MA32134B1 - Composés hétérocycliques - Google Patents
Composés hétérocycliquesInfo
- Publication number
- MA32134B1 MA32134B1 MA33139A MA33139A MA32134B1 MA 32134 B1 MA32134 B1 MA 32134B1 MA 33139 A MA33139 A MA 33139A MA 33139 A MA33139 A MA 33139A MA 32134 B1 MA32134 B1 MA 32134B1
- Authority
- MA
- Morocco
- Prior art keywords
- heterocyclic compounds
- compounds
- substituents
- salts
- formula
- Prior art date
Links
- 150000002391 heterocyclic compounds Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 102000004022 Protein-Tyrosine Kinases Human genes 0.000 abstract 1
- 108090000412 Protein-Tyrosine Kinases Proteins 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- 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
-
- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Psychiatry (AREA)
- Transplantation (AREA)
- Obesity (AREA)
- Hospice & Palliative Care (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Cette invention concerne des composés de formule i et leurs sels, les substituants étant tels que définis dans la description, ainsi que des procédés permettant de les préparer; des composés pharmaceutiques contenant ces composés, en particulier pour une utilisation dans le cadre d'une ou plusieurs maladies associées avec la tyrosine kinase.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08151137 | 2008-02-06 | ||
| PCT/EP2009/051281 WO2009098236A1 (fr) | 2008-02-06 | 2009-02-04 | Composés hétérocycliques |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA32134B1 true MA32134B1 (fr) | 2011-03-01 |
Family
ID=39739330
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA33139A MA32134B1 (fr) | 2008-02-06 | 2010-09-02 | Composés hétérocycliques |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US8420657B2 (fr) |
| EP (1) | EP2247591A1 (fr) |
| JP (1) | JP5323095B2 (fr) |
| KR (2) | KR20130066703A (fr) |
| CN (1) | CN101981036B (fr) |
| AR (1) | AR070558A1 (fr) |
| AU (1) | AU2009211338B2 (fr) |
| BR (1) | BRPI0908433A2 (fr) |
| CA (1) | CA2714177A1 (fr) |
| CL (1) | CL2009000255A1 (fr) |
| CO (1) | CO6321262A2 (fr) |
| CR (1) | CR11614A (fr) |
| DO (1) | DOP2010000242A (fr) |
| EA (1) | EA017952B1 (fr) |
| EC (1) | ECSP10010463A (fr) |
| IL (1) | IL207224A0 (fr) |
| MA (1) | MA32134B1 (fr) |
| MX (1) | MX2010008719A (fr) |
| NI (1) | NI201000137A (fr) |
| NZ (1) | NZ587271A (fr) |
| PA (1) | PA8815201A1 (fr) |
| PE (1) | PE20091485A1 (fr) |
| SM (1) | SMP201000104B (fr) |
| TW (1) | TW200938202A (fr) |
| UY (1) | UY31631A1 (fr) |
| WO (1) | WO2009098236A1 (fr) |
| ZA (1) | ZA201005338B (fr) |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JO3235B1 (ar) | 2006-05-26 | 2018-03-08 | Astex Therapeutics Ltd | مركبات بيررولوبيريميدين و استعمالاتها |
| JP2011513493A (ja) * | 2008-03-10 | 2011-04-28 | コーネル ユニバーシティー | 血液脳関門透過性の調節方法 |
| KR101353857B1 (ko) | 2008-08-22 | 2014-01-21 | 노파르티스 아게 | Cdk 억제제로서 피롤로피리미딘 화합물 |
| WO2010124042A2 (fr) * | 2009-04-23 | 2010-10-28 | Abbott Laboratories | Modulateurs des récepteurs 5-ht et méthodes d'utilisation de ceux-ci |
| US8518933B2 (en) * | 2009-04-23 | 2013-08-27 | Abbvie Inc. | Modulators of 5-HT receptors and methods of use thereof |
