WO2008124085A3 - Méthodes d'utilisation de combinaisons d'inhibiteurs de mek et de jak-2 - Google Patents
Méthodes d'utilisation de combinaisons d'inhibiteurs de mek et de jak-2 Download PDFInfo
- Publication number
- WO2008124085A3 WO2008124085A3 PCT/US2008/004434 US2008004434W WO2008124085A3 WO 2008124085 A3 WO2008124085 A3 WO 2008124085A3 US 2008004434 W US2008004434 W US 2008004434W WO 2008124085 A3 WO2008124085 A3 WO 2008124085A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- jak
- mek
- formula
- compound
- effective amount
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
L'invention concerne une méthode destinée au traitement d'une maladie chez un mammifère, consistant à lui administrer une dose thérapeutique d'un composé à base de MEK représenté par la formule générale I(M), ou une composition pharmaceutique comprenant une dose thérapeutique d'un composé à base de MEK représenté par la formule générale I(M) et un excipient de qualité pharmaceutique, conjointement avec une dose thérapeutique d'un composé à base de JAK-2 représenté par la formule générale I(J), ou une composition pharmaceutique comprenant une dose thérapeutique d'un composé à base de JAK-2 représenté par la formule générale I(J) et un excipient de qualité pharmaceutique, le composé à base de MEK représenté par la formule générale I(M) et le composé à base de JAK-2 représenté par la formule générale I(J) étant définis dans la description de la présente demande.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US92187807P | 2007-04-03 | 2007-04-03 | |
| US60/921,878 | 2007-04-03 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2008124085A2 WO2008124085A2 (fr) | 2008-10-16 |
| WO2008124085A3 true WO2008124085A3 (fr) | 2010-04-15 |
Family
ID=39722502
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2008/004434 Ceased WO2008124085A2 (fr) | 2007-04-03 | 2008-04-03 | Méthodes d'utilisation de combinaisons d'inhibiteurs de mek et de jak-2 |
Country Status (1)
| Country | Link |
|---|---|
| WO (1) | WO2008124085A2 (fr) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8697689B2 (en) | 2008-10-16 | 2014-04-15 | Janssen Pharmaceuticals, Inc. | Indole and benzomorpholine derivatives as modulators of metabotropic glutamate receptors |
| US8937060B2 (en) | 2009-05-12 | 2015-01-20 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo [4,3-A] pyridine derivatives and their use for the treatment of prevention of neurological and psychiatric disorders |
| US8946205B2 (en) | 2009-05-12 | 2015-02-03 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mGluR2 receptors |
| US9012448B2 (en) | 2010-11-08 | 2015-04-21 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of MGLUR2 receptors |
| US9271967B2 (en) | 2010-11-08 | 2016-03-01 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mGluR2 receptors |
| US9290468B2 (en) | 2012-01-17 | 2016-03-22 | Shanghai Kechow Pharma, Inc. | Benzoheterocyclic compounds and use thereof |
Families Citing this family (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0420722D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
| TWI417095B (zh) | 2006-03-15 | 2013-12-01 | Janssen Pharmaceuticals Inc | 1,4-二取代之3-氰基-吡啶酮衍生物及其作為mGluR2-受體之正向異位性調節劑之用途 |
| TW200900065A (en) | 2007-03-07 | 2009-01-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives |
