MX2007014619A - Pirrolopiridinas de utilidad como inhibidores de proteina quinasa. - Google Patents
Pirrolopiridinas de utilidad como inhibidores de proteina quinasa.Info
- Publication number
- MX2007014619A MX2007014619A MX2007014619A MX2007014619A MX2007014619A MX 2007014619 A MX2007014619 A MX 2007014619A MX 2007014619 A MX2007014619 A MX 2007014619A MX 2007014619 A MX2007014619 A MX 2007014619A MX 2007014619 A MX2007014619 A MX 2007014619A
- Authority
- MX
- Mexico
- Prior art keywords
- sup
- inhibitors
- protein kinase
- useful
- pyrrolopyridines
- Prior art date
Links
- 102000001253 Protein Kinase Human genes 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 108060006633 protein kinase Proteins 0.000 title abstract 2
- 150000005255 pyrrolopyridines Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 102000042838 JAK family Human genes 0.000 abstract 1
- 108091082332 JAK family Proteins 0.000 abstract 1
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
- 239000011435 rock Substances 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
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- 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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- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
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- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P9/00—Drugs for disorders of the cardiovascular system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Pulmonology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Oncology (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Cardiology (AREA)
- Virology (AREA)
- Heart & Thoracic Surgery (AREA)
- Communicable Diseases (AREA)
- Psychiatry (AREA)
- Reproductive Health (AREA)
- Gynecology & Obstetrics (AREA)
- Dermatology (AREA)
- Psychology (AREA)
- Hematology (AREA)
- Vascular Medicine (AREA)
- Transplantation (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
Abstract
La presente invención se relaciona con compuestos de la fórmula (I) en donde Q, Z, R1, R2 y R3 son como se describe en la reivindicación 1 útiles como inhibidores de proteínas cinasas, en particular las cinasas de la familia JAK y la familia ROCK. La invención también proporciona las composiciones farmacéuticamente aceptables que comprenden los compuestos y métodos para utilizar las composiciones en el tratamiento de diversas enfermedades, condiciones, o trastornos.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US68355405P | 2005-05-20 | 2005-05-20 | |
PCT/US2006/019711 WO2006127587A1 (en) | 2005-05-20 | 2006-05-22 | Pyrrolopyridines useful as inhibitors of protein kinase |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2007014619A true MX2007014619A (es) | 2009-02-13 |
Family
ID=36940144
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2007014619A MX2007014619A (es) | 2005-05-20 | 2006-05-22 | Pirrolopiridinas de utilidad como inhibidores de proteina quinasa. |
Country Status (16)
Country | Link |
---|---|
US (1) | US8921376B2 (es) |
EP (3) | EP1881983B1 (es) |
JP (3) | JP2008545660A (es) |
KR (1) | KR20080016659A (es) |
CN (1) | CN101228161B (es) |
AT (1) | ATE540948T1 (es) |
AU (1) | AU2006251623A1 (es) |
CA (1) | CA2609126A1 (es) |
ES (1) | ES2380795T3 (es) |
IL (1) | IL187438A0 (es) |
MX (1) | MX2007014619A (es) |
NO (1) | NO20076502L (es) |
NZ (1) | NZ564065A (es) |
RU (2) | RU2435769C2 (es) |
WO (1) | WO2006127587A1 (es) |
ZA (1) | ZA200710379B (es) |
Families Citing this family (169)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2527118T3 (es) | 2003-12-19 | 2015-01-20 | Plexxikon Inc. | Compuestos y procedimientos de desarrollo de moduladores de Ret |
