ZA200803894B - Imidazopyrazines as protein kinase inhibitors - Google Patents
Imidazopyrazines as protein kinase inhibitorsInfo
- Publication number
- ZA200803894B ZA200803894B ZA200803894A ZA200803894A ZA200803894B ZA 200803894 B ZA200803894 B ZA 200803894B ZA 200803894 A ZA200803894 A ZA 200803894A ZA 200803894 A ZA200803894 A ZA 200803894A ZA 200803894 B ZA200803894 B ZA 200803894B
- Authority
- ZA
- South Africa
- Prior art keywords
- imidazopyrazines
- protein kinase
- kinase inhibitors
- inhibitors
- protein
- Prior art date
Links
- 229940045988 antineoplastic drug protein kinase inhibitors Drugs 0.000 title 1
- 150000005235 imidazopyrazines Chemical class 0.000 title 1
- 239000003909 protein kinase inhibitor Substances 0.000 title 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)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Virology (AREA)
- Neurology (AREA)
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- Dermatology (AREA)
- Biotechnology (AREA)
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- Vascular Medicine (AREA)
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- Toxicology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73598205P | 2005-11-10 | 2005-11-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200803894B true ZA200803894B (en) | 2009-03-25 |
Family
ID=38008330
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200803894A ZA200803894B (en) | 2005-11-10 | 2008-05-07 | Imidazopyrazines as protein kinase inhibitors |
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 |
| US20070105864A1 (en) * | 2005-11-10 | 2007-05-10 | Schering Corporation | Methods for inhibiting protein kinases |
| KR20090026288A (ko) * | 2006-05-31 | 2009-03-12 | 갈라파고스 엔.브이. | 퇴행성 및 염증성 질환의 치료에 유용한 트리아졸로피라진 화합물 |
| US20080125358A1 (en) * | 2006-10-26 | 2008-05-29 | University Of Massachusetts Medical School | Methods for Chk2 inhibitor patient selection |
| EP2079746A2 (en) * | 2006-11-08 | 2009-07-22 | Schering Corporation | Imidazopyrazines as protein kinase inhibitors |
| WO2008065198A1 (en) * | 2006-12-01 | 2008-06-05 | 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 |
| CA2690557A1 (en) * | 2007-06-14 | 2008-12-24 | Schering Corporation | Imidazopyrazines as protein kinase inhibitors |
| 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 |
| TW200922628A (en) * | 2007-10-30 | 2009-06-01 | Nihon Mediphysics Co Ltd | Use of novel compound having affinity for amyloid, and process for production of the same |
| 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 |
| AU2008341953B2 (en) * | 2007-12-26 | 2013-05-02 | Msd K.K. | Sulfonyl substituted 6-membered ring derivative |
| WO2009097233A1 (en) * | 2008-01-28 | 2009-08-06 | Schering Corporation | Imidazopyrazines as protein kinase inhibitors |
| NZ587039A (en) | 2008-02-13 | 2013-01-25 | Gilead Connecticut Inc | 6-aryl-imidazo[1, 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 |
| UY31679A1 (es) * | 2008-03-03 | 2009-09-30 | 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 |
| JP5567587B2 (ja) * | 2008-12-08 | 2014-08-06 | ギリアード コネチカット, インコーポレイテッド | イミダゾピラジンSyk阻害剤 |
| SG171993A1 (en) | 2008-12-08 | 2011-07-28 | Gilead Connecticut Inc | Imidazopyrazine syk inhibitors |
| TW201107329A (en) * | 2009-07-30 | 2011-03-01 | Oncotherapy Science Inc | Fused imidazole derivative having ttk inhibitory action |
| EP2473041B1 (en) | 2009-09-04 | 2018-03-07 | Merck Sharp & Dohme Corp. | Modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors |
| BR112012010041A2 (pt) | 2009-10-30 | 2016-05-24 | Janssen Pharmaceutica Nv | derivados de imidazo [1,2-b] piridazina e seu uso como inibidores de pde10 |
| EP2523955B1 (en) | 2010-01-15 | 2014-07-16 | Janssen Pharmaceuticals, Inc. | 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 |
| US8658794B2 (en) * | 2010-02-08 | 2014-02-25 | Merck Sharp & Dohme B.V. | 8-methyl-1-phenyl-imidazol[1,5-a]pyrazine compounds as Lck inhibitors and uses thereof |
| 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 |
| US9562056B2 (en) | 2010-03-11 | 2017-02-07 | Gilead Connecticut, Inc. | Imidazopyridines Syk inhibitors |
| ES2551407T3 (es) | 2010-03-18 | 2015-11-18 | Bayer Intellectual Property Gmbh | Imidazopirazinas |
| WO2011151259A1 (en) | 2010-06-01 | 2011-12-08 | Bayer Pharma Aktiengesellschaft | Substituted imidazopyrazines |
| TWI541243B (zh) * | 2010-09-10 | 2016-07-11 | 拜耳知識產權公司 | 經取代咪唑并嗒 |
| CA2821834A1 (en) | 2010-12-17 | 2012-06-21 | Bayer Intellectual Property Gmbh | 6 substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders |
| WO2012080228A1 (en) | 2010-12-17 | 2012-06-21 | Bayer Pharma Aktiengesellschaft | 6-thio-substituted imidazopyrazines for use as mps-1 and tkk inhibitors in the treatment of hyperproliferative disorders |
| 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 |
| JP2014508794A (ja) | 2011-03-24 | 2014-04-10 | ジヤンセン・フアーマシユーチカルズ・インコーポレーテツド | γ−セクレターゼ調節剤としての新規な置換トリアゾリルピペラジンおよびトリアゾリルピペラジン誘導体 |
| WO2013000924A1 (en) | 2011-06-27 | 2013-01-03 | Janssen Pharmaceutica Nv | 1-ARYL-4-METHYL-[1,2,4]TRIAZOLO[4,3-a]QUINOXALINE DERIVATIVES |
| CN102363618A (zh) * | 2011-07-04 | 2012-02-29 | 华东理工大学 | 一种表皮生长因子受体的新型抑制剂及其应用 |
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- 2006-11-08 CA CA002628455A patent/CA2628455A1/en not_active Abandoned
- 2006-11-08 RU RU2008122967/04A patent/RU2008122967A/ru not_active Application Discontinuation
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- 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 KR KR1020087013635A patent/KR20080074963A/ko not_active Withdrawn
- 2006-11-08 JP JP2008540211A patent/JP5031760B2/ja not_active Expired - Fee Related
- 2006-11-08 US US11/598,186 patent/US20070117804A1/en not_active Abandoned
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| NO20082530L (no) | 2008-08-07 |
| JP5031760B2 (ja) | 2012-09-26 |
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| US20070117804A1 (en) | 2007-05-24 |
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| AR056785A1 (es) | 2007-10-24 |
| WO2007058942A3 (en) | 2007-11-15 |
| RU2008122967A (ru) | 2009-12-20 |
| ECSP088440A (es) | 2008-06-30 |
| AU2006315718B2 (en) | 2012-10-04 |
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| BRPI0618520A2 (pt) | 2011-09-06 |
| JP2009515888A (ja) | 2009-04-16 |
| PE20070805A1 (es) | 2007-08-13 |
| CA2628455A1 (en) | 2007-05-24 |
| AU2006315718A1 (en) | 2007-05-24 |
| KR20080074963A (ko) | 2008-08-13 |
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