ATE255093T1 - Benzamidverbindung und ihre medizinische verwendung - Google Patents
Benzamidverbindung und ihre medizinische verwendungInfo
- Publication number
- ATE255093T1 ATE255093T1 AT95915333T AT95915333T ATE255093T1 AT E255093 T1 ATE255093 T1 AT E255093T1 AT 95915333 T AT95915333 T AT 95915333T AT 95915333 T AT95915333 T AT 95915333T AT E255093 T1 ATE255093 T1 AT E255093T1
- Authority
- AT
- Austria
- Prior art keywords
- compound
- renal
- action
- cerebral
- therapeutic agents
- Prior art date
Links
- -1 BENZAMIDE COMPOUND Chemical class 0.000 title 1
- KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 title 1
- 239000003814 drug Substances 0.000 abstract 6
- 229940124597 therapeutic agent Drugs 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 4
- 206010002383 Angina Pectoris Diseases 0.000 abstract 2
- 229940127291 Calcium channel antagonist Drugs 0.000 abstract 2
- 206010020772 Hypertension Diseases 0.000 abstract 2
- 208000006673 asthma Diseases 0.000 abstract 2
- 230000002490 cerebral effect Effects 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 239000003112 inhibitor Substances 0.000 abstract 2
- 208000001286 intracranial vasospasm Diseases 0.000 abstract 2
- 230000003836 peripheral circulation Effects 0.000 abstract 2
- 230000002093 peripheral effect Effects 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 230000000996 additive effect Effects 0.000 abstract 1
- 239000000556 agonist Substances 0.000 abstract 1
- 210000001367 artery Anatomy 0.000 abstract 1
- 150000003936 benzamides Chemical class 0.000 abstract 1
- 230000008602 contraction Effects 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 230000001077 hypotensive effect Effects 0.000 abstract 1
- 239000003509 long acting drug Substances 0.000 abstract 1
- 230000005923 long-lasting effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- 230000002040 relaxant effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 210000002460 smooth muscle Anatomy 0.000 abstract 1
- 238000011282 treatment Methods 0.000 abstract 1
- 230000002792 vascular Effects 0.000 abstract 1
- 230000000304 vasodilatating effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- 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
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/38—Nitrogen atoms
- C07D215/42—Nitrogen atoms attached in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms 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
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/32—Nitrogen atom
- C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7828094 | 1994-04-18 | ||
| PCT/JP1995/000747 WO1995028387A1 (en) | 1994-04-18 | 1995-04-17 | Benzamide compound and medicinal use thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE255093T1 true ATE255093T1 (de) | 2003-12-15 |
Family
ID=13657559
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT95915333T ATE255093T1 (de) | 1994-04-18 | 1995-04-17 | Benzamidverbindung und ihre medizinische verwendung |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US5958944A (de) |
| EP (3) | EP1195372A1 (de) |
| KR (1) | KR100311438B1 (de) |
| AT (1) | ATE255093T1 (de) |
| CA (1) | CA2188164C (de) |
| DE (1) | DE69532195T2 (de) |
| ES (2) | ES2388917T3 (de) |
| WO (1) | WO1995028387A1 (de) |
Families Citing this family (80)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR9711154A (pt) | 1996-08-12 | 1999-08-17 | Yoshitomi Pharmaceutical | Agente farmac-utico contendo inibidor cinase rho |
