ATE420883T1 - Pyrrolopyrimidine verwendbar als protein kinase inhibitoren - Google Patents
Pyrrolopyrimidine verwendbar als protein kinase inhibitorenInfo
- Publication number
- ATE420883T1 ATE420883T1 AT06734381T AT06734381T ATE420883T1 AT E420883 T1 ATE420883 T1 AT E420883T1 AT 06734381 T AT06734381 T AT 06734381T AT 06734381 T AT06734381 T AT 06734381T AT E420883 T1 ATE420883 T1 AT E420883T1
- Authority
- AT
- Austria
- Prior art keywords
- pyrrolopyrimidines
- protein kinase
- kinase inhibitors
- compositions
- compounds
- Prior art date
Links
Classifications
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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
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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
- A61K31/495—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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- A—HUMAN NECESSITIES
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- A61P9/08—Vasodilators for multiple indications
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- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US64978105P | 2005-02-03 | 2005-02-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
ATE420883T1 true ATE420883T1 (de) | 2009-01-15 |
Family
ID=36498734
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT06734381T ATE420883T1 (de) | 2005-02-03 | 2006-02-02 | Pyrrolopyrimidine verwendbar als protein kinase inhibitoren |
Country Status (17)
Country | Link |
---|---|
US (2) | US8633205B2 (de) |
EP (1) | EP1844050B1 (de) |
JP (2) | JP5227032B2 (de) |
KR (1) | KR20070104641A (de) |
CN (1) | CN101142218B (de) |
AT (1) | ATE420883T1 (de) |
AU (1) | AU2006221065A1 (de) |
CA (1) | CA2596830A1 (de) |
DE (1) | DE602006004844D1 (de) |
ES (1) | ES2320487T3 (de) |
HK (1) | HK1116349A1 (de) |
IL (1) | IL184898A0 (de) |
MX (1) | MX2007009429A (de) |
NO (1) | NO20074431L (de) |
RU (1) | RU2434871C2 (de) |
WO (1) | WO2006096270A1 (de) |
ZA (1) | ZA200707342B (de) |
Families Citing this family (78)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7884109B2 (en) | 2005-04-05 | 2011-02-08 | Wyeth Llc | Purine and imidazopyridine derivatives for immunosuppression |
CA2609126A1 (en) * | 2005-05-20 | 2006-11-30 | Vertex Pharmaceuticals Incorporated | Pyrrolopyridines useful as inhibitors of protein kinase |
EP2270014A1 (de) | 2005-09-22 | 2011-01-05 | Incyte Corporation | Azepinhemmer von Janus-Kinasen |
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 |
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 |
CA2636189A1 (en) | 2006-01-17 | 2007-07-26 | Vertex Pharmaceuticals Incorporated | 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 |
SG170828A1 (en) * | 2006-04-05 | 2011-05-30 | Vertex Pharmaceuticals Inc Us | Deazapurines useful as inhibitors of janus kinases |
WO2008043019A1 (en) | 2006-10-04 | 2008-04-10 | Pharmacopeia, Inc | 8-substituted 2-(benzimidazolyl) purine derivatives for immunosuppression |
US7919490B2 (en) | 2006-10-04 | 2011-04-05 | Wyeth Llc | 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 |
JP2010508363A (ja) | 2006-11-01 | 2010-03-18 | 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三環系ヘテロアリール化合物 |
WO2008060301A1 (en) * | 2006-11-16 | 2008-05-22 | Pharmacopeia , Llc | 7-substituted purine derivatives for immunosuppression |
CA2673472A1 (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 |
US8513270B2 (en) * | 2006-12-22 | 2013-08-20 | Incyte Corporation | Substituted heterocycles as Janus kinase inhibitors |
CN101679440A (zh) * | 2007-04-02 | 2010-03-24 | 帕劳制药股份有限公司 | 作为jak3抑制剂的吡咯并嘧啶衍生物 |
RS58449B1 (sr) * | 2007-06-13 | 2019-04-30 | Incyte Holdings Corp | Upotreba soli inhibitora janus kinaze (r)-3-(4-(7h-pirolo[2,3-d]pirimidin-4-il)-1h- pirazol-1-il)-3-ciklopentilpropionitrila |
