JP2005526765A - Cdk−阻害性2−ヘテロアリール−ピリミジン類、それらの生成及び医薬としての使用 - Google Patents
Cdk−阻害性2−ヘテロアリール−ピリミジン類、それらの生成及び医薬としての使用 Download PDFInfo
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- JP2005526765A JP2005526765A JP2003574654A JP2003574654A JP2005526765A JP 2005526765 A JP2005526765 A JP 2005526765A JP 2003574654 A JP2003574654 A JP 2003574654A JP 2003574654 A JP2003574654 A JP 2003574654A JP 2005526765 A JP2005526765 A JP 2005526765A
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-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Oncology (AREA)
- Immunology (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Urology & Nephrology (AREA)
- Psychology (AREA)
- Dermatology (AREA)
- Transplantation (AREA)
- Hematology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2002112100 DE10212100A1 (de) | 2002-03-11 | 2002-03-11 | CDK inhibitorische 2-Heteroaryl-Pyrimidine, deren Herstellung und Verwendung als Arzneimittel |
| DE10255984A DE10255984A1 (de) | 2002-11-26 | 2002-11-26 | CDK inhibitorische 2-Heteroaryl-Pyrimidine, deren Herstellung und Verwendung als Arnzeimittel |
| PCT/EP2003/001995 WO2003076437A1 (fr) | 2002-03-11 | 2003-02-26 | 2-heteroaryle-pyrimidines inhibitrices de la kinase dependante des cyclines, leur production et leur utilisation comme medicaments |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2005526765A true JP2005526765A (ja) | 2005-09-08 |
Family
ID=27806091
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003574654A Pending JP2005526765A (ja) | 2002-03-11 | 2003-02-26 | Cdk−阻害性2−ヘテロアリール−ピリミジン類、それらの生成及び医薬としての使用 |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP1483260A1 (fr) |
| JP (1) | JP2005526765A (fr) |
| AR (1) | AR038922A1 (fr) |
| AU (1) | AU2003212282A1 (fr) |
| PE (1) | PE20040156A1 (fr) |
| TW (1) | TW200406406A (fr) |
| UY (1) | UY27714A1 (fr) |
| WO (1) | WO2003076437A1 (fr) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010516788A (ja) * | 2007-01-31 | 2010-05-20 | サイトピア・リサーチ・ピーティーワイ・リミテッド | チオピリミジンベースの化合物およびその使用 |
| JP2011513230A (ja) * | 2008-02-22 | 2011-04-28 | ライジェル ファーマシューティカルズ, インコーポレイテッド | アテローム性動脈硬化症の治療のための2,4−ピリミジンジアミンの使用 |
| JP2013545741A (ja) * | 2010-11-10 | 2013-12-26 | エフ.ホフマン−ラ ロシュ アーゲー | Lrrk2調節薬としてのピラゾールアミノピリミジン誘導体 |
| JP2021522349A (ja) * | 2018-05-04 | 2021-08-30 | インフレイゾーム リミテッド | 新規な化合物 |
| JP2024506116A (ja) * | 2020-11-27 | 2024-02-09 | オールオリオン セラピューティクス インコーポレイテッド | アミノヘテロアリールキナーゼ阻害剤 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
| IL166241A0 (en) | 2002-07-29 | 2006-01-15 | Rigel Pharmaceuticals Inc | Method of treating or preventing autoimmune diseases with 2,4-pyrimidinedinediamine compounds |
| RS53109B (sr) | 2003-07-30 | 2014-06-30 | Rigel Pharmaceuticals Inc. | Jedinjenja 2,4 pirimidindiamina za upotrebu u tretmanu ili prevenciji autoimunih bolesti |
