MA27713A1 - Composes aminoheteroaryliques servant d'inhibiteurs de proteine-kinases - Google Patents
Composes aminoheteroaryliques servant d'inhibiteurs de proteine-kinasesInfo
- Publication number
- MA27713A1 MA27713A1 MA28457A MA28457A MA27713A1 MA 27713 A1 MA27713 A1 MA 27713A1 MA 28457 A MA28457 A MA 28457A MA 28457 A MA28457 A MA 28457A MA 27713 A1 MA27713 A1 MA 27713A1
- Authority
- MA
- Morocco
- Prior art keywords
- compounds
- inhibitors
- protein
- aminoheteroarylic
- kinases
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 102000001253 Protein Kinase Human genes 0.000 title 1
- 108060006633 protein kinase Proteins 0.000 title 1
- 239000003909 protein kinase inhibitor Substances 0.000 abstract 2
- 125000005214 aminoheteroaryl group Chemical group 0.000 abstract 1
- 150000003927 aminopyridines Chemical class 0.000 abstract 1
- 229940045988 antineoplastic drug protein kinase inhibitors Drugs 0.000 abstract 1
- 229940043355 kinase inhibitor Drugs 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- XFTQRUTUGRCSGO-UHFFFAOYSA-N pyrazin-2-amine Chemical class NC1=CN=CC=N1 XFTQRUTUGRCSGO-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/73—Unsubstituted amino or imino radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
-
- 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
- A61K31/4965—Non-condensed pyrazines
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
-
- 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
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/68—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D211/72—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/12—Heterocyclic 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Urology & Nephrology (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Gastroenterology & Hepatology (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Emergency Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Vascular Medicine (AREA)
- Endocrinology (AREA)
- Dermatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
DEPOSANT Société dite : SUGEN, INC. REVENDICATION DE PRIORITES US 26 Février 2003 60/449,588 US 29 Janvier 2004 60/540,229 Composés aminohétéroaryliques servant d'inhibiteurs de protéine-kinases Des aminopyridines et aminopyrazines de formule (I), des compositions comprenant ces composés et des méthodes d'utilisation sont proposés. Les composés préférés de formule (I) ont une activité d'inhibiteurs de protéine-kinases, y compris comme inhibiteurs de c-MET.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US44958803P | 2003-02-26 | 2003-02-26 | |
| US54022904P | 2004-01-29 | 2004-01-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA27713A1 true MA27713A1 (fr) | 2006-01-02 |
Family
ID=32930516
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA28457A MA27713A1 (fr) | 2003-02-26 | 2005-08-26 | Composes aminoheteroaryliques servant d'inhibiteurs de proteine-kinases |
Country Status (29)
| Country | Link |
|---|---|
| US (2) | US7230098B2 (fr) |
| EP (2) | EP1603570B9 (fr) |
| JP (1) | JP4695588B2 (fr) |
| KR (1) | KR101106905B1 (fr) |
| CN (1) | CN103265477B (fr) |
| AP (1) | AP2114A (fr) |
| AU (1) | AU2004215428B2 (fr) |
| BR (1) | BRPI0407827B8 (fr) |
| CA (1) | CA2517256C (fr) |
| CY (2) | CY1113837T1 (fr) |
| DK (2) | DK1603570T5 (fr) |
| EA (1) | EA010727B1 (fr) |
| EC (1) | ECSP055988A (fr) |
| ES (2) | ES2401330T3 (fr) |
| GE (1) | GEP20084341B (fr) |
| HR (1) | HRP20050714B1 (fr) |
| IL (1) | IL170291A (fr) |
| IS (1) | IS2910B (fr) |
| MA (1) | MA27713A1 (fr) |
| ME (1) | MEP52808A (fr) |
| MX (1) | MXPA05009063A (fr) |
| NO (1) | NO332188B1 (fr) |
| NZ (1) | NZ541861A (fr) |
| OA (1) | OA13151A (fr) |
| PL (1) | PL216368B1 (fr) |
| PT (2) | PT2476667E (fr) |
| RS (1) | RS53118B (fr) |
| TN (1) | TNSN05208A1 (fr) |
| WO (1) | WO2004076412A2 (fr) |
Families Citing this family (188)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7230098B2 (en) * | 2003-02-26 | 2007-06-12 | Sugen, Inc. | Aminoheteroaryl compounds as protein kinase inhibitors |
| JP2007523188A (ja) * | 2004-02-23 | 2007-08-16 | スゲン,インコーポレイティド | C−met阻害薬及びm−tor阻害薬を使用する異常な細胞増殖の治療法 |
| CN1906166A (zh) | 2004-02-27 | 2007-01-31 | 卫材株式会社 | 新型吡啶衍生物及嘧啶衍生物(1) |
| MXPA06010520A (es) * | 2004-03-30 | 2007-03-26 | Chiron Corp | Derivados de tiofeno sustituidos como agentes anticancerosos. |
| US8008301B2 (en) | 2004-04-01 | 2011-08-30 | Eli Lilly And Company | Histamine H3 receptor agents, preparation and therapeutic uses |
| JP4777974B2 (ja) * | 2004-04-01 | 2011-09-21 | イーライ リリー アンド カンパニー | ヒスタミンh3受容体作用物質、製剤および治療的使用 |
| BRPI0514553A (pt) | 2004-08-23 | 2008-06-17 | Lilly Co Eli | composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, métodos para inibir o receptor de histamina h3 em um mamìfero, para o tratamento de um distúrbio do sistema nervoso, para o tratamento de obesidade e para o tratamento de um distúrbio ou doença, e, uso de um composto ou um sal do mesmo |
| CA2578066C (fr) * | 2004-08-26 | 2011-10-11 | Pfizer Inc. | Composes d'aminoheteroaryle enantiomeriquement purs utilises comme inhibiteurs de proteine kinase |
| EP1786777A1 (fr) * | 2004-08-26 | 2007-05-23 | Pfizer, Inc. | Composes aminoheteroaryles en tant qu'inhibiteurs des proteines tyrosine kinases |
