process Effects 0.000 description 16
- 238000004128 high performance liquid chromatography Methods 0.000 description 15
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 15
- 108010052343 Gastrins Proteins 0.000 description 13
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- 102400000921 Gastrin Human genes 0.000 description 12
- AOXOCDRNSPFDPE-UKEONUMOSA-N chembl413654 Chemical compound C([C@H](C(=O)NCC(=O)N[C@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@H](CCSC)C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CC=1C=CC=CC=1)C(N)=O)NC(=O)[C@@H](C)NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@@H](CCC(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H]1N(CCC1)C(=O)CNC(=O)[C@@H](N)CCC(O)=O)C1=CC=C(O)C=C1 AOXOCDRNSPFDPE-UKEONUMOSA-N 0.000 description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 11
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 11
- 210000001616 monocyte Anatomy 0.000 description 11
- 125000006239 protecting group Chemical group 0.000 description 11
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 10
- 239000001257 hydrogen Substances 0.000 description 10
- 229910052727 yttrium Inorganic materials 0.000 description 10
- WKBAPRRMZYHPNB-BXBUPLCLSA-N QYNAD Chemical compound OC(=O)C[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)CCC(N)=O)CC1=CC=C(O)C=C1 WKBAPRRMZYHPNB-BXBUPLCLSA-N 0.000 description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 230000033228 biological regulation Effects 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- IZXIZTKNFFYFOF-UHFFFAOYSA-N 2-Oxazolidone Chemical compound O=C1NCCO1 IZXIZTKNFFYFOF-UHFFFAOYSA-N 0.000 description 8
- 208000024827 Alzheimer disease Diseases 0.000 description 8
- 101100439665 Arabidopsis thaliana SWI2 gene Proteins 0.000 description 8
- 201000010374 Down Syndrome Diseases 0.000 description 8
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 description 8
- 230000004770 neurodegeneration Effects 0.000 description 8
- 235000002639 sodium chloride Nutrition 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000005160 1H NMR spectroscopy Methods 0.000 description 7
- 101100495911 Arabidopsis thaliana CHR10 gene Proteins 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 230000006870 function Effects 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- OKKJLVBELUTLKV-MZCSYVLQSA-N Deuterated methanol Chemical compound [2H]OC([2H])([2H])[2H] OKKJLVBELUTLKV-MZCSYVLQSA-N 0.000 description 6
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
- 241000124008 Mammalia Species 0.000 description 6
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 6
- XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Chemical compound [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 description 6
- PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 description 6
- 201000010099 disease Diseases 0.000 description 6
- 210000004188 enterochromaffin-like cell Anatomy 0.000 description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 108090000765 processed proteins & peptides Proteins 0.000 description 6
- 239000000651 prodrug Substances 0.000 description 6
- 229940002612 prodrug Drugs 0.000 description 6
- 238000000746 purification Methods 0.000 description 6
- 201000001320 Atherosclerosis Diseases 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 102000002512 Orexin Human genes 0.000 description 5
- XTZNCVSCVHTPAI-UHFFFAOYSA-N Salmeterol xinafoate Chemical compound C1=CC=CC2=C(O)C(C(=O)O)=CC=C21.C1=C(O)C(CO)=CC(C(O)CNCCCCCCOCCCCC=2C=CC=CC=2)=C1 XTZNCVSCVHTPAI-UHFFFAOYSA-N 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- 229910052801 chlorine Inorganic materials 0.000 description 5
- 239000003814 drug Substances 0.000 description 5
- 229910052731 fluorine Inorganic materials 0.000 description 5
- 239000011737 fluorine Substances 0.000 description 5
- 125000005843 halogen group Chemical group 0.000 description 5
- 230000003284 homeostatic effect Effects 0.000 description 5
- 210000000440 neutrophil Anatomy 0.000 description 5
- 108060005714 orexin Proteins 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 4
- 108010052164 Sodium Channels Proteins 0.000 description 4
- 102000018674 Sodium Channels Human genes 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 4
- 210000001744 T-lymphocyte Anatomy 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 229960000583 acetic acid Drugs 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- 150000001413 amino acids Chemical group 0.000 description 4
- DZHSAHHDTRWUTF-SIQRNXPUSA-N amyloid-beta polypeptide 42 Chemical compound C([C@@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)NCC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](C)C(O)=O)[C@@H](C)CC)C(C)C)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C(C)C)C1=CC=CC=C1 DZHSAHHDTRWUTF-SIQRNXPUSA-N 0.000 description 4
- 210000003050 axon Anatomy 0.000 description 4
- 125000005605 benzo group Chemical group 0.000 description 4
- 125000000319 biphenyl-4-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 4
- 239000012267 brine Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000003399 chemotactic effect Effects 0.000 description 4
- 239000005482 chemotactic factor Substances 0.000 description 4
- 239000012043 crude product Substances 0.000 description 4
- 229940079593 drug Drugs 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229960001340 histamine Drugs 0.000 description 4
- 150000002431 hydrogen Chemical group 0.000 description 4
- CFHGBZLNZZVTAY-UHFFFAOYSA-N lawesson's reagent Chemical compound C1=CC(OC)=CC=C1P1(=S)SP(=S)(C=2C=CC(OC)=CC=2)S1 CFHGBZLNZZVTAY-UHFFFAOYSA-N 0.000 description 4
- 210000004698 lymphocyte Anatomy 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 201000006417 multiple sclerosis Diseases 0.000 description 4
- OFNHNCAUVYOTPM-IIIOAANCSA-N orexin-a Chemical compound C([C@@H](C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(N)=O)NC(=O)[C@H](CC(N)=O)NC(=O)CNC(=O)[C@H](C)NC(=O)CNC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H]1NC(=O)[C@H](CO)NC(=O)[C@@H]2CSSC[C@@H](C(=O)N[C@H](C(N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(=O)N2)[C@@H](C)O)=O)CSSC1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CC(C)C)NC(=O)[C@H]1N(CCC1)C(=O)[C@H]1NC(=O)CC1)C1=CNC=N1 OFNHNCAUVYOTPM-IIIOAANCSA-N 0.000 description 4
- 210000001711 oxyntic cell Anatomy 0.000 description 4
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 4
- 210000002784 stomach Anatomy 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- NOAPIRGEHUOPGG-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(4-methoxyphenyl)imidazolidin-2-one Chemical compound C1=CC(OC)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 NOAPIRGEHUOPGG-UHFFFAOYSA-N 0.000 description 3
- OMUHBVDRMKRVLW-UHFFFAOYSA-N 3-(4-chlorophenyl)-2,3-dihydroisoindol-1-one Chemical compound C1=CC(Cl)=CC=C1C1C2=CC=CC=C2C(=O)N1 OMUHBVDRMKRVLW-UHFFFAOYSA-N 0.000 description 3
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 description 3
- WFRXSXUDWCVSPI-UHFFFAOYSA-N 3h-benzimidazol-5-amine Chemical compound NC1=CC=C2NC=NC2=C1 WFRXSXUDWCVSPI-UHFFFAOYSA-N 0.000 description 3
- FUOSRKZBOIVBOS-UHFFFAOYSA-N 4-iodobenzene-1,2-diamine Chemical compound NC1=CC=C(I)C=C1N FUOSRKZBOIVBOS-UHFFFAOYSA-N 0.000 description 3
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 3
- ODHCTXKNWHHXJC-VKHMYHEASA-N 5-oxo-L-proline Chemical compound OC(=O)[C@@H]1CCC(=O)N1 ODHCTXKNWHHXJC-VKHMYHEASA-N 0.000 description 3
- 108010090849 Amyloid beta-Peptides Proteins 0.000 description 3
- 102000013455 Amyloid beta-Peptides Human genes 0.000 description 3
- 102100023700 C-C motif chemokine 16 Human genes 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 208000035895 Guillain-Barré syndrome Diseases 0.000 description 3
- 101000978375 Homo sapiens C-C motif chemokine 16 Proteins 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 206010049567 Miller Fisher syndrome Diseases 0.000 description 3
- 206010028980 Neoplasm Diseases 0.000 description 3
- 102400001103 Neurotensin Human genes 0.000 description 3
- 101800001814 Neurotensin Proteins 0.000 description 3
- ZJPGOXWRFNKIQL-JYJNAYRXSA-N Phe-Pro-Pro Chemical compound C([C@H](N)C(=O)N1[C@@H](CCC1)C(=O)N1[C@@H](CCC1)C(O)=O)C1=CC=CC=C1 ZJPGOXWRFNKIQL-JYJNAYRXSA-N 0.000 description 3
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 3
- 230000037424 autonomic function Effects 0.000 description 3
- 210000001124 body fluid Anatomy 0.000 description 3
- 239000010839 body fluid Substances 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- GBRBMTNGQBKBQE-UHFFFAOYSA-L copper;diiodide Chemical compound I[Cu]I GBRBMTNGQBKBQE-UHFFFAOYSA-L 0.000 description 3
- YMHQVDAATAEZLO-UHFFFAOYSA-N cyclohexane-1,1-diamine Chemical compound NC1(N)CCCCC1 YMHQVDAATAEZLO-UHFFFAOYSA-N 0.000 description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
- 230000037149 energy metabolism Effects 0.000 description 3
- 210000003979 eosinophil Anatomy 0.000 description 3
- 230000037406 food intake Effects 0.000 description 3
- 235000012631 food intake Nutrition 0.000 description 3
- 230000003054 hormonal effect Effects 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 238000001727 in vivo Methods 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 3
- 210000000265 leukocyte Anatomy 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000005012 migration Effects 0.000 description 3
- 238000013508 migration Methods 0.000 description 3
- 125000004312 morpholin-2-yl group Chemical group [H]N1C([H])([H])C([H])([H])OC([H])(*)C1([H])[H] 0.000 description 3
- 125000002757 morpholinyl group Chemical group 0.000 description 3
- 210000004877 mucosa Anatomy 0.000 description 3
- PCJGZPGTCUMMOT-ISULXFBGSA-N neurotensin Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(C)C)C(O)=O)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CCCCN)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CC(C)C)NC(=O)[C@H]1NC(=O)CC1)C1=CC=C(O)C=C1 PCJGZPGTCUMMOT-ISULXFBGSA-N 0.000 description 3
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- 230000035755 proliferation Effects 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- 206010039073 rheumatoid arthritis Diseases 0.000 description 3
- 230000028327 secretion Effects 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 3
- LEIMLDGFXIOXMT-UHFFFAOYSA-N trimethylsilyl cyanide Chemical compound C[Si](C)(C)C#N LEIMLDGFXIOXMT-UHFFFAOYSA-N 0.000 description 3
- RLFNSKPXUSVZSQ-HXUWFJFHSA-N (3r)-2-(3h-benzimidazol-5-yl)-3-(4-chlorophenyl)-3h-isoindol-1-one Chemical compound C1=CC(Cl)=CC=C1[C@@H]1C2=CC=CC=C2C(=O)N1C1=CC=C(NC=N2)C2=C1 RLFNSKPXUSVZSQ-HXUWFJFHSA-N 0.000 description 2
- RLFNSKPXUSVZSQ-FQEVSTJZSA-N (3s)-2-(3h-benzimidazol-5-yl)-3-(4-chlorophenyl)-3h-isoindol-1-one Chemical compound C1=CC(Cl)=CC=C1[C@H]1C2=CC=CC=C2C(=O)N1C1=CC=C(NC=N2)C2=C1 RLFNSKPXUSVZSQ-FQEVSTJZSA-N 0.000 description 2
- CAYQIZIAYYNFCS-UHFFFAOYSA-N (4-chlorophenyl)boronic acid Chemical compound OB(O)C1=CC=C(Cl)C=C1 CAYQIZIAYYNFCS-UHFFFAOYSA-N 0.000 description 2
- YKERBJOANKTOPU-RRPNLBNLSA-N (4s,5r)-3-(3h-benzimidazol-5-yl)-4,5-bis(4-propoxyphenyl)-1,3-oxazolidin-2-one Chemical compound C1=CC(OCCC)=CC=C1[C@@H]1[C@H](C=2C=CC(OCCC)=CC=2)N(C=2C=C3NC=NC3=CC=2)C(=O)O1 YKERBJOANKTOPU-RRPNLBNLSA-N 0.000 description 2
- ORHXOPCPCOZZEF-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(1-phenylpiperidin-4-yl)imidazolidin-2-one Chemical compound C=1C=C2N=CNC2=CC=1N1C(=O)NCC1C(CC1)CCN1C1=CC=CC=C1 ORHXOPCPCOZZEF-UHFFFAOYSA-N 0.000 description 2
- IIKKMYFJIJUIKI-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(2,3-dihydro-1,4-benzodioxin-6-yl)pyrrolidin-2-one Chemical compound O1CCOC2=CC(C3CCC(N3C=3C=C4N=CNC4=CC=3)=O)=CC=C21 IIKKMYFJIJUIKI-UHFFFAOYSA-N 0.000 description 2
- XPBIYIWYDFOLML-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(4-phenylcyclohexyl)imidazolidin-2-one Chemical compound C=1C=C2NC=NC2=CC=1N1C(=O)NCC1C(CC1)CCC1C1=CC=CC=C1 XPBIYIWYDFOLML-UHFFFAOYSA-N 0.000 description 2
- NXFFJDQHYLNEJK-UHFFFAOYSA-N 2-[4-[(4-chlorophenyl)methyl]-7-fluoro-5-methylsulfonyl-2,3-dihydro-1h-cyclopenta[b]indol-3-yl]acetic acid Chemical compound C1=2C(S(=O)(=O)C)=CC(F)=CC=2C=2CCC(CC(O)=O)C=2N1CC1=CC=C(Cl)C=C1 NXFFJDQHYLNEJK-UHFFFAOYSA-N 0.000 description 2
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 2
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 description 2
- 125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 description 2
- SHDVFMMSBPSHFK-UHFFFAOYSA-N 3-(4-propoxyphenyl)-2,3-dihydroisoindol-1-one Chemical compound C1=CC(OCCC)=CC=C1C1C2=CC=CC=C2C(=O)N1 SHDVFMMSBPSHFK-UHFFFAOYSA-N 0.000 description 2
- 244000215068 Acacia senegal Species 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical class [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 101710137189 Amyloid-beta A4 protein Proteins 0.000 description 2
- 102100022704 Amyloid-beta precursor protein Human genes 0.000 description 2
- 101710151993 Amyloid-beta precursor protein Proteins 0.000 description 2
- 241000416162 Astragalus gummifer Species 0.000 description 2
- 101800000285 Big gastrin Proteins 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- 102100031151 C-C chemokine receptor type 2 Human genes 0.000 description 2
- 101710149815 C-C chemokine receptor type 2 Proteins 0.000 description 2
- 102100023701 C-C motif chemokine 18 Human genes 0.000 description 2
- 102100021943 C-C motif chemokine 2 Human genes 0.000 description 2
- 102100032366 C-C motif chemokine 7 Human genes 0.000 description 2
- 102100034871 C-C motif chemokine 8 Human genes 0.000 description 2
- 108010078239 Chemokine CX3CL1 Proteins 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 206010057645 Chronic Inflammatory Demyelinating Polyradiculoneuropathy Diseases 0.000 description 2
- 208000030939 Chronic inflammatory demyelinating polyneuropathy Diseases 0.000 description 2
- 239000004471 Glycine Substances 0.000 description 2
- 229920000084 Gum arabic Polymers 0.000 description 2
- 206010019375 Helicobacter infections Diseases 0.000 description 2
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 102000003797 Neuropeptides Human genes 0.000 description 2
- 108090000189 Neuropeptides Proteins 0.000 description 2
- 206010033645 Pancreatitis Diseases 0.000 description 2
- 206010062519 Poor quality sleep Diseases 0.000 description 2
- 201000004681 Psoriasis Diseases 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 208000005718 Stomach Neoplasms Diseases 0.000 description 2
- 230000024932 T cell mediated immunity Effects 0.000 description 2
- 102400000336 Thyrotropin-releasing hormone Human genes 0.000 description 2
- 101800004623 Thyrotropin-releasing hormone Proteins 0.000 description 2
- 229920001615 Tragacanth Polymers 0.000 description 2
- 239000000205 acacia gum Substances 0.000 description 2
- 235000010489 acacia gum Nutrition 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 230000009858 acid secretion Effects 0.000 description 2
- 125000006241 alcohol protecting group Chemical group 0.000 description 2
- 108010064397 amyloid beta-protein (1-40) Proteins 0.000 description 2
- 108010064539 amyloid beta-protein (1-42) Proteins 0.000 description 2
- 108010087587 amyloid beta-protein (11-40) Proteins 0.000 description 2
- 108010087299 amyloid beta-protein (11-42) Proteins 0.000 description 2
- 230000000259 anti-tumor effect Effects 0.000 description 2
- 210000003719 b-lymphocyte Anatomy 0.000 description 2
- 210000003651 basophil Anatomy 0.000 description 2
- 230000006399 behavior Effects 0.000 description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 2
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 230000037396 body weight Effects 0.000 description 2
- 210000004556 brain Anatomy 0.000 description 2
- 125000006243 carbonyl protecting group Chemical group 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 210000003169 central nervous system Anatomy 0.000 description 2
- 210000001175 cerebrospinal fluid Anatomy 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 208000010877 cognitive disease Diseases 0.000 description 2
- 238000004440 column chromatography Methods 0.000 description 2
- 230000000295 complement effect Effects 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 208000035475 disorder Diseases 0.000 description 2
- 239000003937 drug carrier Substances 0.000 description 2
- 230000004064 dysfunction Effects 0.000 description 2
- 239000003480 eluent Substances 0.000 description 2
- 210000003038 endothelium Anatomy 0.000 description 2
- 230000035558 fertility Effects 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 206010017758 gastric cancer Diseases 0.000 description 2
- 239000003102 growth factor Substances 0.000 description 2
- 229960002897 heparin Drugs 0.000 description 2
- 229920000669 heparin Polymers 0.000 description 2
- 230000028996 humoral immune response Effects 0.000 description 2
- 150000004677 hydrates Chemical class 0.000 description 2
- 230000028709 inflammatory response Effects 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 239000002502 liposome Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 210000001165 lymph node Anatomy 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
- NSPJNIDYTSSIIY-UHFFFAOYSA-N methoxy(methoxymethoxy)methane Chemical compound COCOCOC NSPJNIDYTSSIIY-UHFFFAOYSA-N 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- 208000027061 mild cognitive impairment Diseases 0.000 description 2
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 2
- 230000035772 mutation Effects 0.000 description 2
- 210000003643 myeloid progenitor cell Anatomy 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 230000009826 neoplastic cell growth Effects 0.000 description 2
- 239000002858 neurotransmitter agent Substances 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 108010067535 pentapeptide QYNAD Proteins 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 239000008194 pharmaceutical composition Substances 0.000 description 2
- 125000006245 phosphate protecting group Chemical group 0.000 description 2
- 125000004193 piperazinyl group Chemical group 0.000 description 2
- 125000003386 piperidinyl group Chemical group 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 230000003389 potentiating effect Effects 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- RZIMNEGTIDYAGZ-HNSJZBNRSA-N pro-gastrin Chemical compound N([C@@H](CC(C)C)C(=O)NCC(=O)NCC(=O)N[C@@H](CCC(N)=O)C(=O)NCC(=O)N1CCC[C@H]1C(=O)NCC(=O)NCC(=O)NCC(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](CC(O)=O)C(=O)NCC(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(=O)NCC(=O)N1CCC[C@H]1C(=O)NCC(=O)NCC(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)NCC(=O)N[C@@H](C)C(=O)NCC(=O)NCC(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC=1C=CC=CC=1)C(N)=O)C(=O)[C@@H]1CCC(=O)N1 RZIMNEGTIDYAGZ-HNSJZBNRSA-N 0.000 description 2
- 102000004196 processed proteins & peptides Human genes 0.000 description 2
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- XNSAINXGIQZQOO-SRVKXCTJSA-N protirelin Chemical compound NC(=O)[C@@H]1CCCN1C(=O)[C@@H](NC(=O)[C@H]1NC(=O)CC1)CC1=CN=CN1 XNSAINXGIQZQOO-SRVKXCTJSA-N 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 208000037803 restenosis Diseases 0.000 description 2
- 210000000582 semen Anatomy 0.000 description 2
- 238000011894 semi-preparative HPLC Methods 0.000 description 2
- 230000016160 smooth muscle contraction Effects 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 201000011549 stomach cancer Diseases 0.000 description 2
- 239000000758 substrate Substances 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
- FGTJJHCZWOVVNH-UHFFFAOYSA-N tert-butyl-[tert-butyl(dimethyl)silyl]oxy-dimethylsilane Chemical compound CC(C)(C)[Si](C)(C)O[Si](C)(C)C(C)(C)C FGTJJHCZWOVVNH-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 229940034199 thyrotropin-releasing hormone Drugs 0.000 description 2
- 239000000196 tragacanth Substances 0.000 description 2
- 235000010487 tragacanth Nutrition 0.000 description 2
- 229940116362 tragacanth Drugs 0.000 description 2
- LGSAOJLQTXCYHF-UHFFFAOYSA-N tri(propan-2-yl)-tri(propan-2-yl)silyloxysilane Chemical compound CC(C)[Si](C(C)C)(C(C)C)O[Si](C(C)C)(C(C)C)C(C)C LGSAOJLQTXCYHF-UHFFFAOYSA-N 0.000 description 2
- AQRLNPVMDITEJU-UHFFFAOYSA-N triethylsilane Chemical compound CC[SiH](CC)CC AQRLNPVMDITEJU-UHFFFAOYSA-N 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- 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 2
- 230000001228 trophic effect Effects 0.000 description 2
- 239000002691 unilamellar liposome Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- QDZOEBFLNHCSSF-PFFBOGFISA-N (2S)-2-[[(2R)-2-[[(2S)-1-[(2S)-6-amino-2-[[(2S)-1-[(2R)-2-amino-5-carbamimidamidopentanoyl]pyrrolidine-2-carbonyl]amino]hexanoyl]pyrrolidine-2-carbonyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]-N-[(2R)-1-[[(2S)-1-[[(2R)-1-[[(2S)-1-[[(2S)-1-amino-4-methyl-1-oxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]pentanediamide Chemical compound C([C@@H](C(=O)N[C@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(N)=O)NC(=O)[C@@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CCCCN)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](N)CCCNC(N)=N)C1=CC=CC=C1 QDZOEBFLNHCSSF-PFFBOGFISA-N 0.000 description 1