NZ549880A (en) | 2004-03-30 | 2010-04-30 | Vertex Pharma | Azaindoles useful as inhibitors of JAK and other protein kinases |
US7498342B2 (en) | 2004-06-17 | 2009-03-03 | Plexxikon, Inc. | Compounds modulating c-kit activity |
NZ563444A (en) | 2005-05-17 | 2011-04-29 | Plexxikon Inc | Pyrrolo(2,3-b)pyridine derivatives as protein kinase inhibitors |
WO2006127587A1 (en) * | 2005-05-20 | 2006-11-30 | Vertex Pharmaceuticals Incorporated | Pyrrolopyridines useful as inhibitors of protein kinase |
KR101125919B1 (ko) | 2005-06-22 | 2012-06-12 | 플렉시콘, 인코퍼레이티드 | 단백질 키나제 억제제로서의 피롤로[2,3-b]피리딘 유도체 |
WO2007007919A2 (en) | 2005-07-14 | 2007-01-18 | Astellas Pharma Inc. | Heterocyclic janus kinase 3 inhibitors |
EP2251341A1 (en) * | 2005-07-14 | 2010-11-17 | Astellas Pharma Inc. | Heterocyclic Janus kinase 3 inhibitors |
EP2270014A1 (en) | 2005-09-22 | 2011-01-05 | Incyte Corporation | Azepine inhibitors of janus kinases |
WO2007070514A1 (en) * | 2005-12-13 | 2007-06-21 | Incyte Corporation | Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as janus kinase inhibitors |
AU2015201850B2 (en) * | 2005-12-13 | 2017-03-02 | Incyte Holdings Corporation | Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as Janus kinase inhibitors |
EP1968568A4 (en) * | 2005-12-22 | 2011-04-13 | Glaxosmithkline Llc | HEMMER OF NUTS ACTIVITY |
WO2007084557A2 (en) | 2006-01-17 | 2007-07-26 | Vertex Pharmaceuticals Incorporated | Azaindoles useful as inhibitors of janus kinases |
KR101081293B1 (ko) * | 2006-01-18 | 2011-11-08 | 에프. 호프만-라 로슈 아게 | 11 베타-에이치에스디1 억제제로서 티아졸 |
WO2007084667A2 (en) * | 2006-01-19 | 2007-07-26 | Osi Pharmaceutical, Inc. | Fused heterobicyclic kinase inhibitors |
JP2009532475A (ja) * | 2006-04-05 | 2009-09-10 | 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 | ヤヌスキナーゼの阻害剤として有用なデアザプリン |
WO2007136790A2 (en) * | 2006-05-18 | 2007-11-29 | Mannkind Corporation | Intracellular kinase inhibitors |
US8063050B2 (en) | 2006-07-06 | 2011-11-22 | Array Biopharma Inc. | Hydroxylated and methoxylated pyrimidyl cyclopentanes as AKT protein kinase inhibitors |
KR20150041164A (ko) * | 2006-07-06 | 2015-04-15 | 어레이 바이오파마 인크. | Akt 단백질 키나제 억제제로서의 시클로펜타〔d〕피리미딘 |
CN101516891B (zh) | 2006-07-06 | 2013-06-05 | 阵列生物制药公司 | 作为akt蛋白激酶抑制剂的二氢噻吩并嘧啶 |
EP2049546B1 (en) | 2006-07-06 | 2010-12-29 | Array Biopharma, Inc. | Dihydrofuro pyrimidines as akt protein kinase inhibitors |
US8148361B2 (en) * | 2006-11-10 | 2012-04-03 | Bristol-Myers Squibb Company | Kinase inhibitors |
WO2008063888A2 (en) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Compounds modulating c-fms and/or c-kit activity and uses therefor |
US8071779B2 (en) | 2006-12-18 | 2011-12-06 | Inspire Pharmaceuticals, Inc. | Cytoskeletal active rho kinase inhibitor compounds, composition and use |
WO2008079909A1 (en) | 2006-12-21 | 2008-07-03 | Plexxikon, Inc. | Pyrrolo [2,3-b] pyridines as kinase modulators |
AU2007338754A1 (en) | 2006-12-21 | 2008-07-03 | Vertex Pharmaceuticals Incorporated | 5-cyan0-4- (pyrrolo [2, 3B] pyridine-3-yl) -pyrimidine derivatives useful as protein kinase inhibitors |
CA2673736A1 (en) | 2006-12-21 | 2008-07-03 | Plexxikon, Inc. | Compounds and methods for kinase modulation, and indications therefor |
PE20121126A1 (es) | 2006-12-21 | 2012-08-24 | Plexxikon Inc | Compuestos pirrolo [2,3-b] piridinas como moduladores de quinasa |
US8513270B2 (en) | 2006-12-22 | 2013-08-20 | Incyte Corporation | Substituted heterocycles as Janus kinase inhibitors |
CN101578285A (zh) | 2007-01-12 | 2009-11-11 | 安斯泰来制药株式会社 | 稠合吡啶化合物 |
KR20090129488A (ko) | 2007-03-22 | 2009-12-16 | 버텍스 파마슈티칼스 인코포레이티드 | 야누스 키나아제의 억제제로서 유용한 n-헤테로사이클릭 화합물 |
