BG103655A - Disubstituted bicyclic heterocyclic compounds, their preparation and application as medicamentous forms - Google Patents
Disubstituted bicyclic heterocyclic compounds, their preparation and application as medicamentous formsInfo
- Publication number
- BG103655A BG103655A BG103655A BG10365599A BG103655A BG 103655 A BG103655 A BG 103655A BG 103655 A BG103655 A BG 103655A BG 10365599 A BG10365599 A BG 10365599A BG 103655 A BG103655 A BG 103655A
- Authority
- BG
- Bulgaria
- Prior art keywords
- compounds
- preparation
- application
- heterocyclic compounds
- bicyclic heterocyclic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- 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
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/02—Suppositories; Bougies; Bases therefor; Ovules
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/19—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles lyophilised, i.e. freeze-dried, solutions or dispersions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/2027—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4841—Filling excipients; Inactive ingredients
- A61K9/4858—Organic compounds
-
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/04—Antihaemorrhagics; Procoagulants; Haemostatic agents; Antifibrinolytic agents
-
- 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
- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/12—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/14—Radicals substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/16—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/28—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
- C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
- C07D241/40—Benzopyrazines
- C07D241/44—Benzopyrazines with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/64—Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D277/70—Sulfur atoms
- C07D277/74—Sulfur atoms substituted by carbon atoms
-
- 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
-
- 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
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
The compounds can be applied in medicine. They have the general formula ra-A-Het-B-Ar-E where A, B, Ar, Het and Ra have the meanings listed in the descripiton. When E is a cyanogroup the compounds are valuable intermediate products for making other compounds with the same general formula. In case E means RbNH-C(=NH)-group the compounds show valuable pharmaceological properties, in particular thrombin inhibition effect and thrombin time elongation effect. The invention also relates to tautomers, stereoisomers, mixtures and salts of the above compounds. 15 claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19706229A DE19706229A1 (en) | 1997-02-18 | 1997-02-18 | New aryl-substituted bi:cyclic heterocyclic compounds |
DE1997151939 DE19751939A1 (en) | 1997-11-24 | 1997-11-24 | New aryl-substituted bi:cyclic heterocyclic compounds |
Publications (2)
Publication Number | Publication Date |
---|---|
BG103655A true BG103655A (en) | 2000-02-29 |
BG64558B1 BG64558B1 (en) | 2005-07-29 |
Family
ID=26034058
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BG103655A Active BG64558B1 (en) | 1997-02-18 | 1999-08-10 | Disubstituted bicyclic heterocyclic compounds, their preparation and application as medicamentous forms |
Country Status (39)
Country | Link |
---|---|
EP (1) | EP0966454B1 (en) |
JP (1) | JP3343359B2 (en) |
KR (1) | KR100619458B1 (en) |
CN (1) | CN1088702C (en) |
AR (1) | AR010896A1 (en) |
AT (1) | ATE239712T1 (en) |
AU (1) | AU742593C (en) |
BG (1) | BG64558B1 (en) |
BR (1) | BR9807843B1 (en) |
CA (1) | CA2277949C (en) |
CO (1) | CO4920237A1 (en) |
CZ (1) | CZ297768B6 (en) |
DE (2) | DE59808281D1 (en) |
DK (1) | DK0966454T3 (en) |
EA (1) | EA003697B1 (en) |
EE (1) | EE04716B1 (en) |
EG (1) | EG24144A (en) |
ES (1) | ES2199426T4 (en) |
FR (1) | FR08C0025I2 (en) |
HK (1) | HK1025096A1 (en) |
HR (1) | HRP980082B1 (en) |
HU (1) | HU223754B1 (en) |
IL (1) | IL130812A (en) |
LT (1) | LTC0966454I2 (en) |
LU (1) | LU91437I2 (en) |
MY (1) | MY129408A (en) |
NL (1) | NL300349I2 (en) |
NO (3) | NO313879B1 (en) |
NZ (1) | NZ337323A (en) |
PE (1) | PE121699A1 (en) |
PL (1) | PL195551B1 (en) |
PT (1) | PT966454E (en) |
RS (1) | RS49686B (en) |
SA (1) | SA98190047B1 (en) |
SI (1) | SI0966454T1 (en) |
SK (1) | SK285432B6 (en) |
TR (1) | TR199902017T2 (en) |
TW (1) | TW588047B (en) |
WO (1) | WO1998037075A1 (en) |
Families Citing this family (171)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU1608399A (en) * | 1997-11-26 | 1999-06-15 | Axys Pharmaceuticals, Inc. | Substituted amidinoaryl derivatives and their use as anticoagulants |
