MA30428B1 - Derives de dihydropyrazolopyrimidinones - Google Patents
Derives de dihydropyrazolopyrimidinonesInfo
- Publication number
- MA30428B1 MA30428B1 MA31411A MA31411A MA30428B1 MA 30428 B1 MA30428 B1 MA 30428B1 MA 31411 A MA31411 A MA 31411A MA 31411 A MA31411 A MA 31411A MA 30428 B1 MA30428 B1 MA 30428B1
- Authority
- MA
- Morocco
- Prior art keywords
- group
- formula
- compounds represented
- alkyl group
- dihydropyrazolopyrimidinones
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/4162—1,2-Diazoles condensed with heterocyclic ring 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
L'INVENTION A TRAIT À DES COMPOSÉS REPRÉSENTÉS PAR LA FORMULE (I), DANS LAQUELLE : A1 EST SÉLECTIONNÉ PARMI LES COMPOSÉS REPRÉSENTÉS PAR LA FORMULE (AA1); R1 REPRÉSENTE UN GROUPE ALCÉNYLE INFÉRIEUR OU UN GROUPE ALCYNYLE INFÉRIEUR; R2 REPRÉSENTE UN GROUPE PHÉNYLE, PYRIDYLE OU THIÉNYLE; R5 ET R6 REPRÉSENTENT UN ATOME D'HYDROGÈNE, UN GROUPE ALKYLE INFÉRIEUR OU UN GROUPE HYDROXY ALKYLE INFÉRIEUR, ETC. LES COMPOSÉS SELON L'INVENTION PRÉSENTENT UN EFFET INHIBITEUR DE LA KINASE WEE1 ET SONT DONC UTILES DANS LE DOMAINE MÉDICAL, NOTAMMENT POUR LE TRAITEMENT DE DIVERS CANCERS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2006124208 | 2006-04-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA30428B1 true MA30428B1 (fr) | 2009-05-04 |
Family
ID=38655640
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA31411A MA30428B1 (fr) | 2006-04-27 | 2008-11-24 | Derives de dihydropyrazolopyrimidinones |
Country Status (38)
| Country | Link |
|---|---|
| US (4) | US7834019B2 (fr) |
| EP (2) | EP2016080B1 (fr) |
| JP (2) | JP4513919B2 (fr) |
| KR (1) | KR101409161B1 (fr) |
| CN (1) | CN101432284B (fr) |
| AR (1) | AR060635A1 (fr) |
| AT (1) | ATE475662T1 (fr) |
| AU (1) | AU2007244185B2 (fr) |
| BR (1) | BRPI0710081A2 (fr) |
| CA (1) | CA2650119C (fr) |
| CR (1) | CR10359A (fr) |
| CY (2) | CY1111069T1 (fr) |
| DE (1) | DE602007008085D1 (fr) |
| DK (2) | DK2017278T3 (fr) |
| DO (1) | DOP2007000084A (fr) |
| EC (1) | ECSP088812A (fr) |
| ES (2) | ES2348751T3 (fr) |
| GT (1) | GT200800211A (fr) |
| HN (1) | HN2008001532A (fr) |
| HR (2) | HRP20161763T1 (fr) |
| HU (1) | HUE032987T2 (fr) |
| IL (1) | IL194367A (fr) |
| LT (1) | LT2017278T (fr) |
| MA (1) | MA30428B1 (fr) |
| MX (1) | MX2008013063A (fr) |
| MY (1) | MY145408A (fr) |
| NO (1) | NO341617B1 (fr) |
| NZ (1) | NZ571196A (fr) |
| PE (1) | PE20080695A1 (fr) |
| PL (2) | PL2016080T3 (fr) |
| PT (2) | PT2016080E (fr) |
| RU (1) | RU2437885C2 (fr) |
| SI (2) | SI2016080T1 (fr) |
| SV (1) | SV2009003060A (fr) |
| TW (1) | TWI409262B (fr) |
| UA (1) | UA96152C2 (fr) |
| WO (2) | WO2007126128A1 (fr) |
| ZA (1) | ZA200807748B (fr) |
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| AR060635A1 (es) | 2006-04-27 | 2008-07-02 | Banyu Pharma Co Ltd | Derivados de 1,2-dihidro-3h-pirazolo[3,4-d]pirimidin-3-ona, composiciones farmaceuticas que los comprenden y su uso en el tratamiento del cancer |
