ATE532781T1 - 5-(acylamino)indazol-derivate als kinase- inhibitoren - Google Patents
5-(acylamino)indazol-derivate als kinase- inhibitorenInfo
- Publication number
- ATE532781T1 ATE532781T1 AT04755699T AT04755699T ATE532781T1 AT E532781 T1 ATE532781 T1 AT E532781T1 AT 04755699 T AT04755699 T AT 04755699T AT 04755699 T AT04755699 T AT 04755699T AT E532781 T1 ATE532781 T1 AT E532781T1
- Authority
- AT
- Austria
- Prior art keywords
- acylamino
- kinase inhibitors
- indazole derivatives
- indazolo
- tetrahydropyrimidine
- Prior art date
Links
- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical class C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 title 1
- 229940043355 kinase inhibitor Drugs 0.000 title 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 title 1
- 229940053202 antiepileptics carboxamide derivative Drugs 0.000 abstract 2
- 239000003814 drug Substances 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
Classifications
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- 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
- C07D401/14—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 three or more hetero rings
-
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- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—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 two hetero rings
- C07D403/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Cardiology (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Diabetes (AREA)
- Oncology (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Reproductive Health (AREA)
- Hospice & Palliative Care (AREA)
- Pulmonology (AREA)
- Communicable Diseases (AREA)
- Obesity (AREA)
- Psychology (AREA)
- Vascular Medicine (AREA)
- Psychiatry (AREA)
- Immunology (AREA)
- Gynecology & Obstetrics (AREA)
- Emergency Medicine (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US47975303P | 2003-06-19 | 2003-06-19 | |
| PCT/US2004/019692 WO2004112719A2 (en) | 2003-06-19 | 2004-06-18 | Chemical compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE532781T1 true ATE532781T1 (de) | 2011-11-15 |
Family
ID=33539215
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT04755699T ATE532781T1 (de) | 2003-06-19 | 2004-06-18 | 5-(acylamino)indazol-derivate als kinase- inhibitoren |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7560467B2 (OSRAM) |
| EP (1) | EP1633740B1 (OSRAM) |
| JP (1) | JP4869068B2 (OSRAM) |
| AT (1) | ATE532781T1 (OSRAM) |
| ES (1) | ES2374272T3 (OSRAM) |
| WO (1) | WO2004112719A2 (OSRAM) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1718638A4 (en) * | 2004-02-20 | 2009-04-22 | Smithkline Beecham Corp | NEW COMPOUNDS |
| DE102004028862A1 (de) * | 2004-06-15 | 2005-12-29 | Merck Patent Gmbh | 3-Aminoindazole |
| JP2008503492A (ja) * | 2004-06-17 | 2008-02-07 | スミスクライン・ビーチャム・コーポレイション | Rho−キナーゼの新規阻害剤 |
| WO2006074293A2 (en) * | 2005-01-07 | 2006-07-13 | President And Fellows Of Harvard College | Bicyclic dihydropyrimidines as eg5 inhibitors |
| JP5188988B2 (ja) * | 2006-02-10 | 2013-04-24 | トランステック ファーマ,インコーポレイティド | ベンゾアゾール誘導体、組成物、及びオーロラキナーゼ阻害剤としての使用方法 |
| US20080153810A1 (en) * | 2006-11-15 | 2008-06-26 | Forest Laboratories Holdings Limited | Indazole derivatives useful as melanin concentrating receptor ligands |
| CN101679348A (zh) | 2007-01-10 | 2010-03-24 | 阿尔巴尼分子研究公司 | 5-吡啶酮取代的吲唑 |
| ATE544759T1 (de) | 2007-07-21 | 2012-02-15 | Albany Molecular Res Inc | 5-pyridinon-substituierte indazole und pharmazeutische zusammensetzungen davon |
| CA2768396A1 (en) * | 2009-07-30 | 2011-02-03 | F. Hoffmann-La Roche Ag | Dihydropyrimidone amides as p2x7 modulators |
| SG185431A1 (en) | 2010-05-07 | 2012-12-28 | Glaxosmithkline Llc | Indoles |
| WO2011140325A1 (en) | 2010-05-07 | 2011-11-10 | Glaxosmithkline Llc | Indazoles |
| DK2638149T3 (da) | 2010-11-12 | 2019-08-12 | Univ Georgetown | Immortalisering af epitelceller og fremgangsmåder til anvendelse |
| JO3438B1 (ar) | 2011-04-13 | 2019-10-20 | Epizyme Inc | مركبات بنزين مستبدلة بأريل أو أريل غير متجانس |
| WO2013062945A1 (en) | 2011-10-24 | 2013-05-02 | Glaxosmithkline Intellectual Property Development Limited | Chemical compounds |
| JP6005753B2 (ja) | 2011-11-04 | 2016-10-12 | グラクソスミスクライン、インテレクチュアル、プロパティー、(ナンバー2)、リミテッドGlaxosmithkline Intellectual Property (No.2) Limited | 治療の方法 |