US6114532A (en) * | 1998-02-03 | 2000-09-05 | Boehringer Ingelheim Pharma Kg | Bicyclic heterocycles, the preparation thereof, and their use as pharmaceuticals |
WO1999040072A1 (en) * | 1998-02-03 | 1999-08-12 | Boehringer Ingelheim Pharma Kg | Five-membered, benzo-condensed heterocycles used as antithrombotic agents |
NZ506507A (en) * | 1998-02-09 | 2003-08-29 | Dimensional Pharm Inc | Heteroaryl amidine, methylamidine or guanidine derivatives useful as urokinase inhibitors |
US6291514B1 (en) | 1998-02-09 | 2001-09-18 | 3-Dimensional Pharmaceuticals, Inc. | Heteroaryl amidines, methylamidines and guanidines, preparation thereof, and use thereof as protease inhibitors |
TWI248435B (en) * | 1998-07-04 | 2006-02-01 | Boehringer Ingelheim Pharma | Benzimidazoles, the preparation thereof and their use as pharmaceutical compositions |
US6248770B1 (en) | 1998-07-09 | 2001-06-19 | Boehringer Ingelheim Pharma Kg | Benzimidazoles having antithrombotic activity |
BR9917036A (en) * | 1999-02-09 | 2002-07-30 | Dimensional Pharm Inc | Heteroaryl amidines, methylamidines and guanidines as protease inhibitors |
DE19907813A1 (en) * | 1999-02-24 | 2000-08-31 | Boehringer Ingelheim Pharma | Substituted bicyclic heterocycles, their preparation and their use as pharmaceuticals |
AR023510A1 (en) | 1999-04-21 | 2002-09-04 | Astrazeneca Ab | A TEAM OF PARTS, PHARMACEUTICAL FORMULATION AND USE OF A THROMBIN INHIBITOR. |
US6512000B1 (en) | 1999-08-20 | 2003-01-28 | Boehringer Ingelheim Pharma Kg | Aminocarbonyl-substituted benzimidazoles having tryptase-inhibitory activity |
DE19939463A1 (en) * | 1999-08-20 | 2001-02-22 | Boehringer Ingelheim Pharma | Tryptase inhibitors useful e.g. for treating inflammatory or allergic disease, arteriosclerosis or neoplasia, comprising new or known 2-phenethyl-benzimidazole-5-carboxamides |
DE50001742D1 (en) * | 1999-09-24 | 2003-05-15 | Boehringer Ingelheim Pharma | ARYLSULFONAMIDE SUBSTITUTED BENZIMIDAZOLE DERIVATIVES AND THEIR USE AS TRYPTASE INHIBITORS |
DE19945787A1 (en) | 1999-09-24 | 2001-03-29 | Boehringer Ingelheim Pharma | New 2-(amidino- or aminomethyl-phenethyl)-5-sulfonylamino-benzimidazoles, are tryptase inhibitors useful e.g. for treating inflammatory or allergic disease such as asthma, urticaria or arthritis |
DE19945810A1 (en) * | 1999-09-24 | 2001-03-29 | Boehringer Ingelheim Pharma | Substituted benzimidazole derivatives, process for their preparation and their use as medicaments |
US6413990B1 (en) | 1999-09-24 | 2002-07-02 | Boehringer Ingelheim Pharma Kg | Arylsulphonamide-substituted benzimidazoles having tryptase-inhibiting activity |
US6407130B1 (en) | 1999-11-10 | 2002-06-18 | Boehringer Ingelheim Pharma Kg | Carboxamide-substituted benzimidazoles having tryptase-inhibiting activity |
US6451832B2 (en) | 1999-12-23 | 2002-09-17 | Boehringer Ingelheim Pharma Kg | Benzimidazoles with antithrombotic activity |
US6448281B1 (en) * | 2000-07-06 | 2002-09-10 | Boehringer Ingelheim (Canada) Ltd. | Viral polymerase inhibitors |
CN1243735C (en) * | 2001-04-19 | 2006-03-01 | 卫材株式会社 | 2-lminopyrrolidine derivatives |
DE10133786A1 (en) * | 2001-07-16 | 2003-02-06 | Boehringer Ingelheim Pharma | Use of thrombin inhibitors for the treatment of arthritis |
US20030181488A1 (en) * | 2002-03-07 | 2003-09-25 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Administration form for the oral application of 3-[(2-{[4-(hexyloxycarbonylamino-imino-methyl)-phenylamino]-methyl}-1-methyl-1H-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionic acid ethyl ester and the salts thereof |
PT1870100E (en) * | 2002-03-07 | 2012-04-17 | Boehringer Ingelheim Int | Ethyl 3-(2-(4-(hexyloxycarbonylamidino)phenylaminomethyl)-1-methyl-1h-benzimidazole-5-carbonyl)-2-pyridylamino)propionate methansulfonate |
DE10235639A1 (en) * | 2002-08-02 | 2004-02-19 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | New prodrugs of benzimidazole-5-carboxamide derivative thrombin inhibitor, useful for treating or preventing thrombotic diseases, are well tolerated on subcutaneous injection |
AU2003265398A1 (en) | 2002-08-09 | 2004-02-25 | Transtech Pharma, Inc. | Aryl and heteroaryl compounds and methods to modulate coagulation |
PE20040804A1 (en) | 2002-12-19 | 2004-12-31 | Boehringer Ingelheim Pharma | CARBOXAMID DERIVATIVES AS INHIBITORS OF THE Xa FACTOR |
DE10260730A1 (en) * | 2002-12-23 | 2004-07-01 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Novel substituted nitrogen-containing heterobicyclene, their preparation and their use as pharmaceuticals |
