JP2013530958A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2013530958A5 JP2013530958A5 JP2013513401A JP2013513401A JP2013530958A5 JP 2013530958 A5 JP2013530958 A5 JP 2013530958A5 JP 2013513401 A JP2013513401 A JP 2013513401A JP 2013513401 A JP2013513401 A JP 2013513401A JP 2013530958 A5 JP2013530958 A5 JP 2013530958A5
- Authority
- JP
- Japan
- Prior art keywords
- chlorophenyl
- pharmaceutically acceptable
- oxopiperidin
- methylbutan
- isopropylsulfonyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- DRLCSJFKKILATL-YWCVFVGNSA-N 2-[(3r,5r,6s)-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methyl-1-[(2s)-3-methyl-1-propan-2-ylsulfonylbutan-2-yl]-2-oxopiperidin-3-yl]acetic acid Chemical compound C1([C@@H]2[C@H](N(C([C@@](C)(CC(O)=O)C2)=O)[C@H](CS(=O)(=O)C(C)C)C(C)C)C=2C=CC(Cl)=CC=2)=CC=CC(Cl)=C1 DRLCSJFKKILATL-YWCVFVGNSA-N 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US35182710P | 2010-06-04 | 2010-06-04 | |
| US61/351,827 | 2010-06-04 | ||
| US35232210P | 2010-06-07 | 2010-06-07 | |
| US61/352,322 | 2010-06-07 | ||
| US201161452578P | 2011-03-14 | 2011-03-14 | |
| US61/452,578 | 2011-03-14 | ||
| PCT/US2011/039184 WO2011153509A1 (en) | 2010-06-04 | 2011-06-03 | Piperidinone derivatives as mdm2 inhibitors for the treatment of cancer |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013192621A Division JP5908446B2 (ja) | 2010-06-04 | 2013-09-18 | 癌の治療用ｍｄｍ２阻害剤としてのピペリジノン誘導体 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013530958A JP2013530958A (ja) | 2013-08-01 |
| JP2013530958A5 true JP2013530958A5 (enExample) | 2013-11-07 |
| JP5420797B2 JP5420797B2 (ja) | 2014-02-19 |
Family
ID=44504412
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013513401A Active JP5420797B2 (ja) | 2010-06-04 | 2011-06-03 | 癌の治療用ｍｄｍ２阻害剤としてのピペリジノン誘導体 |
| JP2013192621A Active JP5908446B2 (ja) | 2010-06-04 | 2013-09-18 | 癌の治療用ｍｄｍ２阻害剤としてのピペリジノン誘導体 |
| JP2016056518A Active JP6077695B2 (ja) | 2010-06-04 | 2016-03-22 | 癌の治療用ｍｄｍ２阻害剤としてのピペリジノン誘導体 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013192621A Active JP5908446B2 (ja) | 2010-06-04 | 2013-09-18 | 癌の治療用ｍｄｍ２阻害剤としてのピペリジノン誘導体 |
| JP2016056518A Active JP6077695B2 (ja) | 2010-06-04 | 2016-03-22 | 癌の治療用ｍｄｍ２阻害剤としてのピペリジノン誘導体 |
Country Status (41)
Families Citing this family (51)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0811643D0 (en) | 2008-06-25 | 2008-07-30 | Cancer Rec Tech Ltd | New therapeutic agents |
| JO2998B1 (ar) | 2010-06-04 | 2016-09-05 | Amgen Inc | مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان |
| US20130267699A1 (en) | 2011-06-24 | 2013-10-10 | California Institute Of Technology | Quaternary heteroatom containing compounds |
| US8822679B2 (en) * | 2011-06-24 | 2014-09-02 | California Institute Of Technology | Quaternary heteroatom containing compounds |
| WO2013049250A1 (en) | 2011-09-27 | 2013-04-04 | Amgen Inc. | Heterocyclic compounds as mdm2 inhibitors for the treatment of cancer |
| HUE032240T2 (en) | 2011-10-24 | 2017-09-28 | Asana Biosciences Llc | cyclohexylamines |
| US9376409B2 (en) | 2012-05-09 | 2016-06-28 | Boehringer Ingelheim International Gmbh | Methods for making oxetan-3-ylmethanamines |
| CA2895504A1 (en) | 2012-12-20 | 2014-06-26 | Merck Sharp & Dohme Corp. | Substituted imidazopyridines as hdm2 inhibitors |
| EP2958902B1 (en) * | 2013-02-19 | 2017-11-15 | Amgen Inc. | Cis-morpholinone and other compounds as mdm2 inhibitors for the treatment of cancer |
