NO20082530L - Imidazopyraziner som proteinkinaseinhibitorer - Google Patents
Imidazopyraziner som proteinkinaseinhibitorerInfo
- Publication number
- NO20082530L NO20082530L NO20082530A NO20082530A NO20082530L NO 20082530 L NO20082530 L NO 20082530L NO 20082530 A NO20082530 A NO 20082530A NO 20082530 A NO20082530 A NO 20082530A NO 20082530 L NO20082530 L NO 20082530L
- Authority
- NO
- Norway
- Prior art keywords
- compounds
- imidazopyrazines
- protein kinase
- kinase inhibitors
- protein
- Prior art date
Links
- 150000005235 imidazopyrazines Chemical class 0.000 title abstract 2
- 229940045988 antineoplastic drug protein kinase inhibitors Drugs 0.000 title 1
- 239000003909 protein kinase inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- 238000000034 method Methods 0.000 abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 2
- 102000004169 proteins and genes Human genes 0.000 abstract 2
- 108090000623 proteins and genes Proteins 0.000 abstract 2
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 102000001253 Protein Kinase Human genes 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 108060006633 protein kinase 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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- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (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)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Urology & Nephrology (AREA)
- Molecular Biology (AREA)
- Dermatology (AREA)
- Biotechnology (AREA)
- Endocrinology (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Obesity (AREA)
- Tropical Medicine & Parasitology (AREA)
- Psychiatry (AREA)
- Ophthalmology & Optometry (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73598205P | 2005-11-10 | 2005-11-10 | |
| PCT/US2006/043786 WO2007058942A2 (en) | 2005-11-10 | 2006-11-08 | Imidazopyrazines as protein kinase inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO20082530L true NO20082530L (no) | 2008-08-07 |
Family
ID=38008330
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20082530A NO20082530L (no) | 2005-11-10 | 2008-06-06 | Imidazopyraziner som proteinkinaseinhibitorer |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US20070117804A1 (de) |
| EP (1) | EP1945644A2 (de) |
| JP (1) | JP5031760B2 (de) |
| KR (1) | KR20080074963A (de) |
| CN (1) | CN101370811A (de) |
| AR (1) | AR056785A1 (de) |
| AU (1) | AU2006315718B2 (de) |
| BR (1) | BRPI0618520A2 (de) |
| CA (1) | CA2628455A1 (de) |
| EC (1) | ECSP088440A (de) |
| IL (1) | IL191294A0 (de) |
| NO (1) | NO20082530L (de) |
| PE (1) | PE20070805A1 (de) |
| RU (1) | RU2008122967A (de) |
| TW (1) | TW200804386A (de) |
| WO (1) | WO2007058942A2 (de) |
| ZA (1) | ZA200803894B (de) |
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 |
| TW200803863A (en) * | 2005-11-10 | 2008-01-16 | Schering Corp | Method for inhibiting protein kinases |
| PT2029602E (pt) * | 2006-05-31 | 2010-07-08 | Galapagos Nv | Compostos de triazolopirazina uteis para o tratamento de doenãas degenerativas e inflamatërias |
| US20080125358A1 (en) * | 2006-10-26 | 2008-05-29 | University Of Massachusetts Medical School | Methods for Chk2 inhibitor patient selection |
| EP2079746A2 (de) * | 2006-11-08 | 2009-07-22 | Schering Corporation | Imidazopyrazine als proteinkinasehemmer |
| WO2008065198A1 (en) * | 2006-12-01 | 2008-06-05 | Galapagos N.V. | Triazolopyridine compounds useful for the treatment of degenerative & inflammatory diseases |
| US8148369B2 (en) | 2007-05-10 | 2012-04-03 | Janssen Pharmaceutica Nv | Fused pyrazine compounds useful for the treatment of degenerative and inflammatory diseases |
| CA2690557A1 (en) * | 2007-06-14 | 2008-12-24 | Schering Corporation | Imidazopyrazines as protein kinase inhibitors |
| US20100249030A1 (en) * | 2007-07-31 | 2010-09-30 | 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 |