US7429597B2 (en) | 2002-12-23 | 2008-09-30 | Boehringer Ingelheim Pharma Gmbh & Co., Kg | Substituted nitrogen-containing heterobicycles, the preparation thereof and their use as pharmaceutical compositions |
EP2444393A1 (en) | 2003-02-19 | 2012-04-25 | Eisai R&D Management Co., Ltd. | Methods for producing cyclic benzamidine derivatives |
DE10310278A1 (en) * | 2003-03-10 | 2004-09-23 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | New N-(benzazinyl)-(hetero)aralkylamine derivatives, are inhibitors of factor Xa and/or related serine proteases, useful e.g. as antithrombotic agents and intermediates |
RU2005136383A (en) | 2003-04-24 | 2007-06-10 | БЕРИНГЕР ИНГЕЛЬХАЙМ ИНТЕРНАЦИОНАЛЬ ГмбХ (DE) | APPLICATION OF DIPYRIDAMOL OR MOPIDAMOL FOR TREATMENT AND PREVENTION OF THROMBOEMBOLIC DISEASES AND DISORDERS CAUSED BY REDUCED EDUCATION AND / OR HIGH LEVEL OF EXPRESSION OF TROMBRINES |
CN1832920A (en) * | 2003-08-08 | 2006-09-13 | 特兰斯泰克制药公司 | Aryl and heteroaryl compounds, compositions, and methods of use |
US7208601B2 (en) | 2003-08-08 | 2007-04-24 | Mjalli Adnan M M | Aryl and heteroaryl compounds, compositions, and methods of use |
US7501538B2 (en) | 2003-08-08 | 2009-03-10 | Transtech Pharma, Inc. | Aryl and heteroaryl compounds, compositions and methods of use |
DE10337697A1 (en) * | 2003-08-16 | 2005-03-24 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Tablet containing 3 - [(2 - {[4- (hexyloxycarbonylamino-iminomethyl) -phenyl-amino] -methyl} -1-methyl-1H-benzimidazole-5-carbonyl) -pyridin-2-yl-amino] - propionic acid ethyl ester or its salts |
DE10339862A1 (en) * | 2003-08-29 | 2005-03-24 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | New crystalline forms of ethyl 3-(N-(2-(4-(hexyloxycarbonylamidino)phenylaminomethyl)-1-methyl-1H-benzimidazole-5-carbonyl)-N-(2-pyridyl)amino)propionate methanesulfonate used for post-operative prophylaxis of deep vein thrombosis |
DE10341043A1 (en) * | 2003-09-03 | 2005-03-31 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | New Oral Dosage Form for 3 - [(2 - {[4-hexyloxycarbonylamino-imino-methyl) -phenyl-amino] -methyl} -1-methyl-1H-benzimidazole-5-carbonyl) -pyridin-2-yl-amino] Propionic acid ethyl ester and its salts |
EP1609784A1 (en) * | 2004-06-25 | 2005-12-28 | Boehringer Ingelheim Pharma GmbH & Co.KG | Process for the preparation of 4-(benzimidazolylmethylamino)-benzamidines |
US20060222640A1 (en) * | 2005-03-29 | 2006-10-05 | Boehringer Ingelheim International Gmbh | New pharmaceutical compositions for treatment of thrombosis |
DE102005020002A1 (en) * | 2005-04-27 | 2006-11-02 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | New hexyloxycarbonylamino-imino-methyl-phenylamino-methyl-benzimidazole-pyridine-propionic acid-ethyl ester salts such as hydrochloride useful for the prophylaxis of vein thrombosis and stroke |
DE102005025728A1 (en) * | 2005-06-04 | 2006-12-07 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Polymorphs of 3 - [(2 - {[4- (hexyloxycarbonylamino-imino-methyl) -phenyl-amino] -methyl} -1-methyl-1H-benzimidazole-5-carbonyl) -pyridin-2-yl-amino] -propionic acid ethyl ester |
WO2007002635A2 (en) | 2005-06-27 | 2007-01-04 | Bristol-Myers Squibb Company | C-linked cyclic antagonists of p2y1 receptor useful in the treatment of thrombotic conditions |
DE102005061624A1 (en) * | 2005-12-21 | 2007-06-28 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Improved process for the preparation of salts of 4- (benzimidazolylmethylamino) -benzamidines |
DE102005061623A1 (en) | 2005-12-21 | 2007-06-28 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Improved process for the preparation of 4- (benzimidazolylmethylamino) -benzamidines and their salts |
WO2007103996A1 (en) | 2006-03-09 | 2007-09-13 | Bristol-Myers Squibb Company | 2-(aryloxy)acetamide factor viia inhibitors useful as anticoagulants |
EP2061756B1 (en) | 2006-06-08 | 2013-09-25 | Bristol-Myers Squibb Company | 2-aminocarbonylphenylamino-2-phenilacetamides as factor viia inhibitors useful as anticoagulants |
CA2657269A1 (en) * | 2006-07-17 | 2008-01-24 | Boehringer Ingelheim International Gmbh | New indications for direct thrombin inhibitors |
CL2007002068A1 (en) * | 2006-07-17 | 2008-01-18 | Boehringer Ingelheim Int | Use of dabigatran, dabigatran ethoxylate, (n-2-pyridyl-n-2-ethoxycarbonylethyl) amide of 1-methyl-2- [4- (n-hydroxyamidino) phenylaminoethyl] benzimidazol-5-yl-carboxylic acid, melagatran, ximelagatran, hirudin, hirulog and argatroban for the treatment of cerebral infarction, myocardial infarction, thrombosis, pulmonary embolism, among others. |
US20100087488A1 (en) * | 2006-10-10 | 2010-04-08 | Boehringer Ingelheim International Gmgh | Physiologically Acceptable Salts of 3-[(2--1-methyl-1H-benzimidazol-5-carbonyl)-pyridin-2-yl-amino]-propionic acid ethyl ester |