| US11407721B2 (en) | 2013-02-19 | 2022-08-09 | Amgen Inc. | CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancer |
| CN105121407B (zh) | 2013-02-28 | 2017-07-18 | 美国安进公司 | 用于治疗癌症的苯甲酸衍生物mdm2抑制剂 |
| WO2014151863A1 (en) * | 2013-03-14 | 2014-09-25 | Amgen Inc. | Heteroaryl acid morpholinone compounds as mdm2 inhibitors for the treatment of cancer |
| JOP20200296A1 (ar) | 2013-06-10 | 2017-06-16 | Amgen Inc | عمليات صنع وأشكال بلورية من mdm2 مثبط |
| PT3068393T (pt) * | 2013-11-11 | 2022-06-14 | Amgen Inc | Terapia de combinação, incluindo um inibidor de mdm2 e um ou mais agentes farmaceuticamente ativos adicionais para o tratamento de cancros |
| CA2926307C (en) * | 2013-12-05 | 2021-11-16 | F. Hoffmann-La Roche Ag | Novel combination treatment for acute myeloid leukemia (aml) |
| CN106794171B (zh) | 2014-04-17 | 2020-03-24 | 密歇根大学董事会 | Mdm2抑制剂和使用其的治疗方法 |
| CN103992334A (zh) * | 2014-05-29 | 2014-08-20 | 中国人民解放军第二军医大学 | 吲哚酮螺四氢硫代吡喃类抗肿瘤衍生物及其制备方法 |
| JP6503386B2 (ja) | 2014-07-03 | 2019-04-17 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | ＭＤＭ２−ｐ５３阻害剤としての新しいスピロ［３Ｈ−インドール−３，２’−ピロリジン］−２（１Ｈ）−オン化合物および誘導体 |
| EA038071B1 (ru) | 2014-08-21 | 2021-07-01 | Бёрингер Ингельхайм Интернациональ Гмбх | СОЕДИНЕНИЕ СПИРО[3H-ИНДОЛ-3,2'-ПИРРОЛИДИН]-2(1H)-ОНА И ЕГО ПРОИЗВОДНЫЕ В КАЧЕСТВЕ ИНГИБИТОРОВ MDM2-p53 |
| TW201702218A (zh) | 2014-12-12 | 2017-01-16 | 美國杰克森實驗室 | 關於治療癌症、自體免疫疾病及神經退化性疾病之組合物及方法 |
| US10421696B2 (en) | 2014-12-18 | 2019-09-24 | California Institute Of Technology | Enantioselective synthesis of α-quaternary mannich adducts by palladium-catalyzed allylic alkylation |
| CA2981041C (en) | 2015-03-27 | 2023-09-05 | California Institute Of Technology | Asymmetric catalytic decarboxylative alkyl alkylation using low catalyst concentrations and a robust precatalyst |
| GB201517216D0 (en) | 2015-09-29 | 2015-11-11 | Cancer Res Technology Ltd And Astex Therapeutics Ltd | Pharmaceutical compounds |
| GB201517217D0 (en) | 2015-09-29 | 2015-11-11 | Astex Therapeutics Ltd And Cancer Res Technology Ltd | Pharmaceutical compounds |
| MX377009B (es) * | 2015-10-09 | 2025-03-07 | Boehringer Ingelheim Int | Nuevos compuestos de espiro[3h-indol-3,2´-pirrolidin]-2(1h)-ona y derivados como inhibidores de mdm2-p53. |
| WO2017156239A1 (en) | 2016-03-11 | 2017-09-14 | California Institute Of Technology | Compositions and methods for acylating lactams |
| JP7037500B2 (ja) * | 2016-04-06 | 2022-03-16 | ザ リージェンツ オブ ザ ユニヴァシティ オブ ミシガン | Ｍｄｍ２タンパク質分解剤 |
| AU2017250076B2 (en) * | 2016-04-12 | 2021-07-22 | The Regents Of The University Of Michigan | Bet protein degraders |
| TWI794171B (zh) | 2016-05-11 | 2023-03-01 | 美商滬亞生物國際有限公司 | Ｈｄａｃ抑制劑與ｐｄ-ｌ１抑制劑之組合治療 |
| TWI808055B (zh) | 2016-05-11 | 2023-07-11 | 美商滬亞生物國際有限公司 | Hdac 抑制劑與 pd-1 抑制劑之組合治療 |
| CN109152843A (zh) | 2016-05-20 | 2019-01-04 | 豪夫迈·罗氏有限公司 | Protac抗体缀合物及其使用方法 |
| GB201704966D0 (en) | 2017-03-28 | 2017-05-10 | Astex Therapeutics Ltd | Pharmaceutical compounds |
| GB201704965D0 (en) | 2017-03-28 | 2017-05-10 | Astex Therapeutics Ltd | Pharmaceutical compounds |
| EP3480190B1 (en) | 2017-11-01 | 2023-01-04 | California Institute of Technology | Methods for enantioselective allylic alkylation of esters, lactones, and lactams with unactivated allylic alcohols |
| WO2019166629A1 (en) | 2018-03-02 | 2019-09-06 | Inflazome Limited | Novel compounds |
