EA200701771A1 - Низкомолекулярные ингибиторы mdm2 и их применение - Google Patents
Низкомолекулярные ингибиторы mdm2 и их применениеInfo
- Publication number
- EA200701771A1 EA200701771A1 EA200701771A EA200701771A EA200701771A1 EA 200701771 A1 EA200701771 A1 EA 200701771A1 EA 200701771 A EA200701771 A EA 200701771A EA 200701771 A EA200701771 A EA 200701771A EA 200701771 A1 EA200701771 A1 EA 200701771A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- mdm2
- application
- low molecular
- molecular inhibitors
- inhibitors
- Prior art date
Links
- 102000012199 E3 ubiquitin-protein ligase Mdm2 Human genes 0.000 title abstract 2
- 108050002772 E3 ubiquitin-protein ligase Mdm2 Proteins 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 230000025084 cell cycle arrest Effects 0.000 abstract 1
- 230000030833 cell death Effects 0.000 abstract 1
- 230000010261 cell growth Effects 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000001939 inductive effect Effects 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 230000003993 interaction Effects 0.000 abstract 1
- 230000001235 sensitizing effect Effects 0.000 abstract 1
- 150000003384 small molecules Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/54—Spiro-condensed
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- C07D487/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Indole Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Изобретение относится к малым молекулам, которые функционируют как ингибиторы взаимодействия между р53 и MDM2. Изобретение также относится к применению этих соединений для ингибирования клеточного роста, включая клеточную гибель, индукцию остановки клеточного цикла и/или сенсибилизацию клеток к дополнительному агенту(ам).
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US65513505P | 2005-02-22 | 2005-02-22 | |
| PCT/US2006/006221 WO2006091646A2 (en) | 2005-02-22 | 2006-02-22 | Small molecule inhibitors of mdm2 and uses thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA200701771A1 true EA200701771A1 (ru) | 2008-06-30 |
| EA014445B1 EA014445B1 (ru) | 2010-12-30 |
Family
ID=36927977
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA200701771A EA014445B1 (ru) | 2005-02-22 | 2006-02-22 | Низкомолекулярные ингибиторы mdm2 и их применения |
| EA201001255A EA019566B1 (ru) | 2005-02-22 | 2006-02-22 | Низкомолекулярные ингибиторы mdm2 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA201001255A EA019566B1 (ru) | 2005-02-22 | 2006-02-22 | Низкомолекулярные ингибиторы mdm2 |
Country Status (11)
| Country | Link |
|---|---|
| EP (1) | EP1856123B1 (ru) |
| JP (2) | JP5248866B2 (ru) |
| KR (1) | KR100944301B1 (ru) |
| CN (2) | CN101160314B (ru) |
| AU (2) | AU2006216780B8 (ru) |
| BR (1) | BRPI0609172A2 (ru) |
| CA (2) | CA2752738C (ru) |
| EA (2) | EA014445B1 (ru) |
| MX (1) | MX2007010272A (ru) |
| NO (1) | NO20074853L (ru) |
| WO (1) | WO2006091646A2 (ru) |
