ECSP055560A - Compuestos heteroaromáticos bicíclicos arilamina sustituidos como inhibidores de la quinasa p38 - Google Patents
Compuestos heteroaromáticos bicíclicos arilamina sustituidos como inhibidores de la quinasa p38Info
- Publication number
- ECSP055560A ECSP055560A EC2005005560A ECSP055560A ECSP055560A EC SP055560 A ECSP055560 A EC SP055560A EC 2005005560 A EC2005005560 A EC 2005005560A EC SP055560 A ECSP055560 A EC SP055560A EC SP055560 A ECSP055560 A EC SP055560A
- Authority
- EC
- Ecuador
- Prior art keywords
- group
- atom
- optionally substituted
- inhibitors
- bilyclic
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 150000002390 heteroarenes Chemical class 0.000 title 1
- 125000004429 atom Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 150000002829 nitrogen Chemical class 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 101100490437 Mus musculus Acvrl1 gene Proteins 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 229910052799 carbon Chemical class 0.000 abstract 1
- 125000004432 carbon atom Chemical class C* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 208000026278 immune system disease Diseases 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 102000002574 p38 Mitogen-Activated Protein Kinases Human genes 0.000 abstract 1
- 230000003389 potentiating effect Effects 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 238000011282 treatment Methods 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- 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
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- A—HUMAN NECESSITIES
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- A61P11/06—Antiasthmatics
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- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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- A—HUMAN NECESSITIES
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- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- A—HUMAN NECESSITIES
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- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
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- A61P31/22—Antivirals for DNA viruses for herpes viruses
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- A—HUMAN NECESSITIES
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- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
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- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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- 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
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
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- 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
- A61P37/08—Antiallergic agents
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P7/06—Antianaemics
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- 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
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Physical Education & Sports Medicine (AREA)
- Virology (AREA)
- Neurology (AREA)
- Hematology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Pulmonology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Molecular Biology (AREA)
- Psychology (AREA)
- Psychiatry (AREA)
- Cardiology (AREA)
- Pain & Pain Management (AREA)
- Obesity (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Vascular Medicine (AREA)
- Endocrinology (AREA)
Abstract
