UY28778A1 - Derivados de pirrol como inhibidores del factor xa - Google Patents
Derivados de pirrol como inhibidores del factor xaInfo
- Publication number
- UY28778A1 UY28778A1 UY28778A UY28778A UY28778A1 UY 28778 A1 UY28778 A1 UY 28778A1 UY 28778 A UY28778 A UY 28778A UY 28778 A UY28778 A UY 28778A UY 28778 A1 UY28778 A1 UY 28778A1
- Authority
- UY
- Uruguay
- Prior art keywords
- factor
- compounds
- formulas
- factor viia
- inhibitors
- Prior art date
Links
Classifications
-
- 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- 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
- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrrole Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
La presente invención se refiere a los compuestos de las fórmulas I y Ia, en las que R0; R1; R3; R4; R22; Q, V, G y M tienen los significados indicados más adelante. Los compuestos de las fórmulas I y Ia son compuestos valiosos farmacológicamente activos. Presentan un efecto antitrombótico fuerte y son adecuados, por ejemplo, para la terapia y la profilaxis de los trastornos cardiovasculares como enfermedades tromboembólicas o restenosis. Son inhibidores reversibles del factor Xa (FXa) y/o del factor VIIa (FVIIa) de las enzimas de coagulación de la sangre, y se pueden aplicar en general en condiciones en las que está presente una actividad no deseada del factor Xa y/o del factor VIIa o para la curación o prevención cuya inhibición del factor Xa y/o el factor VIIa se pretende. La invención se refiere además a los procedimientos para la preparación de compuestos de las fórmulas I Ia, a su utilización, en particular como ingredientes activos en productos farmacéuticos, y a las preparaciones farmacéuticas que los comprenden.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04004503A EP1568698A1 (en) | 2004-02-27 | 2004-02-27 | Pyrrole-derivatives as factor Xa inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
UY28778A1 true UY28778A1 (es) | 2005-09-30 |
Family
ID=34745922
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UY28778A UY28778A1 (es) | 2004-02-27 | 2005-02-25 | Derivados de pirrol como inhibidores del factor xa |
Country Status (12)
Country | Link |
---|---|
US (1) | US7465806B2 (es) |
EP (2) | EP1568698A1 (es) |
JP (1) | JP4861306B2 (es) |
CN (1) | CN1926137A (es) |
AU (1) | AU2005219507A1 (es) |
BR (1) | BRPI0508048A (es) |
CA (1) | CA2557270A1 (es) |
IL (1) | IL177253A0 (es) |
PE (1) | PE20051170A1 (es) |
TW (1) | TW200538110A (es) |
UY (1) | UY28778A1 (es) |
WO (1) | WO2005085239A2 (es) |
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7358268B2 (en) * | 2002-12-04 | 2008-04-15 | Sanofi-Aventis Deutschland Gmbh | Imidazole derivatives as factor Xa inhibitors |
US7429581B2 (en) | 2002-12-23 | 2008-09-30 | Sanofi-Aventis Deutschland Gmbh | Pyrazole-derivatives as factor Xa inhibitors |
EP1479675A1 (en) * | 2003-05-19 | 2004-11-24 | Aventis Pharma Deutschland GmbH | Indazole-derivatives as factor Xa inhibitors |
