ATE331708T1 - Substituierte 3-alkyl- und 3-arylalkyl-1h-indol-1-yl-essigsäure-derivate als plasminogen aktivator inhibitor-1 (pai-1) inhibitoren - Google Patents
Substituierte 3-alkyl- und 3-arylalkyl-1h-indol-1-yl-essigsäure-derivate als plasminogen aktivator inhibitor-1 (pai-1) inhibitorenInfo
- Publication number
- ATE331708T1 ATE331708T1 AT03796792T AT03796792T ATE331708T1 AT E331708 T1 ATE331708 T1 AT E331708T1 AT 03796792 T AT03796792 T AT 03796792T AT 03796792 T AT03796792 T AT 03796792T AT E331708 T1 ATE331708 T1 AT E331708T1
- Authority
- AT
- Austria
- Prior art keywords
- sub
- pai
- arylalkyl
- inhibitors
- alkyl
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 102000012335 Plasminogen Activator Inhibitor 1 Human genes 0.000 title 2
- 108010022233 Plasminogen Activator Inhibitor 1 Proteins 0.000 title 2
- 102000010752 Plasminogen Inactivators Human genes 0.000 abstract 2
- 108010077971 Plasminogen Inactivators Proteins 0.000 abstract 2
- 239000002797 plasminogen activator inhibitor Substances 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 1
- 150000002148 esters Chemical group 0.000 abstract 1
- 239000003527 fibrinolytic agent Substances 0.000 abstract 1
- 230000003480 fibrinolytic effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- 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
- C07D409/06—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 carbon chain containing only aliphatic carbon atoms
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- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
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- A61P7/08—Plasma substitutes; Perfusion solutions; Dialytics or haemodialytics; Drugs for electrolytic or acid-base disorders, e.g. hypovolemic shock
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- A—HUMAN NECESSITIES
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- A61P9/00—Drugs for disorders of the cardiovascular system
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- A61P9/00—Drugs for disorders of the cardiovascular system
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
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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
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth 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)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Pulmonology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Vascular Medicine (AREA)
- Virology (AREA)
- Immunology (AREA)
- Dermatology (AREA)
- Hospice & Palliative Care (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Child & Adolescent Psychology (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US43233002P | 2002-12-10 | 2002-12-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE331708T1 true ATE331708T1 (de) | 2006-07-15 |
Family
ID=32507902
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT03796792T ATE331708T1 (de) | 2002-12-10 | 2003-12-09 | Substituierte 3-alkyl- und 3-arylalkyl-1h-indol-1-yl-essigsäure-derivate als plasminogen aktivator inhibitor-1 (pai-1) inhibitoren |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US7348351B2 (de) |
| EP (1) | EP1569899B1 (de) |
| JP (1) | JP2006514640A (de) |
| CN (1) | CN1723197A (de) |
| AT (1) | ATE331708T1 (de) |
| AU (1) | AU2003297727A1 (de) |
| BR (1) | BR0316583A (de) |
| CA (1) | CA2509170A1 (de) |
