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
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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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)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (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)
- Diabetes (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Dermatology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Psychology (AREA)
- Toxicology (AREA)
- Obesity (AREA)
- Ophthalmology & Optometry (AREA)
- Endocrinology (AREA)
- Hospice & Palliative Care (AREA)
Abstract
Det tilveiebringes en ny klasse imidazopyrazinforbindelser som inhibitorer av protein- og/eller kontrollpunktkinaser, fremgangsmåter for fremstilling av slike forbindelser, farmasøytiske preparater innbefattende én eller flere slike forbindelser, fremgangsmåter for å fremstille farmasøytiske formuleringer som innbefatter én eller flere slike forbindelser, og anvendelse ved behandling, forhindring, inhibering eller lindring av én eller flere sykdommer forbundet med protein eller kontrollpunktkinasene når det benyttes slike forbindelser eller farmasøytiske preparater.
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 (no) |
| EP (1) | EP1945644A2 (no) |
| JP (1) | JP5031760B2 (no) |
| KR (1) | KR20080074963A (no) |
| CN (1) | CN101370811A (no) |
| AR (1) | AR056785A1 (no) |
| AU (1) | AU2006315718B2 (no) |
| BR (1) | BRPI0618520A2 (no) |
| CA (1) | CA2628455A1 (no) |
| EC (1) | ECSP088440A (no) |
| IL (1) | IL191294A0 (no) |
| NO (1) | NO20082530L (no) |
| PE (1) | PE20070805A1 (no) |
| RU (1) | RU2008122967A (no) |
| TW (1) | TW200804386A (no) |
| WO (1) | WO2007058942A2 (no) |
| ZA (1) | ZA200803894B (no) |
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 |
| CA2628534A1 (en) * | 2005-11-10 | 2007-05-18 | Schering Corporation | Methods for inhibiting protein kinases |
| DK2029602T3 (da) * | 2006-05-31 | 2010-08-09 | Galapagos Nv | Triazolopyrazinforbindelser, der kan anvendes til behandling af degenerative og inflammatoriske sygdomme |
| US20080125358A1 (en) * | 2006-10-26 | 2008-05-29 | University Of Massachusetts Medical School | Methods for Chk2 inhibitor patient selection |
| WO2008057512A2 (en) * | 2006-11-08 | 2008-05-15 | Schering Corporation | Imidazopyrazines as protein kinase inhibitors |
| DE602007012133D1 (de) * | 2006-12-01 | 2011-03-03 | Andrew Burritt | Triazolopyridinverbindungen zur behandlung von degenerations- und entzündungskrankheiten |
| WO2008138842A1 (en) | 2007-05-10 | 2008-11-20 | Galapagos N.V. | Imidazopyrazines and triazolopyrazine for the treatment of joint degenerative and inflammatory diseases |
| MX2009013729A (es) * | 2007-06-14 | 2010-01-25 | Schering Corp | Imidazopirazinas como inhibidores de proteina quinasa. |
| 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 |
| KR20100101576A (ko) * | 2007-10-30 | 2010-09-17 | 니혼 메디피직스 가부시키가이샤 | 신규 아밀로이드 친화성 화합물의 사용 및 제조 방법 |
| US8603998B2 (en) * | 2007-11-07 | 2013-12-10 | Merck Sharp & Dohme Corp. | Modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors |
| EP2236494B1 (en) * | 2007-12-26 | 2016-08-31 | Msd K.K. | Sulfonyl substituted 6-membered ring derivative |
| WO2009097233A1 (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 |
| PE20091577A1 (es) * | 2008-03-03 | 2009-11-05 | Novartis Ag | 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 |
| KR101745732B1 (ko) | 2008-12-08 | 2017-06-12 | 질레드 코네티컷 인코포레이티드 | 이미다조피라진 syk 억제제 |
| AU2009325133B2 (en) | 2008-12-08 | 2016-02-04 | Gilead Connecticut, 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 |
| 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 |
| CA2778949C (en) | 2009-10-30 | 2018-02-27 | Janssen Pharmaceutica Nv | Imidazo[1,2-b]pyridazine derivatives and their use as pde10 inhibitors |
| US9145399B2 (en) | 2010-01-15 | 2015-09-29 | Janssen Pharmaceuticals, Inc. | Substituted bicyclic triazole derivatives as gamma secretase modulators |
| US8470820B2 (en) | 2010-01-22 | 2013-06-25 | Hoffman-La Roche Inc. | Nitrogen-containing heteroaryl derivatives |
| KR101661383B1 (ko) * | 2010-02-08 | 2016-09-29 | 머크 샤프 앤 도메 비.브이. | 8-메틸-1-페닐-이미다졸[1,5-a]피라진 화합물 |
| 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 |
| CA2793279A1 (en) | 2010-03-18 | 2011-09-22 | Ulrich Klar | Imidazopyrazines |
| US9199999B2 (en) | 2010-06-01 | 2015-12-01 | Bayer Intellectual Property Gmbh | Substituted imidazopyrazines |
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- 2006-11-08 CN CNA2006800507096A patent/CN101370811A/zh active Pending
- 2006-11-08 WO PCT/US2006/043786 patent/WO2007058942A2/en not_active Ceased
- 2006-11-08 CA CA002628455A patent/CA2628455A1/en not_active Abandoned
- 2006-11-08 EP EP06837322A patent/EP1945644A2/en not_active Withdrawn
- 2006-11-08 RU RU2008122967/04A patent/RU2008122967A/ru not_active Application Discontinuation
- 2006-11-08 KR KR1020087013635A patent/KR20080074963A/ko not_active Withdrawn
- 2006-11-08 BR BRPI0618520-7A patent/BRPI0618520A2/pt not_active IP Right Cessation
- 2006-11-08 TW TW095141238A patent/TW200804386A/zh unknown
- 2006-11-08 JP JP2008540211A patent/JP5031760B2/ja not_active Expired - Fee Related
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| CN101370811A (zh) | 2009-02-18 |
| AU2006315718B2 (en) | 2012-10-04 |
| AR056785A1 (es) | 2007-10-24 |
| RU2008122967A (ru) | 2009-12-20 |
| BRPI0618520A2 (pt) | 2011-09-06 |
| WO2007058942A2 (en) | 2007-05-24 |
| WO2007058942A3 (en) | 2007-11-15 |
| PE20070805A1 (es) | 2007-08-13 |
| US20070117804A1 (en) | 2007-05-24 |
| CA2628455A1 (en) | 2007-05-24 |
| JP5031760B2 (ja) | 2012-09-26 |
| JP2009515888A (ja) | 2009-04-16 |
| ECSP088440A (es) | 2008-06-30 |
| EP1945644A2 (en) | 2008-07-23 |
| KR20080074963A (ko) | 2008-08-13 |
| ZA200803894B (en) | 2009-03-25 |
| TW200804386A (en) | 2008-01-16 |
| AU2006315718A1 (en) | 2007-05-24 |
| IL191294A0 (en) | 2009-02-11 |
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