| TW200845978A (en) | 2007-03-07 | 2008-12-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives |
| EP2200436B1 (fr) | 2007-09-04 | 2015-01-21 | The Scripps Research Institute | Pyrimidinyl-amines substituées en tant qu'inhibiteurs de la protéine kinase |
| MY152078A (en) | 2007-09-14 | 2014-08-15 | Ortho Mcneil Janssen Pharm | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h,1'h-[1,4']bipyridinyl-2'-ones |
| CA2697399C (fr) | 2007-09-14 | 2016-01-19 | Ortho-Mcneil-Janssen Pharmaceuticals, Inc. | 4-(aryl-x-phenyl)-1h-pyridine-2-ones 1,3-disubstituees |
| NZ584148A (en) | 2007-09-14 | 2011-05-27 | Ortho Mcneil Janssen Pharm | 1,3-disubstituted-4-phenyl-1 h-pyridin-2-ones |
| RU2492170C9 (ru) | 2007-11-14 | 2013-12-27 | Орто-Макнейл-Янссен Фармасьютикалз, Инк. | Имидазо[1,2-а]пиридиновые производные и их применение в качестве положительных аллостерических модуляторов рецепторов mglur2 |
| AU2009289784B2 (en) | 2008-09-02 | 2012-03-22 | Addex Pharma S.A. | 3-azabicyclo[3.1.0]hexyl derivatives as modulators of metabotropic glutamate receptors |
| WO2010060589A1 (fr) | 2008-11-28 | 2010-06-03 | Ortho-Mcneil-Janssen Pharmaceuticals, Inc. | Dérivés d'indole et de benzoxazine comme modulateurs des récepteurs métabotropiques au glutamate |
| FR2941696B1 (fr) | 2009-02-05 | 2011-04-15 | Sanofi Aventis | Derives d'azaspiranyl-alkylcarbamates d'heterocycles a 5 chainons, leur preparation et leur application en therapeutique |
| FR2945531A1 (fr) | 2009-05-12 | 2010-11-19 | Sanofi Aventis | Derives de 7-aza-spiro°3,5!nonane-7-carboxylates, leur preparation et leur application en therapeutique |
| MY153913A (en) | 2009-05-12 | 2015-04-15 | Janssen Pharmaceuticals Inc | 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
| ES2528948T3 (es) | 2009-09-21 | 2015-02-13 | Chemocentryx, Inc. | Derivados de pirrolidinona carboxamida como moduladores de quemerina-R (ChemR23) |
| MX2012013274A (es) | 2010-05-21 | 2013-05-28 | Chemilia Ab | Novedosos derivados de la pirimidina. |
| GB201012105D0 (en) | 2010-07-19 | 2010-09-01 | Domainex Ltd | Novel pyrimidine compounds |
| CN102020651B (zh) | 2010-11-02 | 2012-07-18 | 北京赛林泰医药技术有限公司 | 6-芳基氨基吡啶酮甲酰胺mek抑制剂 |
| EP2661435B1 (fr) | 2010-11-08 | 2015-08-19 | Janssen Pharmaceuticals, Inc. | Dérivés 1,2,4-triazolo[4,3-a]pyridine et leur utilisation en tant que modulateurs allostériques positifs des récepteurs mglur2 |
| JP5886411B2 (ja) | 2011-03-24 | 2016-03-16 | ノビガ・リサーチ・エービーNoviga Research AB | 新規のピリミジン誘導体 |
| CN102718750B (zh) * | 2011-03-31 | 2015-03-11 | 中国人民解放军军事医学科学院毒物药物研究所 | 含吖啶环的氨基吡啶类衍生物及其用途 |
| BR112013025387B1 (pt) * | 2011-04-01 | 2021-07-27 | University Of Utah Research Foundation | Compostos análogos substituídos da n-fenilpirimidin-2-amina como inibidores da quinase axl, uso dos ditos compostos para o tratamento de um distúrbio de proliferação celular descontrolada, bem como kit compreendendo ditos compostos |
| WO2013109142A1 (fr) | 2012-01-16 | 2013-07-25 | Stichting Het Nederlands Kanker Instituut | Inhibition de la voie des mapk/erk et pdk combinée dans des cas de néoplasie |
| AU2013337702A1 (en) | 2012-11-02 | 2015-05-21 | Merck Patent Gmbh | Method of reducing adverse effects in a cancer patient undergoing treatment with a MEK inhibitor |
| AU2014236820B2 (en) | 2013-03-14 | 2018-08-02 | Sumitomo Pharma Oncology, Inc. | JAK2 and ALK2 inhibitors and methods for their use |
