NL300760I2 - Edoxaban, a salt thereof, a solvate thereof or an N-oxide thereof, in particular edoxaban tosylate - Google Patents
Edoxaban, a salt thereof, a solvate thereof or an N-oxide thereof, in particular edoxaban tosylateInfo
- Publication number
- NL300760I2 NL300760I2 NL300760C NL300760C NL300760I2 NL 300760 I2 NL300760 I2 NL 300760I2 NL 300760 C NL300760 C NL 300760C NL 300760 C NL300760 C NL 300760C NL 300760 I2 NL300760 I2 NL 300760I2
- Authority
- NL
- Netherlands
- Prior art keywords
- edoxaban
- solvate
- salt
- oxide
- tosylate
- Prior art date
Links
- HGVDHZBSSITLCT-JLJPHGGASA-N Edoxaban Chemical compound N([C@H]1CC[C@@H](C[C@H]1NC(=O)C=1SC=2CN(C)CCC=2N=1)C(=O)N(C)C)C(=O)C(=O)NC1=CC=C(Cl)C=N1 HGVDHZBSSITLCT-JLJPHGGASA-N 0.000 title 1
- 150000001204 N-oxides Chemical class 0.000 title 1
- 229960000622 edoxaban Drugs 0.000 title 1
- 229960005378 edoxaban tosylate Drugs 0.000 title 1
- ZLFZITWZOYXXAW-QXXZOGQOSA-N edoxaban tosylate Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1.N([C@H]1CC[C@@H](C[C@H]1NC(=O)C=1SC=2CN(C)CCC=2N=1)C(=O)N(C)C)C(=O)C(=O)NC1=CC=C(Cl)C=N1 ZLFZITWZOYXXAW-QXXZOGQOSA-N 0.000 title 1
- 150000003839 salts Chemical class 0.000 title 1
- 239000012453 solvate Substances 0.000 title 1
Classifications
-
- 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
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/428—Thiazoles condensed with carbocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/429—Thiazoles condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4365—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system having sulfur as a ring hetero atom, e.g. ticlopidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- 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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- 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
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/42—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
- 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
- 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
- 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
- C07D417/14—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 three or more hetero rings
-
- 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
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—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
-
- 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
- C07D513/12—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 three hetero rings
- C07D513/14—Ortho-condensed systems
-
- 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
- C07K5/06191—Dipeptides containing heteroatoms different from O, S, or N
-
- 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
- C07K5/08—Tripeptides
- C07K5/0827—Tripeptides containing heteroatoms different from O, S, or N
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biophysics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Heart & Thoracic Surgery (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001187105 | 2001-06-20 | ||
| JP2001243046 | 2001-08-09 | ||
| JP2001311808 | 2001-10-09 | ||
| JP2001398708 | 2001-12-28 | ||
| PCT/JP2002/002683 WO2003000657A1 (fr) | 2001-06-20 | 2002-03-20 | Derives de diamine |
| PCT/JP2002/006141 WO2003000680A1 (fr) | 2001-06-20 | 2002-06-20 | Derives de diamine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL300760I2 true NL300760I2 (en) | 2017-07-20 |
Family
ID=27482359
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL300760C NL300760I2 (en) | 2001-06-20 | 2015-09-29 | Edoxaban, a salt thereof, a solvate thereof or an N-oxide thereof, in particular edoxaban tosylate |
Country Status (12)
| Country | Link |
|---|---|
| US (7) | US7365205B2 (h) |
| EP (1) | EP2343290A1 (h) |
| AR (1) | AR036102A1 (h) |
| BE (1) | BE2015C046I2 (h) |
| CY (2) | CY1113054T1 (h) |
| FR (1) | FR15C0068I2 (h) |
| MY (1) | MY153231A (h) |
| NL (1) | NL300760I2 (h) |
| PT (1) | PT1405852E (h) |
| TW (1) | TWI298066B (h) |
| WO (1) | WO2003000657A1 (h) |
| ZA (1) | ZA200309866B (h) |
Families Citing this family (118)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI290136B (en) * | 2000-04-05 | 2007-11-21 | Daiichi Seiyaku Co | Ethylenediamine derivatives |
