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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- 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
- A61K31/495—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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- A—HUMAN NECESSITIES
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- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Virology (AREA)
- Oncology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Communicable Diseases (AREA)
- Physical Education & Sports Medicine (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Molecular Biology (AREA)
- Dermatology (AREA)
- Biotechnology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Vascular Medicine (AREA)
- Obesity (AREA)
- Psychiatry (AREA)
- Ophthalmology & Optometry (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 |
| JP2009515882A (ja) * | 2005-11-10 | 2009-04-16 | シェーリング コーポレイション | プロテインキナーゼを阻害するための方法 |
| EA200870592A1 (ru) * | 2006-05-31 | 2009-08-28 | Галапагос Н.В. | Триазолопиразиновые соединения, пригодные для лечения дегенеративных и воспалительных заболеваний |
| US20080125358A1 (en) * | 2006-10-26 | 2008-05-29 | University Of Massachusetts Medical School | Methods for Chk2 inhibitor patient selection |
| AR063581A1 (es) * | 2006-11-08 | 2009-02-04 | Schering Corp | Imidazopirazinas como inhibidores de proteina quinasa |
| JP2010511018A (ja) * | 2006-12-01 | 2010-04-08 | ガラパゴス・ナムローゼ・フェンノートシャップ | 変性疾患及び炎症性疾患の治療に有用なトリアゾロピリジン化合物 |
| WO2008138842A1 (en) | 2007-05-10 | 2008-11-20 | Galapagos N.V. | Imidazopyrazines and triazolopyrazine for the treatment of joint degenerative and inflammatory diseases |
| CN101772500A (zh) * | 2007-06-14 | 2010-07-07 | 先灵公司 | 作为蛋白质激酶抑制剂的咪唑并吡嗪 |
| EP2182986A2 (en) * | 2007-07-31 | 2010-05-12 | Schering Corporation | Anti-mitotic agent and aurora kinase inhibitor combination as anti-cancer treatment |
| GB0716292D0 (en) | 2007-08-21 | 2007-09-26 | Biofocus Dpi Ltd | Imidazopyrazine compounds |
| CN102702195A (zh) * | 2007-10-30 | 2012-10-03 | 日本医事物理股份有限公司 | 对淀粉样蛋白具有亲和性的新化合物的应用及制备方法 |
| PE20091195A1 (es) * | 2007-11-07 | 2009-08-06 | Schering Corp | Nuevos moduladores de los puntos de control del ciclo celular y su uso en combinacion con inhibidores de quinasa de punto de control |
| WO2009081789A1 (ja) * | 2007-12-26 | 2009-07-02 | Banyu Pharmaceutical Co., Ltd. | スルホニル置換六員環誘導体 |
| 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 |
| UY31679A1 (es) * | 2008-03-03 | 2009-09-30 | Inhibidores de cinasa pim y metodos para su uso | |
| US8168794B2 (en) | 2008-03-03 | 2012-05-01 | Novartis Ag | Pim kinase inhibitors and methods of their use |
| 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 |
| SG171991A1 (en) | 2008-12-08 | 2011-07-28 | Gilead Connecticut Inc | Imidazopyrazine syk inhibitors |
| EA021293B1 (ru) * | 2008-12-08 | 2015-05-29 | Джилид Коннектикут, Инк. | ИМИДАЗОПИРАЗИНОВЫЕ ИНГИБИТОРЫ Syk, ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ, СОДЕРЖАЩАЯ ИМИДАЗОПИРАЗИНОВЫЕ ИНГИБИТОРЫ Syk, И СПОСОБЫ ИХ ПРИМЕНЕНИЯ |
| 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 |
| US8993535B2 (en) | 2009-09-04 | 2015-03-31 | Merck Sharp & Dohme Corp. | Modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors |
| JP5641664B2 (ja) | 2009-10-30 | 2014-12-17 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプJanssen Pharmaceutica Naamloze Vennootschap | イミダゾ[1,2−b]ピリダジン誘導体およびPDE10阻害剤としてのそれらの使用 |
| PE20121511A1 (es) | 2010-01-15 | 2012-12-06 | Janssen Pharmaceuticals Inc | Novedosos derivados biciclicos de triazol sustituidos como moduladores de gamma secretasa |
| US8470820B2 (en) | 2010-01-22 | 2013-06-25 | Hoffman-La Roche Inc. | Nitrogen-containing heteroaryl derivatives |
| EP2534151B1 (en) * | 2010-02-08 | 2018-11-14 | Merck Sharp & Dohme B.V. | 8-methyl-1-phenyl-imidazol[1,5-a]pyrazine compounds |
| 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 |
| PT2545052E (pt) | 2010-03-11 | 2015-02-18 | Gilead Connecticut Inc | Inibidores da syk à base de imidazopiridinas |
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- 2006-11-08 EP EP06837322A patent/EP1945644A2/en not_active Withdrawn
- 2006-11-08 KR KR1020087013635A patent/KR20080074963A/ko not_active Withdrawn
- 2006-11-08 PE PE2006001398A patent/PE20070805A1/es not_active Application Discontinuation
- 2006-11-08 CN CNA2006800507096A patent/CN101370811A/zh active Pending
- 2006-11-08 AR ARP060104896A patent/AR056785A1/es unknown
- 2006-11-08 RU RU2008122967/04A patent/RU2008122967A/ru not_active Application Discontinuation
- 2006-11-08 AU AU2006315718A patent/AU2006315718B2/en not_active Ceased
- 2006-11-08 BR BRPI0618520-7A patent/BRPI0618520A2/pt not_active IP Right Cessation
- 2006-11-08 US US11/598,186 patent/US20070117804A1/en not_active Abandoned
- 2006-11-08 JP JP2008540211A patent/JP5031760B2/ja not_active Expired - Fee Related
- 2006-11-08 TW TW095141238A patent/TW200804386A/zh unknown
- 2006-11-08 CA CA002628455A patent/CA2628455A1/en not_active Abandoned
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| WO2007058942A2 (en) | 2007-05-24 |
| WO2007058942A3 (en) | 2007-11-15 |
| AR056785A1 (es) | 2007-10-24 |
| JP5031760B2 (ja) | 2012-09-26 |
| ZA200803894B (en) | 2009-03-25 |
| CA2628455A1 (en) | 2007-05-24 |
| AU2006315718A1 (en) | 2007-05-24 |
| EP1945644A2 (en) | 2008-07-23 |
| AU2006315718B2 (en) | 2012-10-04 |
| RU2008122967A (ru) | 2009-12-20 |
| KR20080074963A (ko) | 2008-08-13 |
| BRPI0618520A2 (pt) | 2011-09-06 |
| NO20082530L (no) | 2008-08-07 |
| IL191294A0 (en) | 2009-02-11 |
| PE20070805A1 (es) | 2007-08-13 |
| JP2009515888A (ja) | 2009-04-16 |
| TW200804386A (en) | 2008-01-16 |
| US20070117804A1 (en) | 2007-05-24 |
| CN101370811A (zh) | 2009-02-18 |
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