JP2007509058A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2007509058A5 JP2007509058A5 JP2006535367A JP2006535367A JP2007509058A5 JP 2007509058 A5 JP2007509058 A5 JP 2007509058A5 JP 2006535367 A JP2006535367 A JP 2006535367A JP 2006535367 A JP2006535367 A JP 2006535367A JP 2007509058 A5 JP2007509058 A5 JP 2007509058A5
- Authority
- JP
- Japan
- Prior art keywords
- lower alkyl
- cancer
- compound
- halo
- hydrogen
- 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
- 0 *C(N(*)c1cc(Oc(c(*)c2)cc3c2[n](*)c(Nc2c(*)c(*)c(*)c(*)c2*)n3)ccn1)=O Chemical compound *C(N(*)c1cc(Oc(c(*)c2)cc3c2[n](*)c(Nc2c(*)c(*)c(*)c(*)c2*)n3)ccn1)=O 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US51196603P | 2003-10-16 | 2003-10-16 | |
| US60/511,966 | 2003-10-16 | ||
| PCT/US2004/034179 WO2005037273A1 (en) | 2003-10-16 | 2004-10-15 | Substituted benzazoles and use thereof as inhibitors of raf kinase |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2007509058A JP2007509058A (ja) | 2007-04-12 |
| JP2007509058A5 true JP2007509058A5 (enExample) | 2007-11-15 |
| JP4755991B2 JP4755991B2 (ja) | 2011-08-24 |
Family
ID=34465300
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006535367A Expired - Fee Related JP4755991B2 (ja) | 2003-10-16 | 2004-10-15 | Rafキナーゼインヒビターとしての置換ベンゾアゾールおよびその使用 |
Country Status (16)
| Country | Link |
|---|---|
| US (3) | US7423150B2 (enExample) |
| EP (1) | EP1682126B1 (enExample) |
| JP (1) | JP4755991B2 (enExample) |
| KR (1) | KR20060118472A (enExample) |
| CN (1) | CN1889951A (enExample) |
| AT (1) | ATE435015T1 (enExample) |
| AU (1) | AU2004281151A1 (enExample) |
| CA (1) | CA2542653A1 (enExample) |
| DE (1) | DE602004021838D1 (enExample) |
| ES (1) | ES2327418T3 (enExample) |
| IL (1) | IL174965A0 (enExample) |
| MX (1) | MXPA06004236A (enExample) |
| PL (1) | PL1682126T3 (enExample) |
| PT (1) | PT1682126E (enExample) |
| TW (1) | TW200526208A (enExample) |
| WO (1) | WO2005037273A1 (enExample) |
Families Citing this family (53)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7351834B1 (en) | 1999-01-13 | 2008-04-01 | Bayer Pharmaceuticals Corporation | ω-Carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| US8124630B2 (en) | 1999-01-13 | 2012-02-28 | Bayer Healthcare Llc | ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| ATE538794T1 (de) | 1999-01-13 | 2012-01-15 | Bayer Healthcare Llc | Gamma carboxyarylsubstituierte diphenylharnstoffverbindungen als p38 kinasehemmer |
| WO2003068229A1 (en) | 2002-02-11 | 2003-08-21 | Bayer Pharmaceuticals Corporation | Pyridine, quinoline, and isoquinoline n-oxides as kinase inhibitors |
| MXPA04007832A (es) | 2002-02-11 | 2005-09-08 | Bayer Pharmaceuticals Corp | Aril-ureas con actividad inhibitoria de angiogenesis. |
| UY28213A1 (es) | 2003-02-28 | 2004-09-30 | Bayer Pharmaceuticals Corp | Nuevos derivados de cianopiridina útiles en el tratamiento de cáncer y otros trastornos. |
