ATE533766T1 - Chinolinderivate als ep4-antagonisten - Google Patents
Chinolinderivate als ep4-antagonistenInfo
- Publication number
- ATE533766T1 ATE533766T1 AT06741503T AT06741503T ATE533766T1 AT E533766 T1 ATE533766 T1 AT E533766T1 AT 06741503 T AT06741503 T AT 06741503T AT 06741503 T AT06741503 T AT 06741503T AT E533766 T1 ATE533766 T1 AT E533766T1
- Authority
- AT
- Austria
- Prior art keywords
- derivatives
- group
- quinoline derivatives
- antagonists
- formula
- Prior art date
Links
- 229940027991 antiseptic and disinfectant quinoline derivative Drugs 0.000 title abstract 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical class N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 title 1
- 239000005557 antagonist Substances 0.000 title 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 208000002193 Pain Diseases 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 208000000094 Chronic Pain Diseases 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 230000001154 acute effect Effects 0.000 abstract 1
- 208000005298 acute pain Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- XEYBRNLFEZDVAW-ARSRFYASSA-N dinoprostone Chemical compound CCCCC[C@H](O)\C=C\[C@H]1[C@H](O)CC(=O)[C@@H]1C\C=C/CCCC(O)=O XEYBRNLFEZDVAW-ARSRFYASSA-N 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 201000008482 osteoarthritis Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000002943 quinolinyl group Chemical class N1=C(C=CC2=CC=CC=C12)* 0.000 abstract 1
- 239000002464 receptor antagonist Substances 0.000 abstract 1
- 229940044551 receptor antagonist Drugs 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 0.000 abstract 1
Classifications
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- 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
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Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Addiction (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Psychiatry (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Ophthalmology & Optometry (AREA)
- Obesity (AREA)
- Dermatology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Pulmonology (AREA)
- Psychology (AREA)
- Urology & Nephrology (AREA)
- Virology (AREA)
- Toxicology (AREA)
- Vascular Medicine (AREA)
- AIDS & HIV (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US68258905P | 2005-05-19 | 2005-05-19 | |
| PCT/CA2006/000789 WO2006122403A1 (en) | 2005-05-19 | 2006-05-15 | Quinoline derivatives as ep4 antagonists |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE533766T1 true ATE533766T1 (de) | 2011-12-15 |
Family
ID=37430885
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT06741503T ATE533766T1 (de) | 2005-05-19 | 2006-05-15 | Chinolinderivate als ep4-antagonisten |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8013159B2 (de) |
| EP (1) | EP1885722B1 (de) |
| JP (1) | JP5289046B2 (de) |
| AT (1) | ATE533766T1 (de) |
| AU (1) | AU2006246930C1 (de) |
| CA (1) | CA2608214C (de) |
| WO (1) | WO2006122403A1 (de) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR057023A1 (es) * | 2005-05-16 | 2007-11-14 | Gilead Sciences Inc | Compuestos heterociclicos con propiedades inhibidoras de hiv-integrasa |
| UY30121A1 (es) | 2006-02-03 | 2007-08-31 | Glaxo Group Ltd | Nuevos compuestos |
| WO2008071736A1 (en) | 2006-12-15 | 2008-06-19 | Glaxo Group Limited | Benzamide derivatives as ep4 receptor agonists |
| US8158671B2 (en) * | 2007-02-26 | 2012-04-17 | Merck Canada Inc. | Indole and indoline cyclopropyl amide derivatives as EP4 receptor antagonists |
| JP2010522218A (ja) * | 2007-03-26 | 2010-07-01 | メルク フロスト カナダ リミテツド | Ep4受容体アンタゴニストとしてのナフタレン及びキノリンスルホニル尿素誘導体 |
| GB0721611D0 (en) | 2007-11-02 | 2007-12-12 | Glaxo Group Ltd | Novel compounds |
| CN102224154A (zh) | 2008-09-25 | 2011-10-19 | 默克弗罗斯特加拿大有限公司 | 作为EP4受体拮抗剂的β-咔啉磺酰脲衍生物 |
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| EP2555773A1 (de) * | 2010-04-08 | 2013-02-13 | Boehringer Ingelheim International GmbH | Arzneimittelkombinationen enthaltend pde4-inhibitoren und ep4-rezeptor-antagonisten |