- ICKMOIBSQQCIKY-JOCHJYFZSA-N (3r)-2-(3h-benzimidazol-5-yl)-3-(3,4-dimethoxyphenyl)-3h-isoindol-1-one Chemical compound C1=C(OC)C(OC)=CC=C1[C@@H]1C2=CC=CC=C2C(=O)N1C1=CC=C(NC=N2)C2=C1 ICKMOIBSQQCIKY-JOCHJYFZSA-N 0.000 description 1
- XZDCCRWIGKXYPP-HSZRJFAPSA-N (3r)-2-(3h-benzimidazol-5-yl)-3-(4-propoxyphenyl)-3h-isoindol-1-one Chemical compound C1=CC(OCCC)=CC=C1[C@@H]1C2=CC=CC=C2C(=O)N1C1=CC=C(NC=N2)C2=C1 XZDCCRWIGKXYPP-HSZRJFAPSA-N 0.000 description 1
- ICKMOIBSQQCIKY-QFIPXVFZSA-N (3s)-2-(3h-benzimidazol-5-yl)-3-(3,4-dimethoxyphenyl)-3h-isoindol-1-one Chemical compound C1=C(OC)C(OC)=CC=C1[C@H]1C2=CC=CC=C2C(=O)N1C1=CC=C(NC=N2)C2=C1 ICKMOIBSQQCIKY-QFIPXVFZSA-N 0.000 description 1
- XZDCCRWIGKXYPP-QHCPKHFHSA-N (3s)-2-(3h-benzimidazol-5-yl)-3-(4-propoxyphenyl)-3h-isoindol-1-one Chemical compound C1=CC(OCCC)=CC=C1[C@H]1C2=CC=CC=C2C(=O)N1C1=CC=C(NC=N2)C2=C1 XZDCCRWIGKXYPP-QHCPKHFHSA-N 0.000 description 1
- GKWRIUUYOSRZHB-HNNXBMFYSA-N (4r)-3-(3h-benzimidazol-5-yl)-4-phenyl-1,3-oxazolidin-2-one Chemical compound C1([C@@H]2COC(N2C=2C=C3NC=NC3=CC=2)=O)=CC=CC=C1 GKWRIUUYOSRZHB-HNNXBMFYSA-N 0.000 description 1
- CBXQUSJYJPWADE-PIGZYNQJSA-N (4r,5s)-1-(3h-benzimidazol-5-yl)-5-(4-methoxyphenyl)-4-methylimidazolidin-2-one Chemical compound C1=CC(OC)=CC=C1[C@@H]1N(C=2C=C3NC=NC3=CC=2)C(=O)N[C@@H]1C CBXQUSJYJPWADE-PIGZYNQJSA-N 0.000 description 1
- ADDXBMUZVNJAIC-MRXNPFEDSA-N (4s)-3-(2-methyl-3h-benzimidazol-5-yl)-4-phenyl-1,3-oxazolidin-2-one Chemical compound C1([C@@H]2N(C(OC2)=O)C2=CC=C3N=C(NC3=C2)C)=CC=CC=C1 ADDXBMUZVNJAIC-MRXNPFEDSA-N 0.000 description 1
- ZTCQMGYVXSYDJK-HXUWFJFHSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-(1-phenylpiperidin-4-yl)-1,3-oxazolidin-2-one Chemical compound C1CC([C@H]2COC(N2C=2C=C3N=CNC3=CC=2)=O)CCN1C1=CC=CC=C1 ZTCQMGYVXSYDJK-HXUWFJFHSA-N 0.000 description 1
- TWOIKTSKRQFXLB-CQSZACIVSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-(2,3-difluorophenyl)-1,3-oxazolidin-2-one Chemical compound FC1=CC=CC([C@@H]2N(C(=O)OC2)C=2C=C3NC=NC3=CC=2)=C1F TWOIKTSKRQFXLB-CQSZACIVSA-N 0.000 description 1
- NVVJFURBSKHDDM-OAHLLOKOSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-(2,3-dihydro-1,4-benzodioxin-6-yl)-1,3-oxazolidin-2-one Chemical compound O1CCOC2=CC([C@H]3COC(N3C=3C=C4NC=NC4=CC=3)=O)=CC=C21 NVVJFURBSKHDDM-OAHLLOKOSA-N 0.000 description 1
- ZRRRITHHERRTOL-HNNXBMFYSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-(2-phenylethyl)-1,3-oxazolidin-2-one Chemical compound C([C@H]1COC(N1C=1C=C2N=CNC2=CC=1)=O)CC1=CC=CC=C1 ZRRRITHHERRTOL-HNNXBMFYSA-N 0.000 description 1
- FTYRNMQUVSKKOM-OAHLLOKOSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-(3-chlorophenyl)-1,3-oxazolidin-2-one Chemical compound ClC1=CC=CC([C@@H]2N(C(=O)OC2)C=2C=C3NC=NC3=CC=2)=C1 FTYRNMQUVSKKOM-OAHLLOKOSA-N 0.000 description 1
- ZPMHBHUZAKYRBJ-OAHLLOKOSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-(3-fluorophenyl)-1,3-oxazolidin-2-one Chemical compound FC1=CC=CC([C@@H]2N(C(=O)OC2)C=2C=C3NC=NC3=CC=2)=C1 ZPMHBHUZAKYRBJ-OAHLLOKOSA-N 0.000 description 1
- AGIHWNYSJKBMSF-LJQANCHMSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-(3-morpholin-4-ylphenyl)-1,3-oxazolidin-2-one Chemical compound C=1C([C@H]2COC(N2C=2C=C3N=CNC3=CC=2)=O)=CC=CC=1N1CCOCC1 AGIHWNYSJKBMSF-LJQANCHMSA-N 0.000 description 1
- WWZUYLAZWSCSRE-HXUWFJFHSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-(3-piperidin-1-ylphenyl)-1,3-oxazolidin-2-one Chemical compound C=1C([C@H]2COC(N2C=2C=C3N=CNC3=CC=2)=O)=CC=CC=1N1CCCCC1 WWZUYLAZWSCSRE-HXUWFJFHSA-N 0.000 description 1
- YJVABIMVWXEWGM-OAHLLOKOSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-(4-chlorophenyl)-1,3-oxazolidin-2-one Chemical compound C1=CC(Cl)=CC=C1[C@@H]1N(C=2C=C3NC=NC3=CC=2)C(=O)OC1 YJVABIMVWXEWGM-OAHLLOKOSA-N 0.000 description 1
- NZICRTJYORZSDU-LJQANCHMSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-(4-morpholin-4-ylphenyl)-1,3-oxazolidin-2-one Chemical compound C1=CC([C@H]2COC(N2C=2C=C3N=CNC3=CC=2)=O)=CC=C1N1CCOCC1 NZICRTJYORZSDU-LJQANCHMSA-N 0.000 description 1
- RAUDIXMQSUIFIX-MYKUNDNFSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-(4-phenylcyclohexyl)-1,3-oxazolidin-2-one Chemical compound C1CC([C@H]2COC(N2C=2C=C3N=CNC3=CC=2)=O)CCC1C1=CC=CC=C1 RAUDIXMQSUIFIX-MYKUNDNFSA-N 0.000 description 1
- GPAWLADRRFWXQH-OAQYLSRUSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-(4-phenylphenyl)-1,3-oxazolidin-2-one Chemical compound C1=CC([C@H]2COC(N2C=2C=C3NC=NC3=CC=2)=O)=CC=C1C1=CC=CC=C1 GPAWLADRRFWXQH-OAQYLSRUSA-N 0.000 description 1
- GAQQUOTYMMOEAB-HXUWFJFHSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-(4-piperidin-1-ylphenyl)-1,3-oxazolidin-2-one Chemical compound C1=CC([C@H]2COC(N2C=2C=C3N=CNC3=CC=2)=O)=CC=C1N1CCCCC1 GAQQUOTYMMOEAB-HXUWFJFHSA-N 0.000 description 1
- QZFGQBUTFFRJKB-GOSISDBHSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-(4-propoxyphenyl)-1,3-oxazolidin-2-one Chemical compound C1=CC(OCCC)=CC=C1[C@@H]1N(C=2C=C3NC=NC3=CC=2)C(=O)OC1 QZFGQBUTFFRJKB-GOSISDBHSA-N 0.000 description 1
- UXALLQDCNCAADT-AWEZNQCLSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-(cyclohexylmethyl)-1,3-oxazolidin-2-one Chemical compound C([C@H]1COC(N1C=1C=C2N=CNC2=CC=1)=O)C1CCCCC1 UXALLQDCNCAADT-AWEZNQCLSA-N 0.000 description 1
- JPJDVVDNQGOHAD-SFHVURJKSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-[(4-cyclohexyloxyphenyl)methyl]-1,3-oxazolidin-2-one Chemical compound C([C@H]1COC(N1C=1C=C2N=CNC2=CC=1)=O)C(C=C1)=CC=C1OC1CCCCC1 JPJDVVDNQGOHAD-SFHVURJKSA-N 0.000 description 1
- OYOLARFSOLGLBG-INIZCTEOSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-[(4-propan-2-yloxyphenyl)methyl]-1,3-oxazolidin-2-one Chemical compound C1=CC(OC(C)C)=CC=C1C[C@@H]1N(C=2C=C3N=CNC3=CC=2)C(=O)OC1 OYOLARFSOLGLBG-INIZCTEOSA-N 0.000 description 1
- YZOLXOXPGRZJJE-INIZCTEOSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-[(4-propoxyphenyl)methyl]-1,3-oxazolidin-2-one Chemical compound C1=CC(OCCC)=CC=C1C[C@@H]1N(C=2C=C3N=CNC3=CC=2)C(=O)OC1 YZOLXOXPGRZJJE-INIZCTEOSA-N 0.000 description 1
- JMUKIVPFJWLYFN-OAQYLSRUSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-[3-(3-chlorophenyl)phenyl]-1,3-oxazolidin-2-one Chemical compound ClC1=CC=CC(C=2C=C(C=CC=2)[C@@H]2N(C(=O)OC2)C=2C=C3NC=NC3=CC=2)=C1 JMUKIVPFJWLYFN-OAQYLSRUSA-N 0.000 description 1
- QMAZKUBVZPELIU-HXUWFJFHSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-[3-(4-methylpiperazin-1-yl)phenyl]-1,3-oxazolidin-2-one Chemical compound C1CN(C)CCN1C1=CC=CC([C@@H]2N(C(=O)OC2)C=2C=C3NC=NC3=CC=2)=C1 QMAZKUBVZPELIU-HXUWFJFHSA-N 0.000 description 1
- ALESAWAFANYGAL-RUZDIDTESA-N (4s)-3-(3h-benzimidazol-5-yl)-4-[3-(4-phenylpiperazin-1-yl)phenyl]-1,3-oxazolidin-2-one Chemical compound C=1C([C@H]2COC(N2C=2C=C3NC=NC3=CC=2)=O)=CC=CC=1N(CC1)CCN1C1=CC=CC=C1 ALESAWAFANYGAL-RUZDIDTESA-N 0.000 description 1
- WRRXGSIKEAHCCU-OAHLLOKOSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-[3-fluoro-5-(trifluoromethyl)phenyl]-1,3-oxazolidin-2-one Chemical compound FC(F)(F)C1=CC(F)=CC([C@@H]2N(C(=O)OC2)C=2C=C3NC=NC3=CC=2)=C1 WRRXGSIKEAHCCU-OAHLLOKOSA-N 0.000 description 1
- SBSCDPPTPKGBST-OAQYLSRUSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-[4-(3-chlorophenyl)phenyl]-1,3-oxazolidin-2-one Chemical compound ClC1=CC=CC(C=2C=CC(=CC=2)[C@@H]2N(C(=O)OC2)C=2C=C3NC=NC3=CC=2)=C1 SBSCDPPTPKGBST-OAQYLSRUSA-N 0.000 description 1
- XJFXWKHDCZOALW-LJQANCHMSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-[4-(3-methoxypropyl)phenyl]-1,3-oxazolidin-2-one Chemical compound C1=CC(CCCOC)=CC=C1[C@@H]1N(C=2C=C3N=CNC3=CC=2)C(=O)OC1 XJFXWKHDCZOALW-LJQANCHMSA-N 0.000 description 1
- RGGOCMGTWDMKAU-HXUWFJFHSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-[4-(4-methylpiperazin-1-yl)phenyl]-1,3-oxazolidin-2-one Chemical compound C1CN(C)CCN1C1=CC=C([C@@H]2N(C(=O)OC2)C=2C=C3NC=NC3=CC=2)C=C1 RGGOCMGTWDMKAU-HXUWFJFHSA-N 0.000 description 1
- GCUQCDXDDFSUNF-RUZDIDTESA-N (4s)-3-(3h-benzimidazol-5-yl)-4-[4-(4-phenylpiperazin-1-yl)phenyl]-1,3-oxazolidin-2-one Chemical compound C1=CC([C@H]2COC(N2C=2C=C3NC=NC3=CC=2)=O)=CC=C1N(CC1)CCN1C1=CC=CC=C1 GCUQCDXDDFSUNF-RUZDIDTESA-N 0.000 description 1
- SWHIOMWCCVFQRY-OAQYLSRUSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-[4-(dicyclopropylamino)phenyl]-1,3-oxazolidin-2-one Chemical compound C1=CC([C@H]2COC(N2C=2C=C3N=CNC3=CC=2)=O)=CC=C1N(C1CC1)C1CC1 SWHIOMWCCVFQRY-OAQYLSRUSA-N 0.000 description 1
- BYQZAHIVCADZCY-LJQANCHMSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-[4-(diethylamino)phenyl]-1,3-oxazolidin-2-one Chemical compound C1=CC(N(CC)CC)=CC=C1[C@@H]1N(C=2C=C3N=CNC3=CC=2)C(=O)OC1 BYQZAHIVCADZCY-LJQANCHMSA-N 0.000 description 1
- ULTZAPHRZBZYHB-LJQANCHMSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-[4-[2-(dimethylamino)ethoxy]phenyl]-1,3-oxazolidin-2-one Chemical compound C1=CC(OCCN(C)C)=CC=C1[C@@H]1N(C=2C=C3N=CNC3=CC=2)C(=O)OC1 ULTZAPHRZBZYHB-LJQANCHMSA-N 0.000 description 1
- JXKFKBYYJDDRRB-OAQYLSRUSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-[4-[bis(2-methoxyethyl)amino]phenyl]-1,3-oxazolidin-2-one Chemical compound C1=CC(N(CCOC)CCOC)=CC=C1[C@@H]1N(C=2C=C3N=CNC3=CC=2)C(=O)OC1 JXKFKBYYJDDRRB-OAQYLSRUSA-N 0.000 description 1
- NNGKNMPVYJTPTQ-AWEZNQCLSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-benzyl-1,3-oxazolidin-2-one Chemical compound C([C@H]1COC(N1C=1C=C2N=CNC2=CC=1)=O)C1=CC=CC=C1 NNGKNMPVYJTPTQ-AWEZNQCLSA-N 0.000 description 1
- USNMMLGWMAQCPM-OAHLLOKOSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-cyclohexyl-1,3-oxazolidin-2-one Chemical compound C1([C@H]2COC(N2C=2C=C3N=CNC3=CC=2)=O)CCCCC1 USNMMLGWMAQCPM-OAHLLOKOSA-N 0.000 description 1
- GKWRIUUYOSRZHB-OAHLLOKOSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-phenyl-1,3-oxazolidin-2-one Chemical compound C1([C@H]2COC(N2C=2C=C3NC=NC3=CC=2)=O)=CC=CC=C1 GKWRIUUYOSRZHB-OAHLLOKOSA-N 0.000 description 1
- VRZCMTOZDIPXRX-GFCCVEGCSA-N (4s)-3-(3h-benzimidazol-5-yl)-4-propan-2-yl-1,3-oxazolidin-2-one Chemical compound CC(C)[C@H]1COC(=O)N1C1=CC=C(NC=N2)C2=C1 VRZCMTOZDIPXRX-GFCCVEGCSA-N 0.000 description 1
- BHFAKXZGAQRIPX-INIZCTEOSA-N (4s)-3-(3h-benzimidazol-5-yl)-5,5-dimethyl-4-phenyl-1,3-oxazolidin-2-one Chemical compound C1([C@@H]2N(C(=O)OC2(C)C)C=2C=C3NC=NC3=CC=2)=CC=CC=C1 BHFAKXZGAQRIPX-INIZCTEOSA-N 0.000 description 1
- VMYWOEMVFMSMFH-LJQANCHMSA-N (4s)-3-(6,7-dimethyl-3h-benzimidazol-5-yl)-4-(4-propoxyphenyl)-1,3-oxazolidin-2-one Chemical compound C1=CC(OCCC)=CC=C1[C@@H]1N(C=2C(=C(C)C=3NC=NC=3C=2)C)C(=O)OC1 VMYWOEMVFMSMFH-LJQANCHMSA-N 0.000 description 1
- BNGIDVKMNFTOKJ-OAHLLOKOSA-N (4s)-3-(6-fluoro-1h-benzimidazol-5-yl)-4-phenyl-1,3-oxazolidin-2-one Chemical compound C1([C@@H]2N(C(OC2)=O)C2=CC=3N=CNC=3C=C2F)=CC=CC=C1 BNGIDVKMNFTOKJ-OAHLLOKOSA-N 0.000 description 1
- RBCOOZSDDHBCLK-CQSZACIVSA-N (4s)-3-(7-fluoro-3h-benzimidazol-5-yl)-4-phenyl-1,3-oxazolidin-2-one Chemical compound C1([C@@H]2N(C(OC2)=O)C=2C=C(C=3NC=NC=3C=2)F)=CC=CC=C1 RBCOOZSDDHBCLK-CQSZACIVSA-N 0.000 description 1
- ATSKZZYZECAMAQ-GOSISDBHSA-N (4s)-3-(7-methyl-3h-benzimidazol-5-yl)-4-(4-propoxyphenyl)-1,3-oxazolidin-2-one Chemical compound C1=CC(OCCC)=CC=C1[C@@H]1N(C=2C=C3N=CNC3=C(C)C=2)C(=O)OC1 ATSKZZYZECAMAQ-GOSISDBHSA-N 0.000 description 1
- UNIGZWBFVWNWKZ-OAHLLOKOSA-N (4s)-3-(7-methyl-3h-benzimidazol-5-yl)-4-phenyl-1,3-oxazolidin-2-one Chemical compound C1([C@@H]2N(C(OC2)=O)C=2C=C(C=3NC=NC=3C=2)C)=CC=CC=C1 UNIGZWBFVWNWKZ-OAHLLOKOSA-N 0.000 description 1
- SVLOXMITWWZIEF-MRXNPFEDSA-N (4s)-4-(1-acetylpiperidin-4-yl)-3-(3h-benzimidazol-5-yl)-1,3-oxazolidin-2-one Chemical compound C1CN(C(=O)C)CCC1[C@@H]1N(C=2C=C3N=CNC3=CC=2)C(=O)OC1 SVLOXMITWWZIEF-MRXNPFEDSA-N 0.000 description 1
- FHTWCLUEQMSJIX-LEWJYISDSA-N (4s,5r)-3-(3h-benzimidazol-5-yl)-4,5-diphenyl-1,3-oxazolidin-2-one Chemical compound C1([C@H]2[C@H](OC(N2C=2C=C3NC=NC3=CC=2)=O)C=2C=CC=CC=2)=CC=CC=C1 FHTWCLUEQMSJIX-LEWJYISDSA-N 0.000 description 1
- CVAPQNMJDHCBSC-MEDUHNTESA-N (4s,5s)-3-(3h-benzimidazol-5-yl)-5-methyl-4-phenyl-1,3-oxazolidin-2-one Chemical compound C1([C@@H]2N(C(=O)O[C@H]2C)C=2C=C3NC=NC3=CC=2)=CC=CC=C1 CVAPQNMJDHCBSC-MEDUHNTESA-N 0.000 description 1
- XHIKZWOEFZENIX-SFHVURJKSA-N (5r)-1-(3h-benzimidazol-5-yl)-5-(4-propoxyphenyl)imidazolidin-2-one Chemical compound C1=CC(OCCC)=CC=C1[C@H]1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 XHIKZWOEFZENIX-SFHVURJKSA-N 0.000 description 1
- XHIKZWOEFZENIX-GOSISDBHSA-N (5s)-1-(3h-benzimidazol-5-yl)-5-(4-propoxyphenyl)imidazolidin-2-one Chemical compound C1=CC(OCCC)=CC=C1[C@@H]1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 XHIKZWOEFZENIX-GOSISDBHSA-N 0.000 description 1
- GAAIFWIYYLVRBP-OAQYLSRUSA-N (5s)-1-(3h-benzimidazol-5-yl)-5-[4-(1-methylpiperidin-4-yl)phenyl]imidazolidin-2-one Chemical compound C1CN(C)CCC1C1=CC=C([C@@H]2N(C(=O)NC2)C=2C=C3N=CNC3=CC=2)C=C1 GAAIFWIYYLVRBP-OAQYLSRUSA-N 0.000 description 1
- WLYKMFXDVWSKFU-HXUWFJFHSA-N (5s)-1-(3h-benzimidazol-5-yl)-5-[4-(4,4-difluorocyclohexyl)phenyl]imidazolidin-2-one Chemical compound C1CC(F)(F)CCC1C1=CC=C([C@@H]2N(C(=O)NC2)C=2C=C3N=CNC3=CC=2)C=C1 WLYKMFXDVWSKFU-HXUWFJFHSA-N 0.000 description 1
- YUVOZTFCKZHKKL-LJQANCHMSA-N (5s)-1-(3h-benzimidazol-5-yl)-5-[4-(diethylamino)phenyl]imidazolidin-2-one Chemical compound C1=CC(N(CC)CC)=CC=C1[C@@H]1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 YUVOZTFCKZHKKL-LJQANCHMSA-N 0.000 description 1
- UNARJRXATYBLGH-LJQANCHMSA-N (5s)-1-(3h-benzimidazol-5-yl)-5-[4-[2-(dimethylamino)ethoxy]phenyl]imidazolidin-2-one Chemical compound C1=CC(OCCN(C)C)=CC=C1[C@@H]1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 UNARJRXATYBLGH-LJQANCHMSA-N 0.000 description 1
- YBFZGUKMCSQDRP-OAQYLSRUSA-N (5s)-1-(3h-benzimidazol-5-yl)-5-[4-[bis(2-methoxyethyl)amino]phenyl]imidazolidin-2-one Chemical compound C1=CC(N(CCOC)CCOC)=CC=C1[C@@H]1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 YBFZGUKMCSQDRP-OAQYLSRUSA-N 0.000 description 1
- JYCSQPKGHASGMV-LJQANCHMSA-N (5s)-4-(3h-benzimidazol-5-yl)-5-(4-propoxyphenyl)morpholin-3-one Chemical compound C1=CC(OCCC)=CC=C1[C@@H]1N(C=2C=C3NC=NC3=CC=2)C(=O)COC1 JYCSQPKGHASGMV-LJQANCHMSA-N 0.000 description 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
- AFDXODALSZRGIH-QPJJXVBHSA-N (E)-3-(4-methoxyphenyl)prop-2-enoic acid Chemical compound COC1=CC=C(\C=C\C(O)=O)C=C1 AFDXODALSZRGIH-QPJJXVBHSA-N 0.000 description 1
- YQYZHMRBCDCVOR-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(2,2-difluoro-1,3-benzodioxol-5-yl)imidazolidin-2-one Chemical compound C1=C2NC=NC2=CC(N2C(=O)NCC2C2=CC=C3OC(OC3=C2)(F)F)=C1 YQYZHMRBCDCVOR-UHFFFAOYSA-N 0.000 description 1
- BRQLZTQDJCRVLF-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(2,3,5-trifluorophenyl)imidazolidin-4-one Chemical compound FC1=CC(F)=C(F)C(C2C(NCN2C=2C=C3N=CNC3=CC=2)=O)=C1 BRQLZTQDJCRVLF-UHFFFAOYSA-N 0.000 description 1
- SKLPRNTUXRWDGF-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(2,3-dihydro-1,4-benzodioxin-6-yl)imidazolidin-2-one Chemical compound O1CCOC2=CC(C3CNC(N3C=3C=C4N=CNC4=CC=3)=O)=CC=C21 SKLPRNTUXRWDGF-UHFFFAOYSA-N 0.000 description 1
- CGSHNOXGHZBPLD-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(2,4-dihydroxyphenyl)imidazolidin-2-one Chemical compound OC1=CC(O)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 CGSHNOXGHZBPLD-UHFFFAOYSA-N 0.000 description 1
- BMVLGILWYACRJJ-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(2,6-difluoro-4-methoxyphenyl)imidazolidin-2-one Chemical compound FC1=CC(OC)=CC(F)=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 BMVLGILWYACRJJ-UHFFFAOYSA-N 0.000 description 1
- LXLZQHXIYRTXLA-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(2-fluoro-4-propoxyphenyl)imidazolidin-2-one Chemical compound FC1=CC(OCCC)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 LXLZQHXIYRTXLA-UHFFFAOYSA-N 0.000 description 1
- XQSDITKQBFZEAY-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(2-hydroxyphenyl)imidazolidin-2-one Chemical compound OC1=CC=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 XQSDITKQBFZEAY-UHFFFAOYSA-N 0.000 description 1
- SPBCIMRZPXOFIM-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(2-methoxyphenyl)imidazolidin-2-one Chemical compound COC1=CC=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 SPBCIMRZPXOFIM-UHFFFAOYSA-N 0.000 description 1
- IISSIWXPIUGGQV-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(3,4-dihydroxyphenyl)imidazolidin-2-one Chemical compound C1=C(O)C(O)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 IISSIWXPIUGGQV-UHFFFAOYSA-N 0.000 description 1
- UXEYFDDPDOUKPX-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(3-chloro-4-morpholin-4-ylphenyl)imidazolidin-2-one Chemical compound ClC1=CC(C2N(C(=O)NC2)C=2C=C3N=CNC3=CC=2)=CC=C1N1CCOCC1 UXEYFDDPDOUKPX-UHFFFAOYSA-N 0.000 description 1
- LNLXPRNACORALX-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(3-fluoro-4-methoxyphenyl)imidazolidin-2-one Chemical compound C1=C(F)C(OC)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 LNLXPRNACORALX-UHFFFAOYSA-N 0.000 description 1
- YNPGVERNVJCADR-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(3-fluoro-4-propoxyphenyl)imidazolidin-2-one Chemical compound C1=C(F)C(OCCC)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 YNPGVERNVJCADR-UHFFFAOYSA-N 0.000 description 1
- UZAYUABXIDMCMD-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(3-hydroxyphenyl)imidazolidin-2-one Chemical compound OC1=CC=CC(C2N(C(=O)NC2)C=2C=C3N=CNC3=CC=2)=C1 UZAYUABXIDMCMD-UHFFFAOYSA-N 0.000 description 1
- DGHUQCPDKHYNNC-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(3-methoxyphenyl)imidazolidin-2-one Chemical compound COC1=CC=CC(C2N(C(=O)NC2)C=2C=C3N=CNC3=CC=2)=C1 DGHUQCPDKHYNNC-UHFFFAOYSA-N 0.000 description 1
- BPMIYWJABFZDBX-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(3-phenylphenyl)imidazolidin-2-one Chemical compound C=1C=C2NC=NC2=CC=1N1C(=O)NCC1C(C=1)=CC=CC=1C1=CC=CC=C1 BPMIYWJABFZDBX-UHFFFAOYSA-N 0.000 description 1
- MJJZZJSYZRLDKU-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(4-butoxyphenyl)imidazolidin-2-one Chemical compound C1=CC(OCCCC)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 MJJZZJSYZRLDKU-UHFFFAOYSA-N 0.000 description 1
- IFFDLCBKIXXANL-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(4-cyclohexyloxyphenyl)imidazolidin-2-one Chemical compound C=1C=C2NC=NC2=CC=1N1C(=O)NCC1C(C=C1)=CC=C1OC1CCCCC1 IFFDLCBKIXXANL-UHFFFAOYSA-N 0.000 description 1
- JNLGPDKBXLBBQW-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(4-cyclohexylphenyl)imidazolidin-2-one Chemical compound C=1C=C2NC=NC2=CC=1N1C(=O)NCC1C(C=C1)=CC=C1C1CCCCC1 JNLGPDKBXLBBQW-UHFFFAOYSA-N 0.000 description 1
- ASONZIYLOLQTDU-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(4-ethoxyphenyl)imidazolidin-2-one Chemical compound C1=CC(OCC)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 ASONZIYLOLQTDU-UHFFFAOYSA-N 0.000 description 1
- KMXQPKIJVJRGNZ-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(4-fluoro-3-methoxyphenyl)imidazolidin-2-one Chemical compound C1=C(F)C(OC)=CC(C2N(C(=O)NC2)C=2C=C3N=CNC3=CC=2)=C1 KMXQPKIJVJRGNZ-UHFFFAOYSA-N 0.000 description 1
- GSJXYPUQIVLTAO-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(4-fluorophenyl)pyrrolidin-2-one Chemical compound C1=CC(F)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)CC1 GSJXYPUQIVLTAO-UHFFFAOYSA-N 0.000 description 1
- CGPOLIDOBGOGKX-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(4-hydroxyphenyl)imidazolidin-2-one Chemical compound C1=CC(O)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 CGPOLIDOBGOGKX-UHFFFAOYSA-N 0.000 description 1
- GAOKCTXXKJPIDL-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(4-methoxyphenyl)pyrrolidin-2-one Chemical compound C1=CC(OC)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)CC1 GAOKCTXXKJPIDL-UHFFFAOYSA-N 0.000 description 1
- DLTPTOQUQFPYRK-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(4-morpholin-4-ylphenyl)imidazolidin-2-one Chemical compound C=1C=C2NC=NC2=CC=1N1C(=O)NCC1C(C=C1)=CC=C1N1CCOCC1 DLTPTOQUQFPYRK-UHFFFAOYSA-N 0.000 description 1
- RAMGEBXRKHKRND-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(4-pentoxyphenyl)imidazolidin-2-one Chemical compound C1=CC(OCCCCC)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 RAMGEBXRKHKRND-UHFFFAOYSA-N 0.000 description 1
- OOZUHXDNVHWMQK-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(4-propan-2-yloxyphenyl)imidazolidin-2-one Chemical compound C1=CC(OC(C)C)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 OOZUHXDNVHWMQK-UHFFFAOYSA-N 0.000 description 1
- XHIKZWOEFZENIX-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(4-propoxyphenyl)imidazolidin-2-one Chemical compound C1=CC(OCCC)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 XHIKZWOEFZENIX-UHFFFAOYSA-N 0.000 description 1
- LAVLGHQMEANVDC-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(4-propoxyphenyl)pyrrolidin-2-one Chemical compound C1=CC(OCCC)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)CC1 LAVLGHQMEANVDC-UHFFFAOYSA-N 0.000 description 1
