MA32911B1 - Derives de benzothiazole convenant comme agents agents anticancereux - Google Patents
Derives de benzothiazole convenant comme agents agents anticancereuxInfo
- Publication number
- MA32911B1 MA32911B1 MA33985A MA33985A MA32911B1 MA 32911 B1 MA32911 B1 MA 32911B1 MA 33985 A MA33985 A MA 33985A MA 33985 A MA33985 A MA 33985A MA 32911 B1 MA32911 B1 MA 32911B1
- Authority
- MA
- Morocco
- Prior art keywords
- agents
- benzothiazole derivatives
- anticancer
- formula
- relates
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles 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 in position 2
- C07D277/82—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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/428—Thiazoles condensed with carbocyclic rings
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
- 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
- C07D277/22—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 only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Genetics & Genomics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Zoology (AREA)
- Biomedical Technology (AREA)
- Wood Science & Technology (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Molecular Biology (AREA)
- Plant Pathology (AREA)
- Microbiology (AREA)
- Biophysics (AREA)
- Oncology (AREA)
- Biochemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
La présente invention concerne un dérivé hétérocyclique fusionné présentant une forte activité inhibitrice de Raf. L'invention concerne ainsi un composé représenté par la formule (I) ou l'un de ses sels. Dans cette formule (I), chaque symbole est tel que défini dans les présentes spécifications.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008307581 | 2008-12-02 | ||
| JP2009125256 | 2009-05-25 | ||
| PCT/JP2009/070447 WO2010064722A1 (fr) | 2008-12-02 | 2009-12-01 | Dérivés de benzothiazole convenant comme agents anticancéreux |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA32911B1 true MA32911B1 (fr) | 2011-12-01 |
Family
ID=42026212
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA33985A MA32911B1 (fr) | 2008-12-02 | 2011-06-30 | Derives de benzothiazole convenant comme agents agents anticancereux |
Country Status (40)
| Country | Link |
|---|---|
| US (2) | US8143258B2 (fr) |
| EP (1) | EP2358689B9 (fr) |
| JP (1) | JP5640014B2 (fr) |
| KR (1) | KR101639092B1 (fr) |
| CN (1) | CN102300854B (fr) |
| AR (1) | AR074435A1 (fr) |
| AU (1) | AU2009323274B2 (fr) |
| BR (1) | BRPI0922109A2 (fr) |
| CA (1) | CA2745144C (fr) |
| CL (1) | CL2011001299A1 (fr) |
| CO (1) | CO6400140A2 (fr) |
| CR (1) | CR20110366A (fr) |
| CY (1) | CY1117178T1 (fr) |
| DK (1) | DK2358689T5 (fr) |
| DO (1) | DOP2011000165A (fr) |
| EA (1) | EA019447B1 (fr) |
| EC (1) | ECSP11011165A (fr) |
| ES (1) | ES2557304T3 (fr) |
| GE (1) | GEP20146003B (fr) |
| HR (1) | HRP20151370T1 (fr) |
| HU (1) | HUE026491T4 (fr) |