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 |
TWI444382B (zh) | 2008-03-11 | 2014-07-11 | Incyte Corp | 作為jak抑制劑之氮雜環丁烷及環丁烷衍生物 |
MX2010014005A (es) * | 2008-06-20 | 2011-02-15 | Genentech Inc | Compuestos de triazolopiridina inhibidores de jak y los metodos. |
KR20110031475A (ko) * | 2008-06-20 | 2011-03-28 | 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 |
CA2752885A1 (en) * | 2009-02-27 | 2010-09-02 | Ambit Biosciences Corporation | Jak kinase modulating quinazoline derivatives and methods of use thereof |
EP3643312A1 (de) | 2009-05-22 | 2020-04-29 | Incyte Holdings Corporation | 3-[4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl]octan- oder heptannitril als jak-inhibitoren |
AU2010249380B2 (en) | 2009-05-22 | 2015-08-20 | Incyte Holdings 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 |
RS55341B1 (sr) | 2009-06-17 | 2017-03-31 | Vertex Pharma | Inhibitori replikacije virusa gripa |
JP5690823B2 (ja) | 2009-07-08 | 2015-03-25 | レオ ファーマ アクティーゼルスカブ | Jak受容体およびタンパク質チロシンキナーゼ阻害薬としての複素環化合物 |
AR078012A1 (es) * | 2009-09-01 | 2011-10-05 | Incyte Corp | Derivados heterociclicos de las pirazol-4-il- pirrolo (2,3-d) pirimidinas como inhibidores de la quinasa janus |
KR20180126619A (ko) | 2009-10-09 | 2018-11-27 | 인사이트 홀딩스 코포레이션 | 3-(4-(7H-피롤로〔2,3-d〕피리미딘-4-일)-1H-피라졸-1-일)-3-사이클로펜틸프로판니트릴의 하이드록실, 케토 및 글루쿠로나이드 유도체 |
BR112012020693B1 (pt) * | 2010-02-18 | 2020-05-12 | Incyte Holdings Corporation | Derivados de ciclobutano e metilciclobutano como inibidores de janus quinase e composição que os compreende |
CN102985417B (zh) * | 2010-03-10 | 2015-01-28 | 因塞特公司 | 作为jak1抑制剂的哌啶-4-基氮杂环丁烷衍生物 |
US8518945B2 (en) * | 2010-03-22 | 2013-08-27 | Hoffmann-La Roche Inc. | Pyrrolopyrazine kinase inhibitors |
EA035981B1 (ru) | 2010-05-21 | 2020-09-09 | Инсайт Холдингс Корпорейшн | Композиция ингибитора jak для местного применения |
EA201300282A1 (ru) * | 2010-08-27 | 2013-08-30 | Мерк Патент Гмбх | Производные триазолопиразина |
EP2640725B1 (de) | 2010-11-19 | 2015-01-07 | Incyte Corporation | Heterocyclensubstituierte pyrrolopyridine und pyrrolopyrimidine als jak-inhibitoren |
TW201249845A (en) | 2010-11-19 | 2012-12-16 | Incyte Corp | Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as JAK inhibitors |
RU2013132681A (ru) | 2010-12-16 | 2015-01-27 | Вертекс Фармасьютикалз Инкорпорейтед | Ингибиторы репликации вирусов гриппа |
WO2012093169A1 (en) | 2011-01-07 | 2012-07-12 | Leo Pharma A/S | Novel sulfamide piperazine derivatives as protein tyrosine kinase inhibitors and pharmaceutical use thereof |
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GB9604361D0 (en) * | 1996-02-29 | 1996-05-01 | Pharmacia Spa | 4-Substituted pyrrolopyrimidine compounds as tyrosine kinase inhibitors |
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JP5227032B2 (ja) | 2013-07-03 |
JP2008528705A (ja) | 2008-07-31 |
MX2007009429A (es) | 2008-03-18 |
RU2007132908A (ru) | 2009-03-10 |
KR20070104641A (ko) | 2007-10-26 |
US8633205B2 (en) | 2014-01-21 |
ES2320487T3 (es) | 2009-05-22 |
CA2596830A1 (en) | 2006-09-14 |
ZA200707342B (en) | 2009-03-25 |
US20140171454A1 (en) | 2014-06-19 |
AU2006221065A1 (en) | 2006-09-14 |
RU2434871C2 (ru) | 2011-11-27 |
WO2006096270A1 (en) | 2006-09-14 |
JP2009102361A (ja) | 2009-05-14 |
US20070004762A9 (en) | 2007-01-04 |
IL184898A0 (en) | 2007-12-03 |
US20060183761A1 (en) | 2006-08-17 |
HK1116349A1 (en) | 2008-12-19 |
NO20074431L (no) | 2007-08-31 |
CN101142218B (zh) | 2013-02-06 |
CN101142218A (zh) | 2008-03-12 |
EP1844050A1 (de) | 2007-10-17 |
EP1844050B1 (de) | 2009-01-14 |
DE602006004844D1 (de) | 2009-03-05 |
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