| EP2216052A4 (de) * | 2007-10-30 | 2012-11-21 | Nihon Mediphysics Co Ltd | Verwendung einer neuen verbindung mit affinität für amyloid und verfahren zu ihrer herstellung |
| JP2011503084A (ja) * | 2007-11-07 | 2011-01-27 | シェーリング コーポレイション | 新規の細胞周期チェックポイント調節剤およびこれらの調節剤とチェックポイント阻害剤との併用 |
| JP5377329B2 (ja) * | 2007-12-26 | 2013-12-25 | Msd株式会社 | スルホニル置換六員環誘導体 |
| CA2710929A1 (en) * | 2008-01-28 | 2009-08-06 | Schering Corporation | Imidazopyrazines as protein kinase inhibitors |
| WO2009102468A1 (en) | 2008-02-13 | 2009-08-20 | 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 |
| 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 |
| PL2716157T3 (pl) | 2008-12-08 | 2017-06-30 | Gilead Connecticut, Inc. | Imidazopirazynowe inhibitory Syk |
| PE20120121A1 (es) | 2008-12-08 | 2012-02-20 | Gilead Connecticut Inc | Derivados de imidazopirazina como inhibidores de syk |
| TW201107329A (en) | 2009-07-30 | 2011-03-01 | Oncotherapy Science Inc | Fused imidazole derivative having ttk inhibitory action |
| EP2473041B1 (de) | 2009-09-04 | 2018-03-07 | Merck Sharp & Dohme Corp. | Modulatoren von zellzyklus-kontrollpunkten und ihre verwendung in kombination mit kontrollpunkt-kinasehemmern |
| KR101774035B1 (ko) | 2009-10-30 | 2017-09-01 | 얀센 파마슈티카 엔.브이. | 이미다조[1,2―b]피리다진 유도체 및 PDE10 저해제로서의 그의 용도 |
| EP2523949B1 (de) | 2010-01-15 | 2014-08-20 | Janssen Pharmaceuticals Inc. | Neuartige substituierte Triazolderivate als Gamma-Sekretase-Modulatoren |
| US8470820B2 (en) | 2010-01-22 | 2013-06-25 | Hoffman-La Roche Inc. | Nitrogen-containing heteroaryl derivatives |
| JP5764145B2 (ja) * | 2010-02-08 | 2015-08-12 | メルク・シャープ・エンド・ドーム・ベー・フェー | 8−メチル−1−フェニル−イミダゾル[1,5−a]ピラジン化合物 |
| 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 |
| AU2011226689B2 (en) | 2010-03-11 | 2016-09-01 | Kronos Bio, Inc. | Imidazopyridines Syk inhibitors |
| WO2011113862A1 (en) | 2010-03-18 | 2011-09-22 | Bayer Pharma Aktiengesellschaft | Imidazopyrazines |
| JP5824040B2 (ja) * | 2010-06-01 | 2015-11-25 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | 置換イミダゾピラジン |
| TWI541243B (zh) * | 2010-09-10 | 2016-07-11 | 拜耳知識產權公司 | 經取代咪唑并嗒 |
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| JP2013545776A (ja) | 2010-12-17 | 2013-12-26 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | 過剰増殖性障害の治療におけるmps−1およびtkk阻害剤として使用するための6置換イミダゾピラジン |
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- 2006-11-08 CN CNA2006800507096A patent/CN101370811A/zh active Pending
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- 2006-11-08 KR KR1020087013635A patent/KR20080074963A/ko not_active Withdrawn
- 2006-11-08 AR ARP060104896A patent/AR056785A1/es unknown
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- 2006-11-08 RU RU2008122967/04A patent/RU2008122967A/ru not_active Application Discontinuation
- 2006-11-08 BR BRPI0618520-7A patent/BRPI0618520A2/pt not_active IP Right Cessation
- 2006-11-08 JP JP2008540211A patent/JP5031760B2/ja not_active Expired - Fee Related
- 2006-11-08 EP EP06837322A patent/EP1945644A2/de not_active Withdrawn
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| AU2006315718A1 (en) | 2007-05-24 |
| BRPI0618520A2 (pt) | 2011-09-06 |
| AU2006315718B2 (en) | 2012-10-04 |
| IL191294A0 (en) | 2009-02-11 |
| EP1945644A2 (de) | 2008-07-23 |
| TW200804386A (en) | 2008-01-16 |
| CA2628455A1 (en) | 2007-05-24 |
| JP2009515888A (ja) | 2009-04-16 |
| AR056785A1 (es) | 2007-10-24 |
| ECSP088440A (es) | 2008-06-30 |
| PE20070805A1 (es) | 2007-08-13 |
| ZA200803894B (en) | 2009-03-25 |
| CN101370811A (zh) | 2009-02-18 |
| JP5031760B2 (ja) | 2012-09-26 |
| RU2008122967A (ru) | 2009-12-20 |
| WO2007058942A3 (en) | 2007-11-15 |
| US20070117804A1 (en) | 2007-05-24 |
| KR20080074963A (ko) | 2008-08-13 |
| WO2007058942A2 (en) | 2007-05-24 |
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