NO20091647L - Trypsinlignende serinproteaseinhibitorer og deres fremstilling og anvendelse - Google Patents
Trypsinlignende serinproteaseinhibitorer og deres fremstilling og anvendelseInfo
- Publication number
- NO20091647L NO20091647L NO20091647A NO20091647A NO20091647L NO 20091647 L NO20091647 L NO 20091647L NO 20091647 A NO20091647 A NO 20091647A NO 20091647 A NO20091647 A NO 20091647A NO 20091647 L NO20091647 L NO 20091647L
- Authority
- NO
- Norway
- Prior art keywords
- trypsin
- preparation
- protease inhibitors
- serine protease
- heart
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/56—Amides
-
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/89—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06078—Dipeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06086—Dipeptides with the first amino acid being basic
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Epidemiology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
- Materials For Medical Uses (AREA)
- Emergency Medicine (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102006050672A DE102006050672A1 (de) | 2006-10-24 | 2006-10-24 | Hemmstoffe des Plasmins und des Plasmakallikreins |
PCT/EP2007/009220 WO2008049595A1 (fr) | 2006-10-24 | 2007-10-24 | Inhibiteurs de sérine protéase de type trypsine, leur fabrication et leur utilisation |
Publications (1)
Publication Number | Publication Date |
---|---|
NO20091647L true NO20091647L (no) | 2009-07-14 |
Family
ID=38961973
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20091647A NO20091647L (no) | 2006-10-24 | 2009-04-24 | Trypsinlignende serinproteaseinhibitorer og deres fremstilling og anvendelse |
Country Status (14)
Country | Link |
---|---|
US (3) | US8207378B2 (fr) |
EP (2) | EP2054380B8 (fr) |
JP (1) | JP5356237B2 (fr) |
CN (1) | CN101541742A (fr) |
AU (1) | AU2007308421B2 (fr) |
BR (1) | BRPI0718286A2 (fr) |
CA (1) | CA2667507C (fr) |
DE (1) | DE102006050672A1 (fr) |
EA (1) | EA018998B1 (fr) |
ES (1) | ES2439244T3 (fr) |
MX (1) | MX2009004320A (fr) |
NO (1) | NO20091647L (fr) |
NZ (1) | NZ577008A (fr) |
WO (1) | WO2008049595A1 (fr) |
Families Citing this family (39)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7838560B2 (en) * | 2002-03-11 | 2010-11-23 | The Medicines Company (Leipzig) Gmbh | Urokinase inhibitors, production and use thereof |
DE10301300B4 (de) | 2003-01-15 | 2009-07-16 | Curacyte Chemistry Gmbh | Verwendung von acylierten 4-Amidino- und 4-Guanidinobenzylaminen zur Inhibierung von Plasmakallikrein |
DE102005044319A1 (de) * | 2005-09-16 | 2007-03-22 | Curacyte Chemistry Gmbh | 2-(Aminomethyl)-5-Chlor-Benzylamid-Derivate und ihre Verwendung als Hemmstoffe des Gerinnungsfaktors Xa |
DE102006050672A1 (de) | 2006-10-24 | 2008-04-30 | Curacyte Discovery Gmbh | Hemmstoffe des Plasmins und des Plasmakallikreins |
WO2010048941A2 (fr) | 2008-10-29 | 2010-05-06 | Philipps-Universität Marburg | Dérivé tétrapeptidique modifié en position n-terminale avec un mimétique d'arginine en position c-terminale |
CA2788417C (fr) * | 2010-01-28 | 2017-02-14 | The Medicines Company (Leipzig) Gmbh | Inhibiteurs de serine protease de type trypsine, et leur preparation et utilisation |
WO2012004678A2 (fr) | 2010-07-07 | 2012-01-12 | The Medicines Company (Leipzig) Gmbh | Inhibiteurs de la sérine protéase |
