ECSP088350A - Pirazolopirimidinas como inhibidores de protein quinasas - Google Patents
Pirazolopirimidinas como inhibidores de protein quinasasInfo
- Publication number
- ECSP088350A ECSP088350A EC2008008350A ECSP088350A ECSP088350A EC SP088350 A ECSP088350 A EC SP088350A EC 2008008350 A EC2008008350 A EC 2008008350A EC SP088350 A ECSP088350 A EC SP088350A EC SP088350 A ECSP088350 A EC SP088350A
- Authority
- EC
- Ecuador
- Prior art keywords
- compounds
- inhibitors
- methods
- pirazolopirimidinas
- protein kinases
- Prior art date
Links
Classifications
-
- 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
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
Abstract
En sus muchas realizaciones, la presente invención provee una nueva clase de compuestos pirazolo[1,5-a]pirimidina amino-sustituidos como inhibidores de las proteínas y/o quinasas checkpoint, métodos para preparar dichos compuestos, composiciones farmacéuticas que incluyen uno o más de dichos compuestos, métodos para la preparación de las formulaciones farmacéuticas que incluyen uno o más de dichos compuestos, y métodos de tratamiento prevención, inhibición o mejoramiento de una o más enfermedades asociadas con las proteínas o checkpoint quinasas usando dichos compuestos o composiciones farmacéuticas.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US72419705P | 2005-10-06 | 2005-10-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
ECSP088350A true ECSP088350A (es) | 2008-05-30 |
Family
ID=37560916
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EC2008008350A ECSP088350A (es) | 2005-10-06 | 2008-04-04 | Pirazolopirimidinas como inhibidores de protein quinasas |
Country Status (18)
Country | Link |
---|---|
US (1) | US7776865B2 (es) |
EP (1) | EP1931676B1 (es) |
JP (2) | JP5052518B2 (es) |
KR (1) | KR20080063806A (es) |
CN (1) | CN101321760A (es) |
AR (1) | AR056206A1 (es) |
AT (1) | ATE533770T1 (es) |
AU (1) | AU2006299338A1 (es) |
BR (1) | BRPI0617150A2 (es) |
CA (1) | CA2624882C (es) |
EC (1) | ECSP088350A (es) |
IL (1) | IL190598A0 (es) |
NO (1) | NO20082092L (es) |
PE (1) | PE20070543A1 (es) |
RU (1) | RU2008117298A (es) |
TW (1) | TW200745123A (es) |
WO (1) | WO2007041712A1 (es) |
ZA (1) | ZA200802995B (es) |
Families Citing this family (64)
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CA2627623C (en) * | 2005-10-06 | 2014-04-22 | Schering Corporation | Methods for inhibiting protein kinases |
AU2007223865A1 (en) * | 2006-03-08 | 2007-09-13 | Novartis Ag | Use of pyrazolo[1,5A]pyrimidin-7-yl amine derivatives in the treatment of neurological disorders |
RU2008150419A (ru) * | 2006-05-22 | 2010-09-20 | Шеринг Корпорейшн (US) | ПИРАЗОЛО[1,5-a]ПИРИМИДИНЫ В КАЧЕСТВЕ ИНГИБИТОРОВ CDK |
ES2403546T3 (es) | 2006-11-03 | 2013-05-20 | Pharmacyclics, Inc. | Sonda de actividad de la tirosina-cinasa de Bruton y procedimiento de utilización |
MY146474A (en) * | 2006-11-06 | 2012-08-15 | Supergen Inc | Imidazo[1,2-b]pyridazine and pyrazolo[1,5-a]pyrimidine derivatives and their use as protein kinase inhibitors |
TW200845962A (en) | 2007-05-08 | 2008-12-01 | Schering Corp | Methods of treatment using intravenous formulations comprising temozolomide |