JP5342450B2 (en) | 2006-12-15 | 2013-11-13 | ブリストル−マイヤーズ スクイブ カンパニー | Arylpropionamide, arylacrylamide, arylpropinamide, or arylmethylurea analogs as factor XIa inhibitors |
PE20081775A1 (en) | 2006-12-20 | 2008-12-18 | Bristol Myers Squibb Co | MACROCYCLIC COMPOUNDS AS INHIBITORS OF FACTOR VIIA |
EP1956018A1 (en) * | 2007-02-06 | 2008-08-13 | Boehringer Ingelheim Pharma GmbH & Co. KG | Method of preparing a derivative of benzimidazole |
BRPI0810462A2 (en) | 2007-04-23 | 2014-10-14 | Sanofi Aventis | KINOLIN-CARBOXAMIDE DERIVATIVES AS P2Y12 ANTAGONISTS |
EP2178849A1 (en) | 2007-07-31 | 2010-04-28 | Mallinckrodt Inc. | Integrated photoactive agents and uses thereof |
EP2238128B1 (en) | 2007-12-26 | 2012-08-22 | Sanofi | Heterocyclic pyrazole-carboxamides as p2y12 antagonists |
CZ305085B6 (en) * | 2008-03-14 | 2015-04-29 | Zentiva, K.S. | Process for preparing dabigatran |
NZ589746A (en) | 2008-07-14 | 2012-10-26 | Boehringer Ingelheim Int | Method for manufacturing medicinal compounds containing dabigatran |
EP2328581A1 (en) * | 2008-08-19 | 2011-06-08 | Boehringer Ingelheim International GmbH | Use of dabigatranetexilate for treating patients with pulmonary hypertension |
CZ2008669A3 (en) * | 2008-10-24 | 2010-05-05 | Zentiva, A. S. | Process for preparing dabigatran and intermediates thereof |
NZ593787A (en) * | 2009-02-02 | 2013-09-27 | Boehringer Ingelheim Int | Lyophilised dabigatran |
WO2010130757A1 (en) | 2009-05-14 | 2010-11-18 | Boehringer Ingelheim International Gmbh | New combination therapy in treatment of oncological and fibrotic diseases |
CN102481317B (en) | 2009-08-24 | 2014-09-03 | 贝林格尔.英格海姆国际有限公司 | Emergency interventions of active charcoal with dabigatran etexilate overdosing |
CN102050814B (en) * | 2009-11-06 | 2014-05-28 | 北京美倍他药物研究有限公司 | Ester derivatives of dabigatran |
CN102050815B (en) * | 2009-11-06 | 2014-04-02 | 北京美倍他药物研究有限公司 | Dabigatran ester derivatives as prodrug |
US8399678B2 (en) * | 2009-11-18 | 2013-03-19 | Boehringer Ingelheim International Gmbh | Process for the manufacture of dabigatran etexilate |
AR079944A1 (en) | 2010-01-20 | 2012-02-29 | Boehringer Ingelheim Int | NEUTRALIZING ANTIBODY OF THE ACTIVITY OF AN ANTICOAGULANT |
HUP1000069A2 (en) | 2010-02-02 | 2012-05-02 | Egis Gyogyszergyar Nyilvanosan M Kod Ruszvunytarsasag | New salts for the preparation of pharmaceutical composition |
EP3786165A1 (en) | 2010-02-11 | 2021-03-03 | Bristol-Myers Squibb Company | Synthetic intermediates for producing macrocycles as factor xia inhibitors |
SI2542224T1 (en) | 2010-03-01 | 2014-10-30 | Ratiopharm Gmbh | Dabigatran etexilate-containing oral pharmaceutical composition |
JP2013521318A (en) | 2010-03-08 | 2013-06-10 | ラティオファルム ゲー・エム・ベー・ハー | Pharmaceutical composition containing dabigatran etexilate |
PT2588090T (en) | 2010-07-01 | 2017-06-26 | Krka Tovarna Zdravil D D Novo Mesto | Pharmaceutical oral dosage forms comprising dabigatran etexilate and its pharmaceutically acceptable salts |
MX2013000295A (en) | 2010-07-09 | 2013-05-28 | Esteve Quimica Sa | Process of preparing a thrombin specific inhibitor. |
JP2013531004A (en) | 2010-07-09 | 2013-08-01 | エステヴェ キミカ, エス.エー. | Intermediates and methods for the preparation of thrombin specific inhibitors |
WO2012027543A1 (en) | 2010-08-25 | 2012-03-01 | Teva Pharmaceuticals Usa, Inc. | Solid state forms of dabigatran etexilate, dabigatran etexilate mesylate and processes for preparation thereof |
EP2649060B1 (en) | 2010-12-06 | 2017-04-05 | MSN Laboratories Limited | Process for the preparation of benzimidazole derivatives and its salts |
EP2671582B1 (en) | 2011-02-01 | 2016-07-13 | Kyowa Hakko Kirin Co., Ltd. | Ring-fused heterocyclic derivative |
EP2691156A1 (en) | 2011-03-30 | 2014-02-05 | Boehringer Ingelheim International GmbH | Anticoagulant antidotes |
HUP1100244A2 (en) | 2011-05-11 | 2012-11-28 | Egis Gyogyszergyar Nyilvanosan Muekoedoe Reszvenytarsasag | Pharmaceutical intermediates and process for their production |
CN102250099B (en) * | 2011-05-16 | 2013-10-16 | 中国药科大学 | Non-peptide thrombin inhibitors as well as preparation method and medical application thereof |
CN102838588B (en) * | 2011-06-24 | 2014-03-19 | 中国药科大学 | Oral thrombin inhibitors, preparation methods and medical uses thereof |
EP2550966B1 (en) * | 2011-07-25 | 2016-10-19 | Dritte Patentportfolio Beteiligungsgesellschaft mbH & Co. KG | Amidoxime carboxylic acid esters of dabigatran as prodrugs and their use as medicament |
TW201311689A (en) | 2011-08-05 | 2013-03-16 | 必治妥美雅史谷比公司 | Novel macrocycles as factor XIa inhibitors |
