TNSN08445A1 - Derives de triazolopyrazine utiles comme agent anticancereux - Google Patents
Derives de triazolopyrazine utiles comme agent anticancereuxInfo
- Publication number
- TNSN08445A1 TNSN08445A1 TNP2008000445A TNSN08445A TNSN08445A1 TN SN08445 A1 TNSN08445 A1 TN SN08445A1 TN P2008000445 A TNP2008000445 A TN P2008000445A TN SN08445 A TNSN08445 A TN SN08445A TN SN08445 A1 TNSN08445 A1 TN SN08445A1
- Authority
- TN
- Tunisia
- Prior art keywords
- anticancer agent
- derivatives useful
- formula
- compounds
- triazolopyrazine derivatives
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
L'invention concerne des composés de formule (I) ou un de leurs sels pharmaceutiquement acceptables, formule dans laquelle R1, R2, R3 et R4 sont tels que definis dans le present memoire. L'invention concerne egalement des compositions pharmaceutiques contenant les composés de formule I, ainsi que des methodes pour le traitement de troubles hyperproliferatifs chez un mammifère par administration des composés de formule (I).
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79996606P | 2006-05-11 | 2006-05-11 | |
| US89323107P | 2007-03-06 | 2007-03-06 | |
| PCT/IB2007/001142 WO2007132308A1 (fr) | 2006-05-11 | 2007-04-30 | Dérivés de triazolopyrazine utiles en tant qu'agents anti-cancereux |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TNSN08445A1 true TNSN08445A1 (fr) | 2010-04-14 |
Family
ID=38441445
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TNP2008000445A TNSN08445A1 (fr) | 2006-05-11 | 2008-11-06 | Derives de triazolopyrazine utiles comme agent anticancereux |
Country Status (32)
| Country | Link |
|---|---|
| US (2) | US7732604B2 (fr) |
| EP (1) | EP2018383B1 (fr) |
| JP (1) | JP4377962B2 (fr) |
| KR (1) | KR101099161B1 (fr) |
| CN (1) | CN101443331A (fr) |
| AP (1) | AP2008004674A0 (fr) |
| AR (1) | AR060994A1 (fr) |
| AT (1) | ATE532785T1 (fr) |
| AU (1) | AU2007251283A1 (fr) |
| BR (1) | BRPI0711809A2 (fr) |
| CA (1) | CA2651363C (fr) |
| CR (1) | CR10383A (fr) |
| EA (1) | EA016204B1 (fr) |
| EC (1) | ECSP088871A (fr) |
| ES (1) | ES2376913T3 (fr) |
| GE (1) | GEP20115174B (fr) |
| GT (1) | GT200700039A (fr) |
| HN (1) | HN2007015177A (fr) |
| IL (1) | IL194813A0 (fr) |
| MA (1) | MA30411B1 (fr) |
| ME (1) | MEP36508A (fr) |
| MX (1) | MX2008014399A (fr) |
| NL (1) | NL2000613C2 (fr) |
| NO (1) | NO20085060L (fr) |
| NZ (1) | NZ572361A (fr) |
| PE (1) | PE20080067A1 (fr) |
| RS (1) | RS20080533A (fr) |
| TN (1) | TNSN08445A1 (fr) |
| TW (1) | TWI346115B (fr) |
| UY (1) | UY30334A1 (fr) |
| WO (1) | WO2007132308A1 (fr) |
| ZA (1) | ZA200809020B (fr) |
Families Citing this family (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8198448B2 (en) * | 2006-07-14 | 2012-06-12 | Amgen Inc. | Fused heterocyclic derivatives and methods of use |
| PE20121506A1 (es) | 2006-07-14 | 2012-11-26 | Amgen Inc | Compuestos triazolopiridinas como inhibidores de c-met |
