TW200911811A - Imidazopyrazines as protein kinase inhibitors - Google Patents
Imidazopyrazines as protein kinase inhibitors Download PDFInfo
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- TW200911811A TW200911811A TW097121942A TW97121942A TW200911811A TW 200911811 A TW200911811 A TW 200911811A TW 097121942 A TW097121942 A TW 097121942A TW 97121942 A TW97121942 A TW 97121942A TW 200911811 A TW200911811 A TW 200911811A
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- alkyl
- compound
- heteroaryl
- aryl
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- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 108700012359 toxins Proteins 0.000 description 1
- 230000026683 transduction Effects 0.000 description 1
- 238000010361 transduction Methods 0.000 description 1
- 102000027257 transmembrane receptors Human genes 0.000 description 1
- 108091008578 transmembrane receptors Proteins 0.000 description 1
- 230000016596 traversing start control point of mitotic cell cycle Effects 0.000 description 1
- GYUURHMITDQTRU-UHFFFAOYSA-N tributyl(pyridin-2-yl)stannane Chemical compound CCCC[Sn](CCCC)(CCCC)C1=CC=CC=N1 GYUURHMITDQTRU-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- BBIUWPMGWINSFC-UHFFFAOYSA-N tridecane-1,2,3-triol Chemical compound CCCCCCCCCCC(O)C(O)CO BBIUWPMGWINSFC-UHFFFAOYSA-N 0.000 description 1
- VFJYIHQDILEQNR-UHFFFAOYSA-M trimethylsulfanium;iodide Chemical compound [I-].C[S+](C)C VFJYIHQDILEQNR-UHFFFAOYSA-M 0.000 description 1
- FIQMHBFVRAXMOP-UHFFFAOYSA-N triphenylphosphane oxide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C1=CC=CC=C1 FIQMHBFVRAXMOP-UHFFFAOYSA-N 0.000 description 1
- 239000001226 triphosphate Substances 0.000 description 1
- RMNIZOOYFMNEJJ-UHFFFAOYSA-K tripotassium;phosphate;hydrate Chemical compound O.[K+].[K+].[K+].[O-]P([O-])([O-])=O RMNIZOOYFMNEJJ-UHFFFAOYSA-K 0.000 description 1
- 238000001665 trituration Methods 0.000 description 1
- 230000005747 tumor angiogenesis Effects 0.000 description 1
- 230000005760 tumorsuppression Effects 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 238000007631 vascular surgery Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 230000001755 vocal effect Effects 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 210000004885 white matter Anatomy 0.000 description 1
- 235000014101 wine Nutrition 0.000 description 1
- 230000029663 wound healing Effects 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
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
- 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
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US94399907P | 2007-06-14 | 2007-06-14 | |
| US98793207P | 2007-11-14 | 2007-11-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW200911811A true TW200911811A (en) | 2009-03-16 |
Family
ID=40002934
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW097121942A TW200911811A (en) | 2007-06-14 | 2008-06-12 | Imidazopyrazines as protein kinase inhibitors |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP2170892A2 (fr) |
| JP (1) | JP2010529195A (fr) |
| CN (1) | CN101772500A (fr) |
| AR (1) | AR066958A1 (fr) |
| CA (1) | CA2690557A1 (fr) |
| CL (1) | CL2008001745A1 (fr) |
| MX (1) | MX2009013729A (fr) |
| PE (1) | PE20090365A1 (fr) |
| TW (1) | TW200911811A (fr) |
| WO (1) | WO2008156614A2 (fr) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102428087B (zh) | 2009-04-16 | 2015-06-17 | 卡洛斯三世国家癌症研究中心基金会 | 用作激酶抑制剂的咪唑并吡嗪类化合物 |
