ECSP088440A - Imidazopirazinas como inhibidores de proteinquinasa - Google Patents
Imidazopirazinas como inhibidores de proteinquinasaInfo
- Publication number
- ECSP088440A ECSP088440A EC2008008440A ECSP088440A ECSP088440A EC SP088440 A ECSP088440 A EC SP088440A EC 2008008440 A EC2008008440 A EC 2008008440A EC SP088440 A ECSP088440 A EC SP088440A EC SP088440 A ECSP088440 A EC SP088440A
- Authority
- EC
- Ecuador
- Prior art keywords
- compounds
- inhibitors
- methods
- kinases
- proteinquinasa
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 4
- 238000000034 method Methods 0.000 abstract 3
- 102000001253 Protein Kinase Human genes 0.000 abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 2
- 108060006633 protein kinase Proteins 0.000 abstract 2
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 150000005235 imidazopyrazines Chemical class 0.000 abstract 1
- 230000006872 improvement Effects 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 102000004169 proteins and genes Human genes 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
Classifications
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- 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
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- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
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Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Virology (AREA)
- Neurology (AREA)
- Oncology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Communicable Diseases (AREA)
- Physical Education & Sports Medicine (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Dermatology (AREA)
- Hospice & Palliative Care (AREA)
- Ophthalmology & Optometry (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Pain & Pain Management (AREA)
- Tropical Medicine & Parasitology (AREA)
- Psychology (AREA)
Abstract
En sus muchas realizaciones, la presente invención provee una nueva clase de compuestos imidazopirazina como inhibidores de proteína y/o de quinasas checkpoint, los métodos de preparación de dichos compuestos, las composiciones farmacéuticas que incluyen uno o más de dichos compuestos, métodos de preparación de las formulaciones farmacéuticas que incluyen uno o más de dichos compuestos y métodos de tratamiento, prevención, inhibición o mejoramiento de una o más enfermedades asociadas con las proteinquinasas o quinasas checkpoint usando dichos compuestos o composiciones farmacéuticas.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73598205P | 2005-11-10 | 2005-11-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP088440A true ECSP088440A (es) | 2008-06-30 |
Family
ID=38008330
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EC2008008440A ECSP088440A (es) | 2005-11-10 | 2008-05-08 | Imidazopirazinas como inhibidores de proteinquinasa |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US20070117804A1 (es) |
| EP (1) | EP1945644A2 (es) |
| JP (1) | JP5031760B2 (es) |
| KR (1) | KR20080074963A (es) |
| CN (1) | CN101370811A (es) |
| AR (1) | AR056785A1 (es) |
| AU (1) | AU2006315718B2 (es) |
| BR (1) | BRPI0618520A2 (es) |
| CA (1) | CA2628455A1 (es) |
| EC (1) | ECSP088440A (es) |
| IL (1) | IL191294A0 (es) |
| NO (1) | NO20082530L (es) |
| PE (1) | PE20070805A1 (es) |
| RU (1) | RU2008122967A (es) |
| TW (1) | TW200804386A (es) |
| WO (1) | WO2007058942A2 (es) |
| ZA (1) | ZA200803894B (es) |
Families Citing this family (84)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7576085B2 (en) * | 2002-09-23 | 2009-08-18 | Schering Corporation | Imidazopyrazines as cyclin dependent kinase inhibitors |
| WO2007056468A1 (en) * | 2005-11-10 | 2007-05-18 | Schering Corporation | Methods for inhibiting protein kinases |
| CA2653506A1 (en) * | 2006-05-31 | 2007-12-06 | Galapagos Nv. | Triazolopyrazine compounds useful for the treatment of degenerative & inflammatory diseases |
| US20080125358A1 (en) * | 2006-10-26 | 2008-05-29 | University Of Massachusetts Medical School | Methods for Chk2 inhibitor patient selection |
| CN101589045A (zh) * | 2006-11-08 | 2009-11-25 | 先灵公司 | 作为蛋白质激酶抑制剂的咪唑并吡嗪 |
| EP2086540B8 (en) * | 2006-12-01 | 2011-03-02 | Galapagos N.V. | Triazolopyridine compounds useful for the treatment of degenerative & inflammatory diseases |
| WO2008138842A1 (en) | 2007-05-10 | 2008-11-20 | Galapagos N.V. | Imidazopyrazines and triazolopyrazine for the treatment of joint degenerative and inflammatory diseases |
| WO2008156614A2 (en) * | 2007-06-14 | 2008-12-24 | Schering Corporation | Imidazopyrazines as protein kinase inhibitors |
| CN101808666A (zh) * | 2007-07-31 | 2010-08-18 | 先灵公司 | 作为抗癌治疗的抗有丝分裂剂和激光激酶抑制剂组合 |
| GB0716292D0 (en) | 2007-08-21 | 2007-09-26 | Biofocus Dpi Ltd | Imidazopyrazine compounds |
| EP2216052A4 (en) * | 2007-10-30 | 2012-11-21 | Nihon Mediphysics Co Ltd | USE OF A NEW COMPOUND WITH AFFINITY FOR AMYLOID AND METHOD FOR THE PRODUCTION THEREOF |