- PSDNQBQDZMNVKM-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-(7-methoxy-1,3-benzodioxol-5-yl)imidazolidin-2-one Chemical compound C1=C2NC=NC2=CC(N2C(=O)NCC2C=2C=C(C=3OCOC=3C=2)OC)=C1 PSDNQBQDZMNVKM-UHFFFAOYSA-N 0.000 description 1
- XVQXSBBZNYESFI-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-[2-fluoro-4-(trifluoromethyl)phenyl]imidazolidin-2-one Chemical compound FC1=CC(C(F)(F)F)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 XVQXSBBZNYESFI-UHFFFAOYSA-N 0.000 description 1
- YWAXQEVHXLZLMM-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-[2-fluoro-5-(trifluoromethyl)phenyl]imidazolidin-2-one Chemical compound FC1=CC=C(C(F)(F)F)C=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 YWAXQEVHXLZLMM-UHFFFAOYSA-N 0.000 description 1
- NMGYQWOGTXDGLT-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-[3-(3-chlorophenyl)phenyl]imidazolidin-2-one Chemical compound ClC1=CC=CC(C=2C=C(C=CC=2)C2N(C(=O)NC2)C=2C=C3N=CNC3=CC=2)=C1 NMGYQWOGTXDGLT-UHFFFAOYSA-N 0.000 description 1
- GEKJXKIWDRDNBM-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-[3-fluoro-4-(trifluoromethyl)phenyl]imidazolidin-2-one Chemical compound C1=C(C(F)(F)F)C(F)=CC(C2N(C(=O)NC2)C=2C=C3N=CNC3=CC=2)=C1 GEKJXKIWDRDNBM-UHFFFAOYSA-N 0.000 description 1
- SCIAZXQFLMVDHZ-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-[3-fluoro-5-(trifluoromethyl)phenyl]imidazolidin-2-one Chemical compound FC(F)(F)C1=CC(F)=CC(C2N(C(=O)NC2)C=2C=C3N=CNC3=CC=2)=C1 SCIAZXQFLMVDHZ-UHFFFAOYSA-N 0.000 description 1
- CCZBHLPIMLZZQH-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-[4-(1,1,2,2-tetrafluoroethoxy)phenyl]imidazolidin-2-one Chemical compound C1=CC(OC(F)(F)C(F)F)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 CCZBHLPIMLZZQH-UHFFFAOYSA-N 0.000 description 1
- SFYPJOURINDDDQ-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-[4-(2-methoxyethoxy)phenyl]imidazolidin-2-one Chemical compound C1=CC(OCCOC)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 SFYPJOURINDDDQ-UHFFFAOYSA-N 0.000 description 1
- FOYOUTDTJICONH-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-[4-(3-methoxypropyl)phenyl]imidazolidin-2-one Chemical compound C1=CC(CCCOC)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)NC1 FOYOUTDTJICONH-UHFFFAOYSA-N 0.000 description 1
- IVJVPOPTXDKMTO-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-[4-(4-morpholin-4-ylcyclohexyl)phenyl]imidazolidin-2-one Chemical compound C=1C=C2NC=NC2=CC=1N1C(=O)NCC1C(C=C1)=CC=C1C(CC1)CCC1N1CCOCC1 IVJVPOPTXDKMTO-UHFFFAOYSA-N 0.000 description 1
- QSIOUMPIIOLJNV-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-[4-(4-oxocyclohexyl)phenyl]imidazolidin-2-one Chemical compound C=1C=C2NC=NC2=CC=1N1C(=O)NCC1C(C=C1)=CC=C1C1CCC(=O)CC1 QSIOUMPIIOLJNV-UHFFFAOYSA-N 0.000 description 1
- FCBIEHRSWNOZRH-UHFFFAOYSA-N 1-(3h-benzimidazol-5-yl)-5-cyclohexylimidazolidin-2-one Chemical compound C=1C=C2NC=NC2=CC=1N1C(=O)NCC1C1CCCCC1 FCBIEHRSWNOZRH-UHFFFAOYSA-N 0.000 description 1
- AZIGPOLIHOZKLO-UHFFFAOYSA-N 1-amino-3-(3h-benzimidazol-5-yl)-4-(4-methoxyphenyl)imidazolidin-2-one Chemical compound C1=CC(OC)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)N(N)C1 AZIGPOLIHOZKLO-UHFFFAOYSA-N 0.000 description 1
- QXQAPNSHUJORMC-UHFFFAOYSA-N 1-chloro-4-propylbenzene Chemical compound CCCC1=CC=C(Cl)C=C1 QXQAPNSHUJORMC-UHFFFAOYSA-N 0.000 description 1
- RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical class CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 description 1
- MRCAAFFMZODJBP-UHFFFAOYSA-N 1-fluoro-3-phenylbenzene Chemical group FC1=CC=CC(C=2C=CC=CC=2)=C1 MRCAAFFMZODJBP-UHFFFAOYSA-N 0.000 description 1
- GPAAEZIXSQCCES-UHFFFAOYSA-N 1-methoxy-2-(2-methoxyethoxymethoxymethoxy)ethane Chemical compound COCCOCOCOCCOC GPAAEZIXSQCCES-UHFFFAOYSA-N 0.000 description 1
- SDTORDSXCYSNTD-UHFFFAOYSA-N 1-methoxy-4-[(4-methoxyphenyl)methoxymethyl]benzene Chemical compound C1=CC(OC)=CC=C1COCC1=CC=C(OC)C=C1 SDTORDSXCYSNTD-UHFFFAOYSA-N 0.000 description 1
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 1
- LLSKXGRDUPMXLC-UHFFFAOYSA-N 1-phenylpiperidine Chemical compound C1CCCCN1C1=CC=CC=C1 LLSKXGRDUPMXLC-UHFFFAOYSA-N 0.000 description 1
- PRQRNNQMKUAVAB-UHFFFAOYSA-N 1-phenylpiperidine-4-carbaldehyde Chemical compound C1CC(C=O)CCN1C1=CC=CC=C1 PRQRNNQMKUAVAB-UHFFFAOYSA-N 0.000 description 1
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 1
- YQTCQNIPQMJNTI-UHFFFAOYSA-N 2,2-dimethylpropan-1-one Chemical group CC(C)(C)[C]=O YQTCQNIPQMJNTI-UHFFFAOYSA-N 0.000 description 1
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 description 1
- KLIDCXVFHGNTTM-UHFFFAOYSA-N 2,6-dimethoxyphenol Chemical group COC1=CC=CC(OC)=C1O KLIDCXVFHGNTTM-UHFFFAOYSA-N 0.000 description 1
- PYKJFEPAUKAXNN-UHFFFAOYSA-N 2-(2-methyl-8-phenylmethoxy-3-imidazo[1,2-a]pyridinyl)acetonitrile Chemical compound C=1C=CN2C(CC#N)=C(C)N=C2C=1OCC1=CC=CC=C1 PYKJFEPAUKAXNN-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- ICKMOIBSQQCIKY-UHFFFAOYSA-N 2-(3h-benzimidazol-5-yl)-3-(3,4-dimethoxyphenyl)-3h-isoindol-1-one Chemical compound C1=C(OC)C(OC)=CC=C1C1C2=CC=CC=C2C(=O)N1C1=CC=C(NC=N2)C2=C1 ICKMOIBSQQCIKY-UHFFFAOYSA-N 0.000 description 1
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical group C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 1
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 1
- XQYVOLNWZPSTGZ-UHFFFAOYSA-N 2-fluoro-n-[5-oxo-2-phenyl-4-(trifluoromethyl)-1h-imidazol-4-yl]benzamide Chemical compound FC1=CC=CC=C1C(=O)NC1(C(F)(F)F)C(=O)NC(C=2C=CC=CC=2)=N1 XQYVOLNWZPSTGZ-UHFFFAOYSA-N 0.000 description 1
- OPJKGTJXHVPYIM-UHFFFAOYSA-N 2-methylprop-2-enamide;phenol Chemical compound CC(=C)C(N)=O.OC1=CC=CC=C1 OPJKGTJXHVPYIM-UHFFFAOYSA-N 0.000 description 1
- 125000004361 3,4,5-trifluorophenyl group Chemical group [H]C1=C(F)C(F)=C(F)C([H])=C1* 0.000 description 1
- 125000005809 3,4,5-trimethoxyphenyl group Chemical group [H]C1=C(OC([H])([H])[H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 description 1
- 125000002774 3,4-dimethoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C(OC([H])([H])[H])=C1OC([H])([H])[H])C([H])([H])* 0.000 description 1
- ZEMIYZVGYNGUJX-UHFFFAOYSA-N 3-(3H-benzimidazol-5-yl)-1-(1-phenylethyl)-4-(4-propoxyphenyl)imidazolidin-2-one Chemical compound N1C=NC2=C1C=CC(=C2)N1C(N(CC1C1=CC=C(C=C1)OCCC)C(C)C1=CC=CC=C1)=O ZEMIYZVGYNGUJX-UHFFFAOYSA-N 0.000 description 1
- PEBGOQRITGIEFJ-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-1-(3-phenylpropyl)-4-(4-propoxyphenyl)imidazolidin-2-one Chemical compound C1=CC(OCCC)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)N(CCCC=2C=CC=CC=2)C1 PEBGOQRITGIEFJ-UHFFFAOYSA-N 0.000 description 1
- VRSNMNXYHMZZHS-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-1-(naphthalen-2-ylmethyl)-4-(4-propoxyphenyl)imidazolidin-2-one Chemical compound C1=CC(OCCC)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)N(CC=2C=C3C=CC=CC3=CC=2)C1 VRSNMNXYHMZZHS-UHFFFAOYSA-N 0.000 description 1
- HLTJUZONECAICT-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-1-benzyl-4-(4-propoxyphenyl)imidazolidin-2-one Chemical compound C1=CC(OCCC)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)N(CC=2C=CC=CC=2)C1 HLTJUZONECAICT-UHFFFAOYSA-N 0.000 description 1
- KOKPUOPWVZTPIS-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-2-(4-chlorophenyl)-1,3-thiazolidin-4-one Chemical compound C1=CC(Cl)=CC=C1C1N(C=2C=C3NC=NC3=CC=2)C(=O)CS1 KOKPUOPWVZTPIS-UHFFFAOYSA-N 0.000 description 1
- UXWIJKIVHBXZDC-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-2-(4-fluorophenyl)-1,3-thiazolidin-4-one Chemical compound C1=CC(F)=CC=C1C1N(C=2C=C3NC=NC3=CC=2)C(=O)CS1 UXWIJKIVHBXZDC-UHFFFAOYSA-N 0.000 description 1
- AZGQSLANURPRRR-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-2-(4-phenoxyphenyl)-1,3-thiazolidin-4-one Chemical compound C=1C=C2N=CNC2=CC=1N1C(=O)CSC1C(C=C1)=CC=C1OC1=CC=CC=C1 AZGQSLANURPRRR-UHFFFAOYSA-N 0.000 description 1
- GRBJTPWEDVCXHU-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-2-(4-phenoxyphenyl)-1,3-thiazolidine-4-thione Chemical compound C=1C=C2N=CNC2=CC=1N1C(=S)CSC1C(C=C1)=CC=C1OC1=CC=CC=C1 GRBJTPWEDVCXHU-UHFFFAOYSA-N 0.000 description 1
- RTCKSAFCQAVYNF-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-2-phenyl-1,3-thiazolidin-4-one Chemical compound C=1C=C2NC=NC2=CC=1N1C(=O)CSC1C1=CC=CC=C1 RTCKSAFCQAVYNF-UHFFFAOYSA-N 0.000 description 1
- BIVMFHDKYBEAJA-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-2-phenyl-1,3-thiazolidine-4-thione Chemical compound C=1C=C2NC=NC2=CC=1N1C(=S)CSC1C1=CC=CC=C1 BIVMFHDKYBEAJA-UHFFFAOYSA-N 0.000 description 1
- RBEIZNCAABSDBL-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-2-thiophen-3-yl-1,3-thiazolidin-4-one Chemical compound C=1C=C2N=CNC2=CC=1N1C(=O)CSC1C=1C=CSC=1 RBEIZNCAABSDBL-UHFFFAOYSA-N 0.000 description 1
- CYFZZMHCTFJPAG-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-4-(1-phenylethyl)-1,3-oxazolidin-2-one Chemical compound C1OC(=O)N(C=2C=C3N=CNC3=CC=2)C1C(C)C1=CC=CC=C1 CYFZZMHCTFJPAG-UHFFFAOYSA-N 0.000 description 1
- NOIWGLSIDMKBAM-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-4-(4-cyclohexyloxyphenyl)-1,3-oxazolidin-2-one Chemical compound C=1C=C2NC=NC2=CC=1N1C(=O)OCC1C(C=C1)=CC=C1OC1CCCCC1 NOIWGLSIDMKBAM-UHFFFAOYSA-N 0.000 description 1
- GFRLKSGDHRJCNV-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-4-(4-propoxyphenyl)-1,3-oxazinan-2-one Chemical compound C1=CC(OCCC)=CC=C1C1N(C=2C=C3NC=NC3=CC=2)C(=O)OCC1 GFRLKSGDHRJCNV-UHFFFAOYSA-N 0.000 description 1
- LRCAIIKYEMPGIF-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-4-(4-pyrrolidin-1-ylphenyl)-1,3-oxazolidin-2-one Chemical compound C=1C=C2NC=NC2=CC=1N1C(=O)OCC1C(C=C1)=CC=C1N1CCCC1 LRCAIIKYEMPGIF-UHFFFAOYSA-N 0.000 description 1
- FLEBUSLQFOYZHY-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-4-[4-(4,4-difluorocyclohexyl)phenyl]-1,3-oxazolidin-2-one Chemical compound C1CC(F)(F)CCC1C1=CC=C(C2N(C(=O)OC2)C=2C=C3N=CNC3=CC=2)C=C1 FLEBUSLQFOYZHY-UHFFFAOYSA-N 0.000 description 1
- UHIWZRXMRYDNOR-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-4-[4-(4-hydroxycyclohexyl)phenyl]-1,3-oxazolidin-2-one Chemical compound C1CC(O)CCC1C1=CC=C(C2N(C(=O)OC2)C=2C=C3N=CNC3=CC=2)C=C1 UHIWZRXMRYDNOR-UHFFFAOYSA-N 0.000 description 1
- VPEVIWZMPRBZME-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-4-[4-(4-methoxycyclohexyl)phenyl]-1,3-oxazolidin-2-one Chemical compound C1CC(OC)CCC1C1=CC=C(C2N(C(=O)OC2)C=2C=C3N=CNC3=CC=2)C=C1 VPEVIWZMPRBZME-UHFFFAOYSA-N 0.000 description 1
- TZVFDTNQCPWWTI-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-4-[4-(4-morpholin-4-ylcyclohexyl)phenyl]-1,3-oxazolidin-2-one Chemical compound C=1C=C2NC=NC2=CC=1N1C(=O)OCC1C(C=C1)=CC=C1C(CC1)CCC1N1CCOCC1 TZVFDTNQCPWWTI-UHFFFAOYSA-N 0.000 description 1
- UCCBYBIZZWTOKV-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-4-[4-(4-oxocyclohexyl)phenyl]-1,3-oxazolidin-2-one Chemical compound C=1C=C2NC=NC2=CC=1N1C(=O)OCC1C(C=C1)=CC=C1C1CCC(=O)CC1 UCCBYBIZZWTOKV-UHFFFAOYSA-N 0.000 description 1
- LUDICTAVQMUGML-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-4-[4-[3-(dimethylamino)propyl]phenyl]-1,3-oxazolidin-2-one Chemical compound C1=CC(CCCN(C)C)=CC=C1C1N(C=2C=C3N=CNC3=CC=2)C(=O)OC1 LUDICTAVQMUGML-UHFFFAOYSA-N 0.000 description 1
- HAJRKXXFIWTQEM-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-5-methyl-2-phenyl-1,3-thiazolidin-4-one Chemical compound C=1C=C2N=CNC2=CC=1N1C(=O)C(C)SC1C1=CC=CC=C1 HAJRKXXFIWTQEM-UHFFFAOYSA-N 0.000 description 1
- BPNUFMWEIQORLP-UHFFFAOYSA-N 3-(3h-benzimidazol-5-yl)-5-phenyl-4-(4-propoxyphenyl)-1,3-oxazolidin-2-one Chemical compound C1=CC(OCCC)=CC=C1C1N(C=2C=C3NC=NC3=CC=2)C(=O)OC1C1=CC=CC=C1 BPNUFMWEIQORLP-UHFFFAOYSA-N 0.000 description 1
- VSFSDXSEWVOTIK-UHFFFAOYSA-N 3-(4-fluorophenyl)-2,3-dihydroisoindol-1-one Chemical compound FC1=CC=C(C=C1)C1NC(C2=CC=CC=C12)=O VSFSDXSEWVOTIK-UHFFFAOYSA-N 0.000 description 1
- JPDCTZYCUZRESY-UHFFFAOYSA-N 3-(4-methoxyphenyl)-2,3-dihydroisoindol-1-one Chemical compound C1=CC(OC)=CC=C1C1C2=CC=CC=C2C(=O)N1 JPDCTZYCUZRESY-UHFFFAOYSA-N 0.000 description 1
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 description 1
- MDCJIADEOATVKA-UHFFFAOYSA-N 3-imidazo[1,2-a]pyridin-7-yl-4-(4-propoxyphenyl)-1,3-oxazinan-2-one Chemical compound C1=CC(OCCC)=CC=C1C1N(C2=CC3=NC=CN3C=C2)C(=O)OCC1 MDCJIADEOATVKA-UHFFFAOYSA-N 0.000 description 1
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 description 1
- WSKBLLFHGABBEW-UHFFFAOYSA-N 3-phenyl-2,3-dihydroisoindol-1-one Chemical compound C12=CC=CC=C2C(=O)NC1C1=CC=CC=C1 WSKBLLFHGABBEW-UHFFFAOYSA-N 0.000 description 1
- YNLSYJFBGQCXRH-UHFFFAOYSA-N 4-(2-chlorophenyl)imidazolidin-2-one Chemical compound ClC1=CC=CC=C1C1NC(=O)NC1 YNLSYJFBGQCXRH-UHFFFAOYSA-N 0.000 description 1
- QQUZSGXDUHPSKW-UHFFFAOYSA-N 4-(3,4-difluorophenyl)imidazolidin-2-one Chemical compound C1=C(F)C(F)=CC=C1C1NC(=O)NC1 QQUZSGXDUHPSKW-UHFFFAOYSA-N 0.000 description 1
- YCGMHNUIFVCQHA-UHFFFAOYSA-N 4-(3-chlorophenyl)imidazolidin-2-one Chemical compound ClC1=CC=CC(C2NC(=O)NC2)=C1 YCGMHNUIFVCQHA-UHFFFAOYSA-N 0.000 description 1
- DSNTVQQMWLKKAL-UHFFFAOYSA-N 4-(3-pyrrolidin-1-ylphenyl)imidazolidin-2-one Chemical compound N1(CCCC1)C=1C=C(C=CC=1)C1CNC(N1)=O DSNTVQQMWLKKAL-UHFFFAOYSA-N 0.000 description 1
- WUYWHIAAQYQKPP-UHFFFAOYSA-N 4-(4-fluorophenyl)-4-oxobutanoic acid Chemical compound OC(=O)CCC(=O)C1=CC=C(F)C=C1 WUYWHIAAQYQKPP-UHFFFAOYSA-N 0.000 description 1
- XFRVACCGEKPJDI-UHFFFAOYSA-N 4-(4-oxocyclohexyl)benzonitrile Chemical compound C1CC(=O)CCC1C1=CC=C(C#N)C=C1 XFRVACCGEKPJDI-UHFFFAOYSA-N 0.000 description 1
- RURHILYUWQEGOS-VOTSOKGWSA-N 4-Methylcinnamic acid Chemical group CC1=CC=C(\C=C\C(O)=O)C=C1 RURHILYUWQEGOS-VOTSOKGWSA-N 0.000 description 1
- SDUKSJXMMCQTGT-UHFFFAOYSA-N 4-[4-(1-methylpiperidin-4-yl)phenyl]-1,3-oxazolidin-2-one Chemical compound C1CN(C)CCC1C1=CC=C(C2NC(=O)OC2)C=C1 SDUKSJXMMCQTGT-UHFFFAOYSA-N 0.000 description 1
- AFOGIDWAVVJKIN-UHFFFAOYSA-N 4-[4-(4-phenylpiperazin-1-yl)phenyl]imidazolidin-2-one Chemical compound C1(=CC=CC=C1)N1CCN(CC1)C1=CC=C(C=C1)C1CNC(N1)=O AFOGIDWAVVJKIN-UHFFFAOYSA-N 0.000 description 1
- HQOIMRVBGLRBCH-UHFFFAOYSA-N 4-[4-(oxan-4-yl)phenyl]-1,3-oxazolidin-2-one Chemical compound C1OC(=O)NC1C1=CC=C(C2CCOCC2)C=C1 HQOIMRVBGLRBCH-UHFFFAOYSA-N 0.000 description 1
- XYWIPYBIIRTJMM-IBGZPJMESA-N 4-[[(2S)-2-[4-[5-chloro-2-[4-(trifluoromethyl)triazol-1-yl]phenyl]-5-methoxy-2-oxopyridin-1-yl]butanoyl]amino]-2-fluorobenzamide Chemical compound CC[C@H](N1C=C(OC)C(=CC1=O)C1=C(C=CC(Cl)=C1)N1C=C(N=N1)C(F)(F)F)C(=O)NC1=CC(F)=C(C=C1)C(N)=O XYWIPYBIIRTJMM-IBGZPJMESA-N 0.000 description 1
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 description 1
- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 description 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 1
- 125000005274 4-hydroxybenzoic acid group Chemical group 0.000 description 1
- HFKIYIBJKBDTBZ-UHFFFAOYSA-N 4-phenylimidazolidin-2-one Chemical compound N1C(=O)NCC1C1=CC=CC=C1 HFKIYIBJKBDTBZ-UHFFFAOYSA-N 0.000 description 1
- IQBLOWAQCJSQIG-UHFFFAOYSA-N 5-(4-methoxyphenyl)pyrrolidin-2-one Chemical compound C1=CC(OC)=CC=C1C1NC(=O)CC1 IQBLOWAQCJSQIG-UHFFFAOYSA-N 0.000 description 1
- FXZDLYKFOLGSFW-UHFFFAOYSA-N 5-(4-propoxyphenyl)pyrrolidin-2-one Chemical compound C1=CC(OCCC)=CC=C1C1NC(=O)CC1 FXZDLYKFOLGSFW-UHFFFAOYSA-N 0.000 description 1
- TVESJBDGOZUZRH-UHFFFAOYSA-N 5-phenylpyrrolidin-2-one Chemical compound N1C(=O)CCC1C1=CC=CC=C1 TVESJBDGOZUZRH-UHFFFAOYSA-N 0.000 description 1
- VKZUQPKYHDKAOH-UHFFFAOYSA-N 6-[2-[(4-chlorophenyl)methyl]pyrrolidin-1-yl]-1h-benzimidazole Chemical compound C1=CC(Cl)=CC=C1CC1N(C=2C=C3N=CNC3=CC=2)CCC1 VKZUQPKYHDKAOH-UHFFFAOYSA-N 0.000 description 1
- HFZMQPITEANRSW-UHFFFAOYSA-N 6-[2-[(4-fluorophenyl)methyl]pyrrolidin-1-yl]-1h-benzimidazole Chemical compound C1=CC(F)=CC=C1CC1N(C=2C=C3N=CNC3=CC=2)CCC1 HFZMQPITEANRSW-UHFFFAOYSA-N 0.000 description 1
- SBOJSSBBYLTRKR-UHFFFAOYSA-N 6-[2-[(4-methoxyphenyl)methyl]pyrrolidin-1-yl]-1h-benzimidazole Chemical compound C1=CC(OC)=CC=C1CC1N(C=2C=C3N=CNC3=CC=2)CCC1 SBOJSSBBYLTRKR-UHFFFAOYSA-N 0.000 description 1
- 125000004939 6-pyridyl group Chemical group N1=CC=CC=C1* 0.000 description 1
- APZDRBPCYOOGAF-UHFFFAOYSA-N 6-pyrrolidin-1-yl-1h-benzimidazole Chemical compound C1CCCN1C1=CC=C(NC=N2)C2=C1 APZDRBPCYOOGAF-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 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 1
- ORILYTVJVMAKLC-UHFFFAOYSA-N Adamantane Natural products C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 102000004400 Aminopeptidases Human genes 0.000 description 1
- 108090000915 Aminopeptidases Proteins 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 208000023275 Autoimmune disease Diseases 0.000 description 1
- GUBGYTABKSRVRQ-DCSYEGIMSA-N Beta-Lactose Chemical compound OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-DCSYEGIMSA-N 0.000 description 1
- 102100021257 Beta-secretase 1 Human genes 0.000 description 1
- 206010068597 Bulbospinal muscular atrophy congenital 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
- 102100031172 C-C chemokine receptor type 1 Human genes 0.000 description 1
- 101710149814 C-C chemokine receptor type 1 Proteins 0.000 description 1
- 102100024167 C-C chemokine receptor type 3 Human genes 0.000 description 1
- 101710149862 C-C chemokine receptor type 3 Proteins 0.000 description 1
- 102100037853 C-C chemokine receptor type 4 Human genes 0.000 description 1
- 101710149863 C-C chemokine receptor type 4 Proteins 0.000 description 1
- 101710112526 C-C motif chemokine 18 Proteins 0.000 description 1
- 101710155857 C-C motif chemokine 2 Proteins 0.000 description 1
- 102100032367 C-C motif chemokine 5 Human genes 0.000 description 1
- 101710155834 C-C motif chemokine 7 Proteins 0.000 description 1
- 101710155833 C-C motif chemokine 8 Proteins 0.000 description 1
- 125000006539 C12 alkyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- OKPCGRXDAHEIOP-UHFFFAOYSA-N C1C(=O)NC(S1)C2=C(C=CC=C2F)F Chemical compound C1C(=O)NC(S1)C2=C(C=CC=C2F)F OKPCGRXDAHEIOP-UHFFFAOYSA-N 0.000 description 1
- JWRRLAUBBPWSFS-UHFFFAOYSA-N C1CCN(CC1)C2=CC=C(C=C2)C3CNC(=O)N3 Chemical compound C1CCN(CC1)C2=CC=C(C=C2)C3CNC(=O)N3 JWRRLAUBBPWSFS-UHFFFAOYSA-N 0.000 description 1
- 108090000835 CX3C Chemokine Receptor 1 Proteins 0.000 description 1
- 102100039196 CX3C chemokine receptor 1 Human genes 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 108010055166 Chemokine CCL5 Proteins 0.000 description 1
- 108010089448 Cholecystokinin B Receptor Proteins 0.000 description 1
- 206010009944 Colon cancer Diseases 0.000 description 1
- 208000001333 Colorectal Neoplasms Diseases 0.000 description 1
- 108090000695 Cytokines Proteins 0.000 description 1
- 102000004127 Cytokines Human genes 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
- 206010061825 Duodenal neoplasm Diseases 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 102000012673 Follicle Stimulating Hormone Human genes 0.000 description 1
- 108010079345 Follicle Stimulating Hormone Proteins 0.000 description 1
- 102000013818 Fractalkine Human genes 0.000 description 1
- 102100020997 Fractalkine Human genes 0.000 description 1
- 210000000712 G cell Anatomy 0.000 description 1
- 241000713444 Gastrina Species 0.000 description 1
- 206010017886 Gastroduodenal ulcer Diseases 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 101000930822 Giardia intestinalis Dipeptidyl-peptidase 4 Proteins 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- NMJREATYWWNIKX-UHFFFAOYSA-N GnRH Chemical compound C1CCC(C(=O)NCC(N)=O)N1C(=O)C(CC(C)C)NC(=O)C(CC=1C2=CC=CC=C2NC=1)NC(=O)CNC(=O)C(NC(=O)C(CO)NC(=O)C(CC=1C2=CC=CC=C2NC=1)NC(=O)C(CC=1NC=NC=1)NC(=O)C1NC(=O)CC1)CC1=CC=C(O)C=C1 NMJREATYWWNIKX-UHFFFAOYSA-N 0.000 description 1
- 108010086677 Gonadotropins Proteins 0.000 description 1
- 102000006771 Gonadotropins Human genes 0.000 description 1
- 241000590002 Helicobacter pylori Species 0.000 description 1
- 102100033798 Homeobox protein aristaless-like 4 Human genes 0.000 description 1
- 101000894895 Homo sapiens Beta-secretase 1 Proteins 0.000 description 1
- 101000978371 Homo sapiens C-C motif chemokine 18 Proteins 0.000 description 1
- 101000797758 Homo sapiens C-C motif chemokine 7 Proteins 0.000 description 1
- 101000946794 Homo sapiens C-C motif chemokine 8 Proteins 0.000 description 1
- 101000969553 Homo sapiens Cell surface glycoprotein CD200 receptor 1 Proteins 0.000 description 1
- 101000967222 Homo sapiens Homeobox protein MSX-2 Proteins 0.000 description 1
- 101000779608 Homo sapiens Homeobox protein aristaless-like 4 Proteins 0.000 description 1
- 101001074035 Homo sapiens Zinc finger protein GLI2 Proteins 0.000 description 1
- 208000023105 Huntington disease Diseases 0.000 description 1
- 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 1
- 208000027747 Kennedy disease Diseases 0.000 description 1
- XNSAINXGIQZQOO-UHFFFAOYSA-N L-pyroglutamyl-L-histidyl-L-proline amide Natural products NC(=O)C1CCCN1C(=O)C(NC(=O)C1NC(=O)CC1)CC1=CN=CN1 XNSAINXGIQZQOO-UHFFFAOYSA-N 0.000 description 1