Se describen derivados heteroaromáticos bicíclicos de fórmula (1): donde:la línea discontinua que une a A y C(Ra) está presente y representa un enlace yA es un átomo -N= o un grupo -C(Rb)=, o la línea discontinua está ausente y A es un grupo -N(Rb)-, o -C(Rb)(Rc)-;X es un átomo de -O-, -S- o de nitrógeno sustituido o un grupo -S(O)-, -S(O2)- o -NH-;Y es un átomo de nitrógeno o de carbono sustituido o un grupo -CH=;n es cero o el número entero 1;Alk1 es una cadena alifática o heteroalifática opcionalmente sustituidaL1 es un enlace covalente o un átomo o grupo de unión;Cy1 es un átomo de hidrógeno o un grupo cicloalifático, policicloalifático, heterocicloalifático, poliheterocicloalifático, aromático o heteroaromático opcionalmente sustituido;Ar es un grupo aromático o heteroaromático opcionalmente sustituido; y los sustituyentes restantes fueron definidos en la especificación.Los compuestos son inhibidores selectivos y potentes de la quinasa p38 y son útiles en la profilaxis y el tratamiento de los trastornos inmunitarios o inflamatorios.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0214268.5A GB0214268D0 (en) | 2002-06-20 | 2002-06-20 | Chemical compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP055560A true ECSP055560A (es) | 2005-05-30 |
Family
ID=9938990
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EC2005005560A ECSP055560A (es) | 2002-06-20 | 2005-01-20 | Compuestos heteroaromáticos bicíclicos arilamina sustituidos como inhibidores de la quinasa p38 |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US7423047B2 (es) |
| EP (1) | EP1551848A1 (es) |
| JP (1) | JP2005530838A (es) |
| KR (1) | KR20060013331A (es) |
| CN (1) | CN100390179C (es) |
| AU (1) | AU2003253087B2 (es) |
| BR (1) | BR0311842A (es) |
| CA (1) | CA2487718A1 (es) |
| EA (1) | EA008410B1 (es) |
| EC (1) | ECSP055560A (es) |
| GB (1) | GB0214268D0 (es) |
| IS (1) | IS7652A (es) |
| MX (1) | MXPA04012746A (es) |
| NO (1) | NO20050306L (es) |
| NZ (1) | NZ537740A (es) |
| PL (1) | PL375083A1 (es) |
| UA (1) | UA78578C2 (es) |
| WO (1) | WO2004000846A1 (es) |
| ZA (1) | ZA200500524B (es) |
Families Citing this family (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0214268D0 (en) * | 2002-06-20 | 2002-07-31 | Celltech R&D Ltd | Chemical compounds |
| GB0218800D0 (en) * | 2002-08-13 | 2002-09-18 | Celltech R&D Ltd | Chemical compounds |
| AU2004249495A1 (en) | 2003-06-20 | 2004-12-29 | Ucb Pharma S.A. | Thienopyridone derivatives as kinase inhibitors |
| DE602004017609D1 (de) * | 2003-06-20 | 2008-12-18 | Ucb Pharma Sa | Verfahren zur herstellung von 3-aminothienopyridon-derivaten |
| CA2528603A1 (en) * | 2003-06-20 | 2004-12-29 | Celltech R & D Limited | Thienopyridone derivatives as kinase inhibitors |
| WO2005042540A1 (en) * | 2003-10-24 | 2005-05-12 | Celltech R & D Limited | Thieno-pyridinone derivatives as kinase inhibitors |
| WO2006056412A1 (en) * | 2004-11-24 | 2006-06-01 | Ucb Pharma, S.A. | Process for pd-catalysed c-n coupling in specific solvent systems |
| AP2007004244A0 (en) | 2005-05-10 | 2007-12-31 | Intermune Inc | Method of modulating stress-activated protein kinase system |
| AU2006284751A1 (en) * | 2005-09-01 | 2007-03-08 | Array Biopharma Inc. | Raf inhibitor compounds and methods of use thereof |
| NZ567140A (en) * | 2005-10-07 | 2011-09-30 | Exelixis Inc | Azetidines as MEK inhibitors for the treatment of proliferative diseases |
| US20110034495A1 (en) * | 2005-11-23 | 2011-02-10 | Intermune, Inc. | Method of Modulating Stress-Activated Protein Kinase System |
| GB0601962D0 (en) | 2006-01-31 | 2006-03-15 | Ucb Sa | Therapeutic agents |