| US8217177B2 (en) | 2006-07-14 | 2012-07-10 | Amgen Inc. | Fused heterocyclic derivatives and methods of use |
| DE102007026341A1 (de) | 2007-06-06 | 2008-12-11 | Merck Patent Gmbh | Benzoxazolonderivate |
| DE102007032507A1 (de) | 2007-07-12 | 2009-04-02 | Merck Patent Gmbh | Pyridazinonderivate |
| US20110039856A1 (en) * | 2007-11-29 | 2011-02-17 | Pfizer Inc. | Polymorphs of a c-met/hgfr inhibitor |
| DE102007061963A1 (de) | 2007-12-21 | 2009-06-25 | Merck Patent Gmbh | Pyridazinonderivate |
| US20110009421A1 (en) * | 2008-02-27 | 2011-01-13 | Takeda Pharmaceutical Company Limited | Compound having 6-membered aromatic ring |
| AR070487A1 (es) * | 2008-02-28 | 2010-04-07 | Novartis Ag | Derivados de 3- metil- imidazo -( 1,2-b)- piridazina |
| US8598184B2 (en) * | 2008-03-03 | 2013-12-03 | Tiger Pharmatech | Protein kinase inhibitors |
| DE102008019907A1 (de) | 2008-04-21 | 2009-10-22 | Merck Patent Gmbh | Pyridazinonderivate |
| DE102008028905A1 (de) | 2008-06-18 | 2009-12-24 | Merck Patent Gmbh | 3-(3-Pyrimidin-2-yl-benzyl)-[1,2,4]triazolo[4,3-b]pyridazinderivate |
| US20110130384A1 (en) * | 2008-06-25 | 2011-06-02 | Takeda Pharmaceutical Company Limited | Amide compound |
| DE102008037790A1 (de) | 2008-08-14 | 2010-02-18 | Merck Patent Gmbh | Bicyclische Triazolderivate |
| JP2012509342A (ja) * | 2008-11-20 | 2012-04-19 | オーエスアイ・フアーマスーテイカルズ・インコーポレーテツド | 置換ピロロ[2,3−b]−ピリジンおよび−ピラジン |
| CA2744563A1 (fr) * | 2008-12-12 | 2010-06-17 | Ariad Pharmaceuticals, Inc. | Derives d'azaindole en tant qu'inhibiteurs de kinases |
| EA019320B1 (ru) | 2008-12-22 | 2014-02-28 | Мерк Патент Гмбх | Новые полиморфные формы дигидрофосфата 6-(1-метил-1h-пиразол-4-ил)-2-{3-[5-(2-морфолин-4-илэтокси)пиримидин-2-ил]бензил}-2h-пиридазин-3-она и способы их получения |
| JOP20190230A1 (ar) | 2009-01-15 | 2017-06-16 | Incyte Corp | طرق لاصلاح مثبطات انزيم jak و المركبات الوسيطة المتعلقة به |
| SG176574A1 (en) * | 2009-05-28 | 2012-01-30 | Vertex Pharma | Aminopyrazole triazolothiadiazole inhibitors of c-met protien kinase |
| US8389526B2 (en) | 2009-08-07 | 2013-03-05 | Novartis Ag | 3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives |
| JP5781510B2 (ja) * | 2009-08-12 | 2015-09-24 | ノバルティス アーゲー | ヘテロ環式ヒドラゾン化合物および癌および炎症の処置のためのそれらの使用 |
| MX2012002179A (es) | 2009-08-20 | 2012-03-16 | Novartis Ag | Compuestos heterociclicos de oxima. |
| DE102009056886A1 (de) | 2009-12-03 | 2011-06-09 | Bayer Schering Pharma Aktiengesellschaft | cMet-Inhibitoren zur Behandlung der Endometriose |
| EP2719699B1 (fr) | 2009-12-31 | 2015-07-08 | Hutchison Medipharma Limited | Certaines triazolopyrazines, leurs compositions et leurs procédés d'utilisation |
| TWI423974B (zh) * | 2010-02-11 | 2014-01-21 | Hutchison Medipharma Ltd | 三氮唑並吡啶和三氮唑並吡嗪化合物及其組合物和應用 |
| AR081039A1 (es) | 2010-05-14 | 2012-05-30 | Osi Pharmaceuticals Llc | Inhibidores biciclicos fusionados de quinasa |