WO2008141140A1 (en) * | 2007-05-09 | 2008-11-20 | Abbott Laboratories | Condensed heterocyclic compounds as inhibitors of protein kinases |
US8124759B2 (en) | 2007-05-09 | 2012-02-28 | Abbott Laboratories | Inhibitors of protein kinases |
MX2009012079A (es) * | 2007-05-09 | 2009-11-19 | Abbott Lab | Compuestos heterociclicos condensados como inhibidores de proteina cinasas. |
WO2009004329A1 (en) * | 2007-07-02 | 2009-01-08 | Cancer Research Technology Limited | 9h-pyrimido[4,5-b]indoles, 9h-pyrido[4',3':4,5]pyrrolo[2,3-d]pyridines, and 9h-1,3,6,9-tetraaza-fluorenes as chk1 kinase function inhibitors |
MX2010005095A (es) * | 2007-11-07 | 2010-08-03 | Schering Corp | Moduladores novedosos de puntos de verificación del ciclo celular y su uso en combinacion con inhibidores de cinasa de puntos de verificacion. |
JP5643105B2 (ja) | 2007-12-14 | 2014-12-17 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | 新規イミダゾ[1,2−a]ピリジン及びイミダゾ[1,2−b]ピリダジン誘導体 |
US8426441B2 (en) * | 2007-12-14 | 2013-04-23 | Roche Palo Alto Llc | Inhibitors of bruton's tyrosine kinase |
EP2265603B1 (en) | 2008-03-13 | 2014-05-07 | The General Hospital Corporation | Inhibitors of the bmp signaling pathway |
JP2011519972A (ja) * | 2008-05-12 | 2011-07-14 | アムネスティックス・インコーポレーテッド | Rhoキナーゼ阻害のためのならびに学習及び記憶を改善するための化合物 |
CL2009001152A1 (es) | 2008-05-13 | 2009-10-16 | Array Biopharma Inc | Compuestos derivados de n-(4-(cicloalquilo nitrogenado-1-il)-1h-pirrolo[2,3-b]piridin-3-il)amida, inhibidores de cinasa; proceso de preparacion; composicion farmaceutica; y su uso para el tratamiento de una enfermedad proliferativa. |
PA8851101A1 (es) * | 2008-12-16 | 2010-07-27 | Lilly Co Eli | Compuesto amino pirazol |
MX2011008583A (es) * | 2009-02-13 | 2011-12-12 | Bayer Pharma AG | Pirimidinas fusionadas. |
US8691825B2 (en) | 2009-04-01 | 2014-04-08 | Merck Sharp & Dohme Corp. | Inhibitors of AKT activity |
UA110324C2 (en) * | 2009-07-02 | 2015-12-25 | Genentech Inc | Jak inhibitory compounds based on pyrazolo pyrimidine |
US8993535B2 (en) | 2009-09-04 | 2015-03-31 | Merck Sharp & Dohme Corp. | Modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors |
UY33071A (es) * | 2009-12-01 | 2011-05-31 | Abbott Lab | Nuevos compuestos tricíclicos |
CA2805015A1 (en) * | 2010-07-13 | 2012-01-19 | Stuart Ince | Bicyclic pyrimidines |
EP2598505B1 (en) * | 2010-07-28 | 2015-03-18 | Bayer Intellectual Property GmbH | Substituted imidazo[1,2-b]pyridazines |
JP2014517079A (ja) | 2011-06-22 | 2014-07-17 | 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 |
PL3409278T3 (pl) | 2011-07-21 | 2021-02-22 | Sumitomo Pharma Oncology, Inc. | Heterocykliczne inhibitory kinazy białkowej |
CN104105696B (zh) | 2011-11-09 | 2017-11-14 | 癌症研究技术有限公司 | 5‑(吡啶‑2‑基‑氨基)‑吡嗪‑2‑腈化合物及其治疗用途 |
ES2589955T3 (es) * | 2012-01-10 | 2016-11-17 | Bayer Intellectual Property Gmbh | Pirazolopirimidinas sustituidas como inhibidores de la quinasa Akt |
SG11201407238VA (en) | 2012-05-15 | 2014-12-30 | Cancer Rec Tech Ltd | 5-[[4-[[morpholin-2-yl]methylamino]-5-(trifluoromethyl)-2-pyridyl]amino]pyrazine-2-carbonitrile and therapeutic uses thereof |
SI3808749T1 (sl) | 2012-12-07 | 2023-07-31 | Vertex Pharmaceuticals Incorporated | Pirazolo(1,5-A)pirimidini za uporabo kot zaviralci ATR kinaze pri zdravljenju rakavih bolezni |
