PE20060197A1 - Heterociclos biciclicos como inhibidores de cinasa - Google Patents
Heterociclos biciclicos como inhibidores de cinasaInfo
- Publication number
- PE20060197A1 PE20060197A1 PE2005000454A PE2005000454A PE20060197A1 PE 20060197 A1 PE20060197 A1 PE 20060197A1 PE 2005000454 A PE2005000454 A PE 2005000454A PE 2005000454 A PE2005000454 A PE 2005000454A PE 20060197 A1 PE20060197 A1 PE 20060197A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- cycloalkyl
- halogen
- heterocycles
- bicycle
- Prior art date
Links
- 229940043355 kinase inhibitor Drugs 0.000 title 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 title 1
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- CJNGZHDUTJNVGB-UHFFFAOYSA-N 2-(4-fluorophenyl)-N-(phenylcarbamoyl)acetamide Chemical compound C1=CC(F)=CC=C1CC(=O)NC(=O)NC1=CC=CC=C1 CJNGZHDUTJNVGB-UHFFFAOYSA-N 0.000 abstract 1
- -1 CYANE Inorganic materials 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 102000004022 Protein-Tyrosine Kinases Human genes 0.000 abstract 1
- 108090000412 Protein-Tyrosine Kinases Proteins 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- WRIRWRKPLXCTFD-UHFFFAOYSA-N malonamide Chemical compound NC(=O)CC(N)=O WRIRWRKPLXCTFD-UHFFFAOYSA-N 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
SE REFIERE A UN COMPUESTO DE FORMULA I O II, DONDE R1 ES H, ALQUILO, ALQUILO SUSTITUIDO, ALQUENILO, CICLOALQUILO, ENTRE OTROS; R2 ES H, HALOGENO, CIANO, NO2, CICLOALQUILO, ENTRE OTROS; V ES CH2, NR8; W Y X SON CADA UNO C, N; Y ES O, S, NR9; Z ES -CR10R11, (CR10R11)mNR12-; m ES 0-2; A ES A, B, ENTRE OTROS; G ES C-HALOGENO, ALQUILO, CICLOALQUILO, ENTRE OTROS; Q ES O, NH, N-ALQUILO, ENTRE OTROS; R3, R4, R8 Y R12 SON CADA UNO H, ALQUILO, ALQUENILO, ALQUINILO SUSTITUIDO, ENTRE OTROS; R9 ES H, ALQUILO, CN, NO2, SO2AMINO; R10 Y R11 SON CADA UNO H, HALOGENO, ALQUILO, HETEROARILO, ENTRE OTROS; R13, R15, R16, R17, R18, R19, R20, R21, R22, R23, R24 Y R25 SON CADA UNO H, HALOGENO, ALQUILO, CICLOALQUILO, HETEROCICLOALQUILO, ARILO, HETEROARILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 1-(4-(4-AMINO-1H-PIRROLO[3,2-c]PIRIDIN-1-IL)FENIL-3-(2-(4-FLUOROFENIL)ACETIL)UREA, SALDE CLOHIDRATO; N1-(4-(4-AMINO-1H-PIRROLO[3,2-c]PIRIDIN-1-IL)FENIL-N3-(4-FLUOROFENIL)MALONAMIDA, SALDE CLOHIDRATO; ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA PROTEINA TIROSINA CINASA UTILES EN EL TRATAMIENTO DE CANCER
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US56538104P | 2004-04-26 | 2004-04-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20060197A1 true PE20060197A1 (es) | 2006-03-15 |
Family
ID=35159810
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2005000454A PE20060197A1 (es) | 2004-04-26 | 2005-04-25 | Heterociclos biciclicos como inhibidores de cinasa |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7566784B2 (es) |
| EP (1) | EP1742948A2 (es) |
| AR (1) | AR049263A1 (es) |
| PE (1) | PE20060197A1 (es) |
| TW (1) | TW200538453A (es) |
| WO (1) | WO2005116028A2 (es) |
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| WO2006114180A1 (de) | 2005-04-25 | 2006-11-02 | Merck Patent Gmbh | Neuartige aza-heterozyklen als kinase-inhibitoren |
| KR101378716B1 (ko) * | 2005-05-20 | 2014-04-10 | 메틸진 인코포레이티드 | Vegf 수용체 및 hgf 수용체 신호전달의 억제제 |
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| JP5734193B2 (ja) | 2008-10-14 | 2015-06-17 | クイ ニング | 化合物及び使用方法 |
| AU2009305669A1 (en) * | 2008-10-16 | 2010-04-22 | The Regents Of The University Of California | Fused ring heteroaryl kinase inhibitors |
| JP5583751B2 (ja) * | 2009-03-21 | 2014-09-03 | クイ ニング | アミノエステル誘導体、その塩、及び使用方法 |
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| MX370814B (es) | 2011-09-02 | 2020-01-08 | Univ California | Pirazolo[3,4-d]pirimidinas sustituidas y usos de las mismas. |
| EA201490451A1 (ru) | 2011-09-14 | 2014-12-30 | Проксимаген Лимитед | Новые соединения - ингибиторы ферментов |
| KR20130118612A (ko) * | 2012-04-20 | 2013-10-30 | (주)네오믹스 | 신규한 아미노피리딘 유도체 및 이의 용도 |