| IL308399B2 (en) | 2018-04-30 | 2025-08-01 | Kartos Therapeutics Inc | Methods of treating cancer |
| BR112021003839A2 (pt) * | 2018-08-31 | 2021-07-27 | Amgen Inc. | processos para preparar um inibidor mdm2 |
| CN110963958B (zh) * | 2018-09-30 | 2025-10-10 | 上海长森药业有限公司 | 一种mdm2抑制剂，及其制备方法、药物组合物和应用 |
| EP3699173A1 (en) | 2018-10-18 | 2020-08-26 | California Institute of Technology | Gem-disubstituted pyrrolidines, piperazines, and diazepanes, and compositions and methods of making the same |
| AR116904A1 (es) * | 2018-12-11 | 2021-06-23 | Kartos Therapeutics Inc | Métodos y composiciones para el tratamiento de un trastorno oftálmico |
| GB201919219D0 (en) | 2019-12-23 | 2020-02-05 | Otsuka Pharma Co Ltd | Cancer biomarkers |
| EP4041736A4 (en) * | 2020-01-23 | 2023-06-07 | Ascentage Pharma (Suzhou) Co., Ltd. | AMORPHOUS FORM OR CRYSTALLINE FORM OF 2-INDOLINOLINOLOLYLSPIRONONE COMPOUNDS OR THEIR SALTS, SOLVENT COMPLEXES |
| WO2021170881A1 (en) | 2020-02-27 | 2021-09-02 | Syngenta Crop Protection Ag | Pesticidally active diazine-bisamide compounds |
| AU2021333983A1 (en) | 2020-08-27 | 2023-01-05 | Otsuka Pharmaceutical Co., Ltd. | Biomarkers for cancer therapy using MDM2 antagonists |
| CN112213428A (zh) * | 2020-10-13 | 2021-01-12 | 辽宁科技大学 | 一种超临界co2中进行非催化乙酰基化反应及其在线检测方法 |
| GB202103080D0 (en) | 2021-03-04 | 2021-04-21 | Otsuka Pharma Co Ltd | Cancer biomarkers |
| WO2023056069A1 (en) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Degrader-antibody conjugates and methods of using same |
| WO2023230059A1 (en) * | 2022-05-24 | 2023-11-30 | Newave Pharmaceutical Inc. | Mdm2 degrader |
| WO2023239697A1 (en) * | 2022-06-06 | 2023-12-14 | Kymera Therapeutics, Inc. | Mdm2 degraders and uses thereof |
| CN115322126B (zh) * | 2022-09-13 | 2023-04-28 | 九江学院 | 一种多芳烃类化合物及其制备方法和应用 |
| WO2024240858A1 (en) | 2023-05-23 | 2024-11-28 | Valerio Therapeutics | Protac molecules directed against dna damage repair system and uses thereof |
Family Cites Families (84)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1016828A (en) | 1961-11-13 | 1966-01-12 | Mcneilab Inc | Substituted morpholines and process for preparing same |
| DE3246148A1 (de) | 1982-12-14 | 1984-06-14 | Troponwerke GmbH & Co KG, 5000 Köln | Pyrazolo(4.3-b)(1.4)oxazine, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel |
| WO1995023135A1 (en) | 1991-03-07 | 1995-08-31 | Fisons Corporation | Diphenyl-2-piperidinone and -2-pyrrolidinone derivatives having anti-convulsant and neuroprotective activity |
| US5334720A (en) | 1991-03-07 | 1994-08-02 | Fisons Corporation | Diphenyl-1-(aminoalkyl)-2-piperidinone and -2-pyrrolidinone derivatives having anticonvulsant properties |
| EP0776324B1 (en) | 1994-08-19 | 2002-06-12 | Abbott Laboratories | Endothelin antagonists |
| EP0885215B1 (en) | 1996-02-13 | 2006-04-19 | Abbott Laboratories | Novel benzo-1,3-dioxolyl- and benzofuranyl substituted pyrrolidine derivatives as endothelin antagonists |
| US6159990A (en) | 1997-06-18 | 2000-12-12 | Synaptic Pharmaceutical Corporation | Oxazolidinones as α1A receptor antagonists |
| TR200101234T2 (tr) | 1997-08-04 | 2002-06-21 | Abbott Laboratories | Endotelin antagonistleri. |
| WO1999031507A1 (en) | 1997-12-18 | 1999-06-24 | Eli Lilly And Company | Peptidomimetic template-based combinatorial libraries |
| US6770658B2 (en) | 1998-09-09 | 2004-08-03 | Inflazyme Pharmaceuticals Ltd. | Substituted γ-phenyl-Δ-lactams and uses related thereto |