| JP2013526570A (ja) | 2010-05-14 | 2013-06-24 | オーエスアイ・ファーマシューティカルズ,エルエルシー | 縮合二環式キナーゼ阻害剤 |
| ES2715611T3 (es) * | 2010-05-17 | 2019-06-05 | Incozen Therapeutics Pvt Ltd | Compuestos novedosos de 3H-imidazo[4,5-b]piridina-3,5-disustituida y 3H-[1,2,3]triazolo[4,5-b]piridina 3,5-disustituida como moduladores de proteína cinasas |
| US20130315895A1 (en) | 2010-07-01 | 2013-11-28 | Takeda Pharmaceutical Company Limited | COMBINATION OF A cMET INHIBITOR AND AN ANTIBODY TO HGF AND/OR cMET |
| WO2012042421A1 (fr) | 2010-09-29 | 2012-04-05 | Pfizer Inc. | Procédé de traitement de la croissance cellulaire anormale |
| CN102532141A (zh) | 2010-12-08 | 2012-07-04 | 中国科学院上海药物研究所 | [1,2,4]三唑并[4,3-b][1,2,4]三嗪类化合物、其制备方法和用途 |
| US20140088114A1 (en) | 2011-05-16 | 2014-03-27 | OSI Pharmaceuticals ,LLC | Fused bicyclic kinase inhibitors |
| WO2013038362A1 (fr) | 2011-09-15 | 2013-03-21 | Novartis Ag | 3-(quinolin-6-ylthio)-[1,2,4]triazolo[4,3-a]pyradines substituées en position 6 à activité tyrosine kinase |
| CN102516263B (zh) * | 2011-10-25 | 2015-04-08 | 南方医科大学 | 一种螺三环类化合物及其制备方法、以及含该类化合物的药物组合物及其应用 |
| CN102503959B (zh) * | 2011-10-25 | 2015-04-08 | 南方医科大学 | 一种稠三环类化合物及其制备方法、以及含该类化合物的药物组合物及其应用 |
| CN103204844A (zh) * | 2012-01-17 | 2013-07-17 | 上海艾力斯医药科技有限公司 | 氨基杂芳基化合物及其制备方法与应用 |
| KR102164317B1 (ko) | 2012-03-30 | 2020-10-13 | 리젠 파마슈티컬스 소시에떼 아노님 | C-met 단백질 키나제의 조절제로서의 신규한 3,5-디치환-3h-이미다조[4,5-b]피리딘 및 3,5- 디치환 -3h-[1,2,3]트리아졸로[4,5-b] 피리딘 화합물 |
| WO2013149581A1 (fr) | 2012-04-03 | 2013-10-10 | Novartis Ag | Produits combinés comprenant des inhibiteurs de tyrosine kinase et leur utilisation |
| US20150051210A1 (en) | 2012-04-03 | 2015-02-19 | Novartis Ag | Tyrosine Kinase Inhibitor Combinations and their Use |
| CN107312009B (zh) * | 2013-04-17 | 2022-09-20 | 上海医药集团股份有限公司 | 喹啉类化合物、其制备方法、中间体、药物组合物和应用 |
| WO2014174478A1 (fr) | 2013-04-26 | 2014-10-30 | Novartis Ag | Combinaisons pharmaceutiques d'un inhibiteur de la pkc et d'un inhibiteur du récepteur tyrosine-kinase c-met |
| ES2675355T3 (es) * | 2013-09-30 | 2018-07-10 | Korea Research Institute Of Chemical Technology | Derivados de triazolopirazina como inhibidores de tirosina cinasa |
| ES2764299T3 (es) | 2014-12-09 | 2020-06-02 | Inst Nat Sante Rech Med | Anticuerpos monoclonales humanos contra AXL |
| WO2016135041A1 (fr) | 2015-02-26 | 2016-09-01 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Protéines de fusion et anticorps les contenant pour favoriser l'apoptose |
| JP2018123059A (ja) * | 2015-06-10 | 2018-08-09 | 石原産業株式会社 | 1−シクロプロピルエチルアミン又はその塩の製造方法 |
| WO2017015267A1 (fr) * | 2015-07-20 | 2017-01-26 | Genzyme Corporation | Inhibiteurs du récepteur de facteur-1 de stimulation de colonies (csf-1r) |
| CN105272995B (zh) | 2015-09-24 | 2017-10-27 | 上海海聚生物科技有限公司 | 喹啉类衍生物、其药物组合物、制备方法及应用 |
| EP3398951B1 (fr) * | 2015-12-31 | 2021-04-07 | Shanghai Pharmaceuticals Holding Co., Ltd. | Sel de composé de quinolone, ses polymorphes, son procédé de préparation, sa composition et les applications associées |
