JP2008156336A5 - - Google Patents
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- Publication number
- JP2008156336A5 JP2008156336A5 JP2007267377A JP2007267377A JP2008156336A5 JP 2008156336 A5 JP2008156336 A5 JP 2008156336A5 JP 2007267377 A JP2007267377 A JP 2007267377A JP 2007267377 A JP2007267377 A JP 2007267377A JP 2008156336 A5 JP2008156336 A5 JP 2008156336A5
- Authority
- JP
- Japan
- Prior art keywords
- cyclohepta
- benzo
- pyridin
- oxo
- methyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US69322905P | 2005-06-23 | 2005-06-23 | |
| US60/693,229 | 2005-06-23 | ||
| US72906105P | 2005-10-21 | 2005-10-21 | |
| US60/729,061 | 2005-10-21 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008506834A Division JP4119478B1 (ja) | 2005-06-23 | 2006-06-22 | チロシンキナーゼインヒビター |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008156336A JP2008156336A (ja) | 2008-07-10 |
| JP2008156336A5 true JP2008156336A5 (cg-RX-API-DMAC7.html) | 2009-07-09 |
| JP5086762B2 JP5086762B2 (ja) | 2012-11-28 |
Family
ID=37478833
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008506834A Expired - Fee Related JP4119478B1 (ja) | 2005-06-23 | 2006-06-22 | チロシンキナーゼインヒビター |
| JP2007267377A Expired - Fee Related JP5086762B2 (ja) | 2005-06-23 | 2007-10-15 | チロシンキナーゼインヒビター |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008506834A Expired - Fee Related JP4119478B1 (ja) | 2005-06-23 | 2006-06-22 | チロシンキナーゼインヒビター |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US8207186B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP1896421B1 (cg-RX-API-DMAC7.html) |
| JP (2) | JP4119478B1 (cg-RX-API-DMAC7.html) |
| AT (1) | ATE524445T1 (cg-RX-API-DMAC7.html) |
| AU (1) | AU2006262172B2 (cg-RX-API-DMAC7.html) |
| CA (1) | CA2611530C (cg-RX-API-DMAC7.html) |
| DK (1) | DK1896421T3 (cg-RX-API-DMAC7.html) |
| HR (1) | HRP20110804T1 (cg-RX-API-DMAC7.html) |
| RU (1) | RU2408584C2 (cg-RX-API-DMAC7.html) |
| SI (1) | SI1896421T1 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2007002254A2 (cg-RX-API-DMAC7.html) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8207186B2 (en) | 2005-06-23 | 2012-06-26 | Merck Sharp & Dohme Corp. | Benzocycloheptapyridines as inhibitors of the receptor tyrosine kinase MET |
| JP2009512706A (ja) | 2005-10-21 | 2009-03-26 | メルク エンド カムパニー インコーポレーテッド | チロシンキナーゼインヒビター |
| TW200813021A (en) * | 2006-07-10 | 2008-03-16 | Merck & Co Inc | Tyrosine kinase inhibitors |
| US8642067B2 (en) | 2007-04-02 | 2014-02-04 | Allergen, Inc. | Methods and compositions for intraocular administration to treat ocular conditions |
| WO2009023846A2 (en) * | 2007-08-15 | 2009-02-19 | The Research Foundation Of State University Of New York | Methods for heat shock protein dependent cancer treatment |
| US7893081B2 (en) | 2007-12-20 | 2011-02-22 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
| WO2011039527A1 (en) | 2009-09-30 | 2011-04-07 | Merck Sharp & Dohme Ltd | Formulations for c-met kinase inhibitors |
| EP2482821A4 (en) | 2009-09-30 | 2013-03-06 | Merck Sharp & Dohme | CRYSTALLINE HYDROCHLORIDE SALTS FROM C-MET KINASE INHIBITORS |
| AU2010322800A1 (en) * | 2009-11-30 | 2012-07-12 | Proteologics, Ltd. | Small pyrimidine derivatives and methods of use thereof |