| JO3368B1 (ar) | 2013-06-04 | 2019-03-13 | Janssen Pharmaceutica Nv | مركبات 6، 7- ثاني هيدرو بيرازولو [5،1-a] بيرازين- 4 (5 يد)- اون واستخدامها بصفة منظمات تفارغية سلبية لمستقبلات ميجلور 2 |
| JO3367B1 (ar) | 2013-09-06 | 2019-03-13 | Janssen Pharmaceutica Nv | مركبات 2،1، 4- ثلاثي زولو [3،4-a] بيريدين واستخدامها بصفة منظمات تفارغية موجبة لمستقبلات ميجلور 2 |
| WO2015041533A1 (fr) | 2013-09-20 | 2015-03-26 | Stichting Het Nederlands Kanker Instituut | Association de rock et de la voie mapk |
| WO2015041534A1 (fr) | 2013-09-20 | 2015-03-26 | Stichting Het Nederlands Kanker Instituut | P90rsk en combinaison avec raf/erk/mek |
| DK3096790T3 (da) | 2014-01-21 | 2019-10-07 | Janssen Pharmaceutica Nv | Kombinationer omfattende positive allosteriske modulatorer eller orthosteriske agonister af metabotrop glutamaterg subtype 2-receptor og anvendelse af disse |
| KR20220038826A (ko) | 2014-01-21 | 2022-03-29 | 얀센 파마슈티카 엔.브이. | 대사 조절형 글루탐산 작동성 수용체 제2아형의 양성 알로스테릭 조절제 또는 오르토스테릭 작동제를 포함하는 조합 및 그 용도 |
| US20170027940A1 (en) | 2014-04-10 | 2017-02-02 | Stichting Het Nederlands Kanker Instituut | Method for treating cancer |
| WO2015178770A1 (fr) | 2014-05-19 | 2015-11-26 | Stichting Het Nederlands Kanker Instituut | Compositions pour le traitement du cancer |
| US20170114323A1 (en) | 2014-06-19 | 2017-04-27 | Whitehead Institute For Biomedical Research | Uses of kinase inhibitors for inducing and maintaining pluripotency |
| AR105483A1 (es) | 2015-06-30 | 2017-10-11 | Exelixis Inc | Sal de fumarato cristalina de (s)-[3,4-difluoro-2-(2-fluoro-4-yodofenilamino)fenil][3-hidroxi-3-(piperidin-2-il)azetidin-1-il]-metanona |
| IL291017B2 (en) | 2015-10-21 | 2023-11-01 | Otsuka Pharma Co Ltd | Benzolactam compounds as protein kinase inhibitors |
| CN106810536A (zh) | 2015-11-30 | 2017-06-09 | 甘李药业股份有限公司 | 一种蛋白激酶抑制剂及其制备方法和医药用途 |
| CN105330643B (zh) | 2015-12-09 | 2017-12-05 | 苏州明锐医药科技有限公司 | 卡比替尼的制备方法 |
| CN106045969B (zh) * | 2016-05-27 | 2019-04-12 | 湖南欧亚药业有限公司 | 一种卡比替尼的合成方法 |
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| SI3658552T1 (sl) | 2017-07-28 | 2023-11-30 | Yuhan Corporation | Postopek za pripravo N-(5-((4-(4-((dimetilamino)metil)-3-fenil-1H-pirazol-1-il)pirimidin-2-il )amino)-4-metoksi-2-morfolinofenil)akrilamida z reagiranjem ustreznega amina s 3-halo-propionil kloridom |
| WO2019195753A1 (fr) | 2018-04-05 | 2019-10-10 | Tolero Pharmaceuticals, Inc. | Inhibiteurs de kinases axl et leur utilisation |
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| CN114302878A (zh) | 2019-07-03 | 2022-04-08 | 大日本住友制药肿瘤公司 | 酪氨酸激酶非受体1(tnk1)抑制剂及其用途 |
| CN110330484B (zh) * | 2019-07-18 | 2022-08-26 | 中国药科大学 | 取代类苯基嘧啶衍生物作为jak激酶抑制剂或其可药用的盐、制备方法及用途 |
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| CN113735859A (zh) * | 2021-08-12 | 2021-12-03 | 安徽医科大学 | 一种激酶抑制剂 |
| CA3256792A1 (fr) * | 2022-04-29 | 2023-11-02 | Beigene , Ltd. | Composés 6-(pyrimidin-4-yl) quinoléiques substitués utilisés comme inhibiteurs de kinase dépendante des cyclines |
| WO2024088323A1 (fr) * | 2022-10-27 | 2024-05-02 | Beigene, Ltd. | Composés de 6-(pyrimidin-4-yl)quinoléine substituée utilisés en tant qu'inhibiteurs de kinase dépendante des cyclines |
| CN117088851A (zh) * | 2023-07-13 | 2023-11-21 | 特科罗生物科技(成都)有限公司 | 一种嘧啶胺类nuak抑制剂及其制备方法和用途 |
Citations (9)
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| WO2001057022A2 (fr) * | 2000-02-05 | 2001-08-09 | Vertex Pharmaceuticals Incorporated | Compositions de pyrazole utiles comme inhibiteurs de erk |