| DE (1) | DE60306547T2 (de) |
| DK (1) | DK1569899T3 (de) |
| ES (1) | ES2268480T3 (de) |
| MX (1) | MXPA05006282A (de) |
| WO (1) | WO2004052853A2 (de) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI224101B (en) * | 2001-06-20 | 2004-11-21 | Wyeth Corp | Substituted naphthyl indole derivatives as inhibitors of plasminogen activator inhibitor type-1 (PAI-1) |
| DK1397130T3 (da) | 2001-06-20 | 2007-11-12 | Wyeth Corp | Substituerede indolsyrederivater som inhibitorer af plasminogenaktivatorinhibitor-1 (PAI-1) |
| AU2003256926A1 (en) * | 2002-07-26 | 2004-02-16 | The Institutes For Pharmaceutical Discovery, Llc | Substituted indolealkanoic acids derivative and formulations containing same for use in treatment of diabetic complications |
| DK1569901T3 (da) * | 2002-12-10 | 2009-02-16 | Wyeth Corp | Aryl-, aryloxy- og alkoxysubstituerede 1H-indol-3-yl-glyoxylsyrederivater som inhibitorer af plasminogenaktivatorinhibitor-1 (PAI-1) |
| UA80453C2 (en) * | 2002-12-10 | 2007-09-25 | Derivatives of substituted dyhydropyranoindol-3,4-dion as inhibitors of plasminogen activator inhibitor-1 (pai-1) | |
| CN1726190A (zh) * | 2002-12-10 | 2006-01-25 | 惠氏公司 | 作为纤溶酶原激活物抑制剂-1(pai-1)的抑制剂的取代3-羰基-1h-吲哚-1-基乙酸衍生物 |
| US7163954B2 (en) * | 2003-09-25 | 2007-01-16 | Wyeth | Substituted naphthyl benzothiophene acids |
| US7411083B2 (en) * | 2003-09-25 | 2008-08-12 | Wyeth | Substituted acetic acid derivatives |
| US7534894B2 (en) * | 2003-09-25 | 2009-05-19 | Wyeth | Biphenyloxy-acids |
| US7442805B2 (en) * | 2003-09-25 | 2008-10-28 | Wyeth | Substituted sulfonamide-indoles |
| US7265148B2 (en) * | 2003-09-25 | 2007-09-04 | Wyeth | Substituted pyrrole-indoles |
| US7268159B2 (en) * | 2003-09-25 | 2007-09-11 | Wyeth | Substituted indoles |
| US7342039B2 (en) * | 2003-09-25 | 2008-03-11 | Wyeth | Substituted indole oximes |
| US7332521B2 (en) * | 2003-09-25 | 2008-02-19 | Wyeth | Substituted indoles |
| US7351726B2 (en) * | 2003-09-25 | 2008-04-01 | Wyeth | Substituted oxadiazolidinediones |
| US7420083B2 (en) * | 2003-09-25 | 2008-09-02 | Wyeth | Substituted aryloximes |
| US7446201B2 (en) * | 2003-09-25 | 2008-11-04 | Wyeth | Substituted heteroaryl benzofuran acids |
| US7141592B2 (en) * | 2003-09-25 | 2006-11-28 | Wyeth | Substituted oxadiazolidinediones |
| US7582773B2 (en) * | 2003-09-25 | 2009-09-01 | Wyeth | Substituted phenyl indoles |
| GB0324763D0 (en) * | 2003-10-23 | 2003-11-26 | Oxagen Ltd | Use of compounds in therapy |
| US7605172B2 (en) * | 2004-08-23 | 2009-10-20 | Wyeth | Thiazolo-naphthyl acids |
| KR20070055563A (ko) * | 2004-08-23 | 2007-05-30 | 와이어쓰 | 혈전증 및 심혈관 질병의 치료에 유용한 플라스미노겐활성화제 억제제 타입-1(pai-1)의 조절제로서의옥사졸로-나프틸 산 |
| BRPI0514549A (pt) * | 2004-08-23 | 2008-06-17 | Wyeth Corp | ácidos de pirrol-naftila como inibidores de pai-1 |
| US7683091B2 (en) | 2005-08-17 | 2010-03-23 | Wyeth | Substituted indoles and methods of their use |
| TW200744585A (en) * | 2006-02-27 | 2007-12-16 | Wyeth Corp | Inhibitors of PAI-1 for treatment of muscular conditions |
| US7750027B2 (en) | 2008-01-18 | 2010-07-06 | Oxagen Limited | Compounds having CRTH2 antagonist activity |
| JP2011509991A (ja) * | 2008-01-22 | 2011-03-31 | オキサジェン リミテッド | Crth2アンタゴニスト活性を有する化合物 |
| WO2009093026A1 (en) | 2008-01-22 | 2009-07-30 | Oxagen Limited | Compounds having crth2 antagonist activity |