| RU2319699C2 (ru) * | 2001-06-20 | 2008-03-20 | Дайити Санкио Компани, Лимитед | Производные диаминов |
| WO2003000657A1 (fr) * | 2001-06-20 | 2003-01-03 | Daiichi Pharmaceutical Co., Ltd. | Derives de diamine |
| PL368402A1 (en) * | 2001-08-09 | 2005-03-21 | Daiichi Pharmaceutical Co, Ltd. | Diamine derivatives |
| KR20050110612A (ko) * | 2002-12-25 | 2005-11-23 | 다이이찌 세이야꾸 가부시기가이샤 | 디아민 유도체 |
| US7205318B2 (en) * | 2003-03-18 | 2007-04-17 | Bristol-Myers Squibb Company | Lactam-containing cyclic diamines and derivatives as a factor Xa inhibitors |
| US7378409B2 (en) | 2003-08-21 | 2008-05-27 | Bristol-Myers Squibb Company | Substituted cycloalkylamine derivatives as modulators of chemokine receptor activity |
| US7115646B2 (en) * | 2003-10-08 | 2006-10-03 | Bristol Myers Squibb, Co. | Cyclic diamines and derivatives as factor Xa inhibitors |
| CA2545730C (en) * | 2003-11-12 | 2014-07-08 | Daiichi Pharmaceutical Co., Ltd. | Process for producing thiazole derivative |
| RU2361862C2 (ru) * | 2003-12-29 | 2009-07-20 | Сепракор Инк. | Пиррольные и пиразольные ингибиторы daao |
| TWI350168B (en) * | 2004-05-07 | 2011-10-11 | Incyte Corp | Amido compounds and their use as pharmaceuticals |
| EP1773780A4 (en) * | 2004-06-24 | 2008-01-09 | Incyte Corp | AMIDO COMPOUNDS AND USES THEREOF AS PHARMACEUTICAL PRODUCTS |
| WO2006002350A1 (en) * | 2004-06-24 | 2006-01-05 | Incyte Corporation | Amido compounds and their use as pharmaceuticals |
| WO2006002361A2 (en) * | 2004-06-24 | 2006-01-05 | Incyte Corporation | 2-methylpropanamides and their use as pharmaceuticals |
| WO2006012173A1 (en) * | 2004-06-24 | 2006-02-02 | Incyte Corporation | Amido compounds and their use as pharmaceuticals |
| EA200700117A1 (ru) * | 2004-06-24 | 2007-06-29 | Инсайт Корпорейшн | N-замещенные пиперидины и их применение в качестве фармацевтических препаратов |
| KR20070024639A (ko) * | 2004-06-24 | 2007-03-02 | 인사이트 산 디에고 인코포레이티드 | 아미도 화합물 및 약제로서의 이의 용도 |
| JP2008509910A (ja) * | 2004-08-10 | 2008-04-03 | インサイト・コーポレイション | アミド化合物およびその医薬としての使用 |
| US7499687B2 (en) * | 2004-11-09 | 2009-03-03 | Theta Microelectronics, Inc. | Wireless transmitter DC offset recalibration |
| US8110581B2 (en) * | 2004-11-10 | 2012-02-07 | Incyte Corporation | Lactam compounds and their use as pharmaceuticals |
| CA2587153A1 (en) * | 2004-11-18 | 2006-05-26 | Incyte Corporation | Inhibitors of 11-.beta. hydroxyl steroid dehydrogenase type 1 and methods of using the same |
| NZ556800A (en) * | 2005-02-18 | 2011-01-28 | Acino Pharma Ag | Novel processes for the preparation of a 2H-chromene (Iclaprim) |
| EP1864982B1 (en) | 2005-03-31 | 2012-10-24 | Daiichi Sankyo Company, Limited | Triamine derivative |
| CA2614282A1 (en) | 2005-07-06 | 2007-01-11 | Sepracor Inc. | Combinations of eszopiclone and trans 4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-n-methyl-1-napthalenamine or trans 4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-napthalenamine, and methods of treatment of menopause and mood, anxiety, and cognitive disorders |
| EP1935883A4 (en) | 2005-09-14 | 2010-07-21 | Dainippon Sumitomo Pharma Co | OXINDOL DERIVATIVES AS A MEANS FOR CONTROLLING FOOD RECEPTION |
| KR101361441B1 (ko) * | 2005-09-16 | 2014-02-10 | 다이이찌 산쿄 가부시키가이샤 | 광학활성인 디아민 유도체 및 그의 제조방법 |
| US20070066584A1 (en) * | 2005-09-21 | 2007-03-22 | Wenqing Yao | Amido compounds and their use as pharmaceuticals |
| EA200870019A1 (ru) * | 2005-12-05 | 2008-12-30 | Инсайт Корпорейшн | Лактамовые соединения и способы их применения |
| CA2636324C (en) | 2006-01-06 | 2012-03-20 | Sepracor Inc. | Cycloalkylamines as monoamine reuptake inhibitors |
| US8053603B2 (en) * | 2006-01-06 | 2011-11-08 | Sunovion Pharmaceuticals Inc. | Tetralone-based monoamine reuptake inhibitors |
| US7998959B2 (en) * | 2006-01-12 | 2011-08-16 | Incyte Corporation | Modulators of 11-β hydroxyl steroid dehydrogenase type 1, pharmaceutical compositions thereof, and methods of using the same |
| JP2009525333A (ja) * | 2006-01-31 | 2009-07-09 | インサイト・コーポレイション | アミド化合物およびその医薬としての使用 |
| WO2007101270A1 (en) * | 2006-03-02 | 2007-09-07 | Incyte Corporation | MODULATORS OF 11-β HYDROXYL STEROID DEHYDROGENASE TYPE 1, PHARMACEUTICAL COMPOSITIONS THEREOF, AND METHODS OF USING THE SAME |