EP1571154A1 (en) * | 2004-03-03 | 2005-09-07 | Aventis Pharma Deutschland GmbH | Beta-aminoacid-derivatives as factor Xa inhibitors |
TW200840815A (en) * | 2007-04-13 | 2008-10-16 | Chang Chun Plastics Co Ltd | Method for preparing melamine salt of bis(pentaerythritol phosphate)phosphoric acid |
US8299115B2 (en) * | 2007-06-08 | 2012-10-30 | Debnath Bhuniya | Pyrrole-2-carboxamide derivatives as glucokinase activators, their process and pharmaceutical application |
KR101897881B1 (ko) | 2008-01-04 | 2018-09-12 | 인텔리카인, 엘엘씨 | 특정 화학 물질, 조성물 및 방법 |
US8193182B2 (en) | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
WO2010137017A2 (en) | 2009-05-27 | 2010-12-02 | Yeda Research And Development Co. Ltd. | Proteasome inhibitors and uses thereof |
ES2637113T3 (es) | 2011-01-10 | 2017-10-10 | Infinity Pharmaceuticals, Inc. | Procedimientos para preparar isoquinolinonas y formas sólidas de isoquinolinonas |
US8828998B2 (en) | 2012-06-25 | 2014-09-09 | Infinity Pharmaceuticals, Inc. | Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors |
PH12015501492A1 (en) | 2013-01-08 | 2015-09-28 | Kalvista Pharmaceuticals Ltd | Benzylamine derivatives |
GB201300304D0 (en) | 2013-01-08 | 2013-02-20 | Kalvista Pharmaceuticals Ltd | Benzylamine derivatives |
TWI636047B (zh) | 2013-08-14 | 2018-09-21 | 英商卡爾維斯塔製藥有限公司 | 雜環衍生物 |
US20150320755A1 (en) | 2014-04-16 | 2015-11-12 | Infinity Pharmaceuticals, Inc. | Combination therapies |
GB201421085D0 (en) | 2014-11-27 | 2015-01-14 | Kalvista Pharmaceuticals Ltd | New enzyme inhibitors |
GB201421083D0 (en) | 2014-11-27 | 2015-01-14 | Kalvista Pharmaceuticals Ltd | Enzyme inhibitors |
BR112018074395A2 (pt) | 2016-05-31 | 2019-03-06 | Kalvista Pharmaceuticals Limited | derivados de pirazol como inibidores de calicreína plasmática |
GB201609603D0 (en) | 2016-06-01 | 2016-07-13 | Kalvista Pharmaceuticals Ltd | Polymorphs of N-[(6-cyano-2-fluoro-3-methoxyphenyl)Methyl]-3-(methoxymethyl)-1-({4-[(2-ox opyridin-1-YL)Methyl]phenyl}methyl)pyrazole-4-carboxamide |
GB201609607D0 (en) | 2016-06-01 | 2016-07-13 | Kalvista Pharmaceuticals Ltd | Polymorphs of N-(3-Fluoro-4-methoxypyridin-2-yl)methyl)-3-(methoxymethyl)-1-({4-((2-oxopy ridin-1-yl)methyl)phenyl}methyl)pyrazole-4-carboxamide and salts |
EP3474856B1 (en) | 2016-06-24 | 2022-09-14 | Infinity Pharmaceuticals, Inc. | Combination therapies |
GB201719881D0 (en) | 2017-11-29 | 2018-01-10 | Kalvista Pharmaceuticals Ltd | Solid forms of plasma kallikrein inhibitor and salts thereof |
LT3716952T (lt) | 2017-11-29 | 2022-04-11 | Kalvista Pharmaceuticals Limited | Vaisto formos, apimančios plazmos kalikreino inhibitorių |
WO2021028645A1 (en) | 2019-08-09 | 2021-02-18 | Kalvista Pharmaceuticals Limited | Plasma kallikrein inhibitors |
CN113192004B (zh) * | 2021-04-01 | 2022-01-18 | 温州医科大学附属第二医院(温州医科大学附属育英儿童医院) | 一种基于冠脉多模影像裂纹形成和扩展的简化计算方法与斑块破裂风险量化的评估系统 |
Family Cites Families (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ZA873607B (en) * | 1986-06-13 | 1988-12-28 | Warner Lambert Co | N-1h-tetrazol-5-yl-2-thiophene carboxamides,n-1h-tetrazol-5-yl-2-pyrrole carboxamides n-1h-tetrazol-5-yl-2-furan carboxamides |
