AP2806A - 3H-imidazo[4,5-C] pyridine-6-carboxamides as anti-infammatory agents - Google Patents
3H-imidazo[4,5-C] pyridine-6-carboxamides as anti-infammatory agentsInfo
- Publication number
- AP2806A AP2806A AP2011005807A AP2011005807A AP2806A AP 2806 A AP2806 A AP 2806A AP 2011005807 A AP2011005807 A AP 2011005807A AP 2011005807 A AP2011005807 A AP 2011005807A AP 2806 A AP2806 A AP 2806A
- Authority
- AP
- ARIPO
- Prior art keywords
- carboxamides
- imidazo
- pyridine
- infammatory
- agents
- Prior art date
Links
- QIYBKHZLGLSNJX-UHFFFAOYSA-N 3h-imidazo[4,5-c]pyridine-6-carboxamide Chemical class C1=NC(C(=O)N)=CC2=C1N=CN2 QIYBKHZLGLSNJX-UHFFFAOYSA-N 0.000 title 1
Classifications
-
- 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
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/30—Nitrogen atoms not forming part of a nitro radical
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Pain & Pain Management (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09154414 | 2009-03-05 | ||
| EP09179618 | 2009-12-17 | ||
| PCT/EP2010/052799 WO2010100249A1 (fr) | 2009-03-05 | 2010-03-05 | 3h-imidazo[4,5-c]pyridine-6-carboxamides en tant qu'anti-inflammatoires |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AP2011005807A0 AP2011005807A0 (en) | 2011-08-31 |
| AP2806A true AP2806A (en) | 2013-11-30 |
Family
ID=42111729
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AP2011005807A AP2806A (en) | 2009-03-05 | 2010-03-05 | 3H-imidazo[4,5-C] pyridine-6-carboxamides as anti-infammatory agents |
Country Status (36)
| Country | Link |
|---|---|
| US (3) | US20100256188A1 (fr) |
| EP (1) | EP2403852B8 (fr) |
| JP (1) | JP5433708B2 (fr) |
| KR (1) | KR20110123764A (fr) |
| CN (1) | CN102341395B (fr) |
| AP (1) | AP2806A (fr) |
| AR (1) | AR075789A1 (fr) |
| AU (1) | AU2010220263B2 (fr) |
| BR (1) | BRPI1009118A2 (fr) |
| CA (1) | CA2753149A1 (fr) |
| CL (1) | CL2011002180A1 (fr) |
| CO (1) | CO6450668A2 (fr) |
| CY (1) | CY1115959T1 (fr) |
| DK (1) | DK2403852T3 (fr) |
| EA (1) | EA020282B1 (fr) |
| EC (1) | ECSP11011324A (fr) |
| ES (1) | ES2528730T3 (fr) |
| GE (1) | GEP20146034B (fr) |
| HR (1) | HRP20150096T1 (fr) |
| IL (1) | IL214033A0 (fr) |
| MA (1) | MA33239B1 (fr) |
| ME (1) | ME02117B (fr) |
| MX (1) | MX2011008948A (fr) |
| MY (1) | MY161092A (fr) |
| NZ (1) | NZ594589A (fr) |
| PE (1) | PE20120589A1 (fr) |
| PL (1) | PL2403852T3 (fr) |
| PT (1) | PT2403852E (fr) |
| RS (1) | RS53757B1 (fr) |
| SG (1) | SG174250A1 (fr) |
| SI (1) | SI2403852T1 (fr) |
| SM (1) | SMT201500053B (fr) |
| TN (1) | TN2011000446A1 (fr) |
| TW (1) | TWI466869B (fr) |
| UY (1) | UY32470A (fr) |
| WO (1) | WO2010100249A1 (fr) |
Families Citing this family (85)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UY32138A (es) | 2008-09-25 | 2010-04-30 | Boehringer Ingelheim Int | Amidas sustituidas del ácido 2-(2,6-dicloro-fenilamino)-6-fluoro-1-metil-1h-bencimidazol-5-carboxílico y sus sales farmacéuticamente aceptables |
| UY32470A (es) | 2009-03-05 | 2010-10-29 | Boehringer Ingelheim Int | Derivados de 2-{2-cloro-5-[(sustituido) metil]fenilamino} -1-metil]fenilamino}-1-metilbencimidazol-5-carboxamidas-n-(sustituidas) y sus sales fisiológicamente aceptables, composiciones conteniéndolos y aplicaciones |