TW201319068A (en) | 2011-08-05 | 2013-05-16 | 必治妥美雅史谷比公司 | Cyclic P1 linkers as factor XIa inhibitors |
WO2013024394A1 (en) * | 2011-08-12 | 2013-02-21 | Alembic Pharmaceuticals Limited | Novel reference markers of dabigatran etexilate |
CN102993174A (en) * | 2011-09-08 | 2013-03-27 | 天津药物研究院 | Dabigatran etexilate derivative as a prodrug |
CN102993175B (en) * | 2011-09-08 | 2014-08-13 | 天津药物研究院 | Dabigatran derivatives, and preparation method and application thereof |
ES2699226T3 (en) | 2011-10-14 | 2019-02-08 | Bristol Myers Squibb Co | Substituted tetrahydroisoquinoline compounds as inhibitors of factor XIa |
ES2579832T3 (en) | 2011-10-14 | 2016-08-17 | Bristol-Myers Squibb Company | Substituted tetrahydroisoquinoline compounds as factor XIa inhibitors |
CA2851810C (en) | 2011-10-14 | 2020-01-07 | Bristol-Myers Squibb Company | Substituted tetrahydroisoquinoline compounds as factor xia inhibitors |
MX2014007331A (en) | 2011-12-22 | 2014-09-01 | Boehringer Ingelheim Int | Immediate release multi unit pellet system. |
WO2013111163A2 (en) | 2012-01-20 | 2013-08-01 | Cadila Healthcare Limited | Process for the preparation of dabigatran etexilate mesylate and polymorphs of intermediates thereof |
JP2015504903A (en) | 2012-01-24 | 2015-02-16 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | New dabigatran formulation for oral administration |
ES2895918T3 (en) | 2012-02-21 | 2022-02-23 | Towa Pharmaceutical Europe S L | Dabigatran etexilate oral pharmaceutical compositions |
EP2631234A1 (en) | 2012-02-23 | 2013-08-28 | Esteve Química, S.A. | Solid forms of dabigatran etexilate mesylate and processes for their preparation |
WO2013144971A1 (en) | 2012-03-27 | 2013-10-03 | Cadila Healthcare Limited | New solid forms of dabigatran etexilate bisulfate and mesylate and processes to prepare them |
US9273030B2 (en) | 2012-04-02 | 2016-03-01 | Msn Laboratories Private Limited | Process for the preparation of benzimidazole derivatives and salts thereof |
CN103387566B (en) * | 2012-05-09 | 2015-09-09 | 上海医药工业研究院 | Prepare the method for 3-[[[2-[[(4-cyano-phenyl) is amino] methyl]-1-methyl isophthalic acid H-benzoglyoxaline-5-base] carbonyl] (pyridine-2-base) is amino] ethyl propionate |
CN103420980A (en) * | 2012-05-22 | 2013-12-04 | 北京美倍他药物研究有限公司 | Dabigatran derivatives |
US20130345262A1 (en) | 2012-06-25 | 2013-12-26 | Boehringer Ingelheim International Gmbh | Method for prevention of stroke |
EP2872499A1 (en) | 2012-07-16 | 2015-05-20 | Interquim, S.A. | Process for the preparation of intermediates for the synthesis of dabigatran etexilate, and crystalline forms of said intermediates |
CN102766134B (en) * | 2012-07-19 | 2014-06-25 | 北京普禄德医药科技有限公司 | Dabigatran etexilate derivative and preparation method and application thereof |
EP2881394B1 (en) * | 2012-07-31 | 2018-03-21 | Kyowa Hakko Kirin Co., Ltd. | Condensed ring heterocyclic compound |
EA028581B1 (en) | 2012-08-03 | 2017-12-29 | Бристол-Маерс Сквибб Компани | DIHYDROPYRIDONE P1 AS FACTOR XIa INHIBITORS |
EA025392B1 (en) | 2012-08-03 | 2016-12-30 | Бристол-Маерс Сквибб Компани | DIHYDROPYRIDONE P1 AS FACTOR XIa INHIBITORS |
WO2014041559A2 (en) * | 2012-08-27 | 2014-03-20 | Glenmark Pharmaceuticals Limited; Glenmark Generics Limited | Process for the preparation of dabigatran etexilate and intermediates thereof |
WO2014060561A1 (en) | 2012-10-19 | 2014-04-24 | Sanovel Ilac Sanayi Ve Ticaret A.S. | Oral pharmaceutical formulations comprising dabigatran |
WO2014060545A1 (en) | 2012-10-19 | 2014-04-24 | Sanovel Ilac Sanayi Ve Ticaret A.S. | Pharmaceutical compositions of dabigatran free base |
US9399616B2 (en) | 2012-10-22 | 2016-07-26 | Boehringer Ingelheim International Gmbh | Process for the manufacture of 4-aminobenzoamidine dihydrochloride |
US10077251B2 (en) | 2012-10-29 | 2018-09-18 | Biophore India Pharmaceuticals Pvt. Ltd. | Process for the synthesis of Dabigatran Etexilate and its intermediates |
US9533971B2 (en) | 2012-10-29 | 2017-01-03 | Biophore India Pharmaceuticals Pvt. Ltd | Process for the synthesis of dabigatran and its intermediates |
CN102977077A (en) * | 2012-11-28 | 2013-03-20 | 浙江燎原药业有限公司 | Method for preparing dabigatran etexilate intermediate |
EP2740471B1 (en) | 2012-12-07 | 2015-05-27 | Hexal AG | Oral pharmaceutical composition comprising dabigatran etexilate |
CN103044404A (en) * | 2013-01-14 | 2013-04-17 | 中国药科大学 | Dabigatran derivatives, and preparation method and application thereof in antithrombosis |
WO2014160668A1 (en) | 2013-03-25 | 2014-10-02 | Bristol-Myers Squibb Company | Tetrahydroisoquinolines containing substituted azoles as factor xia inhibitors |
