MX2007004276A - 1,5-naftiridin-azolidinonas que tienen actividad antiproliferativa de cdk-1. - Google Patents
1,5-naftiridin-azolidinonas que tienen actividad antiproliferativa de cdk-1.Info
- Publication number
- MX2007004276A MX2007004276A MX2007004276A MX2007004276A MX2007004276A MX 2007004276 A MX2007004276 A MX 2007004276A MX 2007004276 A MX2007004276 A MX 2007004276A MX 2007004276 A MX2007004276 A MX 2007004276A MX 2007004276 A MX2007004276 A MX 2007004276A
- Authority
- MX
- Mexico
- Prior art keywords
- azolidinones
- naphthyridine
- antiproliferative activity
- cdk1
- cdk1 antiproliferative
- Prior art date
Links
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
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Abstract
La presente invencion se refiere a las 1,5-naftiridin-azolidinonas de la formula (I) a los procesos para la fabricacion de dichos compuestos, asi como los medicamentos que los contienen. Estos compuestos soninhibidores de CDKl y muestran actividad antiproliferativa. Estos son por lo tanto Utiles como agentes anti-cancerosos.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US61880704P | 2004-10-14 | 2004-10-14 | |
PCT/EP2005/010716 WO2006040052A1 (en) | 2004-10-14 | 2005-10-05 | 1,5-naphthyridine azolidinones having cdk1 antiproliferative activity |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2007004276A true MX2007004276A (es) | 2007-05-16 |
Family
ID=36013291
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2007004276A MX2007004276A (es) | 2004-10-14 | 2005-10-05 | 1,5-naftiridin-azolidinonas que tienen actividad antiproliferativa de cdk-1. |
Country Status (11)
Country | Link |
---|---|
US (1) | US7268231B2 (es) |
EP (1) | EP1805174A1 (es) |
JP (1) | JP2008516905A (es) |
KR (2) | KR100875408B1 (es) |
CN (1) | CN101039944B (es) |
AU (1) | AU2005293835A1 (es) |
BR (1) | BRPI0516488A (es) |
CA (1) | CA2583192A1 (es) |
MX (1) | MX2007004276A (es) |
RU (1) | RU2405781C2 (es) |
WO (1) | WO2006040052A1 (es) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7304074B2 (en) * | 2005-04-05 | 2007-12-04 | Hoffmann-La Roche Inc. | Substituted 1,5-naphthyridine azolinones |
TW200745066A (en) | 2005-09-16 | 2007-12-16 | Torrent Pharmaceuticals Ltd | Novel PTP1B inhibitors |
FR2919608B1 (fr) * | 2007-08-01 | 2012-10-05 | Univ Rennes | Derives d'imidazolones,procede de preparation et applications biologiques |
CN101555248B (zh) * | 2009-05-22 | 2011-06-22 | 北京欧凯纳斯科技有限公司 | 一种多取代1,5-萘啶化合物的制备方法 |
GB201007286D0 (en) | 2010-04-30 | 2010-06-16 | Astex Therapeutics Ltd | New compounds |
GB201020179D0 (en) | 2010-11-29 | 2011-01-12 | Astex Therapeutics Ltd | New compounds |
GB201118652D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
GB201118675D0 (en) | 2011-10-28 | 2011-12-14 | Astex Therapeutics Ltd | New compounds |
GB201118656D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
GB201118654D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
GB201209613D0 (en) | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
GB201209609D0 (en) | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
RU2521390C1 (ru) * | 2013-03-14 | 2014-06-27 | Общество с ограниченной ответственностью "Тиацен" | Производное роданина и средство для профилактики опухолевых заболеваний |
JO3512B1 (ar) | 2014-03-26 | 2020-07-05 | Astex Therapeutics Ltd | مشتقات كينوكسالين مفيدة كمعدلات لإنزيم fgfr كيناز |
PT3122358T (pt) | 2014-03-26 | 2021-03-04 | Astex Therapeutics Ltd | Combinações de inibidores do fgfr e cmet para o tratamento do cancro |