| JP5411847B2 (ja) * | 2007-04-25 | 2014-02-12 | Msd株式会社 | Weelキナーゼインヒビターとしてのジヒドロピラゾロピリミジノン誘導体の多形 |
| WO2008141385A1 (fr) * | 2007-05-21 | 2008-11-27 | Biota Scientific Management Pty Ltd | Inhibiteurs de polymérases virales |
| EP2213673B1 (fr) * | 2007-10-23 | 2013-06-05 | Msd K.K. | Dérivé de dihydropyrazolopyrimidinone substitué par pyridone |
| WO2009151997A1 (fr) * | 2008-06-12 | 2009-12-17 | Merck & Co., Inc. | Procédé de production de dérivés de bicycloaniline |
| WO2010067888A1 (fr) | 2008-12-12 | 2010-06-17 | Banyu Pharmaceutical Co.,Ltd. | Dérivés de dihydropyrimidopirymidine |
| WO2010076887A1 (fr) * | 2009-01-05 | 2010-07-08 | Banyu Pharmaceutical Co.,Ltd. | Biomarqueurs prédictifs utiles pour une thérapie anticancéreuse à médiation par un inhibiteur de wee1 |
| WO2010098367A1 (fr) * | 2009-02-25 | 2010-09-02 | Banyu Pharmaceutical Co.,Ltd. | Dérivé de pyrimido-pyrimido-indazole |
| WO2011027800A1 (fr) * | 2009-09-02 | 2011-03-10 | Banyu Pharmaceutical Co.,Ltd. | Utilisation de biomarqueur(s) pour identifier un patient répondant à l'inhibiteur de wee1 et méthodes de traitement du cancer à médiation par p53 dysfonctionnel ou adhérent par l'administration d'un inhibiteur de wee1 |
| US8703779B2 (en) | 2009-09-15 | 2014-04-22 | Merck Sharp & Dohme Corp. | Preparation of crystalline forms of dihydropyrazolopyrimidinone |
| CA2817968C (fr) | 2010-11-16 | 2019-03-12 | Array Biopharma Inc. | Combinaison d'inhibiteurs de la checkpoint kinase 1 et d'inhibiteurs de la wee 1 kinase |
| EP3266764B1 (fr) * | 2011-04-27 | 2019-01-09 | Zeon Corporation | Composé polymérisable, composition polymérisable, polymère et matériau optiquement anisotrope |
| US8796289B2 (en) | 2011-07-19 | 2014-08-05 | Abbvie Inc. | Pyridazino[4,5-D]pyrimidin-5(6H)-one inhibitors of kinases |
| US9345705B2 (en) | 2011-09-15 | 2016-05-24 | Merck Sharp & Dohme Corp. | Compositions and methods for treating cancer |
| WO2013059485A1 (fr) * | 2011-10-20 | 2013-04-25 | Abbvie Inc. | Composés de pyridopyrimidinone inhibiteurs de kinases |
| US9718821B2 (en) * | 2012-02-23 | 2017-08-01 | Abbvie Inc. | Pyridopyrimidinone inhibitors of kinases |
| WO2014062454A1 (fr) * | 2012-10-15 | 2014-04-24 | Merck Sharp & Dohme Corp. | Compositions et procédés de traitement du cancer |
| AU2013352568B2 (en) | 2012-11-28 | 2019-09-19 | Merck Sharp & Dohme Llc | Compositions and methods for treating cancer |
| WO2014168941A1 (fr) | 2013-04-09 | 2014-10-16 | Lixte Biotechnology, Inc. | Formulations d'oxabicycloheptanes et d'oxabicycloheptènes |
| GB201306610D0 (en) * | 2013-04-11 | 2013-05-29 | Almac Discovery Ltd | Pharmaceutical compounds |
| GB201322602D0 (en) | 2013-12-19 | 2014-02-05 | Almac Discovery Ltd | Pharmaceutical compounds |
| EP3235505B1 (fr) * | 2014-12-17 | 2020-05-06 | Delta-Fly Pharma, Inc. | Composition pharmaceutique pour le traitement ou la palliation d'un patient âgé atteint d'un cancer ou d'un patient atteint d'un cancer en phase terminale |
