PE20041000A1 - Pirazolopirimidinas como inhibidores de la quinasa dependientes de ciclina - Google Patents
Pirazolopirimidinas como inhibidores de la quinasa dependientes de ciclinaInfo
- Publication number
- PE20041000A1 PE20041000A1 PE2003000900A PE2003000900A PE20041000A1 PE 20041000 A1 PE20041000 A1 PE 20041000A1 PE 2003000900 A PE2003000900 A PE 2003000900A PE 2003000900 A PE2003000900 A PE 2003000900A PE 20041000 A1 PE20041000 A1 PE 20041000A1
- Authority
- PE
- Peru
- Prior art keywords
- kinase inhibitors
- cycline
- pyrazolopyrimidines
- dependent kinase
- alkyl
- Prior art date
Links
- 229940043355 kinase inhibitor Drugs 0.000 title abstract 2
- 239000003757 phosphotransferase inhibitor Substances 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 206010061218 Inflammation Diseases 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 206010003246 arthritis Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 230000002526 effect on cardiovascular system Effects 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 230000004054 inflammatory process Effects 0.000 abstract 1
- 230000000626 neurodegenerative effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 102000004169 proteins and genes Human genes 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
- 230000003612 virological effect Effects 0.000 abstract 1
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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Landscapes
- Health & Medical Sciences (AREA)
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- Organic Chemistry (AREA)
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- Chemical Kinetics & Catalysis (AREA)
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- Cardiology (AREA)
- Hematology (AREA)
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- Dermatology (AREA)
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- Rheumatology (AREA)
- Urology & Nephrology (AREA)
- Communicable Diseases (AREA)
- Virology (AREA)
- Diabetes (AREA)
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- Otolaryngology (AREA)
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Abstract
SE REFIERE A UN COMPUESTO DE FORMULA I DONDE R ES ARILO, SUSTITUIDO O NO; R2 ES ALQUINILALQUILO, CN, ALQUILO, ENTRE OTROS; R3 ES H, HALOGENO, ALQUILO, ENTRE OTROS; R4 ES H, HALO, ALQUILO. SON COMPUESTOS PREFERIDOS: A, B, C, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA SIENDO INHIBIDORES DE CINASA DE PROTEINAS UTILES EN EL TRATAMIENTO DE CANCER, INFLAMACION, ARTRITIS, ENFERMEDADES VIRALES Y ENFERMEDADES NEURODEGENERATIVAS, CARDIOVASCULARES Y FUNGICAS
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US40802902P | 2002-09-04 | 2002-09-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20041000A1 true PE20041000A1 (es) | 2004-12-29 |
Family
ID=32030632
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2003000900A PE20041000A1 (es) | 2002-09-04 | 2003-09-04 | Pirazolopirimidinas como inhibidores de la quinasa dependientes de ciclina |
Country Status (18)
| Country | Link |
|---|---|
| US (2) | US7067661B2 (es) |
| EP (1) | EP1534712B1 (es) |
| JP (2) | JP4790265B2 (es) |
| KR (1) | KR20050033659A (es) |
| CN (1) | CN1701073B (es) |
| AR (1) | AR041133A1 (es) |
| AT (1) | ATE362474T1 (es) |
| AU (1) | AU2003298571B2 (es) |
| CA (1) | CA2497544C (es) |
| DE (1) | DE60313872T2 (es) |
| ES (1) | ES2283868T3 (es) |
| MX (1) | MXPA05002572A (es) |
| MY (2) | MY137843A (es) |
| NZ (1) | NZ539161A (es) |
| PE (1) | PE20041000A1 (es) |
| TW (1) | TWI329645B (es) |
| WO (1) | WO2004026229A2 (es) |
