IN2014DN06567A - - Google Patents
Info
- Publication number
- IN2014DN06567A IN2014DN06567A IN6567DEN2014A IN2014DN06567A IN 2014DN06567 A IN2014DN06567 A IN 2014DN06567A IN 6567DEN2014 A IN6567DEN2014 A IN 6567DEN2014A IN 2014DN06567 A IN2014DN06567 A IN 2014DN06567A
- Authority
- IN
- India
- Prior art keywords
- kinase
- inhibitors
- compounds
- heteroaryl
- aryl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 abstract 2
- 102000004022 Protein-Tyrosine Kinases Human genes 0.000 abstract 1
- 108090000412 Protein-Tyrosine Kinases Proteins 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 229940043355 kinase inhibitor Drugs 0.000 abstract 1
- 102000002574 p38 Mitogen-Activated Protein Kinases Human genes 0.000 abstract 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- 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
- C07D417/02—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 two hetero rings
- C07D417/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/28—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and unsaturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/28—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton
- C07C237/42—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Virology (AREA)
- Hematology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US54249004P | 2004-02-06 | 2004-02-06 | |
| US62493704P | 2004-11-04 | 2004-11-04 | |
| PCT/US2005/003728 WO2005077945A2 (fr) | 2004-02-06 | 2005-02-04 | Procede de preparation de carboxamides 2-aminothiazole-5-aromatiques utiles comme inhibiteurs de kinases |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IN2014DN06567A true IN2014DN06567A (fr) | 2015-07-10 |
Family
ID=34864498
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IN6567DEN2014 IN2014DN06567A (fr) | 2004-02-06 | 2005-02-04 |
Country Status (26)
| Country | Link |
|---|---|
| EP (1) | EP1711481B2 (fr) |
| JP (2) | JP5148115B2 (fr) |
| KR (2) | KR101310427B1 (fr) |
| AR (1) | AR047533A1 (fr) |
| AT (1) | ATE453630T1 (fr) |
| AU (1) | AU2005212405B2 (fr) |
| BR (1) | BRPI0507476B8 (fr) |
| CA (1) | CA2555291C (fr) |
| CY (1) | CY1109907T1 (fr) |
| DE (1) | DE602005018601D1 (fr) |
| DK (1) | DK1711481T4 (fr) |
| ES (1) | ES2337272T5 (fr) |
| GE (1) | GEP20094804B (fr) |
| HR (1) | HRP20100166T4 (fr) |
| IL (1) | IL177280A (fr) |
| IN (1) | IN2014DN06567A (fr) |
| NO (1) | NO338049B1 (fr) |
| NZ (1) | NZ548613A (fr) |
| PE (1) | PE20050691A1 (fr) |
| PL (1) | PL1711481T5 (fr) |
| PT (1) | PT1711481E (fr) |
| RU (1) | RU2382039C2 (fr) |
| SI (1) | SI1711481T2 (fr) |
| TW (1) | TWI338004B (fr) |
| WO (1) | WO2005077945A2 (fr) |
| ZA (1) | ZA200606242B (fr) |
Families Citing this family (65)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2450777C (fr) | 2001-08-10 | 2013-04-09 | Novartis Ag | Utilisation d'inhibiteurs c-src seuls ou en combinaison avec sti571 pour le traitement de leucemies |