CN103224469A (en) * | 2013-05-16 | 2013-07-31 | 上海应用技术学院 | Pradaxa analogue with fluorine-containing group modified benzene ring as center and synthesis method thereof |
EP3004086A1 (en) | 2013-06-03 | 2016-04-13 | Bayer Pharma Aktiengesellschaft | Substituted benzoxazoles |
UY35592A (en) | 2013-06-03 | 2014-12-31 | Bayer Pharma AG | BENZOXAZOLES REPLACED |
CN103288744A (en) * | 2013-06-04 | 2013-09-11 | 上海应用技术学院 | Fluorine group-containing-modified dabigatran etexilate analogue and synthetic method thereof |
EP2853260A1 (en) | 2013-09-27 | 2015-04-01 | ratiopharm GmbH | Pharmaceutical preparation comprising dabigatran etexilate bismesylate |
NO2760821T3 (en) | 2014-01-31 | 2018-03-10 | ||
RS57659B1 (en) | 2014-01-31 | 2018-11-30 | Bristol Myers Squibb Co | Macrocycles with hetrocyclic p2' groups as factor xia inhibitors |
WO2015128875A2 (en) | 2014-02-26 | 2015-09-03 | Megafine Pharma (P) Ltd. | A process for preparation of dabigatran etexilate mesylate and intermediates thereof |
WO2015137680A1 (en) * | 2014-03-10 | 2015-09-17 | 동아에스티 주식회사 | Pharmaceutical composition for treating or preventing stroke and systemic embolism |
IN2014MU01042A (en) | 2014-03-26 | 2015-10-02 | Cadila Healthcare Ltd | |
EP2929884A1 (en) | 2014-04-11 | 2015-10-14 | Sanovel Ilac Sanayi ve Ticaret A.S. | Pharmaceutical combinations of dabigatran and h2-receptor antagonists |
US10130618B2 (en) | 2014-04-11 | 2018-11-20 | Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi | Pharmaceutical combinations of dabigatran and proton pump inhibitors |
CN104230888A (en) * | 2014-06-03 | 2014-12-24 | 长春工业大学 | Preparation method of benzimidazole compound |
CN105218519A (en) * | 2014-06-04 | 2016-01-06 | 天津药物研究院 | A kind of preparation method of dabigatran etexilate intermediate |
CN104003977B (en) * | 2014-06-05 | 2016-04-13 | 雅本化学股份有限公司 | The preparation method of N-(2-chloromethyl-1-methyl isophthalic acid H-benzoglyoxaline-5-acyl group)-N-(pyridine-2-base)-3-alanine ethyl ester |
DE102014108210A1 (en) | 2014-06-11 | 2015-12-17 | Dietrich Gulba | rodenticide |
CN104045628B (en) * | 2014-06-13 | 2019-04-09 | 深圳翰宇药业股份有限公司 | The purification process of benzimidizole derivatives |
CN105315257A (en) * | 2014-06-24 | 2016-02-10 | 华仁药业股份有限公司 | Synthetic and purifying method of dabigatran etexilate |
CN107027308A (en) * | 2014-08-06 | 2017-08-08 | 四川海思科制药有限公司 | A kind of dabigatran thioes derivatives and preparation method thereof and purposes pharmaceutically |
WO2016019849A1 (en) * | 2014-08-06 | 2016-02-11 | 四川海思科制药有限公司 | Dabigatran carboalkoxy derivative, preparation method therefor, and pharmaceutical use thereof |
NO2721243T3 (en) | 2014-10-01 | 2018-10-20 | ||
CA3001495C (en) | 2014-11-03 | 2021-07-20 | Solipharma Llc | Formulations of dabigatran etexilate or dabigatran etexilate salts and preparation methods thereof |
CN104592204B (en) * | 2014-12-26 | 2017-05-17 | 华润赛科药业有限责任公司 | Dabigatran derivatives as well as preparation method and application thereof |
CN104650037A (en) * | 2014-12-30 | 2015-05-27 | 青岛黄海制药有限责任公司 | Synthesis method of dabigatran etexilate |
TR201502223A2 (en) | 2015-02-25 | 2016-09-21 | Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi | Pharmaceutical combinations of dronedarone and dabigatran |
CN104628733A (en) * | 2015-03-02 | 2015-05-20 | 中国药科大学 | Tetrahydrobenzo[4,5] imidazo[1,2-a] pyrazine thrombin inhibitors |
US10160750B2 (en) | 2015-06-19 | 2018-12-25 | Bristol-Myers Squibb Company | Diamide macrocycles as factor XIa inhibitors |
CN104987323B (en) * | 2015-07-10 | 2017-08-22 | 浙江美诺华药物化学有限公司 | A kind of preparation method of dabigatran etcxilate |
EP3324946A1 (en) | 2015-07-20 | 2018-05-30 | Sanovel Ilac Sanayi ve Ticaret A.S. | Pharmaceutical formulations of dabigatran free base |
WO2017019821A1 (en) | 2015-07-29 | 2017-02-02 | Bristol-Myers Squibb Company | Factor xia new macrocycle bearing a non-aromatic p2' group |
EP3331872B1 (en) | 2015-08-05 | 2019-09-25 | Bristol-Myers Squibb Company | Novel substituted glycine derived fxia inhibitors |
CN105294651A (en) * | 2015-09-23 | 2016-02-03 | 烟台东诚药业集团股份有限公司 | Method for synthesizing and preparing pradaxa formamidine intermediates |
CN106866626A (en) * | 2015-12-14 | 2017-06-20 | 天津药物研究院有限公司 | A kind of preparation method of dabigatran etexilate intermediate |
CN105481831B (en) * | 2015-12-16 | 2018-06-12 | 开封明仁药业有限公司 | A kind of method for preparing dabigatran etexilate intermediate |
WO2017111637A1 (en) | 2015-12-23 | 2017-06-29 | Zaklady Farmaceutyczne Polpharma Sa | Pharmaceutical composition comprising dabigatran or a pharmaceutically acceptable salt thereof |
CN105566297A (en) * | 2015-12-31 | 2016-05-11 | 哈药集团技术中心 | Preparation method of dabigatran etexilate mesylate |