| RU2007106863A (ru) * | 2004-08-26 | 2008-08-27 | Пфайзер Инк. (US) | Энантиоселективное биопреобразование для получения промежуточных соединений ингибитора белка тирозинкиназы |
| ATE492544T1 (de) * | 2004-08-26 | 2011-01-15 | Pfizer | Pyrazol-substituierte aminoheteroarylverbindungen als proteinkinasehemmer |
| GT200600042A (es) * | 2005-02-10 | 2006-09-27 | Aventis Pharma Inc | Compuestos de bis arilo y heteroarilo sustituido como antagonistas selectivos de 5ht2a |
| CA2599989A1 (fr) * | 2005-03-03 | 2006-09-08 | Sirtris Pharmaceuticals, Inc. | Derives de n-phenylbenzamide en tant qu'agents regulant la sirtuine |
| EP1893212B1 (fr) * | 2005-05-13 | 2013-10-16 | Lexicon Pharmaceuticals, Inc. | Composes polycycliques et procedes pour les utiliser |
| US8088928B2 (en) * | 2005-08-04 | 2012-01-03 | Sirtris Pharmaceuticals, Inc. | Sirtuin modulating compounds |
| CA2617557A1 (fr) | 2005-08-04 | 2007-02-15 | Sirtris Pharmaceuticals, Inc. | Derives de benzimidazole en tant que modulateur du sirtuin |
| US7855289B2 (en) * | 2005-08-04 | 2010-12-21 | Sirtris Pharmaceuticals, Inc. | Sirtuin modulating compounds |
| US8093401B2 (en) * | 2005-08-04 | 2012-01-10 | Sirtris Pharmaceuticals, Inc. | Sirtuin modulating compounds |
| JP4077028B2 (ja) | 2005-08-24 | 2008-04-16 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 新規ピリジン誘導体およびピリミジン誘導体(3) |
| BRPI0619424B1 (pt) * | 2005-12-05 | 2022-02-08 | Pfizer Products Inc | Uso de inibidores c-met/hgfrs para a fabricação de medicamentos |
| KR101146852B1 (ko) * | 2005-12-05 | 2012-05-16 | 화이자 프로덕츠 인크. | C?met/hgfr 억제제의 다형체 |
| PE20070978A1 (es) * | 2006-02-14 | 2007-11-15 | Novartis Ag | COMPUESTOS HETEROCICLICOS COMO INHIBIDORES DE FOSFATIDILINOSITOL 3-QUINASAS (PI3Ks) |
| MX2008011220A (es) | 2006-03-07 | 2008-09-11 | Array Biopharma Inc | Compuestos de pirazol heterobiciclicos y metodos de uso. |
| DE602007004092D1 (de) * | 2006-03-22 | 2010-02-11 | Vertex Pharma | C-met-proteinkinasehemmer zur behandlung proliferativer erkrankungen |
| ES2561406T3 (es) | 2006-04-14 | 2016-02-26 | Cell Signaling Technology, Inc. | Defectos de genes y quinasa ALK mutante en tumores sólidos humanos |
| US8168383B2 (en) | 2006-04-14 | 2012-05-01 | Cell Signaling Technology, Inc. | Gene defects and mutant ALK kinase in human solid tumors |
| US7601716B2 (en) | 2006-05-01 | 2009-10-13 | Cephalon, Inc. | Pyridopyrazines and derivatives thereof as ALK and c-Met inhibitors |
| JP2009538317A (ja) * | 2006-05-26 | 2009-11-05 | バイエル ヘルスケア リミティド ライアビリティ カンパニー | 癌治療のための置換ジアリールウレアを用いた薬物の組み合わせ |
| WO2007146824A2 (fr) * | 2006-06-08 | 2007-12-21 | Array Biopharma Inc. | Quinolines et méthodes d'utilisation |
| EP2057164A1 (fr) | 2006-08-07 | 2009-05-13 | Incyte Corporation | Utilisation de triazolotriazines en tant qu'inhibiteurs des kinases |
| AU2007288793B2 (en) | 2006-08-23 | 2012-04-19 | Eisai R & D Management Co., Ltd. | Salt of phenoxypyridine derivative or crystal thereof and process for producing the same |
| US7790885B2 (en) * | 2006-08-31 | 2010-09-07 | Eisai R&D Management Co., Ltd. | Process for preparing phenoxypyridine derivatives |
| WO2008042867A2 (fr) * | 2006-09-29 | 2008-04-10 | Emiliem Inc. | Modulateurs de kinases multiples |
| MX2009004426A (es) | 2006-10-23 | 2009-08-12 | Cephalon Inc | Derivados biciclicos fusionados de 2,4-diaminopirimidina como inhibidores alk y c-met. |
| GB0621607D0 (en) * | 2006-10-31 | 2006-12-06 | Chroma Therapeutics Ltd | Inhibitors of c-Met |
| EP3443958A1 (fr) | 2006-11-22 | 2019-02-20 | Incyte Holdings Corporation | Imidazotriazines et imidazopyrimidines utilisées en tant qu'inhibiteurs de kinase |
| BRPI0719991A2 (pt) | 2006-12-14 | 2014-03-18 | Bayer Schering Pharma Ag | Derivados de di-hidropiridina úteis como inibidores de proteína cinase |
| JPWO2008087736A1 (ja) * | 2007-01-19 | 2010-05-06 | 宇部興産株式会社 | アラルキルオキシ又はヘテロアラルキルオキシ基を有する芳香族アミンの製法 |
| ES2531002T3 (es) * | 2007-01-19 | 2015-03-09 | Xcovery Inc | Compuestos inhibidores de quinasa |
| AU2008239594B2 (en) | 2007-04-13 | 2013-10-24 | Beth Israel Deaconess Medical Center | Methods for treating cancer resistant to ErbB therapeutics |
| JP5496876B2 (ja) | 2007-04-16 | 2014-05-21 | アッヴィ・インコーポレイテッド | 7−置換されていないインドール系Mcl−1阻害薬 |
| US8263585B2 (en) | 2007-05-04 | 2012-09-11 | Novartis Ag | Organic compounds |
| CL2008001822A1 (es) * | 2007-06-20 | 2009-03-13 | Sirtris Pharmaceuticals Inc | Compuestos derivados de tiazolo[5,4-b]piridina; composicion farmaceutica que comprende a dichos compuestos; y uso del compuesto en el tratamiento de la resistencia a la insulina, sindrome metabolico, diabetes, entre otras. |
| MX2010000617A (es) * | 2007-07-17 | 2010-05-17 | Plexxikon Inc | Compuestos y metodos para modulacion de cinasa, e indicaciones de estos. |
| WO2009013348A2 (fr) * | 2007-07-26 | 2009-01-29 | Novartis Ag | Composés organiques |
| WO2009036404A2 (fr) | 2007-09-13 | 2009-03-19 | Codexis, Inc. | Polypeptides de cétoréductase pour la réduction d'acétophénones |
| EP2215084B1 (fr) * | 2007-10-23 | 2016-09-28 | Allergan, Inc. | Lactames substitués à usage thérapeutique |
| EP2215066A1 (fr) * | 2007-11-01 | 2010-08-11 | Sirtris Pharmaceuticals, Inc. | Dérivés d'amide comme modulateurs de sirtuines |
| CA2705138A1 (fr) * | 2007-11-08 | 2009-05-14 | Sirtris Pharmaceuticals, Inc. | Thiazolopyridines solubilisees |
| JP2009132660A (ja) * | 2007-11-30 | 2009-06-18 | Eisai R & D Management Co Ltd | 食道癌治療用組成物 |
