HRP20100563T1 - Derivati dihidropirazolopirimidinona - Google Patents
Derivati dihidropirazolopirimidinona Download PDFInfo
- Publication number
- HRP20100563T1 HRP20100563T1 HR20100563T HRP20100563T HRP20100563T1 HR P20100563 T1 HRP20100563 T1 HR P20100563T1 HR 20100563 T HR20100563 T HR 20100563T HR P20100563 T HRP20100563 T HR P20100563T HR P20100563 T1 HRP20100563 T1 HR P20100563T1
- Authority
- HR
- Croatia
- Prior art keywords
- group
- phenyl
- dihydro
- amino
- salt
- 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)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Oncology (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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2006124208 | 2006-04-27 | ||
| PCT/JP2007/059408 WO2007126122A1 (en) | 2006-04-27 | 2007-04-25 | Dihydropyrazolopyrimidinone derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HRP20100563T1 true HRP20100563T1 (hr) | 2010-11-30 |
Family
ID=38655640
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HR20100563T HRP20100563T1 (hr) | 2006-04-27 | 2007-04-25 | Derivati dihidropirazolopirimidinona |
| HRP20161763TT HRP20161763T1 (hr) | 2006-04-27 | 2007-04-25 | Derivati dihidropirazolopirimidinona |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HRP20161763TT HRP20161763T1 (hr) | 2006-04-27 | 2007-04-25 | Derivati dihidropirazolopirimidinona |
Country Status (38)
| Country | Link |
|---|---|
| US (4) | US7834019B2 (lt) |
| EP (2) | EP2017278B1 (lt) |
| JP (2) | JP4513919B2 (lt) |
| KR (1) | KR101409161B1 (lt) |
| CN (1) | CN101432284B (lt) |
| AR (1) | AR060635A1 (lt) |
| AT (1) | ATE475662T1 (lt) |
| AU (1) | AU2007244185B2 (lt) |
| BR (1) | BRPI0710081A2 (lt) |
| CA (1) | CA2650119C (lt) |
| CR (1) | CR10359A (lt) |
| CY (2) | CY1111069T1 (lt) |
| DE (1) | DE602007008085D1 (lt) |
| DK (2) | DK2016080T3 (lt) |
| DO (1) | DOP2007000084A (lt) |
| EC (1) | ECSP088812A (lt) |
| ES (2) | ES2348751T3 (lt) |
| GT (1) | GT200800211A (lt) |
| HN (1) | HN2008001532A (lt) |
| HR (2) | HRP20100563T1 (lt) |
| HU (1) | HUE032987T2 (lt) |
| IL (1) | IL194367A (lt) |
| LT (1) | LT2017278T (lt) |
| MA (1) | MA30428B1 (lt) |
| MX (1) | MX2008013063A (lt) |
| MY (1) | MY145408A (lt) |
| NO (1) | NO341617B1 (lt) |
| NZ (1) | NZ571196A (lt) |
| PE (1) | PE20080695A1 (lt) |
| PL (2) | PL2016080T3 (lt) |
| PT (2) | PT2017278T (lt) |
| RU (1) | RU2437885C2 (lt) |
| SI (2) | SI2016080T1 (lt) |
| SV (1) | SV2009003060A (lt) |
| TW (1) | TWI409262B (lt) |
| UA (1) | UA96152C2 (lt) |
| WO (2) | WO2007126122A1 (lt) |
| ZA (1) | ZA200807748B (lt) |
Families Citing this family (81)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20080695A1 (es) | 2006-04-27 | 2008-06-28 | Banyu Pharma Co Ltd | Derivados de dihidropirazolopirimidinona como inhibidores de quinasa weel |