| WO2002044166A1 (fr) * | 2000-11-02 | 2002-06-06 | Astrazeneca Ab | Quinolines substituees comme agents antitumoraux |
| WO2003015689A2 (fr) * | 2001-08-08 | 2003-02-27 | MedInnova Gesellschaft für medizinische Innovationen aus akademischer Forschung mbH | Composition pharmaceutique de prevention et/ou de traitement de maladies virales |
| WO2004113347A1 (fr) * | 2003-06-20 | 2004-12-29 | Celltech R & D Limited | Derives de thienopyridone en tant qu'inhibiteurs de kinase |
| WO2006017443A2 (fr) * | 2004-08-02 | 2006-02-16 | Osi Pharmaceuticals, Inc. | Composes a base de pyrrolopyrimidine a substitution arylamine inhibiteurs de kinases multiples |
| WO2006045514A1 (fr) * | 2004-10-20 | 2006-05-04 | Applied Research Systems Ars Holding N.V. | Derives de 3-arylamino pyridine |
| WO2006061712A2 (fr) * | 2004-12-10 | 2006-06-15 | Pfizer Inc. | Utilisation d'inhibiteurs de mek dans le traitement d'une croissance cellulaire anormale |
| WO2007044515A1 (fr) * | 2005-10-07 | 2007-04-19 | Exelixis, Inc. | Inhibiteurs de mek et procedes pour les utiliser |
| WO2008021389A2 (fr) * | 2006-08-16 | 2008-02-21 | Exelixis, Inc. | Procédés d'utilisation de modulateurs pi3k etmek |
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2008
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| WO2001057022A2 (fr) * | 2000-02-05 | 2001-08-09 | Vertex Pharmaceuticals Incorporated | Compositions de pyrazole utiles comme inhibiteurs de erk |
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| WO2004113347A1 (fr) * | 2003-06-20 | 2004-12-29 | Celltech R & D Limited | Derives de thienopyridone en tant qu'inhibiteurs de kinase |
| WO2006017443A2 (fr) * | 2004-08-02 | 2006-02-16 | Osi Pharmaceuticals, Inc. | Composes a base de pyrrolopyrimidine a substitution arylamine inhibiteurs de kinases multiples |
| WO2006045514A1 (fr) * | 2004-10-20 | 2006-05-04 | Applied Research Systems Ars Holding N.V. | Derives de 3-arylamino pyridine |
| WO2006061712A2 (fr) * | 2004-12-10 | 2006-06-15 | Pfizer Inc. | Utilisation d'inhibiteurs de mek dans le traitement d'une croissance cellulaire anormale |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8697689B2 (en) | 2008-10-16 | 2014-04-15 | Janssen Pharmaceuticals, Inc. | Indole and benzomorpholine derivatives as modulators of metabotropic glutamate receptors |
| US8937060B2 (en) | 2009-05-12 | 2015-01-20 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo [4,3-A] pyridine derivatives and their use for the treatment of prevention of neurological and psychiatric disorders |
| US8946205B2 (en) | 2009-05-12 | 2015-02-03 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mGluR2 receptors |
| US9012448B2 (en) | 2010-11-08 | 2015-04-21 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of MGLUR2 receptors |
| US9271967B2 (en) | 2010-11-08 | 2016-03-01 | Janssen Pharmaceuticals, Inc. | 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mGluR2 receptors |
| US9290468B2 (en) | 2012-01-17 | 2016-03-22 | Shanghai Kechow Pharma, Inc. | Benzoheterocyclic compounds and use thereof |
| US9937158B2 (en) | 2012-01-17 | 2018-04-10 | Shanghai Kechow Pharma, Inc. | Benzoheterocyclic compounds and use thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2008124085A2 (fr) | 2008-10-16 |
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