| TW201107329A (en) * | 2009-07-30 | 2011-03-01 | Oncotherapy Science Inc | Fused imidazole derivative having ttk inhibitory action |
| WO2011028638A1 (fr) | 2009-09-04 | 2011-03-10 | Schering Corporation | Modulateurs de points de contrôle du cycle cellulaire et leur utilisation en combinaison avec des inhibiteurs de kinase de point de contrôle |
| EP2493889B1 (fr) | 2009-10-30 | 2017-09-06 | Janssen Pharmaceutica, N.V. | Dérivés d'imidazo[1,2-b]pyridazine et leur utilisation en tant qu'inhibiteurs pde10 |
| AR080754A1 (es) | 2010-03-09 | 2012-05-09 | Janssen Pharmaceutica Nv | Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10 |
| JP5824040B2 (ja) * | 2010-06-01 | 2015-11-25 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | 置換イミダゾピラジン |
| ES2541054T3 (es) * | 2010-10-20 | 2015-07-15 | Université De Bordeaux | Firmas del resultado clínico en tumores estromales gastrointestinales y método de tratamiento de tumores estromales gastrointestinales |
| EP2444084A1 (fr) | 2010-10-21 | 2012-04-25 | Centro Nacional de Investigaciones Oncológicas (CNIO) | Utilisation d'inhibiteurs de PI3K pour le traitement de l'obésité |
| WO2012052745A1 (fr) | 2010-10-21 | 2012-04-26 | Centro Nacional De Investigaciones Oncológicas (Cnio) | Combinaisons d'inhibiteurs de pi3k avec un second agent antitumoral |
| WO2012080230A1 (fr) * | 2010-12-17 | 2012-06-21 | Bayer Pharma Aktiengesellschaft | Imidazopyrazines 6-substituées pour l'utilisation en tant qu'inhibiteurs de mps-1 et de tkk dans le traitement de troubles d'hyperprolifération |
| US8673905B2 (en) * | 2011-03-17 | 2014-03-18 | Hoffmann-La Roche Inc. | Imidazo pyrazines |
| JP2014521595A (ja) | 2011-05-25 | 2014-08-28 | ブリストル−マイヤーズ スクイブ カンパニー | 抗アポトーシスBcl阻害剤として有用な置換スルホンアミド |
| MX344600B (es) | 2011-06-27 | 2016-12-20 | Janssen Pharmaceutica Nv | Derivados de 1-aril-4-metil-[1,2,4]triazolo[4,3-a]quinoxalina. |
| HK1206250A1 (en) | 2012-06-26 | 2016-01-08 | Janssen Pharmaceutica Nv | Combinations comprising pde 2 inhibitors such as 1-aryl-4-methyl-[1,2,4] triazolo [4,3-a] quinoxaline compounds and ped 10 inhibitors for use in the treatment of neurological or metabolic disorders |
| CN104411314B (zh) | 2012-07-09 | 2017-10-20 | 詹森药业有限公司 | 磷酸二酯酶10的抑制剂 |
| HRP20181795T1 (hr) | 2014-01-13 | 2019-01-25 | Aurigene Discovery Technologies Limited | Biciklički heterociklilni derivati kao inhibitori irak4 |
| EP3105219B9 (fr) | 2014-02-13 | 2018-10-03 | Incyte Corporation | Cyclopropylamines en tant qu'inhibiteurs de lsd1 |
| US9527835B2 (en) | 2014-02-13 | 2016-12-27 | Incyte Corporation | Cyclopropylamines as LSD1 inhibitors |
| PT3105218T (pt) | 2014-02-13 | 2019-12-05 | Incyte Corp | Ciclopropilaminas como inibidores de lsd1 |
| DK3105226T3 (da) | 2014-02-13 | 2019-10-14 | Incyte Corp | Cyclopropylaminer som lsd1-inhibitorer |
| TWI687419B (zh) | 2014-07-10 | 2020-03-11 | 美商英塞特公司 | 作為lsd1抑制劑之咪唑并吡啶及咪唑并吡嗪 |
| TW201613925A (en) | 2014-07-10 | 2016-04-16 | Incyte Corp | Imidazopyrazines as LSD1 inhibitors |
| US9758523B2 (en) | 2014-07-10 | 2017-09-12 | Incyte Corporation | Triazolopyridines and triazolopyrazines as LSD1 inhibitors |
| WO2016007722A1 (fr) | 2014-07-10 | 2016-01-14 | Incyte Corporation | Triazolopyridines et triazolopyrazines utilisables comme inhibiteurs de lsd1 |
| EP3626720A1 (fr) | 2015-04-03 | 2020-03-25 | Incyte Corporation | Composés hétérocycliques utilisés en tant qu'inhibiteurs de lsd1 |
| KR102710120B1 (ko) | 2015-08-12 | 2024-09-27 | 인사이트 홀딩스 코포레이션 | Lsd1 저해제의 염 |
