RU2008147543A - Агонисты мускариновых рецепторов, эффективные при лечении боли, болезни альцгеймера и шизофрении - Google Patents
Агонисты мускариновых рецепторов, эффективные при лечении боли, болезни альцгеймера и шизофрении Download PDFInfo
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- RU2008147543A RU2008147543A RU2008147543/04A RU2008147543A RU2008147543A RU 2008147543 A RU2008147543 A RU 2008147543A RU 2008147543/04 A RU2008147543/04 A RU 2008147543/04A RU 2008147543 A RU2008147543 A RU 2008147543A RU 2008147543 A RU2008147543 A RU 2008147543A
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- Prior art keywords
- alkyl
- alkoxy
- heteroaryl
- heterocycloalkyl
- aryl
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- 208000024827 Alzheimer disease Diseases 0.000 title claims 3
- 201000000980 schizophrenia Diseases 0.000 title claims 3
- UQOFGTXDASPNLL-XHNCKOQMSA-N Muscarine Chemical compound C[C@@H]1O[C@H](C[N+](C)(C)C)C[C@H]1O UQOFGTXDASPNLL-XHNCKOQMSA-N 0.000 title 1
- 239000000018 receptor agonist Substances 0.000 title 1
- 229940044601 receptor agonist Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract 53
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims abstract 52
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 50
- 150000002431 hydrogen Chemical class 0.000 claims abstract 48
- 239000001257 hydrogen Substances 0.000 claims abstract 48
- 229910052736 halogen Inorganic materials 0.000 claims abstract 33
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims abstract 32
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract 31
- 150000002367 halogens Chemical class 0.000 claims abstract 31
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract 29
- 125000005553 heteroaryloxy group Chemical group 0.000 claims abstract 23
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 13
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract 13
- 125000002947 alkylene group Chemical group 0.000 claims abstract 12
- -1 C1-6 alkyl halogen Chemical class 0.000 claims abstract 9
- 150000003839 salts Chemical class 0.000 claims abstract 6
- 239000000203 mixture Substances 0.000 claims abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract 3
- 125000000217 alkyl group Chemical group 0.000 claims 174
- 125000003545 alkoxy group Chemical group 0.000 claims 133
- 125000001072 heteroaryl group Chemical group 0.000 claims 42
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 32
- 125000003118 aryl group Chemical group 0.000 claims 31
- 125000004104 aryloxy group Chemical group 0.000 claims 22
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 22
- 125000000753 cycloalkyl group Chemical group 0.000 claims 21
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 12
- PBVFROWIWWGIFK-UHFFFAOYSA-N fluoromethyl-(2-hydroxyethyl)-dimethylazanium Chemical compound FC[N+](C)(C)CCO PBVFROWIWWGIFK-UHFFFAOYSA-N 0.000 claims 12
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 11
- 238000000034 method Methods 0.000 claims 9
- 125000003282 alkyl amino group Chemical group 0.000 claims 8
