ZA200701366B - Quinazolinone derivatives and their use as B-Raf inhibitors - Google Patents
Quinazolinone derivatives and their use as B-Raf inhibitorsInfo
- Publication number
- ZA200701366B ZA200701366B ZA200701366A ZA200701366A ZA200701366B ZA 200701366 B ZA200701366 B ZA 200701366B ZA 200701366 A ZA200701366 A ZA 200701366A ZA 200701366 A ZA200701366 A ZA 200701366A ZA 200701366 B ZA200701366 B ZA 200701366B
- Authority
- ZA
- South Africa
- Prior art keywords
- raf inhibitors
- quinazolinone derivatives
- quinazolinone
- derivatives
- raf
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/88—Oxygen atoms
- C07D239/90—Oxygen atoms with acyclic radicals attached in position 2 or 3
-
- 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
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- 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
-
- 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
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)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US60653504P | 2004-09-01 | 2004-09-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200701366B true ZA200701366B (en) | 2008-09-25 |
Family
ID=35149373
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200701366A ZA200701366B (en) | 2004-09-01 | 2007-02-15 | Quinazolinone derivatives and their use as B-Raf inhibitors |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US20090054469A1 (pt) |
| EP (1) | EP1789400A1 (pt) |
| JP (1) | JP2008511600A (pt) |
| KR (1) | KR20070055575A (pt) |
| CN (1) | CN101010303A (pt) |
| AR (1) | AR050545A1 (pt) |
| AU (1) | AU2005278961A1 (pt) |
| BR (1) | BRPI0514679A (pt) |
| CA (1) | CA2577278A1 (pt) |
| IL (1) | IL181213A0 (pt) |
| MX (1) | MX2007002433A (pt) |
| NO (1) | NO20071245L (pt) |
| TW (1) | TW200621259A (pt) |
| UY (1) | UY29092A1 (pt) |
| WO (1) | WO2006024836A1 (pt) |
| ZA (1) | ZA200701366B (pt) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8119655B2 (en) | 2005-10-07 | 2012-02-21 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
| ES2604539T3 (es) | 2005-11-14 | 2017-03-07 | Genentech, Inc. | Inhibidores de tipo bisamida de la señalización hedgehog |
| JP2009532450A (ja) * | 2006-04-05 | 2009-09-10 | アストラゼネカ アクチボラグ | 化合物 |
| CN101421253A (zh) * | 2006-04-18 | 2009-04-29 | 阿斯利康(瑞典)有限公司 | 喹唑啉-4-酮衍生物、其制备方法及含有它们的药用组合物 |
| US20100216791A1 (en) * | 2006-08-17 | 2010-08-26 | Astrazeneca | Pyridinylquinazolinamine derivatives and their use as b-raf inhibitors |
| SG158147A1 (en) | 2006-10-09 | 2010-01-29 | Takeda Pharmaceutical | Kinase 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 |
| JP2011513331A (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 | ピラゾール[3,4−b]ピリジンRAF阻害剤 |
| KR20100122505A (ko) * | 2008-02-29 | 2010-11-22 | 어레이 바이오파마 인크. | Raf 저해물질 화합물 및 이들의 이용 방법 |
| CA2716947A1 (en) * | 2008-02-29 | 2009-09-11 | Array Biopharma Inc. | Imidazo [4,5-b] pyridine derivatives used as raf inhibitors |
| WO2010068738A1 (en) | 2008-12-10 | 2010-06-17 | Dana-Farber Cancer Institute, Inc. | Mek mutations conferring resistance to mek inhibitors |
| BR112012022801B8 (pt) | 2010-03-09 | 2019-10-29 | Dana Farber Cancer Inst Inc | método de identificar um indivíduo que tem câncer que é provável beneficiar-se do tratamento com uma terapia de combinação com um inibidor de raf e um segundo inibidor e uso de um inibidor de raf e um segundo inibidor para a fabricação de um medicamento para tratar câncer |
| US8669256B2 (en) | 2010-05-28 | 2014-03-11 | Merck Sharp & Dohme B.V. | Substituted thieno[2,3-b]pyrazine compounds as modulators of B-Raf kinase activity |
| PT2580322T (pt) | 2010-06-09 | 2018-03-01 | Dana Farber Cancer Inst Inc | Uma mutação em mek1 que confere resistência aos inibidores de raf e mek |