| IL (1) | IL213184A0 (fr) |
| JO (1) | JO3101B1 (fr) |
| MA (1) | MA32911B1 (fr) |
| ME (1) | ME02331B (fr) |
| MX (1) | MX2011005836A (fr) |
| MY (1) | MY150989A (fr) |
| NZ (1) | NZ593759A (fr) |
| PE (1) | PE20110588A1 (fr) |
| PL (1) | PL2358689T3 (fr) |
| PT (1) | PT2358689E (fr) |
| RS (1) | RS54370B9 (fr) |
| SG (1) | SG171426A1 (fr) |
| SI (1) | SI2358689T1 (fr) |
| SM (1) | SMT201500316B (fr) |
| TN (1) | TN2011000280A1 (fr) |
| TW (1) | TWI436987B (fr) |
| UY (1) | UY32281A (fr) |
| WO (1) | WO2010064722A1 (fr) |
| ZA (1) | ZA201104659B (fr) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR066845A1 (es) * | 2007-06-05 | 2009-09-16 | Takeda Pharmaceutical | Derivados de triazolopiridina e imidazopiridina una composicion farmaceutica que los comprende y su uso en la preparacion de un medicamento para el tratamiento del cancer |
| JP5270553B2 (ja) * | 2007-08-23 | 2013-08-21 | 武田薬品工業株式会社 | 複素環化合物およびその用途 |
| US8445509B2 (en) * | 2008-05-08 | 2013-05-21 | Takeda Pharmaceutical Company Limited | Fused heterocyclic derivatives and use thereof |
| EP2399921B1 (fr) | 2008-12-01 | 2015-08-12 | Takeda Pharmaceutical Company Limited | Composé hétérocyclique et applications |
| WO2013138753A1 (fr) | 2012-03-16 | 2013-09-19 | Fox Chase Chemical Diversity Center, Inc. | Promédicaments de riluzole et leur méthode d'utilisation |
| CA2868954A1 (fr) * | 2012-03-30 | 2013-10-03 | Takeda Pharmaceutical Company Limited | Administration d'un inhibiteur de raf et d'un inhibiteur de mek dans le traitement du melanome |
| DK2888010T3 (da) | 2012-08-22 | 2021-06-28 | Univ Cornell | Fremgangsmåder til at hæmme fascin |
| EP3013797B1 (fr) | 2013-06-28 | 2018-01-03 | BeiGene, Ltd. | Composés amides tricycliques condensés comme inhibiteurs de kinases multiples |
| CN105452223B (zh) | 2013-06-28 | 2018-10-02 | 百济神州有限公司 | 作为Raf激酶和/或Raf激酶二聚体抑制剂的稠合三环脲类化合物 |
| CN103435572B (zh) * | 2013-07-16 | 2015-02-04 | 浙江医药高等专科学校 | 噻唑并环己烷类化合物、其制备方法和抗肿瘤用途 |
| CN103382190B (zh) * | 2013-07-16 | 2015-01-14 | 浙江医药高等专科学校 | 一类噻唑并环己烷类化合物、其制备方法和用途 |
| CN103435573B (zh) * | 2013-07-16 | 2015-04-01 | 浙江医药高等专科学校 | 苄基取代的噻唑并环己烷类化合物、其制备方法和用途 |
| CN103408541B (zh) * | 2013-07-16 | 2015-04-01 | 浙江医药高等专科学校 | 吲哚取代的噻唑并环己烷类化合物、及其抗肿瘤用途 |
| WO2015127125A1 (fr) | 2014-02-20 | 2015-08-27 | Cornell University | Composés et procédés d'inhibition de la fascine |
| CA2954764A1 (fr) | 2014-07-15 | 2016-01-21 | Ontario Institute For Cancer Research | Procedes et dispositifs permettant de predire l'efficacite d'un traitement a l'anthracycline |
| CA2972189A1 (fr) * | 2014-12-23 | 2016-06-30 | Millennium Pharmaceuticals, Inc. | Combinaison d'inhibiteurs de raf et de taxanes |
| WO2017066664A1 (fr) * | 2015-10-16 | 2017-04-20 | Millennium Pharmaceuticals, Inc. | Polythérapie comprenant un inhibiteur de raf pour le traitement du cancer colorectal |
| TW201735949A (zh) | 2016-03-24 | 2017-10-16 | 千禧製藥公司 | 治療抗ctla4及抗pd-1組合治療中的胃腸道免疫相關不良事件之方法 |