| JP6250561B2 (ja) | 2012-02-08 | 2017-12-20 | サノビオン ファーマシューティカルズ インクSunovion Pharmaceuticals Inc. | ヘテロアリール化合物およびそれらの使用方法 |
| CN105102431B (zh) | 2012-10-15 | 2018-03-02 | Epizyme股份有限公司 | 经取代的苯化合物 |
| EP3046557A1 (en) | 2013-09-20 | 2016-07-27 | Stichting Het Nederlands Kanker Instituut | Rock in combination with mapk-pathway |
| CN107075469A (zh) | 2014-06-27 | 2017-08-18 | 加利福尼亚大学董事会 | 培养的哺乳动物角膜缘干细胞、其产生方法和其用途 |
| US10023564B2 (en) | 2014-08-08 | 2018-07-17 | The Regents Of The University Of Michigan | G protein-coupled receptor kinase 2 inhibitors and methods for use of the same |
| US10100285B2 (en) | 2015-04-03 | 2018-10-16 | Propagenix Inc. | Ex vivo proliferation of epithelial cells |
| AU2016243750B2 (en) | 2015-04-03 | 2022-02-03 | Propagenix Inc. | Ex vivo proliferation of epithelial cells |
| ES2913117T3 (es) | 2015-06-26 | 2022-05-31 | Univ Michigan Regents | Inhibidores de quinasa receptora acoplada a proteína G y métodos para el uso de los mismos |
| JP6869231B2 (ja) | 2015-09-11 | 2021-05-12 | プロパジェニクス インコーポレイテッド | ex vivoでの上皮細胞の増殖 |
| CN110087687A (zh) | 2016-07-29 | 2019-08-02 | 赛诺维信制药公司 | 化合物、组合物及其用途 |
| CA3032302A1 (en) | 2016-07-29 | 2018-02-01 | Taleen G. Hanania | Compounds and compositions and uses thereof |
| WO2019018853A1 (en) * | 2017-07-21 | 2019-01-24 | Kadmon Corporation, Llc | INHIBITORS OF PROTEIN KINASE CONTAINING RHO-ASSOCIATED ROLL COIL |
| CN111183138A (zh) | 2017-08-02 | 2020-05-19 | 赛诺维信制药公司 | 异色满化合物以及用途 |
| WO2020041065A1 (en) | 2018-08-20 | 2020-02-27 | Propagenix Inc. | Epithelial cell spheroids |
| CA3110661A1 (en) | 2018-08-29 | 2020-03-05 | University Of Massachusetts | Inhibition of protein kinases to treat friedreich ataxia |
| UY38427A (es) | 2018-10-26 | 2020-05-29 | Novartis Ag | Métodos y composiciones para terapia con células oculares |
| MX2021010880A (es) | 2019-03-14 | 2022-01-18 | Sunovion Pharmaceuticals Inc | Sales de un compuesto de isocromanilo y formas cristalinas, procesos de preparacion, usos terapeuticos y composiciones farmaceuticas de las mismas. |
| US20230172929A1 (en) * | 2019-08-08 | 2023-06-08 | Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. | Novel peripheral cannabinoid-1 receptor antagonists |
| JP2023522784A (ja) | 2020-04-27 | 2023-05-31 | ノバルティス アーゲー | 眼細胞療法のための方法及び組成物 |
| US20240174637A1 (en) * | 2021-01-22 | 2024-05-30 | Grazia Piizzi | Degraders of grk2 and uses thereof |
| US20240425816A1 (en) | 2021-10-18 | 2024-12-26 | Evia Life Sciences Inc. | Compositions and methods of use thereof for treating liver fibrosis |
| JP2024539220A (ja) | 2021-10-22 | 2024-10-28 | エヴィア ライフ サイエンシズ インコーポレイテッド | 細胞外小胞を作製するための方法、組成物、およびその使用方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1223170B1 (en) | 1999-10-12 | 2005-12-28 | Takeda Pharmaceutical Company Limited | Pyrimidine-5-carboxamide compounds, process for producing the same and use thereof |
| AP2003002825A0 (en) * | 2000-12-21 | 2003-09-30 | Vertex Pharma | Pyrazole compounds useful as protein kinase inhibitors |
| WO2002066443A2 (en) * | 2001-02-21 | 2002-08-29 | Ono Pharmaceutical Co., Ltd. | 2-thioxo-1,2,3,4-tetrahydropyrimidine derivatives |
| AU2002255263B2 (en) | 2001-04-16 | 2006-12-14 | Eisai R&D Management Co., Ltd. | Novel 1H-indazole compound |
| EP1403255A4 (en) * | 2001-06-12 | 2005-04-06 | Sumitomo Pharma | RHO KINASE INHIBITORS |
| JP2008503492A (ja) * | 2004-06-17 | 2008-02-07 | スミスクライン・ビーチャム・コーポレイション | Rho−キナーゼの新規阻害剤 |
-
2004
- 2004-06-18 US US10/560,502 patent/US7560467B2/en not_active Expired - Fee Related
- 2004-06-18 WO PCT/US2004/019692 patent/WO2004112719A2/en not_active Ceased
- 2004-06-18 AT AT04755699T patent/ATE532781T1/de active
- 2004-06-18 EP EP04755699A patent/EP1633740B1/en not_active Expired - Lifetime
- 2004-06-18 JP JP2006517466A patent/JP4869068B2/ja not_active Expired - Fee Related
- 2004-06-18 ES ES04755699T patent/ES2374272T3/es not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| US20070099944A1 (en) | 2007-05-03 |
| JP4869068B2 (ja) | 2012-02-01 |
| WO2004112719A2 (en) | 2004-12-29 |
| EP1633740A4 (en) | 2008-11-19 |
| WO2004112719A8 (en) | 2005-05-26 |
| US7560467B2 (en) | 2009-07-14 |
| JP2007516173A (ja) | 2007-06-21 |
| ES2374272T3 (es) | 2012-02-15 |
| WO2004112719A3 (en) | 2005-04-07 |
| EP1633740B1 (en) | 2011-11-09 |
| EP1633740A2 (en) | 2006-03-15 |
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