Families Citing this family (67)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7759383B2 (en) | 2005-02-22 | 2010-07-20 | The Regents Of The University Of Michigan | Small molecule inhibitors of MDM2 and the uses thereof |
| MY144968A (en) | 2005-04-11 | 2011-11-30 | Xenon Pharmaceuticals Inc | Spiro-oxindole compounds and their uses as therapeutic agents |
| MY145694A (en) | 2005-04-11 | 2012-03-30 | Xenon Pharmaceuticals Inc | Spiroheterocyclic compounds and their uses as therapeutic agents |
| CN101528223B (zh) * | 2006-08-30 | 2013-05-01 | 密执安州立大学董事会 | Mdm2的新型小分子抑制剂和其用途 |
| US8222288B2 (en) | 2006-08-30 | 2012-07-17 | The Regents Of The University Of Michigan | Small molecule inhibitors of MDM2 and the uses thereof |
| ATE467413T1 (de) * | 2006-09-21 | 2010-05-15 | Hoffmann La Roche | Oxindolderivate als antikrebsmittel |
| ATE545416T1 (de) | 2006-10-12 | 2012-03-15 | Xenon Pharmaceuticals Inc | Verwendung von spiro-oxindol-verbindungen als therapeutika |
| US7638548B2 (en) * | 2006-11-09 | 2009-12-29 | Hoffmann-La Roche Inc. | Spiroindolinone derivatives |
| CN101605798A (zh) | 2006-12-14 | 2009-12-16 | 第一三共株式会社 | 咪唑并噻唑衍生物 |
| EA200901212A1 (ru) | 2007-03-29 | 2010-04-30 | Новартис Аг | 3-имидазолилиндолы, предназначенные для лечения пролиферативных заболеваний |
| WO2008144507A2 (en) * | 2007-05-16 | 2008-11-27 | President And Fellows Of Harvard College | Spirooxindole inhibitors of aurora kinase |
| US7834179B2 (en) * | 2007-05-23 | 2010-11-16 | Hoffmann-La Roche Inc. | Spiroindolinone derivatives |
| US7776875B2 (en) * | 2007-12-19 | 2010-08-17 | Hoffman-La Roche Inc. | Spiroindolinone derivatives |
| US7723372B2 (en) * | 2008-03-19 | 2010-05-25 | Hoffman-La Roche Inc. | Spiroindolinone derivatives |
| WO2009151069A1 (ja) | 2008-06-12 | 2009-12-17 | 第一三共株式会社 | 4,7-ジアザスピロ[2.5]オクタン環構造を有するイミダゾチアゾール誘導体 |
| PE20110367A1 (es) | 2008-09-18 | 2011-06-13 | Hoffmann La Roche | DERIVADOS DE 4-CIANO-4-FENIL-PIRROLIDIN-2-CARBOXAMIDAS SUSTITUIDAS COMO INHIBIDORES DE LA INTERACCION p53-MDM2 |
| US8354444B2 (en) * | 2008-09-18 | 2013-01-15 | Hoffmann-La Roche Inc. | Substituted pyrrolidine-2-carboxamides |
| CN103664973B (zh) | 2008-10-17 | 2017-04-19 | 泽农医药公司 | 螺羟吲哚化合物及其作为治疗剂的用途 |
| WO2010045197A1 (en) | 2008-10-17 | 2010-04-22 | Xenon Pharmaceuticals, Inc. | Spiro-oxindole compounds and their use as therapeutic agents |
| US7928233B2 (en) | 2009-02-10 | 2011-04-19 | Hoffmann-La Roche Inc. | Spiroindolinone pyridine derivatives |
| US8217051B2 (en) | 2009-02-17 | 2012-07-10 | Hoffmann-La Roche Inc. | Spiroindolinone derivatives |
| US8076482B2 (en) | 2009-04-23 | 2011-12-13 | Hoffmann-La Roche Inc. | 3,3′-spiroindolinone derivatives |
| AR077252A1 (es) | 2009-06-29 | 2011-08-10 | Xenon Pharmaceuticals Inc | Enantiomeros de compuestos de espirooxindol y sus usos como agentes terapeuticos |
| US8017607B2 (en) | 2009-10-14 | 2011-09-13 | Hoffmann-La Roche Inc. | N-substituted-pyrrolidines as inhibitors of MDM2-P-53 interactions |