- 102000009151 Luteinizing Hormone Human genes 0.000 description 1
- 108010073521 Luteinizing Hormone Proteins 0.000 description 1
- 108700018351 Major Histocompatibility Complex Proteins 0.000 description 1
- 102000001776 Matrix metalloproteinase-9 Human genes 0.000 description 1
- 108010015302 Matrix metalloproteinase-9 Proteins 0.000 description 1
- 206010027476 Metastases Diseases 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
- ZWEMAVPSPUDXHF-UHFFFAOYSA-N N1(CCCCC1)C=1C=C(C=CC=1)C1CNC(N1)=O Chemical compound N1(CCCCC1)C=1C=C(C=CC=1)C1CNC(N1)=O ZWEMAVPSPUDXHF-UHFFFAOYSA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- 102100037588 Orexin receptor type 2 Human genes 0.000 description 1
- 102100028141 Orexin/Hypocretin receptor type 1 Human genes 0.000 description 1
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium on carbon Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 1
- 208000018737 Parkinson disease Diseases 0.000 description 1
- 208000008469 Peptic Ulcer Diseases 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 108010039918 Polylysine Proteins 0.000 description 1
- 229920001710 Polyorthoester Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 208000028017 Psychotic disease Diseases 0.000 description 1
- 206010054184 Small intestine carcinoma Diseases 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 1
- 101000857870 Squalus acanthias Gonadoliberin Proteins 0.000 description 1
- 102400000096 Substance P Human genes 0.000 description 1
- 101800003906 Substance P Proteins 0.000 description 1
- 102000003141 Tachykinin Human genes 0.000 description 1
- 239000000627 Thyrotropin-Releasing Hormone Substances 0.000 description 1
- 208000025865 Ulcer Diseases 0.000 description 1
- 208000006269 X-Linked Bulbo-Spinal Atrophy Diseases 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 102100035558 Zinc finger protein GLI2 Human genes 0.000 description 1
- WLYPBMBWKYALCG-UHFFFAOYSA-N [2,4-bis(trifluoromethyl)phenyl]boronic acid Chemical group OB(O)C1=CC=C(C(F)(F)F)C=C1C(F)(F)F WLYPBMBWKYALCG-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical group 0.000 description 1
- WEVYAHXRMPXWCK-UHFFFAOYSA-N acetonitrile Substances CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 230000036982 action potential Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 235000010419 agar Nutrition 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- 230000002152 alkylating effect Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- FEWOUVRMGWFWIH-ILZZQXMPSA-N amyloid-beta polypeptide 40 Chemical compound C([C@@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](C(=O)NCC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)NCC(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(O)=O)[C@@H](C)CC)C(C)C)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C(C)C)C1=CC=CC=C1 FEWOUVRMGWFWIH-ILZZQXMPSA-N 0.000 description 1
- 206010002022 amyloidosis Diseases 0.000 description 1
- 210000004198 anterior pituitary gland Anatomy 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 208000037979 autoimmune inflammatory disease Diseases 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000003542 behavioural effect Effects 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- 235000012216 bentonite Nutrition 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 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
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 229920002988 biodegradable polymer Polymers 0.000 description 1
- 239000004621 biodegradable polymer Substances 0.000 description 1
- 230000001851 biosynthetic effect Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- SIPUZPBQZHNSDW-UHFFFAOYSA-N bis(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 230000017531 blood circulation Effects 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
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 230000003185 calcium uptake Effects 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000002490 cerebral effect Effects 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 230000000112 colonic effect Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000013270 controlled release Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 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
- HCAJEUSONLESMK-UHFFFAOYSA-N cyclohexylsulfamic acid Chemical compound OS(=O)(=O)NC1CCCCC1 HCAJEUSONLESMK-UHFFFAOYSA-N 0.000 description 1
- 231100000433 cytotoxic Toxicity 0.000 description 1
- 210000001151 cytotoxic T lymphocyte Anatomy 0.000 description 1
- 230000001472 cytotoxic effect Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 210000004443 dendritic cell Anatomy 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 230000004069 differentiation Effects 0.000 description 1
- 102000038379 digestive enzymes Human genes 0.000 description 1
- 108091007734 digestive enzymes Proteins 0.000 description 1
- 210000002249 digestive system Anatomy 0.000 description 1
- 125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 201000000312 duodenum cancer Diseases 0.000 description 1
- 230000002124 endocrine Effects 0.000 description 1
- 210000002889 endothelial cell Anatomy 0.000 description 1
- 210000002919 epithelial cell Anatomy 0.000 description 1
- 230000008556 epithelial cell proliferation Effects 0.000 description 1
- BDWFYHUDXIDTIU-UHFFFAOYSA-N ethanol;propane-1,2,3-triol Chemical compound CCO.OCC(O)CO BDWFYHUDXIDTIU-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- VFRSADQPWYCXDG-LEUCUCNGSA-N ethyl (2s,5s)-5-methylpyrrolidine-2-carboxylate;2,2,2-trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.CCOC(=O)[C@@H]1CC[C@H](C)N1 VFRSADQPWYCXDG-LEUCUCNGSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229940028334 follicle stimulating hormone Drugs 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 230000027119 gastric acid secretion Effects 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 210000002406 gastrin-secreting cell Anatomy 0.000 description 1
- OKGNKPYIPKMGLR-ZPCKCTIPSA-N gastrins Chemical class C([C@@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)N[C@@H](C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(=O)NCC(=O)N1CCC[C@H]1C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)NCC(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC=1C=CC=CC=1)C(N)=O)C(C)C)NC(=O)[C@H]1N(CCC1)C(=O)[C@H]1N(CCC1)C(=O)CNC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)CNC(=O)[C@H](CC(C)C)NC(=O)[C@H]1N(CCC1)C(=O)[C@H]1NC(=O)CC1)C1=CN=CN1 OKGNKPYIPKMGLR-ZPCKCTIPSA-N 0.000 description 1
- 231100000029 gastro-duodenal ulcer Toxicity 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
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 229960004666 glucagon Drugs 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229930195712 glutamate Natural products 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 125000000291 glutamic acid group Chemical group N[C@@H](CCC(O)=O)C(=O)* 0.000 description 1
- ZDXPYRJPNDTMRX-UHFFFAOYSA-N glutamine Natural products OC(=O)C(N)CCC(N)=O ZDXPYRJPNDTMRX-UHFFFAOYSA-N 0.000 description 1
- 125000000404 glutamine group Chemical group N[C@@H](CCC(N)=O)C(=O)* 0.000 description 1
- 239000002622 gonadotropin Substances 0.000 description 1
- 210000003714 granulocyte Anatomy 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 229940037467 helicobacter pylori Drugs 0.000 description 1
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 1
- 239000000017 hydrogel Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- GVONPBONFIJAHJ-UHFFFAOYSA-N imidazolidin-4-one Chemical compound O=C1CNCN1 GVONPBONFIJAHJ-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000000338 in vitro 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
- 230000001939 inductive effect Effects 0.000 description 1
- 208000000509 infertility Diseases 0.000 description 1
- 230000036512 infertility Effects 0.000 description 1
- 231100000535 infertility Toxicity 0.000 description 1
- 230000002757 inflammatory effect Effects 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 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
- 239000000314 lubricant Substances 0.000 description 1
- 229940040129 luteinizing hormone Drugs 0.000 description 1
- 210000002540 macrophage Anatomy 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 230000003211 malignant effect Effects 0.000 description 1
- 210000005171 mammalian brain Anatomy 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 201000001441 melanoma Diseases 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 210000004379 membrane Anatomy 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- FJQXCDYVZAHXNS-UHFFFAOYSA-N methadone hydrochloride Chemical compound Cl.C=1C=CC=CC=1C(CC(C)N(C)C)(C(=O)CC)C1=CC=CC=C1 FJQXCDYVZAHXNS-UHFFFAOYSA-N 0.000 description 1
- GPKUICFDWYEPTK-UHFFFAOYSA-N methoxycyclohexatriene Chemical compound COC1=CC=C=C[CH]1 GPKUICFDWYEPTK-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical group 0.000 description 1
- 150000005217 methyl ethers Chemical class 0.000 description 1
- CPZBTYRIGVOOMI-UHFFFAOYSA-N methylsulfanyl(methylsulfanylmethoxy)methane Chemical compound CSCOCSC CPZBTYRIGVOOMI-UHFFFAOYSA-N 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 125000004572 morpholin-3-yl group Chemical group N1C(COCC1)* 0.000 description 1
- 230000003039 myelosuppressive effect Effects 0.000 description 1
- IHECHUNKORJULE-UHFFFAOYSA-N n-(2,6-difluorophenyl)-2-pyridin-2-ylquinoline-4-carboxamide Chemical compound FC1=CC=CC(F)=C1NC(=O)C1=CC(C=2N=CC=CC=2)=NC2=CC=CC=C12 IHECHUNKORJULE-UHFFFAOYSA-N 0.000 description 1
- RHLMXWCISNJNDH-UHFFFAOYSA-N n-[2-[3-[[5-[3-(dimethylcarbamoyl)phenyl]-2-methoxyphenyl]sulfonylamino]anilino]ethyl]-3-methylbenzamide Chemical compound COC1=CC=C(C=2C=C(C=CC=2)C(=O)N(C)C)C=C1S(=O)(=O)NC(C=1)=CC=CC=1NCCNC(=O)C1=CC=CC(C)=C1 RHLMXWCISNJNDH-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- YZMHQCWXYHARLS-UHFFFAOYSA-N naphthalene-1,2-disulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(S(=O)(=O)O)=CC=C21 YZMHQCWXYHARLS-UHFFFAOYSA-N 0.000 description 1
- 229920001206 natural gum Polymers 0.000 description 1
- 230000001537 neural effect Effects 0.000 description 1
- 210000002569 neuron Anatomy 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- 150000002905 orthoesters Chemical group 0.000 description 1
- KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- AFDXODALSZRGIH-UHFFFAOYSA-N p-coumaric acid methyl ether Natural products COC1=CC=C(C=CC(O)=O)C=C1 AFDXODALSZRGIH-UHFFFAOYSA-N 0.000 description 1
- 125000001312 palmitoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- WLJNZVDCPSBLRP-UHFFFAOYSA-N pamoic acid Chemical compound C1=CC=C2C(CC=3C4=CC=CC=C4C=C(C=3O)C(=O)O)=C(O)C(C(O)=O)=CC2=C1 WLJNZVDCPSBLRP-UHFFFAOYSA-N 0.000 description 1
- 210000000496 pancreas Anatomy 0.000 description 1
- 230000003076 paracrine Effects 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 230000008506 pathogenesis Effects 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 230000007310 pathophysiology Effects 0.000 description 1
- 239000000813 peptide hormone Substances 0.000 description 1
- 210000001428 peripheral nervous system Anatomy 0.000 description 1
- 150000008105 phosphatidylcholines Chemical class 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 230000006461 physiological response Effects 0.000 description 1
- 229920000747 poly(lactic acid) Polymers 0.000 description 1
- 229920002721 polycyanoacrylate Polymers 0.000 description 1
- 239000004626 polylactic acid Substances 0.000 description 1
- 229920000656 polylysine Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 238000002953 preparative HPLC Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 229940043131 pyroglutamate Drugs 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 102000005962 receptors Human genes 0.000 description 1
- 230000007115 recruitment Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 201000000980 schizophrenia 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
- 230000000580 secretagogue effect Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 210000002460 smooth muscle Anatomy 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 210000000278 spinal cord Anatomy 0.000 description 1
- 210000000130 stem cell Anatomy 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 108060008037 tachykinin Proteins 0.000 description 1
- SKQBOMOZPWGHAX-UHFFFAOYSA-N tert-butyl-[[tert-butyl(dimethyl)silyl]oxymethoxymethoxy]-dimethylsilane Chemical compound CC(C)(C)[Si](C)(C)OCOCO[Si](C)(C)C(C)(C)C SKQBOMOZPWGHAX-UHFFFAOYSA-N 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000005329 tetralinyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- VBEQCZHXXJYVRD-GACYYNSASA-N uroanthelone Chemical compound C([C@@H](C(=O)N[C@H](C(=O)N[C@@H](CS)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CS)C(=O)N[C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C(C)C)[C@@H](C)O)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CC=1NC=NC=1)NC(=O)[C@H](CCSC)NC(=O)[C@H](CS)NC(=O)[C@@H](NC(=O)CNC(=O)CNC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CS)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CS)NC(=O)CNC(=O)[C@H]1N(CCC1)C(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC(N)=O)C(C)C)[C@@H](C)CC)C1=CC=C(O)C=C1 VBEQCZHXXJYVRD-GACYYNSASA-N 0.000 description 1
- 229940124549 vasodilator Drugs 0.000 description 1
- 239000003071 vasodilator agent Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 229930195724 β-lactose Natural products 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5355—Non-condensed oxazines and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
-
- 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
- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
-
- 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
- C07D403/14—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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D417/02—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 two hetero rings
- C07D417/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D471/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Psychiatry (AREA)
- Reproductive Health (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Psychology (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Transplantation (AREA)
- Oncology (AREA)
- Anesthesiology (AREA)
- Dermatology (AREA)
- Hospice & Palliative Care (AREA)
- Gynecology & Obstetrics (AREA)
- Pregnancy & Childbirth (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US24143209P | 2009-09-11 | 2009-09-11 | |
| US241432P | 2009-09-11 | ||
| PCT/EP2010/063341 WO2011029920A1 (en) | 2009-09-11 | 2010-09-13 | Heterocylcic derivatives as inhibitors of glutaminyl cyclase |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2548913T3 true ES2548913T3 (es) | 2015-10-21 |
Family
ID=43732030
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES10751952.2T Active ES2548913T3 (es) | 2009-09-11 | 2010-09-13 | Derivados heterocíclicos como inhibidores de glutaminil ciclasa |
Country Status (18)
| Country | Link |
|---|---|
| US (3) | US8486940B2 (enExample) |
| EP (1) | EP2475428B1 (enExample) |
| JP (1) | JP5934645B2 (enExample) |
| KR (1) | KR101755737B1 (enExample) |
| CN (1) | CN102695546B (enExample) |
| AU (1) | AU2010294214B2 (enExample) |
| BR (1) | BR112012008346B1 (enExample) |
| CA (1) | CA2772488C (enExample) |
| DK (1) | DK2475428T3 (enExample) |
| EA (1) | EA022007B1 (enExample) |
| ES (1) | ES2548913T3 (enExample) |
| IL (1) | IL218259A (enExample) |
| MX (1) | MX2012002993A (enExample) |
| NZ (1) | NZ598685A (enExample) |
| PL (1) | PL2475428T3 (enExample) |
| SG (1) | SG178953A1 (enExample) |
| WO (1) | WO2011029920A1 (enExample) |
| ZA (1) | ZA201201366B (enExample) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012123563A1 (en) * | 2011-03-16 | 2012-09-20 | Probiodrug Ag | Benz imidazole derivatives as inhibitors of glutaminyl cyclase |
| JP2014515364A (ja) * | 2011-05-27 | 2014-06-30 | プロビオドルグ エージー | 放射能標識グルタミニルシクラーゼ阻害剤 |
| AU2014233168B2 (en) | 2013-03-15 | 2018-11-22 | Cancer Research Technology, Llc | Methods and compositions for Gamma-glutamyl cycle modulation |
| JP6454651B2 (ja) * | 2013-03-15 | 2019-01-23 | プロビオドルグ エージー | 新規阻害剤 |
| TWI477479B (zh) * | 2013-07-18 | 2015-03-21 | Daxin Materials Corp | 二胺苯化合物、聚合物、配向膜用組成物、配向膜以及液晶顯示元件 |
| DE102015011780A1 (de) * | 2015-09-16 | 2017-03-16 | Hochschule Anhalt | Neue Glutaminylcyclase-lnhibitoren |
| GB201705263D0 (en) | 2017-03-31 | 2017-05-17 | Probiodrug Ag | Novel inhibitors |
| FI3658141T3 (fi) | 2017-07-24 | 2023-03-02 | Patologisten tilojen hoitaminen suoralla tai epäsuoralla siralfa-cd47-vuorovaikutukseen kohdentamisella | |
| DK3461819T3 (da) * | 2017-09-29 | 2020-08-10 | Probiodrug Ag | Inhibitorer af glutaminylcyklase |
| JP7364558B2 (ja) | 2017-10-10 | 2023-10-18 | ダグラス ファーマシューティカルズ エルティーディー. | 持続放出医薬製剤及び治療方法 |
| US10869838B2 (en) | 2017-10-10 | 2020-12-22 | Douglas Pharmaceuticals, Ltd. | Extended release pharmaceutical formulation |
| EP3521308B1 (en) | 2018-01-31 | 2024-03-13 | Vivoryon Therapeutics N.V. | Humanized and de-immunized antibodies |
| EP3750885A4 (en) * | 2018-02-06 | 2021-10-27 | Shanghai Haihe Pharmaceutical Co., Ltd. | COMPOUND PRESENTING AN INHIBITORING ACTIVITY OF BET, ITS PREPARATION PROCESS AND ITS USE |
| MY202227A (en) * | 2018-02-23 | 2024-04-18 | Fraunhofer Ges Zur Frderung Der Angewandten Forschung E V | Novel inhibitors of bacterial glutaminyl cyclases for use in the treatment of periodontal and related diseases |
| TWI715156B (zh) * | 2018-08-31 | 2021-01-01 | 財團法人國家衛生研究院 | 苯并咪唑化合物及其用於治療阿茲海默症或亨丁頓氏症之用途 |
| WO2020047360A1 (en) * | 2018-08-31 | 2020-03-05 | National Health Research Institutes | Benzimidazole compounds and use thereof for treating alzheimer's disease or huntington's disease |
| GB201918410D0 (en) * | 2019-12-13 | 2020-01-29 | Z Factor Ltd | Compounds and their use for the treatment of alpha1-antitrypsin deficiency |
| AU2022298746A1 (en) * | 2021-06-24 | 2023-11-30 | Insilico Medicine Ip Limited | Beta-lactam derivatives for the treatment of diseases |
| AU2022203580A1 (en) * | 2021-09-17 | 2023-04-06 | Academia Sinica | Methods of Increasing Cell Phagocytosis |
| CN115448892B (zh) * | 2022-09-19 | 2023-07-07 | 郑州铁路职业技术学院 | 一种苯并噻二唑杂环化合物的合成方法 |
| EP4455142A1 (en) | 2023-04-26 | 2024-10-30 | Scenic Immunology B.V. | Novel inhibitor of qpctl and/or qc |
| WO2024256618A1 (en) | 2023-06-16 | 2024-12-19 | Vivoryon Therapeutics N.V. | Crystalline pharmaceutically acceptable salt and polymorphic form of the glutaminyl cyclase inhibitor varoglutamstat |
| WO2025021012A1 (en) * | 2023-07-21 | 2025-01-30 | Insilico Medicine Ip Limited | Crystalline beta-lactam derivatives and uses thereof |
| WO2025224169A1 (en) | 2024-04-23 | 2025-10-30 | Vivoryon Therapeutics N.V. | Dose regimens for the glutaminyl cyclase inhibitor varoglutamstat |
| WO2025224179A1 (en) | 2024-04-23 | 2025-10-30 | Vivoryon Therapeutics N.V. | Glutaminyl cyclase inhbitors for use in the treatment of kidney disease |
Family Cites Families (596)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6137764A (ja) | 1984-07-31 | 1986-02-22 | Suntory Ltd | 抗プロリルエンドペプチダ−ゼ活性を有する新規生理活性化合物 |
| JPS6172439A (ja) | 1984-09-18 | 1986-04-14 | Sanyo Electric Co Ltd | デ−タ転送方式 |
| US4873342A (en) | 1985-04-16 | 1989-10-10 | Suntory Limited | Dipeptide derivative and synthesis and use thereof |
| JPH0623190B2 (ja) | 1985-04-16 | 1994-03-30 | サントリー株式会社 | インヒビタ−活性を有するn−アシルピロリジン誘導体及びその製法並びに用途 |
| CA1298033C (en) | 1985-04-16 | 1992-03-24 | Takaharu Tanaka | Dipeptide derivative of fatty acid |
| JPS62114957A (ja) | 1985-11-13 | 1987-05-26 | Suntory Ltd | プロリルエンドペプチダ−ゼ阻害作用を有する新規ピロリジン誘導体およびその製法並びに用途 |
| JPH0714878B2 (ja) | 1985-11-14 | 1995-02-22 | サントリー株式会社 | ピロリジンアミドを有効成分とするプロリルエンドペプチダーゼ阻害剤 |
| JPH0764834B2 (ja) | 1985-11-29 | 1995-07-12 | サントリー株式会社 | プロリルエンドペプチダーゼ阻害活性を有する新規ピロリジンアミド誘導体およびその製法並びに用途 |
| US5198458A (en) | 1986-02-04 | 1993-03-30 | Suntory Limited | Pyrrolidineamide derivatives of acylamino acid and pharmaceutical composition containing the same |
| CA1320734C (en) | 1986-02-04 | 1993-07-27 | Suntory Limited | Pyrrolidineamide derivative of acylamino acid and pharmaceutical composition containing the same |
| CA1334092C (en) | 1986-07-11 | 1995-01-24 | David John Carini | Angiotensin ii receptor blocking imidazoles |
| US5223482A (en) | 1986-11-17 | 1993-06-29 | Scios Nova Inc. | Recombinant Alzheimer's protease inhibitory amyloid protein and method of use |
| JPH08806B2 (ja) | 1986-11-18 | 1996-01-10 | サントリー株式会社 | プロリルエンドペプチダ−ゼ阻害作用を有する新規ピロリジンアミド誘導体 |
| US5254550A (en) | 1986-11-20 | 1993-10-19 | Ono Pharmaceutical Co., Ltd. | Prolinal derivatives and pharmaceutical compositions thereof |
| EP0268190B1 (en) | 1986-11-20 | 1993-06-16 | Ono Pharmaceutical Co., Ltd. | Prolinal derivatives |
