WO2010127152A3 - Compounds and compositions as microsomal prostaglandin e synthase-1 inhibitors - Google Patents
Compounds and compositions as microsomal prostaglandin e synthase-1 inhibitors Download PDFInfo
- Publication number
- WO2010127152A3 WO2010127152A3 PCT/US2010/033022 US2010033022W WO2010127152A3 WO 2010127152 A3 WO2010127152 A3 WO 2010127152A3 US 2010033022 W US2010033022 W US 2010033022W WO 2010127152 A3 WO2010127152 A3 WO 2010127152A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- compounds
- inhibitors
- compositions
- synthase
- microsomal prostaglandin
- 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
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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]
- A61P29/02—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
-
- 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
- C07D403/02—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
-
- 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
- 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
- C07D409/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms 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
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Provided herein are compounds, and pharmaceutical compositions comprising such compounds, wherein the compounds are inhibitors of mPGES-1 activity. Also provided herein are methods of using such compounds and composition to treat or prevent diseases or disorders associated with the activity of mPGES-1.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17379509P | 2009-04-29 | 2009-04-29 | |
| US61/173,795 | 2009-04-29 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2010127152A2 WO2010127152A2 (en) | 2010-11-04 |
| WO2010127152A3 true WO2010127152A3 (en) | 2011-09-29 |
Family
ID=42272690
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2010/033022 Ceased WO2010127152A2 (en) | 2009-04-29 | 2010-04-29 | Compounds and compositions as microsomal prostaglandin e synthase-1 inhibitors |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2010127152A2 (en) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9447049B2 (en) | 2010-03-01 | 2016-09-20 | University Of Tennessee Research Foundation | Compounds for treatment of cancer |
| ES2620027T3 (en) | 2008-09-03 | 2017-06-27 | Biomarin Pharmaceutical Inc. | Compositions that include 6-aminohexanoic acid derivatives as HDAC inhibitors |
| JP2013516480A (en) | 2010-01-07 | 2013-05-13 | セレクサゲン セラピューティクス,インク. | Hedgehog inhibitor |
| EP2552208A4 (en) * | 2010-03-31 | 2014-07-09 | Glaxo Group Ltd | Imidazolyl-imidazoles as kinase inhibitors |
| AR084174A1 (en) * | 2010-12-21 | 2013-04-24 | Lilly Co Eli | IMIDAZOL-2-BENZAMIDA COMPOUNDS USEFUL FOR THE TREATMENT OF OSTEOARTRITIS AND A PHARMACEUTICAL COMPOSITION |
| US10059723B2 (en) | 2011-02-28 | 2018-08-28 | Biomarin Pharmaceutical Inc. | Histone deacetylase inhibitors |
| US8957066B2 (en) | 2011-02-28 | 2015-02-17 | Biomarin Pharmaceutical Inc. | Histone deacetylase inhibitors |
| US9540395B2 (en) | 2011-02-28 | 2017-01-10 | Biomarin Pharmaceutical Inc. | Histone deacetylase inhibitors |
| AR086254A1 (en) * | 2011-05-26 | 2013-11-27 | Lilly Co Eli | USEFUL IMIDAZOL DERIVATIVES FOR THE TREATMENT OF ARTHRITIS |
| US20130165472A1 (en) * | 2011-12-23 | 2013-06-27 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| US9056874B2 (en) | 2012-05-04 | 2015-06-16 | Novartis Ag | Complement pathway modulators and uses thereof |
