PE20040171A1 - BICYCLE HETEROCYCLES, MEDICINES CONTAINING THESE COMPOUNDS, THEIR USE AND PROCEDURES FOR THEIR PREPARATION - Google Patents
BICYCLE HETEROCYCLES, MEDICINES CONTAINING THESE COMPOUNDS, THEIR USE AND PROCEDURES FOR THEIR PREPARATIONInfo
- Publication number
- PE20040171A1 PE20040171A1 PE2003000384A PE2003000384A PE20040171A1 PE 20040171 A1 PE20040171 A1 PE 20040171A1 PE 2003000384 A PE2003000384 A PE 2003000384A PE 2003000384 A PE2003000384 A PE 2003000384A PE 20040171 A1 PE20040171 A1 PE 20040171A1
- Authority
- PE
- Peru
- Prior art keywords
- amino
- bicycle
- phenyl
- ilo
- buten
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/02—Nasal agents, e.g. decongestants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic 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
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- 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
- C07D471/08—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/08—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/08—Bridged systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Urology & Nephrology (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Oncology (AREA)
- Otolaryngology (AREA)
- Gastroenterology & Hepatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Indole Compounds (AREA)
Abstract
SE REFIERE A HETEROCICLOS BICICLICOS DE FORMULA I DONDE Ra ES HIDROGENO, ALQUILO C1-C4; Rb ES FENILO, BENCILO O 1-FENILETILO, ENTRE OTROS; Rc ES HIDROGENO, FLUOR, CLORO, BROMO, HIDROXI, ENTRE OTROS; A ES GRUPO IMINO O ALQUIL(C1-C4)-IMINO; B ES CARBONILO O SULFONILO; C ES 1,3-ALENILENO, 1,1-VINILENO, 1,2-VINILENO, ENTRE OTROS; D ES ALQUILENO C1-C4 DE CADENA LINEAL O RAMIFICADO; E ES PIRROLIDIN-1-ILO, PIPERIDIN-1-ILO U HOMOPIPERIDIN -1-ILO, ENTRE OTROS; X ES UN GRUPO METINO SUSTITUIDO CON GRUPO CIANO, NITROGENO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS:4-[(3-CLORO-4-FLUORO-FENIL)AMINO]-6-{[4-((1S,4S)-2-OXA-5-AZA-BICICLO[2.2.1]HEPT-5-IL)-1-OXO-2-BUTEN-1-IL]AMINO}-7-CICLOPROPILMETOXI-QUINAZOLINA,4-[(3-CLORO-4-FLUORO-FENIL)AMINO]-6-{[4-((1S,4S)-2-OXA-5-AZA-BICICLO[2.2.1]HEPT-5-IL)-1-OXO-2-BUTEN-1-IL]AMINO}-7-CICLOPETILOXI-QUINAZOLINA,4-[(3-CLORO-4-FLUORO-FENIL)AMINO]-6-{[4-((1S,4S)-2-OXA-5-AZA-BICICLO[2.2.1]HEPT-5-IL)-1-OXO-2-BUTEN-1-IL]AMINO}-7-[(S)-(TETRAHIDROFURAN-3-IL)OXI]-QUINAZOLINA, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO PARA LA PREPARACION. LOS COMPUESTOS MENCIONADOS TIENEN ACCION INHIBIDORA SOBRE LA TRANSDUCCION DE SENAL MEDIADA POR TIROSINCINASAS Y SON UTILES PARA EL TRATAMIENTO DE ENFERMEDADES TUMORALES E HIPERPLASIA PROSTATICA BENIGNA (BHP)REFERS TO BICYCLE HETEROCYCLES OF FORMULA I WHERE Ra IS HYDROGEN, C1-C4 ALKYL; Rb IS PHENYL, BENZYL OR 1-PHENYLETHYL, AMONG OTHERS; Rc IS HYDROGEN, FLUORINE, CHLORINE, BROMINE, HYDROXY, AMONG OTHERS; A ES GROUP IMINO OR ALQUIL (C1-C4) -IMINO; B IS CARBONYL OR SULPHONYL; C IS 1,3-ALENYLENE, 1,1-VINYLENE, 1,2-VINYLENE, AMONG OTHERS; D IS LINEAR OR BRANCHED CHAIN C1-C4 ALKYLENE; E IS PIRROLIDIN-1-ILO, PIPERIDIN-1-ILO OR HOMOPIPERIDIN -1-ILO, AMONG OTHERS; X IS A METINO GROUP SUBSTITUTED BY CIANO GROUP, NITROGENO, AMONG OTHERS. THE PREFERRED COMPOUNDS ARE: 4 - [(3-CHLORO-4-FLUORO-PHENYL) AMINO] -6 - {[4 - ((1S, 4S) -2-OXA-5-AZA-BICICLO [2.2.1] HEPT- 5-IL) -1-OXO-2-BUTEN-1-IL] AMINO} -7-CYCLOPROPYLMETOXY-QUINAZOLINE, 4 - [(3-CHLORO-4-FLUORO-PHENYL) AMINO] -6 - {[4- ( (1S, 4S) -2-OXA-5-AZA-BICYCLE [2.2.1] HEPT-5-IL) -1-OXO-2-BUTEN-1-IL] AMINO} -7-CYCLOPETHYLOXY-QUINAZOLINE, 4- [(3-CHLORO-4-FLUORO-PHENYL) AMINO] -6 - {[4 - ((1S, 4S) -2-OXA-5-AZA-BICYCLE [2.2.1] HEPT-5-IL) -1 -OXO-2-BUTEN-1-IL] AMINO} -7 - [(S) - (TETRAHIDROFURAN-3-IL) OXY] -QUINAZOLINE, AMONG OTHERS. IT ALSO REFERS TO A PROCEDURE FOR PREPARATION. THE MENTIONED COMPOUNDS HAVE INHIBITING ACTION ON SIGNAL TRANSDUCTION MEDIATED BY TIROSINKINASES AND ARE USEFUL FOR THE TREATMENT OF TUMOR DISEASES AND BENIGN PROSTATIC HYPERPLASIA (BHP)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10217689A DE10217689A1 (en) | 2002-04-19 | 2002-04-19 | Bicyclic heterocycles, medicaments containing these compounds, their use and processes for their preparation |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20040171A1 true PE20040171A1 (en) | 2004-06-02 |