| 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 (en) * | 2007-05-21 | 2008-11-27 | Biota Scientific Management Pty Ltd | Viral polymerase inhibitors |
| WO2009054332A1 (ja) * | 2007-10-23 | 2009-04-30 | Banyu Pharmaceutical Co., Ltd. | ピリドン置換ジヒドロピラゾロピリミジノン誘導体 |
| WO2009151997A1 (en) * | 2008-06-12 | 2009-12-17 | Merck & Co., Inc. | Process for producing bicycloaniline derivatives |
| AU2009325400A1 (en) * | 2008-12-12 | 2010-06-17 | Msd K.K. | Dihydropyrimidopyrimidine derivatives |
| WO2010076887A1 (en) * | 2009-01-05 | 2010-07-08 | Banyu Pharmaceutical Co.,Ltd. | Predictive biomarkers useful for cancer therapy mediated by a wee1 inhibitor |
| AU2010218781A1 (en) * | 2009-02-25 | 2011-07-28 | Msd K.K. | Pyrimidopyrimidoindazole derivative |
| US20120157342A1 (en) * | 2009-09-02 | 2012-06-21 | Shinji Mizuarai | Predictive biomarkers useful for cancer therapy mediated by a wee1 inhibitor |
| EP2477628B1 (en) | 2009-09-15 | 2014-08-20 | Merck Sharp & Dohme Corp. | Preparation of crystalline hemihydrate forms of dihydropyrazolopyrimidinone |
| RU2017127088A (ru) | 2010-11-16 | 2019-02-04 | Эррэй Биофарма Инк. | Комбинация ингибиторов чекпойнт-киназы 1 и ингибиторов киназы wee 1 |
| CN103492363B (zh) * | 2011-04-27 | 2016-08-24 | 日本瑞翁株式会社 | 聚合性化合物、聚合性组合物、高分子以及光学各向异性体 |
| US8796289B2 (en) | 2011-07-19 | 2014-08-05 | Abbvie Inc. | Pyridazino[4,5-D]pyrimidin-5(6H)-one inhibitors of kinases |
| WO2013039854A1 (en) | 2011-09-15 | 2013-03-21 | Merck Sharp & Dohme Corp. | Compositions and methods for treating cancer |
| US9181239B2 (en) | 2011-10-20 | 2015-11-10 | Abbvie Inc. | Pyridopyrimidinone inhibitors of kinases |
| MX2014010176A (es) * | 2012-02-23 | 2014-11-10 | Abbvie Inc | Inhibidores de cinasas de piridopirimidinona. |
| WO2014062454A1 (en) * | 2012-10-15 | 2014-04-24 | Merck Sharp & Dohme Corp. | Compositions and methods for treating cancer |
| RS56680B1 (sr) | 2012-11-28 | 2018-03-30 | Merck Sharp & Dohme | Kompozicije i postupci za lečenje kancera |
| EP2983661B1 (en) | 2013-04-09 | 2024-05-29 | Lixte Biotechnology, Inc. | Formulations of oxabicycloheptanes and oxabicycloheptenes |
| 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 |
| KR102032933B1 (ko) * | 2014-12-17 | 2019-10-16 | 데루타-후라이 화마 가부시키가이샤 | 고령이나 말기의 암환자를 치료 또는 경감하기 위한 의약 조성물 |
| US20160304496A1 (en) | 2015-04-17 | 2016-10-20 | Abbvie Inc. | Indazolones as modulators of tnf signaling |
| AR104291A1 (es) | 2015-04-17 | 2017-07-12 | Abbvie Inc | Moduladores tricíclicos de la señalización por tnf |
| US9879016B2 (en) | 2015-04-17 | 2018-01-30 | Abbvie Inc. | Indazolones as modulators of TNF signaling |
| JP6141568B1 (ja) * | 2015-09-01 | 2017-06-07 | 大鵬薬品工業株式会社 | 新規なピラゾロ[3,4−d]ピリミジン化合物又はその塩 |
| 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 |
| JP6692423B2 (ja) * | 2015-11-01 | 2020-05-13 | ザ リージェンツ オブ ザ ユニヴァーシティ オブ コロラド,ア ボディ コーポレイト | Wee1キナーゼ阻害剤、並びにそれを作製及び使用する方法 |