| SG11201807965YA (en) | 2016-03-15 | 2018-10-30 | Oryzon Genomics Sa | Combinations of lsd1 inhibitors for use in the treatment of solid tumors |
| US11091489B2 (en) * | 2016-06-20 | 2021-08-17 | Novartis Ag | Crystalline forms of a triazolopyrimidine compound |
| KR20180092096A (ko) * | 2017-02-08 | 2018-08-17 | 에이비온 주식회사 | 트리아졸로 피라진 유도체의 신규한 다형체 및 이의 제조 방법 |
| CN108570053A (zh) * | 2017-03-13 | 2018-09-25 | 中国科学院上海药物研究所 | 五元并六元杂环化合物、制备方法、中间体、组合和应用 |
| CN108276418A (zh) * | 2018-03-20 | 2018-07-13 | 北京凯恩梅格医药科技有限公司 | 化合物、含有该化合物的药用组合物及其用途 |
| CA3122575A1 (fr) | 2018-12-14 | 2020-06-18 | Beta Pharma, Inc. | Composes substitues par organophosphore en tant qu'inhibiteurs de c-met et leurs utilisations therapeutiques |
| JP2024500919A (ja) | 2020-12-23 | 2024-01-10 | ジェンザイム・コーポレーション | 重水素化コロニー刺激因子-1受容体(csf-1r)阻害剤 |
| WO2025098425A1 (fr) * | 2023-11-09 | 2025-05-15 | 浙江华海药业股份有限公司 | Procédé de préparation de modulateur du récepteur de la chimiokine et utilisation |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FI941572L (fi) | 1991-10-07 | 1994-05-27 | Oncologix Inc | Anti-erbB-2-monoklonaalisten vasta-aineiden yhdistelmä ja käyttömenetelmä |
| ATE419355T1 (de) | 1992-02-06 | 2009-01-15 | Novartis Vaccines & Diagnostic | Marker für krebs und biosynthetisches bindeprotein dafür |
| IL112248A0 (en) | 1994-01-25 | 1995-03-30 | Warner Lambert Co | Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them |
| GB9520822D0 (en) | 1995-10-11 | 1995-12-13 | Wellcome Found | Therapeutically active compounds |
| EP0912559B1 (fr) | 1996-07-13 | 2002-11-06 | Glaxo Group Limited | Composes heterocycliques condenses en tant qu'inhibiteurs de la proteine tyrosine kinase |
| DE69718472T2 (de) | 1996-07-13 | 2003-11-06 | Glaxo Group Ltd., Greenford | Bicyclische heteroaromatische verbindungen als protein tyrosine kinase inhibitoren |
| GB9800569D0 (en) | 1998-01-12 | 1998-03-11 | Glaxo Group Ltd | Heterocyclic compounds |
| GB9800575D0 (en) | 1998-01-12 | 1998-03-11 | Glaxo Group Ltd | Heterocyclic compounds |
| PT1212327E (pt) * | 1999-09-17 | 2004-01-30 | Abbott Gmbh & Co Kg | Pirazolopirimidinas como agentes terapeuticos |
| JP2007516180A (ja) * | 2003-07-02 | 2007-06-21 | スゲン,インコーポレイティド | c−Met阻害薬としてのアリールメチルトリアゾロおよびイミダゾピラジン類 |
| WO2005028480A2 (fr) | 2003-09-03 | 2005-03-31 | Neurogen Corporation | 5-aryl-pyrazolo[4,3-d]pyrimidines, pyridines, et pyrazines et composes associes |
| US9672526B2 (en) | 2012-03-13 | 2017-06-06 | American Express Travel Related Services Company, Inc. | Systems and methods for tailoring marketing |
| US10884952B2 (en) | 2016-09-30 | 2021-01-05 | Intel Corporation | Enforcing memory operand types using protection keys |
-
2007
- 2007-04-26 NL NL2000613A patent/NL2000613C2/nl not_active IP Right Cessation
- 2007-04-30 BR BRPI0711809-0A patent/BRPI0711809A2/pt not_active IP Right Cessation
- 2007-04-30 EP EP07734459A patent/EP2018383B1/fr active Active