| AR059898A1 (es) | 2006-03-15 | 2008-05-07 | Janssen Pharmaceutica Nv | Derivados de 3-ciano-piridona 1,4-disustituida y su uso como moduladores alostericos de los receptores mglur2 |
| US20090192164A1 (en) * | 2006-06-28 | 2009-07-30 | Aska Pharmaceutical Co., Ltd. | Treating agent of inflammatory bowel disease |
| WO2008024724A1 (en) * | 2006-08-21 | 2008-02-28 | Genentech, Inc. | Aza-benzothiophenyl compounds and methods of use |
| ZA200901009B (en) * | 2006-08-21 | 2010-05-26 | Genentech Inc | Aza-benzothiophenyl compounds and methods of use |
| WO2008064829A2 (en) * | 2006-11-30 | 2008-06-05 | Ucb Pharma, S.A. | Novel aminothienopyridinone derivatives processes for preparing them and pharmaceutical compositions thereof |
| US20100093777A1 (en) | 2007-01-25 | 2010-04-15 | Takeda Pharmaceutical Company Limited | Spiro-ring compound |
| KR101434706B1 (ko) * | 2007-02-16 | 2014-08-26 | 아스카 세이야쿠 가부시키가이샤 | 미립자 유성 현탁액을 포함하는 의약 조성물 |
| EP2123652A1 (en) | 2007-02-20 | 2009-11-25 | Takeda Pharmaceutical Company Limited | Heterocyclic compound |
| 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 |
| GB0714384D0 (en) | 2007-07-23 | 2007-09-05 | Ucb Pharma Sa | theraputic agents |
| EA017648B1 (ru) | 2007-09-14 | 2013-02-28 | Орто-Макнейл-Янссен Фармасьютикалз, Инк. | 1',3'-двузамещенные-4-фенил-3,4,5,6-тетрагидро-2н,1'н-[1,4']бипириди-нил-2'-оны |
| WO2009093008A1 (en) | 2008-01-21 | 2009-07-30 | Ucb Pharma S.A. | Thieno-pyridine derivatives as mek inhibitors |
| US8980210B2 (en) * | 2008-01-28 | 2015-03-17 | Battelle Memorial Institute | Capture and release of acid-gasses with acid-gas binding organic compounds |
| US7799299B2 (en) * | 2008-01-28 | 2010-09-21 | Batelle Memorial Institute | Capture and release of mixed acid gasses with binding organic liquids |
| KR101630466B1 (ko) * | 2008-04-11 | 2016-06-14 | 메르크 파텐트 게엠베하 | Amp-활성화 단백질 키나아제(ampk) 활성화제로서의 티에노피리돈 유도체 |
| EP2296653B1 (en) | 2008-06-03 | 2016-01-27 | Intermune, Inc. | Compounds and methods for treating inflammatory and fibrotic disorders |
| GB0811304D0 (en) | 2008-06-19 | 2008-07-30 | Ucb Pharma Sa | Therapeutic agents |
| JP5547194B2 (ja) | 2008-09-02 | 2014-07-09 | ジャンセン ファーマシューティカルズ, インコーポレイテッド. | 代謝型グルタミン酸受容体の調節因子としての3−アザビシクロ[3.1.0]ヘキシル誘導体 |
| WO2010043396A1 (en) | 2008-10-16 | 2010-04-22 | Ortho-Mcneil-Janssen Pharmaceuticals, Inc. | Indole and benzomorpholine derivatives as modulators of metabotropic glutamate receptors |
| JP5690277B2 (ja) | 2008-11-28 | 2015-03-25 | ジャンセン ファーマシューティカルズ, インコーポレイテッド. | 代謝型グルタミン酸受容体の調節因子としてのインドールおよびベンゾオキサジン誘導体 |
| HRP20131122T1 (hr) | 2009-05-12 | 2013-12-20 | Janssen Pharmaceuticals, Inc. | Derivati 1,2,4-triazolo[4,3-a] piridina i njihova uporaba u lijeäśenju ili prevenciji neuroloških i psihijatrijskih poremeä†aja |
| CN102439015B (zh) | 2009-05-12 | 2015-05-13 | 杨森制药有限公司 | 1,2,4-三唑并[4,3-a]吡啶衍生物和其作为mGluR2受体的正向变构调节剂的用途 |
| 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 |
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| US3935222A (en) * | 1975-04-16 | 1976-01-27 | E. R. Squibb & Sons, Inc. | 1,4,5,7-Tetrahydropyrazolo[3,4-b]pyridin-6-ones |
| US6048863A (en) | 1994-04-19 | 2000-04-11 | Takeda Chemical Industries, Ltd. | Condensed-ring thiophene derivatives and thienopyrimidine derivatives, their production and use |
| GB9614718D0 (en) * | 1996-07-12 | 1996-09-04 | Bayer Ag | 3-ureido-pyridofurans and -pyridothiophenes |
| MY132496A (en) * | 1998-05-11 | 2007-10-31 | Vertex Pharma | Inhibitors of p38 |
| AU4429799A (en) * | 1998-06-12 | 1999-12-30 | Vertex Pharmaceuticals Incorporated | Inhibitors of p38 |