| DK1618092T3 (da) | 2003-05-01 | 2011-01-31 | Bristol Myers Squibb Co | Aryl-substituerede pyrazol-amidforbindelser, der er anvendelige som kinasehæmmere |
| US7652146B2 (en) | 2004-02-06 | 2010-01-26 | Bristol-Myers Squibb Company | Process for preparing 2-aminothiazole-5-carboxamides useful as kinase inhibitors |
| TWI338004B (en) * | 2004-02-06 | 2011-03-01 | Bristol Myers Squibb Co | Process for preparing 2-aminothiazole-5-aromatic carboxamides as kinase inhibitors |
| TW200600513A (en) | 2004-06-30 | 2006-01-01 | Bristol Myers Squibb Co | A method for preparing pyrrolotriazine compounds |
| PT1885339E (pt) * | 2005-05-05 | 2015-10-12 | Bristol Myers Squibb Holdings Ireland | Formulações de um inibidor src/abl |
| EP1919885B1 (fr) | 2005-08-05 | 2010-04-28 | Brystol-Myers Squibb Company | Preparation de derives d'acide 2-amino-thiazole-5-carboxylique |
| WO2007035874A1 (fr) * | 2005-09-21 | 2007-03-29 | Bristol-Myers Squibb Company | Administration par voie orale de n-(2-chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1-piperazinyl]-2-methyl-4-pyrimidinyl]amino]-1,3-thiazole-5-carboxamide et sels de celui-ci |
| US20070219370A1 (en) * | 2006-03-15 | 2007-09-20 | Bristol-Myers Squibb Company | Process for preparing n-(2-chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1-piperazinyl]-2-methyl-4-pyrimidinyl]amino] -5-thiazolecarboxamide and related metabolites thereof |
| AU2007296743B2 (en) | 2006-09-11 | 2012-02-16 | Curis, Inc. | Tyrosine kinase inhibitors containing a zinc binding moiety |
| AR062927A1 (es) | 2006-10-11 | 2008-12-17 | Bayer Healthcare Ag | 4- [4-( [ [ 4- cloro-3-( trifluorometil) fenil) carbamoil] amino] -3- fluorofenoxi) -n- metilpiridin-2- carboxamida monohidratada |
| JP5528807B2 (ja) | 2006-10-12 | 2014-06-25 | アステックス、セラピューティックス、リミテッド | 複合薬剤 |
| WO2008044041A1 (fr) | 2006-10-12 | 2008-04-17 | Astex Therapeutics Limited | Combinaisons pharmaceutiques |
| EP1992344A1 (fr) | 2007-05-18 | 2008-11-19 | Institut Curie | P38 alpha comme cible therapeutique pour les maladies associées á une mutation de FGFR3 |
| EP2508523B2 (fr) | 2007-10-23 | 2019-04-17 | Teva Pharmaceutical Industries Ltd. | Polymorphes de dasatinib et leur procédé de préparation |
| WO2010062715A2 (fr) * | 2008-11-03 | 2010-06-03 | Teva Pharmaceutical Industries Ltd. | Polymorphes de dasatinib et leur procédé de préparation |
| WO2010067374A2 (fr) * | 2008-12-08 | 2010-06-17 | Hetero Research Foundation | Polymorphes de dasatinib |
| WO2010129208A1 (fr) * | 2009-05-05 | 2010-11-11 | Merck Sharp & Dohme Corp. | Agents inhibiteurs de la p38 kinase |
| CN101812060B (zh) * | 2010-02-02 | 2011-08-17 | 南京卡文迪许生物工程技术有限公司 | 一种简捷制备高纯度达沙替尼的新方法以及中间体化合物 |
| EP2359813A1 (fr) | 2010-02-04 | 2011-08-24 | Ratiopharm GmbH | Composition pharmaceutique comprenant du N-(2-chloro-6-méthylphényl)-2-[[6-[4-(2-hydroxyéthyl)-1-pipérazinyl]-2-méthyl-4-pyrimidinyl]amino]-5-thiazolecarboxamide |
