BE2015C046I2 - - Google Patents
Download PDFInfo
- Publication number
- BE2015C046I2 BE2015C046I2 BE2015C046C BE2015C046C BE2015C046I2 BE 2015C046 I2 BE2015C046 I2 BE 2015C046I2 BE 2015C046 C BE2015C046 C BE 2015C046C BE 2015C046 C BE2015C046 C BE 2015C046C BE 2015C046 I2 BE2015C046 I2 BE 2015C046I2
- Authority
- BE
- Belgium
Links
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)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (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 (en) | 2001-06-20 | 2002-03-20 | Diamine derivatives |
PCT/JP2002/006141 WO2003000680A1 (en) | 2001-06-20 | 2002-06-20 | Diamine derivatives |
Publications (1)
Publication Number | Publication Date |
---|---|
BE2015C046I2 true BE2015C046I2 (en) | 2021-07-19 |
Family
ID=27482359
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE2015C046C BE2015C046I2 (en) | 2001-06-20 | 2015-07-16 |
Country Status (13)
Country | Link |
---|---|
US (7) | US7365205B2 (en) |
EP (1) | EP2343290A1 (en) |
AR (1) | AR036102A1 (en) |
BE (1) | BE2015C046I2 (en) |
CY (2) | CY1113054T1 (en) |
FR (1) | FR15C0068I2 (en) |
HK (1) | HK1092461A1 (en) |
MY (1) | MY153231A (en) |
NL (1) | NL300760I2 (en) |
PT (1) | PT1405852E (en) |
TW (1) | TWI298066B (en) |
WO (1) | WO2003000657A1 (en) |
ZA (1) | ZA200309866B (en) |
Families Citing this family (112)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI290136B (en) | 2000-04-05 | 2007-11-21 | Daiichi Seiyaku Co | Ethylenediamine derivatives |
PL214669B1 (en) * | 2001-06-20 | 2013-08-30 | Daiichi Sankyo Company | Diamine derivatives |
US7365205B2 (en) * | 2001-06-20 | 2008-04-29 | Daiichi Sankyo Company, Limited | Diamine derivatives |
RU2314303C2 (en) * | 2001-08-09 | 2008-01-10 | Дайити Фармасьютикал Ко., Лтд. | Diamine derivatives |
WO2008011131A2 (en) * | 2006-07-21 | 2008-01-24 | Takeda Pharmaceutical Company Limited | Amide compounds |
JP4109288B2 (en) * | 2002-12-25 | 2008-07-02 | 第一三共株式会社 | Diamine derivatives |
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 |
US7488747B2 (en) * | 2003-12-29 | 2009-02-10 | Sepracor Inc. | Pyrrole and pyrazole DAAO inhibitors |
TWI350168B (en) * | 2004-05-07 | 2011-10-11 | Incyte Corp | Amido compounds and their use as pharmaceuticals |
CA2570694A1 (en) * | 2004-06-24 | 2006-02-02 | Incyte Corporation | Amido compounds and their use as pharmaceuticals |
EP1758582A4 (en) * | 2004-06-24 | 2008-01-09 | Incyte Corp | Amido compounds and their use as pharmaceuticals |
EP1768954A4 (en) * | 2004-06-24 | 2008-05-28 | Incyte Corp | 2-methylpropanamides and their use as pharmaceuticals |
WO2006012173A1 (en) * | 2004-06-24 | 2006-02-02 | Incyte Corporation | Amido compounds and their use as pharmaceuticals |
US20060009491A1 (en) * | 2004-06-24 | 2006-01-12 | Incyte Corporation | Amido compounds and their use as pharmaceuticals |
US8071624B2 (en) | 2004-06-24 | 2011-12-06 | Incyte Corporation | N-substituted piperidines and their use as pharmaceuticals |