JP5603770B2 (ja) | 2007-05-31 | 2014-10-08 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Ccr2受容体拮抗薬およびその使用 |
GB0710528D0 (en) * | 2007-06-01 | 2007-07-11 | Glaxo Group Ltd | Novel compounds |
SI3070090T1 (sl) | 2007-06-13 | 2019-04-30 | Incyte Holdings Corporation | Uporaba soli zaviralca Janus kinaze (R)-3-(4-(7H-pirolo (2,3-D)pirimidin-4-il)-1H-pirazol-1-il)-3-ciklopentilpropannitrila |
CL2008001709A1 (es) | 2007-06-13 | 2008-11-03 | Incyte Corp | Compuestos derivados de pirrolo [2,3-b]pirimidina, moduladores de quinasas jak; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como cancer, psoriasis, artritis reumatoide, entre otras. |
CN103396409B (zh) | 2007-07-05 | 2015-03-11 | 阵列生物制药公司 | 作为akt蛋白激酶抑制剂的嘧啶基环戊烷 |
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EP2170830B1 (en) | 2007-07-17 | 2014-10-15 | Plexxikon, Inc. | 2-FLUORO-BENZENESULFONAMIDE COMPOUNDS AS Raf KINASE MODULATORS |
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-
2006
- 2006-05-22 WO PCT/US2006/019711 patent/WO2006127587A1/en active Application Filing
- 2006-05-22 EP EP06770824A patent/EP1881983B1/en not_active Not-in-force
- 2006-05-22 ES ES06770824T patent/ES2380795T3/es active Active
- 2006-05-22 MX MX2007014619A patent/MX2007014619A/es not_active Application Discontinuation
- 2006-05-22 EP EP10188694A patent/EP2354139A1/en not_active Withdrawn
- 2006-05-22 KR KR1020077029764A patent/KR20080016659A/ko not_active Ceased
- 2006-05-22 CA CA002609126A patent/CA2609126A1/en not_active Abandoned
- 2006-05-22 EP EP10188700A patent/EP2354140A1/en not_active Withdrawn
- 2006-05-22 US US11/438,748 patent/US8921376B2/en not_active Expired - Fee Related
- 2006-05-22 ZA ZA200710379A patent/ZA200710379B/xx unknown
- 2006-05-22 NZ NZ564065A patent/NZ564065A/en not_active IP Right Cessation
- 2006-05-22 AU AU2006251623A patent/AU2006251623A1/en not_active Abandoned
- 2006-05-22 AT AT06770824T patent/ATE540948T1/de active
- 2006-05-22 RU RU2007147455/04A patent/RU2435769C2/ru not_active IP Right Cessation
- 2006-05-22 CN CN2006800263918A patent/CN101228161B/zh not_active Expired - Fee Related
- 2006-05-22 JP JP2008512591A patent/JP2008545660A/ja active Pending
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2007
- 2007-11-18 IL IL187438A patent/IL187438A0/en unknown
- 2007-12-18 NO NO20076502A patent/NO20076502L/no not_active Application Discontinuation
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2009
- 2009-05-21 JP JP2009123635A patent/JP2009179644A/ja active Pending
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2011
- 2011-08-11 RU RU2011133825/04A patent/RU2011133825A/ru not_active Application Discontinuation
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Also Published As
Publication number | Publication date |
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RU2007147455A (ru) | 2009-06-27 |
JP2008545660A (ja) | 2008-12-18 |
CN101228161B (zh) | 2012-10-10 |
JP2009179644A (ja) | 2009-08-13 |
EP2354140A1 (en) | 2011-08-10 |
RU2435769C2 (ru) | 2011-12-10 |
EP2354139A1 (en) | 2011-08-10 |
CN101228161A (zh) | 2008-07-23 |
RU2011133825A (ru) | 2013-02-20 |
JP2013253114A (ja) | 2013-12-19 |
ATE540948T1 (de) | 2012-01-15 |
CA2609126A1 (en) | 2006-11-30 |
AU2006251623A1 (en) | 2006-11-30 |
IL187438A0 (en) | 2008-02-09 |
ES2380795T3 (es) | 2012-05-18 |
NZ564065A (en) | 2011-03-31 |
EP1881983A1 (en) | 2008-01-30 |
WO2006127587A1 (en) | 2006-11-30 |
NO20076502L (no) | 2008-02-19 |
EP1881983B1 (en) | 2012-01-11 |
KR20080016659A (ko) | 2008-02-21 |
ZA200710379B (en) | 2009-05-27 |
US20070135466A1 (en) | 2007-06-14 |
US8921376B2 (en) | 2014-12-30 |
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