| EP2356116A1 (de) * | 2008-11-20 | 2011-08-17 | OSI Pharmaceuticals, Inc. | Substituierte pyrrolo[2,3-b]pyridine und pyrazine |
| JP2013526570A (ja) | 2010-05-14 | 2013-06-24 | オーエスアイ・ファーマシューティカルズ,エルエルシー | 縮合二環式キナーゼ阻害剤 |
| AR081039A1 (es) | 2010-05-14 | 2012-05-30 | Osi Pharmaceuticals Llc | Inhibidores biciclicos fusionados de quinasa |
| GB201322273D0 (en) | 2013-12-17 | 2014-01-29 | Atopix Therapeutics Ltd | Process |
| GB201407807D0 (en) | 2014-05-02 | 2014-06-18 | Atopix Therapeutics Ltd | Polymorphic form |
| GB201407820D0 (en) | 2014-05-02 | 2014-06-18 | Atopix Therapeutics Ltd | Polymorphic form |
| CN110167582A (zh) * | 2016-12-15 | 2019-08-23 | 泰伦基国际有限公司 | 一种预防和治疗药物性肾损伤的方法 |
| CN110191718A (zh) | 2016-12-15 | 2019-08-30 | 泰伦基国际有限公司 | 一种预防和治疗组织器官纤维化的方法 |
| JP7335609B2 (ja) | 2017-06-19 | 2023-08-30 | タレンゲン インターナショナル リミテッド | Glp-1/glp-1rを調節制御する方法および薬剤 |
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| GB1321433A (en) | 1968-01-11 | 1973-06-27 | Roussel Uclaf | 1,2,3,6-tetrasubstituted indoles |
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| US5151435A (en) | 1991-04-08 | 1992-09-29 | Merck & Co., Inc. | Angiotensin ii antagonists incorporating an indole or dihydroindole |
| IL101785A0 (en) | 1991-05-10 | 1992-12-30 | Fujisawa Pharmaceutical Co | Urea derivatives,processes for the preparation thereof and pharmaceutical compositions containing the same |
| GB9123396D0 (en) | 1991-11-04 | 1991-12-18 | Hoffmann La Roche | A process for the manufacture of substituted maleimides |
| US5502187A (en) | 1992-04-03 | 1996-03-26 | The Upjohn Company | Pharmaceutically active bicyclic-heterocyclic amines |
| US5612360A (en) | 1992-06-03 | 1997-03-18 | Eli Lilly And Company | Angiotensin II antagonists |
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-
2003
- 2003-12-09 AT AT03796792T patent/ATE331708T1/de not_active IP Right Cessation
- 2003-12-09 MX MXPA05006282A patent/MXPA05006282A/es active IP Right Grant
- 2003-12-09 JP JP2004559409A patent/JP2006514640A/ja active Pending
- 2003-12-09 CN CNA200380105448XA patent/CN1723197A/zh not_active Withdrawn
- 2003-12-09 AU AU2003297727A patent/AU2003297727A1/en not_active Withdrawn
- 2003-12-09 ES ES03796792T patent/ES2268480T3/es not_active Expired - Lifetime
- 2003-12-09 BR BR0316583-3A patent/BR0316583A/pt not_active IP Right Cessation
- 2003-12-09 DK DK03796792T patent/DK1569899T3/da active
- 2003-12-09 CA CA002509170A patent/CA2509170A1/en not_active Abandoned
- 2003-12-09 WO PCT/US2003/038930 patent/WO2004052853A2/en not_active Ceased
- 2003-12-09 EP EP03796792A patent/EP1569899B1/de not_active Expired - Lifetime
- 2003-12-09 DE DE60306547T patent/DE60306547T2/de not_active Expired - Lifetime
- 2003-12-09 US US10/730,951 patent/US7348351B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| MXPA05006282A (es) | 2005-08-19 |
| EP1569899A2 (de) | 2005-09-07 |
| US20040116488A1 (en) | 2004-06-17 |
| US7348351B2 (en) | 2008-03-25 |
| BR0316583A (pt) | 2005-10-04 |
| WO2004052853A2 (en) | 2004-06-24 |
| CA2509170A1 (en) | 2004-06-24 |
| WO2004052853A3 (en) | 2004-09-16 |
| DE60306547D1 (de) | 2006-08-10 |
| ES2268480T3 (es) | 2007-03-16 |
| DE60306547T2 (de) | 2007-06-28 |
| EP1569899B1 (de) | 2006-06-28 |
| JP2006514640A (ja) | 2006-05-11 |
| AU2003297727A1 (en) | 2004-06-30 |
| DK1569899T3 (da) | 2006-10-23 |
| CN1723197A (zh) | 2006-01-18 |
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