| JPS63162672A (ja) | 1986-12-25 | 1988-07-06 | Ono Pharmaceut Co Ltd | 新規なプロリナ−ル誘導体、それらの製造方法およびそれらを含有する抗健忘症剤 |
| JPH089591B2 (ja) | 1986-12-29 | 1996-01-31 | 小野薬品工業株式会社 | 新規なプロリナール誘導体 |
| US5262431A (en) | 1986-12-29 | 1993-11-16 | Ono Pharmaceutical Co., Ltd. | Prolinal derivatives and pharmaceutical compositions thereof |
| EP0275482B1 (en) | 1986-12-29 | 1993-01-20 | Ono Pharmaceutical Co., Ltd. | Proline derivatives |
| JP2528343B2 (ja) | 1987-02-04 | 1996-08-28 | 小野薬品工業株式会社 | 新規なプロリナ―ル誘導体 |
| EP0277588B1 (en) | 1987-02-04 | 1993-03-24 | Ono Pharmaceutical Co., Ltd. | Prolinal derivatives |
| DE3855875T2 (de) | 1987-02-23 | 1997-08-28 | Ono Pharmaceutical Co | Thiazolidin-Derivate |
| JPS6442465A (en) | 1987-08-07 | 1989-02-14 | Wakunaga Pharma Co Ltd | N-acylprolylpyrrolidine derivative, production and use thereof |
| JP2649237B2 (ja) | 1988-03-07 | 1997-09-03 | キッセイ薬品工業 株式会社 | チアゾリジン誘導体 |
| US4857524A (en) | 1987-08-08 | 1989-08-15 | Kissei Pharmaceutical Co., Ltd. | Thiazolidine compounds and therapeutic method |
| JP2515558B2 (ja) | 1987-09-10 | 1996-07-10 | 株式会社ヤクルト本社 | 新規なペプチドおよびそれを有効成分とする抗健忘症剤 |
| CA1339014C (en) | 1987-10-08 | 1997-03-25 | Ronald E. Majocha | Antibodies to a4 amyloid peptide |
| JPH0742309B2 (ja) | 1987-11-30 | 1995-05-10 | キッセイ薬品工業株式会社 | チアゾリジン誘導体 |
| JPH01250370A (ja) | 1987-12-23 | 1989-10-05 | Zeria Pharmaceut Co Ltd | 新規アミノ酸イミド誘導体、製法ならびに用途 |
| US5053414A (en) | 1988-04-08 | 1991-10-01 | Ono Pharmaceutical Co., Ltd. | Heterocyclic compounds |
| US5328899A (en) | 1988-07-15 | 1994-07-12 | The Salk Institute For Biological Studies | NPY peptide analogs |
| ZA896376B (en) | 1988-08-26 | 1990-05-30 | Merrell Dow Pharma | Neuropeptide y agonists |
| ZA896374B (en) | 1988-08-26 | 1990-05-30 | Merrell Dow Pharma | Neuropeptide y antagonists |
| JP2531989B2 (ja) | 1988-09-14 | 1996-09-04 | 吉富製薬株式会社 | ピリジン化合物 |
| CA2004028C (en) | 1988-12-08 | 1998-09-22 | Motoki Torizuka | Condensed benzene derivative |
| JPH02207070A (ja) | 1989-02-07 | 1990-08-16 | Zeria Pharmaceut Co Ltd | アミノ酸イミド誘導体、それを含有する医薬及び該化合物の製造中間体 |
| WO1990012005A1 (fr) | 1989-04-13 | 1990-10-18 | Japan Tobacco Inc. | Nouveaux derives aminoacides possedant une activite d'inhibiteur de la prolylendopeptidase |
| AU5525090A (en) | 1989-04-14 | 1990-11-16 | Research Foundation For Mental Hygiene, Inc. | Monoclonal antibody to amyloid peptide |
| AU5439790A (en) | 1989-04-14 | 1990-11-16 | Research Foundation For Mental Hygiene, Inc. | Cerebrovascular amyloid protein-specific monoclonal antibody sv17-6e10 |
| ES2207091T3 (es) | 1989-06-14 | 2004-05-16 | Smithkline Beecham Corporation | Acido imidazolil-alquenoico. |
| JPH082791B2 (ja) | 1989-07-24 | 1996-01-17 | キッセイ薬品工業株式会社 | 健忘症治療剤 |
| DE3939797A1 (de) | 1989-12-01 | 1991-06-06 | Basf Ag | Neue vom neuropeptid y abgeleitete peptide |
| US4985560A (en) | 1990-01-12 | 1991-01-15 | American Home Products Corporation | Pyridazino(4,5-b)indolizines |
| IL97219A (en) | 1990-02-19 | 1995-12-08 | Ciba Geigy Ag | Biphenyl substituted aliphatic amino compounds process for their preparation and pharmaceutical compositions containing them |
| JPH04211648A (ja) | 1990-07-27 | 1992-08-03 | Nippon Kayaku Co Ltd | ケト酸アミド誘導体 |
| JPH03255080A (ja) | 1990-03-05 | 1991-11-13 | Yoshitomi Pharmaceut Ind Ltd | ベンゼン化合物 |
| NZ237476A (en) | 1990-03-20 | 1994-01-26 | Sanofi Sa | N-substituted heterocyclic compounds and pharmaceutical compositions. |
| US4999349A (en) | 1990-03-22 | 1991-03-12 | Bristol-Myers Squibb Co. | BU-4164E - A and B, prolyl endopeptidase inhibitors |
| US5073549A (en) | 1990-03-22 | 1991-12-17 | Bristol-Myers Squibb Company | BU-4164E - A and B, prolyl endopeptidase inhibitors and their methods of use |
| US5196444A (en) | 1990-04-27 | 1993-03-23 | Takeda Chemical Industries, Ltd. | 1-(cyclohexyloxycarbonyloxy)ethyl 2-ethoxy-1-[[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]benzimidazole-7-carboxylate and compositions and methods of pharmaceutical use thereof |
| JPH049367A (ja) | 1990-04-26 | 1992-01-14 | Zeria Pharmaceut Co Ltd | アリールアルカノイル誘導体,該化合物の製造中間体及びそれらを含有する医薬 |
| WO1991018891A1 (en) | 1990-06-04 | 1991-12-12 | Pfizer Inc. | Aromatic pyrrolidine and thiazolidine amides |
| EP0536399B1 (en) | 1990-06-07 | 1996-01-24 | Zeria Pharmaceutical Co., Ltd. | Novel arylalkanoylamine derivative and drug containing the same |
| US5506256A (en) | 1990-07-27 | 1996-04-09 | Yoshitomi Pharmaceutical Industries, Ltd. | Proline derivatives possessing prolyl endopeptidase-inhibitory activity |
| JPH05186498A (ja) | 1991-12-27 | 1993-07-27 | Japan Tobacco Inc | プロリン誘導体 |
| JPH07108897B2 (ja) | 1990-07-27 | 1995-11-22 | 日本たばこ産業株式会社 | 新規なプロリン誘導体 |
| EP0468469A2 (en) | 1990-07-27 | 1992-01-29 | Japan Tobacco Inc. | Proline derivatives |
| JPH04235162A (ja) | 1990-08-09 | 1992-08-24 | Zeria Pharmaceut Co Ltd | 新規コハク酸アミド誘導体およびそれを含有する医薬 |
| JPH04208299A (ja) | 1990-11-30 | 1992-07-29 | Ajinomoto Co Inc | プロリルエンドペプチターゼ阻害ペプチド |
| IS1756B (is) | 1991-02-21 | 2000-12-28 | Sankyo Company Limited | Hliðstæðuaðferð til framleiðslu 1-Biphenylmethylimidazole afleiða |
| US5104880A (en) | 1991-05-01 | 1992-04-14 | Mayo Foundation For Medical Education And Research | Huperzine a analogs as acetylcholinesterase inhibitors |
| WO1992021333A2 (en) | 1991-05-24 | 1992-12-10 | Pharmavene, Inc. | Treatment of drug withdrawal symptoms and drug craving with type b monoamine oxidase inhibitors |
| WO1993000361A1 (en) | 1991-06-20 | 1993-01-07 | Snow Brand Milk Products Co., Ltd. | Novel prolyl endopeptidase inhibitors sna-115 and sna-115t, production thereof, and strain which produces said inhibitors |
| DE4121975A1 (de) | 1991-07-03 | 1993-01-07 | Basf Ag | Thermoplastische formmassen auf der basis von polycarbonaten, styrol/acrylnitril-polymerisaten und polyolefinen |
| JP3010795B2 (ja) | 1991-07-04 | 2000-02-21 | 不二製油株式会社 | ペプチドの苦味除去方法 |
| CZ281628B6 (cs) | 1991-07-29 | 1996-11-13 | Warner-Lambert Company | Deriváty chinazolinu a farmaceutické přípravky na jejich bázi |
| TW226375B (enExample) | 1991-10-24 | 1994-07-11 | American Home Prod | |
| JPH08501055A (ja) | 1991-12-19 | 1996-02-06 | ガーヴァン インスティチュート オブ メディカル リサーチ | 神経ペプチドチロシンの生物学的機能を抑制する新規な分子 |
| JPH05301826A (ja) | 1991-12-24 | 1993-11-16 | Snow Brand Milk Prod Co Ltd | プロリルエンドペプチダーゼ阻害剤 |
| JPH05201970A (ja) | 1992-01-24 | 1993-08-10 | Japan Tobacco Inc | 新規プロリン誘導体 |
| JP3318622B2 (ja) | 1992-05-27 | 2002-08-26 | 独立行政法人産業技術総合研究所 | プロリルエンドペプチダーゼ阻害剤 |
| GB9212308D0 (en) | 1992-06-10 | 1992-07-22 | Ici Plc | Therapeutic compositions |
| GB9213215D0 (en) | 1992-06-20 | 1992-08-05 | Wellcome Found | Peptides |
| JPH06116284A (ja) | 1992-10-02 | 1994-04-26 | Yamanouchi Pharmaceut Co Ltd | 新規ペプチド |
| US5610303A (en) | 1992-10-05 | 1997-03-11 | Ube Industries, Ltd. | Arylamino pyrimidine compound |
| US5260286A (en) | 1992-10-16 | 1993-11-09 | Japan Tobacco, Inc. | 2-piperidinecarboxylic acid derivatives useful as NMDA receptor antagonists |
| EP0670309A1 (en) | 1992-11-20 | 1995-09-06 | Japan Tobacco Inc. | Compound with prolyl endopeptidase inhibitor activity and pharmaceutical use thereof |
| US5354758A (en) | 1992-12-16 | 1994-10-11 | Japan Tobacco Inc. | Benzomorphans useful as NMDA receptor antagonists |
| JPH06192298A (ja) | 1992-12-24 | 1994-07-12 | Mitsui Toatsu Chem Inc | 新規機能性ペプチド |
| DE4326465A1 (de) | 1993-01-20 | 1995-02-09 | Thomae Gmbh Dr K | Aminosäurederivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
| US5750349A (en) | 1993-01-25 | 1998-05-12 | Takeda Chemical Industries Ltd. | Antibodies to β-amyloids or their derivatives and use thereof |
| JPH06234693A (ja) | 1993-02-09 | 1994-08-23 | Snow Brand Milk Prod Co Ltd | 新規イソテトラセノン系物質及びその製造法 |
| FR2701480B1 (fr) | 1993-02-15 | 1995-05-24 | Sanofi Elf | Composés à groupe sulfamoyle et amidino, leur procédé de préparation et les compositions pharmaceutiques les contenant. |
| EP0611769A1 (en) | 1993-02-16 | 1994-08-24 | Merrell Dow Pharmaceuticals Inc. | Silylated acetylcholinesterase inhibitors |
| WO1994020476A1 (fr) | 1993-03-02 | 1994-09-15 | Fujisawa Pharmaceutical Co., Ltd. | Nouveau compose heterocyclique |
| FR2702150B1 (fr) | 1993-03-03 | 1995-04-07 | Rhone Poulenc Rorer Sa | Application de dérivés de 2H-1,2-4-benzothiadiazine-3(4H)-one-1,1-dioxyde comme antagonistes non compétitifs du récepteur NMDA. |
| FR2703050B1 (fr) | 1993-03-24 | 1995-04-28 | Adir | Nouveaux dérivés bicycliques azotés, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent. |
| EP0627400A1 (en) | 1993-06-04 | 1994-12-07 | Merrell Dow Pharmaceuticals Inc. | Aromatic acetylcholinesterase inhibitors |
| CA2165200A1 (en) | 1993-06-18 | 1995-01-05 | Ambikaipakan Balasubramaniam | Neuropeptide y antagonists and agonists |
| AU6983894A (en) | 1993-06-30 | 1995-01-24 | Zeria Pharmaceutical Co., Ltd. | Thiazolidine derivative and medicine containing the same |
| FR2707645B1 (fr) | 1993-07-16 | 1995-08-11 | Rhone Poulenc Rorer Sa | Dérivés d'imidazo[1,2-a]pirazine-4-one, leur préparation et les médicaments les contenant. |
| FR2707643B1 (fr) | 1993-07-16 | 1995-08-11 | Rhone Poulenc Rorer Sa | Dérivés d'imidazo[1,2-a]pyrazine-4-one, leur préparation et les médicaments les contenant. |
| WO1995003277A1 (en) | 1993-07-23 | 1995-02-02 | Zaidan Hojin Biseibutsu Kagaku Kenkyukai | Novel pyrrolidine derivative |
| FR2711993B1 (fr) | 1993-11-05 | 1995-12-01 | Rhone Poulenc Rorer Sa | Médicaments contenant des dérivés de 7H-imidazol[1,2-a]pyrazine-8-one, les nouveaux composés et leur préparation. |
| HUT74687A (en) | 1993-12-02 | 1997-01-28 | Merrell Pharma Inc | Pyrrole and thiazolidine derivatives of prolyl endopeptidase inhibitor activity and pharmaceutical compositions containing the same |
| IL111785A0 (en) | 1993-12-03 | 1995-01-24 | Ferring Bv | Dp-iv inhibitors and pharmaceutical compositions containing them |
| FR2717811B1 (fr) | 1994-03-28 | 1996-04-26 | Rhone Poulenc Rorer Sa | Dérivés d'imidazo[1,2-a]pyrazine-4-one, leur préparation et les médicaments les contenant. |
| FR2717812B1 (fr) | 1994-03-28 | 1996-05-10 | Rhone Poulenc Rorer Sa | Indeno[1,2-e]pyrazine-4-ones, leur préparation et les médicaments les contenant. |
| FR2717805B1 (fr) | 1994-03-28 | 1996-05-10 | Rhone Poulenc Rorer Sa | Dérivés de 5H-indeno[1,2-b]pyrazine-2,3-dione, leur préparation et les médicaments les contenant . |
| FR2717813B1 (fr) | 1994-03-28 | 1996-05-10 | Rhone Poulenc Rorer Sa | Dérivés d'imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one, leur préparation et les médicaments les contenant . |
| JPH07267988A (ja) | 1994-03-31 | 1995-10-17 | Yamanouchi Pharmaceut Co Ltd | 新規ペプチド |
| GB9410320D0 (en) | 1994-05-24 | 1994-07-13 | Fisons Corp | Novel therapeutic method |
| GB9418443D0 (en) | 1994-09-13 | 1994-11-02 | Pfizer Ltd | Therapeutic agents |
| US6562862B1 (en) | 1994-10-20 | 2003-05-13 | Eli Lilly And Company | Methods of inhibiting physiological conditions associated with an excess of neuropeptide Y |
| US5663192A (en) | 1994-10-20 | 1997-09-02 | Eli Lilly And Company | Heterocyclic neuropeptide Y receptor antagonists |
| AU3953795A (en) | 1994-10-20 | 1996-05-15 | Eli Lilly And Company | Bicyclic neuropeptide y receptor antagonists |
| FR2726275B1 (fr) | 1994-11-02 | 1996-12-06 | Rhone Poulenc Rorer Sa | Spiro heterocycle-imidazo(1,2-a)indeno(1,2-e)pyrazine)-4'- ones, leur preparation et les medicaments les contenants |
| IL116584A0 (en) | 1994-12-29 | 1996-03-31 | Res Dev Foundation | Novel flavin adenine dinucleotide analogue inhibitors of monoamine oxidase |
| US5691368A (en) | 1995-01-11 | 1997-11-25 | Hoechst Marion Roussel, Inc. | Substituted oxazolidine calpain and/or cathepsin B inhibitors |
| GB9500601D0 (en) | 1995-01-12 | 1995-03-01 | Wellcome Found | Modified peptides |
| US5786180A (en) | 1995-02-14 | 1998-07-28 | Bayer Corporation | Monoclonal antibody 369.2B specific for β A4 peptide |
| US5552411A (en) | 1995-05-26 | 1996-09-03 | Warner-Lambert Company | Sulfonylquinolines as central nervous system and cardiovascular agents |
| US5554621A (en) | 1995-06-07 | 1996-09-10 | Bristol-Myers Squibb Company | Dihydropyridine NPY antagonists: nitrogen heterocyclic derivatives |
| US5668151A (en) | 1995-06-07 | 1997-09-16 | Bristol-Myers Squibb Company | Dihydropyridine NPY antagonists: piperidine derivatives |
| IL117997A0 (en) | 1995-06-07 | 1996-10-31 | Pfizer | Neuropeptide Y1 specific ligands |
| US5635503A (en) | 1995-06-07 | 1997-06-03 | Bristol-Myers Squibb Company | Dihydropyridine npy antagonists: piperazine derivatives |
| JP3727383B2 (ja) | 1995-07-31 | 2005-12-14 | 月桂冠株式会社 | プロリルエンドペプチダーゼ阻害剤 |
| NZ318228A (en) | 1995-09-01 | 1999-07-29 | Lilly Co Eli | Indolyl neuropeptide y receptor antagonists |
| WO1997012613A1 (en) | 1995-10-05 | 1997-04-10 | Warner-Lambert Company | Method for treating and preventing inflammation and atherosclerosis |
| ES2100129B1 (es) | 1995-10-11 | 1998-02-16 | Medichem Sa | Nuevos compuestos aminopiridinicos policiclicos inhibidores de acetilcolinesterasa, procedimiento para su preparacion y su utilizacion. |
| DE19544685A1 (de) | 1995-11-30 | 1997-06-05 | Thomae Gmbh Dr K | Aminosäurederivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
| DE19544687A1 (de) | 1995-11-30 | 1997-06-05 | Thomae Gmbh Dr K | Aminosäurederivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
| DE19544686A1 (de) | 1995-11-30 | 1997-06-05 | Thomae Gmbh Dr K | Aminosäurederivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
| WO1997020822A1 (en) | 1995-12-01 | 1997-06-12 | Novartis Ag | Quinazolin-2,4-diazirines as npy receptor antagonist |
| AU7692996A (en) | 1995-12-01 | 1997-06-27 | Ciba-Geigy Ag | Receptor antagonists |
| WO1997020821A1 (en) | 1995-12-01 | 1997-06-12 | Novartis Ag | Heteroaryl derivatives |
| WO1997020820A1 (en) | 1995-12-01 | 1997-06-12 | Novartis Ag | Heteroaryl compounds |
| WO1997019682A1 (en) | 1995-12-01 | 1997-06-05 | Synaptic Pharmaceutical Corporation | Aryl sulfonamide and sulfamide derivatives and uses thereof |
| JPH09157253A (ja) | 1995-12-12 | 1997-06-17 | Yamanouchi Pharmaceut Co Ltd | 新規アミノ酸誘導体 |
| ZA9610741B (en) | 1995-12-22 | 1997-06-24 | Warner Lambert Co | 4-Substituted piperidine analogs and their use as subtype selective nmda receptor antagonists |
| ZA9610736B (en) | 1995-12-22 | 1997-06-27 | Warner Lambert Co | 2-Substituted piperidine analogs and their use as subtypeselective nmda receptor antagonists |
| ZA9610745B (en) | 1995-12-22 | 1997-06-24 | Warner Lambert Co | 4-Subsituted piperidine analogs and their use as subtype selective nmda receptor antagonists |
| EP0871442A1 (en) | 1996-01-09 | 1998-10-21 | Eli Lilly And Company | Benzimidzolyl neuropeptide y receptor antagonists |
| GB9605027D0 (en) | 1996-03-09 | 1996-05-08 | Pfizer Ltd | Quinoxalinediones |
| US5662723A (en) | 1996-03-22 | 1997-09-02 | Libbey Glass Inc. | Apparatus and method for forming a decorative pattern on glassware having an edge |
| WO1997038993A1 (en) | 1996-04-12 | 1997-10-23 | Hoechst Marion Roussel, Inc. | Isatin derivatives as acetylcholinesterase inhibitors and analgesics |
| DE122010000020I1 (de) | 1996-04-25 | 2010-07-08 | Prosidion Ltd | Verfahren zur Senkung des Blutglukosespiegels in Säugern |
| WO1997046250A1 (en) | 1996-06-04 | 1997-12-11 | Synaptic Pharmaceutical Corporation | Methods of modifying feeding behavior, compounds useful in such methods, and dna encoding a hypothalamic atypical neuropeptide y/peptide yy receptor (y5) |
| AU3451797A (en) | 1996-07-05 | 1998-02-02 | Andrew Peter Worsley | Compositions for the treatment of peripheral neuropathies containing antidepressants and/or monoamine oxidase inhibitors and/or vitamin b12 and/or precursors or inducers of a neurotransmitter |
| ATE239002T1 (de) | 1996-07-23 | 2003-05-15 | Neurogen Corp | Einige amido-und amino-substituierte benzylaminderivate: eine neue klasse von neuropeptid y1 spezifischen liganden |
| US5985873A (en) | 1996-07-23 | 1999-11-16 | Neurogen Corporation | Certain substituted benzylamine derivatives a new class of Neuropeptide-Y1 specific ligands |
| ES2186907T3 (es) | 1996-07-23 | 2003-05-16 | Neurogen Corp | Ciertos derivados de bencilamina sustituidos; una nueva clase de ligandos especificos del neuropeptido y1. |
| WO1998005337A1 (en) | 1996-08-01 | 1998-02-12 | Cocensys, Inc. | Use of gaba and nmda receptor ligands for the treatment of migraine headache |
| JP2000516611A (ja) | 1996-08-14 | 2000-12-12 | ワーナー―ランバート・コンパニー | Mcp―1アンタゴニストとしての2―フェニルベンズイミダゾール誘導体 |
| DE69713402T2 (de) | 1996-08-23 | 2002-11-07 | Agouron Pharma | Liganden des neuropeptids y |
| JP3880664B2 (ja) | 1996-09-04 | 2007-02-14 | 月桂冠株式会社 | プロリルエンドペプチダーゼ阻害ペプチド |
| WO1998010757A2 (en) | 1996-09-11 | 1998-03-19 | The Government Of The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | The use of functional n-methyl-d-aspartate antagonists to ameliorate or prevent aminoglycoside-induced ototoxicity |
| WO1998015647A1 (en) | 1996-10-08 | 1998-04-16 | Novartis Ag | Modulation of apoptosis |
| FR2754709B1 (fr) | 1996-10-23 | 1999-03-05 | Sanofi Sa | Composition cosmetique contenant un antagoniste des recepteurs du neuropeptide gamma et alpha 2 antagonistes susceptibles d'etre incorpores dans une telle composition |
| US6011155A (en) | 1996-11-07 | 2000-01-04 | Novartis Ag | N-(substituted glycyl)-2-cyanopyrrolidines, pharmaceutical compositions containing them and their use in inhibiting dipeptidyl peptidase-IV |
| TW492957B (en) | 1996-11-07 | 2002-07-01 | Novartis Ag | N-substituted 2-cyanopyrrolidnes |
| WO1998030243A1 (en) | 1997-01-08 | 1998-07-16 | Warner-Lambert Company | Acetylcholinesterase inhibitors in combination with muscarinic agonists for the treatment of alzheimer's disease |
| US20030068316A1 (en) | 1997-02-05 | 2003-04-10 | Klein William L. | Anti-ADDL antibodies and uses thereof |
| JP2894445B2 (ja) | 1997-02-12 | 1999-05-24 | 日本たばこ産業株式会社 | Cetp活性阻害剤として有効な化合物 |
| WO1998040102A1 (en) | 1997-03-13 | 1998-09-17 | The Provost, Fellows And Scholars Of The College Of The Holy And Undivided Trinity Of Queen Elizabeth Near Dublin | Cytoprotective agents comprising monoamine oxidase inhibitors |
| AU743827B2 (en) | 1997-04-09 | 2002-02-07 | Intellect Neurosciences, Inc. | Recombinant antibodies specific for beta-amyloid ends, DNA encoding and methods of use thereof |
| US8173127B2 (en) | 1997-04-09 | 2012-05-08 | Intellect Neurosciences, Inc. | Specific antibodies to amyloid beta peptide, pharmaceutical compositions and methods of use thereof |
| WO1998046559A1 (en) | 1997-04-16 | 1998-10-22 | Arqule, Inc. | SYNTHESIS AND USE OF α-KETOAMIDE DERIVATIVES AND ARRAYS |
| WO1998050044A1 (en) | 1997-05-07 | 1998-11-12 | Algos Pharmaceutical Corporation | Composition and method combining an antidepressant with an nmda receptor antagonist, for treating neuropathic pain |
| AU7472798A (en) | 1997-05-07 | 1998-11-27 | Algos Pharmaceutical Corporation | Cox-2 inhibitors in combination with nmda-blockers for treating pain |
| AU724974B2 (en) | 1997-06-30 | 2000-10-05 | Merz Pharma Gmbh & Co. Kgaa | 1-amino-alkylcyclohexane NMDA receptor antagonists |
| GB9716657D0 (en) | 1997-08-07 | 1997-10-15 | Zeneca Ltd | Chemical compounds |
| GB9716879D0 (en) | 1997-08-08 | 1997-10-15 | Shire Int Licensing Bv | Treatment of attention deficit disorders |
| AU7696098A (en) | 1997-08-11 | 1999-03-01 | Algos Pharmaceutical Corporation | Substance p inhibitors in combination with nmda-blockers for treating pain |
| SE9703376D0 (sv) | 1997-09-18 | 1997-09-18 | Astra Ab | A new combination |
| SE9703414D0 (sv) | 1997-09-23 | 1997-09-23 | Astra Ab | New compounds |
| TWI239847B (en) | 1997-12-02 | 2005-09-21 | Elan Pharm Inc | N-terminal fragment of Abeta peptide and an adjuvant for preventing and treating amyloidogenic disease |
| US7179892B2 (en) | 2000-12-06 | 2007-02-20 | Neuralab Limited | Humanized antibodies that recognize beta amyloid peptide |
| US7964192B1 (en) | 1997-12-02 | 2011-06-21 | Janssen Alzheimer Immunotherapy | Prevention and treatment of amyloidgenic disease |
| AU766219B2 (en) | 1998-02-02 | 2003-10-09 | 1149336 Ontario Inc. | Method of regulating glucose metabolism, and reagents related thereto |
| AU3034299A (en) | 1998-03-09 | 1999-09-27 | Fondatech Benelux N.V. | Serine peptidase modulators |
| US6007841A (en) | 1998-03-13 | 1999-12-28 | Algos Pharmaceutical Corporation | Analgesic composition and method for treating pain |
| GB9805561D0 (en) | 1998-03-16 | 1998-05-13 | Merck Sharp & Dohme | A combination of therapeutic agents |
| US6541208B1 (en) | 1998-03-17 | 2003-04-01 | University Of Maryland Biotechnology Institute | Diagnostic method for distinguishing HIV-associated dementia from other forms of dementia |
| DE19812331A1 (de) | 1998-03-20 | 1999-09-23 | Merck Patent Gmbh | Piperidinderivate |
| US6054451A (en) | 1998-04-21 | 2000-04-25 | Algos Pharmaceutical Corporation | Analgesic composition and method for alleviating pain |
| WO1999057119A1 (en) | 1998-05-04 | 1999-11-11 | Neotherapeutics, Inc. | Novel dopamine-like 9-substituted hypoxanthine and methods of use |