MX2007001540A (en) * | 2004-08-10 | 2007-04-23 | Incyte Corp | Amido compounds and their use as pharmaceuticals. |
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 |
HUP0700604A3 (en) * | 2005-02-18 | 2008-02-28 | Arpida Ag | Novel processes for preparation of a 2h-chromene |
BRPI0609419A2 (en) * | 2005-03-31 | 2010-03-30 | Daiichi Sankyo Co Ltd | thiamine derivatives |
AU2006264317B2 (en) | 2005-07-06 | 2012-02-23 | Sunovion Pharmaceuticals 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 |
TW200745033A (en) | 2005-09-14 | 2007-12-16 | Dainippon Sumitomo Pharma Co | Oxindole derivative as feeding control agent |
KR101361441B1 (en) * | 2005-09-16 | 2014-02-10 | 다이이찌 산쿄 가부시키가이샤 | Optically active diamine derivative and process for producing the same |
JP2009508963A (en) * | 2005-09-21 | 2009-03-05 | インサイト・コーポレイション | Amide compounds and their use as pharmaceutical compositions |
US8193207B2 (en) * | 2005-12-05 | 2012-06-05 | Incyte Corporation | Lactam compounds and methods of using the same |
CN101426372A (en) * | 2006-01-06 | 2009-05-06 | 塞普拉柯公司 | Tetralone-based monoamine reuptake inhibitors |
ES2594156T3 (en) * | 2006-01-06 | 2016-12-16 | Sunovion Pharmaceuticals Inc. | Cycloalkylamines as 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 |
CA2635814A1 (en) * | 2006-01-31 | 2007-08-09 | Incyte Corporation | Amido compounds and their use as pharmaceuticals |
US20070213311A1 (en) * | 2006-03-02 | 2007-09-13 | Yun-Long Li | Modulators of 11-beta 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 |
US8097760B2 (en) | 2006-03-31 | 2012-01-17 | Sunovion Pharmacuticals Inc. | Preparation of chiral amides and amines |
JP2009535420A (en) * | 2006-05-01 | 2009-10-01 | インサイト・コーポレイション | Tetra-substituted ureas as modulators of 11-beta hydroxyl steroid dehydrogenase type 1 |
EP2018378A2 (en) * | 2006-05-17 | 2009-01-28 | Incyte Corporation | Heterocyclic inhibitors of 11-b hydroxyl steroid dehydrogenase type i and methods of using the same |
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 |
US8344180B2 (en) | 2006-08-30 | 2013-01-01 | Shionogi & Co., Ltd. | Hydrazine amide derivative |
ZA200904686B (en) * | 2007-01-18 | 2010-09-29 | Sepracor Inc | Inhibitiors of D-amino acid oxidase |
US7902252B2 (en) * | 2007-01-18 | 2011-03-08 | Sepracor, Inc. | Inhibitors of D-amino acid oxidase |
FI2140867T4 (en) * | 2007-03-29 | 2023-09-14 | Pharmaceutical composition | |
MX2009012685A (en) | 2007-05-31 | 2009-12-14 | Sepracor Inc | Phenyl substituted cycloalkylamines as monoamine reuptake inhibitors. |
DE102007028319A1 (en) | 2007-06-20 | 2008-12-24 | Bayer Healthcare Ag | Substituted oxazolidinones and their use |
DE102007028407A1 (en) | 2007-06-20 | 2008-12-24 | Bayer Healthcare Ag | Substituted oxazolidinones and their use |
DE102007028406A1 (en) | 2007-06-20 | 2008-12-24 | Bayer Healthcare Ag | Substituted oxazolidinones and their use |
