NO20083448L - Benzo(f)isoindol-2-ylfenyleddiksyrederivater som EP4 receptoragonister - Google Patents
Benzo(f)isoindol-2-ylfenyleddiksyrederivater som EP4 receptoragonisterInfo
- Publication number
- NO20083448L NO20083448L NO20083448A NO20083448A NO20083448L NO 20083448 L NO20083448 L NO 20083448L NO 20083448 A NO20083448 A NO 20083448A NO 20083448 A NO20083448 A NO 20083448A NO 20083448 L NO20083448 L NO 20083448L
- Authority
- NO
- Norway
- Prior art keywords
- isoindol
- benzo
- acid derivatives
- receptor agonists
- ylphenylacetic
- Prior art date
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
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Abstract
En forbindelse med formel (I) eller et farmasøytisk akseptabelt derivat derav, hvor R1 R2 R3, R4, R5, R6, X og Y er som definert i spesifikasjonen; en prosess for å lage slike forbindelser; en farmasøytisk sammensetning som omfatter slike forbindelser; og anvendelsen av slike forbindelser i medisin.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0602237A GB0602237D0 (en) | 2006-02-03 | 2006-02-03 | Novel compounds |
| GB0608976A GB0608976D0 (en) | 2006-05-05 | 2006-05-05 | Novel compounds |
| PCT/EP2007/050992 WO2007088190A1 (en) | 2006-02-03 | 2007-02-01 | Benzo (f) isoindol-2-ylphenyl acetic acid derivatives as ep4 receptor agonists |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO20083448L true NO20083448L (no) | 2008-10-23 |
Family
ID=37944208
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20083448A NO20083448L (no) | 2006-02-03 | 2008-08-07 | Benzo(f)isoindol-2-ylfenyleddiksyrederivater som EP4 receptoragonister |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US8252833B2 (no) |
| EP (2) | EP1979316B1 (no) |
| JP (2) | JP5250427B2 (no) |
| KR (1) | KR20080097417A (no) |
| AR (1) | AR059282A1 (no) |
| AU (1) | AU2007211484A1 (no) |
| BR (1) | BRPI0708024A2 (no) |
| CA (1) | CA2640277A1 (no) |
| CR (1) | CR10207A (no) |
| EA (1) | EA200870224A1 (no) |
| ES (1) | ES2390491T3 (no) |
| IL (1) | IL192934A0 (no) |
| MA (1) | MA30209B1 (no) |
| NO (1) | NO20083448L (no) |
| PE (1) | PE20070949A1 (no) |
| SG (1) | SG169380A1 (no) |
| TW (1) | TW200808722A (no) |
| UY (1) | UY30121A1 (no) |
| WO (1) | WO2007088190A1 (no) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2008014450A (es) * | 2006-05-18 | 2009-03-09 | Mannkind Corp | Inhibidores de cinasa intracelular. |
| GB0615111D0 (en) * | 2006-07-28 | 2006-09-06 | Glaxo Group Ltd | Novel compounds |
| GB0620619D0 (en) * | 2006-10-17 | 2006-11-29 | Glaxo Group Ltd | Novel compounds |
| GB0623203D0 (en) * | 2006-11-21 | 2007-01-03 | Glaxo Group Ltd | Novel compounds |
| EP2147672A4 (en) | 2007-05-08 | 2011-11-02 | Nat University Corp Hamamatsu University School Of Medicine | CYTOTOXIC T CELL ACTIVATOR WITH AN EP4 AGONIST |
| GB0721611D0 (en) | 2007-11-02 | 2007-12-12 | Glaxo Group Ltd | Novel compounds |
| CN103012111B (zh) * | 2012-09-12 | 2016-01-13 | 衢州学院 | 一种2,4,5-三氟苯乙酸的制备方法 |