| JP4783774B2 (ja) * | 1996-08-12 | 2011-09-28 | 田辺三菱製薬株式会社 | Ｒｈｏキナーゼ阻害剤を含有する医薬 |
| CA2307285C (en) | 1998-08-17 | 2009-03-31 | Senju Pharmaceutical Co., Ltd. | Agent for prophylaxis and treatment of glaucoma |
| US6316503B1 (en) * | 1999-03-15 | 2001-11-13 | Tularik Inc. | LXR modulators |
| AU3987800A (en) * | 1999-04-22 | 2000-11-10 | Mitsubishi Pharma Corporation | Preventives/remedies for angiostenosis |
| EP1177796B1 (de) * | 1999-04-27 | 2011-04-27 | Mitsubishi Tanabe Pharma Corporation | Arzneimittel zur präventiven oder therapeutische Behandlung von Lebererkrankungen |
| EP1200086A4 (de) * | 1999-08-04 | 2009-05-27 | Icagen Inc | Methoden zur behandlung oder vorbeugung von schmerzen und angstzuständen |
| US7217722B2 (en) | 2000-02-01 | 2007-05-15 | Kirin Beer Kabushiki Kaisha | Nitrogen-containing compounds having kinase inhibitory activity and drugs containing the same |
| WO2001082924A1 (en) * | 2000-05-02 | 2001-11-08 | Smithkline Beecham Corporation | Phosphate transport inhibitors |
| EP1318985A2 (de) * | 2000-09-20 | 2003-06-18 | MERCK PATENT GmbH | 4-amino chinazolinen |
| JP2004509876A (ja) | 2000-09-20 | 2004-04-02 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフトング | ４−アミノ−キナゾリン |
| US6995162B2 (en) * | 2001-01-12 | 2006-02-07 | Amgen Inc. | Substituted alkylamine derivatives and methods of use |
| US20030134836A1 (en) * | 2001-01-12 | 2003-07-17 | Amgen Inc. | Substituted arylamine derivatives and methods of use |
| US7105682B2 (en) | 2001-01-12 | 2006-09-12 | Amgen Inc. | Substituted amine derivatives and methods of use |
| US7102009B2 (en) | 2001-01-12 | 2006-09-05 | Amgen Inc. | Substituted amine derivatives and methods of use |
| US6878714B2 (en) * | 2001-01-12 | 2005-04-12 | Amgen Inc. | Substituted alkylamine derivatives and methods of use |
| PE20020958A1 (es) * | 2001-03-23 | 2002-11-14 | Bayer Corp | Inhibidores de la rho-quinasa |
| UY27224A1 (es) * | 2001-03-23 | 2002-10-31 | Bayer Corp | Inhibidores de la rho-quinasa |
| US7109208B2 (en) * | 2001-04-11 | 2006-09-19 | Senju Pharmaceutical Co., Ltd. | Visual function disorder improving agents |
| US7074801B1 (en) * | 2001-04-26 | 2006-07-11 | Eisai Co., Ltd. | Nitrogen-containing condensed cyclic compound having a pyrazolyl group as a substituent group and pharmaceutical composition thereof |
| US7829566B2 (en) * | 2001-09-17 | 2010-11-09 | Werner Mederski | 4-amino-quinazolines |
| JP4505228B2 (ja) * | 2002-01-10 | 2010-07-21 | バイエル・シェーリング・ファルマ・アクチェンゲゼルシャフト | Ｒｈｏ−キナーゼ阻害剤 |
| MXPA04007196A (es) * | 2002-01-23 | 2005-06-08 | Bayer Pharmaceuticals Corp | Inhibidores de rho-quinasa. |
| EP1470121B1 (de) * | 2002-01-23 | 2012-07-11 | Bayer HealthCare LLC | Pyrimidin-derivate als rho kinase inhibitoren |
| CA2474702A1 (en) * | 2002-01-30 | 2003-08-07 | Tularik Inc | Heterocyclic arylsulfonamidobenzylic compounds |
| JP4434744B2 (ja) * | 2002-01-30 | 2010-03-17 | アムジェン インコーポレイテッド | アリールスルホンアミドベンジル化合物 |
| US20040028716A1 (en) * | 2002-06-14 | 2004-02-12 | Marks Andrew R. | Use of Y-27632 as an agent to prevent restenosis after coronary artery angioplasty/stent implantation |
| DE60319714T2 (de) | 2002-06-19 | 2009-04-02 | Schering Corp. | Agonisten des cannabinoidrezeptors |
| US7307088B2 (en) | 2002-07-09 | 2007-12-11 | Amgen Inc. | Substituted anthranilic amide derivatives and methods of use |
| AU2003280812A1 (en) | 2002-11-18 | 2004-06-15 | Santen Pharmaceutical Co., Ltd. | REMEDY FOR GLAUCOMA COMPRISING Rho KINASE INHIBITOR AND Beta-BLOCKER |