| GB201612092D0 (en) | 2016-07-12 | 2016-08-24 | Almac Discovery Ltd | Pharmaceutical compounds |
| AU2017327539B2 (en) | 2016-09-15 | 2020-12-24 | Boehringer Ingelheim International Gmbh | Heteroaryl carboxamide compounds as inhibitors of RIPK2 |
| 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. |
| JP6717457B2 (ja) * | 2017-01-23 | 2020-07-01 | シージャーズォアン サガシティ ニュー ドラッグ デベロップメント カンパニー リミテッド | Wee1阻害剤としての1,2−ジヒドロ−3H−ピラゾロ[3,4−d]ピリミジン−3−オン誘導体 |
| GB201703881D0 (en) * | 2017-03-10 | 2017-04-26 | Almac Discovery Ltd | Pharmaceutical compounds |
| US11248006B2 (en) | 2017-03-23 | 2022-02-15 | Shanghai De Novo Pharmatech Co., Ltd. | Macrocyclic derivative of pyrazol[3,4-d]pyrimidin-3-one, pharmaceutical composition and use thereof |
| CN110678169A (zh) | 2017-03-31 | 2020-01-10 | 西雅图遗传学公司 | Chk1-抑制剂与weel-抑制剂的组合 |
| MX2020001235A (es) | 2017-08-01 | 2020-07-20 | Recurium Ip Holdings Llc | Análogos de 1,2-dihidro-3h-pirazolo[3,4-d]pirimidin-3-ona. |
| 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 |
| EP3694861A4 (en) * | 2017-10-09 | 2021-05-19 | Nuvation Bio Inc. | HETEROCYCLIC COMPOUNDS AND USES THEREOF |
| AU2018347307A1 (en) | 2017-10-09 | 2020-04-23 | Nuvation Bio Inc. | Heterocyclic compounds and uses thereof |
| SG11202003974XA (en) | 2017-11-01 | 2020-05-28 | Shijiazhuang Sagacity New Drug Development Co Ltd | Macrocyclic compound serving as weel inhibitor and applications thereof |
| CN109810111B (zh) * | 2017-11-20 | 2023-10-27 | 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 |
| WO2019134539A1 (zh) * | 2018-01-05 | 2019-07-11 | 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 |
| WO2019165204A1 (en) * | 2018-02-23 | 2019-08-29 | Newave Pharmaceutical Inc. | 1,2-dihydro-3h-pyrazolo[3,4-d]pyrimidine-3-one compounds as inhibitors of wee-1 kinase |
| US12220415B2 (en) | 2018-02-28 | 2025-02-11 | The Regents Of The University Of Colorado, A Body Corporate | WEE1 kinase inhibitors and methods of treating cancer using the same |
| EP4566612A3 (en) | 2018-03-09 | 2025-08-20 | Recurium IP Holdings, LLC | Substituted 1,2-dihydro-3h-pyrazolo[3,4-d]pyrimidin-3-ones |
| 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 |
| US12180184B2 (en) | 2018-10-26 | 2024-12-31 | Wuxi Biocity Biopharmaceutics Co., Ltd. | Pyrimidopyrazolone derivative as Wee1 inhibitor and use thereof |
| CN113480541B (zh) * | 2019-03-07 | 2022-09-02 | 湖南化工研究院有限公司 | 咪唑并吡啶化合物及其中间体的制备方法 |
| KR102697799B1 (ko) * | 2019-03-22 | 2024-08-23 | 쇼우야오 홀딩스 (베이징) 코., 엘티디. | Wee1 억제제 및 이의 제조 및 용도 |
| US20220220115A1 (en) * | 2019-04-09 | 2022-07-14 | Nuvation Bio Inc. | Heterocyclic compounds and uses thereof |
| JP2022526831A (ja) | 2019-04-09 | 2022-05-26 | ニューベイション・バイオ・インコーポレイテッド | ヘテロ環式化合物およびその使用 |
| WO2020210320A1 (en) * | 2019-04-11 | 2020-10-15 | Recurium Ip Holdings, Llc | Substituted l,2-dihydro-3h-pyrazolo[3,4-d]pyrimidin-3-ones |