| AR104291A1 (es) | 2015-04-17 | 2017-07-12 | Abbvie Inc | Moduladores tricíclicos de la señalización por tnf |
| UY36628A (es) | 2015-04-17 | 2016-11-30 | Abbvie Inc | Indazolonas como moduladores de la señalización de tnf |
| EP3294726A1 (fr) | 2015-04-17 | 2018-03-21 | AbbVie Inc. | Indazolones utilisées en tant que modulateurs de la signalisation du tnf |
| DK3345907T3 (da) * | 2015-09-01 | 2020-06-22 | Taiho Pharmaceutical Co Ltd | Pyrazolo[3,4-d]pyrimidinforbindelser eller salte deraf |
| CN105130986B (zh) * | 2015-09-30 | 2017-07-18 | 广州科擎新药开发有限公司 | 嘧啶或吡啶并吡啶酮类化合物及其应用 |
| AU2016344040B2 (en) * | 2015-11-01 | 2020-12-10 | The Regents Of The University Of Colorado, A Body Corporate | Wee 1 kinase inhibitors and methods of making and using the same |
| GB201612092D0 (en) | 2016-07-12 | 2016-08-24 | Almac Discovery Ltd | Pharmaceutical compounds |
| CN110023290B (zh) | 2016-09-15 | 2022-08-12 | 勃林格殷格翰国际有限公司 | 作为ripk2抑制剂的杂芳基甲酰胺化合物 |
| CN106719769A (zh) * | 2016-11-28 | 2017-05-31 | 山东农业大学 | 一种含香菇多糖、苯醚甲环唑和噻虫啉的病虫兼治农药组合物 |
| MX2019006694A (es) | 2016-12-08 | 2019-08-21 | Lixte Biotechnology Inc | Oxabicicloheptanos para la modulacion de la respuesta inmunitaria. |
| WO2018133829A1 (fr) | 2017-01-23 | 2018-07-26 | 南京明德新药研发股份有限公司 | Dérivé de 1,2-dihydro-3h-pyrazolo[3,4-d]pyrimidin-3-one utilisé en tant qu'inhibiteur de wee1 |
| GB201703881D0 (en) * | 2017-03-10 | 2017-04-26 | Almac Discovery Ltd | Pharmaceutical compounds |
| CN108623615B (zh) * | 2017-03-23 | 2022-12-13 | 上海迪诺医药科技有限公司 | 吡唑[3,4-d]嘧啶-3-酮的大环衍生物、其药物组合物及应用 |
| KR20190130621A (ko) | 2017-03-31 | 2019-11-22 | 시애틀 지네틱스, 인크. | Chk1 저해제와 wee1 저해제의 조합물 |
| KR20200034781A (ko) | 2017-08-01 | 2020-03-31 | 리커리엄 아이피 홀딩스, 엘엘씨 | 1,2-다이하이드로-3H-피라졸로[3,4-d]피리미딘-3-온 유사체 |
| CN109422754A (zh) * | 2017-08-24 | 2019-03-05 | 上海迪诺医药科技有限公司 | 吡唑并[3,4-d]嘧啶-3-酮衍生物、其药物组合物及应用 |
| WO2019074981A1 (fr) | 2017-10-09 | 2019-04-18 | GiraFpharma LLC | Composés hétérocycliques et leurs utilisations |
| EP3694861A4 (fr) * | 2017-10-09 | 2021-05-19 | Nuvation Bio Inc. | Composés hétérocycliques et leurs utilisations |
| PT3712150T (pt) * | 2017-11-01 | 2024-08-22 | Wuxi Biocity Biopharmaceutics Co Ltd | Composto macrocíclico que serve como inibidor wee1 e aplicações do mesmo |
| WO2019096322A1 (fr) * | 2017-11-20 | 2019-05-23 | 上海医药集团股份有限公司 | Composé de pyrazolone-pyrimidine, son procédé de préparation et son application |
| CN111315747B (zh) * | 2018-01-05 | 2023-05-02 | 四川科伦博泰生物医药股份有限公司 | 二氢吡唑酮并嘧啶类化合物及其制备方法和用途 |
| US11479555B2 (en) | 2018-02-23 | 2022-10-25 | Newave Pharmaceutical Inc. | Substituted 1,2-dihydro-3H-pyrazolo[3,4-D]pyrimidin-3-ones as inhibitors of WEE-1 kinase |
| AU2019227823B2 (en) * | 2018-02-28 | 2024-12-12 | The Regents Of The University Of Colorado, A Body Corporate | WEE1 kinase inhibitors and methods of treating cancer using the same |
| EP3762385B1 (fr) * | 2018-03-09 | 2025-02-12 | Recurium IP Holdings, LLC | 1,2-dihydro-3h-pyrazolo[3,4-d]pyrimidin-3-ones substituées |