KR101878361B1 (ko) * | 2010-09-20 | 2018-08-20 | 시르나 쎄러퓨틱스 인코퍼레이티드 | 올리고뉴클레오티드 전달을 위한 신규 저분자량 양이온성 지질 |
WO2012083436A1 (fr) | 2010-12-21 | 2012-06-28 | The Medicines Company (Leipzig) Gmbh | Inhibiteurs de protéases à sérine semblables à la trypsine, leur synthèse et leur utilisation comme inhibiteurs sélectifs des facteurs de coagulation iia et xa |
EP2543676A1 (fr) * | 2011-07-07 | 2013-01-09 | Philipps-Universität Marburg | Mimes tripeptides cycliques |
GB2494851A (en) * | 2011-07-07 | 2013-03-27 | Kalvista Pharmaceuticals Ltd | Plasma kallikrein inhibitors |
GB201212081D0 (en) | 2012-07-06 | 2012-08-22 | Kalvista Pharmaceuticals Ltd | New polymorph |
GB201300304D0 (en) | 2013-01-08 | 2013-02-20 | Kalvista Pharmaceuticals Ltd | Benzylamine derivatives |
IL239682B (en) | 2013-01-08 | 2018-10-31 | Kalvista Pharmaceuticals Ltd | History of benzylamine and 2-(aminomethyl)pyridine |
GB2510407A (en) | 2013-02-04 | 2014-08-06 | Kalvista Pharmaceuticals Ltd | Aqueous suspensions of kallikrein inhibitors for parenteral administration |
KR102276700B1 (ko) | 2013-05-23 | 2021-07-12 | 칼비스타 파마슈티컬즈 리미티드 | 헤테로사이클릭 유도체 |
JP6527147B2 (ja) | 2013-08-14 | 2019-06-05 | カルヴィスタ ファーマシューティカルズ リミテッド | 血漿カリクレインの阻害薬 |
GB2517908A (en) | 2013-08-14 | 2015-03-11 | Kalvista Pharmaceuticals Ltd | Bicyclic inhibitors |
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 |
GB201421088D0 (en) | 2014-11-27 | 2015-01-14 | Kalvista Pharmaceuticals Ltd | New enzyme inhibitors |
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 |
KR20160111657A (ko) | 2015-03-17 | 2016-09-27 | 김순철 | 절수형 변기 |
LT3464271T (lt) | 2016-05-31 | 2020-09-10 | Kalvista Pharmaceuticals Limited | Pirazolo dariniai kaip plazmos kalikreino inhibitoriai |
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 |
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 |
GB201719881D0 (en) | 2017-11-29 | 2018-01-10 | Kalvista Pharmaceuticals Ltd | Solid forms of plasma kallikrein inhibitor and salts thereof |
IL274557B2 (en) | 2017-11-29 | 2024-09-01 | Kalvista Pharmaceuticals Ltd | Dosage forms containing a plasma kallikrein inhibitor |
GB201910116D0 (en) | 2019-07-15 | 2019-08-28 | Kalvista Pharmaceuticals Ltd | Treatments of hereditary angioedema |
GB201910125D0 (en) | 2019-07-15 | 2019-08-28 | Kalvista Pharmaceuticals Ltd | Treatments of angioedema |
EP4010333A1 (fr) | 2019-08-09 | 2022-06-15 | Kalvista Pharmaceuticals Limited | Inhibiteurs de la kallicréine plasmatique |
GB2591730A (en) | 2019-12-09 | 2021-08-11 | Kalvista Pharmaceuticals Ltd | New polymorphs |
GB201918994D0 (en) | 2019-12-20 | 2020-02-05 | Kalvista Pharmaceuticals Ltd | Treatments of diabetic macular edema and impaired visual acuity |
TW202228686A (zh) | 2020-10-15 | 2022-08-01 | 英商卡爾維斯塔製藥有限公司 | 血管性水腫之治療 |
US20230381162A1 (en) | 2020-10-23 | 2023-11-30 | Kalvista Pharmaceuticals Limited | Treatments of angioedema |
US20240122909A1 (en) | 2021-02-09 | 2024-04-18 | Kalvista Pharmaceuticals Limited | Treatments of hereditary angioedema |
WO2023002219A1 (fr) | 2021-07-23 | 2023-01-26 | Kalvista Pharmaceuticals Limited | Traitements de l'angio-oedème héréditaire |
WO2023209381A1 (fr) | 2022-04-27 | 2023-11-02 | Kalvista Pharmaceuticals Limited | Formulations d'un inhibiteur de la kallicréine plasmatique |
