CN101808516B - 作为mek抑制剂的包括多晶型物的n-(芳氨基)磺酰胺衍生物和组合物、其使用方法和制备方法 - Google Patents
作为mek抑制剂的包括多晶型物的n-(芳氨基)磺酰胺衍生物和组合物、其使用方法和制备方法 Download PDFInfo
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- CN101808516B CN101808516B CN2008801088296A CN200880108829A CN101808516B CN 101808516 B CN101808516 B CN 101808516B CN 2008801088296 A CN2008801088296 A CN 2008801088296A CN 200880108829 A CN200880108829 A CN 200880108829A CN 101808516 B CN101808516 B CN 101808516B
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- C07C311/22—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
- C07C311/28—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring
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- A—HUMAN NECESSITIES
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
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Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201310317815.8A CN103479604B (zh) | 2007-07-30 | 2008-07-28 | 作为mek抑制剂的包括多晶型物的n-(芳氨基)磺酰胺衍生物和组合物、其使用方法和制备方法 |
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/830,733 | 2007-07-30 | ||
| US11/830,733 US8101799B2 (en) | 2005-07-21 | 2007-07-30 | Derivatives of N-(arylamino) sulfonamides as inhibitors of MEK |
| US3446608P | 2008-03-06 | 2008-03-06 | |
| US3446408P | 2008-03-06 | 2008-03-06 | |
| US61/034,466 | 2008-03-06 | ||
| US61/034,464 | 2008-03-06 | ||
| US4488608P | 2008-04-14 | 2008-04-14 | |
| US61/044,886 | 2008-04-14 | ||
| PCT/US2008/071392 WO2009018233A1 (en) | 2007-07-30 | 2008-07-28 | Derivatives of n-(arylamino) sulfonamides including polymorphs as inhibitors of mek as well as compositions, methods of use and methods for preparing the same |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201310317815.8A Division CN103479604B (zh) | 2007-07-30 | 2008-07-28 | 作为mek抑制剂的包括多晶型物的n-(芳氨基)磺酰胺衍生物和组合物、其使用方法和制备方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101808516A CN101808516A (zh) | 2010-08-18 |
| CN101808516B true CN101808516B (zh) | 2013-08-28 |
Family
ID=40304796
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2008801088296A Expired - Fee Related CN101808516B (zh) | 2007-07-30 | 2008-07-28 | 作为mek抑制剂的包括多晶型物的n-(芳氨基)磺酰胺衍生物和组合物、其使用方法和制备方法 |
| CN201310317815.8A Expired - Fee Related CN103479604B (zh) | 2007-07-30 | 2008-07-28 | 作为mek抑制剂的包括多晶型物的n-(芳氨基)磺酰胺衍生物和组合物、其使用方法和制备方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201310317815.8A Expired - Fee Related CN103479604B (zh) | 2007-07-30 | 2008-07-28 | 作为mek抑制剂的包括多晶型物的n-(芳氨基)磺酰胺衍生物和组合物、其使用方法和制备方法 |
Country Status (22)
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|---|---|
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| JP (3) | JP2010535232A (enExample) |
| KR (3) | KR20100092424A (enExample) |
| CN (2) | CN101808516B (enExample) |
| AP (1) | AP2817A (enExample) |
| AU (2) | AU2008282338B2 (enExample) |
| BR (1) | BRPI0815659A2 (enExample) |
| CA (1) | CA2693390C (enExample) |
| CO (1) | CO6470808A2 (enExample) |
| CR (1) | CR11244A (enExample) |
| DO (1) | DOP2010000045A (enExample) |
| EA (2) | EA032294B1 (enExample) |
| EC (1) | ECSP109910A (enExample) |