DK3122359T3 (da) | 2014-03-26 | 2021-03-08 | Astex Therapeutics Ltd | Kombinationer af en fgfr-inhibitor og en igf1r-hæmmer |
JOP20200201A1 (ar) | 2015-02-10 | 2017-06-16 | Astex Therapeutics Ltd | تركيبات صيدلانية تشتمل على n-(3.5- ثنائي ميثوكسي فينيل)-n'-(1-ميثيل إيثيل)-n-[3-(ميثيل-1h-بيرازول-4-يل) كينوكسالين-6-يل]إيثان-1.2-ثنائي الأمين |
US10478494B2 (en) | 2015-04-03 | 2019-11-19 | Astex Therapeutics Ltd | FGFR/PD-1 combination therapy for the treatment of cancer |
CA2996989C (en) | 2015-09-23 | 2023-10-03 | Janssen Pharmaceutica Nv | Bi-heteroaryl substituted 1,4-benzodiazepines and uses thereof for the treatment of cancer |
LT3353177T (lt) | 2015-09-23 | 2020-08-25 | Janssen Pharmaceutica Nv | Tricikliniai heterociklai, skirti vėžio gydymui |
JP7311620B2 (ja) | 2019-03-08 | 2023-07-19 | メビオン・メディカル・システムズ・インコーポレーテッド | 粒子線治療システムのためのコリメータおよびエネルギーデグレーダ |
US20230167104A1 (en) * | 2020-04-30 | 2023-06-01 | Perha Pharmaceuticals | New imidazolone derivatives as inhibitors of protein kinases in particular dyrk1a, clk1 and/or clk4 |
EP3904354A1 (en) * | 2020-04-30 | 2021-11-03 | Perha Pharmaceuticals | New imidazolone derivatives as inhibitors of protein kinases in particular dyrk1a, clk1 and/or clk4 |
TW202237585A (zh) | 2020-11-27 | 2022-10-01 | 瑞士商瑞森製藥公司 | Cdk抑制劑 |
WO2022149057A1 (en) | 2021-01-05 | 2022-07-14 | Rhizen Pharmaceuticals Ag | Cdk inhibitors |
EP4173674A1 (en) | 2021-10-26 | 2023-05-03 | Perha Pharmaceuticals | Imidazolone derivatives as inhibitors of protein kinases in particular dyrk1a, clk1 and/or clk4 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1681811B (zh) * | 2002-07-10 | 2010-05-26 | 默克雪兰诺有限公司 | 唑烷酮-乙烯基稠合的-苯衍生物 |
SI1567112T1 (sl) * | 2002-11-22 | 2009-02-28 | Smithkline Beecham Corp | Thiazolidin-4-oni za inhibiranje proteinov hyak3 |
-
2005
- 2005-10-05 CA CA002583192A patent/CA2583192A1/en not_active Abandoned
- 2005-10-05 BR BRPI0516488-5A patent/BRPI0516488A/pt not_active IP Right Cessation
- 2005-10-05 AU AU2005293835A patent/AU2005293835A1/en not_active Abandoned
- 2005-10-05 EP EP05791894A patent/EP1805174A1/en not_active Withdrawn
- 2005-10-05 WO PCT/EP2005/010716 patent/WO2006040052A1/en active Application Filing
- 2005-10-05 US US11/244,022 patent/US7268231B2/en not_active Expired - Fee Related
- 2005-10-05 RU RU2007117765/04A patent/RU2405781C2/ru not_active IP Right Cessation
- 2005-10-05 CN CN2005800351115A patent/CN101039944B/zh not_active Expired - Fee Related
- 2005-10-05 KR KR1020077008407A patent/KR100875408B1/ko not_active IP Right Cessation
- 2005-10-05 MX MX2007004276A patent/MX2007004276A/es active IP Right Grant
- 2005-10-05 KR KR1020087018586A patent/KR20080075235A/ko not_active Application Discontinuation
- 2005-10-05 JP JP2007536046A patent/JP2008516905A/ja not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
AU2005293835A1 (en) | 2006-04-20 |
CN101039944A (zh) | 2007-09-19 |
US7268231B2 (en) | 2007-09-11 |
US20060084673A1 (en) | 2006-04-20 |
JP2008516905A (ja) | 2008-05-22 |
RU2405781C2 (ru) | 2010-12-10 |
RU2007117765A (ru) | 2008-11-20 |
KR100875408B1 (ko) | 2008-12-23 |
CA2583192A1 (en) | 2006-04-20 |
BRPI0516488A (pt) | 2008-09-09 |
EP1805174A1 (en) | 2007-07-11 |
CN101039944B (zh) | 2010-05-05 |
KR20070053332A (ko) | 2007-05-23 |
KR20080075235A (ko) | 2008-08-14 |
WO2006040052A1 (en) | 2006-04-20 |
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