CL2008001839A1 (en) | 2007-06-21 | 2009-01-16 | Incyte Holdings Corp | Compounds derived from 2,7-diazaspirocycles, inhibitors of 11-beta hydroxyl steroid dehydrogenase type 1; pharmaceutical composition comprising said compounds; Useful to treat obesity, diabetes, glucose intolerance, type II diabetes, among other diseases. |
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 |
US9776963B2 (en) | 2008-11-10 | 2017-10-03 | The Trustees Of The University Of Pennsylvania | Small molecule CD4 mimetics and uses thereof |
KR20110106840A (en) * | 2008-12-12 | 2011-09-29 | 다이이찌 산쿄 가부시키가이샤 | Process for producing optically active carboxylic acid |
KR101463653B1 (en) | 2008-12-17 | 2014-11-19 | 다이이찌 산쿄 가부시키가이샤 | Method for producing diamine derivative |
JPWO2010082531A1 (en) | 2009-01-13 | 2012-07-05 | 第一三共株式会社 | Activated blood coagulation factor inhibitor |
JP5666424B2 (en) | 2009-03-10 | 2015-02-12 | 第一三共株式会社 | Method for producing diamine derivative |
CN102348680B (en) | 2009-03-13 | 2014-11-05 | 第一三共株式会社 | Method for producing optically active diamine derivative |
WO2010131663A1 (en) * | 2009-05-15 | 2010-11-18 | 第一三共株式会社 | Oxamide derivative |
CN102481296A (en) | 2009-06-18 | 2012-05-30 | 第一三共株式会社 | Daiichi sankyo co ltd |
FR2948372B1 (en) | 2009-07-21 | 2011-07-22 | Servier Lab | NOVEL CHROMENIC DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME |
US20110034434A1 (en) * | 2009-08-07 | 2011-02-10 | Sepracor Inc. | Prodrugs of fused heterocyclic inhibitors of d-amino acid oxidase |
EP2540317A4 (en) | 2010-02-22 | 2014-04-16 | Daiichi Sankyo Co Ltd | Sustained-release solid preparation for oral use |
JP5749247B2 (en) * | 2010-02-22 | 2015-07-15 | 第一三共株式会社 | Oral sustained-release solid preparation |
TW201200165A (en) | 2010-02-22 | 2012-01-01 | Daiichi Sankyo Co Ltd | Oral solid extended release dosage form |
HUE031059T2 (en) | 2010-03-19 | 2017-06-28 | Daiichi Sankyo Co Ltd | Method for improving dissolvability of anticoagulant |
KR101708528B1 (en) * | 2010-03-19 | 2017-02-20 | 다이이찌 산쿄 가부시키가이샤 | Crystal of diamine derivative and method of producing same |
WO2011149110A1 (en) | 2010-05-28 | 2011-12-01 | Daiichi Sankyo Company, Limited | Novel composition for the prevention and/or treatment of thromboembolism |
EP2589590B1 (en) | 2010-07-02 | 2016-12-28 | Daiichi Sankyo Company, Limited | Process for preparation of optically active diamine derivative salt |
HUP1000598A2 (en) | 2010-11-05 | 2012-09-28 | Richter Gedeon Nyrt | Indole derivatives |
US20140050743A1 (en) | 2011-01-19 | 2014-02-20 | Bayer Intellectual Property Gmbh | Binding proteins to inhibitors of coagulation factors |
EP2730269B1 (en) | 2011-07-08 | 2017-08-23 | Daiichi Sankyo Company, Limited | Product quality control method |
CN103732227B (en) | 2011-08-10 | 2017-04-12 | 第一三共株式会社 | Pharmaceutical composition containing diamine derivative |
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 (en) * | 2012-04-24 | 2013-11-06 | 南京药石药物研发有限公司 | Intermediate synthesizing 5-chlorothiophene-3-carbo and preparation method thereof |