| MA44483A (fr) | 2016-03-24 | 2019-01-30 | Millennium Pharm Inc | Procédés pour traiter des événements indésirables gastro-intestinaux d'origine immunitaire dans des traitements oncologiques immunitaires |
| WO2017165491A1 (fr) * | 2016-03-24 | 2017-09-28 | Millennium Pharmaceuticals, Inc. | Utilisation d'un antagoniste de pd-1 et d'un inhibiteur de raf dans le traitement du cancer |
| CN109053630B (zh) * | 2018-08-22 | 2022-04-01 | 中国人民解放军第二军医大学 | 一种苯并噻唑类衍生物及其用途 |
| EP3876939A4 (fr) | 2018-11-07 | 2022-08-10 | Dana-Farber Cancer Institute, Inc. | Dérivés benzothiazoles et dérivés 7-aza benzothiazoles comme inhibiteurs de la janus kinase 2 et leurs utilisations |
| WO2020232445A1 (fr) * | 2019-05-16 | 2020-11-19 | The Regents Of The University Of California | Modulateurs des voies de biosynthèse des nucléotides de pyrimidine |
| CA3181537A1 (fr) | 2020-05-06 | 2021-11-11 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles et azabenzimidazoles en tant qu'inhibiteurs de jak2 |
| CN112094248B (zh) * | 2020-09-17 | 2023-05-12 | 中国人民解放军海军军医大学 | 一种取代苯并噻唑类化合物及其用途 |
| US12043632B2 (en) | 2020-12-23 | 2024-07-23 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as JAK2 inhibitors |
| TW202325289A (zh) | 2021-11-09 | 2023-07-01 | 美商雅捷可斯治療公司 | Jak2抑制劑之形式及組合物 |
| CA3234638A1 (fr) | 2021-11-09 | 2023-05-19 | Ajax Therapeutics, Inc. | 6-hetero-aryloxy-benzimidazoles et azabenzimidazoles en tant qu'inhibiteurs de jak2 |
| CN115724837B (zh) * | 2022-10-26 | 2024-07-23 | 中国人民解放军海军军医大学 | 一种抑制程序性细胞坏死的苯并噻唑衍生物及其应用 |
Family Cites Families (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2399026A (en) * | 1941-02-06 | 1946-04-23 | Chem Ind Basel | Amides of 2-aminoarylenethiazoles |
| US4096264A (en) | 1975-12-09 | 1978-06-20 | Merck & Co., Inc. | Certain substituted imidazo [1,2-a] pyridines |
| CO4950519A1 (es) | 1997-02-13 | 2000-09-01 | Novartis Ag | Ftalazinas, preparaciones farmaceuticas que las comprenden y proceso para su preparacion |
| GB9716557D0 (en) | 1997-08-06 | 1997-10-08 | Glaxo Group Ltd | Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity |
| US6093728A (en) | 1997-09-26 | 2000-07-25 | Asta Medica Aktiengesellschaft | Methods of modulating serine/threonine protein kinase function with azabenzimidazole-based compounds |
| WO2000042012A1 (fr) | 1999-01-13 | 2000-07-20 | Bayer Corporation | DIPHENYLUREES A SUBSTITUANTS φ-CARBOXYARYLES, INHIBITRICES DE KINASE RAF |
| EP1158985B1 (fr) | 1999-01-13 | 2011-12-28 | Bayer HealthCare LLC | DIPHENYLE UREES A SUBSTITUTION OMEGA-CARBOXY ARYLE EN TANT QU'INHIBITEURS DE LA KINASE p38 |
| EE04913B1 (et) * | 1999-01-13 | 2007-10-15 | Bayer Corporation | Omega-karboksarlasendatud difenlkarbamiidid kui RAF-kinaasi inhibiitorid ja neid sisaldavad farmatseutilised kompositsioonid |
| US7928239B2 (en) | 1999-01-13 | 2011-04-19 | Bayer Healthcare Llc | Inhibition of RAF kinase using quinolyl, isoquinolyl or pyridyl ureas |