WO2024180100A1 (fr) | 2023-02-27 | 2024-09-06 | Kalvista Pharmaceuticals Limited | Nouvelle forme solide d'un inhibiteur de la kallicréine plasmatique |
Family Cites Families (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0183271B1 (fr) | 1984-11-30 | 1990-05-16 | Shosuke Okamoto | Dérivé de lysine et inhibiteur de protéinase |
AU8868991A (en) | 1990-11-15 | 1992-06-11 | Pentapharm Ag | Meta-substituted phenyl alanine derivatives |
DE4243858A1 (de) | 1992-12-23 | 1994-06-30 | Thomae Gmbh Dr K | Aminosäurederivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
CA2133761A1 (fr) | 1993-02-10 | 1994-08-18 | Jorg Sturzebecher | Piperazides de derives de substitution de la phenylalamine utilises comme inhibiteurs de la thrombine |
SE9301916D0 (sv) | 1993-06-03 | 1993-06-03 | Ab Astra | New peptides derivatives |
US5550213A (en) | 1993-12-27 | 1996-08-27 | Rutgers, The State University Of New Jersey | Inhibitors of urokinase plasminogen activator |
CA2140598C (fr) | 1994-01-27 | 2010-03-09 | Masahiro Ohshima | Derives de la prolineamide |
ZA951617B (en) | 1994-03-04 | 1997-02-27 | Lilly Co Eli | Antithrombotic agents. |
US5726159A (en) | 1994-03-04 | 1998-03-10 | Eli Lilly And Company | Antithrombotic agents |
US5705487A (en) | 1994-03-04 | 1998-01-06 | Eli Lilly And Company | Antithrombotic agents |
US5707966A (en) | 1994-03-04 | 1998-01-13 | Eli Lilly And Company | Antithrombotic agents |
ZA953361B (en) | 1994-04-26 | 1996-01-12 | Selectide Corp | Factor Xa inhibitors |
SK104697A3 (en) | 1995-02-17 | 1998-11-04 | Basf Ag | Novel dipeptide amidines as thrombin inhibitors |
US5710130A (en) | 1995-02-27 | 1998-01-20 | Eli Lilly And Company | Antithrombotic agents |
US5914319A (en) | 1995-02-27 | 1999-06-22 | Eli Lilly And Company | Antithrombotic agents |
CH689611A5 (de) | 1995-03-01 | 1999-07-15 | Pentapharm Ag | Urokinase-Inhibitoren. |
US5786328A (en) | 1995-06-05 | 1998-07-28 | Genentech, Inc. | Use of kunitz type plasma kallikrein inhibitors |
AR005245A1 (es) | 1995-12-21 | 1999-04-28 | Astrazeneca Ab | Prodrogas de inhibidores de trombina, una formulación farmaceutica que las comprende, el uso de dichas prodrogas para la manufactura de un medicamento y un procedimiento para su preparacion |
AU3496297A (en) | 1996-06-25 | 1998-01-14 | Eli Lilly And Company | Anticoagulant agents |
ZA986594B (en) | 1997-07-25 | 1999-01-27 | Abbott Lab | Urokinase inhibitors |
JP4603162B2 (ja) | 1998-07-20 | 2010-12-22 | ヴィレックス アクチェンゲゼルシャフト | 新規ウロキナーゼインヒビター |
US7342018B2 (en) | 1998-07-20 | 2008-03-11 | Wilex Ag | Urokinase inhibitors and uses thereof |
US6576613B1 (en) | 1998-07-24 | 2003-06-10 | Corvas International, Inc. | Title inhibitors of urokinase |
SE9802974D0 (sv) | 1998-09-03 | 1998-09-03 | Astra Ab | New crystalline forms |
AU9059798A (en) | 1998-09-18 | 2000-04-10 | Pentapharm Ag | Urokinase inhibitors |
BR0008755A (pt) | 1999-01-13 | 2007-05-29 | Genentech Inc | compostos inibidores de protease de serina, composição, método de inibição da atividade de tf/fator viia, fator xa, trombina ou calicreìna, método de tratamento de uma disfunção mediada por tf/fator viia, fator xa, trombina ou calicreìna e método de prevenção de trombose ou tratamento de trombose anormal |