| CN110003129B (zh) * | 2019-04-18 | 2021-04-06 | 济南立德医药技术有限公司 | 一种佐米曲普坦中间体的制备方法 |
| WO2021082705A1 (zh) | 2019-10-29 | 2021-05-06 | 宁波舜宇光电信息有限公司 | 摄像模组及其光学镜头、光学镜片和制造方法以及大广角摄像模组的组装方法 |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT947165B (it) | 1971-05-17 | 1973-05-21 | Grefco | Composizioni e processo per la eliminazione selettiva di prodot ti oleosi dall acqua |
| JPH10265454A (ja) | 1997-01-27 | 1998-10-06 | Ono Pharmaceut Co Ltd | 3,7−ジチアプロスタン酸誘導体、それらの製造方法およびそれらを有効成分として含有する薬剤 |
| AUPO713297A0 (en) | 1997-06-02 | 1997-06-26 | Fujisawa Pharmaceutical Co., Ltd. | Oxazole compound |
| US6043275A (en) | 1998-04-16 | 2000-03-28 | Ono Pharmaceutical Co., Ltd. | 3,7-dithiaprostanoic acid derivative |
| TWI249520B (en) | 1998-07-15 | 2006-02-21 | Ono Pharmaceutical Co | 5-Thia-omega-substituted phenyl prostaglandin E derivatives, method for producing the same and medicines containing the same as the active ingredient |
| KR20010074981A (ko) | 1998-09-14 | 2001-08-09 | 우에노 도시오 | ω치환된 페닐프로스타그란딘 E 유도체 및 그 유도체를유효 성분으로 하는 약제 |
| AUPP608898A0 (en) | 1998-09-23 | 1998-10-15 | Fujisawa Pharmaceutical Co., Ltd. | New use of prostaglandin E2 antagonists |
| US6437146B1 (en) | 1998-09-25 | 2002-08-20 | Fujisawa Pharmaceutical Co., Ltd. | Oxazole compounds as prostaglandin e2 agonists or antagonists |
| AU1444200A (en) | 1998-10-15 | 2000-05-01 | Merck & Co., Inc. | Methods for inhibiting bone resorption |
| DE60012751T2 (de) | 1999-08-10 | 2005-01-20 | Glaxo Group Ltd., Greenford | Verwendung von EP 4 Rezeptorliganden zur Behandlung von neuropathischem Schmerz |
| GB0030541D0 (en) | 2000-12-14 | 2001-01-31 | Glaxo Group Ltd | Medical uses |
| GB0031315D0 (en) | 2000-12-21 | 2001-02-07 | Glaxo Group Ltd | Indole derivatives |
| 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 |
| WO2003077910A1 (en) | 2002-03-18 | 2003-09-25 | Pfizer Products Inc. | Methods of treatment with selective ep4 receptor agonists |
| EP1499305A2 (en) | 2002-04-12 | 2005-01-26 | Pfizer Japan Inc. | Use of ep4 receptor ligands in the treatment of il-6 involved diseases |
| JP4754820B2 (ja) | 2002-06-10 | 2011-08-24 | メルク セローノ ソシエテ アノニム | プロスタグランジン作動薬としてのγラクタムおよびその使用 |
| US20040142993A1 (en) | 2002-07-01 | 2004-07-22 | Carlo Battistini | Inhibitors of HCV NS5B polymerase |
| WO2004037813A1 (en) | 2002-10-25 | 2004-05-06 | Merck Frosst Canada & Co. | Pyrrolidin-2-on derivatives as ep4 receptor agonists |
| US7053085B2 (en) | 2003-03-26 | 2006-05-30 | Merck & Co. Inc. | EP4 receptor agonist, compositions and methods thereof |
| ES2308139T3 (es) | 2003-01-29 | 2008-12-01 | Asterand Uk Limited | Antagonista de receptos ep4. |
| CN1867551B (zh) | 2003-09-03 | 2013-09-11 | 拉夸里亚创药株式会社 | 作为前列腺素e2拮抗剂的苯基或吡啶基酰胺化合物 |
| GB0324269D0 (en) | 2003-10-16 | 2003-11-19 | Pharmagene Lab Ltd | EP4 receptor antagonists |
| WO2005080367A1 (en) | 2004-02-12 | 2005-09-01 | Pharmagene Laboratories Limited | Ep2 receptor agonists |