| US20070208001A1 (en) * | 2006-03-03 | 2007-09-06 | Jincong Zhuo | Modulators of 11- beta hydroxyl steroid dehydrogenase type 1, pharmaceutical compositions thereof, and methods of using the same |
| CN101421228B (zh) | 2006-03-31 | 2014-05-21 | 塞普拉柯公司 | 手性酰胺和胺的制备 |
| CA2649677A1 (en) * | 2006-05-01 | 2007-11-15 | Incyte Corporation | Tetrasubstituted ureas as modulators of 11-.beta. hydroxyl steroid dehydrogenase type 1 |
| JP2009537564A (ja) * | 2006-05-17 | 2009-10-29 | インサイト・コーポレイション | 11−βヒドロキシルステロイドデヒドロゲナーゼタイプIの複素環阻害剤およびそれを用いる方法 |
| US7579370B2 (en) * | 2006-06-30 | 2009-08-25 | Sepracor Inc. | Fused heterocycles |
| US7884124B2 (en) * | 2006-06-30 | 2011-02-08 | Sepracor Inc. | Fluoro-substituted inhibitors of D-amino acid oxidase |
| JP2009544616A (ja) * | 2006-07-21 | 2009-12-17 | 武田薬品工業株式会社 | アミド化合物 |
| JP5187901B2 (ja) | 2006-08-30 | 2013-04-24 | 塩野義製薬株式会社 | ヒドラジンアミド誘導体 |
| US7902252B2 (en) * | 2007-01-18 | 2011-03-08 | Sepracor, Inc. | Inhibitors of D-amino acid oxidase |
| KR20090111322A (ko) * | 2007-01-18 | 2009-10-26 | 세프라코 아이엔시. | 디 아미노산 옥시다제의 억제제 |
| AU2008241982B2 (en) * | 2007-03-29 | 2013-02-21 | Daiichi Sankyo Company, Limited | Pharmaceutical composition |
| MX2009012685A (es) | 2007-05-31 | 2009-12-14 | Sepracor Inc | Cicloalquilaminas sustituidas con fenilo como inhibidores de la reabsorcion de monoamina. |
| DE102007028407A1 (de) | 2007-06-20 | 2008-12-24 | Bayer Healthcare Ag | Substituierte Oxazolidinone und ihre Verwendung |
| DE102007028406A1 (de) | 2007-06-20 | 2008-12-24 | Bayer Healthcare Ag | Substituierte Oxazolidinone und ihre Verwendung |
| DE102007028319A1 (de) | 2007-06-20 | 2008-12-24 | Bayer Healthcare Ag | Substituierte Oxazolidinone und ihre Verwendung |
| CL2008001839A1 (es) | 2007-06-21 | 2009-01-16 | Incyte Holdings Corp | Compuestos derivados de 2,7-diazaespirociclos, inhibidores de 11-beta hidroxil esteroide deshidrogenasa tipo 1; composicion farmaceutica que comprende a dichos compuestos; utiles para tratar la obesidad, diabetes, intolerancia a la glucosa, diabetes tipo ii, entre otras enfermedades. |
| GB0721333D0 (en) * | 2007-10-31 | 2007-12-12 | Motac Neuroscience Ltd | Medicaments |
| US20100120740A1 (en) * | 2008-08-07 | 2010-05-13 | Sepracor Inc. | Prodrugs of fused heterocyclic inhibitors of d-amino acid oxidase |
| WO2010053583A2 (en) * | 2008-11-10 | 2010-05-14 | Dana Farber Cancer Institute | Small molecule cd4 mimetics and uses thereof |
| WO2010067824A1 (ja) | 2008-12-12 | 2010-06-17 | 第一三共株式会社 | 光学活性カルボン酸の製造方法 |
| EP2371830B1 (en) | 2008-12-17 | 2013-10-02 | Daiichi Sankyo Company, Limited | Method for producing diamine derivative |
| EP2383272A4 (en) | 2009-01-13 | 2012-07-25 | Daiichi Sankyo Co Ltd | ACTIVE BLOOD CREATION FACTOR HEMMER |
| EP2407457B1 (en) * | 2009-03-10 | 2015-04-22 | Daiichi Sankyo Company, Limited | Process for producing diamine derivative |
| WO2010104106A1 (ja) | 2009-03-13 | 2010-09-16 | 第一三共株式会社 | 光学活性なジアミン誘導体の製造方法 |
| WO2010131663A1 (ja) * | 2009-05-15 | 2010-11-18 | 第一三共株式会社 | オキサミド誘導体 |
| SG176934A1 (en) | 2009-06-18 | 2012-01-30 | Daiichi Sankyo Co Ltd | Pharmaceutical composition having improved solubility |
| FR2948372B1 (fr) | 2009-07-21 | 2011-07-22 | Servier Lab | Nouveaux derives chromeniques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| US20110034434A1 (en) * | 2009-08-07 | 2011-02-10 | Sepracor Inc. | Prodrugs of fused heterocyclic inhibitors of d-amino acid oxidase |
| JP5714562B2 (ja) | 2010-02-22 | 2015-05-07 | 第一三共株式会社 | 経口用徐放性固形製剤 |
| EP2540318B1 (en) * | 2010-02-22 | 2018-10-24 | Daiichi Sankyo Company, Limited | Sustained-release solid preparation for oral use |
| JP5870023B2 (ja) * | 2010-02-22 | 2016-02-24 | 第一三共株式会社 | 経口用徐放性固形製剤 |
| JP5390014B2 (ja) | 2010-03-19 | 2014-01-15 | 第一三共株式会社 | 抗凝固剤の溶出改善方法 |
| JP5692873B2 (ja) | 2010-03-19 | 2015-04-01 | 第一三共株式会社 | ジアミン誘導体の結晶およびその製造方法 |
| WO2011149110A1 (en) | 2010-05-28 | 2011-12-01 | Daiichi Sankyo Company, Limited | Novel composition for the prevention and/or treatment of thromboembolism |
| ES2619374T3 (es) | 2010-07-02 | 2017-06-26 | Daiichi Sankyo Company, Limited | Procedimiento de preparación de sal derivada de diamina ópticamente activa |