| GB9900752D0 (en) | 1999-01-15 | 1999-03-03 | Angiogene Pharm Ltd | Benzimidazole vascular damaging agents |
| IL144461A0 (en) * | 1999-01-22 | 2002-05-23 | Kirin Brewery | Quinoline and quinazoline derivatives and pharmaceutical compositions containing them |
| MXPA02000253A (es) * | 1999-07-01 | 2002-06-21 | Ajinomoto Kk | Compuestos heterociclicos y uso medico de los mismos. |
| BRPI0015203B8 (pt) | 1999-11-05 | 2021-05-25 | Astrazeneca Ab | derivado de quinazolina, composição farmacêutica, e, uso de um composto |
| PL357099A1 (en) | 2000-02-07 | 2004-07-12 | Abbott Gmbh & Co.Kg | 2-benzothiazolyl urea derivatives and their use as protein kinase inhibitors |
| IL151127A0 (en) | 2000-02-15 | 2003-04-10 | Sugen Inc | Pyrrole substituted 2-indolinone protein kinase inhibitors |
| AU2001235838A1 (en) | 2000-03-06 | 2001-09-17 | Smithkline Beecham Plc | Imidazol derivatives as raf kinase inhibitors |
| GB0005357D0 (en) | 2000-03-06 | 2000-04-26 | Smithkline Beecham Plc | Compounds |
| DK1303272T3 (da) | 2000-06-21 | 2008-05-26 | Hoffmann La Roche | Benzothiazolderivater til behandling af Alzheimers sygdom og Parkinsons sygdom |
| MXPA03002449A (es) | 2000-09-21 | 2003-06-19 | Smithkline Beecham Plc | Derivados de imidazol como inhibidores de cinasa raf. |
| JP3712393B2 (ja) | 2000-10-20 | 2005-11-02 | エーザイ株式会社 | 含窒素芳香環誘導体 |
| US7238813B2 (en) | 2000-11-29 | 2007-07-03 | Smithkline Beecham Corporation | Chemical compounds |
| GB0112348D0 (en) | 2001-05-19 | 2001-07-11 | Smithkline Beecham Plc | Compounds |
| EP1432703A1 (fr) | 2001-09-05 | 2004-06-30 | Smithkline Beecham Plc | Derives heterocycles de carboxamide utilises comme inhibiteurs de raf kinase |
| GB0121488D0 (en) | 2001-09-05 | 2001-10-24 | Smithkline Beecham Plc | Compounds |
| WO2003022838A1 (fr) | 2001-09-05 | 2003-03-20 | Smithkline Beecham Plc | Derives furaniques substitues par une pyridine servant d'inhibiteurs de raf kinase |
| GB0121494D0 (en) | 2001-09-05 | 2001-10-24 | Smithkline Beecham Plc | Compounds |
| AU2003220970A1 (en) | 2002-03-01 | 2003-09-16 | Smithkline Beecham Corporation | Diamino-pyrimidines and their use as angiogenesis inhibitors |
| US8299108B2 (en) | 2002-03-29 | 2012-10-30 | Novartis Ag | Substituted benzazoles and methods of their use as inhibitors of raf kinase |
| CN100515419C (zh) | 2002-03-29 | 2009-07-22 | 诺华疫苗和诊断公司 | 取代的吲哚及其作为Raf激酶抑制剂的应用 |
| EP2258365B1 (fr) | 2003-03-28 | 2013-05-29 | Novartis Vaccines and Diagnostics, Inc. | Utilisation de composés organiques pour potentialiser l'immunité |
| US7378233B2 (en) * | 2003-04-12 | 2008-05-27 | The Johns Hopkins University | BRAF mutation T1796A in thyroid cancers |
| DE10334663A1 (de) * | 2003-07-30 | 2005-03-10 | Merck Patent Gmbh | Harnstoffderivate |
| DE10337942A1 (de) | 2003-08-18 | 2005-03-17 | Merck Patent Gmbh | Aminobenzimidazolderivate |