| WO2009073224A1 (fr) * | 2007-12-07 | 2009-06-11 | Ambit Biosciences Corp. | Procédés de traitement de certaines maladies à l'aide de dérivés de la pyrimidine |
| JP2009203226A (ja) * | 2008-01-31 | 2009-09-10 | Eisai R & D Management Co Ltd | ピリジン誘導体およびピリミジン誘導体を含有するレセプターチロシンキナーゼ阻害剤 |
| WO2009096198A1 (fr) * | 2008-02-01 | 2009-08-06 | Pharma Ip Limited Liability Intermediary Corporations | Nouveau derive de biaryle |
| EP2265270A1 (fr) | 2008-02-04 | 2010-12-29 | OSI Pharmaceuticals, Inc. | Inhibiteurs de 2-aminopyridine kinases |
| AR070317A1 (es) * | 2008-02-06 | 2010-03-31 | Osi Pharm Inc | Furo (3,2-c) piridina y tieno (3,2-c) piridinas |
| US20100311972A1 (en) * | 2008-02-18 | 2010-12-09 | Mitsuo Nagai | Method for producing phenoxypyridine derivative |
| US20110092452A1 (en) * | 2008-03-05 | 2011-04-21 | The Regents Of The University Of Michigan | Compositions and methods for diagnosing and treating pancreatic cancer |
| US8268834B2 (en) | 2008-03-19 | 2012-09-18 | Novartis Ag | Pyrazine derivatives that inhibit phosphatidylinositol 3-kinase enzyme |
| FR2928922B1 (fr) | 2008-03-21 | 2010-04-23 | Sanofi Aventis | Derives de 2-aryl-6-phenyl-imidazo°1,2-a!pyridines polysubstitues, leur preparation et leur application en therapeutique |
| FR2928924B1 (fr) | 2008-03-21 | 2010-04-23 | Sanofi Aventis | Derives polysubstitues de 6-heteroaryle-imidazo°1,2-a! pyridines, leur preparation et leur application en therapeutique |
| FR2928923B1 (fr) | 2008-03-21 | 2010-04-23 | Sanofi Aventis | Derives polysubstitues de 2-heteroaryl-6-phenyl-imidazo °1,2-a!pyridines, leur preparation et leur application en therapeutiques |
| US20110039860A1 (en) * | 2008-05-07 | 2011-02-17 | Cangming Yang | Soluble epoxide hydrolase inhibitors, compositions containing such compounds and methods of treatment |
| NZ589622A (en) | 2008-05-21 | 2012-10-26 | Incyte Corp | Salts of 2-fluoro-N-methyl-4-[7-(quinolin-6-yl-methyl)-imidazo[1,2-b][1,2,4]triazin-2-yl]benzamide and processes related to preparing the same |
| ES2670665T3 (es) * | 2008-06-19 | 2018-05-31 | Xcovery Holding Company Llc | Compuestos de piridazina carboxamida sustituidos como compuestos inhibidores de quinasa |
| CA2734172A1 (fr) * | 2008-08-29 | 2010-03-04 | Genentech, Inc. | Diagnostics et traitements de tumeurs independantes du vegf |
| WO2010046780A2 (fr) * | 2008-10-22 | 2010-04-29 | Institut Pasteur Korea | Composés antiviraux |
| AT507187B1 (de) | 2008-10-23 | 2010-03-15 | Helmut Dr Buchberger | Inhalator |
| JP2012509342A (ja) | 2008-11-20 | 2012-04-19 | オーエスアイ・フアーマスーテイカルズ・インコーポレーテツド | 置換ピロロ[2,3−b]−ピリジンおよび−ピラジン |
| EP2375904B1 (fr) * | 2008-12-09 | 2014-05-28 | Merck Sharp & Dohme Corp. | Biaryl carboxamides |
| CN106518856B (zh) | 2008-12-19 | 2020-04-28 | 沃泰克斯药物股份有限公司 | 用作atr激酶抑制剂的化合物 |
| EP2376502B1 (fr) | 2008-12-19 | 2015-06-17 | GlaxoSmithKline LLC | Composés thiazolopyridines de modulation des sirtuines |
| JP2012102018A (ja) * | 2009-03-03 | 2012-05-31 | Astellas Pharma Inc | アミド化合物 |
| TW201100441A (en) * | 2009-06-01 | 2011-01-01 | Osi Pharm Inc | Amino pyrimidine anticancer compounds |
| DE102009056886A1 (de) | 2009-12-03 | 2011-06-09 | Bayer Schering Pharma Aktiengesellschaft | cMet-Inhibitoren zur Behandlung der Endometriose |
| ES2608329T3 (es) | 2010-02-03 | 2017-04-07 | Incyte Holdings Corporation | Imidazo[1,2-b][1,2,4]triazinas como inhibidores de c-Met |
| JP2013525476A (ja) * | 2010-05-04 | 2013-06-20 | ファイザー・インク | Alk阻害剤としての複素環式誘導体 |
| US9062008B2 (en) * | 2010-05-12 | 2015-06-23 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of ATR kinase |
| JP2013526540A (ja) | 2010-05-12 | 2013-06-24 | バーテックス ファーマシューティカルズ インコーポレイテッド | Atrキナーゼ阻害剤として有用な化合物 |
| SG185524A1 (en) | 2010-05-12 | 2012-12-28 | Vertex Pharma | Compounds useful as inhibitors of atr kinase |
| AR081039A1 (es) | 2010-05-14 | 2012-05-30 | Osi Pharmaceuticals Llc | Inhibidores biciclicos fusionados de quinasa |
| EP2569315A1 (fr) | 2010-05-14 | 2013-03-20 | OSI Pharmaceuticals, LLC | Inhibiteurs de kinases bicycliques fusionnés |
| US10010439B2 (en) | 2010-06-13 | 2018-07-03 | Synerz Medical, Inc. | Intragastric device for treating obesity |
| US9526648B2 (en) | 2010-06-13 | 2016-12-27 | Synerz Medical, Inc. | Intragastric device for treating obesity |
| US10420665B2 (en) | 2010-06-13 | 2019-09-24 | W. L. Gore & Associates, Inc. | Intragastric device for treating obesity |
| US8628554B2 (en) | 2010-06-13 | 2014-01-14 | Virender K. Sharma | Intragastric device for treating obesity |
| BR112012032462A2 (pt) | 2010-06-25 | 2016-11-08 | Eisai R&D Man Co Ltd | agente antitumoral empregando compostos que, em combinação, têm efeito inibidor de quinase. |
| WO2012007836A1 (fr) | 2010-07-16 | 2012-01-19 | Purdue Pharma .Lp. | Composés pyridines comme bloqueurs des canaux sodiques |
| WO2012042421A1 (fr) | 2010-09-29 | 2012-04-05 | Pfizer Inc. | Procédé de traitement de la croissance cellulaire anormale |
| EP2625176B1 (fr) | 2010-10-08 | 2016-08-17 | Xcovery Holding Company LLC | Composés substitués de 6-amino-pyridazin-3-yle carboxamide comme modulateurs de protéine kinases |
| PT2646448T (pt) | 2010-11-29 | 2017-10-04 | Osi Pharmaceuticals Llc | Inibidores macrocíclicos de cinases |
| GB201021103D0 (en) * | 2010-12-13 | 2011-01-26 | Univ Leuven Kath | New compounds for the treatment of neurodegenerative diseases |
