PE20080974A1 - Nuevas pirozolopirimidinas como inhibidores de quinasa dependientes de ciclina - Google Patents
Nuevas pirozolopirimidinas como inhibidores de quinasa dependientes de ciclinaInfo
- Publication number
- PE20080974A1 PE20080974A1 PE2007001331A PE2007001331A PE20080974A1 PE 20080974 A1 PE20080974 A1 PE 20080974A1 PE 2007001331 A PE2007001331 A PE 2007001331A PE 2007001331 A PE2007001331 A PE 2007001331A PE 20080974 A1 PE20080974 A1 PE 20080974A1
- Authority
- PE
- Peru
- Prior art keywords
- pyrimidine
- cycline
- dependent kinase
- pyrozolopyrimidines
- pirazolo
- 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
- 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
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
SE REFIERE A UN COMPUESTO DERIVADO DE PIRAZOLO[1,5-a]PIRIMIDINA SELECCIONADA DE 3-(TIAZOL-4-IL)-5-(PIPERAZIN-3-IL)-6-BROMO-7-AMINO-PIRAZOLO[1,5-a]PIRIMIDINA; 3-(1-METIL-PIRAZOL-4-IL)-5-(PIPERAZIN-3-IL)-6-IODO-7-AMINO-PIRAZOLO[1,5-a]PIRIMIDINA; 3-(1-METILPIRAZOL-4-IL)-5-(1-AMINOCICLOPENTIL-3-IL)-6-BROMO-7-AMINO-PIRAZOLO[1,5-a]PIRIMIDINA; ENTRE OTROS. DICHOS COMPUESTOS SON INHIBIDORES DE QUINASA DEPENDIENTE DE CICLINA CDK1, CDK2, CDK9, UTILES EN EL TRATAMIENTO DE UNA ENFERMEDAD PROLIFERATIVA SELECCIONADA DE CANCER DE VEJIGA, MAMA, COLON, RINON, HIGADO, PULMON, OVARIO, ENTRE OTROS
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/542,920 US7605155B2 (en) | 2002-09-04 | 2006-10-04 | Substituted pyrazolo[1,5-a]pyrimidines as protein kinase inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20080974A1 true PE20080974A1 (es) | 2008-07-19 |
Family
ID=39111854
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2007001331A PE20080974A1 (es) | 2006-10-04 | 2007-10-02 | Nuevas pirozolopirimidinas como inhibidores de quinasa dependientes de ciclina |
Country Status (10)
Country | Link |
---|---|
US (1) | US7605155B2 (es) |
EP (1) | EP2069349B1 (es) |
JP (1) | JP2010505839A (es) |
CN (1) | CN101573363B (es) |
AR (1) | AR063096A1 (es) |
CA (1) | CA2665127A1 (es) |
CL (1) | CL2007002856A1 (es) |
PE (1) | PE20080974A1 (es) |
TW (1) | TW200821313A (es) |
WO (1) | WO2008045267A2 (es) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5152922B2 (ja) * | 2005-10-06 | 2013-02-27 | メルク・シャープ・アンド・ドーム・コーポレーション | プロテインキナーゼを阻害するためのピラゾロ[1,5−a]ピリミジン誘導体の使用およびプロテインキナーゼを阻害する方法 |
WO2007139732A1 (en) * | 2006-05-22 | 2007-12-06 | Schering Corporation | Pyrazolo [1, 5-a] pyrimidines as cdk 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 |
MX2010014005A (es) * | 2008-06-20 | 2011-02-15 | Genentech Inc | Compuestos de triazolopiridina inhibidores de jak y los metodos. |
WO2011028638A1 (en) | 2009-09-04 | 2011-03-10 | Schering Corporation | Modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors |
WO2011049625A1 (en) | 2009-10-20 | 2011-04-28 | Mansour Samadpour | Method for aflatoxin screening of products |
CA3022722A1 (en) | 2009-11-05 | 2011-05-12 | Rhizen Pharmaceuticals S.A. | Pi3k protein kinase modulators |
WO2011090935A1 (en) * | 2010-01-19 | 2011-07-28 | Merck Sharp & Dohme Corp. | PYRAZOLO[1,5-a]PYRIMIDINE COMPOUNDS AS mTOR INHIBITORS |
WO2011119457A1 (en) * | 2010-03-26 | 2011-09-29 | Schering Corporation | Process for synthesizing 6-bromo-3-(1-methyl-1h-pyrazol-4-yl)-5-(3(r)-piperidinyl)pyrazolo[1,5-a]pyrimidin-7-amine |
US8883801B2 (en) | 2010-08-23 | 2014-11-11 | Merck Sharp & Dohme Corp. | Substituted pyrazolo[1,5-a]pyrimidines as mTOR inhibitors |
EP2608668B1 (en) * | 2010-08-23 | 2016-06-01 | Merck Sharp & Dohme Corp. | Fused tricyclic inhibitors of mammalian target of rapamycin |