| HUP1000598A2 (en) | 2010-11-05 | 2012-09-28 | Richter Gedeon Nyrt | Indole derivatives |
| CA2824885A1 (en) | 2011-01-19 | 2012-07-26 | Bayer Intellectual Property Gmbh | Binding proteins to inhibitors of coagulation factors |
| US9977846B2 (en) | 2011-07-08 | 2018-05-22 | Daiichi Sankyo Company, Limited | Product quality control method |
| CA2844604C (en) | 2011-08-10 | 2017-07-18 | Daiichi Sankyo Company, Limited | Pharmaceutical composition containing ethanediamide derivatives |
| US20130158069A1 (en) | 2011-12-14 | 2013-06-20 | Daiichi Sankyo Company, Limited | Preventive and/or therapeutic agent for thromboembolism in thromboembolism patient with severe renal impairment |
| CN102659757B (zh) * | 2012-04-24 | 2013-11-06 | 南京药石药物研发有限公司 | 一种合成5-氯-3-噻吩甲醛的中间体及其制备方法 |
| KR102127625B1 (ko) | 2012-09-03 | 2020-06-29 | 다이이찌 산쿄 가부시키가이샤 | 하이드로모르폰염산염 함유의 경구용 서방성 의약 조성물 |
| BR112015004666B1 (pt) | 2012-09-07 | 2022-04-26 | Novartis Ag | Derivados de indol carboxamida, seu uso, e composição farmacêutica |
| WO2014081047A1 (en) | 2012-11-23 | 2014-05-30 | Daiichi Sankyo Company,Limited | Process for the preparation of (1s,4s,5s)-4-bromo-6-oxabicyclo[3.2.1] octan-7-one |
| MY181020A (en) | 2013-03-15 | 2020-12-16 | Sanofi Sa | Heteroaryl compounds and uses thereof |
| EA036160B1 (ru) | 2013-03-15 | 2020-10-08 | Селджен Кар Ллс | Гетероарильные соединения и их применение |
| TWI602803B (zh) | 2013-03-29 | 2017-10-21 | 第一三共股份有限公司 | 光學活性二胺衍生物之製造方法 |
| WO2014157612A1 (ja) | 2013-03-29 | 2014-10-02 | 第一三共株式会社 | (1s,4s,5s)-4-ブロモ-6-オキサビシクロ[3.2.1]オクタン-7-オンの製造方法 |
| EP3038620A1 (en) | 2013-08-29 | 2016-07-06 | Daiichi Sankyo Co., Ltd. | Agent for the treatment and prevention of cancer |
| WO2015150950A1 (en) | 2014-03-31 | 2015-10-08 | Daiichi Sankyo Company, Limited | Use of a factor xa inhibitor for treating and preventing bleeding events and related disorders in patients having sensitivity to vitamin k antagonists used as anticoagulants |
| DE102014108210A1 (de) | 2014-06-11 | 2015-12-17 | Dietrich Gulba | Rodentizid |
| US9975848B2 (en) | 2014-08-13 | 2018-05-22 | The Trustees Of The University Of Pennsylvania | Inhibitors of HIV-1 entry and methods of use thereof |
| CN104529729B (zh) * | 2014-12-31 | 2016-03-30 | 浙江永太科技股份有限公司 | 一种2-氟-3-氯苯甲醛的制备方法 |
| TWI571460B (zh) | 2016-03-14 | 2017-02-21 | 中化合成生技股份有限公司 | 二胺衍生物之製造方法 |
| EP3484893A1 (en) | 2016-07-13 | 2019-05-22 | Mylan Laboratories Ltd. | Salt of amine-protected (1s,2r,4s)-1,2-amino-n,n-dimethylcyclohexane-4-carboxamide |
| WO2018069769A1 (en) | 2016-10-13 | 2018-04-19 | Daiichi Sankyo Company, Limited | Pharmaceutical composition for inhibiting neointima formation of blood vessel |
| US10301322B2 (en) | 2016-12-27 | 2019-05-28 | Apotex Inc. | Processes for the preparation of edoxaban and intermediates thereof |
| EP3592736A1 (en) | 2017-03-10 | 2020-01-15 | Rutgers, the State University of New Jersey | Indole derivatives as efflux pump inhibitors |
| GB201807014D0 (en) | 2018-04-30 | 2018-06-13 | Univ Leeds Innovations Ltd | Factor xlla inhibitors |
| TWI826474B (zh) | 2018-06-27 | 2023-12-21 | 日商第一三共股份有限公司 | 包含二胺衍生物之顆粒劑、以及其用途及製造方法 |
| EP3858386A4 (en) | 2018-09-26 | 2022-10-12 | Jiangsu Hengrui Medicine Co., Ltd. | LIGAND-DRUG CONJUGATE OF AN EXATECAN ANALOG, METHOD FOR PREPARATION AND THEIR USE |
| KR20210068457A (ko) | 2018-09-30 | 2021-06-09 | 지앙수 헨그루이 메디슨 컴퍼니 리미티드 | 항-b7h3 항체-엑사테칸 유사체 접합체 및 이의 의약 용도 |
| CN109942600B (zh) * | 2019-04-15 | 2021-08-20 | 内蒙古京东药业有限公司 | 一种依度沙班的制备方法 |
| US20220251112A1 (en) * | 2019-07-04 | 2022-08-11 | Glenmark Life Sciences Limited | Process for preparation of edoxaban |
| EP3997075A1 (de) | 2019-07-10 | 2022-05-18 | Bayer Aktiengesellschaft | Verfahren zur herstellung von 2-(phenylimino)-1,3-thiazolidin-4-onen |
| KR102333564B1 (ko) | 2019-11-28 | 2021-12-01 | 동방에프티엘(주) | 광학 활성 다이아민 유도체 및 티아졸 유도체의 생산을 위한 새로운 합성경로 |
| KR20220113728A (ko) | 2019-12-12 | 2022-08-16 | 지앙수 헨그루이 파마슈티컬스 컴퍼니 리미티드 | 항 클라우딘 항체 약물 접합체 및 그 의약 용도 |
| WO2021147993A1 (zh) | 2020-01-22 | 2021-07-29 | 江苏恒瑞医药股份有限公司 | 抗trop-2抗体-依喜替康类似物偶联物及其医药用途 |
| TWI885105B (zh) | 2020-03-25 | 2025-06-01 | 大陸商江蘇恆瑞醫藥股份有限公司 | 一種含抗體藥物偶聯物的醫藥組成物及其用途 |
| WO2021190583A1 (zh) | 2020-03-25 | 2021-09-30 | 江苏恒瑞医药股份有限公司 | 抗psma抗体-依喜替康类似物偶联物及其医药用途 |
