CL2008001297A1 - N-[(1s)-1-(5-fluoropirim idin-2-i1 )etil]-3-(5-isopropoxi-1 h-pirazol-3-il )-3h-imidazo[4,5-b]piridin-5amina o una sal farmacéuticamente aceptabie del mismo; composición farmacéutica que lo comprende; y su uso en el tratamiento del cáncer. - Google Patents
N-[(1s)-1-(5-fluoropirim idin-2-i1 )etil]-3-(5-isopropoxi-1 h-pirazol-3-il )-3h-imidazo[4,5-b]piridin-5amina o una sal farmacéuticamente aceptabie del mismo; composición farmacéutica que lo comprende; y su uso en el tratamiento del cáncer.Info
- Publication number
- CL2008001297A1 CL2008001297A1 CL2008001297A CL2008001297A CL2008001297A1 CL 2008001297 A1 CL2008001297 A1 CL 2008001297A1 CL 2008001297 A CL2008001297 A CL 2008001297A CL 2008001297 A CL2008001297 A CL 2008001297A CL 2008001297 A1 CL2008001297 A1 CL 2008001297A1
- Authority
- CL
- Chile
- Prior art keywords
- pharmaceutically acceptable
- acceptable salt
- 5amine
- imidazo
- cancer
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 title abstract 5
- 206010028980 Neoplasm Diseases 0.000 title abstract 2
- 201000011510 cancer Diseases 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 239000008280 blood Substances 0.000 abstract 1
- 210000004369 blood Anatomy 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000000546 pharmaceutical excipient Substances 0.000 abstract 1
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- 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
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- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
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- 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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- 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
- C07D471/22—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 systems contains four or more hetero rings
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- C07D491/22—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains four or more hetero rings
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- C07D498/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
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- Ophthalmology & Optometry (AREA)
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- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
N-[(1S)-1-(5-FLUOROPIRIM IDIN-2-IL)ETIL]-3-(5-I50PROPOXI-1 H-PIRAZOL-3-IL )-3H-IMIDAZO[4,5-B]PIRIDIN-5AMINA O UNA SAL FARMACÉUTICAMENTE ACEPTABLE DEL MISMO. DICHO COMPUESTO O UNA SAL FARMACÉUTICAMENTE ACEPTABLE DEL MISMO, PARA USAR COMO UN MEDICAMENTO. USO DE DICHO COMPUESTO O UNA SAL FARMACÉUTICAMENTE ACEPTABLE DEL MISMO, PARA EL TRATAMIENTO DEL CÁNCER EN UN ANIMAL E SANGRE CALIENTE.<br /> COMPOSICIÓN FARMACÉUTICA QUE COMPRENDE DICHO COMPUESTO O UNA SAL FARMACÉUTICAMENTE ACEPTABLE DEL MISMO Y POR LO MENOS UN PORTADOR, DILUYENTE O EXCIPIENTE FARMACÉUTICAMENTE ACEPTABLE.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US91627007P | 2007-05-04 | 2007-05-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2008001297A1 true CL2008001297A1 (es) | 2009-01-16 |
Family
ID=39592016