BR112015004190A2 (en) | 2012-09-03 | 2017-07-04 | Daiichi Sankyo Co Ltd | sustained release pharmaceutical composition, and method for producing a sustained release pharmaceutical composition |
EA028093B1 (en) | 2012-09-07 | 2017-10-31 | Новартис Аг | Indole carboxamide derivatives and uses thereof |
JP2016503389A (en) | 2012-11-23 | 2016-02-04 | 第一三共株式会社 | Process for the preparation of (1S, 4S, 5S) -4-bromo-6-oxabicyclo [3.2.1] octan-7-one |
MX2015011514A (en) | 2013-03-15 | 2016-08-11 | Celgene Avilomics Res Inc | Heteroaryl compounds and uses thereof. |
EP3943087A1 (en) | 2013-03-15 | 2022-01-26 | Celgene CAR LLC | Heteroaryl compounds and uses thereof |
TWI602803B (en) | 2013-03-29 | 2017-10-21 | 第一三共股份有限公司 | Preparation method of optically active diamine compound |
WO2014157612A1 (en) | 2013-03-29 | 2014-10-02 | 第一三共株式会社 | Method for producing (1s,4s,5s)-4-bromo-6- oxabicyclo[3.2.1]octane-7-one |
JP2016529279A (en) | 2013-08-29 | 2016-09-23 | 第一三共株式会社 | Agents for the treatment or 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 (en) | 2014-06-11 | 2015-12-17 | Dietrich Gulba | rodenticide |
WO2016025681A1 (en) | 2014-08-13 | 2016-02-18 | The Trustees Of The University Of Pennsylvania | Inhibitors of hiv-1 entry and methods of use thereof |
CN104529729B (en) * | 2014-12-31 | 2016-03-30 | 浙江永太科技股份有限公司 | The preparation method of the fluoro-3-chlorobenzaldehyde of a kind of 2- |
TWI571460B (en) | 2016-03-14 | 2017-02-21 | 中化合成生技股份有限公司 | Process for producing diamine derivative |
WO2018011823A1 (en) | 2016-07-13 | 2018-01-18 | Mylan Laboratories Limited | 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 |
JP7323179B2 (en) * | 2017-03-10 | 2023-08-08 | ラトガーズ, ザ ステイト ユニバーシティ オブ ニュー ジャージー | Indole derivatives as efflux pump inhibitors |
GB201807014D0 (en) | 2018-04-30 | 2018-06-13 | Univ Leeds Innovations Ltd | Factor xlla inhibitors |
TWI826474B (en) | 2018-06-27 | 2023-12-21 | 日商第一三共股份有限公司 | Granules containing diamine derivative, as well as use and manufacturing method thereof |
WO2020063676A1 (en) | 2018-09-26 | 2020-04-02 | 江苏恒瑞医药股份有限公司 | Ligand-drug conjugate of exatecan analogue, preparation method therefor and application thereof |
AU2019351427A1 (en) | 2018-09-30 | 2021-04-15 | Changzhou Hansoh Pharmaceutical Co., Ltd. | Anti-B7H3 antibody-exatecan analog conjugate and medicinal use thereof |
CN109942600B (en) * | 2019-04-15 | 2021-08-20 | 内蒙古京东药业有限公司 | Preparation method of edoxaban |
MX2022000421A (en) | 2019-07-10 | 2022-02-10 | Bayer Ag | Process of preparing 2-(phenylimino)-1,3-thiazolidin-4-ones. |
KR102333564B1 (en) | 2019-11-28 | 2021-12-01 | 동방에프티엘(주) | A novel synthetic route for the production of optically active diamine derivative and thiazole derivate |
JP2023505708A (en) | 2019-12-12 | 2023-02-10 | 江蘇恒瑞医薬股▲ふん▼有限公司 | Anti-claudin antibody drug conjugate and pharmaceutical use thereof |