CA2897200C (en) | 2013-01-14 | 2021-07-06 | Incyte Corporation | Bicyclic aromatic carboxamide compounds useful as pim kinase inhibitors |
US9200004B2 (en) | 2013-01-15 | 2015-12-01 | Incyte Holdings Corporation | Thiazolecarboxamides and pyridinecarboxamide compounds useful as Pim kinase inhibitors |
EP2970311A4 (en) | 2013-03-14 | 2016-11-23 | Brigham & Womens Hospital | BMP INHIBITORS AND METHODS OF USE |
EP2970288A1 (en) | 2013-03-15 | 2016-01-20 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
WO2014143241A1 (en) | 2013-03-15 | 2014-09-18 | Vertex Pharmaceuticals Incorporated | Compounds useful as inhibitors of atr kinase |
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 |
TW201536293A (zh) | 2013-07-18 | 2015-10-01 | Taiho Pharmaceutical Co Ltd | 對fgfr抑制劑具耐受性之癌的治療藥 |
US20160193210A1 (en) * | 2013-07-18 | 2016-07-07 | Taiho Pharmaceutical Co., Ltd. | Antitumor drug for intermittent administration of fgfr inhibitor |
SG11201601259YA (en) | 2013-08-23 | 2016-03-30 | Incyte Corp | Furo- and thieno-pyridine carboxamide compounds useful as pim kinase inhibitors |
RU2687276C2 (ru) | 2013-12-06 | 2019-05-13 | Вертекс Фармасьютикалз Инкорпорейтед | Соединения, пригодные для использования в качестве ингибиторов atr киназы |
NZ764151A (en) | 2014-06-05 | 2023-12-22 | Vertex Pharma | Radiolabelled derivatives of a 2-amino-6-fluoro-n-[5-fluoro-pyridin-3-yl]- pyrazolo[1,5-a]pyrimidin-3-carboxamide compound useful as atr kinase inhibitor, the preparation of said compound and different solid forms thereof |
CA2950780C (en) | 2014-06-17 | 2023-05-16 | Vertex Pharmaceuticals Incorporated | Method for treating cancer using a combination of chk1 and atr inhibitors |
US9580418B2 (en) | 2014-07-14 | 2017-02-28 | Incyte Corporation | Bicyclic aromatic carboxamide compounds useful as Pim kinase inhibitors |
US9822124B2 (en) | 2014-07-14 | 2017-11-21 | Incyte Corporation | Bicyclic heteroaromatic carboxamide compounds useful as Pim kinase inhibitors |
WO2016011019A1 (en) | 2014-07-15 | 2016-01-21 | The Brigham And Women's Hospital, Inc. | Compositions and methods for inhibiting bmp |
TW201702218A (zh) | 2014-12-12 | 2017-01-16 | 美國杰克森實驗室 | 關於治療癌症、自體免疫疾病及神經退化性疾病之組合物及方法 |
CN107406455B (zh) | 2015-03-31 | 2020-05-12 | 大鹏药品工业株式会社 | 3,5-二取代的苯炔基化合物晶体 |
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TWI734699B (zh) | 2015-09-09 | 2021-08-01 | 美商英塞特公司 | Pim激酶抑制劑之鹽 |
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US11883404B2 (en) | 2016-03-04 | 2024-01-30 | Taiho Pharmaceuticals Co., Ltd. | Preparation and composition for treatment of malignant tumors |
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DE3130633A1 (de) * | 1981-08-01 | 1983-02-17 | Basf Ag, 6700 Ludwigshafen | 7-amino-azolo(1,5-a)pyrimidine und diese enthaltende fungizide |
US5688949A (en) | 1991-04-22 | 1997-11-18 | Otsuka Pharmaceutical Factory, Inc. | Pyrazolo 1,5-A!pyrimidine derivatives and anti-inflammatory agent containing the same |
EP0628559B1 (en) | 1993-06-10 | 2002-04-03 | Beiersdorf-Lilly GmbH | Pyrimidine compounds and their use as pharmaceuticals |
US5571813A (en) | 1993-06-10 | 1996-11-05 | Beiersdorf-Lilly Gmbh | Fused pyrimidine compounds and their use as pharmaceuticals |