| EP1636585B2 (en) | 2003-05-20 | 2012-06-13 | Bayer HealthCare LLC | Diaryl ureas with kinase inhibiting activity |
| HRP20060073B1 (hr) | 2003-07-23 | 2014-03-14 | Bayer Healthcare Llc | Fluoro supstituirana omega-karboksiaril difenil urea za lijeäśenje i prevenciju bolesti i stanja |
| CA2542653A1 (en) * | 2003-10-16 | 2005-04-28 | Chiron Corporation | Substituted benzazoles and use thereof as inhibitors of raf kinase |
| WO2006124874A2 (en) * | 2005-05-12 | 2006-11-23 | Kalypsys, Inc. | Inhibitors of b-raf kinase |
| DE602006015957D1 (de) * | 2005-06-23 | 2010-09-16 | Siemens Healthcare Diagnostics | Quantitative assays für ras p21 in körperflüssigkeiten |
| PE20070427A1 (es) * | 2005-08-30 | 2007-04-21 | Novartis Ag | Compuestos derivados de benzimidazoles sustituidos como inhibidores de tirosina quinasas |
| EP2295432A1 (en) * | 2006-02-10 | 2011-03-16 | TransTech Pharma Inc. | Process for the preparation of aminobenzimidazole derivatives |
| PE20080359A1 (es) * | 2006-04-19 | 2008-06-06 | Novartis Ag | Compuestos de benzoxazol y benzotiazol 6-0-sustituidos y metodos de inhibicion de la senalizacion de csf-1r |
| CA2685967A1 (en) | 2007-05-21 | 2008-11-21 | Novartis Ag | Csf-1r inhibitors, compositions, and methods of use |
| WO2008147782A1 (en) * | 2007-05-23 | 2008-12-04 | Novartis Ag | Raf inhibitors for the treatment of thyroid cancer |
| 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 |
| EP2181987B9 (en) | 2007-08-23 | 2014-09-03 | Takeda Pharmaceutical Company Limited | 2-Carbonylaminobenzothiazoles and their use for the prophylaxis and treatment of cancer |
| WO2009028655A1 (ja) * | 2007-08-30 | 2009-03-05 | Takeda Pharmaceutical Company Limited | 複素環化合物およびその用途 |
| WO2009050228A2 (en) * | 2007-10-18 | 2009-04-23 | Novartis Ag | Csf-1r inhibitors for treatment of cancer and bone diseases |
| KR20100122505A (ko) * | 2008-02-29 | 2010-11-22 | 어레이 바이오파마 인크. | Raf 저해물질 화합물 및 이들의 이용 방법 |
| US20110003809A1 (en) * | 2008-02-29 | 2011-01-06 | Array Biopharma Inc. | Imidazo [4,5-b] pyridine derivatives used as raf inhibitors |
| WO2009111279A1 (en) * | 2008-02-29 | 2009-09-11 | Array Biopharma Inc. | Pyrazole [3, 4-b] pyridine raf inhibitors |
| JP2011513332A (ja) * | 2008-02-29 | 2011-04-28 | アレイ バイオファーマ、インコーポレイテッド | 癌の治療のためのraf阻害剤としてのn−(6−アミノピリジン−3−イル)−3−(スルホンアミド)ベンズアミド誘導体 |
| US9540322B2 (en) * | 2008-08-18 | 2017-01-10 | Yale University | MIF modulators |
| WO2010064611A1 (ja) | 2008-12-01 | 2010-06-10 | 武田薬品工業株式会社 | 複素環化合物およびその用途 |
| JO3101B1 (ar) | 2008-12-02 | 2017-09-20 | Takeda Pharmaceuticals Co | مشتقات بنزوثيازول كعوامل مضادة للسرطان |
| AU2011224410B2 (en) * | 2010-03-09 | 2015-05-28 | Dana-Farber Cancer Institute, Inc. | Methods of diagnosing and treating cancer in patients having or developing resistance to a first cancer therapy |
| EP2661434A4 (en) * | 2011-01-06 | 2014-07-09 | Beta Pharma Canada Inc | NEW URGES FOR THE TREATMENT AND PREVENTION OF CANCER |
| US9408885B2 (en) | 2011-12-01 | 2016-08-09 | Vib Vzw | Combinations of therapeutic agents for treating melanoma |