CA3168260A1 (en) | 2020-01-22 | 2021-07-29 | Jiangsu Hengrui Medicine Co., Ltd. | Anti-trop-2 antidody-exatecan analog conjugate and medical use thereof |
JP2023518583A (en) | 2020-03-25 | 2023-05-02 | 江蘇恒瑞医薬股▲ふん▼有限公司 | PHARMACEUTICAL COMPOSITIONS CONTAINING AN ANTIBODY-DRUG CONJUGATE AND USES THEREOF (Application No. CN 202110287012.7). |
MX2022011808A (en) | 2020-03-25 | 2022-12-06 | Jiangsu Hengrui Pharmaceuticals Co Ltd | Anti-psma antibody-exatecan analogue conjugate and medical use thereof. |
TW202144014A (en) | 2020-03-25 | 2021-12-01 | 大陸商江蘇恆瑞醫藥股份有限公司 | Method for the preparation of an antibody drug conjugate |
BR112022024930A2 (en) | 2020-06-08 | 2022-12-27 | Baili Bio Chengdu Pharmaceutical Co Ltd | CAMPTOTHECIN DRUG HAVING HIGH STABILITY HYDROPHILIC CONNECTION UNIT AND CONJUGATE THEREOF |
KR20220087933A (en) | 2020-12-18 | 2022-06-27 | 엠에프씨 주식회사 | Method For Producing Diamine Derivative |
WO2022129535A1 (en) | 2020-12-18 | 2022-06-23 | Krka, D.D., Novo Mesto | Edoxaban formulation containing no sugar alcohols |
EP4070658A1 (en) | 2021-04-06 | 2022-10-12 | BIORoxx GmbH | Use of anticoagulant active compounds as rodenticide |
GB202107722D0 (en) | 2021-05-28 | 2021-07-14 | Lunac Therapeutics Ltd | Factor XIIA Inhibitors |
WO2023083381A1 (en) | 2021-11-15 | 2023-05-19 | 成都百利多特生物药业有限责任公司 | Bispecific antibody-camptothecin drug conjugate and pharmaceutical use thereof |
CN114456194B (en) * | 2021-12-14 | 2023-07-07 | 浙江九洲药业股份有限公司 | Intermediate of Ai Duosha class tosylate and preparation method thereof |
CN115583900A (en) * | 2022-04-29 | 2023-01-10 | 张邦成都生物医药科技有限公司 | Preparation method of high-purity ixaban intermediate |
WO2023223346A1 (en) | 2022-05-16 | 2023-11-23 | Mylan Laboratories Limited | An improved process for the preparation of edoxaban intermediate |
Family Cites Families (92)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3376268A (en) * | 1964-02-26 | 1968-04-02 | Monsanto Co | Amide-heterocyclic polymers |
JPS63500796A (en) | 1985-06-07 | 1988-03-24 | ジ・アップジョン・カンパニ− | Antiarrhythmic use of aminocycloalkylamides |
WO1992004017A1 (en) | 1990-09-10 | 1992-03-19 | The Upjohn Company | Cis-n-(2-aminocyclohexyl)benzamide and their enantiomers as anticonvulsants |
IL100576A (en) | 1991-01-18 | 1995-11-27 | Eli Lilley And Company | Cephalosporin antibiotics |
WO1993010022A1 (en) | 1991-11-14 | 1993-05-27 | Frutin Bernard D | 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 |
DE69410193T2 (en) | 1993-03-17 | 1998-09-03 | Meiji Seika Co | NEW CONNECTIONS WITH BLOOD PLAGUE AGGREGATING ACTIVITY |
KR970001164B1 (en) | 1993-06-09 | 1997-01-29 | 한국과학기술연구원 | Cephalosporin antibiotics and their process for preparing them |
CA2174516A1 (en) | 1993-10-19 | 1995-04-27 | Yoshiharu Ikeda | 2,3-diaminopropionic acid derivative |
TW270114B (en) | 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 (en) | 1994-06-01 | 1995-12-07 | Yamanouchi Pharmaceutical Co. Ltd. | Oxadiazole derivative and medicinal composition thereof |