| US7214540B2 (en) | 1999-04-06 | 2007-05-08 | Uab Research Foundation | Method for screening crystallization conditions in solution crystal growth |
| US6630006B2 (en) | 1999-06-18 | 2003-10-07 | The Regents Of The University Of California | Method for screening microcrystallizations for crystal formation |
| US7195670B2 (en) | 2000-06-27 | 2007-03-27 | California Institute Of Technology | High throughput screening of crystallization of materials |
| US7052545B2 (en) | 2001-04-06 | 2006-05-30 | California Institute Of Technology | High throughput screening of crystallization of materials |
| WO2002017912A1 (en) | 2000-08-31 | 2002-03-07 | Abbott Laboratories | Endothelin antagonists |
| AU2002228598A1 (en) | 2000-11-20 | 2002-06-03 | Parallel Synthesis Technologies, Inc. | Methods and devices for high throughput crystallization |
| JP2004518688A (ja) | 2001-01-30 | 2004-06-24 | ブリストル−マイヤーズ スクイブ カンパニー | ファクターＸａ阻害剤のスルホンアミドラクタムおよびその方法 |
| DE60229059D1 (de) | 2001-05-08 | 2008-11-06 | Univ Yale | Proteomimetische verbindungen und verfahren |
| WO2002094787A1 (en) | 2001-05-23 | 2002-11-28 | Ucb, S.A. | 2-oxo-piperidinyl- and 2-oxo-azepanyl alkanoic acid derivativ es for the treatment of epilepsy and other neurological disorders |
| AU2002366278B2 (en) | 2001-12-18 | 2007-07-19 | F. Hoffmann-La Roche Ag | CIS-2,4,5- triphenyl-imidazolines and their use in the treatment of tumors |
| US6860940B2 (en) | 2002-02-11 | 2005-03-01 | The Regents Of The University Of California | Automated macromolecular crystallization screening |
| US6916833B2 (en) * | 2003-03-13 | 2005-07-12 | Hoffmann-La Roche Inc. | Substituted piperidines |
| US7425638B2 (en) | 2003-06-17 | 2008-09-16 | Hoffmann-La Roche Inc. | Cis-imidazolines |
| JP4814228B2 (ja) | 2004-05-18 | 2011-11-16 | エフ．ホフマン−ラ ロシュ アーゲー | 新規ｃｉｓ−イミダゾリン |
| US7893278B2 (en) | 2004-06-17 | 2011-02-22 | Hoffman-La Roche Inc. | CIS-imidazolines |
| MX2007004551A (es) | 2004-10-18 | 2007-05-23 | Amgen Inc | Compuestos tiadiazol y metodos de uso. |
| CN101155784A (zh) | 2005-03-16 | 2008-04-02 | 霍夫曼-拉罗奇有限公司 | 顺式-2,4,5-三芳基-咪唑啉类化合物及其作为抗癌药物的应用 |
| HRP20110524T1 (hr) | 2005-04-04 | 2011-08-31 | Eisai R&D Management Co. | Spojevi dihidropiridina za neurodegenerativne bolesti i demenciju |
| EP2130822A1 (en) | 2005-12-01 | 2009-12-09 | F. Hoffmann-La Roche AG | 2,4,5-triphenyl imidazoline derivatives as inhibitors of the interaction between p53 and mdm2 proteins for use as anticancer agents |
| WO2007084319A2 (en) * | 2006-01-13 | 2007-07-26 | Schering Corporation | Diaryl piperidines as cb1 modulators |
| EP1981884B1 (en) | 2006-01-18 | 2012-06-13 | Amgen, Inc | Thiazole compounds as protein kinase b (pkb) inhibitors |
| US20070213341A1 (en) | 2006-03-13 | 2007-09-13 | Li Chen | Spiroindolinone derivatives |
| GB0606283D0 (en) | 2006-03-29 | 2006-05-10 | Cyclacel Ltd | Process |
| KR20090042779A (ko) | 2006-06-30 | 2009-04-30 | 쉐링 코포레이션 | Ｐ53 활성을 증가시키는 치환된 피페리딘 및 이의 사용 |
| WO2008010953A2 (en) | 2006-07-19 | 2008-01-24 | University Of Georgia Research Foundation, Inc. | Pyridinone diketo acids: inhibitors of hiv replication in combination therapy |
| US20080045560A1 (en) | 2006-08-15 | 2008-02-21 | Wyeth | Pyrrolidine and related derivatives useful as PR modulators |
| US7618989B2 (en) | 2006-08-15 | 2009-11-17 | Wyeth | Tricyclic oxazolidone derivatives useful as PR modulators |