ES2164153T3 (es) | 1994-06-21 | 2002-02-16 | Otsuka Pharma Co Ltd | Derivado de pirazolo(1,5-a)pirimidina. |
US6313124B1 (en) | 1997-07-23 | 2001-11-06 | Dupont Pharmaceuticals Company | Tetrazine bicyclic compounds |
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ZA9811178B (en) | 1997-12-13 | 2000-06-07 | Bristol Myers Squibb Co | Use of pyrazolo (3,4-b) pyridine as cyclin dependent kinase inhibitors. |
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KR20030016429A (ko) | 2000-07-26 | 2003-02-26 | 브리스톨-마이어스스퀴브컴파니 | 시클린 의존성 키나제의n-[5-[[[5-알킬-2-옥사졸릴]메틸]티오]-2-티아졸릴]카르복스아미드 저해제 |
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AU2003227437A1 (en) | 2002-04-23 | 2003-11-10 | Shionogi And Co., Ltd. | PYRAZOLO(1,5-a)PYRIMIDINE DERIVATIVE AND NAD(P)H OXIDASE INHIBITOR CONTAINING THE SAME |
DE10223917A1 (de) | 2002-05-29 | 2003-12-11 | Bayer Cropscience Ag | Pyrazolopyrimidine |
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-
2006
- 2006-10-04 EP EP06816408A patent/EP1931676B1/en active Active
- 2006-10-04 RU RU2008117298/04A patent/RU2008117298A/ru not_active Application Discontinuation
- 2006-10-04 BR BRPI0617150-8A patent/BRPI0617150A2/pt not_active IP Right Cessation
- 2006-10-04 TW TW095136815A patent/TW200745123A/zh unknown
- 2006-10-04 WO PCT/US2006/039136 patent/WO2007041712A1/en active Application Filing
- 2006-10-04 CA CA2624882A patent/CA2624882C/en not_active Expired - Fee Related
- 2006-10-04 AT AT06816408T patent/ATE533770T1/de active
- 2006-10-04 CN CNA2006800455049A patent/CN101321760A/zh active Pending
- 2006-10-04 PE PE2006001206A patent/PE20070543A1/es not_active Application Discontinuation
- 2006-10-04 AU AU2006299338A patent/AU2006299338A1/en not_active Abandoned
- 2006-10-04 JP JP2008534711A patent/JP5052518B2/ja not_active Expired - Fee Related
- 2006-10-04 AR ARP060104364A patent/AR056206A1/es not_active Application Discontinuation
- 2006-10-04 US US11/542,921 patent/US7776865B2/en active Active
- 2006-10-04 KR KR1020087010465A patent/KR20080063806A/ko not_active Application Discontinuation
-
2008
- 2008-04-03 IL IL190598A patent/IL190598A0/en unknown
- 2008-04-04 EC EC2008008350A patent/ECSP088350A/es unknown
- 2008-04-04 ZA ZA200802995A patent/ZA200802995B/xx unknown
- 2008-05-05 NO NO20082092A patent/NO20082092L/no not_active Application Discontinuation
-
2012
- 2012-01-27 JP JP2012015794A patent/JP2012082233A/ja not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
JP2009511491A (ja) | 2009-03-19 |
KR20080063806A (ko) | 2008-07-07 |
CN101321760A (zh) | 2008-12-10 |
WO2007041712A1 (en) | 2007-04-12 |
AR056206A1 (es) | 2007-09-26 |
JP2012082233A (ja) | 2012-04-26 |
ATE533770T1 (de) | 2011-12-15 |
EP1931676B1 (en) | 2011-11-16 |
CA2624882A1 (en) | 2007-04-12 |
IL190598A0 (en) | 2008-11-03 |
BRPI0617150A2 (pt) | 2011-07-12 |
PE20070543A1 (es) | 2007-06-14 |
EP1931676A1 (en) | 2008-06-18 |
CA2624882C (en) | 2014-05-20 |
AU2006299338A1 (en) | 2007-04-12 |
ZA200802995B (en) | 2009-02-25 |
JP5052518B2 (ja) | 2012-10-17 |
TW200745123A (en) | 2007-12-16 |
US7776865B2 (en) | 2010-08-17 |
RU2008117298A (ru) | 2009-11-20 |
US20070083044A1 (en) | 2007-04-12 |
NO20082092L (no) | 2008-07-04 |
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