| HN (1) | HN2010000203A (enExample) |
| IL (1) | IL203296A (enExample) |
| MA (1) | MA31881B1 (enExample) |
| MX (1) | MX2010001244A (enExample) |
| NZ (1) | NZ582929A (enExample) |
| PH (1) | PH12015501914A1 (enExample) |
| SV (1) | SV2010003469A (enExample) |
| TN (1) | TN2010000049A1 (enExample) |
| WO (1) | WO2009018233A1 (enExample) |
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| US7723477B2 (en) | 2005-10-31 | 2010-05-25 | Oncomed Pharmaceuticals, Inc. | Compositions and methods for inhibiting Wnt-dependent solid tumor cell growth |
| WO2009129246A2 (en) * | 2008-04-14 | 2009-10-22 | Ardea Biosciences, Inc. | Compositions and methods for preparing and using same |
| CA3086566C (en) * | 2008-09-09 | 2025-09-02 | Hoffmann La Roche | Polymorphs of acyl sulfonamides |
| AU2009296246B2 (en) | 2008-09-26 | 2015-07-30 | Oncomed Pharmaceuticals, Inc. | Frizzled-binding agents and uses thereof |
| BRPI1009448A2 (pt) * | 2009-03-11 | 2016-03-01 | Ardea Biosciences Inc | combinações farmacêuticas compreendendo edea119/bay 869766 para o tratamento de cânceres específicos |
| UY32486A (es) * | 2009-03-11 | 2010-10-29 | Ardea Biosciences Inc | Tratamiento del cáncer de páncreas |
| CA2814617C (en) | 2009-10-13 | 2017-12-19 | Allostem Therapeutics Llc | Novel mek inhibitors, useful in the treatment of diseases |
| CA2777304A1 (en) * | 2009-10-21 | 2011-04-28 | Marion Hitchcock | Substituted benzosulphonamides |
| TWI535445B (zh) | 2010-01-12 | 2016-06-01 | 安可美德藥物股份有限公司 | Wnt拮抗劑及治療和篩選方法 |
| CN102020651B (zh) | 2010-11-02 | 2012-07-18 | 北京赛林泰医药技术有限公司 | 6-芳基氨基吡啶酮甲酰胺mek抑制剂 |
| CN102649773A (zh) * | 2011-02-23 | 2012-08-29 | 苏州波锐生物医药科技有限公司 | 氨基芳香烃类化合物及其在制备抗恶性肿瘤药物中的用途 |
| CA2833390A1 (en) * | 2011-04-28 | 2012-11-01 | Sloan-Kettering Institute For Cancer Research | Hsp90 combination therapy |
| AR086553A1 (es) * | 2011-05-27 | 2014-01-08 | Bayer Ip Gmbh | Sintesis quiral de n-{3,4-difluoro-2-[(2-fluoro-4-yodofenil)amino]-6-metoxifenil}-1-[2,3-dihidroxi-propil]ciclopropano sulfonamidas |
| JP2015502958A (ja) * | 2011-12-09 | 2015-01-29 | オンコメッド ファーマシューティカルズ インコーポレイテッド | がんの処置のための併用療法 |
| WO2013109142A1 (en) | 2012-01-16 | 2013-07-25 | Stichting Het Nederlands Kanker Instituut | Combined pdk and mapk/erk pathway inhibition in neoplasia |
| JP2015527874A (ja) * | 2012-05-31 | 2015-09-24 | バイエル ファーマ アクチエンゲゼルシャフト | 肝細胞癌(hcc)患者の治療の有効な応答を決定するためのバイオマーカー |
| TWI662964B (zh) | 2012-06-04 | 2019-06-21 | 美商製藥有限責任公司 | 布魯頓氏酪胺酸激酶抑制劑之結晶形式 |
| SI3702351T1 (sl) * | 2012-10-19 | 2024-03-29 | Array Biopharma Inc., | Formulacija, ki obsega inhibitor mek |
| WO2014071183A1 (en) | 2012-11-02 | 2014-05-08 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Method of reducing adverse effects in a cancer patient undergoing treatment with a mek inhibitor |
| CN105073195A (zh) | 2013-02-04 | 2015-11-18 | 昂科梅德制药有限公司 | 使用Wnt途径抑制剂进行治疗的方法及对该治疗的监测 |
| EP2848246A1 (en) | 2013-09-13 | 2015-03-18 | Bayer Pharma Aktiengesellschaft | Pharmaceutical compositions containing refametinib |
| WO2015041533A1 (en) | 2013-09-20 | 2015-03-26 | Stichting Het Nederlands Kanker Instituut | Rock in combination with mapk-pathway |