| WO1999057120A1 (en) | 1998-05-04 | 1999-11-11 | Neotherapeutics, Inc. | Novel serotonin-like 9-substituted hypoxanthine and methods of use |
| CA2325600A1 (en) | 1998-05-21 | 1999-11-25 | The University Of Tennessee Research Corporation | Methods for amyloid removal using anti-amyloid antibodies |
| DE19823831A1 (de) | 1998-05-28 | 1999-12-02 | Probiodrug Ges Fuer Arzneim | Neue pharmazeutische Verwendung von Isoleucyl Thiazolidid und seinen Salzen |
| DE19828113A1 (de) | 1998-06-24 | 2000-01-05 | Probiodrug Ges Fuer Arzneim | Prodrugs von Inhibitoren der Dipeptidyl Peptidase IV |
| DE19828114A1 (de) | 1998-06-24 | 2000-01-27 | Probiodrug Ges Fuer Arzneim | Produgs instabiler Inhibitoren der Dipeptidyl Peptidase IV |
| PE20000728A1 (es) | 1998-06-26 | 2000-08-21 | Cocensys Inc | Heterociclos 4-bencil piperidina alquilsulfoxido y su uso como antagonistas receptores subtipo-selectivo nmda |
| DE19834591A1 (de) | 1998-07-31 | 2000-02-03 | Probiodrug Ges Fuer Arzneim | Verfahren zur Steigerung des Blutglukosespiegels in Säugern |
| IT1304904B1 (it) | 1998-09-11 | 2001-04-05 | Eisai Co Ltd | Derivati anticolinesterasici per il trattamento delle sindromidolorose funzionali e/o organiche |
| CA2351224A1 (en) | 1998-11-12 | 2000-05-25 | Algos Pharmaceutical Corporation | Cox-2 inhibitors in combination with nmda-blockers for treating pain |
| WO2000030674A1 (en) | 1998-11-26 | 2000-06-02 | Ferring Bv | Neuropeptide y y4 agents in the treatment of reproductive disorders |
| GB9902455D0 (en) | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
| GB9902461D0 (en) | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
| GB9902453D0 (en) | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
| GB9902452D0 (en) | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
| GB9902459D0 (en) | 1999-02-05 | 1999-03-24 | Zeneca Ltd | Chemical compounds |
| AU3195600A (en) | 1999-03-23 | 2000-10-09 | Sumitomo Pharmaceuticals Company, Limited | Tricyclic indole-2-carboxylic acid compound used as nmda receptor antagonist |
| CA2363984A1 (en) | 1999-04-15 | 2000-10-26 | Merck Frosst Canada & Co. | Antibodies that recognize app cleaved by caspases and methods of use |
| US6121311A (en) | 1999-04-28 | 2000-09-19 | Japan Tobacco Inc. | Method for treating cocainism |
| HK1041263A1 (zh) | 1999-05-05 | 2002-07-05 | Ortho-Mcneil Pharmaceutical, Inc. | 可用於治疗肥胖和其他疾病的3a,4,5,9b-四氢-1h-苯并[e]吲-2-基胺衍生的神经肽y受体配体 |
| JP3148739B2 (ja) | 1999-05-19 | 2001-03-26 | ドーマー株式会社 | プロリルエンドペプチダーゼ阻害剤 |
| ATE405636T1 (de) | 1999-06-16 | 2008-09-15 | Boston Biomedical Res Inst | Immunologische kontrolle des beta-amyloid gehaltes in vivo |
| US6107317A (en) | 1999-06-24 | 2000-08-22 | Novartis Ag | N-(substituted glycyl)-thiazolidines, pharmaceutical compositions containing them and their use in inhibiting dipeptidyl peptidase-IV |
| US6172081B1 (en) | 1999-06-24 | 2001-01-09 | Novartis Ag | Tetrahydroisoquinoline 3-carboxamide derivatives |
| US6110949A (en) | 1999-06-24 | 2000-08-29 | Novartis Ag | N-(substituted glycyl)-4-cyanothiazolidines, pharmaceutical compositions containing them and their use in inhibiting dipeptidyl peptidase-IV |
| AU6053900A (en) | 1999-06-25 | 2001-01-31 | Morris Notelovitz | Compositions for treating or preventing neurodegeneration and cognitive decline |
| US6316449B1 (en) | 1999-07-08 | 2001-11-13 | Millennium Pharmaceuticals, Inc. | Chemokine receptor antagonists |
| DE19936719A1 (de) | 1999-08-06 | 2001-02-15 | Gruenenthal Gmbh | Substituierte 1,5-Dihydropyrrol-2-on-Derivate |
| DE19936521A1 (de) | 1999-08-06 | 2001-02-15 | Gruenenthal Gmbh | Substituierte Pyrrolidin-2,3,4-trion-3-oxim-Derivate |
| CA2382095A1 (en) | 1999-08-13 | 2001-02-22 | The Trustees Of Columbia University In The City Of New York | Methods of inhibiting binding of .beta.-sheet fibril to rage and consequences thereof |
| EP1078632A1 (en) | 1999-08-16 | 2001-02-28 | Sanofi-Synthelabo | Use of monoamine oxydase inhibitors for the manufacture of drugs intended for the treatment of obesity |
| DE19940130A1 (de) | 1999-08-24 | 2001-03-01 | Probiodrug Ges Fuer Arzneim | Neue Effektoren der Dipeptidyl Peptidase IV zur topischen Anwendung |
| TWI283577B (en) | 1999-10-11 | 2007-07-11 | Sod Conseils Rech Applic | Pharmaceutical composition of imidazole derivatives acting as modulators of sodium channels and the use thereof |
| UA72558C2 (uk) | 1999-11-01 | 2005-03-15 | Мерц Фарма Гмбх Унд Ко. Кгаа | 1-аміноалкілциклогексанові антагоністи рецептора nmda |
| WO2001034594A1 (en) | 1999-11-12 | 2001-05-17 | Guilford Pharmaceuticals, Inc. | Dipeptidyl peptidase iv inhibitors and methods of making and using dipeptidyl peptidase iv inhibitors |
| US20020094335A1 (en) | 1999-11-29 | 2002-07-18 | Robert Chalifour | Vaccine for the prevention and treatment of alzheimer's and amyloid related diseases |
| GB9928330D0 (en) | 1999-11-30 | 2000-01-26 | Ferring Bv | Novel antidiabetic agents |
| EP1254108A1 (en) | 2000-01-24 | 2002-11-06 | MERCK SHARP & DOHME LTD. | Gamma-secretase inhibitors |
| JP2003520849A (ja) | 2000-01-24 | 2003-07-08 | ノボ ノルディスク アクティーゼルスカブ | 酵素dpp−ivの阻害剤であるn−置換2−シアノピロールおよび−ピロリン |
| CA2399080C (en) | 2000-02-03 | 2013-05-21 | Millennium Pharmaceuticals, Inc. | Humanized anti-ccr2 antibodies and methods of use therefor |
| SK288711B6 (sk) | 2000-02-24 | 2019-11-05 | Univ Washington | Humanizovaná protilátka, jej fragment a ich použitie, polynukleová kyselina, expresný vektor, bunka a farmaceutický prostriedok |
| GB0005251D0 (en) | 2000-03-03 | 2000-04-26 | Merck Sharp & Dohme | Therapeutic compounds |
| AU2001239052A1 (en) | 2000-03-06 | 2001-09-17 | Immune Network Ltd. | Compositions for prevention and treatment of dementia |
| US6395767B2 (en) | 2000-03-10 | 2002-05-28 | Bristol-Myers Squibb Company | Cyclopropyl-fused pyrrolidine-based inhibitors of dipeptidyl peptidase IV and method |
| ES2275675T3 (es) | 2000-03-23 | 2007-06-16 | Elan Pharmaceuticals, Inc. | Compuestos y metodos para tratar la enfermedad de alzheimer. |
| US6992081B2 (en) | 2000-03-23 | 2006-01-31 | Elan Pharmaceuticals, Inc. | Compounds to treat Alzheimer's disease |
| GB0008710D0 (en) | 2000-04-07 | 2000-05-31 | Merck Sharp & Dohme | Therapeutic compounds |
| EP1285656A4 (en) | 2000-04-13 | 2006-07-12 | Eisai Co Ltd | ACETYLCHOLINESTERASE HEMMER CONTAINING 1-BENZYLPYRIDINIUM SALT |
| GB0010183D0 (en) | 2000-04-26 | 2000-06-14 | Ferring Bv | Inhibitors of dipeptidyl peptidase IV |
| EP1278716B1 (en) | 2000-04-26 | 2006-08-23 | Warner-Lambert Company LLC | Trans-n-¬4-(4-hydroxyphenyl)cyclohexyl|-3-phenylpropionamide as subtype selective nmda receptor antagonist |
| GB0010188D0 (en) | 2000-04-26 | 2000-06-14 | Ferring Bv | Inhibitors of dipeptidyl peptidase IV |
| US20010036949A1 (en) | 2000-05-09 | 2001-11-01 | Coe Jotham Wadsworth | Pharmaceutical composition and method of treatment of diseases of cognitive dysfunction in a mammal |
| BR0111279A (pt) | 2000-06-01 | 2003-11-04 | Warner Lambert Co | Derivados da ciclohexilamina como antagonistas para o receptor do nmda seletivo ao subtipo |
| DE60112574T2 (de) | 2000-06-06 | 2006-06-08 | Warner-Lambert Co. Llc | Bicyclische cyclohexylamine und ihre verwendung als nmda-rezeptor antagonisten |
| DE60125541T2 (de) | 2000-06-22 | 2007-10-11 | Pharmos Corp. | Neue nicht psychotropische cannabinoide |
| GB0015488D0 (en) | 2000-06-23 | 2000-08-16 | Merck Sharp & Dohme | Therapeutic agents |
| US6713276B2 (en) | 2000-06-28 | 2004-03-30 | Scios, Inc. | Modulation of Aβ levels by β-secretase BACE2 |
| CN1217920C (zh) | 2000-06-30 | 2005-09-07 | 艾兰制药公司 | 治疗早老性痴呆的化合物 |
| US6686449B2 (en) | 2000-06-30 | 2004-02-03 | Pharmacia & Upjohn Company | Mutant presenilin 1 polypeptides |
| WO2002002560A2 (en) | 2000-07-04 | 2002-01-10 | Novo Nordisk A/S | Purine-2,6-diones which are inhibitors of the enzyme dipeptidyl peptidase iv (dpp-iv) |
| GB0016681D0 (en) | 2000-07-06 | 2000-08-23 | Merck Sharp & Dohme | Therapeutic compounds |
| US6556971B1 (en) | 2000-09-01 | 2003-04-29 | Snap-On Technologies, Inc. | Computer-implemented speech recognition system training |
| EP1351946A2 (en) * | 2000-09-01 | 2003-10-15 | Icos Corporation | Materials and methods to potentiate cancer treatment |
| WO2002027418A2 (en) | 2000-09-25 | 2002-04-04 | Motorwiz, Inc. | Model-based machine diagnostics and prognostics using theory of noise and communications |
| US20020151591A1 (en) | 2000-10-17 | 2002-10-17 | Anabella Villalobos | Combination use of acetylcholinesterase inhibitors and GABAa inverse agonists for the treatment of cognitive disorders |
| HU227197B1 (en) | 2000-10-24 | 2010-10-28 | Richter Gedeon Nyrt | Nmda receptor antagonist carboxylic acid amide derivatives and pharmaceutical compositions containing them |
| AU2002210747B2 (en) | 2000-11-02 | 2006-06-01 | Merck Sharp & Dohme Limited | Sulfamides as gamma-secretase inhibitors |
| WO2002041842A2 (en) | 2000-11-03 | 2002-05-30 | Proteotech. Inc. | Antibody pti-hs7 for treatment of alzheimer's disease and other amyloidoses and parkinson's disease |
| TWI243162B (en) | 2000-11-10 | 2005-11-11 | Taisho Pharmaceutical Co Ltd | Cyanopyrrolidine derivatives |
| PE20020574A1 (es) | 2000-12-06 | 2002-07-02 | Wyeth Corp | Anticuerpos humanizados que reconocen el peptido amiloideo beta |
| US6495335B2 (en) | 2000-12-07 | 2002-12-17 | Mario Chojkier | Compositions and methods for diagnosing alzheimer's disease |
| US6670364B2 (en) | 2001-01-31 | 2003-12-30 | Telik, Inc. | Antagonists of MCP-1 function and methods of use thereof |
| TWI245761B (en) | 2001-03-01 | 2005-12-21 | Telik Inc | Antagonists of MCP-1 function and methods of use thereof |
| JP2005506292A (ja) | 2001-03-08 | 2005-03-03 | エモリー ユニバーシティ | pHに依存するNMDAレセプターアンタゴニスト |
| US6649196B2 (en) | 2001-03-12 | 2003-11-18 | Mayo Foundation For Medical Education And Research | Methods of reducing β-amyloid polypeptides |
| US6815175B2 (en) | 2001-03-16 | 2004-11-09 | Cornell Research Foundation, Inc. | Anti-amyloid peptide antibody based diagnosis and treatment of a neurological disease or disorder |
| TWI236474B (en) | 2001-04-03 | 2005-07-21 | Telik Inc | Antagonists of MCP-1 function and methods of use thereof |
| US6573287B2 (en) | 2001-04-12 | 2003-06-03 | Bristo-Myers Squibb Company | 2,1-oxazoline and 1,2-pyrazoline-based inhibitors of dipeptidyl peptidase IV and method |
| EP1385545B1 (en) | 2001-04-30 | 2009-01-07 | Eli Lilly And Company | Humanized antibodies recognizing the beta-amyloid peptide |
| EP1385544B1 (en) | 2001-04-30 | 2008-09-24 | Eli Lilly And Company | Humanized antibodies |
| FR2824825B1 (fr) | 2001-05-15 | 2005-05-06 | Servier Lab | Nouveaux derives d'alpha-amino-acides, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| SI20922A (sl) | 2001-05-18 | 2002-12-31 | Krka Tovarna Zdravil, D.D., Novo Mesto | Monoklonsko protitelo, ki nevtralizira aktivnost katepsina B, in njegove uporabe |
| US6562783B2 (en) | 2001-05-30 | 2003-05-13 | Neurologic, Inc. | Phosphinylmethyl and phosphorylmethyl succinic and glutauric acid analogs as β-secretase inhibitors |
| EP1395551B1 (en) | 2001-06-01 | 2008-05-21 | Elan Pharmaceuticals, Inc. | Hydroxy alkyl amine derivatives as beta-secretase inhibitors and their use for the treatment of alzheimer's disease and similar diseases |
| US7253172B2 (en) | 2001-06-20 | 2007-08-07 | Merck & Co., Inc. | Dipeptidyl peptidase inhibitors for the treatment of diabetes |
| WO2003000180A2 (en) | 2001-06-20 | 2003-01-03 | Merck & Co., Inc. | Dipeptidyl peptidase inhibitors for the treatment of diabetes |
| GB0115517D0 (en) | 2001-06-25 | 2001-08-15 | Ferring Bv | Novel antidiabetic agents |
| ATE370943T1 (de) | 2001-06-27 | 2007-09-15 | Smithkline Beecham Corp | Fluoropyrrolidine als dipeptidyl-peptidase inhibitoren |
| CN1990468A (zh) | 2001-06-27 | 2007-07-04 | 史密丝克莱恩比彻姆公司 | 作为二肽酶抑制剂的氟代吡咯烷 |
| CA2419888A1 (en) | 2001-06-27 | 2003-01-09 | Probiodrug Ag | Peptide structures useful for competitive modulation of dipeptidyl peptidase iv catalysis |
| DE10150203A1 (de) | 2001-10-12 | 2003-04-17 | Probiodrug Ag | Peptidylketone als Inhibitoren der DPIV |
| DE10154689A1 (de) | 2001-11-09 | 2003-05-22 | Probiodrug Ag | Substituierte Aminoketonverbindungen |
| EP1401452A1 (en) | 2001-06-27 | 2004-03-31 | Elan Pharmaceuticals, Inc. | Beta-hydroxyamine derivatives useful in the treatment of alzheimer's disease |
| EP1399471B1 (en) | 2001-06-27 | 2008-01-30 | Probiodrug AG | Use of dipeptidyl peptidase iv inhibitors as therapeutics for neurological disorders |
| JP4300108B2 (ja) | 2001-06-27 | 2009-07-22 | スミスクライン ビーチャム コーポレーション | ジペプチジルペプチダーゼ阻害剤としてのピロリジン類 |
| EP1404675B1 (en) | 2001-07-03 | 2008-03-12 | Novo Nordisk A/S | Dpp-iv-inhibiting purine derivatives for the treatment of diabetes |
| UA74912C2 (en) | 2001-07-06 | 2006-02-15 | Merck & Co Inc | Beta-aminotetrahydroimidazo-(1,2-a)-pyrazines and tetratriazolo-(4,3-a)-pyrazines as inhibitors of dipeptylpeptidase for the treatment or prevention of diabetes |
| CZ2004233A3 (cs) | 2001-07-24 | 2004-12-15 | Richter Gedeon Vegyészeti Gyár Rt. | Nové amidové sloučeniny karboxylové kyseliny |
| US20040234990A1 (en) | 2001-07-31 | 2004-11-25 | Hiroto Komano | Method of screening alzheimer's disease-associated gene |
| IL159848A0 (en) | 2001-08-03 | 2004-06-20 | Schering Corp | Novel gamma secretase inhibitors |
| WO2003014162A1 (en) | 2001-08-03 | 2003-02-20 | Medical & Biological Laboratories Co., Ltd. | ANTIBODY RECOGNIZING GM1 GANGLIOSIDE-BOUND AMYLOID β-PROTEIN AND DNA ENCODING THE ANTIBODY |
| WO2003013527A1 (en) | 2001-08-03 | 2003-02-20 | Schering Corporation | Sulfonamide derivatives as gamma secretase inhibitors |
| AU2002324468A1 (en) | 2001-08-17 | 2003-03-03 | Eli Lilly And Company | Rapid improvement of cognition in conditions related to abeta |
| EP1432444A4 (en) | 2001-08-17 | 2005-11-02 | Lilly Co Eli | ANTI-BETA ANTIBODIES |
| CA2459146A1 (en) | 2001-08-30 | 2003-03-13 | Ortho-Mcneil Pharmaceutical, Inc. | Treatment of dementia and memory disorders with anticonvulsants and acetylcholinesterase inhibitors |
| WO2003024942A1 (en) | 2001-09-14 | 2003-03-27 | Mitsubishi Pharma Corporation | Thiazolidine derivative and medicinal use thereof |
| EP1463727A2 (en) | 2001-09-19 | 2004-10-06 | Novo Nordisk A/S | Heterocyclic compounds that are inhibitors of the enzyme dpp-iv |
| GB0125445D0 (en) | 2001-10-23 | 2001-12-12 | Ferring Bv | Protease Inhibitors |
| EP1448218A4 (en) | 2001-10-23 | 2009-01-14 | Oklahoma Med Res Found | BETA SECRETASE INHIBITORS AND METHODS OF USE |
| GB0125446D0 (en) | 2001-10-23 | 2001-12-12 | Ferring Bv | Novel anti-diabetic agents |
| US6861440B2 (en) | 2001-10-26 | 2005-03-01 | Hoffmann-La Roche Inc. | DPP IV inhibitors |
| EP1448601A4 (en) | 2001-11-02 | 2006-04-26 | Diagenics Internat Corp | METHOD AND COMPOSITIONS OF MONOCLONAL ANTIBODIES SPECIFIC TO BETA-AMYLOIDE PROTEINS |
| WO2003037376A1 (fr) | 2001-11-02 | 2003-05-08 | Kensuke Egashira | Prophylactiques et/ou remedes pour le traitement de l'arteriosclerose apres transplantation dans le cas de rejet de greffe |
| WO2003040183A2 (en) | 2001-11-09 | 2003-05-15 | The Genetics Company, Inc | Compounds for the diagnosis/prevention/treatment of alzheimer's disease |
| KR20050044533A (ko) | 2001-11-19 | 2005-05-12 | 엘란 파마슈티칼스, 인크. | 알츠하이머병을 치료하기 위한 베타-세크레타아제억제제로서의(4-페닐)피페리딘-3-일-페닐카르복실레이트유도체 및 관련 화합물 |
| EP1572894B1 (en) | 2001-11-21 | 2016-04-13 | New York University | Synthetic immunogenic but non-deposit-forming polypeptides and peptides homologous to amyloid beta, prion protein, amylin, alpha synuclein, or polyglutamine repeats for induction of an immune response thereto |
| JP4771661B2 (ja) | 2001-11-26 | 2011-09-14 | トラスティーズ オブ タフツ カレッジ | Post−プロリン開裂酵素の擬ペプチド性阻害剤 |
| AU2002354433A1 (en) | 2001-12-06 | 2003-06-17 | Japan As Represented By Secretary Of Chubu National Hospital | Alzheimer's disease-associated gene and protein and use thereof |
| US20050227941A1 (en) | 2001-12-17 | 2005-10-13 | Karen Duff | Sequestration of ass in the periphery in the absence of immunomodulating agent as a therapeutic approach for the treatment or prevention of beta-amyloid related diseases |
| MXPA04005864A (es) | 2001-12-19 | 2004-10-29 | Atherogenics Inc | Derivados de charcona y su uso para tratar enfermedades. |
| US20060210555A1 (en) | 2001-12-21 | 2006-09-21 | Antigenics, Inc. | Compositions comprising immunoreactive reagents and saponins, and methods of use thereof |
| AU2002360732A1 (en) | 2001-12-26 | 2003-07-24 | Guilford Pharmaceuticals | Change inhibitors of dipeptidyl peptidase iv |
| US6727261B2 (en) | 2001-12-27 | 2004-04-27 | Hoffman-La Roche Inc. | Pyrido[2,1-A]Isoquinoline derivatives |
| AU2003235799A1 (en) | 2002-01-08 | 2003-07-24 | Nordic Bioscience A/S | Modulation of iamt (pimt or pcmt) in immune system |
| JP2005516967A (ja) | 2002-01-18 | 2005-06-09 | ザ ジェネティクス カンパニー インコーポレーティッド | β−セクレターゼインヒビター |
| AU2003207973A1 (en) | 2002-01-31 | 2003-09-02 | Tel Aviv University Future Technology Development L.P. | Peptides antibodies directed thereagainst and methods using same for diagnosing and treating amyloid-associated diseases |
| US20040171614A1 (en) | 2002-02-06 | 2004-09-02 | Schering-Plough Corporation | Novel gamma secretase inhibitors |
| TW200302717A (en) | 2002-02-06 | 2003-08-16 | Schering Corp | Novel gamma secretase inhibitors |
| BR0307665A (pt) | 2002-02-13 | 2005-01-04 | Hoffmann La Roche | Compostos, processo para a sua manufatura, composições farmacêuticas que compreendem os mesmos, método para o tratamento e/ou profilaxia de enfermidades associadas com dpp iv e utilização dos compostos |
| WO2003068748A1 (en) | 2002-02-13 | 2003-08-21 | F. Hoffmann-La Roche Ag | Novel pyridine- and quinoline-derivatives |
| AR038568A1 (es) | 2002-02-20 | 2005-01-19 | Hoffmann La Roche | Anticuerpos anti-a beta y su uso |
| HUP0200849A2 (hu) | 2002-03-06 | 2004-08-30 | Sanofi-Synthelabo | N-aminoacetil-2-ciano-pirrolidin-származékok, e vegyületeket tartalmazó gyógyszerkészítmények és eljárás előállításukra |
| MY139983A (en) | 2002-03-12 | 2009-11-30 | Janssen Alzheimer Immunotherap | Humanized antibodies that recognize beta amyloid peptide |
| AU2003225916A1 (en) | 2002-03-25 | 2003-10-13 | Merck & Co., Inc. | Beta-amino heterocyclic dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| ES2297141T3 (es) | 2002-03-29 | 2008-05-01 | EISAI R&D MANAGEMENT CO., LTD. | Derivados de (1-indanona)-(1,2,3,6-tetrahidropiridina). |
| AU2003226356A1 (en) | 2002-04-12 | 2003-10-27 | Ramot At Tel Aviv University Ltd. | Prevention of brain inflammation as a result of induced autoimmune response |
| EP1497321B1 (en) | 2002-04-19 | 2011-06-29 | The Governing Council Of The University Of Toronto | Immunological methods and compositions for the treatment of alzheimer's disease |
| EP1498421B1 (en) | 2002-04-24 | 2009-11-11 | Hiroshi Mori | Gamma-secretase inhibitors |
| ATE413388T1 (de) | 2002-04-26 | 2008-11-15 | Schering Corp | Muskarin antagonisten |
| AU2003230392A1 (en) | 2002-05-17 | 2003-12-12 | Merck And Co., Inc. | Beta-secretase inhibitors |
| IL165255A0 (en) | 2002-05-31 | 2005-12-18 | Lundbeck & Co As H | A combination of an nmda-antagonist and acetylcholine esterase inhibitors for teh treatment of alzheimer's disease |
| EP1513808A2 (en) | 2002-06-04 | 2005-03-16 | Pfizer Products Inc. | Fluorinated cyclic amides as dipeptidyl peptidase iv inhibitors |
| AU2003233010A1 (en) | 2002-06-04 | 2003-12-19 | Pfizer Products Inc. | Process for the preparation of 3,3,4,4-tetrafluoropyrrolidine and derivatives thereof |
| TWI273104B (en) | 2002-06-06 | 2007-02-11 | Eisai Co Ltd | Novel fused imidazole derivative |
| CN100369991C (zh) | 2002-06-19 | 2008-02-20 | 舒飞士特种化工有限公司 | 半光粉末涂料组合物 |
| WO2004007446A1 (ja) | 2002-07-10 | 2004-01-22 | Yamanouchi Pharmaceutical Co., Ltd. | 新規なアゼチジン誘導体又はその塩 |
| WO2004007468A1 (en) | 2002-07-15 | 2004-01-22 | Merck & Co., Inc. | Piperidino pyrimidine dipeptidyl peptidase inhibitors for the treatment of diabetes |
| TW200410672A (en) | 2002-07-19 | 2004-07-01 | Merz Pharma Gmbh & Co Kgaa | NMDA receptor antagonists and their use in inhibiting abnormal hyperphosphorylation of microtubule associated protein tau |
| US7557137B2 (en) | 2002-08-05 | 2009-07-07 | Bristol-Myers Squibb Company | Gamma-lactams as beta-secretase inhibitors |
| HRP20050157B1 (en) | 2002-08-21 | 2013-01-31 | Boehringer Ingelheim Pharma | 8-[3-amino-piperidin-1-yl]-xanthines,the production thereof and the use of the same as medicaments |
| DE10238470A1 (de) | 2002-08-22 | 2004-03-04 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Xanthinderivate, deren Herstellung und deren Verwendung als Arzneimittel |
| DE10238477A1 (de) | 2002-08-22 | 2004-03-04 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Purinderivate, deren Herstellung und deren Verwendung als Arzneimittel |
| ES2201929B1 (es) | 2002-09-12 | 2005-05-16 | Araclon Biotech, S.L. | Anticuerpos policlonales, metodo de preparacion y uso de los mismos. |