KR20180117156A (en) | 2016-03-02 | 2018-10-26 | 브리스톨-마이어스 스큅 컴퍼니 | Diamide macrocycle with factor XIa inhibitory activity |
CN105669651B (en) * | 2016-03-07 | 2018-03-06 | 山东罗欣药业集团股份有限公司 | A kind of preparation technology of dabigatran etexilate methanesulfonate |
CN106397400A (en) * | 2016-04-14 | 2017-02-15 | 江苏康缘药业股份有限公司 | Preparation method for dabigatran etexilate |
TR201606697A2 (en) | 2016-05-20 | 2017-12-21 | Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi | NEW ORAL PHARMACEUTICAL FORMULATIONS OF DABIGATRA |
CN106349221A (en) * | 2016-08-29 | 2017-01-25 | 常州市阳光药业有限公司 | Preparation method of high-purity dabigatran etexilate |
TR201617984A2 (en) | 2016-12-07 | 2018-06-21 | Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi | PHARMACEUTICAL COMPOSITIONS OF DABIGATRAN |
EP3332771A1 (en) | 2016-12-07 | 2018-06-13 | Sanovel Ilac Sanayi ve Ticaret A.S. | Multilayered tablet compositions of dabigatran |
JP2018184375A (en) | 2017-04-27 | 2018-11-22 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Tablet comprising dabigatran etexilate or pharmaceutically acceptable salt thereof and method for producing the same |
WO2019004980A2 (en) | 2017-05-10 | 2019-01-03 | Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi | Solid oral pharmaceutical compositions of dabigatran etexilate |
TR201706848A2 (en) | 2017-05-10 | 2018-11-21 | Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi | SOLID ORAL PHARMACEUTICAL COMPOSITIONS CONTAINING DABIGATRAN ETEXCLATE |
CN109010249A (en) * | 2017-06-08 | 2018-12-18 | 上海美悦生物科技发展有限公司 | Injection dabigatran etcxilate pharmaceutical composition and its preparation method and application |
KR20190036857A (en) | 2017-09-28 | 2019-04-05 | 한미약품 주식회사 | Composite capsule formulation comprising dabigatran etexilate |
TR201722323A2 (en) | 2017-12-27 | 2019-07-22 | Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi | Oral pharmaceutical compositions of dabigatran |
TR201722186A2 (en) | 2017-12-27 | 2019-07-22 | Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi | Pharmaceutical compositions of dabigatran |
TR201722630A2 (en) | 2017-12-28 | 2019-07-22 | Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi | |
CN111954532A (en) * | 2018-04-13 | 2020-11-17 | 上海交通大学医学院附属瑞金医院 | Anti-tumor multi-drug resistance of heteroaryl amide compounds, application of heteroaryl amide compounds in treating cancer and protein-drug molecular compound |
CN108864047A (en) * | 2018-07-02 | 2018-11-23 | 河南师范大学 | A kind of preparation method of non-peptide batroxobin inhibitor dabigatran etcxilate |
EP3771465A1 (en) | 2019-08-01 | 2021-02-03 | Zaklady Farmaceutyczne Polpharma SA | Pharmaceutical composition comprising dabigatran etexilate |
CN111606885A (en) * | 2020-06-18 | 2020-09-01 | 安徽鼎旺医药有限公司 | Dabigatran etexilate mesylate and preparation method thereof |
CN113929661A (en) * | 2020-06-29 | 2022-01-14 | 石药集团恩必普药业有限公司 | Dabigatran etexilate intermediate and preparation method thereof |
EP4070658A1 (en) | 2021-04-06 | 2022-10-12 | BIORoxx GmbH | Use of anticoagulant active compounds as rodenticide |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4675405A (en) * | 1984-09-21 | 1987-06-23 | American Home Products Corporation | Quinoline compounds as antiallergic and antithrombotic agents |
DE4129603A1 (en) * | 1991-09-06 | 1993-03-11 | Thomae Gmbh Dr K | CONDENSED 5-LOW HETEROCYCLES, METHOD FOR THE PRODUCTION THEREOF, AND MEDICAMENTS CONTAINING THESE COMPOUNDS |
US5416099A (en) * | 1991-10-29 | 1995-05-16 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
ZA928276B (en) * | 1991-10-31 | 1993-05-06 | Daiichi Seiyaku Co | Aromatic amidine derivates and salts thereof. |
CA2134192A1 (en) * | 1993-11-12 | 1995-05-13 | Michael L. Denney | 5, 6-bicyclic glycoprotein iib/iiia antagonists |
-
1998
- 1998-01-15 PE PE1998000030A patent/PE121699A1/en not_active IP Right Cessation
- 1998-01-23 MY MYPI98000290A patent/MY129408A/en unknown
- 1998-02-16 PL PL98335154A patent/PL195551B1/en unknown
- 1998-02-16 BR BRPI9807843-7A patent/BR9807843B1/en not_active IP Right Cessation
- 1998-02-16 CZ CZ0291599A patent/CZ297768B6/en not_active IP Right Cessation
- 1998-02-16 ES ES98909468T patent/ES2199426T4/en not_active Expired - Lifetime
- 1998-02-16 EA EA199900746A patent/EA003697B1/en active IP Right Grant
- 1998-02-16 CN CN98802623A patent/CN1088702C/en not_active Expired - Lifetime
- 1998-02-16 DE DE59808281T patent/DE59808281D1/en not_active Expired - Lifetime
- 1998-02-16 EE EEP199900359A patent/EE04716B1/en active Protection Beyond IP Right Term
- 1998-02-16 RS YUP-387/99A patent/RS49686B/en unknown
- 1998-02-16 SI SI9830479T patent/SI0966454T1/en unknown