| AU2012214085B2 (en) | 2011-02-11 | 2015-07-09 | Nicoventures Trading Limited | Inhaler component |
| WO2012116050A2 (fr) * | 2011-02-24 | 2012-08-30 | Eternity Bioscience Inc. | Composés contenant du phosphore en tant qu'inhibiteurs de la protéine kinase |
| US9145390B2 (en) | 2011-03-03 | 2015-09-29 | Concert Pharmaceuticals, Inc. | Derivatives of pyrazole-substituted amino-heteroaryl compounds |
| JO3438B1 (ar) * | 2011-04-13 | 2019-10-20 | Epizyme Inc | مركبات بنزين مستبدلة بأريل أو أريل غير متجانس |
| EP2707373A1 (fr) | 2011-05-10 | 2014-03-19 | Bayer Intellectual Property GmbH | (thio)carbonylamidines bicycliques |
| EP2710003A1 (fr) | 2011-05-16 | 2014-03-26 | OSI Pharmaceuticals, LLC | Inhibiteurs de kinases bicycliques fusionnés |
| US9309250B2 (en) | 2011-06-22 | 2016-04-12 | Vertex Pharmaceuticals Incorporated | Substituted pyrrolo[2,3-b]pyrazines as ATR kinase inhibitors |
| US9226923B2 (en) * | 2011-07-27 | 2016-01-05 | Nanjing Allgen Pharma Co. Ltd. | Spirocyclic molecules as protein kinase inhibitors |
| RU2014102935A (ru) | 2011-08-02 | 2015-09-10 | Пфайзер Инк. | Кризотиниб для применения в лечении рака |
| CA2850566C (fr) | 2011-09-30 | 2022-05-03 | Vertex Pharmaceuticals Incorporated | Procede de fabrication d'un derive de 4-[chloro-n- hydroxycarbonimidoyl]phenyle |
| EP3733185B1 (fr) | 2011-09-30 | 2022-12-07 | Vertex Pharmaceuticals Incorporated | Traitement du cancer du poumon non à petites cellules avec des inhibiteurs de l'atr |
| BR112014022106B1 (pt) | 2012-03-06 | 2022-08-02 | Pfizer Inc | Derivados macrocíclicos, combinação, composição e usos na fabricação de um medicamento para o tratamento de doenças |
| WO2013136170A1 (fr) | 2012-03-16 | 2013-09-19 | Purdue Pharma L.P. | Pyridines substituées en tant que bloqueurs des canaux sodiques |
| EP2833973B1 (fr) | 2012-04-05 | 2017-09-13 | Vertex Pharmaceuticals Incorporated | Composés utiles comme inhibiteurs d'atr kinase et thérapies combinées les utilisant |
| WO2013152252A1 (fr) | 2012-04-06 | 2013-10-10 | OSI Pharmaceuticals, LLC | Polythérapie antinéoplasique |
| IL308807B2 (en) * | 2012-04-13 | 2025-08-01 | Epizyme Inc | Combination therapy for treating cancer |
| CN103387535B (zh) * | 2012-05-10 | 2016-06-01 | 广东东阳光药业有限公司 | 取代的炔基吡啶化合物及其使用方法和用途 |
| WO2013177092A1 (fr) * | 2012-05-23 | 2013-11-28 | Sunshine Lake Pharma Co., Ltd. | Composés d'alcynylpyridine substitués et procédés d'utilisation |
| GB201211310D0 (en) | 2012-06-26 | 2012-08-08 | Chroma Therapeutics Ltd | CSF-1R kinase inhibitors |
| US20150182490A1 (en) | 2012-06-26 | 2015-07-02 | Del Mar Pharmaceuticals | Methods for treating tyrosine-kinase-inhibitor-resistant malignancies in patients with genetic polymorphisms or ahi1 dysregulations or mutations employing dianhydrogalactitol, diacetyldianhydrogalactitol, dibromodulcitol, or analogs or derivatives thereof |
| US9651555B2 (en) | 2012-09-24 | 2017-05-16 | Ventana Medical Systems, Inc. | Method of identifying treatment responsive non-small cell lung cancer using anaplastic lymphoma kinase (ALK) as a marker |
| US8999632B2 (en) | 2012-10-04 | 2015-04-07 | Vertex Pharmaceuticals Incorporated | Method for measuring ATR inhibition mediated increases in DNA damage |
| WO2014081816A1 (fr) * | 2012-11-21 | 2014-05-30 | Concert Pharmaceuticals, Inc. | Dérivés fluorés de composés amino-hétéroaryle substitués par pyrazole |
| DK3418281T3 (da) | 2012-12-07 | 2020-12-07 | Vertex Pharma | Pyrazolo[1,5-a]pyrimidiner, der er anvendelige som inhibitorer af atr-kinase til behandling af cancersygdomme |
| US9714252B2 (en) | 2012-12-20 | 2017-07-25 | Purdue Pharma L.P. | Cyclic sulfonamides as sodium channel blockers |
| RU2015115397A (ru) | 2012-12-21 | 2017-01-25 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Аморфная форма производного хинолина и способ его получения |
| EP2952510B1 (fr) * | 2013-02-02 | 2018-12-26 | Chia Tai Tianqing Pharmaceutical Group Co.,Ltd | Inhibiteur de protéine-kinase de 2-aminopyridine substituée |
| JP2016512815A (ja) | 2013-03-15 | 2016-05-09 | バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated | Atrキナーゼの阻害剤として有用な縮合ピラゾロピリミジン誘導体 |
| KR20160061911A (ko) | 2013-04-08 | 2016-06-01 | 데니스 엠. 브라운 | 최적하 투여된 화학 화합물의 치료 효과 |
| CN105264380B (zh) | 2013-05-14 | 2017-09-05 | 卫材R&D管理有限公司 | 用于预测和评价子宫内膜癌受试者对乐伐替尼化合物响应性的生物标志 |
| WO2015034729A1 (fr) * | 2013-09-05 | 2015-03-12 | Calitor Sciences, Llc | Composés de pyridine substituée et leurs méthodes d'utilisation |
| US20160214961A1 (en) * | 2013-09-10 | 2016-07-28 | Shilpa Medicare Limited | Novel salts of crizotinib and their preparation |
| RU2550346C2 (ru) | 2013-09-26 | 2015-05-10 | Общество с ограниченной ответственностью "Отечественные Фармацевтические Технологии" ООО"ФармТех" | Новые химические соединения (варианты) и их применение для лечения онкологических заболеваний |
| EP3053923B1 (fr) | 2013-09-30 | 2018-04-11 | Korea Research Institute of Chemical Technology | Dérivés de triazolopyrazine en tant qu'inhibiteurs de tyrosine kinase |
| WO2015069922A2 (fr) | 2013-11-06 | 2015-05-14 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Anticorps anti-alk, conjugues, et recepteurs antigeniques chimeriques, et leur utilisation |