| US9535076B2 (en) | 2002-09-12 | 2017-01-03 | The Regents Of The University Of California | Methods and compositions for eliciting an amyloid-selective immune response |
| US8871447B2 (en) | 2002-09-12 | 2014-10-28 | The Regents Of The University Of California | Immunogens and corresponding antibodies specific for high molecular weight aggregation intermediates common to amyloids formed from proteins of differing sequence |
| WO2010012004A2 (en) | 2008-07-25 | 2010-01-28 | The Regents Of The University Of California | Monoclonal antibodies specific for pathological amyoid aggregates common to amyloids formed from proteins of differing sequence |
| DK1538207T3 (da) | 2002-09-12 | 2010-07-05 | Chemo Sero Therapeut Res Inst | Humant anti-human MCP-1-antistof og antistoffragment deraf |
| NZ538567A (en) | 2002-09-19 | 2007-04-27 | Abbott Lab | Pyrrolidine-2-carbonitrile derivatives and their pharmaceutical compositions as inhibitors of dipeptidyl peptidase-IV (DPP-IV) |
| WO2004026851A1 (en) | 2002-09-20 | 2004-04-01 | Axys Pharmaceuticals, Inc. | 3-(3,5-disubstituted-4-hydroxyphenyl)propionamide derivatives as cathepsin b inhibitors |
| US7273889B2 (en) | 2002-09-25 | 2007-09-25 | Innovative Drug Delivery Systems, Inc. | NMDA receptor antagonist formulation with reduced neurotoxicity |
| WO2004029629A1 (en) | 2002-09-27 | 2004-04-08 | Janssen Pharmaceutica N.V. | N-11 truncated amyloid-beta nomoclonal antibodies, compositions, methods and uses |
| WO2004031400A2 (en) | 2002-10-01 | 2004-04-15 | Northwestern University | Amyloid beta-derived diffusible ligands (addls), addl-surrogates, addl-binding molecules, and uses thereof |
| GB0223038D0 (en) | 2002-10-04 | 2002-11-13 | Merck Sharp & Dohme | Therapeutic compounds |
| GB0223039D0 (en) | 2002-10-04 | 2002-11-13 | Merck Sharp & Dohme | Therapeutic compounds |
| CA2499586A1 (en) | 2002-10-07 | 2004-04-22 | Merck & Co., Inc. | Antidiabetic beta-amino heterocyclic dipeptidyl peptidase inhibitors |
| AU2003269850A1 (en) | 2002-10-08 | 2004-05-04 | Novo Nordisk A/S | Hemisuccinate salts of heterocyclic dpp-iv inhibitors |
| GB0223494D0 (en) | 2002-10-09 | 2002-11-13 | Neuropharma Sa | Dual binding site acetylcholinesterase inhibitors for the treatment of alzheimer's disease |
| JP2006519762A (ja) | 2002-10-09 | 2006-08-31 | ライナット ニューロサイエンス コーポレイション | アミロイドβペプチド及びその組成物に対する抗体を使用して、アルツハイマー病を治療する方法 |
| MXPA05004063A (es) | 2002-10-18 | 2005-06-08 | Merck & Co Inc | Inhibidores de la beta-amino heterociclico dipeptidil peptidasa para el tratamiento o prevencion de diabetes. |
| GEP20094759B (en) | 2002-10-24 | 2009-08-25 | Merz Pharma Gmbh & Co Kgaa | Combination therapy using 1-aminocyclohexane derivatives and acetylcholinesterase inhibitors |
| US20040082543A1 (en) | 2002-10-29 | 2004-04-29 | Pharmacia Corporation | Compositions of cyclooxygenase-2 selective inhibitors and NMDA receptor antagonists for the treatment or prevention of neuropathic pain |
| WO2004041795A1 (en) | 2002-10-30 | 2004-05-21 | Guilford Pharmaceuticals Inc. | Novel inhibitors of dipeptidyl peptidase iv |
| WO2004039773A2 (en) | 2002-10-30 | 2004-05-13 | Nordic Bioscience A/S | Coumpounds modulating the activity of gapdh and/or iamt |
| US7452911B2 (en) * | 2002-10-31 | 2008-11-18 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Alkyne compounds with MCH antagonistic activity and medicaments comprising these compounds |
| GB0225474D0 (en) | 2002-11-01 | 2002-12-11 | Merck Sharp & Dohme | Therapeutic agents |
| FR2846667B1 (fr) | 2002-11-06 | 2004-12-31 | Pasteur Institut | Fragments variables d'anticorps de camelides a chaine unique diriges contre le peptide beta-amyloide 1-42 et leurs applications pour le diagnostic et le traitement des maladies neuroagregatives |
| MXPA05004890A (es) | 2002-11-07 | 2005-07-22 | Merck & Co Inc | Derivados de fenilalanina como inhibidores de dipeptidilpeptidasa para el tratamiento o prevencion de diabetes. |
| EP1562897B1 (en) | 2002-11-12 | 2009-09-16 | Merck & Co., Inc. | Phenylcarboxamide beta-secretase inhibitors for the treatment of alzheimer s disease |
| AU2002952946A0 (en) | 2002-11-27 | 2002-12-12 | Fujisawa Pharmaceutical Co., Ltd. | Dpp-iv inhibitor |
| AU2003297564A1 (en) | 2002-12-04 | 2004-06-23 | Merck & Co., Inc. | Phenylalanine derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| US7420079B2 (en) | 2002-12-09 | 2008-09-02 | Bristol-Myers Squibb Company | Methods and compounds for producing dipeptidyl peptidase IV inhibitors and intermediates thereof |
| US20040181075A1 (en) | 2002-12-19 | 2004-09-16 | Weingarten M. David | Process of making chalcone derivatives |
| WO2004058266A1 (en) | 2002-12-20 | 2004-07-15 | Merck & Co., Inc. | 3-amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| CA2512111A1 (en) | 2003-01-07 | 2004-07-29 | Merck And Co., Inc. | Macrocyclic beta-secretase inhibitors for treatment of alzheimer's disease |
| WO2004064778A2 (en) | 2003-01-17 | 2004-08-05 | Merck & Co. Inc. | 3-amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| WO2004069162A2 (en) | 2003-01-31 | 2004-08-19 | Merck & Co., Inc. | 3-amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| DE10303974A1 (de) | 2003-01-31 | 2004-08-05 | Abbott Gmbh & Co. Kg | Amyloid-β(1-42)-Oligomere, Verfahren zu deren Herstellung und deren Verwendung |
| EP1594969B1 (en) | 2003-02-01 | 2015-05-20 | Janssen Sciences Ireland UC | Active immunization to generate antibodies to soluble a-beta |
| NZ541324A (en) | 2003-02-04 | 2008-10-31 | Hoffmann La Roche | Malonamide derivatives as gamma-secretase inhibitors |
| US7575747B2 (en) | 2003-02-10 | 2009-08-18 | Applied Molecular Evolution | Aβ binding molecules |
| WO2004071454A2 (en) | 2003-02-13 | 2004-08-26 | Guilford Pharmaceuticals Inc. | Substituted azetidine compounds as inhibitors of dipeptidyl peptidase iv |
| EP1596878A4 (en) | 2003-02-18 | 2008-05-28 | Roskamp Res Llc | ANTIANGIOGENIC AND ANTITUMORAL PROPERTIES OF BETA AND GAMMA SECRETASE INHIBITORS |
| US8663650B2 (en) | 2003-02-21 | 2014-03-04 | Ac Immune Sa | Methods and compositions comprising supramolecular constructs |
| WO2004076434A1 (en) | 2003-02-28 | 2004-09-10 | Aic | Dipeptidyl peptidase inhibitors |
| AU2003207881A1 (en) | 2003-02-28 | 2004-09-17 | Aic | Dipeptidyl peptidase inhibitors |
| EP1454627A1 (en) | 2003-03-06 | 2004-09-08 | MyoContract Ltd. | Alpha-Keto carbonyl calpain inhibitors |
| WO2004084830A2 (en) | 2003-03-21 | 2004-10-07 | Buck Institute | Method for treating alzheimer’s dementia |
| US20040191334A1 (en) | 2003-03-24 | 2004-09-30 | Pang-Chui Shaw | Use of transhinone derivates as cholinesterase inhibitors in treating related diseases |
| KR20050122220A (ko) | 2003-03-25 | 2005-12-28 | 다케다 샌디에고, 인코포레이티드 | 디펩티딜 펩티다제 억제제 |
| EP1613321A2 (en) | 2003-03-28 | 2006-01-11 | Acadia Pharmaceuticals Inc. | Muscarinic m1 receptor agonists for pain management |
| CA2520853A1 (en) | 2003-03-28 | 2005-03-31 | Centocor, Inc. | Anti-amyloid antibodies, compositions, methods and uses |
| MXPA05010760A (es) | 2003-04-09 | 2005-12-12 | Wyeth Corp | Derivados de acido 2-(8,9-dioxo-2,6-diazabiciclo[5.2.0]non-1(7)-en-2-il)alquil fosfonico y su uso como antagonistas de receptor de n-metil-d-aspartato (nmda). |
| GB0308382D0 (en) | 2003-04-10 | 2003-05-21 | Univ Cambridge Tech | Therapeutic methods and means |
| GB0308318D0 (en) | 2003-04-10 | 2003-05-14 | Merck Sharp & Dohme | Therapeutic agents |
| WO2004089362A1 (en) | 2003-04-11 | 2004-10-21 | Novo Nordisk A/S | 2-cyanopyrroles and their analogues as ddp-iv inhibitors |
| ATE464889T1 (de) | 2003-05-05 | 2010-05-15 | Probiodrug Ag | Medizinische verwendung von hemmern von glutaminyl und glutamatcyclasen |
| EP1622870A2 (en) | 2003-05-05 | 2006-02-08 | Prosidion Ltd. | Glutaminyl based dp iv-inhibitors |
| ATE462432T1 (de) | 2003-05-05 | 2010-04-15 | Probiodrug Ag | Glutaminylcyclase-hemmer |
| ES2246178B1 (es) | 2003-05-08 | 2007-03-01 | Universidad De Zaragoza. | Uso de anticuerpos para el tratamiento de enfermedades amiloideas. |
| AU2003902260A0 (en) | 2003-05-09 | 2003-05-29 | Fujisawa Pharmaceutical Co., Ltd. | Dpp-iv inhibitor |
| ES2308206T3 (es) | 2003-05-13 | 2008-12-01 | Schering Corporation | N-arilsulfonilpiperidinas con fuentes como inhibidores de gamma-secretasa. |
| US7560455B2 (en) | 2003-05-14 | 2009-07-14 | Merck & Co., Inc. | 3-Amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| EP1625122A1 (en) | 2003-05-14 | 2006-02-15 | Takeda San Diego, Inc. | Dipeptidyl peptidase inhibitors |
| NZ542797A (en) | 2003-05-16 | 2007-12-21 | Merck Sharp & Dohme | Cyclohexyl sulfones comprising an additional fused ring cyclic sulfonamide group suitable for inhibition of gamma-secretase |
| MXPA05012493A (es) | 2003-05-27 | 2006-05-25 | Forest Laboratories | Combinacion de un antagonista del receptor de nmda y un inhibidor selectivo de reabsorcion de serotonina para el tratamiento de depresion y otros trastornos de estado de animo. |
| TWI306458B (en) | 2003-05-30 | 2009-02-21 | Elan Pharma Int Ltd | Humanized antibodies that recognize beta amyloid peptide |
| AU2003902828A0 (en) | 2003-06-05 | 2003-06-26 | Fujisawa Pharmaceutical Co., Ltd. | Dpp-iv inhibitor |
| AU2004247068A1 (en) | 2003-06-06 | 2004-12-23 | Merck & Co., Inc. | Fused indoles as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
| AU2003902946A0 (en) | 2003-06-12 | 2003-06-26 | Fujisawa Pharmaceutical Co., Ltd. | Dpp-iv inhibitor |
| EP1638950A4 (en) | 2003-06-17 | 2010-06-30 | Merck Sharp & Dohme | CYCLOHEXYLGLYCIN DERIVATIVES AS DIPEPTIDYLPEPTIDASEINHIBITORS FOR THE TREATMENT OF BZW. PREVENTION OF DIABETES |
| ES2327740T3 (es) | 2003-06-20 | 2009-11-03 | F. Hoffmann-La Roche Ag | Hexahidropiridoisoquinolinas como inhibidoras de la dpp-iv. |
| HRP20110018T1 (hr) | 2003-06-20 | 2011-02-28 | F. Hoffmann - La Roche Ag | Derivati pirido(2,1-a)-izokinolina kao inhibitori dpp-iv |
| CN101415724B (zh) | 2003-06-30 | 2015-12-02 | 特拉维夫大学未来科技开发有限公司 | 肽、抗肽抗体以及用它们来诊断和治疗淀粉样蛋白相关疾病的方法 |
| CA2529994A1 (en) | 2003-06-30 | 2005-01-20 | Merck & Co., Inc. | N-alkyl phenylcarboxamide beta-secretase inhibitors for the treatment of alzheimer's disease |
| CN1909897A (zh) | 2003-07-01 | 2007-02-07 | 默克公司 | 用于治疗阿尔茨海默病的苯基羧化物β-分泌酶抑制剂 |
| WO2005007614A1 (en) | 2003-07-03 | 2005-01-27 | The Government Of The United States Of America As Represented By The Secretary, Department Of Health And Human Services 6011 | Monoamine oxidase inhibitors |
| EP1648520B1 (en) | 2003-07-16 | 2010-05-05 | RVX Therapeutics, Inc. | Compounds and methods for downregulating the effects of tgf-beta |
| EP1671129A1 (en) | 2003-07-21 | 2006-06-21 | Angiogenetics Sweden AB | Compounds and methods for promoting angiogenesis by using a gamma-secretase inhibitor or inhibiting the gamma-secretase pathway |
| WO2005014041A2 (en) | 2003-07-24 | 2005-02-17 | Novartis Ag | Use of an amyloid beta dna vaccine for the treatment and/or prevention of amyloid diseases |
| EP1660058A2 (en) | 2003-07-28 | 2006-05-31 | Merz Pharma GmbH & Co. KGaA | The use of 1-amino-alkylcyclohexane compounds in the treatment of pain hypersensitivity |
| WO2005011581A2 (en) | 2003-07-31 | 2005-02-10 | Merck & Co., Inc. | Hexahydrodiazepinones as dipeptidyl peptidase-iv inhibitors for the treatment or prevention of diabetes |
| WO2005011599A2 (en) | 2003-08-01 | 2005-02-10 | Northwestern University | Antibodies specific for toxic amyloid beta protein oligomers |
| GB0318447D0 (en) | 2003-08-05 | 2003-09-10 | Merck Sharp & Dohme | Therapeutic agents |
| US7579357B2 (en) | 2003-08-13 | 2009-08-25 | Takeda Pharmaceutical Company Limited | Dipeptidyl peptidase inhibitors |
| US7329746B2 (en) | 2003-08-14 | 2008-02-12 | Merck & Co., Inc. | Macrocyclic beta-secretase inhibitors for the treatment of Alzheimer's disease |
| WO2005018424A2 (en) | 2003-08-18 | 2005-03-03 | Research Foundation For Mental Hygiene, Inc. | Antibodies specific for fibrillar amyloid and a procedure to detect fibrillar amyloid deposits |
| WO2005023762A1 (en) | 2003-09-04 | 2005-03-17 | Abbott Laboratories | Pyrrolidine-2-carbonitrile derivatives and their use as inhibitors of dipeptidyl peptidase-iv (dpp-iv) |
| AU2003298171A1 (en) | 2003-09-05 | 2005-03-29 | Cellzome Ag | Protein complexes associated with app-processing |
| WO2005026148A1 (en) | 2003-09-08 | 2005-03-24 | Takeda San Diego, Inc. | Dipeptidyl peptidase inhibitors |
| WO2005030751A2 (en) | 2003-09-08 | 2005-04-07 | Takeda Pharmaceutical Company Limited | Dipeptidyl peptidase inhibitors |
| US20070031416A1 (en) | 2003-09-09 | 2007-02-08 | Takeda Pharmaceutical Company Limited | Use of antibody |
| TW200530157A (en) | 2003-09-09 | 2005-09-16 | Japan Tobacco Inc | Dipeptidyl peptidase iv inhibitor |
| US20070110750A1 (en) | 2003-09-12 | 2007-05-17 | The Regents Of The University Of California | Monoclonal antibodies specific for high molecular weight aggregation intermediates common to amyloids formed from proteins of differing sequence |
| GB0322140D0 (en) | 2003-09-22 | 2003-10-22 | Pfizer Ltd | Combinations |
| US7514459B2 (en) | 2003-09-24 | 2009-04-07 | Merck Sharp & Dohme Ltd. | Gamma-secretase inhibitors |
| DE602004014170D1 (de) | 2003-10-03 | 2008-07-10 | Merck & Co Inc | Benzylether- und benzylamino-beta-sekretase-hemmer zur behandlung von alzheimer-krankheit |
| EP1682540A1 (en) | 2003-10-06 | 2006-07-26 | Alangudi Sankaranarayanan | Azolidinecarbonitriles and their use as dpp-iv inhibitors |
| DK1673347T3 (en) | 2003-10-06 | 2015-10-12 | Hoffmann La Roche | SUBSTITUTED DIBENZO-AZEPINE AND BENZO-DIAZEPINE DERIVATIVES USED AS GAMMA SECRETASE INHIBITORS |
| US20070021414A1 (en) | 2003-10-08 | 2007-01-25 | Pfizer, Inc. | 1-'2-(4-Hydroxyphenyl)-2-hydroxyethyl!-piperidin-4-ol compounds as nmda receptor antagonists |
| NZ546322A (en) | 2003-10-15 | 2008-11-28 | Probiodrug Ag | Use of effectors of glutaminyl and glutamate cyclases |
| EP2269608A3 (en) | 2003-10-16 | 2011-02-16 | NeuroSearch AS | Pharmaceutical composition comprising a monoamine neurotransmitter re-uptake inhibitor and an acetylcholinesterase inhibitor |
| GB0324236D0 (en) | 2003-10-16 | 2003-11-19 | Astrazeneca Ab | Chemical compounds |
| TW200519105A (en) | 2003-10-20 | 2005-06-16 | Lg Life Science Ltd | Novel inhibitors of DPP-IV, methods of preparing the same, and pharmaceutical compositions containing the same as an active agent |
| CN1870984A (zh) | 2003-10-22 | 2006-11-29 | 莫茨药物股份两合公司 | 1-氨基环己烷衍生物用于调节淀粉样病变中原纤维生成Aβ肽的沉积的用途 |
| WO2006058720A2 (en) | 2003-11-03 | 2006-06-08 | Probiodrug Ag | Novel compounds for the treatment of neurological disorders |
| JP2007510651A (ja) | 2003-11-04 | 2007-04-26 | メルク エンド カムパニー インコーポレーテッド | 糖尿病の治療又は予防のためのジペプチジルペプチダーゼ−iv阻害剤としての縮合フェニルアラニン誘導体 |
| CA2544203A1 (en) | 2003-11-11 | 2005-05-19 | F. Hoffmann-La Roche Ag | Phosphinic acids derivatives, beta-secretase inhibitors for the treatment of alzheimer's disease |
| DK1689757T3 (en) | 2003-11-12 | 2014-12-08 | Sino Med Internat Alliance Inc | HETEROCYCLIC DRY ACID COMPOUNDS |
| AU2004293416B2 (en) | 2003-11-24 | 2009-09-24 | Merck & Co., Inc. | Benzylether and benzylamino beta-secretase inhibitors for the treatment of Alzheimer's disease |
| DE10355304A1 (de) | 2003-11-27 | 2005-06-23 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue 8-(Piperazin-1-yl)-und 8-([1,4]Diazepan-1-yl)-xanthine, deren Herstellung und deren Verwendung als Arzneimittel |
| UY28650A1 (es) | 2003-12-05 | 2005-02-28 | Forest Laboratories | Memantina para la prevencion o disminucion de la conducta suicida y para el tratamiento de la depresion mayor asociada con esta conducta |
| EP1541143A1 (en) | 2003-12-09 | 2005-06-15 | Graffinity Pharmaceuticals Aktiengesellschaft | Dpp-iv inhibitors |
| EP1541148A1 (en) | 2003-12-09 | 2005-06-15 | Graffinity Pharmaceuticals Aktiengesellschaft | Dpp-iv inhibitors |
| WO2005058849A1 (en) | 2003-12-15 | 2005-06-30 | Glenmark Pharmaceuticals Ltd. | New dipeptidyl peptidase in inhibitors; process for their preparation and compositions containing them |
| EP1697308B1 (en) | 2003-12-19 | 2014-03-19 | Merck Sharp & Dohme Corp. | Phenylamide and pyridylamide beta-secretase inhibitors for the treatment of alzheimer's disease |
| CA2554617A1 (en) | 2004-01-22 | 2005-08-04 | Boehringer Ingelheim International Gmbh | Pharmaceutical composition comprising a monoamine neurotransmitter re-uptake inhibitor and an n-methyl-d-aspartate (nmda) receptors antagonist |
| CA2554959A1 (en) | 2004-01-29 | 2005-08-11 | Neuromolecular, Inc. | Combination of a nmda receptor antagonist and a mao-inhibitor or a gadpf-inhibitor for the treatment of central nervous system-related conditions |
| WO2005075426A1 (en) | 2004-02-03 | 2005-08-18 | Glenmark Pharmaceuticals Ltd. | Novel dipeptidyl peptidase iv inhibitors; processes for their preparation and compositions thereof |
| CN1918131B (zh) * | 2004-02-05 | 2011-05-04 | 前体生物药物股份公司 | 谷氨酰胺酰基环化酶抑制剂 |
| US20050209218A1 (en) | 2004-02-13 | 2005-09-22 | Meyerson Laurence R | Methods and compositions for the treatment of psychiatric conditions |
| US20050182044A1 (en) | 2004-02-17 | 2005-08-18 | Bruinsma Gosse B. | Combinatorial therapy with an acetylcholinesterase inhibitor and (3aR)-1,3a,8-trimethyl-1,2,3,3a,8,8a-hexahydropyrrolo[2,3,-b]indol-5-yl phenylcarbamate |
| EA010854B1 (ru) | 2004-02-18 | 2008-12-30 | Бёрингер Ингельхайм Интернациональ Гмбх | 8-[3-аминопиперидин-1-ил]ксантины, их получение и их применение в качестве ингибиторов dpp-iv |
| JP4824547B2 (ja) | 2004-02-20 | 2011-11-30 | インテレクト ニュウロサイエンシス,インク. | モノクローナル抗体およびその利用 |
| US20050203027A1 (en) | 2004-02-23 | 2005-09-15 | Trustees Of Tufts College | Inhibitors of dipeptidylpeptidase IV |
| EP1593671A1 (en) | 2004-03-05 | 2005-11-09 | Graffinity Pharmaceuticals AG | DPP-IV inhibitors |
| CN1942186B (zh) | 2004-03-09 | 2010-10-06 | 国家卫生研究院 | 吡咯烷化合物 |
| MXPA06010571A (es) | 2004-03-15 | 2007-02-16 | Takeda Pharmaceutical | Inhibidores de dipeptidil peptidasa. |
| EP1740172A4 (en) | 2004-03-19 | 2007-10-10 | Axonyx Inc | ACETYLCHOLINESTERASE INHIBITORS AND N-METHYL-D-ASPARTATE ANTAGONISTS FOR THE TREATMENT OF COGNITIVE DISORDER |
| WO2005095339A1 (en) | 2004-03-31 | 2005-10-13 | Pfizer Products Inc. | Dicyanopyrrolidines as dipeptidyl peptidase iv inhibitors |
| WO2005097103A2 (en) | 2004-04-01 | 2005-10-20 | Axys Pharmaceuticals, Inc. | Diabetes and metabolic syndrome therapy utilizing cathepsin b inhibitors |
| AU2005230681B2 (en) | 2004-04-05 | 2009-07-30 | Schering Corporation | Novel gamma secretase inhibitors |
| CA2563639A1 (en) | 2004-04-20 | 2005-11-03 | Merck & Co., Inc. | 2, 4, 6-substituted pyridyl derivative compounds useful as beta-secretase inhibitors for the treatment of alzheimer's disease |
| JP2007533743A (ja) | 2004-04-20 | 2007-11-22 | メルク エンド カムパニー インコーポレーテッド | アルツハイマー病治療のためのβ−セクレターゼ阻害薬として有用な1,3,5−置換フェニル誘導体化合物 |
| WO2005102390A2 (en) | 2004-04-22 | 2005-11-03 | Pfizer Japan, Inc. | Combinations comprising alpha-2-delta ligands and nmda receptor antagonists |
| US9549895B2 (en) | 2004-04-23 | 2017-01-24 | Massachusetts Eye And Ear Infirmary | Methods and compositions for preserving the viability of photoreceptor cells |
| WO2005105998A1 (ja) | 2004-04-27 | 2005-11-10 | Juridical Foundation The Chemo-Sero-Therapeutic Research Institute | ヒト抗アミロイドβペプチド抗体およびその抗体フラグメント |
| WO2005108382A1 (en) | 2004-05-04 | 2005-11-17 | Merck & Co., Inc. | 1,2,4-oxadiazole derivatives as dipeptidyl peptidase-iv inhibitors for the treatment or prevention of diabetes |
| ES2327857T3 (es) | 2004-05-12 | 2009-11-04 | Pfizer Products Inc. | Derivados de prolina y su uso como inhibidores de la dipeptidil peptidasa iv. |
| CA2566053A1 (en) | 2004-05-13 | 2005-12-01 | Merck & Co., Inc. | Phenyl carboxamide compounds useful as beta-secretase inhibitors for the treatment of alzheimer's disease |
| CA2564884A1 (en) | 2004-05-18 | 2005-12-08 | Merck & Co., Inc. | Cyclohexylalanine derivatives as dipeptidyl peptidase-iv inhibitors for the treatment or prevention of diabetes |
| EP1598341A1 (en) | 2004-05-21 | 2005-11-23 | Santhera Pharmaceuticals (Deutschland) Aktiengesellschaft | DPP-IV inhibitors |
| US7687638B2 (en) | 2004-06-04 | 2010-03-30 | Takeda San Diego, Inc. | Dipeptidyl peptidase inhibitors |
| DE602005022871D1 (de) | 2004-06-07 | 2010-09-23 | Univ Ramot | Verfahren zur passiven immunisierung gegen eine durch amyloidaggregation gekennzeichnete krankheit oder erkrankung mit vermindertem nervenentzündungsrisiko |
| EP1604989A1 (en) | 2004-06-08 | 2005-12-14 | Santhera Pharmaceuticals (Deutschland) Aktiengesellschaft | DPP-IV inhibitors |
| EP1604980A1 (en) | 2004-06-08 | 2005-12-14 | Santhera Pharmaceuticals (Deutschland) Aktiengesellschaft | DPP-IV inhibitors |
| EP1604662A1 (en) | 2004-06-08 | 2005-12-14 | Santhera Pharmaceuticals (Deutschland) Aktiengesellschaft | 1-[(3R)-Amino-4-(2-fluoro-phenyl)-butyl]-pyrrolidine-(2R)-carboxylic acid benzyl amine derivatives and related compounds as dipeptidyl peptidase IV (DPP-IV) inhibitors for the treatment of type 2 diabetes mellitus |