| SI3964510T1 (sl) | 2019-04-30 | 2024-10-30 | Wuxi Biocity Biopharmaceutics Co., Ltd. | Kristalna oblika WEE1 inhibitorske spojine in njena uporaba |
| 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 |
| BR112021026618A2 (pt) | 2019-06-28 | 2022-06-07 | Shanghai Pharmaceuticals Holding Co Ltd | Composto de pirazolpirimidina, método de preparação do mesmo e aplicações do mesmo |
| EP4048277A1 (en) | 2019-10-25 | 2022-08-31 | Astrazeneca AB | Methods of treating cancer |
| JP2023507797A (ja) * | 2019-12-20 | 2023-02-27 | リキュリウム アイピー ホールディングス リミテッド ライアビリティー カンパニー | 組み合わせ |
| CN113387962A (zh) * | 2020-03-12 | 2021-09-14 | 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 |
| CA3180664A1 (en) | 2020-06-17 | 2021-12-23 | Yuli Xie | Pyrazolo[3,4-d]pyrimidine-3-one derivative as wee-1 inhibitor |
| US12551584B1 (en) | 2020-12-07 | 2026-02-17 | Actinium Pharmaceuticals, Inc. | Lewis Y radioimmunotherapy for the treatment of cancer |
| KR102549484B1 (ko) * | 2020-12-08 | 2023-06-29 | 한국화학연구원 | 피라졸로피리미딘 설폰아마이드 유도체 및 이를 유효성분으로 포함하는 암 관련 질환의 예방 또는 치료용 약학적 조성물 |
| WO2022171088A1 (zh) * | 2021-02-09 | 2022-08-18 | 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 (zh) * | 2021-02-09 | 2022-08-18 | 微境生物医药科技(上海)有限公司 | 作为Wee-1抑制剂的稠环化合物 |
| CN116848118A (zh) * | 2021-02-09 | 2023-10-03 | 微境生物医药科技(上海)有限公司 | 作为Wee-1抑制剂的吡唑并[3,4-d]嘧啶-3-酮衍生物 |
| 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 |
| KR20240004584A (ko) | 2021-04-29 | 2024-01-11 | 노파르티스 아게 | 탈유비퀴티나아제-표적화 키메라 및 관련된 방법 |
| KR20240004539A (ko) | 2021-04-30 | 2024-01-11 | 위겐 바이오메더슨 테크널러지 (상하이) 컴퍼니 리미티드 | Wee-1 억제제로서의 축합 고리 화합물, 그를 위한 제조 방법 및 그의 용도 |
| EP4349838A4 (en) | 2021-05-28 | 2025-08-13 | Jiangsu Tasly Diyi Pharmaceutical Co Ltd | WEE1 INHIBITOR AND ITS USE |
| CN117794932A (zh) * | 2021-06-04 | 2024-03-29 | 阿普里治疗股份有限公司 | 可用作wee1激酶抑制剂的吡啶并嘧啶衍生物 |
| TW202328142A (zh) * | 2021-09-18 | 2023-07-16 | 香港商優領醫藥科技(香港)有限公司 | 含嘧啶并二氫吡唑啉酮類衍生物、其藥學上可接受的鹽及其製備方法和應用 |
| CN113880844B (zh) * | 2021-09-29 | 2023-02-14 | 武汉九州钰民医药科技有限公司 | Wee1蛋白激酶抑制剂adavosertib的化学合成方法 |
| CN113735863A (zh) * | 2021-09-29 | 2021-12-03 | 武汉九州钰民医药科技有限公司 | Wee1抑制剂adavosertib的制备工艺 |
| WO2023072301A1 (zh) * | 2021-11-01 | 2023-05-04 | 正大天晴药业集团股份有限公司 | 吡唑[3,4-d]嘧啶-3-酮类化合物及其医药用途 |
| CN116462687B (zh) | 2022-01-18 | 2025-01-07 | 江苏天士力帝益药业有限公司 | Wee1抑制剂及其制备和用途 |
| CN116836184B (zh) * | 2022-03-25 | 2025-07-25 | 药雅科技(上海)有限公司 | Wee1激酶抑制剂的制备及其应用 |
| 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 (zh) * | 2022-07-15 | 2024-01-18 | 映恩生物制药(苏州)有限公司 | 一种嘧啶并五元杂环化合物、其制备方法和用途 |
| 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 |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| OA07174A (fr) | 1981-08-24 | 1984-04-30 | May & Baker Ltd | Nouvelles imidazotétrazionones, leur préparation et les médicaments qui les contiennent. |