| CN1889951A (zh) | 2003-10-16 | 2007-01-03 | 希龙公司 | 取代的苯并唑及其用作raf激酶抑制剂的应用 |
| WO2005112932A2 (fr) | 2004-05-07 | 2005-12-01 | Exelixis, Inc. | Modulateurs de raf et methodes d'utilisation |
| MX2007001155A (es) | 2004-07-29 | 2007-08-14 | Creabilis Therapeutics Spa | Uso de inhibidores de k-252a y de quinasa para la prevencion o el tratamiento de patologias asociadas con hmgb1. |
| GB0420719D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
| WO2006071035A1 (fr) | 2004-12-31 | 2006-07-06 | Lg Life Sciences, Ltd. | Nouveaux derives de ([1,3]thiazolo[5,4-b]pyridin-2-yl)-2-carboxamide |
| WO2006076376A1 (fr) | 2005-01-11 | 2006-07-20 | Medicinova, Inc. | Traitement topique de tumeurs solides et de la neovascularisation oculaire |
| AU2006209183B2 (en) * | 2005-01-26 | 2009-11-19 | Irm Llc | Compounds and compositions as protein kinase inhibitors |
| RU2420525C2 (ru) | 2005-07-11 | 2011-06-10 | Мицубиси Танабе Фарма Корпорейшн | Производные оксимов и их получение |
| PE20070335A1 (es) | 2005-08-30 | 2007-04-21 | Novartis Ag | Benzimidazoles sustituidos y metodos para su preparacion |
| GT200600429A (es) | 2005-09-30 | 2007-04-30 | Compuestos organicos | |
| KR20070052207A (ko) | 2005-11-16 | 2007-05-21 | 주식회사 엘지생명과학 | 신규한 kdr 억제제 |
| EA018917B1 (ru) | 2006-04-19 | 2013-11-29 | Новартис Аг | 6-о-замещенные бензоксазолы и бензотиазолы и способы подавления передачи сигналов от csf-1r |
| WO2008016131A1 (fr) | 2006-08-04 | 2008-02-07 | Takeda Pharmaceutical Company Limited | Composé hétérocyclique à cycles fusionnés |
| EP2049541B1 (fr) | 2006-08-04 | 2015-09-23 | Takeda Pharmaceutical Company Limited | N-[5-({2-[(cyclopropylcarbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}oxy)-2-methylphenyl]-1,3-dimethyl-1h-pyrazole-5-carboxamide en tant qu'inhibiteurs de vegfr |
| JP4328820B2 (ja) | 2007-01-10 | 2009-09-09 | 田辺三菱製薬株式会社 | 医薬組成物 |
| WO2008084873A1 (fr) | 2007-01-10 | 2008-07-17 | Mitsubishi Tanabe Pharma Corporation | Dérivé oxime |
| CN101260106A (zh) * | 2007-03-06 | 2008-09-10 | 中国药科大学 | Raf激酶抑制剂及其制备方法和用途 |
| WO2008125633A2 (fr) | 2007-04-13 | 2008-10-23 | Rikshospitalet - Radiumhospitalet Hf | Traitement et diagnostic du cancer métastatique de la prostate par des inhibiteurs de récepteur de facteur de croissance epidermique (egfr) |
| CA2690281A1 (fr) | 2007-05-11 | 2008-11-20 | The Johns Hopkins University | Biomarqueurs pour melanomes |
| WO2008147782A1 (fr) | 2007-05-23 | 2008-12-04 | Novartis Ag | Inhibiteurs de raf pour le traitement du cancer de la thyroïde |
| AR066845A1 (es) | 2007-06-05 | 2009-09-16 | Takeda Pharmaceutical | Derivados de triazolopiridina e imidazopiridina una composicion farmaceutica que los comprende y su uso en la preparacion de un medicamento para el tratamiento del cancer |
| JP2008307581A (ja) | 2007-06-15 | 2008-12-25 | Sanyo Special Steel Co Ltd | 管材の洗浄装置 |
| JP5270553B2 (ja) | 2007-08-23 | 2013-08-21 | 武田薬品工業株式会社 | 複素環化合物およびその用途 |