| US9295665B2 (en) | 2013-03-12 | 2016-03-29 | Allergan, Inc. | Inhibition of neovascularization by simultaneous inhibition of prostanoid IP and EP4 receptors |
| CR20180323A (es) | 2015-11-20 | 2018-08-06 | Idorsia Pharmaceuticals Ltd | Derivados de indol n-sustituídos como moduladores de los receptores de pge2 |
| US10342785B2 (en) | 2016-11-04 | 2019-07-09 | Askat Inc. | Use of EP4 receptor antagonists for the treatment of NASH-associated liver cancer |
| AR111941A1 (es) | 2017-05-18 | 2019-09-04 | Idorsia Pharmaceuticals Ltd | Derivados de pirimidina como moduladores del receptor de pge2 |
| EP3625223B1 (de) | 2017-05-18 | 2021-08-11 | Idorsia Pharmaceuticals Ltd | Pyrimidinderivate |
| MX388257B (es) | 2017-05-18 | 2025-03-19 | Idorsia Pharmaceuticals Ltd | Derivados de pirimidina como moduladores del receptor de pge2. |
| US20200069686A1 (en) | 2017-05-18 | 2020-03-05 | Idorsia Pharmaceuticals Ltd | N-substituted indole derivatives |
| JP7093791B2 (ja) | 2017-05-18 | 2022-06-30 | イドーシア ファーマシューティカルズ リミテッド | Pge2レセプター調節剤としてのベンゾフラン及びベンゾチオフェン誘導体 |
| EP4245301A4 (de) | 2020-11-13 | 2024-08-21 | ONO Pharmaceutical Co., Ltd. | Krebsbehandlung durch kombinierte verwendung eines ep4-antagonisten und eines immuncheckpoint-inhibitors |
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| AU8807882A (en) * | 1981-09-21 | 1983-03-31 | Mobil Oil Corp. | Catalyst composition with zeolite support |
| GB9417532D0 (en) | 1994-08-31 | 1994-10-19 | Zeneca Ltd | Aromatic compounds |
| GB9420557D0 (en) * | 1994-10-12 | 1994-11-30 | Zeneca Ltd | Aromatic compounds |
| EP0752421B1 (de) | 1995-07-07 | 2005-10-12 | AstraZeneca AB | Ortho-substituierte aromatische Verbindungen, die drei (Het)aryl-Ringe enthalten, deren Herstellung und deren Verwendung als Prostaglandin-E2-(PGE2)-Antagonisten |
| EP1121133A1 (de) * | 1998-10-15 | 2001-08-08 | Merck & Co., Inc. | Methoden zur stimulierung der knochenbildung |
| GB0031302D0 (en) * | 2000-12-21 | 2001-01-31 | Glaxo Group Ltd | Napthalene derivatives |
| GB0031295D0 (en) | 2000-12-21 | 2001-01-31 | Glaxo Group Ltd | Naphthalene derivatives |
| GB0103269D0 (en) * | 2001-02-09 | 2001-03-28 | Glaxo Group Ltd | Napthalene derivatives |
| CA2369967A1 (en) | 2001-02-12 | 2002-08-12 | Joseph Anthony Cornicelli | Methods of treating nuclear factor-kappa b mediated diseases and disorders |
| WO2003047513A2 (en) * | 2001-12-03 | 2003-06-12 | Merck & Co., Inc. | Method for treating ocular hypertension |
| US7348433B2 (en) * | 2001-12-14 | 2008-03-25 | Merck Frosst Canada & Co. | Quinolinones as prostaglandin receptor ligands |
| WO2004019932A1 (en) | 2002-08-30 | 2004-03-11 | Pharmacia & Upjohn Company | Method of preventing or treating atherosclerosis or restenosis |
| AU2003301439A1 (en) | 2002-10-16 | 2004-05-04 | Gilead Sciences, Inc. | Pre-organized tricyclic integrase inhibitor compounds |
| JP2006505572A (ja) * | 2002-10-25 | 2006-02-16 | メルク フロスト カナダ アンド カンパニー | Ep4受容体アゴニストとしての2−ピロリドン |
| EP1625130A2 (de) | 2003-04-28 | 2006-02-15 | Tibotec Pharmaceuticals Ltd. | Hiv-integrasehemmer |
| WO2005097738A1 (ja) | 2004-04-06 | 2005-10-20 | Dainippon Sumitomo Pharma Co., Ltd. | 新規スルホンアミド誘導体 |
| PL1742642T3 (pl) | 2004-04-14 | 2009-06-30 | Gilead Sciences Inc | Analogi fosfonianowe związków inhibitorów integrazy HIV |
| JP5137574B2 (ja) | 2004-08-30 | 2013-02-06 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | 11−ベータヒドロキシステロイドヒドロゲナーゼ阻害剤としての三環式ラクタム誘導体 |
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| EP1885722A1 (de) | 2008-02-13 |
| EP1885722A4 (de) | 2010-02-24 |
| JP5289046B2 (ja) | 2013-09-11 |
| WO2006122403A1 (en) | 2006-11-23 |
| CA2608214A1 (en) | 2006-11-23 |
| JP2008540584A (ja) | 2008-11-20 |
| US20090099226A1 (en) | 2009-04-16 |
| CA2608214C (en) | 2013-08-20 |
| EP1885722B1 (de) | 2011-11-16 |
| AU2006246930C1 (en) | 2012-01-19 |
| US8013159B2 (en) | 2011-09-06 |
| AU2006246930A1 (en) | 2006-11-23 |
| AU2006246930B2 (en) | 2011-08-18 |
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