| US8586604B2 (en) | 2010-08-20 | 2013-11-19 | Boehringer Ingelheim International Gmbh | Inhibitors of the microsomal prostaglandin E2 synthase-1 |
| US8759537B2 (en) * | 2010-08-20 | 2014-06-24 | Boehringer Ingelheim International Gmbh | 3H-imidazo [4, 5-C] pyridine-6-carboxamides as anti-inflammatory agents |
| TW201305178A (zh) | 2010-10-29 | 2013-02-01 | Glenmark Pharmaceuticals Sa | 作為mPGES-1抑制物的三環化合物 |
| US8466186B2 (en) * | 2010-12-10 | 2013-06-18 | Boehringer Ingelheim International Gmbh | Compounds |
| UY33779A (es) * | 2010-12-10 | 2012-07-31 | Boehringer Ingelheim Int | ?2-(fenilamino)-1H-bencimidazol-5-carboxamidas novedosas? |
| US8486968B2 (en) * | 2010-12-10 | 2013-07-16 | Boehringer Ingelheim International Gmbh | Compounds |
| AR084174A1 (es) | 2010-12-21 | 2013-04-24 | Lilly Co Eli | Compuestos de imidazol-2-benzamida utiles para el tratamiento de osteoartritis y una composicion farmaceutica |
| AR086254A1 (es) | 2011-05-26 | 2013-11-27 | Lilly Co Eli | Derivados de imidazol utiles para el tratamiento de artritis |
| WO2013038308A1 (fr) | 2011-09-15 | 2013-03-21 | Glenmark Pharmaceuticals S.A. | Composés à base d'hétéroaryle bicyclique substitué capables d'inhiber mpges-1 |
| MY167575A (en) * | 2011-10-14 | 2018-09-20 | Ambit Biosciences Corp | Heterocyclic compounds and use thereof as modulators of type iii receptor tyrosine kinases |
| WO2013072825A1 (fr) | 2011-11-16 | 2013-05-23 | Glenmark Pharmaceuticals S.A. | Dérivés de phtalazinone en tant qu'inhibiteurs de mpges-1 |
| US9006257B2 (en) | 2012-02-09 | 2015-04-14 | Glenmark Pharmaceuticals S.A. | Bicyclic compounds as mPGES-1 inhibitors |
| US9580398B2 (en) | 2012-04-02 | 2017-02-28 | The Trustees Of Columbia University In The City Of New York | Compounds, compositions, and methods for modulating ferroptosis and treating excitotoxic disorders |
| WO2013153535A1 (fr) | 2012-04-13 | 2013-10-17 | Glenmark Pharmaceuticals S.A. | Composés tricycliques à titre d'inhibiteurs de la mpges-1 |
| CN103450329B (zh) * | 2012-05-29 | 2015-05-27 | 首都医科大学 | 3h-咪唑并吡啶-6-甲酰氨基酸苄酯、其合成、抗肿瘤活性和应用 |
| TWI568722B (zh) * | 2012-06-15 | 2017-02-01 | 葛蘭馬克製藥公司 | 作爲mPGES-1抑制劑之三唑酮化合物 |
| WO2014167444A1 (fr) | 2013-04-08 | 2014-10-16 | Glenmark Pharmaceuticals S.A. | Composés bicycliques substitués utilisés en tant qu'inhibiteurs de mpges-1 |
| EP3010912A4 (fr) * | 2013-06-20 | 2016-12-07 | Novasaid Ab | Nouveaux dérivés pipéridinyle benzoimidazole utilisés comme inhibiteurs de la mpges-1 |
| WO2015059618A1 (fr) | 2013-10-22 | 2015-04-30 | Glenmark Pharmaceuticals S.A. | Composés de pyrimidine substitués utilisés en tant qu'inhibiteurs de mpges-1 |
| CA2939021C (fr) | 2014-02-11 | 2022-07-12 | Bayer Pharma Aktiengesellschaft | Benzimidazol-2-amines utilisees en tant qu'inhibiteurs de midh1 |
| BR112016018604A2 (pt) | 2014-02-11 | 2017-08-08 | Bayer Pharma AG | Benzimidazol-2-aminas como inibidores de midh1 |
| CN105198960B (zh) * | 2014-06-13 | 2018-10-19 | 首都医科大学 | 咪唑并吡啶-6-甲酰-Met-AA-OBzl,其合成,活性和应用 |