| WO2013109142A1 (en) | 2012-01-16 | 2013-07-25 | Stichting Het Nederlands Kanker Instituut | Combined pdk and mapk/erk pathway inhibition in neoplasia |
| US20150141470A1 (en) | 2012-05-08 | 2015-05-21 | The Broad Institute, Inc. | Diagnostic and treatment methods in patients having or at risk of developing resistance to cancer therapy |
| AU2014243816B2 (en) * | 2013-03-13 | 2019-01-31 | Bioasis Technologies Inc. | Fragments of p97 and uses thereof |
| WO2015041534A1 (en) | 2013-09-20 | 2015-03-26 | Stichting Het Nederlands Kanker Instituut | P90rsk in combination with raf/erk/mek |
| US9629851B2 (en) | 2013-09-20 | 2017-04-25 | Stitching Het Nederlands Kanker Institut—Antoni Van Leeuwenhoek Ziekenhuis | ROCK in combination with MAPK pathway |
| JP6038212B2 (ja) * | 2015-03-18 | 2016-12-07 | ザ ガバメント オブ ザ ユナイテッド ステイツ オブ アメリカ アズ リプレゼンテッド バイ ザ セクレタリー オブ ザ デパートメント オブ ヘルス アンド ヒューマン サービシーズ | 甲状腺刺激ホルモン受容体(tshr)の低分子量アゴニスト |
| EA202192575A1 (ru) | 2019-03-21 | 2022-01-14 | Онксео | Соединения dbait в сочетании с ингибиторами киназ для лечения рака |
| CN114761006A (zh) | 2019-11-08 | 2022-07-15 | Inserm(法国国家健康医学研究院) | 对激酶抑制剂产生耐药性的癌症的治疗方法 |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| WO2025073765A1 (en) | 2023-10-03 | 2025-04-10 | Institut National de la Santé et de la Recherche Médicale | Methods of prognosis and treatment of patients suffering from melanoma |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2444606A (en) * | 1945-12-15 | 1948-07-06 | Gen Aniline & Film Corp | Stabilizers for photographic emulsions |
| GB9623833D0 (en) * | 1996-11-16 | 1997-01-08 | Zeneca Ltd | Chemical compound |
| WO2000007991A1 (en) * | 1998-08-04 | 2000-02-17 | Astrazeneca Ab | Amide derivatives useful as inhibitors of the production of cytokines |
| GB0005357D0 (en) * | 2000-03-06 | 2000-04-26 | Smithkline Beecham Plc | Compounds |
| WO2003082272A1 (en) * | 2002-03-29 | 2003-10-09 | Chiron Corporation | Substituted benzazoles and use thereof as raf kinase inhibitors |
-
2005
- 2005-08-26 MX MX2007002433A patent/MX2007002433A/es not_active Application Discontinuation
- 2005-08-26 BR BRPI0514679-8A patent/BRPI0514679A/pt not_active Application Discontinuation
- 2005-08-26 AU AU2005278961A patent/AU2005278961A1/en not_active Abandoned
- 2005-08-26 CN CNA2005800293196A patent/CN101010303A/zh active Pending
- 2005-08-26 CA CA002577278A patent/CA2577278A1/en not_active Abandoned
- 2005-08-26 WO PCT/GB2005/003336 patent/WO2006024836A1/en not_active Ceased
- 2005-08-26 KR KR1020077007040A patent/KR20070055575A/ko not_active Withdrawn
- 2005-08-26 EP EP05775543A patent/EP1789400A1/en not_active Withdrawn
- 2005-08-26 JP JP2007528984A patent/JP2008511600A/ja active Pending
- 2005-08-28 US US11/574,036 patent/US20090054469A1/en not_active Abandoned
- 2005-08-30 UY UY29092A patent/UY29092A1/es not_active Application Discontinuation
- 2005-08-30 AR ARP050103625A patent/AR050545A1/es unknown
- 2005-09-02 TW TW094130101A patent/TW200621259A/zh unknown
-
2007
- 2007-02-07 IL IL181213A patent/IL181213A0/en unknown
- 2007-02-15 ZA ZA200701366A patent/ZA200701366B/xx unknown
- 2007-03-07 NO NO20071245A patent/NO20071245L/no unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2577278A1 (en) | 2006-03-09 |
| KR20070055575A (ko) | 2007-05-30 |
| MX2007002433A (es) | 2007-05-04 |
| US20090054469A1 (en) | 2009-02-26 |
| BRPI0514679A (pt) | 2008-06-17 |
| TW200621259A (en) | 2006-07-01 |
| IL181213A0 (en) | 2007-07-04 |
| UY29092A1 (es) | 2006-04-28 |
| EP1789400A1 (en) | 2007-05-30 |
| WO2006024836A1 (en) | 2006-03-09 |
| JP2008511600A (ja) | 2008-04-17 |
| AU2005278961A1 (en) | 2006-03-09 |
| CN101010303A (zh) | 2007-08-01 |
| AR050545A1 (es) | 2006-11-01 |
| NO20071245L (no) | 2007-05-24 |
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