| US8820639B2 (en) | 2006-11-03 | 2014-09-02 | Assa Abloy Ab | Security feature RFID card |
| TW200831080A (en) | 2006-12-15 | 2008-08-01 | Irm Llc | Compounds and compositions as inhibitors of cannabinoid receptor 1 activity |
| GB0722769D0 (en) | 2007-11-21 | 2008-01-02 | Biolipox Ab | New compounds |
| JP2010521444A (ja) * | 2007-03-12 | 2010-06-24 | バイオリポックス エービー | 炎症の治療において有用なピペリジノン類 |
| PL2137186T3 (pl) | 2007-03-23 | 2016-09-30 | Związki heterocykliczne i ich zastosowania | |
| AU2008231384B2 (en) | 2007-03-23 | 2011-09-15 | Amgen Inc. | Heterocyclic compounds and their use |
| US7705018B2 (en) | 2007-03-23 | 2010-04-27 | Amgen Inc. | Substituted quinolines and their uses in treatment of inflammatory and related conditions |
| BRPI0810082A2 (pt) * | 2007-03-29 | 2014-10-21 | Novartis Ag | 3-imidazolil-indóis para o tratamento de doenças proliferativas |
| US7625895B2 (en) | 2007-04-12 | 2009-12-01 | Hoffmann-Le Roche Inc. | Diphenyl-dihydro-imidazopyridinones |
| WO2008130614A2 (en) | 2007-04-20 | 2008-10-30 | University Of Pittsburg-Of The Commonwealth System Of Higher Education | Selective and dual-action p53/mdm2/mdm4 antagonists |
| US7834179B2 (en) * | 2007-05-23 | 2010-11-16 | Hoffmann-La Roche Inc. | Spiroindolinone derivatives |
| WO2009004430A1 (en) | 2007-06-29 | 2009-01-08 | Pfizer Inc. | N-benzyl oxazolidinones and related heterocycleic compounds as potentiators of glutamate receptors |
| CA2692720A1 (en) | 2007-07-09 | 2009-01-15 | Astrazeneca Ab | Morpholino pyrimidine derivatives used in diseases linked to mtor kinase and/or pi3k |
| AU2008276512A1 (en) | 2007-07-17 | 2009-01-22 | Amgen Inc. | Thiadiazole modulators of PKB |
| AU2008276521B2 (en) | 2007-07-17 | 2011-11-03 | Amgen Inc. | Heterocyclic modulators of PKB |
| ES2401557T3 (es) | 2007-08-02 | 2013-04-22 | Amgen, Inc | Moduladores de Pl3 cinasas y métodos de uso |
| RU2487127C2 (ru) | 2007-10-09 | 2013-07-10 | Ф.Хоффманн-Ля Рош Аг | Хиральные цис-имидазолины |
| CA2709202C (en) | 2007-12-19 | 2013-04-23 | Amgen Inc. | Fused pyridine, pyrimidine and triazine compounds as cell cycle inhibitors |
| US7776875B2 (en) | 2007-12-19 | 2010-08-17 | Hoffman-La Roche Inc. | Spiroindolinone derivatives |
| US7820665B2 (en) | 2007-12-19 | 2010-10-26 | Amgen Inc. | Imidazopyridazine inhibitors of PI3 kinase for cancer treatment |
| EP2222296A2 (en) | 2007-12-26 | 2010-09-01 | Eisai R&D Management Co., Ltd. | Ampa receptor antagonists and zonisamide for epilepsy |
| WO2009114950A1 (en) | 2008-03-21 | 2009-09-24 | Chlorion Pharma, Inc. | Substituted pyrrolidine and piperidine compounds, derivatives thereof, and methods for treating pain |
| WO2009126584A1 (en) | 2008-04-07 | 2009-10-15 | Amgen Inc. | Gem-disubstituted and spirocyclic amino pyridines/pyrimidines as cell cycle inhibitors |
| WO2009155121A2 (en) | 2008-05-30 | 2009-12-23 | Amgen Inc. | Inhibitors of pi3 kinase |
| GB0811643D0 (en) | 2008-06-25 | 2008-07-30 | Cancer Rec Tech Ltd | New therapeutic agents |
| TW201011009A (en) * | 2008-09-15 | 2010-03-16 | Priaxon Ag | Novel pyrrolidin-2-ones |
| KR101380013B1 (ko) | 2008-09-18 | 2014-04-10 | 에프. 호프만-라 로슈 아게 | 치환 피롤리딘-2-카르복사미드 |
| US20110263647A1 (en) | 2009-01-15 | 2011-10-27 | Amgen Inc. | Fluoroisoquinoline substituted thiazole compounds and methods of use |
| CA2752527C (en) | 2009-02-18 | 2014-09-23 | Amgen Inc. | Indole/benzimidazole compounds as mtor kinase inhibitors |
