CN101142218B - 可用作蛋白激酶抑制剂的吡咯并嘧啶 - Google Patents
可用作蛋白激酶抑制剂的吡咯并嘧啶 Download PDFInfo
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- CN101142218B CN101142218B CN2006800087780A CN200680008778A CN101142218B CN 101142218 B CN101142218 B CN 101142218B CN 2006800087780 A CN2006800087780 A CN 2006800087780A CN 200680008778 A CN200680008778 A CN 200680008778A CN 101142218 B CN101142218 B CN 101142218B
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- 0 C*1C*#CC1 Chemical compound C*1C*#CC1 0.000 description 4
- OLNDFAVAFVCDPN-UHFFFAOYSA-N C(c1ccccc1)=C/c1c(cc[nH]2)c2ncn1 Chemical compound C(c1ccccc1)=C/c1c(cc[nH]2)c2ncn1 OLNDFAVAFVCDPN-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- 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
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- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Neurology (AREA)
- Physical Education & Sports Medicine (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Cardiology (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Oncology (AREA)
- Endocrinology (AREA)
- Ophthalmology & Optometry (AREA)
- Virology (AREA)
- Pain & Pain Management (AREA)
- Psychology (AREA)
- Gynecology & Obstetrics (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Communicable Diseases (AREA)
- Vascular Medicine (AREA)
- Reproductive Health (AREA)
- Psychiatry (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US64978105P | 2005-02-03 | 2005-02-03 | |
| US60/649,781 | 2005-02-03 | ||
| PCT/US2006/004019 WO2006096270A1 (en) | 2005-02-03 | 2006-02-02 | Pyrrolopyrimidines useful as inhibitors of protein kinase |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101142218A CN101142218A (zh) | 2008-03-12 |
| CN101142218B true CN101142218B (zh) | 2013-02-06 |
Family
ID=36498734
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2006800087780A Expired - Fee Related CN101142218B (zh) | 2005-02-03 | 2006-02-02 | 可用作蛋白激酶抑制剂的吡咯并嘧啶 |
Country Status (16)
| Country | Link |
|---|---|
| US (2) | US8633205B2 (enExample) |
| EP (1) | EP1844050B1 (enExample) |
| JP (2) | JP5227032B2 (enExample) |
| KR (1) | KR20070104641A (enExample) |
| CN (1) | CN101142218B (enExample) |
| AT (1) | ATE420883T1 (enExample) |
| AU (1) | AU2006221065A1 (enExample) |
| CA (1) | CA2596830A1 (enExample) |
| DE (1) | DE602006004844D1 (enExample) |
| ES (1) | ES2320487T3 (enExample) |
| IL (1) | IL184898A0 (enExample) |
| MX (1) | MX2007009429A (enExample) |
| NO (1) | NO20074431L (enExample) |
| RU (1) | RU2434871C2 (enExample) |
| WO (1) | WO2006096270A1 (enExample) |
| ZA (1) | ZA200707342B (enExample) |
Families Citing this family (81)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7884109B2 (en) | 2005-04-05 | 2011-02-08 | Wyeth Llc | Purine and imidazopyridine derivatives for immunosuppression |
| US8921376B2 (en) * | 2005-05-20 | 2014-12-30 | Vertex Pharmaceuticals Incorporated | Pyrrolopyridines useful as inhibitors of protein kinase |
| WO2007038215A1 (en) | 2005-09-22 | 2007-04-05 | Incyte Corporation | Tetracyclic inhibitors of janus kinases |
| ATE525374T1 (de) | 2005-12-13 | 2011-10-15 | Incyte Corp | Heteroarylsubstituierte pyrroloä2,3-büpyridine und pyrroloä2,3-büpyrimidine als januskinaseinhibitoren |
| 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 |
| EP2537849A3 (en) | 2006-01-17 | 2013-04-03 | Vertex Pharmaceuticals, Inc. | Azaindoles useful as inhibitors of janus kinases |
| US7989459B2 (en) | 2006-02-17 | 2011-08-02 | Pharmacopeia, Llc | Purinones and 1H-imidazopyridinones as PKC-theta inhibitors |
| CA2648250A1 (en) * | 2006-04-05 | 2007-10-18 | Vertex Pharmaceuticals Incorporated | Deazapurines useful as inhibitors of janus kinases |
| TW200831104A (en) | 2006-10-04 | 2008-08-01 | Pharmacopeia Inc | 6-substituted 2-(benzimidazolyl)purine and purinone derivatives for immunosuppression |
| US7902187B2 (en) | 2006-10-04 | 2011-03-08 | Wyeth Llc | 6-substituted 2-(benzimidazolyl)purine and purinone derivatives for immunosuppression |
| WO2008043019A1 (en) | 2006-10-04 | 2008-04-10 | Pharmacopeia, Inc | 8-substituted 2-(benzimidazolyl) purine derivatives for immunosuppression |