| CN105198959B (zh) * | 2014-06-13 | 2018-09-07 | 首都医科大学 | 咪唑并吡啶-6-甲酰-Met-Glu(OBzl)2,其合成,活性和应用 |
| CN105294829B (zh) * | 2014-06-13 | 2018-07-27 | 首都医科大学 | 咪唑并吡啶-6-甲酰-氨基酸苄酯,其合成,活性及应用 |
| CN105315326A (zh) * | 2014-07-10 | 2016-02-10 | 首都医科大学 | 咪唑并吡啶-6-甲酰-氨基酸苄酯,合成,活性和应用 |
| CN105315335A (zh) * | 2014-07-10 | 2016-02-10 | 首都医科大学 | 咪唑并吡啶-6-甲酰-Met-Gln-OBzl,其合成,活性和应用 |
| CN105315325A (zh) * | 2014-07-10 | 2016-02-10 | 首都医科大学 | 咪唑并吡啶-6-甲酰-Met-Arg(NO2)-OBzl,其合成,活性和应用 |
| HUE044602T2 (hu) | 2014-08-01 | 2019-11-28 | Glenmark Pharmaceuticals Sa | Nanorészecskés készítmény, amely egy MPGES-1 inhibitorot tartalmaz |
| EP3209660B1 (fr) | 2014-10-23 | 2020-06-17 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | 1-cyclohexyl -2-phénylaminobenzimidazoles en tant qu'inhibiteurs de midh1 dans le traitement de tumeurs |
| WO2016062677A1 (fr) | 2014-10-23 | 2016-04-28 | Bayer Pharma Aktiengesellschaft | Benzimidazol-2-amines en tant qu'inhibiteurs midh1 |
| AR102361A1 (es) | 2014-10-29 | 2017-02-22 | Lilly Co Eli | Compuestos de metil-quinolina útiles para inhibir la sintasa-1 de prostaglandina microsomal e2 |
| JO3581B1 (ar) * | 2014-10-29 | 2020-07-05 | Lilly Co Eli | مركبات ميثيل-بيبيريدين جديدة مفيدة لتثبيط إنزيم سينثاز -1 بروستاجلاندين e2 ميكروسومي |
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| US10414734B2 (en) | 2015-07-16 | 2019-09-17 | Bayer Pharma Aktiengesellschaft | 5-hydroxyalkylbenzimidazoles as mIDH1 inhibitors |
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| WO2020097400A1 (fr) | 2018-11-07 | 2020-05-14 | Dana-Farber Cancer Institute, Inc. | Dérivés d'imidazopyridine et dérivés d'aza-imidazopyridine utilisés comme inhibiteurs de la janus kinase 2 et utilisations associées |
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| EP3876939A4 (fr) | 2018-11-07 | 2022-08-10 | Dana-Farber Cancer Institute, Inc. | Dérivés benzothiazoles et dérivés 7-aza benzothiazoles comme inhibiteurs de la janus kinase 2 et leurs utilisations |
| AU2020301161B2 (en) | 2019-06-25 | 2023-10-26 | Gilead Sciences, Inc. | FLT3L-Fc fusion proteins and methods of use |
| WO2021040393A1 (fr) * | 2019-08-26 | 2021-03-04 | 국제약품 주식회사 | Dérivé d'indole carboxamide et composition pharmaceutique le contenant |
| KR102902719B1 (ko) | 2019-10-18 | 2025-12-24 | 포티 세븐, 엘엘씨 | 골수이형성 증후군 및 급성 골수성 백혈병을 치료하기 위한 조합 치료 |
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Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000068213A1 (fr) * | 1999-05-05 | 2000-11-16 | Aventis Pharma Limited | Composes bicycliques substitues |
| WO2001025238A2 (fr) * | 1999-10-06 | 2001-04-12 | Boehringer Ingelheim Pharmaceuticals, Inc. | Composes heterocycliques utiles comme inhibiteurs de tyrosine kinases |
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| WO2000068213A1 (fr) * | 1999-05-05 | 2000-11-16 | Aventis Pharma Limited | Composes bicycliques substitues |
| WO2001025238A2 (fr) * | 1999-10-06 | 2001-04-12 | Boehringer Ingelheim Pharmaceuticals, Inc. | Composes heterocycliques utiles comme inhibiteurs de tyrosine kinases |
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