| CN101857594B (zh) * | 2010-06-18 | 2013-04-03 | 南方医科大学 | 一种四氢吡啶并吲哚类化合物及其制备方法和应用 |
| WO2012003338A1 (en) | 2010-07-01 | 2012-01-05 | Takeda Pharmaceutical Company Limited | COMBINATION OF A cMET INHIBITOR AND AN ANTIBODY TO HGF AND/OR cMET |
| EP2727920B1 (en) | 2011-07-29 | 2016-11-02 | FUJIFILM Corporation | 1,5-naphthyridine derivative or salt thereof |
| WO2013131089A2 (en) | 2012-03-02 | 2013-09-06 | The Board Of Trustees Of The University Of Illinois | Potent anticancer activity via dual compound activation |
| CN104507479B (zh) | 2012-03-06 | 2017-08-18 | 伊利诺伊大学评议会 | 通过联合治疗的半胱天冬酶‑3酶原激活 |
| RU2636234C2 (ru) * | 2012-03-06 | 2017-11-21 | Зэ Борд оф Трастиз оф зэ Юниверсити оф Иллинойс | Прокаспазная комбинированная терапия при глиобластоме |
| MX367055B (es) | 2012-06-26 | 2019-08-02 | Del Mar Pharmaceuticals | El uso de una composición que comprende dianhidrogalactitol, diacetildianhidrogalactitol, y dibromodulcitol, y análogos o derivados de cada uno para el tratamiento de malignidades resistentes a inhibidores de tirosina cinasa. |
| WO2014150996A1 (en) * | 2013-03-15 | 2014-09-25 | Cba Pharma, Inc. | Cancer treatment |
| CN105492011A (zh) | 2013-04-08 | 2016-04-13 | 丹尼斯·M·布朗 | 不理想给药化学化合物的治疗增效 |
| JP6864953B2 (ja) | 2014-12-09 | 2021-04-28 | アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル | Ａｘｌに対するヒトモノクローナル抗体 |
| WO2016094361A1 (en) * | 2014-12-10 | 2016-06-16 | Southern Research Institute | Antiviral agents |
| WO2016135041A1 (en) | 2015-02-26 | 2016-09-01 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Fusion proteins and antibodies comprising thereof for promoting apoptosis |
| WO2017161004A1 (en) * | 2016-03-15 | 2017-09-21 | University Of South Florida | PKCδ INHIBITOR FORMULATIONS AND USES THEREOF CROSS-REFERENCE TO RELATED APPLICATIONS |
| AU2018368453B2 (en) | 2017-11-17 | 2024-05-30 | The Board Of Trustees Of The University Of Illinois | Cancer therapy by degrading dual MEK signaling |
| US12090153B2 (en) | 2018-10-05 | 2024-09-17 | The Board Of Trustees Of The University Of Illinois | Combination therapy for the treatment of uveal melanoma |
| CN114364798A (zh) | 2019-03-21 | 2022-04-15 | 欧恩科斯欧公司 | 用于治疗癌症的Dbait分子与激酶抑制剂的组合 |
| US20230115865A1 (en) * | 2019-10-01 | 2023-04-13 | Sanofi | Novel Substituted 6,7-Dihydro-5H-Benzo[7]Annulene Compounds, Processes for Their Preparation and Therapeutic Uses Thereof |
| US20220401436A1 (en) | 2019-11-08 | 2022-12-22 | INSERM (Institute National de la Santé et de la Recherche Médicale) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| AU2022379973A1 (en) | 2021-11-08 | 2024-06-27 | Progentos Therapeutics, Inc. | Platelet-derived growth factor receptor (pdgfr) alpha inhibitors and uses thereof |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL132137C (cg-RX-API-DMAC7.html) | 1963-04-24 | |||
| US4826853A (en) | 1986-10-31 | 1989-05-02 | Schering Corporation | 6,11-Dihydro-11-(N-substituted-4-piperidylidene)-5H-benzo(5,6)cyclohepta(1,2-B)pyridines and compositions and methods of use |
| JP2852659B2 (ja) | 1988-03-03 | 1999-02-03 | 富山化学工業株式会社 | ピペラジン誘導体およびその塩 |