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 5
- 230000003993 interaction Effects 0.000 claims 5
- 239000003814 drug Substances 0.000 claims 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 4
- 238000004519 manufacturing process Methods 0.000 claims 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 3
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 3
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims 2
- 230000015572 biosynthetic process Effects 0.000 claims 2
- 239000003153 chemical reaction reagent Substances 0.000 claims 2
- 239000003638 chemical reducing agent Substances 0.000 claims 2
- 125000006545 (C1-C9) alkyl group Chemical group 0.000 claims 1
- DMQNYYUSRGZMNA-IBGZPJMESA-N 1-methyl-3-[1-[(3s)-1-[3-(2-oxopyrrolidin-1-yl)propanoyl]pyrrolidin-3-yl]piperidin-4-yl]benzimidazol-2-one Chemical compound C([C@@H](C1)N2CCC(CC2)N2C3=CC=CC=C3N(C2=O)C)CN1C(=O)CCN1CCCC1=O DMQNYYUSRGZMNA-IBGZPJMESA-N 0.000 claims 1
- WQMADGKABXWRPB-UHFFFAOYSA-N 3-[1-(1-butanoylpyrrolidin-3-yl)piperidin-4-yl]-1h-benzimidazol-2-one Chemical compound C1N(C(=O)CCC)CCC1N1CCC(N2C(NC3=CC=CC=C32)=O)CC1 WQMADGKABXWRPB-UHFFFAOYSA-N 0.000 claims 1
- KIKVFRJEORTHAK-SFHVURJKSA-N 3-[1-[(3s)-1-(cyclopentanecarbonyl)pyrrolidin-3-yl]piperidin-4-yl]-1h-benzimidazol-2-one Chemical compound C([C@H](CC1)N2CCC(CC2)N2C(NC3=CC=CC=C32)=O)N1C(=O)C1CCCC1 KIKVFRJEORTHAK-SFHVURJKSA-N 0.000 claims 1
- JNOJPZRLZGKCBU-LPHOPBHVSA-N 3-[1-[(3s)-1-[(2s)-oxolane-2-carbonyl]pyrrolidin-3-yl]piperidin-4-yl]-1h-benzimidazol-2-one Chemical compound C([C@H](CC1)N2CCC(CC2)N2C(NC3=CC=CC=C32)=O)N1C(=O)[C@@H]1CCCO1 JNOJPZRLZGKCBU-LPHOPBHVSA-N 0.000 claims 1
- VTIHIQFWUKTACE-UHFFFAOYSA-N 3-[1-[1-(3-methylbutanoyl)pyrrolidin-3-yl]piperidin-4-yl]-1h-benzimidazol-2-one Chemical compound C1N(C(=O)CC(C)C)CCC1N1CCC(N2C(NC3=CC=CC=C32)=O)CC1 VTIHIQFWUKTACE-UHFFFAOYSA-N 0.000 claims 1
- 208000019901 Anxiety disease Diseases 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 230000036506 anxiety Effects 0.000 claims 1
- HPTPNUOHRVVTRL-UHFFFAOYSA-N benzyl 3-[4-(2-oxo-3h-benzimidazol-1-yl)piperidin-1-yl]pyrrolidine-1-carboxylate Chemical compound C1CC(N2CCC(CC2)N2C(NC3=CC=CC=C32)=O)CN1C(=O)OCC1=CC=CC=C1 HPTPNUOHRVVTRL-UHFFFAOYSA-N 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- HXYQHTSHRKZZEB-OAHLLOKOSA-N ethyl (3r)-3-[4-(2-oxo-3h-benzimidazol-1-yl)piperidin-1-yl]pyrrolidine-1-carboxylate Chemical compound C1N(C(=O)OCC)CC[C@H]1N1CCC(N2C(NC3=CC=CC=C32)=O)CC1 HXYQHTSHRKZZEB-OAHLLOKOSA-N 0.000 claims 1
- HXYQHTSHRKZZEB-HNNXBMFYSA-N ethyl (3s)-3-[4-(2-oxo-3h-benzimidazol-1-yl)piperidin-1-yl]pyrrolidine-1-carboxylate Chemical compound C1N(C(=O)OCC)CC[C@@H]1N1CCC(N2C(NC3=CC=CC=C32)=O)CC1 HXYQHTSHRKZZEB-HNNXBMFYSA-N 0.000 claims 1
- UGVSPMUTKNEWKD-HNNXBMFYSA-N ethyl (3s)-3-[4-[2-oxo-6-(trifluoromethyl)-3h-benzimidazol-1-yl]piperidin-1-yl]pyrrolidine-1-carboxylate Chemical compound C1N(C(=O)OCC)CC[C@@H]1N1CCC(N2C(NC3=CC=C(C=C32)C(F)(F)F)=O)CC1 UGVSPMUTKNEWKD-HNNXBMFYSA-N 0.000 claims 1