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2008001297A CL2008001297A1 (es) | 2007-05-04 | 2008-05-05 | N-[(1s)-1-(5-fluoropirim idin-2-i1 )etil]-3-(5-isopropoxi-1 h-pirazol-3-il )-3h-imidazo[4,5-b]piridin-5amina o una sal farmacéuticamente aceptabie del mismo; composición farmacéutica que lo comprende; y su uso en el tratamiento del cáncer. |
Country Status (24)
| Country | Link |
|---|---|
| US (3) | US8486966B2 (es) |
| EP (1) | EP2152705A1 (es) |
| JP (1) | JP5415403B2 (es) |
| KR (1) | KR101563372B1 (es) |
| CN (1) | CN101679426A (es) |
| AR (1) | AR066429A1 (es) |
| AU (1) | AU2008247159B2 (es) |
| BR (1) | BRPI0811534A2 (es) |
| CA (1) | CA2684693C (es) |
| CL (1) | CL2008001297A1 (es) |
| CO (1) | CO6251294A2 (es) |
| EC (1) | ECSP099751A (es) |
| IL (1) | IL201691A0 (es) |
| MX (1) | MX2009011944A (es) |
| MY (1) | MY147890A (es) |
| NZ (1) | NZ581633A (es) |
| PE (1) | PE20090238A1 (es) |
| RU (1) | RU2481348C2 (es) |
| SA (1) | SA08290271B1 (es) |
| TW (1) | TWI406864B (es) |
| UA (1) | UA99459C2 (es) |
| UY (1) | UY31065A1 (es) |
| WO (1) | WO2008135785A1 (es) |
| ZA (1) | ZA200907679B (es) |
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| UA99459C2 (en) * | 2007-05-04 | 2012-08-27 | Астразенека Аб | 9-(pyrazol-3-yl)- 9h-purine-2-amine and 3-(pyraz0l-3-yl)-3h-imidazo[4,5-b]pyridin-5-amine derivatives and their use for the treatment of cancer |
| EA201000561A1 (ru) | 2007-10-09 | 2010-10-29 | Мерк Патент Гмбх | Производные пиридина, пригодные в качестве активаторов глюкокиназы |
| GB0725218D0 (en) * | 2007-12-24 | 2008-02-06 | Syngenta Ltd | Chemical compounds |
| US8299070B2 (en) * | 2009-11-25 | 2012-10-30 | Japan Tobacco Inc. | Indole compounds and pharmaceutical use thereof |
| EP2397482A1 (en) | 2010-06-15 | 2011-12-21 | Almirall, S.A. | Heteroaryl imidazolone derivatives as jak inhibitors |
| UA110259C2 (uk) * | 2011-09-22 | 2015-12-10 | Пфайзер Інк. | Похідні піролопіримідину і пурину |
| CN102952084A (zh) * | 2012-11-15 | 2013-03-06 | 大连九信生物化工科技有限公司 | 一种4,6-二氯-2-甲硫基-5-硝基嘧啶的合成方法 |
| US9370515B2 (en) | 2013-03-07 | 2016-06-21 | Califia Bio, Inc. | Mixed lineage kinase inhibitors and method of treatments |
| CN104003943A (zh) * | 2014-05-06 | 2014-08-27 | 南通常佑药业科技有限公司 | 一种替格瑞洛中间体的制备方法 |
| KR20190043437A (ko) * | 2017-10-18 | 2019-04-26 | 씨제이헬스케어 주식회사 | 단백질 키나제 억제제로서의 헤테로고리 화합물 |
| GB201717260D0 (en) | 2017-10-20 | 2017-12-06 | Galapagos Nv | Novel compounds and pharma ceutical compositions thereof for the treatment of inflammatory disorders |
| KR102195348B1 (ko) | 2018-11-15 | 2020-12-24 | 에이치케이이노엔 주식회사 | 단백질 키나제 억제제로서의 신규 화합물 및 이를 포함하는 약제학적 조성물 |
| EP3942045A1 (en) | 2019-03-21 | 2022-01-26 | Onxeo | A dbait molecule in combination with kinase inhibitor for the treatment of cancer |
| WO2021062163A1 (en) | 2019-09-27 | 2021-04-01 | Disc Medicine, Inc. | Methods for treating myelofibrosis and related conditions |
| KR20220098759A (ko) | 2019-11-08 | 2022-07-12 | 인쎄름 (엥스띠뛰 나씨오날 드 라 쌍떼 에 드 라 흐쉐르슈 메디깔) | 키나제 억제제에 대해 내성을 획득한 암의 치료 방법 |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| CA3169286A1 (en) * | 2020-02-25 | 2021-09-02 | Dana-Farber Cancer Institute, Inc. | Potent and selective degraders of alk |
| CA3177830A1 (en) | 2020-05-13 | 2021-11-18 | Maria BECONI | Anti-hemojuvelin (hjv) antibodies for treating myelofibrosis |
| AR124526A1 (es) * | 2020-12-29 | 2023-04-05 | Pyramid Biosciences Inc | Composiciones farmacéuticas tópicas y métodos |