| RU2009120622A (ru) | 2006-11-01 | 2010-12-10 | Вертекс Фармасьютикалз Инкорпорейтед (Us) | Трициклические гетероарильные соединения в качестве ингибиторов янус-киназы |
| CA2669686A1 (en) * | 2006-11-16 | 2008-05-22 | Pharmacopeia, Llc | 7-substituted purine derivatives for immunosuppression |
| NZ577798A (en) | 2006-12-21 | 2012-04-27 | Vertex Pharma | 5-cyano-4- (pyrrolo [2, 3b] pyridine-3-yl) -pyrimidine derivatives useful as protein kinase inhibitors |
| JP5492565B2 (ja) | 2006-12-22 | 2014-05-14 | インサイト・コーポレイション | Janusキナーゼ阻害剤としての置換複素環 |
| PE20090996A1 (es) * | 2007-04-02 | 2009-07-15 | Palau Pharma Sa | Derivados de pirrolopirimidina como inhibidores de cinasa jak3 |
| ES2467665T5 (es) * | 2007-06-13 | 2022-11-03 | Incyte Holdings Corp | Sales del inhibidor de cinasas Janus (R)-3-(4-(7H-pirrolo[2,3-d]pirimidin-4-il)-1H-pirazol-1-il)-3-ciclopentilpropanonitrilo |
| 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. |
| AU2009211338B2 (en) * | 2008-02-06 | 2011-12-15 | Novartis Ag | Pyrrolo[2, 3-D] pyrimidines and use thereof as tyrosine kinase inhibitors |
| SG191660A1 (en) | 2008-03-11 | 2013-07-31 | Incyte Corp | Azetidine and cyclobutane derivatives as jak inhibitors |
| PE20110063A1 (es) * | 2008-06-20 | 2011-02-16 | Genentech Inc | DERIVADOS DE [1, 2, 4]TRIAZOLO[1, 5-a]PIRIDINA COMO INHIBIDORES DE JAK |
| KR20110033223A (ko) | 2008-06-20 | 2011-03-30 | 제넨테크, 인크. | 트리아졸로피리딘 jak 억제제 화합물 및 방법 |
| CL2009001884A1 (es) * | 2008-10-02 | 2010-05-14 | Incyte Holdings Corp | Uso de 3-ciclopentil-3-[4-(7h-pirrolo[2,3-d]pirimidin-4-il)-1h-pirazol-1-il)propanonitrilo, inhibidor de janus quinasa, y uso de una composición que lo comprende para el tratamiento del ojo seco. |
| JOP20190231A1 (ar) | 2009-01-15 | 2017-06-16 | Incyte Corp | طرق لاصلاح مثبطات انزيم jak و المركبات الوسيطة المتعلقة به |
| WO2010093808A1 (en) * | 2009-02-11 | 2010-08-19 | Reaction Biology Corp. | Selective kinase inhibitors |
| CN105601619A (zh) * | 2009-02-27 | 2016-05-25 | 埃姆比特生物科学公司 | 调控jak激酶的喹唑啉衍生物和其使用方法 |
| WO2010135650A1 (en) | 2009-05-22 | 2010-11-25 | Incyte Corporation | N-(HETERO)ARYL-PYRROLIDINE DERIVATIVES OF PYRAZOL-4-YL-PYRROLO[2,3-d]PYRIMIDINES AND PYRROL-3-YL-PYRROLO[2,3-d]PYRIMIDINES AS JANUS KINASE INHIBITORS |
| JP6172939B2 (ja) * | 2009-05-22 | 2017-08-02 | インサイト・ホールディングス・コーポレイションIncyte Holdings Corporation | Jak阻害薬としての3−[4−(7h−ピロロ[2,3−d]ピリミジン−4−イル)−1h−ピラゾール−1−イル]オクタン−またはヘプタン−ニトリル |
| SG10201405826RA (en) | 2009-06-17 | 2014-12-30 | Vertex Pharma | Inhibitors of influenza viruses replication |
| CN102574857B (zh) | 2009-07-08 | 2015-06-10 | 利奥制药有限公司 | 作为jak受体和蛋白酪氨酸激酶抑制剂的杂环化合物 |
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| ATE247469T1 (de) * | 1995-06-07 | 2003-09-15 | Pfizer | Heterocyclische kondensierte pyrimidin-derivate |
| GB9604361D0 (en) * | 1996-02-29 | 1996-05-01 | Pharmacia Spa | 4-Substituted pyrrolopyrimidine compounds as tyrosine kinase inhibitors |
| EP1506962B1 (en) * | 2000-10-20 | 2008-07-02 | Eisai R&D Management Co., Ltd. | Nitrogen-containing aromatic heterocycles |
| CA2515132C (en) * | 2003-02-07 | 2012-01-03 | Vertex Pharmaceuticals Incorporated | Heteroaryl substituted pyrroles useful as inhibitors of protein kinases |
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| RU2007132908A (ru) | 2009-03-10 |
| HK1116349A1 (en) | 2008-12-19 |
| ES2320487T3 (es) | 2009-05-22 |
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| MX2007009429A (es) | 2008-03-18 |
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| EP1844050A1 (en) | 2007-10-17 |
| DE602006004844D1 (de) | 2009-03-05 |
| JP5227032B2 (ja) | 2013-07-03 |
| US8633205B2 (en) | 2014-01-21 |
| ZA200707342B (en) | 2009-03-25 |
| US20060183761A1 (en) | 2006-08-17 |
| US20140171454A1 (en) | 2014-06-19 |
| JP2009102361A (ja) | 2009-05-14 |
| JP2008528705A (ja) | 2008-07-31 |
| CA2596830A1 (en) | 2006-09-14 |
| WO2006096270A1 (en) | 2006-09-14 |
| RU2434871C2 (ru) | 2011-11-27 |
| EP1844050B1 (en) | 2009-01-14 |
| IL184898A0 (en) | 2007-12-03 |
| US20070004762A9 (en) | 2007-01-04 |
| CN101142218A (zh) | 2008-03-12 |
| AU2006221065A1 (en) | 2006-09-14 |
| NO20074431L (no) | 2007-08-31 |
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