WO2007034278A3 - Antagonistes du recepteur du c3a - Google Patents
Antagonistes du recepteur du c3a Download PDFInfo
- Publication number
- WO2007034278A3 WO2007034278A3 PCT/IB2006/002561 IB2006002561W WO2007034278A3 WO 2007034278 A3 WO2007034278 A3 WO 2007034278A3 IB 2006002561 W IB2006002561 W IB 2006002561W WO 2007034278 A3 WO2007034278 A3 WO 2007034278A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- receptor antagonists
- imidazole derivatives
- fused imidazole
- treating
- compounds
- Prior art date
Links
- 150000002460 imidazoles Chemical class 0.000 title 1
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 title 1
- 239000002464 receptor antagonist Substances 0.000 title 1
- 229940044551 receptor antagonist Drugs 0.000 title 1
- UBOOKRVGOBKDMM-UHFFFAOYSA-N 3h-imidazo[4,5-c]pyridine Chemical class C1=NC=C2NC=NC2=C1 UBOOKRVGOBKDMM-UHFFFAOYSA-N 0.000 abstract 1
- 239000005557 antagonist Substances 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 230000024203 complement activation Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- 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
-
- 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]
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pain & Pain Management (AREA)
- Pharmacology & Pharmacy (AREA)
- Rheumatology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
L'invention porte sur des composés imidazo[4,5-c] pyridine à substitution aryle. Ces composés sont utiles dans des compositions pharmaceutiques comme antagonistes du C3a pour traiter différentes affections médicales associées à la cascade du complément. L'invention porte également sur des méthodes de traitement correspondantes.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71845105P | 2005-09-19 | 2005-09-19 | |
| US60/718,451 | 2005-09-19 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2007034278A2 WO2007034278A2 (fr) | 2007-03-29 |
| WO2007034278A3 true WO2007034278A3 (fr) | 2007-05-18 |
Family
ID=37779396
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/IB2006/002561 WO2007034278A2 (fr) | 2005-09-19 | 2006-09-18 | Antagonistes du recepteur du c3a |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2007034278A2 (fr) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2485113C2 (ru) * | 2007-11-02 | 2013-06-20 | Хатчисон Медифарма Энтерпрайзис | Ингибиторы цитокинов |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007063946A1 (fr) * | 2005-11-30 | 2007-06-07 | Fujifilm Ri Pharma Co., Ltd. | Diagnostic et remede pour une maladie provoquee par l’aggregation et/ou le depot d’amyloide |
| EP2063962A2 (fr) * | 2006-09-07 | 2009-06-03 | Biogen Idec MA Inc. | Irak modulateurs pour le traitement d'une condition inflammatoire,d'une trouble proliferatif,immunologique |
| EP2184273A1 (fr) | 2008-11-05 | 2010-05-12 | Bayer CropScience AG | Composés substitués par l'halogène comme pesticides |
| BR112012023576B1 (pt) * | 2010-03-18 | 2022-08-23 | Institut Pasteur Korea | Compostos anti-infecciosos e composições compreendendo os mesmos |
| WO2011137587A1 (fr) * | 2010-05-06 | 2011-11-10 | Hutchison Medipharma Limited | Inhibiteurs de cytokines |
| AU2012272706B2 (en) | 2011-06-22 | 2017-07-06 | Apellis Pharmaceuticals, Inc. | Methods of treating chronic disorders with complement inhibitors |
| US9730447B2 (en) | 2013-04-15 | 2017-08-15 | E I Du Pont De Nemours And Company | Fungicidal amides |
| CA3026154A1 (fr) | 2015-06-03 | 2016-12-08 | The University Of Queensland | Agents mobilisateurs et leurs utilisations |
| CN115745848A (zh) * | 2022-12-07 | 2023-03-07 | 上海优合生物科技有限公司 | 一种氨基胍的加工合成工艺 |
| WO2025166319A1 (fr) | 2024-02-02 | 2025-08-07 | The Broad Institute, Inc. | Inhibiteurs de la cascade du complément |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001030778A1 (fr) * | 1999-10-27 | 2001-05-03 | Novartis Ag | Composes thiazole et imidazo [4,5-b] pyridine et leur utilisation pharmaceutique |
| EP1104762A1 (fr) * | 1998-08-03 | 2001-06-06 | Laboratorios S.A.L.V.A.T., S.A. | Imidazo 1,2a]azines substituees servant d'inhibiteurs selectifs de la cox-2 |
| WO2001057038A1 (fr) * | 2000-02-01 | 2001-08-09 | Basf Aktiengesellschaft | Composes heterocycliques et leur utilisation comme inhibiteurs de parp |
| WO2003051890A1 (fr) * | 2001-12-14 | 2003-06-26 | Aegera Therapeutics Inc. | Imidazo [2,1-b]-1,3,4-thiadiazole sulfonamides |
| WO2004111060A1 (fr) * | 2003-06-13 | 2004-12-23 | Aegera Therapeutics Inc. | Imidazo[2,1-b]-1,3,4-thiadiazole sulfoxydes et sulfones |
| WO2004111061A1 (fr) * | 2003-06-13 | 2004-12-23 | Aegera Therapeutics Inc. | Imidazo[2,1-b]-1,3,4,-thiadiazole-2-sulfonamides acyles et non acyles, et utilisations associees |
-
2006
- 2006-09-18 WO PCT/IB2006/002561 patent/WO2007034278A2/fr active Application Filing
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1104762A1 (fr) * | 1998-08-03 | 2001-06-06 | Laboratorios S.A.L.V.A.T., S.A. | Imidazo 1,2a]azines substituees servant d'inhibiteurs selectifs de la cox-2 |
| WO2001030778A1 (fr) * | 1999-10-27 | 2001-05-03 | Novartis Ag | Composes thiazole et imidazo [4,5-b] pyridine et leur utilisation pharmaceutique |
| WO2001057038A1 (fr) * | 2000-02-01 | 2001-08-09 | Basf Aktiengesellschaft | Composes heterocycliques et leur utilisation comme inhibiteurs de parp |
| WO2003051890A1 (fr) * | 2001-12-14 | 2003-06-26 | Aegera Therapeutics Inc. | Imidazo [2,1-b]-1,3,4-thiadiazole sulfonamides |
| WO2004111060A1 (fr) * | 2003-06-13 | 2004-12-23 | Aegera Therapeutics Inc. | Imidazo[2,1-b]-1,3,4-thiadiazole sulfoxydes et sulfones |
| WO2004111061A1 (fr) * | 2003-06-13 | 2004-12-23 | Aegera Therapeutics Inc. | Imidazo[2,1-b]-1,3,4,-thiadiazole-2-sulfonamides acyles et non acyles, et utilisations associees |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2485113C2 (ru) * | 2007-11-02 | 2013-06-20 | Хатчисон Медифарма Энтерпрайзис | Ингибиторы цитокинов |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2007034278A2 (fr) | 2007-03-29 |
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