- 2007-04-30 JP JP2009508530A patent/JP4377962B2/ja not_active Expired - Fee Related
- 2007-04-30 AP AP2008004674A patent/AP2008004674A0/xx unknown
- 2007-04-30 ME MEP-365/08A patent/MEP36508A/xx unknown
- 2007-04-30 KR KR1020087027474A patent/KR101099161B1/ko not_active Expired - Fee Related
- 2007-04-30 CA CA2651363A patent/CA2651363C/fr not_active Expired - Fee Related
- 2007-04-30 AU AU2007251283A patent/AU2007251283A1/en not_active Abandoned
- 2007-04-30 GE GEAP200710971A patent/GEP20115174B/en unknown
- 2007-04-30 CN CNA2007800170852A patent/CN101443331A/zh active Pending
- 2007-04-30 AT AT07734459T patent/ATE532785T1/de active
- 2007-04-30 NZ NZ572361A patent/NZ572361A/en not_active IP Right Cessation
- 2007-04-30 EA EA200870423A patent/EA016204B1/ru not_active IP Right Cessation
- 2007-04-30 WO PCT/IB2007/001142 patent/WO2007132308A1/fr not_active Ceased
- 2007-04-30 MX MX2008014399A patent/MX2008014399A/es active IP Right Grant
- 2007-04-30 RS RSP-2008/0533A patent/RS20080533A/sr unknown
- 2007-04-30 ES ES07734459T patent/ES2376913T3/es active Active
- 2007-05-08 US US11/745,921 patent/US7732604B2/en not_active Expired - Fee Related
- 2007-05-09 PE PE2007000559A patent/PE20080067A1/es not_active Application Discontinuation
- 2007-05-09 GT GT200700039A patent/GT200700039A/es unknown
- 2007-05-09 AR ARP070102012A patent/AR060994A1/es not_active Application Discontinuation
- 2007-05-09 UY UY30334A patent/UY30334A1/es unknown
- 2007-05-09 HN HN2007015177A patent/HN2007015177A/es unknown
- 2007-05-10 TW TW096116645A patent/TWI346115B/zh not_active IP Right Cessation
-
2008
- 2008-10-21 CR CR10383A patent/CR10383A/es not_active Application Discontinuation
- 2008-10-21 ZA ZA2008/09020A patent/ZA200809020B/en unknown
- 2008-10-22 IL IL194813A patent/IL194813A0/en unknown
- 2008-11-06 TN TNP2008000445A patent/TNSN08445A1/fr unknown
- 2008-11-07 EC EC2008008871A patent/ECSP088871A/es unknown
- 2008-11-11 MA MA31378A patent/MA30411B1/fr unknown
- 2008-12-03 NO NO20085060A patent/NO20085060L/no not_active Application Discontinuation
-
2010
- 2010-01-04 US US12/651,984 patent/US20100105656A1/en not_active Abandoned
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| MA30403B1 (fr) | Derives d'acides cycloalkylamines et leurs compositions pharmaceutiques | |
| MA27774A1 (fr) | Inhibiteurs de phosphatidylinositol 3-kinase | |
| MA30333B1 (fr) | Aminotetrahydropyranes utiles en tant qu'inhibiteurs de la dipeptidyle peptidase-iv pour le traitement ou la prevention du diabete. | |
| TNSN98084A1 (fr) | Derives de macrolides substitues en position c-4 | |
| TNSN07145A1 (fr) | Derives de 2-amido-4-phenylthiazole, leur preparation et leur application en therapeutique | |
| MA29170B1 (fr) | Derives puriniques agissant comme des agonistes du recepteur a2a | |
| MA30696B1 (fr) | Derives de l'acide (3-amino-1,2,3,4-tetrahydro-9h-carbazol-9-yl)-acetique |