| US8546377B2 (en) | 2009-04-23 | 2013-10-01 | Abbvie Inc. | Modulators of 5-HT receptors and methods of use thereof |
| AU2010309882B2 (en) | 2009-10-20 | 2016-01-28 | Cellzome Limited | Heterocyclyl pyrazolopyrimidine analogues as JAK inhibitors |
| ME02800B (fr) * | 2009-12-01 | 2018-01-20 | Abbvie Inc | Composés tricycliques innovants |
| US8791100B2 (en) | 2010-02-02 | 2014-07-29 | Novartis Ag | Aryl benzylamine compounds |
| UY33226A (es) * | 2010-02-19 | 2011-09-30 | Novartis Ag | Compuestos de pirrolopirimidina deuterada como inhibidores de la cdk4/6 |
| UY33227A (es) * | 2010-02-19 | 2011-09-30 | Novartis Ag | Compuestos de pirrolopirimidina como inhibidores de la cdk4/6 |
| EP2566867A1 (fr) | 2010-04-30 | 2013-03-13 | Cellzome Limited | Composés de pyrazole comme inhibiteurs de jak |
| TW201204732A (en) | 2010-07-09 | 2012-02-01 | Leo Pharma As | Novel homopiperazine derivatives as protein tyrosine kinase inhibitors and pharmaceutical use thereof |
| JP2013534233A (ja) * | 2010-08-20 | 2013-09-02 | セルゾーム リミティッド | 選択的jak阻害剤としてのヘテロシクリルピラゾロピリミジン類似体 |
| JP2013540748A (ja) * | 2010-09-16 | 2013-11-07 | コーネル ユニバーシティー | 血液脳関門の透過性を調節するためのアデノシン受容体シグナル伝達の使用法 |
| WO2012143320A1 (fr) | 2011-04-18 | 2012-10-26 | Cellzome Limited | Composés (7h-pyrrolo[2,3-d]pyrimidin-2-yl)amine comme inhibiteurs de la jak3 |
| MY161237A (en) | 2011-07-01 | 2017-04-14 | Novartis Ag | Combination therapy comprising a cdk4/6 inhibitor and a p13k inhibitor for use in the treatment of cancer |
| EP2760863A1 (fr) | 2011-09-20 | 2014-08-06 | Cellzome Limited | Dérivés de pyrazolo[4,3-c]pyridine comme inhibiteurs de kinases |
| AU2012338869A1 (en) | 2011-11-15 | 2014-06-05 | Novartis Ag | Combination of a phosphoinositide 3-kinase inhibitor and a modulator of the Janus Kinase 2-Signal Transducer and Activator of Transcription 5 pathway |
| CN102627646A (zh) * | 2012-03-19 | 2012-08-08 | 苏州四同医药科技有限公司 | 一种3-碘-5-溴-4,7-二氮杂吲哚的制备方法 |
| CN102633802B (zh) * | 2012-04-11 | 2014-03-19 | 南京药石药物研发有限公司 | 一种合成2-氯-7H-吡咯并[2,3-d]嘧啶的中间体及其制法 |
| CN106008511B (zh) * | 2012-05-14 | 2018-08-14 | 华东理工大学 | 蝶啶酮衍生物及其作为egfr、blk、flt3抑制剂的应用 |
| CN103059030B (zh) * | 2012-12-28 | 2015-04-29 | 北京师范大学 | 一种具有粘着斑激酶抑制作用的嘧啶类化合物及其制备方法和应用 |
| WO2014145576A2 (fr) | 2013-03-15 | 2014-09-18 | Northwestern University | Pyrrolo(2,3-d)pyrimidines substituées pour le traitement du cancer |
| LT3033086T (lt) | 2013-08-14 | 2021-12-27 | Novartis Ag | Kombinuota terapija vėžiui gydyti |
| CN106458914B (zh) * | 2014-03-28 | 2020-01-14 | 常州捷凯医药科技有限公司 | 作为axl抑制剂的杂环化合物 |
| WO2015168269A1 (fr) | 2014-05-01 | 2015-11-05 | Novartis Ag | Composés et compositions utilisés en tant qu'agonistes du récepteur de type toll-7 |
| WO2015168279A1 (fr) | 2014-05-01 | 2015-11-05 | Novartis Ag | Composés et compositions utiles en tant qu'agonistes du récepteur 7 de type toll |
| CN108430515B (zh) | 2015-10-29 | 2021-11-12 | 诺华股份有限公司 | 包含toll-样受体激动剂的抗体缀合物 |
| PT3773593T (pt) | 2018-03-30 | 2024-06-25 | Incyte Corp | Tratamento da hidradenite supurativa com inibidores de jak |
| CN111484496B (zh) * | 2019-01-29 | 2022-11-29 | 江苏开元药业有限公司 | 2-氨基-吡咯并嘧啶和吡唑并嘧啶类化合物及其制备方法和用途 |
| KR102916168B1 (ko) | 2019-05-08 | 2026-01-21 | 비말란 바이오사이언스즈, 인크. | Jak 억제제 |