| DE10349423A1 (de) * | 2003-10-16 | 2005-06-16 | Schering Ag | Sulfoximinsubstituierte Parimidine als CDK- und/oder VEGF-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel |
| WO2006034872A1 (fr) * | 2004-09-29 | 2006-04-06 | Bayer Schering Pharma Aktiengesellschaft | 2-anilinopyrimidine substituee utilisee en tant que kinase a cycle cellulaire ou recepteur de la tyrosine kinase, leur production et leur utilisation en tant que medicament |
| ES2380550T3 (es) | 2004-11-24 | 2012-05-16 | Rigel Pharmaceuticals, Inc. | Compuestos de espiro-2,4-pirimidindiamina y sus usos |
| NZ555947A (en) | 2005-01-19 | 2010-11-26 | Rigel Pharmaceuticals Inc | Prodrugs of 2,4-pyrimidinediamine compounds and their uses |
| EP1710246A1 (fr) * | 2005-04-08 | 2006-10-11 | Schering Aktiengesellschaft | Macrocycles de sulfoximine-pyrmidine et leurs sels correspondants, leurs procédé de fabrication, et leurs utilisation pharmaceutique contre le cancer |
| MX286273B (es) | 2005-06-08 | 2011-05-04 | Rigel Pharmaceuticals Inc | Composiciones y metodos para inhibicion de la via jak. |
| US20070203161A1 (en) | 2006-02-24 | 2007-08-30 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
| EP2258359A3 (fr) | 2005-08-26 | 2011-04-06 | Braincells, Inc. | Neurogenèse par modulation des récepteurs muscariniques avec sabcomeline |
| US7678363B2 (en) | 2005-08-26 | 2010-03-16 | Braincells Inc | Methods of treating psychiatric conditions comprising administration of muscarinic agents in combination with SSRIs |
| WO2007047978A2 (fr) | 2005-10-21 | 2007-04-26 | Braincells, Inc. | Modulation de la neurogenese par inhibition de la pde |
| AU2006308889A1 (en) | 2005-10-31 | 2007-05-10 | Braincells, Inc. | GABA receptor mediated modulation of neurogenesis |
| EP1803723A1 (fr) | 2006-01-03 | 2007-07-04 | Bayer Schering Pharma Aktiengesellschaft | Dérivés (2,4,9-triaza-1(2,4)-pyrimidina-3(1,3)-benzenacyclononaphan-3^4-yl)-sulfoximide en tant qu'inhibiteurs de la kinase aurora pour le traitement de cancer |
| TW200736195A (en) | 2006-02-17 | 2007-10-01 | Wyeth Corp | Methods for preparing sulfonamide substituted alcohols and intermediates thereof |
| RU2008131051A (ru) | 2006-02-17 | 2010-03-27 | Вайет (Us) | Избирательное n-сульфонилирование 2-амино трифторалкильнзамещенных спиртов |
| CA2642229C (fr) | 2006-02-24 | 2015-05-12 | Rigel Pharmaceuticals, Inc. | Compositions et methodes destinees a l'inhibition de la voie jak |
| US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
| CA2651813A1 (fr) | 2006-05-09 | 2007-11-22 | Braincells, Inc. | Neurogenese par modulation de l'angiotensine |
| US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
| DE102007010801A1 (de) | 2007-03-02 | 2008-09-04 | Bayer Cropscience Ag | Diaminopyrimidine als Fungizide |
| CN101970417A (zh) * | 2008-03-14 | 2011-02-09 | 巴斯夫欧洲公司 | 作为杀真菌剂使用的取代的吡嗪基甲基磺酰胺 |
| CN102203086A (zh) | 2008-09-03 | 2011-09-28 | 拜尔农作物科学股份公司 | 作为杀真菌剂的噻吩基氨基嘧啶类化合物 |