Family
ID=29224623
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2003000384A PE20040171A1 (en) | 2002-04-19 | 2003-04-15 | BICYCLE HETEROCYCLES, MEDICINES CONTAINING THESE COMPOUNDS, THEIR USE AND PROCEDURES FOR THEIR PREPARATION |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP1499619A1 (en) |
JP (1) | JP4527406B2 (en) |
AR (1) | AR039571A1 (en) |
AU (1) | AU2003226806A1 (en) |
CA (1) | CA2484395C (en) |
DE (1) | DE10217689A1 (en) |
PE (1) | PE20040171A1 (en) |
TW (1) | TW200408643A (en) |
UY (1) | UY27767A1 (en) |
WO (1) | WO2003089439A1 (en) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100709909B1 (en) | 1999-06-21 | 2007-04-24 | 베링거 잉겔하임 파르마 게엠베하 운트 코 카게 | Bicyclic heterocycles, medicaments containing these compounds and methods for the production thereof |
US7019012B2 (en) | 2000-12-20 | 2006-03-28 | Boehringer Ingelheim International Pharma Gmbh & Co. Kg | Quinazoline derivatives and pharmaceutical compositions containing them |
US20040044014A1 (en) | 2002-04-19 | 2004-03-04 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Bicyclic heterocycles, pharmaceutical compositions containing these compounds, their use and processes for the preparation thereof |
ES2400339T3 (en) | 2002-07-15 | 2013-04-09 | Symphony Evolution, Inc. | Compounds, pharmaceutical compositions thereof and their use in the treatment of cancer |
US8309562B2 (en) | 2003-07-03 | 2012-11-13 | Myrexis, Inc. | Compounds and therapeutical use thereof |
JP4638436B2 (en) | 2003-09-26 | 2011-02-23 | エグゼリクシス, インコーポレイテッド | c-Met modulators and uses thereof |
CA2565812C (en) * | 2004-05-06 | 2012-03-13 | Warner-Lambert Company Llc | 4-phenylamino-quinazolin-6-yl-amides |
EP1833482A4 (en) | 2005-01-03 | 2011-02-16 | Myriad Genetics Inc | Compounds and therapeutical use thereof |
US8258145B2 (en) | 2005-01-03 | 2012-09-04 | Myrexis, Inc. | Method of treating brain cancer |
KR100832594B1 (en) | 2005-11-08 | 2008-05-27 | 한미약품 주식회사 | Quinazoline derivatives as an multiplex inhibitor and method for the preparation thereof |
US8404697B2 (en) | 2005-11-11 | 2013-03-26 | Boehringer Ingelheim International Gmbh | Quinazoline derivatives for the treatment of cancer diseases |
NZ576065A (en) | 2006-09-18 | 2011-12-22 | Boehringer Ingelheim Int | Method for treating cancer harboring egfr mutations |
TWI577664B (en) | 2009-01-16 | 2017-04-11 | 艾克塞里克斯公司 | Malate salt of n-(4-{[6,7-bis(methyloxy)quinolin-4-yl]oxy}phenyl)-n'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide, pharmaceutical composition comprising the same and use thereof |
CN102711472B (en) | 2009-07-02 | 2015-12-02 | 江苏康缘药业股份有限公司 | Phosphorous quinazoline compound and using method thereof |
SI2451445T1 (en) | 2009-07-06 | 2019-07-31 | Boehringer Ingelheim International Gmbh | Process for drying of bibw2992, of its salts and of solid pharmaceutical formulations comprising this active ingredient |
UA108618C2 (en) | 2009-08-07 | 2015-05-25 | APPLICATION OF C-MET-MODULATORS IN COMBINATION WITH THEMOSOLOMID AND / OR RADIATION THERAPY FOR CANCER TREATMENT | |
CN102020639A (en) | 2009-09-14 | 2011-04-20 | 上海恒瑞医药有限公司 | 6-amido quinazoline or 3-cyano quinoline derivative, preparation method thereof and application of derivative to medicament |
CN103748080B (en) | 2011-05-26 | 2016-09-28 | 山东轩竹医药科技有限公司 | Quinazoline derivative species tyrosine kinase inhibitor and preparation method and application |