| MX2011009796A (es) | 2009-03-20 | 2011-12-14 | Amgen Inc | Inhibidores de la cinasa pi3. |
| US8076482B2 (en) | 2009-04-23 | 2011-12-13 | Hoffmann-La Roche Inc. | 3,3′-spiroindolinone derivatives |
| UY32582A (es) | 2009-04-28 | 2010-11-30 | Amgen Inc | Inhibidores de fosfoinositida 3 cinasa y/u objetivo mamífero |
| JP2012526836A (ja) | 2009-05-13 | 2012-11-01 | アムジエン・インコーポレーテツド | Ｐｉｋｋ阻害薬としてのヘテロアリール化合物 |
| WO2010151791A1 (en) | 2009-06-25 | 2010-12-29 | Amgen Inc. | Heterocyclic compounds and their uses |
| CA2765819A1 (en) | 2009-06-25 | 2010-12-29 | Amgen Inc. | Heterocyclic compounds and their uses as inhibitors of pi3 k activity |
| SG176986A1 (en) | 2009-06-25 | 2012-02-28 | Amgen Inc | Polycyclic derivatives of pyridine and their use in the treatment of (inter alia) rheumatoid arthritis and similar diseases |
| US8754089B2 (en) | 2009-06-25 | 2014-06-17 | Amgen Inc. | Heterocyclic compounds and their uses |
| EA201200321A1 (ru) | 2009-08-26 | 2012-09-28 | Новартис Аг | Тетразамещенные гетероарильные соединения и их применение в качестве модуляторов mdm2 и/или mdm4 |
| US8088815B2 (en) | 2009-12-02 | 2012-01-03 | Hoffman-La Roche Inc. | Spiroindolinone pyrrolidines |
| US8440693B2 (en) | 2009-12-22 | 2013-05-14 | Novartis Ag | Substituted isoquinolinones and quinazolinones |
| JO2998B1 (ar) | 2010-06-04 | 2016-09-05 | Amgen Inc | مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان |
| CN102153557B (zh) | 2011-01-21 | 2013-03-20 | 中国科学院上海有机化学研究所 | 具有乙二胺骨架的多手性中心氮杂环卡宾前体盐、合成方法及用途 |
| WO2013049250A1 (en) | 2011-09-27 | 2013-04-04 | Amgen Inc. | Heterocyclic compounds as mdm2 inhibitors for the treatment of cancer |
| EP2958902B1 (en) | 2013-02-19 | 2017-11-15 | Amgen Inc. | Cis-morpholinone and other compounds as mdm2 inhibitors for the treatment of cancer |
| CN105121407B (zh) | 2013-02-28 | 2017-07-18 | 美国安进公司 | 用于治疗癌症的苯甲酸衍生物mdm2抑制剂 |
| WO2014151863A1 (en) | 2013-03-14 | 2014-09-25 | Amgen Inc. | Heteroaryl acid morpholinone compounds as mdm2 inhibitors for the treatment of cancer |
| JOP20200296A1 (ar) | 2013-06-10 | 2017-06-16 | Amgen Inc | عمليات صنع وأشكال بلورية من mdm2 مثبط |
-
2011
- 2011-06-02 JO JOP/2011/0182A patent/JO2998B1/ar active
- 2011-06-03 CA CA3157177A patent/CA3157177C/en active Active
- 2011-06-03 BR BR122020013151-9A patent/BR122020013151B1/pt active IP Right Grant
- 2011-06-03 IL IL317703A patent/IL317703A/en unknown
- 2011-06-03 SI SI201130499T patent/SI2576510T1/sl unknown
- 2011-06-03 MY MYPI2018000697A patent/MY202394A/en unknown
- 2011-06-03 PT PT117265819T patent/PT2576510E/pt unknown
- 2011-06-03 SI SI201131669T patent/SI2927213T1/sl unknown
- 2011-06-03 CA CA2799972A patent/CA2799972C/en active Active
- 2011-06-03 UY UY0001039338A patent/UY39338A/es not_active Application Discontinuation
- 2011-06-03 RS RS20240056A patent/RS65141B1/sr unknown
- 2011-06-03 PL PL15159363T patent/PL2927213T3/pl unknown
- 2011-06-03 EP EP18197155.7A patent/EP3483143B1/en active Active
- 2011-06-03 AR ARP110101928A patent/AR082763A1/es active IP Right Grant
- 2011-06-03 TW TW104140967A patent/TWI582076B/zh active
- 2011-06-03 MX MX2016001932A patent/MX343587B/es unknown
- 2011-06-03 KR KR1020137000287A patent/KR101456801B1/ko active Active
- 2011-06-03 FI FIEP18197155.7T patent/FI3483143T3/fi active
- 2011-06-03 HU HUE18197155A patent/HUE066050T2/hu unknown
- 2011-06-03 RS RS20150364A patent/RS54030B1/sr unknown