| EP2184285B1 (fr) | 2007-08-29 | 2015-11-04 | Takeda Pharmaceutical Company Limited | Composé hétérocyclique et son utilisation |
| WO2009028655A1 (fr) | 2007-08-30 | 2009-03-05 | Takeda Pharmaceutical Company Limited | Composé hétérocyclique et son utilisation |
| JP2009125256A (ja) | 2007-11-22 | 2009-06-11 | Kandado:Kk | 安眠枕 |
| CN101220024A (zh) * | 2007-12-11 | 2008-07-16 | 杜晓敏 | 一组抑制激酶的抗癌化合物 |
| US20110081362A1 (en) | 2008-01-31 | 2011-04-07 | The Brigham And Women's Hospital, Inc. | Treatment of cancer |
| US20090275546A1 (en) * | 2008-04-10 | 2009-11-05 | Istituto Superiore Di Sanita | Diagnostic tests and personalized treatment regimes for cancer stem cells |
| US8445509B2 (en) | 2008-05-08 | 2013-05-21 | Takeda Pharmaceutical Company Limited | Fused heterocyclic derivatives and use thereof |
-
2009
- 2009-11-25 JO JOP/2009/0448A patent/JO3101B1/ar active
- 2009-12-01 HU HUE09775337A patent/HUE026491T4/en unknown
- 2009-12-01 WO PCT/JP2009/070447 patent/WO2010064722A1/fr not_active Ceased
- 2009-12-01 PL PL09775337T patent/PL2358689T3/pl unknown
- 2009-12-01 CN CN200980155786.1A patent/CN102300854B/zh not_active Expired - Fee Related
- 2009-12-01 EP EP09775337.0A patent/EP2358689B9/fr active Active
- 2009-12-01 AR ARP090104620A patent/AR074435A1/es active IP Right Grant
- 2009-12-01 EA EA201170735A patent/EA019447B1/ru not_active IP Right Cessation
- 2009-12-01 RS RS20150768A patent/RS54370B9/sr unknown
- 2009-12-01 TW TW098140940A patent/TWI436987B/zh not_active IP Right Cessation
- 2009-12-01 SG SG2011038247A patent/SG171426A1/en unknown
- 2009-12-01 CA CA2745144A patent/CA2745144C/fr active Active
- 2009-12-01 AU AU2009323274A patent/AU2009323274B2/en not_active Ceased
- 2009-12-01 DK DK09775337.0T patent/DK2358689T5/en active
- 2009-12-01 PT PT97753370T patent/PT2358689E/pt unknown
- 2009-12-01 JP JP2011538209A patent/JP5640014B2/ja not_active Expired - Fee Related
- 2009-12-01 US US12/628,697 patent/US8143258B2/en not_active Expired - Fee Related
- 2009-12-01 PE PE2011001128A patent/PE20110588A1/es active IP Right Grant
- 2009-12-01 HR HRP20151370TT patent/HRP20151370T1/hr unknown
- 2009-12-01 SI SI200931334T patent/SI2358689T1/sl unknown
- 2009-12-01 GE GEAP200912278A patent/GEP20146003B/en unknown
- 2009-12-01 MX MX2011005836A patent/MX2011005836A/es active IP Right Grant
- 2009-12-01 ME MEP-2016-203A patent/ME02331B/fr unknown
- 2009-12-01 MY MYPI20112494 patent/MY150989A/en unknown
- 2009-12-01 ES ES09775337.0T patent/ES2557304T3/es active Active
- 2009-12-01 UY UY0001032281A patent/UY32281A/es not_active Application Discontinuation
- 2009-12-01 KR KR1020117015343A patent/KR101639092B1/ko not_active Expired - Fee Related
- 2009-12-01 NZ NZ593759A patent/NZ593759A/en not_active IP Right Cessation
- 2009-12-01 BR BRPI0922109-3A patent/BRPI0922109A2/pt not_active IP Right Cessation
-
2011
- 2011-05-26 IL IL213184A patent/IL213184A0/en active IP Right Grant