| WO2013170774A1 (en) * | 2012-05-16 | 2013-11-21 | 上海医药集团股份有限公司 | Acetylene derivative having antineoplastic activity |
| JP2015525223A (en) | 2012-06-14 | 2015-09-03 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | Pest control method using substituted 3-pyridylthiazole compounds and derivatives for controlling animal pests |
| JP6387391B2 (en) | 2013-03-14 | 2018-09-05 | ノバルティス アーゲー | 2- (1H-Indol-4-ylmethyl) -3H-imidazo [4,5-b] pyridine-6-carbonitrile derivatives as complement factor B inhibitors useful for the treatment of ophthalmic diseases |
| KR20150132345A (en) | 2013-03-15 | 2015-11-25 | 바이오마린 파머수티컬 인크. | Hdac inhibitors |
| EP3089963A1 (en) | 2013-10-30 | 2016-11-09 | Novartis AG | 2-benzyl-benzimidazole complement factor b inhibitors and uses thereof |
| CN105899504A (en) * | 2014-01-21 | 2016-08-24 | 豪夫迈·罗氏有限公司 | Imidazoles for the treatment and prophylaxis of respiratory syncytial virus infection |
| CA3079483A1 (en) | 2017-11-22 | 2019-05-31 | Khondrion Ip B.V. | Compounds as mpges-1 inhibitors |
| JP2025527659A (en) * | 2022-08-24 | 2025-08-22 | インシリコ メディシン アイピー リミテッド | Method for producing kinase inhibitors |
| WO2025007950A1 (en) * | 2023-07-06 | 2025-01-09 | Insilico Medicine Ip Limited | Crystalline tnik inhibitor and uses thereof |
| WO2025151705A1 (en) * | 2024-01-10 | 2025-07-17 | Vrise Therapeutics, Inc. | Novel inhibitors of dna damage repair pathway |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005123673A1 (en) * | 2004-06-18 | 2005-12-29 | Biolipox Ab | Indoles useful in the treatment of inflammation |
| US20070208017A1 (en) * | 2004-12-17 | 2007-09-06 | Anh Chau | 2-(Phenyl or heterocyclic)-1H-phenantrho[9,10-d]imidazoles as mPGES-1 inhibitors |
| WO2008084218A1 (en) * | 2007-01-12 | 2008-07-17 | Boehringer Ingelheim International Gmbh | Benzazole derivatives for the treatment of inflammations |
| WO2008139161A1 (en) * | 2007-05-10 | 2008-11-20 | Sareum Limited | Oxazole tyrosine kinase inhibitors |
-
2010
- 2010-04-29 WO PCT/US2010/033022 patent/WO2010127152A2/en not_active Ceased
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005123673A1 (en) * | 2004-06-18 | 2005-12-29 | Biolipox Ab | Indoles useful in the treatment of inflammation |
| US20070208017A1 (en) * | 2004-12-17 | 2007-09-06 | Anh Chau | 2-(Phenyl or heterocyclic)-1H-phenantrho[9,10-d]imidazoles as mPGES-1 inhibitors |
| WO2008084218A1 (en) * | 2007-01-12 | 2008-07-17 | Boehringer Ingelheim International Gmbh | Benzazole derivatives for the treatment of inflammations |
| WO2008139161A1 (en) * | 2007-05-10 | 2008-11-20 | Sareum Limited | Oxazole tyrosine kinase inhibitors |
Non-Patent Citations (2)
| Title |
|---|
| ST. LAURANT DR ET AL: "Preparation of 5-substituted 2-(2-alkyl/aryl-1H-imidazol-4-yl)oxazoles and 5-substituted 2-(2-alkyl/arylthiazol-4-yl)oxazoles by utilizing 5-substituted 2-(2-bromo-1,1-diethoxyethyl)oxazole as a synthon", SYNTHESIS, no. 9, 25 March 2009 (2009-03-25), pages 1445 - 1458, XP002589898 * |
| TANAKA ET AL: "Studies on antiplatelet agents i. Synthesis and platelet inhibitory activity of 5-alkyl-2-aryl-4-pyridylimidazoles", CHEMICAL AND PHARMACEUTICAL BULLETIN, vol. 40, no. 12, 1 January 1992 (1992-01-01), pages 3206 - 3213, XP002651273 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2010127152A2 (en) | 2010-11-04 |
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