MA32272B1 - Inhibiteurs de raf de pyrazole [3,4-b]pyridine - Google Patents
Inhibiteurs de raf de pyrazole [3,4-b]pyridineInfo
- Publication number
- MA32272B1 MA32272B1 MA33203A MA33203A MA32272B1 MA 32272 B1 MA32272 B1 MA 32272B1 MA 33203 A MA33203 A MA 33203A MA 33203 A MA33203 A MA 33203A MA 32272 B1 MA32272 B1 MA 32272B1
- Authority
- MA
- Morocco
- Prior art keywords
- raf
- pyrazole
- pyridine
- inhibitors
- compounds
- Prior art date
Links
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 title 2
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 235000007688 Lycopersicon esculentum Nutrition 0.000 abstract 1
- 240000003768 Solanum lycopersicum Species 0.000 abstract 1
- 239000002671 adjuvant Substances 0.000 abstract 1
- 238000003745 diagnosis Methods 0.000 abstract 1
- 238000000338 in vitro Methods 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 210000004962 mammalian cell Anatomy 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 102000009929 raf Kinases Human genes 0.000 abstract 1
- 108010077182 raf Kinases Proteins 0.000 abstract 1
- 150000003839 salts Chemical class 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
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/08—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
La présente invention concerne des composés de formule i qui sont utiles pour l'inhibition de kinases raf. La présente invention concerne des procédés d'utilisation de composés de formule i et des stéréo-isomères, tautomères, promédicaments et sels pharmaceutiquement acceptables de ceux-ci, pour le diagnostic, la prévention ou le traitement in vitro, in situ, et in vivo de tels troubles dans des cellules de mammifère, ou des états pathologiques associés.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3281308P | 2008-02-29 | 2008-02-29 | |
| PCT/US2009/035381 WO2009111279A1 (fr) | 2008-02-29 | 2009-02-27 | Inhibiteurs de raf de pyrazole[3,4-b]pyridine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA32272B1 true MA32272B1 (fr) | 2011-05-02 |
Family
ID=40677552
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA33203A MA32272B1 (fr) | 2008-02-29 | 2010-09-24 | Inhibiteurs de raf de pyrazole [3,4-b]pyridine |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US8394795B2 (fr) |
| EP (1) | EP2265610B1 (fr) |
| JP (1) | JP2011513331A (fr) |
| KR (1) | KR20100117686A (fr) |
| CN (1) | CN102149712A (fr) |
| AR (1) | AR072657A1 (fr) |
| AU (1) | AU2009222144A1 (fr) |
| BR (1) | BRPI0908268A2 (fr) |
| CA (1) | CA2716952A1 (fr) |
| CL (1) | CL2009000448A1 (fr) |
| CR (1) | CR11690A (fr) |
| EC (1) | ECSP10010507A (fr) |
| ES (1) | ES2400202T3 (fr) |
| IL (1) | IL207845A0 (fr) |
| MA (1) | MA32272B1 (fr) |
| MX (1) | MX2010009411A (fr) |
| PE (1) | PE20091623A1 (fr) |
| TW (1) | TW200940539A (fr) |
| WO (1) | WO2009111279A1 (fr) |
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| WO2008063888A2 (fr) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Composés modulant l'activité de c-fms et/ou de c-kit et utilisations associées |
| WO2009012283A1 (fr) | 2007-07-17 | 2009-01-22 | Plexxikon Inc. | Composés et procédés pour la modulation des kinases et leurs indications |
| CN101970415A (zh) | 2008-01-09 | 2011-02-09 | 阵列生物制药公司 | 作为AKT蛋白激酶抑制剂的5H-环戊二烯并[d]嘧啶 |