| AP2006003769A0 (en) | 2004-05-04 | 2006-10-31 | Pfizer | Ortho substituted aryl or heteroaryl amide compounds |
| CN1950333A (zh) | 2004-05-04 | 2007-04-18 | 辉瑞大药厂 | 取代的甲基芳基或杂芳基酰胺化合物 |
| WO2005116010A1 (en) | 2004-05-26 | 2005-12-08 | Merck Frosst Canada Ltd. | Ep4 receptor agonist, compositions and methods thereof |
| US8013159B2 (en) | 2005-05-19 | 2011-09-06 | Merck Canada Inc. | Quinoline derivatives as EP4 antagonists |
| GB0602900D0 (en) * | 2006-02-13 | 2006-03-22 | Glaxo Group Ltd | Novel Compounds |
-
2007
- 2007-01-30 UY UY30121A patent/UY30121A1/es not_active Application Discontinuation
- 2007-02-01 US US12/278,019 patent/US8252833B2/en not_active Expired - Fee Related
- 2007-02-01 BR BRPI0708024-7A patent/BRPI0708024A2/pt not_active IP Right Cessation
- 2007-02-01 KR KR1020087018920A patent/KR20080097417A/ko not_active Ceased
- 2007-02-01 CA CA002640277A patent/CA2640277A1/en not_active Abandoned
- 2007-02-01 AU AU2007211484A patent/AU2007211484A1/en not_active Abandoned
- 2007-02-01 EP EP07704313A patent/EP1979316B1/en active Active
- 2007-02-01 SG SG201100788-7A patent/SG169380A1/en unknown
- 2007-02-01 EP EP12154482A patent/EP2457897A1/en not_active Withdrawn
- 2007-02-01 EA EA200870224A patent/EA200870224A1/ru unknown
- 2007-02-01 TW TW096103620A patent/TW200808722A/zh unknown
- 2007-02-01 PE PE2007000114A patent/PE20070949A1/es not_active Application Discontinuation
- 2007-02-01 ES ES07704313T patent/ES2390491T3/es active Active
- 2007-02-01 AR ARP070100429A patent/AR059282A1/es not_active Application Discontinuation
- 2007-02-01 JP JP2008552809A patent/JP5250427B2/ja not_active Expired - Fee Related
- 2007-02-01 WO PCT/EP2007/050992 patent/WO2007088190A1/en not_active Ceased
-
2008
- 2008-07-21 IL IL192934A patent/IL192934A0/en unknown
- 2008-08-06 MA MA31159A patent/MA30209B1/fr unknown
- 2008-08-07 NO NO20083448A patent/NO20083448L/no not_active Application Discontinuation
- 2008-08-14 CR CR10207A patent/CR10207A/es unknown
-
2013
- 2013-01-04 JP JP2013000193A patent/JP2013082734A/ja not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| EA200870224A1 (ru) | 2009-02-27 |
| WO2007088190A1 (en) | 2007-08-09 |
| KR20080097417A (ko) | 2008-11-05 |
| JP5250427B2 (ja) | 2013-07-31 |
| PE20070949A1 (es) | 2007-11-22 |
| CR10207A (es) | 2008-09-22 |
| EP1979316A1 (en) | 2008-10-15 |
| AU2007211484A1 (en) | 2007-08-09 |
| EP1979316B1 (en) | 2012-07-11 |
| US20110201663A1 (en) | 2011-08-18 |
| TW200808722A (en) | 2008-02-16 |
| ES2390491T3 (es) | 2012-11-13 |
| MA30209B1 (fr) | 2009-02-02 |
| JP2013082734A (ja) | 2013-05-09 |
| SG169380A1 (en) | 2011-03-30 |
| BRPI0708024A2 (pt) | 2011-05-17 |
| JP2009525309A (ja) | 2009-07-09 |
| UY30121A1 (es) | 2007-08-31 |
| CA2640277A1 (en) | 2007-08-09 |
| IL192934A0 (en) | 2009-02-11 |
| EP2457897A1 (en) | 2012-05-30 |
| AR059282A1 (es) | 2008-03-19 |
| US8252833B2 (en) | 2012-08-28 |
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