| PT3077397T (pt) | 2013-12-06 | 2020-01-22 | Vertex Pharma | Composto de 2-amino-6-fluoro-n-[5-fluoro-piridin-3-il]pirazolo[1,5-a]pirimidin-3-carboxamida útil como inibidor da atr quinase, a sua preparação, diferentes formas sólidas e derivados radiomarcados do mesmo |
| KR20160100329A (ko) | 2013-12-20 | 2016-08-23 | 3-브이 바이오사이언시스, 인코포레이티드 | 지질 합성의 헤테로사이클릭 조절물질 및 이들의 조합물 |
| CN103755627B (zh) * | 2014-01-09 | 2016-02-17 | 定陶县友帮化工有限公司 | 2-氨基-3-羟基-5-氯吡啶的合成方法 |
| TWI672141B (zh) | 2014-02-20 | 2019-09-21 | 美商醫科泰生技 | 投予ros1突變癌細胞之分子 |
| KR20160137599A (ko) | 2014-03-24 | 2016-11-30 | 제넨테크, 인크. | C-met 길항제로의 암 치료 및 이것과 hgf 발현과의 상관관계 |
| US10730866B2 (en) | 2014-04-07 | 2020-08-04 | Purdue Pharma L.P. | Indole derivatives and use thereof |
| EP3137074B1 (fr) * | 2014-04-29 | 2020-08-05 | Emory University | Antagonistes du récepteur ep2 des prostaglandines, dérivés, compositions et utilisations associées |
| WO2015172747A1 (fr) * | 2014-05-16 | 2015-11-19 | Zhaoyin Wang | Molécules spirocycliques servant d'inhibiteurs de mth1 |
| KR102575125B1 (ko) | 2014-06-05 | 2023-09-07 | 버텍스 파마슈티칼스 인코포레이티드 | Atr 키나제의 저해제로서 유용한 2-아미노-6-플루오로-n-[5-플루오로-피리딘-3-일]-피라졸로[1,5-a]피리미딘-3-카복스아미드 화합물의 방사성표지된 유도체, 상기 화합물의 제조 및 이의 다양한 고체 형태 |
| DK3157566T3 (da) | 2014-06-17 | 2019-07-22 | Vertex Pharma | Fremgangsmåde til behandling af cancer under anvendelse af en kombination chk1- og atr-inhibitorer |
| WO2016019909A1 (fr) * | 2014-08-07 | 2016-02-11 | 江苏豪森药业股份有限公司 | Nouvelle forme cristalline de composé anticancéreux, procédé de préparation et utilisation correspondants |
| EP3183248B1 (fr) | 2014-08-21 | 2020-11-11 | Bristol-Myers Squibb Company | Dérivés rattachés de benzamide utilisés comme puissants inhibiteurs de rock |
| LT3524595T (lt) | 2014-08-28 | 2022-09-26 | Eisai R&D Management Co., Ltd. | Aukšto grynumo chinolino darinys ir jo gamybos būdas |
| AU2015333738B2 (en) * | 2014-10-13 | 2020-03-26 | Atrin Pharmaceuticals LLC | Ataxia telengiectasia and Rad3-related (ATR) protein kinase inhibitors |
| GB2535427A (en) | 2014-11-07 | 2016-08-24 | Nicoventures Holdings Ltd | Solution |
| AR102537A1 (es) * | 2014-11-05 | 2017-03-08 | Flexus Biosciences Inc | Agentes inmunomoduladores |
| EP3215150B1 (fr) | 2014-11-07 | 2022-07-20 | The Regents of The University of Michigan | Inhibiteurs de la transcription de gènes médiée par le facteur apparenté à la myocardine et le facteur de réponse sérique (mrtf/srf) et procédés pour les utiliser |
| WO2016089760A1 (fr) | 2014-12-02 | 2016-06-09 | Ignyta, Inc. | Combinaisons pour le traitement du neuroblastome |
| CN107530430A (zh) | 2015-01-13 | 2018-01-02 | 国立大学法人京都大学 | 用于预防和/或治疗肌萎缩性侧索硬化症的药剂 |
| US20180028662A1 (en) | 2015-02-25 | 2018-02-01 | Eisai R&D Management Co., Ltd. | Method for Suppressing Bitterness of Quinoline Derivative |
| MA41598A (fr) * | 2015-02-25 | 2018-01-02 | Constellation Pharmaceuticals Inc | Composés thérapeutiques de pyridazine et leurs utilisations |
| WO2016140717A1 (fr) | 2015-03-04 | 2016-09-09 | Merck Sharp & Dohme Corp. | Association d'un antagoniste de pd-1 et d'un inhibiteur des tyrosines kinases vegfr/fgfr/ret pour traiter le cancer |
| CN107709314A (zh) | 2015-06-11 | 2018-02-16 | 巴斯利尔药物国际股份公司 | 外排泵抑制剂及其治疗性用途 |
| MX373231B (es) | 2015-06-16 | 2020-05-08 | Eisai R&D Man Co Ltd | Agente anticancerigeno. |
| US10405627B2 (en) * | 2015-07-14 | 2019-09-10 | Michael Charles Boland, III | Luggage with fold out table |
| CN108135894B (zh) | 2015-08-20 | 2021-02-19 | 卫材R&D管理有限公司 | 肿瘤治疗剂 |
| MX395066B (es) | 2015-09-30 | 2025-03-24 | Vertex Pharma | Método para tratar cáncer usando una combinación de agentes que dañan el adn e inhibidores de proteína relacionada con ataxia telangiectasia y rad3 (atr). |
| GB2542838B (en) | 2015-10-01 | 2022-01-12 | Nicoventures Trading Ltd | Aerosol provision system |
| JP7061068B2 (ja) | 2015-12-18 | 2022-04-27 | イグナイタ インコーポレイテッド | 癌治療のための併用薬 |
| US11129808B2 (en) | 2016-03-15 | 2021-09-28 | University Of South Florida | PKC-delta-I inhibitor formulations and uses thereof |
| WO2017180723A1 (fr) | 2016-04-12 | 2017-10-19 | Atrin Pharmaceuticals LLC | Inhibiteurs de l'atr (ataxia telangiectasia and rad3 related) et leurs méthodes d'utilisation |
| US10779980B2 (en) | 2016-04-27 | 2020-09-22 | Synerz Medical, Inc. | Intragastric device for treating obesity |
| US10933068B2 (en) * | 2016-05-26 | 2021-03-02 | Sonic Master Limited | Modulators of DUX4 for regulation of muscle function |
| TWI646094B (zh) * | 2016-06-01 | 2019-01-01 | 大陸商貝達藥業股份有限公司 | Crystal form of inhibitory protein kinase active compound and application thereof |
| JP7120549B2 (ja) | 2016-12-15 | 2022-08-17 | 小野薬品工業株式会社 | Trek(twik関連kチャネル)チャネルのアクチベータ |
| CN106866627B (zh) * | 2017-01-24 | 2021-09-14 | 南方医科大学 | 3-(1-(氨基吡啶氧基)乙基)苯甲酰胺衍生物及其合成方法和应用 |
| JP6581320B2 (ja) | 2017-02-08 | 2019-09-25 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 腫瘍治療用医薬組成物 |
| RU2019134940A (ru) | 2017-05-16 | 2021-06-16 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Лечение гепатоцеллюлярной карциномы |
| JP2020527588A (ja) | 2017-07-18 | 2020-09-10 | ニューベイション・バイオ・インコーポレイテッドNuvation Bio Inc. | アデノシンアンタゴニストとしてのヘテロ環式化合物 |
| MX2020000693A (es) | 2017-07-18 | 2020-07-29 | Nuvation Bio Inc | Compuestos de 1,8-naftiridinona, y usos de los mismos. |
| US10398693B2 (en) | 2017-07-19 | 2019-09-03 | Ignyta, Inc. | Pharmaceutical compositions and dosage forms |