US5506134A (en) | 1990-10-22 | 1996-04-09 | Corvas International, Inc. | Hypridoma and monoclonal antibody which inhibits blood coagulation tissue factor/factor VIIa complex |
US5788965A (en) | 1991-02-28 | 1998-08-04 | Novo Nordisk A/S | Modified factor VII |
US5833982A (en) | 1991-02-28 | 1998-11-10 | Zymogenetics, Inc. | Modified factor VII |
SK286094B6 (sk) | 1994-04-26 | 2008-03-05 | Aventis Pharmaceuticals Inc. | Zlúčenina špecificky inhibujúca aktivitu faktora Xa, farmaceutická kompozícia s jej obsahom a jej použitie |
IT1282797B1 (it) * | 1995-04-21 | 1998-03-31 | Colla Paolo | Pirril-(indolil)-aril-sulfoni e relativo processo di produzione ed impiego nella terapia delle infezioni da virus dell'aids |
AU730224B2 (en) * | 1996-12-23 | 2001-03-01 | Du Pont Pharmaceuticals Company | Nitrogen containing heteroaromatics as factor Xa inhibitors |
US6020357A (en) * | 1996-12-23 | 2000-02-01 | Dupont Pharmaceuticals Company | Nitrogen containing heteroaromatics as factor Xa inhibitors |
US6432947B1 (en) * | 1997-02-19 | 2002-08-13 | Berlex Laboratories, Inc. | N-heterocyclic derivatives as NOS inhibitors |
CA2314401A1 (en) * | 1997-12-22 | 1999-07-01 | Du Pont Pharmaceuticals Company | Nitrogen containing heteroaromatics with ortho-substituted p1's as factor xa inhibitors |
JP4589529B2 (ja) * | 1997-12-24 | 2010-12-01 | サノフィ−アベンティス・ドイチュラント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | Xa因子阻害剤としてのインドール誘導体 |
US6410561B1 (en) * | 1998-03-26 | 2002-06-25 | Japan Tobacco Inc. | Amide derivatives and nociceptin antagonists |
EP0987274A1 (en) | 1998-09-15 | 2000-03-22 | Hoechst Marion Roussel Deutschland GmbH | Factor VIIa Inhibitors |
CA2362381C (en) * | 1999-02-10 | 2009-12-22 | Welfide Corporation | Amide compounds and medicinal use thereof |
EP1226123A1 (en) * | 1999-11-03 | 2002-07-31 | Du Pont Pharmaceuticals Company | Cyano compounds as factor xa inhibitors |
MY138097A (en) * | 2000-03-22 | 2009-04-30 | Du Pont | Insecticidal anthranilamides |
WO2002000651A2 (en) * | 2000-06-27 | 2002-01-03 | Bristol-Myers Squibb Pharma Company | Factor xa inhibitors |
AU2001295098A1 (en) | 2000-09-05 | 2002-03-22 | Medical Research Council | Monoclonal antibody against ovarian carcinoma |
EP1217000A1 (en) | 2000-12-23 | 2002-06-26 | Aventis Pharma Deutschland GmbH | Inhibitors of factor Xa and factor VIIa |
WO2002053155A1 (en) * | 2000-12-30 | 2002-07-11 | Geron Corporation | Telomerase inhibitor |
WO2002053157A1 (en) * | 2000-12-30 | 2002-07-11 | Geron Corporation | Thiazolidine derivative |
PE20020870A1 (es) * | 2001-02-13 | 2002-11-18 | Aventis Pharma Gmbh | 6,7,8,9-tetrahidro-5h-benzocicloheptenil aminas aciladas |
TWI243164B (en) * | 2001-02-13 | 2005-11-11 | Aventis Pharma Gmbh | Acylated indanyl amines and their use as pharmaceuticals |
EP1314733A1 (en) | 2001-11-22 | 2003-05-28 | Aventis Pharma Deutschland GmbH | Indole-2-carboxamides as factor Xa inhibitors |