| US6861422B2 (en) * | 2003-02-26 | 2005-03-01 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Dihydropteridinones, processes for preparing them and their use as pharmaceutical compositions |
| MXPA06001566A (es) * | 2003-08-12 | 2006-05-15 | Amgen Inc | Compuestos arilsulfonamidobencilicos. |
| CN1925855B (zh) | 2003-12-19 | 2010-06-16 | 普莱希科公司 | 开发Ret调节剂的化合物和方法 |
| GB0403635D0 (en) * | 2004-02-18 | 2004-03-24 | Devgen Nv | Pyridinocarboxamides with improved activity as kinase inhibitors |
| US7485654B2 (en) * | 2004-06-03 | 2009-02-03 | Senju Pharmaceutical Co., Ltd. | Corneal perception recovery drug containing amide compound |
| DE102004033670A1 (de) * | 2004-07-09 | 2006-02-02 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Pyridodihydropyrazinone, Verfahren zu Ihrer Herstellung und Ihre Verwendung als Arzneimittel |
| US7728134B2 (en) * | 2004-08-14 | 2010-06-01 | Boehringer Ingelheim International Gmbh | Hydrates and polymorphs of 4[[(7R)-8-cyclopentyl-7-ethyl-5,6,7,8-tetrahydro-5-methyl-6-oxo-2-pteridinyl]amino]-3-methoxy-N-(1-methyl-4-piperidinyl)-benzamide, process for their manufacture and their use as medicament |
| US20060074088A1 (en) * | 2004-08-14 | 2006-04-06 | Boehringer Ingelheim International Gmbh | Dihydropteridinones for the treatment of cancer diseases |
| US20060058311A1 (en) | 2004-08-14 | 2006-03-16 | Boehringer Ingelheim International Gmbh | Combinations for the treatment of diseases involving cell proliferation |
| US7759485B2 (en) * | 2004-08-14 | 2010-07-20 | Boehringer Ingelheim International Gmbh | Process for the manufacture of dihydropteridinones |
| US20060035903A1 (en) * | 2004-08-14 | 2006-02-16 | Boehringer Ingelheim International Gmbh | Storage stable perfusion solution for dihydropteridinones |
| DE102004058337A1 (de) | 2004-12-02 | 2006-06-14 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Verfahren zur Herstellung von annelierten Piperazin-2-on Derivaten |
| US20100168102A9 (en) * | 2005-07-11 | 2010-07-01 | Devgen Nv | Amide Derivatives as Kinase Inhibitors |
| EP1934181A2 (de) * | 2005-10-13 | 2008-06-25 | Devgen NV | Kinaseinhibitoren |
| US8247556B2 (en) * | 2005-10-21 | 2012-08-21 | Amgen Inc. | Method for preparing 6-substituted-7-aza-indoles |
| US7439358B2 (en) * | 2006-02-08 | 2008-10-21 | Boehringer Ingelheim International Gmbh | Specific salt, anhydrous and crystalline form of a dihydropteridione derivative |
| BRPI0714782A2 (pt) | 2006-07-31 | 2013-07-16 | Senju Pharma Co | preparaÇço lÍquida aquosa contendo composto de amida |
| US8071625B2 (en) * | 2006-08-02 | 2011-12-06 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
| US8063082B2 (en) * | 2006-08-02 | 2011-11-22 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
| US20090036465A1 (en) * | 2006-10-18 | 2009-02-05 | United Therapeutics Corporation | Combination therapy for pulmonary arterial hypertension |
| WO2008063888A2 (en) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
| WO2008070823A2 (en) * | 2006-12-07 | 2008-06-12 | University Of South Florida | Substrate-mimetic akt inhibitor |
| WO2009012283A1 (en) | 2007-07-17 | 2009-01-22 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| WO2009019205A1 (en) * | 2007-08-03 | 2009-02-12 | Boehringer Ingelheim International Gmbh | Crystalline form of a dihydropteridione derivative |
| US8088793B2 (en) | 2007-08-15 | 2012-01-03 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