EA024842B9 (ru) | 2011-05-04 | 2017-08-31 | Ризен Фармасьютикалз Са | Соединения в качестве модуляторов протеинкиназы pi3k |
DK3260455T3 (da) | 2012-07-04 | 2019-06-11 | Rhizen Pharmaceuticals S A | Selektive pi3k delta-hæmmere |
AU2013344716B2 (en) | 2012-11-16 | 2018-03-01 | University Health Network | Pyrazolopyrimidine compounds |
LT3033086T (lt) * | 2013-08-14 | 2021-12-27 | Novartis Ag | Kombinuota terapija vėžiui gydyti |
US9505767B2 (en) | 2013-09-05 | 2016-11-29 | Genentech, Inc. | Pyrazolo[1,5-A]pyrimidin-7(4H)-onehistone demethylase inhibitors |
CN106727474A (zh) * | 2017-01-04 | 2017-05-31 | 仪修南 | 苯氧乙酸类除草剂作为化学治疗剂治疗疾病的应用 |
CN108653282B (zh) * | 2018-06-28 | 2020-08-14 | 中国科学院昆明植物研究所 | 苯并噻唑类及苯并吡咯类化合物在制备抗肿瘤药物中的应用 |
EP3866789A4 (en) * | 2018-10-15 | 2022-07-06 | Nimbus Lakshmi, Inc. | TYK2 INHIBITORS AND USES THEREOF |
CN112996790B (zh) * | 2018-10-30 | 2023-11-03 | 克洛诺斯生物公司 | 用于调节cdk9活性的化合物、组合物和方法 |
CN111393447B (zh) * | 2020-05-14 | 2021-01-15 | 苏州信诺维医药科技有限公司 | 一种嘧啶并吡唑类化合物、其制备方法及应用 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HUP0302991A3 (en) | 2000-09-15 | 2009-10-28 | Vertex Pharma | Isoxazoles and their use as inhibitors of erk and pharmaceutical compositions containing the compounds |
CN1880317B (zh) * | 2002-09-04 | 2012-10-10 | 先灵公司 | 作为细胞周期蛋白依赖性激酶抑制剂的吡唑并嘧啶 |
WO2004022559A1 (en) * | 2002-09-04 | 2004-03-18 | Schering Corporation | Pyrazolopyrimidines as cyclin dependent kinase inhibitors |
EP1537116B1 (en) * | 2002-09-04 | 2010-06-02 | Schering Corporation | Pyrazolopyrimidines suitable for the treatment of cancer diseases |
US7196078B2 (en) * | 2002-09-04 | 2007-03-27 | Schering Corpoartion | Trisubstituted and tetrasubstituted pyrazolopyrimidines as cyclin dependent kinase inhibitors |
EP1608652A1 (en) * | 2003-03-31 | 2005-12-28 | Vernalis (Cambridge) Limited | Pyrazolopyrimidine compounds and their use in medicine |
PE20051089A1 (es) * | 2004-01-22 | 2006-01-25 | Novartis Ag | Derivados de pirazolo [1,5-a] pirimidin-7-il-amina como inhibidores de quinasa de proteina |
JP5152922B2 (ja) * | 2005-10-06 | 2013-02-27 | メルク・シャープ・アンド・ドーム・コーポレーション | プロテインキナーゼを阻害するためのピラゾロ[1,5−a]ピリミジン誘導体の使用およびプロテインキナーゼを阻害する方法 |
-
2006
- 2006-10-04 US US11/542,920 patent/US7605155B2/en not_active Expired - Lifetime
-
2007
- 2007-10-02 EP EP07839218.0A patent/EP2069349B1/en active Active
- 2007-10-02 WO PCT/US2007/021274 patent/WO2008045267A2/en active Application Filing
- 2007-10-02 JP JP2009531445A patent/JP2010505839A/ja not_active Ceased
- 2007-10-02 CN CN2007800446523A patent/CN101573363B/zh not_active Expired - Fee Related
- 2007-10-02 PE PE2007001331A patent/PE20080974A1/es not_active Application Discontinuation
- 2007-10-02 AR ARP070104358A patent/AR063096A1/es not_active Application Discontinuation
- 2007-10-02 CA CA002665127A patent/CA2665127A1/en not_active Abandoned
- 2007-10-03 TW TW096137089A patent/TW200821313A/zh unknown
- 2007-10-03 CL CL2007002856A patent/CL2007002856A1/es unknown
Also Published As
Publication number | Publication date |
---|---|
US20070072881A1 (en) | 2007-03-29 |
EP2069349B1 (en) | 2016-06-15 |
CN101573363B (zh) | 2013-03-06 |
TW200821313A (en) | 2008-05-16 |
CL2007002856A1 (es) | 2008-01-18 |
JP2010505839A (ja) | 2010-02-25 |
WO2008045267A3 (en) | 2008-07-31 |
WO2008045267A2 (en) | 2008-04-17 |
CN101573363A (zh) | 2009-11-04 |
AR063096A1 (es) | 2008-12-30 |
EP2069349A2 (en) | 2009-06-17 |
CA2665127A1 (en) | 2008-04-17 |
US7605155B2 (en) | 2009-10-20 |
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Legal Events
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