| JP7311498B2 (ja) | 2017-10-17 | 2023-07-19 | イグナイタ インコーポレイテッド | 薬学的組成物および剤形 |
| CN107794282B (zh) * | 2017-11-20 | 2020-12-25 | 浙江工业大学 | 一种克唑替尼手性中间体的制备方法及菌株 |
| WO2019154665A1 (fr) * | 2018-02-07 | 2019-08-15 | Basf Se | Nouveaux pyridine carboxamides |
| KR102556742B1 (ko) | 2018-03-15 | 2023-07-18 | 푸지안 하이시 파마슈티칼스 컴퍼니 리미티드 | 키나제 억제제로서의 헤테로아릴 화합물 |
| CN110372664A (zh) * | 2018-04-13 | 2019-10-25 | 华东理工大学 | 选择性jak2抑制剂及其应用 |
| WO2019206049A1 (fr) * | 2018-04-25 | 2019-10-31 | Zhuhai Yufan Biotechnologies Co., Ltd | Inhibiteurs d'hpk1, procédé de préparation et utilisation associés |
| CN110396087A (zh) * | 2018-04-25 | 2019-11-01 | 珠海宇繁生物科技有限责任公司 | Hpk1激酶抑制剂、制备方法及其应用 |
| CN108947895B (zh) * | 2018-08-22 | 2021-09-24 | 肇庆中彩机电技术研发有限公司 | 一种抗癌活性的化合物 |
| JP2022517418A (ja) * | 2019-01-18 | 2022-03-08 | ニューベイション・バイオ・インコーポレイテッド | アデノシンアンタゴニストとしてのヘテロ環式化合物 |
| AU2020208644A1 (en) | 2019-01-18 | 2021-08-26 | Nuvation Bio Inc. | Heterocyclic compounds as adenosine antagonists |
| EP3911324A4 (fr) | 2019-01-18 | 2022-08-17 | Nuvation Bio Inc. | Composés de 1,8-naphthyridinone et leurs utilisations |
| US12240829B2 (en) | 2019-03-20 | 2025-03-04 | Emory University | Prostaglandin receptor EP2 antagonists, derivatives, and uses related thereto |
| KR20220004206A (ko) | 2019-05-14 | 2022-01-11 | 텔리진 엘티디. | 키네이스 억제제로 유용한 치환된 거대고리화합물 |
| KR102426921B1 (ko) | 2019-09-24 | 2022-07-29 | 주식회사 이노보테라퓨틱스 | 헤테로아릴아미도피리딘올 유도체 및 이를 유효성분으로 포함하는 자가면역질환의 예방 또는 치료용 약학적 조성물 |
| CN112552293A (zh) * | 2019-09-25 | 2021-03-26 | 珠海宇繁生物科技有限责任公司 | 一种protac小分子化合物及其应用 |
| KR102344185B1 (ko) * | 2020-02-26 | 2021-12-27 | 계명대학교 산학협력단 | 신규한 Pim 키나아제 억제제 및 이의 용도 |
| CN113493437B (zh) * | 2020-04-03 | 2022-07-26 | 中国药科大学 | 含苯并咪唑结构的化合物及其制备方法和用途 |
| WO2021196655A1 (fr) * | 2020-04-03 | 2021-10-07 | 中国药科大学 | Composé contenant une structure benzimidazole, son procédé de préparation et application de celui-ci |
| WO2023086671A1 (fr) * | 2021-11-15 | 2023-05-19 | The Broad Institute, Inc. | Composés, compositions et méthodes pour induire une activité intracellulaire antimicrobienne et pour prévenir et traiter des infections microbiennes |
| JPWO2024009921A1 (fr) | 2022-07-04 | 2024-01-11 | ||
| KR20250055574A (ko) | 2022-08-30 | 2025-04-24 | 추가이 세이야쿠 가부시키가이샤 | 병용 의약 |
Family Cites Families (71)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4725601A (en) | 1985-06-04 | 1988-02-16 | Fujisawa Pharmaceutical Co., Ltd. | Certain imidazo[1,2-a]pyridines useful in the treatment of ulcers |
| US4966849A (en) | 1985-09-20 | 1990-10-30 | President And Fellows Of Harvard College | CDNA and genes for human angiogenin (angiogenesis factor) and methods of expression |
| US5217999A (en) | 1987-12-24 | 1993-06-08 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Styryl compounds which inhibit EGF receptor protein tyrosine kinase |
| GB8827305D0 (en) | 1988-11-23 | 1988-12-29 | British Bio Technology | Compounds |
| EP0526488B1 (fr) | 1990-04-02 | 1994-11-30 | Pfizer Inc. | Composes d'acide benzylphosphonique utilises comme inhibiteurs de la tyrosine kinase |
| US5302606A (en) | 1990-04-16 | 1994-04-12 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Styryl-substituted pyridyl compounds which inhibit EGF receptor tyrosine kinase |
| EP0584222B1 (fr) | 1991-05-10 | 1997-10-08 | Rhone-Poulenc Rorer International (Holdings) Inc. | Composes aryle et heteroaryle bis monocycliques et/ou bicycliques qui inhibent la tyrosine kinase d'un recepteur du egf et/ou du pdgf |
| CA2108889A1 (fr) | 1991-05-29 | 1992-11-30 | Robert Lee Dow | Inhibiteurs tricycliques et polyhydroxyliques de la tyrosine kinase |
| FI941572A7 (fi) | 1991-10-07 | 1994-05-27 | Oncologix Inc | Anti-erbB-2-monoklonaalisten vasta-aineiden yhdistelmä ja käyttömenete lmä |
| GB9201693D0 (en) | 1992-01-27 | 1992-03-11 | Smithkline Beecham Intercredit | Compounds |
| EP1514934B1 (fr) | 1992-02-06 | 2008-12-31 | Novartis Vaccines and Diagnostics, Inc. | Protéine de liaison biosynthétique pour marqueur de cancer |
| WO1994003427A1 (fr) | 1992-08-06 | 1994-02-17 | Warner-Lambert Company | 2-thioindoles (selenoindoles) et disulfures associes (seleniures) inhibant les tyrosine kinases et presentant des proprietes antitumorales |
| US5330992A (en) | 1992-10-23 | 1994-07-19 | Sterling Winthrop Inc. | 1-cyclopropyl-4-pyridyl-quinolinones |
| DK1975181T3 (da) | 1992-10-28 | 2011-06-06 | Genentech Inc | Anvendelse af vaskulære endothelcelle-vækstfaktor-antagonister |
| US6177401B1 (en) | 1992-11-13 | 2001-01-23 | Max-Planck-Gesellschaft Zur Forderung Der Wissenschaften | Use of organic compounds for the inhibition of Flk-1 mediated vasculogenesis and angiogenesis |
| GB9226855D0 (en) | 1992-12-23 | 1993-02-17 | Erba Carlo Spa | Vinylene-azaindole derivatives and process for their preparation |
| US5455258A (en) | 1993-01-06 | 1995-10-03 | Ciba-Geigy Corporation | Arylsulfonamido-substituted hydroxamic acids |
| US5521190A (en) * | 1993-05-27 | 1996-05-28 | Fmc Corporation | Insecticidal pterdines and 8-deazapteridines |
| JPH07109260A (ja) | 1993-10-12 | 1995-04-25 | Fuji Photo Film Co Ltd | 5−アミノ−2−ニトロピリジン誘導体及び2,5−ジアミノ−3−ヒドロキシピリジン誘導体の製造方法 |
| IL112248A0 (en) | 1994-01-25 | 1995-03-30 | Warner Lambert Co | Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them |
| US5863949A (en) | 1995-03-08 | 1999-01-26 | Pfizer Inc | Arylsulfonylamino hydroxamic acid derivatives |