| PE20190377A1 (es) | 2016-04-22 | 2019-03-08 | Incyte Corp | Formulaciones de un inhibidor de lsd 1 |
| WO2018102552A1 (fr) | 2016-11-30 | 2018-06-07 | Case Western Reserve University | Combinaisons d'inhibiteurs de 15-pgdh avec des corcostéroïdes et/ou des inhibiteurs du tnf et leurs utilisations |
| JP2020514323A (ja) | 2017-02-06 | 2020-05-21 | ケース ウエスタン リザーブ ユニバーシティ | 短鎖デヒドロゲナーゼ活性を調節する組成物と方法 |
| US11419875B2 (en) * | 2017-03-31 | 2022-08-23 | Aurigene Discovery Technologies Limited | Compounds and compositions for treating hematological disorders |
| CN107954977A (zh) * | 2017-12-15 | 2018-04-24 | 上海鼎雅药物化学科技有限公司 | 雷替曲塞中间体的合成方法 |
| US10968200B2 (en) | 2018-08-31 | 2021-04-06 | Incyte Corporation | Salts of an LSD1 inhibitor and processes for preparing the same |
| EA202191422A1 (ru) | 2018-11-21 | 2021-10-21 | Кейс Вестерн Ризерв Юниверсити | Композиции и способы модулирования активности короткоцепочечной дегидрогеназы |
| CN115485279A (zh) * | 2020-04-29 | 2022-12-16 | 豪夫迈·罗氏有限公司 | 抗菌8-苯基氨基-3-(吡唑-4-基)咪唑并[1,2-a]吡嗪衍生物 |
| EP4178571A4 (fr) * | 2020-07-10 | 2024-07-17 | The Regents Of The University Of Michigan | Inhibiteurs de gas41 et leurs méthodes d'utilisation |
| KR20240004476A (ko) | 2021-04-08 | 2024-01-11 | 쿠리스 인코퍼레이션 | 암 치료를 위한 병용 요법 |
| WO2022222995A1 (fr) * | 2021-04-23 | 2022-10-27 | 南京明德新药研发有限公司 | Composé picolinamide |
| CN116715668A (zh) * | 2022-03-07 | 2023-09-08 | 上海凌达生物医药有限公司 | 一类含氮杂环类细胞周期抑制剂化合物、制备方法和用途 |
| WO2024088192A1 (fr) * | 2022-10-26 | 2024-05-02 | Js Innopharm (Suzhou) Ltd. | Inhibiteur d'aurora a destiné à être utilisé dans des traitements anticancéreux |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7576085B2 (en) * | 2002-09-23 | 2009-08-18 | Schering Corporation | Imidazopyrazines as cyclin dependent kinase inhibitors |
| ATE377600T1 (de) * | 2002-09-23 | 2007-11-15 | Schering Corp | Imidazopyrazine als cdk-inhibitoren |
| WO2006053121A2 (fr) * | 2004-11-10 | 2006-05-18 | Cgi Pharmaceuticals, Inc. | Certaines imidazo[1,2-a] pyrazin-8-ylamines et les procédés de fabrication et d'utilisation correspondants |
| AR056785A1 (es) * | 2005-11-10 | 2007-10-24 | Schering Corp | COMPUESTOS DE IMIDAZO[1,2-A]PIRAZINAS, uTILES COMO INHIBIDORES, REGULADORES O MODULADORES DE PROTEINQUINASAS |
-
2008
- 2008-06-11 PE PE2008001001A patent/PE20090365A1/es not_active Application Discontinuation
- 2008-06-11 EP EP08768351A patent/EP2170892A2/fr not_active Withdrawn
- 2008-06-11 WO PCT/US2008/007295 patent/WO2008156614A2/fr not_active Ceased
- 2008-06-11 CN CN200880101960A patent/CN101772500A/zh active Pending
- 2008-06-11 AR ARP080102481A patent/AR066958A1/es not_active Application Discontinuation
- 2008-06-11 JP JP2010512177A patent/JP2010529195A/ja not_active Withdrawn
- 2008-06-11 MX MX2009013729A patent/MX2009013729A/es not_active Application Discontinuation
- 2008-06-11 CA CA2690557A patent/CA2690557A1/fr not_active Abandoned
- 2008-06-12 TW TW097121942A patent/TW200911811A/zh unknown
- 2008-06-12 CL CL2008001745A patent/CL2008001745A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2010529195A (ja) | 2010-08-26 |
| MX2009013729A (es) | 2010-01-25 |
| CL2008001745A1 (es) | 2008-12-05 |
| CN101772500A (zh) | 2010-07-07 |
| CA2690557A1 (fr) | 2008-12-24 |
| WO2008156614A3 (fr) | 2009-02-12 |
| WO2008156614A2 (fr) | 2008-12-24 |
| PE20090365A1 (es) | 2009-04-04 |
| AR066958A1 (es) | 2009-09-23 |
| EP2170892A2 (fr) | 2010-04-07 |
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