PE20070805A1 - Imidazopirazinas como inhibidores de proteinquinasa - Google Patents
Imidazopirazinas como inhibidores de proteinquinasaInfo
- Publication number
- PE20070805A1 PE20070805A1 PE2006001398A PE2006001398A PE20070805A1 PE 20070805 A1 PE20070805 A1 PE 20070805A1 PE 2006001398 A PE2006001398 A PE 2006001398A PE 2006001398 A PE2006001398 A PE 2006001398A PE 20070805 A1 PE20070805 A1 PE 20070805A1
- Authority
- PE
- Peru
- Prior art keywords
- halo
- inhibitors
- heteroaryl
- alkyl
- proteinquinase
- Prior art date
Links
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
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- 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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- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- A—HUMAN NECESSITIES
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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)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
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- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Virology (AREA)
- Neurology (AREA)
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- Neurosurgery (AREA)
- Communicable Diseases (AREA)
- Physical Education & Sports Medicine (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Urology & Nephrology (AREA)
- Molecular Biology (AREA)
- Dermatology (AREA)
- Biotechnology (AREA)
- Transplantation (AREA)
- Obesity (AREA)
- Hospice & Palliative Care (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Psychiatry (AREA)
- Psychology (AREA)
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE IMIDAZO[1,2-a]PIRAZINA DE FORMULA (I) DONDE R ES H, CN, CICLOALQUILO(C3-C10), HETEROARILO DE 5 A 14 MIEMBROS, ENTRE OTROS; R1 ES H, HALO, ARILO(C6-C14) O HETEROARILO DE 5 A 14 MIEMBROS OPCIONALMENTE SUSTITUIDOS CON HALO, ALQUILO(C1-C20), ALQUENILO(C2-C15), ALQUINILO(C2-C15), ENTRE OTROS SUSTITUYENTES; R2 ES H, HALO, ARILO(C6-C14), ARILALQUILO O HETEROARILO DE 5 A 14 MIEMBROS OPCIONALMENTE SUSTITUIDOS CON HALO, AMIDA, ALQUILO(C1-C20), ENTRE OTROS SUSTITUYENTES; R3 ES H, ALQUILO(C1-C20), CICLOALQUILO(C3-C10), ENTRE OTROS. SON COMPUESTOS PREFERIDOS: (a), (b), ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE PROTEINQUINASA SIENDO UTILES PARA EL TRATAMIENTO DE CANCER DE VEJIGA, LEUCEMIA, FIBROSARCOMA, GLIOMA, MELANOMA
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73598205P | 2005-11-10 | 2005-11-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20070805A1 true PE20070805A1 (es) | 2007-08-13 |
Family
ID=38008330
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2006001398A PE20070805A1 (es) | 2005-11-10 | 2006-11-08 | 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 |
| CA2628534A1 (en) * | 2005-11-10 | 2007-05-18 | Schering Corporation | Methods for inhibiting protein kinases |
| MX2008015057A (es) * | 2006-05-31 | 2008-12-10 | Galapagos Nv | Compuestos de triazolopirazina utiles para el tratamiento de enfermedades degenerativas e inflamatorias. |
| 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 |
| 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 |
| EP2170892A2 (en) * | 2007-06-14 | 2010-04-07 | Schering Corporation | Imidazopyrazines as protein kinase inhibitors |
| MX2010001340A (es) * | 2007-07-31 | 2010-06-02 | Schering Corp | Combianacion de agente antimitotico e inhibidor de aurora quinasa como tratamiento anticancerigeno. |
| 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 |
| CA2705092A1 (en) * | 2007-11-07 | 2009-05-14 | Schering Corporation | 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 |
| AU2009215191A1 (en) | 2008-02-13 | 2009-08-20 | Gilead Connecticut, 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 |
| AR070531A1 (es) * | 2008-03-03 | 2010-04-14 | 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 |
| NZ593460A (en) | 2008-12-08 | 2013-11-29 | Gilead Connecticut Inc | Imidazopyrazine syk inhibitors |
| 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 |
| 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 |
| US20120220581A1 (en) | 2009-10-30 | 2012-08-30 | Janssen-Cilag, S.A. | IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE10 INHIBITORS |
| EP2523949B1 (en) | 2010-01-15 | 2014-08-20 | Janssen Pharmaceuticals Inc. | Novel substituted 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 |
| JP5938352B2 (ja) | 2010-03-11 | 2016-06-22 | ギリアード コネチカット, インコーポレイテッド | イミダゾピリジンsyk阻害剤 |
| ES2551407T3 (es) | 2010-03-18 | 2015-11-18 | Bayer Intellectual Property Gmbh | Imidazopirazinas |
| EP2576560B1 (en) | 2010-06-01 | 2015-09-30 | Bayer Intellectual Property GmbH | 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 |
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- 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 WO PCT/US2006/043786 patent/WO2007058942A2/en not_active Ceased
- 2006-11-08 PE PE2006001398A patent/PE20070805A1/es not_active Application Discontinuation
- 2006-11-08 AR ARP060104896A patent/AR056785A1/es unknown
- 2006-11-08 AU AU2006315718A patent/AU2006315718B2/en not_active Ceased
- 2006-11-08 TW TW095141238A patent/TW200804386A/zh unknown
- 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 JP JP2008540211A patent/JP5031760B2/ja not_active Expired - Fee Related
- 2006-11-08 BR BRPI0618520-7A patent/BRPI0618520A2/pt not_active IP Right Cessation
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- 2008-05-07 ZA ZA200803894A patent/ZA200803894B/xx unknown
- 2008-05-08 EC EC2008008440A patent/ECSP088440A/es unknown
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| JP2009515888A (ja) | 2009-04-16 |
| BRPI0618520A2 (pt) | 2011-09-06 |
| CA2628455A1 (en) | 2007-05-24 |
| AR056785A1 (es) | 2007-10-24 |
| NO20082530L (no) | 2008-08-07 |
| AU2006315718A1 (en) | 2007-05-24 |
| ZA200803894B (en) | 2009-03-25 |
| US20070117804A1 (en) | 2007-05-24 |
| WO2007058942A3 (en) | 2007-11-15 |
| WO2007058942A2 (en) | 2007-05-24 |
| JP5031760B2 (ja) | 2012-09-26 |
| RU2008122967A (ru) | 2009-12-20 |
| EP1945644A2 (en) | 2008-07-23 |
| IL191294A0 (en) | 2009-02-11 |
| TW200804386A (en) | 2008-01-16 |
| ECSP088440A (es) | 2008-06-30 |
| AU2006315718B2 (en) | 2012-10-04 |
| KR20080074963A (ko) | 2008-08-13 |
| CN101370811A (zh) | 2009-02-18 |
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