EP1388341A1 (en) * | 2002-08-07 | 2004-02-11 | Aventis Pharma Deutschland GmbH | Acylamino-substituted heteroaromatic compounds and their use as pharmaceuticals |
US7250443B2 (en) * | 2002-08-23 | 2007-07-31 | Chiron Corporation | Pyrrole based inhibitors of glycogen synthase kinase 3 |
WO2004039318A2 (en) * | 2002-10-25 | 2004-05-13 | Genesoft Pharmaceuticals, Inc. | Anti-infective biaryl compounds |
US7358268B2 (en) | 2002-12-04 | 2008-04-15 | Sanofi-Aventis Deutschland Gmbh | Imidazole derivatives as factor Xa inhibitors |
US7429581B2 (en) | 2002-12-23 | 2008-09-30 | Sanofi-Aventis Deutschland Gmbh | Pyrazole-derivatives as factor Xa inhibitors |
WO2004060870A1 (en) * | 2003-01-02 | 2004-07-22 | F. Hoffmann-La Roche Ag | Novel cb 1 receptour inverse agonists |
US7741341B2 (en) | 2003-05-19 | 2010-06-22 | Sanofi-Aventis Deutschland Gmbh | Benzimidazole-derivatives as factor Xa inhibitors |
EP1479675A1 (en) | 2003-05-19 | 2004-11-24 | Aventis Pharma Deutschland GmbH | Indazole-derivatives as factor Xa inhibitors |
US7317027B2 (en) | 2003-05-19 | 2008-01-08 | Sanofi-Aventis Deutschland Gmbh | Azaindole-derivatives as factor Xa inhibitors |
EP1571154A1 (en) | 2004-03-03 | 2005-09-07 | Aventis Pharma Deutschland GmbH | Beta-aminoacid-derivatives as factor Xa inhibitors |
-
2004
- 2004-02-27 EP EP04004503A patent/EP1568698A1/en not_active Withdrawn
-
2005
- 2005-02-12 BR BRPI0508048-7A patent/BRPI0508048A/pt not_active IP Right Cessation
- 2005-02-12 WO PCT/EP2005/001423 patent/WO2005085239A2/en active Application Filing
- 2005-02-12 EP EP05707352A patent/EP1725550A2/en not_active Withdrawn
- 2005-02-12 AU AU2005219507A patent/AU2005219507A1/en not_active Abandoned
- 2005-02-12 CN CNA2005800062350A patent/CN1926137A/zh active Pending
- 2005-02-12 CA CA002557270A patent/CA2557270A1/en not_active Abandoned
- 2005-02-12 JP JP2007500094A patent/JP4861306B2/ja not_active Expired - Fee Related
- 2005-02-15 PE PE2005000176A patent/PE20051170A1/es not_active Application Discontinuation
- 2005-02-24 TW TW094105507A patent/TW200538110A/zh unknown
- 2005-02-25 UY UY28778A patent/UY28778A1/es unknown
-
2006
- 2006-08-02 IL IL177253A patent/IL177253A0/en unknown
- 2006-08-25 US US11/467,277 patent/US7465806B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP4861306B2 (ja) | 2012-01-25 |
WO2005085239A2 (en) | 2005-09-15 |
KR20070000487A (ko) | 2007-01-02 |
PE20051170A1 (es) | 2006-02-07 |
EP1725550A2 (en) | 2006-11-29 |
CA2557270A1 (en) | 2005-09-15 |
JP2007523927A (ja) | 2007-08-23 |
BRPI0508048A (pt) | 2007-07-17 |
EP1568698A1 (en) | 2005-08-31 |
US20070049573A1 (en) | 2007-03-01 |
US7465806B2 (en) | 2008-12-16 |
WO2005085239A3 (en) | 2005-10-13 |
IL177253A0 (en) | 2006-12-10 |
CN1926137A (zh) | 2007-03-07 |
TW200538110A (en) | 2005-12-01 |
AU2005219507A1 (en) | 2005-09-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
DESI | Application deemed to be withdrawn |
Effective date: 20120418 |