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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 PDF

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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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alkyl
hydroxy
alkoxy
cycloalkyl
halogen
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リュッキンク,ウルリッヒ
クリューガー,マルティン
ヤウテラト,ロルフ
プリエン,オラフ
ジーマイスター,ゲルト
エルンスト,アレクサンダー
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シエーリング アクチエンゲゼルシャフト
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Priority claimed from DE2002112100 external-priority patent/DE10212100A1/de
Priority claimed from DE10255984A external-priority patent/DE10255984A1/de
Application filed by シエーリング アクチエンゲゼルシャフト filed Critical シエーリング アクチエンゲゼルシャフト
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    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P25/16Anti-Parkinson drugs
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
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    • C07D417/02Heterocyclic 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
    • C07D417/12Heterocyclic 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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  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Oncology (AREA)
  • Immunology (AREA)
  • Virology (AREA)
  • Communicable Diseases (AREA)
  • Urology & Nephrology (AREA)
  • Psychology (AREA)
  • Dermatology (AREA)
  • Transplantation (AREA)
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  • Cardiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
JP2003574654A 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 Pending JP2005526765A (ja)

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)

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JP2005526765A true JP2005526765A (ja) 2005-09-08

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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

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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)

* Cited by examiner, † Cited by third party
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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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
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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
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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
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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

Cited By (6)

* Cited by examiner, † Cited by third party
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

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AR038922A1 (es) 2005-02-02
AU2003212282A1 (en) 2003-09-22
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