FR2791683A1 (fr) * | 1999-03-30 | 2000-10-06 | Synthelabo | Derives de n-sulfonyl-dipeptides, leur preparation et leur application en therapeutique |
AR023510A1 (es) | 1999-04-21 | 2002-09-04 | Astrazeneca Ab | Un equipo de partes, formulacion farmaceutica y uso de un inhibidor de trombina. |
DE19940389A1 (de) | 1999-08-25 | 2001-03-01 | Wilex Biotechnology Gmbh | Selektive Inhibitoren des Urokinase-Plasminogen Aktivators |
US6797504B1 (en) | 2000-09-08 | 2004-09-28 | Dendreon San Diego Llc | Inhibitors of serine protease activity of matriptase or MTSP1 |
DE10005631A1 (de) | 2000-02-09 | 2001-08-23 | Max Planck Gesellschaft | Arginin-Mimetika als Faktor X¶a¶-Inhibitoren |
DE10013715A1 (de) | 2000-03-20 | 2001-09-27 | Wilex Biotechnology Gmbh | Hochselektive Inhibitoren des Urokinase-Plasminogenaktivators |
EP1276722B1 (fr) | 2000-04-25 | 2006-03-08 | Abbott Laboratories | Inhibiteur de naphthamidine urokinase |
DE10029014A1 (de) | 2000-06-15 | 2001-12-20 | Univ Schiller Jena | Urokinase-Hemmstoffe |
DE10029015A1 (de) | 2000-06-15 | 2001-12-20 | Curacyte Ag | Hemmstoffe für den Gerinnungsfaktor Xa |
DE10029001C2 (de) | 2000-06-17 | 2003-03-27 | Rainer Seidel | Automatische Warnvorrichtung vor einer kritischen Schiffsneigung z.B. bei Wellenbildung oder Krängung |
AU2001266838A1 (en) | 2000-06-21 | 2002-01-02 | Georgetown University | Inhibitors of matriptase for the treatment of cancer |
AU2002222933A1 (en) | 2000-07-13 | 2002-01-30 | Millennium Pharamaceuticals, Inc. | Inhibitors of factor xa |
NZ518195A (en) | 2000-08-11 | 2005-04-29 | Corvas Int Inc | Non-covalent inhibitors of urokinase and blood vessel formation |
EP1808440B1 (fr) | 2000-08-11 | 2011-07-27 | Wilex AG | Inhibiteurs non covalents d'urokinase et formation de vaisseaux sanguins |
JP2004516286A (ja) | 2000-12-18 | 2004-06-03 | メルク エンド カムパニー インコーポレーテッド | ベンジルアミン誘導体およびそれのトロンビン阻害薬としての使用 |
DE10102878A1 (de) | 2001-01-23 | 2002-08-01 | Haemosys Gmbh | Oligo- oder Polyalkylengekoppelte Thrombininhibitoren |
EP1364960A4 (fr) | 2001-02-02 | 2005-05-18 | Chugai Pharmaceutical Co Ltd | Derives de peptide |
DK1453852T3 (da) | 2001-12-12 | 2007-05-21 | Wilex Ag | Selektive arylguanidinpeptider som urokinaseinhibitorer |
AU2003206945A1 (en) * | 2002-02-22 | 2003-09-09 | Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften E.V. | Use of proteinase inhibitors in the treatment of autoimmune diseases |
DE10210590A1 (de) * | 2002-03-11 | 2003-10-02 | Curacyte Ag | Hemmstoffe des Gerinnungsfaktors Xa, ihre Herstellung und Verwendung |
US7838560B2 (en) | 2002-03-11 | 2010-11-23 | The Medicines Company (Leipzig) Gmbh | Urokinase inhibitors, production and use thereof |
DE10212555A1 (de) | 2002-03-15 | 2003-09-25 | Univ Schiller Jena | Verwendung von Hemmstoffen des Gerinnungsfaktors Xa als Wirkstoffe zur Erkennung und Unterdrückung des Wachstums maligner Tumore sowie der von diesen ausgehenden Metastasierung |
DE10225876A1 (de) | 2002-06-11 | 2003-12-24 | Wilex Ag | Guanidinophenylalaninverbindungen als Urokinase-Inhibitoren |
AU2002349247A1 (en) | 2002-10-04 | 2004-04-23 | Pentapharm Ag | Substrate for tafi (a) |
DE10301300B4 (de) | 2003-01-15 | 2009-07-16 | Curacyte Chemistry Gmbh | Verwendung von acylierten 4-Amidino- und 4-Guanidinobenzylaminen zur Inhibierung von Plasmakallikrein |