| ZA (1) | ZA200501846B (es) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69734362T2 (de) * | 1996-12-03 | 2006-07-20 | Sloan-Kettering Institute For Cancer Research | Synthese von epothilonen, zwischenprodukte dazu, analoga und verwendungen davon |
| EP1388541A1 (en) * | 2002-08-09 | 2004-02-11 | Centre National De La Recherche Scientifique (Cnrs) | Pyrrolopyrazines as kinase inhibitors |
| US7649006B2 (en) | 2002-08-23 | 2010-01-19 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
| US6921769B2 (en) | 2002-08-23 | 2005-07-26 | Sloan-Kettering Institute For Cancer Research | Synthesis of epothilones, intermediates thereto and analogues thereof |
| ES2281692T3 (es) | 2002-08-23 | 2007-10-01 | Sloan-Kettering Institute For Cancer Research | Sintesis de epotilones, sus intermediarios, sus analogos y sus usos. |
| US7205308B2 (en) * | 2002-09-04 | 2007-04-17 | Schering Corporation | Trisubstituted 7-aminopyrazolopyrimidines as cyclin dependent kinase inhibitors |
| ATE362474T1 (de) * | 2002-09-04 | 2007-06-15 | Schering Corp | Pyrazolo(1,5-a)pyrimidine als hemmstoffe cyclin- abhängiger kinasen |
| US7601724B2 (en) * | 2002-09-04 | 2009-10-13 | Schering Corporation | Substituted pyrazolo[1,5-a]pyrimidines as protein kinase inhibitors |
| WO2004076458A1 (en) * | 2003-02-28 | 2004-09-10 | Teijin Pharma Limited | Pyrazolo[1,5-a]pyrimidine derivatives |
| WO2004087707A1 (en) * | 2003-03-31 | 2004-10-14 | Vernalis (Cambridge) Limited | Pyrazolopyrimidine compounds and their use in medicine |
| EP1671962A1 (en) * | 2003-10-10 | 2006-06-21 | Ono Pharmaceutical Co., Ltd. | Novel fused heterocyclic compound and use thereof |
| WO2005112936A1 (en) * | 2004-05-14 | 2005-12-01 | The Regents Of The University Of Michigan | Compositions and methods relating to protein kinase inhibitors |
| CA2578384A1 (en) * | 2004-09-06 | 2006-03-16 | Altana Pharma Ag | Novel pyrazolopyrimidines |
| FR2876582B1 (fr) * | 2004-10-15 | 2007-01-05 | Centre Nat Rech Scient Cnrse | Utilisation de derives de pyrrolo-pyrazines pour la fabrication de medicaments pour le traitement de la mucoviscidose et de maladies liees a un defaut d'adressage des proteines dans les cellules |
| US7741318B2 (en) | 2004-12-21 | 2010-06-22 | Schering Corporation | Pyrazolo [1,5-A]pyrimidine adenosine A2a receptor antagonists |
| EP2258359A3 (en) | 2005-08-26 | 2011-04-06 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation with sabcomelin |
| CA2620333A1 (en) | 2005-08-26 | 2007-03-01 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation |
| ES2349476T3 (es) | 2005-09-09 | 2011-01-03 | Schering Corporation | Nuevos derivados de 4-ciano, 4-amino y 4-aminometilo de compuestos de pirazolo[1,5-a]piridinas, pirazolo[1,5-c]pirimidinas y 2h-indazol y derivados de 5-ciano, 5-amino y 5-aminometilo de compuestos de imidazo[1,2-a]piridinas e imidazo[1,5-a]pirazinas, como inhibidores de cinasa dependiente de ciclina. |
| AU2006304787A1 (en) | 2005-10-21 | 2007-04-26 | Braincells, Inc. | Modulation of neurogenesis by PDE inhibition |
| EP2314289A1 (en) | 2005-10-31 | 2011-04-27 | Braincells, Inc. | Gaba receptor mediated modulation of neurogenesis |
| US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
| WO2007118844A1 (de) * | 2006-04-13 | 2007-10-25 | Basf Se | Substituierte pyrazolopyrimidine, verfahren zu ihrer herstellung und ihre verwendung zur bekämpfung von schadpilzen sowie sie enthaltende mittel |
| EP2021000A2 (en) | 2006-05-09 | 2009-02-11 | Braincells, Inc. | Neurogenesis by modulating angiotensin |
| CN101495481A (zh) * | 2006-05-22 | 2009-07-29 | 先灵公司 | 作为CDK抑制剂的吡唑并[1,5-α]嘧啶 |