| US20230241242A1 (en) | 2020-03-25 | 2023-08-03 | Jiangsu Hengrui Pharmaceuticals Co., Ltd. | Preparation method for antibody medicament conjugate |
| KR20230022211A (ko) | 2020-06-08 | 2023-02-14 | 바이리-바이오 (청두) 파마슈티칼 컴퍼니, 리미티드 | 고안정성 친수성 연결 단위를 갖는 캄프토테신 약물 및 이의 접합체 |
| KR20220087933A (ko) | 2020-12-18 | 2022-06-27 | 엠에프씨 주식회사 | 디아민 유도체의 제조방법 |
| WO2022129535A1 (en) | 2020-12-18 | 2022-06-23 | Krka, D.D., Novo Mesto | Edoxaban formulation containing no sugar alcohols |
| EP4070658A1 (de) | 2021-04-06 | 2022-10-12 | BIORoxx GmbH | Verwendung von blutgerinnungshemmenden verbindungen als rodentizide |
| GB202107722D0 (en) | 2021-05-28 | 2021-07-14 | Lunac Therapeutics Ltd | Factor XIIA Inhibitors |
| US20250059296A1 (en) | 2021-11-15 | 2025-02-20 | Systimmune, Inc. | Bispecific antibody-camptothecin drug conjugate and pharmaceutical use thereof |
| CN116178251A (zh) * | 2021-11-26 | 2023-05-30 | 上海汇伦医药股份有限公司 | 一种依度沙班中间体的制备方法 |
| CN116212044A (zh) | 2021-12-03 | 2023-06-06 | 成都百利多特生物药业有限责任公司 | 抗人Trop2抗体-喜树碱类药物偶联物及其医药用途 |
| CN114456194B (zh) * | 2021-12-14 | 2023-07-07 | 浙江九洲药业股份有限公司 | 甲苯磺酸艾多沙班的中间体及其制备方法 |
| CN115583900A (zh) * | 2022-04-29 | 2023-01-10 | 张邦成都生物医药科技有限公司 | 一种高纯度依度沙班中间体的制备方法 |
| WO2023223346A1 (en) | 2022-05-16 | 2023-11-23 | Mylan Laboratories Limited | An improved process for the preparation of edoxaban intermediate |
| CN117752813A (zh) | 2022-09-26 | 2024-03-26 | 成都百利多特生物药业有限责任公司 | 抗cd33抗体和抗cd33抗体-药物偶联物及其用途 |
| CN115724792A (zh) * | 2022-11-24 | 2023-03-03 | 上海柏狮生物科技有限公司 | 一种依度沙班关键中间体及其合成方法 |
| NL2036011B1 (en) | 2023-10-12 | 2025-04-30 | Synapse Res Institute | Molecules for reversing anti-coagulant activity of direct oral anticoagulants |
Family Cites Families (92)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3324086A (en) * | 1964-02-26 | 1967-06-06 | Monsanto Co | Polyamides containing fused heterocycle units |
| WO1986007257A2 (en) | 1985-06-07 | 1986-12-18 | The Upjohn Company | Antiarrhythmic use for aminocycloalkylamides |
| AU8501291A (en) | 1990-09-10 | 1992-03-30 | Upjohn Company, The | Cis-n-(2-aminocyclohexyl)benzamide and their enantiomers as anticonvulsants |
| IL100576A (en) | 1991-01-18 | 1995-11-27 | Eli Lilley And Company | Cephalosporin antibiotics |
| AU2913292A (en) | 1991-11-14 | 1993-06-15 | Bernard Derek Frutin | A pressurised container |
| US5430150A (en) * | 1992-12-16 | 1995-07-04 | American Cyanamid Company | Retroviral protease inhibitors |
| AU6252794A (en) | 1993-03-03 | 1994-09-26 | Eli Lilly And Company | Balanoids |
| ATE166047T1 (de) | 1993-03-17 | 1998-05-15 | Meiji Seika Co | Neue verbindungen mit blutplättchenaggregationshemmender aktivität |
| KR970001164B1 (ko) | 1993-06-09 | 1997-01-29 | 한국과학기술연구원 | 세팔로스포린계 항생제 및 그의 제조방법 |
| CN1076345C (zh) | 1993-10-19 | 2001-12-19 | 住友制药株式会社 | 2,3-二氨基丙酸衍生物 |
| TW270114B (h) | 1993-10-22 | 1996-02-11 | Hoffmann La Roche | |
| US5525042A (en) | 1993-11-08 | 1996-06-11 | Clearline Systems, Inc. | Liquid pump with compressed gas motive fluid |
| US5849736A (en) | 1993-11-24 | 1998-12-15 | The Dupont Merck Pharmaceutical Company | Isoxazoline and isoxazole fibrinogen receptor antagonists |
| WO1995032965A1 (fr) | 1994-06-01 | 1995-12-07 | Yamanouchi Pharmaceutical Co. Ltd. | Derive de l'oxadiazole et composition medicinale a base de ce dernier |
| IL115420A0 (en) | 1994-09-26 | 1995-12-31 | Zeneca Ltd | Aminoheterocyclic derivatives |
| US5719144A (en) | 1995-02-22 | 1998-02-17 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| ES2194986T3 (es) | 1995-04-07 | 2003-12-01 | Schering Corp | Compuestos de carbonil-piperazinilo y piperidinilo que inhiben la farnesil-protein-transferasa. |
| ZA963391B (en) | 1995-05-24 | 1997-10-29 | Du Pont Merck Pharma | Isoxazoline fibrinogen receptor antagonists. |
| US5726126A (en) | 1995-06-02 | 1998-03-10 | American Cyanamid Company | 1-(3-heterocyclyphenyl)-S-triazine-2,6,6-oxo or thiotrione herbicidal agents |
| US5741819A (en) | 1995-06-07 | 1998-04-21 | 3-Dimensional Pharmaceuticals, Inc. | Arylsulfonylaminobenzene derivatives and the use thereof as factor Xa inhibitors |
| GB9516709D0 (en) | 1995-08-15 | 1995-10-18 | Zeneca Ltd | Medicament |
| DE19536783A1 (de) | 1995-09-21 | 1997-03-27 | Diagnostikforschung Inst | Bifunktionelle Nicotinamid-Chelatbildner vom Typ N¶2¶S¶2¶ für radioaktive Isotope |