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 |
AU5432696A (en) | 1995-04-07 | 1996-10-23 | Pharmacopeia, Inc. | Carbonyl-piperazinyl and piperidinil compounds which inhibit farnesyl protein transferase |
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 (en) * | 1995-09-21 | 1997-03-27 | Diagnostikforschung Inst | Bifunctional nicotinamide chelating agents of the type N¶2¶S¶2¶ for radioactive isotopes |
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 |
JP2002503207A (en) | 1996-04-17 | 2002-01-29 | デュポン ファーマシューティカルズ カンパニー | N- (amidinophenyl) -N '-(substituted) -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 |
PL331599A1 (en) | 1996-08-14 | 1999-08-02 | Zeneca Ltd | Substituted derivatives of pyrimidine and their pharmaceutical application |
UA56197C2 (en) | 1996-11-08 | 2003-05-15 | Зенека Лімітед | Heterocyclic derivatives |
JP2001511798A (en) | 1997-02-13 | 2001-08-14 | ゼネカ・リミテッド | Heterocyclic compounds useful as oxide-squalene cyclase inhibitors |
IT1291823B1 (en) | 1997-04-08 | 1999-01-21 | Menarini Ricerche Spa | PSEUDO-PEPTIDE COMPOUNDS, THEIR PREPARATION AND USE IN PHARMACEUTICAL FORMULATIONS |
DE69835430T2 (en) | 1997-05-30 | 2007-03-08 | Takeda Pharmaceutical Co. Ltd. | Sulphonamide derivatives, their preparation and their use |
US6207679B1 (en) * | 1997-06-19 | 2001-03-27 | Sepracor, Inc. | Antimicrobial agents uses and compositions related thereto |
WO1999000126A1 (en) | 1997-06-26 | 1999-01-07 | Eli Lilly And Company | Antithrombotic agents |
CA2294126A1 (en) | 1997-06-26 | 1999-01-07 | Douglas Wade Beight | Antithrombotic agents |
WO1999000121A1 (en) | 1997-06-26 | 1999-01-07 | Eli Lilly And Company | Antithrombotic agents |
GB9715895D0 (en) | 1997-07-29 | 1997-10-01 | Zeneca Ltd | Heterocyclic compounds |
GB9715894D0 (en) | 1997-07-29 | 1997-10-01 | Zeneca Ltd | Heterocyclic derivatives |
DE69833036T2 (en) | 1997-09-30 | 2006-06-22 | Daiichi Pharmaceutical Co., Ltd. | sulfonyl |
AR013693A1 (en) | 1997-10-23 | 2001-01-10 | Uriach & Cia Sa J | NEW PIPERIDINES AND PIPERAZINAS AS INHIBITORS OF THE PLAQUETARY AGREGATION |
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 |
EP0937723A1 (en) | 1998-02-18 | 1999-08-25 | Roche Diagnostics GmbH | Novel sulfonamides, process for their preparation and medicaments containing them |
EP0937711A1 (en) | 1998-02-18 | 1999-08-25 | Roche Diagnostics GmbH | Thiobenzamides, process for their preparation and medicaments containing them |
GB9807104D0 (en) | 1998-04-02 | 1998-06-03 | Chirotech Technology Ltd | The preparation of phosphine ligands |
DE19814801A1 (en) | 1998-04-02 | 1999-10-07 | Basf Ag | Process for the preparation of 1,3,4-trisubstituted 1,2,4-triazolium salts |
DE69940951D1 (en) * | 1998-04-21 | 2009-07-16 | Bristol Myers Squibb Pharma Co | ND GROWTH-INHIBITED MEANS |
TR200003200T2 (en) | 1998-05-02 | 2001-02-21 | Astrazeneca Ab | Heterocyclic derivatives that prevent factor XA. |