- HXYQHTSHRKZZEB-UHFFFAOYSA-N ethyl 3-[4-(2-oxo-3h-benzimidazol-1-yl)piperidin-1-yl]pyrrolidine-1-carboxylate Chemical compound C1N(C(=O)OCC)CCC1N1CCC(N2C(NC3=CC=CC=C32)=O)CC1 HXYQHTSHRKZZEB-UHFFFAOYSA-N 0.000 claims 1
- CYPTXTYYWOUWKO-UHFFFAOYSA-N ethyl 3-[4-(5-chloro-2-oxo-3h-benzimidazol-1-yl)piperidin-1-yl]pyrrolidine-1-carboxylate Chemical compound C1N(C(=O)OCC)CCC1N1CCC(N2C(NC3=CC(Cl)=CC=C32)=O)CC1 CYPTXTYYWOUWKO-UHFFFAOYSA-N 0.000 claims 1
- RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical compound C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 claims 1
- PCODWIPXFMYUEX-AWEZNQCLSA-N methyl (3s)-3-[4-(2-oxo-3h-benzimidazol-1-yl)piperidin-1-yl]pyrrolidine-1-carboxylate Chemical compound C1N(C(=O)OC)CC[C@@H]1N1CCC(N2C(NC3=CC=CC=C32)=O)CC1 PCODWIPXFMYUEX-AWEZNQCLSA-N 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- NYCVCXMSZNOGDH-UHFFFAOYSA-N pyrrolidine-1-carboxylic acid Chemical compound OC(=O)N1CCCC1 NYCVCXMSZNOGDH-UHFFFAOYSA-N 0.000 claims 1
- 238000006722 reduction reaction Methods 0.000 claims 1
- 238000006268 reductive amination reaction Methods 0.000 claims 1
- VKQFQFLXAGPJKI-INIZCTEOSA-N tert-butyl (3s)-3-[4-(2-oxo-3h-benzimidazol-1-yl)piperidin-1-yl]pyrrolidine-1-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CC[C@@H]1N1CCC(N2C(NC3=CC=CC=C32)=O)CC1 VKQFQFLXAGPJKI-INIZCTEOSA-N 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 3
- 0 *C(N(CC1)CC1=O)=O Chemical compound *C(N(CC1)CC1=O)=O 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
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- 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
- A61K31/439—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 the ring forming part of a bridged ring system, e.g. quinuclidine
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
- C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
-
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- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Addiction (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Psychology (AREA)
- Communicable Diseases (AREA)
- Hematology (AREA)
- Virology (AREA)
- Transplantation (AREA)
- Oncology (AREA)
- Cardiology (AREA)
- Hospice & Palliative Care (AREA)
- Child & Adolescent Psychology (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US81220806P | 2006-06-09 | 2006-06-09 | |
| US60/812,208 | 2006-06-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2008147543A true RU2008147543A (ru) | 2010-07-20 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2008147543/04A RU2008147543A (ru) | 2006-06-09 | 2007-06-08 | Агонисты мускариновых рецепторов, эффективные при лечении боли, болезни альцгеймера и шизофрении |
Country Status (18)
| Country | Link |
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| US (1) | US20100173935A1 (OSRAM) |
| EP (1) | EP2035412A4 (OSRAM) |
| JP (1) | JP2009539833A (OSRAM) |
| KR (1) | KR20090016636A (OSRAM) |
| CN (1) | CN101501024A (OSRAM) |
| AR (1) | AR061306A1 (OSRAM) |
| AU (1) | AU2007256014B2 (OSRAM) |
| BR (1) | BRPI0712415A2 (OSRAM) |
| CA (1) | CA2654147A1 (OSRAM) |
| EC (1) | ECSP088967A (OSRAM) |