| JP2008502684A (ja) | 2004-06-15 | 2008-01-31 | メルク エンド カムパニー インコーポレーテッド | アルツハイマー病を治療するためのベータ−セクレターゼ阻害剤として有用なピロリジン−3−イル化合物 |
| GB0413389D0 (en) | 2004-06-16 | 2004-07-21 | Astrazeneca Ab | Chemical compounds |
| SE0401601D0 (sv) | 2004-06-21 | 2004-06-21 | Bioarctic Neuroscience Ab | Protofibril specific antibodies and uses thereof |
| AU2005265148B2 (en) | 2004-06-21 | 2011-01-20 | Merck Sharp & Dohme Corp. | Aminocyclohexanes as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes |
| CA2572289A1 (en) | 2004-06-30 | 2006-08-17 | Centocor, Inc. | Anti-mcp-1 antibodies, compositions, methods and uses |
| JP2008505100A (ja) | 2004-06-30 | 2008-02-21 | シェーリング コーポレイション | ガンマ−セクレターゼ阻害剤としての置換n−アリールスルホニル複素環アミン |
| EP1769002A1 (en) | 2004-07-02 | 2007-04-04 | Northwestern University | Monolocal antibodies that target pathological assemblies of amyloid beta; (abeta) |
| US7786163B2 (en) | 2004-07-12 | 2010-08-31 | Forest Laboratories Holdings Limited (BM) | Constrained cyano compounds |
| WO2006019965A2 (en) | 2004-07-16 | 2006-02-23 | Takeda San Diego, Inc. | Dipeptidyl peptidase inhibitors |
| WO2006008661A2 (en) | 2004-07-19 | 2006-01-26 | Neurochem (International) Limited | Diagnostic methods of multiple organ amyloidosis |
| WO2006014638A2 (en) | 2004-07-19 | 2006-02-09 | The General Hospital Corporation | ANTIBODIES TO CROSS-LINKED AMYLOID β OLIGOMERS |
| AR049726A1 (es) | 2004-07-22 | 2006-08-30 | Schering Corp | Amidas sustituidas inhibidoras de beta secretasa |
| CN101027297B (zh) | 2004-07-28 | 2010-09-08 | 先灵公司 | 大环β-分泌酶抑制剂 |
| HUP0401523A3 (en) | 2004-07-29 | 2007-05-02 | Richter Gedeon Vegyeszet | Indole-2-carboxamide derivatives, pharmaceutical compositions containing them and process for producing them |
| BRPI0513959A (pt) | 2004-07-30 | 2008-05-20 | Rinat Neuroscience Corp | anticorpos dirigidos contra o peptìdeo beta-amilóide, suas composições farmacêuticas, kit e métodos de fabricação dos mesmos |
| EP1623983A1 (en) | 2004-08-05 | 2006-02-08 | Santhera Pharmaceuticals (Deutschland) Aktiengesellschaft | Heterocyclic compounds useful as DPP-IV inhibitors |
| US8168188B1 (en) | 2004-08-11 | 2012-05-01 | Kyoto University | Antibody and utilization of the same |
| EP1784188B1 (en) | 2004-08-23 | 2010-07-14 | Merck Sharp & Dohme Corp. | Fused triazole derivatives as dipeptidyl peptidase-iv inhibitors for the treatment or prevention of diabetes |
| WO2006021409A1 (en) | 2004-08-25 | 2006-03-02 | Santhera Pharmaceuticals (Schweiz) Ag | Alpha-keto carbonyl calpain inhibitors |
| AU2005276635A1 (en) | 2004-08-25 | 2006-03-02 | Santhera Pharmaceuticals (Schweiz) Ag | Alpha-keto carbonyl calpain inhibitors |
| US7388007B2 (en) | 2004-08-26 | 2008-06-17 | Bristol-Myers Squibb Company | Gamma-lactams as beta-secretase inhibitors |
| TWI374935B (en) | 2004-08-27 | 2012-10-21 | Pfizer Ireland Pharmaceuticals | Production of α-abeta |
| CA2579472A1 (en) | 2004-09-14 | 2006-03-23 | The Genetics Company, Inc. | Hydrazone derivatives and their use as beta secretase inhibitors |
| EP1797052A1 (en) | 2004-09-17 | 2007-06-20 | Comentis, Inc. | Bicyclic compounds which inhibit beta-secretase activity and methods of use thereof |
| WO2006034296A2 (en) | 2004-09-17 | 2006-03-30 | Comentis, Inc. | Amino-containing compounds which inhibit memapsin 2 beta-secretase activity and methods of use thereof |
| EP1799260A4 (en) | 2004-09-29 | 2011-09-28 | Centocor Inc | ANTI-AMYLOID ANTIBODIES, COMPOSITIONS, TECHNIQUES AND USES |
| CN101031300A (zh) | 2004-10-01 | 2007-09-05 | 默克公司 | 用于治疗或预防糖尿病的作为二肽基肽酶-ⅳ抑制剂的氨基哌啶化合物 |
| WO2006042103A2 (en) | 2004-10-05 | 2006-04-20 | Axys Pharmaceuticals, Inc. | Reversible inhibitors of cathepsin b |
| AU2005294320A1 (en) | 2004-10-08 | 2006-04-20 | Novartis Ag | Combination of organic compounds |
| WO2006040688A2 (en) | 2004-10-12 | 2006-04-20 | Ernir Snorrason | Inhibitors of acetylcholinesterase for treating skin diseases |
| CN101068545A (zh) | 2004-10-13 | 2007-11-07 | 默克公司 | 作为β-分泌酶抑制剂用于治疗阿尔茨海默病的螺哌啶化合物 |
| EP1816996A4 (en) | 2004-10-15 | 2009-08-12 | Biopharmacopae Design Internat | THERAPEUTIC METHODS AND COMPOSITIONS COMPRISING PLANT EXTRACTS FOR THE TREATMENT OF CANCER |
| US7811563B2 (en) | 2004-10-25 | 2010-10-12 | Northwestern University | Anti-addl antibodies and uses thereof |
| CN101035522B (zh) | 2004-10-25 | 2011-12-07 | 诺瓦提斯公司 | Dpp-ⅳ抑制剂、ppar抗糖尿病剂和二甲双胍的组合 |
| US20080199879A1 (en) | 2004-10-28 | 2008-08-21 | Sanko Junyaku Co., Ltd. | Method of Assaying Alzheimer's Disease and Diagnostic Reagent |
| AU2005310239A1 (en) | 2004-10-29 | 2006-06-08 | Merck & Co., Inc. | 2-aminopyridine compounds useful as beta-secretase inhibitors for the treatment of Alzheimer's disease |
| EP1814537B1 (en) | 2004-11-17 | 2014-11-12 | Merck Sharp & Dohme Corp. | Macrocyclic tertiary amine beta-secretase inhibitors for the treatment of alzheimer's disease |
| JP2008520718A (ja) | 2004-11-23 | 2008-06-19 | メルク エンド カムパニー インコーポレーテッド | アルツハイマー病の治療のためのβ−セクレターゼ阻害剤として有用な2,3,4,6−置換ピリジル誘導体化合物 |
| CA2587256A1 (en) | 2004-11-23 | 2006-06-01 | Merck & Co., Inc. | Macrocyclic aminopyridyl beta-secretase inhibitors for the treatment of alzheimer's disease |
| RU2404750C2 (ru) | 2004-11-23 | 2010-11-27 | Адамас Фармасьютикалс, Инк. | Композиция, содержащая основу или покрытие для замедленного высвобождения и антагонист nmda рецептора, способ введения такого nmda антагониста субъекту |
| EP1845968A2 (en) | 2004-11-24 | 2007-10-24 | Neuromolecular Pharmaceuticals, Inc | Composition comprising an nmda receptor antagonist and levodopa and use thereof for treating neurological disease |
| AU2005309606B2 (en) | 2004-11-29 | 2011-01-06 | Merck Sharp & Dohme Corp. | Fused aminopiperidines as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes |
| RU2401267C2 (ru) | 2004-11-30 | 2010-10-10 | Ф.Хоффманн-Ля Рош Аг | Замещенные производные бензохинолизина |
| WO2006060473A2 (en) | 2004-12-03 | 2006-06-08 | Mucosal Therapeutics Llc | Methods of treatment of injured or diseased joints with lubricin compositions |
| AR052051A1 (es) | 2004-12-15 | 2007-02-28 | Neuralab Ltd | Anticuerpos ab humanizados usados en mejorar la cognicion |
| US20060240486A1 (en) | 2004-12-15 | 2006-10-26 | Johnson-Wood Kelly L | Immunoprecipitation-based assay for predicting in vivo efficacy of beta-amyloid antibodies |
| CA2589017A1 (en) | 2004-12-15 | 2006-06-22 | Neuralab Limited | Amyloid beta antibodies for use in improving cognition |
| WO2006066049A2 (en) | 2004-12-15 | 2006-06-22 | Neuralab Limited | Humanized antibodies that recognize beta amyloid peptide |
| US7411093B2 (en) | 2004-12-20 | 2008-08-12 | Hoffman-La Roche Inc. | Aminocycloalkanes as DPP-IV inhibitors |
| KR100904829B1 (ko) | 2004-12-20 | 2009-06-25 | 에프. 호프만-라 로슈 아게 | 4-아미노피페리딘 유도체 |
| EP1828192B1 (en) | 2004-12-21 | 2014-12-03 | Takeda Pharmaceutical Company Limited | Dipeptidyl peptidase inhibitors |
| EP2425846A1 (en) | 2004-12-23 | 2012-03-07 | Voyager Pharmaceutical Corporation | Acetylcholinesterase Inhibitors and leuprolide acetate for the treatment of Alzheimer's disease |
| EP1831172B1 (en) | 2004-12-28 | 2009-02-18 | Council of Scientific and Industrial Research | Substituted carbamic acid quinolin-6-yl esters useful as acetylcholinesterase inhibitors |
| WO2006074265A2 (en) | 2005-01-06 | 2006-07-13 | Merck & Co., Inc. | Drug combination therapy and pharmaceutical compositions for treating inflammatory disorders |
| CA2594943A1 (en) | 2005-01-19 | 2006-07-27 | Merck & Co., Inc. | Aminomethyl beta-secretase inhibitors for the treatment of alzheimer's disease |
| WO2006081171A1 (en) | 2005-01-24 | 2006-08-03 | Amgen Inc. | Humanized anti-amyloid antibody |
| TW200640529A (en) | 2005-02-28 | 2006-12-01 | Thomas Christian Lines | Composition for treating mental health disorders |
| US20080194698A1 (en) | 2005-03-07 | 2008-08-14 | Michael Hermanussen | Nmda Receptor Antagonists in the Medical Intervention of Metabolic Disorders |
| ES2259270B1 (es) | 2005-03-09 | 2007-11-01 | Consejo Superior De Investigaciones Cientificas | Metodo de diagnostico in vitro de la enfermedad de alzheimer mediante un anticuerpo monoclonal. |
| US7745470B2 (en) | 2005-03-10 | 2010-06-29 | Bristol-Myers Squibb Company | Isophthalates as beta-secretase inhibitors |
| FR2883285B1 (fr) | 2005-03-17 | 2007-05-18 | Sanofi Aventis Sa | Sel besylate de la 7-(2-(4-(3-trifluoromethyl-phenyl) -1,2,3,6-tetrahudro-pyrid-1-yl)ethyl) isoquinoleine, sa preparation et son utilisation en therapeutique |
| ES2318918B1 (es) | 2005-04-01 | 2010-02-16 | Biotherapix Molecular Medicines, S.L.U. | Anticuerpos humanos con capacidad de union al peptido beta-amiloide y sus aplicaciones. |
| MX2007013471A (es) | 2005-04-27 | 2008-01-22 | Novartis Ag | Metodos de tratamiento de aterosclerosis. |
| UY29504A1 (es) | 2005-04-29 | 2006-10-31 | Rinat Neuroscience Corp | Anticuerpos dirigidos contra el péptido amiloide beta y métodos que utilizan los mismos. |
| PE20110071A1 (es) | 2005-05-19 | 2011-01-31 | Centocor Inc | Anticuerpos anti-mcp-1, composiciones y metodos |
| WO2006128693A2 (en) | 2005-06-01 | 2006-12-07 | Ucb Pharma, S.A. | 2 -oxo-i -pyrrolidine derivatives/ processes for preparing them and their therapeutic use on the central nervous system |
| WO2006137354A1 (ja) | 2005-06-21 | 2006-12-28 | Medical & Biological Laboratories Co., Ltd. | アミロイド線維形成に対する阻害活性を有する抗体 |
| CN101238124A (zh) | 2005-07-18 | 2008-08-06 | 默克公司 | 用于治疗阿尔茨海默氏病的螺哌啶β-分泌酶抑制剂 |
| WO2007019078A2 (en) | 2005-08-03 | 2007-02-15 | Merck & Co., Inc. | Tricyclic beta-secretase inhibitors for the treatment of alzheimer's disease |
| US20090182021A1 (en) | 2005-08-03 | 2009-07-16 | Nanternet Philippe G | Tricyclic Beta-Secretase Inhibitors for the Treatment of Alzheimer's Disease |
| US7338974B2 (en) | 2005-08-12 | 2008-03-04 | Bristol-Myers Squibb Company | Macrocyclic diaminopropanes as beta-secretase inhibitors |
| US8124076B2 (en) | 2005-08-18 | 2012-02-28 | Ramot At Tel Aviv University Ltd. | Single chain antibodies against β-amyloid peptide |
| DE602006020052D1 (de) | 2005-09-28 | 2011-03-24 | Robert Ternansky | Neue arzneimittel gegen demenz |
| WO2007051333A1 (en) | 2005-11-02 | 2007-05-10 | Oncalis Ag | Triazine beta-secretase inhibitors |
| DK1959991T3 (da) | 2005-12-12 | 2013-06-17 | Ac Immune Sa | Terapeutisk vaccine |
| EP2808032B1 (en) | 2005-12-12 | 2018-08-01 | AC Immune S.A. | A beta 1-42 specific monoclonal antibodies with therapeutic properties |
| AU2007207481B2 (en) | 2006-01-20 | 2012-08-23 | Merck Sharp & Dohme Corp. | Carbocyclic and heterocyclic arylsulfones as gamma secretase inhibitors |
| CA2638775A1 (en) | 2006-02-22 | 2007-08-30 | Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkyujo | Peptide vaccine for inducing production of anti-amyloid-.beta.-peptide antibody |
| GB0704100D0 (en) | 2006-03-17 | 2007-04-11 | Vodafone Plc | Improvements in an ehspa architecture |
| KR20120093400A (ko) | 2006-03-30 | 2012-08-22 | 글락소 그룹 리미티드 | 아밀로이드?베타 펩티드에 대한 항체 |
| CL2007002070A1 (es) | 2006-07-14 | 2008-02-08 | Ac Immune S A Genentech Inc | Anticuerpo quimerico o humanizado, o fragmentos de ellos, que se adhieren especificamente a por lo menos un epitopo en la proteina beta-amiloide; molecula de acido nucleico que lo codifica; composicion que lo comprende; su uso para tratar enfermedade |
| ES2640095T3 (es) | 2006-10-02 | 2017-10-31 | Ac Immune S.A. | Anticuerpo humanizado contra beta-amiloide |
| WO2008054698A2 (en) | 2006-10-30 | 2008-05-08 | Merck & Co., Inc. | Spiropiperidine beta-secretase inhibitors for the treatment of alzheimer's disease |
| US8278345B2 (en) | 2006-11-09 | 2012-10-02 | Probiodrug Ag | Inhibitors of glutaminyl cyclase |
| JP5599614B2 (ja) | 2006-11-09 | 2014-10-01 | プロビオドルグ エージー | グルタミニルシクラーゼの新規阻害剤 |
| ES2468546T3 (es) * | 2006-11-09 | 2014-06-16 | Probiodrug Ag | Nuevos inhibidores de glutaminil ciclasa |
| SI2091948T1 (sl) | 2006-11-30 | 2012-07-31 | Probiodrug Ag | Novi inhibitorji glutaminil ciklaze |
| US20100216875A1 (en) | 2006-12-20 | 2010-08-26 | Gregory Hook | Methods of treating alzheimer's disease |
| CA2672213C (en) * | 2006-12-22 | 2016-02-16 | Astex Therapeutics Limited | Bicyclic amine derivatives as protein tyrosine kinase inhibitors |
| US7803810B2 (en) | 2007-03-09 | 2010-09-28 | Probiodrug Ag | Inhibitors |
| WO2008128981A1 (en) | 2007-04-18 | 2008-10-30 | Probiodrug Ag | Nitrovinyl-diamine derivatives as glutaminyl cyclase inhibitors |
| WO2008128986A1 (en) | 2007-04-18 | 2008-10-30 | Probiodrug Ag | Urea derivatives as glutaminyl cyclase inhibitors |
| EP2160380B1 (en) | 2007-04-18 | 2014-04-02 | Probiodrug AG | Cyano-guanidine derivatives as glutaminyl cyclase inhibitors |
| WO2008128987A1 (en) | 2007-04-18 | 2008-10-30 | Probiodrug Ag | Novel inhibitors |
| DK2160389T3 (da) | 2007-04-18 | 2014-06-23 | Probiodrug Ag | Thioxoquinazolinonderivater som glutaminylcyclaseinhibitorer |
| EP2142514B1 (en) | 2007-04-18 | 2014-12-24 | Probiodrug AG | Thiourea derivatives as glutaminyl cyclase inhibitors |
| EP2142536B1 (en) | 2007-04-20 | 2015-10-21 | Probiodrug AG | Aminopyrimidine derivatives as glutaminyl cyclase inhibitors |
| CA2684594C (en) * | 2007-04-20 | 2015-10-06 | The Research Foundation Of State University Of New York | Benzimidazoles and pharmaceutical compositions thereof for treating mycobacterium tuberculosis or francisella tulerensis infection |
| WO2008147800A1 (en) | 2007-05-25 | 2008-12-04 | Elan Pharmaceuticals, Inc. | Pyrazolopyrrolidines as inhibitors of gamma secretase |
| TWI516500B (zh) | 2007-06-12 | 2016-01-11 | Ac免疫公司 | 抗β類澱粉蛋白單株抗體 |
| WO2008151927A2 (en) | 2007-06-15 | 2008-12-18 | Nycomed Gmbh | 6-n-substituted benz imidazole derivatives as acid pump antagonists |
| EP2435416B1 (en) | 2007-07-05 | 2016-03-30 | Merck Sharp & Dohme Corp. | Tetrahydropyranochromene gamma secretase inhibitors |
| PE20090447A1 (es) | 2007-07-17 | 2009-04-18 | Schering Corp | Bencensulfonil-cromano, tiocromano, tetrahidronaftaleno e inhibidores relacionados de la gamma secretasa |
| WO2009029272A2 (en) | 2007-08-27 | 2009-03-05 | Agadjanyan Michael G | Epitope vaccine for prevention and reversion of ad pathology |
| US20100239570A1 (en) | 2007-09-13 | 2010-09-23 | Roger Nitsch | Moncolonal amyloid beta (abeta) - specific antibody and uses thereof |
| CN101868457B (zh) | 2007-09-24 | 2013-02-13 | 科门蒂斯公司 | 作为β-分泌酶抑制剂用于治疗的(3-羟基-4-氨基-丁-2-基)-3-(2-噻唑-2-基-吡咯烷-1-羰基)苯甲酰胺衍生物和相关化合物 |
| WO2009042907A1 (en) | 2007-09-27 | 2009-04-02 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Isoindoline compounds for the treatment of spinal muscular atrophy and other uses |
| GB0720912D0 (en) | 2007-10-25 | 2007-12-05 | Univ Cardiff | Monoclonal Anitbody for APP |
| WO2009054537A1 (ja) | 2007-10-25 | 2009-04-30 | Kagoshima University | アミロイドβペプチドのミミック分子を用いたペプチドワクチン |
| EA201070539A1 (ru) | 2007-10-29 | 2010-10-29 | Энсэрм (Энститю Насьональ Де Ля Санте Э Де Ля Решерш Медикаль) | НОВЫЕ АНТИТЕЛА, СПЕЦИФИЧНЫЕ К β-АМИЛОИДНЫМ ПЕПТИДАМ, И ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ ДИАГНОСТИЧЕСКИХ ИЛИ ЛЕКАРСТВЕННЫХ СРЕДСТВ |
| DK2207568T3 (en) | 2007-11-16 | 2017-09-18 | Univ Rockefeller | ANTIBODIES SPECIFIC TO THE PROTOFIBRILE FORM OF BETA AMYLOID PROTEIN |
| EP2231180B1 (en) | 2008-01-16 | 2016-08-17 | Ben-gurion University Of The Negev Research And Development Authority | Vaccine for alzheimer's disease |
| ITNA20080006A1 (it) | 2008-01-28 | 2009-07-29 | Consiglio Nazionale Ricerche | Proteine chimeriche capaci di formare particelle virus-like, che contengono sequenze peptidiche del beta-amiloide e la componente e2 della alfachetoacido deidrogenasi di "geobacillus stearothermophilus", utili per l'induzione di una risposta anticorp |
| WO2009108550A1 (en) | 2008-02-28 | 2009-09-03 | Merck & Co., Inc. | 2-aminoimidazole beta-secretase inhibitors for the treatment of alzheimer's disease |
| WO2009134750A1 (en) | 2008-04-28 | 2009-11-05 | Janssen Pharmaceutica Nv | Benzoimidazoles as prolyl hydroxylase inhibitors |
| AU2009271019A1 (en) * | 2008-07-14 | 2010-01-21 | Gilead Sciences, Inc. | Fused heterocyclyc inhibitors of histone deacetylase and/or cyclin-dependent kinases |
| WO2010011947A2 (en) | 2008-07-25 | 2010-01-28 | Abbott Laboratories | AMYLOID ß PEPTIDE ANALOGUES, OLIGOMERS THEREOF, PROCESSES FOR PREPARING AND COMPOSITIONS COMPRISING SAID ANALOGUES OR OLIGOMERS, AND THEIR USES |
| WO2010016912A2 (en) | 2008-08-07 | 2010-02-11 | Mercia Pharma, Llc | Immunotherapeutic compositions for the treatment of alzheimer's disease |
| EP2324032B1 (en) | 2008-08-19 | 2014-10-01 | Vitae Pharmaceuticals, Inc. | Inhibitors of beta-secretase |
| EP2344157B1 (en) * | 2008-09-04 | 2016-05-25 | Probiodrug AG | Novel inhibitors |
| KR101640147B1 (ko) | 2008-10-16 | 2016-07-18 | 잇빤 자이단호진 가가쿠오요비겟세이료호겐쿠쇼 | 변성된 아밀로이드 베타 펩티드 |
| US20110224231A1 (en) | 2008-11-23 | 2011-09-15 | Pfizer Inc. | Novel Lactams as Beta Secretase Inhibitors |
| EP2393776B1 (en) | 2009-02-06 | 2014-05-14 | Merck Sharp & Dohme Corp. | Novel trifluoromethylsulfonamide gamma secretase inhibitor |
| WO2010094242A1 (en) | 2009-02-20 | 2010-08-26 | Merck Sharp & Dohme Corp. | Spiropyrrolidine beta-secretase inhibitors for the treatment of alzheimer's disease |
-
2010
- 2010-09-13 CN CN201080050870.XA patent/CN102695546B/zh active Active
- 2010-09-13 ES ES10751952.2T patent/ES2548913T3/es active Active
- 2010-09-13 SG SG2012014817A patent/SG178953A1/en unknown
- 2010-09-13 NZ NZ598685A patent/NZ598685A/xx unknown
- 2010-09-13 CA CA2772488A patent/CA2772488C/en active Active
- 2010-09-13 PL PL10751952T patent/PL2475428T3/pl unknown
- 2010-09-13 AU AU2010294214A patent/AU2010294214B2/en active Active
- 2010-09-13 US US12/880,369 patent/US8486940B2/en active Active
- 2010-09-13 DK DK10751952.2T patent/DK2475428T3/en active
- 2010-09-13 MX MX2012002993A patent/MX2012002993A/es active IP Right Grant
- 2010-09-13 BR BR112012008346-5A patent/BR112012008346B1/pt active IP Right Grant
- 2010-09-13 KR KR1020127008546A patent/KR101755737B1/ko active Active
- 2010-09-13 EP EP10751952.2A patent/EP2475428B1/en active Active
- 2010-09-13 JP JP2012528379A patent/JP5934645B2/ja active Active
- 2010-09-13 WO PCT/EP2010/063341 patent/WO2011029920A1/en not_active Ceased
- 2010-09-13 EA EA201200474A patent/EA022007B1/ru unknown
-
2012
- 2012-02-22 IL IL218259A patent/IL218259A/en active IP Right Grant
- 2012-02-23 ZA ZA2012/01366A patent/ZA201201366B/en unknown
-
2013
- 2013-06-05 US US13/910,702 patent/US9173885B2/en active Active
-
2015
- 2015-09-23 US US14/862,245 patent/US9650362B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| CN102695546A (zh) | 2012-09-26 |
| DK2475428T3 (en) | 2015-09-28 |
| EP2475428A1 (en) | 2012-07-18 |
| NZ598685A (en) | 2013-05-31 |
| CA2772488A1 (en) | 2011-03-17 |
| US20140065095A1 (en) | 2014-03-06 |
| WO2011029920A1 (en) | 2011-03-17 |
| JP5934645B2 (ja) | 2016-06-15 |
| KR101755737B1 (ko) | 2017-07-07 |
| US8486940B2 (en) | 2013-07-16 |
| SG178953A1 (en) | 2012-04-27 |
| EP2475428B1 (en) | 2015-07-01 |
| CN102695546B (zh) | 2014-09-10 |
| MX2012002993A (es) | 2012-04-19 |
| KR20120105421A (ko) | 2012-09-25 |
| US9173885B2 (en) | 2015-11-03 |
| AU2010294214A1 (en) | 2012-03-29 |
| US20110092501A1 (en) | 2011-04-21 |
| EA022007B1 (ru) | 2015-10-30 |
| JP2013504544A (ja) | 2013-02-07 |
| IL218259A (en) | 2016-09-29 |
| EA201200474A1 (ru) | 2012-10-30 |
| US20160039795A1 (en) | 2016-02-11 |
| BR112012008346A2 (pt) | 2020-09-15 |
| PL2475428T3 (pl) | 2015-12-31 |
| BR112012008346B1 (pt) | 2021-12-21 |
| AU2010294214B2 (en) | 2015-05-07 |
| US9650362B2 (en) | 2017-05-16 |
| CA2772488C (en) | 2018-04-17 |
| HK1175135A1 (en) | 2013-06-28 |
| IL218259A0 (en) | 2012-04-30 |
| ZA201201366B (en) | 2013-09-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2548913T3 (es) | Derivados heterocíclicos como inhibidores de glutaminil ciclasa | |
| ES2599621T3 (es) | Nuevos inhibidores | |
| CN110382503B (zh) | 制备acc抑制剂及其固体形式的方法 | |
| US11040035B2 (en) | 3-oxo-2,6-diphenyl-2,3-dihydropyridazine-4-carboxamides | |
| ES2478673T3 (es) | Derivados de tioxoquinazolinona como inhibidores de la glutaminil ciclasa | |
| RU2518073C2 (ru) | Новое бициклическое гетероциклическое соединение | |
| ES2586231T3 (es) | Inhibidores de glutaminil ciclasa | |
| US8952158B2 (en) | Tricyclic compound and use thereof | |
| EA029451B1 (ru) | Новые ингибиторы | |
| US20200289509A1 (en) | 2-hetarylpyrimidine-4-carboxamides as aryl hydrocarbon receptor anatgonists | |
| KR20170102885A (ko) | 삼환성 스피로 화합물 | |
| US20200283395A1 (en) | 2-phenylpyrimidine-4-carboxamides as ahr inhibitors | |
| JP6204983B2 (ja) | Ccr2のオクタヒドロ−シクロペンタピロリル拮抗薬 | |
| JP2002511085A (ja) | α1aアドレナリン受容体拮抗薬 | |
| CN101262864A (zh) | 饱和o-杂环取代的烷酰胺 | |
| JP3273777B2 (ja) | 複素環化合物、その製造法および用途 | |
| JP7713954B2 (ja) | 核内受容体に対して活性な化合物 | |
| BR112022019057B1 (pt) | Aminotiazóis substituídos como inibidores de dgkzeta para ativação imune, seus usos, composição e combinação farmacêuticas, e kit | |
| JP2002069070A (ja) | 複素環化合物、その製造法および用途 | |
| HK1178528B (en) | Heterocyclic inhibitors of glutaminyl cyclase (qc, ec 2.3.2.5) |