GB9809350D0 (en) | 1998-05-02 | 1998-07-01 | Zeneca Ltd | Novel salt |
GB9809349D0 (en) | 1998-05-02 | 1998-07-01 | Zeneca Ltd | Heterocyclic derivatives |
EP1090016B1 (en) | 1998-06-30 | 2002-10-30 | Chirotech Technology Limited | The preparation of arylphosphines |
JP2000086659A (en) | 1998-07-14 | 2000-03-28 | Takeda Chem Ind Ltd | Octahydropyrido[1,2-alpha]pyrazine derivative |
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 |
EP1104754A1 (en) | 1998-08-11 | 2001-06-06 | Daiichi Pharmaceutical Co., Ltd. | Novel sulfonyl derivatives |
EP1140905B1 (en) | 1998-12-23 | 2003-05-14 | Eli Lilly And Company | Heteroaromatic amides as inhibitor of factor xa |
JP2004522689A (en) | 1998-12-23 | 2004-07-29 | イーライ・リリー・アンド・カンパニー | Antithrombotic amides |
CA2361149A1 (en) | 1998-12-23 | 2000-07-06 | Eli Lilly And Company | Aromatic amides |
ES2217879T3 (en) | 1998-12-24 | 2004-11-01 | Eli Lilly And Company | HETEROCICLIC AMIDAS. |
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 (en) | 1999-04-23 | 2009-12-24 | アステラス製薬株式会社 | Novel diazepane derivatives or salts thereof |
GB9909592D0 (en) | 1999-04-26 | 1999-06-23 | Chirotech Technology Ltd | Process for the preparation of calanolide precursors |
EP1185511A2 (en) | 1999-05-24 | 2002-03-13 | Cor Therapeutics, Inc. | Inhibitors of factor xa |
ES2248084T3 (en) | 1999-06-14 | 2006-03-16 | Eli Lilly And Company | SERINPROTEASA INHIBITORS. |
AU6448200A (en) * | 1999-06-15 | 2001-01-02 | Rhodia Chimie | Sulphonylamides and carboxamides and their use in asymmetrical catalysis |
GB9914342D0 (en) | 1999-06-19 | 1999-08-18 | Zeneca Ltd | Compound |
JP2001011071A (en) | 1999-06-25 | 2001-01-16 | Mochida Pharmaceut Co Ltd | Aminoalkylsulfonamide derivative |
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 |
DK1212300T3 (en) | 1999-09-13 | 2004-03-15 | Dimensional Pharm Inc | Azacyclolol alkanone serine protease inhibitors |
RU2002110295A (en) | 1999-09-17 | 2003-12-10 | Милленниум Фармасьютикалс, Инк. (Us) | Factor Xa Inhibitors |
CZ2002961A3 (en) | 1999-09-17 | 2002-08-14 | Millennium Pharmaceuticals, Inc. | Benzamides and related compounds for inhibition of Xa factor |
WO2001038309A1 (en) | 1999-11-24 | 2001-05-31 | Cor Therapeutics, Inc. | β-AMINO ACID-, ASPARTIC ACID- AND DIAMINOPROPIONIC-BASED INHIBITORS OF FACTOR Xa |
ATE311366T1 (en) | 2000-02-29 | 2005-12-15 | Millennium Pharm Inc | BENZAMIDE AND SIMILAR FACTOR XA INHIBITORS |
TWI290136B (en) * | 2000-04-05 | 2007-11-21 | Daiichi Seiyaku Co | Ethylenediamine derivatives |
CA2413241A1 (en) | 2000-06-29 | 2002-01-10 | Bristol-Myers Squibb Pharma Company | Thrombin or factor xa inhibitors |
AU2001294824A1 (en) | 2000-09-29 | 2002-04-08 | Millennium Pharmaceuticals, Inc. | Piperazine based inhibitors of factor xa |
US20040067938A1 (en) | 2000-09-29 | 2004-04-08 | Penglie Zhang | Quaternary amines and related inhibitors of factor xa |