| US5861510A (en) | 1995-04-20 | 1999-01-19 | Pfizer Inc | Arylsulfonyl hydroxamic acid derivatives as MMP and TNF inhibitors |
| US5747498A (en) | 1996-05-28 | 1998-05-05 | Pfizer Inc. | Alkynyl and azido-substituted 4-anilinoquinazolines |
| US5880141A (en) | 1995-06-07 | 1999-03-09 | Sugen, Inc. | Benzylidene-Z-indoline compounds for the treatment of disease |
| GB9520822D0 (en) | 1995-10-11 | 1995-12-13 | Wellcome Found | Therapeutically active compounds |
| GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
| ATE225343T1 (de) | 1995-12-20 | 2002-10-15 | Hoffmann La Roche | Matrix-metalloprotease inhibitoren |
| KR100489174B1 (ko) | 1996-03-05 | 2005-09-30 | 제네카-파마 소시에떼아노님 | 4-아닐리노퀴나졸린유도체 |
| BR9710362A (pt) | 1996-07-13 | 1999-08-17 | Glaxo Group Ltd | Composto formula-ao farmaceutica utiliza-ao de um composto processos de tratamento de um ser humano ou animal sofrendo de uma mediada por atividade anormal de cinase de proteina tirosina e para a prepara-ao de um composto |
| HRP970371A2 (en) | 1996-07-13 | 1998-08-31 | Kathryn Jane Smith | Heterocyclic compounds |
| EP0912559B1 (fr) | 1996-07-13 | 2002-11-06 | Glaxo Group Limited | Composes heterocycliques condenses en tant qu'inhibiteurs de la proteine tyrosine kinase |
| BR9710381A (pt) | 1996-07-18 | 1999-08-17 | Pfizer | Inibidores de metaloproteases de matriz - base de fosfinato |
| CN1228083A (zh) | 1996-08-23 | 1999-09-08 | 美国辉瑞有限公司 | 芳基磺酰氨基异羟肟酸衍生物 |
| ID18494A (id) | 1996-10-02 | 1998-04-16 | Novartis Ag | Turunan pirazola leburan dan proses pembuatannya |
| WO1998030566A1 (fr) | 1997-01-06 | 1998-07-16 | Pfizer Inc. | Derives de sulfone cyclique |
| TR199901849T2 (xx) | 1997-02-03 | 2000-02-21 | Pfizer Products Inc. | Arils�lfonilamino hidroksamik asit t�revleri. |
| CA2279863A1 (fr) | 1997-02-07 | 1998-08-13 | Pfizer Inc. | Derives du n-hxdroxy-beta-sulfonyl-propionamide et leur utilisation comme inhibiteurs des metalloproteases matrices |
| EA002546B1 (ru) | 1997-02-11 | 2002-06-27 | Пфайзер Инк. | Производные арилсульфонилгидроксамовой кислоты |
| SE9700661D0 (sv) * | 1997-02-25 | 1997-02-25 | Astra Ab | New compounds |
| WO1998050356A1 (fr) | 1997-05-07 | 1998-11-12 | Sugen, Inc. | Derives de 2-indolinone utilises en tant que modulateurs de l'activite de la proteine kinase |
| CA2291709A1 (fr) | 1997-05-30 | 1998-12-03 | Merck & Co., Inc. | Nouveaux inhibiteurs d'angiogenese |
| ES2289791T3 (es) | 1997-08-22 | 2008-02-01 | Astrazeneca Ab | Derivados de oxindolilquinazolina como inhibidores de la angiogenesis. |
| EP1017682A4 (fr) | 1997-09-26 | 2000-11-08 | Merck & Co Inc | Nouveaux inhibiteurs de l'angiogenese |
| HUP0100287A3 (en) | 1997-11-11 | 2003-04-28 | Pfizer Prod Inc | Thienopyrimidine and thienopyridine derivatives useful as anticancer agents |
| GB9725782D0 (en) | 1997-12-05 | 1998-02-04 | Pfizer Ltd | Therapeutic agents |
| GB9800575D0 (en) | 1998-01-12 | 1998-03-11 | Glaxo Group Ltd | Heterocyclic compounds |
| GB9800569D0 (en) | 1998-01-12 | 1998-03-11 | Glaxo Group Ltd | Heterocyclic compounds |
| GB9801690D0 (en) | 1998-01-27 | 1998-03-25 | Pfizer Ltd | Therapeutic agents |
| PA8469501A1 (es) | 1998-04-10 | 2000-09-29 | Pfizer Prod Inc | Hidroxamidas del acido (4-arilsulfonilamino)-tetrahidropiran-4-carboxilico |
| PA8469401A1 (es) | 1998-04-10 | 2000-05-24 | Pfizer Prod Inc | Derivados biciclicos del acido hidroxamico |
| SE9801526D0 (sv) * | 1998-04-29 | 1998-04-29 | Astra Ab | New compounds |
| EP1082305A4 (fr) | 1998-05-29 | 2001-09-26 | Sugen Inc | Inhibiteurs de la proteine kinase 2-indolinone a substitution pyrrole |
| US20010002396A1 (en) * | 1998-07-16 | 2001-05-31 | Charles Achkar | Compositions and methods of treating skin conditions |
| SK11002001A3 (sk) | 1999-02-11 | 2002-05-09 | Pfizer Products Inc. | Heteroarylom substituované chinolin-2-ónové deriváty použiteľné ako protinádorové prostriedky |
| GB9908410D0 (en) | 1999-04-13 | 1999-06-09 | Pfizer Ltd | Pyridines |
| WO2001000213A1 (fr) * | 1999-06-30 | 2001-01-04 | Merck & Co., Inc. | Composes inhibiteurs de la src kinase |
| HN2001000008A (es) * | 2000-01-21 | 2003-12-11 | Inc Agouron Pharmaceuticals | Compuesto de amida y composiciones farmaceuticas para inhibir proteinquinasas, y su modo de empleo |
| MY130363A (en) | 2000-02-15 | 2007-06-29 | Sugen Inc | "pyrrole substituted 2-indolinone protein kinase inhibitors" |
| DK1255740T3 (da) | 2000-02-16 | 2006-02-06 | Neurogen Corp | Substituerede arylpyraziner |
| AU7164201A (en) | 2000-07-07 | 2002-01-21 | Tufts College | 7-substituted tetracycline compounds |
| JP2004523474A (ja) * | 2000-09-20 | 2004-08-05 | オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド | チロシンキナーゼモジュレーターとしてのピラジン誘導体 |
| GB0101577D0 (en) | 2001-01-22 | 2001-03-07 | Smithkline Beecham Plc | Compounds |
| DE60206363T2 (de) * | 2001-02-12 | 2006-07-06 | F. Hoffmann-La Roche Ag | 6-substituierte pyridopyrimidine |
| US6825198B2 (en) * | 2001-06-21 | 2004-11-30 | Pfizer Inc | 5-HT receptor ligands and uses thereof |
| DK1446387T3 (da) | 2001-11-21 | 2009-12-21 | Pharmacia & Upjohn Co Llc | Substituerede aryl, 1,4-pyrazinderivater |
| US7230098B2 (en) * | 2003-02-26 | 2007-06-12 | Sugen, Inc. | Aminoheteroaryl compounds as protein kinase inhibitors |