| US8008307B2 (en) | 2006-08-08 | 2011-08-30 | Millennium Pharmaceuticals, Inc. | Heteroaryl compounds useful as inhibitors of E1 activating enzymes |
| US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
| US8299241B2 (en) * | 2006-12-05 | 2012-10-30 | Arena Pharmaceuticals, Inc. | Processes for preparing (R)-8-chloro-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine and intermediates thereof |
| BRPI0910979A2 (pt) * | 2008-04-07 | 2016-01-05 | Irm Llc | compostos e composições como inibidores de quinase |
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| EP2473041B1 (en) | 2009-09-04 | 2018-03-07 | Merck Sharp & Dohme Corp. | Modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors |
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2003
- 2003-09-03 AT AT03796321T patent/ATE362474T1/de not_active IP Right Cessation
- 2003-09-03 WO PCT/US2003/027491 patent/WO2004026229A2/en not_active Ceased
- 2003-09-03 NZ NZ539161A patent/NZ539161A/en not_active IP Right Cessation
- 2003-09-03 MY MYPI20033315A patent/MY137843A/en unknown
- 2003-09-03 MY MYPI20071385A patent/MY145332A/en unknown
- 2003-09-03 US US10/653,776 patent/US7067661B2/en not_active Expired - Lifetime
- 2003-09-03 TW TW092124336A patent/TWI329645B/zh active
- 2003-09-03 AR ARP030103188A patent/AR041133A1/es unknown
- 2003-09-03 KR KR1020057003527A patent/KR20050033659A/ko not_active Ceased
- 2003-09-03 CN CN038247011A patent/CN1701073B/zh not_active Expired - Fee Related
- 2003-09-03 ES ES03796321T patent/ES2283868T3/es not_active Expired - Lifetime
- 2003-09-03 JP JP2004537708A patent/JP4790265B2/ja not_active Expired - Fee Related
- 2003-09-03 EP EP03796321A patent/EP1534712B1/en not_active Expired - Lifetime
- 2003-09-03 DE DE60313872T patent/DE60313872T2/de not_active Expired - Lifetime
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- 2003-09-03 CA CA2497544A patent/CA2497544C/en not_active Expired - Fee Related
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- 2003-09-04 PE PE2003000900A patent/PE20041000A1/es not_active Application Discontinuation
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2005
- 2005-03-03 ZA ZA200501846A patent/ZA200501846B/en unknown
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2006
- 2006-03-31 US US11/395,676 patent/US7514442B2/en not_active Expired - Lifetime
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- 2010-04-06 JP JP2010088212A patent/JP2010180235A/ja not_active Withdrawn
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| WO2004026229A2 (en) | 2004-04-01 |
| DE60313872T2 (de) | 2008-01-17 |
| AR041133A1 (es) | 2005-05-04 |
| EP1534712B1 (en) | 2007-05-16 |
| CN1701073A (zh) | 2005-11-23 |
| US7514442B2 (en) | 2009-04-07 |
| ES2283868T3 (es) | 2007-11-01 |
| NZ539161A (en) | 2006-05-26 |
| ATE362474T1 (de) | 2007-06-15 |
| CA2497544A1 (en) | 2004-04-01 |
| WO2004026229A3 (en) | 2004-06-17 |
| TW200413376A (en) | 2004-08-01 |
| US20060178371A1 (en) | 2006-08-10 |
| TWI329645B (en) | 2010-09-01 |
| MY137843A (en) | 2009-03-31 |
| MXPA05002572A (es) | 2005-09-08 |
| JP2010180235A (ja) | 2010-08-19 |
| JP4790265B2 (ja) | 2011-10-12 |
| AU2003298571A1 (en) | 2004-04-08 |
| ZA200501846B (en) | 2005-09-12 |
| JP2006502184A (ja) | 2006-01-19 |
| EP1534712A2 (en) | 2005-06-01 |
| HK1071572A1 (en) | 2005-07-22 |
| US20040106624A1 (en) | 2004-06-03 |
| DE60313872D1 (de) | 2007-06-28 |
| CA2497544C (en) | 2010-11-02 |
| US7067661B2 (en) | 2006-06-27 |
| MY145332A (en) | 2012-01-31 |
| AU2003298571B2 (en) | 2006-10-19 |
| KR20050033659A (ko) | 2005-04-12 |
| CN1701073B (zh) | 2011-06-22 |
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