CA2422873A1 (en) | 2000-09-29 | 2002-04-04 | Wenhao Li | Piperazin-2-one amides as 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 |
WO2002042270A1 (en) | 2000-11-22 | 2002-05-30 | Yamanouchi Pharmaceutical Co., Ltd. | Substituted benzene derivatives or salts thereof |
US6706712B2 (en) | 2000-12-20 | 2004-03-16 | Bristol-Myers Squibb Pharma Company | Cyclic derivatives as modulators of chemokine receptor activity |
ATE368643T1 (en) | 2001-03-30 | 2007-08-15 | Millennium Pharm Inc | FACTOR XA BENZAMIDINE INHIBITORS |
PL214669B1 (en) | 2001-06-20 | 2013-08-30 | Daiichi Sankyo Company | Diamine derivatives |
US7365205B2 (en) | 2001-06-20 | 2008-04-29 | Daiichi Sankyo Company, Limited | Diamine derivatives |
RU2314303C2 (en) | 2001-08-09 | 2008-01-10 | Дайити Фармасьютикал Ко., Лтд. | Diamine derivatives |
BRPI0212726B8 (en) | 2001-09-21 | 2021-05-25 | Bristol Myers Squibb Co | compounds containing lactams, and derivatives thereof, pharmaceutical composition comprising them and their uses |
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 |
PL378215A1 (en) * | 2002-12-24 | 2006-03-20 | Daiichi Pharmaceutical Co., Ltd. | Novel ethylenediamine derivatives |
JP4109288B2 (en) * | 2002-12-25 | 2008-07-02 | 第一三共株式会社 | Diamine derivatives |
-
2002
- 2002-03-20 US US10/481,262 patent/US7365205B2/en active Active
- 2002-03-20 WO PCT/JP2002/002683 patent/WO2003000657A1/en active Application Filing
- 2002-06-19 MY MYPI20022307A patent/MY153231A/en unknown
- 2002-06-20 PT PT02743653T patent/PT1405852E/en unknown
- 2002-06-20 EP EP11002212A patent/EP2343290A1/en not_active Withdrawn
- 2002-06-20 TW TW091113510A patent/TWI298066B/en active
- 2002-06-20 AR ARP020102322A patent/AR036102A1/en active IP Right Grant
-
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
-
2006
- 2006-11-24 HK HK06112922.2A patent/HK1092461A1/en not_active IP Right Cessation
-
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/en unknown
-
2015
- 2015-07-16 BE BE2015C046C patent/BE2015C046I2/fr unknown
- 2015-08-20 CY CY2015034C patent/CY2015034I2/en unknown
- 2015-09-29 NL NL300760C patent/NL300760I2/en unknown
- 2015-10-09 FR FR15C0068C patent/FR15C0068I2/en active Active
Also Published As
Publication number | Publication date |
---|---|
HK1092461A1 (en) | 2007-02-09 |
MY153231A (en) | 2015-01-29 |
NL300760I2 (en) | 2017-07-20 |
US20080015215A1 (en) | 2008-01-17 |
CY2015034I1 (en) | 2016-04-13 |
FR15C0068I2 (en) | 2016-04-22 |
US20110077266A1 (en) | 2011-03-31 |
EP2343290A1 (en) | 2011-07-13 |
AR036102A1 (en) | 2004-08-11 |
US20050119486A1 (en) | 2005-06-02 |
CY2015034I2 (en) | 2016-04-13 |
FR15C0068I1 (en) | 2015-12-04 |
US20050020645A1 (en) | 2005-01-27 |
PT1405852E (en) | 2012-10-30 |
WO2003000657A1 (en) | 2003-01-03 |
US7342014B2 (en) | 2008-03-11 |
TWI298066B (en) | 2008-06-21 |
US20090270446A1 (en) | 2009-10-29 |
CY1113054T1 (en) | 2016-04-13 |
ZA200309866B (en) | 2005-03-30 |
US20100093785A1 (en) | 2010-04-15 |
US20110312990A1 (en) | 2011-12-22 |
US7365205B2 (en) | 2008-04-29 |