| CA2716947A1 (fr) * | 2008-02-29 | 2009-09-11 | Array Biopharma Inc. | Derives d'imidazo[4,5-b]pyridine utilises comme inhibiteurs de raf |
| KR20100122505A (ko) * | 2008-02-29 | 2010-11-22 | 어레이 바이오파마 인크. | Raf 저해물질 화합물 및 이들의 이용 방법 |
| JP2011513332A (ja) * | 2008-02-29 | 2011-04-28 | アレイ バイオファーマ、インコーポレイテッド | 癌の治療のためのraf阻害剤としてのn−(6−アミノピリジン−3−イル)−3−(スルホンアミド)ベンズアミド誘導体 |
| MY172424A (en) | 2009-04-03 | 2019-11-25 | Hoffmann La Roche | Propane- i-sulfonic acid {3- (4-chloro-phenyl)-1h-pyrrolo [2, 3-b] pyridine-3-carconyl] -2, 4-difluoro-phenyl} -amide compositions and uses thereof |
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| CN106220623A (zh) | 2009-11-06 | 2016-12-14 | 普莱希科公司 | 用于激酶调节的化合物和方法及其适应症 |
| EP2661434A4 (fr) | 2011-01-06 | 2014-07-09 | Beta Pharma Canada Inc | Nouvelles urées pour le traitement et la prévention du cancer |
| US9624213B2 (en) | 2011-02-07 | 2017-04-18 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| AR085279A1 (es) | 2011-02-21 | 2013-09-18 | Plexxikon Inc | Formas solidas de {3-[5-(4-cloro-fenil)-1h-pirrolo[2,3-b]piridina-3-carbonil]-2,4-difluor-fenil}-amida del acido propano-1-sulfonico |
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-
2009
- 2009-02-27 JP JP2010548886A patent/JP2011513331A/ja not_active Withdrawn
- 2009-02-27 MX MX2010009411A patent/MX2010009411A/es not_active Application Discontinuation
- 2009-02-27 CA CA2716952A patent/CA2716952A1/fr not_active Abandoned
- 2009-02-27 AR ARP090100688A patent/AR072657A1/es unknown
- 2009-02-27 AU AU2009222144A patent/AU2009222144A1/en not_active Abandoned
- 2009-02-27 PE PE2009000310A patent/PE20091623A1/es not_active Application Discontinuation
- 2009-02-27 BR BRPI0908268A patent/BRPI0908268A2/pt not_active IP Right Cessation
- 2009-02-27 CL CL2009000448A patent/CL2009000448A1/es unknown
- 2009-02-27 EP EP09718306A patent/EP2265610B1/fr active Active
- 2009-02-27 KR KR1020107021611A patent/KR20100117686A/ko not_active Withdrawn
- 2009-02-27 TW TW098106512A patent/TW200940539A/zh unknown
- 2009-02-27 ES ES09718306T patent/ES2400202T3/es active Active
- 2009-02-27 WO PCT/US2009/035381 patent/WO2009111279A1/fr not_active Ceased
- 2009-02-27 US US12/920,050 patent/US8394795B2/en not_active Expired - Fee Related
- 2009-02-27 CN CN2009801155134A patent/CN102149712A/zh active Pending
-
2010
- 2010-08-29 IL IL207845A patent/IL207845A0/en unknown
- 2010-09-24 MA MA33203A patent/MA32272B1/fr unknown
- 2010-09-27 CR CR11690A patent/CR11690A/es unknown
- 2010-09-28 EC EC2010010507A patent/ECSP10010507A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CL2009000448A1 (es) | 2009-11-27 |
| PE20091623A1 (es) | 2009-11-19 |
| EP2265610A1 (fr) | 2010-12-29 |
| EP2265610B1 (fr) | 2012-12-12 |
| US20110092479A1 (en) | 2011-04-21 |
| WO2009111279A1 (fr) | 2009-09-11 |
| CA2716952A1 (fr) | 2009-09-11 |
| JP2011513331A (ja) | 2011-04-28 |
| MX2010009411A (es) | 2010-11-30 |
| ECSP10010507A (es) | 2010-10-30 |
| IL207845A0 (en) | 2010-12-30 |
| BRPI0908268A2 (pt) | 2018-10-30 |
| US8394795B2 (en) | 2013-03-12 |
| ES2400202T3 (es) | 2013-04-08 |
| AR072657A1 (es) | 2010-09-15 |
| TW200940539A (en) | 2009-10-01 |
| CN102149712A (zh) | 2011-08-10 |
| AU2009222144A1 (en) | 2009-09-11 |
| KR20100117686A (ko) | 2010-11-03 |
| CR11690A (es) | 2010-11-02 |
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