| IL (1) | IL195427A0 (OSRAM) |
| MX (1) | MX2008015155A (OSRAM) |
| NO (1) | NO20085271L (OSRAM) |
| RU (1) | RU2008147543A (OSRAM) |
| TW (1) | TW200815405A (OSRAM) |
| UY (1) | UY30393A1 (OSRAM) |
| WO (1) | WO2007142585A1 (OSRAM) |
| ZA (1) | ZA200809976B (OSRAM) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200813018A (en) * | 2006-06-09 | 2008-03-16 | Astrazeneca Ab | Novel compounds |
| KR20140139125A (ko) | 2007-08-31 | 2014-12-04 | 퍼듀 퍼머 엘피 | 치환-퀴녹살린-형 피페리딘 화합물 및 그의 용도 |
| UY31672A1 (es) * | 2008-02-28 | 2009-09-30 | "agonistas de receptores muscarínicos composiciones farmacéuticas métodos de tratamiento de los mismos, y procedimientos para su preparación" | |
| US20090221642A1 (en) * | 2008-03-03 | 2009-09-03 | Astrazeneca Ab | Muscarinic receptor agonists, compositions, methods of treatment thereof, and processes for preparation thereof-176 |
| HRP20120841T4 (hr) | 2008-07-21 | 2015-07-03 | Purdue Pharma L.P. | Premošteni piperidinski spojevi substituiranog kinoksalin-tipa i njihova uporaba |
| GB0817982D0 (en) * | 2008-10-01 | 2008-11-05 | Glaxo Group Ltd | Compounds |
| TW201211028A (en) * | 2010-08-10 | 2012-03-16 | Dainippon Sumitomo Pharma Co | Fused ring pyrrolidine derivatives |
| CA2835261C (en) | 2011-05-06 | 2019-06-04 | Zafgen, Inc. | Partially saturated tricyclic compounds and methods of making and using same |
| JP2015083543A (ja) * | 2012-02-14 | 2015-04-30 | 大日本住友製薬株式会社 | 新規縮環ピロリジン誘導体 |
| US20140171466A1 (en) * | 2012-08-14 | 2014-06-19 | Regents Of The University Of Minnesota | Pain management in sickle cell anemia |
| DK2897948T3 (en) * | 2012-09-18 | 2016-12-05 | Heptares Therapeutics Ltd | BICYCLIC AZA RELATIONS AS MUSCARIN M1 RECEPTOR AGONISTS |
| NZ707773A (en) | 2012-11-05 | 2019-05-31 | Zafgen Inc | Methods of treating liver diseases |
| CN121824387A (zh) * | 2026-03-12 | 2026-04-10 | 济南国鼎医药科技有限公司 | 一种(R)-1-Boc-3-氨基吡咯烷的制备方法 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5524326A (en) * | 1993-01-21 | 1996-06-11 | Markowitz; Eli | Interactive game between pet and owner |
| EP0786997A4 (en) * | 1994-10-27 | 1998-03-11 | Merck & Co Inc | MUSCARINE ANTAGONISTS |
| US5756508A (en) * | 1995-10-31 | 1998-05-26 | Merck & Co., Inc. | Muscarine antagonists |
| WO1999032481A1 (en) * | 1997-12-23 | 1999-07-01 | Alcon Laboratories, Inc. | Muscarinic agents and use thereof to treat glaucoma, myopia and various other conditions |
| ES2223588T3 (es) * | 1999-10-13 | 2005-03-01 | Banyu Pharmaceutical Co., Ltd. | Derivados de imidazolidinona sustituidos. |
| US7164024B2 (en) * | 2001-04-20 | 2007-01-16 | Banyu Pharmaceutical Co., Ltd. | Benzimidazolone derivatives |
| WO2004089942A2 (en) * | 2001-10-02 | 2004-10-21 | Acadia Pharmaceuticals Inc. | Benzimidazolidinone derivatives as muscarinic agents |
| CA2488845A1 (en) * | 2002-06-17 | 2003-12-24 | Merck & Co., Inc. | Opthalmic compositions containing selective m1 muscarinic agonists for treating ocular hypertension |
| JPWO2004069828A1 (ja) * | 2003-02-04 | 2006-05-25 | 三菱ウェルファーマ株式会社 | ピペリジン化合物およびその医薬用途 |