| EP2179992A1 (fr) | 2008-10-21 | 2010-04-28 | Bayer Schering Pharma Aktiengesellschaft | Dérivés d'anilino-pyrimidine substitués par sulfone en tant qu'inhibiteurs de CDK, leur fabrication et leur utilisation en tant que médicaments |
| EP2179991A1 (fr) * | 2008-10-21 | 2010-04-28 | Bayer Schering Pharma Aktiengesellschaft | Dérivés d'anilino-pyrimidine substitués par sulfoximine en tant qu'inhibiteurs de CDK, leur fabrication et leur utilisation en tant que médicaments |
| EP2179993A1 (fr) | 2008-10-21 | 2010-04-28 | Bayer Schering Pharma Aktiengesellschaft | Dérivés d'anilino-pyrimidine substitués par sulfoxide en tant qu'inhibiteurs de CDK, leur fabrication et leur utilisation en tant que médicaments |
| WO2010099217A1 (fr) | 2009-02-25 | 2010-09-02 | Braincells, Inc. | Modulation de neurogenèse à l'aide de combinaisons de d-cyclosérine |
| DE102009001438A1 (de) | 2009-03-10 | 2010-09-16 | Bayer Schering Pharma Aktiengesellschaft | Carbonylamino-substituierte Anilino-Pyrimidinderivate als Tyk-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel |
| DE102009015070A1 (de) | 2009-03-30 | 2010-10-14 | Bayer Schering Pharma Aktiengesellschaft | Aminocabonylamino-substituierte Anilino-Pyrimidinderivate als Tyk-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel |
| US8466155B2 (en) * | 2009-10-02 | 2013-06-18 | Boehringer Ingelheim International Gmbh | Pyrimidines |
| DE102010014427A1 (de) | 2010-04-01 | 2011-10-06 | Bayer Schering Pharma Aktiengesellschaft | Kombinationen neuer pan-CDK-Inhibitoren zur Behandlung von Tumoren |
| DE102010014426A1 (de) | 2010-04-01 | 2011-10-06 | Bayer Schering Pharma Aktiengesellschaft | Verwendung neuer pan-CDK-Inhibitoren zur Behandlung von Tumoren |
| EP2827871A1 (fr) | 2012-03-21 | 2015-01-28 | Bayer Intellectual Property GmbH | Utilisation de (rs)-s-cyclopropyl-s-(4-{[4-{[(1r, 2r)-2-hydroxy-1-méthylpropyl]oxy}-5-(trifluorméthyl)pyrimidin-2-yl]amino}phényl)sulfoximide pour traiter des tumeurs spécifiques |
| HK1215256A1 (zh) | 2012-11-20 | 2016-08-19 | Vertex Pharmaceuticals Incorporated | 用作吲哚胺2,3-二氧化酶的抑制劑的化合物 |
| WO2014173815A1 (fr) | 2013-04-23 | 2014-10-30 | Bayer Pharma Aktiengesellschaft | Utilisation de (rs)-s-cyclopropyl-s-(4-{[4-{[(1r, 2r)-2-hydroxy-1-méthylpropyl]oxy}-5-(trifluorométhyl)pyrimidin-2-yl]amino}phényl)sulfoximide dans le traitement de tumeurs spécifiques |
| WO2019157020A1 (fr) | 2018-02-06 | 2019-08-15 | The Board Of Trustees Of The University Of Illinois | Analogues de benzothiophène substitués en tant qu'agents de dégradation sélectifs du récepteur d'œstrogènes |
| US11066404B2 (en) | 2018-10-11 | 2021-07-20 | Incyte Corporation | Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors |
| WO2020168197A1 (fr) | 2019-02-15 | 2020-08-20 | Incyte Corporation | Composés de pyrrolo[2,3-d]pyrimidinone en tant qu'inhibiteurs de cdk2 |
| TW202100520A (zh) | 2019-03-05 | 2021-01-01 | 美商英塞特公司 | 作為cdk2 抑制劑之吡唑基嘧啶基胺化合物 |