| JPS6019790A (ja) | 1983-07-14 | 1985-01-31 | Yakult Honsha Co Ltd | 新規なカンプトテシン誘導体 |
| IL85035A0 (en) | 1987-01-08 | 1988-06-30 | Int Genetic Eng | Polynucleotide molecule,a chimeric antibody with specificity for human b cell surface antigen,a process for the preparation and methods utilizing the same |
| JP2628707B2 (ja) * | 1987-08-26 | 1997-07-09 | 三井製薬工業株式会社 | ピリミジン類及びその薬学的に許容される塩類 |
| US5223608A (en) | 1987-08-28 | 1993-06-29 | Eli Lilly And Company | Process for and intermediates of 2',2'-difluoronucleosides |
| FI931384A7 (fi) | 1990-09-28 | 1993-03-26 | Smithkline Beecham Corp | Vesiliukoisia kamptotekiinianalogeja, prosesseja ja menetelmiä |
| US5247089A (en) | 1990-12-20 | 1993-09-21 | North Carolina State University | Method of making intermediates useful for the manufacture of camptothecin and camptothecin analogs |
| US5243050A (en) | 1990-12-20 | 1993-09-07 | North Carolina State University | Alkylpyridone DE ring intermediates useful for the manufacture of camptothecin and camptothecin analogs |
| US5191082A (en) | 1990-12-20 | 1993-03-02 | North Carolina State University | Camptothecin intermediate and method of making camptothecin intermediates |
| US5200524A (en) | 1990-12-20 | 1993-04-06 | North Carolina State University | Camptothecin intermediates and method of making same |
| US5162532A (en) | 1990-12-20 | 1992-11-10 | North Carolina State University | Intermediates and method of making camptothecin and camptothecin analogs |
| AU687727B2 (en) | 1992-10-28 | 1998-03-05 | Genentech Inc. | Vascular endothelial cell growth factor antagonists |
| JP3025602B2 (ja) | 1993-05-21 | 2000-03-27 | デビオファーム エス.アー. | 光学的に高純度なシス−オキザラート(トランス−l−1,2−シクロヘキサンジアミン)白金(II)錯体の製造方法 |
| GB9508538D0 (en) | 1995-04-27 | 1995-06-14 | Zeneca Ltd | Quinazoline derivatives |
| JPH11507535A (ja) | 1995-06-07 | 1999-07-06 | イムクローン システムズ インコーポレイテッド | 腫瘍の成長を抑制する抗体および抗体フラグメント類 |
| JP3154399B2 (ja) | 1996-07-04 | 2001-04-09 | デビオファーム エス.アー. | 白金化合物の製造方法 |
| CZ27399A3 (cs) | 1999-01-26 | 2000-08-16 | Ústav Experimentální Botaniky Av Čr | Substituované dusíkaté heterocyklické deriváty, způsob jejich přípravy, tyto deriváty pro použití jako léčiva, farmaceutická kompozice a kombinovaný farmaceutický přípravek tyto deriváty obsahující a použití těchto derivátů pro výrobu léčiv |
| SE0103649D0 (sv) | 2001-11-01 | 2001-11-01 | Astrazeneca Ab | Therapeutic quinoline compounds |
| WO2003091255A1 (en) | 2002-04-26 | 2003-11-06 | Warner-Lambert Company Llc | Inhibitors of checkpoint kinases (wee1 and chk1) |
| UA80767C2 (en) | 2002-12-20 | 2007-10-25 | Pfizer Prod Inc | Pyrimidine derivatives for the treatment of abnormal cell growth |
| MXPA05007503A (es) * | 2003-01-17 | 2005-09-21 | Warner Lambert Co | Heterociclicos 2-aminopiridina sustituidos como inhibidores de proliferacion celular. |