| MY172424A (en) | 2009-04-03 | 2019-11-25 | Hoffmann La Roche | Propane- i-sulfonic acid {3- (4-chloro-phenyl)-1h-pyrrolo [2, 3-b] pyridine-3-carconyl] -2, 4-difluoro-phenyl} -amide compositions and uses thereof |
| TW201103904A (en) * | 2009-06-11 | 2011-02-01 | Hoffmann La Roche | Janus kinase inhibitor compounds and methods |
| US8329724B2 (en) | 2009-08-03 | 2012-12-11 | Hoffmann-La Roche Inc. | Process for the manufacture of pharmaceutically active compounds |
| GB0914726D0 (en) * | 2009-08-24 | 2009-09-30 | Univ Manchester | Kinase inhibitors |
| CN106220623A (zh) | 2009-11-06 | 2016-12-14 | 普莱希科公司 | 用于激酶调节的化合物和方法及其适应症 |
| WO2011080984A1 (en) | 2009-12-29 | 2011-07-07 | Senju Pharmaceutical Co., Ltd. | Therapeutic agent (y - 39983 ) for corneal endothelial dysfunction |
| US8546566B2 (en) | 2010-10-12 | 2013-10-01 | Boehringer Ingelheim International Gmbh | Process for manufacturing dihydropteridinones and intermediates thereof |
| US9358233B2 (en) | 2010-11-29 | 2016-06-07 | Boehringer Ingelheim International Gmbh | Method for treating acute myeloid leukemia |
| US9624213B2 (en) | 2011-02-07 | 2017-04-18 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| AR085279A1 (es) | 2011-02-21 | 2013-09-18 | Plexxikon Inc | Formas solidas de {3-[5-(4-cloro-fenil)-1h-pirrolo[2,3-b]piridina-3-carbonil]-2,4-difluor-fenil}-amida del acido propano-1-sulfonico |
| US9370535B2 (en) | 2011-05-17 | 2016-06-21 | Boehringer Ingelheim International Gmbh | Method for treatment of advanced solid tumors |
| ES2897740T3 (es) | 2011-12-28 | 2022-03-02 | Kyoto Prefectural Public Univ Corp | Normalización del cultivo de células endoteliales de la córnea |
| US9150570B2 (en) | 2012-05-31 | 2015-10-06 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
| EP3024464A1 (de) | 2013-07-26 | 2016-06-01 | Boehringer Ingelheim International GmbH | Behandlung des myelodysplastischen syndroms |
| EP3029140A4 (de) | 2013-07-30 | 2017-06-28 | Kyoto Prefectural Public University Corporation | Hornhautendothel-zellmarker |
| CA2927898C (en) | 2013-10-31 | 2021-11-16 | Kyoto Prefectural Public University Corporation | Therapeutic drug for diseases related to endoplasmic reticulum cell death in corneal endothelium |
| WO2015080297A1 (en) | 2013-11-27 | 2015-06-04 | Kyoto Prefectural Public University Corporation | Application of laminin to corneal endothelial cell culture |
| US9867831B2 (en) | 2014-10-01 | 2018-01-16 | Boehringer Ingelheim International Gmbh | Combination treatment of acute myeloid leukemia and myelodysplastic syndrome |
| EP3416658B1 (de) | 2016-02-15 | 2023-03-22 | Kyoto Prefectural Public University Corporation | Menschliche funktionelle hornhautendothelzelle und anwendung davon |
| US20210207088A1 (en) | 2018-08-31 | 2021-07-08 | The Doshisha | Composition and method for preserving or culturing ocular cells |
| CA3109705A1 (en) | 2018-10-02 | 2020-04-09 | The Doshisha | Method and vessel for preserving corneal endothelial cells |
| US12473284B2 (en) * | 2019-12-30 | 2025-11-18 | Memorial Sloan Kettering Cancer Center | Small molecule inhibitors of ULK1 |
| WO2021172554A1 (ja) | 2020-02-27 | 2021-09-02 | 京都府公立大学法人 | ヒト機能性角膜内皮細胞およびその応用 |
| AU2021366805B2 (en) | 2020-10-22 | 2025-04-24 | Kyoto Prefectural Public University Corporation | A storage method of human corneal endothelial cells and/or human corneal endothelial precursor cells |