| CN102250084A (zh) * | 2010-02-08 | 2011-11-23 | 南京卡文迪许生物工程技术有限公司 | 达沙替尼多晶型物及其制备方法和药用组合物 |
| JP5589097B2 (ja) * | 2010-02-08 | 2014-09-10 | 南京▲か▼文迪許生物工程技術有限公司 | ダサチニブ多結晶体、並びにその調製方法及び薬物組成物 |
| WO2013065063A1 (fr) | 2011-11-03 | 2013-05-10 | Cadila Healthcare Limited | Forme anhydre du dasatinib, son procédé de préparation et son utilisation |
| CN104379582A (zh) | 2012-06-15 | 2015-02-25 | 巴斯夫欧洲公司 | 包含达沙替尼和所选择的共晶体形成剂的多组分晶体 |
| CN102827156A (zh) * | 2012-09-11 | 2012-12-19 | 湖南欧亚生物有限公司 | 一种达沙替尼的新的工业合成方法 |
| CN103819469A (zh) * | 2012-11-16 | 2014-05-28 | 重庆医药工业研究院有限责任公司 | 一种达沙替尼的晶型及其制备方法 |
| CZ306598B6 (cs) | 2012-12-06 | 2017-03-22 | Zentiva, K.S. | Způsob přípravy a čištění nových i známých polymorfů a solvátů dasatinibu |
| CN103880833B (zh) * | 2012-12-19 | 2018-04-06 | 北京本草天源药物研究院 | 达沙替尼一水合物的新晶形及其制备方法和药物组合物 |
| WO2014102759A2 (fr) | 2012-12-31 | 2014-07-03 | Ranbaxy Laboratories Limited | Procédé de préparation de dasatinib et de ses intermédiaires |
| CN103319476B (zh) * | 2013-06-13 | 2015-12-02 | 济南德爱医药技术有限公司 | 一种激酶抑制剂 |
| WO2015011120A2 (fr) * | 2013-07-25 | 2015-01-29 | Basf Se | Sels de dasatinib se présentant sous forme cristalline |
| MX2016001096A (es) | 2013-07-25 | 2016-04-25 | Basf Se | Sales de dasatinib en forma amorfa. |
| CN104341410A (zh) * | 2013-08-09 | 2015-02-11 | 上海科胜药物研发有限公司 | 一种达沙替尼新晶型及其制备方法 |
| CN103483289B (zh) * | 2013-09-06 | 2016-01-27 | 浙江科源化工有限公司 | 一种2-氨基-n-(2-氯-6-甲基苯基)噻唑-5-甲酰胺的合成方法 |
| WO2015107545A1 (fr) | 2013-12-18 | 2015-07-23 | Dharmesh Mahendrabhai Shah | Sels solubles dans l'eau d'hydrate de dasatinib |
| CZ306732B6 (cs) * | 2013-12-19 | 2017-05-31 | Zentiva, K.S. | Způsob přípravy bezvodé polymorfní formy N-6 Dasatinibu |
| CA2882438A1 (fr) | 2014-03-11 | 2015-09-11 | Cerbios-Pharma Sa | Procedes et intermediaires pour la preparation de dasatinib |
| RU2567537C1 (ru) * | 2014-04-23 | 2015-11-10 | Олег Ростиславович Михайлов | Кристаллическая безводная дельта-модификация n-(2-хлор-6-метилфенил)-2-[[6-[4-(2-гидроксиэтил)-1-пиперазинил]-2-метил-4-пиримидинил]амино]-5-тиазолкарбоксамида, способ ее получения и фармацевтическая композиция на ее основе |
| HU231013B1 (hu) | 2014-05-26 | 2019-11-28 | Egis Gyógyszergyár Zrt. | Dasatinib sók |
| WO2017002131A1 (fr) * | 2015-06-29 | 2017-01-05 | Msn Laboratories Private Limited | Formes cristallines de n-(2-chloro-6-méthylphényl)-2-[[6-[4-(2-hydroxyéthyl)-1-pipérazinyl]-2-méthyl-4-pyrimidinyl]amino]-5-thiazolecarboxamide et leurs procédés associés |
| WO2017098391A1 (fr) * | 2015-12-11 | 2017-06-15 | Shilpa Medicare Limited | Procédé de préparation du dasatinib |
| WO2017108605A1 (fr) | 2015-12-22 | 2017-06-29 | Synthon B.V. | Composition pharmaceutique comprenant du dasatinib amorphe |
| CN105503854A (zh) * | 2015-12-31 | 2016-04-20 | 哈药集团技术中心 | 一种达沙替尼无水合物的新晶型物及其制备方法 |
| WO2017134615A1 (fr) | 2016-02-03 | 2017-08-10 | Dr. Reddy's Laboratories Limited | Formes solides de dasatinib et leurs procédés de préparation |