CN103874696B (en) * | 2011-10-12 | 2015-06-03 | 苏州韬略生物科技有限公司 | Quinazoline derivatives as kinases inhibitors and methods of use thereof |
US9242965B2 (en) | 2013-12-31 | 2016-01-26 | Boehringer Ingelheim International Gmbh | Process for the manufacture of (E)-4-N,N-dialkylamino crotonic acid in HX salt form and use thereof for synthesis of EGFR tyrosine kinase inhibitors |
WO2020068867A1 (en) | 2018-09-25 | 2020-04-02 | Black Diamond Therapeutics, Inc. | Quinazoline derivatives as tyrosine kinase inhibitor, compositions, methods of making them and their use |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK0892789T4 (en) * | 1996-04-12 | 2010-04-06 | Warner Lambert Co | Irreversible inhibitors of tyrosine kinases |
TW436485B (en) * | 1997-08-01 | 2001-05-28 | American Cyanamid Co | Substituted quinazoline derivatives |
SI2253620T1 (en) * | 1998-09-29 | 2014-06-30 | Wyeth Holdings Llc | Substituted 3-cyanoquinolines as protein tyrosine kinases inhibitors |
JP3751201B2 (en) * | 1999-02-27 | 2006-03-01 | ベーリンガー インゲルハイム ファルマ ゲゼルシャフト ミット ベシュレンクテル ハフツング ウント コンパニー コマンディトゲゼルシャフト | 4-Amino-quinazoline derivatives and quinoline derivatives having an inhibitory effect on signal transduction mediated by tyrosine kinases |
DE19908567A1 (en) * | 1999-02-27 | 2000-08-31 | Boehringer Ingelheim Pharma | New 4-amino-quinazoline or quinoline derivatives, are tyrosine kinase-mediated signal transduction inhibitors useful e.g. for treating tumors, polyps or respiratory or gastrointestinal diseases |
KR100709909B1 (en) * | 1999-06-21 | 2007-04-24 | 베링거 잉겔하임 파르마 게엠베하 운트 코 카게 | Bicyclic heterocycles, medicaments containing these compounds and methods for the production thereof |
ATE350378T1 (en) * | 2000-04-08 | 2007-01-15 | Boehringer Ingelheim Pharma | BICYCLIC HETEROCYCLES, MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS, THEIR USE AND METHOD FOR THEIR PRODUCTION |
DE10017539A1 (en) * | 2000-04-08 | 2001-10-11 | Boehringer Ingelheim Pharma | New 6-acylamino-4-amino-quinazoline or quinoline derivatives, are tyrosine kinase-mediated signal transduction inhibitors useful e.g. for treating tumors or respiratory or gastrointestinal diseases |
DE10042061A1 (en) * | 2000-08-26 | 2002-03-07 | Boehringer Ingelheim Pharma | Bicyclic heterocycles, medicaments containing these compounds, their use and processes for their preparation |
DE10042062A1 (en) * | 2000-08-26 | 2002-03-07 | Boehringer Ingelheim Pharma | Bicyclic heterocycles, medicaments containing these compounds, their use and methods of preparation |
-
2002
- 2002-04-19 DE DE10217689A patent/DE10217689A1/en not_active Withdrawn
-
2003
- 2003-04-14 JP JP2003586159A patent/JP4527406B2/en not_active Expired - Fee Related
- 2003-04-14 CA CA2484395A patent/CA2484395C/en not_active Expired - Fee Related
- 2003-04-14 EP EP03746824A patent/EP1499619A1/en not_active Withdrawn
- 2003-04-14 AU AU2003226806A patent/AU2003226806A1/en not_active Abandoned
- 2003-04-14 WO PCT/EP2003/003828 patent/WO2003089439A1/en active Application Filing
- 2003-04-15 PE PE2003000384A patent/PE20040171A1/en not_active Application Discontinuation
- 2003-04-16 TW TW092108807A patent/TW200408643A/en unknown
- 2003-04-16 UY UY27767A patent/UY27767A1/en not_active Application Discontinuation
- 2003-04-16 AR ARP030101330A patent/AR039571A1/en not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
AU2003226806A1 (en) | 2003-11-03 |
CA2484395C (en) | 2011-11-22 |
WO2003089439A1 (en) | 2003-10-30 |
JP2005526837A (en) | 2005-09-08 |
EP1499619A1 (en) | 2005-01-26 |
DE10217689A1 (en) | 2003-11-13 |
JP4527406B2 (en) | 2010-08-18 |
UY27767A1 (en) | 2003-11-28 |
TW200408643A (en) | 2004-06-01 |
AR039571A1 (en) | 2005-02-23 |
CA2484395A1 (en) | 2003-10-30 |
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