| EP2217611B1 (en) * | 2007-11-07 | 2013-07-31 | Merck Sharp & Dohme Corp. | Novel modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors |
| US8124807B2 (en) * | 2007-12-26 | 2012-02-28 | Msd K.K. | Sulfonyl-substituted 6-membered ring derivative |
| WO2009097233A1 (en) * | 2008-01-28 | 2009-08-06 | Schering Corporation | Imidazopyrazines as protein kinase inhibitors |
| EP2252617A1 (en) | 2008-02-13 | 2010-11-24 | CGI Pharmaceuticals, Inc. | 6-aryl-imidaz0[l, 2-a]pyrazine derivatives, method of making, and method of use thereof |
| US20090207142A1 (en) * | 2008-02-20 | 2009-08-20 | Nokia Corporation | Apparatus, method, computer program and user interface for enabling user input |
| US8168794B2 (en) | 2008-03-03 | 2012-05-01 | Novartis Ag | Pim kinase inhibitors and methods of their use |
| PE20091577A1 (es) * | 2008-03-03 | 2009-11-05 | Novartis Ag | Inhibidores de cinasa pim y metodos para su uso |
| FR2933409B1 (fr) * | 2008-07-03 | 2010-08-27 | Centre Nat Rech Scient | NOUVEAUX PYRROLO °2,3-a! CARBAZOLES ET LEUR UTILISATION COMME INHIBITEURS DES KINASES PIM |
| ES2590804T3 (es) | 2008-12-08 | 2016-11-23 | Gilead Connecticut, Inc. | Inhibidores de Imidazopyrazine Syk |
| WO2010068258A1 (en) | 2008-12-08 | 2010-06-17 | Cgi Pharmaceuticals, Inc. | Imidazopyrazine syk inhibitors |
| US8450321B2 (en) | 2008-12-08 | 2013-05-28 | Gilead Connecticut, Inc. | 6-(1H-indazol-6-yl)-N-[4-(morpholin-4-yl)phenyl]imidazo-[1,2-A]pyrazin-8-amine, or a pharmaceutically acceptable salt thereof, as a SYK inhibitor |
| TW201107329A (en) | 2009-07-30 | 2011-03-01 | Oncotherapy Science Inc | Fused imidazole derivative having ttk inhibitory action |
| WO2011028638A1 (en) | 2009-09-04 | 2011-03-10 | Schering Corporation | Modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors |
| WO2011051342A1 (en) | 2009-10-30 | 2011-05-05 | Janssen Pharmaceutica Nv | IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE10 INHIBITORS |
| AU2011206634B2 (en) | 2010-01-15 | 2014-11-13 | Cellzome Limited | Novel substituted bicyclic triazole derivatives as gamma secretase modulators |
| US8470820B2 (en) | 2010-01-22 | 2013-06-25 | Hoffman-La Roche Inc. | Nitrogen-containing heteroaryl derivatives |
| MX2012009208A (es) * | 2010-02-08 | 2012-09-07 | Msd Oss Bv | Compuestos de 8-metil-1-fenil-imidazol[1, 5-a]pirazina. |
| AR080754A1 (es) | 2010-03-09 | 2012-05-09 | Janssen Pharmaceutica Nv | Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10 |
| KR101717809B1 (ko) | 2010-03-11 | 2017-03-17 | 질레드 코네티컷 인코포레이티드 | 이미다조피리딘 syk 억제제 |
| WO2011113862A1 (en) | 2010-03-18 | 2011-09-22 | Bayer Pharma Aktiengesellschaft | Imidazopyrazines |
| CN103038235B (zh) * | 2010-06-01 | 2015-07-29 | 拜耳知识产权有限责任公司 | 取代的咪唑并吡嗪 |
| TWI541243B (zh) * | 2010-09-10 | 2016-07-11 | 拜耳知識產權公司 | 經取代咪唑并嗒 |
| CA2821819A1 (en) | 2010-12-17 | 2012-06-21 | Marcus Koppitz | 6-substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders |
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| WO2007056468A1 (en) * | 2005-11-10 | 2007-05-18 | Schering Corporation | Methods for inhibiting protein kinases |
-
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- 2006-11-08 TW TW095141238A patent/TW200804386A/zh unknown
- 2006-11-08 RU RU2008122967/04A patent/RU2008122967A/ru not_active Application Discontinuation
- 2006-11-08 EP EP06837322A patent/EP1945644A2/en not_active Withdrawn
- 2006-11-08 AR ARP060104896A patent/AR056785A1/es unknown
- 2006-11-08 BR BRPI0618520-7A patent/BRPI0618520A2/pt not_active IP Right Cessation
- 2006-11-08 CN CNA2006800507096A patent/CN101370811A/zh active Pending
- 2006-11-08 PE PE2006001398A patent/PE20070805A1/es not_active Application Discontinuation
- 2006-11-08 CA CA002628455A patent/CA2628455A1/en not_active Abandoned
- 2006-11-08 JP JP2008540211A patent/JP5031760B2/ja not_active Expired - Fee Related
- 2006-11-08 WO PCT/US2006/043786 patent/WO2007058942A2/en not_active Ceased
- 2006-11-08 AU AU2006315718A patent/AU2006315718B2/en not_active Ceased
- 2006-11-08 US US11/598,186 patent/US20070117804A1/en not_active Abandoned
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| AU2006315718B2 (en) | 2012-10-04 |
| US20070117804A1 (en) | 2007-05-24 |
| WO2007058942A3 (en) | 2007-11-15 |
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| TW200804386A (en) | 2008-01-16 |
| WO2007058942A2 (en) | 2007-05-24 |
| ZA200803894B (en) | 2009-03-25 |
| PE20070805A1 (es) | 2007-08-13 |
| BRPI0618520A2 (pt) | 2011-09-06 |
| RU2008122967A (ru) | 2009-12-20 |
| JP2009515888A (ja) | 2009-04-16 |
| IL191294A0 (en) | 2009-02-11 |
| NO20082530L (no) | 2008-08-07 |
| AR056785A1 (es) | 2007-10-24 |
| CA2628455A1 (en) | 2007-05-24 |
| JP5031760B2 (ja) | 2012-09-26 |
| CN101370811A (zh) | 2009-02-18 |
| AU2006315718A1 (en) | 2007-05-24 |
| EP1945644A2 (en) | 2008-07-23 |
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