| US5852045A (en) | 1995-10-19 | 1998-12-22 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| US6274715B1 (en) | 1995-11-08 | 2001-08-14 | Abbott Laboratories | Tricyclic erythromycin derivatives |
| GB9602294D0 (en) | 1996-02-05 | 1996-04-03 | Zeneca Ltd | Heterocyclic compounds |
| IL126610A0 (en) | 1996-04-17 | 1999-08-17 | Du Pont Pharm Co | N-(amidinophenyl)-n'-(subst.)-3h-2,4-benzodiazepin-3- one derivatives as factor xa inhibitors |
| US5668159A (en) | 1996-05-08 | 1997-09-16 | The Dupont Merck Pharmaceutical Company | 1,3,4-thiadiazoles and 1,3,4-oxadiazoles as IIb/IIIa antagonists |
| IL128428A0 (en) | 1996-08-14 | 2000-01-31 | Zeneca Ltd | Substituted pyrimidine derivatives and their pharmaceutical use |
| UA56197C2 (uk) | 1996-11-08 | 2003-05-15 | Зенека Лімітед | Гетероциклічні похідні |
| WO1998035956A1 (en) | 1997-02-13 | 1998-08-20 | Zeneca Limited | Heterocyclic compounds useful as oxido-squalene cyclase inhibitors |
| IT1291823B1 (it) | 1997-04-08 | 1999-01-21 | Menarini Ricerche Spa | Composti pseudo-peptidici, loro preparazione ed uso in formulazioni farmaceutiche |
| ATE334975T1 (de) | 1997-05-30 | 2006-08-15 | Takeda Pharmaceutical | Sulfonamidderivate, ihre herstellung und verwendung |
| US6207679B1 (en) * | 1997-06-19 | 2001-03-27 | Sepracor, Inc. | Antimicrobial agents uses and compositions related thereto |
| US6313122B1 (en) | 1997-06-26 | 2001-11-06 | Eli Lilly And Company | Antithrombotic agents |
| EP0999834B1 (en) | 1997-06-26 | 2005-10-12 | Eli Lilly And Company | Antithrombotic agents |
| EP1007037A4 (en) | 1997-06-26 | 2004-10-06 | Lilly Co Eli | ANTITHROMBOTIC AGENTS |
| GB9715894D0 (en) | 1997-07-29 | 1997-10-01 | Zeneca Ltd | Heterocyclic derivatives |
| GB9715895D0 (en) | 1997-07-29 | 1997-10-01 | Zeneca Ltd | Heterocyclic compounds |
| DE69833036T2 (de) | 1997-09-30 | 2006-06-22 | Daiichi Pharmaceutical Co., Ltd. | Sulfonylderivate |
| AR013693A1 (es) | 1997-10-23 | 2001-01-10 | Uriach & Cia Sa J | Nuevas piperidinas y piperazinas como inhibidores de la agregacion plaquetaria |
| US6130349A (en) | 1997-12-19 | 2000-10-10 | The Board Of Trustees Of The Leland Stanford Junior University | Catalytic compositions and methods for asymmetric allylic alkylation |
| EP0937711A1 (de) | 1998-02-18 | 1999-08-25 | Roche Diagnostics GmbH | Neue Thiobenzamide, Verfahren zu ihrer Herstellung sowie diese enthaltende Arzneimittel |
| EP0937723A1 (de) | 1998-02-18 | 1999-08-25 | Roche Diagnostics GmbH | Neue Sulfonamide, Verfahren zu ihrer Herstellung sowie diese enthaltende Arzneimittel |
| DE19814801A1 (de) | 1998-04-02 | 1999-10-07 | Basf Ag | Verfahren zur Herstellung von 1,3,4-trisubstituierten 1,2,4-Triazoliumsalzen |
| GB9807104D0 (en) | 1998-04-02 | 1998-06-03 | Chirotech Technology Ltd | The preparation of phosphine ligands |
| EP1071668B1 (en) | 1998-04-21 | 2009-06-03 | Bristol-Myers Squibb Pharma Company | 5-aminoindeno[1,2-c]pyrazol-4-ones as anti-cancer and anti-proliferative agents |
| GB9809349D0 (en) | 1998-05-02 | 1998-07-01 | Zeneca Ltd | Heterocyclic derivatives |
| DE69921994T2 (de) | 1998-05-02 | 2005-12-01 | Astrazeneca Ab | Heterozyklische verbindungen mit faktor xa hemmender wirkung |
| GB9809350D0 (en) | 1998-05-02 | 1998-07-01 | Zeneca Ltd | Novel salt |
| AU4631499A (en) | 1998-06-30 | 2000-01-17 | Chirotech Technology Limited | The preparation of arylphosphines |
| JP2000086659A (ja) | 1998-07-14 | 2000-03-28 | Takeda Chem Ind Ltd | オクタヒドロピリド[1,2―a]ピラジン誘導体 |
| TW434207B (en) | 1998-07-24 | 2001-05-16 | Everlight Chem Ind Corp | Chiral ligand and method for preparing cyanohydrins from aldehydes |
| US6303625B1 (en) | 1998-07-27 | 2001-10-16 | Ortho-Mcneil Pharmaceutical, Inc. | Triazolopyridines for the treatment of thrombosis disorders |
| WO2000009480A1 (fr) | 1998-08-11 | 2000-02-24 | Daiichi Pharmaceutical Co., Ltd. | Nouveaux derives sulfonyle |
| CA2358091A1 (en) | 1998-12-23 | 2000-07-06 | Eli Lilly And Company | Antithrombotic amides |
| AU2364600A (en) | 1998-12-23 | 2000-07-31 | Eli Lilly And Company | Heteroroaromatic amides as inhibitor of factor xa |
| CA2361149A1 (en) | 1998-12-23 | 2000-07-06 | Eli Lilly And Company | Aromatic amides |