- 2011-05-30 TN TN2011000280A patent/TN2011000280A1/fr unknown
- 2011-06-01 CL CL2011001299A patent/CL2011001299A1/es unknown
- 2011-06-01 DO DO2011000165A patent/DOP2011000165A/es unknown
- 2011-06-23 ZA ZA2011/04659A patent/ZA201104659B/en unknown
- 2011-06-24 CR CR20110366A patent/CR20110366A/es unknown
- 2011-06-29 EC EC2011011165A patent/ECSP11011165A/es unknown
- 2011-06-30 MA MA33985A patent/MA32911B1/fr unknown
- 2011-06-30 CO CO11082152A patent/CO6400140A2/es active IP Right Grant
-
2012
- 2012-01-10 US US13/347,302 patent/US8497274B2/en not_active Expired - Fee Related
-
2015
- 2015-12-15 SM SM201500316T patent/SMT201500316B/it unknown
- 2015-12-17 CY CY20151101155T patent/CY1117178T1/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MA32911B1 (fr) | Derives de benzothiazole convenant comme agents agents anticancereux | |
| MA31770B1 (fr) | Derives pyrrolidine dione spiroheterocyclique utiles en tant que pesticides. | |
| MA31741B1 (fr) | Derives fongicides de 2-alkylthio-2-quinolinyloxy- acetamide | |
| MA31759B1 (fr) | Compose amide | |
| MA33330B1 (fr) | Quinazolines substituées comme fongicides | |
| MA31574B1 (fr) | Dérivés de pyrazole et leur utilisation comme inhibiteurs de raf | |
| TN2011000654A1 (fr) | Sulfonamides heterocycliques leurs utilisations et compositions pharmaceutiques les contenant | |
| MA30427B1 (fr) | Derives bicycliques utilises comme inhibiteurs de cetp | |
| MA33519B1 (fr) | Hétérocycles microbicides | |
| MA31690B1 (fr) | Nouveaux fongicides | |
| MA28076A1 (fr) | Derives de 2,4-di(hetero)-arylamino-pyrimidine comme inhibiteurs des kinases zap-70 et/ou syk | |
| CR11021A (es) | Derivados de quinolina como fungicidas | |
| MA32882B1 (fr) | Nouveaux pyrazole-4-n-alkoxycarboxamides en tant que microbiocides | |
| EA201070186A1 (ru) | Способы и соединения, предназначенные для получения ингибиторов котранспортера натрий-глюкозы 2 типа | |
| MA32903B1 (fr) | Inhibiteurs de proteine-kinases | |
| RU2711869C3 (ru) | Имидазопирролопиразиновые производные, полезные для лечения заболеваний, вызванных аномальной активностью протеинкиназ Jak1, Jak3 или Syk | |
| UY30842A1 (es) | Derivados de n-(amino-heteroaril)-1h-pirrolopiridin-2-carboxamidas, su preparacion y su aplicacion en terapéutica | |
| MA33209B1 (fr) | Inhibiteurs de la replication du virus de l'hepatite c | |
| MA39152B1 (fr) | Cyclopentanes substitués en 1,2 utilisés comme antagonistes du récepteur d'orexine | |
| CO6190578A2 (es) | Novedosos derivados de imidazol | |
| MA32296B1 (fr) | Derives de piperidine 3,4-substitues comme inhibiteurs de la renine | |
| EP1650194A4 (fr) | Inhibiteur de la proteine kinase | |
| MA37719A1 (fr) | Dérivés de pyrimidinone en tant qu'agents anti-malaria | |
| MA32553B1 (fr) | Composition pharmaceutique solide | |
| DE602006010540D1 (de) | (3,4-dihydro-chinazolin-2-yl)-(2-aryloxy-ethyl)-amine mit aktivität am 5-ht-rezeptor |