| BR112015001528B1 (pt) * | 2012-07-28 | 2020-12-22 | Calitor Sciences, Llc E Sunshine Lake Pharma Co., Ltd. | composto, composição farmacêutica, e, uso de um composto ou de uma composição farmacêutica |
| US9242969B2 (en) | 2013-03-14 | 2016-01-26 | Novartis Ag | Biaryl amide compounds as kinase inhibitors |
| UY36294A (es) | 2014-09-12 | 2016-04-29 | Novartis Ag | Compuestos y composiciones como inhibidores de quinasa |
| WO2016100184A1 (en) | 2014-12-16 | 2016-06-23 | Forum Pharmaceuticals, Inc. | Geminal substituted quinuclidine amide compounds as agonists of alpha-7 nicotinic acetylcholine receptors |
| CN105949178B (zh) * | 2015-03-09 | 2020-05-26 | 西格莱(苏州)生物医药有限公司 | 一种苯并咪唑类化合物、其制备方法、中间体及应用 |
| JP2018516973A (ja) | 2015-06-10 | 2018-06-28 | フォーラム・ファーマシューティカルズ・インコーポレイテッドForum Pharmaceuticals Inc. | α7−ニコチン性アセチルコリン受容体のアゴニストとしてのアミノベンゾイソオキサゾール化合物 |
| EP3334740A4 (en) | 2015-08-12 | 2019-02-06 | Axovant Sciences GmbH | GEMINAL SUBSTITUTED AMINOBENZISOXAZOLE COMPOUNDS AS AGONISTS OF ALPHA 7-NICOTINIC ACETYLCHOLINE RECEPTORS |
| CA3037456A1 (en) | 2016-09-19 | 2018-03-22 | Novartis Ag | Therapeutic combinations comprising a raf inhibitor and a erk inhibitor |
| WO2018064557A1 (en) * | 2016-09-30 | 2018-04-05 | Epizyme, Inc. | Substituted fused bi- or tri- heterocyclic compounds as ehmt2 inhibitors |
| US11471538B2 (en) | 2017-02-10 | 2022-10-18 | INSERM (Institut National de la Santéet de la Recherche Medicale) | Methods and pharmaceutical compositions for the treatment of cancers associated with activation of the MAPK pathway |
| EP3612181A4 (en) | 2017-04-21 | 2021-01-06 | Epizyme, Inc. | Combination therapies with ehmt2 inhibitors |
| IL270224B1 (en) | 2017-05-02 | 2024-04-01 | Novartis Ag | Combination therapy employing trametinib and a defined raf inhibitor |
| CN108102093A (zh) * | 2017-12-19 | 2018-06-01 | 中科院广州化学有限公司 | 一种含芴及吡啶基团的二胺单体及由其合成的聚酰亚胺 |
| EP3732285A1 (en) | 2017-12-28 | 2020-11-04 | Tract Pharmaceuticals, Inc. | Stem cell culture systems for columnar epithelial stem cells, and uses related thereto |
| JP2022500385A (ja) | 2018-09-10 | 2022-01-04 | ミラティ セラピューティクス, インコーポレイテッド | 組み合わせ療法 |
| WO2020097398A1 (en) * | 2018-11-07 | 2020-05-14 | Dana-Farber Cancer Institute, Inc. | Benzothiazole derivatives and 7-aza-benzothiazole derivatives as janus kinase 2 inhibitors and uses thereof |
| WO2020097396A1 (en) * | 2018-11-07 | 2020-05-14 | Dana-Farber Cancer Institute, Inc. | Benzimidazole derivatives and aza-benzimidazole derivatives as janus kinase 2 inhibitors and uses thereof |
| EP4563150A3 (en) | 2019-05-13 | 2025-07-23 | Novartis AG | New crystalline forms of n-(3-(2-(2-hydroxyethoxy)-6-morpholinopyridin-4-yl)-4-methvlphenyl)-2(trifluoromethyl) isonicotinamide as raf inhibitors for the treatment of cancer |
| CA3181537A1 (en) | 2020-05-06 | 2021-11-11 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors |
| WO2022140527A1 (en) | 2020-12-23 | 2022-06-30 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors |
| WO2023009708A1 (en) * | 2021-07-29 | 2023-02-02 | Ajax Therapeutics, Inc. | Heteroaryloxy triazolo- and imidazo-azines 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 (en) * | 2021-11-09 | 2023-05-19 | Ajax Therapeutics, Inc. | 6-heteroaryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6358932B1 (en) | 1994-05-31 | 2002-03-19 | Isis Pharmaceticals, Inc. | Antisense oligonucleotide inhibition of raf gene expression |
| US5717100A (en) | 1995-10-06 | 1998-02-10 | Merck & Co., Inc. | Substituted imidazoles having anti-cancer and cytokine inhibitory activity |
| DE19613976C1 (de) * | 1996-04-09 | 1997-11-20 | Gruenenthal Gmbh | Thalidomid-Prodrugs mit immunmodulatorischer Wirkung |
| NZ510991A (en) * | 1997-03-05 | 2002-11-26 | Sugen Inc | Use of formulations for hydrophobic pharmaceutical agents in treatment or prevention of cell proliferative disorders |
| AR012634A1 (es) | 1997-05-02 | 2000-11-08 | Sugen Inc | Compuesto basado en quinazolina, composicion famaceutica que lo comprende, metodo para sintetizarlo, su uso, metodos de modulacion de la funcion deserina/treonina proteinaquinasa con dicho compuesto y metodo in vitro para identificar compuestos que modulan dicha funcion |
| GB9711650D0 (en) | 1997-06-05 | 1997-07-30 | Pfizer Ltd | Compounds useful in therapy |
| GB9716557D0 (en) | 1997-08-06 | 1997-10-08 | Glaxo Group Ltd | Benzylidene-1,3-dihydro-indol-2-one derivatives having anti-cancer activity |
| US6022884A (en) | 1997-11-07 | 2000-02-08 | Amgen Inc. | Substituted pyridine compounds and methods of use |
| US6211177B1 (en) * | 1998-11-24 | 2001-04-03 | Cell Pathways, Inc. | Method for treating neoplasia by exposure to substituted 2-aryl-benzimidazole derivatives |
| WO2000042012A1 (en) | 1999-01-13 | 2000-07-20 | Bayer Corporation | φ-CARBOXYARYL SUBSTITUTED DIPHENYL UREAS AS RAF KINASE INHIBITORS |
| EP2308833A3 (en) | 1999-04-15 | 2011-09-28 | Bristol-Myers Squibb Company | Cyclic protein tyrosine kinase inhibitors |
| ATE339406T1 (de) * | 1999-09-23 | 2006-10-15 | Astrazeneca Ab | Chinazoline verbindungen als heilmittel |
| JP2003525936A (ja) | 2000-03-06 | 2003-09-02 | スミスクライン ビーチャム パブリック リミテッド カンパニー | Rafキナーゼ阻害物質としてのイミダゾール誘導体 |
| HUP0400651A2 (hu) | 2000-11-07 | 2004-06-28 | Bristol-Myers Squibb Company | Szerin proteáz inhibitorokként alkalmazható savszármazékok és ezeket tartalmazó gyógyszerkészítmények |
| EP1341771A2 (en) | 2000-11-29 | 2003-09-10 | Glaxo Group Limited | Benzimidazole derivatives useful as tie-2 and/or vegfr-2 inhibitors |
| US20030009034A1 (en) | 2001-03-22 | 2003-01-09 | Neil Wishart | Transition metal mediated process |
| GB0112348D0 (en) | 2001-05-19 | 2001-07-11 | Smithkline Beecham Plc | Compounds |
| JP4628678B2 (ja) * | 2002-03-29 | 2011-02-09 | ノバルティス バクシンズ アンド ダイアグノスティックス,インコーポレーテッド | 置換ベンズアゾールおよびRafキナーゼ阻害剤としてのそれらの使用 |