| IE68935B1 (en) | 1990-06-22 | 1996-07-24 | Schering Corp | Bis-benzo or benzopyrido cyclohepta piperidene piperidylidene and piperazine compounds compositions and methods of use |
| US6365588B1 (en) | 1993-10-15 | 2002-04-02 | Schering Corporation | Tricyclic amide and urea compounds useful for inhibition of G-protein function and for treatment of proliferative diseases |
| CN1168133A (zh) | 1995-10-16 | 1997-12-17 | 协和发酵工业株式会社 | 三环化合物 |
| CA2264569C (en) | 1996-09-13 | 2003-11-11 | Schering Corporation | Tricyclic compounds useful for inhibition of g-protein function and for treatment of proliferative diseases |
| AU4337597A (en) | 1996-09-13 | 1998-04-02 | Schering Corporation | Substituted benzocycloheptapyridine useful as inhibitors of farnesyl-protein tr ansferase |
| TR200003580T2 (tr) * | 1997-06-17 | 2002-10-21 | Schering Corporation | Farnesil protein transferazı'nın önlenmesine mahsus benzo(5,6)siklohepta(1,2-B)piridin türevleri |
| US7018979B1 (en) | 2000-01-26 | 2006-03-28 | Cedars-Sinai Medical Center | Method for using potassium channel agonists for delivering a medicant to an abnormal brain region and/or a malignant tumor |
| JP2003523965A (ja) * | 2000-01-26 | 2003-08-12 | シーダース シナイ メディカル センター | 異常な脳領域および／または悪性腫瘍に薬剤をデリバリーするためにカリウムチャンネルアゴニストを使用する方法 |
| ATE363473T1 (de) | 2001-09-19 | 2007-06-15 | Pharmacia Corp | Substituierte pyrazoloverbindungen zur behandlung von entzündungen |
| AU2003230758A1 (en) | 2002-04-02 | 2003-10-20 | Merck And Co., Inc. | 5h-benzo(4,5)cyclohepta(1,2-b)pyridine nmda/nr2b antagonists |
| ES2211315B1 (es) | 2002-11-12 | 2005-10-16 | Almirall Prodesfarma, S.A. | Nuevos compuestos triciclicos. |
| JP2006151809A (ja) | 2002-12-26 | 2006-06-15 | Ube Ind Ltd | ベンゾシクロヘプタピリジン化合物 |
| US8207186B2 (en) | 2005-06-23 | 2012-06-26 | Merck Sharp & Dohme Corp. | Benzocycloheptapyridines as inhibitors of the receptor tyrosine kinase MET |
| JP2009512707A (ja) | 2005-10-21 | 2009-03-26 | メルク エンド カムパニー インコーポレーテッド | チロシンキナーゼインヒビター |
| CA2624656A1 (en) | 2005-10-21 | 2007-05-03 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
| JP2009512706A (ja) | 2005-10-21 | 2009-03-26 | メルク エンド カムパニー インコーポレーテッド | チロシンキナーゼインヒビター |
| TW200813021A (en) | 2006-07-10 | 2008-03-16 | Merck & Co Inc | Tyrosine kinase inhibitors |
-
2006
- 2006-06-22 US US11/921,350 patent/US8207186B2/en active Active
- 2006-06-22 AT AT06785313T patent/ATE524445T1/de not_active IP Right Cessation
- 2006-06-22 SI SI200631207T patent/SI1896421T1/sl unknown
- 2006-06-22 EP EP06785313A patent/EP1896421B1/en active Active
- 2006-06-22 JP JP2008506834A patent/JP4119478B1/ja not_active Expired - Fee Related
- 2006-06-22 DK DK06785313.5T patent/DK1896421T3/da active
- 2006-06-22 RU RU2008102381/04A patent/RU2408584C2/ru not_active IP Right Cessation
- 2006-06-22 CA CA2611530A patent/CA2611530C/en active Active
- 2006-06-22 WO PCT/US2006/024247 patent/WO2007002254A2/en not_active Ceased
- 2006-06-22 HR HR20110804T patent/HRP20110804T1/hr unknown
- 2006-06-22 US US11/473,273 patent/US7550478B2/en active Active
- 2006-06-22 AU AU2006262172A patent/AU2006262172B2/en not_active Ceased
-
2007
- 2007-10-15 JP JP2007267377A patent/JP5086762B2/ja not_active Expired - Fee Related
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