| WO2017144109A1 (fr) | 2016-02-25 | 2017-08-31 | Remedica Ltd | Composition de dasatinib |
| GB201608587D0 (en) | 2016-05-16 | 2016-06-29 | Univ Dundee | Treatment of opiod tolerance |
| CN106117195A (zh) * | 2016-06-09 | 2016-11-16 | 青岛辰达生物科技有限公司 | 一种用于治疗白血病的药物达沙替尼的合成方法 |
| IT201700006157A1 (it) * | 2017-01-20 | 2018-07-20 | Cerbios Pharma Sa | Co-cristalli di un composto antitumorale |
| IT201700006145A1 (it) * | 2017-01-20 | 2018-07-20 | Cerbios Pharma Sa | Co-cristallo di un composto antitumorale |
| JP6597727B2 (ja) | 2017-05-11 | 2019-10-30 | 東洋インキScホールディングス株式会社 | 表面保護用粘着剤および粘着シート |
| WO2019008555A1 (fr) * | 2017-07-07 | 2019-01-10 | Biocon Limited | Formes polymorphes de dasatinib |
| WO2019071147A1 (fr) | 2017-10-05 | 2019-04-11 | Fulcrum Therapeutics, Inc. | Inhibiteurs de la kinase p38 réduisant l'expression du gène dux4 et des gènes aval pour le traitement de la fshd |
| US10342786B2 (en) | 2017-10-05 | 2019-07-09 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD |
| CN113292537B (zh) | 2018-06-15 | 2024-04-05 | 汉达癌症医药责任有限公司 | 激酶抑制剂的盐类及其组合物 |
| DK3643713T3 (da) | 2018-10-23 | 2025-11-03 | Iomx Therapeutics Ag | Heterocykliske kinaseinhibitorer og deres anvendelse |
| CN109369638B (zh) * | 2018-11-21 | 2020-07-07 | 山东罗欣药业集团股份有限公司 | 一种达沙替尼的制备工艺 |
| CN109503568B (zh) * | 2018-12-29 | 2020-08-07 | 山东罗欣药业集团股份有限公司 | 一种达沙替尼的制备方法 |
| WO2021028518A1 (fr) * | 2019-08-15 | 2021-02-18 | Bayer Aktiengesellschaft | Procédé de préparation de 2-(phénylimino)-3-alkyl-1,3-thiazolidin-4-ones |
| CN112409349A (zh) * | 2019-08-20 | 2021-02-26 | 湖南华纳大药厂股份有限公司 | 激酶抑制剂及其制备、药物组合物和用途 |
| EP4714503A2 (fr) | 2020-01-24 | 2026-03-25 | Handa Therapeutics, LLC | Dispersions solides amorphes de dasatinib et leurs utilisations |
| GB2592680A (en) | 2020-03-06 | 2021-09-08 | Zentiva Ks | Pharmaceutical compositions comprising dasatinib anhydrous and uses thereof |
| EP4071248A1 (fr) | 2021-04-07 | 2022-10-12 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Moyens et procédés pour améliorer le transfert de gènes ciblé par des récepteurs |
| US11980619B2 (en) | 2021-07-28 | 2024-05-14 | Nanocopoeia, Llc | Pharmaceutical compositions and crushable tablets including amorphous solid dispersions of dasatinib and uses |
| CN114634421A (zh) * | 2022-02-24 | 2022-06-17 | 济宁晟泰药业有限公司 | 一种达沙替尼中间体的制备方法 |
| TW202523302A (zh) | 2023-11-02 | 2025-06-16 | 美商阿克思生物科學有限公司 | 噻唑化合物及其使用方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3547917A (en) * | 1966-12-07 | 1970-12-15 | Uniroyal Inc | 2-amino-4-methylthiazole-5-carboxamides |
| US5514643A (en) * | 1993-08-16 | 1996-05-07 | Lucky Ltd. | 2-aminothiazolecarboxamide derivatives, processes for preparing the same and use thereof for controlling phytopathogenic organisms |
| HU224812B1 (en) * | 1997-06-24 | 2006-02-28 | Janssen Pharmaceutica Nv | Angiogenesis inhibiting 5-substituted-1,2,4-thiadiazolyl derivatives, process for producing them and pharmaceutical compositions containing the same |