| AR030053A1 (es) * | 2000-03-02 | 2003-08-13 | Smithkline Beecham Corp | 1h-pirimido [4,5-d] pirimidin-2-onas y sales, composiciones farmaceuticas, uso para la fabricacion de un medicamento y procedimiento para producirlas |
| DE60139506D1 (de) * | 2000-12-28 | 2009-09-17 | Shionogi & Co | 2-pyridonderivate mit affinität für den cannabinoid-typ-2-rezeptor |
| GB0124848D0 (en) | 2001-10-16 | 2001-12-05 | Celltech R&D Ltd | Chemical compounds |
| US6974870B2 (en) * | 2002-06-06 | 2005-12-13 | Boehringer Ingelheim Phamaceuticals, Inc. | Substituted 3-amino-thieno [2,3-b]pyridine-2-carboxylic acid amide compounds and processes for preparing and their uses |
| BR0311605A (pt) * | 2002-06-06 | 2005-02-22 | Boehringer Ingelheim Pharma | Compostos de amida de ácido 3-aminotieno[2,3-b]piridina-2-carboxìlico substituìdo e processos para preparação e seus usos |
| GB0214268D0 (en) | 2002-06-20 | 2002-07-31 | Celltech R&D Ltd | Chemical compounds |
| GB0218800D0 (en) * | 2002-08-13 | 2002-09-18 | Celltech R&D Ltd | Chemical compounds |
| AU2004249495A1 (en) * | 2003-06-20 | 2004-12-29 | Ucb Pharma S.A. | Thienopyridone derivatives as kinase inhibitors |
-
2002
- 2002-06-20 GB GBGB0214268.5A patent/GB0214268D0/en not_active Ceased
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2003
- 2003-06-20 NZ NZ537740A patent/NZ537740A/xx unknown
- 2003-06-20 BR BR0311842-8A patent/BR0311842A/pt not_active IP Right Cessation
- 2003-06-20 EA EA200500042A patent/EA008410B1/ru not_active IP Right Cessation
- 2003-06-20 JP JP2004515043A patent/JP2005530838A/ja active Pending
- 2003-06-20 CN CNB038183714A patent/CN100390179C/zh not_active Expired - Fee Related
- 2003-06-20 CA CA002487718A patent/CA2487718A1/en not_active Abandoned
- 2003-06-20 KR KR1020047020770A patent/KR20060013331A/ko not_active Ceased
- 2003-06-20 WO PCT/GB2003/002667 patent/WO2004000846A1/en not_active Ceased
- 2003-06-20 US US10/518,725 patent/US7423047B2/en not_active Expired - Fee Related
- 2003-06-20 AU AU2003253087A patent/AU2003253087B2/en not_active Ceased
- 2003-06-20 EP EP03760802A patent/EP1551848A1/en not_active Withdrawn
- 2003-06-20 PL PL03375083A patent/PL375083A1/xx not_active Application Discontinuation
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- 2003-06-20 UA UAA200500509A patent/UA78578C2/uk unknown
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2005
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- 2005-01-19 ZA ZA200500524A patent/ZA200500524B/xx unknown
- 2005-01-20 EC EC2005005560A patent/ECSP055560A/es unknown
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2008
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| Publication number | Publication date |
|---|---|
| MXPA04012746A (es) | 2005-03-23 |
| US20060004025A1 (en) | 2006-01-05 |
| PL375083A1 (en) | 2005-11-14 |
| BR0311842A (pt) | 2005-03-15 |
| US7423047B2 (en) | 2008-09-09 |
| NO20050306L (no) | 2005-03-16 |
| EP1551848A1 (en) | 2005-07-13 |
| CN1671715A (zh) | 2005-09-21 |
| NZ537740A (en) | 2006-03-31 |
| EA008410B1 (ru) | 2007-04-27 |
| GB0214268D0 (en) | 2002-07-31 |
| EA200500042A1 (ru) | 2005-08-25 |
| WO2004000846A1 (en) | 2003-12-31 |
| US20090042877A1 (en) | 2009-02-12 |
| AU2003253087A1 (en) | 2004-01-06 |
| CN100390179C (zh) | 2008-05-28 |
| ZA200500524B (en) | 2006-08-30 |
| UA78578C2 (en) | 2007-04-10 |
| IS7652A (is) | 2005-01-18 |
| KR20060013331A (ko) | 2006-02-09 |
| CA2487718A1 (en) | 2003-12-31 |
| US7763729B2 (en) | 2010-07-27 |
| JP2005530838A (ja) | 2005-10-13 |
| AU2003253087B2 (en) | 2008-10-16 |
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