| EP1753748B1 (en) * | 2004-05-12 | 2009-07-29 | Pfizer Products Inc. | Proline derivatives and their use as dipeptidyl peptidase iv inhibitors |
| CA2568524A1 (en) * | 2004-05-28 | 2005-12-15 | Vertex Pharmaceuticals Incorporated | Modulators of muscarinic receptors |
| TW200815351A (en) * | 2006-05-02 | 2008-04-01 | Astrazeneca Ab | Novel compounds |
| TW200813018A (en) * | 2006-06-09 | 2008-03-16 | Astrazeneca Ab | Novel compounds |
| US8119661B2 (en) * | 2007-09-11 | 2012-02-21 | Astrazeneca Ab | Piperidine derivatives and their use as muscarinic receptor modulators |
| UY31672A1 (es) * | 2008-02-28 | 2009-09-30 | "agonistas de receptores muscarínicos composiciones farmacéuticas métodos de tratamiento de los mismos, y procedimientos para su preparación" | |
| US20090221642A1 (en) * | 2008-03-03 | 2009-09-03 | Astrazeneca Ab | Muscarinic receptor agonists, compositions, methods of treatment thereof, and processes for preparation thereof-176 |
| US20090275574A1 (en) * | 2008-05-05 | 2009-11-05 | Astrazeneca Ab | Novel compounds-300 |
-
2007
- 2007-05-29 TW TW096119136A patent/TW200815405A/zh unknown
- 2007-06-06 UY UY30393A patent/UY30393A1/es unknown
- 2007-06-08 KR KR1020097000416A patent/KR20090016636A/ko not_active Withdrawn
- 2007-06-08 CN CNA2007800294554A patent/CN101501024A/zh active Pending
- 2007-06-08 RU RU2008147543/04A patent/RU2008147543A/ru not_active Application Discontinuation
- 2007-06-08 CA CA002654147A patent/CA2654147A1/en not_active Abandoned
- 2007-06-08 JP JP2009514233A patent/JP2009539833A/ja active Pending
- 2007-06-08 AU AU2007256014A patent/AU2007256014B2/en not_active Expired - Fee Related
- 2007-06-08 MX MX2008015155A patent/MX2008015155A/es not_active Application Discontinuation
- 2007-06-08 EP EP07748219A patent/EP2035412A4/en not_active Withdrawn
- 2007-06-08 AR ARP070102508A patent/AR061306A1/es unknown
- 2007-06-08 US US12/303,641 patent/US20100173935A1/en not_active Abandoned
- 2007-06-08 WO PCT/SE2007/000556 patent/WO2007142585A1/en not_active Ceased
- 2007-06-08 BR BRPI0712415-5A patent/BRPI0712415A2/pt not_active IP Right Cessation
-
2008
- 2008-11-20 IL IL195427A patent/IL195427A0/en unknown
- 2008-11-24 ZA ZA2008/09976A patent/ZA200809976B/en unknown
- 2008-12-12 EC EC2008008967A patent/ECSP088967A/es unknown
- 2008-12-16 NO NO20085271A patent/NO20085271L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AU2007256014B2 (en) | 2011-06-30 |
| ZA200809976B (en) | 2011-04-28 |
| BRPI0712415A2 (pt) | 2012-09-04 |
| CN101501024A (zh) | 2009-08-05 |
| IL195427A0 (en) | 2009-08-03 |
| CA2654147A1 (en) | 2007-12-13 |
| ECSP088967A (es) | 2009-01-30 |
| MX2008015155A (es) | 2008-12-12 |
| US20100173935A1 (en) | 2010-07-08 |
| KR20090016636A (ko) | 2009-02-16 |
| TW200815405A (en) | 2008-04-01 |
| AR061306A1 (es) | 2008-08-20 |
| UY30393A1 (es) | 2009-04-30 |
| NO20085271L (no) | 2009-01-06 |
| AU2007256014A1 (en) | 2007-12-13 |
| JP2009539833A (ja) | 2009-11-19 |
| EP2035412A1 (en) | 2009-03-18 |
| EP2035412A4 (en) | 2011-02-16 |
| WO2007142585A1 (en) | 2007-12-13 |
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