| JP2006518381A (ja) * | 2003-02-07 | 2006-08-10 | バーテックス ファーマシューティカルズ インコーポレイテッド | プロテインキナーゼのインヒビターとして有用なヘテロアリール置換ピロール |
| US7320992B2 (en) | 2003-08-25 | 2008-01-22 | Amgen Inc. | Substituted 2,3-dihydro-1h-isoindol-1-one derivatives and methods of use |
| US20050250836A1 (en) * | 2004-05-03 | 2005-11-10 | Pfizer Inc | Inhibitors of checkpoint kinases (Wee1 and Chk1) |
| WO2006004040A1 (ja) | 2004-07-01 | 2006-01-12 | Daiichi Asubio Pharma Co., Ltd. | Pde7阻害作用を有するチエノピラゾール誘導体 |
| EP1846408B1 (en) | 2005-01-14 | 2013-03-20 | Janssen Pharmaceutica NV | 5-membered annelated heterocyclic pyrimidines as kinase inhibitors |
| WO2006091737A1 (en) * | 2005-02-24 | 2006-08-31 | Kemia, Inc. | Modulators of gsk-3 activity |
| PE20080695A1 (es) * | 2006-04-27 | 2008-06-28 | Banyu Pharma Co Ltd | Derivados de dihidropirazolopirimidinona como inhibidores de quinasa weel |
-
2007
- 2007-04-24 PE PE2007000511A patent/PE20080695A1/es active IP Right Grant
- 2007-04-24 AR ARP070101763A patent/AR060635A1/es active IP Right Grant
- 2007-04-25 PL PL07742843T patent/PL2016080T3/pl unknown
- 2007-04-25 DK DK07742843.1T patent/DK2016080T3/da active
- 2007-04-25 PT PT77428514T patent/PT2017278T/pt unknown
- 2007-04-25 LT LTEP07742851.4T patent/LT2017278T/lt unknown
- 2007-04-25 PL PL07742851T patent/PL2017278T3/pl unknown
- 2007-04-25 RU RU2008146759/04A patent/RU2437885C2/ru active
- 2007-04-25 BR BRPI0710081-7A patent/BRPI0710081A2/pt not_active Application Discontinuation
- 2007-04-25 KR KR1020087026239A patent/KR101409161B1/ko not_active Expired - Fee Related
- 2007-04-25 MX MX2008013063A patent/MX2008013063A/es active IP Right Grant
- 2007-04-25 EP EP07742851.4A patent/EP2017278B1/en active Active
- 2007-04-25 WO PCT/JP2007/059408 patent/WO2007126122A1/en not_active Ceased
- 2007-04-25 ES ES07742843T patent/ES2348751T3/es active Active
- 2007-04-25 US US11/789,548 patent/US7834019B2/en active Active
- 2007-04-25 EP EP07742843A patent/EP2016080B1/en active Active
- 2007-04-25 AU AU2007244185A patent/AU2007244185B2/en not_active Ceased
- 2007-04-25 SI SI200730373T patent/SI2016080T1/sl unknown
- 2007-04-25 PT PT07742843T patent/PT2016080E/pt unknown
- 2007-04-25 DE DE602007008085T patent/DE602007008085D1/de active Active
- 2007-04-25 HR HR20100563T patent/HRP20100563T1/hr unknown
- 2007-04-25 DK DK07742851.4T patent/DK2017278T3/en active
- 2007-04-25 WO PCT/JP2007/059416 patent/WO2007126128A1/ja not_active Ceased
- 2007-04-25 ES ES07742851.4T patent/ES2609087T3/es active Active
- 2007-04-25 UA UAA200813667A patent/UA96152C2/ru unknown
- 2007-04-25 HU HUE07742851A patent/HUE032987T2/en unknown
- 2007-04-25 CA CA2650119A patent/CA2650119C/en active Active
- 2007-04-25 NZ NZ571196A patent/NZ571196A/en not_active IP Right Cessation
- 2007-04-25 JP JP2008513330A patent/JP4513919B2/ja not_active Expired - Fee Related
- 2007-04-25 US US12/226,707 patent/US7935708B2/en active Active