| US6660739B1 (en) | 1998-12-24 | 2003-12-09 | Eli Lilly And Company | Heterocyclic amides as inhibitors of factor Xa |
| GB9902989D0 (en) | 1999-02-11 | 1999-03-31 | Zeneca Ltd | Heterocyclic derivatives |
| AU2241400A (en) * | 1999-04-06 | 2000-10-12 | Yamanouchi Pharmaceutical Co., Ltd. | Novel thiazolobenzoimidazole derivative |
| JP4390024B2 (ja) | 1999-04-23 | 2009-12-24 | アステラス製薬株式会社 | 新規なジアゼパン誘導体又はその塩 |
| GB9909592D0 (en) * | 1999-04-26 | 1999-06-23 | Chirotech Technology Ltd | Process for the preparation of calanolide precursors |
| JP2003500390A (ja) | 1999-05-24 | 2003-01-07 | シーオーアール セラピューティクス インコーポレイテッド | Xa因子阻害剤 |
| US6855715B1 (en) | 1999-06-14 | 2005-02-15 | Eli Lilly And Company | Serine protease inhibitors |
| JP2003502296A (ja) * | 1999-06-15 | 2003-01-21 | ロディア・シミ | スルホニルアミド及びカルボキサミド並びに不斉触媒作用におけるそれらの使用 |
| GB9914342D0 (en) | 1999-06-19 | 1999-08-18 | Zeneca Ltd | Compound |
| JP2001011071A (ja) | 1999-06-25 | 2001-01-16 | Mochida Pharmaceut Co Ltd | アミノアルキルスルホンアミド誘導体 |
| US6492408B1 (en) | 1999-07-21 | 2002-12-10 | Boehringer Ingelheim Pharmaceuticals, Inc. | Small molecules useful in the treatment of inflammatory disease |
| GB9917344D0 (en) | 1999-07-24 | 1999-09-22 | Zeneca Ltd | Novel salt |
| HK1050005A1 (zh) | 1999-09-13 | 2003-06-06 | 三维药物公司 | 氮杂环烷酮丝氨酸蛋白酶抑制剂 |
| CZ2002961A3 (cs) | 1999-09-17 | 2002-08-14 | Millennium Pharmaceuticals, Inc. | Benzamidy a příbuzné sloučeniny pro inhibici faktoru Xa |
| TR200201413T2 (tr) | 1999-09-17 | 2003-02-21 | Millennium Pharmaceuticals, Inc. | Faktör Xa' nın inhibitörleri. |
| WO2001038309A1 (en) | 1999-11-24 | 2001-05-31 | Cor Therapeutics, Inc. | β-AMINO ACID-, ASPARTIC ACID- AND DIAMINOPROPIONIC-BASED INHIBITORS OF FACTOR Xa |
| ATE311366T1 (de) | 2000-02-29 | 2005-12-15 | Millennium Pharm Inc | Benzamide und ähnliche inhibitoren vom faktor xa |
| TWI290136B (en) * | 2000-04-05 | 2007-11-21 | Daiichi Seiyaku Co | Ethylenediamine derivatives |
| WO2002002519A2 (en) | 2000-06-29 | 2002-01-10 | Bristol-Myers Squibb Pharma Company | THROMBIN OR FACTOR Xa INHIBITORS |
| US20040082786A1 (en) | 2000-09-29 | 2004-04-29 | Bing-Yan Zhu | Piperazine based inhibitors of factor xa |
| BR0107282A (pt) | 2000-09-29 | 2004-07-06 | Cor Therapeutics Inc | Composto, composição farmacêutica e métodos para prevenir ou tratar uma condição em um mamìfero e para inibir a coagulação de amostras biológicas |
| AU2002214626A1 (en) | 2000-09-29 | 2002-04-08 | Cor Therapeutics, Inc. | Quaternary amines and related inhibitors of factor xa |
| US6710058B2 (en) | 2000-11-06 | 2004-03-23 | Bristol-Myers Squibb Pharma Company | Monocyclic or bicyclic carbocycles and heterocycles as factor Xa inhibitors |
| AU2406402A (en) | 2000-11-22 | 2002-06-03 | Yamanouchi Pharma Co Ltd | Substituted benzene derivatives or salts thereof |
| HUP0303652A2 (hu) | 2000-12-20 | 2004-03-01 | Bristol-Myers Squibb Company | Ciklikus származékok, mint kemokin receptor aktivitás modulátorai és ezeket tartalmazó gyógyszerkészítmények |
| WO2002079145A1 (en) | 2001-03-30 | 2002-10-10 | Millennium Pharmaceuticals, Inc. | BENZAMIDE INHIBITORS OF FACTOR Xa |
| WO2003000657A1 (fr) | 2001-06-20 | 2003-01-03 | Daiichi Pharmaceutical Co., Ltd. | Derives de diamine |
| RU2319699C2 (ru) * | 2001-06-20 | 2008-03-20 | Дайити Санкио Компани, Лимитед | Производные диаминов |
| PL368402A1 (en) | 2001-08-09 | 2005-03-21 | Daiichi Pharmaceutical Co, Ltd. | Diamine derivatives |
| EP1427415B1 (en) | 2001-09-21 | 2009-08-12 | Brystol-Myers Squibb Company | Lactam-containing compounds and derivatives thereof as factor xa inhibitors |
| US7030141B2 (en) | 2001-11-29 | 2006-04-18 | Christopher Franklin Bigge | Inhibitors of factor Xa and other serine proteases involved in the coagulation cascade |
| WO2003048081A2 (en) | 2001-12-04 | 2003-06-12 | Bristol-Myers Squibb Company | Glycinamides as factor xa inhibitors |
| US7312214B2 (en) | 2002-05-10 | 2007-12-25 | Bristol-Myers Squibb Company | 1, 1-disubstituted cycloalkyl derivatives as factor Xa inhibitors |
| KR20050092373A (ko) * | 2002-12-24 | 2005-09-21 | 다이이찌 세이야꾸 가부시기가이샤 | 신규한 에틸렌디아민 유도체 |
| KR20050110612A (ko) * | 2002-12-25 | 2005-11-23 | 다이이찌 세이야꾸 가부시기가이샤 | 디아민 유도체 |
-
2002
- 2002-03-20 WO PCT/JP2002/002683 patent/WO2003000657A1/ja active Application Filing