| SG11201502331RA (en) | 2012-09-26 | 2015-04-29 | Univ California | Modulation of ire1 |
| BR112015006990A2 (pt) | 2012-09-28 | 2017-07-04 | Merck Sharp & Dohme | composto, composição farmacêutica, e, uso de pelo menos um composto |
| US9226922B2 (en) | 2012-09-28 | 2016-01-05 | Merck Sharp & Dohme Corp. | Compounds that are ERK inhibitors |
| CN111423366B (zh) * | 2020-04-28 | 2022-05-27 | 山东汇海医药化工有限公司 | 一种吡非尼酮的制备方法 |
| CN114262322A (zh) * | 2020-09-16 | 2022-04-01 | 中国科学院上海有机化学研究所 | 一类细胞程序性坏死抑制剂及其制备方法和用途 |
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| TW200407143A (en) | 2002-05-21 | 2004-05-16 | Bristol Myers Squibb Co | Pyrrolotriazinone compounds and their use to treat diseases |
| TW200401638A (en) | 2002-06-20 | 2004-02-01 | Bristol Myers Squibb Co | Heterocyclic inhibitors of kinases |
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| WO2004032846A2 (en) | 2002-10-07 | 2004-04-22 | Bristol-Myers Squibb Company | Triazolone and triazolethione derivatives |
| CL2003002287A1 (es) | 2002-11-25 | 2005-01-14 | Wyeth Corp | COMPUESTOS DERIVADOS DE TIENO[3,2-b]-PIRIDINA-6-CARBONITRILOS Y TIENEO[2,3-b]-PIRIDINA-5-CARBONITRILOS, COMPOSICION FARMACEUTICA, PROCEDIMIENTO DE PREPARACION Y COMPUESTOS INTERMEDIARIOS, Y SU USO EN EL TRATAMIENTO DEL CANCER, APOPLEJIA, OSTEOPOROSIS |
| TW200420565A (en) | 2002-12-13 | 2004-10-16 | Bristol Myers Squibb Co | C-6 modified indazolylpyrrolotriazines |
| TW200427688A (en) | 2002-12-18 | 2004-12-16 | Glaxo Group Ltd | Antibacterial agents |
| US7144911B2 (en) | 2002-12-31 | 2006-12-05 | Deciphera Pharmaceuticals Llc | Anti-inflammatory medicaments |
| US7030112B2 (en) * | 2003-03-25 | 2006-04-18 | Bristol-Myers Squibb Company | Pyrrolopyridazine compounds and methods of use thereof for the treatment of proliferative disorders |
| US20070213374A1 (en) | 2003-07-07 | 2007-09-13 | Merck Patent Gmbh | Malonamide Derivatives |
| US20050026944A1 (en) | 2003-07-24 | 2005-02-03 | Patrick Betschmann | Thienopyridine and furopyridine kinase inhibitors |
| ES2314444T3 (es) | 2003-08-29 | 2009-03-16 | Pfizer Inc. | Tienopiridina-fenilacetaminasy sus derivados utiles como nuevos agentes antiangiogenicos. |
| SE0302487D0 (sv) | 2003-09-18 | 2003-09-18 | Astrazeneca Ab | Novel compounds |
| PT2213661E (pt) | 2003-09-26 | 2011-12-15 | Exelixis Inc | Moduladores de c-met e métodos de uso |
| US7419978B2 (en) * | 2003-10-22 | 2008-09-02 | Bristol-Myers Squibb Company | Phenyl-aniline substituted bicyclic compounds useful as kinase inhibitors |
| DE10357510A1 (de) | 2003-12-09 | 2005-07-07 | Bayer Healthcare Ag | Heteroarylsubstituierte Benzole |
| AU2005217325B2 (en) | 2004-02-27 | 2007-11-29 | Eisai R & D Management Co., Ltd. | Novel pyridine derivative and pyrimidine derivative (1) |
| DE102004017438A1 (de) | 2004-04-08 | 2005-11-03 | Bayer Healthcare Ag | Hetaryloxy-substituierte Phenylaminopyrimidine |
| US7459562B2 (en) * | 2004-04-23 | 2008-12-02 | Bristol-Myers Squibb Company | Monocyclic heterocycles as kinase inhibitors |
| US7173031B2 (en) * | 2004-06-28 | 2007-02-06 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
| US7432373B2 (en) * | 2004-06-28 | 2008-10-07 | Bristol-Meyers Squibb Company | Processes and intermediates useful for preparing fused heterocyclic kinase inhibitors |
-
2005
- 2005-04-20 TW TW094112576A patent/TW200538453A/zh unknown
- 2005-04-25 PE PE2005000454A patent/PE20060197A1/es not_active Application Discontinuation
- 2005-04-25 US US11/113,838 patent/US7566784B2/en active Active
- 2005-04-25 AR ARP050101631A patent/AR049263A1/es unknown
- 2005-04-26 EP EP05779223A patent/EP1742948A2/en not_active Withdrawn
- 2005-04-26 WO PCT/US2005/014164 patent/WO2005116028A2/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| WO2005116028A3 (en) | 2006-03-30 |
| TW200538453A (en) | 2005-12-01 |
| US20050239820A1 (en) | 2005-10-27 |
| EP1742948A2 (en) | 2007-01-17 |
| US7566784B2 (en) | 2009-07-28 |
| AR049263A1 (es) | 2006-07-12 |
| WO2005116028A2 (en) | 2005-12-08 |
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