- 2007-04-25 CN CN2007800150647A patent/CN101432284B/zh not_active Expired - Fee Related
- 2007-04-25 SI SI200731875A patent/SI2017278T1/sl unknown
- 2007-04-25 AT AT07742843T patent/ATE475662T1/de active
- 2007-04-25 HR HRP20161763TT patent/HRP20161763T1/hr unknown
- 2007-04-27 TW TW096114902A patent/TWI409262B/zh not_active IP Right Cessation
- 2007-04-27 DO DO2007000084A patent/DOP2007000084A/es unknown
-
2008
- 2008-09-09 ZA ZA200807748A patent/ZA200807748B/xx unknown
- 2008-09-18 MY MYPI20083651A patent/MY145408A/en unknown
- 2008-09-25 IL IL194367A patent/IL194367A/en active IP Right Grant
- 2008-10-09 EC EC2008008812A patent/ECSP088812A/es unknown
- 2008-10-10 GT GT200800211A patent/GT200800211A/es unknown
- 2008-10-10 CR CR10359A patent/CR10359A/es unknown
- 2008-10-10 HN HN2008001532A patent/HN2008001532A/es unknown
- 2008-10-10 SV SV2008003060A patent/SV2009003060A/es unknown
- 2008-11-24 MA MA31411A patent/MA30428B1/fr unknown
- 2008-11-26 NO NO20084968A patent/NO341617B1/no unknown
-
2010
- 2010-02-08 JP JP2010025458A patent/JP5167291B2/ja not_active Expired - Fee Related
- 2010-10-27 CY CY20101100973T patent/CY1111069T1/el unknown
-
2011
- 2011-03-22 US US13/053,798 patent/US8791125B2/en active Active
-
2014
- 2014-06-24 US US14/312,982 patent/US20140303178A1/en not_active Abandoned
-
2017
- 2017-01-27 CY CY20171100129T patent/CY1118526T1/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| HRP20100563T1 (hr) | Derivati dihidropirazolopirimidinona | |
| HRP20161536T1 (hr) | Derivat bicikloanilina | |
| EP2213673B1 (en) | Pyridone-substituted-dihydropyrazolopyrimidinone derivative | |
| ES2580779T3 (es) | Pirimidinas fusionadas | |
| AU2009279944B2 (en) | Dihydropyridophthalazinone inhibitors of poly(ADP-ribose)polymerase (PARP) | |
| EP2376493B1 (en) | Dihydropyrimidopyrimidine derivative | |
| EP2155752B1 (en) | Polymorph of dihydropyrazolopyrimidinone derivative as weel kinase.inhibitor | |
| IL292229A (en) | Pharmacological combination of prmt5 inhibitors | |
| ES2435804T3 (es) | Pirimidinas condensadas como inhibidores de Akt | |
| JP2012518598A5 (lt) | ||
| JP2010525057A5 (lt) | ||
| AU2008288392B2 (en) | Fused bicyclic pyrimidines | |
| RU2009111599A (ru) | Новые аминопиридиновые производные с селективной ингибирующей активностью в отношении авроры а | |
| CA2745959A1 (en) | Dihydropyrimidopyrimidine derivatives | |
| AU2023342153A1 (en) | Brm targeting compounds and associated methods of use | |
| RU2007119776A (ru) | Новые аминопиридиновые производные, обладающие селективной aurora a ингибирующей активностью | |
| EP2651949B1 (en) | Substituted pyrimido[1,2-b]indazoles and their use as modulators of the pi3k/akt pathway | |
| WO2025184459A1 (en) | Brm and brg1 targeting compounds and associated methods of use | |
| HK1166984B (en) | Fused pyrimidines as akt inhibitors |