| CN110305140B (zh) * | 2019-07-30 | 2020-08-04 | 上海勋和医药科技有限公司 | 二氢吡咯并嘧啶类选择性jak2抑制剂 |
| WO2021026465A1 (fr) * | 2019-08-08 | 2021-02-11 | Vimalan Biosciences, Inc. | Inhibiteurs de jak |
| GB201911868D0 (en) * | 2019-08-19 | 2019-10-02 | Galapagos Nv | Novel compounds and pharmaceutical compositions thereof for the treatment of inflammatory disorders |
| US20220348590A1 (en) * | 2019-09-13 | 2022-11-03 | The Board Institute, Inc. | Cyclooxygenase-2 inhibitors and uses thereof |
| GB201914910D0 (en) * | 2019-10-15 | 2019-11-27 | Sentinel Oncology Ltd | Pharmaceutical compounds |
| WO2023036252A1 (fr) * | 2021-09-08 | 2023-03-16 | 希格生科(深圳)有限公司 | Dérivé de pyrrolopyrimidine ou de pyrrolopyridine et son utilisation médicale |
| CN114957248B (zh) * | 2022-05-09 | 2023-12-29 | 南开大学 | 一种吡咯并嘧啶化合物及其制备方法、药物组合物和应用 |
| CN116813624B (zh) * | 2023-06-29 | 2025-10-03 | 成都金瑞基业生物科技有限公司 | 一种jak2抑制剂的晶型及制备方法 |
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| US7917643B2 (en) * | 1996-09-12 | 2011-03-29 | Audible, Inc. | Digital information library and delivery system |
| US20030074530A1 (en) * | 1997-12-11 | 2003-04-17 | Rupaka Mahalingaiah | Load/store unit with fast memory data access mechanism |
| US6887224B2 (en) * | 1998-06-15 | 2005-05-03 | Ilse Rubio | Close fitting leakage resistant feminine hygiene pad |
| TW505646B (en) | 1998-06-19 | 2002-10-11 | Pfizer Prod Inc | Pyrrolo [2,3-d] pyrimidine compounds |
| PT1382339E (pt) | 1999-12-10 | 2008-02-06 | Pfizer Prod Inc | Composições que contêm derivados de pirrolo[2,3-d]- pirimidina |
| WO2002076985A1 (fr) * | 2001-03-23 | 2002-10-03 | Smithkline Beecham Corporation | Composes utiles en tant qu'inhibiteurs de kinases pour le traitement des maladies hyperproliferatives |
| AU2003210388B2 (en) | 2002-03-07 | 2007-05-17 | F. Hoffmann-La Roche Ag | Bicyclic pyridine and pyrimidine P38 Kinase inhibitors |
| US7132221B2 (en) * | 2003-09-12 | 2006-11-07 | Headway Technologies, Inc. | Method to print photoresist lines with negative sidewalls |
| US7532909B2 (en) * | 2003-10-15 | 2009-05-12 | Nextel Communications Inc. | System and method for providing dedicated paging channels for walkie-talkie services |
| US7319102B1 (en) * | 2003-12-09 | 2008-01-15 | The Procter & Gamble Company | Pyrrolo[2,3-d]pyrimidine cytokine inhibitors |
| CN1918158B (zh) * | 2004-02-14 | 2011-03-02 | Irm责任有限公司 | 作为蛋白激酶抑制剂的化合物和组合物 |
| EP1725562A1 (fr) | 2004-03-05 | 2006-11-29 | Taisho Pharmaceutical Co., Ltd | D riv s pyrrolopyrimidine |
| WO2005107760A1 (fr) * | 2004-04-30 | 2005-11-17 | Irm Llc | Composes et compositions en tant qu'inducteurs de la differenciation de keratinocytes |
| WO2006045828A1 (fr) * | 2004-10-29 | 2006-05-04 | Tibotec Pharmaceuticals Ltd. | Derives de pyrimidine bicycliques inhibant le vih |
| US20060122003A1 (en) * | 2004-12-03 | 2006-06-08 | Kim Jong H | Portable golf swing position training aid kit |
| ES2411975T3 (es) | 2005-01-14 | 2013-07-09 | Janssen Pharmaceutica Nv | Pirimidinas heterocíclicas anilladas de 5 miembros como inhibidores de cinasas |
| RU2434871C2 (ru) * | 2005-02-03 | 2011-11-27 | Вертекс Фармасьютикалз Инкорпорейтед | Пирролопиримидины, применимые в качестве ингибиторов протеинкиназы |