- 1998-02-16 NZ NZ337323A patent/NZ337323A/en not_active IP Right Cessation
- 1998-02-16 IL IL13081298A patent/IL130812A/en active Protection Beyond IP Right Term
- 1998-02-16 WO PCT/EP1998/000865 patent/WO1998037075A1/en active IP Right Grant
- 1998-02-16 SK SK1121-99A patent/SK285432B6/en active Protection Beyond IP Right Term
- 1998-02-16 AT AT98909468T patent/ATE239712T1/en active
- 1998-02-16 AU AU63991/98A patent/AU742593C/en not_active Expired
- 1998-02-16 JP JP53623498A patent/JP3343359B2/en not_active Expired - Lifetime
- 1998-02-16 DE DE122008000020C patent/DE122008000020I1/en active Pending
- 1998-02-16 HU HU0001116A patent/HU223754B1/en active Protection Beyond IP Right Term
- 1998-02-16 TR TR1999/02017T patent/TR199902017T2/en unknown
- 1998-02-16 EP EP98909468A patent/EP0966454B1/en not_active Expired - Lifetime
- 1998-02-16 PT PT98909468T patent/PT966454E/en unknown
- 1998-02-16 KR KR1019997007335A patent/KR100619458B1/en active IP Right Review Request
- 1998-02-16 DK DK98909468T patent/DK0966454T3/en active
- 1998-02-16 CA CA002277949A patent/CA2277949C/en not_active Expired - Lifetime
- 1998-02-17 EG EG18498A patent/EG24144A/en active
- 1998-02-17 HR HR980082A patent/HRP980082B1/en not_active IP Right Cessation
- 1998-02-17 CO CO98008407A patent/CO4920237A1/en unknown
- 1998-02-18 AR ARP980100722A patent/AR010896A1/en active Pending
- 1998-02-18 TW TW087102265A patent/TW588047B/en not_active IP Right Cessation
- 1998-05-06 SA SA98190047A patent/SA98190047B1/en unknown
-
1999
- 1999-08-10 BG BG103655A patent/BG64558B1/en active Active
- 1999-08-17 NO NO19993945A patent/NO313879B1/en not_active IP Right Cessation
-
2000
- 2000-07-10 HK HK00104207A patent/HK1025096A1/en not_active IP Right Cessation
-
2008
- 2008-05-09 LT LTPA2008008C patent/LTC0966454I2/en unknown
- 2008-05-14 LU LU91437C patent/LU91437I2/en unknown
- 2008-05-28 NL NL300349C patent/NL300349I2/en unknown
- 2008-06-06 FR FR08C0025C patent/FR08C0025I2/en active Active
- 2008-07-31 NO NO2008012C patent/NO2008012I2/en not_active IP Right Cessation
-
2021
- 2021-02-05 NO NO2021005C patent/NO2021005I1/en unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BG103655A (en) | Disubstituted bicyclic heterocyclic compounds, their preparation and application as medicamentous forms | |
WO2000008014A8 (en) | Disubstituted bicyclic heterocycles having, in particular, a thrombin inhibitive effect | |
MX9803954A (en) | Amino acid derivatives, pharmaceutical compositions containing these compounds and processes for preparing them. | |
YU84700A (en) | Benzimidazoles, production thereof and use thereof as medicaments | |
AU7453498A (en) | Sulfonamide derivatives, their production and use | |
NO933248L (en) | Cyclic urea derivatives, drugs containing these compounds, and process for their preparation | |
TW200504067A (en) | New substituted imidazo-pyridinones and imidazo-pyridazinones, the preparation thereof and their use as pharmaceutical compositions | |
BG100946A (en) | New amino acid derivatives, method for their preparation and pharmaceutical compositions containing them | |
TW289757B (en) | ||
MX9706069A (en) | Novel dipeptide amidines as thrombin inhibitors. | |
BG103417A (en) | Condensed pyrimidine bicyclic derivatives | |
MY125749A (en) | Aralkyl and aralkylidene heterocyclic lactams and imides | |
BG103947A (en) | Derivatives of 9-oxymerythromycin | |
HUT74736A (en) | 2,5-dioxo imidazolodine derivatives, pharmaceutical compositions containing them, and process for producing them | |
YU30902A (en) | Novel cyclopropanes as cgrp antagonists, medicaments containing said compounds and method for the production thereof | |
IL117209A0 (en) | 1-aryl-2-acylamino-ethane compounds and pharmaceutical compositions containing them | |
MY115466A (en) | Substituted cinnamic acid guanidides, a process for their preparation, their use as medicaments or diagnostic agents and medicaments comprising them. | |
BG101220A (en) | N-substituted 3-azabicyclo (93.2.0) heptane derivatives,their preparation and use | |
ATE177424T1 (en) | N-SUBSTITUTED NAPHTHALIMIDES, THEIR PRODUCTION AND USE | |
WO1999029670A3 (en) | Aminocarbonyltetralin and dihydronaphtalene derivates as thrombin inhibitors | |
UA66785C2 (en) | Disubstituted bicyclic heterocycles, preparation and use thereof as medicaments | |
GR3036023T3 (en) | Substituted phenyl amidines, medicaments containing these compounds and process for producing them | |
YU3701A (en) | Substituted phenylamidines with antithrombotic action | |
WO2000011951A3 (en) | Use of 5-amino-pyrazol-derivatives for combating micro-organisms | |
BG105329A (en) | N-substituted azabicycloheptane derivatives, production and use thereof |