- 2011-06-03 ME MEP-2015-84A patent/ME02150B/me unknown
- 2011-06-03 ES ES11726581.9T patent/ES2540992T3/es active Active
- 2011-06-03 NZ NZ627385A patent/NZ627385A/en unknown
- 2011-06-03 JP JP2013513401A patent/JP5420797B2/ja active Active
- 2011-06-03 DK DK15159363.9T patent/DK2927213T3/en active
- 2011-06-03 PT PT181971557T patent/PT3483143T/pt unknown
- 2011-06-03 KR KR1020147013519A patent/KR101863407B1/ko active Active
- 2011-06-03 SM SM20190099T patent/SMT201900099T1/it unknown
- 2011-06-03 MX MX2012014044A patent/MX337178B/es active IP Right Grant
- 2011-06-03 MA MA35504A patent/MA34342B1/fr unknown
- 2011-06-03 TW TW103105903A patent/TWI519519B/zh active
- 2011-06-03 EP EP22160459.8A patent/EP4092012A1/en active Pending
- 2011-06-03 PL PL11726581T patent/PL2576510T3/pl unknown
- 2011-06-03 RS RS20190184A patent/RS58366B1/sr unknown
- 2011-06-03 SG SG10201604817QA patent/SG10201604817QA/en unknown
- 2011-06-03 SG SG10202112488SA patent/SG10202112488SA/en unknown
- 2011-06-03 KR KR1020217016376A patent/KR20210068144A/ko not_active Ceased
- 2011-06-03 US US13/153,345 patent/US8569341B2/en active Active
- 2011-06-03 PH PH12016501048A patent/PH12016501048A1/en unknown
- 2011-06-03 PH PH1/2012/502410A patent/PH12012502410A1/en unknown
- 2011-06-03 IL IL295076A patent/IL295076B2/en unknown
- 2011-06-03 LT LTEP18197155.7T patent/LT3483143T/lt unknown
- 2011-06-03 KR KR1020237037399A patent/KR20230156431A/ko not_active Ceased
- 2011-06-03 EA EA201291356A patent/EA023004B1/ru not_active IP Right Cessation
- 2011-06-03 KR KR1020187014728A patent/KR20180059574A/ko not_active Ceased
- 2011-06-03 SG SG10202006923RA patent/SG10202006923RA/en unknown
- 2011-06-03 WO PCT/US2011/039184 patent/WO2011153509A1/en not_active Ceased
- 2011-06-03 PT PT15159363T patent/PT2927213T/pt unknown
- 2011-06-03 KR KR1020257008612A patent/KR20250044461A/ko active Pending
- 2011-06-03 KR KR1020227017268A patent/KR20220083817A/ko not_active Ceased
- 2011-06-03 DK DK11726581.9T patent/DK2576510T3/en active
- 2011-06-03 HU HUE15159363A patent/HUE041488T2/hu unknown
- 2011-06-03 ES ES18197155T patent/ES2971445T3/es active Active
- 2011-06-03 EP EP15159363.9A patent/EP2927213B1/en active Active
- 2011-06-03 KR KR1020197014475A patent/KR20190058694A/ko not_active Ceased
- 2011-06-03 TW TW100119640A patent/TWI433844B/zh active
- 2011-06-03 IL IL277579A patent/IL277579B/en unknown
- 2011-06-03 AU AU2011261263A patent/AU2011261263C1/en active Active
- 2011-06-03 SI SI201132100T patent/SI3483143T1/sl unknown
- 2011-06-03 LT LTEP15159363.9T patent/LT2927213T/lt unknown
- 2011-06-03 CN CN201510205985.6A patent/CN105153014B/zh active Active
- 2011-06-03 SM SM20240024T patent/SMT202400024T1/it unknown
- 2011-06-03 NZ NZ604074A patent/NZ604074A/en unknown
- 2011-06-03 ES ES15159363T patent/ES2717306T3/es active Active
- 2011-06-03 KR KR1020207014861A patent/KR20200063255A/ko not_active Ceased
- 2011-06-03 DK DK18197155.7T patent/DK3483143T3/da active
- 2011-06-03 HR HRP20150704TT patent/HRP20150704T1/hr unknown
- 2011-06-03 SG SG2012088837A patent/SG186147A1/en unknown
- 2011-06-03 UY UY0001033430A patent/UY33430A/es unknown
- 2011-06-03 UA UAA201300192 patent/UA110481C2/ru unknown
- 2011-06-03 PL PL18197155.7T patent/PL3483143T3/pl unknown
- 2011-06-03 PE PE2012002267A patent/PE20130229A1/es active IP Right Grant
- 2011-06-03 ME MEP-2019-41A patent/ME03322B/me unknown