| JP2006241089A (ja) | 2005-03-04 | 2006-09-14 | Astellas Pharma Inc | ピロロピリミジン誘導体またはその塩 |
| EP1877411B9 (fr) | 2005-05-05 | 2012-08-29 | Ardea Biosciences, Inc. | Diaryl-purine, -azapurines et -deazapurines inhibiteurs non nucleosidiques de la transcriptase inverse utilises dans le traitement du vih |
| US7749527B2 (en) | 2005-05-24 | 2010-07-06 | Wyeth Llc | Gel compositions for control of ecto-parasites |
| AR056691A1 (es) | 2005-10-13 | 2007-10-17 | Glaxo Group Ltd | Derivados pirrolopirimidina como inhibidores de syk |
| AU2006316605B2 (en) * | 2005-11-17 | 2012-04-26 | Osi Pharmaceuticals, Inc. | Fused bicyclic mTOR inhibitors |
| TWI630207B (zh) * | 2005-12-13 | 2018-07-21 | 英塞特控股公司 | 作為傑納斯激酶(JANUS KINASE)抑制劑之經雜芳基取代之吡咯并〔2,3-b〕吡啶及吡咯并〔2,3-b〕嘧啶 |
| EP2001476A4 (fr) | 2006-03-20 | 2010-12-22 | Synta Pharmaceuticals Corp | Composés à base de benzoimidazolyl-parazine pour utilisations contre l'inflammation et des troubles immunitaires |
| JO3235B1 (ar) | 2006-05-26 | 2018-03-08 | Astex Therapeutics Ltd | مركبات بيررولوبيريميدين و استعمالاتها |
| JP4861772B2 (ja) * | 2006-08-28 | 2012-01-25 | 富士通株式会社 | 移動体標定プログラム、該プログラムを記録した記録媒体、移動体標定装置、および移動体標定方法 |
| CL2007002994A1 (es) | 2006-10-19 | 2008-02-08 | Wyeth Corp | Compuestos derivados heterociclicos que contienen sulfamoilo, inhibidores de hsp90; composicion farmaceutica; y uso para el tratamiento del cancer, tal como cancer de mama, de colon y prostata, entre otros. |
| CL2008001709A1 (es) | 2007-06-13 | 2008-11-03 | Incyte Corp | Compuestos derivados de pirrolo [2,3-b]pirimidina, moduladores de quinasas jak; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como cancer, psoriasis, artritis reumatoide, entre otras. |
| KR20090033605A (ko) * | 2007-10-01 | 2009-04-06 | 삼성전자주식회사 | 적층형 반도체 패키지, 그 형성방법 및 이를 구비하는전자장치 |
| WO2009070524A1 (fr) | 2007-11-27 | 2009-06-04 | Wyeth | Composés de pyrrolo[3,2-d]pyrimidine et leur utilisation comme inhibiteurs de la pi3 kinase et de la mtor kinase |
| WO2009085185A1 (fr) | 2007-12-19 | 2009-07-09 | Amgen Inc. | Composés condensés de pyridine, de pyrimidine et de triazine en tant qu'inhibiteurs du cycle cellulaire |
| US20090192176A1 (en) * | 2008-01-30 | 2009-07-30 | Wyeth | 1H-PYRAZOLO[3,4-D]PYRIMIDINE, PURINE, 7H-PURIN-8(9H)-ONE, 3H-[1,2,3]TRIAZOLO[4,5-D]PYRIMIDINE, AND THIENO[3,2-D]PYRIMIDINE COMPOUNDS, THEIR USE AS mTOR KINASE AND PI3 KINASE INHIBITORS, AND THEIR SYNTHESES |
-
2009
- 2009-02-04 CN CN2009801117630A patent/CN101981036B/zh not_active Expired - Fee Related
- 2009-02-04 EA EA201001242A patent/EA017952B1/ru not_active IP Right Cessation
- 2009-02-04 WO PCT/EP2009/051281 patent/WO2009098236A1/fr not_active Ceased
- 2009-02-04 MX MX2010008719A patent/MX2010008719A/es active IP Right Grant
- 2009-02-04 BR BRPI0908433A patent/BRPI0908433A2/pt not_active IP Right Cessation
- 2009-02-04 JP JP2010545458A patent/JP5323095B2/ja not_active Expired - Fee Related
- 2009-02-04 KR KR1020137011455A patent/KR20130066703A/ko not_active Withdrawn
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- 2009-02-04 EP EP09708802A patent/EP2247591A1/fr not_active Withdrawn
- 2009-02-04 UY UY031631A patent/UY31631A1/es not_active Application Discontinuation
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