| WO2015041534A1 (en) | 2013-09-20 | 2015-03-26 | Stichting Het Nederlands Kanker Instituut | P90rsk in combination with raf/erk/mek |
| WO2015156674A2 (en) | 2014-04-10 | 2015-10-15 | Stichting Het Nederlands Kanker Instituut | Method for treating cancer |
| WO2015178770A1 (en) | 2014-05-19 | 2015-11-26 | Stichting Het Nederlands Kanker Instituut | Compositions for cancer treatment |
| WO2015196072A2 (en) | 2014-06-19 | 2015-12-23 | Whitehead Institute For Biomedical Research | Uses of kinase inhibitors for inducing and maintaining pluripotency |
| US11197896B2 (en) | 2014-08-25 | 2021-12-14 | Société des Produits Nestlé S.A. | Egg protein formulations and methods of manufacture thereof |
| IL315294A (en) | 2015-03-03 | 2024-10-01 | Pharmacyclics Llc | Pharmaceutical formulations of bruton's tyrosine kinase inhibitor |
| AU2018283289B2 (en) * | 2017-06-16 | 2021-03-25 | Beta Pharma, Inc. | Pharmaceutical formulations of N-(2-(2-(dimethylamino)ethoxy)-4-methoxy-5-((4-(1-methyl-1H-indol-3-yl)pyrimidin-2-yl)amino)phenyl)acrylamide and salts thereof |
| MX2021009863A (es) | 2019-03-21 | 2021-11-12 | Onxeo | Una molecula dbait en combinacion con inhibidor de quinasa para el tratamiento del cancer. |
| US20220380348A1 (en) * | 2019-10-04 | 2022-12-01 | Sumitomo Dainippon Pharma Oncology, Inc. | Axl inhibitor formulations |
| WO2021089791A1 (en) | 2019-11-08 | 2021-05-14 | INSERM (Institut 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 |
| US12371667B2 (en) | 2021-05-13 | 2025-07-29 | Washington University | Enhanced methods for inducing and maintaining naive human pluripotent stem cells |
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| CN118834328B (zh) * | 2024-07-02 | 2025-09-16 | 江苏海洋大学 | 金属蛋白酶9抗原决定基印迹纳米颗粒的制备方法及应用 |
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| JP3657002B2 (ja) * | 1992-08-25 | 2005-06-08 | ジー.ディー.サール アンド カンパニー | レトロウイルスプロテアーゼ阻害剤として有用なα−およびβ−アミノ酸ヒドロキシエチルアミノスルホンアミド |
| US7115632B1 (en) * | 1999-05-12 | 2006-10-03 | G. D. Searle & Co. | Sulfonyl aryl or heteroaryl hydroxamic acid compounds |
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| US7235567B2 (en) * | 2000-06-15 | 2007-06-26 | Schering Corporation | Crystalline polymorph of a bisulfate salt of a thrombin receptor antagonist |
| AU2002330088B2 (en) * | 2001-09-24 | 2009-09-03 | Jessie L.-S. Au | Methods and compositions to determine the chemosensitizing dose of suramin used in combination therapy |
| KR20050040907A (ko) * | 2002-07-17 | 2005-05-03 | 타이탄 파머슈티컬즈 인코퍼레이티드 | 항종양 활성 증강용 화학요법제의 조합 |
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| DK1912636T3 (da) * | 2005-07-21 | 2014-07-21 | Ardea Biosciences Inc | N-(arylamino)-sulfonamid-inhibitorer af mek |
| JP2007099763A (ja) * | 2005-09-08 | 2007-04-19 | Toyama Chem Co Ltd | ピペラシリンナトリウム・1水和物の新規な結晶及びその製造方法 |
| TW200800150A (en) * | 2005-12-21 | 2008-01-01 | Organon Nv | Compounds with medicinal effects due to interaction with the glucocorticoid receptor |
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