| NZ599334A (en) | 2009-10-14 | 2014-03-28 | Xenon Pharmaceuticals Inc | Synthetic methods for spiro-oxindole compounds |
| AU2010319595B2 (en) * | 2009-11-12 | 2015-09-17 | The Regents Of The University Of Michigan | Spiro-oxindole MDM2 antagonists |
| US20110118283A1 (en) * | 2009-11-17 | 2011-05-19 | Qingjie Ding | Substituted Pyrrolidine-2-Carboxamides |
| US8088815B2 (en) | 2009-12-02 | 2012-01-03 | Hoffman-La Roche Inc. | Spiroindolinone pyrrolidines |
| US8288431B2 (en) | 2010-02-17 | 2012-10-16 | Hoffmann-La Roche Inc. | Substituted spiroindolinones |
| US9504671B2 (en) | 2010-02-26 | 2016-11-29 | Xenon Pharmaceuticals Inc. | Pharmaceutical compositions of spiro-oxindole compound for topical administration and their use as therapeutic agents |
| CN103153302A (zh) * | 2010-04-09 | 2013-06-12 | 密歇根大学董事会 | 针对用于治疗疾病的mdm2抑制剂的生物标记 |
| US8217044B2 (en) | 2010-04-28 | 2012-07-10 | Hoffmann-La Roche Inc. | Spiroindolinone pyrrolidines |
| US20120046306A1 (en) * | 2010-08-18 | 2012-02-23 | David Joseph Bartkovitz | Substituted Heteroaryl Spiropyrrolidine MDM2 Antagonists |
| US20120065210A1 (en) * | 2010-09-15 | 2012-03-15 | Xin-Jie Chu | Substituted hexahydropyrrolo[1,2-c]imidazolones |
| US20120071499A1 (en) * | 2010-09-20 | 2012-03-22 | Xin-Jie Chu | Substituted Spiro[3H-Indole-3,6'(5'H)-[1H]Pyrrolo[1,2c]Imidazole-1',2(1H,2'H)-diones |
| FR2967072B1 (fr) | 2010-11-05 | 2013-03-29 | Univ Dundee | Procede pour ameliorer la production de virus et semences vaccinales influenza |
| CA2817585A1 (en) * | 2010-11-12 | 2012-05-18 | The Regents Of The University Of Michigan | Spiro-oxindole mdm2 antagonists |
| HUE038714T2 (hu) | 2011-03-10 | 2018-11-28 | Daiichi Sankyo Co Ltd | Dispiropirrolidin származék |
| CA2835422C (en) * | 2011-05-11 | 2016-10-11 | The Regents Of The University Of Michigan | Spiro-oxindole mdm2 antagonists |
| CN102627650B (zh) * | 2012-03-08 | 2015-07-08 | 徐州师范大学 | 手性四氢吡咯-3,2′-氧化吲哚螺环化合物及其合成方法 |
| TWI586668B (zh) | 2012-09-06 | 2017-06-11 | 第一三共股份有限公司 | 二螺吡咯啶衍生物之結晶 |
| 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 |
| CN103435622B (zh) * | 2013-07-31 | 2015-11-18 | 陕西科技大学 | 一种螺环吲哚二酮哌嗪类生物碱及其合成方法和应用 |
| JP6368311B2 (ja) | 2013-09-04 | 2018-08-01 | 第一三共株式会社 | スピロオキシインドール誘導体の製造方法 |
| TW201613576A (en) | 2014-06-26 | 2016-04-16 | Novartis Ag | Intermittent dosing of MDM2 inhibitor |
| WO2016001376A1 (en) | 2014-07-03 | 2016-01-07 | Boehringer Ingelheim International Gmbh | New spiro[3h-indole-3,2´-pyrrolidin]-2(1h)-one compounds and derivatives as mdm2-p53 inhibitors |
| SI3183254T1 (sl) | 2014-08-21 | 2019-08-30 | Boehringer Ingelheim International Gmbh | Nove spiro(3H-indol-3,2'pirolidin)-2(1H)-onske spojine in derivati kot inhibitorji MDM2-P53 |
| WO2016127068A1 (en) | 2015-02-05 | 2016-08-11 | Teva Pharmaceuticals International Gmbh | Methods of treating postherpetic neuralgia with a topical formulation of a spiro-oxindole compound |
| ES2968789T3 (es) * | 2015-02-20 | 2024-05-14 | Daiichi Sankyo Co Ltd | Procedimiento combinado para el tratamiento del cáncer |
| CN107484415B (zh) * | 2015-03-30 | 2021-01-29 | 特殊治疗有限公司 | 作为usp30抑制剂的1-氰基吡咯烷化合物 |
| JP6823587B2 (ja) | 2015-04-13 | 2021-02-03 | 第一三共株式会社 | Mdm2阻害剤とbtk阻害剤との併用治療法 |
| GB201517217D0 (en) | 2015-09-29 | 2015-11-11 | Astex Therapeutics Ltd And Cancer Res Technology Ltd | Pharmaceutical compounds |
| GB201517216D0 (en) | 2015-09-29 | 2015-11-11 | Cancer Res Technology Ltd And Astex Therapeutics Ltd | Pharmaceutical compounds |
| AR106314A1 (es) | 2015-10-09 | 2018-01-03 | Boehringer Ingelheim Int | COMPUESTOS DE ESPIRO[3H-INDOL-3,2-PIRROLIDIN]-2(1H)-ONA Y DERIVADOS COMO INHIBIDORES DE MDM2 - p53 |
| CN105585570B (zh) * | 2015-12-15 | 2019-10-15 | 贵州大学 | 异恶唑拼接吡咯螺环氧化吲哚化合物及其制备方法及应用 |
| SG11201808728QA (en) | 2016-04-06 | 2018-11-29 | Univ Michigan Regents | Mdm2 protein degraders |
| ES2858151T3 (es) | 2016-05-20 | 2021-09-29 | Hoffmann La Roche | Conjugados de PROTAC-anticuerpo y procedimientos de uso |
| CA3040840A1 (en) | 2016-10-17 | 2018-04-26 | Daiichi Sankyo Company, Limited | Combined use of mdm2 inhibitor and dna methyltransferase inhibitor for cancer treatment |
| 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 |
| CN107353292B (zh) * | 2017-08-23 | 2018-07-10 | 山东博苑医药化学有限公司 | 螺环氧化吲哚乙内酰(硫)脲衍生物及其制备方法和在防治植物病毒、杀菌、杀虫方面的应用 |
| CN108486041A (zh) * | 2018-03-28 | 2018-09-04 | 华南农业大学 | PI3K/Akt信号通路在鸡胚成纤维细胞内对马立克氏病毒增殖的应用及其检测方法 |
| CN110680838B (zh) * | 2019-11-21 | 2021-10-01 | 海门茂发美术图案设计有限公司 | 一种素心腊梅碱的抗前列腺癌用途 |
| CN112876488B (zh) * | 2021-02-18 | 2021-12-21 | 苏州大学 | 螺环吲哚啉衍生物及其制备方法和应用 |
| WO2023056069A1 (en) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Degrader-antibody conjugates and methods of using same |
| CN115417871B (zh) * | 2022-09-21 | 2023-06-02 | 成都理工大学 | 双螺环吡咯螺氧化吲哚化合物及其合成方法和抗真菌活性 |
| WO2024240858A1 (en) | 2023-05-23 | 2024-11-28 | Valerio Therapeutics | Protac molecules directed against dna damage repair system and uses thereof |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3219661A (en) * | 1962-12-14 | 1965-11-23 | Warner Lambert Pharmaceutical | Spirooxindole and spirodehydroindole alkaloids and process therefor |
| GB1056537A (en) * | 1963-07-16 | 1967-01-25 | Smith Kline French Lab | Improvements in or relating to crystalline alkaloids of mitragyna citiata and compositions thereof |
| JPH0423184A (ja) * | 1990-05-18 | 1992-01-27 | Toshiba Corp | 光学的文字読取装置 |
| JP3074281B2 (ja) * | 1990-05-30 | 2000-08-07 | 住友大阪セメント株式会社 | フレキシブルコンテナ |
| JPH07238069A (ja) * | 1994-02-28 | 1995-09-12 | Daicel Chem Ind Ltd | 環状アミド化合物の製造方法 |
| RU2084449C1 (ru) * | 1994-03-02 | 1997-07-20 | Всероссийский научный центр по безопасности биологически активных веществ | 1-бензил-2-оксотриптамин гидрохлорид и его производные, обладающие гепатозащитной активностью |
| US5773455A (en) * | 1996-06-28 | 1998-06-30 | Biomeasure, Incorporated | Inhibitors of prenyl transferases |
| ATE467418T1 (de) * | 1997-01-20 | 2010-05-15 | Immodal Pharmaka Gmbh | Verfahren und stoffe zur freisetzung eines wachstumsfaktors aus endothelzellen, und nach dem verfahren freigesetzter wachstumsfaktor sowie seine verwendung |
| DK0994890T3 (da) * | 1997-06-10 | 2003-12-01 | Univ Michigan | Benzimidazolderivater |
| WO1999012904A1 (en) * | 1997-09-08 | 1999-03-18 | Arqule, Inc. | Spiro[pyrrolidine-2,3'-oxindole] compounds and methods of use |
| CN1182083C (zh) * | 2001-10-08 | 2004-12-29 | 廖宜芳 | 一种杀虫灭菌的配位肥及其制造方法 |
| CA2468783A1 (en) * | 2001-12-18 | 2003-06-26 | F. Hoffmann-La Roche Ag | Cis-imidazolines as mdm2 inhibitors |
-
2006
- 2006-02-22 WO PCT/US2006/006221 patent/WO2006091646A2/en not_active Ceased
- 2006-02-22 AU AU2006216780A patent/AU2006216780B8/en not_active Ceased
- 2006-02-22 CN CN2006800129073A patent/CN101160314B/zh not_active Expired - Fee Related
- 2006-02-22 KR KR1020077021939A patent/KR100944301B1/ko not_active Expired - Fee Related
- 2006-02-22 BR BRPI0609172-5A patent/BRPI0609172A2/pt not_active IP Right Cessation
- 2006-02-22 EP EP06735754.1A patent/EP1856123B1/en active Active
- 2006-02-22 MX MX2007010272A patent/MX2007010272A/es active IP Right Grant
- 2006-02-22 JP JP2007556414A patent/JP5248866B2/ja not_active Expired - Fee Related
- 2006-02-22 CA CA2752738A patent/CA2752738C/en not_active Expired - Fee Related
- 2006-02-22 EA EA200701771A patent/EA014445B1/ru not_active IP Right Cessation
- 2006-02-22 EA EA201001255A patent/EA019566B1/ru not_active IP Right Cessation
- 2006-02-22 CN CN201210066457.3A patent/CN102627649B/zh not_active Expired - Fee Related
- 2006-02-22 CA CA2598690A patent/CA2598690C/en not_active Expired - Fee Related
-
2007
- 2007-09-24 NO NO20074853A patent/NO20074853L/no not_active Application Discontinuation
-
2010
- 2010-06-30 AU AU2010202759A patent/AU2010202759B2/en not_active Ceased
-
2012
- 2012-04-06 JP JP2012086927A patent/JP5638023B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA2598690C (en) | 2011-11-15 |
| EP1856123A4 (en) | 2010-12-29 |
| EA201001255A1 (ru) | 2011-02-28 |
| CN102627649A (zh) | 2012-08-08 |
| AU2006216780B8 (en) | 2010-04-22 |
| EP1856123B1 (en) | 2016-02-17 |
| WO2006091646A3 (en) | 2006-11-30 |
| KR20070108917A (ko) | 2007-11-13 |
| JP2008531504A (ja) | 2008-08-14 |
| CA2752738A1 (en) | 2006-08-31 |
| AU2006216780A1 (en) | 2006-08-31 |
| BRPI0609172A2 (pt) | 2010-02-23 |
| CN101160314A (zh) | 2008-04-09 |
| AU2010202759A1 (en) | 2010-07-22 |
| JP2012162550A (ja) | 2012-08-30 |
| EA019566B1 (ru) | 2014-04-30 |
| CA2598690A1 (en) | 2006-08-31 |
| CA2752738C (en) | 2014-05-27 |
| JP5248866B2 (ja) | 2013-07-31 |
| CN101160314B (zh) | 2012-05-23 |
| MX2007010272A (es) | 2008-03-12 |
| AU2006216780B2 (en) | 2010-04-01 |
| EA014445B1 (ru) | 2010-12-30 |
| EP1856123A2 (en) | 2007-11-21 |
| AU2010202759B2 (en) | 2012-07-19 |
| NO20074853L (no) | 2007-11-21 |
| JP5638023B2 (ja) | 2014-12-10 |
| WO2006091646A2 (en) | 2006-08-31 |
| KR100944301B1 (ko) | 2010-02-24 |
| CN102627649B (zh) | 2015-03-25 |
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