| JPWO2023085369A1 (de) | 2021-11-11 | 2023-05-19 |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3971789A (en) * | 1972-10-21 | 1976-07-27 | John Wyeth & Brother Limited | O-(4-Quinolylamino)benzamides |
| DE2520896A1 (de) * | 1975-05-10 | 1976-11-25 | Basf Ag | Azopigmente der beta-hydroxynaphthoesaeurereihe |
| ES438120A1 (es) * | 1975-06-02 | 1977-02-01 | Gallardo Antonio Sa | Procedimiento para la preparacion de amidas aromaticas. |
| NL7611713A (nl) * | 1975-11-03 | 1977-05-05 | Thomae Gmbh Dr K | Werkwijze voor de bereiding van verbindingen en preparaten met waardevolle farmacologische eigen- schappen. |
| ES456989A1 (es) | 1977-03-18 | 1978-07-16 | Lafarquim | Procedimiento de obtencion de un derivado de 4-aminopiridinay sus sales. |
| IT1126509B (it) * | 1979-12-07 | 1986-05-21 | Medea Res Srl | Benzimidi ad attivita' anestetica locale e antiaritmica,processo per la loro preparazione e composizioni farmaceutiche che le contengono |
| JPS57206662A (en) * | 1981-06-15 | 1982-12-18 | Chugai Pharmaceut Co Ltd | Benzamide derivative |
| DE3662788D1 (en) * | 1985-07-11 | 1989-05-18 | Rhone Poulenc Sante | Substituted amides, their preparation and compositions containing them |
| FR2592882B2 (fr) * | 1986-01-16 | 1988-03-11 | Rhone Poulenc Sante | Nouveaux amides substitues, leur preparation et les medicaments qui les contiennent |
| JPS6229566A (ja) * | 1985-07-30 | 1987-02-07 | Taiyo Yakuhin Kogyo Kk | 新規グアニジノメチル安息香酸誘導体 |
| JPS6290657A (ja) * | 1985-10-17 | 1987-04-25 | Fuji Photo Film Co Ltd | ２当量カプラ−単量体の製造方法 |
| JPS62158253A (ja) * | 1985-12-28 | 1987-07-14 | Kirin Brewery Co Ltd | ４−アミノピリジンアミド誘導体 |
| JPS62158252A (ja) * | 1985-12-28 | 1987-07-14 | Kirin Brewery Co Ltd | ４−アミノピリジンベンズアミド誘導体 |
| JPS6368551A (ja) * | 1986-09-10 | 1988-03-28 | Shiseido Co Ltd | Ｎ−〔２−ヒドロキシ−２−（４−ヒドロキシフエニル）エチル〕ベンズアミドおよび該化合物を有効成分とする循環器疾患治療剤および皮膚外用剤 |
| JPS63126860A (ja) * | 1986-11-17 | 1988-05-30 | Nippon Haipotsukusu:Kk | グアニジノメチル安息香酸誘導体 |
| JPS63277622A (ja) * | 1986-12-17 | 1988-11-15 | グラクソ、グループ、リミテッド | 医薬 |
| US4743610A (en) * | 1987-03-16 | 1988-05-10 | American Cyanamid Company | N-[ω(3-pyridinyl)alkyl]benzamides, useful as thromboxane synthetase enzyme and/or cardioprotective agents |
| EP0303445A1 (de) * | 1987-08-13 | 1989-02-15 | Walton S.A. | Pflaster zur transdermalen Applikation von Cleboprid |
| DE3804346A1 (de) * | 1988-02-12 | 1989-08-24 | Boehringer Mannheim Gmbh | Tert.-butylphenyl-pyridyl-amide - verfahren zu ihrer herstellung sowie diese verbindungen enthaltende arzneimittel |
| US4948891A (en) * | 1988-05-24 | 1990-08-14 | Pfizer Inc. | Benzamide protease inhibitors |
| WO1990005723A1 (fr) * | 1988-11-24 | 1990-05-31 | Yoshitomi Pharmaceutical Industries, Ltd. | Composes de trans-4-amino(alkyl)-1-pyridylcarbamoylcyclohexane et leur utilisation en medecine |
| KR0133372B1 (ko) * | 1991-09-06 | 1998-04-23 | 고야 다다시 | 4-아미노(알킬)시클로헥산-1-카르복사미드 화합물 및 그 용도 |
-
1995
- 1995-04-14 EP EP01127632A patent/EP1195372A1/de not_active Withdrawn
- 1995-04-17 CA CA002188164A patent/CA2188164C/en not_active Expired - Lifetime
- 1995-04-17 ES ES03025765T patent/ES2388917T3/es not_active Expired - Lifetime
- 1995-04-17 KR KR1019960705864A patent/KR100311438B1/ko not_active Expired - Lifetime
- 1995-04-17 AT AT95915333T patent/ATE255093T1/de not_active IP Right Cessation
- 1995-04-17 WO PCT/JP1995/000747 patent/WO1995028387A1/ja not_active Ceased
- 1995-04-17 EP EP95915333A patent/EP0757038B1/de not_active Expired - Lifetime