- 2002-03-20 US US10/481,262 patent/US7365205B2/en active Active
- 2002-06-19 MY MYPI20022307A patent/MY153231A/en unknown
- 2002-06-20 EP EP11002212A patent/EP2343290A1/en not_active Withdrawn
- 2002-06-20 TW TW091113510A patent/TWI298066B/zh active
- 2002-06-20 AR ARP020102322A patent/AR036102A1/es active IP Right Grant
- 2002-06-20 PT PT02743653T patent/PT1405852E/pt unknown
-
2003
- 2003-12-19 ZA ZA2003/09866A patent/ZA200309866B/en unknown
-
2004
- 2004-02-09 US US10/773,344 patent/US7342014B2/en not_active Expired - Lifetime
-
2007
- 2007-09-06 US US11/850,788 patent/US20080015215A1/en not_active Abandoned
-
2008
- 2008-12-30 US US12/259,496 patent/US20100093785A1/en not_active Abandoned
-
2009
- 2009-03-06 US US12/399,702 patent/US20090270446A1/en not_active Abandoned
-
2010
- 2010-05-21 US US12/784,710 patent/US20110077266A1/en not_active Abandoned
- 2010-12-13 US US12/966,640 patent/US20110312990A1/en not_active Abandoned
-
2012
- 2012-08-20 CY CY20121100742T patent/CY1113054T1/el unknown
-
2015
- 2015-07-16 BE BE2015C046C patent/BE2015C046I2/fr unknown
- 2015-08-20 CY CY2015034C patent/CY2015034I1/el unknown
- 2015-09-29 NL NL300760C patent/NL300760I2/en unknown
- 2015-10-09 FR FR15C0068C patent/FR15C0068I2/fr active Active
Also Published As
| Publication number | Publication date |
|---|---|
| TWI298066B (en) | 2008-06-21 |
| CY1113054T1 (el) | 2016-04-13 |
| FR15C0068I2 (fr) | 2016-04-22 |
| AR036102A1 (es) | 2004-08-11 |
| CY2015034I2 (el) | 2016-04-13 |
| US7342014B2 (en) | 2008-03-11 |
| PT1405852E (pt) | 2012-10-30 |
| EP2343290A1 (en) | 2011-07-13 |
| US20080015215A1 (en) | 2008-01-17 |
| US20110312990A1 (en) | 2011-12-22 |
| BE2015C046I2 (h) | 2021-07-19 |
| ZA200309866B (en) | 2005-03-30 |
| US20050119486A1 (en) | 2005-06-02 |
| US20110077266A1 (en) | 2011-03-31 |
| WO2003000657A1 (fr) | 2003-01-03 |
| US7365205B2 (en) | 2008-04-29 |
| CY2015034I1 (el) | 2016-04-13 |
| US20100093785A1 (en) | 2010-04-15 |
| FR15C0068I1 (h) | 2015-12-04 |
| MY153231A (en) | 2015-01-29 |
| HK1092461A1 (en) | 2007-02-09 |
| US20090270446A1 (en) | 2009-10-29 |
| US20050020645A1 (en) | 2005-01-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NL300760I2 (en) | Edoxaban, a salt thereof, a solvate thereof or an N-oxide thereof, in particular edoxaban tosylate | |
| NO2015022I2 (no) | Edoksaban, et salt derav, et solvat derav eller et N-oksid derav, spesielt edoksabantosilat | |
| NL300996I1 (nl) | Naldemedine dan wel een farmaceutisch aanvaardbaar zout of solvaat daarvan, in het bijzonder het tosylaatzout | |
| NL301020I2 (nl) | Avatrombopag, desgewenst in de vorm van een farmaceutisch aanvaardbaar zout daarvan, in het bijzonder avatrombopag-maleaat | |
| NL300913I2 (nl) | Cariprazine, optioneel in de vorm van een zout, waaronder cariprazine hydrochloride | |
| FR17C1012I2 (fr) | 2-(pyridin-2-ylamino)-pyrido [2,3-d]pyrimidin-7-ones | |
| DE602004029145D1 (de) | Pyrazolopyridin-derivate | |
| NO20054220D0 (no) | Substituerte N-arylheterocykler, fremgangsmate for fremstilling derav og deres anvendelse som legemiddel | |
| DE602004026205D1 (de) | Roboterhand | |
| NL1031976A1 (nl) | N-(pyridine-2-yl)sulfonamidederivativen. | |
| EP1668781A4 (en) | CELLULAR BOOSTER WITH SHORT RANGE | |
| DE112004001751D2 (de) | Socke | |
| ATE394659T1 (de) | Probenhomogenisator | |
| DE112004002437D2 (de) | Socke | |
| ITMO20030289A1 (it) | Apparati, metodo e articolo. | |
| DK1667668T3 (da) | Alfabeta3 og altabeta6-integrinantagonister som antifibrotiske midler | |
| DK3184275T3 (da) | Polymere artikler | |
| NL1033403A1 (nl) | Therapeutische pyrazolo[3,4-b]pyridinen en indazolen. | |
| DE602004032218D1 (de) | Kontaktpunkteinrichtung | |
| NL300918I1 (nl) | Naltrexon of een farmaceutisch aanvaardbaar zout daarvan, in het bijzonder naltrexonhydrochloride, en bupropion of een farmaceutisch aanvaardbaar zout daarvan, in het bijzonder bupropionhydrochloride | |
| NO20053805D0 (no) | Diarylmetylindenpiperidinderivater, framgangsmate for fremstilling derav, og anvendelse derav | |
| ITMO20030004A0 (it) | Macchina utensile. | |
| ITMI20031132A0 (it) | Attrezzo da palestra perfezionato | |
| FI20031240L (fi) | Hissin tarraajajärjestely | |
| DE60316540D1 (de) | Brotbackgerät |