| US11919904B2 (en) | 2019-03-29 | 2024-03-05 | Incyte Corporation | Sulfonylamide compounds as CDK2 inhibitors |
| EP3947368B1 (fr) * | 2019-04-04 | 2025-09-03 | Dana-Farber Cancer Institute, Inc. | Composés bifonctionells comprennant un ligand cdk2/5, un lieur et un dégron qui s'attache a la ligase d'ubiquitin e3 pour le traitement du cancer |
| US11447494B2 (en) | 2019-05-01 | 2022-09-20 | Incyte Corporation | Tricyclic amine compounds as CDK2 inhibitors |
| US11440914B2 (en) | 2019-05-01 | 2022-09-13 | Incyte Corporation | Tricyclic amine compounds as CDK2 inhibitors |
| PH12022550361A1 (en) | 2019-08-14 | 2023-02-27 | Incyte Corp | Imidazolyl pyrimidinylamine compounds as cdk2 inhibitors |
| JP7693656B2 (ja) | 2019-10-11 | 2025-06-17 | インサイト・コーポレイション | Cdk2阻害剤としての二環式アミン |
| US11981671B2 (en) | 2021-06-21 | 2024-05-14 | Incyte Corporation | Bicyclic pyrazolyl amines as CDK2 inhibitors |
| US11976073B2 (en) | 2021-12-10 | 2024-05-07 | Incyte Corporation | Bicyclic amines as CDK2 inhibitors |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9828511D0 (en) * | 1998-12-24 | 1999-02-17 | Zeneca Ltd | Chemical compounds |
| GB0004888D0 (en) * | 2000-03-01 | 2000-04-19 | Astrazeneca Uk Ltd | Chemical compounds |
| GB0016877D0 (en) * | 2000-07-11 | 2000-08-30 | Astrazeneca Ab | Chemical compounds |
-
2003
- 2003-02-26 JP JP2003574654A patent/JP2005526765A/ja active Pending
- 2003-02-26 AU AU2003212282A patent/AU2003212282A1/en not_active Abandoned
- 2003-02-26 WO PCT/EP2003/001995 patent/WO2003076437A1/fr not_active Ceased
- 2003-02-26 EP EP03708151A patent/EP1483260A1/fr not_active Withdrawn
- 2003-03-10 PE PE2003000240A patent/PE20040156A1/es not_active Application Discontinuation
- 2003-03-11 TW TW092105221A patent/TW200406406A/zh unknown
- 2003-03-11 UY UY27714A patent/UY27714A1/es not_active Application Discontinuation
- 2003-03-11 AR ARP030100819A patent/AR038922A1/es unknown
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010516788A (ja) * | 2007-01-31 | 2010-05-20 | サイトピア・リサーチ・ピーティーワイ・リミテッド | チオピリミジンベースの化合物およびその使用 |
| JP2011513230A (ja) * | 2008-02-22 | 2011-04-28 | ライジェル ファーマシューティカルズ, インコーポレイテッド | アテローム性動脈硬化症の治療のための2,4−ピリミジンジアミンの使用 |
| JP2013545741A (ja) * | 2010-11-10 | 2013-12-26 | エフ.ホフマン−ラ ロシュ アーゲー | Lrrk2調節薬としてのピラゾールアミノピリミジン誘導体 |
| JP2018109038A (ja) * | 2010-11-10 | 2018-07-12 | ジェネンテック, インコーポレイテッド | Lrrk2調節薬としてのピラゾールアミノピリミジン誘導体 |
| JP2021522349A (ja) * | 2018-05-04 | 2021-08-30 | インフレイゾーム リミテッド | 新規な化合物 |
| JP2024506116A (ja) * | 2020-11-27 | 2024-02-09 | オールオリオン セラピューティクス インコーポレイテッド | アミノヘテロアリールキナーゼ阻害剤 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2003076437A1 (fr) | 2003-09-18 |
| UY27714A1 (es) | 2003-10-31 |
| PE20040156A1 (es) | 2004-06-07 |
| EP1483260A1 (fr) | 2004-12-08 |
| AR038922A1 (es) | 2005-02-02 |
| AU2003212282A1 (en) | 2003-09-22 |
| TW200406406A (en) | 2004-05-01 |
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