NO20083214L - Pyrimidinylarylurea-derivater som omdannes til FGF-inhibitorer - Google Patents
Pyrimidinylarylurea-derivater som omdannes til FGF-inhibitorerInfo
- Publication number
- NO20083214L NO20083214L NO20083214A NO20083214A NO20083214L NO 20083214 L NO20083214 L NO 20083214L NO 20083214 A NO20083214 A NO 20083214A NO 20083214 A NO20083214 A NO 20083214A NO 20083214 L NO20083214 L NO 20083214L
- Authority
- NO
- Norway
- Prior art keywords
- compounds
- pyrimidinylarylurea
- derivatives
- converted
- fgf inhibitors
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 238000000034 method Methods 0.000 abstract 2
- 150000003672 ureas Chemical class 0.000 abstract 2
- 102000001253 Protein Kinase Human genes 0.000 abstract 1
- 230000001419 dependent effect Effects 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 108060006633 protein kinase Proteins 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Foreliggende oppfinnelse angår heteroarylarylureaforbindelser med formelen (IA) hvori radikalene og symbolene har betydningene slik det er definert heri, anvendelsen av slike forbindelser for fremstilling av proteinkinaseavhengige sykdommer; farmasøytiske preparater som innbefatter nevnte heteroarylarylureaforbindelser, fremgangsmåter for fremstilling av slike nye forbindelser og fremgangsmåter for behandling som innbefatter anvendelsen av slike heteroarylarylureaforbindelser.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US75271105P | 2005-12-21 | 2005-12-21 | |
| PCT/EP2006/070046 WO2007071752A2 (en) | 2005-12-21 | 2006-12-20 | Pyrimidinyl aryl urea derivatives being fgf inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO20083214L true NO20083214L (no) | 2008-09-01 |
Family
ID=37946774
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20083214A NO20083214L (no) | 2005-12-21 | 2008-07-18 | Pyrimidinylarylurea-derivater som omdannes til FGF-inhibitorer |
Country Status (22)
| Country | Link |
|---|---|
| US (2) | US8293746B2 (no) |
| EP (1) | EP1976847B1 (no) |
| JP (1) | JP5153645B2 (no) |
| KR (1) | KR101406956B1 (no) |
| CN (1) | CN101336237B (no) |
| AU (1) | AU2006326989B2 (no) |
| BR (1) | BRPI0620408B8 (no) |
| CA (1) | CA2634047C (no) |
| CR (1) | CR10072A (no) |
| EA (1) | EA016438B1 (no) |
| EC (1) | ECSP088561A (no) |
| GE (1) | GEP20105074B (no) |
| HN (1) | HN2008000949A (no) |
| IL (1) | IL192093A0 (no) |
| MA (1) | MA30063B1 (no) |
| ME (2) | MEP3808A (no) |
| NO (1) | NO20083214L (no) |
| SM (1) | SMP200800041B (no) |
| SV (1) | SV2008002967A (no) |
| TN (1) | TNSN08276A1 (no) |
| WO (1) | WO2007071752A2 (no) |
| ZA (1) | ZA200805092B (no) |
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| GB0512324D0 (en) * | 2005-06-16 | 2005-07-27 | Novartis Ag | Organic compounds |
| AU2006326989B2 (en) * | 2005-12-21 | 2011-11-24 | Novartis Ag | Pyrimidinyl aryl urea derivatives being FGF inhibitors |
| US20120214811A1 (en) * | 2009-08-28 | 2012-08-23 | Ignacio Aliagas | Raf inhibitor compounds and methods of use thereof |
| CN102596916B (zh) * | 2009-10-30 | 2015-06-17 | 诺瓦提斯公司 | 3-(2,6-二氯-3,5-二甲氧基-苯基)-1-{6-[4-(4-乙基-哌嗪-1-基)-苯基氨基]-嘧啶-4-基}-1-甲基-脲的n-氧化物 |
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| WO2011075620A1 (en) | 2009-12-18 | 2011-06-23 | Novartis Ag | Method for treating haematological cancers |
| US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
| JP5343177B1 (ja) | 2012-02-28 | 2013-11-13 | アステラス製薬株式会社 | 含窒素芳香族へテロ環化合物 |
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| PH12019502809B1 (en) | 2012-06-13 | 2024-04-24 | Incyte Holdings Corp | Substituted tricyclic compounds as fgfr inhibitors |
| US20150203589A1 (en) | 2012-07-24 | 2015-07-23 | The Trustees Of Columbia University In The City Of New York | Fusion proteins and methods thereof |
| US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| AR094812A1 (es) | 2013-02-20 | 2015-08-26 | Eisai R&D Man Co Ltd | Derivado de piridina monocíclico como inhibidor del fgfr |
| KR20150124941A (ko) * | 2013-03-10 | 2015-11-06 | 고쿠리츠 다이가쿠 호우징 나고야 다이가쿠 | 골 계통 질환 치료약 및 그 용도 |
| EP2968337B1 (en) | 2013-03-15 | 2021-07-21 | Celgene CAR LLC | Heteroaryl compounds and uses thereof |
| CA2907152A1 (en) | 2013-03-15 | 2014-09-25 | The Trustees Of Columbia University In The City Of New York | Fusion proteins and methods thereof |
| KR102350704B1 (ko) | 2013-03-15 | 2022-01-13 | 셀젠 카르 엘엘씨 | 헤테로아릴 화합물 및 이의 용도 |
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| SMT201800127T1 (it) | 2013-04-19 | 2018-05-02 | Incyte Holdings Corp | Eterocilci biciclici come inibitori di fgfr |
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| BR112016008110B1 (pt) | 2013-10-18 | 2019-07-02 | Eisai R&D Management Co., Ltd. | Composto inibidor de pirimidina fgfr4, composição farmacêutica compreendendo dito compoto e usos terapêuticos destes |
| JP6203954B2 (ja) | 2013-10-25 | 2017-09-27 | ノバルティス アーゲー | Fgfr4阻害剤としての縮環二環式ピリジル誘導体 |
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| EP3925979A3 (en) | 2014-12-23 | 2022-03-23 | The Trustees of Columbia University in the City of New York | Fgfr-tacc fusion proteins and methods thereof |
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| SG10201913036RA (en) | 2015-02-20 | 2020-02-27 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
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| TWI808067B (zh) * | 2016-12-19 | 2023-07-11 | 美商雅酶股份有限公司 | 作為ehmt2抑制劑之胺取代的雜環化合物及其使用方法 |
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| JPWO2019189241A1 (ja) | 2018-03-28 | 2021-03-18 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 肝細胞癌治療剤 |
| MA52493A (fr) | 2018-05-04 | 2021-03-10 | Incyte Corp | Sels d'un inhibiteur de fgfr |
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| EP4069696A1 (en) | 2019-12-04 | 2022-10-12 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
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2006
- 2006-12-20 AU AU2006326989A patent/AU2006326989B2/en active Active
- 2006-12-20 EA EA200801565A patent/EA016438B1/ru not_active IP Right Cessation
- 2006-12-20 ME MEP-38/08A patent/MEP3808A/xx unknown
- 2006-12-20 WO PCT/EP2006/070046 patent/WO2007071752A2/en not_active Ceased
- 2006-12-20 BR BRPI0620408A patent/BRPI0620408B8/pt active IP Right Grant
- 2006-12-20 GE GEAP200610763A patent/GEP20105074B/en unknown
- 2006-12-20 KR KR1020087017819A patent/KR101406956B1/ko active Active
- 2006-12-20 EP EP06830765.1A patent/EP1976847B1/en active Active
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