| PL215901B1 (pl) * | 1999-04-15 | 2014-02-28 | Bristol Myers Squibb Co | Cykliczny inhibitor bialkowych kinaz tyrozynowych, jego zastosowanie oraz kompozycja farmaceutyczna zawierajaca taki zwiazek |
| ES2349532T3 (es) * | 2003-02-06 | 2011-01-04 | Bristol-Myers Squibb Company | Compuestos basados en tiazolilo útiles como inhibidores de cinasa. |
| ATE481134T1 (de) * | 2004-01-21 | 2010-10-15 | Univ Emory | Zusammensetzungen und verwendung von tyrosinkinase-hemmern zur behandlung von pathogenen infektionen |
| TWI338004B (en) * | 2004-02-06 | 2011-03-01 | Bristol Myers Squibb Co | Process for preparing 2-aminothiazole-5-aromatic carboxamides as kinase inhibitors |
-
2005
- 2005-02-01 TW TW094103090A patent/TWI338004B/zh not_active IP Right Cessation
- 2005-02-04 AU AU2005212405A patent/AU2005212405B2/en not_active Expired
- 2005-02-04 EP EP05722772.0A patent/EP1711481B2/fr not_active Expired - Lifetime
- 2005-02-04 HR HRP20100166TT patent/HRP20100166T4/hr unknown
- 2005-02-04 GE GEAP20059607A patent/GEP20094804B/en unknown
- 2005-02-04 AT AT05722772T patent/ATE453630T1/de active
- 2005-02-04 ES ES05722772T patent/ES2337272T5/es not_active Expired - Lifetime
- 2005-02-04 CA CA2555291A patent/CA2555291C/fr not_active Expired - Lifetime
- 2005-02-04 PE PE2005000128A patent/PE20050691A1/es active IP Right Grant
- 2005-02-04 SI SI200530905T patent/SI1711481T2/sl unknown
- 2005-02-04 AR ARP050100427A patent/AR047533A1/es not_active Application Discontinuation
- 2005-02-04 PL PL05722772T patent/PL1711481T5/pl unknown
- 2005-02-04 DE DE602005018601T patent/DE602005018601D1/de not_active Expired - Lifetime
- 2005-02-04 WO PCT/US2005/003728 patent/WO2005077945A2/fr not_active Ceased
- 2005-02-04 BR BRPI0507476A patent/BRPI0507476B8/pt not_active IP Right Cessation
- 2005-02-04 DK DK05722772.0T patent/DK1711481T4/da active
- 2005-02-04 IN IN6567DEN2014 patent/IN2014DN06567A/en unknown
- 2005-02-04 KR KR1020067015839A patent/KR101310427B1/ko not_active Expired - Lifetime
- 2005-02-04 NZ NZ548613A patent/NZ548613A/en not_active IP Right Cessation
- 2005-02-04 PT PT05722772T patent/PT1711481E/pt unknown
- 2005-02-04 RU RU2006131591/04A patent/RU2382039C2/ru active
- 2005-02-04 KR KR1020127021611A patent/KR20120097424A/ko not_active Ceased
- 2005-02-04 JP JP2006552303A patent/JP5148115B2/ja not_active Expired - Lifetime
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2006
- 2006-07-27 ZA ZA2006/06242A patent/ZA200606242B/en unknown
- 2006-08-03 IL IL177280A patent/IL177280A/en active IP Right Grant
- 2006-08-24 NO NO20063780A patent/NO338049B1/no unknown
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2010
- 2010-03-19 CY CY20101100253T patent/CY1109907T1/el unknown
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2012
- 2012-06-06 JP JP2012129253A patent/JP2012188446A/ja active Pending
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