WO2007034282A3 - Diaryl-imidazole compounds condensed with a heterocycle as c3a receptor antagonists - Google Patents
Diaryl-imidazole compounds condensed with a heterocycle as c3a receptor antagonists Download PDFInfo
- Publication number
- WO2007034282A3 WO2007034282A3 PCT/IB2006/002568 IB2006002568W WO2007034282A3 WO 2007034282 A3 WO2007034282 A3 WO 2007034282A3 IB 2006002568 W IB2006002568 W IB 2006002568W WO 2007034282 A3 WO2007034282 A3 WO 2007034282A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- diaryl
- heterocycle
- receptor antagonists
- imidazole compounds
- compounds condensed
- 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.)
- Ceased
Links
Classifications
-
- 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
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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]
-
- 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
-
- 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)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurosurgery (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Neurology (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Aryl substituted imidazo[4,5-c] pyridine compounds are provided. These compounds are useful in pharmaceutical compositions as C3a antagonists for treating a variety of medical conditions associated with the Complement cascade. Methods for treating such conditions are also provided.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71851705P | 2005-09-19 | 2005-09-19 | |
| US60/718,517 | 2005-09-19 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2007034282A2 WO2007034282A2 (en) | 2007-03-29 |
| WO2007034282A3 true WO2007034282A3 (en) | 2007-05-18 |
Family
ID=37807741
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/IB2006/002568 Ceased WO2007034282A2 (en) | 2005-09-19 | 2006-09-18 | Diaryl-imidazole compounds condensed with a heterocycle as c3a receptor antagonists |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2007034282A2 (en) |
Cited By (1)
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|---|---|---|---|---|
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| ES2338904T3 (en) | 2004-10-26 | 2010-05-13 | EISAI R&D MANAGEMENT CO., LTD. | FORM AMORFA OF CINAMIDE COMPOUNDS. |
| JP5221144B2 (en) | 2005-11-24 | 2013-06-26 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | Morpholine-type cinnamide compounds |
| TWI370130B (en) | 2005-11-24 | 2012-08-11 | Eisai R&D Man Co Ltd | Two cyclic cinnamide compound |
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| US7563797B2 (en) | 2006-08-28 | 2009-07-21 | Forest Laboratories Holding Limited | Substituted imidazo(1,2-A)pyrimidines and imidazo(1,2-A) pyridines as cannabinoid receptor ligands |
| US20110021513A1 (en) * | 2006-09-07 | 2011-01-27 | Biogen Idec Ma Inc. | Modulators of interleukin-1 receptor-associated kinase |
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| EP1964841A1 (en) * | 2007-02-28 | 2008-09-03 | sanofi-aventis | Imidazo[1,2-a]azine and their use as pharmaceuticals |
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| EP2193134A4 (en) | 2007-09-05 | 2011-09-14 | Univ Alberta | PROCESS FOR THE ORGANOCATALYTIC ACTIVATION OF CARBOXYLIC ACIDS FOR CHEMICAL REACTIONS USING ORTHOSUBSTITUTED ARYLBORONIC ACIDS |
| CN102702195A (en) * | 2007-10-30 | 2012-10-03 | 日本医事物理股份有限公司 | Use of novel compound having affinity for amyloid, and process for production of the same |
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| PH12012501841B1 (en) * | 2010-03-18 | 2018-01-12 | Inst Nat Sante Rech Med | Anti-infective compounds |
| US8410117B2 (en) * | 2010-03-26 | 2013-04-02 | Hoffmann-La Roche Inc. | Imidazopyrimidine derivatives |
| EP2648723A4 (en) | 2010-12-08 | 2014-04-02 | Univ Vanderbilt | USE OF BICYCLIC PYRAZOLE COMPOUNDS AS ALLUSTERIC MODULATORS OF MGLUR5 RECEPTORS |
| WO2012125732A1 (en) * | 2011-03-15 | 2012-09-20 | Vanderbilt University | Substituted imadazapyrinidin-5(6h)-ones as allosteric modulators of mglur5 receptors |
| AU2012272550B2 (en) * | 2011-06-20 | 2017-06-01 | The University Of Queensland | Prevention and treatment of acute inflammatory conditions |
| AU2012272706B2 (en) | 2011-06-22 | 2017-07-06 | Apellis Pharmaceuticals, Inc. | Methods of treating chronic disorders with complement inhibitors |
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| DK2767532T3 (en) | 2012-12-21 | 2016-09-12 | Nat Inst For Quantum And Radiological Science And Tech | New connection for reproduction of tau protein heavy in the brain. |
| EP2951170B1 (en) * | 2013-02-04 | 2018-10-24 | Janssen Pharmaceutica NV | Flap modulators |
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| JP6130055B2 (en) * | 2013-05-23 | 2017-05-17 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | 2-Phenylimidazo [1.2-A] pyrimidine as a contrast agent |
| EP3302710A4 (en) | 2015-06-03 | 2019-02-20 | The University of Queensland | MOBILIZING AGENTS AND USES THEREOF |
| TW201718581A (en) | 2015-10-19 | 2017-06-01 | 英塞特公司 | Heterocyclic compounds as immunomodulators |
| LT3377488T (en) | 2015-11-19 | 2023-01-10 | Incyte Corporation | HETEROCYCLIC COMPOUNDS AS IMMUNOMODULATORS |
| CN105439965B (en) * | 2015-11-20 | 2018-05-22 | 江苏恒安化工有限公司 | The synthetic method of quinoxaline heterocycle and its derivative |
| US20170174679A1 (en) | 2015-12-22 | 2017-06-22 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
| MA44860A (en) | 2016-05-06 | 2019-03-13 | Incyte Holdings Corp | HETEROCYCLIC COMPOUNDS USED AS IMMUNOMODULATORS |
| WO2017205464A1 (en) | 2016-05-26 | 2017-11-30 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
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| WO2018119221A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Pyridine derivatives as immunomodulators |
| JP7303108B2 (en) | 2016-12-22 | 2023-07-04 | インサイト・コーポレイション | Bicyclic heteroaromatic compounds as immunomodulators |
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| CN118812530A (en) * | 2023-04-18 | 2024-10-22 | 中国科学院大连化学物理研究所 | A method for preparing imidazopyridine compounds by catalyzing lignin and model compounds using a Pd/C two-component system |
| WO2025109474A1 (en) * | 2023-11-21 | 2025-05-30 | Novartis Ag | Substituted imidazoarenes and methods of their use |
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-
2006
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11566026B2 (en) | 2016-12-22 | 2023-01-31 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2007034282A2 (en) | 2007-03-29 |
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