- 1995-04-17 US US08/727,669 patent/US5958944A/en not_active Expired - Lifetime
- 1995-04-17 ES ES95915333T patent/ES2208678T3/es not_active Expired - Lifetime
- 1995-04-17 EP EP03025765A patent/EP1391454B1/de not_active Expired - Lifetime
- 1995-04-17 DE DE69532195T patent/DE69532195T2/de not_active Expired - Lifetime
-
1999
- 1999-02-18 US US09/252,079 patent/US6156766A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| KR100311438B1 (ko) | 2002-06-20 |
| EP1391454A1 (de) | 2004-02-25 |
| EP0757038A4 (de) | 1997-08-06 |
| CA2188164A1 (en) | 1995-10-26 |
| CA2188164C (en) | 2005-08-09 |
| ES2388917T3 (es) | 2012-10-19 |
| WO1995028387A1 (en) | 1995-10-26 |
| EP1391454B1 (de) | 2012-05-30 |
| KR970702255A (ko) | 1997-05-13 |
| EP0757038B1 (de) | 2003-11-26 |
| EP1195372A1 (de) | 2002-04-10 |
| DE69532195D1 (de) | 2004-01-08 |
| EP0757038A1 (de) | 1997-02-05 |
| DE69532195T2 (de) | 2004-09-02 |
| US6156766A (en) | 2000-12-05 |
| ES2208678T3 (es) | 2004-06-16 |
| US5958944A (en) | 1999-09-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69532195D1 (de) | Benzamidverbindung und ihre medizinische verwendung | |
| RU93058253A (ru) | Соединения-антибиотики, способы их получения, промежуточные соединения, фармкомпозиция, способ лечения | |
| DE60114994D1 (de) | Blutplättchen-adp-rezeptor-inhibitoren | |
| TWI265931B (en) | Composition and method for inhibiting platelet aggregation | |
| IL152770A (en) | Use of Gabapentin analogues for the preparation of preparations for the treatment of sleep disorders | |
| JP2008526999A5 (de) | ||
| LV12291A (lv) | Savienojums un farmaceitiskas kompozicijas ar triptazes aktivitates izmainam saistitu slimibu arstesanai | |
| KR900700465A (ko) | 화합물 | |
| DK0453042T3 (da) | Hidtil ukendte 2 9-disubstituerede 4H-pyhrido[1 2-a]pyridin-4-oner | |
| EE200000298A (et) | Bifenüülamidiini derivaadid, eelravim, vere koagulatsiooniinhibiitor ning profülaktiline ja terapeutiline toimeaine tromboosi või emboolia vastu | |
| DK0920865T3 (da) | Farmaceutiske sammensætninger indeholdende norastemizol | |
| PL377715A1 (pl) | Antagoniści CCR1 do leczenia między innymi demielizacyjnej choroby zapalnej | |
| ES2053668T3 (es) | Derivados de poliamina como agentes antineoplasicos. | |
| TNSN06440A1 (fr) | Derives de pyrido-pyrimidine, leur preparation, leur application dans le traitement du cancer | |
| DK1557414T3 (da) | IsoquinoIin-forbindelser og medicinsk anvendelse deraf | |
| EA200400547A1 (ru) | Замещенные производные 4-фенил-4-[1h-имидазол-2-ил] пиперидина для снижения ишемического повреждения | |
| SE9900190D0 (sv) | New compounds | |
| MA27492A1 (fr) | Nouveaux derives antagonistes du recepteur de la vitronectine, leur procede de preparation, leur application comme medicaments et les compositions pharmaceutiques les renfermant | |
| IL99434A0 (en) | 3-(1h-indazol-3-yl)-4-pyridinamines,a process and intermediates for their preparation and pharmaceutical compositions containing them | |
| RU2024118959A (ru) | Пиримидин-аннелированные триазольные производные и их применение в ингибировании агрегации тромбоцитов | |
| ATE232848T1 (de) | Benzoesäurederivate und deren medizinische verwendung | |
| ATE95697T1 (de) | Uricosuretische zusammensetzung. | |
| BR0002935A (pt) | Compostos tetrazolilalquil-indol como agentes antiinflamatórios e analgésicos | |
| TH35867A (th) | สารสูตรผสมที่ปรับปรุงชนิดใหม่สำหรับรักษาสภาวะลิ่มเลือดจุกหลอดเลือด |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |