MA31550B1 - Derives de 2,4,5-triphenyl imidazoline en tant qu'inhibiteurs de l'interaction entre les proteines p53 et mdm2, utilises en tant qu'agents anticancereux - Google Patents
Derives de 2,4,5-triphenyl imidazoline en tant qu'inhibiteurs de l'interaction entre les proteines p53 et mdm2, utilises en tant qu'agents anticancereuxInfo
- Publication number
- MA31550B1 MA31550B1 MA30992A MA30992A MA31550B1 MA 31550 B1 MA31550 B1 MA 31550B1 MA 30992 A MA30992 A MA 30992A MA 30992 A MA30992 A MA 30992A MA 31550 B1 MA31550 B1 MA 31550B1
- Authority
- MA
- Morocco
- Prior art keywords
- mdm2
- triphenyl
- inhibitors
- proteins
- interaction
- Prior art date
Links
- 239000002246 antineoplastic agent Substances 0.000 title abstract 2
- UCCFUHZMGXEALP-UHFFFAOYSA-N 2,4,5-triphenyl-4,5-dihydro-1h-imidazole Chemical class N1C(C=2C=CC=CC=2)C(C=2C=CC=CC=2)N=C1C1=CC=CC=C1 UCCFUHZMGXEALP-UHFFFAOYSA-N 0.000 title 1
- 102000012199 E3 ubiquitin-protein ligase Mdm2 Human genes 0.000 title 1
- 108050002772 E3 ubiquitin-protein ligase Mdm2 Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 230000006916 protein interaction Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/20—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D233/22—Radicals substituted by oxygen atoms
-
- 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
- A61K31/4164—1,3-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/20—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D233/26—Radicals substituted by carbon atoms having three bonds to hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
LA PRÉSENTE INVENTION CONCERNE UN COMPOSÉ RÉPONDANT À LA FORMULE (I) AINSI QUE DES SELS ET ESTERS PHARMACEUTIQUEMENT ACCEPTABLES DE CELUI-CI, X1 , X2, R1 , R2, R3, R4, R5 ET R6 ÉTANT TELS QUE DÉCRITS DANS LE PRÉSENT DOCUMENT. LESDITS COMPOSÉS SONT ACTIFS EN TANT QU'AGENTS ANTICANCÉREUX.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US74122305P | 2005-12-01 | 2005-12-01 | |
| US85274706P | 2006-10-19 | 2006-10-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA31550B1 true MA31550B1 (fr) | 2010-08-02 |
Family
ID=37866229
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA30992A MA31550B1 (fr) | 2005-12-01 | 2008-06-02 | Derives de 2,4,5-triphenyl imidazoline en tant qu'inhibiteurs de l'interaction entre les proteines p53 et mdm2, utilises en tant qu'agents anticancereux |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US7851626B2 (fr) |
| EP (3) | EP1960368B1 (fr) |
| JP (1) | JP4870778B2 (fr) |
| KR (2) | KR20100129331A (fr) |
| CN (1) | CN101316823B (fr) |
| AR (1) | AR057990A1 (fr) |
| AU (1) | AU2006319248B2 (fr) |
| BR (1) | BRPI0619236A2 (fr) |
| CA (1) | CA2630410C (fr) |
| CR (1) | CR9980A (fr) |
| ES (1) | ES2538714T3 (fr) |
| MA (1) | MA31550B1 (fr) |
| NO (1) | NO20082389L (fr) |
| NZ (1) | NZ568285A (fr) |
| RU (1) | RU2442779C2 (fr) |
| TW (1) | TWI326681B (fr) |
| WO (1) | WO2007063013A1 (fr) |
Families Citing this family (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2076497B1 (fr) * | 2006-10-19 | 2012-02-22 | F. Hoffmann-La Roche AG | Aminométhyl-4-imidazoles |
| EP2104665A2 (fr) * | 2006-10-19 | 2009-09-30 | F. Hoffmann-Roche AG | Dérivés d'imidazolone et d'imidazolidinone utilisés en tant qu'inhibiteurs de l'enzyme 11b-hsd1 pour le diabète |
| EP2192111A3 (fr) * | 2007-07-06 | 2010-10-06 | Paratek Pharmaceuticals, Inc. | Procédés servant à synthétiser des composés de tétracycline substituée |
| EP2325180A1 (fr) * | 2007-10-09 | 2011-05-25 | F. Hoffmann-La Roche AG | CIS-imidazolines chiraux |
| WO2009085216A2 (fr) | 2007-12-20 | 2009-07-09 | Squicor | Compositions et méthodes de détection ou d'élimination de cellules sénescentes pour le diagnostic ou le traitement de maladies |
| EP2298778A4 (fr) | 2008-06-12 | 2011-10-05 | Daiichi Sankyo Co Ltd | Dérivé d imidazothiazole ayant une structure cyclique de 4,7-diazaspiroý2.5¨octane |
| CN102356085A (zh) | 2009-01-16 | 2012-02-15 | 第一三共株式会社 | 具有脯氨酸环结构的咪唑并噻唑衍生物 |
| IN2012DN01693A (fr) * | 2009-08-26 | 2015-06-05 | Novartis Ag | |
| BR112012008849A2 (pt) | 2009-10-14 | 2015-09-22 | Schering Corp | composto, composição farmacêutica, e, uso de um composto |
| JO2998B1 (ar) | 2010-06-04 | 2016-09-05 | Amgen Inc | مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان |
| US8709419B2 (en) | 2010-08-17 | 2014-04-29 | Hoffmann-La Roche, Inc. | Combination therapy |
| CA2813256A1 (fr) | 2010-09-30 | 2012-04-05 | St. Jude Children's Research Hospital | Imidazoles substitues par aryle |
| FR2967072B1 (fr) | 2010-11-05 | 2013-03-29 | Univ Dundee | Procede pour ameliorer la production de virus et semences vaccinales influenza |
| US9295669B2 (en) | 2010-12-14 | 2016-03-29 | Hoffman La-Roche Inc. | Combination therapy for proliferative disorders |
| KR20130088170A (ko) | 2010-12-16 | 2013-08-07 | 로슈 글리카트 아게 | 비푸코실화 cd20 항체와 mdm2 저해제와의 조합 치료 |
| WO2012177927A1 (fr) | 2011-06-21 | 2012-12-27 | Mayo Foundation For Medical Education And Research | Animaux transgéniques pouvant être induits pour éliminer des cellules sénescentes |
| EP2760845B1 (fr) | 2011-09-27 | 2016-11-16 | Amgen Inc. | Heterocycles utilises comme inhibiteurs de mdm2 dans le traitement du cancer |
| EP2771008A4 (fr) | 2011-10-28 | 2015-04-08 | Merck Sharp & Dohme | Macrocycles augmentant l'activité p53 et leurs utilisations |
| US20140335074A1 (en) | 2011-12-13 | 2014-11-13 | Buck Institute For Research On Aging | Methods for improving medical therapies |
| WO2013096150A1 (fr) | 2011-12-21 | 2013-06-27 | Merck Sharp & Dohme Corp. | Pipéridines substituées en tant qu'inhibiteurs d'hdm2 |
| US9216170B2 (en) | 2012-03-19 | 2015-12-22 | Hoffmann-La Roche Inc. | Combination therapy for proliferative disorders |
| WO2013158664A2 (fr) | 2012-04-17 | 2013-10-24 | Kythera Biopharmaceuticals, Inc. | Utilisation de virus modifiés pour tuer spécifiquement les cellules sénescentes |
| TWI654180B (zh) | 2012-06-29 | 2019-03-21 | 美商艾佛艾姆希公司 | 殺真菌之雜環羧醯胺 |
| US9901081B2 (en) | 2012-08-23 | 2018-02-27 | Buck Institute For Research On Aging | Transgenic mouse for determining the role of senescent cells in cancer |
| US9901080B2 (en) | 2012-08-23 | 2018-02-27 | Buck Institute For Research On Aging | Transgenic mouse having a transgene that converts a prodrug into a cytotoxic compound in senescent cells |
| WO2014082889A1 (fr) * | 2012-11-28 | 2014-06-05 | F. Hoffmann-La Roche Ag | Nouvelles imidazolines utilisées en tant que doubles inhibiteurs de mdm2 et mdmx |
| US10279018B2 (en) | 2012-12-03 | 2019-05-07 | Unity Biotechnology, Inc. | Immunogenic compositions for inducing an immune response for elimination of senescent cells |
| TW201429969A (zh) | 2012-12-20 | 2014-08-01 | Merck Sharp & Dohme | 作爲hdm2抑制劑之經取代咪唑吡啶 |
| CN103012272B (zh) * | 2012-12-21 | 2015-01-28 | 江苏国泰超威新材料有限公司 | 一种咪唑啉化合物的制备方法 |
| US11407721B2 (en) | 2013-02-19 | 2022-08-09 | Amgen Inc. | CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancer |
| EP2961735B1 (fr) | 2013-02-28 | 2017-09-27 | Amgen Inc. | Inhibiteur mdm2 dérivé de l'acide benzoïque pour le traitement du cancer |
| AU2014236812B2 (en) | 2013-03-14 | 2018-03-01 | 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 |
| AU2014286237B2 (en) | 2013-07-03 | 2020-08-20 | F. Hoffmann-La Roche Ag | mRNA-based gene expression for personalizing patient cancer therapy with an MDM2 antagonist |
| US9657351B2 (en) | 2013-12-06 | 2017-05-23 | Hoffman-La Roche Inc. | MRNA-based gene expression for personalizing patient cancer therapy with an MDM2 antagonist |
| US20190269675A1 (en) | 2014-01-28 | 2019-09-05 | Buck Institute for Research and Aging | Treatment of parkinson's disease and other conditions caused or mediated by senescent astrocytes using small molecule senolytic agents |
| US10328058B2 (en) | 2014-01-28 | 2019-06-25 | Mayo Foundation For Medical Education And Research | Treating atherosclerosis by removing senescent foam cell macrophages from atherosclerotic plaques |
| WO2015116735A1 (fr) | 2014-01-28 | 2015-08-06 | Mayo Foundation For Medical Education And Research | Procédés et combinaisons pour tuer des cellules sénescentes et traiter des maladies et troubles associés à une sénescence |
| EP3669881B1 (fr) | 2014-01-28 | 2022-03-30 | Buck Institute for Research on Aging | Compositions pour leur utilisation pour traiter les maladies et les troubles oculaires associés à la sénescence |
| WO2015161032A1 (fr) | 2014-04-17 | 2015-10-22 | The Regents Of The University Of Michigan | Inhibiteurs de hdac et méthodes thérapeutiques les utilisant |
| JP6889661B2 (ja) * | 2015-01-09 | 2021-06-18 | ジェネンテック, インコーポレイテッド | 4,5−ジヒドロイミダゾール誘導体およびヒストンジメチラーゼ(kdm2b)インヒビターとしてのその使用 |
| CA2988430A1 (fr) * | 2015-07-10 | 2017-01-19 | Arvinas, Inc. | Modulateurs de proteolyse a base de mdm2 et methodes d'utilisation associees |
| JP2019522633A (ja) | 2016-05-20 | 2019-08-15 | ジェネンテック, インコーポレイテッド | Protac抗体コンジュゲート及び使用方法 |
| AU2017418538B2 (en) | 2017-06-16 | 2021-10-21 | Unity Biotechnology, Inc. | Synthesis method for producing enantiomerically pure cis-imidazoline compounds for pharmaceutical use |
| AU2019247554A1 (en) | 2018-04-06 | 2020-11-26 | Oncolyze, Inc. | Compositions for use in lysis of selective cancer cells |
| KR102039696B1 (ko) | 2018-04-23 | 2019-11-04 | 충남대학교산학협력단 | 세포내 결핵균 제어를 위한 p53 발현 조절 가능한 조성물 (K279-1558) 또는 방법 |
| CN114075121B (zh) * | 2020-08-19 | 2025-08-29 | 中国科学院上海有机化学研究所 | 一类偶氮化合物的制备方法及其用途 |
| KR102622992B1 (ko) * | 2021-03-29 | 2024-01-10 | 주식회사 퓨전바이오텍 | 이미다졸린 유도체 및 이의 중간체 제조방법 |
| WO2023056069A1 (fr) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Conjugués agent de dégradation-anticorps et leurs procédés d'utilisation |
| WO2024240858A1 (fr) | 2023-05-23 | 2024-11-28 | Valerio Therapeutics | Molécules protac dirigées contre un système de réparation de dommages à l'adn et leurs utilisations |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02101065A (ja) | 1988-10-06 | 1990-04-12 | Tanabe Seiyaku Co Ltd | イミダゾリン誘導体及びその製法 |
| PL183931B1 (pl) * | 1994-09-26 | 2002-08-30 | Shionogi & Co | Nowe związki, pochodne imidazolu i kompozycje farmaceutyczne je zawierające |
| GB2351082A (en) | 1999-06-18 | 2000-12-20 | Lilly Forschung Gmbh | Synthesis of Cyclic Substituted Amidines |
| RU2305095C2 (ru) | 2001-12-18 | 2007-08-27 | Ф.Хоффманн-Ля Рош Аг | Цис-2,4,5-трифенилимидазолины и фармацевтическая композиция на их основе |
| KR100640707B1 (ko) | 2001-12-18 | 2006-10-31 | 에프. 호프만-라 로슈 아게 | Mdm2 저해제로서의 시스-이미다졸린 |
| US7345078B2 (en) * | 2002-05-31 | 2008-03-18 | The Board Of Trustees Of Michigan State University | NF-κB inhibitors and uses thereof |
| US6878735B2 (en) * | 2002-05-31 | 2005-04-12 | Board Of Trustees Of Michigan State University | Multi-substituted imidazolines and method of use thereof |
| US7157455B2 (en) | 2003-02-10 | 2007-01-02 | Hoffmann-La Roche Inc. | 4-Aminopyrimidine-5-one derivatives |
| US7132421B2 (en) | 2003-06-17 | 2006-11-07 | Hoffmann-La Roche Inc. | CIS-imidazoles |
| MXPA05013279A (es) * | 2003-06-17 | 2006-03-09 | Hoffmann La Roche | Cis-2,4,5-triaril-imidazolinas. |
| WO2005002575A1 (fr) * | 2003-06-17 | 2005-01-13 | F. Hoffmann-La Roche Ag | Cis-imidazolines utilisees en tant qu'inhibiteurs de mdm2 |
| 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 |
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2006
- 2006-11-22 ES ES06819663.3T patent/ES2538714T3/es active Active
- 2006-11-22 BR BRPI0619236-0A patent/BRPI0619236A2/pt not_active Application Discontinuation
- 2006-11-22 EP EP20060819663 patent/EP1960368B1/fr active Active
- 2006-11-22 WO PCT/EP2006/068748 patent/WO2007063013A1/fr not_active Ceased
- 2006-11-22 AU AU2006319248A patent/AU2006319248B2/en not_active Ceased
- 2006-11-22 JP JP2008542723A patent/JP4870778B2/ja not_active Expired - Fee Related
- 2006-11-22 CN CN2006800448100A patent/CN101316823B/zh not_active Expired - Fee Related
- 2006-11-22 EP EP09166803A patent/EP2130822A1/fr not_active Withdrawn
- 2006-11-22 KR KR1020107024025A patent/KR20100129331A/ko not_active Ceased
- 2006-11-22 RU RU2008126383/04A patent/RU2442779C2/ru active
- 2006-11-22 NZ NZ568285A patent/NZ568285A/en not_active IP Right Cessation
- 2006-11-22 KR KR1020087013226A patent/KR101109437B1/ko not_active Expired - Fee Related
- 2006-11-22 CA CA2630410A patent/CA2630410C/fr not_active Expired - Fee Related
- 2006-11-22 EP EP10175570A patent/EP2311814A1/fr not_active Withdrawn
- 2006-11-27 US US11/604,558 patent/US7851626B2/en not_active Expired - Fee Related
- 2006-11-29 TW TW095144209A patent/TWI326681B/zh not_active IP Right Cessation
- 2006-11-29 AR ARP060105272A patent/AR057990A1/es not_active Application Discontinuation
-
2008
- 2008-05-16 CR CR9980A patent/CR9980A/es not_active Application Discontinuation
- 2008-05-26 NO NO20082389A patent/NO20082389L/no not_active Application Discontinuation
- 2008-06-02 MA MA30992A patent/MA31550B1/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP2311814A1 (fr) | 2011-04-20 |
| CR9980A (es) | 2008-06-18 |
| RU2442779C2 (ru) | 2012-02-20 |
| EP1960368B1 (fr) | 2015-05-06 |
| TWI326681B (en) | 2010-07-01 |
| AR057990A1 (es) | 2008-01-09 |
| TW200804297A (en) | 2008-01-16 |
| EP2130822A1 (fr) | 2009-12-09 |
| BRPI0619236A2 (pt) | 2011-09-20 |
| CN101316823A (zh) | 2008-12-03 |
| JP4870778B2 (ja) | 2012-02-08 |
| AU2006319248A1 (en) | 2007-06-07 |
| CA2630410A1 (fr) | 2007-06-07 |
| NO20082389L (no) | 2008-08-18 |
| US7851626B2 (en) | 2010-12-14 |
| KR101109437B1 (ko) | 2012-01-31 |
| NZ568285A (en) | 2011-08-26 |
| HK1126216A1 (en) | 2009-08-28 |
| KR20080072894A (ko) | 2008-08-07 |
| US20070129416A1 (en) | 2007-06-07 |
| CA2630410C (fr) | 2014-02-25 |
| AU2006319248B2 (en) | 2012-09-27 |
| JP2009517439A (ja) | 2009-04-30 |
| CN101316823B (zh) | 2013-05-22 |
| EP1960368A1 (fr) | 2008-08-27 |
| ES2538714T3 (es) | 2015-06-23 |
| WO2007063013A1 (fr) | 2007-06-07 |
| RU2008126383A (ru) | 2010-01-10 |
| KR20100129331A (ko) | 2010-12-08 |
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