| CA2578066C (fr) * | 2004-08-26 | 2011-10-11 | Pfizer Inc. | Composes d'aminoheteroaryle enantiomeriquement purs utilises comme inhibiteurs de proteine kinase |
| ATE492544T1 (de) * | 2004-08-26 | 2011-01-15 | Pfizer | Pyrazol-substituierte aminoheteroarylverbindungen als proteinkinasehemmer |
| US20130246300A1 (en) | 2012-03-13 | 2013-09-19 | American Express Travel Related Services Company, Inc. | Systems and Methods for Tailoring Marketing |
| US10884952B2 (en) | 2016-09-30 | 2021-01-05 | Intel Corporation | Enforcing memory operand types using protection keys |
| JP6943759B2 (ja) | 2017-12-28 | 2021-10-06 | 株式会社東海理化電機製作所 | シフト装置 |
-
2004
- 2004-02-26 US US10/786,610 patent/US7230098B2/en not_active Expired - Lifetime
- 2004-02-26 KR KR1020057015999A patent/KR101106905B1/ko not_active Expired - Lifetime
- 2004-02-26 CN CN201310167961.7A patent/CN103265477B/zh not_active Expired - Lifetime
- 2004-02-26 JP JP2006503845A patent/JP4695588B2/ja not_active Expired - Lifetime
- 2004-02-26 BR BRPI0407827A patent/BRPI0407827B8/pt not_active IP Right Cessation
- 2004-02-26 AU AU2004215428A patent/AU2004215428B2/en active Active
- 2004-02-26 PT PT121638555T patent/PT2476667E/pt unknown
- 2004-02-26 PT PT47150016T patent/PT1603570E/pt unknown
- 2004-02-26 EP EP04715001.6A patent/EP1603570B9/fr not_active Expired - Lifetime
- 2004-02-26 MX MXPA05009063A patent/MXPA05009063A/es active IP Right Grant
- 2004-02-26 ES ES04715001T patent/ES2401330T3/es not_active Expired - Lifetime
- 2004-02-26 OA OA1200500243A patent/OA13151A/en unknown
- 2004-02-26 DK DK04715001.6T patent/DK1603570T5/da active
- 2004-02-26 NZ NZ541861A patent/NZ541861A/en not_active IP Right Cessation
- 2004-02-26 ES ES12163855.5T patent/ES2502490T3/es not_active Expired - Lifetime
- 2004-02-26 PL PL378759A patent/PL216368B1/pl unknown
- 2004-02-26 AP AP2005003383A patent/AP2114A/xx active
- 2004-02-26 GE GEAP20048993A patent/GEP20084341B/en unknown
- 2004-02-26 CA CA2517256A patent/CA2517256C/fr not_active Expired - Lifetime
- 2004-02-26 DK DK12163855.5T patent/DK2476667T3/da active
- 2004-02-26 EA EA200501236A patent/EA010727B1/ru active Protection Beyond IP Right Term
- 2004-02-26 EP EP12163855.5A patent/EP2476667B1/fr not_active Expired - Lifetime
- 2004-02-26 WO PCT/US2004/005495 patent/WO2004076412A2/fr not_active Ceased
- 2004-02-26 HR HRP20050714AA patent/HRP20050714B1/hr not_active IP Right Cessation
- 2004-02-26 RS YU20050708A patent/RS53118B/sr unknown
- 2004-02-26 ME MEP-528/08A patent/MEP52808A/xx unknown
-
2005
- 2005-08-15 IL IL170291A patent/IL170291A/en active Protection Beyond IP Right Term
- 2005-08-18 IS IS7990A patent/IS2910B/is unknown
- 2005-08-26 EC EC2005005988A patent/ECSP055988A/es unknown
- 2005-08-26 MA MA28457A patent/MA27713A1/fr unknown
- 2005-08-26 TN TNP2005000208A patent/TNSN05208A1/fr unknown
- 2005-09-01 NO NO20054080A patent/NO332188B1/no unknown
-
2006
- 2006-11-14 US US11/598,765 patent/US8106197B2/en active Active
-
2013
- 2013-03-19 CY CY20131100229T patent/CY1113837T1/el unknown
-
2014
- 2014-08-20 CY CY20141100664T patent/CY1115472T1/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA27713A1 (fr) | Composes aminoheteroaryliques servant d'inhibiteurs de proteine-kinases | |
| MA29141B1 (fr) | Pyrrolopyrazoles, servant de puissants inhibiteurs de kinases | |
| NO20070557L (no) | Ftalazinderivater som PARP-inhibitorer | |
| NO20070526L (no) | Kinazolindionderivater som parp-inhibitorer | |
| NO20070555L (no) | Kinazolinonderivater som parp-inhibitorer | |
| DE59812455D1 (de) | Fluorpyrazol-biphenylamide als fungizide | |
| EP1675552A4 (fr) | Preparation d'azabenzimidazoles 1,6-disubstitues comme inhibiteurs de kinases | |
| NO20034289L (no) | N-(2-aryletyl)benzylaminer som antagonister av 5-HT6- reseptoren | |
| WO2004063151A3 (fr) | Nouveaux inhibiteurs de tyrosine kinase | |
| MXPA05013076A (es) | Compuestos de isoindolina-1-ona como inhibidores de cinasa. | |
| MXPA03004549A (es) | Derivados de 3-arilindola y su uso como agonistas del receptor cb2. | |
| WO2006050109A3 (fr) | Nouveaux inhibiteurs de kinase | |
| MA27467A1 (fr) | Quinolones anti-microbiens, leurs compositions et utilisations | |
| TW200640880A (en) | Quinazoline derivatives having a tyrosine kinase inhibitory activity | |
| MA27991A1 (fr) | Derives d'aminoquinoline et leur utilisation comme ligands d'adenosine a3 | |
| DK1165544T3 (da) | Substituerede 1,4-dihydroindeno[1,2-c]pyrazoler som inhibitorer af tyrosinkinase | |
| TNSN03090A1 (fr) | Derives d'ethers phenyliques d'heterocyclyle servant d' inhibiteurs selectifs de reabsorption de serotonine | |
| DE60314381D1 (de) | Benzylimidazolyl substituierte 2-chinolon und chinazolinon derivate zur verwendung als farnesyl transferase inhibitoren | |
| UA80474C2 (en) | Aminoheteroaryl compounds as inhibitors of protein kinase | |
| TW200607808A (en) | Pyrido-pyrimidine derivatives, preparation thereof and application thereof | |
| ATE332695T1 (de) | Pyrimidin-derivate als selektive inhibitoren von cox-2 | |
| ATE274515T1 (de) | Pyrazolopyridinderivate | |
| PT1351954E (pt) | Derivados 4-heterociclil-quinolina e quinazolina inibidores da farnesil-transferase | |
| TNSN08274A1 (fr) | Carbonylaminopyrrolopyrazoles servant de puissants inhibiteurs de kinases | |
| SI1651596T1 (sl) | Novi derivati ditiobis aminobutan sulfonatov in sestavki ki jih vsebujejo |