| CN108653282B (zh) * | 2018-06-28 | 2020-08-14 | 中国科学院昆明植物研究所 | 苯并噻唑类及苯并吡咯类化合物在制备抗肿瘤药物中的应用 |
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| CN111662283B (zh) * | 2019-03-07 | 2021-11-16 | 湖南化工研究院有限公司 | 咪唑并吡啶类化合物及其中间体、制备方法与应用 |
| JP2022528047A (ja) * | 2019-03-22 | 2022-06-08 | ショウヤオ ホールディングス(ベイジン) カンパニー, リミテッド | Wee1阻害剤、その製造および用途 |
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| WO2020210320A1 (fr) * | 2019-04-11 | 2020-10-15 | Recurium Ip Holdings, Llc | L,2-dihydro-3h-pyrazolo[3,4-d]pyrimidin-3-ones substituées |
| CN113784968B (zh) | 2019-04-30 | 2024-03-15 | 无锡智康弘义生物科技有限公司 | Wee1抑制剂化合物的晶型及其应用 |
| CN112142748B (zh) | 2019-06-28 | 2023-07-04 | 上海医药集团股份有限公司 | 一种吡唑酮并嘧啶类化合物、其制备方法及应用 |
| MX2021015572A (es) | 2019-06-28 | 2022-04-06 | Shanghai Pharmaceuticals Holding Co Ltd | Compuesto de pirazolopirimidina, método de preparación para el mismo y sus aplicaciones. |
| CN114599399A (zh) | 2019-10-25 | 2022-06-07 | 阿斯利康(瑞典)有限公司 | 治疗癌症的方法 |
| AU2020407573A1 (en) * | 2019-12-20 | 2022-07-14 | Recurium Ip Holdings, Llc | Combinations |
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| EP4169919A4 (fr) * | 2020-06-17 | 2024-07-17 | Wigen Biomedicine Technology (Shanghai) Co., Ltd. | Dérivé de pyrazolo[3,4-d]pyrimidine-3-cétone utilisé en tant qu'inhibiteur de wee-1 |
| KR102549484B1 (ko) * | 2020-12-08 | 2023-06-29 | 한국화학연구원 | 피라졸로피리미딘 설폰아마이드 유도체 및 이를 유효성분으로 포함하는 암 관련 질환의 예방 또는 치료용 약학적 조성물 |
| WO2022171128A1 (fr) * | 2021-02-09 | 2022-08-18 | 微境生物医药科技(上海)有限公司 | Dérivé de pyrazolo[3,4-d]pyrimidine-3-cétone servant d'inhibiteur de wee-1 |
| CN116867787A (zh) * | 2021-02-09 | 2023-10-10 | 微境生物医药科技(上海)有限公司 | 吡唑并[3,4-d]嘧啶-3-酮衍生物 |
| WO2022171126A1 (fr) * | 2021-02-09 | 2022-08-18 | 微境生物医药科技(上海)有限公司 | Composé cyclique fusionné utilisé comme inhibiteur de wee-1 |
| CN115197221B (zh) * | 2021-04-02 | 2024-05-24 | 轩竹(北京)医药科技有限公司 | 二氢吡唑并嘧啶酮类大环衍生物及其用途 |
| US20240252655A1 (en) | 2021-04-29 | 2024-08-01 | Novartis Ag | Deubiquitinase-targeting chimeras and related methods |
| BR112023022236A2 (pt) | 2021-04-30 | 2024-02-06 | Wigen Biomedicine Tech Shanghai Co Ltd | Composto de fórmula geral (1) ou seu isômero, forma cristalina, sal farmaceuticamente aceitável, hidrato ou solvato; composição farmacêutica; e; uso do composto ou seu isômero, forma cristalina, sal farmaceuticamente aceitável, hidrato ou solvato |
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| CN115073460B (zh) * | 2022-07-13 | 2023-07-25 | 苏州施安鼎泰生物医药技术有限公司 | 一种嘧啶并[5,4-c][2,6]萘啶衍生物及其制备方法以及药物组合物和应用 |
| CN117402162A (zh) | 2022-07-13 | 2024-01-16 | 江苏天士力帝益药业有限公司 | Wee1抑制剂及其制备和用途 |
| WO2024012549A1 (fr) * | 2022-07-15 | 2024-01-18 | 映恩生物制药(苏州)有限公司 | Composé hétérocyclique à cinq chaînons pyrimido, son procédé de préparation et son utilisation |
| CN119798282A (zh) * | 2023-10-11 | 2025-04-11 | 智擎生技制药股份有限公司 | 基于稠合吡啶环的Myt1抑制剂 |
| TW202519226A (zh) | 2023-11-08 | 2025-05-16 | 美商艾克塞里克斯公司 | 使用抑制pkmyt1之化合物治療癌症之方法 |
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