| WO2023248151A1 (en) | 2022-06-24 | 2023-12-28 | Pyramid Biosciences, Inc. | Method of treating skin field cancerization with actinic keratoses |
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-
2008
- 2008-02-05 UA UAA200912433A patent/UA99459C2/ru unknown
- 2008-04-30 PE PE2008000770A patent/PE20090238A1/es not_active Application Discontinuation
- 2008-04-30 TW TW097115958A patent/TWI406864B/zh not_active IP Right Cessation
- 2008-05-02 NZ NZ581633A patent/NZ581633A/en not_active IP Right Cessation
- 2008-05-02 WO PCT/GB2008/050321 patent/WO2008135785A1/en not_active Ceased
- 2008-05-02 EP EP20080737245 patent/EP2152705A1/en not_active Withdrawn
- 2008-05-02 US US12/598,473 patent/US8486966B2/en not_active Expired - Fee Related
- 2008-05-02 KR KR1020097025268A patent/KR101563372B1/ko not_active Expired - Fee Related
- 2008-05-02 RU RU2009144848/04A patent/RU2481348C2/ru not_active IP Right Cessation
- 2008-05-02 CA CA2684693A patent/CA2684693C/en not_active Expired - Fee Related
- 2008-05-02 MY MYPI20094620A patent/MY147890A/en unknown
- 2008-05-02 JP JP2010507002A patent/JP5415403B2/ja not_active Expired - Fee Related
- 2008-05-02 BR BRPI0811534-6A2A patent/BRPI0811534A2/pt not_active IP Right Cessation
- 2008-05-02 MX MX2009011944A patent/MX2009011944A/es active IP Right Grant
- 2008-05-02 CN CN200880019785A patent/CN101679426A/zh active Pending
- 2008-05-02 UY UY31065A patent/UY31065A1/es not_active Application Discontinuation
- 2008-05-02 AU AU2008247159A patent/AU2008247159B2/en not_active Ceased
- 2008-05-02 AR ARP080101879A patent/AR066429A1/es unknown
- 2008-05-03 SA SA8290271A patent/SA08290271B1/ar unknown
- 2008-05-05 CL CL2008001297A patent/CL2008001297A1/es unknown
-
2009
- 2009-10-22 IL IL201691A patent/IL201691A0/en unknown
- 2009-11-02 ZA ZA200907679A patent/ZA200907679B/xx unknown
- 2009-11-09 CO CO09126884A patent/CO6251294A2/es active IP Right Grant
- 2009-11-20 EC EC2009009751A patent/ECSP099751A/es unknown
-
2013
- 2013-06-21 US US13/923,498 patent/US20140155394A1/en not_active Abandoned
-
2014
- 2014-07-15 US US14/331,302 patent/US20150011545A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| IL201691A0 (en) | 2010-05-31 |
| US8486966B2 (en) | 2013-07-16 |
| EP2152705A1 (en) | 2010-02-17 |
| MY147890A (en) | 2013-01-31 |
| US20140155394A1 (en) | 2014-06-05 |
| UA99459C2 (en) | 2012-08-27 |
| CA2684693A1 (en) | 2008-11-13 |
| AR066429A1 (es) | 2009-08-19 |
| KR101563372B1 (ko) | 2015-10-26 |
| BRPI0811534A2 (pt) | 2014-11-18 |
| RU2481348C2 (ru) | 2013-05-10 |
| CO6251294A2 (es) | 2011-02-21 |
| CA2684693C (en) | 2015-06-23 |
| SA08290271B1 (ar) | 2012-02-07 |
| RU2009144848A (ru) | 2011-06-10 |
| ECSP099751A (es) | 2009-12-28 |
| US20150011545A1 (en) | 2015-01-08 |
| JP2010526128A (ja) | 2010-07-29 |
| ZA200907679B (en) | 2010-07-28 |
| MX2009011944A (es) | 2009-12-11 |
| WO2008135785A1 (en) | 2008-11-13 |
| CN101679426A (zh) | 2010-03-24 |
| PE20090238A1 (es) | 2009-04-21 |
| UY31065A1 (es) | 2009-01-05 |
| KR20100019988A (ko) | 2010-02-19 |
| JP5415403B2 (ja) | 2014-02-12 |
| NZ581633A (en) | 2012-01-12 |
| TWI406864B (zh) | 2013-09-01 |
| US20100324040A1 (en) | 2010-12-23 |
| TW200902530A (en) | 2009-01-16 |
| AU2008247159B2 (en) | 2011-11-10 |
| AU2008247159A1 (en) | 2008-11-13 |
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