DE10322191B4 (de) | 2003-05-16 | 2014-02-27 | The Medicines Company (Leipzig) Gmbh | N-sulfonylierte Aminosäurederivate, Verfahren zu ihrer Herstellung und ihre Verwendung |
DE10323898A1 (de) | 2003-05-26 | 2004-12-23 | Wilex Ag | Hydroxyamidin- und Hydroxyguanidin-Verbindungen als Urokinase-Hemmstoffe |
DE10342108A1 (de) * | 2003-09-11 | 2005-04-14 | Curacyte Chemistry Gmbh | Basisch-substituierte Benzylaminanaloga als Inhibitoren des Gerinnungsfaktors Xa, ihre Herstellung und Verwendung |
DE102005044319A1 (de) | 2005-09-16 | 2007-03-22 | Curacyte Chemistry Gmbh | 2-(Aminomethyl)-5-Chlor-Benzylamid-Derivate und ihre Verwendung als Hemmstoffe des Gerinnungsfaktors Xa |
DE102006050672A1 (de) | 2006-10-24 | 2008-04-30 | Curacyte Discovery Gmbh | Hemmstoffe des Plasmins und des Plasmakallikreins |
-
2006
- 2006-10-24 DE DE102006050672A patent/DE102006050672A1/de not_active Withdrawn
-
2007
- 2007-10-24 WO PCT/EP2007/009220 patent/WO2008049595A1/fr active Application Filing
- 2007-10-24 JP JP2009533726A patent/JP5356237B2/ja not_active Expired - Fee Related
- 2007-10-24 EA EA200970397A patent/EA018998B1/ru not_active IP Right Cessation
- 2007-10-24 BR BRPI0718286-4A patent/BRPI0718286A2/pt not_active IP Right Cessation
- 2007-10-24 NZ NZ577008A patent/NZ577008A/en not_active IP Right Cessation
- 2007-10-24 MX MX2009004320A patent/MX2009004320A/es active IP Right Grant
- 2007-10-24 CA CA2667507A patent/CA2667507C/fr not_active Expired - Fee Related
- 2007-10-24 AU AU2007308421A patent/AU2007308421B2/en not_active Ceased
- 2007-10-24 EP EP07819274.7A patent/EP2054380B8/fr active Active
- 2007-10-24 ES ES07819274.7T patent/ES2439244T3/es active Active
- 2007-10-24 CN CNA2007800436964A patent/CN101541742A/zh active Pending
- 2007-10-24 EP EP12004643.8A patent/EP2502906A3/fr not_active Withdrawn
-
2009
- 2009-04-24 NO NO20091647A patent/NO20091647L/no not_active Application Discontinuation
- 2009-04-24 US US12/429,766 patent/US8207378B2/en not_active Expired - Fee Related
-
2012
- 2012-05-14 US US13/471,007 patent/US8410310B2/en not_active Expired - Fee Related
-
2013
- 2013-02-19 US US13/770,588 patent/US8513461B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
EP2502906A2 (fr) | 2012-09-26 |
EP2054380B8 (fr) | 2013-10-30 |
US20100022781A1 (en) | 2010-01-28 |
US8207378B2 (en) | 2012-06-26 |
JP2010507610A (ja) | 2010-03-11 |
BRPI0718286A2 (pt) | 2013-11-19 |
AU2007308421A1 (en) | 2008-05-02 |
ES2439244T3 (es) | 2014-01-22 |
CA2667507C (fr) | 2015-04-21 |
WO2008049595A9 (fr) | 2009-01-29 |
CN101541742A (zh) | 2009-09-23 |
US20130165510A1 (en) | 2013-06-27 |
AU2007308421B2 (en) | 2012-05-03 |
EA018998B1 (ru) | 2013-12-30 |
US8513461B2 (en) | 2013-08-20 |
EP2502906A3 (fr) | 2013-05-08 |
DE102006050672A1 (de) | 2008-04-30 |
EP2054380A1 (fr) | 2009-05-06 |
US20120225913A1 (en) | 2012-09-06 |
ES2439244T8 (es) | 2014-11-06 |
EA200970397A1 (ru) | 2009-10-30 |
NZ577008A (en) | 2012-02-24 |
EP2054380B1 (fr) | 2013-09-11 |
JP5356237B2 (ja) | 2013-12-04 |
MX2009004320A (es) | 2009-08-28 |
US8410310B2 (en) | 2013-04-02 |
CA2667507A1 (fr) | 2008-05-02 |
WO2008049595A1 (fr) | 2008-05-02 |
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