| US8299108B2 (en) | 2002-03-29 | 2012-10-30 | Novartis Ag | Substituted benzazoles and methods of their use as inhibitors of raf kinase |
| US7531553B2 (en) * | 2003-03-21 | 2009-05-12 | Amgen Inc. | Heterocyclic compounds and methods of use |
| CA2542653A1 (en) | 2003-10-16 | 2005-04-28 | Chiron Corporation | Substituted benzazoles and use thereof as inhibitors of raf kinase |
-
2004
- 2004-10-15 CA CA002542653A patent/CA2542653A1/en not_active Abandoned
- 2004-10-15 MX MXPA06004236A patent/MXPA06004236A/es unknown
- 2004-10-15 JP JP2006535367A patent/JP4755991B2/ja not_active Expired - Fee Related
- 2004-10-15 PL PL04795357T patent/PL1682126T3/pl unknown
- 2004-10-15 PT PT04795357T patent/PT1682126E/pt unknown
- 2004-10-15 EP EP04795357A patent/EP1682126B1/en not_active Expired - Lifetime
- 2004-10-15 CN CNA2004800361998A patent/CN1889951A/zh active Pending
- 2004-10-15 AT AT04795357T patent/ATE435015T1/de not_active IP Right Cessation
- 2004-10-15 DE DE602004021838T patent/DE602004021838D1/de not_active Expired - Lifetime
- 2004-10-15 KR KR1020067009081A patent/KR20060118472A/ko not_active Ceased
- 2004-10-15 WO PCT/US2004/034179 patent/WO2005037273A1/en not_active Ceased
- 2004-10-15 US US10/967,089 patent/US7423150B2/en not_active Expired - Fee Related
- 2004-10-15 AU AU2004281151A patent/AU2004281151A1/en not_active Abandoned
- 2004-10-15 ES ES04795357T patent/ES2327418T3/es not_active Expired - Lifetime
- 2004-10-18 TW TW093131586A patent/TW200526208A/zh unknown
-
2006
- 2006-04-11 IL IL174965A patent/IL174965A0/en unknown
-
2008
- 2008-09-05 US US12/205,028 patent/US8415382B2/en not_active Expired - Fee Related
-
2013
- 2013-04-03 US US13/856,225 patent/US20130224195A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2007509058A5 (enExample) | ||
| JP2007507428A5 (enExample) | ||
| JP2005529089A5 (enExample) | ||
| JP2007509059A5 (enExample) | ||
| JP5384611B2 (ja) | 新規ヘテロ環式化合物およびそれらの使用 | |
| JP6873145B2 (ja) | 5−置換2−(モルホリン−4−イル)−1,7−ナフチリジン | |
| ES2456275T3 (es) | Derivados de quinazolina moduladores de la quinasa JAK y su uso en métodos | |
| ZA200305619B (en) | Substituted triazole diamine derivatives as kinase inhibitors. | |
| JP2012501312A5 (enExample) | ||
| JP2022125283A5 (enExample) | ||
| JP2010510319A5 (enExample) | ||
| RU2009125897A (ru) | Ингибиторы фосфоинозитид-3-киназы и способы их применения | |
| ZA200603418B (en) | Substituted benzazoles and use thereof as inhibitors of Raf kinase | |
| JP5901634B2 (ja) | キナゾリン化合物及びその使用方法 | |
| JP2013516393A5 (enExample) | ||
| CA2671982A1 (en) | Methods of using mek inhibitors | |
| WO2015015318A4 (en) | Novel quinazolinones as bromodomain inhibitors | |
| JP2016522246A5 (enExample) | ||
| JP2010527373A5 (enExample) | ||
| RU2008141761A (ru) | ИНГИБИТОРЫ с-МЕТ ПРОТЕИНКИНАЗЫ | |
| JP2012519179A5 (enExample) | ||
| CN114430740A (zh) | Egfr抑制剂、组合物及其制备方法 | |
| JP2012111761A5 (enExample) | ||
| RU2017118165A (ru) | Ингибиторы энхансера гомолога 2 zestes | |
| JP2017532360A5 (enExample) |