- 2011-06-03 CA CA3060703A patent/CA3060703C/en active Active
- 2011-06-03 EP EP20110726581 patent/EP2576510B1/en active Active
- 2011-06-03 HR HRP20240055TT patent/HRP20240055T1/hr unknown
- 2011-06-03 CA CA3207676A patent/CA3207676A1/en active Pending
- 2011-06-03 BR BR112012030923A patent/BR112012030923B8/pt active IP Right Grant
- 2011-06-03 CN CN201180038476.9A patent/CN103180296B/zh active Active
-
2012
- 2012-11-22 IL IL223201A patent/IL223201A/en active IP Right Grant
- 2012-11-27 TN TNP2012000559A patent/TN2012000559A1/en unknown
- 2012-12-04 CL CL2012003415A patent/CL2012003415A1/es unknown
- 2012-12-10 CO CO12223240A patent/CO6710897A2/es active IP Right Grant
- 2012-12-21 CR CR20120659A patent/CR20120659A/es unknown
-
2013
- 2013-09-12 US US14/025,688 patent/US20140011796A1/en not_active Abandoned
- 2013-09-18 JP JP2013192621A patent/JP5908446B2/ja active Active
-
2014
- 2014-02-07 ZA ZA2014/00948A patent/ZA201400948B/en unknown
- 2014-06-26 US US14/316,586 patent/US9296736B2/en active Active
- 2014-06-26 IL IL233411A patent/IL233411A/en active IP Right Grant
-
2015
- 2015-07-14 SM SM201500168T patent/SMT201500168B/xx unknown
-
2016
- 2016-01-27 US US15/008,342 patent/US9593129B2/en active Active
- 2016-03-22 JP JP2016056518A patent/JP6077695B2/ja active Active
- 2016-06-16 IL IL246296A patent/IL246296A0/en active IP Right Grant
- 2016-07-06 CL CL2016001733A patent/CL2016001733A1/es unknown
-
2017
- 2017-01-23 US US15/412,804 patent/US20170144971A1/en not_active Abandoned
-
2018
- 2018-03-21 US US15/927,426 patent/US20190062276A1/en not_active Abandoned
-
2019
- 2019-02-11 HR HRP20190273TT patent/HRP20190273T1/hr unknown
- 2019-02-13 CY CY20191100192T patent/CY1121265T1/el unknown
- 2019-03-11 IL IL265278A patent/IL265278B/en active IP Right Grant
-
2020
- 2020-08-03 US US16/983,027 patent/US20210179560A1/en not_active Abandoned
-
2022
- 2022-02-15 US US17/672,660 patent/US20220169611A1/en not_active Abandoned
-
2023
- 2023-10-11 US US18/484,675 patent/US20240300892A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2013530958A5 (enExample) | ||
| NL301284I2 (nl) | Etrasimod, of een farmaceutisch aanvaardbaar zout daarvan, zoals etrasimod arginine | |
| NO2025029I1 (no) | Entrectinib or isomers, tautomers, or pharmaceutically acceptable salts therof - forlenget | |
| NL301021I1 (nl) | talazoparib, desgewenst in de vorm van een farmaceutisch aanvaardbaar zout. | |
| CA2914723C (en) | Processes of making and crystalline forms of a mdm2 inhibitor | |
| USD675268S1 (en) | Ball | |
| JP2014515013A5 (enExample) | ||
| EA201490419A1 (ru) | Соединения для лечения и профилактики респираторного синцитиального вирусного заболевания | |
| JP2013519683A5 (enExample) | ||
| USD670089S1 (en) | Table | |
| NL300909I2 (nl) | Ribociclib, desgewenst in de vorm van een farmaceutisch aanvaardbaar zout | |
| JP2010529118A5 (enExample) | ||
| JP2015504870A5 (enExample) | ||
| JP2011168603A5 (enExample) | ||
| JP2013525444A5 (enExample) | ||
| EP2881384A8 (en) | Partially saturated nitrogen-containing heterocyclic compound | |
| USD696792S1 (en) | Barrier structure | |
| JP2011105738A5 (enExample) | ||
| WO2012020848A8 (en) | Heterocyclic compound and use thereof | |
| JP2013032389A5 (enExample) | ||
| JP2013173781A5 (enExample) | ||
| JP2013532687A5 (enExample) | ||
| JP2013507408A5 (enExample) | ||
| JP2013532130A5 (enExample) | ||
| JP2014513036A5 (enExample) |